Item | Value |
---|---|
geneid | 192668 |
ensemblid | ENSG00000205795.5 |
hgncid | 18525 |
symbol | CYS1 |
name | cystin 1 |
refseq_nuc | NM_001037160.3 |
refseq_prot | NP_001032237.1 |
ensembl_nuc | ENST00000381813.5 |
ensembl_prot | ENSP00000371234.4 |
mane_status | MANE Select |
chr | chr2 |
start | 10056473 |
end | 10080411 |
strand | - |
ver | v1.2 |
region | chr2:10056473-10080411 |
region5000 | chr2:10051473-10085411 |
regionname0 | CYS1_chr2_10056473_10080411 |
regionname5000 | CYS1_chr2_10051473_10085411 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 158 | 263 | 59 | 62 | 98 | 15 | 27 | 77 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0002 | 0/0 | 158 | 70 | 18 | 7 | 36 | 1 | 8 | 29 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0003 | 0/0 | 158 | 62 | 18 | 6 | 29 | 0 | 9 | 18 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0004 | 0/0 | 158 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0005 | 0/0 | 158 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0006 | 0/0 | 158 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0007 | 0/0 | 158 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
a0008 | 0/0 | 158 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | MGSGS others(153): Show |
chr2 | 10051473 | 10085411 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 474 | 263 | 59 | 62 | 98 | 15 | 27 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0002c0002 | 0/0 | 474 | 70 | 18 | 7 | 36 | 1 | 8 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0003c0003 | 0/0 | 474 | 62 | 18 | 6 | 29 | 0 | 9 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0004c0007 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0005c0006 | 0/0 | 474 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0006c0005 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0007c0008 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 | ||
a0008c0004 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | ATGGG others(469): Show |
chr2 | 10051473 | 10085411 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3045 | 184 | 21 | 46 | 89 | 8 | 19 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0002 | 1/0 | 3045 | 19 | 11 | 4 | 1 | 0 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0003 | 0/0 | 3045 | 12 | 11 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0004 | 0/0 | 3045 | 10 | 0 | 4 | 1 | 2 | 3 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0005 | 0/0 | 3045 | 9 | 8 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0006 | 0/0 | 3045 | 10 | 1 | 3 | 0 | 4 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0007 | 0/0 | 3045 | 5 | 4 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0008 | 0/0 | 3045 | 5 | 0 | 0 | 5 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0009 | 0/0 | 3045 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0010 | 0/0 | 3045 | 2 | 0 | 2 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0012 | 0/0 | 3045 | 2 | 0 | 0 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0001c0001t0013 | 0/0 | 3045 | 2 | 0 | 1 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0001 | 0/0 | 3045 | 6 | 3 | 2 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0002 | 0/0 | 3045 | 49 | 4 | 4 | 33 | 1 | 7 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0003 | 0/0 | 3045 | 9 | 8 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0004 | 0/0 | 3045 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0005 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0014 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0016 | 0/0 | 3045 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0002c0002t0017 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0003c0003t0001 | 0/0 | 3045 | 56 | 15 | 5 | 27 | 0 | 9 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0003c0003t0003 | 0/0 | 3045 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0003c0003t0005 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0003c0003t0011 | 0/0 | 3045 | 2 | 0 | 0 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0003c0003t0015 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0004c0007t0001 | 0/0 | 3045 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0005c0006t0002 | 0/0 | 3045 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0006c0005t0002 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0007c0008t0001 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
a0008c0004t0001 | 0/0 | 3045 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | GCTCG others(3040): Show |
chr2 | 10051473 | 10085411 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 0 | 6 | 20 | 1 | 3 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0003 | 0/0 | 12 | 1 | 1 | 9 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0005 | 0/0 | 9 | 2 | 5 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0054 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0053 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0005g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0006g0015 | 0/0 | 4 | 0 | 0 | 0 | 3 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0006g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0008g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0009g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0010g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0012g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0001c0001t0013g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0001g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0004 | 0/0 | 12 | 0 | 1 | 9 | 0 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0006 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0033 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0032 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0004g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0016g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0002c0002t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0002 | 0/0 | 21 | 0 | 0 | 16 | 0 | 5 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0011g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0003c0003t0015g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0004c0007t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0005c0006t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0006c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0007c0008t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
a0008c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | GBR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | GBR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00140 | hp2 | a0001 | c0001 | t0013 | g0043 | EUR | GBR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0028 | EUR | FIN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00423 | hp2 | a0003 | c0003 | t0011 | g0078 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00438 | hp2 | a0004 | c0007 | t0001 | g0193 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00639 | hp2 | a0005 | c0006 | t0002 | g0153 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00673 | hp1 | a0003 | c0003 | t0001 | g0075 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0189 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01069 | hp1 | a0001 | c0001 | t0010 | g0040 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0040 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0190 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01109 | hp1 | a0003 | c0003 | t0005 | g0062 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0037 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0034 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0043 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0211 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | IBS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0015 | EUR | IBS | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0184 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02040 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02055 | hp2 | a0003 | c0003 | t0001 | g0070 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02080 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0028 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | CDX | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02165 | hp1 | a0002 | c0002 | t0017 | g0204 | EAS | CDX | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0076 | EAS | CDX | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02258 | hp2 | a0003 | c0003 | t0003 | g0067 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0066 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0085 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02451 | hp2 | a0006 | c0005 | t0002 | g0069 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02523 | hp1 | a0003 | c0003 | t0011 | g0073 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0028 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0017 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0032 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0168 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0206 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0033 