Item | Value |
---|---|
geneid | 7133 |
ensemblid | ENSG00000028137.19 |
hgncid | 11917 |
symbol | TNFRSF1B |
name | TNF receptor superfamily member 1B |
refseq_nuc | NM_001066.3 |
refseq_prot | NP_001057.1 |
ensembl_nuc | ENST00000376259.7 |
ensembl_prot | ENSP00000365435.3 |
mane_status | MANE Select |
chr | chr1 |
start | 12166991 |
end | 12209220 |
strand | + |
ver | v1.2 |
region | chr1:12166991-12209220 |
region5000 | chr1:12161991-12214220 |
regionname0 | TNFRSF1B_chr1_12166991_12209220 |
regionname5000 | TNFRSF1B_chr1_12161991_12214220 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 461 | 292 | 73 | 58 | 117 | 10 | 33 | 81 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0002 | 0/0 | 461 | 56 | 16 | 11 | 18 | 4 | 7 | 15 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0003 | 0/0 | 461 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0004 | 0/1 | 461 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0005 | 0/0 | 461 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0006 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0007 | 0/0 | 461 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0008 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0009 | 0/0 | 461 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
a0010 | 0/0 | 461 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | MAPVA others(456): Show |
chr1 | 12161991 | 12214220 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1383 | 277 | 67 | 58 | 109 | 10 | 32 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0001c0003 | 0/0 | 1383 | 8 | 6 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0001c0004 | 0/0 | 1383 | 7 | 0 | 0 | 7 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0002c0002 | 0/0 | 1383 | 55 | 15 | 11 | 18 | 4 | 7 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0002c0009 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0003c0005 | 0/0 | 1383 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0004c0007 | 0/1 | 1383 | 2 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0005c0006 | 0/0 | 1383 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0006c0010 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0007c0008 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0008c0011 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0009c0012 | 0/0 | 1383 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 | ||
a0010c0013 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | ATGGC others(1378): Show |
chr1 | 12161991 | 12214220 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3687 | 33 | 2 | 14 | 12 | 3 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0002 | 0/0 | 3687 | 45 | 4 | 7 | 28 | 0 | 6 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0003 | 1/0 | 3687 | 41 | 6 | 7 | 21 | 2 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0004 | 0/0 | 3687 | 17 | 2 | 2 | 12 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0005 | 0/0 | 3688 | 16 | 2 | 0 | 12 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0006 | 0/0 | 3688 | 12 | 10 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0007 | 0/0 | 3687 | 3 | 0 | 0 | 2 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0008 | 0/0 | 3687 | 7 | 6 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0009 | 0/0 | 3688 | 7 | 1 | 3 | 1 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0010 | 0/0 | 3687 | 8 | 6 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0011 | 0/0 | 3688 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0012 | 0/0 | 3687 | 6 | 2 | 1 | 2 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0013 | 0/0 | 3687 | 5 | 1 | 0 | 0 | 0 | 4 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0014 | 0/0 | 3687 | 4 | 0 | 2 | 0 | 1 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0015 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0016 | 0/0 | 3691 | 4 | 0 | 4 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3686): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0017 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0018 | 0/0 | 3688 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0019 | 0/0 | 3687 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0020 | 0/0 | 3688 | 3 | 0 | 2 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0021 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0022 | 0/0 | 3687 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0023 | 0/0 | 3688 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0024 | 0/0 | 3687 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0025 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0026 | 0/0 | 3688 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0027 | 0/0 | 3687 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0028 | 0/0 | 3687 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0029 | 0/0 | 3688 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0030 | 0/0 | 3687 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0032 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0033 | 0/0 | 3687 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0035 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0036 | 0/0 | 3691 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3686): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0037 | 0/0 | 3687 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0041 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0042 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0043 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0044 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0045 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0046 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0047 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0049 | 0/0 | 3688 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0050 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0051 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0052 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0053 | 0/0 | 3691 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3686): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0054 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0055 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0056 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0057 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0058 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0061 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0062 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0063 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0064 | 0/0 | 3691 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3686): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0065 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0066 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0001t0068 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3691): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0002 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0003 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0034 | 0/0 | 3688 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0035 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0059 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0067 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3691): Show |
chr1 | 12161991 | 12214220 |
a0001c0003t0069 | 0/0 | 3696 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3691): Show |
chr1 | 12161991 | 12214220 |
a0001c0004t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0004t0007 | 0/0 | 3687 | 5 | 0 | 0 | 5 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0001c0004t0024 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0001 | 0/0 | 3687 | 16 | 0 | 3 | 6 | 1 | 6 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0002 | 0/0 | 3687 | 7 | 1 | 2 | 3 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0003 | 0/0 | 3687 | 3 | 1 | 0 | 1 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0005 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0007 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0008 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0009 | 0/0 | 3688 | 2 | 0 | 1 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0011 | 0/0 | 3688 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0012 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0013 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0014 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0015 | 0/0 | 3688 | 3 | 2 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0017 | 0/0 | 3687 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0019 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0021 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0022 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0025 | 0/0 | 3688 | 2 | 1 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0031 | 0/0 | 3688 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0032 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0034 | 0/0 | 3688 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0038 | 0/0 | 3696 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3691): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0039 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0002t0040 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0002c0009t0018 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0003c0005t0003 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0003c0005t0007 | 0/0 | 3687 | 3 | 0 | 0 | 3 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0003c0005t0019 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0004c0007t0014 | 0/0 | 3687 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0004c0007t0016 | 0/1 | 3691 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3686): Show |
chr1 | 12161991 | 12214220 |
a0005c0006t0001 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0005c0006t0060 | 0/0 | 3688 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3683): Show |
chr1 | 12161991 | 12214220 |
a0006c0010t0048 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0007c0008t0003 | 0/0 | 3687 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0008c0011t0001 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0009c0012t0001 | 0/0 | 3687 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
a0010c0013t0001 | 0/0 | 3687 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | AGTCG others(3682): Show |
chr1 | 12161991 | 12214220 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0007g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0011g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0012g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0013g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0014g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0015g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0016g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0018g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0019g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0020g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0021g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0022g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0022g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0024g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0024g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0025g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0026g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0026g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0027g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0027g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0028g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0028g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0029g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0029g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0030g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0030g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0032g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0033g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0035g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0036g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0036g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0037g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0037g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0041g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0042g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0043g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0044g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0045g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0046g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0047g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0049g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0050g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0051g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0052g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0053g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0054g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0055g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0056g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0057g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0058g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0061g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0062g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0063g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0064g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0065g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0066g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0001t0068g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0034g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0035g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0059g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0067g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0003t0069g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0001c0004t0024g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0008g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0011g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0012g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0013g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0014g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0015g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0017g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0019g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0022g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0025g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0025g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0031g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0031g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0032g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0034g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0038g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0038g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0039g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0002t0040g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0002c0009t0018g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0003c0005t0019g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0004c0007t0014g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0004c0007t0016g0327 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0005c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0005c0006t0060g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0006c0010t0048g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0007c0008t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0008c0011t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0009c0012t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
a0010c0013t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0063 | g0091 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0178 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0318 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0282 | EUR | GBR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00323 | hp2 | a0001 | c0001 | t0022 | g0123 | EUR | FIN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00408 | hp2 | a0001 | c0004 | t0007 | g0148 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00423 | hp2 | a0002 | c0002 | t0034 | g0171 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00438 | hp1 | a0001 | c0004 | t0007 | g0211 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00438 | hp2 | a0001 | c0001 | t0044 | g0205 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00544 | hp1 | a0001 | c0001 | t0030 | g0183 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00544 | hp2 | a0001 | c0001 | t0030 | g0188 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00597 | hp1 | a0003 | c0005 | t0003 | g0224 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00639 | hp1 | a0001 | c0001 | t0014 | g0251 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0082 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00673 | hp1 | a0001 | c0001 | t0019 | g0090 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0143 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00738 | hp2 | a0001 | c0001 | t0020 | g0212 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01069 | hp1 | a0001 | c0001 | t0022 | g0163 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01070 | hp1 | a0001 | c0001 | t0028 | g0302 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0245 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01071 | hp2 | a0001 | c0001 | t0028 | g0303 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01081 | hp2 | a0001 | c0001 | t0065 | g0275 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01099 | hp1 | a0001 | c0001 | t0016 | g0124 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01099 | hp2 | a0001 | c0001 | t0020 | g0065 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01106 | hp2 | a0002 | c0002 | t0013 | g0044 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01109 | hp2 | a0001 | c0001 | t0052 | g0280 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01167 | hp1 | a0001 | c0001 | t0027 | g0262 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0021 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01169 | hp1 | a0001 | c0001 | t0027 | g0057 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01192 | hp1 | a0001 | c0001 | t0018 | g0301 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01192 | hp2 | a0001 | c0001 | t0049 | g0038 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01243 | hp2 | a0002 | c0002 | t0015 | g0046 | AMR | PUR | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0297 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0093 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0323 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01261 | hp1 | a0002 | c0002 | t0031 | g0319 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01358 | hp1 | a0001 | c0001 | t0026 | g0304 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01358 | hp2 | a0004 | c0007 | t0014 | g0328 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01433 | hp1 | a0002 | c0002 | t0009 | g0257 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0095 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01515 | hp1 | a0001 | c0001 | t0009 | g0054 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01515 | hp2 | a0002 | c0002 | t0009 | g0165 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0092 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01516 | hp2 | a0001 | c0001 | t0014 | g0009 | EUR | IBS | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01884 | hp1 | a0001 | c0001 | t0021 | g0238 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0028 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0235 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01934 | hp1 | a0002 | c0002 | t0031 | g0152 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01934 | hp2 | a0001 | c0001 | t0036 | g0012 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0069 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01981 | hp2 | a0001 | c0001 | t0036 | g0071 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02027 | hp1 | a0001 | c0001 | t0058 | g0316 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02040 | hp1 | a0006 | c0010 | t0048 | g0263 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0258 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02055 | hp1 | a0001 | c0001 | t0055 | g0288 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02055 | hp2 | a0002 | c0002 | t0008 | g0333 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02056 | hp1 | a0002 | c0002 | t0022 | g0164 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02056 | hp2 | a0001 | c0001 | t0019 | g0098 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02135 | hp1 | a0003 | c0005 | t0007 | g0204 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02145 | hp1 | a0001 | c0001 | t0015 | g0283 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02145 | hp2 | a0001 | c0001 | t0025 | g0221 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02155 | hp1 | a0001 | c0001 | t0010 | g0202 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02165 | hp1 | a0002 | c0002 | t0007 | g0170 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | CDX | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02257 | hp1 | a0002 | c0002 | t0038 | g0339 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0056 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0058 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0142 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0274 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02280 | hp1 | a0005 | c0006 | t0001 | g0108 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02293 | hp2 | a0002 | c0002 | t0014 | g0278 | AMR | PEL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0296 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02451 | hp2 | a0001 | c0001 | t0011 | g0236 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02523 | hp2 | a0001 | c0001 | t0041 | g0314 | EAS | KHV | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02572 | hp1 | a0002 | c0002 | t0011 | g0041 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02572 | hp2 | a0001 | c0003 | t0067 | g0337 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02615 | hp1 | a0001 | c0003 | t0069 | g0336 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0335 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0256 