Item | Value |
---|---|
geneid | 283316 |
ensemblid | ENSG00000177675.9 |
hgncid | 30375 |
symbol | CD163L1 |
name | CD163 molecule like 1 |
refseq_nuc | NM_174941.6 |
refseq_prot | NP_777601.3 |
ensembl_nuc | ENST00000313599.8 |
ensembl_prot | ENSP00000315945.3 |
mane_status | MANE Select |
chr | chr12 |
start | 7354960 |
end | 7444153 |
strand | - |
ver | v1.2 |
region | chr12:7354960-7444153 |
region5000 | chr12:7349960-7449153 |
regionname0 | CD163L1_chr12_7354960_7444153 |
regionname5000 | CD163L1_chr12_7349960_7449153 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1453 | 250 | 37 | 56 | 123 | 13 | 20 | 100 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0002 | 0/0 | 1453 | 55 | 22 | 4 | 22 | 0 | 7 | 16 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0003 | 0/0 | 1453 | 21 | 8 | 1 | 9 | 0 | 3 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0004 | 0/0 | 1453 | 15 | 8 | 0 | 5 | 0 | 2 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0005 | 0/0 | 1453 | 7 | 6 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0006 | 0/0 | 1453 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0007 | 0/0 | 1455 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1450): Show |
chr12 | 7349960 | 7449153 |
a0008 | 1/0 | 1453 | 3 | 2 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0009 | 0/0 | 1453 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0010 | 0/0 | 1453 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLLQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0011 | 0/0 | 1453 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLLQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0012 | 0/0 | 1453 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0013 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0014 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0015 | 0/0 | 1453 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0016 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0017 | 0/0 | 1453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLLQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0018 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0019 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(829): Show |
chr12 | 7349960 | 7449153 |
a0020 | 0/0 | 1453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0021 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0022 | 0/0 | 1453 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0023 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0024 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
a0025 | 0/0 | 1453 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | MMLPQ others(1448): Show |
chr12 | 7349960 | 7449153 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4359 | 138 | 19 | 27 | 78 | 3 | 10 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0002 | 0/0 | 4359 | 67 | 0 | 19 | 41 | 2 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0004 | 0/0 | 4359 | 21 | 4 | 4 | 2 | 6 | 5 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0007 | 0/0 | 4359 | 9 | 4 | 3 | 0 | 2 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0008 | 0/0 | 4359 | 7 | 6 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0017 | 0/0 | 4359 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0025 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0026 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0027 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0029 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0039 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0001c0041 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0002c0003 | 0/0 | 4359 | 54 | 21 | 4 | 22 | 0 | 7 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0002c0032 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0003c0005 | 0/0 | 4359 | 20 | 7 | 1 | 9 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0003c0033 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0004c0006 | 0/0 | 4359 | 11 | 4 | 0 | 5 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0004c0012 | 0/0 | 4359 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0004c0028 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0005c0013 | 0/0 | 4359 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0005c0014 | 0/0 | 4359 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0005c0030 | 0/0 | 4359 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0006c0009 | 0/0 | 4359 | 6 | 4 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0006c0034 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0007c0010 | 0/0 | 4365 | 5 | 0 | 0 | 5 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4360): Show |
chr12 | 7349960 | 7449153 | ||
a0008c0011 | 1/0 | 4359 | 3 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0009c0015 | 0/0 | 4359 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0010c0018 | 0/0 | 4359 | 2 | 1 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0011c0042 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0011c0043 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0012c0016 | 0/0 | 4359 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0013c0024 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0014c0037 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0015c0040 | 0/0 | 4359 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0016c0019 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0017c0044 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0018c0023 | 0/0 | 4359 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0019c0020 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0020c0038 | 0/0 | 4359 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0021c0021 | 0/0 | 4359 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0022c0036 | 0/0 | 4359 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0023c0031 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0024c0022 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 | ||
a0025c0035 | 0/0 | 4359 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | ATGAT others(4354): Show |
chr12 | 7349960 | 7449153 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4583 | 104 | 12 | 17 | 64 | 2 | 9 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0001t0002 | 0/0 | 4583 | 26 | 7 | 5 | 13 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0001t0003 | 0/1 | 4583 | 7 | 0 | 5 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0001t0004 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0002t0001 | 0/0 | 4583 | 52 | 0 | 13 | 35 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0002t0002 | 0/0 | 4583 | 9 | 0 | 3 | 5 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0002t0003 | 0/0 | 4583 | 6 | 0 | 3 | 1 | 2 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0004t0001 | 0/0 | 4583 | 7 | 2 | 0 | 2 | 3 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0004t0002 | 0/0 | 4583 | 11 | 2 | 3 | 0 | 2 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0004t0003 | 0/0 | 4583 | 3 | 0 | 1 | 0 | 1 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0007t0001 | 0/0 | 4583 | 6 | 4 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0007t0002 | 0/0 | 4583 | 2 | 0 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0007t0003 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0008t0001 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0008t0002 | 0/0 | 4583 | 4 | 3 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0017t0002 | 0/0 | 4583 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0025t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0026t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0027t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0029t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0039t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0001c0041t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0002c0003t0001 | 0/0 | 4583 | 33 | 10 | 2 | 21 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0002c0003t0002 | 0/0 | 4583 | 18 | 11 | 2 | 1 | 0 | 4 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0002c0003t0003 | 0/0 | 4583 | 3 | 0 | 0 | 0 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0002c0032t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0003c0005t0001 | 0/0 | 4583 | 14 | 4 | 1 | 7 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0003c0005t0002 | 0/0 | 4583 | 4 | 3 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0003c0005t0003 | 0/0 | 4583 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0003c0033t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0006t0001 | 0/0 | 4583 | 8 | 2 | 0 | 5 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0006t0002 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0006t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0012t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0012t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0004c0028t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0005c0013t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0005c0013t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0005c0014t0001 | 0/0 | 4583 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0005c0014t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0005c0030t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0006c0009t0001 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0006c0009t0002 | 0/0 | 4583 | 3 | 1 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0006c0034t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0007c0010t0001 | 0/0 | 4589 | 4 | 0 | 0 | 4 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4584): Show |
chr12 | 7349960 | 7449153 |
a0007c0010t0003 | 0/0 | 4589 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4584): Show |
chr12 | 7349960 | 7449153 |
a0008c0011t0001 | 1/0 | 4583 | 2 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0008c0011t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0009c0015t0001 | 0/0 | 4583 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0010c0018t0001 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0010c0018t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0011c0042t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0011c0043t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0012c0016t0001 | 0/0 | 4583 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0013c0024t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0014c0037t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0015c0040t0001 | 0/0 | 4583 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0016c0019t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0017c0044t0002 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0018c0023t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0019c0020t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0020c0038t0001 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0021c0021t0003 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0022c0036t0002 | 0/0 | 4583 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0023c0031t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0024c0022t0001 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
a0025c0035t0002 | 0/0 | 4583 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | AGGAC others(4578): Show |
chr12 | 7349960 | 7449153 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0002t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0004t0003g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0007t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0008t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0008t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0008t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0008t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0017t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0025t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0026t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0027t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0029t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0039t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0001c0041t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0002c0032t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0005t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0003c0033t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0006t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0012t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0012t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0012t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0004c0028t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0013t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0013t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0013t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0014t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0014t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0014t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0005c0030t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0009t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0009t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0009t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0009t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0009t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0006c0034t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0007c0010t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0007c0010t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0007c0010t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0007c0010t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0008c0011t0001g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0008c0011t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0008c0011t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0009c0015t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0009c0015t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0010c0018t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0010c0018t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0011c0042t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0011c0043t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0012c0016t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0012c0016t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0013c0024t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0014c0037t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0015c0040t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0016c0019t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0017c0044t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0018c0023t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0019c0020t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0020c0038t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0021c0021t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0022c0036t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0023c0031t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0024c0022t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
a0025c0035t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0312 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0291 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00140 | hp1 | a0005 | c0030 | t0003 | g0301 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00423 | hp1 | a0003 | c0005 | t0001 | g0050 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0297 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00544 | hp1 | a0013 | c0024 | t0001 | g0262 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0285 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00639 | hp2 | a0001 | c0007 | t0001 | g0027 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00673 | hp2 | a0014 | c0037 | t0001 | g0336 | EAS | CHS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0300 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00738 | hp1 | a0002 | c0003 | t0002 | g0079 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG00738 | hp2 | a0001 | c0004 | t0002 | g0310 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01069 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01074 | hp1 | a0001 | c0004 | t0002 | g0307 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01099 | hp1 | a0003 | c0005 | t0001 | g0008 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0320 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01106 | hp1 | a0001 | c0002 | t0003 | g0316 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01109 | hp2 | a0001 | c0004 | t0002 | g0322 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01167 | hp1 | a0006 | c0009 | t0002 | g0013 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01168 | hp1 | a0001 | c0017 | t0002 | g0019 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01169 | hp1 | a0006 | c0009 | t0002 | g0013 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01169 | hp2 | a0001 | c0017 | t0002 | g0019 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01175 | hp1 | a0001 | c0008 | t0002 | g0235 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01175 | hp2 | a0001 | c0004 | t0003 | g0308 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01243 | hp1 | a0015 | c0040 | t0001 | g0090 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0261 | AMR | PUR | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0299 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01256 | hp2 | a0001 | c0007 | t0002 | g0017 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01261 | hp1 | a0010 | c0018 | t0001 | g0344 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01515 | hp1 | a0001 | c0007 | t0002 | g0017 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01515 | hp2 | a0001 | c0004 | t0001 | g0311 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01516 | hp1 | a0001 | c0004 | t0001 | g0315 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0241 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01517 | hp1 | a0001 | c0004 | t0002 | g0314 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01517 | hp2 | a0001 | c0007 | t0001 | g0163 | EUR | IBS | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01884 | hp1 | a0004 | c0006 | t0002 | g0325 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01884 | hp2 | a0002 | c0003 | t0002 | g0080 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01891 | hp1 | a0008 | c0011 | t0001 | g0127 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01891 | hp2 | a0003 | c0033 | t0002 | g0128 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0037 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0292 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02015 | hp2 | a0001 | c0004 | t0001 | g0304 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02027 | hp1 | a0001 | c0025 | t0002 | g0265 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0084 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02056 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02083 | hp1 | a0001 | c0041 | t0001 | g0113 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02129 | hp1 | a0003 | c0005 | t0003 | g0054 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02129 | hp2 | a0016 | c0019 | t0001 | g0134 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0249 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02145 | hp2 | a0011 | c0043 | t0001 | g0343 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0055 | EAS | CDX | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02257 | hp1 | a0002 | c0003 | t0002 | g0053 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0303 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02258 | hp1 | a0002 | c0003 | t0002 | g0078 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02258 | hp2 | a0006 | c0009 | t0001 | g0039 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02280 | hp1 | a0017 | c0044 | t0002 | g0347 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02280 | hp2 | a0002 | c0003 | t0002 | g0074 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02300 | hp2 | a0002 | c0003 | t0002 | g0056 | AMR | PEL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02451 | hp1 | a0010 | c0018 | t0002 | g0345 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02572 | hp1 | a0008 | c0011 | t0002 | g0124 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02572 | hp2 | a0005 | c0013 | t0001 | g0243 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02615 | hp1 | a0002 | c0003 | t0002 | g0092 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02615 | hp2 | a0002 | c0003 | t0001 | g0031 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02622 | hp1 | a0002 | c0003 | t0001 | g0089 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02622 | hp2 | a0004 | c0006 | t0002 | g0103 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02630 | hp1 | a0004 | c0012 | t0002 | g0324 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02630 | hp2 | a0001 | c0039 | t0001 | g0192 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02647 | hp1 | a0006 | c0009 | t0002 | g0200 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02647 | hp2 | a0002 | c0003 | t0002 | g0083 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02698 | hp1 | a0009 | c0015 | t0001 | g0264 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02698 | hp2 | a0002 | c0003 | t0002 | g0048 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02717 | hp1 | a0001 | c0007 | t0001 | g0131 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02723 | hp1 | a0001 | c0008 | t0002 | g0005 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02723 | hp2 | a0002 | c0032 | t0001 | g0043 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02735 | hp1 | a0018 | c0023 | t0003 | g0257 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02735 | hp2 | a0001 | c0004 | t0002 | g0026 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02809 | hp1 | a0019 | c0020 | t0001 | g0253 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02809 | hp2 | a0002 | c0003 | t0002 | g0087 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0041 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02818 | hp2 | a0001 | c0004 | t0002 | g0121 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02886 | hp1 | a0005 | c0013 | t0001 | g0342 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02886 | hp2 | a0004 | c0006 | t0001 | g0332 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0032 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0085 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0077 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02922 | hp1 | a0011 | c0042 | t0002 | g0346 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02922 | hp2 | a0001 | c0008 | t0002 | g0005 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02970 | hp1 | a0004 | c0012 | t0001 | g0327 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03017 | hp2 | a0002 | c0003 | t0003 | g0073 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03041 | hp1 | a0001 | c0008 | t0001 | g0238 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03041 | hp2 | a0002 | c0003 | t0002 | g0088 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03098 | hp2 | a0001 | c0007 | t0001 | g0330 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03130 | hp1 | a0002 | c0003 | t0001 | g0086 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03130 | hp2 | a0005 | c0014 | t0001 | g0116 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03139 | hp2 | a0004 | c0006 | t0001 | g0335 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03195 | hp1 | a0001 | c0007 | t0001 | g0104 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03195 | hp2 | a0001 | c0008 | t0002 | g0005 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03209 | hp1 | a0003 | c0005 | t0001 | g0190 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03209 | hp2 | a0002 | c0003 | t0002 | g0094 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03453 | hp1 | a0001 | c0008 | t0001 | g0196 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03453 | hp2 | a0003 | c0005 | t0001 | g0076 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03486 | hp2 | a0003 | c0005 | t0002 | g0033 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03491 | hp2 | a0001 | c0004 | t0002 | g0025 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0340 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03492 | hp2 | a0001 | c0004 | t0002 | g0025 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03516 | hp1 | a0020 | c0038 | t0001 | g0132 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | ESN | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03540 | hp1 | a0002 | c0003 | t0002 | g0042 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03540 | hp2 | a0001 | c0027 | t0002 | g0030 | AFR | GWD | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03579 | hp1 | a0006 | c0009 | t0001 | g0118 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0027 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03654 | hp2 | a0003 | c0005 | t0002 | g0052 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0068 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03669 | hp2 | a0004 | c0006 | t0001 | g0334 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03688 | hp1 | a0002 | c0003 | t0003 | g0062 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03688 | hp2 | a0001 | c0004 | t0003 | g0309 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03704 | hp2 | a0021 | c0021 | t0003 | g0258 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03831 | hp1 | a0022 | c0036 | t0002 | g0214 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03927 | hp2 | a0001 | c0004 | t0002 | g0026 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04115 | hp1 | a0002 | c0003 | t0002 | g0049 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04184 | hp1 | a0003 | c0005 | t0001 | g0069 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04199 | hp1 | a0004 | c0006 | t0003 | g0333 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04204 | hp1 | a0002 | c0003 | t0002 | g0044 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04228 | hp1 | a0002 | c0003 | t0003 | g0058 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG04228 | hp2 | a0003 | c0005 | t0001 | g0008 | SAS | STU | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0081 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18522 | hp2 | a0004 | c0012 | t0001 | g0326 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18612 | hp2 | a0004 | c0006 | t0001 | g0328 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18747 | hp1 | a0007 | c0010 | t0001 | g0018 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | CHB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18906 | hp2 | a0003 | c0005 | t0002 | g0093 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18939 | hp2 | a0004 | c0006 | t0001 | g0338 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18944 | hp1 | a0001 | c0004 | t0001 | g0341 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18946 | hp1 | a0012 | c0016 | t0001 | g0038 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18956 | hp1 | a0003 | c0005 | t0001 | g0318 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18960 | hp2 | a0004 | c0006 | t0001 | g0329 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18962 | hp2 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18967 | hp1 | a0004 | c0006 | t0001 | g0339 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0029 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18968 | hp1 | a0003 | c0005 | t0001 | g0319 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18970 | hp2 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18975 | hp1 | a0023 | c0031 | t0001 | g0060 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18979 | hp2 | a0007 | c0010 | t0001 | g0182 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18983 | hp2 | a0002 | c0003 | t0001 | g0098 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18984 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0071 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18994 | hp1 | a0012 | c0016 | t0001 | g0064 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18998 | hp1 | a0007 | c0010 | t0003 | g0185 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19003 | hp1 | a0004 | c0006 | t0001 | g0337 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19009 | hp2 | a0003 | c0005 | t0001 | g0035 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19010 | hp2 | a0003 | c0005 | t0001 | g0057 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0096 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19030 | hp1 | a0005 | c0014 | t0002 | g0117 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19043 | hp1 | a0001 | c0008 | t0001 | g0232 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19043 | hp2 | a0005 | c0014 | t0001 | g0105 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19058 | hp1 | a0024 | c0022 | t0001 | g0268 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19063 | hp2 | a0007 | c0010 | t0001 | g0018 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19064 | hp2 | a0002 | c0003 | t0001 | g0059 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19068 | hp2 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19074 | hp1 | a0025 | c0035 | t0002 | g0227 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19078 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19083 | hp2 | a0007 | c0010 | t0001 | g0177 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19085 | hp2 | a0003 | c0005 | t0003 | g0051 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19087 | hp1 | a0003 | c0005 | t0001 | g0317 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19240 | hp1 | a0001 | c0029 | t0001 | g0122 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0120 | AFR | YRI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20129 | hp1 | a0001 | c0026 | t0002 | g0109 | AFR | ASW | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0302 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0254 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20805 | hp1 | a0001 | c0004 | t0003 | g0306 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01123 | hp1 | a0009 | c0015 | t0001 | g0295 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG01123 | hp2 | a0001 | c0007 | t0003 | g0331 | AMR | CLM | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02109 | hp1 | a0004 | c0028 | t0001 | g0126 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0075 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02486 | hp2 | a0003 | c0005 | t0001 | g0070 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02559 | hp1 | a0001 | c0004 | t0002 | g0305 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG02559 | hp2 | a0006 | c0009 | t0001 | g0040 | AFR | ACB | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0091 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | MSL | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG06807 | hp1 | a0005 | c0013 | t0002 | g0242 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA20300 | hp2 | a0003 | c0005 | t0002 | g0034 | AFR | USA | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
NA21309 | hp2 | a0006 | c0034 | t0001 | g0123 | AFR | LWK | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0240 | REF | REF | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
homoSapiens | grch38p0 | a0008 | c0011 | t0001 | g0125 | REF | REF | CD163L1_chr12_7349960_7449153 | CD163L1 | chr12 | 7349960 | 7449153 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:7355130 | T | G | 8 | a0001 a0002 a0003 others(5): Show |
26 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(23): Show |
splice_region_variant | LOW | c.*25A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | chr12 | 7355130 | |||||||
chr12:7369536 | A | C | 1 | a0018 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.3860T>G | p.Leu1287Arg | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3886/4583 | 3860/4362 | 1287/1453 | chr12 | 7369536 | |||
chr12:7369561 | C | T | 1 | a0014 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.3835G>A | p.Glu1279Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3861/4583 | 3835/4362 | 1279/1453 | chr12 | 7369561 | |||
chr12:7373488 | C | T | 1 | a0020 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3562G>A | p.Glu1188Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/20 | 3588/4583 | 3562/4362 | 1188/1453 | chr12 | 7373488 | |||
chr12:7373524 | T | C | 1 | a0016 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.3526A>G | p.Ile1176Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/20 | 3552/4583 | 3526/4362 | 1176/1453 | chr12 | 7373524 | |||
chr12:7374505 | G | A | 1 | a0013 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.3346C>T | p.Pro1116Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3372/4583 | 3346/4362 | 1116/1453 | chr12 | 7374505 | |||
chr12:7374528 | A | G | 7 | a0003 a0004 a0006 others(4): Show |
49 | HG00423.hp1 HG00673.hp2 HG01099.hp1 others(46): Show |
missense_variant | MODERATE | c.3323T>C | p.Met1108Thr | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3349/4583 | 3323/4362 | 1108/1453 | chr12 | 7374528 | |||
chr12:7374688 | C | T | 1 | a0009 | 2 | HG01123.hp1 HG02698.hp1 |
missense_variant | MODERATE | c.3163G>A | p.Gly1055Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3189/4583 | 3163/4362 | 1055/1453 | chr12 | 7374688 | |||
chr12:7375445 | G | A | 1 | a0012 | 2 | NA18946.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.2837C>T | p.Ala946Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2863/4583 | 2837/4362 | 946/1453 | chr12 | 7375445 | |||
chr12:7375582 | G | GACAGAT | 1 | a0007 | 5 | NA18747.hp1 NA18979.hp2 NA18998.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.2699_2700insATCTGT | p.Val900_Arg901insSe others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2725/4583 | 2699/4362 | 900/1453 | chr12 | 7375582 | |||
chr12:7375883 | C | A | 1 | a0019 | 1 | HG02809.hp1 | stop_gained | HIGH | c.2503G>T | p.Glu835* | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 10/20 | 2529/4583 | 2503/4362 | 835/1453 | chr12 | 7375883 | |||
