Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 717 |
| ensemblid | ENSG00000166278.16 |
| hgncid | 1248 |
| symbol | C2 |
| name | complement C2 |
| refseq_nuc | NM_000063.6 |
| refseq_prot | NP_000054.2 |
| ensembl_nuc | ENST00000299367.10 |
| ensembl_prot | ENSP00000299367.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 31927717 |
| end | 31945672 |
| strand | + |
| ver | v1.2 |
| region | chr6:31927717-31945672 |
| region5000 | chr6:31922717-31950672 |
| regionname0 | C2_chr6_31927717_31945672 |
| regionname5000 | C2_chr6_31922717_31950672 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 752 | 370 | 89 | 73 | 155 | 17 | 35 | 116 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0002 | 0/0 | 752 | 14 | 0 | 4 | 8 | 0 | 2 | 8 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0003 | 0/0 | 283 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(278): Show |
chr6 | 31922717 | 31950672 |
| a0004 | 0/0 | 752 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0005 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0006 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0007 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0008 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0009 | 0/0 | 752 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0010 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| a0011 | 0/0 | 752 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | MGPLM others(747): Show |
chr6 | 31922717 | 31950672 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2256 | 332 | 72 | 65 | 151 | 15 | 28 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0001c0002 | 0/0 | 2256 | 36 | 15 | 8 | 4 | 2 | 7 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0001c0007 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0001c0010 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0002c0003 | 0/0 | 2256 | 7 | 0 | 3 | 2 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0002c0004 | 0/0 | 2256 | 7 | 0 | 1 | 6 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0003c0005 | 0/0 | 2245 | 2 | 0 | 1 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2240): Show |
chr6 | 31922717 | 31950672 | ||
| a0004c0006 | 0/0 | 2256 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0005c0013 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0006c0014 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0007c0011 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0008c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0009c0012 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0010c0008 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 | ||
| a0011c0015 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | ATGGG others(2251): Show |
chr6 | 31922717 | 31950672 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2610 | 332 | 72 | 65 | 151 | 15 | 28 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0001c0002t0001 | 0/0 | 2610 | 36 | 15 | 8 | 4 | 2 | 7 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0001c0007t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0001c0010t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0002c0003t0001 | 0/0 | 2610 | 7 | 0 | 3 | 2 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0002c0004t0001 | 0/0 | 2610 | 7 | 0 | 1 | 6 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0003c0005t0001 | 0/0 | 2599 | 2 | 0 | 1 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2594): Show |
chr6 | 31922717 | 31950672 |
| a0004c0006t0001 | 0/0 | 2610 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0005c0013t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0006c0014t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0007c0011t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0008c0009t0001 | 0/0 | 2610 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0009c0012t0001 | 0/0 | 2610 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0010c0008t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| a0011c0015t0001 | 0/0 | 2610 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | GGCTC others(2605): Show |
chr6 | 31922717 | 31950672 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 39 | 1 | 6 | 24 | 3 | 5 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 9 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0003 | 0/0 | 15 | 1 | 8 | 6 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0004 | 0/0 | 14 | 9 | 4 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0005 | 0/0 | 7 | 2 | 3 | 0 | 2 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0007 | 0/0 | 7 | 5 | 0 | 0 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 1 | 1 | 3 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0015 | 0/0 | 5 | 2 | 2 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0024 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0031 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0053 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0026 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0056 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0007t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0001c0010t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0003t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0004t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0003c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0003c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0004c0006t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0005c0013t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0006c0014t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0007c0011t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0008c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0009c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0010c0008t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| a0011c0015t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00323 | hp2 | a0003 | c0005 | t0001 | g0083 | EUR | FIN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0091 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0082 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0042 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0009 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02015 | hp1 | a0005 | c0013 | t0001 | g0154 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02647 | hp1 | a0001 | c0007 | t0001 | g0076 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02647 | hp2 | a0007 | c0011 | t0001 | g0029 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03098 | hp1 | a0008 | c0009 | t0001 | g0192 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03453 | hp1 | a0001 | c0010 | t0001 | g0178 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0084 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0087 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03704 | hp2 | a0009 | c0012 | t0001 | g0179 