Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 58157 |
| ensemblid | ENSG00000165553.5 |
| hgncid | 14077 |
| symbol | NGB |
| name | neuroglobin |
| refseq_nuc | NM_021257.4 |
| refseq_prot | NP_067080.1 |
| ensembl_nuc | ENST00000298352.5 |
| ensembl_prot | ENSP00000298352.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77265483 |
| end | 77271206 |
| strand | - |
| ver | v1.2 |
| region | chr14:77265483-77271206 |
| region5000 | chr14:77260483-77276206 |
| regionname0 | NGB_chr14_77265483_77271206 |
| regionname5000 | NGB_chr14_77260483_77276206 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 151 | 359 | 86 | 59 | 162 | 8 | 42 | 122 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0002 | 0/0 | 151 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0003 | 0/0 | 151 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0004 | 0/0 | 151 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0005 | 0/0 | 151 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0006 | 0/0 | 110 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | MERPE others(105): Show |
chr14 | 77260483 | 77276206 |
| a0007 | 0/0 | 151 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| a0008 | 0/0 | 151 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | MERPE others(146): Show |
chr14 | 77260483 | 77276206 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 453 | 358 | 86 | 59 | 162 | 7 | 42 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0001c0007 | 0/0 | 453 | 1 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0002c0005 | 0/0 | 453 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0003c0009 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0004c0004 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0005c0008 | 0/0 | 453 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0006c0006 | 0/0 | 453 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0007c0002 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 | ||
| a0008c0003 | 0/0 | 453 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | ATGGA others(448): Show |
chr14 | 77260483 | 77276206 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1778 | 320 | 79 | 56 | 138 | 6 | 39 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0002 | 0/0 | 1778 | 14 | 0 | 0 | 14 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGT others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0003 | 0/0 | 1777 | 11 | 0 | 3 | 7 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1772): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0004 | 0/0 | 1777 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1772): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0005 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0006 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0007 | 0/0 | 1777 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1772): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0008 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0009 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0010 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0011 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0012 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0013 | 0/0 | 1795 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1790): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0014 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0001c0001t0015 | 0/0 | 1777 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGT others(1772): Show |
chr14 | 77260483 | 77276206 |
| a0001c0007t0001 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0002c0005t0001 | 0/0 | 1778 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0003c0009t0001 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0004c0004t0001 | 0/0 | 1778 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0005c0008t0001 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0006c0006t0001 | 0/0 | 1778 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0007c0002t0001 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGC others(1773): Show |
chr14 | 77260483 | 77276206 |
| a0008c0003t0002 | 0/0 | 1778 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | GGGGT others(1773): Show |
chr14 | 77260483 | 77276206 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 63 | 6 | 14 | 35 | 0 | 8 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0002 | 0/0 | 41 | 3 | 5 | 33 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0003 | 0/0 | 22 | 7 | 3 | 3 | 0 | 9 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0004 | 0/0 | 20 | 2 | 3 | 15 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0005 | 0/0 | 19 | 14 | 0 | 0 | 0 | 5 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0006 | 0/0 | 17 | 4 | 1 | 10 | 0 | 2 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0007 | 0/0 | 11 | 2 | 1 | 7 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0009 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0011 | 1/0 | 6 | 2 | 2 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0013 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0015 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0002g0008 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0003g0014 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0010g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0001c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0002c0005t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0003c0009t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0004c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0005c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0006c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0007c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| a0008c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00323 | hp1 | a0001 | c0007 | t0001 | g0093 | EUR | FIN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01943 | hp1 | a0002 | c0005 | t0001 | g0051 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02622 | hp1 | a0003 | c0009 | t0001 | g0047 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0058 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0061 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03239 | hp1 | a0005 | c0008 | t0001 | g0092 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0057 | AFR | GWD | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0050 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04115 | hp2 | a0006 | c0006 | t0001 | g0059 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18945 | hp1 | a0001 | c0001 | t0014 | g0103 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18968 | hp1 | a0007 | c0002 | t0001 | g0039 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18995 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19068 | hp1 | a0001 | c0001 | t0015 | g0109 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19083 | hp1 | a0008 | c0003 | t0002 | g0104 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0043 | SAS | GIH | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02486 | hp2 | a0001 | c0001 | t0013 | g0053 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | NGB_chr14_77260483_77276206 | NGB | chr14 | 77260483 | 77276206 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77266553 | C | A | 1 | a0004 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.439G>T | p.Gly147Cys | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 708/1778 | 439/456 | 147/151 | chr14 | 77266553 | |||