chr12:7379176 | C | G | 1 | a0022 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.2173G>C | p.Glu725Gln | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2199/4583 | 2173/4362 | 725/1453 | chr12 | 7379176 | |||
chr12:7379218 | C | T | 1 | a0025 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2131G>A | p.Val711Met | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2157/4583 | 2131/4362 | 711/1453 | chr12 | 7379218 | |||
chr12:7396338 | G | A | 1 | a0005 | 7 | HG00140.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
missense_variant | MODERATE | c.1807C>T | p.Arg603Trp | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1833/4583 | 1807/4362 | 603/1453 | chr12 | 7396338 | |||
chr12:7396350 | A | T | 1 | a0010 | 2 | HG01261.hp1 HG02451.hp1 |
missense_variant | MODERATE | c.1795T>A | p.Tyr599Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1821/4583 | 1795/4362 | 599/1453 | chr12 | 7396350 | |||
chr12:7396400 | C | G | 7 | a0002 a0003 a0010 others(4): Show |
84 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(81): Show |
missense_variant | MODERATE | c.1745G>C | p.Gly582Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1771/4583 | 1745/4362 | 582/1453 | chr12 | 7396400 | |||
chr12:7396413 | C | T | 8 | a0002 a0003 a0006 others(5): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
missense_variant&splice_region_variant | MODERATE | c.1732G>A | p.Asp578Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/20 | 1758/4583 | 1732/4362 | 578/1453 | chr12 | 7396413 | |||
chr12:7398398 | T | C | 1 | a0015 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.1595A>G | p.Lys532Arg | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1621/4583 | 1595/4362 | 532/1453 | chr12 | 7398398 | |||
chr12:7398426 | A | T | 24 | a0001 a0002 a0003 others(21): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
missense_variant | MODERATE | c.1567T>A | p.Leu523Met | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1593/4583 | 1567/4362 | 523/1453 | chr12 | 7398426 | |||
chr12:7398482 | C | T | 1 | a0023 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.1511G>A | p.Arg504Lys | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1537/4583 | 1511/4362 | 504/1453 | chr12 | 7398482 | |||
chr12:7398533 | C | T | 1 | a0024 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1460G>A | p.Gly487Glu | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1486/4583 | 1460/4362 | 487/1453 | chr12 | 7398533 | |||
chr12:7403681 | C | T | 1 | a0021 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1262G>A | p.Arg421His | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/20 | 1288/4583 | 1262/4362 | 421/1453 | chr12 | 7403681 | |||
chr12:7433523 | C | T | 1 | a0019 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.296G>A | p.Arg99His | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 322/4583 | 296/4362 | 99/1453 | chr12 | 7433523 | |||
chr12:7433550 | C | G | 1 | a0016 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.269G>C | p.Gly90Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 295/4583 | 269/4362 | 90/1453 | chr12 | 7433550 | |||
chr12:7444117 | G | A | 3 | a0010 a0011 a0017 |
5 | HG01261.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.11C>T | p.Pro4Leu | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/20 | 37/4583 | 11/4362 | 4/1453 | chr12 | 7444117 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:7368175 | G | A | 13 | a0001c0008 a0001c0027 a0001c0039 others(10): Show |
26 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(23): Show |
synonymous_variant | LOW | c.4095C>T | p.Ser1365Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/20 | 4121/4583 | 4095/4362 | 1365/1453 | chr12 | 7368175 | |||
chr12:7369556 | C | T | 3 | a0001c0039 a0002c0032 a0005c0013 |
5 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.3840G>A | p.Ala1280Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/20 | 3866/4583 | 3840/4362 | 1280/1453 | chr12 | 7369556 | |||
chr12:7374713 | G | A | 3 | a0010c0018 a0011c0042 a0011c0043 |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
synonymous_variant | LOW | c.3138C>T | p.Ala1046Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/20 | 3164/4583 | 3138/4362 | 1046/1453 | chr12 | 7374713 | |||
chr12:7375396 | C | T | 1 | a0017c0044 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.2886G>A | p.Val962Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/20 | 2912/4583 | 2886/4362 | 962/1453 | chr12 | 7375396 | |||
chr12:7375875 | G | A | 25 | a0001c0001 a0001c0008 a0001c0017 others(22): Show |
209 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(206): Show |
synonymous_variant | LOW | c.2511C>T | p.Asn837Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 10/20 | 2537/4583 | 2511/4362 | 837/1453 | chr12 | 7375875 | |||
chr12:7379291 | C | T | 1 | a0001c0026 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2058G>A | p.Ser686Ser | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/20 | 2084/4583 | 2058/4362 | 686/1453 | chr12 | 7379291 | |||
chr12:7398454 | A | C | 43 | a0001c0001 a0001c0002 a0001c0004 others(40): Show |
380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
synonymous_variant | LOW | c.1539T>G | p.Val513Val | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/20 | 1565/4583 | 1539/4362 | 513/1453 | chr12 | 7398454 | |||
chr12:7432651 | T | C | 29 | a0001c0001 a0001c0007 a0001c0008 others(26): Show |
279 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
synonymous_variant | LOW | c.531A>G | p.Gly177Gly | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/20 | 557/4583 | 531/4362 | 177/1453 | chr12 | 7432651 | |||
chr12:7433375 | A | G | 8 | a0001c0002 a0001c0025 a0009c0015 others(5): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
splice_region_variant&synonymous_variant | LOW | c.444T>C | p.Tyr148Tyr | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 470/4583 | 444/4362 | 148/1453 | chr12 | 7433375 | |||
chr12:7433381 | G | A | 1 | a0001c0017 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.438C>T | p.Asn146Asn | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 464/4583 | 438/4362 | 146/1453 | chr12 | 7433381 | |||
chr12:7433510 | G | A | 1 | a0001c0041 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.309C>T | p.Ala103Ala | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/20 | 335/4583 | 309/4362 | 103/1453 | chr12 | 7433510 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:7355059 | C | T | 1 | a0001c0001t0004 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | 2345 | chr12 | 7355059 | ||||||
chr12:7355061 | T | C | 23 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(20): Show |
94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*94A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 20/20 | 2343 | chr12 | 7355061 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:7355238 | C | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0167 others(3): Show |
6 | NA18942.hp1 NA18968.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.*25-108G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355238 | |||||||
chr12:7355282 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG00609.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.*25-152C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355282 | |||||||
chr12:7355597 | G | A | 1 | a0005c0013t0001g0342 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.*25-467C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355597 | |||||||
chr12:7355741 | T | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0228 a0006c0009t0001g0040 |
4 | HG02559.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.*25-611A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7355741 | |||||||
chr12:7356060 | G | A | 37 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(34): Show |
42 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.*25-930C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356060 | |||||||
chr12:7356214 | G | T | 4 | a0001c0002t0001g0293 a0001c0002t0001g0294 a0001c0002t0001g0296 others(1): Show |
4 | NA18943.hp2 NA18980.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.*25-1084C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356214 | |||||||
chr12:7356272 | A | G | 3 | a0001c0001t0002g0323 a0001c0008t0002g0005 a0002c0003t0002g0094 |
5 | HG02451.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.*24+1108T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356272 | |||||||
chr12:7356462 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*24+918A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356462 | |||||||
chr12:7356570 | G | C | 3 | a0001c0001t0001g0197 a0005c0014t0001g0105 a0019c0020t0001g0253 |
3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.*24+810C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356570 | |||||||
chr12:7356574 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*24+806G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356574 | |||||||
chr12:7356709 | G | T | 1 | a0001c0002t0001g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.*24+671C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356709 | |||||||
chr12:7356732 | A | T | 1 | a0004c0012t0002g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*24+648T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356732 | |||||||
chr12:7356841 | C | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
54 | HG00544.hp1 HG00609.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.*24+539G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356841 | |||||||
chr12:7356850 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0139 |
3 | NA18951.hp1 NA18981.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.*24+530C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7356850 | |||||||
chr12:7357267 | T | G | 4 | a0001c0002t0001g0250 a0002c0003t0001g0098 a0023c0031t0001g0060 others(1): Show |
4 | NA18945.hp2 NA18975.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.*24+113A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357267 | |||||||
chr12:7357306 | A | C | 1 | a0001c0001t0002g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*24+74T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357306 | |||||||
chr12:7357372 | C | T | 2 | a0001c0004t0002g0314 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp1 |
splice_region_variant&intron_variant | LOW | c.*24+8G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 19/19 | chr12 | 7357372 | |||||||
chr12:7357541 | G | A | 1 | a0020c0038t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4280-55C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357541 | |||||||
chr12:7357648 | T | C | 64 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(61): Show |
69 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.4280-162A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357648 | |||||||
chr12:7357668 | A | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0007t0001g0104 others(5): Show |
8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4280-182T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357668 | |||||||
chr12:7357927 | A | G | 82 | a0001c0001t0002g0006 a0001c0001t0002g0107 a0001c0001t0002g0137 others(79): Show |
93 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.4280-441T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7357927 | |||||||
chr12:7358122 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4280-636T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358122 | |||||||
chr12:7358179 | A | C | 45 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(42): Show |
50 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.4280-693T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358179 | |||||||
chr12:7358405 | G | A | 3 | a0001c0001t0001g0197 a0005c0014t0001g0105 a0019c0020t0001g0253 |
3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4280-919C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358405 | |||||||
chr12:7358605 | A | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0191 a0001c0001t0001g0194 others(11): Show |
15 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.4280-1119T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358605 | |||||||
chr12:7358715 | T | C | 5 | a0001c0001t0002g0195 a0002c0003t0002g0053 a0002c0003t0002g0080 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4280-1229A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358715 | |||||||
chr12:7358908 | A | G | 93 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0130 others(90): Show |
95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.4280-1422T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358908 | |||||||
chr12:7358910 | T | C | 1 | a0002c0003t0001g0096 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4280-1424A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358910 | |||||||
chr12:7358948 | G | A | 1 | a0002c0003t0001g0047 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4280-1462C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358948 | |||||||
chr12:7358972 | C | G | 1 | a0002c0003t0001g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4280-1486G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7358972 | |||||||
chr12:7359151 | A | G | 1 | a0001c0002t0002g0252 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4280-1665T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359151 | |||||||
chr12:7359430 | A | C | 330 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.4280-1944T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359430 | |||||||
chr12:7359448 | G | T | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.4280-1962C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359448 | |||||||
chr12:7359477 | A | G | 2 | a0001c0001t0002g0170 a0001c0001t0002g0176 |
2 | NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.4280-1991T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359477 | |||||||
chr12:7359935 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4280-2449A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359935 | |||||||
chr12:7359998 | T | G | 4 | a0001c0001t0002g0231 a0004c0006t0002g0325 a0006c0009t0002g0200 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4280-2512A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7359998 | |||||||
chr12:7360383 | T | C | 8 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0007t0001g0104 others(5): Show |
8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4280-2897A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360383 | |||||||
chr12:7360671 | A | G | 1 | a0003c0005t0001g0318 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4280-3185T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360671 | |||||||
chr12:7360687 | G | A | 11 | a0001c0002t0001g0298 a0001c0002t0001g0300 a0001c0004t0001g0303 others(8): Show |
11 | HG00099.hp1 HG00733.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.4280-3201C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360687 | |||||||
chr12:7360859 | G | T | 1 | a0005c0013t0002g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4280-3373C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360859 | |||||||
chr12:7360945 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0139 others(1): Show |
5 | NA18951.hp1 NA18981.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.4280-3459C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360945 | |||||||
chr12:7360953 | TTTTGGTT others(4): Show |
T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(51): Show |
65 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.4280-3478_4280-346 others(15): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360953 | |||||||
chr12:7360964 | C | CTTTGT | 88 | a0001c0001t0001g0106 a0001c0001t0001g0119 a0001c0001t0001g0130 others(85): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.4280-3483_4280-347 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360964 | |||||||
chr12:7360964 | C | CTTTGTTT others(3): Show |
1 | a0003c0005t0001g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.4280-3488_4280-347 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7360964 | |||||||
chr12:7361197 | T | C | 83 | a0001c0001t0002g0006 a0001c0001t0002g0107 a0001c0001t0002g0137 others(80): Show |
94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.4280-3711A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361197 | |||||||
chr12:7361321 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4280-3835A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361321 | |||||||
chr12:7361497 | TC | T | 3 | a0001c0001t0002g0107 a0001c0001t0002g0188 a0003c0005t0002g0033 |
3 | HG03471.hp2 HG03486.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4280-4012delG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361497 | |||||||
chr12:7361544 | T | C | 83 | a0001c0001t0002g0006 a0001c0001t0002g0107 a0001c0001t0002g0137 others(80): Show |
94 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.4280-4058A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361544 | |||||||
chr12:7361546 | T | C | 12 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0001t0001g0222 others(9): Show |
12 | HG01168.hp2 HG01243.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.4280-4060A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361546 | |||||||
chr12:7361608 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | NA18961.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.4280-4122G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361608 | |||||||
chr12:7361616 | C | T | 12 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0199 others(9): Show |
12 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.4280-4130G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361616 | |||||||
chr12:7361636 | C | T | 37 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(34): Show |
42 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.4280-4150G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361636 | |||||||
chr12:7361720 | T | C | 6 | a0001c0001t0001g0138 a0001c0002t0001g0279 a0002c0003t0001g0007 others(3): Show |
7 | NA18946.hp1 NA18970.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.4280-4234A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361720 | |||||||
chr12:7361837 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4280-4351C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361837 | |||||||
chr12:7361910 | C | T | 4 | a0001c0001t0002g0231 a0004c0006t0002g0325 a0006c0009t0002g0200 others(1): Show |
4 | HG01884.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4280-4424G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7361910 | |||||||
chr12:7362217 | AT | A | 79 | a0001c0001t0002g0006 a0001c0001t0002g0107 a0001c0001t0002g0137 others(76): Show |
90 | HG00558.hp1 HG00558.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.4280-4732delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362217 | |||||||
chr12:7362256 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
121 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.4280-4770C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362256 | |||||||
chr12:7362294 | T | C | 1 | a0002c0003t0001g0082 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4280-4808A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362294 | |||||||
chr12:7362346 | T | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
121 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.4280-4860A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362346 | |||||||
chr12:7362440 | A | G | 3 | a0004c0006t0001g0332 a0004c0006t0001g0335 a0004c0028t0001g0126 |
3 | HG02109.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4279+4796T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362440 | |||||||
chr12:7362526 | A | G | 1 | a0004c0006t0001g0328 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4279+4710T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362526 | |||||||
chr12:7362617 | A | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(51): Show |
65 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.4279+4619T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362617 | |||||||
chr12:7362669 | A | G | 3 | a0001c0001t0001g0222 a0001c0002t0001g0028 a0001c0002t0001g0286 |
3 | HG06807.hp2 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4279+4567T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362669 | |||||||
chr12:7362705 | T | C | 38 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(35): Show |
43 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.4279+4531A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362705 | |||||||
chr12:7362807 | T | C | 16 | a0001c0001t0002g0195 a0001c0026t0002g0109 a0002c0003t0002g0042 others(13): Show |
17 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.4279+4429A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362807 | |||||||
chr12:7362974 | T | A | 1 | a0006c0009t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4279+4262A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362974 | |||||||
chr12:7362975 | A | T | 2 | a0001c0004t0001g0120 a0002c0003t0001g0086 |
2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4279+4261T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7362975 | |||||||
chr12:7363030 | C | G | 1 | a0001c0001t0002g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4279+4206G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363030 | |||||||
chr12:7363043 | G | A | 3 | a0002c0003t0002g0044 a0002c0003t0002g0048 a0002c0003t0002g0049 |
3 | HG02698.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.4279+4193C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363043 | |||||||
chr12:7363347 | G | A | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4279+3889C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363347 | |||||||
chr12:7363418 | A | AAATAAT | 39 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(36): Show |
44 | HG00408.hp1 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.4279+3812_4279+381 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363418 | |||||||
chr12:7363701 | T | C | 1 | a0001c0002t0001g0283 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4279+3535A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363701 | |||||||
chr12:7363718 | C | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0129 a0001c0007t0001g0104 others(5): Show |
8 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4279+3518G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363718 | |||||||
chr12:7363790 | G | GA | 330 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.4279+3445dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7363790 | |||||||
chr12:7364109 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0095 others(33): Show |
43 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.4279+3127G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364109 | |||||||
chr12:7364240 | G | A | 1 | a0001c0017t0002g0019 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4279+2996C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364240 | |||||||
chr12:7364294 | T | C | 1 | a0001c0002t0001g0285 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4279+2942A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364294 | |||||||
chr12:7364446 | A | G | 2 | a0012c0016t0001g0038 a0012c0016t0001g0064 |
2 | NA18946.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.4279+2790T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364446 | |||||||
chr12:7364547 | C | T | 3 | a0001c0001t0003g0221 a0001c0002t0003g0261 a0001c0004t0003g0309 |
3 | HG01243.hp2 HG02148.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.4279+2689G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364547 | |||||||
chr12:7364832 | A | G | 1 | a0001c0002t0001g0290 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.4279+2404T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364832 | |||||||
chr12:7364863 | C | T | 1 | a0003c0005t0003g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4279+2373G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7364863 | |||||||
chr12:7365011 | C | G | 1 | a0002c0003t0001g0045 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.4279+2225G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365011 | |||||||
chr12:7365182 | C | T | 3 | a0001c0001t0001g0197 a0005c0014t0001g0105 a0019c0020t0001g0253 |
3 | HG02809.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4279+2054G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365182 | |||||||
chr12:7365294 | A | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0191 a0001c0001t0001g0194 others(11): Show |
15 | HG01358.hp1 HG01891.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.4279+1942T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365294 | |||||||
chr12:7365346 | T | C | 1 | a0020c0038t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4279+1890A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365346 | |||||||
chr12:7365732 | A | G | 1 | a0005c0013t0001g0342 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4279+1504T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365732 | |||||||
chr12:7365742 | T | C | 2 | a0004c0006t0001g0335 a0004c0028t0001g0126 |
2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4279+1494A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365742 | |||||||
chr12:7365787 | G | C | 99 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(96): Show |
115 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.4279+1449C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365787 | |||||||
chr12:7365794 | C | T | 1 | a0002c0003t0002g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4279+1442G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365794 | |||||||
chr12:7365826 | G | T | 98 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0148 others(95): Show |
114 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.4279+1410C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365826 | |||||||
chr12:7365909 | G | A | 2 | a0001c0001t0001g0212 a0001c0002t0001g0267 |
2 | NA18942.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.4279+1327C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7365909 | |||||||
chr12:7366161 | T | C | 11 | a0002c0003t0001g0031 a0002c0003t0001g0089 a0002c0003t0002g0053 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.4279+1075A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366161 | |||||||
chr12:7366179 | T | G | 10 | a0001c0001t0001g0106 a0001c0001t0001g0197 a0001c0001t0002g0323 others(7): Show |
10 | HG01884.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.4279+1057A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366179 | |||||||
chr12:7366293 | A | G | 3 | a0002c0003t0001g0075 a0002c0003t0001g0077 a0002c0003t0001g0085 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4279+943T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366293 | |||||||
chr12:7366421 | A | G | 1 | a0001c0001t0001g0003 | 3 | HG03017.hp1 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.4279+815T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366421 | |||||||
chr12:7366537 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
171 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.4279+699A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366537 | |||||||
chr12:7366724 | T | C | 1 | a0006c0034t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4279+512A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366724 | |||||||
chr12:7366889 | T | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.4279+347A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366889 | |||||||
chr12:7366918 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0184 a0001c0001t0001g0186 |
3 | NA18961.hp2 NA18981.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.4279+318C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7366918 | |||||||
chr12:7367117 | G | A | 1 | a0001c0002t0001g0102 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.4279+119C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367117 | |||||||
chr12:7367177 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.4279+59G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367177 | |||||||
chr12:7367230 | A | G | 35 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(32): Show |
39 | HG00558.hp2 HG00609.hp2 HG00735.hp2 others(36): Show |
splice_region_variant&intron_variant | LOW | c.4279+6T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 18/19 | chr12 | 7367230 | |||||||
chr12:7367528 | C | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(12): Show |
17 | HG00544.hp2 HG02040.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.4184-197G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/19 | chr12 | 7367528 | |||||||
chr12:7368039 | T | G | 1 | a0001c0002t0002g0292 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4183+48A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 17/19 | chr12 | 7368039 | |||||||
chr12:7368435 | G | A | 24 | a0001c0008t0001g0196 a0001c0008t0001g0232 a0001c0008t0001g0238 others(21): Show |
26 | HG01175.hp1 HG01261.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.4073-238C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368435 | |||||||
chr12:7368529 | C | CT | 32 | a0001c0001t0001g0204 a0001c0001t0002g0107 a0001c0001t0002g0188 others(29): Show |
35 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.4073-333dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368529 | |||||||
chr12:7368529 | C | CTT | 25 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(22): Show |
28 | HG00609.hp2 HG00735.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.4073-334_4073-333d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368529 | |||||||
chr12:7368584 | T | C | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4072+349A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368584 | |||||||
chr12:7368703 | AG | A | 5 | a0001c0004t0002g0121 a0002c0003t0001g0077 a0002c0003t0001g0085 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4072+229delC | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368703 | |||||||
chr12:7368708 | A | T | 5 | a0001c0004t0002g0121 a0002c0003t0001g0077 a0002c0003t0001g0085 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4072+225T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368708 | |||||||
chr12:7368908 | A | G | 2 | a0008c0011t0001g0127 a0008c0011t0002g0124 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.4072+25T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 16/19 | chr12 | 7368908 | |||||||
chr12:7368967 | T | TGA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0187 a0001c0004t0001g0120 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4040-4_4040-3dupTC | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368967 | |||||||
chr12:7368967 | T | TGAGA | 6 | a0001c0007t0001g0131 a0001c0008t0001g0238 a0001c0008t0002g0235 others(3): Show |
6 | HG01175.hp1 HG01261.hp1 HG02451.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4040-6_4040-3dupTC others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368967 | |||||||
chr12:7368979 | A | G | 1 | a0005c0030t0003g0301 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4040-14T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7368979 | |||||||
chr12:7369277 | A | G | 1 | a0002c0003t0001g0061 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4039+80T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7369277 | |||||||
chr12:7369280 | C | A | 2 | a0001c0001t0002g0323 a0002c0003t0001g0031 |
2 | HG02451.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.4039+77G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 15/19 | chr12 | 7369280 | |||||||
chr12:7369752 | G | A | 4 | a0001c0004t0002g0121 a0002c0003t0001g0077 a0002c0003t0001g0085 others(1): Show |
4 | HG02647.hp1 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3731-87C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7369752 | |||||||
chr12:7370072 | T | C | 1 | a0001c0004t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3731-407A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370072 | |||||||
chr12:7370179 | A | G | 5 | a0001c0039t0001g0192 a0002c0032t0001g0043 a0005c0013t0001g0243 others(2): Show |
5 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.3731-514T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370179 | |||||||
chr12:7370367 | T | A | 3 | a0002c0003t0001g0031 a0008c0011t0001g0127 a0008c0011t0002g0124 |
3 | HG01891.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3731-702A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370367 | |||||||
chr12:7370393 | T | C | 2 | a0010c0018t0001g0344 a0010c0018t0002g0345 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3731-728A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370393 | |||||||
chr12:7370413 | T | C | 2 | a0003c0005t0001g0190 a0003c0005t0002g0093 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3731-748A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370413 | |||||||
chr12:7370602 | G | A | 2 | a0003c0005t0001g0057 a0003c0005t0001g0072 |
2 | NA18970.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.3731-937C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370602 | |||||||
chr12:7370636 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3731-971T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370636 | |||||||
chr12:7370757 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(14): Show |
19 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.3731-1092G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370757 | |||||||
chr12:7370866 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3731-1201C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370866 | |||||||
chr12:7370905 | G | C | 1 | a0002c0003t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3731-1240C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370905 | |||||||
chr12:7370956 | G | T | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3731-1291C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7370956 | |||||||
chr12:7371026 | A | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(50): Show |
