Search by Gene
| Item | Value |
|---|---|
| geneid | 84680 |
| ensemblid | ENSG00000110455.14 |
| hgncid | 23989 |
| symbol | ACCS |
| name | 1-aminocyclopropane-1-carboxylate synthase homolog (inactive) |
| refseq_nuc | NM_032592.4 |
| refseq_prot | NP_115981.1 |
| ensembl_nuc | ENST00000263776.9 |
| ensembl_prot | ENSP00000263776.8 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 44066270 |
| end | 44084237 |
| strand | + |
| ver | v1.2 |
| region | chr11:44066270-44084237 |
| region5000 | chr11:44061270-44089237 |
| regionname0 | ACCS_chr11_44066270_44084237 |
| regionname5000 | ACCS_chr11_44061270_44089237 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 501 | 198 | 16 | 44 | 103 | 5 | 29 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0002 | 0/1 | 501 | 111 | 25 | 17 | 53 | 7 | 8 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0003 | 0/0 | 501 | 75 | 18 | 8 | 42 | 3 | 4 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0004 | 0/0 | 501 | 30 | 20 | 1 | 6 | 0 | 3 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0005 | 0/0 | 501 | 8 | 6 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0006 | 0/0 | 501 | 4 | 4 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0007 | 0/0 | 501 | 3 | 3 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0008 | 0/0 | 501 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0009 | 0/0 | 501 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0010 | 0/0 | 501 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0011 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0012 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0013 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| a0014 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | MFTLP others(496): Show |
chr11 | 44061270 | 44089237 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1503 | 197 | 16 | 44 | 103 | 4 | 29 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0001c0017 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0002c0003 | 0/0 | 1503 | 62 | 13 | 10 | 30 | 3 | 6 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0002c0004 | 0/1 | 1503 | 48 | 11 | 7 | 23 | 4 | 2 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0002c0018 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0003c0002 | 0/0 | 1503 | 72 | 16 | 8 | 41 | 3 | 4 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0003c0008 | 0/0 | 1503 | 3 | 2 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0004c0005 | 0/0 | 1503 | 30 | 20 | 1 | 6 | 0 | 3 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0005c0006 | 0/0 | 1503 | 8 | 6 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0006c0007 | 0/0 | 1503 | 4 | 4 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0007c0009 | 0/0 | 1503 | 3 | 3 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0008c0010 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0009c0011 | 0/0 | 1503 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0010c0013 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0011c0014 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0012c0016 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0013c0012 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 | ||
| a0014c0015 | 0/0 | 1503 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ATGTT others(1498): Show |
chr11 | 44061270 | 44089237 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2383 | 169 | 12 | 42 | 83 | 4 | 27 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0002 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0003 | 0/0 | 2383 | 10 | 0 | 1 | 9 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0004 | 0/0 | 2383 | 6 | 4 | 1 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0005 | 0/0 | 2383 | 4 | 0 | 0 | 4 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0006 | 0/0 | 2383 | 4 | 0 | 0 | 3 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0009 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0001t0012 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0001c0017t0005 | 0/0 | 2383 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0003t0001 | 0/0 | 2383 | 58 | 13 | 10 | 26 | 3 | 6 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0003t0002 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0003t0008 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0004t0001 | 0/1 | 2383 | 45 | 11 | 6 | 21 | 4 | 2 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0004t0002 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0004t0007 | 0/0 | 2383 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0004t0010 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0002c0018t0001 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0002t0001 | 0/0 | 2383 | 19 | 13 | 3 | 2 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0002t0002 | 0/0 | 2383 | 47 | 1 | 5 | 35 | 3 | 3 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0002t0003 | 0/0 | 2383 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0002t0007 | 0/0 | 2383 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0002t0011 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0008t0001 | 0/0 | 2383 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0003c0008t0002 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0004c0005t0001 | 0/0 | 2383 | 24 | 20 | 1 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0004c0005t0002 | 0/0 | 2383 | 4 | 0 | 0 | 1 | 0 | 3 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0004c0005t0003 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0005c0006t0001 | 0/0 | 2383 | 8 | 6 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0006c0007t0001 | 0/0 | 2383 | 4 | 4 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0007c0009t0001 | 0/0 | 2383 | 3 | 3 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0008c0010t0001 | 0/0 | 2383 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0009c0011t0001 | 0/0 | 2383 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0010c0013t0001 | 0/0 | 2383 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0011c0014t0001 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0012c0016t0001 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0013c0012t0001 | 0/0 | 2383 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| a0014c0015t0001 | 0/0 | 2383 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | ACACG others(2378): Show |
chr11 | 44061270 | 44089237 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 4 | 8 | 1 | 3 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 4 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0061 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0065 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0005g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0001c0017t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0007 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0026 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0028 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0003t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0050 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0007g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0004t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0002c0018t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0032 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0002t0011g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0008t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0003c0008t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0004c0005t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0005c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0006c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0006c0007t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0006c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0006c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0007c0009t0001g0067 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0007c0009t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0008c0010t0001g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0009c0011t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0010c0013t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0011c0014t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0012c0016t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0013c0012t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| a0014c0015t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0050 | EUR | GBR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00140 | hp1 | a0003 | c0002 | t0002 | g0056 | EUR | GBR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0034 | EUR | GBR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00280 | hp2 | a0010 | c0013 | t0001 | g0119 | EUR | FIN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0127 | EUR | FIN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00323 | hp2 | a0002 | c0004 | t0001 | g0106 | EUR | FIN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00438 | hp1 | a0002 | c0004 | t0001 | g0059 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00438 | hp2 | a0003 | c0002 | t0002 | g0055 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00544 | hp1 | a0002 | c0003 | t0008 | g0007 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00544 | hp2 | a0002 | c0004 | t0001 | g0059 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00597 | hp1 | a0003 | c0002 | t0002 | g0003 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00609 | hp1 | a0002 | c0004 | t0001 | g0029 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00621 | hp1 | a0003 | c0002 | t0002 | g0226 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00639 | hp1 | a0002 | c0004 | t0007 | g0136 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00673 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | CHS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00735 | hp1 | a0003 | c0002 | t0002 | g0219 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00738 | hp1 | a0003 | c0002 | t0002 | g0032 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00741 | hp1 | a0003 | c0002 | t0002 | g0217 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01109 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0108 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0162 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01168 | hp2 | a0003 | c0002 | t0001 | g0053 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01169 | hp1 | a0003 | c0002 | t0001 | g0053 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0256 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0051 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01243 | hp2 | a0002 | c0004 | t0001 | g0069 | AMR | PUR | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0028 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01257 | hp2 | a0002 | c0004 | t0001 | g0049 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0012 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01258 | hp2 | a0002 | c0004 | t0001 | g0049 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01261 | hp1 | a0004 | c0005 | t0001 | g0214 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0168 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01346 | hp2 | a0003 | c0002 | t0002 | g0218 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01433 | hp1 | a0002 | c0003 | t0001 | g0026 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01433 | hp2 | a0003 | c0002 | t0002 | g0220 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01496 | hp1 | a0002 | c0003 | t0001 | g0010 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01516 | hp1 | a0003 | c0002 | t0002 | g0032 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01516 | hp2 | a0002 | c0004 | t0001 | g0184 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01517 | hp1 | a0003 | c0002 | t0002 | g0032 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01517 | hp2 | a0002 | c0003 | t0001 | g0027 | EUR | IBS | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01884 | hp1 | a0004 | c0005 | t0001 | g0008 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01884 | hp2 | a0004 | c0005 | t0001 | g0100 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01891 | hp1 | a0003 | c0002 | t0001 | g0074 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0047 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01978 | hp2 | a0003 | c0002 | t0001 | g0206 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01993 | hp1 | a0002 | c0004 | t0001 | g0239 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02015 | hp2 | a0003 | c0002 | t0002 | g0033 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02027 | hp1 | a0003 | c0002 | t0002 | g0030 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0185 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02040 | hp1 | a0004 | c0005 | t0003 | g0275 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02055 | hp1 | a0002 | c0003 | t0001 | g0178 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0050 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02056 | hp2 | a0003 | c0002 | t0011 | g0222 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02074 | hp1 | a0003 | c0002 | t0002 | g0229 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02080 | hp1 | a0003 | c0002 | t0001 | g0033 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02083 | hp2 | a0003 | c0002 | t0002 | g0030 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02132 | hp1 | a0011 | c0014 | t0001 | g0121 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02135 | hp1 | a0002 | c0003 | t0001 | g0139 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02135 | hp2 | a0002 | c0004 | t0001 | g0247 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02145 | hp1 | a0004 | c0005 | t0001 | g0268 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02145 | hp2 | a0006 | c0007 | t0001 | g0109 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02155 | hp2 | a0002 | c0004 | t0001 | g0246 | EAS | CDX | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02165 | hp1 | a0002 | c0004 | t0001 | g0152 | EAS | CDX | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02257 | hp1 | a0003 | c0002 | t0007 | g0098 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02258 | hp1 | a0004 | c0005 | t0001 | g0204 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02258 | hp2 | a0003 | c0002 | t0001 | g0102 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02300 | hp1 | a0002 | c0004 | t0001 | g0051 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | KHV | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02572 | hp1 | a0004 | c0005 | t0001 | g0008 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02572 | hp2 | a0004 | c0005 | t0001 | g0018 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02615 | hp2 | a0005 | c0006 | t0001 | g0196 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02622 | hp2 | a0007 | c0009 | t0001 | g0067 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02630 | hp2 | a0007 | c0009 | t0001 | g0266 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02647 | hp1 | a0002 | c0004 | t0001 | g0079 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02647 | hp2 | a0003 | c0002 | t0007 | g0099 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02683 | hp2 | a0002 | c0004 | t0001 | g0075 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0252 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02717 | hp1 | a0004 | c0005 | t0001 | g0194 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02717 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02723 | hp2 | a0005 | c0006 | t0001 | g0197 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02735 | hp1 | a0002 | c0003 | t0001 | g0012 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02738 | hp2 | a0004 | c0005 | t0002 | g0215 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02809 | hp2 | a0006 | c0007 | t0001 | g0089 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02818 | hp1 | a0006 | c0007 | t0001 | g0088 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0081 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02886 | hp2 | a0003 | c0002 | t0001 | g0055 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02895 | hp1 | a0003 | c0002 | t0001 | g0009 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02895 | hp2 | a0008 | c0010 | t0001 | g0066 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02896 | hp1 | a0003 | c0008 | t0001 | g0057 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0026 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02897 | hp1 | a0008 | c0010 | t0001 | g0066 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0092 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02922 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02965 | hp1 | a0012 | c0016 | t0001 | g0159 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0035 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02970 | hp1 | a0003 | c0008 | t0001 | g0057 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02976 | hp1 | a0004 | c0005 | t0001 | g0008 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02976 | hp2 | a0003 | c0002 | t0001 | g0202 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03041 | hp1 | a0006 | c0007 | t0001 | g0091 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03041 | hp2 | a0004 | c0005 | t0001 | g0097 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0010 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03139 | hp1 | a0003 | c0002 | t0001 | g0264 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03139 | hp2 | a0002 | c0004 | t0001 | g0157 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03195 | hp1 | a0005 | c0006 | t0001 | g0052 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0160 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03209 | hp1 | a0004 | c0005 | t0001 | g0101 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03209 | hp2 | a0003 | c0002 | t0001 | g0203 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03225 | hp1 | a0004 | c0005 | t0001 | g0265 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03239 | hp2 | a0003 | c0002 | t0002 | g0056 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03453 | hp2 | a0003 | c0002 | t0001 | g0095 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03486 | hp1 | a0002 | c0004 | t0001 | g0267 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03516 | hp1 | a0005 | c0006 | t0001 | g0093 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03516 | hp2 | a0003 | c0002 | t0002 | g0207 | AFR | ESN | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03540 | hp1 | a0007 | c0009 | t0001 | g0067 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03540 | hp2 | a0004 | c0005 | t0001 | g0018 | AFR | GWD | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0068 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0027 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03831 | hp1 | a0003 | c0002 | t0002 | g0225 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03927 | hp1 | a0003 | c0002 | t0002 | g0210 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03927 | hp2 | a0002 | c0004 | t0001 | g0232 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03942 | hp1 | a0004 | c0005 | t0002 | g0228 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0221 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0271 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04184 | hp1 | a0004 | c0005 | t0002 | g0230 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0282 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0169 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18522 | hp1 | a0003 | c0002 | t0001 | g0096 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18612 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | CHB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18747 | hp1 | a0004 | c0005 | t0001 | g0198 | EAS | CHB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18747 | hp2 | a0002 | c0004 | t0001 | g0080 | EAS | CHB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18906 | hp2 | a0005 | c0006 | t0001 | g0094 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0117 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18939 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18941 | hp1 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18943 | hp1 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18947 | hp2 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18948 | hp1 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18950 | hp2 | a0003 | c0002 | t0002 | g0208 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18951 | hp1 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18956 | hp2 | a0002 | c0004 | t0001 | g0190 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18957 | hp1 | a0002 | c0004 | t0001 | g0143 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18959 | hp1 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18960 | hp1 | a0003 | c0002 | t0002 | g0212 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18966 | hp1 | a0003 | c0002 | t0002 | g0211 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18968 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18969 | hp1 | a0002 | c0004 | t0001 | g0086 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18969 | hp2 | a0002 | c0004 | t0010 | g0082 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18972 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18974 | hp2 | a0003 | c0002 | t0002 | g0270 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18977 | hp1 | a0004 | c0005 | t0002 | g0216 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18977 | hp2 | a0002 | c0004 | t0001 | g0085 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18979 | hp1 | a0001 | c0001 | t0012 | g0172 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18980 | hp1 | a0002 | c0003 | t0001 | g0115 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18982 | hp1 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18983 | hp2 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18984 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18986 | hp2 | a0005 | c0006 | t0001 | g0201 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18987 | hp2 | a0003 | c0002 | t0002 | g0031 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18988 | hp2 | a0004 | c0005 | t0001 | g0054 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18990 | hp1 | a0003 | c0002 | t0002 | g0009 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18993 | hp1 | a0003 | c0002 | t0002 | g0033 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18993 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18995 | hp2 | a0014 | c0015 | t0001 | g0151 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA18999 | hp2 | a0009 | c0011 | t0001 | g0024 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19000 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19001 | hp1 | a0003 | c0002 | t0001 | g0195 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19004 | hp1 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19005 | hp2 | a0003 | c0008 | t0002 | g0205 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19006 | hp2 | a0002 | c0004 | t0001 | g0084 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19010 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19012 | hp1 | a0002 | c0004 | t0001 | g0142 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19012 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0070 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19030 | hp2 | a0005 | c0006 | t0001 | g0052 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19043 | hp1 | a0003 | c0002 | t0001 | g0213 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19054 | hp2 | a0003 | c0002 | t0002 | g0031 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19056 | hp1 | a0002 | c0004 | t0001 | g0035 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19056 | hp2 | a0002 | c0004 | t0002 | g0181 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0012 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19064 | hp1 | a0002 | c0004 | t0001 | g0187 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19065 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19066 | hp1 | a0003 | c0002 | t0002 | g0031 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19066 | hp2 | a0004 | c0005 | t0001 | g0054 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19067 | hp2 | a0003 | c0002 | t0003 | g0273 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19072 | hp1 | a0004 | c0005 | t0003 | g0276 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19072 | hp2 | a0003 | c0002 | t0002 | g0223 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19074 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19077 | hp2 | a0009 | c0011 | t0001 | g0024 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19078 | hp2 | a0003 | c0002 | t0002 | g0192 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19079 | hp1 | a0002 | c0004 | t0001 | g0104 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19079 | hp2 | a0003 | c0002 | t0002 | g0209 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19080 | hp1 | a0003 | c0002 | t0002 | g0030 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19081 | hp1 | a0002 | c0003 | t0008 | g0179 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19082 | hp1 | a0002 | c0004 | t0001 | g0034 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19082 | hp2 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19084 | hp1 | a0003 | c0002 | t0003 | g0286 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19085 | hp2 | a0002 | c0004 | t0001 | g0078 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0285 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19088 | hp1 | a0003 | c0002 | t0002 | g0224 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19089 | hp1 | a0003 | c0002 | t0002 | g0003 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19090 | hp2 | a0003 | c0002 | t0003 | g0274 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19091 | hp1 | a0005 | c0006 | t0001 | g0200 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA19240 | hp2 | a0004 | c0005 | t0001 | g0071 | AFR | YRI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20129 | hp1 | a0003 | c0002 | t0001 | g0036 | AFR | ASW | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0008 | AFR | ASW | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20752 | hp1 | a0001 | c0017 | t0005 | g0174 | EUR | TSI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20905 | hp2 | a0003 | c0002 | t0001 | g0009 | SAS | GIH | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0170 | AMR | CLM | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02109 | hp1 | a0003 | c0002 | t0001 | g0036 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02109 | hp2 | a0003 | c0002 | t0001 | g0263 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02486 | hp1 | a0002 | c0018 | t0001 | g0177 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0018 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02559 | hp1 | a0004 | c0005 | t0001 | g0103 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03471 | hp1 | a0002 | c0004 | t0001 | g0158 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG03471 | hp2 | a0004 | c0005 | t0001 | g0193 | AFR | MSL | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG06807 | hp1 | a0013 | c0012 | t0001 | g0227 | AFR | USA | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0010 | AFR | USA | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0199 | AFR | USA | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | USA | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0083 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| NA21309 | hp2 | a0002 | c0004 | t0001 | g0261 | AFR | LWK | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0001 | g0188 | REF | REF | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0257 | REF | REF | ACCS_chr11_44061270_44089237 | ACCS | chr11 | 44061270 | 44089237 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44067802 | G | A | 6 | a0003a0004a0005others(3): Show | 119 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(116): Show |
missense_variant | MODERATE | c.175G>A | p.Asp59Asn | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/15 | 607/2383 | 175/1506 | 59/501 | chr11 | 44067802 | |||
| chr11:44073500 | C | G | 2 | a0007a0008 | 5 | HG02622.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.402C>G | p.Asp134Glu | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/15 | 834/2383 | 402/1506 | 134/501 | chr11 | 44073500 | |||
| chr11:44074637 | C | G | 1 | a0013 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.445C>G | p.Leu149Val | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/15 | 877/2383 | 445/1506 | 149/501 | chr11 | 44074637 | |||
| chr11:44077852 | G | A | 1 | a0005 | 8 | HG02615.hp2 HG02723.hp2 HG03195.hp1 others(5): Show |
missense_variant | MODERATE | c.662G>A | p.Gly221Glu | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/15 | 1094/2383 | 662/1506 | 221/501 | chr11 | 44077852 | |||
| chr11:44079599 | G | A | 1 | a0009 | 2 | NA18999.hp2 NA19077.hp2 |
missense_variant | MODERATE | c.902G>A | p.Arg301His | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/15 | 1334/2383 | 902/1506 | 301/501 | chr11 | 44079599 | |||
| chr11:44081201 | G | A | 1 | a0012 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.992G>A | p.Arg331His | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/15 | 1424/2383 | 992/1506 | 331/501 | chr11 | 44081201 | |||
| chr11:44081213 | T | C | 1 | a0010 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1004T>C | p.Leu335Pro | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/15 | 1436/2383 | 1004/1506 | 335/501 | chr11 | 44081213 | |||
| chr11:44083431 | C | T | 6 | a0002a0003a0006others(3): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
missense_variant | MODERATE | c.1262C>T | p.Pro421Leu | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 14/15 | 1694/2383 | 1262/1506 | 421/501 | chr11 | 44083431 | |||
| chr11:44083467 | G | A | 1 | a0011 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1298G>A | p.Arg433His | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 14/15 | 1730/2383 | 1298/1506 | 433/501 | chr11 | 44083467 | |||
| chr11:44083734 | A | T | 1 | a0014 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1448A>T | p.Gln483Leu | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 1880/2383 | 1448/1506 | 483/501 | chr11 | 44083734 | |||
| chr11:44083751 | C | T | 1 | a0006 | 4 | HG02145.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.1465C>T | p.Arg489Cys | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 1897/2383 | 1465/1506 | 489/501 | chr11 | 44083751 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44077325 | C | T | 1 | a0002c0018 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.603C>T | p.His201His | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/15 | 1035/2383 | 603/1506 | 201/501 | chr11 | 44077325 | |||
| chr11:44077328 | G | A | 1 | a0006c0007 | 4 | HG02145.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
synonymous_variant | LOW | c.606G>A | p.Val202Val | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/15 | 1038/2383 | 606/1506 | 202/501 | chr11 | 44077328 | |||
| chr11:44078695 | C | T | 1 | a0001c0017 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.744C>T | p.Val248Val | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/15 | 1176/2383 | 744/1506 | 248/501 | chr11 | 44078695 | |||
| chr11:44079568 | C | T | 4 | a0002c0003a0002c0018a0003c0008others(1): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.871C>T | p.Leu291Leu | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/15 | 1303/2383 | 871/1506 | 291/501 | chr11 | 44079568 | |||
| chr11:44081244 | C | T | 1 | a0005c0006 | 8 | HG02615.hp2 HG02723.hp2 HG03195.hp1 others(5): Show |
synonymous_variant | LOW | c.1035C>T | p.Ala345Ala | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/15 | 1467/2383 | 1035/1506 | 345/501 | chr11 | 44081244 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44066439 | G | T | 8 | a0001c0001t0002a0001c0001t0012a0002c0003t0002others(5): Show | 59 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-263G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/15 | 1189 | chr11 | 44066439 | ||||||
| chr11:44066529 | C | G | 1 | a0002c0003t0008 | 2 | HG00544.hp1 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-173C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/15 | 1099 | chr11 | 44066529 | ||||||
| chr11:44066581 | G | A | 1 | a0001c0001t0009 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-121G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/15 | 1047 | chr11 | 44066581 | ||||||
| chr11:44066595 | C | G | 4 | a0001c0001t0003a0001c0001t0006a0003c0002t0003others(1): Show | 19 | HG01106.hp1 HG02040.hp1 HG02074.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/15 | 1033 | chr11 | 44066595 | ||||||
| chr11:44066615 | G | A | 1 | a0003c0002t0011 | 1 | HG02056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-87G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/15 | 1013 | chr11 | 44066615 | ||||||
| chr11:44083887 | C | T | 2 | a0002c0004t0007a0003c0002t0007 | 3 | HG00639.hp1 HG02257.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*95C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 95 | chr11 | 44083887 | ||||||
| chr11:44083994 | T | C | 1 | a0001c0001t0004 | 6 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*202T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 202 | chr11 | 44083994 | ||||||
| chr11:44084025 | G | A | 4 | a0001c0001t0005a0001c0001t0006a0001c0001t0012others(1): Show | 10 | HG04204.hp1 NA18945.hp1 NA18962.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*233G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 233 | chr11 | 44084025 | ||||||
| chr11:44084176 | T | A | 1 | a0002c0004t0010 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 15/15 | 384 | chr11 | 44084176 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:44066722 | C | T | 11 | a0001c0001t0003g0017a0001c0001t0003g0277a0001c0001t0003g0278others(8): Show | 14 | HG02074.hp2 HG02080.hp2 HG04204.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1+21C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066722 | |||||||
| chr11:44066746 | G | C | 5 | a0001c0001t0001g0072a0002c0003t0001g0070a0002c0004t0001g0068others(2): Show | 5 | HG01243.hp2 HG03579.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1+45G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066746 | |||||||
| chr11:44066757 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-1+56G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066757 | |||||||
| chr11:44066818 | C | T | 16 | a0001c0001t0003g0017a0001c0001t0003g0272a0001c0001t0003g0277others(13): Show | 19 | HG01106.hp1 HG02040.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.-1+117C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066818 | |||||||
| chr11:44066860 | C | A | 1 | a0003c0002t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1+159C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066860 | |||||||
| chr11:44066960 | C | T | 1 | a0002c0003t0001g0271 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-1+259C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066960 | |||||||
| chr11:44066999 | G | A | 1 | a0001c0001t0003g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-1+298G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44066999 | |||||||
| chr11:44067042 | G | T | 1 | a0003c0002t0002g0270 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-1+341G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067042 | |||||||
| chr11:44067068 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-1+367G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067068 | |||||||