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0019 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02896 | hp1 | a0007 | c0008 | t0001 | g0217 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02896 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0019 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0032 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0058 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0055 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0174 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03130 | hp1 | a0003 | c0003 | t0015 | g0064 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03139 | hp2 | a0002 | c0002 | t0003 | g0055 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0208 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03225 | hp2 | a0002 | c0002 | t0004 | g0058 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0197 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03486 | hp1 | a0002 | c0002 | t0005 | g0196 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0068 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03492 | hp1 | a0003 | c0003 | t0001 | g0036 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03540 | hp1 | a0008 | c0004 | t0001 | g0061 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03579 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0083 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0036 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03710 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0105 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0015 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03927 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03942 | hp2 | a0002 | c0002 | t0016 | g0202 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | BEB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0104 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG04228 | hp2 | a0001 | c0001 | t0007 | g0186 | SAS | STU | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0016 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | CHB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18944 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18948 | hp1 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18949 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18966 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18971 | hp1 | a0001 | c0001 | t0012 | g0115 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18972 | hp1 | a0003 | c0003 | t0001 | g0074 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18975 | hp1 | a0001 | c0001 | t0012 | g0124 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18981 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18984 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18997 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19058 | hp1 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19062 | hp1 | a0002 | c0002 | t0014 | g0060 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19066 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19083 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19086 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19091 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0019 | AFR | ASW | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20129 | hp2 | a0002 | c0002 | t0003 | g0198 | AFR | ASW | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20752 | hp2 | a0002 | c0002 | t0002 | g0212 | EUR | TSI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0052 | EUR | TSI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02109 | hp2 | a0002 | c0002 | t0003 | g0209 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
HG06807 | hp2 | a0003 | c0003 | t0001 | g0034 | AFR | USA | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | USA | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | LWK | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0087 | REF | REF | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0164 | REF | REF | CYS1_chr2_10051473_10085411 | CYS1 | chr2 | 10051473 | 10085411 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10058870 | G | C | 1 | a0006 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.460C>G | p.Arg154Gly | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 648/3045 | 460/477 | 154/158 | chr2 | 10058870 | |||
chr2:10065950 | C | T | 1 | a0005 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.325G>A | p.Ala109Thr | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/3 | 513/3045 | 325/477 | 109/158 | chr2 | 10065950 | |||
chr2:10079964 | G | A | 3 | a0003 a0004 a0006 |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
missense_variant | MODERATE | c.260C>T | p.Pro87Leu | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 448/3045 | 260/477 | 87/158 | chr2 | 10079964 | |||
chr2:10080091 | C | G | 3 | a0003 a0004 a0006 |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
missense_variant | MODERATE | c.133G>C | p.Val45Leu | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 321/3045 | 133/477 | 45/158 | chr2 | 10080091 | |||
chr2:10080120 | C | A | 2 | a0002 a0004 |
71 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
missense_variant | MODERATE | c.104G>T | p.Arg35Leu | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 292/3045 | 104/477 | 35/158 | chr2 | 10080120 | |||
chr2:10080144 | G | T | 1 | a0008 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.80C>A | p.Ala27Glu | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 268/3045 | 80/477 | 27/158 | chr2 | 10080144 | |||
chr2:10080199 | T | C | 1 | a0007 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.25A>G | p.Ser9Gly | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 213/3045 | 25/477 | 9/158 | chr2 | 10080199 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10056907 | A | T | 4 | a0001c0001t0004 a0001c0001t0009 a0002c0002t0004 others(1): Show |
16 | HG00099.hp1 HG01192.hp2 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1946T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 1946 | chr2 | 10056907 | ||||||
chr2:10057143 | T | A | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*1710A>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 1710 | chr2 | 10057143 | ||||||
chr2:10057488 | T | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(21): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1365A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 1365 | chr2 | 10057488 | ||||||
chr2:10057609 | T | C | 1 | a0001c0001t0013 | 2 | HG00140.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1244A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 1244 | chr2 | 10057609 | ||||||
chr2:10057726 | A | G | 1 | a0001c0001t0012 | 2 | NA18971.hp1 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1127T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 1127 | chr2 | 10057726 | ||||||
chr2:10057986 | C | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(13): Show |
273 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*867G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 867 | chr2 | 10057986 | ||||||
chr2:10058059 | C | G | 1 | a0003c0003t0011 | 2 | HG00423.hp2 HG02523.hp1 |
3_prime_UTR_variant | MODIFIER | c.*794G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 794 | chr2 | 10058059 | ||||||
chr2:10058061 | C | G | 3 | a0001c0001t0005 a0002c0002t0005 a0003c0003t0005 |
11 | HG01109.hp1 HG01934.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*792G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 792 | chr2 | 10058061 | ||||||
chr2:10058070 | G | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(1): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*783C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 783 | chr2 | 10058070 | ||||||
chr2:10058135 | G | A | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0009 others(1): Show |
25 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*718C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 718 | chr2 | 10058135 | ||||||
chr2:10058219 | C | T | 1 | a0002c0002t0016 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*634G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 634 | chr2 | 10058219 | ||||||
chr2:10058288 | T | C | 1 | a0001c0001t0008 | 5 | NA18941.hp2 NA18984.hp1 NA19010.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*565A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 565 | chr2 | 10058288 | ||||||
chr2:10058411 | C | G | 2 | a0001c0001t0004 a0002c0002t0004 |
12 | HG00099.hp1 HG01192.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*442G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 442 | chr2 | 10058411 | ||||||
chr2:10058439 | C | T | 1 | a0003c0003t0015 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 414 | chr2 | 10058439 | ||||||
chr2:10058600 | G | T | 1 | a0001c0001t0010 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*253C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 3/3 | 253 | chr2 | 10058600 | ||||||
