Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25988 |
| ensemblid | ENSG00000172273.13 |
| hgncid | 17850 |
| symbol | HINFP |
| name | histone H4 transcription factor |
| refseq_nuc | NM_198971.3 |
| refseq_prot | NP_945322.1 |
| ensembl_nuc | ENST00000350777.7 |
| ensembl_prot | ENSP00000318085.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 119121580 |
| end | 119136059 |
| strand | + |
| ver | v1.2 |
| region | chr11:119121580-119136059 |
| region5000 | chr11:119116580-119141059 |
| regionname0 | HINFP_chr11_119121580_119136059 |
| regionname5000 | HINFP_chr11_119116580_119141059 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 517 | 216 | 74 | 33 | 70 | 11 | 26 | 53 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0002 | 0/0 | 517 | 176 | 15 | 19 | 121 | 3 | 18 | 94 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0003 | 0/0 | 517 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0004 | 0/0 | 517 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0005 | 0/0 | 517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0006 | 0/0 | 517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0007 | 0/0 | 517 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0008 | 0/0 | 517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| a0009 | 0/0 | 517 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | MPPPG others(512): Show |
chr11 | 119116580 | 119141059 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1551 | 204 | 64 | 32 | 70 | 11 | 26 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0003 | 0/0 | 1551 | 6 | 6 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0006 | 1/0 | 1551 | 2 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0008 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0012 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0016 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0001c0017 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0002c0002 | 0/0 | 1551 | 174 | 15 | 18 | 120 | 3 | 18 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0002c0007 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0002c0011 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0003c0004 | 0/0 | 1551 | 4 | 4 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0004c0005 | 0/0 | 1551 | 3 | 1 | 2 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0005c0010 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0006c0014 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0007c0015 | 0/0 | 1551 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0008c0009 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 | ||
| a0009c0013 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | ATGCC others(1546): Show |
chr11 | 119116580 | 119141059 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 3185 | 105 | 32 | 27 | 30 | 8 | 7 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0003 | 0/0 | 3185 | 64 | 4 | 5 | 37 | 1 | 17 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0005 | 0/0 | 3185 | 9 | 9 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0006 | 0/0 | 3185 | 6 | 6 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0007 | 0/0 | 3185 | 8 | 8 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0008 | 0/0 | 3185 | 4 | 3 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0011 | 0/0 | 3185 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0015 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0016 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0017 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0018 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0020 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0001t0021 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0003t0002 | 0/0 | 3185 | 5 | 5 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0003t0008 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0006t0002 | 1/0 | 3185 | 2 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0008t0002 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0012t0019 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0016t0002 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0001c0017t0002 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0001 | 0/0 | 3185 | 144 | 13 | 15 | 101 | 3 | 12 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0004 | 0/0 | 3185 | 16 | 0 | 0 | 16 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0009 | 0/0 | 3185 | 3 | 0 | 0 | 0 | 0 | 3 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0010 | 0/0 | 3185 | 3 | 0 | 2 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0012 | 0/0 | 3188 | 2 | 0 | 1 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3183): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0013 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0014 | 0/0 | 3188 | 2 | 0 | 0 | 0 | 0 | 2 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3183): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0022 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0002t0023 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0007t0001 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0002c0011t0004 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0003c0004t0002 | 0/0 | 3185 | 4 | 4 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0004c0005t0006 | 0/0 | 3185 | 3 | 1 | 2 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0005c0010t0002 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0006c0014t0001 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0007c0015t0002 | 0/0 | 3185 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0008c0009t0002 | 0/0 | 3185 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| a0009c0013t0003 | 0/0 | 3185 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | GCCTC others(3180): Show |
chr11 | 119116580 | 119141059 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/1 | 19 | 2 | 6 | 7 | 3 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0010 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0014 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0006g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0008g0011 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0017g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0018g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0020g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0003t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0003t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0003t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0006t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0006t0002g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0008t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0012t0019g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0016t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0001c0017t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0001 | 0/0 | 30 | 0 | 4 | 23 | 1 | 2 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0002 | 0/0 | 15 | 1 | 2 | 9 | 1 | 2 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0004 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0006 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0009g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0009g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0010g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0012g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0012g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0014g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0014g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0022g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0002t0023g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0007t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0002c0011t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0003c0004t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0003c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0003c0004t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0004c0005t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0004c0005t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0004c0005t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0005c0010t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0006c0014t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0007c0015t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0008c0009t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| a0009c0013t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | GBR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0133 | EUR | GBR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00280 | hp1 | a0001 | c0001 | t0016 | g0086 | EUR | FIN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00609 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00642 | hp1 | a0004 | c0005 | t0006 | g0202 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00673 | hp2 | a0002 | c0011 | t0004 | g0041 | EAS | CHS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00738 | hp2 | a0002 | c0002 | t0010 | g0001 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG00741 | hp2 | a0001 | c0006 | t0002 | g0003 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01069 | hp1 | a0002 | c0007 | t0001 | g0005 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01074 | hp2 | a0004 | c0005 | t0006 | g0200 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01081 | hp1 | a0002 | c0002 | t0012 | g0001 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01167 | hp2 | a0002 | c0002 | t0010 | g0001 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0024 | EUR | IBS | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01884 | hp1 | a0006 | c0014 | t0001 | g0017 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02004 | hp1 | a0007 | c0015 | t0002 | g0003 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02040 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0083 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | CDX | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0206 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0210 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02647 | hp2 | a0002 | c0002 | t0013 | g0153 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02698 | hp1 | a0002 | c0002 | t0009 | g0002 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0011 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0017 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0008 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0204 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02818 | hp2 | a0001 | c0016 | t0002 | g0008 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0030 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02895 | hp2 | a0003 | c0004 | t0002 | g0104 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0120 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02965 | hp1 | a0003 | c0004 | t0002 | g0103 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02965 | hp2 | a0001 | c0008 | t0002 | g0008 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0044 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0077 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0065 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03540 | hp1 | a0002 | c0002 | t0013 | g0154 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03579 | hp1 | a0001 | c0003 | t0002 | g0030 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03834 | hp1 | a0002 | c0002 | t0010 | g0001 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0136 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0011 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03942 | hp2 | a0002 | c0002 | t0009 | g0002 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0107 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04184 | hp2 | a0002 | c0002 | t0014 | g0155 | SAS | BEB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04199 | hp1 | a0001 | c0001 | t0017 | g0203 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04204 | hp1 | a0002 | c0002 | t0014 | g0156 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04228 | hp1 | a0002 | c0002 | t0009 | g0108 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0132 | SAS | STU | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18522 | hp2 | a0003 | c0004 | t0002 | g0013 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | CHB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18747 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | CHB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18906 | hp1 | a0001 | c0012 | t0019 | g0211 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18943 | hp2 | a0002 | c0002 | t0023 | g0006 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18947 | hp1 | a0002 | c0002 | t0004 | g0137 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18953 | hp1 | a0001 | c0001 | t0021 | g0159 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18959 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18969 | hp2 | a0001 | c0001 | t0011 | g0099 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18975 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18981 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18982 | hp2 | a0002 | c0002 | t0004 | g0118 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18997 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18998 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19007 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19009 | hp1 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0171 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19062 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19063 | hp2 | a0002 | c0002 | t0022 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19067 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19068 | hp1 | a0002 | c0002 | t0012 | g0115 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19068 | hp2 | a0009 | c0013 | t0003 | g0193 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19086 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20129 | hp1 | a0001 | c0017 | t0002 | g0009 | AFR | ASW | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20129 | hp2 | a0003 | c0004 | t0002 | g0013 | AFR | ASW | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20752 | hp2 | a0001 | c0001 | t0020 | g0003 | EUR | TSI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0049 | EUR | TSI | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | GIH | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG01123 | hp2 | a0005 | c0010 | t0002 | g0096 | AMR | CLM | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02109 | hp1 | a0001 | c0003 | t0008 | g0054 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02559 | hp1 | a0004 | c0005 | t0006 | g0201 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0079 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | USA | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| HG06807 | hp2 | a0008 | c0009 | t0002 | g0007 | AFR | USA | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | USA | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0061 | AFR | USA | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0003 | REF | REF | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0002 | g0148 | REF | REF | HINFP_chr11_119116580_119141059 | HINFP | chr11 | 119116580 | 119141059 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:119126935 | G | A | 1 | a0001 | 1 | HG02809.hp2 | splice_region_variant | LOW | c.-10G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/10 | chr11 | 119126935 | |||||||
| chr11:119127062 | C | A | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.118C>A | p.Leu40Met | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/10 | 188/3185 | 118/1554 | 40/517 | chr11 | 119127062 | |||
| chr11:119127113 | G | A | 1 | a0005 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.169G>A | p.Asp57Asn | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/10 | 239/3185 | 169/1554 | 57/517 | chr11 | 119127113 | |||
| chr11:119133105 | A | G | 1 | a0007 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.1025A>G | p.Glu342Gly | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/10 | 1095/3185 | 1025/1554 | 342/517 | chr11 | 119133105 | |||
| chr11:119133135 | A | G | 1 | a0006 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1055A>G | p.Lys352Arg | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/10 | 1125/3185 | 1055/1554 | 352/517 | chr11 | 119133135 | |||