63 | HG00558.hp1 HG00735.hp1 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.3731-1361T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371026 | |||||||
chr12:7371103 | C | T | 147 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(144): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.3731-1438G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371103 | |||||||
chr12:7371447 | A | G | 3 | a0002c0003t0001g0031 a0008c0011t0001g0127 a0008c0011t0002g0124 |
3 | HG01891.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3731-1782T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371447 | |||||||
chr12:7371614 | T | C | 1 | a0008c0011t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3730+1706A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371614 | |||||||
chr12:7371775 | A | C | 2 | a0001c0004t0001g0120 a0001c0027t0002g0030 |
2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3730+1545T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371775 | |||||||
chr12:7371835 | G | C | 32 | a0001c0001t0002g0323 a0002c0003t0001g0041 a0002c0003t0002g0042 others(29): Show |
33 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.3730+1485C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371835 | |||||||
chr12:7371882 | T | G | 1 | a0004c0006t0001g0339 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3730+1438A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371882 | |||||||
chr12:7371895 | T | C | 1 | a0003c0005t0001g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3730+1425A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371895 | |||||||
chr12:7371898 | A | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(14): Show |
19 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.3730+1422T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371898 | |||||||
chr12:7371976 | T | C | 2 | a0011c0042t0002g0346 a0011c0043t0001g0343 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3730+1344A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7371976 | |||||||
chr12:7372055 | AAAG | A | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.3730+1262_3730+126 others(7): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372055 | |||||||
chr12:7372079 | T | C | 5 | a0002c0032t0001g0043 a0005c0013t0001g0243 a0005c0013t0001g0342 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.3730+1241A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372079 | |||||||
chr12:7372130 | C | A | 1 | a0001c0002t0003g0291 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3730+1190G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372130 | |||||||
chr12:7372308 | T | C | 1 | a0001c0002t0001g0279 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3730+1012A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372308 | |||||||
chr12:7372314 | C | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(330): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.3730+1006G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372314 | |||||||
chr12:7372809 | T | C | 3 | a0003c0005t0001g0032 a0003c0005t0001g0076 a0015c0040t0001g0090 |
3 | HG01243.hp1 HG02895.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3730+511A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372809 | |||||||
chr12:7372958 | T | A | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3730+362A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7372958 | |||||||
chr12:7373199 | C | T | 268 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(265): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.3730+121G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373199 | |||||||
chr12:7373209 | T | C | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3730+111A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373209 | |||||||
chr12:7373269 | G | C | 173 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(170): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.3730+51C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 14/19 | chr12 | 7373269 | |||||||
chr12:7373711 | A | AT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(58): Show |
69 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.3410-72dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7373711 | |||||||
chr12:7373903 | C | G | 1 | a0025c0035t0002g0227 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3410-263G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7373903 | |||||||
chr12:7374043 | C | A | 2 | a0011c0042t0002g0346 a0011c0043t0001g0343 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3409+399G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374043 | |||||||
chr12:7374142 | C | T | 1 | a0008c0011t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3409+300G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374142 | |||||||
chr12:7374263 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3409+179G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374263 | |||||||
chr12:7374404 | G | A | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3409+38C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 13/19 | chr12 | 7374404 | |||||||
chr12:7374794 | T | C | 18 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(15): Show |
19 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.3094+37A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 12/19 | chr12 | 7374794 | |||||||
chr12:7374987 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | NA18961.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.3002-64A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7374987 | |||||||
chr12:7375064 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3002-141A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7375064 | |||||||
chr12:7375255 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3001+26C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 11/19 | chr12 | 7375255 | |||||||
chr12:7376313 | C | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2372-299G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376313 | |||||||
chr12:7376330 | A | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2372-316T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376330 | |||||||
chr12:7376467 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
209 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(206): Show |
intron_variant | MODIFIER | c.2372-453C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376467 | |||||||
chr12:7376577 | A | G | 5 | a0004c0006t0002g0103 a0004c0006t0002g0325 a0004c0012t0001g0326 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2372-563T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376577 | |||||||
chr12:7376960 | A | G | 23 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(20): Show |
24 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2372-946T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7376960 | |||||||
chr12:7377088 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
209 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(206): Show |
intron_variant | MODIFIER | c.2372-1074G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377088 | |||||||
chr12:7377104 | T | C | 19 | a0003c0005t0001g0190 a0003c0005t0002g0093 a0004c0006t0001g0328 others(16): Show |
19 | HG00673.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2372-1090A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377104 | |||||||
chr12:7377126 | A | G | 1 | a0022c0036t0002g0214 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2372-1112T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377126 | |||||||
chr12:7377291 | T | C | 144 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(141): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.2372-1277A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377291 | |||||||
chr12:7377295 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2372-1281A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377295 | |||||||
chr12:7377326 | C | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(13): Show |
18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2372-1312G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377326 | |||||||
chr12:7377355 | C | T | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2372-1341G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377355 | |||||||
chr12:7377487 | C | T | 2 | a0001c0002t0001g0298 a0001c0002t0003g0299 |
2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2372-1473G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377487 | |||||||
chr12:7377730 | C | A | 1 | a0001c0008t0002g0235 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2371+1248G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377730 | |||||||
chr12:7377749 | C | T | 1 | a0001c0002t0001g0251 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2371+1229G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377749 | |||||||
chr12:7377764 | C | T | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2371+1214G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377764 | |||||||
chr12:7377912 | G | A | 47 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(44): Show |
49 | HG00423.hp1 HG00673.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.2371+1066C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377912 | |||||||
chr12:7377940 | T | C | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2371+1038A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7377940 | |||||||
chr12:7378041 | C | T | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2371+937G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378041 | |||||||
chr12:7378155 | T | A | 1 | a0001c0002t0001g0284 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2371+823A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378155 | |||||||
chr12:7378225 | CT | C | 3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2371+752delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378225 | |||||||
chr12:7378266 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2371+712C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378266 | |||||||
chr12:7378268 | A | G | 18 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(15): Show |
19 | HG00423.hp1 HG01099.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.2371+710T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378268 | |||||||
chr12:7378302 | G | A | 1 | a0001c0002t0001g0286 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2371+676C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378302 | |||||||
chr12:7378369 | C | T | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0007t0001g0131 others(1): Show |
4 | HG02717.hp1 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2371+609G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378369 | |||||||
chr12:7378396 | A | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(6): Show |
11 | HG00544.hp2 HG02056.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2371+582T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378396 | |||||||
chr12:7378407 | A | C | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2371+571T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378407 | |||||||
chr12:7378422 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(13): Show |
18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2371+556A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378422 | |||||||
chr12:7378612 | TA | T | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2371+365delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 9/19 | chr12 | 7378612 | |||||||
chr12:7379313 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2051-15G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379313 | |||||||
chr12:7379373 | C | T | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2051-75G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379373 | |||||||
chr12:7379420 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-122C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379420 | |||||||
chr12:7379736 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2051-438C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379736 | |||||||
chr12:7379803 | A | G | 1 | a0020c0038t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2051-505T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379803 | |||||||
chr12:7379867 | G | GT | 4 | a0001c0001t0001g0213 a0001c0001t0002g0247 a0001c0008t0002g0005 others(1): Show |
6 | HG02723.hp1 HG02922.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-570dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | |||||||
chr12:7379867 | G | GTT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(52): Show |
61 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.2051-571_2051-570d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | |||||||
chr12:7379867 | GT | G | 17 | a0004c0006t0001g0328 a0004c0006t0001g0329 a0004c0006t0001g0332 others(14): Show |
17 | HG00673.hp2 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2051-570delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7379867 | |||||||
chr12:7380205 | A | T | 2 | a0010c0018t0001g0344 a0010c0018t0002g0345 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2051-907T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380205 | |||||||
chr12:7380210 | G | A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-912C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380210 | |||||||
chr12:7380234 | C | T | 1 | a0001c0002t0001g0298 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2051-936G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380234 | |||||||
chr12:7380273 | T | C | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-975A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380273 | |||||||
chr12:7380274 | GGT | G | 15 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(12): Show |
16 | HG00099.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2051-978_2051-977d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | |||||||
chr12:7380274 | GGTGT | G | 144 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(141): Show |
157 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2051-980_2051-977d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | |||||||
chr12:7380274 | GGTGTGT | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0178 a0001c0001t0001g0179 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-982_2051-977d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | |||||||
chr12:7380274 | GGTGTGTG others(1): Show |
G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
190 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.2051-984_2051-977d others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380274 | |||||||
chr12:7380287 | GTGTGTGT others(57): Show |
G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1053_2051-990 others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380287 | |||||||
chr12:7380287 | GTGTGTGT others(85): Show |
G | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2051-1081_2051-990 others(95): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380287 | |||||||
chr12:7380291 | GTGTGTGT others(29): Show |
G | 2 | a0003c0005t0001g0069 a0006c0009t0002g0200 |
2 | HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1029_2051-994 others(39): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380291 | |||||||
chr12:7380293 | G | GTATACAC others(13): Show |
1 | a0004c0012t0002g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-996_2051-995i others(22): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380293 | |||||||
chr12:7380295 | G | A | 1 | a0004c0012t0002g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-997C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380295 | |||||||
chr12:7380295 | G | GTGTATAC others(17): Show |
2 | a0001c0002t0001g0112 a0001c0002t0002g0249 |
2 | HG02135.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2051-998_2051-997i others(26): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380295 | |||||||
chr12:7380299 | G | A | 3 | a0001c0002t0001g0112 a0001c0002t0002g0249 a0004c0012t0002g0324 |
3 | HG02135.hp1 HG02630.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2051-1001C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380299 | |||||||
chr12:7380301 | G | A | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2051-1003C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380301 | |||||||
chr12:7380307 | A | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(18): Show |
23 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.2051-1009T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380307 | |||||||
chr12:7380309 | A | G | 11 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(8): Show |
13 | HG02135.hp1 HG02630.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.2051-1011T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380309 | |||||||
chr12:7380316 | T | C | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2051-1018A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380316 | |||||||
chr12:7380321 | A | G | 21 | a0001c0002t0001g0112 a0001c0002t0002g0249 a0003c0005t0001g0008 others(18): Show |
22 | HG00423.hp1 HG01099.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2051-1023T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380321 | |||||||
chr12:7380327 | A | ATGTATAC others(21): Show |
1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2051-1030_2051-102 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | |||||||
chr12:7380327 | A | ATGTATAC others(21): Show |
2 | a0001c0002t0001g0256 a0001c0002t0001g0270 |
2 | NA19063.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2051-1030_2051-102 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | |||||||
chr12:7380327 | A | G | 21 | a0001c0001t0001g0149 a0001c0002t0001g0111 a0001c0002t0001g0112 others(18): Show |
22 | HG00423.hp1 HG01099.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2051-1029T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | |||||||
chr12:7380327 | ATGTATAC others(21): Show |
A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-1057_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380327 | |||||||
chr12:7380335 | A | ACGTATAC others(49): Show |
2 | a0001c0004t0001g0311 a0001c0004t0001g0312 |
2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2051-1038_2051-103 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380335 | A | ACGTATAC others(21): Show |
133 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(130): Show |
147 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.2051-1065_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380335 | A | ACGTATAC others(49): Show |
3 | a0002c0003t0001g0071 a0009c0015t0001g0264 a0009c0015t0001g0295 |
3 | HG01123.hp1 HG02698.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2051-1038_2051-103 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380335 | A | ACGTATAC others(77): Show |
1 | a0013c0024t0001g0262 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2051-1038_2051-103 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380335 | A | G | 10 | a0001c0001t0001g0149 a0001c0002t0001g0112 a0001c0002t0001g0256 others(7): Show |
11 | HG01167.hp1 HG01169.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.2051-1037T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380335 | ACGTATAC others(21): Show |
A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(12): Show |
17 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.2051-1065_2051-103 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380335 | |||||||
chr12:7380337 | G | A | 2 | a0003c0005t0001g0069 a0006c0009t0002g0200 |
2 | HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1039C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380337 | |||||||
chr12:7380344 | T | C | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-1046A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380344 | |||||||
chr12:7380344 | T | TACATGTA others(21): Show |
1 | a0001c0002t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2051-1047_2051-104 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380344 | |||||||
chr12:7380349 | G | A | 1 | a0006c0009t0002g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2051-1051C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380349 | |||||||
chr12:7380363 | G | A | 6 | a0003c0005t0001g0008 a0003c0005t0001g0069 a0010c0018t0001g0344 others(3): Show |
7 | HG01099.hp1 HG01261.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-1065C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380363 | |||||||
chr12:7380365 | G | A | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1067C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380365 | |||||||
chr12:7380372 | T | C | 17 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0158 others(14): Show |
18 | HG01167.hp1 HG01169.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.2051-1074A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | |||||||
chr12:7380372 | T | TACATGTA others(21): Show |
2 | a0001c0002t0001g0293 a0024c0022t0001g0268 |
2 | NA19058.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2051-1075_2051-107 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | |||||||
chr12:7380372 | T | TACATGTA others(49): Show |
1 | a0002c0003t0003g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2051-1075_2051-107 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | |||||||
chr12:7380372 | TACATGTA others(21): Show |
T | 15 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(12): Show |
16 | HG00423.hp1 HG01099.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.2051-1102_2051-107 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380372 | |||||||
chr12:7380390 | T | C | 18 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0007t0001g0131 others(15): Show |
18 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2051-1092A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380390 | |||||||
chr12:7380391 | G | A | 1 | a0003c0005t0001g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2051-1093C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380391 | |||||||
chr12:7380400 | C | T | 2 | a0003c0005t0001g0069 a0003c0033t0002g0128 |
2 | HG01891.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2051-1102G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380400 | |||||||
chr12:7380413 | G | GTA | 7 | a0002c0032t0001g0043 a0005c0013t0001g0243 a0005c0013t0001g0342 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2051-1117_2051-111 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380413 | |||||||
chr12:7380415 | A | G | 1 | a0001c0002t0003g0316 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2051-1117T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380415 | |||||||
chr12:7380493 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2051-1195A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380493 | |||||||
chr12:7380757 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-1459A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380757 | |||||||
chr12:7380793 | A | T | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-1495T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380793 | |||||||
chr12:7380799 | G | T | 12 | a0001c0001t0001g0191 a0001c0001t0001g0233 a0001c0001t0001g0237 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.2051-1501C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380799 | |||||||
chr12:7380806 | C | T | 2 | a0001c0001t0003g0234 a0001c0007t0001g0330 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2051-1508G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380806 | |||||||
chr12:7380825 | T | C | 1 | a0002c0003t0001g0071 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2051-1527A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380825 | |||||||
chr12:7380833 | G | C | 1 | a0001c0008t0001g0196 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2051-1535C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380833 | |||||||
chr12:7380883 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0205 |
4 | HG00609.hp2 HG02015.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-1585G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380883 | |||||||
chr12:7380903 | A | T | 1 | a0001c0001t0001g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2051-1605T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7380903 | |||||||
chr12:7381130 | C | A | 2 | a0003c0005t0001g0008 a0003c0005t0001g0069 |
3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2051-1832G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381130 | |||||||
chr12:7381440 | C | T | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-2142G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381440 | |||||||
chr12:7381926 | A | G | 3 | a0004c0006t0001g0332 a0004c0006t0001g0335 a0004c0028t0001g0126 |
3 | HG02109.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2051-2628T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381926 | |||||||
chr12:7381961 | AAT | A | 15 | a0003c0005t0001g0008 a0003c0005t0001g0032 a0003c0005t0001g0035 others(12): Show |
16 | HG00423.hp1 HG01099.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.2051-2665_2051-266 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381961 | |||||||
chr12:7381962 | AT | A | 65 | a0001c0001t0001g0204 a0001c0002t0002g0313 a0001c0007t0001g0104 others(62): Show |
67 | HG00408.hp1 HG00673.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.2051-2665delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381962 | |||||||
chr12:7381963 | T | A | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-2665A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381963 | |||||||
chr12:7381965 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-2667A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7381965 | |||||||
chr12:7382018 | T | A | 1 | a0002c0003t0002g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2051-2720A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382018 | |||||||
chr12:7382079 | T | C | 1 | a0001c0008t0002g0235 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2051-2781A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382079 | |||||||
chr12:7382132 | A | G | 1 | a0004c0012t0002g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2051-2834T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382132 | |||||||
chr12:7382270 | T | C | 1 | a0001c0001t0003g0021 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2051-2972A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382270 | |||||||
chr12:7382457 | G | A | 1 | a0002c0003t0001g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2051-3159C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382457 | |||||||
chr12:7382551 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-3253A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382551 | |||||||
chr12:7382702 | C | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-3404G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382702 | |||||||
chr12:7382758 | G | A | 20 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(17): Show |
21 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.2051-3460C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382758 | |||||||
chr12:7382785 | T | C | 1 | a0002c0003t0003g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2051-3487A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7382785 | |||||||
chr12:7383095 | A | G | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2051-3797T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383095 | |||||||
chr12:7383286 | C | T | 15 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(12): Show |
16 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2051-3988G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383286 | |||||||
chr12:7383302 | G | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-4004C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383302 | |||||||
chr12:7383334 | C | A | 1 | a0001c0027t0002g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2051-4036G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383334 | |||||||
chr12:7383360 | G | A | 4 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-4062C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383360 | |||||||
chr12:7383402 | G | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(54): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2051-4104C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383402 | |||||||
chr12:7383408 | A | G | 1 | a0002c0003t0001g0063 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2051-4110T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383408 | |||||||
chr12:7383441 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(5): Show |
10 | HG00544.hp2 HG02056.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.2051-4143G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383441 | |||||||
chr12:7383445 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2051-4147G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383445 | |||||||
chr12:7383532 | G | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0133 others(8): Show |
18 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2051-4234C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383532 | |||||||
chr12:7383697 | A | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2051-4399T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383697 | |||||||
chr12:7383762 | C | G | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2051-4464G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383762 | |||||||
chr12:7383951 | C | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(74): Show |
90 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.2051-4653G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383951 | |||||||
chr12:7383984 | G | A | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2051-4686C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7383984 | |||||||
chr12:7384053 | T | A | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2051-4755A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384053 | |||||||
chr12:7384171 | T | TA | 11 | a0003c0033t0002g0128 a0006c0009t0001g0039 a0006c0009t0001g0040 others(8): Show |
12 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.2051-4874dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384171 | |||||||
chr12:7384171 | T | TAA | 74 | a0001c0007t0001g0104 a0002c0003t0001g0007 a0002c0003t0001g0009 others(71): Show |
77 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.2051-4875_2051-487 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384171 | |||||||
chr12:7384353 | A | G | 1 | a0002c0003t0002g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2051-5055T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384353 | |||||||
chr12:7384499 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2051-5201G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384499 | |||||||
chr12:7384519 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2051-5221T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384519 | |||||||
chr12:7384687 | C | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2051-5389G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384687 | |||||||
chr12:7384772 | T | C | 1 | a0001c0004t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2051-5474A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384772 | |||||||
chr12:7384860 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2051-5562T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384860 | |||||||
chr12:7384868 | A | G | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2051-5570T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7384868 | |||||||
chr12:7385034 | C | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2051-5736G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385034 | |||||||
chr12:7385186 | G | T | 4 | a0001c0002t0001g0248 a0001c0002t0001g0260 a0001c0002t0001g0273 others(1): Show |
4 | NA18951.hp2 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-5888C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385186 | |||||||
chr12:7385250 | T | TA | 74 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(71): Show |
85 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2051-5953dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385250 | |||||||
chr12:7385250 | TA | T | 6 | a0001c0004t0003g0308 a0002c0032t0001g0043 a0010c0018t0001g0344 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2051-5953delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385250 | |||||||
chr12:7385348 | C | T | 1 | a0001c0002t0002g0252 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2051-6050G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385348 | |||||||
chr12:7385356 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2051-6058A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385356 | |||||||
chr12:7385755 | A | C | 1 | a0019c0020t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2051-6457T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385755 | |||||||
chr12:7385930 | A | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(13): Show |
18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2051-6632T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7385930 | |||||||
chr12:7386014 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(57): Show |
71 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.2051-6716T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386014 | |||||||
chr12:7386087 | TAAAAG | T | 3 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0034t0001g0123 |
4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-6794_2051-679 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386087 | |||||||
chr12:7386125 | A | G | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-6827T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386125 | |||||||
chr12:7386190 | C | T | 5 | a0001c0004t0002g0305 a0004c0006t0002g0325 a0004c0012t0001g0326 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-6892G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386190 | |||||||
chr12:7386246 | G | C | 1 | a0001c0026t0002g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2051-6948C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386246 | |||||||