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0141 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02647 | hp2 | a0002 | c0002 | t0015 | g0197 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02683 | hp1 | a0002 | c0002 | t0025 | g0166 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02683 | hp2 | a0001 | c0001 | t0014 | g0220 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02698 | hp2 | a0001 | c0001 | t0064 | g0195 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02717 | hp1 | a0001 | c0001 | t0047 | g0048 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02717 | hp2 | a0002 | c0002 | t0032 | g0036 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0150 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0267 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02809 | hp1 | a0005 | c0006 | t0060 | g0109 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02886 | hp1 | a0002 | c0002 | t0008 | g0035 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02886 | hp2 | a0001 | c0001 | t0023 | g0031 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02895 | hp2 | a0001 | c0001 | t0023 | g0039 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02897 | hp1 | a0001 | c0001 | t0035 | g0222 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0016 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0237 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02970 | hp2 | a0002 | c0002 | t0017 | g0045 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03017 | hp1 | a0001 | c0001 | t0013 | g0252 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03017 | hp2 | a0001 | c0001 | t0033 | g0008 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0234 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03130 | hp2 | a0001 | c0001 | t0068 | g0338 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03195 | hp1 | a0007 | c0008 | t0003 | g0281 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03195 | hp2 | a0001 | c0001 | t0021 | g0230 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0287 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0064 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03239 | hp2 | a0001 | c0001 | t0020 | g0203 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0289 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03486 | hp1 | a0001 | c0003 | t0059 | g0059 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03486 | hp2 | a0002 | c0009 | t0018 | g0062 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03491 | hp1 | a0001 | c0001 | t0037 | g0134 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03491 | hp2 | a0001 | c0001 | t0033 | g0008 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03492 | hp1 | a0001 | c0001 | t0024 | g0321 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03492 | hp2 | a0001 | c0001 | t0037 | g0133 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0290 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03540 | hp1 | a0001 | c0001 | t0051 | g0233 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | GWD | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03579 | hp2 | a0001 | c0001 | t0042 | g0139 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03688 | hp2 | a0001 | c0001 | t0013 | g0010 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03704 | hp1 | a0001 | c0001 | t0013 | g0050 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03704 | hp2 | a0001 | c0001 | t0029 | g0003 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03710 | hp2 | a0001 | c0001 | t0043 | g0246 | SAS | PJL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03831 | hp1 | a0008 | c0011 | t0001 | g0156 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03831 | hp2 | a0001 | c0001 | t0013 | g0153 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03927 | hp1 | a0009 | c0012 | t0001 | g0132 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03942 | hp1 | a0001 | c0001 | t0054 | g0253 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0300 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0053 | SAS | BEB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04199 | hp1 | a0001 | c0003 | t0034 | g0176 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0309 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | STU | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0261 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0030 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | CHB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18906 | hp2 | a0002 | c0002 | t0017 | g0047 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18941 | hp2 | a0001 | c0001 | t0029 | g0119 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18942 | hp2 | a0001 | c0001 | t0057 | g0315 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18943 | hp1 | a0001 | c0001 | t0024 | g0191 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18944 | hp1 | a0002 | c0002 | t0019 | g0168 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18965 | hp2 | a0003 | c0005 | t0019 | g0158 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18966 | hp1 | a0010 | c0013 | t0001 | g0208 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18971 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18978 | hp1 | a0002 | c0002 | t0039 | g0157 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18978 | hp2 | a0001 | c0001 | t0032 | g0131 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18982 | hp2 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18993 | hp2 | a0001 | c0001 | t0012 | g0019 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18995 | hp2 | a0001 | c0001 | t0012 | g0187 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19000 | hp2 | a0001 | c0004 | t0007 | g0007 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19002 | hp2 | a0001 | c0001 | t0056 | g0259 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19005 | hp2 | a0001 | c0001 | t0053 | g0107 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19007 | hp2 | a0002 | c0002 | t0040 | g0250 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19009 | hp1 | a0001 | c0003 | t0001 | g0326 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19011 | hp1 | a0003 | c0005 | t0007 | g0145 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19012 | hp2 | a0002 | c0002 | t0012 | g0249 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19030 | hp1 | a0001 | c0001 | t0045 | g0210 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19030 | hp2 | a0002 | c0002 | t0021 | g0198 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0226 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19055 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19056 | hp2 | a0001 | c0004 | t0007 | g0007 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19063 | hp1 | a0001 | c0004 | t0007 | g0147 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19063 | hp2 | a0001 | c0001 | t0061 | g0159 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19065 | hp2 | a0001 | c0001 | t0010 | g0115 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19066 | hp2 | a0001 | c0004 | t0024 | g0146 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19074 | hp1 | a0002 | c0002 | t0005 | g0173 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0299 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19084 | hp1 | a0001 | c0001 | t0066 | g0254 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19088 | hp2 | a0003 | c0005 | t0007 | g0232 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19089 | hp1 | a0001 | c0001 | t0046 | g0097 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19089 | hp2 | a0001 | c0001 | t0062 | g0106 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19240 | hp1 | a0002 | c0002 | t0038 | g0340 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | YRI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | ASW | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20129 | hp2 | a0002 | c0002 | t0015 | g0025 | AFR | ASW | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0295 | EUR | TSI | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0063 | SAS | GIH | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | GIH | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG01123 | hp2 | a0001 | c0001 | t0050 | g0076 | AMR | CLM | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02109 | hp1 | a0001 | c0003 | t0002 | g0324 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02109 | hp2 | a0001 | c0001 | t0015 | g0013 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02559 | hp1 | a0002 | c0002 | t0025 | g0199 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0011 | AFR | ACB | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03471 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0276 | AFR | MSL | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG06807 | hp1 | a0001 | c0003 | t0035 | g0042 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
HG06807 | hp2 | a0002 | c0002 | t0011 | g0307 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA18955 | hp2 | a0001 | c0004 | t0001 | g0322 | EAS | JPT | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20300 | hp1 | a0001 | c0001 | t0026 | g0010 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0308 | AFR | USA | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0074 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
NA21309 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | LWK | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
homoSapiens | chm13v2 | a0004 | c0007 | t0016 | g0327 | REF | REF | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0136 | REF | REF | TNFRSF1B_chr1_12161991_12214220 | TNFRSF1B | chr1 | 12161991 | 12214220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12188806 | C | T | 1 | a0010 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.89C>T | p.Thr30Ile | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/10 | 190/3687 | 89/1386 | 30/461 | chr1 | 12188806 | |||
chr1:12192870 | G | A | 1 | a0007 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.559G>A | p.Val187Met | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 660/3687 | 559/1386 | 187/461 | chr1 | 12192870 | |||
chr1:12192898 | T | G | 4 | a0002 a0004 a0008 others(1): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
missense_variant | MODERATE | c.587T>G | p.Met196Arg | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 688/3687 | 587/1386 | 196/461 | chr1 | 12192898 | |||
chr1:12192919 | C | T | 1 | a0009 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.608C>T | p.Thr203Met | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 709/3687 | 608/1386 | 203/461 | chr1 | 12192919 | |||
chr1:12193005 | G | A | 2 | a0003 a0004 |
6 | HG00597.hp1 HG01358.hp2 HG02135.hp1 others(3): Show |
missense_variant | MODERATE | c.694G>A | p.Glu232Lys | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/10 | 795/3687 | 694/1386 | 232/461 | chr1 | 12193005 | |||
chr1:12193958 | T | C | 1 | a0005 | 2 | HG02280.hp1 HG02809.hp1 |
missense_variant | MODERATE | c.791T>C | p.Leu264Pro | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/10 | 892/3687 | 791/1386 | 264/461 | chr1 | 12193958 | |||
chr1:12201985 | A | G | 1 | a0006 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.919A>G | p.Lys307Glu | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/10 | 1020/3687 | 919/1386 | 307/461 | chr1 | 12201985 | |||
chr1:12206881 | C | T | 1 | a0008 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1247C>T | p.Pro416Leu | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1348/3687 | 1247/1386 | 416/461 | chr1 | 12206881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12188885 | A | G | 5 | a0001c0003 a0002c0002 a0004c0007 others(2): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
synonymous_variant | LOW | c.168A>G | p.Lys56Lys | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/10 | 269/3687 | 168/1386 | 56/461 | chr1 | 12188885 | |||
chr1:12192516 | C | T | 1 | a0001c0004 | 7 | HG00408.hp2 HG00438.hp1 NA18955.hp2 others(4): Show |
synonymous_variant | LOW | c.543C>T | p.Pro181Pro | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/10 | 644/3687 | 543/1386 | 181/461 | chr1 | 12192516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12167002 | A | C | 4 | a0001c0001t0068 a0001c0003t0067 a0001c0003t0069 others(1): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-90A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 90 | chr1 | 12167002 | ||||||
chr1:12167008 | C | A | 1 | a0002c0002t0039 | 1 | NA18978.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 84 | chr1 | 12167008 | ||||||
chr1:12167017 | G | A | 1 | a0002c0002t0040 | 1 | NA19007.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 75 | chr1 | 12167017 | ||||||
chr1:12167017 | G | T | 1 | a0001c0001t0066 | 1 | NA19084.hp1 | 5_prime_UTR_variant | MODIFIER | c.-75G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 75 | chr1 | 12167017 | ||||||
chr1:12167039 | T | TGCGAGGG others(1): Show |
4 | a0001c0001t0068 a0001c0003t0067 a0001c0003t0069 others(1): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-36_-29dupGCGAGGGC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/10 | 28 | INFO_REALIGN_3_PRIME | chr1 | 12167039 | |||||
chr1:12207208 | A | G | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(51): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*188A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 188 | chr1 | 12207208 | ||||||
chr1:12207213 | T | G | 4 | a0001c0001t0020 a0001c0001t0026 a0001c0001t0027 others(1): Show |
9 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*193T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 193 | chr1 | 12207213 | ||||||
chr1:12207235 | C | T | 43 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(40): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*215C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 215 | chr1 | 12207235 | ||||||
chr1:12207407 | C | A | 20 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0013 others(17): Show |
57 | HG00621.hp1 HG00733.hp2 HG01099.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*387C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 387 | chr1 | 12207407 | ||||||
chr1:12207473 | A | G | 2 | a0001c0001t0021 a0002c0002t0021 |
3 | HG01884.hp1 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*453A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 453 | chr1 | 12207473 | ||||||
chr1:12207490 | C | A | 1 | a0001c0001t0042 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*470C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 470 | chr1 | 12207490 | ||||||
chr1:12207492 | T | C | 3 | a0001c0001t0033 a0001c0001t0037 a0001c0001t0043 |
5 | HG03017.hp2 HG03491.hp1 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*472T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 472 | chr1 | 12207492 | ||||||
chr1:12207498 | C | G | 7 | a0001c0001t0008 a0001c0001t0035 a0001c0001t0049 others(4): Show |
14 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*478C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 478 | chr1 | 12207498 | ||||||
chr1:12207649 | C | T | 1 | a0001c0001t0042 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*629C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 629 | chr1 | 12207649 | ||||||
chr1:12207778 | C | T | 1 | a0006c0010t0048 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 758 | chr1 | 12207778 | ||||||
chr1:12207842 | G | A | 1 | a0001c0001t0044 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 822 | chr1 | 12207842 | ||||||
chr1:12207858 | C | G | 12 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0024 others(9): Show |
22 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*838C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 838 | chr1 | 12207858 | ||||||
chr1:12207914 | G | GA | 35 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0009 others(32): Show |
88 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*904dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 905 | INFO_REALIGN_3_PRIME | chr1 | 12207914 | |||||
chr1:12207942 | C | T | 44 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(41): Show |
120 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 922 | chr1 | 12207942 | ||||||
chr1:12207966 | G | GTGAA | 4 | a0001c0001t0016 a0001c0001t0036 a0001c0001t0053 others(1): Show |
8 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*947_*950dupTGAA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 951 | INFO_REALIGN_3_PRIME | chr1 | 12207966 | |||||
chr1:12208168 | C | T | 2 | a0001c0001t0017 a0002c0002t0017 |
4 | HG02970.hp2 HG03471.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1148C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1148 | chr1 | 12208168 | ||||||
chr1:12208268 | C | T | 1 | a0001c0001t0043 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1248 | chr1 | 12208268 | ||||||
chr1:12208329 | T | C | 2 | a0001c0001t0029 a0001c0001t0054 |
3 | HG03704.hp2 HG03942.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1309T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1309 | chr1 | 12208329 | ||||||
chr1:12208330 | C | T | 2 | a0001c0001t0052 a0001c0001t0063 |
2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1310C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1310 | chr1 | 12208330 | ||||||
chr1:12208331 | C | A | 2 | a0001c0001t0052 a0001c0001t0063 |
2 | HG00099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1311C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1311 | chr1 | 12208331 | ||||||
chr1:12208375 | G | A | 1 | a0001c0001t0056 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1355G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1355 | chr1 | 12208375 | ||||||
chr1:12208438 | T | C | 1 | a0001c0001t0046 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1418 | chr1 | 12208438 | ||||||
chr1:12208442 | G | A | 12 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0018 others(9): Show |
38 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1422 | chr1 | 12208442 | ||||||
chr1:12208514 | A | G | 10 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0036 others(7): Show |
16 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1494A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1494 | chr1 | 12208514 | ||||||
chr1:12208521 | T | G | 2 | a0001c0001t0023 a0002c0002t0038 |
5 | HG02257.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1501T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1501 | chr1 | 12208521 | ||||||
chr1:12208567 | G | A | 1 | a0001c0001t0057 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1547 | chr1 | 12208567 | ||||||
chr1:12208580 | C | T | 4 | a0001c0001t0014 a0001c0001t0028 a0002c0002t0014 others(1): Show |
8 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1560C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1560 | chr1 | 12208580 | ||||||
chr1:12208664 | G | A | 7 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0036 others(4): Show |
13 | HG01099.hp1 HG01255.hp2 HG01433.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1644G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1644 | chr1 | 12208664 | ||||||
chr1:12209005 | A | C | 1 | a0001c0001t0058 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1985A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 1985 | chr1 | 12209005 | ||||||
chr1:12209024 | C | G | 1 | a0001c0001t0051 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2004C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2004 | chr1 | 12209024 | ||||||
chr1:12209097 | C | T | 3 | a0001c0003t0067 a0001c0003t0069 a0005c0006t0060 |
3 | HG02572.hp2 HG02615.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2077C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2077 | chr1 | 12209097 | ||||||
chr1:12209163 | A | C | 1 | a0001c0001t0045 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2143A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 10/10 | 2143 | chr1 | 12209163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12167245 | C | G | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+76C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167245 | |||||||
chr1:12167319 | A | C | 1 | a0001c0001t0006g0335 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+150A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167319 | |||||||
chr1:12167471 | T | C | 1 | a0001c0001t0005g0018 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+302T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167471 | |||||||
chr1:12167674 | G | C | 1 | a0001c0001t0012g0019 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.78+505G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167674 | |||||||
chr1:12167784 | G | C | 14 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+615G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167784 | |||||||
chr1:12167808 | A | G | 14 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+639A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167808 | |||||||
chr1:12167814 | C | G | 14 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+645C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167814 | |||||||
chr1:12167838 | A | C | 1 | a0001c0001t0002g0334 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.78+669A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12167838 | |||||||
chr1:12168115 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.78+946G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168115 | |||||||
chr1:12168176 | G | A | 3 | a0002c0002t0002g0037 a0002c0002t0008g0035 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+1007G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168176 | |||||||
chr1:12168208 | C | T | 2 | a0002c0002t0038g0339 a0002c0002t0038g0340 |
2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.78+1039C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168208 | |||||||
chr1:12168445 | G | A | 1 | a0001c0001t0049g0038 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.78+1276G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168445 | |||||||
chr1:12168534 | C | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+1365C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168534 | |||||||
chr1:12168712 | C | A | 1 | a0001c0001t0023g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.78+1543C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168712 | |||||||
chr1:12168712 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.78+1543C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168712 | |||||||
chr1:12168753 | G | C | 33 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(30): Show |