| chr11:44067133 | A | G | 1 | a0004c0005t0001g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1+432A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067133 | |||||||
| chr11:44067162 | C | G | 1 | a0001c0001t0001g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-1+461C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067162 | |||||||
| chr11:44067262 | C | T | 7 | a0002c0004t0001g0267a0003c0002t0001g0263a0003c0002t0001g0264others(4): Show | 9 | HG02109.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1-366C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067262 | |||||||
| chr11:44067280 | G | A | 24 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(21): Show | 26 | HG00140.hp2 HG00423.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1-348G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067280 | |||||||
| chr11:44067406 | T | C | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1-222T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067406 | |||||||
| chr11:44067604 | C | T | 1 | a0001c0001t0001g0262 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1-24C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067604 | |||||||
| chr11:44067610 | C | T | 1 | a0002c0004t0001g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1-18C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067610 | |||||||
| chr11:44067611 | G | A | 247 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(244): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1-17G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 1/14 | chr11 | 44067611 | |||||||
| chr11:44068020 | G | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(72): Show | 116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.288+105G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068020 | |||||||
| chr11:44068459 | A | G | 119 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(116): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.288+544A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068459 | |||||||
| chr11:44068473 | C | T | 11 | a0001c0001t0003g0017a0001c0001t0003g0272a0001c0001t0003g0277others(8): Show | 14 | HG01106.hp1 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.288+558C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068473 | |||||||
| chr11:44068589 | T | C | 122 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0073others(119): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.288+674T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068589 | |||||||
| chr11:44068820 | C | A | 32 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(29): Show | 38 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.288+905C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068820 | |||||||
| chr11:44068950 | G | A | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(287): Show | 434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.288+1035G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068950 | |||||||
| chr11:44068994 | A | T | 130 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(127): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.288+1079A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44068994 | |||||||
| chr11:44069011 | A | G | 12 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(9): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.288+1096A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069011 | |||||||
| chr11:44069019 | A | G | 30 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0171others(27): Show | 41 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.288+1104A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069019 | |||||||
| chr11:44069092 | G | A | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1177G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069092 | |||||||
| chr11:44069102 | A | G | 12 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(9): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.288+1187A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069102 | |||||||
| chr11:44069177 | G | T | 6 | a0001c0001t0001g0087a0001c0001t0004g0090a0002c0004t0001g0092others(3): Show | 6 | HG02723.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+1262G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069177 | |||||||
| chr11:44069230 | C | CT | 33 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0077others(30): Show | 39 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.288+1325dupT | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 44069230 | ||||||
| chr11:44069282 | T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.288+1367T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069282 | |||||||
| chr11:44069301 | C | A | 1 | a0003c0002t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.288+1386C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069301 | |||||||
| chr11:44069312 | C | T | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1397C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069312 | |||||||
| chr11:44069399 | T | C | 2 | a0001c0001t0001g0233a0002c0004t0001g0232 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.288+1484T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069399 | |||||||
| chr11:44069459 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.288+1544C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069459 | |||||||
| chr11:44069469 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.288+1554C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069469 | |||||||
| chr11:44069479 | A | G | 66 | a0001c0001t0001g0260a0001c0001t0002g0156a0002c0003t0001g0221others(63): Show | 97 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.288+1564A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069479 | |||||||
| chr11:44069481 | T | G | 1 | a0003c0002t0002g0192 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.288+1566T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069481 | |||||||
| chr11:44069509 | G | A | 2 | a0004c0005t0001g0008a0004c0005t0001g0193 | 7 | HG01884.hp1 HG02572.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+1594G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069509 | |||||||
| chr11:44069510 | C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0045others(5): Show | 17 | HG00423.hp1 HG02165.hp1 NA18942.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1595C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069510 | |||||||
| chr11:44069512 | T | C | 207 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(204): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.288+1597T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069512 | |||||||
| chr11:44069541 | C | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0161others(9): Show | 21 | HG00738.hp2 HG01074.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+1626C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069541 | |||||||
| chr11:44069545 | G | A | 1 | a0014c0015t0001g0151 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.288+1630G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069545 | |||||||
| chr11:44069625 | G | T | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-1631G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069625 | |||||||
| chr11:44069692 | C | T | 19 | a0001c0001t0001g0024a0001c0001t0001g0041a0001c0001t0001g0042others(16): Show | 23 | HG00609.hp2 HG02040.hp2 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.289-1564C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069692 | |||||||
| chr11:44069722 | C | G | 1 | a0004c0005t0002g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.289-1534C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069722 | |||||||
| chr11:44069849 | A | G | 51 | a0001c0001t0001g0260a0001c0001t0002g0156a0002c0003t0001g0221others(48): Show | 76 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.289-1407A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44069849 | |||||||
| chr11:44070037 | A | G | 1 | a0003c0002t0001g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.289-1219A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070037 | |||||||
| chr11:44070079 | T | C | 13 | a0003c0002t0001g0195a0003c0002t0001g0202a0003c0002t0001g0203others(10): Show | 19 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.289-1177T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070079 | |||||||
| chr11:44070088 | G | A | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-1168G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070088 | |||||||
| chr11:44070122 | G | A | 1 | a0002c0004t0001g0104 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.289-1134G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070122 | |||||||
| chr11:44070128 | A | T | 98 | a0001c0001t0001g0260a0001c0001t0002g0156a0001c0001t0003g0017others(95): Show | 137 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.289-1128A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070128 | |||||||
| chr11:44070187 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.289-1069G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070187 | |||||||
| chr11:44070236 | T | A | 2 | a0001c0001t0005g0235a0001c0001t0005g0236 | 2 | NA18962.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.289-1020T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070236 | |||||||
| chr11:44070467 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.289-789G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070467 | |||||||
| chr11:44070542 | C | T | 1 | a0004c0005t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.289-714C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070542 | |||||||
| chr11:44070582 | G | A | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.289-674G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070582 | |||||||
| chr11:44070595 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.289-661C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070595 | |||||||
| chr11:44070595 | C | T | 11 | a0001c0001t0003g0017a0001c0001t0003g0272a0001c0001t0003g0277others(8): Show | 14 | HG01106.hp1 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.289-661C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070595 | |||||||
| chr11:44070600 | C | G | 14 | a0003c0002t0001g0036a0003c0002t0001g0095a0003c0002t0001g0096others(11): Show | 17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-656C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070600 | |||||||
| chr11:44070678 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.289-578G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070678 | |||||||
| chr11:44070740 | C | A | 1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.289-516C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070740 | |||||||
| chr11:44070915 | C | T | 1 | a0002c0003t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.289-341C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070915 | |||||||
| chr11:44070929 | G | A | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.289-327G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44070929 | |||||||
| chr11:44071176 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.289-80G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 2/14 | chr11 | 44071176 | |||||||
| chr11:44071330 | C | T | 30 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0171others(27): Show | 41 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.348+15C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071330 | |||||||
| chr11:44071630 | G | T | 1 | a0002c0004t0007g0136 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.348+315G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071630 | |||||||
| chr11:44071744 | G | A | 1 | a0005c0006t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.348+429G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071744 | |||||||
| chr11:44071747 | T | C | 259 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.348+432T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071747 | |||||||