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | PJL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0186 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | STU | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18970 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18985 | hp2 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18991 | hp1 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18997 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | LWK | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19054 | hp2 | a0010 | c0008 | t0001 | g0185 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19056 | hp2 | a0011 | c0015 | t0001 | g0188 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19060 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19068 | hp2 | a0002 | c0004 | t0001 | g0079 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19074 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19081 | hp1 | a0004 | c0006 | t0001 | g0030 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19086 | hp2 | a0002 | c0004 | t0001 | g0037 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ASW | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | GIH | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01123 | hp1 | a0003 | c0005 | t0001 | g0086 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02109 | hp2 | a0006 | c0014 | t0001 | g0183 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0160 | REF | REF | C2_chr6_31922717_31950672 | C2 | chr6 | 31922717 | 31950672 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31928758 | T | G | 1 | a0010 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.283T>G | p.Phe95Val | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/18 | 319/2610 | 283/2259 | 95/752 | chr6 | 31928758 | |||
| chr6:31934288 | ATGGTGGA others(21): Show |
A | 1 | a0003 | 2 | HG00323.hp2 HG01123.hp1 |
splice_donor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.841_849+19delGTGGA others(23): Show |
p.Val281_Arg283del | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/18 | 877/2610 | 841/2259 | 281/752 | INFO_REALIGN_3_PRIME | chr6 | 31934288 | ||
| chr6:31936009 | C | G | 1 | a0011 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.936C>G | p.Asn312Lys | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/18 | 972/2610 | 936/2259 | 312/752 | chr6 | 31936009 | |||
| chr6:31936027 | G | C | 2 | a0002 a0003 |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
missense_variant | MODERATE | c.954G>C | p.Glu318Asp | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/18 | 990/2610 | 954/2259 | 318/752 | chr6 | 31936027 | |||
| chr6:31943063 | A | G | 1 | a0006 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1324A>G | p.Thr442Ala | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 10/18 | 1360/2610 | 1324/2259 | 442/752 | chr6 | 31943063 | |||
| chr6:31943455 | G | A | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1495G>A | p.Asp499Asn | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 12/18 | 1531/2610 | 1495/2259 | 499/752 | chr6 | 31943455 | |||
| chr6:31943489 | G | A | 2 | a0004 a0010 |
3 | NA18991.hp1 NA19054.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.1529G>A | p.Arg510His | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 12/18 | 1565/2610 | 1529/2259 | 510/752 | chr6 | 31943489 | |||
| chr6:31944159 | G | A | 1 | a0009 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1835G>A | p.Ser612Asn | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/18 | 1871/2610 | 1835/2259 | 612/752 | chr6 | 31944159 | |||
| chr6:31945269 | C | T | 1 | a0008 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.2171C>T | p.Pro724Leu | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 18/18 | 2207/2610 | 2171/2259 | 724/752 | chr6 | 31945269 | |||
| chr6:31945298 | C | T | 1 | a0005 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2200C>T | p.Arg734Cys | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 18/18 | 2236/2610 | 2200/2259 | 734/752 | chr6 | 31945298 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31928115 | G | A | 1 | a0001c0007 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.207G>A | p.Gln69Gln | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 2/18 | 243/2610 | 207/2259 | 69/752 | chr6 | 31928115 | |||
| chr6:31937353 | G | A | 5 | a0001c0002 a0004c0006 a0008c0009 others(2): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
synonymous_variant | LOW | c.1023G>A | p.Ala341Ala | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/18 | 1059/2610 | 1023/2259 | 341/752 | chr6 | 31937353 | |||
| chr6:31937393 | C | A | 1 | a0001c0010 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1063C>A | p.Arg355Arg | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/18 | 1099/2610 | 1063/2259 | 355/752 | chr6 | 31937393 | |||
| chr6:31944996 | A | G | 1 | a0002c0004 | 7 | HG01993.hp1 NA18985.hp2 NA18997.hp2 others(4): Show |
synonymous_variant | LOW | c.2046A>G | p.Ala682Ala | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 17/18 | 2082/2610 | 2046/2259 | 682/752 | chr6 | 31944996 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:31927842 | G | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0199 a0001c0001t0001g0201 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+44G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 1/17 | chr6 | 31927842 | |||||||
| chr6:31928196 | C | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
69 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.256+32C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 2/17 | chr6 | 31928196 | |||||||
| chr6:31928335 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
6 | HG00423.hp2 HG02738.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.256+171G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 2/17 | chr6 | 31928335 | |||||||
| chr6:31928440 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.256+276G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 2/17 | chr6 | 31928440 | |||||||
| chr6:31928591 | CAT | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(2): Show |
15 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(12): Show |
intron_variant | MODIFIER | c.257-140_257-139del others(2): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 2/17 | chr6 | 31928591 | |||||||
| chr6:31929097 | G | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(2): Show |
15 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(12): Show |
intron_variant | MODIFIER | c.442+180G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929097 | |||||||
| chr6:31929277 | G | A | 1 | a0001c0001t0001g0033 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.442+360G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929277 | |||||||
| chr6:31929284 | G | T | 1 | a0001c0002t0001g0166 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+367G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929284 | |||||||