33 | HG01106.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.78+1584G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168753 | |||||||
chr1:12168791 | C | G | 1 | a0001c0001t0002g0331 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.78+1622C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168791 | |||||||
chr1:12168804 | C | G | 2 | a0001c0001t0002g0330 a0001c0001t0003g0329 |
2 | NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.78+1635C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168804 | |||||||
chr1:12168921 | C | A | 1 | a0001c0001t0003g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.78+1752C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168921 | |||||||
chr1:12168953 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.78+1784C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168953 | |||||||
chr1:12168960 | C | T | 3 | a0002c0002t0002g0037 a0002c0002t0008g0035 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+1791C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12168960 | |||||||
chr1:12168974 | TC | T | 14 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+1810delC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12168974 | ||||||
chr1:12169649 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.78+2480C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169649 | |||||||
chr1:12169650 | G | A | 1 | a0001c0001t0013g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.78+2481G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169650 | |||||||
chr1:12169954 | G | A | 1 | a0001c0001t0005g0018 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.78+2785G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169954 | |||||||
chr1:12169990 | G | C | 1 | a0001c0001t0005g0051 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.78+2821G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12169990 | |||||||
chr1:12170024 | G | A | 7 | a0001c0003t0035g0042 a0002c0002t0002g0043 a0002c0002t0003g0040 others(4): Show |
7 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+2855G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170024 | |||||||
chr1:12170070 | C | T | 1 | a0001c0003t0002g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.78+2901C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170070 | |||||||
chr1:12170175 | CCATT | C | 33 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(30): Show |
33 | HG01106.hp2 HG01167.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.78+3024_78+3027del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12170175 | ||||||
chr1:12170248 | G | C | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+3079G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170248 | |||||||
chr1:12170388 | G | T | 14 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.78+3219G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170388 | |||||||
chr1:12170472 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.78+3303G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170472 | |||||||
chr1:12170492 | C | T | 1 | a0001c0001t0068g0338 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.78+3323C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170492 | |||||||
chr1:12170574 | G | C | 19 | a0001c0001t0002g0023 a0001c0001t0003g0029 a0001c0001t0006g0027 others(16): Show |
19 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.78+3405G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170574 | |||||||
chr1:12170833 | A | AT | 7 | a0001c0001t0004g0017 a0001c0001t0004g0323 a0001c0001t0008g0017 others(4): Show |
7 | HG01257.hp2 HG01358.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+3678dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12170833 | ||||||
chr1:12170866 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.78+3697G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170866 | |||||||
chr1:12170936 | A | C | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.78+3767A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12170936 | |||||||
chr1:12171176 | C | CT | 12 | a0001c0001t0005g0320 a0001c0001t0023g0039 a0001c0003t0001g0326 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.78+4024dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12171176 | ||||||
chr1:12171176 | CT | C | 13 | a0001c0001t0002g0060 a0001c0001t0003g0049 a0001c0001t0003g0061 others(10): Show |
13 | HG01074.hp1 HG01169.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+4024delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12171176 | ||||||
chr1:12171197 | A | G | 1 | a0002c0002t0031g0319 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.78+4028A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171197 | |||||||
chr1:12171294 | G | A | 1 | a0001c0001t0020g0065 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.78+4125G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171294 | |||||||
chr1:12171447 | G | T | 1 | a0002c0002t0003g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.78+4278G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171447 | |||||||
chr1:12171597 | C | T | 7 | a0001c0001t0003g0029 a0001c0001t0006g0027 a0001c0001t0011g0028 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+4428C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12171597 | |||||||
chr1:12172231 | C | T | 1 | a0001c0001t0002g0317 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.78+5062C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172231 | |||||||
chr1:12172297 | C | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA19055.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.78+5128C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172297 | |||||||
chr1:12172459 | T | A | 3 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0002c0002t0017g0047 |
3 | HG02717.hp1 HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.78+5290T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172459 | |||||||
chr1:12172597 | A | G | 8 | a0001c0001t0002g0311 a0001c0001t0002g0312 a0001c0001t0002g0313 others(5): Show |
8 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+5428A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172597 | |||||||
chr1:12172747 | A | G | 1 | a0001c0001t0005g0309 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.78+5578A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172747 | |||||||
chr1:12172749 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(88): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.78+5580T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172749 | |||||||
chr1:12172948 | A | G | 3 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 |
3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.78+5779A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172948 | |||||||
chr1:12172951 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+5782C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12172951 | |||||||
chr1:12173004 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.78+5835A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173004 | |||||||
chr1:12173205 | C | T | 3 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 |
3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.78+6036C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173205 | |||||||
chr1:12173697 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(261): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.78+6528T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173697 | |||||||
chr1:12173776 | T | C | 1 | a0003c0005t0007g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.78+6607T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12173776 | |||||||
chr1:12174122 | T | TTTC | 10 | a0001c0001t0003g0294 a0001c0001t0003g0295 a0001c0001t0004g0293 others(7): Show |
10 | HG00639.hp1 HG02027.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+6994_78+6996dup others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTC | 7 | a0001c0001t0006g0298 a0001c0001t0009g0063 a0001c0001t0013g0252 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6991_78+6996dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(2): Show |
6 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0001c0001t0007g0299 others(3): Show |
6 | HG00741.hp2 HG01192.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6988_78+6996dup others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(5): Show |
8 | a0001c0001t0001g0305 a0001c0001t0005g0309 a0001c0001t0006g0335 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+6985_78+6996dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(8): Show |
4 | a0001c0001t0004g0258 a0001c0001t0004g0306 a0001c0003t0002g0324 others(1): Show |
4 | HG02040.hp2 HG02109.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6982_78+6996dup others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(11): Show |
2 | a0001c0001t0004g0308 a0001c0001t0056g0259 |
2 | NA19002.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.78+6979_78+6996dup others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(14): Show |
2 | a0001c0003t0003g0064 a0002c0002t0002g0043 |
2 | HG02004.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.78+6976_78+6996dup others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(17): Show |
1 | a0001c0001t0001g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.78+6973_78+6996dup others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(20): Show |
1 | a0001c0001t0006g0261 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.78+6970_78+6996dup others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(23): Show |
2 | a0001c0001t0001g0144 a0001c0001t0012g0143 |
2 | HG00733.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.78+6967_78+6996dup others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | T | TTTCTTCT others(26): Show |
1 | a0001c0001t0058g0316 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.78+6964_78+6996dup others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | TTTC | T | 10 | a0001c0001t0002g0155 a0001c0001t0003g0006 a0001c0001t0003g0068 others(7): Show |
10 | HG00735.hp2 HG01934.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.78+6994_78+6996del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174122 | TTTCTTC | T | 3 | a0001c0004t0007g0147 a0001c0004t0007g0148 a0001c0004t0024g0146 |
3 | HG00408.hp2 NA19063.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.78+6991_78+6996del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174122 | ||||||
chr1:12174139 | TCTTCTTC others(50): Show |
T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6976_78+7032del others(57): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174139 | ||||||
chr1:12174148 | T | TCTCCTTC others(20): Show |
1 | a0001c0001t0001g0094 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.78+6981_78+6982ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | T | TCTCCTTC others(26): Show |
2 | a0001c0001t0001g0085 a0001c0001t0022g0123 |
2 | HG00323.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.78+6981_78+6982ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | T | TCTTCTCC others(11): Show |
1 | a0001c0001t0016g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.78+6984_78+6985ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | T | TCTTCTCC others(29): Show |
2 | a0001c0001t0016g0124 a0002c0002t0039g0157 |
2 | HG01099.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.78+6984_78+6985ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | TCTTCTTC others(11): Show |
T | 2 | a0001c0001t0008g0020 a0001c0004t0001g0322 |
2 | HG01891.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.78+6985_78+7002del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | TCTTCTTC others(23): Show |
T | 3 | a0001c0001t0008g0021 a0001c0001t0008g0022 a0001c0001t0008g0024 |
3 | HG01167.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.78+6985_78+7014del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | TCTTCTTC others(29): Show |
T | 2 | a0001c0001t0002g0023 a0001c0001t0017g0026 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.78+6985_78+7020del others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174148 | TCTTCTTC others(41): Show |
T | 1 | a0002c0002t0015g0025 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.78+6985_78+7032del others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174148 | ||||||
chr1:12174151 | TCTTCTTC others(26): Show |
T | 2 | a0001c0001t0006g0027 a0001c0001t0011g0028 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.78+6988_78+7020del others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174151 | ||||||
chr1:12174151 | TCTTCTTC others(32): Show |
T | 2 | a0001c0001t0003g0029 a0002c0002t0008g0333 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.78+6988_78+7026del others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174151 | ||||||
chr1:12174154 | T | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0016g0093 others(4): Show |
7 | HG00323.hp2 HG01099.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6985T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174154 | |||||||
chr1:12174154 | T | TCTC | 5 | a0001c0001t0002g0247 a0001c0001t0005g0102 a0002c0002t0001g0167 others(2): Show |
5 | HG00423.hp1 HG01952.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTCCTTC others(8): Show |
4 | a0001c0001t0001g0186 a0001c0001t0005g0089 a0001c0003t0034g0176 others(1): Show |
4 | HG04199.hp1 NA18954.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTCCTTC others(14): Show |
1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.78+6987_78+6988ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTCCTTC others(20): Show |
2 | a0001c0001t0001g0070 a0002c0002t0005g0173 |
2 | HG01123.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.78+6987_78+6988ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(5): Show |
2 | a0001c0001t0003g0274 a0003c0005t0019g0158 |
2 | HG02273.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(11): Show |
3 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0001t0006g0244 |
3 | HG01175.hp2 HG01496.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(17): Show |
2 | a0001c0001t0009g0082 a0001c0001t0015g0013 |
2 | HG00639.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(23): Show |
1 | a0001c0001t0019g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.78+6990_78+6991ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(29): Show |
3 | a0001c0001t0001g0110 a0002c0002t0001g0162 a0002c0002t0007g0170 |
3 | HG02165.hp1 HG02818.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(35): Show |
2 | a0001c0001t0002g0317 a0001c0001t0019g0098 |
2 | HG00408.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.78+6990_78+6991ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | T | TCTTCTCC others(41): Show |
1 | a0005c0006t0060g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.78+6990_78+6991ins others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | TCTTCTTC others(11): Show |
T | 1 | a0002c0002t0013g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.78+6991_78+7008del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174154 | TCTTCTTC others(17): Show |
T | 1 | a0002c0002t0015g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.78+6991_78+7014del others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174154 | ||||||
chr1:12174157 | TCTTCTTC others(2): Show |
T | 5 | a0001c0001t0009g0074 a0001c0001t0030g0183 a0001c0001t0032g0131 others(2): Show |
5 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+6994_78+7002del others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174157 | ||||||
chr1:12174157 | TCTTCTTC others(8): Show |
T | 1 | a0002c0002t0017g0045 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.78+6994_78+7008del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174157 | ||||||
chr1:12174160 | T | C | 45 | a0001c0001t0001g0070 a0001c0001t0001g0081 a0001c0001t0001g0085 others(42): Show |
45 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.78+6991T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174160 | |||||||
chr1:12174160 | T | TCTC | 3 | a0001c0001t0002g0079 a0001c0001t0016g0069 a0002c0002t0031g0319 |
3 | HG01261.hp1 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(2): Show |
8 | a0001c0001t0001g0190 a0001c0001t0002g0066 a0001c0001t0002g0100 others(5): Show |
8 | HG00099.hp1 HG01074.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(8): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0122 a0001c0001t0002g0052 others(4): Show |
7 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(14): Show |
6 | a0001c0001t0001g0002 a0001c0001t0002g0067 a0001c0001t0003g0092 others(3): Show |
6 | HG00673.hp2 HG01496.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(20): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0005g0112 |
3 | HG01243.hp1 HG01257.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(26): Show |
2 | a0001c0001t0001g0073 a0001c0001t0005g0051 |
2 | HG01258.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(32): Show |
2 | a0001c0001t0003g0004 a0001c0001t0005g0088 |
2 | NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTCCTTC others(38): Show |
2 | a0001c0001t0002g0004 a0001c0001t0005g0078 |
2 | NA19009.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.78+6993_78+6994ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTC | 4 | a0001c0001t0002g0213 a0001c0001t0003g0116 a0001c0001t0003g0182 others(1): Show |
4 | HG01261.hp2 HG02523.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+7087_78+7092dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(5): Show |
1 | a0001c0001t0002g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.78+7081_78+7092dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(11): Show |
6 | a0001c0001t0002g0077 a0001c0001t0002g0231 a0001c0001t0022g0163 others(3): Show |
6 | HG00423.hp2 HG01069.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+7075_78+7092dup others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(17): Show |
4 | a0001c0001t0001g0101 a0001c0001t0002g0125 a0001c0001t0004g0270 others(1): Show |
4 | HG00621.hp2 HG01981.hp2 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+7069_78+7092dup others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(23): Show |
5 | a0001c0001t0001g0084 a0001c0001t0001g0325 a0001c0001t0002g0096 others(2): Show |
5 | HG00735.hp1 HG04115.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.78+7063_78+7092dup others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(29): Show |
3 | a0001c0001t0002g0004 a0001c0001t0004g0225 a0001c0001t0024g0321 |
3 | HG00621.hp1 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.78+7057_78+7092dup others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTCC others(35): Show |
1 | a0005c0006t0001g0108 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.78+7051_78+7092dup others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(2): Show |
4 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0004g0075 others(1): Show |
4 | HG01175.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(8): Show |
9 | a0001c0001t0001g0206 a0001c0001t0002g0331 a0001c0001t0003g0196 others(6): Show |
9 | HG01891.hp2 HG02683.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(14): Show |
9 | a0001c0001t0001g0121 a0001c0001t0003g0013 a0001c0001t0003g0185 others(6): Show |
9 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(6): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(20): Show |
3 | a0001c0001t0009g0005 a0001c0001t0062g0106 a0002c0002t0002g0055 |
4 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(32): Show |
2 | a0001c0001t0002g0228 a0001c0001t0005g0018 |
2 | NA18948.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(38): Show |
1 | a0001c0001t0001g0219 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(44): Show |
2 | a0001c0001t0003g0001 a0001c0001t0003g0003 |
2 | NA18966.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(51): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(50): Show |
1 | a0001c0001t0003g0003 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(57): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(5): Show |
6 | a0001c0001t0001g0332 a0001c0001t0004g0207 a0001c0001t0021g0238 others(3): Show |
6 | HG00438.hp2 HG01884.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(11): Show |
7 | a0001c0001t0001g0239 a0001c0001t0003g0014 a0001c0001t0005g0118 others(4): Show |
7 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(17): Show |
7 | a0001c0001t0002g0161 a0001c0001t0002g0330 a0001c0001t0007g0266 others(4): Show |
7 | HG01934.hp2 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(23): Show |
7 | a0001c0001t0001g0012 a0001c0001t0001g0223 a0001c0001t0002g0001 others(4): Show |
7 | HG01981.hp1 HG02293.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(29): Show |
5 | a0001c0001t0002g0229 a0001c0001t0003g0209 a0001c0001t0003g0215 others(2): Show |
5 | HG03209.hp1 NA18945.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(41): Show |
1 | a0001c0001t0035g0222 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(8): Show |
2 | a0001c0001t0005g0216 a0001c0001t0013g0050 |
2 | HG03704.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(14): Show |
7 | a0001c0001t0006g0241 a0001c0001t0011g0276 a0001c0001t0012g0019 others(4): Show |
7 | HG01516.hp2 HG02976.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(20): Show |
2 | a0001c0001t0061g0159 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(26): Show |
4 | a0001c0001t0001g0217 a0001c0001t0002g0104 a0001c0001t0003g0329 others(1): Show |
4 | HG01256.hp1 HG02273.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(32): Show |
3 | a0001c0001t0002g0103 a0001c0001t0002g0126 a0001c0001t0033g0008 |
4 | HG03017.hp2 HG03491.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(38): Show |
1 | a0001c0001t0002g0334 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(44): Show |
1 | a0001c0001t0002g0189 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(51): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(11): Show |
4 | a0001c0001t0004g0009 a0001c0001t0004g0218 a0001c0001t0006g0011 others(1): Show |
4 | HG02622.hp2 HG03579.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(17): Show |
4 | a0001c0001t0003g0001 a0001c0001t0003g0138 a0001c0001t0003g0140 others(1): Show |
4 | HG01109.hp1 HG02083.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(23): Show |
1 | a0001c0001t0004g0323 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(29): Show |
3 | a0001c0001t0002g0313 a0001c0001t0003g0113 a0001c0001t0008g0226 |
3 | HG00558.hp2 HG02129.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(35): Show |
3 | a0001c0001t0002g0312 a0001c0001t0003g0243 a0001c0001t0030g0188 |