| chr11:44071773 | C | G | 61 | a0002c0003t0001g0221a0003c0002t0001g0009a0003c0002t0001g0033others(58): Show | 92 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.348+458C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071773 | |||||||
| chr11:44071798 | C | T | 1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.348+483C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071798 | |||||||
| chr11:44071813 | T | G | 11 | a0001c0001t0003g0017a0001c0001t0003g0272a0001c0001t0003g0277others(8): Show | 14 | HG01106.hp1 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+498T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44071813 | |||||||
| chr11:44072068 | A | G | 54 | a0001c0001t0001g0072a0001c0001t0001g0171a0001c0001t0001g0175others(51): Show | 75 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.348+753A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072068 | |||||||
| chr11:44072074 | A | G | 1 | a0003c0002t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.348+759A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072074 | |||||||
| chr11:44072092 | C | T | 1 | a0002c0004t0001g0261 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348+777C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072092 | |||||||
| chr11:44072148 | T | TTTTATTT others(5): Show |
14 | a0002c0003t0001g0111a0002c0003t0001g0112a0002c0003t0001g0113others(11): Show | 15 | HG02109.hp1 HG02559.hp1 HG03041.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+850_348+861dup others(12): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 44072148 | ||||||
| chr11:44072148 | T | TTTTATTT others(9): Show |
67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 118 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.348+846_348+861dup others(16): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 44072148 | ||||||
| chr11:44072148 | T | TTTTATTT others(13): Show |
58 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0041others(55): Show | 81 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.348+842_348+861dup others(20): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 44072148 | ||||||
| chr11:44072148 | T | TTTTATTT others(17): Show |
4 | a0001c0001t0001g0161a0002c0003t0001g0185a0002c0004t0001g0104others(1): Show | 4 | HG01516.hp2 HG02027.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+838_348+861dup others(24): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 44072148 | ||||||
| chr11:44072332 | A | G | 8 | a0002c0004t0001g0086a0003c0002t0001g0033a0003c0002t0002g0033others(5): Show | 9 | HG00621.hp1 HG02015.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.348+1017A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072332 | |||||||
| chr11:44072344 | G | C | 1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.348+1029G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072344 | |||||||
| chr11:44072402 | C | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.349-1045C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072402 | |||||||
| chr11:44072445 | T | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0163a0001c0001t0001g0253 | 5 | HG01074.hp1 HG01257.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1002T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072445 | |||||||
| chr11:44072451 | C | T | 33 | a0001c0001t0001g0161a0001c0001t0001g0176a0001c0001t0001g0183others(30): Show | 50 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.349-996C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072451 | |||||||
| chr11:44072588 | TA | T | 4 | a0004c0005t0001g0265a0007c0009t0001g0067a0007c0009t0001g0266others(1): Show | 6 | HG02622.hp2 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-854delA | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 44072588 | ||||||
| chr11:44072615 | A | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0183 | 2 | NA18943.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.349-832A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072615 | |||||||
| chr11:44072690 | A | G | 6 | a0001c0001t0001g0046a0003c0002t0001g0036a0004c0005t0001g0097others(3): Show | 8 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.349-757A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072690 | |||||||
| chr11:44072866 | C | T | 93 | a0001c0001t0001g0161a0001c0001t0001g0176a0001c0001t0001g0189others(90): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.349-581C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44072866 | |||||||
| chr11:44073071 | G | A | 61 | a0001c0001t0001g0046a0002c0004t0001g0059a0002c0004t0001g0068others(58): Show | 86 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.349-376G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44073071 | |||||||
| chr11:44073193 | A | G | 1 | a0002c0003t0001g0160 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349-254A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44073193 | |||||||
| chr11:44073328 | T | C | 8 | a0001c0001t0005g0064a0001c0001t0005g0235a0001c0001t0005g0236others(5): Show | 9 | HG04204.hp1 NA18945.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-119T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44073328 | |||||||
| chr11:44073332 | C | G | 1 | a0003c0002t0001g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.349-115C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 3/14 | chr11 | 44073332 | |||||||
| chr11:44073532 | T | C | 3 | a0002c0004t0007g0136a0003c0002t0007g0098a0003c0002t0007g0099 | 3 | HG00639.hp1 HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.419+15T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073532 | |||||||
| chr11:44073700 | C | T | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.419+183C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073700 | |||||||
| chr11:44073742 | C | T | 1 | a0005c0006t0001g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.419+225C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073742 | |||||||
| chr11:44073751 | A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.419+234A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073751 | |||||||
| chr11:44073939 | G | A | 1 | a0002c0004t0001g0152 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.419+422G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073939 | |||||||
| chr11:44073953 | C | T | 1 | a0003c0002t0002g0229 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.419+436C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44073953 | |||||||
| chr11:44074103 | C | G | 10 | a0001c0001t0003g0272a0001c0001t0005g0064a0001c0001t0005g0235others(7): Show | 11 | HG01106.hp1 HG04204.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.420-509C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074103 | |||||||
| chr11:44074153 | T | C | 3 | a0002c0004t0001g0106a0003c0002t0001g0053a0003c0002t0001g0206 | 4 | HG00323.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.420-459T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074153 | |||||||
| chr11:44074231 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.420-381T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074231 | |||||||
| chr11:44074232 | GA | G | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.420-378delA | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 44074232 | ||||||
| chr11:44074235 | G | A | 5 | a0002c0004t0001g0158a0003c0002t0001g0074a0003c0002t0001g0095others(2): Show | 5 | HG01891.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.420-377G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074235 | |||||||
| chr11:44074273 | T | G | 1 | a0003c0002t0002g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.420-339T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074273 | |||||||
| chr11:44074292 | A | C | 1 | a0003c0002t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.420-320A>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074292 | |||||||
| chr11:44074295 | A | G | 1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.420-317A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074295 | |||||||
| chr11:44074412 | T | G | 1 | a0001c0001t0001g0138 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.420-200T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074412 | |||||||
| chr11:44074565 | G | A | 47 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(44): Show | 68 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.420-47G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 4/14 | chr11 | 44074565 | |||||||
| chr11:44074688 | G | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
splice_region_variant&intron_variant | LOW | c.489+7G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074688 | |||||||
| chr11:44074732 | A | ATCTCTTT others(65): Show |
1 | a0007c0009t0001g0266 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(70): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074732 | ||||||
| chr11:44074732 | A | ATCTCTTT others(87): Show |
1 | a0005c0006t0001g0094 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.489+74_489+75insTT others(92): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074732 | ||||||
| chr11:44074732 | A | ATCTCTTT others(79): Show |
1 | a0005c0006t0001g0197 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.489+74_489+75insTT others(84): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074732 | ||||||
| chr11:44074734 | C | CCCTTTCT others(21): Show |
1 | a0003c0002t0003g0286 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.489+53_489+54insCC others(26): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074734 | |||||||
| chr11:44074734 | C | CCCTTTCT others(25): Show |
1 | a0003c0002t0002g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.489+53_489+54insCC others(30): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074734 | |||||||
| chr11:44074734 | C | CTCTTTCT others(13): Show |
5 | a0002c0004t0001g0068a0002c0004t0001g0075a0003c0002t0001g0102others(2): Show | 5 | HG00735.hp1 HG01433.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+75_489+94dupCT others(18): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(17): Show |
5 | a0001c0001t0004g0110a0001c0001t0004g0169a0002c0004t0007g0136others(2): Show | 5 | HG00639.hp1 HG02040.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+71_489+94dupCT others(22): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(21): Show |
16 | a0001c0001t0004g0090a0002c0004t0001g0029a0002c0004t0001g0035others(13): Show | 21 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.489+67_489+94dupCT others(26): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(25): Show |
16 | a0001c0001t0002g0156a0001c0001t0004g0037a0002c0004t0001g0049others(13): Show | 23 | HG00673.hp2 HG00741.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.489+63_489+94dupCT others(30): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(29): Show |
15 | a0001c0001t0004g0108a0002c0004t0001g0069a0002c0004t0001g0081others(12): Show | 20 | HG00140.hp1 HG01109.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+59_489+94dupCT others(34): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(33): Show |
19 | a0001c0001t0001g0260a0002c0004t0001g0034a0002c0004t0001g0080others(16): Show | 29 | HG00140.hp2 HG00597.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.489+55_489+94dupCT others(38): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(37): Show |
7 | a0002c0004t0001g0050a0002c0004t0001g0079a0002c0004t0001g0086others(4): Show | 11 | HG00099.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(42): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(41): Show |
4 | a0002c0004t0001g0078a0003c0002t0002g0030a0004c0005t0001g0054others(1): Show | 7 | HG02027.hp1 HG02083.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(46): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(101): Show |
1 | a0005c0006t0001g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(106): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(45): Show |