chr12:7386346 | A | AC | 4 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-7049dupG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386346 | |||||||
chr12:7386403 | A | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2051-7105T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386403 | |||||||
chr12:7386536 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2051-7238T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386536 | |||||||
chr12:7386604 | C | CA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(113): Show |
128 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(125): Show |
intron_variant | MODIFIER | c.2051-7307dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386604 | |||||||
chr12:7386604 | CA | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(193): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2051-7307delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386604 | |||||||
chr12:7386619 | A | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-7321T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386619 | |||||||
chr12:7386664 | T | C | 76 | a0001c0007t0001g0104 a0002c0003t0001g0007 a0002c0003t0001g0009 others(73): Show |
79 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.2051-7366A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386664 | |||||||
chr12:7386971 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2051-7673G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7386971 | |||||||
chr12:7387253 | C | A | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2051-7955G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387253 | |||||||
chr12:7387362 | G | A | 11 | a0001c0002t0001g0023 a0001c0002t0001g0250 a0001c0002t0001g0256 others(8): Show |
12 | HG00544.hp1 NA18747.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.2051-8064C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387362 | |||||||
chr12:7387427 | T | C | 3 | a0002c0003t0002g0044 a0002c0003t0002g0048 a0002c0003t0002g0049 |
3 | HG02698.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2051-8129A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387427 | |||||||
chr12:7387641 | C | T | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2051-8343G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387641 | |||||||
chr12:7387759 | C | T | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050+8336G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387759 | |||||||
chr12:7387881 | A | G | 80 | a0001c0007t0001g0104 a0002c0003t0001g0007 a0002c0003t0001g0009 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.2050+8214T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387881 | |||||||
chr12:7387923 | A | C | 1 | a0002c0003t0002g0048 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2050+8172T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387923 | |||||||
chr12:7387934 | T | G | 7 | a0002c0032t0001g0043 a0005c0013t0001g0243 a0005c0013t0001g0342 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2050+8161A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7387934 | |||||||
chr12:7388137 | T | C | 1 | a0001c0002t0003g0299 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2050+7958A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388137 | |||||||
chr12:7388163 | A | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+7932T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388163 | |||||||
chr12:7388236 | A | C | 1 | a0006c0009t0002g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+7859T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388236 | |||||||
chr12:7388294 | T | C | 1 | a0003c0005t0003g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2050+7801A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388294 | |||||||
chr12:7388321 | G | T | 1 | a0004c0006t0001g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2050+7774C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388321 | |||||||
chr12:7388339 | G | A | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7756C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388339 | |||||||
chr12:7388509 | A | AC | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7585_2050+758 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388509 | |||||||
chr12:7388510 | A | T | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7585T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388510 | |||||||
chr12:7388511 | G | T | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7584C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388511 | |||||||
chr12:7388515 | G | C | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7580C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388515 | |||||||
chr12:7388516 | G | C | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7579C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388516 | |||||||
chr12:7388517 | C | CG | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7577_2050+757 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388517 | |||||||
chr12:7388518 | A | G | 8 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(5): Show |
8 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+7577T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388518 | |||||||
chr12:7388625 | T | C | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2050+7470A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388625 | |||||||
chr12:7388677 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(13): Show |
18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+7418C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388677 | |||||||
chr12:7388743 | C | CA | 66 | a0001c0001t0001g0108 a0001c0001t0001g0165 a0001c0001t0001g0173 others(63): Show |
69 | HG00140.hp2 HG00639.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.2050+7351dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388743 | |||||||
chr12:7388743 | C | CAA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
56 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.2050+7350_2050+735 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388743 | |||||||
chr12:7388766 | G | GC | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0136 others(13): Show |
18 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+7328_2050+732 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388766 | |||||||
chr12:7388771 | G | GT | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7323_2050+732 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388771 | |||||||
chr12:7388816 | G | A | 11 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(8): Show |
12 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2050+7279C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7388816 | |||||||
chr12:7389001 | A | G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+7094T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389001 | |||||||
chr12:7389094 | T | A | 12 | a0001c0001t0001g0191 a0001c0001t0001g0233 a0001c0001t0001g0237 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.2050+7001A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389094 | |||||||
chr12:7389118 | C | T | 1 | a0001c0002t0001g0340 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2050+6977G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389118 | |||||||
chr12:7389174 | C | T | 1 | a0001c0002t0001g0256 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2050+6921G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389174 | |||||||
chr12:7389340 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+6755G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389340 | |||||||
chr12:7389944 | T | TTTTATAT others(7): Show |
5 | a0002c0003t0001g0031 a0002c0003t0001g0089 a0003c0005t0001g0032 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050+6137_2050+615 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389944 | |||||||
chr12:7389946 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0215 a0022c0036t0002g0214 |
2 | HG03831.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.2050+6137_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | |||||||
chr12:7389946 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2050+6148_2050+614 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | |||||||
chr12:7389946 | T | TTATATAT others(25): Show |
1 | a0001c0001t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2050+6148_2050+614 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389946 | |||||||
chr12:7389948 | A | ATATATAT others(5): Show |
1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+6135_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389948 | |||||||
chr12:7389950 | A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0245 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2050+6144_2050+614 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389950 | |||||||
chr12:7389960 | T | A | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG00558.hp2 HG03831.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+6135A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(52): Show |
68 | HG00099.hp1 HG00609.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.2050+6133_2050+613 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATA | 48 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
53 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2050+6131_2050+613 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATA | 45 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(42): Show |
51 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.2050+6129_2050+613 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0179 others(1): Show |
4 | HG02040.hp2 NA18946.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2050+6127_2050+613 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(3): Show |
1 | a0004c0006t0003g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2050+6125_2050+613 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(5): Show |
1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2050+6123_2050+613 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(7): Show |
1 | a0001c0041t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2050+6121_2050+613 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(9): Show |
2 | a0010c0018t0001g0344 a0010c0018t0002g0345 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2050+6119_2050+613 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2050+6134_2050+613 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(23): Show |
1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2050+6134_2050+613 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389960 | T | TTATATAT others(9): Show |
8 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(5): Show |
9 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2050+6134_2050+613 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389960 | |||||||
chr12:7389962 | A | ATATATAT others(6): Show |
1 | a0002c0003t0001g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2050+6120_2050+613 others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389962 | |||||||
chr12:7389962 | A | ATATATAT others(5): Show |
69 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0036 others(66): Show |
72 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.2050+6132_2050+613 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389962 | |||||||
chr12:7389964 | A | ATATATAT others(3): Show |
1 | a0002c0003t0003g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2050+6130_2050+613 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7389964 | |||||||
chr12:7390128 | C | T | 87 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(84): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2050+5967G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390128 | |||||||
chr12:7390212 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
279 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.2050+5883T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390212 | |||||||
chr12:7390865 | A | G | 1 | a0001c0004t0002g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2050+5230T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7390865 | |||||||
chr12:7391013 | C | T | 1 | a0001c0002t0001g0280 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2050+5082G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391013 | |||||||
chr12:7391019 | A | G | 1 | a0004c0028t0001g0126 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2050+5076T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391019 | |||||||
chr12:7391420 | T | C | 1 | a0006c0009t0002g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+4675A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391420 | |||||||
chr12:7391542 | C | T | 19 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(16): Show |
20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+4553G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391542 | |||||||
chr12:7391655 | G | A | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2050+4440C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391655 | |||||||
chr12:7391659 | G | T | 4 | a0001c0001t0002g0231 a0001c0007t0001g0104 a0001c0008t0001g0232 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+4436C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391659 | |||||||
chr12:7391712 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2050+4383A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391712 | |||||||
chr12:7391765 | G | A | 56 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(53): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+4330C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391765 | |||||||
chr12:7391805 | C | A | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+4290G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391805 | |||||||
chr12:7391830 | C | T | 56 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(53): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+4265G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391830 | |||||||
chr12:7391990 | CCACT | C | 87 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(84): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.2050+4101_2050+410 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391990 | |||||||
chr12:7391992 | A | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(83): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.2050+4103T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7391992 | |||||||
chr12:7392100 | C | T | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2050+3995G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392100 | |||||||
chr12:7392116 | T | C | 19 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(16): Show |
20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+3979A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392116 | |||||||
chr12:7392121 | AT | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.2050+3973delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392121 | |||||||
chr12:7392224 | C | T | 56 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(53): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.2050+3871G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392224 | |||||||
chr12:7392230 | G | C | 2 | a0006c0009t0002g0013 a0006c0034t0001g0123 |
3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2050+3865C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392230 | |||||||
chr12:7392238 | C | T | 1 | a0001c0002t0001g0320 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2050+3857G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392238 | |||||||
chr12:7392248 | T | C | 1 | a0001c0002t0001g0320 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2050+3847A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392248 | |||||||
chr12:7392335 | A | G | 19 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(16): Show |
20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.2050+3760T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392335 | |||||||
chr12:7392349 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2050+3746T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392349 | |||||||
chr12:7392418 | T | G | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2050+3677A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392418 | |||||||
chr12:7392460 | C | T | 1 | a0002c0003t0001g0045 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2050+3635G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392460 | |||||||
chr12:7392663 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2050+3432A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392663 | |||||||
chr12:7392896 | C | T | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+3199G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392896 | |||||||
chr12:7392914 | A | G | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0025c0035t0002g0227 |
3 | NA18950.hp2 NA18994.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2050+3181T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392914 | |||||||
chr12:7392998 | G | T | 2 | a0003c0005t0001g0008 a0003c0005t0001g0069 |
3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2050+3097C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7392998 | |||||||
chr12:7393175 | A | C | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2050+2920T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393175 | |||||||
chr12:7393191 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2050+2904C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393191 | |||||||
chr12:7393231 | A | G | 5 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(2): Show |
7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+2864T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393231 | |||||||
chr12:7393309 | G | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2050+2786C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393309 | |||||||
chr12:7393329 | T | C | 5 | a0001c0002t0001g0002 a0001c0002t0001g0102 a0001c0002t0001g0269 others(2): Show |
8 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2050+2766A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393329 | |||||||
chr12:7393853 | C | T | 4 | a0001c0002t0001g0248 a0001c0002t0001g0260 a0001c0002t0001g0273 others(1): Show |
4 | NA18951.hp2 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050+2242G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393853 | |||||||
chr12:7393975 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+2120G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7393975 | |||||||
chr12:7394081 | G | A | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050+2014C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394081 | |||||||
chr12:7394106 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2050+1989G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394106 | |||||||
chr12:7394123 | A | AC | 86 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(83): Show |
90 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.2050+1971_2050+197 others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394123 | |||||||
chr12:7394123 | A | C | 1 | a0006c0009t0002g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2050+1972T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394123 | |||||||
chr12:7394474 | T | C | 62 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(59): Show |
68 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.2050+1621A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394474 | |||||||
chr12:7394695 | C | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2050+1400G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394695 | |||||||
chr12:7394774 | G | T | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2050+1321C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394774 | |||||||
chr12:7394868 | G | C | 1 | a0001c0002t0001g0269 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2050+1227C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7394868 | |||||||
chr12:7395158 | G | A | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2050+937C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395158 | |||||||
chr12:7395179 | G | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | NA18943.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2050+916C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395179 | |||||||
chr12:7395358 | A | AC | 11 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0133 others(8): Show |
18 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2050+736dupG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395358 | |||||||
chr12:7395579 | A | G | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2050+516T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395579 | |||||||
chr12:7395587 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0002g0218 a0001c0001t0003g0221 |
3 | HG00735.hp2 HG02148.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2050+508C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7395587 | |||||||
chr12:7396017 | TACTG | T | 10 | a0001c0002t0001g0251 a0001c0002t0001g0271 a0001c0002t0001g0272 others(7): Show |
11 | HG00408.hp2 NA18947.hp1 NA18965.hp2 others(8): Show |
intron_variant | MODIFIER | c.2050+74_2050+77del others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 8/19 | chr12 | 7396017 | |||||||
chr12:7396494 | C | A | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1730-79G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396494 | |||||||
chr12:7396494 | C | T | 1 | a0001c0004t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1730-79G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396494 | |||||||
chr12:7396495 | C | G | 87 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(84): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1730-80G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396495 | |||||||
chr12:7396559 | C | G | 1 | a0001c0001t0001g0181 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1730-144G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396559 | |||||||
chr12:7396629 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1730-214A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396629 | |||||||
chr12:7396742 | C | G | 1 | a0001c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1730-327G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396742 | |||||||
chr12:7396770 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1730-355G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396770 | |||||||
chr12:7396856 | C | A | 56 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(53): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1730-441G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | |||||||
chr12:7396856 | C | CAGAG | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(56): Show |
70 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.1730-445_1730-442d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | |||||||
chr12:7396856 | C | G | 4 | a0001c0004t0001g0120 a0001c0004t0001g0341 a0001c0004t0002g0121 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1730-441G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396856 | |||||||
chr12:7396874 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(57): Show |
71 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.1730-459T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396874 | |||||||
chr12:7396924 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.1730-509G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7396924 | |||||||
chr12:7397083 | A | C | 1 | a0004c0006t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1730-668T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397083 | |||||||
chr12:7397083 | A | G | 15 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(12): Show |
17 | HG00099.hp1 HG00140.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1730-668T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397083 | |||||||
chr12:7397166 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0002g0202 |
2 | HG00558.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1730-751G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397166 | |||||||
chr12:7397184 | T | C | 19 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(16): Show |
20 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1730-769A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397184 | |||||||
chr12:7397294 | A | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(53): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.1730-879T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397294 | |||||||
chr12:7397346 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1729+918G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397346 | |||||||
chr12:7397536 | AC | A | 3 | a0001c0007t0001g0104 a0001c0008t0001g0232 a0001c0008t0001g0238 |
3 | HG03041.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1729+727delG | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397536 | |||||||
chr12:7397576 | C | A | 3 | a0002c0003t0001g0041 a0002c0003t0002g0042 a0002c0032t0001g0043 |
3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1729+688G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397576 | |||||||
chr12:7397590 | G | A | 87 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(84): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1729+674C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397590 | |||||||
chr12:7397925 | G | C | 3 | a0002c0003t0001g0041 a0002c0003t0002g0042 a0002c0032t0001g0043 |
3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1729+339C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 7/19 | chr12 | 7397925 | |||||||
chr12:7398626 | G | C | 87 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(84): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1409-42C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398626 | |||||||
chr12:7398711 | A | G | 87 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(84): Show |
91 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.1409-127T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398711 | |||||||
chr12:7398760 | G | A | 1 | a0001c0002t0001g0275 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1409-176C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398760 | |||||||
chr12:7398792 | G | A | 2 | a0010c0018t0001g0344 a0010c0018t0002g0345 |
2 | HG01261.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1409-208C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7398792 | |||||||
chr12:7399143 | TCTTC | T | 3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1409-563_1409-560d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399143 | |||||||
chr12:7399172 | C | T | 1 | a0023c0031t0001g0060 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1409-588G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399172 | |||||||
chr12:7399207 | CT | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.1409-624delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399207 | |||||||
chr12:7399300 | C | CCT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
277 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.1409-718_1409-717d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399300 | |||||||
chr12:7399319 | TTC | T | 32 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(29): Show |
34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-737_1409-736d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399319 | |||||||
chr12:7399321 | C | CTCTCTCT others(8): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1409-752_1409-738d others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399321 | |||||||
chr12:7399321 | CTCTCTCT others(8): Show |
C | 8 | a0004c0006t0001g0328 a0004c0006t0001g0329 a0004c0006t0001g0334 others(5): Show |
8 | HG00673.hp2 HG03669.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.1409-752_1409-738d others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399321 | |||||||
chr12:7399389 | TTTTC | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
28 | HG00544.hp2 HG00609.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1409-809_1409-806d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399389 | |||||||
chr12:7399430 | T | TCTTCTTC others(83): Show |
1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1409-847_1409-846i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | |||||||
chr12:7399430 | T | TCTTCTTC others(41): Show |
182 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(179): Show |
193 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.1409-894_1409-847d others(50): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | |||||||
chr12:7399430 | T | TCTTCTTC others(83): Show |
2 | a0001c0002t0001g0256 a0001c0002t0001g0270 |
2 | NA19063.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1409-847_1409-846i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | |||||||
chr12:7399430 | T | TCTTCTTC others(89): Show |
74 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(71): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.1409-847_1409-846i others(98): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399430 | |||||||
chr12:7399441 | C | CTCTTCCT others(83): Show |
1 | a0001c0025t0002g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1409-858_1409-857i others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399441 | |||||||
chr12:7399550 | G | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(35): Show |
41 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1409-966C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399550 | |||||||
chr12:7399550 | GCTTT | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0108 others(18): Show |
24 | HG00558.hp2 HG01358.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.1409-970_1409-967d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399550 | |||||||
chr12:7399554 | T | G | 36 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(33): Show |
39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-970A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399554 | |||||||
chr12:7399554 | T | TCTTTCTT others(2): Show |
3 | a0001c0002t0001g0287 a0001c0002t0001g0288 a0002c0003t0001g0065 |
3 | HG01975.hp1 HG01978.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1409-979_1409-971d others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399554 | |||||||
chr12:7399584 | C | T | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1409-1000G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399584 | |||||||
chr12:7399703 | T | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1409-1119A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399703 | |||||||
chr12:7399881 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1409-1297G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7399881 | |||||||
chr12:7400017 | C | A | 84 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1409-1433G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400017 | |||||||
chr12:7400259 | A | G | 85 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(82): Show |
89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1675T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400259 | |||||||
chr12:7400325 | C | T | 85 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(82): Show |
89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1741G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400325 | |||||||
chr12:7400455 | G | T | 85 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(82): Show |
89 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(86): Show |
intron_variant | MODIFIER | c.1409-1871C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400455 | |||||||
chr12:7400614 | C | T | 1 | a0001c0002t0001g0269 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1409-2030G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400614 | |||||||
chr12:7400720 | A | G | 1 | a0002c0003t0001g0059 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1409-2136T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400720 | |||||||
chr12:7400734 | T | C | 1 | a0001c0002t0001g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1409-2150A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400734 | |||||||
chr12:7400899 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1409-2315A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400899 | |||||||
chr12:7400951 | A | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-2367T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400951 | |||||||
chr12:7400968 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1409-2384G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7400968 | |||||||
chr12:7401029 | G | C | 86 | a0001c0004t0002g0322 a0002c0003t0001g0007 a0002c0003t0001g0009 others(83): Show |
90 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1409-2445C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401029 | |||||||
chr12:7401039 | A | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1409-2455T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401039 | |||||||
chr12:7401101 | A | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1408+2434T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401101 | |||||||
chr12:7401145 | T | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+2390A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401145 | |||||||
chr12:7401223 | C | A | 85 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.1408+2312G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401223 | |||||||
chr12:7401645 | G | A | 1 | a0004c0006t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1408+1890C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401645 | |||||||
chr12:7401790 | A | T | 1 | a0002c0003t0002g0056 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1408+1745T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401790 | |||||||
chr12:7401792 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1408+1743G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401792 | |||||||