3 | HG00544.hp2 NA18747.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(47): Show |
1 | a0001c0001t0002g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(54): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(14): Show |
3 | a0001c0001t0015g0283 a0001c0001t0025g0221 a0002c0002t0015g0197 |
3 | HG02145.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(20): Show |
1 | a0006c0010t0048g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(26): Show |
1 | a0001c0001t0041g0314 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(32): Show |
2 | a0001c0001t0002g0311 a0001c0001t0011g0011 |
2 | HG02080.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(38): Show |
1 | a0001c0001t0064g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(56): Show |
1 | a0001c0001t0002g0227 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(63): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(23): Show |
4 | a0001c0001t0003g0135 a0001c0001t0012g0058 a0001c0001t0037g0133 others(1): Show |
4 | HG02258.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(29): Show |
1 | a0002c0009t0018g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(47): Show |
1 | a0001c0001t0002g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(54): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(20): Show |
1 | a0001c0001t0004g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(27): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(38): Show |
2 | a0001c0001t0003g0265 a0001c0001t0007g0267 |
2 | HG02735.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(45): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(23): Show |
2 | a0001c0001t0027g0057 a0001c0001t0027g0262 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.78+6996_78+6997ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(29): Show |
1 | a0001c0001t0043g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(35): Show |
1 | a0001c0001t0057g0315 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(26): Show |
1 | a0001c0001t0003g0061 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(33): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(32): Show |
1 | a0001c0001t0002g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(35): Show |
1 | a0001c0001t0004g0310 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | T | TCTTCTTC others(32): Show |
1 | a0001c0001t0003g0049 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.78+6996_78+6997ins others(39): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | TCTTCTC | T | 8 | a0001c0001t0003g0034 a0001c0001t0008g0017 a0001c0001t0020g0065 others(5): Show |
8 | HG00738.hp2 HG01099.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.78+7087_78+7092del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | TCTTCTCC others(5): Show |
T | 2 | a0001c0001t0004g0017 a0002c0002t0001g0279 |
2 | HG02630.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.78+7081_78+7092del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | TCTTCTCC others(11): Show |
T | 3 | a0001c0001t0002g0277 a0001c0001t0006g0289 a0001c0003t0059g0059 |
3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.78+7075_78+7092del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | TCTTCTCC others(23): Show |
T | 3 | a0001c0001t0023g0039 a0002c0002t0002g0037 a0002c0002t0017g0047 |
3 | HG02895.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.78+7063_78+7092del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174160 | TCTTCTCC others(35): Show |
T | 1 | a0001c0001t0047g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.78+7051_78+7092del others(42): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174160 | ||||||
chr1:12174163 | TCTC | T | 12 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0003g0184 others(9): Show |
13 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.78+6997_78+6999del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | ||||||
chr1:12174163 | TCTCCTTC others(2): Show |
T | 4 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0011g0032 others(1): Show |
4 | HG02280.hp2 HG03195.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+6997_78+7005del others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | ||||||
chr1:12174163 | TCTCCTTC others(8): Show |
T | 4 | a0001c0001t0006g0290 a0001c0001t0008g0284 a0001c0001t0020g0203 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+6997_78+7011del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | ||||||
chr1:12174163 | TCTCCTTC others(14): Show |
T | 2 | a0002c0002t0008g0035 a0002c0002t0032g0036 |
2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.78+6997_78+7017del others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174163 | ||||||
chr1:12174166 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0144 a0001c0001t0001g0292 others(28): Show |
31 | HG00140.hp1 HG00140.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.78+6997C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174166 | |||||||
chr1:12174172 | C | T | 34 | a0001c0001t0001g0292 a0001c0001t0003g0034 a0001c0001t0003g0214 others(31): Show |
35 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.78+7003C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174172 | |||||||
chr1:12174178 | C | T | 28 | a0001c0001t0001g0292 a0001c0001t0002g0285 a0001c0001t0002g0286 others(25): Show |
28 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.78+7009C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174178 | |||||||
chr1:12174184 | C | T | 20 | a0001c0001t0002g0277 a0001c0001t0002g0286 a0001c0001t0003g0034 others(17): Show |
20 | HG00140.hp1 HG00140.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.78+7015C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174184 | |||||||
chr1:12174190 | C | CCTTCTCC others(22): Show |
1 | a0001c0001t0005g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.78+7023_78+7051dup others(29): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12174190 | ||||||
chr1:12174190 | C | T | 5 | a0001c0003t0059g0059 a0002c0002t0001g0279 a0002c0002t0008g0035 others(2): Show |
5 | HG02717.hp2 HG02886.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7021C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174190 | |||||||
chr1:12174196 | C | T | 2 | a0002c0002t0001g0279 a0002c0002t0032g0036 |
2 | HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.78+7027C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174196 | |||||||
chr1:12174246 | T | C | 1 | a0008c0011t0001g0156 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.78+7077T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174246 | |||||||
chr1:12174250 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7081C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174250 | |||||||
chr1:12174256 | C | T | 6 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(3): Show |
6 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.78+7087C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174256 | |||||||
chr1:12174262 | T | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(7): Show |
13 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.78+7093T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174262 | |||||||
chr1:12174263 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7094C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174263 | |||||||
chr1:12174266 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7097C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174266 | |||||||
chr1:12174267 | T | A | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+7098T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174267 | |||||||
chr1:12174267 | T | TCCTTCTC others(23): Show |
1 | a0001c0003t0001g0326 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.78+7098_78+7099ins others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174267 | |||||||
chr1:12174461 | T | A | 2 | a0001c0001t0023g0039 a0002c0002t0017g0047 |
2 | HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.78+7292T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174461 | |||||||
chr1:12174468 | G | C | 2 | a0001c0001t0008g0020 a0001c0001t0008g0021 |
2 | HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.78+7299G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174468 | |||||||
chr1:12174540 | G | A | 1 | a0003c0005t0019g0158 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.78+7371G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174540 | |||||||
chr1:12174550 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.78+7381C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174550 | |||||||
chr1:12174565 | A | G | 7 | a0001c0001t0068g0338 a0001c0003t0001g0326 a0001c0003t0067g0337 others(4): Show |
7 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+7396A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174565 | |||||||
chr1:12174685 | G | A | 2 | a0001c0001t0005g0130 a0001c0001t0032g0131 |
2 | NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.78+7516G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174685 | |||||||
chr1:12174710 | C | A | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.78+7541C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174710 | |||||||
chr1:12174720 | G | A | 3 | a0001c0001t0004g0017 a0001c0001t0004g0323 a0001c0001t0008g0017 |
3 | HG01257.hp2 HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.78+7551G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174720 | |||||||
chr1:12174736 | A | G | 1 | a0001c0001t0023g0039 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.78+7567A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174736 | |||||||
chr1:12174769 | G | C | 1 | a0001c0001t0061g0159 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.78+7600G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174769 | |||||||
chr1:12174828 | T | C | 7 | a0001c0001t0068g0338 a0001c0003t0001g0326 a0001c0003t0067g0337 others(4): Show |
7 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+7659T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174828 | |||||||
chr1:12174926 | G | A | 4 | a0001c0001t0003g0029 a0001c0001t0006g0027 a0001c0001t0007g0299 others(1): Show |
4 | HG01884.hp2 HG02976.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+7757G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174926 | |||||||
chr1:12174983 | C | T | 1 | a0001c0001t0017g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.78+7814C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12174983 | |||||||
chr1:12175075 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0006g0160 |
2 | HG03209.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78+7906G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175075 | |||||||
chr1:12175114 | G | A | 3 | a0001c0001t0009g0074 a0001c0001t0022g0163 a0002c0002t0001g0162 |
3 | HG01069.hp1 HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.78+7945G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175114 | |||||||
chr1:12175223 | C | T | 3 | a0001c0001t0002g0155 a0001c0001t0002g0247 a0001c0001t0003g0154 |
3 | HG00423.hp1 HG02129.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.78+8054C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175223 | |||||||
chr1:12175242 | C | T | 1 | a0001c0001t0043g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.78+8073C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175242 | |||||||
chr1:12175374 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0006g0014 a0001c0001t0006g0245 |
3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.78+8205A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175374 | |||||||
chr1:12175391 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0006g0244 a0001c0001t0015g0013 |
3 | HG02109.hp2 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.78+8222C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175391 | |||||||
chr1:12175399 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.78+8230C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175399 | |||||||
chr1:12175667 | C | G | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.78+8498C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175667 | |||||||
chr1:12175820 | C | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+8651C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12175820 | |||||||
chr1:12176053 | G | GA | 53 | a0001c0001t0001g0186 a0001c0001t0002g0066 a0001c0001t0002g0067 others(50): Show |
53 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.78+8900dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176053 | ||||||
chr1:12176053 | GA | G | 10 | a0001c0001t0002g0060 a0001c0001t0003g0061 a0001c0001t0003g0127 others(7): Show |
10 | HG01358.hp2 HG02109.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.78+8900delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176053 | ||||||
chr1:12176060 | A | G | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+8891A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176060 | |||||||
chr1:12176103 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+8934C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176103 | |||||||
chr1:12176161 | G | T | 1 | a0001c0001t0002g0126 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.78+8992G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176161 | |||||||
chr1:12176173 | C | T | 1 | a0001c0001t0003g0243 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.78+9004C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176173 | |||||||
chr1:12176175 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.78+9006C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12176175 | |||||||
chr1:12176269 | AG | A | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+9102delG | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176269 | ||||||
chr1:12176971 | TCCTGAGC | T | 7 | a0001c0001t0068g0338 a0001c0003t0001g0326 a0001c0003t0067g0337 others(4): Show |
7 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+9819_78+9825del others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12176971 | ||||||
chr1:12177148 | G | A | 26 | a0001c0001t0001g0305 a0001c0001t0002g0311 a0001c0001t0002g0312 others(23): Show |
27 | HG00558.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.78+9979G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177148 | |||||||
chr1:12177282 | C | T | 1 | a0002c0002t0009g0257 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.78+10113C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177282 | |||||||
chr1:12177313 | G | A | 1 | a0001c0001t0006g0335 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+10144G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177313 | |||||||
chr1:12177364 | G | A | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+10195G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177364 | |||||||
chr1:12177394 | G | A | 1 | a0001c0004t0007g0007 | 2 | NA19000.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.78+10225G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177394 | |||||||
chr1:12177520 | C | T | 4 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0002c0002t0008g0333 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.78+10351C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177520 | |||||||
chr1:12177717 | C | T | 4 | a0001c0003t0067g0337 a0001c0003t0069g0336 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.78+10548C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177717 | |||||||
chr1:12177751 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.78+10582G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177751 | |||||||
chr1:12177760 | C | G | 1 | a0001c0001t0002g0242 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.78+10591C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177760 | |||||||
chr1:12177764 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.78+10595A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177764 | |||||||
chr1:12177794 | C | CA | 37 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0305 others(34): Show |
38 | HG00558.hp1 HG00558.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.78+10641dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12177794 | ||||||
chr1:12177794 | CA | C | 17 | a0001c0001t0001g0239 a0001c0001t0002g0291 a0001c0001t0006g0241 others(14): Show |
17 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.78+10641delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12177794 | ||||||
chr1:12177821 | C | T | 1 | a0001c0001t0016g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.78+10652C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177821 | |||||||
chr1:12177921 | C | T | 7 | a0001c0001t0068g0338 a0001c0003t0001g0326 a0001c0003t0067g0337 others(4): Show |
7 | HG01358.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.78+10752C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12177921 | |||||||
chr1:12178139 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-10657C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178139 | |||||||
chr1:12178303 | G | A | 1 | a0001c0001t0065g0275 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.79-10493G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178303 | |||||||
chr1:12178582 | G | C | 1 | a0001c0001t0024g0191 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79-10214G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178582 | |||||||
chr1:12178689 | G | A | 3 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 |
3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.79-10107G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178689 | |||||||
chr1:12178772 | C | G | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-10024C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178772 | |||||||
chr1:12178830 | C | T | 5 | a0001c0001t0068g0338 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-9966C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178830 | |||||||
chr1:12178913 | C | T | 11 | a0001c0001t0002g0161 a0001c0001t0003g0256 a0001c0001t0006g0241 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-9883C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178913 | |||||||
chr1:12178970 | G | T | 3 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0002c0002t0017g0047 |
3 | HG02717.hp1 HG02895.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.79-9826G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178970 | |||||||
chr1:12178972 | G | A | 3 | a0001c0001t0011g0276 a0001c0001t0018g0296 a0002c0002t0011g0307 |
3 | HG02451.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.79-9824G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12178972 | |||||||
chr1:12179032 | G | A | 16 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0001c0003t0001g0326 others(13): Show |
16 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.79-9764G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179032 | |||||||
chr1:12179094 | C | T | 3 | a0001c0003t0001g0326 a0002c0002t0015g0025 a0004c0007t0014g0328 |
3 | HG01358.hp2 NA19009.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.79-9702C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179094 | |||||||
chr1:12179299 | C | T | 2 | a0001c0001t0002g0231 a0003c0005t0007g0232 |
2 | NA18975.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.79-9497C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179299 | |||||||
chr1:12179308 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.79-9488G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179308 | |||||||
chr1:12179463 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-9333C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179463 | |||||||
chr1:12179473 | G | A | 14 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0001c0003t0035g0042 others(11): Show |
14 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-9323G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179473 | |||||||
chr1:12179756 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.79-9040G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12179756 | |||||||
chr1:12180031 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.79-8765G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180031 | |||||||
chr1:12180040 | G | A | 4 | a0001c0003t0067g0337 a0001c0003t0069g0336 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-8756G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180040 | |||||||
chr1:12180089 | A | T | 2 | a0001c0001t0022g0163 a0002c0002t0001g0162 |
2 | HG01069.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.79-8707A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180089 | |||||||
chr1:12180152 | G | A | 1 | a0001c0001t0002g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.79-8644G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180152 | |||||||
chr1:12180358 | C | G | 1 | a0001c0001t0022g0123 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.79-8438C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180358 | |||||||
chr1:12180539 | A | T | 4 | a0001c0003t0067g0337 a0001c0003t0069g0336 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-8257A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180539 | |||||||
chr1:12180619 | G | A | 47 | a0001c0001t0001g0186 a0001c0001t0002g0066 a0001c0001t0002g0067 others(44): Show |
47 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-8177G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180619 | |||||||
chr1:12180635 | C | T | 3 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 |
3 | HG01106.hp2 HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.79-8161C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180635 | |||||||
chr1:12180665 | T | G | 14 | a0001c0001t0023g0039 a0001c0001t0047g0048 a0001c0003t0035g0042 others(11): Show |
14 | HG01106.hp2 HG01243.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-8131T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180665 | |||||||
chr1:12180751 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.79-8045C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180751 | |||||||
chr1:12180767 | T | G | 70 | a0001c0001t0001g0186 a0001c0001t0002g0066 a0001c0001t0002g0067 others(67): Show |
70 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.79-8029T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180767 | |||||||
chr1:12180833 | A | G | 2 | a0001c0001t0002g0330 a0001c0001t0003g0329 |
2 | NA18944.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.79-7963A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180833 | |||||||
chr1:12180993 | T | C | 13 | a0001c0001t0002g0277 a0001c0001t0018g0056 a0001c0001t0023g0039 others(10): Show |
13 | HG01192.hp2 HG01358.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-7803T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12180993 | |||||||