2 | a0002c0004t0001g0190a0003c0002t0002g0270 | 2 | NA18956.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(50): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(123): Show |
1 | a0001c0001t0006g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(128): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(131): Show |
1 | a0001c0001t0006g0283 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(136): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(87): Show |
1 | a0001c0001t0003g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(92): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(135): Show |
1 | a0001c0001t0005g0064 | 2 | NA18972.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(140): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(131): Show |
1 | a0001c0001t0006g0284 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(136): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(143): Show |
1 | a0001c0001t0005g0235 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(148): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(131): Show |
1 | a0001c0001t0006g0285 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(136): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(151): Show |
1 | a0001c0001t0005g0236 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(156): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(147): Show |
1 | a0001c0001t0012g0172 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(152): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(97): Show |
1 | a0004c0005t0001g0199 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(102): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | C | CTCTTTCT others(81): Show |
1 | a0001c0001t0001g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(86): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | CTCTT | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0255a0001c0001t0001g0258 | 3 | HG02523.hp1 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.489+91_489+94delCT others(2): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | CTCTTTCT others(1): Show |
C | 23 | a0001c0001t0001g0001a0001c0001t0001g0048a0001c0001t0001g0058others(20): Show | 42 | HG00423.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.489+87_489+94delCT others(6): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074734 | CTCTTTCT others(5): Show |
C | 4 | a0001c0001t0001g0025a0001c0001t0001g0163a0001c0001t0001g0250others(1): Show | 6 | HG01074.hp1 HG01257.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+83_489+94delCT others(10): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074734 | ||||||
| chr11:44074736 | C | CTTTCTTT others(119): Show |
1 | a0001c0017t0005g0174 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(124): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074736 | ||||||
| chr11:44074738 | T | TTCTTTCT others(77): Show |
1 | a0007c0009t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(82): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(73): Show |
1 | a0008c0010t0001g0066 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(78): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(65): Show |
1 | a0007c0009t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(70): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(25): Show |
1 | a0004c0005t0001g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.489+86_489+87insTT others(30): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(79): Show |
1 | a0005c0006t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.489+74_489+75insTT others(84): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(75): Show |
2 | a0005c0006t0001g0052a0005c0006t0001g0196 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.489+74_489+75insTT others(80): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074738 | T | TTCTTTCT others(71): Show |
1 | a0005c0006t0001g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.489+74_489+75insTT others(76): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074738 | ||||||
| chr11:44074742 | T | TTCTTTCT others(77): Show |
1 | a0005c0006t0001g0201 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(82): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(74): Show |
1 | a0004c0005t0001g0018 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(79): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(85): Show |
1 | a0004c0005t0001g0018 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(90): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(77): Show |
2 | a0001c0001t0001g0046a0001c0001t0001g0165 | 2 | HG02257.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(82): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(73): Show |
1 | a0004c0005t0001g0008 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(78): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(69): Show |
5 | a0001c0001t0001g0046a0004c0005t0001g0008a0004c0005t0001g0018others(2): Show | 6 | HG01243.hp1 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(74): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(65): Show |
2 | a0001c0001t0001g0087a0004c0005t0001g0008 | 4 | HG01884.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(70): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(61): Show |
1 | a0001c0001t0001g0161 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(66): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074742 | T | TTCTTTCT others(37): Show |
1 | a0004c0005t0001g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(42): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074742 | ||||||
| chr11:44074745 | T | TTTCTTTC others(52): Show |
1 | a0002c0003t0001g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(57): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074745 | ||||||
| chr11:44074746 | T | TTCTTTCT others(51): Show |
1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(56): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074746 | ||||||
| chr11:44074748 | C | CTTTCTTT others(47): Show |
1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(52): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074748 | ||||||
| chr11:44074749 | T | TTTCTTTC others(58): Show |
1 | a0002c0003t0001g0182 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(63): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074749 | ||||||
| chr11:44074750 | T | TTCTTTCT others(31): Show |
2 | a0002c0003t0001g0010a0002c0003t0001g0160 | 6 | HG01109.hp1 HG01496.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(36): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(27): Show |
1 | a0002c0018t0001g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(32): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(35): Show |
1 | a0002c0003t0001g0047 | 2 | HG01891.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(40): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(31): Show |
1 | a0002c0003t0001g0178 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(36): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(39): Show |
1 | a0012c0016t0001g0159 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(44): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(35): Show |
2 | a0002c0003t0001g0117a0002c0003t0001g0125 | 2 | NA18939.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(40): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(39): Show |
5 | a0002c0003t0001g0022a0002c0003t0001g0026a0002c0003t0001g0111others(2): Show | 10 | HG00558.hp1 HG01123.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(44): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(43): Show |
9 | a0002c0003t0001g0007a0002c0003t0001g0070a0002c0003t0001g0113others(6): Show | 12 | HG00544.hp1 HG01168.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(48): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(47): Show |
8 | a0002c0003t0001g0012a0002c0003t0001g0040a0002c0003t0001g0063others(5): Show | 12 | HG00558.hp2 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(52): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(51): Show |
6 | a0002c0003t0001g0027a0002c0003t0001g0115a0002c0003t0001g0116others(3): Show | 8 | HG01515.hp2 HG01517.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(56): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(55): Show |
4 | a0002c0003t0001g0028a0002c0003t0001g0127a0002c0003t0001g0150others(1): Show | 6 | HG00323.hp1 HG01255.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(60): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(59): Show |
1 | a0002c0003t0001g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(64): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(63): Show |
1 | a0002c0003t0001g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(68): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(87): Show |
1 | a0001c0001t0001g0153 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(92): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(67): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0240 | 2 | NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(72): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(85): Show |
1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(90): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(81): Show |
1 | a0001c0001t0001g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(86): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(77): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0130 | 2 | HG02293.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(82): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(73): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0041a0001c0001t0001g0105others(3): Show | 10 | HG00280.hp2 HG01069.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(78): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(69): Show |
12 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0042others(9): Show | 18 | HG01069.hp2 HG01074.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(74): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(65): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0043others(14): Show | 29 | HG00609.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(70): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(61): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0023others(16): Show | 34 | HG00099.hp2 HG00621.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(66): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(57): Show |
8 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0062others(5): Show | 13 | HG00423.hp1 HG00673.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(62): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(53): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0155a0001c0001t0001g0167others(2): Show | 14 | HG01071.hp2 HG02129.hp2 NA18953.hp2 others(11): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(58): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(49): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0124a0001c0001t0001g0134others(1): Show | 6 | HG00597.hp2 HG01993.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(54): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(45): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0244a0001c0001t0003g0281others(1): Show | 6 | HG01952.hp1 HG01952.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+94_489+95insCT others(50): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074750 | T | TTCTTTCT others(41): Show |
1 | a0001c0001t0001g0039 | 2 | HG01255.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.489+94_489+95insCT others(46): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074750 | ||||||
| chr11:44074753 | T | TTTCTTTC others(42): Show |
1 | a0002c0003t0001g0112 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(47): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074753 | ||||||