| chr11:119134347 | A | G | 2 | a0003 a0005 |
5 | HG01123.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
missense_variant | MODERATE | c.1403A>G | p.Asn468Ser | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1473/3185 | 1403/1554 | 468/517 | chr11 | 119134347 | |||
| chr11:119134356 | A | G | 1 | a0004 | 3 | HG00642.hp1 HG01074.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.1412A>G | p.Asn471Ser | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1482/3185 | 1412/1554 | 471/517 | chr11 | 119134356 | |||
| chr11:119134422 | C | T | 2 | a0002 a0006 |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
missense_variant | MODERATE | c.1478C>T | p.Ala493Val | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1548/3185 | 1478/1554 | 493/517 | chr11 | 119134422 | |||
| chr11:119134463 | G | C | 1 | a0009 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.1519G>C | p.Gly507Arg | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1589/3185 | 1519/1554 | 507/517 | chr11 | 119134463 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:119127004 | G | A | 1 | a0002c0007 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.60G>A | p.Gly20Gly | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/10 | 130/3185 | 60/1554 | 20/517 | chr11 | 119127004 | |||
| chr11:119127049 | T | C | 1 | a0001c0008 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.105T>C | p.His35His | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/10 | 175/3185 | 105/1554 | 35/517 | chr11 | 119127049 | |||
| chr11:119131543 | C | T | 1 | a0001c0017 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.420C>T | p.Phe140Phe | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 4/10 | 490/3185 | 420/1554 | 140/517 | chr11 | 119131543 | |||
| chr11:119131609 | C | T | 1 | a0001c0016 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.486C>T | p.Val162Val | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 4/10 | 556/3185 | 486/1554 | 162/517 | chr11 | 119131609 | |||
| chr11:119131849 | G | A | 1 | a0002c0011 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.543G>A | p.Lys181Lys | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/10 | 613/3185 | 543/1554 | 181/517 | chr11 | 119131849 | |||
| chr11:119131855 | C | A | 1 | a0001c0012 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.549C>A | p.Arg183Arg | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/10 | 619/3185 | 549/1554 | 183/517 | chr11 | 119131855 | |||
| chr11:119131976 | T | C | 1 | a0001c0003 | 6 | HG01891.hp1 HG02109.hp1 HG02886.hp1 others(3): Show |
synonymous_variant | LOW | c.670T>C | p.Leu224Leu | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/10 | 740/3185 | 670/1554 | 224/517 | chr11 | 119131976 | |||
| chr11:119134378 | C | T | 16 | a0001c0001 a0001c0003 a0001c0008 others(13): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
synonymous_variant | LOW | c.1434C>T | p.Ile478Ile | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1504/3185 | 1434/1554 | 478/517 | chr11 | 119134378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:119134532 | C | T | 1 | a0002c0002t0023 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 34 | chr11 | 119134532 | ||||||
| chr11:119134597 | A | G | 1 | a0002c0002t0022 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*99A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 99 | chr11 | 119134597 | ||||||
| chr11:119134775 | C | T | 12 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(9): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*277C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 277 | chr11 | 119134775 | ||||||
| chr11:119134798 | C | G | 1 | a0001c0001t0021 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 300 | chr11 | 119134798 | ||||||
| chr11:119134851 | C | T | 2 | a0002c0002t0004 a0002c0011t0004 |
17 | HG00609.hp1 HG00673.hp2 HG02040.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*353C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 353 | chr11 | 119134851 | ||||||
| chr11:119135005 | G | T | 1 | a0001c0001t0020 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*507G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 507 | chr11 | 119135005 | ||||||
| chr11:119135101 | G | A | 1 | a0001c0001t0011 | 2 | NA18969.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*603G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 603 | chr11 | 119135101 | ||||||
| chr11:119135190 | C | G | 2 | a0001c0001t0003 a0009c0013t0003 |
65 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*692C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 692 | chr11 | 119135190 | ||||||
| chr11:119135282 | G | A | 1 | a0001c0001t0016 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 784 | chr11 | 119135282 | ||||||
| chr11:119135481 | A | G | 1 | a0002c0002t0014 | 2 | HG04184.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*983A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 983 | chr11 | 119135481 | ||||||
| chr11:119135588 | T | C | 1 | a0001c0001t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1090T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1090 | chr11 | 119135588 | ||||||
| chr11:119135590 | C | A | 12 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(9): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1092C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1092 | chr11 | 119135590 | ||||||
| chr11:119135617 | C | T | 1 | a0002c0002t0013 | 2 | HG02647.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1119C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1119 | chr11 | 119135617 | ||||||
| chr11:119135752 | A | G | 18 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(15): Show |
260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*1254A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1254 | chr11 | 119135752 | ||||||
| chr11:119135804 | G | A | 1 | a0002c0002t0009 | 3 | HG02698.hp1 HG03942.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1306G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1306 | chr11 | 119135804 | ||||||
| chr11:119135806 | A | G | 1 | a0001c0001t0005 | 9 | HG02145.hp2 HG02976.hp2 HG03130.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1308A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1308 | chr11 | 119135806 | ||||||
| chr11:119135952 | G | A | 1 | a0001c0001t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1454 | chr11 | 119135952 | ||||||
| chr11:119136003 | G | A | 1 | a0002c0002t0010 | 3 | HG00738.hp2 HG01167.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1505G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1505 | chr11 | 119136003 | ||||||
| chr11:119136012 | T | C | 20 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(17): Show |
262 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*1514T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1514 | chr11 | 119136012 | ||||||
| chr11:119136041 | T | G | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(3): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1543T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1543 | chr11 | 119136041 | ||||||
| chr11:119136045 | G | T | 19 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(16): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1547G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1547 | chr11 | 119136045 | ||||||
| chr11:119136048 | AG | A | 10 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(7): Show |
171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1551delG | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1551 | chr11 | 119136048 | ||||||
| chr11:119136049 | G | T | 5 | a0001c0001t0006 a0001c0001t0021 a0002c0002t0012 others(2): Show |
14 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1551G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1551 | chr11 | 119136049 | ||||||
| chr11:119136050 | A | AAAT | 2 | a0002c0002t0012 a0002c0002t0014 |
4 | HG01081.hp1 HG04184.hp2 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1554_*1555insTAA | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1555 | INFO_REALIGN_3_PRIME | chr11 | 119136050 | |||||