chr1:12181017 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-7779G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181017 | |||||||
chr1:12181086 | G | A | 1 | a0001c0001t0008g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.79-7710G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181086 | |||||||
chr1:12181126 | A | G | 2 | a0001c0001t0018g0056 a0001c0001t0049g0038 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.79-7670A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181126 | |||||||
chr1:12181205 | T | C | 4 | a0001c0003t0067g0337 a0001c0003t0069g0336 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-7591T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181205 | |||||||
chr1:12181267 | T | C | 1 | a0001c0001t0056g0259 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.79-7529T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181267 | |||||||
chr1:12181412 | A | G | 11 | a0001c0001t0001g0121 a0001c0001t0018g0056 a0001c0001t0021g0230 others(8): Show |
11 | HG00597.hp2 HG01192.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.79-7384A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181412 | |||||||
chr1:12181546 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79-7250C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181546 | |||||||
chr1:12181554 | G | A | 1 | a0001c0001t0002g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-7242G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181554 | |||||||
chr1:12181615 | G | A | 3 | a0001c0001t0004g0308 a0001c0001t0028g0302 a0001c0001t0028g0303 |
3 | HG01070.hp1 HG01071.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.79-7181G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181615 | |||||||
chr1:12181780 | G | A | 1 | a0002c0002t0014g0278 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.79-7016G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181780 | |||||||
chr1:12181798 | T | G | 24 | a0001c0001t0002g0277 a0001c0001t0003g0013 a0001c0001t0009g0063 others(21): Show |
24 | HG00140.hp1 HG01106.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.79-6998T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181798 | |||||||
chr1:12181934 | G | A | 57 | a0001c0001t0001g0305 a0001c0001t0002g0277 a0001c0001t0002g0311 others(54): Show |
58 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.79-6862G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12181934 | |||||||
chr1:12182022 | C | T | 4 | a0001c0003t0067g0337 a0001c0003t0069g0336 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-6774C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182022 | |||||||
chr1:12182039 | C | T | 4 | a0001c0001t0021g0230 a0001c0003t0001g0326 a0002c0002t0008g0333 others(1): Show |
4 | HG01358.hp2 HG02055.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-6757C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182039 | |||||||
chr1:12182140 | G | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-6656G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182140 | |||||||
chr1:12182148 | G | A | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-6648G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182148 | |||||||
chr1:12182401 | T | C | 68 | a0001c0001t0004g0293 a0001c0001t0008g0022 a0001c0001t0008g0024 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.79-6395T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182401 | |||||||
chr1:12182520 | T | C | 1 | a0001c0001t0017g0030 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.79-6276T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182520 | |||||||
chr1:12182562 | T | C | 2 | a0001c0001t0008g0022 a0001c0001t0008g0024 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.79-6234T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182562 | |||||||
chr1:12182562 | T | TTGAA | 59 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-6216_79-6213dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12182562 | ||||||
chr1:12182647 | G | A | 2 | a0001c0001t0002g0200 a0001c0001t0002g0201 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.79-6149G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182647 | |||||||
chr1:12182702 | T | A | 7 | a0002c0002t0001g0279 a0002c0002t0002g0043 a0002c0002t0003g0040 others(4): Show |
7 | HG00140.hp1 HG02004.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-6094T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182702 | |||||||
chr1:12182736 | T | G | 63 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.79-6060T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182736 | |||||||
chr1:12182813 | G | A | 38 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0034g0176 others(35): Show |
38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-5983G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182813 | |||||||
chr1:12182857 | G | A | 2 | a0001c0001t0027g0057 a0001c0001t0027g0262 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.79-5939G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182857 | |||||||
chr1:12182892 | A | G | 60 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.79-5904A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12182892 | |||||||
chr1:12183084 | C | T | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5712C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183084 | |||||||
chr1:12183133 | C | T | 4 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0229 others(1): Show |
4 | HG02132.hp2 NA18984.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5663C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183133 | |||||||
chr1:12183217 | C | T | 63 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.79-5579C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183217 | |||||||
chr1:12183320 | G | C | 66 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-5476G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183320 | |||||||
chr1:12183446 | T | TTC | 10 | a0001c0001t0005g0309 a0001c0003t0002g0324 a0001c0003t0003g0064 others(7): Show |
10 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5324_79-5323dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183446 | ||||||
chr1:12183446 | TTC | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.79-5324_79-5323del others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183446 | ||||||
chr1:12183492 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79-5304A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183492 | |||||||
chr1:12183545 | A | T | 1 | a0001c0001t0005g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.79-5251A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183545 | |||||||
chr1:12183587 | T | A | 1 | a0002c0002t0001g0162 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.79-5209T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183587 | |||||||
chr1:12183597 | TTATC | T | 4 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0002c0002t0011g0041 others(1): Show |
4 | HG01358.hp2 HG02572.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5185_79-5182del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183597 | ||||||
chr1:12183605 | CTATCTAT others(5): Show |
C | 3 | a0002c0002t0001g0180 a0002c0002t0001g0181 a0002c0002t0031g0152 |
3 | HG01168.hp2 HG01169.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.79-5189_79-5178del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183605 | ||||||
chr1:12183609 | CTATCTGT others(1): Show |
C | 35 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0034g0176 others(32): Show |
35 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.79-5185_79-5178del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183609 | ||||||
chr1:12183617 | T | C | 25 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(22): Show |
25 | HG00140.hp1 HG01106.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.79-5179T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183617 | |||||||
chr1:12183654 | TTTTATCT others(3): Show |
T | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-5140_79-5131del others(10): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183654 | ||||||
chr1:12183656 | T | TTATC | 56 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0099 others(53): Show |
59 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.79-5088_79-5085dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | T | TTATCTAT others(1): Show |
18 | a0001c0001t0001g0110 a0001c0001t0002g0247 a0001c0001t0002g0317 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5092_79-5085dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | T | TTATCTAT others(5): Show |
2 | a0001c0001t0002g0114 a0001c0001t0007g0267 |
2 | HG02083.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.79-5096_79-5085dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | TTATC | T | 80 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(77): Show |
82 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.79-5088_79-5085del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | TTATCTAT others(1): Show |
T | 31 | a0001c0001t0001g0085 a0001c0001t0001g0144 a0001c0001t0001g0239 others(28): Show |
31 | HG00558.hp1 HG00738.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.79-5092_79-5085del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | TTATCTAT others(5): Show |
T | 19 | a0001c0001t0001g0206 a0001c0001t0001g0219 a0001c0001t0001g0332 others(16): Show |
19 | HG00438.hp2 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.79-5096_79-5085del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183656 | TTATCTAT others(9): Show |
T | 5 | a0001c0001t0002g0104 a0001c0001t0003g0138 a0001c0001t0003g0140 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-5100_79-5085del others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183656 | ||||||
chr1:12183675 | T | G | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5121T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183675 | |||||||
chr1:12183679 | TCTA | T | 3 | a0002c0002t0002g0178 a0002c0002t0002g0179 a0009c0012t0001g0132 |
3 | HG00099.hp2 HG03927.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.79-5116_79-5114del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183679 | |||||||
chr1:12183683 | TCTA | T | 20 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0162 others(17): Show |
20 | HG00423.hp2 HG01074.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-5112_79-5110del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183683 | |||||||
chr1:12183687 | TCTA | T | 11 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0151 others(8): Show |
11 | HG01168.hp2 HG01169.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-5108_79-5106del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183687 | |||||||
chr1:12183695 | T | A | 2 | a0002c0002t0011g0041 a0002c0002t0015g0197 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.79-5101T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183695 | |||||||
chr1:12183699 | T | G | 6 | a0001c0003t0003g0064 a0002c0002t0013g0044 a0002c0002t0015g0046 others(3): Show |
6 | HG01106.hp2 HG01243.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-5097T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183699 | |||||||
chr1:12183699 | T | TCTATCTA others(9): Show |
1 | a0001c0003t0002g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183699 | ||||||
chr1:12183699 | T | TCTATCTA others(13): Show |
1 | a0001c0003t0059g0059 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(20): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183699 | ||||||
chr1:12183702 | A | ATCTAGCT others(14): Show |
1 | a0002c0002t0002g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(21): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183702 | ||||||
chr1:12183703 | T | A | 2 | a0002c0002t0002g0043 a0002c0002t0003g0318 |
2 | HG00140.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.79-5093T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | |||||||
chr1:12183703 | T | G | 2 | a0002c0002t0008g0333 a0002c0002t0011g0307 |
2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.79-5093T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | |||||||
chr1:12183703 | TCTATCTA others(5): Show |
T | 1 | a0002c0002t0003g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-5092_79-5081del others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183703 | |||||||
chr1:12183706 | A | AGCTAGCT others(10): Show |
1 | a0001c0003t0069g0336 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.79-5090_79-5089ins others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183706 | |||||||
chr1:12183707 | T | A | 2 | a0002c0002t0001g0279 a0002c0002t0014g0278 |
2 | HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.79-5089T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183707 | |||||||
chr1:12183707 | T | G | 4 | a0001c0003t0035g0042 a0002c0002t0008g0035 a0002c0002t0011g0307 others(1): Show |
4 | HG02717.hp2 HG02886.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5089T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183707 | |||||||
chr1:12183710 | A | AGCTAGCT others(17): Show |
1 | a0001c0003t0067g0337 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183710 | |||||||
chr1:12183710 | A | AGCTATCT others(9): Show |
1 | a0001c0003t0035g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.79-5086_79-5085ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183710 | |||||||
chr1:12183710 | AT | A | 38 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0149 others(35): Show |
38 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.79-5084delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183710 | ||||||
chr1:12183711 | T | A | 3 | a0001c0003t0035g0042 a0001c0003t0067g0337 a0002c0002t0011g0307 |
3 | HG02572.hp2 HG06807.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.79-5085T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | |||||||
chr1:12183711 | T | TCTAGCTA others(9): Show |
1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79-5085_79-5084ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | |||||||
chr1:12183711 | T | TTCTA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0190 others(64): Show |
70 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.79-5080_79-5077dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | ||||||
chr1:12183711 | T | TTCTATCT others(5): Show |
1 | a0002c0002t0032g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.79-5077_79-5076ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | ||||||
chr1:12183711 | T | TTCTATCT others(9): Show |
1 | a0001c0001t0002g0004 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.79-5077_79-5076ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | ||||||
chr1:12183711 | T | TTCTATCT others(17): Show |
2 | a0001c0001t0002g0229 a0001c0001t0024g0191 |
2 | NA18943.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.79-5077_79-5076ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183711 | ||||||
chr1:12183711 | TTCTATCT others(42): Show |
T | 6 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0002c0002t0002g0193 others(3): Show |
6 | HG02572.hp1 HG02647.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5084_79-5036del others(49): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183711 | |||||||
chr1:12183716 | T | G | 1 | a0002c0002t0011g0307 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-5080T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183716 | |||||||
chr1:12183720 | C | A | 1 | a0002c0002t0003g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.79-5076C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183720 | |||||||
chr1:12183720 | C | CCTAT | 27 | a0001c0001t0002g0114 a0001c0001t0002g0126 a0001c0001t0002g0285 others(24): Show |
27 | HG00597.hp1 HG00621.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.79-5048_79-5045dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | ||||||
chr1:12183720 | C | CCTATCTA others(1): Show |
4 | a0001c0001t0011g0276 a0001c0001t0055g0288 a0002c0009t0018g0062 others(1): Show |
4 | HG02055.hp1 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5052_79-5045dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | ||||||
chr1:12183720 | C | CCTATCTA others(5): Show |
3 | a0001c0001t0003g0140 a0001c0001t0006g0289 a0001c0001t0010g0141 |
3 | HG01109.hp1 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.79-5056_79-5045dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | ||||||
chr1:12183720 | C | CCTATCTA others(9): Show |
1 | a0001c0001t0006g0290 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.79-5060_79-5045dup others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | ||||||
chr1:12183720 | C | T | 64 | a0001c0001t0002g0004 a0001c0001t0002g0229 a0001c0001t0003g0004 others(61): Show |
65 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.79-5076C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183720 | |||||||
chr1:12183720 | CCTAT | C | 18 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0002g0079 others(15): Show |
18 | HG01081.hp2 HG01168.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5048_79-5045del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183720 | ||||||
chr1:12183724 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0005g0320 |
2 | HG03098.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.79-5072T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183724 | |||||||
chr1:12183728 | T | C | 1 | a0001c0001t0066g0254 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.79-5068T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183728 | |||||||
chr1:12183728 | TCTATCTA others(33): Show |
T | 4 | a0002c0002t0001g0167 a0002c0002t0002g0043 a0002c0002t0002g0179 others(1): Show |
4 | HG00140.hp1 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5059_79-5020del others(40): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183728 | ||||||
chr1:12183732 | TCTATCTA others(29): Show |
T | 13 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0172 others(10): Show |
13 | HG00099.hp2 HG01433.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.79-5055_79-5020del others(36): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183732 | ||||||
chr1:12183736 | TCTATCTA others(25): Show |
T | 10 | a0002c0002t0001g0151 a0002c0002t0001g0162 a0002c0002t0001g0169 others(7): Show |
10 | HG01168.hp2 HG01169.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5051_79-5020del others(32): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183736 | ||||||
chr1:12183740 | TCTATCTA others(21): Show |
T | 9 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0174 others(6): Show |
9 | HG00423.hp2 HG01074.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-5047_79-5020del others(28): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183740 | ||||||
chr1:12183744 | T | G | 2 | a0001c0001t0007g0266 a0001c0001t0016g0095 |
2 | HG01433.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.79-5052T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183744 | |||||||
chr1:12183744 | T | TCTAG | 3 | a0001c0001t0002g0023 a0001c0001t0017g0026 a0001c0001t0018g0296 |
3 | HG02451.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.79-5049_79-5048ins others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183744 | ||||||
chr1:12183744 | TCTATCTA others(17): Show |
T | 3 | a0002c0002t0003g0040 a0002c0002t0009g0165 a0002c0002t0031g0152 |
3 | HG01515.hp2 HG01934.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.79-5044_79-5021del others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183744 | ||||||
chr1:12183748 | T | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(78): Show |
84 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.79-5048T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183748 | |||||||
chr1:12183748 | T | TCTAG | 14 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(11): Show |
14 | HG00639.hp2 HG00673.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.79-5028_79-5025dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTAGCTA others(1): Show |
13 | a0001c0001t0001g0219 a0001c0001t0002g0200 a0001c0001t0002g0201 others(10): Show |
13 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-5032_79-5025dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTATCTA others(1): Show |
32 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0260 others(29): Show |
34 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTATCTA others(5): Show |
1 | a0001c0001t0014g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79-5045_79-5044ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTATCTA others(5): Show |
11 | a0001c0001t0001g0001 a0001c0001t0002g0242 a0001c0001t0002g0312 others(8): Show |
11 | HG02040.hp2 HG02132.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTATCTA others(33): Show |
1 | a0001c0001t0001g0325 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.79-5045_79-5044ins others(40): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | T | TCTATCTA others(9): Show |
8 | a0001c0001t0001g0012 a0001c0001t0001g0217 a0001c0001t0001g0223 others(5): Show |
8 | HG01069.hp1 HG01934.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-5045_79-5044ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183748 | TCTAGCTA others(1): Show |
T | 4 | a0001c0001t0001g0144 a0001c0001t0003g0135 a0001c0001t0012g0142 others(1): Show |
4 | HG00733.hp2 HG02258.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-5032_79-5025del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183748 | ||||||
chr1:12183752 | G | T | 15 | a0001c0001t0008g0022 a0001c0001t0008g0024 a0001c0003t0002g0324 others(12): Show |
15 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.79-5044G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183752 | |||||||
chr1:12183755 | A | ATCTATCT others(2): Show |
8 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(5): Show |
8 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-5041_79-5040ins others(9): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183755 | |||||||
chr1:12183755 | AGCTAGCT others(8): Show |
A | 1 | a0001c0003t0003g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.79-5040_79-5026del others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183755 | |||||||
chr1:12183756 | G | T | 18 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0035g0042 others(15): Show |
18 | HG01106.hp2 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-5040G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183756 | |||||||
chr1:12183759 | AGCTAGCT others(4): Show |
A | 1 | a0001c0003t0002g0324 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.79-5036_79-5026del others(11): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183759 | |||||||