| chr11:44074754 | T | TTCTTTCT others(31): Show |
1 | a0002c0003t0001g0271 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(36): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074754 | ||||||
| chr11:44074772 | C | CTTTCTTT others(32): Show |
1 | a0002c0004t0001g0084 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(37): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074772 | ||||||
| chr11:44074773 | T | TTTCTTTC others(42): Show |
1 | a0002c0003t0001g0126 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(47): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074773 | ||||||
| chr11:44074773 | T | TTTCTTTC others(28): Show |
1 | a0003c0002t0002g0212 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(33): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074773 | ||||||
| chr11:44074773 | T | TTTCTTTC others(36): Show |
1 | a0003c0002t0002g0211 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(41): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074773 | ||||||
| chr11:44074773 | T | TTTCTTTC others(40): Show |
1 | a0003c0002t0002g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(45): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074773 | ||||||
| chr11:44074775 | T | TCTTTCTT others(42): Show |
1 | a0003c0002t0002g0209 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(47): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074775 | |||||||
| chr11:44074775 | T | TCTTTCTT others(46): Show |
1 | a0003c0002t0002g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.489+94_489+95insCT others(51): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074775 | |||||||
| chr11:44074775 | T | TCTTTCTT others(35): Show |
1 | a0003c0002t0002g0192 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.489+94_489+95insCT others(40): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074775 | |||||||
| chr11:44074807 | C | T | 9 | a0001c0001t0005g0064a0001c0001t0005g0235a0001c0001t0005g0236others(6): Show | 10 | HG04204.hp1 NA18945.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+126C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074807 | |||||||
| chr11:44074812 | C | CT | 6 | a0002c0004t0001g0157a0005c0006t0001g0052a0005c0006t0001g0093others(3): Show | 7 | HG02615.hp2 HG02723.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+145dupT | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074812 | ||||||
| chr11:44074812 | CT | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.489+145delT | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074812 | ||||||
| chr11:44074812 | CTT | C | 11 | a0001c0001t0001g0147a0001c0001t0005g0064a0001c0001t0005g0235others(8): Show | 12 | HG04204.hp1 NA18945.hp1 NA18962.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+144_489+145del others(2): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr11 | 44074812 | ||||||
| chr11:44074818 | T | A | 5 | a0002c0003t0001g0149a0002c0003t0001g0150a0002c0003t0001g0180others(2): Show | 5 | HG00558.hp2 HG02523.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+137T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074818 | |||||||
| chr11:44074820 | T | A | 1 | a0003c0002t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+139T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074820 | |||||||
| chr11:44074825 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.489+144T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074825 | |||||||
| chr11:44074826 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+145T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074826 | |||||||
| chr11:44074827 | A | T | 1 | a0001c0001t0001g0166 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.489+146A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074827 | |||||||
| chr11:44074848 | T | A | 48 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(45): Show | 69 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.489+167T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074848 | |||||||
| chr11:44074861 | G | T | 2 | a0003c0002t0002g0225a0003c0002t0002g0226 | 2 | HG00621.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.489+180G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074861 | |||||||
| chr11:44074864 | A | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.489+183A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074864 | |||||||
| chr11:44074941 | C | T | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+260C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074941 | |||||||
| chr11:44074991 | T | G | 5 | a0001c0001t0004g0037a0001c0001t0004g0090a0001c0001t0004g0108others(2): Show | 6 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+310T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44074991 | |||||||
| chr11:44075043 | C | T | 1 | a0002c0004t0001g0069 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+362C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075043 | |||||||
| chr11:44075061 | T | A | 1 | a0003c0002t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489+380T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075061 | |||||||
| chr11:44075092 | G | A | 1 | a0002c0004t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+411G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075092 | |||||||
| chr11:44075249 | G | T | 5 | a0001c0001t0004g0037a0001c0001t0004g0090a0001c0001t0004g0108others(2): Show | 6 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-277G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075249 | |||||||
| chr11:44075365 | C | T | 1 | a0002c0003t0001g0127 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.490-161C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075365 | |||||||
| chr11:44075437 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.490-89C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075437 | |||||||
| chr11:44075447 | G | T | 5 | a0002c0004t0001g0092a0002c0004t0001g0157a0002c0004t0007g0136others(2): Show | 5 | HG00639.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-79G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 5/14 | chr11 | 44075447 | |||||||
| chr11:44075676 | A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 144 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.556+84A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44075676 | |||||||
| chr11:44075704 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.556+112T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44075704 | |||||||
| chr11:44075943 | T | G | 1 | a0004c0005t0002g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.556+351T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44075943 | |||||||
| chr11:44076045 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.556+453G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076045 | |||||||
| chr11:44076314 | C | T | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.556+722C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076314 | |||||||
| chr11:44076450 | T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.557-829T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076450 | |||||||
| chr11:44076624 | C | T | 1 | a0004c0005t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.557-655C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076624 | |||||||
| chr11:44076636 | G | T | 1 | a0005c0006t0001g0196 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.557-643G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076636 | |||||||
| chr11:44076643 | G | C | 1 | a0001c0001t0006g0285 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.557-636G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076643 | |||||||
| chr11:44076658 | T | A | 5 | a0002c0004t0001g0158a0003c0002t0001g0074a0003c0002t0001g0095others(2): Show | 5 | HG01891.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-621T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076658 | |||||||
| chr11:44076933 | A | G | 1 | a0002c0003t0008g0179 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.557-346A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44076933 | |||||||
| chr11:44077089 | C | T | 5 | a0002c0004t0001g0092a0002c0004t0001g0157a0002c0004t0007g0136others(2): Show | 5 | HG00639.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-190C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44077089 | |||||||
| chr11:44077146 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.557-133G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44077146 | |||||||
| chr11:44077201 | G | A | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.557-78G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44077201 | |||||||
| chr11:44077245 | A | G | 5 | a0002c0004t0001g0158a0003c0002t0001g0074a0003c0002t0001g0095others(2): Show | 5 | HG01891.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-34A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44077245 | |||||||
| chr11:44077261 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.557-18G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 6/14 | chr11 | 44077261 | |||||||
| chr11:44077419 | G | A | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.654+43G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077419 | |||||||
| chr11:44077428 | T | C | 5 | a0001c0001t0004g0037a0001c0001t0004g0090a0001c0001t0004g0108others(2): Show | 6 | HG01109.hp2 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+52T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077428 | |||||||
| chr11:44077435 | G | A | 145 | a0001c0001t0001g0260a0001c0001t0004g0037a0001c0001t0004g0090others(142): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.654+59G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077435 | |||||||
| chr11:44077604 | A | G | 7 | a0005c0006t0001g0052a0005c0006t0001g0093a0005c0006t0001g0094others(4): Show | 8 | HG02615.hp2 HG02723.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+228A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077604 | |||||||
| chr11:44077610 | A | G | 7 | a0005c0006t0001g0052a0005c0006t0001g0093a0005c0006t0001g0094others(4): Show | 8 | HG02615.hp2 HG02723.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+234A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077610 | |||||||
| chr11:44077640 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.655-205A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077640 | |||||||
| chr11:44077800 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655-45A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 7/14 | chr11 | 44077800 | |||||||
| chr11:44078038 | A | C | 89 | a0001c0001t0001g0260a0001c0001t0002g0156a0001c0001t0004g0037others(86): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.732+116A>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078038 | |||||||
| chr11:44078214 | G | A | 1 | a0002c0003t0001g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.732+292G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078214 | |||||||
| chr11:44078308 | G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(254): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.733-376G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078308 | |||||||
| chr11:44078333 | G | A | 1 | a0011c0014t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.733-351G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078333 | |||||||
| chr11:44078448 | T | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.733-236T>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078448 | |||||||
| chr11:44078471 | T | C | 89 | a0001c0001t0001g0260a0001c0001t0002g0156a0001c0001t0004g0037others(86): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.733-213T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078471 | |||||||
| chr11:44078577 | C | T | 1 | a0003c0002t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.733-107C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078577 | |||||||