| chr11:119136050 | A | T | 10 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(7): Show |
173 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1552A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1552 | chr11 | 119136050 | ||||||
| chr11:119136054 | G | T | 12 | a0002c0002t0001 a0002c0002t0004 a0002c0002t0009 others(9): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*1556G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 10/10 | 1556 | chr11 | 119136054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:119121792 | T | G | 85 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-11+153T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119121792 | |||||||
| chr11:119122137 | A | G | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-11+498A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122137 | |||||||
| chr11:119122209 | A | C | 151 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(148): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-11+570A>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122209 | |||||||
| chr11:119122240 | A | G | 1 | a0001c0001t0007g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11+601A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122240 | |||||||
| chr11:119122407 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-11+768C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122407 | |||||||
| chr11:119122431 | T | G | 1 | a0001c0001t0021g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+792T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122431 | |||||||
| chr11:119122481 | G | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0052 others(5): Show |
14 | HG01891.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-11+842G>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122481 | |||||||
| chr11:119122501 | C | T | 1 | a0001c0001t0005g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-11+862C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122501 | |||||||
| chr11:119122608 | G | A | 1 | a0001c0001t0021g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+969G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122608 | |||||||
| chr11:119122650 | A | G | 1 | a0002c0002t0001g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-11+1011A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122650 | |||||||
| chr11:119122657 | A | T | 1 | a0001c0001t0003g0051 | 2 | HG02015.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-11+1018A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122657 | |||||||
| chr11:119122712 | A | G | 1 | a0001c0001t0007g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11+1073A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122712 | |||||||
| chr11:119122795 | A | G | 1 | a0001c0001t0007g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-11+1156A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122795 | |||||||
| chr11:119122839 | T | C | 148 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-11+1200T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122839 | |||||||
| chr11:119122922 | G | A | 148 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-11+1283G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122922 | |||||||
| chr11:119122959 | C | T | 2 | a0003c0004t0002g0103 a0003c0004t0002g0104 |
2 | HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-11+1320C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122959 | |||||||
| chr11:119122993 | C | T | 2 | a0002c0002t0014g0155 a0002c0002t0014g0156 |
2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-11+1354C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119122993 | |||||||
| chr11:119123021 | C | A | 1 | a0001c0001t0002g0055 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-11+1382C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123021 | |||||||
| chr11:119123036 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-11+1397G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123036 | |||||||
| chr11:119123062 | A | G | 2 | a0002c0002t0013g0153 a0002c0002t0013g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-11+1423A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123062 | |||||||
| chr11:119123084 | C | T | 2 | a0002c0002t0001g0043 a0002c0002t0001g0152 |
3 | NA18944.hp2 NA18960.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-11+1445C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123084 | |||||||
| chr11:119123091 | G | A | 50 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(47): Show |
68 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-11+1452G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123091 | |||||||
| chr11:119123128 | C | CAA | 65 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(62): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-11+1511_-11+1512d others(4): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | C | CAAA | 18 | a0001c0001t0002g0013 a0001c0001t0002g0031 a0001c0001t0002g0032 others(15): Show |
24 | HG00642.hp2 HG01069.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11+1510_-11+1512d others(5): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | C | CAAAAA | 57 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0002c0002t0001g0001 others(54): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-11+1508_-11+1512d others(7): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | C | CAAAAAA | 20 | a0002c0002t0001g0004 a0002c0002t0001g0012 a0002c0002t0001g0016 others(17): Show |
39 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-11+1507_-11+1512d others(8): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | C | CAAAAAAA | 7 | a0001c0001t0006g0198 a0001c0001t0006g0199 a0001c0001t0007g0210 others(4): Show |
7 | HG00642.hp1 HG01074.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+1506_-11+1512d others(9): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | CA | C | 40 | a0001c0001t0003g0020 a0001c0001t0003g0027 a0001c0001t0003g0028 others(37): Show |
56 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-11+1512delA | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123128 | CAAAAAAA others(5): Show |
C | 2 | a0002c0002t0001g0042 a0002c0002t0001g0151 |
3 | NA18950.hp2 NA18979.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-11+1501_-11+1512d others(14): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123128 | ||||||
| chr11:119123189 | G | A | 85 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-11+1550G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123189 | |||||||
| chr11:119123200 | C | G | 8 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-11+1561C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123200 | |||||||
| chr11:119123346 | G | A | 4 | a0001c0001t0002g0057 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | NA18967.hp2 NA18990.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1707G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123346 | |||||||
| chr11:119123506 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+1867C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123506 | |||||||
| chr11:119123512 | A | G | 2 | a0001c0001t0011g0099 a0001c0001t0011g0100 |
2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-11+1873A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123512 | |||||||
| chr11:119123548 | CT | C | 143 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(140): Show |
217 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.-11+1923delT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123548 | ||||||
| chr11:119123647 | T | A | 148 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-11+2008T>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123647 | |||||||
| chr11:119123706 | G | GA | 20 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0032 others(17): Show |
29 | HG00642.hp1 HG00642.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-11+2067_-11+2068i others(3): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123706 | |||||||
| chr11:119123706 | G | GT | 54 | a0001c0001t0007g0207 a0001c0001t0007g0208 a0002c0002t0001g0001 others(51): Show |
134 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.-11+2092dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123706 | ||||||