| chr6:31929442 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(25): Show |
55 | HG00423.hp2 HG00558.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.442+525G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929442 | |||||||
| chr6:31929446 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0007t0001g0076 |
3 | HG01515.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.442+529T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929446 | |||||||
| chr6:31929521 | C | T | 17 | a0001c0002t0001g0030 a0001c0002t0001g0056 a0001c0002t0001g0186 others(14): Show |
19 | HG02683.hp2 HG02698.hp2 HG02886.hp2 others(16): Show |
intron_variant | MODIFIER | c.442+604C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929521 | |||||||
| chr6:31929667 | G | A | 1 | a0010c0008t0001g0185 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.442+750G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929667 | |||||||
| chr6:31929717 | C | CA | 30 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(27): Show |
47 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.442+824dupA | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31929717 | ||||||
| chr6:31929717 | C | CAA | 5 | a0001c0001t0001g0051 a0001c0007t0001g0076 a0002c0003t0001g0037 others(2): Show |
6 | HG01952.hp1 HG02148.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+823_442+824dup others(2): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31929717 | ||||||
| chr6:31929717 | CA | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(85): Show |
175 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.442+824delA | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31929717 | ||||||
| chr6:31929717 | CAA | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG01516.hp2 HG02083.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+823_442+824del others(2): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31929717 | ||||||
| chr6:31929766 | G | A | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.442+849G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929766 | |||||||
| chr6:31929820 | T | C | 2 | a0001c0002t0001g0189 a0011c0015t0001g0188 |
2 | NA18941.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.442+903T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929820 | |||||||
| chr6:31929840 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
6 | HG01952.hp2 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+923G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929840 | |||||||
| chr6:31929850 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.442+933C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929850 | |||||||
| chr6:31929905 | A | G | 1 | a0002c0003t0001g0091 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.442+988A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929905 | |||||||
| chr6:31929915 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.442+998G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929915 | |||||||
| chr6:31929974 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442+1057T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31929974 | |||||||
| chr6:31930012 | A | AAAAC | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0161 |
3 | HG01261.hp1 HG01361.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.442+1119_442+1122d others(6): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31930012 | ||||||
| chr6:31930012 | AAAAC | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(15): Show |
35 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.442+1119_442+1122d others(6): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31930012 | ||||||
| chr6:31930084 | CT | C | 13 | a0001c0001t0001g0078 a0001c0001t0001g0201 a0002c0003t0001g0009 others(10): Show |
17 | HG00323.hp2 HG00741.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.442+1181delT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31930084 | ||||||
| chr6:31930134 | T | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(21): Show |
38 | HG01884.hp2 HG02683.hp2 HG02698.hp2 others(35): Show |
intron_variant | MODIFIER | c.442+1217T>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31930134 | |||||||
| chr6:31930244 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG00621.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.442+1327G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31930244 | |||||||
| chr6:31930508 | A | G | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.442+1591A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31930508 | |||||||
| chr6:31930643 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0121 a0001c0001t0001g0122 others(2): Show |
6 | NA18941.hp2 NA18965.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+1726G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31930643 | |||||||
| chr6:31930953 | G | T | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.442+2036G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31930953 | |||||||
| chr6:31931262 | C | CT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0073 others(7): Show |
16 | HG00738.hp2 HG01934.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.443-2329dupT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931262 | ||||||
| chr6:31931262 | CT | C | 27 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0044 others(24): Show |
36 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.443-2329delT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931262 | ||||||
| chr6:31931282 | A | T | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-2328A>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931282 | |||||||
| chr6:31931395 | G | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0113 others(1): Show |
4 | HG01358.hp1 HG01515.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-2215G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931395 | |||||||
| chr6:31931424 | T | C | 2 | a0001c0001t0001g0060 a0006c0014t0001g0183 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.443-2186T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931424 | |||||||
| chr6:31931470 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0170 |
7 | HG01934.hp2 HG01952.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-2140G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931470 | |||||||
| chr6:31931518 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0129 |
3 | NA18975.hp2 NA18983.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.443-2092G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931518 | |||||||
| chr6:31931520 | T | C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-2090T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931520 | |||||||
| chr6:31931739 | C | A | 1 | a0011c0015t0001g0188 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.443-1871C>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931739 | |||||||