chr12:7401816 | AT | A | 8 | a0001c0002t0001g0028 a0001c0002t0001g0286 a0001c0002t0001g0287 others(5): Show |
8 | HG01975.hp1 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1408+1718delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7401816 | |||||||
chr12:7402004 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1408+1531G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402004 | |||||||
chr12:7402190 | A | T | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1408+1345T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402190 | |||||||
chr12:7402362 | A | G | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+1173T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402362 | |||||||
chr12:7402369 | T | TTG | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.1408+1164_1408+116 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402369 | |||||||
chr12:7402638 | A | AT | 12 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(9): Show |
13 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.1408+896dupA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402638 | |||||||
chr12:7402638 | AT | A | 99 | a0001c0001t0001g0020 a0001c0001t0001g0194 a0001c0001t0001g0197 others(96): Show |
106 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.1408+896delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402638 | |||||||
chr12:7402820 | G | C | 81 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(78): Show |
84 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.1408+715C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402820 | |||||||
chr12:7402921 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1408+614G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402921 | |||||||
chr12:7402930 | G | A | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1408+605C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7402930 | |||||||
chr12:7403040 | A | G | 88 | a0001c0001t0001g0222 a0001c0002t0001g0002 a0001c0002t0001g0010 others(85): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.1408+495T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403040 | |||||||
chr12:7403100 | A | G | 1 | a0001c0002t0001g0298 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1408+435T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403100 | |||||||
chr12:7403198 | TA | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
279 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.1408+336delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403198 | |||||||
chr12:7403295 | G | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408+240C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403295 | |||||||
chr12:7403375 | T | C | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+160A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403375 | |||||||
chr12:7403505 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1408+30C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 6/19 | chr12 | 7403505 | |||||||
chr12:7403863 | G | A | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.1088-8C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7403863 | |||||||
chr12:7404007 | AATTTTAA others(17): Show |
A | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1088-176_1088-153d others(26): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404007 | |||||||
chr12:7404194 | A | G | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088-339T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404194 | |||||||
chr12:7404370 | T | TTCTCATA others(330): Show |
1 | a0001c0004t0001g0312 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1088-516_1088-515i others(339): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404370 | |||||||
chr12:7404370 | T | TTCTCATA others(340): Show |
1 | a0001c0004t0001g0311 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1088-516_1088-515i others(349): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404370 | |||||||
chr12:7404377 | A | G | 1 | a0004c0006t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1088-522T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404377 | |||||||
chr12:7404388 | C | T | 1 | a0001c0002t0001g0251 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1088-533G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404388 | |||||||
chr12:7404487 | C | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1088-632G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404487 | |||||||
chr12:7404538 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1088-683T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404538 | |||||||
chr12:7404622 | T | G | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1088-767A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404622 | |||||||
chr12:7404653 | C | T | 6 | a0001c0001t0001g0237 a0001c0001t0002g0236 a0001c0001t0003g0021 others(3): Show |
7 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1088-798G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404653 | |||||||
chr12:7404876 | T | C | 1 | a0002c0032t0001g0043 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1088-1021A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404876 | |||||||
chr12:7404896 | G | C | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1088-1041C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404896 | |||||||
chr12:7404966 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1088-1111A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7404966 | |||||||
chr12:7405039 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1088-1184C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405039 | |||||||
chr12:7405158 | T | C | 11 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(8): Show |
12 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.1088-1303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405158 | |||||||
chr12:7405229 | T | C | 1 | a0002c0003t0001g0055 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1087+1303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405229 | |||||||
chr12:7405283 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
183 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.1087+1249A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405283 | |||||||
chr12:7405412 | T | C | 1 | a0003c0005t0001g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1087+1120A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405412 | |||||||
chr12:7405563 | G | A | 4 | a0001c0001t0002g0231 a0001c0007t0001g0104 a0001c0008t0001g0232 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+969C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405563 | |||||||
chr12:7405979 | T | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+553A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7405979 | |||||||
chr12:7406410 | A | T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+122T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 5/19 | chr12 | 7406410 | |||||||
chr12:7406991 | C | A | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-139G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7406991 | |||||||
chr12:7407171 | A | T | 1 | a0024c0022t0001g0268 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.767-319T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407171 | |||||||
chr12:7407205 | G | A | 58 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(55): Show |
64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.767-353C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407205 | |||||||
chr12:7407214 | T | G | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.767-362A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407214 | |||||||
chr12:7407328 | C | T | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-476G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407328 | |||||||
chr12:7407509 | G | T | 1 | a0001c0001t0003g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.767-657C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407509 | |||||||
chr12:7407541 | C | A | 3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.767-689G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407541 | |||||||
chr12:7407565 | T | A | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-713A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407565 | |||||||
chr12:7407652 | C | T | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-800G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407652 | |||||||
chr12:7407674 | C | T | 84 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(81): Show |
88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-822G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407674 | |||||||
chr12:7407688 | T | C | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-836A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407688 | |||||||
chr12:7407692 | G | C | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-840C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407692 | |||||||
chr12:7407782 | T | TAC | 67 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(64): Show |
80 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.767-932_767-931dup others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | |||||||
chr12:7407782 | T | TACAC | 17 | a0001c0001t0001g0233 a0001c0007t0001g0027 a0001c0007t0001g0163 others(14): Show |
19 | HG00140.hp2 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-934_767-931dup others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | |||||||
chr12:7407782 | TAC | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(29): Show |
37 | HG01099.hp1 HG01256.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.767-932_767-931del others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407782 | |||||||
chr12:7407816 | C | A | 58 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(55): Show |
64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.767-964G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407816 | |||||||
chr12:7407828 | T | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-976A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407828 | |||||||
chr12:7407872 | C | T | 71 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(68): Show |
74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.767-1020G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7407872 | |||||||
chr12:7408076 | C | CAT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(74): Show |
88 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.767-1226_767-1225d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408076 | |||||||
chr12:7408076 | CAT | C | 21 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0007t0001g0027 others(18): Show |
22 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.767-1226_767-1225d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408076 | |||||||
chr12:7408093 | A | ATATC | 84 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(81): Show |
88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-1242_767-1241i others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408093 | |||||||
chr12:7408205 | T | C | 1 | a0002c0003t0002g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.767-1353A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408205 | |||||||
chr12:7408388 | GTAT | G | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-1539_767-1537d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408388 | |||||||
chr12:7408432 | C | T | 84 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(81): Show |
88 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.767-1580G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408432 | |||||||
chr12:7408492 | G | T | 1 | a0001c0004t0001g0341 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.767-1640C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408492 | |||||||
chr12:7408615 | C | A | 4 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0009t0002g0200 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-1763G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408615 | |||||||
chr12:7408663 | C | T | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.767-1811G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408663 | |||||||
chr12:7408870 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(5): Show |
10 | HG00544.hp2 HG02056.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.767-2018C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7408870 | |||||||
chr12:7409109 | C | T | 1 | a0001c0004t0001g0303 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.767-2257G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409109 | |||||||
chr12:7409137 | C | T | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-2285G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409137 | |||||||
chr12:7409276 | G | A | 1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.767-2424C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409276 | |||||||
chr12:7409294 | T | C | 1 | a0004c0006t0001g0339 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.767-2442A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409294 | |||||||
chr12:7409423 | C | G | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-2571G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409423 | |||||||
chr12:7409478 | T | C | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.767-2626A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409478 | |||||||
chr12:7409651 | G | A | 1 | a0001c0004t0003g0308 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.767-2799C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7409651 | |||||||
chr12:7410018 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.767-3166A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410018 | |||||||
chr12:7410243 | A | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-3391T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410243 | |||||||
chr12:7410572 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-3720G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410572 | |||||||
chr12:7410573 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-3721G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410573 | |||||||
chr12:7410604 | C | CA | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-3753dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410604 | |||||||
chr12:7410604 | CA | C | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.767-3753delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410604 | |||||||
chr12:7410648 | G | A | 71 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(68): Show |
74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.767-3796C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410648 | |||||||
chr12:7410760 | G | T | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-3908C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410760 | |||||||
chr12:7410794 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-3942G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410794 | |||||||
chr12:7410813 | G | C | 2 | a0001c0002t0002g0024 a0001c0002t0002g0252 |
3 | HG01167.hp2 HG01361.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.767-3961C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410813 | |||||||
chr12:7410817 | G | A | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-3965C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7410817 | |||||||
chr12:7411539 | C | A | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-4687G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411539 | |||||||
chr12:7411671 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.767-4819T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411671 | |||||||
chr12:7411886 | A | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.767-5034T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411886 | |||||||
chr12:7411969 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-5117G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7411969 | |||||||
chr12:7412007 | A | G | 1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.767-5155T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412007 | |||||||
chr12:7412144 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-5292C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412144 | |||||||
chr12:7412162 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-5310G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412162 | |||||||
chr12:7412300 | T | C | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.767-5448A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412300 | |||||||
chr12:7412425 | T | C | 79 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(76): Show |
87 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.767-5573A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412425 | |||||||
chr12:7412620 | T | C | 79 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(76): Show |
87 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.767-5768A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412620 | |||||||
chr12:7412752 | C | T | 1 | a0003c0005t0001g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.767-5900G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412752 | |||||||
chr12:7412824 | C | T | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-5972G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412824 | |||||||
chr12:7412862 | C | T | 21 | a0002c0003t0001g0075 a0002c0003t0001g0077 a0002c0003t0001g0082 others(18): Show |
21 | HG00738.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.767-6010G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412862 | |||||||
chr12:7412988 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-6136G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7412988 | |||||||
chr12:7413011 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.767-6159C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413011 | |||||||
chr12:7413044 | C | T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6192G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413044 | |||||||
chr12:7413091 | C | CA | 64 | a0001c0001t0001g0115 a0001c0001t0001g0133 a0001c0001t0001g0139 others(61): Show |
67 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.767-6240dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | |||||||
chr12:7413091 | C | CAA | 77 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0108 others(74): Show |
83 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.767-6241_767-6240d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | |||||||
chr12:7413091 | C | CAAA | 6 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0191 others(3): Show |
6 | HG01358.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-6242_767-6240d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | |||||||
chr12:7413091 | CAAAAAAA others(5): Show |
C | 4 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6251_767-6240d others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413091 | |||||||
chr12:7413311 | A | G | 12 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(9): Show |
13 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.767-6459T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413311 | |||||||
chr12:7413534 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-6682G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413534 | |||||||
chr12:7413552 | C | A | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-6700G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413552 | |||||||
chr12:7413562 | T | C | 1 | a0021c0021t0003g0258 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.767-6710A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413562 | |||||||
chr12:7413694 | C | T | 1 | a0003c0005t0001g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.767-6842G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413694 | |||||||
chr12:7413825 | T | C | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-6973A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7413825 | |||||||
chr12:7414266 | T | C | 2 | a0001c0001t0001g0237 a0001c0001t0003g0239 |
2 | HG00733.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.767-7414A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414266 | |||||||
chr12:7414325 | T | G | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.767-7473A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414325 | |||||||
chr12:7414545 | AAATT | A | 80 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.767-7697_767-7694d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414545 | |||||||
chr12:7414724 | A | G | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-7872T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414724 | |||||||
chr12:7414799 | G | A | 2 | a0002c0003t0002g0094 a0003c0005t0002g0093 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.767-7947C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414799 | |||||||
chr12:7414827 | A | G | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.767-7975T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414827 | |||||||
chr12:7414866 | T | A | 1 | a0008c0011t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.767-8014A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414866 | |||||||
chr12:7414960 | G | T | 85 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.767-8108C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7414960 | |||||||
chr12:7415141 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.767-8289A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415141 | |||||||
chr12:7415152 | T | C | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-8300A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415152 | |||||||
chr12:7415286 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.767-8434A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415286 | |||||||
chr12:7415608 | G | A | 1 | a0001c0002t0001g0289 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.767-8756C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415608 | |||||||
chr12:7415762 | G | A | 1 | a0001c0025t0002g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.767-8910C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415762 | |||||||
chr12:7415798 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.767-8946C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7415798 | |||||||
chr12:7416195 | A | G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-9343T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416195 | |||||||
chr12:7416428 | T | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-9576A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416428 | |||||||
chr12:7416664 | C | T | 80 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.767-9812G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416664 | |||||||
chr12:7416849 | C | T | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.767-9997G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7416849 | |||||||
chr12:7417039 | C | A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-10187G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417039 | |||||||
chr12:7417086 | T | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-10234A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417086 | |||||||
chr12:7417234 | C | G | 2 | a0003c0005t0002g0033 a0003c0005t0002g0034 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.767-10382G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417234 | |||||||
chr12:7417382 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-10530G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417382 | |||||||
chr12:7417422 | G | T | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.767-10570C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417422 | |||||||
chr12:7417476 | C | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(83): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.767-10624G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417476 | |||||||
chr12:7417802 | G | A | 1 | a0004c0006t0001g0335 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.767-10950C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417802 | |||||||
chr12:7417825 | T | A | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-10973A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417825 | |||||||
chr12:7417886 | G | A | 2 | a0001c0002t0001g0290 a0001c0002t0003g0291 |
2 | HG00099.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.767-11034C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417886 | |||||||
chr12:7417961 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.767-11109T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7417961 | |||||||
chr12:7418001 | T | TA | 139 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(136): Show |
148 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.767-11150dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418001 | |||||||
chr12:7418096 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-11244G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418096 | |||||||
chr12:7418117 | T | C | 1 | a0001c0004t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.767-11265A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418117 | |||||||
chr12:7418141 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.767-11289G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418141 | |||||||
chr12:7418234 | C | G | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.767-11382G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418234 | |||||||
chr12:7418322 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.767-11470T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418322 | |||||||
chr12:7418347 | C | G | 1 | a0001c0004t0002g0302 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.767-11495G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418347 | |||||||
chr12:7418351 | C | T | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-11499G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418351 | |||||||
chr12:7418416 | G | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-11564C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418416 | |||||||
chr12:7418861 | A | G | 4 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-12009T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418861 | |||||||
chr12:7418904 | A | G | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.767-12052T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418904 | |||||||
chr12:7418957 | G | T | 1 | a0003c0005t0001g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.767-12105C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7418957 | |||||||
chr12:7419021 | C | A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-12169G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419021 | |||||||
chr12:7419044 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.767-12192A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419044 | |||||||
chr12:7419114 | C | CAAAACAC others(300): Show |
1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.767-12263_767-1226 others(311): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419114 | |||||||
chr12:7419391 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.767-12539T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419391 | |||||||
chr12:7419409 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.767-12557A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419409 | |||||||
chr12:7419462 | C | T | 1 | a0003c0005t0001g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.767-12610G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419462 | |||||||
chr12:7419479 | T | C | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.767-12627A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419479 | |||||||
chr12:7419585 | T | C | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.767-12733A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419585 | |||||||
chr12:7419657 | G | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+12759C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419657 | |||||||
chr12:7419736 | G | A | 1 | a0015c0040t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.766+12680C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7419736 | |||||||
chr12:7420184 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.766+12232G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420184 | |||||||
chr12:7420375 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.766+12041T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420375 | |||||||
chr12:7420415 | C | G | 4 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+12001G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420415 | |||||||
chr12:7420460 | C | T | 3 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 |
4 | HG00639.hp2 HG01123.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11956G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420460 | |||||||
chr12:7420475 | T | A | 80 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.766+11941A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420475 | |||||||
chr12:7420519 | A | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+11897T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420519 | |||||||
chr12:7420550 | A | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(83): Show |
96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.766+11866T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420550 | |||||||
chr12:7420553 | C | G | 3 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 |
4 | HG00639.hp2 HG01123.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11863G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420553 | |||||||
chr12:7420757 | A | C | 1 | a0001c0001t0001g0233 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.766+11659T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420757 | |||||||
chr12:7420892 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.766+11524G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420892 | |||||||
chr12:7420902 | T | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0321 |
3 | NA18943.hp1 NA19009.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.766+11514A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420902 | |||||||
chr12:7420983 | T | TGGTATAT others(57): Show |
1 | a0016c0019t0001g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.766+11369_766+1143 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420983 | |||||||
chr12:7420998 | T | TATATATA others(77): Show |
1 | a0001c0001t0001g0129 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.766+11417_766+1141 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | |||||||
chr12:7420998 | T | TATATATA others(77): Show |
1 | a0001c0001t0001g0130 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.766+11417_766+1141 others(88): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | |||||||
chr12:7420998 | TATATATA others(19): Show |
T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11392_766+1141 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7420998 | |||||||
chr12:7421001 | ATATATAT others(79): Show |
A | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11329_766+1141 others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421001 | |||||||
chr12:7421022 | T | C | 1 | a0005c0014t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.766+11394A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421022 | |||||||
chr12:7421024 | C | CAT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(146): Show |
166 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.766+11390_766+1139 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | |||||||
chr12:7421024 | C | CATATATA others(23): Show |
1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.766+11391_766+1139 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | |||||||
chr12:7421024 | C | CATATATA others(29): Show |
1 | a0001c0007t0001g0027 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.766+11391_766+1139 others(40): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421024 | |||||||
chr12:7421025 | A | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11391T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421025 | |||||||
chr12:7421029 | ATATATAC others(13): Show |
A | 1 | a0001c0025t0002g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.766+11367_766+1138 others(24): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421029 | |||||||
chr12:7421030 | T | C | 2 | a0001c0002t0001g0277 a0001c0002t0002g0022 |
2 | NA18965.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.766+11386A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421030 | |||||||
chr12:7421034 | T | C | 1 | a0001c0004t0001g0341 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.766+11382A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421034 | |||||||
chr12:7421036 | C | T | 4 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11380G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421036 | |||||||
chr12:7421037 | G | A | 4 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11379C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421037 | |||||||
chr12:7421038 | T | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11378A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421038 | |||||||
chr12:7421039 | G | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11377C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421039 | |||||||
chr12:7421041 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.766+11374_766+1137 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421041 | |||||||
chr12:7421041 | A | G | 4 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0002g0218 others(1): Show |
4 | HG00735.hp2 HG03831.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+11375T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421041 | |||||||
chr12:7421045 | A | ATATACAT others(47): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0222 |
3 | HG02135.hp2 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(58): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATACAT others(107): Show |
2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(118): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATACAT others(79): Show |