| chr11:119123706 | G | GTT | 18 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0016 others(15): Show |
30 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-11+2091_-11+2092d others(4): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123706 | ||||||
| chr11:119123706 | GT | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0072 others(8): Show |
13 | HG01099.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+2092delT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119123706 | ||||||
| chr11:119123707 | T | A | 117 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0009 others(114): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.-11+2068T>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123707 | |||||||
| chr11:119123708 | T | A | 11 | a0001c0001t0002g0008 a0001c0001t0002g0071 a0001c0001t0002g0072 others(8): Show |
13 | HG01099.hp1 HG02257.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+2069T>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123708 | |||||||
| chr11:119123719 | T | TG | 4 | a0002c0002t0001g0117 a0002c0002t0001g0119 a0002c0002t0001g0120 others(1): Show |
4 | HG00738.hp1 HG02145.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+2080_-11+2081i others(3): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123719 | |||||||
| chr11:119123734 | G | C | 10 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(7): Show |
11 | HG00642.hp1 HG01074.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-11+2095G>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123734 | |||||||
| chr11:119123805 | C | T | 2 | a0002c0002t0004g0041 a0002c0011t0004g0041 |
2 | HG00609.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.-11+2166C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123805 | |||||||
| chr11:119123806 | G | A | 138 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(135): Show |
211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-11+2167G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123806 | |||||||
| chr11:119123965 | A | G | 3 | a0002c0002t0001g0019 a0002c0002t0001g0037 a0002c0002t0001g0116 |
7 | HG00544.hp1 HG00673.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+2326A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119123965 | |||||||
| chr11:119124100 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-11+2461C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124100 | |||||||
| chr11:119124241 | A | G | 43 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(40): Show |
60 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-11+2602A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124241 | |||||||
| chr11:119124241 | A | T | 1 | a0001c0001t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-11+2602A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124241 | |||||||
| chr11:119124296 | T | G | 3 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0195 |
3 | HG00423.hp2 HG02056.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-10-2639T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124296 | |||||||
| chr11:119124370 | G | T | 1 | a0002c0002t0013g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-10-2565G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124370 | |||||||
| chr11:119124573 | A | T | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-10-2362A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124573 | |||||||
| chr11:119124578 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0058 others(6): Show |
15 | HG00741.hp1 HG01099.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-2357G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124578 | |||||||
| chr11:119124615 | T | C | 205 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(202): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-10-2320T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124615 | |||||||
| chr11:119124633 | G | T | 3 | a0004c0005t0006g0200 a0004c0005t0006g0201 a0004c0005t0006g0202 |
3 | HG00642.hp1 HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-10-2302G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124633 | |||||||
| chr11:119124643 | C | G | 152 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(149): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-10-2292C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124643 | |||||||
| chr11:119124677 | C | T | 1 | a0001c0001t0002g0015 | 4 | NA18939.hp2 NA18968.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-2258C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124677 | |||||||
| chr11:119124764 | A | G | 1 | a0001c0001t0006g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-2171A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124764 | |||||||
| chr11:119124771 | C | T | 85 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-10-2164C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124771 | |||||||
| chr11:119124929 | G | A | 3 | a0004c0005t0006g0200 a0004c0005t0006g0201 a0004c0005t0006g0202 |
3 | HG00642.hp1 HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-10-2006G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124929 | |||||||
| chr11:119124956 | C | T | 1 | a0002c0002t0001g0134 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-10-1979C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119124956 | |||||||
| chr11:119125019 | T | G | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-10-1916T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125019 | |||||||
| chr11:119125019 | T | TTG | 61 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(58): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.-10-1900_-10-1899d others(4): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119125019 | ||||||
| chr11:119125019 | T | TTGTG | 6 | a0001c0001t0002g0007 a0001c0001t0002g0053 a0001c0003t0002g0007 others(3): Show |
10 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1902_-10-1899d others(6): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119125019 | ||||||
| chr11:119125034 | TG | T | 8 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-1900delG | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125034 | |||||||
| chr11:119125035 | G | GT | 58 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(55): Show |
78 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10-1879dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119125035 | ||||||
| chr11:119125035 | G | GTGT | 13 | a0001c0001t0002g0014 a0001c0001t0002g0033 a0001c0001t0002g0062 others(10): Show |
17 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-1899_-10-1898i others(5): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119125035 | ||||||
| chr11:119125035 | G | GTT | 11 | a0001c0001t0003g0028 a0001c0001t0003g0161 a0001c0001t0003g0167 others(8): Show |
11 | HG01109.hp1 HG01257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-10-1880_-10-1879d others(4): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119125035 | ||||||
| chr11:119125035 | G | T | 1 | a0002c0002t0001g0019 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-10-1900G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125035 | |||||||
| chr11:119125036 | T | TG | 3 | a0001c0001t0002g0034 a0001c0001t0002g0056 a0001c0001t0002g0074 |
4 | HG01516.hp1 HG01934.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1899_-10-1898i others(3): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125036 | |||||||
| chr11:119125037 | T | G | 3 | a0001c0001t0002g0073 a0001c0001t0002g0102 a0001c0012t0019g0211 |
3 | HG01074.hp1 HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-10-1898T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125037 | |||||||
| chr11:119125038 | T | G | 2 | a0001c0001t0017g0203 a0002c0002t0001g0122 |
2 | HG04199.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-10-1897T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125038 | |||||||
| chr11:119125045 | T | G | 7 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(4): Show |
8 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-1890T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125045 | |||||||