| chr6:31931741 | T | C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-1869T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931741 | |||||||
| chr6:31931779 | T | C | 12 | a0001c0002t0001g0011 a0001c0002t0001g0042 a0001c0002t0001g0080 others(9): Show |
17 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.443-1831T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931779 | |||||||
| chr6:31931821 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
45 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.443-1789C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931821 | |||||||
| chr6:31931842 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
38 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.443-1768G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931842 | |||||||
| chr6:31931870 | AGGGCGGC others(91): Show |
A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0095 a0001c0001t0001g0099 others(1): Show |
7 | NA18944.hp2 NA18968.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.443-1691_443-1594d others(100): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931870 | ||||||
| chr6:31931897 | CCCCCCCA others(42): Show |
C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(71): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.443-1689_443-1641d others(51): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931897 | ||||||
| chr6:31931898 | CCCCCCAC others(41): Show |
C | 1 | a0001c0001t0001g0001 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.443-1706_443-1659d others(50): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931898 | ||||||
| chr6:31931918 | CGGCGCGG others(169): Show |
C | 2 | a0001c0002t0001g0190 a0001c0002t0001g0198 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.443-1689_443-1514d others(2): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931918 | ||||||
| chr6:31931921 | C | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0014 others(57): Show |
96 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.443-1689C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931921 | |||||||
| chr6:31931921 | CGCGGCTG others(42): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1664_443-1616d others(51): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931921 | ||||||
| chr6:31931931 | C | T | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-1679C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931931 | |||||||
| chr6:31931945 | ATCCCCCC others(41): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.443-1664_443-1617d others(50): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931945 | |||||||
| chr6:31931946 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
11 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.443-1664T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931946 | |||||||
| chr6:31931946 | T | TCCCCCCA others(120): Show |
1 | a0001c0001t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.443-1643_443-1642i others(129): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31931946 | ||||||
| chr6:31931961 | C | G | 1 | a0001c0002t0001g0186 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.443-1649C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931961 | |||||||
| chr6:31931968 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-1642G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931968 | |||||||
| chr6:31931970 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-1640G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931970 | |||||||
| chr6:31931970 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.443-1640G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931970 | |||||||
| chr6:31931972 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
10 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-1638C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931972 | |||||||
| chr6:31931994 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.443-1616A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31931994 | |||||||
| chr6:31932021 | TGGCTGGC others(120): Show |
T | 28 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(25): Show |
37 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.443-1572_443-1446d others(2): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31932021 | ||||||
| chr6:31932030 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.443-1580G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932030 | |||||||
| chr6:31932113 | A | G | 2 | a0001c0002t0001g0190 a0001c0002t0001g0198 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.443-1497A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932113 | |||||||
| chr6:31932144 | G | A | 2 | a0001c0002t0001g0190 a0001c0002t0001g0198 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.443-1466G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932144 | |||||||
| chr6:31932146 | G | A | 2 | a0001c0002t0001g0190 a0001c0002t0001g0198 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.443-1464G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932146 | |||||||
| chr6:31932148 | C | T | 2 | a0001c0002t0001g0190 a0001c0002t0001g0198 |
2 | HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.443-1462C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932148 | |||||||
| chr6:31932162 | G | A | 12 | a0001c0002t0001g0011 a0001c0002t0001g0042 a0001c0002t0001g0080 others(9): Show |
17 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.443-1448G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932162 | |||||||
| chr6:31932190 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(2): Show |
15 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(12): Show |
intron_variant | MODIFIER | c.443-1420G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932190 | |||||||
| chr6:31932222 | G | C | 17 | a0001c0002t0001g0030 a0001c0002t0001g0056 a0001c0002t0001g0186 others(14): Show |
19 | HG02683.hp2 HG02698.hp2 HG02886.hp2 others(16): Show |
intron_variant | MODIFIER | c.443-1388G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932222 | |||||||
| chr6:31932238 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.443-1372C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932238 | |||||||
| chr6:31932341 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.443-1269G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932341 | |||||||
| chr6:31932376 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0169 others(4): Show |
9 | HG01884.hp1 HG02630.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-1234G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932376 | |||||||
| chr6:31932405 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.443-1205G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932405 | |||||||
| chr6:31932435 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.443-1175C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932435 | |||||||