1 | a0001c0001t0001g0108 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.766+11370_766+1137 others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATACAT others(51): Show |
2 | a0001c0001t0001g0106 a0001c0001t0002g0107 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(62): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATACAT others(49): Show |
44 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(41): Show |
49 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.766+11370_766+1137 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATACAT others(81): Show |
2 | a0001c0001t0001g0194 a0001c0001t0001g0203 |
2 | HG01952.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.766+11370_766+1137 others(92): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | ATATATAC others(51): Show |
1 | a0001c0001t0002g0006 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.766+11370_766+1137 others(62): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421045 | A | G | 3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+11371T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421045 | |||||||
chr12:7421047 | A | ATACATAT others(49): Show |
1 | a0004c0012t0002g0324 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.766+11368_766+1136 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421047 | |||||||
chr12:7421048 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.766+11368A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421048 | |||||||
chr12:7421049 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(102): Show |
122 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.766+11367C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | |||||||
chr12:7421049 | G | GTATATAC others(23): Show |
1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766+11366_766+1136 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | |||||||
chr12:7421049 | G | GTATATAC others(23): Show |
1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.766+11337_766+1136 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | |||||||
chr12:7421049 | G | GTATATAC others(139): Show |
2 | a0006c0009t0002g0013 a0006c0034t0001g0123 |
3 | HG01167.hp1 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.766+11366_766+1136 others(150): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | |||||||
chr12:7421049 | G | GTATATAC others(65): Show |
2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.766+11366_766+1136 others(76): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421049 | |||||||
chr12:7421050 | T | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.766+11366A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421050 | |||||||
chr12:7421055 | ACG | A | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11359_766+1136 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421055 | |||||||
chr12:7421056 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.766+11360G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421056 | |||||||
chr12:7421057 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(44): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11359C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421057 | G | GTA | 53 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(50): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.766+11357_766+1135 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421057 | G | GTATATAT others(49): Show |
1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(60): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421057 | G | GTATATAT others(87): Show |
1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(98): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421057 | G | GTATATAT others(27): Show |
1 | a0001c0001t0002g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766+11358_766+1135 others(38): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421057 | G | GTATATAT others(57): Show |
2 | a0001c0001t0001g0217 a0022c0036t0002g0214 |
2 | HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.766+11358_766+1135 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421057 | |||||||
chr12:7421062 | T | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(44): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11354A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421062 | |||||||
chr12:7421063 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(44): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11353T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421063 | |||||||
chr12:7421064 | T | C | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11352A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421064 | |||||||
chr12:7421064 | T | TGTATATA others(57): Show |
1 | a0001c0001t0001g0215 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.766+11351_766+1135 others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421064 | |||||||
chr12:7421065 | G | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11351C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421065 | |||||||
chr12:7421067 | A | G | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11349T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421067 | |||||||
chr12:7421073 | ACG | A | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11341_766+1134 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421073 | |||||||
chr12:7421073 | ACGTATAT others(41): Show |
A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(44): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11295_766+1134 others(52): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421073 | |||||||
chr12:7421074 | CGT | C | 14 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(11): Show |
15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.766+11340_766+1134 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421074 | |||||||
chr12:7421075 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.766+11341C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421075 | |||||||
chr12:7421077 | A | ATATATAC others(19): Show |
3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+11338_766+1133 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421077 | |||||||
chr12:7421077 | A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.766+11338_766+1133 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421077 | |||||||
chr12:7421080 | T | C | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11336A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421080 | |||||||
chr12:7421085 | ACG | A | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11329_766+1133 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421085 | |||||||
chr12:7421087 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.766+11329C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421087 | |||||||
chr12:7421089 | A | ATATATGT others(227): Show |
1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+11326_766+1132 others(238): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421089 | |||||||
chr12:7421093 | A | T | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11323T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421093 | |||||||
chr12:7421094 | T | C | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11322A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421094 | |||||||
chr12:7421095 | A | G | 77 | a0001c0007t0001g0163 a0001c0007t0002g0017 a0002c0003t0001g0007 others(74): Show |
81 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.766+11321T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421095 | |||||||
chr12:7421096 | T | TACGTATA others(109): Show |
1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11319_766+1132 others(120): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421096 | |||||||
chr12:7421097 | G | A | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.766+11319C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421097 | |||||||
chr12:7421105 | ACATTTGG others(9): Show |
A | 2 | a0001c0007t0001g0163 a0001c0007t0002g0017 |
3 | HG01256.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766+11295_766+1131 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421105 | |||||||
chr12:7421123 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.766+11293T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421123 | |||||||
chr12:7421139 | G | GTA | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.766+11275_766+1127 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421139 | |||||||
chr12:7421153 | A | T | 1 | a0002c0003t0001g0047 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.766+11263T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421153 | |||||||
chr12:7421154 | A | T | 2 | a0002c0003t0001g0097 a0002c0003t0001g0098 |
2 | NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.766+11262T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421154 | |||||||
chr12:7421195 | G | GTA | 5 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | NA18945.hp1 NA18952.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+11219_766+1122 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421195 | |||||||
chr12:7421241 | T | C | 1 | a0001c0002t0002g0263 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.766+11175A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421241 | |||||||
chr12:7421271 | A | ATG | 5 | a0002c0003t0001g0031 a0002c0003t0001g0075 a0003c0005t0001g0032 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+11143_766+1114 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421271 | |||||||
chr12:7421274 | T | C | 1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.766+11142A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421274 | |||||||
chr12:7421277 | GTA | G | 8 | a0001c0001t0002g0231 a0001c0007t0001g0104 a0001c0008t0001g0232 others(5): Show |
8 | HG02572.hp2 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+11137_766+1113 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421277 | |||||||
chr12:7421287 | A | ATG | 74 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(71): Show |
77 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.766+11127_766+1112 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421287 | |||||||
chr12:7421287 | A | G | 5 | a0002c0003t0001g0031 a0002c0003t0001g0075 a0003c0005t0001g0032 others(2): Show |
5 | HG02109.hp2 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+11129T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421287 | |||||||
chr12:7421291 | GTGTATAT others(47): Show |
G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+11071_766+1112 others(58): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421291 | |||||||
chr12:7421298 | TATGTATA others(39): Show |
T | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.766+11072_766+1111 others(50): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421298 | |||||||
chr12:7421304 | TATATACA others(74): Show |
T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11031_766+1111 others(85): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421304 | |||||||
chr12:7421328 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11088C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421328 | |||||||
chr12:7421329 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11087A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421329 | |||||||
chr12:7421330 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0220 |
2 | HG01975.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.766+11086T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421330 | |||||||
chr12:7421347 | G | GTA | 43 | a0002c0003t0001g0041 a0002c0003t0001g0047 a0002c0003t0001g0055 others(40): Show |
43 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.766+11067_766+1106 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421347 | |||||||
chr12:7421352 | T | C | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+11064A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421352 | |||||||
chr12:7421355 | ATGTG | A | 14 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(11): Show |
15 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+11057_766+1106 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421355 | |||||||
chr12:7421357 | G | A | 31 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(28): Show |
34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11059C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421357 | |||||||
chr12:7421359 | G | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11057C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421359 | |||||||
chr12:7421360 | T | C | 13 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(10): Show |
14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11056A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421360 | |||||||
chr12:7421361 | A | G | 31 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(28): Show |
34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11055T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421361 | |||||||
chr12:7421365 | A | G | 1 | a0003c0005t0001g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.766+11051T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421365 | |||||||
chr12:7421366 | TGTATATA others(37): Show |
T | 31 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(28): Show |
34 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.766+11006_766+1104 others(48): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421366 | |||||||
chr12:7421368 | T | TAC | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+11047_766+1104 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421368 | |||||||
chr12:7421370 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11046A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421370 | |||||||
chr12:7421372 | TATACATT others(31): Show |
T | 1 | a0003c0005t0001g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.766+11006_766+1104 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421372 | |||||||
chr12:7421375 | ACATTTGG others(31): Show |
A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+11003_766+1104 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421375 | |||||||
chr12:7421376 | CATTTGGA others(4): Show |
C | 43 | a0002c0003t0001g0041 a0002c0003t0001g0047 a0002c0003t0001g0055 others(40): Show |
43 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.766+11029_766+1103 others(15): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421376 | |||||||
chr12:7421378 | TTTGGA | T | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+11033_766+1103 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421378 | |||||||
chr12:7421379 | T | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11037A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421379 | |||||||
chr12:7421382 | G | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11034C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421382 | |||||||
chr12:7421385 | G | T | 13 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(10): Show |
14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11031C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421385 | |||||||
chr12:7421387 | T | C | 13 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(10): Show |
14 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+11029A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421387 | |||||||
chr12:7421396 | A | G | 63 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(60): Show |
69 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.766+11020T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421396 | |||||||
chr12:7421397 | T | C | 56 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(53): Show |
57 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+11019A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421397 | |||||||
chr12:7421398 | ATATATCT others(8): Show |
A | 1 | a0002c0003t0002g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.766+11003_766+1101 others(19): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421398 | |||||||
chr12:7421400 | ATATCTTC others(6): Show |
A | 42 | a0002c0003t0001g0041 a0002c0003t0001g0047 a0002c0003t0001g0055 others(39): Show |
42 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+11003_766+1101 others(17): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421400 | |||||||
chr12:7421403 | TCTTCCAA | T | 16 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(13): Show |
17 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.766+11006_766+1101 others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421403 | |||||||
chr12:7421404 | C | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11012G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421404 | |||||||
chr12:7421406 | T | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11010A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421406 | |||||||
chr12:7421408 | C | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11008G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421408 | |||||||
chr12:7421410 | A | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+11006T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421410 | |||||||
chr12:7421412 | T | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+11004A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421412 | |||||||
chr12:7421413 | G | A | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+11003C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421413 | |||||||
chr12:7421416 | T | C | 4 | a0001c0001t0002g0323 a0002c0003t0001g0041 a0002c0003t0002g0042 others(1): Show |
4 | HG02451.hp2 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+11000A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421416 | |||||||
chr12:7421416 | TATATACA others(17): Show |
T | 1 | a0001c0025t0002g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.766+10976_766+1099 others(28): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421416 | |||||||
chr12:7421420 | T | C | 1 | a0003c0005t0001g0072 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.766+10996A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421420 | |||||||
chr12:7421427 | A | G | 1 | a0002c0003t0002g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.766+10989T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421427 | |||||||
chr12:7421434 | TATATAC | T | 16 | a0001c0001t0001g0201 a0001c0001t0001g0233 a0001c0001t0001g0237 others(13): Show |
17 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.766+10976_766+1098 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421434 | |||||||
chr12:7421438 | TAC | T | 23 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(20): Show |
25 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.766+10976_766+1097 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421438 | |||||||
chr12:7421440 | C | CATATACA others(21): Show |
4 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0001g0211 others(1): Show |
4 | HG01975.hp2 HG02004.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10948_766+1097 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421440 | |||||||
chr12:7421440 | C | T | 2 | a0002c0003t0003g0058 a0002c0003t0003g0062 |
2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.766+10976G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421440 | |||||||
chr12:7421453 | G | A | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10963C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421453 | |||||||
chr12:7421454 | T | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.766+10962A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421454 | |||||||
chr12:7421456 | C | T | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10960G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421456 | |||||||
chr12:7421456 | CAT | C | 4 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0246 others(1): Show |
4 | HG00558.hp2 NA18964.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10958_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421456 | |||||||
chr12:7421458 | TATATACA others(37): Show |
T | 1 | a0002c0003t0001g0065 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.766+10914_766+1095 others(48): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421458 | |||||||
chr12:7421461 | A | ATG | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10954_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421461 | |||||||
chr12:7421461 | A | G | 2 | a0003c0033t0002g0128 a0009c0015t0001g0264 |
2 | HG01891.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.766+10955T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421461 | |||||||
chr12:7421462 | TAC | T | 7 | a0002c0003t0001g0031 a0003c0005t0002g0033 a0003c0005t0002g0034 others(4): Show |
7 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.766+10952_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421462 | |||||||
chr12:7421463 | A | G | 11 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(8): Show |
12 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10953T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421463 | |||||||
chr12:7421464 | C | CAT | 6 | a0001c0002t0002g0252 a0005c0013t0001g0243 a0005c0013t0001g0342 others(3): Show |
6 | HG01167.hp2 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10950_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | |||||||
chr12:7421464 | C | T | 11 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(8): Show |
12 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10952G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | |||||||
chr12:7421464 | CAT | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
24 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.766+10950_766+1095 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | |||||||
chr12:7421464 | CATAT | C | 76 | a0001c0001t0001g0020 a0001c0001t0001g0228 a0001c0002t0002g0263 others(73): Show |
80 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.766+10948_766+1095 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | |||||||
chr12:7421464 | CATATATA others(55): Show |
C | 3 | a0002c0003t0001g0041 a0002c0003t0002g0042 a0002c0032t0001g0043 |
3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766+10890_766+1095 others(66): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421464 | |||||||
chr12:7421466 | T | C | 11 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(8): Show |
12 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10950A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421466 | |||||||
chr12:7421467 | ATATATAC others(7): Show |
A | 1 | a0001c0002t0001g0259 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.766+10935_766+1094 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421467 | |||||||
chr12:7421468 | T | C | 7 | a0002c0003t0001g0031 a0003c0005t0002g0033 a0003c0005t0002g0034 others(4): Show |
7 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.766+10948A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | |||||||
chr12:7421468 | T | TAC | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10947_766+1094 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | |||||||
chr12:7421468 | T | TATATATA others(1): Show |
3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0007c0010t0001g0177 |
3 | HG01433.hp2 HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10947_766+1094 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421468 | |||||||
chr12:7421470 | T | C | 3 | a0001c0001t0001g0210 a0001c0002t0003g0261 a0005c0030t0003g0301 |
3 | HG00140.hp1 HG01243.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.766+10946A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421470 | |||||||
chr12:7421471 | A | G | 1 | a0001c0008t0001g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.766+10945T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421471 | |||||||
chr12:7421472 | TAC | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(37): Show |
51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10942_766+1094 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421472 | |||||||
chr12:7421474 | CATAT | C | 17 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(14): Show |
17 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.766+10938_766+1094 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421474 | |||||||
chr12:7421477 | ATATG | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0159 others(3): Show |
6 | HG02148.hp1 NA18954.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10935_766+1093 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421477 | |||||||
chr12:7421478 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(37): Show |
51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10938A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421478 | |||||||
chr12:7421481 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(37): Show |
51 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.766+10935C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421481 | |||||||
chr12:7421484 | C | CATATATA others(21): Show |
1 | a0001c0001t0001g0153 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.766+10931_766+1093 others(32): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421484 | |||||||
chr12:7421486 | T | C | 1 | a0001c0008t0001g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.766+10930A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | |||||||
chr12:7421486 | T | TATATAC | 5 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(2): Show |
7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+10924_766+1092 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | |||||||
chr12:7421486 | TATATACA others(9): Show |
T | 28 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(25): Show |
30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10914_766+1092 others(20): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421486 | |||||||
chr12:7421490 | T | C | 11 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(8): Show |
12 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10926A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421490 | |||||||
chr12:7421491 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10925T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421491 | |||||||
chr12:7421492 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10924G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421492 | |||||||
chr12:7421492 | CATATATG others(27): Show |
C | 41 | a0002c0003t0001g0047 a0002c0003t0001g0055 a0002c0003t0001g0075 others(38): Show |
42 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+10890_766+1092 others(38): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421492 | |||||||
chr12:7421494 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10922A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | |||||||
chr12:7421494 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+10921_766+1092 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | |||||||
chr12:7421494 | TATATGTA others(7): Show |
T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
22 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+10908_766+1092 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421494 | |||||||
chr12:7421496 | TATGTACA others(5): Show |
T | 27 | a0001c0002t0001g0255 a0001c0002t0001g0260 a0001c0002t0002g0263 others(24): Show |
29 | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.766+10908_766+1091 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421496 | |||||||
chr12:7421499 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(116): Show |
138 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.766+10917C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421499 | |||||||
chr12:7421502 | C | CAT | 5 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+10912_766+1091 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | |||||||
chr12:7421502 | C | CATATATG others(5): Show |
2 | a0001c0001t0001g0108 a0001c0001t0002g0107 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.766+10913_766+1091 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | |||||||
chr12:7421502 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+10914G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421502 | |||||||
chr12:7421504 | T | TATATAC | 5 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(2): Show |
7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+10911_766+1091 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421504 | |||||||
chr12:7421505 | A | G | 1 | a0004c0006t0001g0328 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.766+10911T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421505 | |||||||
chr12:7421506 | T | TATGTAC | 3 | a0001c0001t0001g0020 a0001c0001t0001g0106 a0001c0001t0001g0228 |
4 | HG02055.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10909_766+1091 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421506 | |||||||
chr12:7421506 | TAC | T | 4 | a0001c0002t0001g0259 a0002c0003t0001g0091 a0003c0005t0001g0057 others(1): Show |
4 | HG01891.hp2 HG03471.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10908_766+1090 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421506 | |||||||
chr12:7421508 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(51): Show |
68 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.766+10908G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421508 | |||||||
chr12:7421511 | A | ATATACAT others(5): Show |
1 | a0004c0006t0001g0328 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.766+10904_766+1090 others(16): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421511 | |||||||
chr12:7421511 | A | G | 2 | a0002c0003t0001g0091 a0003c0005t0001g0057 |
2 | HG03471.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.766+10905T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421511 | |||||||
chr12:7421512 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10904A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421512 | |||||||
chr12:7421516 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10900A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421516 | |||||||
chr12:7421521 | G | A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+10895C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421521 | |||||||
chr12:7421522 | TAC | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(43): Show |
57 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.766+10892_766+1089 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421522 | |||||||
chr12:7421523 | A | G | 11 | a0001c0002t0001g0251 a0001c0002t0001g0271 a0001c0002t0001g0272 others(8): Show |
12 | HG00408.hp2 HG00423.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10893T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421523 | |||||||
chr12:7421526 | T | C | 6 | a0002c0003t0001g0031 a0002c0003t0001g0091 a0003c0005t0001g0032 others(3): Show |
6 | HG02615.hp2 HG02895.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+10890A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421526 | |||||||
chr12:7421526 | T | TATAC | 3 | a0001c0001t0001g0020 a0001c0001t0001g0220 a0001c0001t0001g0228 |
4 | HG02004.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10889_766+1089 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421526 | |||||||
chr12:7421529 | A | ATGTACAT others(53): Show |
1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.766+10886_766+1088 others(64): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421529 | |||||||
chr12:7421536 | TACGTACA others(1): Show |
T | 9 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10872_766+1087 others(12): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421536 | |||||||
chr12:7421537 | ACG | A | 13 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(10): Show |
16 | HG00140.hp1 HG00544.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766+10877_766+1087 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421537 | |||||||
chr12:7421538 | C | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
239 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(236): Show |
intron_variant | MODIFIER | c.766+10878G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421538 | |||||||
chr12:7421538 | CGTACACA others(25): Show |
C | 4 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10846_766+1087 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421538 | |||||||
chr12:7421539 | G | A | 2 | a0001c0001t0001g0152 a0007c0010t0001g0177 |
2 | HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10877C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421539 | |||||||
chr12:7421540 | TAC | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
151 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.766+10874_766+1087 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421540 | |||||||
chr12:7421542 | C | CACACATA others(19): Show |
2 | a0001c0001t0001g0152 a0007c0010t0001g0177 |
2 | HG01993.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.766+10873_766+1087 others(30): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | |||||||
chr12:7421542 | C | CATATACA others(31): Show |
4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG03831.hp1 NA18966.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10873_766+1087 others(42): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | |||||||
chr12:7421542 | C | CATATACA others(25): Show |
1 | a0001c0004t0002g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.766+10873_766+1087 others(36): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | |||||||
chr12:7421542 | C | T | 13 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(10): Show |
16 | HG00140.hp1 HG00544.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.766+10874G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421542 | |||||||
chr12:7421544 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0228 a0003c0033t0002g0128 others(4): Show |
8 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+10872G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421544 | |||||||
chr12:7421547 | A | G | 8 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10869T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421547 | |||||||