| chr11:119125108 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-10-1827G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125108 | |||||||
| chr11:119125195 | C | T | 2 | a0002c0002t0001g0132 a0002c0002t0001g0133 |
2 | HG00140.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-10-1740C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125195 | |||||||
| chr11:119125803 | T | G | 1 | a0002c0002t0001g0123 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-10-1132T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125803 | |||||||
| chr11:119125981 | A | G | 2 | a0002c0002t0013g0153 a0002c0002t0013g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-10-954A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119125981 | |||||||
| chr11:119126070 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-10-865C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126070 | |||||||
| chr11:119126071 | A | G | 151 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(148): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.-10-864A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126071 | |||||||
| chr11:119126107 | C | T | 3 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0172 |
3 | HG02055.hp1 HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-10-828C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126107 | |||||||
| chr11:119126192 | C | T | 2 | a0002c0002t0001g0114 a0002c0002t0001g0141 |
2 | HG02129.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-10-743C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126192 | |||||||
| chr11:119126224 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0102 |
2 | HG01074.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-10-711C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126224 | |||||||
| chr11:119126238 | C | A | 85 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(82): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-10-697C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126238 | |||||||
| chr11:119126354 | C | CA | 16 | a0001c0001t0002g0058 a0001c0001t0002g0063 a0001c0001t0002g0069 others(13): Show |
18 | HG01175.hp1 HG01192.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-10-562dupA | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119126354 | ||||||
| chr11:119126354 | CA | C | 8 | a0001c0001t0002g0088 a0001c0001t0003g0163 a0001c0001t0003g0175 others(5): Show |
8 | HG01256.hp1 HG04184.hp1 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-562delA | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119126354 | ||||||
| chr11:119126354 | CAA | C | 58 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(55): Show |
77 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.-10-563_-10-562del others(2): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr11 | 119126354 | ||||||
| chr11:119126533 | GGTC | G | 5 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(2): Show |
6 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-401_-10-399del others(3): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126533 | |||||||
| chr11:119126706 | G | T | 1 | a0009c0013t0003g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-10-229G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126706 | |||||||
| chr11:119126767 | T | C | 1 | a0002c0002t0001g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-10-168T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 1/9 | chr11 | 119126767 | |||||||
| chr11:119127159 | C | T | 87 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(84): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.181+34C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127159 | |||||||
| chr11:119127420 | C | CT | 148 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.181+303dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127420 | ||||||
| chr11:119127473 | G | GT | 12 | a0001c0001t0002g0063 a0001c0001t0002g0074 a0001c0001t0002g0097 others(9): Show |
12 | HG00140.hp2 HG01175.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.181+368dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127473 | ||||||
| chr11:119127473 | G | GTT | 45 | a0001c0001t0002g0087 a0001c0001t0003g0020 a0001c0001t0003g0026 others(42): Show |
63 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.181+367_181+368dup others(2): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127473 | ||||||
| chr11:119127473 | G | GTTT | 9 | a0001c0001t0003g0169 a0001c0001t0003g0189 a0001c0001t0003g0190 others(6): Show |
9 | HG01496.hp2 HG02056.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.181+366_181+368dup others(3): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127473 | ||||||
| chr11:119127473 | GT | G | 51 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
74 | HG00642.hp1 HG00741.hp1 HG01074.hp2 others(71): Show |
intron_variant | MODIFIER | c.181+368delT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127473 | ||||||
| chr11:119127499 | TC | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0080 others(1): Show |
7 | NA18961.hp1 NA18971.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+375delC | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127499 | |||||||
| chr11:119127502 | A | T | 4 | a0001c0001t0002g0023 a0001c0001t0002g0031 a0001c0001t0002g0080 others(1): Show |
7 | NA18961.hp1 NA18971.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.181+377A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127502 | |||||||
| chr11:119127503 | G | A | 8 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+378G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127503 | |||||||
| chr11:119127506 | T | G | 1 | a0001c0001t0017g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.181+381T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127506 | |||||||
| chr11:119127530 | T | C | 3 | a0004c0005t0006g0200 a0004c0005t0006g0201 a0004c0005t0006g0202 |
3 | HG00642.hp1 HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.181+405T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127530 | |||||||
| chr11:119127656 | A | G | 1 | a0001c0001t0007g0171 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181+531A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127656 | |||||||
| chr11:119127670 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.181+545T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127670 | |||||||
| chr11:119127788 | A | G | 1 | a0002c0002t0001g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.181+663A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127788 | |||||||
| chr11:119127810 | G | T | 1 | a0001c0001t0007g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.181+685G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127810 | |||||||
| chr11:119127857 | A | AT | 8 | a0001c0001t0003g0194 a0002c0002t0001g0107 a0002c0002t0001g0109 others(5): Show |
8 | HG02738.hp2 HG04115.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.181+749dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119127857 | ||||||
| chr11:119127876 | A | T | 8 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(5): Show |
9 | HG00642.hp1 HG01074.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.181+751A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119127876 | |||||||
| chr11:119128000 | C | T | 4 | a0002c0002t0001g0036 a0002c0002t0001g0040 a0002c0002t0001g0110 others(1): Show |
6 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+875C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128000 | |||||||
| chr11:119128002 | C | T | 4 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0204 others(1): Show |
5 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.181+877C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128002 | |||||||
| chr11:119128011 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.181+886G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128011 | |||||||
| chr11:119128094 | C | A | 1 | a0001c0001t0005g0077 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.181+969C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128094 | |||||||
| chr11:119128350 | G | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0067 a0001c0001t0002g0078 others(1): Show |