| chr6:31932455 | A | C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-1155A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932455 | |||||||
| chr6:31932476 | T | C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-1134T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932476 | |||||||
| chr6:31932485 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0109 |
2 | HG04204.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443-1125C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932485 | |||||||
| chr6:31932522 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.443-1088G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932522 | |||||||
| chr6:31932534 | CGCTCCTC others(110): Show |
C | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-1066_443-950de others(1): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31932534 | ||||||
| chr6:31932537 | T | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0106 others(1): Show |
5 | HG01361.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-1073T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932537 | |||||||
| chr6:31932575 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG00438.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.443-1035G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932575 | |||||||
| chr6:31932595 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0012 others(61): Show |
140 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.443-1015G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932595 | |||||||
| chr6:31932601 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0007t0001g0076 |
3 | HG01515.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.443-1009G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932601 | |||||||
| chr6:31932604 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.443-1006C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932604 | |||||||
| chr6:31932614 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(4): Show |
19 | HG01884.hp2 HG02723.hp2 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.443-996C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932614 | |||||||
| chr6:31932676 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG00621.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.443-934T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932676 | |||||||
| chr6:31932691 | G | A | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-919G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932691 | |||||||
| chr6:31932704 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.443-906C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932704 | |||||||
| chr6:31932705 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.443-905A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932705 | |||||||
| chr6:31932793 | A | G | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.443-817A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932793 | |||||||
| chr6:31932800 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0057 others(2): Show |
7 | HG00423.hp2 HG01069.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-810C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932800 | |||||||
| chr6:31932880 | G | A | 12 | a0002c0003t0001g0009 a0002c0003t0001g0037 a0002c0003t0001g0082 others(9): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.443-730G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932880 | |||||||
| chr6:31932990 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.443-620C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31932990 | |||||||
| chr6:31933008 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
14 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.443-602C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933008 | |||||||
| chr6:31933064 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0069 |
3 | HG02451.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443-546C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933064 | |||||||
| chr6:31933091 | C | CAGAGGGA others(18): Show |
12 | a0002c0003t0001g0009 a0002c0003t0001g0037 a0002c0003t0001g0082 others(9): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.443-507_443-483dup others(25): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 31933091 | ||||||
| chr6:31933115 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0007t0001g0076 |
3 | HG01515.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.443-495G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933115 | |||||||
| chr6:31933131 | G | C | 12 | a0002c0003t0001g0009 a0002c0003t0001g0037 a0002c0003t0001g0082 others(9): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.443-479G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933131 | |||||||
| chr6:31933313 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.443-297G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933313 | |||||||
| chr6:31933545 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.443-65C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933545 | |||||||
| chr6:31933572 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.443-38G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933572 | |||||||
| chr6:31933594 | C | T | 2 | a0001c0001t0001g0060 a0006c0014t0001g0183 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.443-16C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933594 | |||||||
| chr6:31933606 | G | A | 2 | a0001c0001t0001g0060 a0006c0014t0001g0183 |
2 | HG02109.hp2 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.443-4G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 3/17 | chr6 | 31933606 | |||||||
| chr6:31933996 | G | A | 1 | a0001c0002t0001g0026 | 3 | HG00738.hp2 HG02257.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.715+31G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 5/17 | chr6 | 31933996 | |||||||
| chr6:31934118 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0170 |
7 | HG01934.hp2 HG01952.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-48G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 5/17 | chr6 | 31934118 | |||||||
| chr6:31934512 | C | G | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.849+213C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31934512 | |||||||
| chr6:31934577 | C | T | 1 | a0001c0001t0001g0049 | 2 | NA18612.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.849+278C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31934577 | |||||||
| chr6:31934600 | C | A | 1 | a0005c0013t0001g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.849+301C>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31934600 | |||||||
| chr6:31934868 | A | G | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.849+569A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31934868 | |||||||