| chr14:77266592 | T | C | 1 | a0002 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.400A>G | p.Ser134Gly | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 669/1778 | 400/456 | 134/151 | chr14 | 77266592 | |||
| chr14:77266661 | C | A | 1 | a0006 | 1 | HG04115.hp2 | stop_gained | HIGH | c.331G>T | p.Glu111* | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 600/1778 | 331/456 | 111/151 | chr14 | 77266661 | |||
| chr14:77269238 | C | G | 1 | a0008 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.178G>C | p.Glu60Gln | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/4 | 447/1778 | 178/456 | 60/151 | chr14 | 77269238 | |||
| chr14:77269241 | G | A | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.175C>T | p.Pro59Ser | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/4 | 444/1778 | 175/456 | 59/151 | chr14 | 77269241 | |||
| chr14:77269273 | T | A | 1 | a0003 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.143A>T | p.Gln48Leu | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/4 | 412/1778 | 143/456 | 48/151 | chr14 | 77269273 | |||
| chr14:77270912 | A | G | 1 | a0007 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.26T>C | p.Ile9Thr | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/4 | 295/1778 | 26/456 | 9/151 | chr14 | 77270912 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77268478 | G | C | 1 | a0001c0007 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.309C>G | p.Leu103Leu | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/4 | 578/1778 | 309/456 | 103/151 | chr14 | 77268478 | |||
| chr14:77270911 | G | A | 1 | a0007c0002 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.27C>T | p.Ile9Ile | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/4 | 296/1778 | 27/456 | 9/151 | chr14 | 77270911 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77265554 | A | G | 1 | a0001c0001t0011 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 982 | chr14 | 77265554 | ||||||
| chr14:77265555 | C | A | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0015 |
13 | HG00140.hp2 HG01099.hp1 HG01243.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*981G>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 981 | chr14 | 77265555 | ||||||
| chr14:77265780 | C | T | 1 | a0001c0001t0010 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 756 | chr14 | 77265780 | ||||||
| chr14:77265901 | G | A | 1 | a0001c0001t0012 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*635C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 635 | chr14 | 77265901 | ||||||
| chr14:77265926 | G | T | 1 | a0001c0001t0009 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*610C>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 610 | chr14 | 77265926 | ||||||
| chr14:77266007 | C | T | 1 | a0001c0001t0007 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 529 | chr14 | 77266007 | ||||||
| chr14:77266152 | G | T | 1 | a0001c0001t0008 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384C>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 384 | chr14 | 77266152 | ||||||
| chr14:77266205 | C | CTCCACCT others(10): Show |
1 | a0001c0001t0013 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330_*331insTGAGCT others(11): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 330 | chr14 | 77266205 | ||||||
| chr14:77266279 | CA | C | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(1): Show |
15 | HG00140.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*256delT | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 256 | chr14 | 77266279 | ||||||
| chr14:77266417 | C | G | 1 | a0001c0001t0006 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*119G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 4/4 | 119 | chr14 | 77266417 | ||||||
| chr14:77270997 | C | A | 1 | a0001c0001t0014 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60G>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/4 | 60 | chr14 | 77270997 | ||||||
| chr14:77271081 | C | T | 1 | a0001c0001t0005 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/4 | 144 | chr14 | 77271081 | ||||||
| chr14:77271202 | G | A | 3 | a0001c0001t0002 a0001c0001t0015 a0008c0003t0002 |
16 | HG00544.hp2 HG00558.hp1 HG02027.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-265C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/4 | 265 | chr14 | 77271202 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77266774 | CT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.322-105delA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77266774 | |||||||
| chr14:77266850 | T | C | 1 | a0001c0001t0013g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.322-180A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77266850 | |||||||
| chr14:77267048 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.322-378T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267048 | |||||||
| chr14:77267186 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.322-516C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267186 | |||||||
| chr14:77267224 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0055 others(1): Show |
5 | HG02257.hp2 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-554G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267224 | |||||||
| chr14:77267513 | C | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0063 |
5 | HG01167.hp1 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.322-843G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267513 | |||||||
| chr14:77267617 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.321+849C>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267617 | |||||||
| chr14:77267900 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
128 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.321+566C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77267900 | |||||||
| chr14:77268085 | A | G | 1 | a0001c0001t0003g0066 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.321+381T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268085 | |||||||