chr1:12183760 | G | T | 17 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0059g0059 others(14): Show |
17 | HG01243.hp2 HG01358.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.79-5036G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183760 | |||||||
chr1:12183764 | G | C | 8 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(5): Show |
8 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.79-5032G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183764 | |||||||
chr1:12183764 | G | T | 20 | a0001c0001t0002g0060 a0001c0001t0003g0013 a0001c0001t0003g0061 others(17): Show |
20 | HG01106.hp2 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-5032G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183764 | |||||||
chr1:12183767 | AGCT | A | 3 | a0002c0002t0015g0046 a0002c0002t0017g0045 a0002c0002t0038g0339 |
3 | HG01243.hp2 HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.79-5028_79-5026del others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183767 | |||||||
chr1:12183768 | G | C | 10 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(7): Show |
10 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-5028G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183768 | |||||||
chr1:12183768 | G | T | 10 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0002c0002t0002g0193 others(7): Show |
10 | HG01106.hp2 HG01358.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.79-5028G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183768 | |||||||
chr1:12183771 | A | T | 7 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.79-5025A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183771 | |||||||
chr1:12183772 | T | C | 2 | a0002c0002t0021g0198 a0002c0002t0025g0199 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-5024T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183772 | |||||||
chr1:12183775 | AT | A | 13 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(10): Show |
13 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.79-5019delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183775 | ||||||
chr1:12183776 | T | TCTA | 6 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5020_79-5019ins others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183776 | |||||||
chr1:12183781 | T | C | 9 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(6): Show |
9 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-5015T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183781 | |||||||
chr1:12183785 | C | G | 6 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-5011C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183785 | |||||||
chr1:12183785 | C | T | 4 | a0002c0002t0002g0037 a0002c0002t0021g0198 a0002c0002t0025g0199 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-5011C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183785 | |||||||
chr1:12183789 | C | CCTAT | 47 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0034g0176 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.79-4995_79-4992dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183789 | ||||||
chr1:12183789 | C | G | 2 | a0002c0002t0002g0037 a0002c0002t0032g0036 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79-5007C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183789 | |||||||
chr1:12183789 | C | T | 17 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(14): Show |
17 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.79-5007C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183789 | |||||||
chr1:12183793 | T | G | 2 | a0002c0002t0021g0198 a0002c0002t0025g0199 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-5003T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183793 | |||||||
chr1:12183796 | A | AT | 6 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.79-4999dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183796 | ||||||
chr1:12183805 | G | C | 5 | a0001c0003t0035g0042 a0001c0003t0067g0337 a0001c0003t0069g0336 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-4991G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183805 | |||||||
chr1:12183805 | G | T | 5 | a0001c0001t0029g0003 a0001c0001t0054g0253 a0001c0003t0001g0326 others(2): Show |
5 | HG02717.hp2 HG03579.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.79-4991G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183805 | |||||||
chr1:12183808 | A | T | 2 | a0002c0002t0021g0198 a0002c0002t0025g0199 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-4988A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183808 | |||||||
chr1:12183809 | T | C | 2 | a0002c0002t0002g0037 a0002c0002t0032g0036 |
2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.79-4987T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183809 | |||||||
chr1:12183816 | AT | A | 10 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(7): Show |
10 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-4978delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183816 | ||||||
chr1:12183817 | T | TTCTATCT others(1): Show |
3 | a0002c0002t0002g0043 a0002c0002t0038g0339 a0002c0002t0038g0340 |
3 | HG02004.hp2 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.79-4978_79-4971dup others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | ||||||
chr1:12183817 | T | TTCTATCT others(5): Show |
6 | a0002c0002t0001g0279 a0002c0002t0003g0040 a0002c0002t0003g0318 others(3): Show |
6 | HG00140.hp1 HG02056.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-4971_79-4970ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | ||||||
chr1:12183817 | T | TTCTATCT others(9): Show |
1 | a0002c0002t0011g0041 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.79-4971_79-4970ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183817 | ||||||
chr1:12183826 | C | CCTAT | 20 | a0001c0001t0001g0012 a0001c0001t0001g0122 a0001c0001t0001g0192 others(17): Show |
20 | HG01069.hp1 HG01167.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.79-4946_79-4943dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183826 | ||||||
chr1:12183826 | C | CCTATCTA others(5): Show |
1 | a0002c0002t0011g0307 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-4954_79-4943dup others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183826 | ||||||
chr1:12183826 | C | T | 58 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.79-4970C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183826 | |||||||
chr1:12183842 | T | C | 1 | a0001c0003t0001g0326 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.79-4954T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183842 | |||||||
chr1:12183846 | T | C | 1 | a0001c0003t0001g0326 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.79-4950T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183846 | |||||||
chr1:12183850 | T | C | 4 | a0001c0001t0010g0202 a0001c0003t0001g0326 a0001c0003t0035g0042 others(1): Show |
4 | HG02155.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4946T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12183850 | |||||||
chr1:12183850 | T | TCTATCTA others(5): Show |
18 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0162 others(15): Show |
18 | HG00099.hp2 HG00423.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | ||||||
chr1:12183850 | T | TCTATCTA others(9): Show |
1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.79-4943_79-4942ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | ||||||
chr1:12183850 | T | TCTATCTA others(9): Show |
9 | a0002c0002t0001g0167 a0002c0002t0001g0177 a0002c0002t0001g0180 others(6): Show |
9 | HG01074.hp1 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | ||||||
chr1:12183850 | T | TCTATCTA others(13): Show |
10 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0002c0002t0001g0149 others(7): Show |
10 | HG01106.hp2 HG01243.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.79-4943_79-4942ins others(20): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | ||||||
chr1:12183850 | T | TCTATCTA others(17): Show |
1 | a0002c0002t0025g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.79-4943_79-4942ins others(24): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12183850 | ||||||
chr1:12184111 | A | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0122 a0005c0006t0001g0108 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-4685A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184111 | |||||||
chr1:12184201 | A | G | 66 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-4595A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184201 | |||||||
chr1:12184261 | T | C | 67 | a0001c0001t0004g0270 a0001c0001t0037g0133 a0001c0001t0037g0134 others(64): Show |
67 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.79-4535T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184261 | |||||||
chr1:12184345 | AT | A | 7 | a0001c0001t0001g0121 a0001c0001t0004g0323 a0001c0001t0051g0233 others(4): Show |
7 | HG00597.hp2 HG01106.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-4436delT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12184345 | ||||||
chr1:12184443 | A | G | 4 | a0002c0002t0021g0198 a0002c0002t0025g0199 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4353A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184443 | |||||||
chr1:12184482 | G | C | 1 | a0001c0001t0011g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.79-4314G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184482 | |||||||
chr1:12184570 | G | A | 1 | a0002c0002t0011g0307 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.79-4226G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184570 | |||||||
chr1:12184594 | C | T | 1 | a0001c0001t0024g0191 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.79-4202C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184594 | |||||||
chr1:12184647 | C | T | 4 | a0001c0001t0006g0011 a0001c0001t0011g0011 a0001c0001t0025g0221 others(1): Show |
4 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-4149C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184647 | |||||||
chr1:12184657 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0009g0082 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.79-4139G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184657 | |||||||
chr1:12184855 | C | T | 1 | a0001c0001t0014g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.79-3941C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184855 | |||||||
chr1:12184949 | C | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-3847C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184949 | |||||||
chr1:12184972 | T | C | 66 | a0001c0001t0023g0039 a0001c0001t0037g0133 a0001c0001t0037g0134 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-3824T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12184972 | |||||||
chr1:12185095 | G | A | 2 | a0001c0001t0002g0231 a0003c0005t0003g0224 |
2 | HG00597.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.79-3701G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185095 | |||||||
chr1:12185095 | GCAGTTAG others(23): Show |
G | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-3700_79-3671del others(30): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185095 | |||||||
chr1:12185179 | G | A | 1 | a0001c0001t0009g0083 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79-3617G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185179 | |||||||
chr1:12185298 | G | A | 1 | a0001c0001t0009g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79-3498G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185298 | |||||||
chr1:12185303 | CCTTTTT | C | 63 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.79-3482_79-3477del others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12185303 | ||||||
chr1:12185344 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-3452C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185344 | |||||||
chr1:12185437 | T | TC | 38 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0034g0176 others(35): Show |
38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-3353dupC | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12185437 | ||||||
chr1:12185443 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.79-3353C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185443 | |||||||
chr1:12185559 | G | T | 1 | a0001c0001t0003g0295 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.79-3237G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185559 | |||||||
chr1:12185651 | T | G | 66 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0001g0326 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-3145T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185651 | |||||||
chr1:12185675 | T | A | 38 | a0001c0001t0037g0133 a0001c0001t0037g0134 a0001c0003t0034g0176 others(35): Show |
38 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.79-3121T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12185675 | |||||||
chr1:12186118 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0190 others(72): Show |
79 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.79-2678C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186118 | |||||||
chr1:12186126 | C | A | 7 | a0001c0003t0035g0042 a0001c0003t0067g0337 a0001c0003t0069g0336 others(4): Show |
7 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.79-2670C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186126 | |||||||
chr1:12186143 | G | A | 1 | a0001c0001t0026g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.79-2653G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186143 | |||||||
chr1:12186212 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.79-2584G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186212 | |||||||
chr1:12186275 | C | T | 1 | a0001c0001t0029g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.79-2521C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186275 | |||||||
chr1:12186419 | G | A | 1 | a0001c0001t0003g0185 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.79-2377G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186419 | |||||||
chr1:12186526 | ATATGTTA others(41): Show |
A | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-2269_79-2222del others(48): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186526 | |||||||
chr1:12186723 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.79-2073G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186723 | |||||||
chr1:12186951 | C | G | 36 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0149 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-1845C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12186951 | |||||||
chr1:12187071 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.79-1725C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187071 | |||||||
chr1:12187253 | A | G | 42 | a0001c0001t0001g0305 a0001c0001t0002g0066 a0001c0001t0002g0067 others(39): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.79-1543A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187253 | |||||||
chr1:12187309 | A | G | 4 | a0002c0002t0021g0198 a0002c0002t0025g0199 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-1487A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187309 | |||||||
chr1:12187438 | C | T | 3 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 |
3 | HG02109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-1358C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187438 | |||||||
chr1:12187453 | C | T | 1 | a0002c0002t0008g0333 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-1343C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187453 | |||||||
chr1:12187470 | C | T | 3 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 |
3 | HG02109.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.79-1326C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187470 | |||||||
chr1:12187681 | A | AAGTCTTG others(3): Show |
1 | a0001c0001t0032g0131 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.79-1112_79-1103dup others(10): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12187681 | ||||||
chr1:12187883 | C | T | 9 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(6): Show |
9 | HG01358.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.79-913C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187883 | |||||||
chr1:12187886 | G | T | 8 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(5): Show |
8 | HG01106.hp2 HG01243.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.79-910G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187886 | |||||||
chr1:12187953 | G | A | 1 | a0002c0002t0040g0250 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.79-843G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12187953 | |||||||
chr1:12188183 | ATG | A | 36 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0149 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-612_79-611delTG | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188183 | |||||||
chr1:12188234 | G | C | 66 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-562G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188234 | |||||||
chr1:12188290 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.79-506C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188290 | |||||||
chr1:12188293 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0125 |
2 | HG02071.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.79-503G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188293 | |||||||
chr1:12188368 | T | A | 66 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.79-428T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188368 | |||||||
chr1:12188446 | G | A | 36 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0149 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.79-350G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188446 | |||||||
chr1:12188470 | C | T | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-326C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188470 | |||||||
chr1:12188501 | G | A | 4 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-295G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188501 | |||||||
chr1:12188542 | A | T | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-254A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188542 | |||||||
chr1:12188596 | G | GGGGGAGG others(74): Show |
1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-199_79-198insGG others(79): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 12188596 | ||||||
chr1:12188598 | T | A | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-198T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188598 | |||||||
chr1:12188628 | G | A | 4 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.79-168G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188628 | |||||||
chr1:12188639 | C | T | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-157C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188639 | |||||||
chr1:12188655 | G | A | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-141G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188655 | |||||||
chr1:12188682 | A | T | 6 | a0001c0001t0002g0060 a0001c0001t0003g0013 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-114A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188682 | |||||||
chr1:12188683 | G | C | 2 | a0001c0001t0018g0056 a0001c0001t0049g0038 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.79-113G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188683 | |||||||
chr1:12188710 | C | A | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-86C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188710 | |||||||
chr1:12188722 | G | A | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-74G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188722 | |||||||
chr1:12188739 | G | A | 1 | a0002c0002t0040g0250 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.79-57G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188739 | |||||||
chr1:12188744 | G | C | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-52G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188744 | |||||||
chr1:12188748 | A | G | 1 | a0001c0001t0005g0078 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.79-48A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 1/9 | chr1 | 12188748 | |||||||
chr1:12188908 | A | G | 66 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.178+13A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188908 | |||||||
chr1:12188963 | C | T | 62 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.178+68C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188963 | |||||||
chr1:12188974 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0190 others(205): Show |
212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.178+79A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12188974 | |||||||
chr1:12189027 | C | G | 6 | a0001c0003t0035g0042 a0001c0003t0067g0337 a0001c0003t0069g0336 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+132C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189027 | |||||||
chr1:12189069 | C | T | 2 | a0002c0002t0021g0198 a0002c0002t0025g0199 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.178+174C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189069 | |||||||
chr1:12189157 | C | A | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+262C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189157 | |||||||
chr1:12189175 | T | A | 50 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0034g0176 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.178+280T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189175 | |||||||
chr1:12189175 | T | C | 12 | a0001c0003t0001g0326 a0001c0003t0035g0042 a0001c0003t0067g0337 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+280T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189175 | |||||||
chr1:12189248 | C | T | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.178+353C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189248 | |||||||
chr1:12189265 | G | T | 2 | a0001c0001t0018g0056 a0001c0001t0049g0038 |
2 | HG01192.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.178+370G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189265 | |||||||
chr1:12189287 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.178+392T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189287 | |||||||
chr1:12189369 | C | A | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.178+474C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189369 | |||||||
chr1:12189417 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.178+522C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189417 | |||||||