chr2:10080257 | G | T | 1 | a0002c0002t0014 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/3 | 34 | chr2 | 10080257 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:10059042 | T | G | 1 | a0006c0005t0002g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.372-84A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059042 | |||||||
chr2:10059123 | G | T | 1 | a0002c0002t0003g0032 | 3 | HG01109.hp2 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.372-165C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059123 | |||||||
chr2:10059212 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.372-254C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059212 | |||||||
chr2:10059382 | G | C | 2 | a0002c0002t0002g0031 a0002c0002t0002g0213 |
4 | HG00673.hp2 NA18941.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-424C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059382 | |||||||
chr2:10059451 | C | T | 1 | a0001c0001t0006g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.372-493G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059451 | |||||||
chr2:10059474 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
276 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.372-516T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059474 | |||||||
chr2:10059643 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.372-685T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059643 | |||||||
chr2:10059758 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-800C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059758 | |||||||
chr2:10059953 | C | T | 4 | a0001c0001t0002g0151 a0002c0002t0002g0030 a0002c0002t0002g0205 others(1): Show |
6 | NA18947.hp2 NA18952.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.372-995G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059953 | |||||||
chr2:10059996 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.372-1038G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10059996 | |||||||
chr2:10060004 | C | T | 1 | a0001c0001t0006g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.372-1046G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060004 | |||||||
chr2:10060188 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.372-1230A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060188 | |||||||
chr2:10060189 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(35): Show |
79 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.372-1231C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060189 | |||||||
chr2:10060199 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0136 |
2 | NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.372-1241G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060199 | |||||||
chr2:10060319 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.372-1361C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060319 | |||||||
chr2:10060383 | G | A | 2 | a0003c0003t0001g0035 a0007c0008t0001g0217 |
3 | HG01070.hp2 HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.372-1425C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060383 | |||||||
chr2:10060413 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.372-1455C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060413 | |||||||
chr2:10060520 | C | A | 1 | a0001c0001t0001g0046 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.372-1562G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060520 | |||||||
chr2:10060583 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.372-1625C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060583 | |||||||
chr2:10060605 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.372-1647G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060605 | |||||||
chr2:10060697 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02056.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.372-1739G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060697 | |||||||
chr2:10060712 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.372-1754G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060712 | |||||||
chr2:10060824 | C | A | 1 | a0002c0002t0014g0060 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.372-1866G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060824 | |||||||
chr2:10060877 | A | G | 2 | a0002c0002t0002g0200 a0002c0002t0002g0203 |
2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.372-1919T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060877 | |||||||
chr2:10060956 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.372-1998C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10060956 | |||||||
chr2:10061009 | T | C | 1 | a0001c0001t0009g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.372-2051A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061009 | |||||||
chr2:10061218 | C | T | 1 | a0001c0001t0009g0048 | 2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.372-2260G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061218 | |||||||
chr2:10061248 | C | CCAAA | 15 | a0001c0001t0003g0051 a0001c0001t0003g0128 a0001c0001t0003g0161 others(12): Show |
19 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.372-2291_372-2290i others(6): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061248 | |||||||
chr2:10061252 | C | A | 35 | a0001c0001t0003g0051 a0001c0001t0003g0128 a0001c0001t0003g0161 others(32): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.372-2294G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061252 | |||||||
chr2:10061256 | A | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.372-2298T>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061256 | |||||||
chr2:10061271 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(186): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.372-2313C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061271 | |||||||
chr2:10061387 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.372-2429T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061387 | |||||||
chr2:10061396 | C | T | 1 | a0001c0001t0007g0133 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.372-2438G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061396 | |||||||
chr2:10061459 | C | T | 2 | a0003c0003t0001g0063 a0003c0003t0001g0066 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.372-2501G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061459 | |||||||
chr2:10061599 | G | A | 6 | a0001c0001t0003g0128 a0001c0001t0003g0188 a0002c0002t0001g0216 others(3): Show |
7 | HG02280.hp1 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.372-2641C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061599 | |||||||
chr2:10061610 | CA | C | 3 | a0001c0001t0001g0187 a0003c0003t0001g0063 a0003c0003t0001g0066 |
3 | HG02280.hp2 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.372-2653delT | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061610 | |||||||
chr2:10061702 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.372-2744T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10061702 | |||||||
chr2:10062195 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0158 |
4 | NA18942.hp1 NA18956.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-3237G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062195 | |||||||
chr2:10062244 | A | C | 1 | a0001c0001t0004g0052 | 2 | HG01255.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.372-3286T>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062244 | |||||||
chr2:10062401 | C | CT | 6 | a0001c0001t0001g0091 a0001c0001t0001g0180 a0001c0001t0003g0177 others(3): Show |
10 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.372-3444dupA | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062401 | |||||||
chr2:10062536 | G | A | 1 | a0006c0005t0002g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371+3368C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062536 | |||||||
chr2:10062681 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(16): Show |
34 | HG00408.hp1 HG00733.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.371+3223C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062681 | |||||||
chr2:10062774 | A | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0039 |
5 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+3130T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10062774 | |||||||
chr2:10063020 | T | C | 7 | a0001c0001t0002g0023 a0001c0001t0002g0045 a0001c0001t0002g0130 others(4): Show |
10 | HG00639.hp2 HG01175.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.371+2884A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063020 | |||||||
chr2:10063157 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.371+2747G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063157 | |||||||
chr2:10063379 | T | A | 2 | a0001c0001t0002g0157 a0001c0001t0005g0014 |
5 | HG01934.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+2525A>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063379 | |||||||
chr2:10063425 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.371+2479T>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063425 | |||||||
chr2:10063449 | T | A | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.371+2455A>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063449 | |||||||