| chr14:77268113 | A | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0029 a0001c0001t0003g0030 others(6): Show |
15 | HG00140.hp2 HG01099.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+353T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268113 | |||||||
| chr14:77268149 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0082 |
3 | HG02109.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.321+317T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268149 | |||||||
| chr14:77268209 | T | A | 1 | a0007c0002t0001g0039 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.321+257A>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268209 | |||||||
| chr14:77268237 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.321+229A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268237 | |||||||
| chr14:77268329 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02809.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.321+137A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 3/3 | chr14 | 77268329 | |||||||
| chr14:77268707 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.202-122C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77268707 | |||||||
| chr14:77268785 | A | G | 2 | a0001c0001t0004g0065 a0001c0001t0004g0067 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.202-200T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77268785 | |||||||
| chr14:77268906 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.201+309T>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77268906 | |||||||
| chr14:77268994 | T | C | 1 | a0007c0002t0001g0039 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.201+221A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77268994 | |||||||
| chr14:77269130 | G | C | 2 | a0001c0001t0004g0065 a0001c0001t0004g0067 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.201+85C>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77269130 | |||||||
| chr14:77269162 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.201+53C>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 2/3 | chr14 | 77269162 | |||||||
| chr14:77269419 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0098 |
2 | HG01433.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.90-93G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269419 | |||||||
| chr14:77269450 | G | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0022 others(11): Show |
36 | HG01167.hp2 HG01891.hp2 HG02257.hp2 others(33): Show |
intron_variant | MODIFIER | c.90-124C>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269450 | |||||||
| chr14:77269549 | G | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
10 | HG01109.hp1 HG01243.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-223C>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269549 | |||||||
| chr14:77269665 | CCTTTCTC others(53): Show |
C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0060 a0001c0007t0001g0093 |
3 | HG00323.hp1 HG01106.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.90-399_90-340delAG others(58): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269665 | |||||||
| chr14:77269665 | CCTTTCTC others(76): Show |
C | 1 | a0001c0001t0010g0061 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.90-422_90-340delAG others(81): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269665 | |||||||
| chr14:77269666 | CT | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0033 |
3 | HG02056.hp2 HG02572.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.90-341delA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269666 | |||||||
| chr14:77269667 | TTTCTCTC others(18): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.90-366_90-342delGA others(23): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(26): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.90-374_90-342delGA others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(28): Show |
T | 1 | a0001c0001t0001g0037 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.90-376_90-342delGA others(33): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(40): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.90-388_90-342delGA others(45): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(42): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.90-390_90-342delGA others(47): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(46): Show |
T | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.90-394_90-342delGA others(51): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(52): Show |
T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
15 | HG01496.hp2 HG01884.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.90-400_90-342delGA others(57): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(57): Show |
T | 2 | a0001c0001t0001g0001 a0003c0009t0001g0047 |
3 | HG01346.hp2 HG02622.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.90-405_90-342delGA others(62): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(59): Show |
T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0007 |
2 | HG00408.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.90-407_90-342delGA others(64): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269667 | TTTCTCTC others(61): Show |
T | 2 | a0001c0001t0001g0003 a0001c0001t0002g0008 |
2 | HG00558.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.90-409_90-342delGA others(66): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269667 | |||||||
| chr14:77269668 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0077 |
4 | HG00735.hp2 HG01258.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-342A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269668 | |||||||
| chr14:77269668 | TTCTCTCT others(54): Show |
T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0002g0107 |
3 | HG01192.hp2 NA18978.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.90-403_90-343delGA others(59): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269668 | |||||||
| chr14:77269668 | TTCTCTCT others(56): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0027 others(1): Show |
4 | HG02572.hp1 HG02922.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-405_90-343delGA others(61): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269668 | |||||||
| chr14:77269668 | TTCTCTCT others(58): Show |
T | 2 | a0001c0001t0001g0007 a0006c0006t0001g0059 |
4 | HG00408.hp2 HG02809.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-407_90-343delGA others(63): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269668 | |||||||
| chr14:77269670 | CTCTCTCT others(50): Show |
C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(3): Show |