chr12:7421550 | C | T | 8 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10866G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421550 | |||||||
chr12:7421556 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10860G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421556 | |||||||
chr12:7421557 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10859T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421557 | |||||||
chr12:7421559 | A | G | 71 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(68): Show |
74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.766+10857T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421559 | |||||||
chr12:7421560 | T | C | 1 | a0001c0002t0002g0292 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.766+10856A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421560 | |||||||
chr12:7421560 | TATGTACA others(7): Show |
T | 2 | a0003c0005t0001g0008 a0003c0005t0001g0069 |
3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.766+10842_766+1085 others(18): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421560 | |||||||
chr12:7421562 | T | C | 11 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(8): Show |
12 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.766+10854A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421562 | |||||||
chr12:7421563 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10853C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421563 | |||||||
chr12:7421565 | A | G | 5 | a0001c0001t0001g0183 a0007c0010t0001g0018 a0007c0010t0001g0177 others(2): Show |
6 | HG02027.hp2 NA18747.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10851T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421565 | |||||||
chr12:7421568 | T | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10848A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421568 | |||||||
chr12:7421570 | TATAC | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10842_766+1084 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421570 | |||||||
chr12:7421573 | A | G | 4 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10843T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421573 | |||||||
chr12:7421574 | C | CATATACA others(3): Show |
4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10841_766+1084 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421574 | |||||||
chr12:7421574 | C | T | 4 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+10842G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421574 | |||||||
chr12:7421576 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.766+10840A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421576 | |||||||
chr12:7421576 | T | TATAC | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
176 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.766+10839_766+1084 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421576 | |||||||
chr12:7421577 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10839C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421577 | |||||||
chr12:7421582 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
183 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.766+10834A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421582 | |||||||
chr12:7421584 | TATAC | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10828_766+1083 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421584 | |||||||
chr12:7421588 | CATATACA others(29): Show |
C | 98 | a0001c0001t0001g0108 a0001c0001t0001g0233 a0001c0001t0001g0237 others(95): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.766+10792_766+1082 others(40): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421588 | |||||||
chr12:7421590 | T | A | 6 | a0004c0006t0001g0328 a0004c0006t0001g0329 a0004c0006t0001g0337 others(3): Show |
6 | HG00673.hp2 NA18612.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10826A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421590 | |||||||
chr12:7421591 | A | G | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10825T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421591 | |||||||
chr12:7421597 | A | G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10819T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421597 | |||||||
chr12:7421600 | TGTAC | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10812_766+1081 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421600 | |||||||
chr12:7421606 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
182 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.766+10810G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421606 | |||||||
chr12:7421609 | A | G | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10807T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421609 | |||||||
chr12:7421610 | TACATATA others(23): Show |
T | 48 | a0002c0003t0001g0031 a0002c0003t0001g0041 a0002c0003t0001g0047 others(45): Show |
48 | HG00423.hp1 HG00738.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.766+10776_766+1080 others(34): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421610 | |||||||
chr12:7421613 | A | ATG | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
181 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.766+10802_766+1080 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421613 | |||||||
chr12:7421616 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
181 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.766+10800A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421616 | |||||||
chr12:7421616 | T | TAC | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10799_766+1080 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421616 | |||||||
chr12:7421618 | T | C | 30 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(27): Show |
33 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.766+10798A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421618 | |||||||
chr12:7421618 | TGTAC | T | 9 | a0001c0001t0001g0153 a0001c0001t0001g0194 a0001c0001t0001g0197 others(6): Show |
9 | HG01433.hp2 HG01952.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10794_766+1079 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421618 | |||||||
chr12:7421619 | G | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
215 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.766+10797C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421619 | |||||||
chr12:7421622 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
215 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(212): Show |
intron_variant | MODIFIER | c.766+10794G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421622 | |||||||
chr12:7421624 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
194 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(191): Show |
intron_variant | MODIFIER | c.766+10792A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | |||||||
chr12:7421624 | T | TATATACA others(85): Show |
1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10791_766+1079 others(96): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | |||||||
chr12:7421624 | TATATACA others(11): Show |
T | 1 | a0001c0002t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10774_766+1079 others(22): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421624 | |||||||
chr12:7421625 | A | G | 27 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(24): Show |
30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10791T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421625 | |||||||
chr12:7421626 | T | C | 1 | a0005c0014t0001g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.766+10790A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421626 | |||||||
chr12:7421628 | T | C | 27 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(24): Show |
30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10788A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421628 | |||||||
chr12:7421634 | TATGTAC | T | 27 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(24): Show |
30 | HG00408.hp1 HG00673.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.766+10776_766+1078 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421634 | |||||||
chr12:7421640 | C | CACATAT | 3 | a0003c0033t0002g0128 a0011c0042t0002g0346 a0011c0043t0001g0343 |
3 | HG01891.hp2 HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.766+10770_766+1077 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421640 | |||||||
chr12:7421654 | T | C | 1 | a0001c0002t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10762A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421654 | |||||||
chr12:7421657 | A | G | 1 | a0001c0002t0001g0296 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.766+10759T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421657 | |||||||
chr12:7421686 | T | C | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10730A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421686 | |||||||
chr12:7421686 | TATAC | T | 4 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10726_766+1072 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421686 | |||||||
chr12:7421720 | C | T | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.766+10696G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421720 | |||||||
chr12:7421745 | GTA | G | 5 | a0001c0001t0002g0323 a0001c0002t0001g0293 a0003c0033t0002g0128 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+10669_766+1067 others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | |||||||
chr12:7421745 | GTATA | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.766+10667_766+1067 others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | |||||||
chr12:7421745 | GTATATA | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0138 others(4): Show |
9 | HG01358.hp1 HG02280.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.766+10665_766+1067 others(10): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421745 | |||||||
chr12:7421747 | A | G | 7 | a0001c0007t0001g0131 a0002c0003t0001g0096 a0003c0005t0001g0050 others(4): Show |
8 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+10669T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421747 | |||||||
chr12:7421749 | A | G | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+10667T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421749 | |||||||
chr12:7421760 | TATATA | T | 5 | a0001c0001t0001g0233 a0001c0001t0002g0231 a0001c0007t0001g0104 others(2): Show |
5 | HG00140.hp2 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.766+10651_766+1065 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421760 | |||||||
chr12:7421760 | TATATATA others(2): Show |
T | 17 | a0002c0003t0001g0031 a0002c0003t0001g0046 a0002c0003t0001g0055 others(14): Show |
17 | HG00408.hp1 HG01243.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.766+10647_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421760 | |||||||
chr12:7421761 | ATATATAT others(2): Show |
A | 54 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(51): Show |
57 | HG00423.hp1 HG00673.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.766+10646_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421761 | |||||||
chr12:7421761 | ATATATAT others(3): Show |
A | 1 | a0002c0003t0002g0078 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.766+10645_766+1065 others(14): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421761 | |||||||
chr12:7421762 | TATATA | T | 9 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0237 others(6): Show |
10 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.766+10649_766+1065 others(9): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421762 | |||||||
chr12:7421762 | TATATATA | T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10647_766+1065 others(11): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421762 | |||||||
chr12:7421763 | ATATATAT others(2): Show |
A | 3 | a0002c0003t0001g0047 a0002c0003t0002g0079 a0003c0005t0003g0054 |
3 | HG00738.hp1 HG02129.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.766+10644_766+1065 others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421763 | |||||||
chr12:7421764 | TATA | T | 3 | a0006c0009t0001g0118 a0006c0009t0002g0013 a0006c0034t0001g0123 |
4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+10649_766+1065 others(7): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421764 | |||||||
chr12:7421765 | A | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0110 others(47): Show |
58 | HG00099.hp2 HG00423.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.766+10651T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421765 | |||||||
chr12:7421767 | A | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(193): Show |
217 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.766+10649T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421767 | |||||||
chr12:7421769 | A | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(259): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.766+10647T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421769 | |||||||
chr12:7421776 | C | T | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10640G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421776 | |||||||
chr12:7421785 | G | A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10631C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421785 | |||||||
chr12:7421865 | T | G | 10 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0001g0149 others(7): Show |
10 | NA18941.hp1 NA18943.hp1 NA18945.hp1 others(7): Show |
intron_variant | MODIFIER | c.766+10551A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421865 | |||||||
chr12:7421886 | T | C | 30 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
35 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.766+10530A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7421886 | |||||||
chr12:7422056 | T | G | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10360A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422056 | |||||||
chr12:7422072 | G | A | 1 | a0001c0004t0001g0312 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.766+10344C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422072 | |||||||
chr12:7422108 | T | C | 1 | a0001c0002t0001g0294 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.766+10308A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422108 | |||||||
chr12:7422111 | C | G | 2 | a0001c0001t0002g0188 a0001c0001t0002g0189 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.766+10305G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422111 | |||||||
chr12:7422112 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.766+10304G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422112 | |||||||
chr12:7422148 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+10268T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422148 | |||||||
chr12:7422225 | G | A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+10191C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422225 | |||||||
chr12:7422257 | G | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+10159C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422257 | |||||||
chr12:7422361 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10055G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422361 | |||||||
chr12:7422373 | A | T | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10043T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422373 | |||||||
chr12:7422375 | A | G | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+10041T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422375 | |||||||
chr12:7422412 | CAAGGGCA others(13): Show |
C | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9984_766+10003 others(23): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422412 | |||||||
chr12:7422435 | T | A | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9981A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422435 | |||||||
chr12:7422439 | T | G | 1 | a0001c0001t0002g0247 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.766+9977A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422439 | |||||||
chr12:7422639 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.766+9777T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422639 | |||||||
chr12:7422643 | CATAT | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+9769_766+9772d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422643 | |||||||
chr12:7422751 | A | ATG | 9 | a0001c0001t0001g0004 a0001c0001t0001g0114 a0001c0001t0001g0172 others(6): Show |
11 | HG02040.hp2 NA18948.hp1 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.766+9663_766+9664d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | |||||||
chr12:7422751 | ATG | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(196): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.766+9663_766+9664d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | |||||||
chr12:7422751 | ATGTG | A | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.766+9661_766+9664d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422751 | |||||||
chr12:7422771 | GTGTA | G | 3 | a0002c0003t0001g0045 a0002c0003t0001g0046 a0004c0012t0002g0324 |
3 | HG02630.hp1 NA18979.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.766+9641_766+9644d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422771 | |||||||
chr12:7422773 | G | A | 2 | a0006c0009t0001g0118 a0016c0019t0001g0134 |
2 | HG02129.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.766+9643C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422773 | |||||||
chr12:7422773 | GTA | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0004t0001g0315 others(5): Show |
8 | HG01516.hp1 HG01517.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+9641_766+9642d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7422773 | |||||||
chr12:7423272 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.766+9144A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423272 | |||||||
chr12:7423347 | T | G | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+9069A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423347 | |||||||
chr12:7423538 | G | T | 71 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(68): Show |
74 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.766+8878C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423538 | |||||||
chr12:7423656 | G | A | 2 | a0002c0003t0001g0067 a0002c0003t0002g0066 |
2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.766+8760C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423656 | |||||||
chr12:7423800 | A | G | 1 | a0001c0007t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.766+8616T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423800 | |||||||
chr12:7423883 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.766+8533G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423883 | |||||||
chr12:7423927 | T | C | 1 | a0009c0015t0001g0295 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.766+8489A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7423927 | |||||||
chr12:7424074 | T | C | 80 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.766+8342A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424074 | |||||||
chr12:7424205 | A | T | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+8211T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424205 | |||||||
chr12:7424288 | TA | T | 293 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(290): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.766+8127delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424288 | |||||||
chr12:7424434 | G | C | 8 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0005c0013t0001g0243 others(5): Show |
8 | HG02572.hp2 HG02717.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.766+7982C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424434 | |||||||
chr12:7424496 | G | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7920C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424496 | |||||||
chr12:7424497 | C | A | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7919G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424497 | |||||||
chr12:7424506 | G | T | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7910C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424506 | |||||||
chr12:7424512 | A | T | 1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.766+7904T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424512 | |||||||
chr12:7424546 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.766+7870C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424546 | |||||||
chr12:7424686 | C | T | 1 | a0001c0002t0003g0254 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.766+7730G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424686 | |||||||
chr12:7424941 | T | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+7475A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424941 | |||||||
chr12:7424944 | C | G | 1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766+7472G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7424944 | |||||||
chr12:7425042 | A | T | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.766+7374T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425042 | |||||||
chr12:7425304 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.766+7112G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425304 | |||||||
chr12:7425422 | G | A | 2 | a0001c0004t0001g0311 a0001c0004t0001g0312 |
2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.766+6994C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7425422 | |||||||
chr12:7426028 | C | A | 1 | a0001c0002t0003g0297 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.766+6388G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426028 | |||||||
chr12:7426098 | A | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+6318T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426098 | |||||||
chr12:7426123 | G | A | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.766+6293C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426123 | |||||||
chr12:7426142 | G | A | 1 | a0025c0035t0002g0227 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.766+6274C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426142 | |||||||
chr12:7426338 | G | A | 1 | a0006c0009t0002g0013 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.766+6078C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426338 | |||||||
chr12:7426439 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.766+5977G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426439 | |||||||
chr12:7426445 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.766+5971G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426445 | |||||||
chr12:7426477 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+5939A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426477 | |||||||
chr12:7426519 | G | A | 2 | a0001c0002t0001g0298 a0001c0002t0003g0299 |
2 | HG01256.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.766+5897C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426519 | |||||||
chr12:7426666 | C | T | 2 | a0001c0001t0001g0136 a0002c0003t0001g0096 |
2 | NA19011.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.766+5750G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426666 | |||||||
chr12:7426667 | G | A | 2 | a0003c0005t0001g0008 a0003c0005t0001g0069 |
3 | HG01099.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.766+5749C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426667 | |||||||
chr12:7426671 | T | C | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+5745A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426671 | |||||||
chr12:7426681 | C | A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+5735G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7426681 | |||||||
chr12:7427058 | G | A | 97 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(94): Show |
101 | HG00408.hp1 HG00423.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.766+5358C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427058 | |||||||
chr12:7427170 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.766+5246C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427170 | |||||||
chr12:7427176 | GAAC | G | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+5237_766+5239d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427176 | |||||||
chr12:7427519 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
22 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.766+4897C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427519 | |||||||
chr12:7427698 | T | C | 3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.766+4718A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427698 | |||||||
chr12:7427723 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(341): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.766+4693G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7427723 | |||||||
chr12:7428153 | T | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+4263A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428153 | |||||||
chr12:7428209 | A | C | 3 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 |
3 | HG02818.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.766+4207T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428209 | |||||||
chr12:7428220 | G | A | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+4196C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428220 | |||||||
chr12:7428285 | A | T | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.766+4131T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428285 | |||||||
chr12:7428288 | T | C | 3 | a0003c0005t0001g0317 a0003c0005t0001g0318 a0003c0005t0001g0319 |
3 | NA18956.hp1 NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766+4128A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428288 | |||||||
chr12:7428463 | C | T | 1 | a0001c0026t0002g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.766+3953G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428463 | |||||||
chr12:7428602 | T | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+3814A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428602 | |||||||
chr12:7428735 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
21 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.766+3681C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428735 | |||||||
chr12:7428963 | C | T | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.766+3453G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7428963 | |||||||
chr12:7429011 | A | C | 1 | a0002c0003t0002g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.766+3405T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429011 | |||||||
chr12:7429182 | A | C | 36 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(33): Show |
39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.766+3234T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429182 | |||||||
chr12:7429517 | C | T | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+2899G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429517 | |||||||
chr12:7429581 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.766+2835A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429581 | |||||||
chr12:7429696 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0151 |
2 | HG01934.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.766+2720T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429696 | |||||||
chr12:7429877 | C | A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.766+2539G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7429877 | |||||||
chr12:7430177 | T | C | 1 | a0003c0005t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.766+2239A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430177 | |||||||
chr12:7430222 | A | G | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+2194T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430222 | |||||||
chr12:7430503 | T | C | 1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.766+1913A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430503 | |||||||
chr12:7430824 | A | G | 3 | a0002c0003t0001g0041 a0002c0003t0002g0042 a0002c0032t0001g0043 |
3 | HG02723.hp2 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.766+1592T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430824 | |||||||
chr12:7430870 | G | C | 1 | a0001c0001t0003g0239 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.766+1546C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430870 | |||||||
chr12:7430934 | A | G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+1482T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7430934 | |||||||
chr12:7431101 | C | T | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+1315G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431101 | |||||||
chr12:7431102 | T | G | 1 | a0002c0003t0001g0071 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.766+1314A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431102 | |||||||
chr12:7431159 | A | T | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+1257T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431159 | |||||||
chr12:7431160 | C | G | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.766+1256G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431160 | |||||||
chr12:7431160 | C | T | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.766+1256G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431160 | |||||||
chr12:7431161 | G | A | 4 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+1255C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431161 | |||||||
chr12:7431274 | G | A | 1 | a0006c0009t0001g0040 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766+1142C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431274 | |||||||
chr12:7431288 | G | T | 1 | a0002c0003t0003g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.766+1128C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431288 | |||||||
chr12:7431335 | C | T | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.766+1081G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431335 | |||||||
chr12:7431420 | C | T | 3 | a0003c0005t0001g0317 a0003c0005t0001g0318 a0003c0005t0001g0319 |
3 | NA18956.hp1 NA18968.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.766+996G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431420 | |||||||
chr12:7431427 | C | CA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
279 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.766+988dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431427 | |||||||
chr12:7431480 | T | A | 1 | a0004c0006t0002g0325 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.766+936A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431480 | |||||||
chr12:7431608 | G | C | 1 | a0001c0002t0003g0299 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.766+808C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431608 | |||||||
chr12:7431730 | C | T | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+686G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431730 | |||||||
chr12:7431731 | T | G | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.766+685A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7431731 | |||||||
chr12:7432317 | G | A | 1 | a0001c0002t0001g0300 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.766+99C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 4/19 | chr12 | 7432317 | |||||||
chr12:7432740 | C | T | 3 | a0001c0001t0001g0150 a0006c0009t0001g0039 a0006c0009t0001g0040 |
3 | HG02258.hp2 HG02559.hp2 NA20805.hp2 |
splice_region_variant&intron_variant | LOW | c.446-4G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432740 | |||||||
chr12:7432808 | G | T | 1 | a0001c0026t0002g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.446-72C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432808 | |||||||
chr12:7432847 | T | TA | 36 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0114 others(33): Show |
39 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.446-112dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7432847 | |||||||
chr12:7433011 | T | C | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.446-275A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433011 | |||||||
chr12:7433137 | G | A | 1 | a0002c0003t0002g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.445+237C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433137 | |||||||
chr12:7433150 | G | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.445+224C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433150 | |||||||
chr12:7433329 | G | A | 1 | a0020c0038t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445+45C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433329 | |||||||
chr12:7433331 | G | T | 2 | a0001c0004t0001g0315 a0001c0004t0002g0314 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.445+43C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 3/19 | chr12 | 7433331 | |||||||
chr12:7433838 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.125-144A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433838 | |||||||
chr12:7433902 | C | T | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-208G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433902 | |||||||
chr12:7433990 | G | C | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-296C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433990 | |||||||
chr12:7433999 | T | C | 85 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.125-305A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7433999 | |||||||
chr12:7434033 | A | G | 4 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-339T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434033 | |||||||
chr12:7434221 | C | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-527G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434221 | |||||||
chr12:7434226 | CAGG | C | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-535_125-533del others(3): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434226 | |||||||