chr2:10063805 | C | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0146 |
2 | HG01952.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.371+2099G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063805 | |||||||
chr2:10063939 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0125 others(1): Show |
10 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.371+1965T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10063939 | |||||||
chr2:10064080 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.371+1824C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064080 | |||||||
chr2:10064093 | C | T | 1 | a0006c0005t0002g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371+1811G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064093 | |||||||
chr2:10064150 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0112 |
10 | HG00280.hp1 HG00558.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.371+1754C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064150 | |||||||
chr2:10064163 | C | T | 5 | a0001c0001t0003g0051 a0001c0001t0003g0161 a0002c0002t0003g0032 others(2): Show |
8 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.371+1741G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064163 | |||||||
chr2:10064180 | A | T | 5 | a0001c0001t0001g0180 a0001c0001t0003g0177 a0003c0003t0001g0016 others(2): Show |
9 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.371+1724T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064180 | |||||||
chr2:10064359 | T | C | 1 | a0003c0003t0001g0079 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.371+1545A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064359 | |||||||
chr2:10064403 | C | T | 1 | a0001c0001t0001g0009 | 5 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+1501G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064403 | |||||||
chr2:10064483 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.371+1421G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064483 | |||||||
chr2:10064599 | C | A | 1 | a0001c0001t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.371+1305G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064599 | |||||||
chr2:10064616 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.371+1288G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064616 | |||||||
chr2:10064677 | C | A | 1 | a0001c0001t0009g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.371+1227G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064677 | |||||||
chr2:10064722 | A | T | 16 | a0001c0001t0001g0131 a0001c0001t0001g0175 a0001c0001t0001g0176 others(13): Show |
23 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.371+1182T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064722 | |||||||
chr2:10064726 | AT | A | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0007g0168 others(4): Show |
8 | HG02258.hp2 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.371+1177delA | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064726 | |||||||
chr2:10064778 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0143 |
2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.371+1126G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064778 | |||||||
chr2:10064781 | G | T | 2 | a0003c0003t0001g0077 a0004c0007t0001g0193 |
2 | HG00438.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.371+1123C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064781 | |||||||
chr2:10064811 | G | A | 1 | a0005c0006t0002g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.371+1093C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064811 | |||||||
chr2:10064838 | C | G | 6 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0007g0085 others(3): Show |
6 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+1066G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064838 | |||||||
chr2:10064865 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0007g0085 |
3 | HG02055.hp1 HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.371+1039C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064865 | |||||||
chr2:10064878 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0007g0085 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.371+1026G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064878 | |||||||
chr2:10064896 | G | GT | 17 | a0001c0001t0001g0112 a0001c0001t0001g0120 a0001c0001t0001g0121 others(14): Show |
20 | HG01109.hp2 HG01884.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.371+1007dupA | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064896 | |||||||
chr2:10064896 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.371+1008C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064896 | |||||||
chr2:10064902 | T | G | 1 | a0001c0001t0003g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.371+1002A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10064902 | |||||||
chr2:10065068 | C | G | 1 | a0001c0001t0002g0185 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.371+836G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065068 | |||||||
chr2:10065190 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.371+714G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065190 | |||||||
chr2:10065437 | G | A | 1 | a0006c0005t0002g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371+467C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065437 | |||||||
chr2:10065484 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0175 others(10): Show |
17 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.371+420C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065484 | |||||||
chr2:10065617 | A | G | 1 | a0002c0002t0003g0208 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.371+287T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065617 | |||||||
chr2:10065798 | C | T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0161 a0002c0002t0003g0032 |
6 | HG01109.hp2 HG01884.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+106G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 2/2 | chr2 | 10065798 | |||||||
chr2:10066319 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.319-363G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066319 | |||||||
chr2:10066340 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0119 |
2 | NA18970.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.319-384C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066340 | |||||||
chr2:10066424 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0039 others(1): Show |
12 | HG00323.hp1 HG01081.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-468G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066424 | |||||||
chr2:10066432 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0003g0128 a0001c0001t0003g0162 |
3 | HG02818.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.319-476G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066432 | |||||||
chr2:10066504 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.319-548T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066504 | |||||||
chr2:10066559 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.319-603A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066559 | |||||||
chr2:10066696 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.319-740C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066696 | |||||||
chr2:10066829 | GA | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(80): Show |
157 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.319-874delT | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066829 | |||||||
chr2:10066839 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.319-883A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066839 | |||||||
chr2:10066854 | G | C | 2 | a0001c0001t0003g0051 a0001c0001t0003g0161 |
3 | HG01884.hp1 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.319-898C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10066854 | |||||||
chr2:10067068 | T | G | 61 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(58): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.319-1112A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067068 | |||||||
chr2:10067164 | C | T | 6 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0127 others(3): Show |
9 | HG00099.hp1 HG01192.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-1208G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067164 | |||||||
chr2:10067175 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
158 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.319-1219C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067175 | |||||||
chr2:10067196 | A | G | 2 | a0001c0001t0007g0174 a0006c0005t0002g0069 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.319-1240T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067196 | |||||||
chr2:10067352 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(143): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.319-1396A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067352 | |||||||
chr2:10067398 | A | T | 2 | a0002c0002t0002g0029 a0002c0002t0002g0056 |