7 | HG02723.hp2 HG02922.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-401_90-345delAG others(55): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269670 | |||||||
| chr14:77269671 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG01123.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.90-345A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269671 | |||||||
| chr14:77269672 | CTCTCTCT others(48): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(3): Show |
9 | HG02293.hp1 HG02886.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.90-401_90-347delAG others(53): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269672 | |||||||
| chr14:77269674 | CTCTCTCT others(46): Show |
C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(4): Show |
11 | HG01070.hp2 HG01099.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-401_90-349delAG others(51): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269674 | |||||||
| chr14:77269676 | CTCTCTCT others(44): Show |
C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(4): Show |
11 | HG00544.hp1 HG02965.hp2 HG03654.hp1 others(8): Show |
intron_variant | MODIFIER | c.90-401_90-351delAG others(49): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269676 | |||||||
| chr14:77269678 | CTCTCTCT others(42): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(2): Show |
8 | HG01978.hp2 HG02071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-401_90-353delAG others(47): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269678 | |||||||
| chr14:77269680 | CTCTCTCT others(40): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0034 |
5 | HG03453.hp2 NA18966.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-401_90-355delAG others(45): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269680 | |||||||
| chr14:77269682 | CTCTCTCT others(38): Show |
C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0088 others(1): Show |
5 | HG00673.hp1 HG02015.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-401_90-357delAG others(43): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269682 | |||||||
| chr14:77269684 | CTCTCTCT others(36): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0071 |
3 | HG00673.hp2 HG01884.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.90-401_90-359delAG others(41): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269684 | |||||||
| chr14:77269686 | CTCTCTCT others(34): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(2): Show |
9 | HG00323.hp2 HG01346.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-401_90-361delAG others(39): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269686 | |||||||
| chr14:77269688 | CTCTCTCT others(32): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 |
3 | NA18953.hp2 NA18975.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.90-401_90-363delAG others(37): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269688 | |||||||
| chr14:77269690 | CTCTCTCT others(30): Show |
C | 1 | a0001c0001t0001g0002 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.90-401_90-365delAG others(35): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269690 | |||||||
| chr14:77269692 | CTCTCTCT others(28): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
2 | NA18969.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.90-401_90-367delAG others(33): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269692 | |||||||
| chr14:77269694 | CTCTCTCT others(26): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.90-401_90-369delAG others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269694 | |||||||
| chr14:77269696 | CTCTCTCT others(24): Show |
C | 1 | a0001c0001t0001g0002 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.90-401_90-371delAG others(29): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269696 | |||||||
| chr14:77269698 | CTCTCTCT others(22): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.90-401_90-373delAG others(27): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269698 | |||||||
| chr14:77269699 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.90-373A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269699 | |||||||
| chr14:77269700 | CTCTCTCT others(20): Show |
C | 1 | a0001c0001t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.90-401_90-375delAG others(25): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269700 | |||||||
| chr14:77269704 | CTCTCTCT others(16): Show |
C | 1 | a0001c0001t0001g0002 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.90-401_90-379delAG others(21): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269704 | |||||||
| chr14:77269705 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.90-379A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269705 | |||||||
| chr14:77269707 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.90-381A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269707 | |||||||
| chr14:77269709 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0005 |
3 | HG02559.hp1 HG03098.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.90-383A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269709 | |||||||
| chr14:77269709 | TCTCTCTC others(88): Show |
T | 1 | a0001c0001t0001g0004 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.90-478_90-384delGG others(93): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269709 | |||||||
| chr14:77269710 | CTCTCTCT others(10): Show |
C | 1 | a0001c0001t0001g0004 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.90-401_90-385delAG others(15): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269710 | |||||||
| chr14:77269711 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
21 | HG01167.hp1 HG01169.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.90-385A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269711 | |||||||
| chr14:77269713 | T | C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(4): Show |
14 | HG00597.hp2 HG01928.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.90-387A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269713 | |||||||
| chr14:77269714 | CT | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0040 |
4 | HG02109.hp1 HG02132.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-389delA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269714 | |||||||
| chr14:77269715 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(7): Show |
22 | HG00621.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.90-389A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269715 | |||||||
| chr14:77269717 | T | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(14): Show |
45 | HG00609.hp2 HG01081.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.90-391A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269717 | |||||||