| chr6:31934980 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0112 |
3 | HG01361.hp2 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.849+681C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31934980 | |||||||
| chr6:31935016 | TAAATAAA others(3): Show |
T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0033 others(7): Show |
28 | HG00558.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.849+738_849+747del others(10): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 31935016 | ||||||
| chr6:31935344 | G | A | 13 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.850-579G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935344 | |||||||
| chr6:31935462 | T | A | 1 | a0006c0014t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.850-461T>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935462 | |||||||
| chr6:31935462 | T | TTTA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
7 | HG01952.hp2 HG03540.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-437_850-435dup others(3): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 31935462 | ||||||
| chr6:31935462 | T | TTTATTA | 12 | a0002c0003t0001g0009 a0002c0003t0001g0037 a0002c0003t0001g0082 others(9): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.850-440_850-435dup others(6): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 31935462 | ||||||
| chr6:31935462 | TTTA | T | 14 | a0001c0001t0001g0077 a0001c0002t0001g0011 a0001c0002t0001g0026 others(11): Show |
21 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.850-437_850-435del others(3): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 31935462 | ||||||
| chr6:31935580 | C | T | 1 | a0001c0001t0001g0048 | 2 | NA18998.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.850-343C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935580 | |||||||
| chr6:31935586 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.850-337C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935586 | |||||||
| chr6:31935604 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.850-319G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935604 | |||||||
| chr6:31935688 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.850-235C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935688 | |||||||
| chr6:31935869 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.850-54A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 6/17 | chr6 | 31935869 | |||||||
| chr6:31936404 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.988+343C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31936404 | |||||||
| chr6:31936529 | G | A | 14 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.988+468G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31936529 | |||||||
| chr6:31936882 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.989-437T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31936882 | |||||||
| chr6:31936952 | TGTA | T | 31 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(28): Show |
40 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.989-363_989-361del others(3): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 31936952 | ||||||
| chr6:31936953 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.989-366G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31936953 | |||||||
| chr6:31937206 | C | CA | 43 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0052 others(40): Show |
67 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.989-97dupA | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 31937206 | ||||||
| chr6:31937206 | CA | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(80): Show |
183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.989-97delA | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 31937206 | ||||||
| chr6:31937207 | A | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0047 others(12): Show |
34 | HG00621.hp2 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.989-112A>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31937207 | |||||||
| chr6:31937208 | A | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0047 others(12): Show |
34 | HG00621.hp2 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.989-111A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31937208 | |||||||
| chr6:31937227 | A | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0123 |
3 | NA18941.hp2 NA18995.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.989-92A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 7/17 | chr6 | 31937227 | |||||||
| chr6:31937551 | G | T | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1129+92G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31937551 | |||||||
| chr6:31937745 | G | A | 4 | a0001c0002t0001g0190 a0001c0002t0001g0193 a0001c0002t0001g0198 others(1): Show |
4 | HG02886.hp2 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129+286G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31937745 | |||||||
| chr6:31937916 | A | G | 1 | a0001c0001t0001g0046 | 2 | NA19010.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1129+457A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31937916 | |||||||
| chr6:31938104 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1129+645C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938104 | |||||||
| chr6:31938344 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp2 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1129+885C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938344 | |||||||
| chr6:31938456 | G | GTA | 16 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(13): Show |
37 | HG00558.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.1130-761_1130-760d others(4): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938456 | ||||||
| chr6:31938456 | GTA | G | 26 | a0001c0001t0001g0060 a0001c0002t0001g0030 a0001c0002t0001g0042 others(23): Show |
29 | HG01074.hp2 HG01099.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.1130-761_1130-760d others(4): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938456 | ||||||
| chr6:31938468 | A | ATG | 8 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0080 others(5): Show |
14 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1130-762_1130-761i others(4): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938468 | ||||||
| chr6:31938472 | G | A | 8 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0080 others(5): Show |
14 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1130-759G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938472 | |||||||
| chr6:31938473 | T | C | 8 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0080 others(5): Show |
14 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1130-758T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938473 | |||||||
| chr6:31938481 | C | CAT | 5 | a0001c0001t0001g0025 a0001c0001t0001g0060 a0001c0001t0001g0138 others(2): Show |