5 | NA18939.hp2 NA18943.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1442T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067398 | |||||||
chr2:10067406 | C | CT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.319-1451dupA | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067406 | |||||||
chr2:10067406 | CT | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(51): Show |
94 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.319-1451delA | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067406 | |||||||
chr2:10067411 | T | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(12): Show |
19 | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.319-1455A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067411 | |||||||
chr2:10067554 | C | T | 31 | a0001c0001t0001g0183 a0001c0001t0002g0041 a0001c0001t0002g0096 others(28): Show |
62 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.319-1598G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067554 | |||||||
chr2:10067638 | C | T | 14 | a0001c0001t0001g0163 a0001c0001t0001g0187 a0001c0001t0002g0157 others(11): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-1682G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067638 | |||||||
chr2:10067700 | C | G | 1 | a0001c0001t0001g0047 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.319-1744G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067700 | |||||||
chr2:10067967 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.319-2011G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067967 | |||||||
chr2:10067968 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(82): Show |
159 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.319-2012T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10067968 | |||||||
chr2:10068032 | TTG | T | 14 | a0001c0001t0001g0163 a0001c0001t0001g0187 a0001c0001t0002g0157 others(11): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-2078_319-2077d others(4): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068032 | |||||||
chr2:10068042 | A | C | 14 | a0001c0001t0001g0163 a0001c0001t0001g0187 a0001c0001t0002g0157 others(11): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-2086T>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068042 | |||||||
chr2:10068290 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319-2334C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068290 | |||||||
chr2:10068307 | T | C | 1 | a0002c0002t0003g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319-2351A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068307 | |||||||
chr2:10068448 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.319-2492T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068448 | |||||||
chr2:10068531 | T | C | 1 | a0001c0001t0003g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.319-2575A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068531 | |||||||
chr2:10068596 | ACTT | A | 11 | a0001c0001t0001g0187 a0001c0001t0002g0157 a0001c0001t0003g0188 others(8): Show |
23 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.319-2643_319-2641d others(5): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068596 | |||||||
chr2:10068759 | G | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(13): Show |
20 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-2803C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068759 | |||||||
chr2:10068936 | C | A | 16 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(13): Show |
20 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.319-2980G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10068936 | |||||||
chr2:10069289 | A | G | 1 | a0001c0001t0006g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.319-3333T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069289 | |||||||
chr2:10069327 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0003g0162 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.319-3371T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069327 | |||||||
chr2:10069425 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-3469C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069425 | |||||||
chr2:10069513 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(143): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.319-3557A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069513 | |||||||
chr2:10069526 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0004g0104 |
2 | HG04228.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.319-3570C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069526 | |||||||
chr2:10069629 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(94): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.319-3673C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069629 | |||||||
chr2:10069661 | C | G | 1 | a0002c0002t0004g0058 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-3705G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069661 | |||||||
chr2:10069679 | T | A | 2 | a0001c0001t0001g0163 a0001c0001t0003g0162 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.319-3723A>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069679 | |||||||
chr2:10069688 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.319-3732A>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069688 | |||||||
chr2:10069722 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.319-3766C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069722 | |||||||
chr2:10069791 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(93): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.319-3835C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069791 | |||||||
chr2:10069806 | A | G | 10 | a0001c0001t0001g0187 a0001c0001t0002g0157 a0001c0001t0003g0188 others(7): Show |
22 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.319-3850T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069806 | |||||||
chr2:10069822 | G | A | 1 | a0002c0002t0016g0202 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319-3866C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069822 | |||||||
chr2:10069866 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(93): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.319-3910G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069866 | |||||||
chr2:10069971 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(65): Show |
138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.319-4015T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069971 | |||||||
chr2:10069977 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319-4021C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069977 | |||||||
chr2:10069998 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0192 |
2 | HG02155.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.319-4042G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10069998 | |||||||
chr2:10070113 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.319-4157G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070113 | |||||||
chr2:10070117 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(141): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.319-4161C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070117 | |||||||
chr2:10070159 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.319-4203T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070159 | |||||||
chr2:10070206 | G | A | 18 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0163 others(15): Show |
22 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.319-4250C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070206 | |||||||
chr2:10070284 | T | C | 11 | a0001c0001t0001g0187 a0001c0001t0002g0157 a0001c0001t0003g0128 others(8): Show |
23 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.319-4328A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070284 | |||||||
chr2:10070302 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(66): Show |
139 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.319-4346A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070302 | |||||||
chr2:10070414 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.319-4458G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070414 | |||||||
chr2:10070476 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.319-4520C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070476 | |||||||
chr2:10070592 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(75): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.319-4636G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070592 | |||||||
chr2:10070637 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(76): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.319-4681G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070637 | |||||||
chr2:10070663 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(44): Show |
89 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.319-4707C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070663 | |||||||
chr2:10070775 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.319-4819G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070775 | |||||||