| chr14:77269717 | TCTCTCTC others(59): Show |
T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0003 |
2 | HG01978.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.90-457_90-392delGA others(64): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269717 | |||||||
| chr14:77269717 | TCTCTCTC others(60): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.90-458_90-392delGG others(65): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269717 | |||||||
| chr14:77269717 | TCTCTCTC others(80): Show |
T | 1 | a0001c0001t0001g0006 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.90-478_90-392delGG others(85): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269717 | |||||||
| chr14:77269719 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(6): Show |
37 | HG00423.hp1 HG00597.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.90-393A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269719 | |||||||
| chr14:77269719 | TCTCTCTC others(57): Show |
T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0042 |
2 | HG03516.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.90-457_90-394delGA others(62): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269719 | |||||||
| chr14:77269719 | TCTCTCTC others(77): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0004g0067 |
4 | HG02559.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-477_90-394delGG others(82): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269719 | |||||||
| chr14:77269721 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(16): Show |
45 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.90-395A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269721 | TCTCTCTT others(55): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
2 | NA18964.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.90-457_90-396delGA others(60): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269721 | TCTCTCTT others(56): Show |
T | 1 | a0001c0001t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.90-458_90-396delGG others(61): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269721 | TCTCTCTT others(74): Show |
T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0004g0065 |
4 | HG01169.hp2 HG02145.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-476_90-396delGG others(79): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269721 | TCTCTCTT others(75): Show |
T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(2): Show |
10 | HG01258.hp1 HG01261.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.90-477_90-396delGG others(80): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269721 | TCTCTCTT others(76): Show |
T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0021 |
8 | HG01167.hp1 HG01256.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-478_90-396delGG others(81): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269721 | |||||||
| chr14:77269723 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(16): Show |
45 | HG00609.hp1 HG00609.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.90-397A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | T | TCCTCCCT others(26): Show |
1 | a0001c0001t0001g0076 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.90-398_90-397insGG others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(67): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(1): Show |
20 | HG00423.hp1 HG01168.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.90-471_90-398delGG others(72): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(68): Show |
T | 1 | a0001c0001t0001g0009 | 7 | HG01256.hp1 HG01361.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-472_90-398delGG others(73): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(71): Show |
T | 1 | a0001c0001t0001g0013 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.90-475_90-398delGG others(76): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(72): Show |
T | 1 | a0001c0001t0001g0007 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.90-476_90-398delGG others(77): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(73): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(1): Show |
9 | HG02080.hp2 HG02148.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-477_90-398delGG others(78): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269723 | TCTCTTCT others(74): Show |
T | 1 | a0001c0001t0001g0006 | 3 | HG01928.hp2 HG02071.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.90-478_90-398delGG others(79): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269723 | |||||||
| chr14:77269725 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0018 others(3): Show |
9 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-399A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | T | TCCCTCCC others(14): Show |
1 | a0001c0001t0001g0010 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.90-400_90-399insGA others(19): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | T | TCCCTCCC others(26): Show |
1 | a0001c0001t0001g0032 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.90-400_90-399insGA others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(65): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(4): Show |
16 | HG00544.hp2 HG00621.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.90-471_90-400delGG others(70): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(66): Show |
T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 |
6 | HG00738.hp1 HG01123.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.90-472_90-400delGG others(71): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(69): Show |
T | 1 | a0001c0001t0001g0013 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.90-475_90-400delGG others(74): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(70): Show |
T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0012g0057 |
4 | HG03540.hp2 NA18974.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-476_90-400delGG others(75): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(71): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0070 |
15 | HG00639.hp2 HG01943.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.90-477_90-400delGG others(76): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269725 | TCTTCTCT others(72): Show |
T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0011g0043 others(1): Show |
5 | HG00621.hp1 HG02451.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-478_90-400delGG others(77): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269725 | |||||||
| chr14:77269726 | C | CCCTCCCT others(26): Show |
1 | a0001c0001t0001g0077 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.90-401_90-400insAG others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269726 | |||||||