| chr11:44078608 | G | A | 2 | a0004c0005t0001g0097a0004c0005t0001g0100 | 2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.733-76G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078608 | |||||||
| chr11:44078671 | C | T | 1 | a0002c0004t0001g0092 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.733-13C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 8/14 | chr11 | 44078671 | |||||||
| chr11:44078816 | G | A | 5 | a0002c0004t0001g0158a0003c0002t0001g0074a0003c0002t0001g0095others(2): Show | 5 | HG01891.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.833+32G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44078816 | |||||||
| chr11:44078841 | C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0076 | 3 | HG00423.hp2 HG04184.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.833+57C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44078841 | |||||||
| chr11:44078911 | G | C | 1 | a0001c0001t0001g0025 | 3 | HG01257.hp1 HG01346.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.833+127G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44078911 | |||||||
| chr11:44078992 | G | T | 146 | a0001c0001t0001g0260a0001c0001t0003g0272a0001c0001t0004g0037others(143): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.833+208G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44078992 | |||||||
| chr11:44079037 | CTCATACA others(18): Show |
C | 7 | a0001c0001t0001g0072a0001c0001t0001g0087a0001c0001t0001g0161others(4): Show | 14 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.833+274_833+298del others(25): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 44079037 | ||||||
| chr11:44079290 | G | A | 5 | a0002c0004t0001g0092a0002c0004t0001g0157a0002c0004t0007g0136others(2): Show | 5 | HG00639.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.834-241G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079290 | |||||||
| chr11:44079296 | G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(75): Show | 135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.834-235G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079296 | |||||||
| chr11:44079469 | C | T | 5 | a0002c0004t0001g0158a0003c0002t0001g0074a0003c0002t0001g0095others(2): Show | 5 | HG01891.hp1 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-62C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079469 | |||||||
| chr11:44079492 | C | T | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.834-39C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079492 | |||||||
| chr11:44079493 | A | C | 5 | a0002c0003t0001g0149a0002c0003t0001g0150a0002c0003t0001g0180others(2): Show | 5 | HG00558.hp2 HG02523.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.834-38A>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079493 | |||||||
| chr11:44079512 | C | T | 1 | a0001c0001t0009g0133 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.834-19C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 9/14 | chr11 | 44079512 | |||||||
| chr11:44079705 | T | C | 8 | a0001c0001t0005g0064a0001c0001t0005g0235a0001c0001t0005g0236others(5): Show | 9 | HG04204.hp1 NA18945.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.923+85T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44079705 | |||||||
| chr11:44079777 | C | G | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.923+157C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44079777 | |||||||
| chr11:44079914 | C | T | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.923+294C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44079914 | |||||||
| chr11:44079945 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.923+325C>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44079945 | |||||||
| chr11:44080009 | C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.923+389C>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080009 | |||||||
| chr11:44080166 | C | T | 50 | a0002c0004t0001g0059a0002c0004t0001g0068a0002c0004t0001g0075others(47): Show | 73 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.923+546C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080166 | |||||||
| chr11:44080206 | G | A | 3 | a0002c0004t0007g0136a0003c0002t0007g0098a0003c0002t0007g0099 | 3 | HG00639.hp1 HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.923+586G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080206 | |||||||
| chr11:44080257 | G | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.923+637G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080257 | |||||||
| chr11:44080297 | C | T | 1 | a0002c0003t0001g0070 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.923+677C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080297 | |||||||
| chr11:44080298 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.923+678G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080298 | |||||||
| chr11:44080332 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.924-688C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080332 | |||||||
| chr11:44080388 | A | G | 1 | a0003c0002t0002g0207 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.924-632A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080388 | |||||||
| chr11:44080397 | G | A | 2 | a0001c0001t0001g0164a0004c0005t0001g0268 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.924-623G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080397 | |||||||
| chr11:44080443 | GTGAT | G | 5 | a0001c0001t0001g0046a0004c0005t0001g0097a0004c0005t0001g0100others(2): Show | 6 | HG01243.hp1 HG01884.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.924-574_924-571del others(4): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr11 | 44080443 | ||||||
| chr11:44080531 | A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.924-489A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080531 | |||||||
| chr11:44080668 | G | T | 1 | a0001c0001t0003g0278 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.924-352G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080668 | |||||||
| chr11:44080669 | A | T | 1 | a0001c0001t0003g0278 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.924-351A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080669 | |||||||
| chr11:44080705 | C | T | 2 | a0003c0002t0002g0217a0003c0002t0002g0220 | 2 | HG00741.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.924-315C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080705 | |||||||
| chr11:44080772 | A | G | 10 | a0001c0001t0003g0272a0001c0001t0005g0064a0001c0001t0005g0235others(7): Show | 11 | HG01106.hp1 HG04204.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.924-248A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080772 | |||||||
| chr11:44080938 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.924-82C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 10/14 | chr11 | 44080938 | |||||||
| chr11:44081392 | T | C | 1 | a0002c0004t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1111+72T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081392 | |||||||
| chr11:44081395 | A | T | 3 | a0003c0002t0001g0074a0003c0002t0001g0095a0003c0002t0001g0096 | 3 | HG01891.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1111+75A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081395 | |||||||
| chr11:44081470 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1111+150A>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081470 | |||||||
| chr11:44081529 | A | T | 83 | a0001c0001t0002g0156a0002c0004t0001g0029a0002c0004t0001g0034others(80): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1111+209A>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081529 | |||||||
| chr11:44081627 | G | T | 98 | a0001c0001t0004g0037a0001c0001t0004g0090a0001c0001t0004g0108others(95): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1111+307G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081627 | |||||||
| chr11:44081684 | G | T | 9 | a0002c0003t0001g0040a0002c0003t0001g0063a0002c0003t0001g0111others(6): Show | 11 | HG02027.hp2 NA18939.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.1111+364G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081684 | |||||||
| chr11:44081810 | G | A | 3 | a0002c0004t0007g0136a0003c0002t0007g0098a0003c0002t0007g0099 | 3 | HG00639.hp1 HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1111+490G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081810 | |||||||
| chr11:44081813 | T | C | 7 | a0001c0001t0001g0072a0001c0001t0001g0087a0001c0001t0001g0161others(4): Show | 14 | HG01884.hp1 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1111+493T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44081813 | |||||||
| chr11:44082114 | A | C | 1 | a0002c0004t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111+794A>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082114 | |||||||
| chr11:44082189 | GAGTGTAA others(2): Show |
G | 83 | a0001c0001t0002g0156a0002c0004t0001g0029a0002c0004t0001g0034others(80): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1111+873_1111+881d others(11): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 44082189 | ||||||
| chr11:44082408 | A | G | 46 | a0002c0003t0001g0007a0002c0003t0001g0010a0002c0003t0001g0012others(43): Show | 67 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1112-761A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082408 | |||||||
| chr11:44082490 | G | C | 1 | a0002c0018t0001g0177 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1112-679G>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082490 | |||||||
| chr11:44082528 | G | A | 1 | a0003c0002t0011g0222 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1112-641G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082528 | |||||||
| chr11:44082666 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1112-503A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082666 | |||||||
| chr11:44082672 | C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1112-497C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082672 | |||||||
| chr11:44082840 | G | T | 2 | a0001c0001t0001g0255a0004c0005t0001g0214 | 2 | HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1112-329G>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44082840 | |||||||
| chr11:44083020 | G | A | 1 | a0002c0004t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1112-149G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44083020 | |||||||
| chr11:44083121 | T | C | 10 | a0001c0001t0003g0272a0001c0001t0005g0064a0001c0001t0005g0235others(7): Show | 11 | HG01106.hp1 HG04204.hp1 NA18945.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-48T>C | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44083121 | |||||||
| chr11:44083124 | A | G | 1 | a0002c0004t0001g0173 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1112-45A>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44083124 | |||||||
| chr11:44083150 | G | A | 1 | a0002c0004t0001g0267 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1112-19G>A | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | chr11 | 44083150 | |||||||
| chr11:44083151 | C | CCT | 241 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1112-15_1112-14dup others(2): Show |
ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 44083151 | ||||||
| chr11:44083335 | T | G | 82 | a0001c0001t0002g0156a0002c0004t0001g0029a0002c0004t0001g0034others(79): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1254+24T>G | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 13/14 | chr11 | 44083335 | |||||||
| chr11:44083391 | C | T | 5 | a0002c0004t0001g0092a0002c0004t0001g0157a0002c0004t0007g0136others(2): Show | 5 | HG00639.hp1 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1255-33C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 13/14 | chr11 | 44083391 | |||||||
| chr11:44083649 | C | T | 1 | a0001c0001t0003g0017 | 4 | NA18953.hp2 NA18970.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1409-46C>T | ACCS | ENSG00000110455.14 | transcript | ENST00000263776.9 | protein_coding | 14/14 | chr11 | 44083649 |