7 | HG02071.hp1 HG02109.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1130-733_1130-732d others(4): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938481 | ||||||
| chr6:31938481 | C | CATAT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0002t0001g0030 others(17): Show |
25 | HG02055.hp1 HG02129.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.1130-735_1130-732d others(6): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938481 | ||||||
| chr6:31938481 | C | CATATATA others(1): Show |
5 | a0001c0002t0001g0042 a0001c0002t0001g0114 a0001c0002t0001g0115 others(2): Show |
6 | HG01074.hp2 HG01099.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1130-739_1130-732d others(10): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938481 | ||||||
| chr6:31938481 | C | T | 8 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0080 others(5): Show |
14 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1130-750C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938481 | |||||||
| chr6:31938481 | CAT | C | 2 | a0001c0001t0001g0014 a0009c0012t0001g0179 |
6 | HG00140.hp2 HG02602.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-733_1130-732d others(4): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 31938481 | ||||||
| chr6:31938500 | T | A | 2 | a0001c0001t0001g0138 a0001c0002t0001g0114 |
2 | HG02129.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1130-731T>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938500 | |||||||
| chr6:31938557 | T | A | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1130-674T>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938557 | |||||||
| chr6:31938721 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1130-510G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938721 | |||||||
| chr6:31938728 | C | T | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1130-503C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938728 | |||||||
| chr6:31938737 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1130-494G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938737 | |||||||
| chr6:31938814 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1130-417C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938814 | |||||||
| chr6:31938820 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0105 |
3 | HG00438.hp1 NA18967.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1130-411A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31938820 | |||||||
| chr6:31939051 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
13 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.1130-180G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31939051 | |||||||
| chr6:31939088 | C | T | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1130-143C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31939088 | |||||||
| chr6:31939129 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1130-102A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31939129 | |||||||
| chr6:31939220 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0050 others(1): Show |
14 | NA18945.hp2 NA18963.hp2 NA18984.hp1 others(11): Show |
intron_variant | MODIFIER | c.1130-11C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 8/17 | chr6 | 31939220 | |||||||
| chr6:31939370 | T | C | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1219+50T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31939370 | |||||||
| chr6:31939391 | C | T | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1219+71C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31939391 | |||||||
| chr6:31939510 | C | CT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0072 others(18): Show |
27 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1219+211dupT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31939510 | ||||||
| chr6:31939510 | CT | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0060 others(12): Show |
17 | HG00099.hp1 HG00323.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219+211delT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31939510 | ||||||
| chr6:31939562 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1219+242A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31939562 | |||||||
| chr6:31939679 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1219+359C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31939679 | |||||||
| chr6:31939721 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1219+401A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31939721 | |||||||
| chr6:31940060 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(89): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1219+740G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940060 | |||||||
| chr6:31940200 | G | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0102 a0001c0001t0001g0131 others(3): Show |
8 | HG02027.hp1 HG02132.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219+880G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940200 | |||||||
| chr6:31940289 | C | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0106 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1219+969C>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940289 | |||||||
| chr6:31940369 | G | A | 1 | a0001c0001t0001g0025 | 3 | HG02280.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1219+1049G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940369 | |||||||
| chr6:31940447 | C | T | 12 | a0001c0002t0001g0011 a0001c0002t0001g0042 a0001c0002t0001g0080 others(9): Show |
17 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219+1127C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940447 | |||||||
| chr6:31940528 | A | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
6 | HG01952.hp2 NA18945.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1219+1208A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940528 | |||||||
| chr6:31940660 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1219+1340C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940660 | |||||||
| chr6:31940662 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1219+1342C>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940662 | |||||||
| chr6:31940790 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1219+1470C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940790 | |||||||
| chr6:31940801 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1219+1481C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940801 | |||||||
| chr6:31940881 | C | T | 1 | a0001c0007t0001g0076 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1219+1561C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940881 | |||||||
| chr6:31940984 | T | C | 32 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(29): Show |
41 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1219+1664T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31940984 | |||||||