| chr14:77269726 | CT | C | 27 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0025 others(24): Show |
40 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.90-401delA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269726 | |||||||
| chr14:77269727 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG00735.hp2 HG01255.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.90-401A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(4): Show |
1 | a0001c0001t0001g0018 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.90-402_90-401insGG others(9): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(12): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0018 |
2 | HG01192.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.90-402_90-401insGG others(17): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(16): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0031 others(2): Show |
5 | HG01106.hp1 HG01123.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-402_90-401insGG others(21): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(20): Show |
1 | a0001c0001t0001g0010 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGG others(25): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(22): Show |
1 | a0001c0001t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGA others(27): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(26): Show |
1 | a0001c0001t0001g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGA others(31): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCCCTCCC others(28): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0079 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.90-402_90-401insGG others(33): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCCCCC others(20): Show |
1 | a0001c0001t0001g0017 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGG others(25): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCCCCC others(22): Show |
1 | a0001c0001t0001g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.90-402_90-401insGA others(27): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCCCCT others(37): Show |
1 | a0001c0001t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGA others(42): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCCTCC others(21): Show |
1 | a0001c0001t0001g0017 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGG others(26): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCCTCC others(25): Show |
1 | a0001c0001t0001g0018 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGG others(30): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCCC others(20): Show |
1 | a0001c0001t0001g0010 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.90-402_90-401insGG others(25): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTC others(18): Show |
1 | a0001c0001t0001g0073 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGG others(23): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTC others(30): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0081 |
2 | HG00140.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.90-402_90-401insGG others(35): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTC others(90): Show |
1 | a0001c0001t0001g0098 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGA others(95): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTC others(106): Show |
1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.90-402_90-401insGA others(111): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTC others(13): Show |
1 | a0001c0001t0001g0099 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.90-402_90-401insGA others(18): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | T | TCTCTCTT others(3): Show |
1 | a0001c0001t0001g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.90-402_90-401insGA others(8): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(62): Show |
T | 1 | a0001c0001t0003g0064 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.90-470_90-402delGG others(67): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(63): Show |
T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(7): Show |
20 | HG00609.hp1 HG00735.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.90-471_90-402delGG others(68): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(64): Show |
T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 |
3 | HG01169.hp1 HG01891.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.90-472_90-402delGG others(69): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(68): Show |
T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0026 |
2 | HG06807.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.90-476_90-402delGG others(73): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(69): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(1): Show |
16 | HG00609.hp2 HG01081.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.90-477_90-402delGG others(74): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269727 | TTCTCTCT others(70): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0002g0105 |
5 | HG01891.hp1 NA18522.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-478_90-402delGG others(75): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269727 | |||||||
| chr14:77269728 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0080 others(1): Show |
4 | HG02148.hp1 HG03516.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.90-402A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269728 | |||||||
| chr14:77269729 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.90-403G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269729 | |||||||
| chr14:77269730 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
17 | HG00639.hp1 HG00738.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.90-404A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269730 | |||||||
| chr14:77269732 | T | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0056 a0001c0001t0001g0078 others(2): Show |
6 | HG01099.hp1 HG01167.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-406A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269732 | |||||||
| chr14:77269734 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
12 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.90-408A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269734 | |||||||
| chr14:77269734 | T | TCCCTCCC others(3): Show |
1 | a0001c0001t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.90-409_90-408insGG others(8): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269734 | |||||||
| chr14:77269736 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0055 a0001c0001t0001g0078 |