chr2:10070795 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(93): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.319-4839G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070795 | |||||||
chr2:10070817 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.319-4861A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070817 | |||||||
chr2:10070865 | T | C | 9 | a0001c0001t0001g0187 a0001c0001t0002g0157 a0001c0001t0003g0188 others(6): Show |
21 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-4909A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070865 | |||||||
chr2:10070881 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0163 others(14): Show |
21 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-4925G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070881 | |||||||
chr2:10070895 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.319-4939G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10070895 | |||||||
chr2:10071020 | GC | G | 1 | a0002c0002t0002g0033 | 3 | HG00733.hp1 HG02735.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.319-5065delG | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071020 | |||||||
chr2:10071090 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.319-5134G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071090 | |||||||
chr2:10071212 | C | T | 2 | a0003c0003t0003g0067 a0003c0003t0003g0068 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.319-5256G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071212 | |||||||
chr2:10071318 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.319-5362A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071318 | |||||||
chr2:10071365 | C | T | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.319-5409G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071365 | |||||||
chr2:10071366 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.319-5410C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071366 | |||||||
chr2:10071494 | C | A | 1 | a0002c0002t0002g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.319-5538G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071494 | |||||||
chr2:10071494 | C | T | 1 | a0001c0001t0009g0167 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.319-5538G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071494 | |||||||
chr2:10071498 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.319-5542G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071498 | |||||||
chr2:10071529 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(150): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.319-5573T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071529 | |||||||
chr2:10071539 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(150): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.319-5583G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071539 | |||||||
chr2:10071709 | T | G | 1 | a0001c0001t0012g0124 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.319-5753A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071709 | |||||||
chr2:10071814 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0170 |
2 | NA18906.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.319-5858C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071814 | |||||||
chr2:10071827 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.319-5871G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071827 | |||||||
chr2:10071849 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319-5893G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071849 | |||||||
chr2:10071917 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.319-5961C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10071917 | |||||||
chr2:10072062 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.319-6106C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072062 | |||||||
chr2:10072123 | G | A | 1 | a0003c0003t0001g0036 | 2 | HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.319-6167C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072123 | |||||||
chr2:10072166 | C | G | 67 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0026 others(64): Show |
115 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.319-6210G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072166 | |||||||
chr2:10072328 | C | T | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0002c0002t0001g0195 others(1): Show |
4 | HG00639.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-6372G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072328 | |||||||
chr2:10072401 | T | G | 21 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(18): Show |
28 | HG00099.hp1 HG01192.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.319-6445A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072401 | |||||||
chr2:10072439 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.319-6483A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072439 | |||||||
chr2:10072513 | A | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(15): Show |
31 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.319-6557T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072513 | |||||||
chr2:10072518 | C | T | 7 | a0002c0002t0001g0216 a0002c0002t0003g0055 a0002c0002t0003g0197 others(4): Show |
9 | HG01070.hp2 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.319-6562G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072518 | |||||||
chr2:10072565 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(15): Show |
31 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.319-6609G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072565 | |||||||
chr2:10072693 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.319-6737C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072693 | |||||||
chr2:10072758 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.319-6802C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072758 | |||||||
chr2:10072923 | G | C | 16 | a0002c0002t0001g0216 a0002c0002t0003g0055 a0002c0002t0003g0197 others(13): Show |
23 | HG01070.hp2 HG01109.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.319-6967C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072923 | |||||||
chr2:10072957 | G | T | 1 | a0002c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.318+6949C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10072957 | |||||||
chr2:10073073 | TG | T | 29 | a0001c0001t0001g0092 a0001c0001t0001g0183 a0001c0001t0001g0187 others(26): Show |
49 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.318+6832delC | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073073 | |||||||
chr2:10073209 | G | GC | 13 | a0001c0001t0001g0012 a0001c0001t0001g0095 a0001c0001t0001g0101 others(10): Show |
19 | HG00733.hp2 HG01099.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.318+6696dupG | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073209 | |||||||
chr2:10073209 | GCCC | G | 25 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0092 others(22): Show |
51 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.318+6694_318+6696d others(5): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073209 | |||||||
chr2:10073209 | GCCCC | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(114): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.318+6693_318+6696d others(6): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073209 | |||||||
chr2:10073209 | GCCCCC | G | 18 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(15): Show |
25 | HG00099.hp1 HG01255.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.318+6692_318+6696d others(7): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073209 | |||||||
chr2:10073217 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.318+6689G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073217 | |||||||
chr2:10073219 | C | T | 1 | a0003c0003t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.318+6687G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073219 | |||||||
chr2:10073220 | C | CA | 2 | a0003c0003t0001g0035 a0003c0003t0003g0068 |
3 | HG01070.hp2 HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.318+6685_318+6686i others(3): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073220 | |||||||
chr2:10073220 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318+6686G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073220 | |||||||
chr2:10073220 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(73): Show |
150 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.318+6686G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073220 | |||||||
chr2:10073221 | C | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0183 a0001c0001t0001g0187 others(10): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+6685G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073221 | |||||||
chr2:10073226 | G | A | 32 | a0001c0001t0001g0147 a0001c0001t0002g0041 a0001c0001t0002g0096 others(29): Show |
62 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+6680C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073226 | |||||||