chr1:12189466 | G | T | 3 | a0002c0002t0002g0037 a0002c0002t0011g0307 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.178+571G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189466 | |||||||
chr1:12189511 | A | C | 18 | a0001c0003t0001g0326 a0002c0002t0001g0279 a0002c0002t0002g0037 others(15): Show |
18 | HG00140.hp1 HG01106.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.178+616A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189511 | |||||||
chr1:12189515 | G | C | 1 | a0002c0002t0003g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.178+620G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189515 | |||||||
chr1:12189558 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.178+663A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189558 | |||||||
chr1:12189586 | A | T | 63 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.178+691A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189586 | |||||||
chr1:12189713 | G | A | 59 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.178+818G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189713 | |||||||
chr1:12189720 | C | T | 3 | a0001c0001t0012g0019 a0001c0001t0012g0187 a0001c0001t0061g0159 |
3 | NA18993.hp2 NA18995.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.178+825C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189720 | |||||||
chr1:12189759 | C | T | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+864C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189759 | |||||||
chr1:12189772 | A | G | 59 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.178+877A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189772 | |||||||
chr1:12189808 | G | C | 59 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.178+913G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189808 | |||||||
chr1:12189826 | A | G | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+931A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189826 | |||||||
chr1:12189881 | G | A | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.178+986G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189881 | |||||||
chr1:12189931 | G | A | 59 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.179-1026G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189931 | |||||||
chr1:12189947 | T | C | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.179-1010T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12189947 | |||||||
chr1:12190037 | T | C | 5 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-920T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190037 | |||||||
chr1:12190131 | C | A | 2 | a0001c0003t0001g0326 a0004c0007t0014g0328 |
2 | HG01358.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.179-826C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190131 | |||||||
chr1:12190380 | G | A | 63 | a0001c0003t0001g0326 a0001c0003t0002g0324 a0001c0003t0003g0064 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.179-577G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190380 | |||||||
chr1:12190458 | C | CA | 41 | a0001c0001t0001g0260 a0001c0001t0002g0086 a0001c0001t0002g0200 others(38): Show |
41 | HG00323.hp1 HG00639.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.179-477dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | ||||||
chr1:12190458 | C | CAAA | 6 | a0001c0003t0002g0324 a0001c0003t0059g0059 a0002c0002t0008g0035 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-479_179-477dup others(3): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | ||||||
chr1:12190458 | C | CAAAAA | 35 | a0001c0003t0034g0176 a0002c0002t0001g0015 a0002c0002t0001g0150 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.179-481_179-477dup others(5): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | ||||||
chr1:12190458 | C | CAAAAAA | 10 | a0002c0002t0001g0149 a0002c0002t0001g0169 a0002c0002t0001g0194 others(7): Show |
10 | HG02683.hp1 HG03654.hp2 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-482_179-477dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | ||||||
chr1:12190458 | CA | C | 7 | a0001c0001t0001g0219 a0001c0001t0001g0239 a0001c0001t0002g0103 others(4): Show |
8 | HG03041.hp1 NA18942.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-477delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 12190458 | ||||||
chr1:12190831 | T | C | 11 | a0001c0001t0001g0144 a0001c0001t0003g0135 a0001c0001t0009g0063 others(8): Show |
11 | HG00733.hp2 HG01109.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-126T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190831 | |||||||
chr1:12190837 | T | G | 6 | a0001c0001t0002g0060 a0001c0001t0003g0013 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-120T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190837 | |||||||
chr1:12190922 | C | T | 9 | a0002c0002t0001g0279 a0002c0002t0002g0043 a0002c0002t0003g0040 others(6): Show |
9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-35C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 2/9 | chr1 | 12190922 | |||||||
chr1:12191134 | T | A | 42 | a0002c0002t0001g0015 a0002c0002t0001g0149 a0002c0002t0001g0150 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.307+49T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191134 | |||||||
chr1:12191195 | T | C | 3 | a0002c0002t0002g0037 a0002c0002t0011g0307 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.307+110T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191195 | |||||||
chr1:12191221 | T | C | 3 | a0001c0001t0003g0029 a0001c0001t0006g0027 a0001c0001t0011g0028 |
3 | HG01884.hp2 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.307+136T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191221 | |||||||
chr1:12191224 | C | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0229 |
2 | NA18984.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.307+139C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191224 | |||||||
chr1:12191261 | G | A | 46 | a0002c0002t0001g0015 a0002c0002t0001g0149 a0002c0002t0001g0150 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.307+176G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191261 | |||||||
chr1:12191284 | A | C | 12 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.307+199A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191284 | |||||||
chr1:12191353 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.307+268G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191353 | |||||||
chr1:12191443 | C | T | 3 | a0001c0001t0003g0014 a0001c0001t0006g0014 a0001c0001t0006g0245 |
3 | HG01069.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.308-331C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191443 | |||||||
chr1:12191465 | A | G | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308-309A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191465 | |||||||
chr1:12191489 | G | A | 3 | a0001c0001t0002g0104 a0001c0001t0002g0331 a0001c0001t0002g0334 |
3 | HG01256.hp1 NA19074.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.308-285G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191489 | |||||||
chr1:12191549 | AGGACTGC others(11): Show |
A | 4 | a0002c0002t0013g0044 a0002c0002t0015g0046 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG01243.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.308-189_308-172del others(18): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 12191549 | ||||||
chr1:12191685 | C | T | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.308-89C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191685 | |||||||
chr1:12191690 | T | G | 1 | a0001c0001t0019g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.308-84T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191690 | |||||||
chr1:12191699 | G | C | 1 | a0002c0002t0034g0171 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.308-75G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191699 | |||||||
chr1:12191708 | T | G | 62 | a0001c0001t0064g0195 a0001c0003t0002g0324 a0001c0003t0003g0064 others(59): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.308-66T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191708 | |||||||
chr1:12191751 | T | G | 108 | a0001c0001t0001g0305 a0001c0001t0002g0066 a0001c0001t0002g0067 others(105): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.308-23T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 3/9 | chr1 | 12191751 | |||||||
chr1:12192276 | C | CTG | 82 | a0001c0001t0001g0002 a0001c0001t0001g0081 a0001c0001t0001g0084 others(79): Show |
86 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.458-125_458-124dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192276 | C | CTGTG | 20 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(17): Show |
21 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.458-127_458-124dup others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192276 | C | CTGTGTG | 10 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(7): Show |
10 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.458-129_458-124dup others(6): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192276 | CTG | C | 11 | a0001c0001t0002g0077 a0001c0001t0002g0114 a0001c0001t0002g0125 others(8): Show |
11 | HG00738.hp2 HG01358.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.458-125_458-124del others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192276 | CTGTG | C | 25 | a0001c0001t0013g0050 a0001c0001t0032g0131 a0002c0002t0001g0149 others(22): Show |
25 | HG00099.hp2 HG00140.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.458-127_458-124del others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192276 | CTGTGTGT others(1): Show |
C | 19 | a0002c0002t0001g0015 a0002c0002t0001g0162 a0002c0002t0001g0172 others(16): Show |
19 | HG00423.hp2 HG01074.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.458-131_458-124del others(8): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 12192276 | ||||||
chr1:12192393 | T | G | 1 | a0003c0005t0019g0158 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.458-38T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 4/9 | chr1 | 12192393 | |||||||
chr1:12192595 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.551+71C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/9 | chr1 | 12192595 | |||||||
chr1:12192835 | C | T | 58 | a0001c0003t0002g0324 a0001c0003t0003g0064 a0001c0003t0059g0059 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.552-28C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 5/9 | chr1 | 12192835 | |||||||
chr1:12193294 | T | C | 53 | a0001c0001t0002g0291 a0002c0002t0001g0015 a0002c0002t0001g0149 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.787+196T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193294 | |||||||
chr1:12193406 | T | A | 1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787+308T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193406 | |||||||
chr1:12193735 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0009g0082 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.788-220G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193735 | |||||||
chr1:12193842 | C | T | 4 | a0002c0002t0021g0198 a0002c0002t0025g0199 a0002c0002t0038g0339 others(1): Show |
4 | HG02257.hp1 HG02559.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-113C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 6/9 | chr1 | 12193842 | |||||||
chr1:12194144 | G | A | 45 | a0002c0002t0001g0015 a0002c0002t0001g0149 a0002c0002t0001g0150 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.865+112G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194144 | |||||||
chr1:12194356 | C | T | 1 | a0001c0004t0007g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.866-228C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194356 | |||||||
chr1:12194381 | G | T | 1 | a0001c0001t0047g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.866-203G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194381 | |||||||
chr1:12194573 | C | G | 1 | a0010c0013t0001g0208 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.866-11C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 7/9 | chr1 | 12194573 | |||||||
chr1:12194986 | A | T | 1 | a0001c0001t0056g0259 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.900+368A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12194986 | |||||||
chr1:12195178 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.900+560T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195178 | |||||||
chr1:12195275 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0004g0207 |
2 | NA18942.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.900+657A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195275 | |||||||
chr1:12195303 | A | C | 44 | a0001c0001t0003g0034 a0001c0001t0006g0335 a0001c0001t0008g0022 others(41): Show |
44 | HG00099.hp2 HG00423.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.900+685A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195303 | |||||||
chr1:12195501 | C | G | 5 | a0002c0002t0002g0037 a0002c0002t0008g0035 a0002c0002t0008g0333 others(2): Show |
5 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+883C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195501 | |||||||
chr1:12195691 | G | C | 25 | a0001c0001t0001g0121 a0001c0001t0001g0206 a0001c0001t0001g0239 others(22): Show |
26 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.900+1073G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195691 | |||||||
chr1:12195747 | C | G | 1 | a0001c0001t0006g0261 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.900+1129C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195747 | |||||||
chr1:12195844 | G | A | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+1226G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12195844 | |||||||
chr1:12196007 | A | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.900+1389A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196007 | |||||||
chr1:12196114 | A | G | 2 | a0001c0001t0008g0022 a0001c0001t0008g0024 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.900+1496A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196114 | |||||||
chr1:12196685 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.900+2067C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196685 | |||||||
chr1:12196782 | C | T | 2 | a0001c0001t0008g0022 a0001c0001t0008g0024 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.900+2164C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196782 | |||||||
chr1:12196800 | G | A | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+2182G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196800 | |||||||
chr1:12196804 | G | A | 1 | a0002c0002t0031g0152 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.900+2186G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196804 | |||||||
chr1:12196813 | G | T | 3 | a0001c0001t0003g0029 a0001c0001t0006g0290 a0001c0001t0055g0288 |
3 | HG02055.hp1 HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.900+2195G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196813 | |||||||
chr1:12196852 | C | T | 1 | a0001c0001t0017g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.900+2234C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196852 | |||||||
chr1:12196884 | C | G | 9 | a0002c0002t0001g0162 a0002c0002t0001g0279 a0002c0002t0002g0043 others(6): Show |
9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.900+2266C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196884 | |||||||
chr1:12196940 | A | AT | 52 | a0001c0001t0003g0034 a0001c0001t0006g0335 a0002c0002t0001g0015 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.900+2332dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12196940 | ||||||
chr1:12196948 | T | C | 1 | a0001c0001t0009g0083 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.900+2330T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196948 | |||||||
chr1:12196963 | T | C | 2 | a0001c0001t0005g0216 a0001c0001t0005g0320 |
2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.900+2345T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196963 | |||||||
chr1:12196987 | G | A | 1 | a0001c0001t0003g0182 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.900+2369G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12196987 | |||||||
chr1:12197310 | T | C | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.900+2692T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197310 | |||||||
chr1:12197333 | A | G | 12 | a0001c0001t0006g0335 a0001c0001t0008g0022 a0001c0001t0008g0024 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.900+2715A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197333 | |||||||
chr1:12197342 | C | G | 45 | a0002c0002t0001g0015 a0002c0002t0001g0149 a0002c0002t0001g0150 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.900+2724C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197342 | |||||||
chr1:12197540 | GGGAGCAT others(16): Show |
G | 1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.900+2923_900+2945d others(25): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197540 | |||||||
chr1:12197599 | T | C | 10 | a0001c0001t0006g0335 a0002c0002t0002g0037 a0002c0002t0008g0035 others(7): Show |
10 | HG01106.hp2 HG01243.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+2981T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197599 | |||||||
chr1:12197708 | C | T | 1 | a0001c0001t0007g0299 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.900+3090C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197708 | |||||||
chr1:12197712 | G | A | 5 | a0001c0001t0006g0335 a0002c0002t0013g0044 a0002c0002t0015g0046 others(2): Show |
5 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+3094G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197712 | |||||||
chr1:12197796 | G | C | 4 | a0002c0002t0002g0037 a0002c0002t0008g0333 a0002c0002t0011g0307 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.900+3178G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197796 | |||||||
chr1:12197897 | G | T | 1 | a0002c0002t0015g0197 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.900+3279G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197897 | |||||||
chr1:12197900 | C | T | 1 | a0001c0001t0016g0095 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.900+3282C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197900 | |||||||
chr1:12197942 | A | G | 4 | a0001c0001t0010g0016 a0001c0001t0010g0287 a0001c0001t0047g0048 others(1): Show |
5 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.900+3324A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197942 | |||||||
chr1:12197953 | A | G | 2 | a0001c0001t0010g0016 a0001c0001t0010g0287 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.900+3335A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197953 | |||||||
chr1:12197998 | G | A | 1 | a0002c0002t0015g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.900+3380G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12197998 | |||||||
chr1:12198036 | A | G | 1 | a0001c0001t0005g0089 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.900+3418A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198036 | |||||||
chr1:12198046 | C | T | 1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.900+3428C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198046 | |||||||
chr1:12198117 | A | G | 63 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0006g0335 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.900+3499A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198117 | |||||||
chr1:12198121 | C | CA | 15 | a0001c0001t0001g0217 a0001c0001t0002g0079 a0001c0001t0002g0213 others(12): Show |
15 | HG00408.hp1 HG01261.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.900+3523dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | ||||||
chr1:12198121 | CA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.900+3523delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | ||||||
chr1:12198121 | CAA | C | 19 | a0001c0001t0002g0023 a0001c0001t0006g0011 a0001c0001t0008g0020 others(16): Show |
19 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.900+3522_900+3523d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198121 | ||||||
chr1:12198174 | T | C | 72 | a0001c0001t0002g0161 a0001c0001t0002g0312 a0001c0001t0002g0313 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.900+3556T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198174 | |||||||
chr1:12198196 | C | T | 1 | a0001c0001t0043g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.900+3578C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198196 | |||||||
chr1:12198231 | C | T | 4 | a0001c0001t0006g0335 a0002c0002t0013g0044 a0002c0002t0017g0045 others(1): Show |
4 | HG01106.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.900+3613C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198231 | |||||||
chr1:12198452 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.901-3515C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198452 | |||||||
chr1:12198517 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0004g0207 |
2 | NA18942.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.901-3450C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198517 | |||||||
chr1:12198659 | TGCTGGCT others(5): Show |
T | 20 | a0001c0001t0002g0023 a0001c0001t0006g0011 a0001c0001t0008g0020 others(17): Show |
20 | HG01167.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.901-3294_901-3283d others(14): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198659 | ||||||
chr1:12198673 | C | A | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3294C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198673 | |||||||
chr1:12198674 | T | A | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3293T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198674 | |||||||
chr1:12198675 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3292G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198675 | |||||||
chr1:12198676 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3291G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198676 | |||||||
chr1:12198680 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3287G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198680 | |||||||
chr1:12198681 | C | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3286C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198681 | |||||||
chr1:12198683 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3284G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198683 | |||||||
chr1:12198684 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3283G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198684 | |||||||