chr12:7434367 | T | C | 1 | a0001c0002t0002g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.125-673A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434367 | |||||||
chr12:7434374 | T | C | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-680A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434374 | |||||||
chr12:7434703 | A | C | 1 | a0001c0041t0001g0113 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.125-1009T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434703 | |||||||
chr12:7434706 | AAGAG | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(56): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.125-1016_125-1013d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434706 | |||||||
chr12:7434724 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.125-1030C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434724 | |||||||
chr12:7434784 | T | G | 2 | a0001c0004t0001g0315 a0001c0004t0002g0314 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.125-1090A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434784 | |||||||
chr12:7434805 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-1111T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434805 | |||||||
chr12:7434884 | G | T | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-1190C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434884 | |||||||
chr12:7434906 | T | C | 1 | a0003c0005t0001g0072 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.125-1212A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434906 | |||||||
chr12:7434938 | T | C | 68 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0095 others(65): Show |
75 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.125-1244A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7434938 | |||||||
chr12:7435031 | G | C | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-1337C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435031 | |||||||
chr12:7435047 | A | G | 2 | a0001c0007t0001g0131 a0020c0038t0001g0132 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-1353T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435047 | |||||||
chr12:7435089 | TAC | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.125-1397_125-1396d others(4): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435089 | |||||||
chr12:7435121 | A | T | 1 | a0006c0034t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125-1427T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435121 | |||||||
chr12:7435156 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.125-1462C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435156 | |||||||
chr12:7435240 | TAAAGAA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(46): Show |
60 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.125-1552_125-1547d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435240 | |||||||
chr12:7435346 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0025c0035t0002g0227 |
3 | NA18950.hp2 NA18994.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.125-1652A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435346 | |||||||
chr12:7435595 | A | G | 4 | a0010c0018t0001g0344 a0010c0018t0002g0345 a0011c0042t0002g0346 others(1): Show |
4 | HG01261.hp1 HG02145.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1901T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435595 | |||||||
chr12:7435598 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-1904A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435598 | |||||||
chr12:7435707 | T | C | 2 | a0002c0003t0002g0094 a0003c0005t0002g0093 |
2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.125-2013A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435707 | |||||||
chr12:7435866 | C | T | 2 | a0004c0006t0001g0328 a0004c0006t0001g0329 |
2 | NA18612.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.125-2172G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7435866 | |||||||
chr12:7436039 | T | C | 1 | a0017c0044t0002g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-2345A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436039 | |||||||
chr12:7436068 | G | A | 1 | a0002c0003t0003g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.125-2374C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436068 | |||||||
chr12:7436280 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.125-2586C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436280 | |||||||
chr12:7436363 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
279 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.125-2669G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436363 | |||||||
chr12:7436471 | C | T | 1 | a0001c0002t0002g0252 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-2777G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436471 | |||||||
chr12:7436508 | A | G | 5 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(2): Show |
7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-2814T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436508 | |||||||
chr12:7436572 | G | C | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.125-2878C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436572 | |||||||
chr12:7436716 | TAAC | T | 85 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.125-3025_125-3023d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436716 | |||||||
chr12:7436892 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0002g0323 |
2 | HG02451.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.125-3198T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436892 | |||||||
chr12:7436997 | T | C | 1 | a0004c0012t0001g0326 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.125-3303A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7436997 | |||||||
chr12:7437009 | T | C | 2 | a0003c0005t0002g0033 a0003c0005t0002g0034 |
2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.125-3315A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437009 | |||||||
chr12:7437117 | T | C | 1 | a0001c0002t0003g0316 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.125-3423A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437117 | |||||||
chr12:7437131 | TTTTA | T | 79 | a0001c0002t0001g0251 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00423.hp1 HG00673.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3441_125-3438d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437131 | |||||||
chr12:7437136 | T | TTTA | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
197 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.125-3445_125-3443d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437136 | |||||||
chr12:7437166 | T | TTAAG | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(247): Show |
277 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.125-3473_125-3472i others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437166 | |||||||
chr12:7437183 | ATTTTTAT others(84): Show |
A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3580_125-3490d others(93): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437183 | |||||||
chr12:7437204 | CTTT | C | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3513_125-3511d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437204 | |||||||
chr12:7437205 | TTTTTTAT others(62): Show |
T | 2 | a0004c0028t0001g0126 a0008c0011t0001g0127 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.125-3580_125-3512d others(71): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437205 | |||||||
chr12:7437235 | T | TAAATACT others(150): Show |
1 | a0001c0027t0002g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(159): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | |||||||
chr12:7437235 | T | TAAATACT others(140): Show |
1 | a0001c0029t0001g0122 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.125-3542_125-3541i others(149): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | |||||||
chr12:7437235 | T | TAAATACT others(151): Show |
1 | a0001c0004t0002g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(160): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | |||||||
chr12:7437235 | T | TAAATACT others(96): Show |
1 | a0001c0004t0001g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.125-3542_125-3541i others(105): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437235 | |||||||
chr12:7437237 | C | A | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3543G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437237 | |||||||
chr12:7437238 | T | TTTTAAAT others(92): Show |
1 | a0001c0002t0003g0291 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(92): Show |
6 | a0001c0002t0001g0023 a0001c0002t0001g0259 a0001c0002t0001g0283 others(3): Show |
7 | HG00544.hp1 HG01071.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(92): Show |
41 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0028 others(38): Show |
44 | HG00408.hp2 HG00423.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(81): Show |
1 | a0001c0002t0001g0251 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(125): Show |
1 | a0001c0002t0001g0294 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(134): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(81): Show |
1 | a0001c0002t0002g0292 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(90): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(59): Show |
1 | a0001c0002t0001g0272 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(68): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(92): Show |
1 | a0001c0002t0001g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125-3545_125-3544i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437238 | T | TTTTAAAT others(70): Show |
1 | a0001c0002t0002g0024 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.125-3545_125-3544i others(79): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437238 | |||||||
chr12:7437239 | T | A | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3545A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(102): Show |
1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(111): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(58): Show |
4 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0034t0001g0123 others(1): Show |
4 | HG02717.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(80): Show |
1 | a0006c0009t0002g0013 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(107): Show |
2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(116): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(212): Show |
1 | a0001c0025t0002g0265 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(221): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(58): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(44): Show |
58 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0004t0002g0302 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(234): Show |
1 | a0001c0002t0001g0289 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(243): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(102): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(111): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
9 | a0001c0004t0001g0303 a0001c0004t0001g0304 a0001c0004t0001g0311 others(6): Show |
10 | HG00099.hp1 HG01074.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
6 | a0001c0004t0001g0315 a0001c0004t0001g0341 a0001c0004t0002g0025 others(3): Show |
7 | HG00140.hp1 HG00738.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
1 | a0001c0002t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(201): Show |
1 | a0019c0020t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(210): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(300): Show |
1 | a0001c0002t0001g0274 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(309): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(212): Show |
3 | a0001c0002t0001g0248 a0001c0002t0001g0260 a0001c0002t0001g0273 |
3 | NA18951.hp2 NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(221): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(47): Show |
6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(56): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(124): Show |
1 | a0001c0004t0002g0322 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(190): Show |
1 | a0001c0026t0002g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(91): Show |
5 | a0001c0002t0001g0002 a0001c0002t0001g0102 a0001c0002t0001g0269 others(2): Show |
8 | HG00639.hp1 HG01074.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(100): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(69): Show |
2 | a0001c0007t0003g0331 a0017c0044t0002g0347 |
2 | HG01123.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(58): Show |
3 | a0001c0001t0001g0183 a0004c0006t0001g0332 a0004c0006t0001g0335 |
3 | HG02027.hp2 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0004t0003g0306 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(168): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(80): Show |
3 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 |
3 | HG01884.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(69): Show |
23 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
28 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(256): Show |
1 | a0008c0011t0002g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(265): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(190): Show |
1 | a0001c0001t0002g0189 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(58): Show |
9 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(6): Show |
10 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(67): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(80): Show |
3 | a0004c0006t0001g0328 a0004c0006t0001g0329 a0004c0006t0001g0337 |
3 | NA18612.hp2 NA18960.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(89): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(124): Show |
1 | a0001c0001t0001g0216 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0001t0002g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0220 others(1): Show |
4 | HG01496.hp1 HG01943.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
1 | a0001c0001t0001g0211 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(190): Show |
1 | a0001c0001t0002g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(199): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(69): Show |
3 | a0001c0007t0001g0104 a0001c0008t0001g0232 a0001c0008t0001g0238 |
3 | HG03041.hp1 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(78): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(135): Show |
1 | a0001c0001t0001g0114 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(124): Show |
1 | a0001c0001t0002g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(91): Show |
3 | a0004c0006t0001g0338 a0004c0006t0001g0339 a0014c0037t0001g0336 |
3 | HG00673.hp2 NA18939.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(100): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(135): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0197 others(4): Show |
7 | HG02165.hp1 HG02738.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(124): Show |
1 | a0001c0001t0001g0215 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(133): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0006 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0001t0001g0224 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(135): Show |
3 | a0001c0001t0002g0245 a0001c0001t0002g0247 a0001c0008t0002g0005 |
3 | HG00558.hp2 HG02723.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
14 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0194 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0001t0001g0212 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0206 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0008t0002g0005 | 2 | HG02922.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(135): Show |
1 | a0001c0001t0001g0217 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(144): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(168): Show |
1 | a0001c0001t0001g0115 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
8 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0001c0001t0001g0222 others(5): Show |
8 | HG00558.hp1 HG01361.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0228 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
1 | a0006c0009t0002g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(146): Show |
1 | a0001c0001t0002g0006 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(155): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(168): Show |
1 | a0001c0001t0002g0006 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(177): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(113): Show |
1 | a0001c0001t0002g0246 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.125-3546_125-3545i others(122): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(157): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0201 |
2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.125-3546_125-3545i others(166): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437239 | T | TTTAAATA others(179): Show |
1 | a0003c0005t0001g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.125-3546_125-3545i others(188): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437239 | |||||||
chr12:7437244 | ATAGTATT others(1469): Show |
A | 1 | a0001c0001t0001g0135 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.124+2434_125-3551d others(2): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437244 | |||||||
chr12:7437247 | G | GTATTTAA others(4): Show |
1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3554_125-3553i others(13): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437247 | |||||||
chr12:7437247 | G | GTATTTAA others(92): Show |
1 | a0001c0002t0001g0112 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.125-3554_125-3553i others(101): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437247 | |||||||
chr12:7437258 | G | C | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3564C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437258 | |||||||
chr12:7437315 | ATTATTT | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
23 | HG00544.hp2 HG00609.hp1 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.125-3627_125-3622d others(8): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437315 | |||||||
chr12:7437318 | ATTT | A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3627_125-3625d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437318 | |||||||
chr12:7437324 | ATTT | A | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3633_125-3631d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437324 | |||||||
chr12:7437350 | ATATT | A | 79 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.125-3660_125-3657d others(6): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437350 | |||||||
chr12:7437370 | T | C | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3676A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437370 | |||||||
chr12:7437373 | ATGTGCAC others(10): Show |
A | 2 | a0006c0009t0001g0039 a0006c0009t0001g0040 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.125-3696_125-3680d others(19): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437373 | |||||||
chr12:7437402 | T | C | 1 | a0003c0033t0002g0128 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-3708A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437402 | |||||||
chr12:7437581 | C | T | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+3573G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437581 | |||||||
chr12:7437630 | C | T | 1 | a0002c0003t0001g0031 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124+3524G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437630 | |||||||
chr12:7437670 | CT | C | 45 | a0001c0001t0001g0228 a0001c0001t0002g0229 a0001c0001t0002g0323 others(42): Show |
46 | HG00639.hp2 HG00673.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.124+3483delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437670 | |||||||
chr12:7437898 | T | TA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0172 a0001c0001t0001g0173 others(17): Show |
23 | HG02027.hp2 NA18612.hp1 NA18747.hp1 others(20): Show |
intron_variant | MODIFIER | c.124+3255dupT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437898 | |||||||
chr12:7437898 | TA | T | 6 | a0001c0007t0001g0131 a0003c0033t0002g0128 a0006c0009t0001g0118 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+3255delT | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437898 | |||||||
chr12:7437967 | T | C | 6 | a0006c0009t0001g0039 a0006c0009t0001g0040 a0010c0018t0001g0344 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+3187A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437967 | |||||||
chr12:7437988 | G | T | 6 | a0005c0013t0001g0243 a0005c0013t0001g0342 a0005c0013t0002g0242 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+3166C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7437988 | |||||||
chr12:7438181 | T | C | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.124+2973A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438181 | |||||||
chr12:7438218 | C | G | 75 | a0002c0003t0001g0007 a0002c0003t0001g0009 a0002c0003t0001g0029 others(72): Show |
78 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.124+2936G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438218 | |||||||
chr12:7438464 | T | C | 5 | a0001c0007t0001g0131 a0006c0009t0001g0118 a0006c0009t0002g0013 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+2690A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438464 | |||||||
chr12:7438593 | T | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124+2561A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438593 | |||||||
chr12:7438681 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(45): Show |
59 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.124+2473A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438681 | |||||||
chr12:7438718 | T | C | 1 | a0001c0001t0003g0241 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.124+2436A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438718 | |||||||
chr12:7438741 | T | A | 1 | a0001c0001t0001g0230 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.124+2413A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438741 | |||||||
chr12:7438771 | C | T | 1 | a0001c0002t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.124+2383G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438771 | |||||||
chr12:7438940 | T | A | 84 | a0001c0001t0001g0095 a0001c0001t0002g0323 a0001c0027t0002g0030 others(81): Show |
87 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(84): Show |
intron_variant | MODIFIER | c.124+2214A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438940 | |||||||
chr12:7438968 | T | C | 1 | a0001c0017t0002g0019 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.124+2186A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7438968 | |||||||
chr12:7439085 | G | A | 14 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(11): Show |
15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+2069C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439085 | |||||||
chr12:7439119 | T | G | 76 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(73): Show |
79 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.124+2035A>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439119 | |||||||
chr12:7439147 | A | C | 1 | a0016c0019t0001g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.124+2007T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439147 | |||||||
chr12:7439213 | C | T | 5 | a0001c0002t0001g0010 a0001c0002t0001g0011 a0001c0002t0001g0111 others(2): Show |
7 | HG02135.hp1 NA18948.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1941G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439213 | |||||||
chr12:7439439 | G | T | 89 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(86): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.124+1715C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439439 | |||||||
chr12:7439543 | G | A | 89 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(86): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.124+1611C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439543 | |||||||
chr12:7439598 | T | C | 80 | a0001c0001t0001g0095 a0001c0001t0002g0323 a0002c0003t0001g0007 others(77): Show |
83 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.124+1556A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439598 | |||||||
chr12:7439629 | C | T | 1 | a0005c0013t0002g0242 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+1525G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439629 | |||||||
chr12:7439783 | A | G | 79 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+1371T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439783 | |||||||
chr12:7439815 | C | A | 2 | a0001c0002t0001g0011 a0001c0002t0001g0112 |
3 | NA18959.hp1 NA18983.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.124+1339G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439815 | |||||||
chr12:7439849 | G | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(85): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.124+1305C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439849 | |||||||
chr12:7439900 | CCTT | C | 58 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0106 others(55): Show |
64 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.124+1251_124+1253d others(5): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439900 | |||||||
chr12:7439943 | A | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0010 a0001c0002t0001g0011 others(84): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.124+1211T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439943 | |||||||
chr12:7439998 | T | C | 1 | a0020c0038t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124+1156A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7439998 | |||||||
chr12:7440038 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.124+1116G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440038 | |||||||
chr12:7440090 | G | A | 1 | a0004c0012t0001g0327 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.124+1064C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440090 | |||||||
chr12:7440233 | G | T | 84 | a0001c0002t0001g0002 a0001c0002t0001g0023 a0001c0002t0001g0028 others(81): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.124+921C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440233 | |||||||
chr12:7440280 | G | C | 79 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+874C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440280 | |||||||
chr12:7440364 | G | C | 79 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.124+790C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440364 | |||||||
chr12:7440377 | C | G | 12 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0004t0001g0120 others(9): Show |
13 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.124+777G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440377 | |||||||
chr12:7440568 | T | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0237 a0001c0001t0002g0231 others(9): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+586A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440568 | |||||||
chr12:7440627 | T | A | 10 | a0001c0001t0002g0244 a0001c0001t0002g0245 a0001c0001t0002g0246 others(7): Show |
10 | HG00558.hp2 HG02572.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+527A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440627 | |||||||
chr12:7440629 | CT | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(318): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.124+524delA | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440629 | |||||||
chr12:7440882 | C | G | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+272G>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440882 | |||||||
chr12:7440922 | C | T | 4 | a0001c0004t0001g0120 a0001c0004t0002g0121 a0001c0027t0002g0030 others(1): Show |
4 | HG02818.hp2 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+232G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7440922 | |||||||
chr12:7441062 | A | G | 2 | a0002c0003t0001g0036 a0002c0003t0001g0037 |
2 | HG01069.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.124+92T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 2/19 | chr12 | 7441062 | |||||||
chr12:7441433 | G | C | 4 | a0004c0006t0002g0325 a0004c0012t0001g0326 a0004c0012t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02630.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.32-187C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441433 | |||||||
chr12:7441579 | C | T | 79 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.32-333G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441579 | |||||||
chr12:7441618 | C | A | 14 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(11): Show |
15 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.32-372G>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441618 | |||||||
chr12:7441758 | T | C | 85 | a0001c0001t0001g0321 a0001c0002t0001g0002 a0001c0002t0001g0023 others(82): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.32-512A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441758 | |||||||
chr12:7441790 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0119 |
3 | HG00609.hp2 HG02165.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.32-544T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441790 | |||||||
chr12:7441812 | A | T | 1 | a0006c0009t0001g0118 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.32-566T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7441812 | |||||||
chr12:7442036 | G | A | 1 | a0001c0001t0002g0323 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32-790C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442036 | |||||||
chr12:7442207 | C | T | 2 | a0005c0014t0001g0116 a0005c0014t0002g0117 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.32-961G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442207 | |||||||
chr12:7442242 | G | T | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0002t0001g0010 others(4): Show |
9 | HG02040.hp2 HG02083.hp1 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-996C>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442242 | |||||||
chr12:7442380 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.32-1134T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442380 | |||||||
chr12:7442429 | A | G | 1 | a0001c0026t0002g0109 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.32-1183T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442429 | |||||||
chr12:7442506 | T | TA | 18 | a0001c0007t0001g0027 a0001c0007t0001g0330 a0001c0007t0003g0331 others(15): Show |
19 | HG00639.hp2 HG00673.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-1261_32-1260ins others(1): Show |
CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442506 | |||||||
chr12:7442535 | C | T | 1 | a0003c0005t0001g0035 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.32-1289G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442535 | |||||||
chr12:7442555 | A | G | 4 | a0002c0003t0001g0031 a0003c0005t0001g0032 a0003c0005t0002g0033 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-1309T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442555 | |||||||
chr12:7442600 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0002g0107 |
3 | HG02055.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.32-1354T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442600 | |||||||
chr12:7442605 | G | A | 8 | a0002c0003t0001g0009 a0002c0003t0001g0029 a0002c0003t0001g0096 others(5): Show |
9 | HG00408.hp1 HG02056.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.32-1359C>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442605 | |||||||
chr12:7442619 | A | G | 1 | a0005c0014t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32-1373T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442619 | |||||||
chr12:7442627 | C | T | 1 | a0001c0007t0001g0104 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.32-1381G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442627 | |||||||
chr12:7442983 | T | A | 1 | a0004c0006t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+1114A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7442983 | |||||||
chr12:7443004 | A | G | 1 | a0004c0006t0002g0103 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31+1093T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443004 | |||||||
chr12:7443054 | A | T | 1 | a0001c0002t0001g0102 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.31+1043T>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443054 | |||||||
chr12:7443138 | T | C | 1 | a0001c0002t0001g0340 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.31+959A>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443138 | |||||||
chr12:7443240 | C | T | 79 | a0001c0001t0001g0095 a0002c0003t0001g0007 a0002c0003t0001g0009 others(76): Show |
82 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.31+857G>A | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443240 | |||||||
chr12:7443267 | A | C | 1 | a0001c0027t0002g0030 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31+830T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443267 | |||||||
chr12:7443783 | T | A | 1 | a0001c0004t0001g0341 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31+314A>T | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443783 | |||||||
chr12:7443973 | A | G | 1 | a0002c0003t0001g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.31+124T>C | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443973 | |||||||
chr12:7443987 | G | C | 1 | a0005c0013t0001g0342 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31+110C>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7443987 | |||||||
chr12:7444081 | A | C | 1 | a0001c0002t0001g0028 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.31+16T>G | CD163L1 | ENSG00000177675.9 | transcript | ENST00000313599.8 | protein_coding | 1/19 | chr12 | 7444081 |