chr2:10073272 | G | T | 1 | a0003c0003t0001g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.318+6634C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073272 | |||||||
chr2:10073283 | G | C | 1 | a0003c0003t0001g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318+6623C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073283 | |||||||
chr2:10073370 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(173): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.318+6536T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073370 | |||||||
chr2:10073594 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0183 a0001c0001t0001g0187 others(10): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+6312C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073594 | |||||||
chr2:10073636 | TTAGGGGC others(2): Show |
T | 13 | a0001c0001t0001g0092 a0001c0001t0001g0183 a0001c0001t0001g0187 others(10): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+6261_318+6269d others(11): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073636 | |||||||
chr2:10073662 | C | T | 2 | a0001c0001t0007g0174 a0006c0005t0002g0069 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.318+6244G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073662 | |||||||
chr2:10073790 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.318+6116A>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073790 | |||||||
chr2:10073883 | CCT | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(15): Show |
29 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.318+6021_318+6022d others(4): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073883 | |||||||
chr2:10073896 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0003g0162 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.318+6010G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073896 | |||||||
chr2:10073929 | A | C | 9 | a0003c0003t0001g0016 a0003c0003t0001g0017 a0003c0003t0001g0034 others(6): Show |
14 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.318+5977T>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073929 | |||||||
chr2:10073976 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(40): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.318+5930G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10073976 | |||||||
chr2:10074018 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.318+5888G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074018 | |||||||
chr2:10074132 | T | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(46): Show |
90 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.318+5774A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074132 | |||||||
chr2:10074134 | GTA | G | 7 | a0001c0001t0002g0023 a0001c0001t0002g0045 a0001c0001t0002g0130 others(4): Show |
10 | HG01175.hp2 HG01891.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.318+5770_318+5771d others(4): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074134 | |||||||
chr2:10074151 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.318+5755T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074151 | |||||||
chr2:10074230 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.318+5676G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074230 | |||||||
chr2:10074317 | C | G | 38 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(35): Show |
54 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.318+5589G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074317 | |||||||
chr2:10074456 | G | A | 13 | a0001c0001t0001g0092 a0001c0001t0001g0183 a0001c0001t0001g0187 others(10): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+5450C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074456 | |||||||
chr2:10074558 | G | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0086 a0001c0001t0001g0088 others(2): Show |
6 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+5348C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074558 | |||||||
chr2:10074772 | C | G | 5 | a0002c0002t0002g0057 a0002c0002t0002g0210 a0002c0002t0003g0032 others(2): Show |
8 | HG01109.hp2 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+5134G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074772 | |||||||
chr2:10074800 | T | C | 1 | a0003c0003t0001g0082 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.318+5106A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074800 | |||||||
chr2:10074946 | T | TA | 3 | a0002c0002t0001g0216 a0002c0002t0003g0055 a0002c0002t0003g0198 |
4 | HG02280.hp1 HG03098.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+4959dupT | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10074946 | |||||||
chr2:10075031 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0135 |
4 | NA18961.hp2 NA18981.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+4875C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075031 | |||||||
chr2:10075069 | G | A | 42 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(39): Show |
80 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.318+4837C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075069 | |||||||
chr2:10075113 | CA | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(64): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.318+4792delT | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075113 | |||||||
chr2:10075113 | CAA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(67): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.318+4791_318+4792d others(4): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075113 | |||||||
chr2:10075310 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.318+4596A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075310 | |||||||
chr2:10075331 | C | T | 1 | a0003c0003t0001g0072 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.318+4575G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075331 | |||||||
chr2:10075377 | A | T | 1 | a0002c0002t0002g0201 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.318+4529T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075377 | |||||||
chr2:10075395 | C | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(39): Show |
80 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.318+4511G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075395 | |||||||
chr2:10075557 | C | T | 1 | a0002c0002t0004g0058 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+4349G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075557 | |||||||
chr2:10075770 | T | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0007g0085 |
3 | HG02055.hp1 HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.318+4136A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075770 | |||||||
chr2:10075848 | T | C | 53 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(50): Show |
94 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.318+4058A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075848 | |||||||
chr2:10075858 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318+4048C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075858 | |||||||
chr2:10075882 | C | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(40): Show |
81 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.318+4024G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10075882 | |||||||
chr2:10076049 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.318+3857G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076049 | |||||||
chr2:10076189 | A | T | 1 | a0001c0001t0001g0046 | 2 | HG03688.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.318+3717T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076189 | |||||||
chr2:10076261 | A | AAATTTCA others(10): Show |
1 | a0001c0001t0001g0106 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.318+3628_318+3644d others(19): Show |
CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076261 | |||||||
chr2:10076315 | G | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(40): Show |
81 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.318+3591C>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076315 | |||||||
chr2:10076357 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0007g0085 |
3 | HG02055.hp1 HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.318+3549G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076357 | |||||||
chr2:10076382 | G | A | 13 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0157 others(10): Show |
26 | HG00140.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+3524C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076382 | |||||||
chr2:10076422 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.318+3484G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076422 | |||||||
chr2:10076444 | T | C | 2 | a0001c0001t0001g0160 a0008c0004t0001g0061 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.318+3462A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076444 | |||||||
chr2:10076513 | G | A | 20 | a0001c0001t0001g0026 a0001c0001t0001g0131 a0001c0001t0001g0169 others(17): Show |