4 | HG01109.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+1225G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128350 | |||||||
| chr11:119128400 | G | A | 1 | a0001c0001t0017g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.181+1275G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128400 | |||||||
| chr11:119128409 | G | A | 2 | a0001c0001t0017g0203 a0001c0012t0019g0211 |
2 | HG04199.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.181+1284G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128409 | |||||||
| chr11:119128543 | G | A | 1 | a0001c0001t0005g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.181+1418G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128543 | |||||||
| chr11:119128543 | G | T | 5 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(2): Show |
6 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.181+1418G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128543 | |||||||
| chr11:119128623 | C | T | 1 | a0001c0001t0017g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.181+1498C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128623 | |||||||
| chr11:119128686 | C | T | 1 | a0002c0002t0001g0127 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.181+1561C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128686 | |||||||
| chr11:119128757 | G | A | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+1632G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128757 | |||||||
| chr11:119128758 | G | C | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+1633G>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128758 | |||||||
| chr11:119128824 | G | A | 4 | a0002c0002t0001g0036 a0002c0002t0001g0040 a0002c0002t0001g0110 others(1): Show |
6 | HG01884.hp2 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.181+1699G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128824 | |||||||
| chr11:119128967 | C | A | 1 | a0002c0002t0001g0125 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.182-1758C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119128967 | |||||||
| chr11:119129043 | A | C | 1 | a0001c0001t0016g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.182-1682A>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129043 | |||||||
| chr11:119129075 | C | T | 2 | a0001c0001t0007g0210 a0001c0001t0021g0159 |
2 | HG02630.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.182-1650C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129075 | |||||||
| chr11:119129079 | T | G | 2 | a0002c0002t0013g0153 a0002c0002t0013g0154 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.182-1646T>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129079 | |||||||
| chr11:119129110 | G | C | 3 | a0001c0001t0003g0178 a0001c0001t0003g0179 a0001c0001t0003g0189 |
3 | HG02602.hp1 HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.182-1615G>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129110 | |||||||
| chr11:119129167 | A | G | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0013 others(40): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.182-1558A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129167 | |||||||
| chr11:119129333 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.182-1392C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129333 | |||||||
| chr11:119129334 | C | G | 148 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(145): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.182-1391C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129334 | |||||||
| chr11:119129360 | A | G | 87 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0008 others(84): Show |
142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.182-1365A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129360 | |||||||
| chr11:119129459 | A | C | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.182-1266A>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129459 | |||||||
| chr11:119129490 | C | CT | 23 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
31 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.182-1220dupT | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTT | 5 | a0001c0001t0007g0044 a0001c0001t0007g0171 a0001c0001t0007g0207 others(2): Show |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-1222_182-1220d others(5): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTCTT others(24): Show |
1 | a0001c0001t0003g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.182-1231_182-1230i others(33): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0003g0020 a0001c0001t0003g0164 a0001c0001t0003g0175 others(4): Show |
10 | HG02647.hp2 HG03540.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.182-1227_182-1220d others(10): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0006g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.182-1227_182-1226i others(18): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0006g0050 a0001c0001t0006g0198 |
3 | HG02723.hp2 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.182-1227_182-1226i others(22): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0006g0204 a0001c0001t0006g0205 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.182-1227_182-1226i others(23): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0181 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.182-1229_182-1220d others(12): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0003g0182 a0001c0001t0007g0210 |
2 | HG02630.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.182-1233_182-1220d others(16): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0021g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.182-1234_182-1220d others(17): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.182-1220_182-1219i others(20): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0165 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.182-1220_182-1219i others(22): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(17): Show |
1 | a0004c0005t0006g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.182-1220_182-1219i others(26): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(18): Show |
2 | a0004c0005t0006g0201 a0004c0005t0006g0202 |
2 | HG00642.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(27): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0003g0166 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.182-1220_182-1219i others(29): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(23): Show |
5 | a0001c0001t0003g0051 a0001c0001t0003g0170 a0001c0001t0003g0173 others(2): Show |
6 | HG02015.hp1 HG02015.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-1220_182-1219i others(32): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(24): Show |
7 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0045 others(4): Show |
12 | HG00423.hp1 HG00423.hp2 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.182-1220_182-1219i others(33): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(25): Show |
5 | a0001c0001t0003g0028 a0001c0001t0003g0162 a0001c0001t0003g0169 others(2): Show |
7 | HG00558.hp1 HG00558.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.182-1220_182-1219i others(34): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(26): Show |
3 | a0001c0001t0003g0047 a0001c0001t0003g0163 a0001c0001t0003g0190 |
4 | HG01346.hp1 HG02683.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-1220_182-1219i others(35): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(27): Show |
2 | a0001c0001t0003g0048 a0001c0001t0003g0167 |
3 | HG02698.hp2 HG02738.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(36): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0007g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.182-1220_182-1219i others(37): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(29): Show |
3 | a0001c0001t0003g0168 a0001c0001t0003g0184 a0001c0001t0003g0196 |
3 | HG02155.hp2 NA18960.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(38): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(30): Show |
1 | a0001c0001t0003g0029 | 3 | HG02135.hp2 NA18965.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(39): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(31): Show |