| chr6:31941037 | T | C | 2 | a0001c0001t0001g0060 a0006c0014t0001g0183 |
2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1219+1717T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941037 | |||||||
| chr6:31941297 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(5): Show |
13 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1220-1662T>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941297 | |||||||
| chr6:31941423 | A | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0102 a0001c0001t0001g0131 others(3): Show |
8 | HG02027.hp1 HG02132.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1220-1536A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941423 | |||||||
| chr6:31941465 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1220-1494G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941465 | |||||||
| chr6:31941563 | G | A | 12 | a0002c0003t0001g0009 a0002c0003t0001g0037 a0002c0003t0001g0082 others(9): Show |
16 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1220-1396G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941563 | |||||||
| chr6:31941606 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1220-1353A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941606 | |||||||
| chr6:31941611 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1220-1348C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31941611 | |||||||
| chr6:31941814 | C | CT | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(61): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1220-1123dupT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTT | 4 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0147 others(1): Show |
8 | HG02083.hp2 HG03486.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.1220-1124_1220-112 others(6): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(3): Show |
17 | a0001c0002t0001g0011 a0001c0002t0001g0030 a0001c0002t0001g0042 others(14): Show |
23 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1220-1132_1220-112 others(14): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(4): Show |
10 | a0001c0002t0001g0056 a0001c0002t0001g0116 a0001c0002t0001g0186 others(7): Show |
11 | HG01361.hp1 HG02055.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1220-1133_1220-112 others(15): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1220-1134_1220-112 others(16): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1220-1135_1220-112 others(17): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(7): Show |
5 | a0001c0001t0001g0027 a0001c0001t0001g0102 a0001c0001t0001g0131 others(2): Show |
7 | HG02027.hp1 HG02132.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1220-1136_1220-112 others(18): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0135 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1220-1137_1220-112 others(19): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31941814 | CT | C | 15 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0148 others(12): Show |
19 | HG00323.hp2 HG00741.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1220-1123delT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31941814 | ||||||
| chr6:31942061 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0106 |
2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1220-898C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31942061 | |||||||
| chr6:31942114 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1220-845C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31942114 | |||||||
| chr6:31942124 | C | CT | 3 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0009c0012t0001g0179 |
8 | HG00140.hp2 HG02602.hp2 HG03704.hp2 others(5): Show |
intron_variant | MODIFIER | c.1220-822dupT | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 31942124 | ||||||
| chr6:31942164 | A | G | 1 | a0001c0001t0001g0005 | 7 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1220-795A>G | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31942164 | |||||||
| chr6:31942385 | G | A | 31 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(28): Show |
40 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1220-574G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31942385 | |||||||
| chr6:31942679 | G | T | 11 | a0001c0002t0001g0011 a0001c0002t0001g0042 a0001c0002t0001g0081 others(8): Show |
16 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1220-280G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 9/17 | chr6 | 31942679 | |||||||
| chr6:31943152 | G | A | 31 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(28): Show |
40 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1360+53G>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 10/17 | chr6 | 31943152 | |||||||
| chr6:31943161 | G | T | 31 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0030 others(28): Show |
40 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1360+62G>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 10/17 | chr6 | 31943161 | |||||||
| chr6:31943545 | CCAGCCTC others(15): Show |
C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0071 |
2 | HG02698.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1567+22_1567+43del others(22): Show |
C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 31943545 | ||||||
| chr6:31944232 | G | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0001g0057 others(4): Show |
9 | HG00140.hp1 HG01123.hp2 HG02738.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1902+6G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/17 | chr6 | 31944232 | |||||||
| chr6:31944323 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1902+97G>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/17 | chr6 | 31944323 | |||||||
| chr6:31944324 | C | T | 1 | a0006c0014t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1902+98C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/17 | chr6 | 31944324 | |||||||
| chr6:31944615 | A | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0182 a0001c0001t0001g0184 |
4 | HG03834.hp1 NA18948.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1903-112A>C | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/17 | chr6 | 31944615 | |||||||
| chr6:31944701 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
12 | HG01891.hp1 HG02145.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1903-26T>A | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 15/17 | chr6 | 31944701 | |||||||
| chr6:31944943 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2030-37C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 16/17 | chr6 | 31944943 | |||||||
| chr6:31945100 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0162 |
2 | NA18965.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2079+71C>T | C2 | ENSG00000166278.16 | transcript | ENST00000299367.10 | protein_coding | 17/17 | chr6 | 31945100 |