28 | HG00099.hp1 HG01192.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.318+3393C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076513 | |||||||
chr2:10076612 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.318+3294G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076612 | |||||||
chr2:10076867 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0006g0184 |
4 | HG01891.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3039C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076867 | |||||||
chr2:10076867 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0003g0162 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.318+3039C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076867 | |||||||
chr2:10076906 | T | C | 58 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(55): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.318+3000A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10076906 | |||||||
chr2:10077038 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.318+2868C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077038 | |||||||
chr2:10077055 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.318+2851T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077055 | |||||||
chr2:10077108 | C | A | 1 | a0001c0001t0003g0054 | 2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.318+2798G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077108 | |||||||
chr2:10077212 | C | A | 2 | a0001c0001t0006g0189 a0001c0001t0006g0190 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.318+2694G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077212 | |||||||
chr2:10077233 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.318+2673G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077233 | |||||||
chr2:10077623 | A | G | 1 | a0002c0002t0001g0195 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.318+2283T>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077623 | |||||||
chr2:10077628 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.318+2278G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077628 | |||||||
chr2:10077653 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+2253A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077653 | |||||||
chr2:10077790 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
8 | HG00558.hp1 HG01106.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+2116A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077790 | |||||||
chr2:10077825 | G | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(36): Show |
80 | HG00408.hp1 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.318+2081C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077825 | |||||||
chr2:10077869 | G | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0027 others(7): Show |
19 | HG00280.hp2 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.318+2037C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077869 | |||||||
chr2:10077884 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.318+2022G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077884 | |||||||
chr2:10077885 | G | A | 3 | a0002c0002t0001g0211 a0002c0002t0002g0033 a0002c0002t0002g0212 |
5 | HG00733.hp1 HG01361.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+2021C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077885 | |||||||
chr2:10077993 | A | T | 1 | a0003c0003t0001g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.318+1913T>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10077993 | |||||||
chr2:10078055 | G | A | 1 | a0002c0002t0004g0058 | 2 | HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+1851C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078055 | |||||||
chr2:10078105 | CA | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(149): Show |
286 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.318+1800delT | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078105 | |||||||
chr2:10078192 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.318+1714A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078192 | |||||||
chr2:10078221 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.318+1685G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078221 | |||||||
chr2:10078223 | C | T | 33 | a0001c0001t0001g0095 a0003c0003t0001g0002 a0003c0003t0001g0016 others(30): Show |
65 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.318+1683G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078223 | |||||||
chr2:10078285 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(9): Show |
20 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+1621G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078285 | |||||||
chr2:10078319 | T | C | 1 | a0008c0004t0001g0061 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.318+1587A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078319 | |||||||
chr2:10078342 | G | A | 2 | a0001c0001t0003g0177 a0001c0001t0003g0178 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.318+1564C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078342 | |||||||
chr2:10078519 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
190 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.318+1387G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078519 | |||||||
chr2:10078573 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.318+1333C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078573 | |||||||
chr2:10078678 | C | A | 1 | a0002c0002t0001g0059 | 2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318+1228G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078678 | |||||||
chr2:10078715 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(9): Show |
20 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+1191G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078715 | |||||||
chr2:10078716 | G | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0027 others(7): Show |
19 | HG00280.hp2 HG00738.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.318+1190C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078716 | |||||||
chr2:10078790 | C | G | 1 | a0001c0001t0001g0094 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.318+1116G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078790 | |||||||
chr2:10078819 | G | A | 50 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(47): Show |
92 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.318+1087C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078819 | |||||||
chr2:10078896 | C | A | 1 | a0002c0002t0002g0215 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.318+1010G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10078896 | |||||||
chr2:10079143 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.318+763C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079143 | |||||||
chr2:10079149 | T | TG | 4 | a0001c0001t0001g0183 a0001c0001t0002g0027 a0001c0001t0003g0054 others(1): Show |
7 | HG01496.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+756dupC | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079149 | |||||||
chr2:10079151 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0007g0186 |
2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.318+755C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079151 | |||||||
chr2:10079289 | T | C | 6 | a0001c0001t0001g0187 a0001c0001t0003g0188 a0001c0001t0005g0011 others(3): Show |
12 | HG00280.hp2 HG00738.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.318+617A>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079289 | |||||||
chr2:10079597 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.318+309C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079597 | |||||||
chr2:10079619 | C | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0038 others(9): Show |
20 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+287G>C | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079619 | |||||||
chr2:10079628 | C | A | 19 | a0003c0003t0001g0002 a0003c0003t0001g0018 a0003c0003t0001g0019 others(16): Show |
45 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.318+278G>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079628 | |||||||
chr2:10079628 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.318+278G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079628 | |||||||
chr2:10079792 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.318+114C>G | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079792 | |||||||
chr2:10079802 | G | A | 32 | a0003c0003t0001g0002 a0003c0003t0001g0016 a0003c0003t0001g0017 others(29): Show |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.318+104C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079802 | |||||||
chr2:10079851 | G | A | 1 | a0002c0002t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.318+55C>T | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079851 | |||||||
chr2:10079879 | C | T | 32 | a0003c0003t0001g0002 a0003c0003t0001g0016 a0003c0003t0001g0017 others(29): Show |
64 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.318+27G>A | CYS1 | ENSG00000205795.5 | transcript | ENST00000381813.5 | protein_coding | 1/2 | chr2 | 10079879 |