2 | a0001c0001t0003g0049 a0001c0001t0003g0177 |
3 | NA18941.hp1 NA19067.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(40): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(32): Show |
4 | a0001c0001t0003g0185 a0001c0001t0003g0191 a0001c0001t0003g0194 others(1): Show |
4 | HG01496.hp2 HG02738.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1220_182-1219i others(41): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(33): Show |
2 | a0001c0001t0003g0186 a0001c0001t0003g0192 |
2 | HG02129.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.182-1220_182-1219i others(42): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(35): Show |
1 | a0001c0001t0003g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.182-1220_182-1219i others(44): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(38): Show |
1 | a0001c0001t0003g0187 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.182-1220_182-1219i others(47): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129490 | C | CTTTTTTT others(39): Show |
1 | a0001c0001t0003g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.182-1220_182-1219i others(48): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119129490 | ||||||
| chr11:119129514 | G | A | 1 | a0001c0001t0007g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.182-1211G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129514 | |||||||
| chr11:119129605 | C | T | 1 | a0001c0001t0017g0203 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.182-1120C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129605 | |||||||
| chr11:119129621 | C | T | 54 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(51): Show |
72 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.182-1104C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129621 | |||||||
| chr11:119129715 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.182-1010C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129715 | |||||||
| chr11:119129905 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.182-820A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119129905 | |||||||
| chr11:119130227 | G | A | 1 | a0001c0001t0021g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.182-498G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119130227 | |||||||
| chr11:119130295 | C | T | 3 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0172 |
3 | HG02055.hp1 HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.182-430C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119130295 | |||||||
| chr11:119130616 | C | T | 1 | a0002c0002t0004g0137 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.182-109C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | chr11 | 119130616 | |||||||
| chr11:119130671 | GTGACCTG others(20): Show |
G | 1 | a0001c0001t0002g0084 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.182-52_182-26delGA others(25): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr11 | 119130671 | ||||||
| chr11:119131128 | G | A | 4 | a0002c0002t0001g0018 a0002c0002t0001g0142 a0002c0002t0001g0144 others(1): Show |
7 | HG00438.hp1 NA18951.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.411+174G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131128 | |||||||
| chr11:119131303 | G | A | 3 | a0004c0005t0006g0200 a0004c0005t0006g0201 a0004c0005t0006g0202 |
3 | HG00642.hp1 HG01074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.412-232G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131303 | |||||||
| chr11:119131309 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0093 |
2 | HG01069.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.412-226G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131309 | |||||||
| chr11:119131384 | C | T | 1 | a0001c0012t0019g0211 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.412-151C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131384 | |||||||
| chr11:119131494 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.412-41T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131494 | |||||||
| chr11:119131496 | C | A | 1 | a0002c0002t0001g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.412-39C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 3/9 | chr11 | 119131496 | |||||||
| chr11:119131729 | A | G | 57 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(54): Show |
75 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.523+83A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 4/9 | chr11 | 119131729 | |||||||
| chr11:119131808 | A | T | 4 | a0001c0001t0002g0059 a0001c0001t0002g0067 a0001c0001t0002g0078 others(1): Show |
4 | HG01109.hp2 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-22A>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 4/9 | chr11 | 119131808 | |||||||
| chr11:119132042 | C | T | 1 | a0001c0001t0021g0159 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.676+60C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/9 | chr11 | 119132042 | |||||||
| chr11:119132058 | G | T | 64 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(61): Show |
83 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.676+76G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/9 | chr11 | 119132058 | |||||||
| chr11:119132158 | C | T | 57 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(54): Show |
75 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.676+176C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 5/9 | chr11 | 119132158 | |||||||
| chr11:119132612 | C | A | 82 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0004 others(79): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.754+39C>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 6/9 | chr11 | 119132612 | |||||||
| chr11:119132614 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.754+41A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 6/9 | chr11 | 119132614 | |||||||
| chr11:119133299 | G | T | 82 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0004 others(79): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1139+80G>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133299 | |||||||
| chr11:119133306 | C | T | 1 | a0001c0001t0016g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1139+87C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133306 | |||||||
| chr11:119133309 | G | A | 7 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(4): Show |
8 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1139+90G>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133309 | |||||||
| chr11:119133316 | C | T | 82 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0004 others(79): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1139+97C>T | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133316 | |||||||
| chr11:119133424 | C | G | 5 | a0001c0001t0006g0050 a0001c0001t0006g0198 a0001c0001t0006g0199 others(2): Show |
6 | HG02257.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1139+205C>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133424 | |||||||
| chr11:119133580 | A | AAAAT | 82 | a0001c0001t0003g0169 a0002c0002t0001g0001 a0002c0002t0001g0002 others(79): Show |
177 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1139+381_1139+384d others(6): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 119133580 | ||||||
| chr11:119133805 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1140-279T>C | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133805 | |||||||
| chr11:119133976 | T | A | 146 | a0001c0001t0003g0020 a0001c0001t0003g0026 a0001c0001t0003g0027 others(143): Show |
260 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(257): Show |
intron_variant | MODIFIER | c.1140-108T>A | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119133976 | |||||||
| chr11:119134059 | G | GCCCTTTA others(5): Show |
1 | a0001c0001t0002g0080 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1140-23_1140-12dup others(12): Show |
HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr11 | 119134059 | ||||||
| chr11:119134074 | A | G | 1 | a0002c0002t0001g0126 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1140-10A>G | HINFP | ENSG00000172273.13 | transcript | ENST00000350777.7 | protein_coding | 9/9 | chr11 | 119134074 |