chr1:12198685 | A | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3282A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198685 | |||||||
chr1:12198686 | A | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3281A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198686 | |||||||
chr1:12198689 | C | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3278C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198689 | |||||||
chr1:12198691 | G | GT | 44 | a0001c0001t0001g0001 a0001c0001t0001g0192 a0001c0001t0001g0223 others(41): Show |
46 | HG00423.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.901-3259dupT | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTT | 8 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0284 others(5): Show |
8 | HG00544.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.901-3260_901-3259d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTGTT others(6): Show |
1 | a0001c0001t0047g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.901-3272_901-3271i others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0013g0050 a0002c0002t0011g0307 |
2 | HG03704.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.901-3268_901-3259d others(12): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(4): Show |
15 | a0001c0001t0001g0305 a0001c0001t0002g0137 a0001c0001t0002g0155 others(12): Show |
15 | HG00323.hp2 HG01255.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.901-3269_901-3259d others(13): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(5): Show |
119 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(116): Show |
123 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.901-3270_901-3259d others(14): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(6): Show |
61 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0101 others(58): Show |
62 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.901-3271_901-3259d others(15): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(7): Show |
10 | a0001c0001t0002g0052 a0001c0001t0002g0077 a0001c0001t0002g0125 others(7): Show |
10 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.901-3272_901-3259d others(16): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0005g0118 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.901-3273_901-3259d others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12198691 | ||||||
chr1:12198691 | G | T | 1 | a0002c0002t0038g0340 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.901-3276G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198691 | |||||||
chr1:12198884 | G | T | 39 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0057g0315 others(36): Show |
39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.901-3083G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198884 | |||||||
chr1:12198972 | T | G | 11 | a0001c0001t0001g0292 a0001c0001t0003g0113 a0001c0001t0003g0209 others(8): Show |
11 | HG00140.hp2 HG02027.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-2995T>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198972 | |||||||
chr1:12198981 | C | T | 1 | a0001c0001t0011g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.901-2986C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12198981 | |||||||
chr1:12199137 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(5): Show |
11 | HG00733.hp1 HG00738.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.901-2830T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199137 | |||||||
chr1:12199278 | G | T | 1 | a0001c0001t0002g0286 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.901-2689G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199278 | |||||||
chr1:12199316 | T | C | 6 | a0001c0001t0008g0022 a0001c0001t0008g0024 a0002c0002t0002g0037 others(3): Show |
6 | HG02055.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-2651T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199316 | |||||||
chr1:12199440 | G | T | 1 | a0001c0001t0010g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.901-2527G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199440 | |||||||
chr1:12199461 | G | A | 1 | a0002c0002t0003g0040 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.901-2506G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199461 | |||||||
chr1:12199495 | G | T | 1 | a0001c0001t0009g0082 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.901-2472G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199495 | |||||||
chr1:12199962 | G | C | 1 | a0001c0001t0014g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2005G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199962 | |||||||
chr1:12199963 | A | C | 1 | a0001c0001t0014g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2004A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199963 | |||||||
chr1:12199964 | A | AGCCAGTG others(8): Show |
1 | a0001c0001t0014g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901-2003_901-2002i others(17): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12199964 | |||||||
chr1:12200167 | G | C | 3 | a0002c0002t0001g0279 a0002c0002t0003g0318 a0002c0002t0014g0278 |
3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.901-1800G>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200167 | |||||||
chr1:12200197 | T | C | 1 | a0002c0002t0032g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.901-1770T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200197 | |||||||
chr1:12200264 | ATAT | A | 9 | a0002c0002t0001g0162 a0002c0002t0001g0279 a0002c0002t0002g0043 others(6): Show |
9 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.901-1692_901-1690d others(5): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12200264 | ||||||
chr1:12200280 | A | G | 5 | a0001c0001t0006g0335 a0002c0002t0008g0035 a0002c0002t0013g0044 others(2): Show |
5 | HG01106.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.901-1687A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200280 | |||||||
chr1:12200323 | C | T | 6 | a0001c0001t0006g0335 a0002c0002t0008g0035 a0002c0002t0013g0044 others(3): Show |
6 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-1644C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200323 | |||||||
chr1:12200342 | C | T | 1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.901-1625C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200342 | |||||||
chr1:12200420 | G | A | 1 | a0002c0002t0015g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.901-1547G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200420 | |||||||
chr1:12200674 | G | A | 1 | a0001c0001t0010g0235 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.901-1293G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200674 | |||||||
chr1:12200722 | A | C | 1 | a0001c0001t0003g0185 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.901-1245A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200722 | |||||||
chr1:12200810 | G | A | 6 | a0001c0001t0006g0335 a0002c0002t0008g0035 a0002c0002t0013g0044 others(3): Show |
6 | HG01106.hp2 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.901-1157G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200810 | |||||||
chr1:12200811 | G | A | 1 | a0001c0001t0018g0301 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.901-1156G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12200811 | |||||||
chr1:12201260 | C | CA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0070 a0001c0001t0001g0072 others(27): Show |
33 | HG00621.hp2 HG00673.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.901-684dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201260 | ||||||
chr1:12201260 | CA | C | 28 | a0001c0001t0001g0239 a0001c0001t0001g0305 a0001c0001t0002g0067 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.901-684delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201260 | ||||||
chr1:12201282 | A | G | 1 | a0001c0001t0012g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.901-685A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201282 | |||||||
chr1:12201417 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.901-550A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201417 | |||||||
chr1:12201471 | T | TA | 52 | a0001c0001t0001g0186 a0001c0001t0001g0325 a0001c0001t0002g0052 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.901-481dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | ||||||
chr1:12201471 | T | TAA | 11 | a0001c0001t0008g0022 a0001c0001t0008g0024 a0002c0002t0001g0162 others(8): Show |
11 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.901-482_901-481dup others(2): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | ||||||
chr1:12201471 | TA | T | 7 | a0001c0001t0001g0239 a0001c0001t0002g0285 a0001c0001t0009g0074 others(4): Show |
7 | HG02717.hp2 HG03239.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-481delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 12201471 | ||||||
chr1:12201556 | T | C | 2 | a0001c0001t0003g0113 a0004c0007t0014g0328 |
2 | HG01358.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.901-411T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201556 | |||||||
chr1:12201733 | T | C | 4 | a0001c0001t0003g0113 a0001c0001t0008g0022 a0001c0001t0008g0024 others(1): Show |
4 | HG01358.hp2 HG02129.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-234T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201733 | |||||||
chr1:12201786 | G | A | 1 | a0002c0002t0002g0178 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.901-181G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201786 | |||||||
chr1:12201915 | A | G | 41 | a0001c0001t0002g0312 a0001c0001t0002g0313 a0001c0001t0008g0022 others(38): Show |
41 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.901-52A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201915 | |||||||
chr1:12201944 | C | T | 5 | a0001c0001t0001g0219 a0001c0001t0002g0104 a0001c0001t0002g0331 others(2): Show |
5 | HG01256.hp1 NA18960.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-23C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 8/9 | chr1 | 12201944 | |||||||
chr1:12202241 | G | A | 57 | a0001c0001t0002g0023 a0001c0001t0002g0312 a0001c0001t0002g0313 others(54): Show |
57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.1105+70G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202241 | |||||||
chr1:12202369 | C | T | 44 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(41): Show |
44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+198C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202369 | |||||||
chr1:12202619 | C | T | 8 | a0001c0001t0006g0335 a0001c0001t0017g0030 a0001c0001t0055g0288 others(5): Show |
8 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+448C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202619 | |||||||
chr1:12202632 | G | A | 45 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(42): Show |
45 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1105+461G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202632 | |||||||
chr1:12202633 | A | C | 44 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(41): Show |
44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+462A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202633 | |||||||
chr1:12202735 | A | G | 44 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(41): Show |
44 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.1105+564A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202735 | |||||||
chr1:12202737 | G | A | 1 | a0001c0001t0066g0254 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1105+566G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202737 | |||||||
chr1:12202817 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1105+646A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202817 | |||||||
chr1:12202830 | A | G | 1 | a0002c0002t0003g0318 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1105+659A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202830 | |||||||
chr1:12202858 | C | T | 3 | a0002c0002t0002g0037 a0002c0002t0011g0307 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1105+687C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12202858 | |||||||
chr1:12203002 | G | A | 1 | a0002c0002t0005g0173 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1105+831G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203002 | |||||||
chr1:12203345 | C | T | 1 | a0001c0001t0053g0107 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1105+1174C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203345 | |||||||
chr1:12203403 | A | T | 2 | a0002c0002t0001g0180 a0002c0002t0001g0181 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1105+1232A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203403 | |||||||
chr1:12203460 | C | A | 5 | a0001c0001t0002g0079 a0001c0001t0003g0068 a0001c0001t0003g0092 others(2): Show |
5 | HG00099.hp1 HG00735.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105+1289C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203460 | |||||||
chr1:12203488 | C | T | 34 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(31): Show |
34 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1105+1317C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203488 | |||||||
chr1:12203529 | G | A | 9 | a0001c0001t0006g0335 a0001c0001t0017g0030 a0001c0001t0055g0288 others(6): Show |
9 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1105+1358G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203529 | |||||||
chr1:12203727 | T | A | 1 | a0002c0002t0001g0174 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1105+1556T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203727 | |||||||
chr1:12203760 | T | C | 34 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1105+1589T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203760 | |||||||
chr1:12203844 | C | A | 1 | a0002c0002t0008g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1105+1673C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203844 | |||||||
chr1:12203862 | C | T | 58 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0277 others(55): Show |
58 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1105+1691C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203862 | |||||||
chr1:12203892 | G | A | 1 | a0001c0001t0005g0282 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1105+1721G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203892 | |||||||
chr1:12203949 | C | G | 3 | a0002c0002t0002g0037 a0002c0002t0011g0307 a0002c0002t0032g0036 |
3 | HG02717.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1105+1778C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203949 | |||||||
chr1:12203974 | T | A | 1 | a0001c0001t0008g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1105+1803T>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12203974 | |||||||
chr1:12204078 | C | T | 1 | a0001c0001t0025g0221 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1105+1907C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204078 | |||||||
chr1:12204166 | T | C | 7 | a0002c0002t0001g0162 a0002c0002t0001g0279 a0002c0002t0002g0043 others(4): Show |
7 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1105+1995T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204166 | |||||||
chr1:12204265 | C | G | 1 | a0001c0001t0022g0163 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1105+2094C>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204265 | |||||||
chr1:12204298 | A | G | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(340): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1105+2127A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204298 | |||||||
chr1:12204404 | G | A | 8 | a0001c0001t0002g0080 a0002c0002t0001g0162 a0002c0002t0001g0279 others(5): Show |
8 | HG00140.hp1 HG01168.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1105+2233G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204404 | |||||||
chr1:12204586 | A | T | 1 | a0002c0002t0032g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1106-2154A>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204586 | |||||||
chr1:12204690 | C | T | 1 | a0002c0002t0032g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1106-2050C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204690 | |||||||
chr1:12204763 | T | C | 2 | a0001c0001t0010g0016 a0001c0001t0010g0287 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1106-1977T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204763 | |||||||
chr1:12204790 | TCAC | T | 24 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(21): Show |
24 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1106-1926_1106-192 others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204790 | ||||||
chr1:12204808 | C | CCAA | 11 | a0001c0001t0006g0335 a0001c0001t0017g0030 a0001c0001t0055g0288 others(8): Show |
11 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-1930_1106-192 others(7): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204808 | ||||||
chr1:12204811 | C | A | 21 | a0001c0001t0002g0080 a0001c0001t0006g0335 a0001c0001t0017g0030 others(18): Show |
21 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1106-1929C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204811 | |||||||
chr1:12204814 | C | A | 27 | a0001c0001t0002g0080 a0001c0001t0006g0335 a0001c0001t0017g0030 others(24): Show |
27 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1106-1926C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204814 | |||||||
chr1:12204818 | C | CA | 12 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0226 others(9): Show |
12 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1106-1915dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12204818 | ||||||
chr1:12204821 | A | C | 1 | a0004c0007t0014g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1106-1919A>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204821 | |||||||
chr1:12204828 | C | T | 1 | a0002c0002t0015g0197 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1106-1912C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12204828 | |||||||
chr1:12205005 | G | A | 2 | a0001c0001t0006g0335 a0001c0001t0055g0288 |
2 | HG02055.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1106-1735G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205005 | |||||||
chr1:12205019 | A | G | 7 | a0002c0002t0001g0162 a0002c0002t0001g0279 a0002c0002t0002g0043 others(4): Show |
7 | HG00140.hp1 HG01261.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1106-1721A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205019 | |||||||
chr1:12205235 | A | G | 2 | a0001c0001t0002g0311 a0001c0001t0010g0202 |
2 | HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1106-1505A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205235 | |||||||
chr1:12205270 | C | T | 2 | a0002c0002t0001g0174 a0002c0002t0005g0173 |
2 | NA18954.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1106-1470C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205270 | |||||||
chr1:12205322 | C | T | 1 | a0001c0001t0053g0107 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1106-1418C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205322 | |||||||
chr1:12205408 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1106-1332G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205408 | |||||||
chr1:12205660 | C | T | 2 | a0001c0001t0005g0078 a0001c0001t0005g0112 |
2 | NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1106-1080C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205660 | |||||||
chr1:12205775 | C | T | 2 | a0001c0001t0027g0057 a0001c0001t0027g0262 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1106-965C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205775 | |||||||
chr1:12205782 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1106-958C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12205782 | |||||||
chr1:12205788 | A | ATT | 17 | a0001c0001t0002g0080 a0001c0001t0006g0335 a0001c0001t0017g0030 others(14): Show |
17 | HG00140.hp1 HG01106.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.1106-942_1106-941d others(4): Show |
TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12205788 | ||||||
chr1:12206359 | C | CA | 10 | a0001c0001t0001g0292 a0001c0001t0003g0264 a0001c0001t0005g0088 others(7): Show |
11 | HG00140.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1106-363dupA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12206359 | ||||||
chr1:12206359 | CA | C | 27 | a0001c0001t0001g0084 a0001c0001t0001g0260 a0001c0001t0006g0335 others(24): Show |
27 | HG00323.hp1 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1106-363delA | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 12206359 | ||||||
chr1:12206396 | T | C | 9 | a0001c0001t0006g0335 a0001c0001t0011g0276 a0001c0001t0017g0030 others(6): Show |
9 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1106-344T>C | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206396 | |||||||
chr1:12206462 | A | G | 2 | a0001c0001t0005g0078 a0001c0001t0005g0112 |
2 | NA18962.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1106-278A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206462 | |||||||
chr1:12206534 | A | G | 35 | a0001c0001t0001g0081 a0001c0001t0002g0096 a0001c0001t0002g0100 others(32): Show |
35 | HG00099.hp2 HG00639.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.1106-206A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206534 | |||||||
chr1:12206544 | G | A | 3 | a0002c0002t0001g0279 a0002c0002t0003g0318 a0002c0002t0014g0278 |
3 | HG00140.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1106-196G>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206544 | |||||||
chr1:12206555 | A | G | 41 | a0001c0001t0001g0081 a0001c0001t0002g0080 a0001c0001t0002g0096 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.1106-185A>G | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206555 | |||||||
chr1:12206585 | C | A | 1 | a0001c0001t0050g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1106-155C>A | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206585 | |||||||
chr1:12206599 | G | T | 3 | a0001c0001t0005g0130 a0004c0007t0014g0328 a0006c0010t0048g0263 |
3 | HG01358.hp2 HG02040.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1106-141G>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206599 | |||||||
chr1:12206625 | C | T | 6 | a0001c0001t0008g0020 a0001c0001t0008g0021 a0001c0001t0008g0226 others(3): Show |
6 | HG01167.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-115C>T | TNFRSF1B | ENSG00000028137.19 | transcript | ENST00000376259.7 | protein_coding | 9/9 | chr1 | 12206625 |