4 | HG02148.hp1 HG02257.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-410A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269736 | |||||||
| chr14:77269736 | T | TCCCTCCC others(19): Show |
1 | a0001c0001t0001g0074 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.90-411_90-410insGG others(24): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269736 | |||||||
| chr14:77269736 | TCTCTCTC others(58): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.90-475_90-411delGG others(63): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269736 | |||||||
| chr14:77269736 | TCTCTCTC others(60): Show |
T | 4 | a0001c0001t0001g0046 a0001c0001t0003g0029 a0001c0001t0003g0066 others(1): Show |
5 | HG01099.hp1 HG01167.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.90-477_90-411delGG others(65): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269736 | |||||||
| chr14:77269737 | CT | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0035 |
3 | HG00423.hp2 HG01517.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.90-412delA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269737 | |||||||
| chr14:77269738 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(4): Show |
9 | HG00639.hp1 HG01192.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.90-412A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269738 | |||||||
| chr14:77269738 | TCTCTCTC others(56): Show |
T | 1 | a0001c0001t0001g0101 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.90-475_90-413delGG others(61): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269738 | |||||||
| chr14:77269738 | TCTCTCTC others(59): Show |
T | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.90-478_90-413delGG others(64): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269738 | |||||||
| chr14:77269740 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0003g0014 |
2 | HG00140.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.90-414A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269740 | |||||||
| chr14:77269740 | TCTCTCTC others(56): Show |
T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0055 |
3 | HG02257.hp2 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.90-477_90-415delGG others(61): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269740 | |||||||
| chr14:77269742 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
4 | HG02280.hp1 HG04184.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-416A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269742 | |||||||
| chr14:77269742 | TCTCTCTC others(54): Show |
T | 1 | a0001c0001t0003g0014 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.90-477_90-417delGG others(59): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269742 | |||||||
| chr14:77269744 | T | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0035 others(3): Show |
7 | HG00423.hp2 HG01243.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.90-418A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269744 | |||||||
| chr14:77269744 | TCTCTCTC others(52): Show |
T | 2 | a0001c0001t0001g0016 a0001c0001t0003g0014 |
2 | HG00140.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.90-477_90-419delGG others(57): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269744 | |||||||
| chr14:77269744 | TCTCTCTC others(53): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.90-478_90-419delGG others(58): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269744 | |||||||
| chr14:77269746 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0091 |
2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.90-420A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269746 | |||||||
| chr14:77269746 | TCTCTCTC others(50): Show |
T | 1 | a0001c0001t0007g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.90-477_90-421delGG others(55): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269746 | |||||||
| chr14:77269748 | TCTCTCTC others(47): Show |
T | 1 | a0001c0001t0001g0037 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.90-476_90-423delGG others(52): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269748 | |||||||
| chr14:77269748 | TCTCTCTC others(48): Show |
T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0035 others(2): Show |
6 | HG00423.hp2 HG01243.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-477_90-423delGG others(53): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269748 | |||||||
| chr14:77269750 | TCTCTCTC others(47): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.90-478_90-425delGG others(52): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269750 | |||||||
| chr14:77269752 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0100 a0001c0001t0003g0014 |
3 | HG01975.hp1 HG03209.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.90-426A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269752 | |||||||
| chr14:77269754 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.90-428A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269754 | |||||||
| chr14:77269756 | T | C | 1 | a0001c0001t0013g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.90-430A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269756 | |||||||
| chr14:77269756 | TCTCTCTC others(38): Show |
T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.90-475_90-431delGG others(43): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269756 | |||||||
| chr14:77269756 | TCTCTCTC others(40): Show |
T | 2 | a0001c0001t0001g0024 a0001c0001t0003g0014 |
2 | HG01975.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.90-477_90-431delGG others(45): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269756 | |||||||
| chr14:77269758 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.90-432A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269758 | |||||||
| chr14:77269758 | TCTCTCTC others(37): Show |
T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0094 |
2 | HG02040.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.90-476_90-433delGG others(42): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269758 | |||||||
| chr14:77269758 | TCTCTCTC others(38): Show |
T | 1 | a0001c0001t0003g0014 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.90-477_90-433delGG others(43): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269758 | |||||||
| chr14:77269760 | TCTCTCTC others(36): Show |
T | 1 | a0001c0001t0013g0053 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.90-477_90-435delGG others(41): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269760 | |||||||
| chr14:77269762 | TCTCTCTC others(34): Show |
T | 1 | a0001c0001t0001g0016 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.90-477_90-437delGG others(39): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269762 | |||||||
| chr14:77269763 | C | A | 1 | a0001c0001t0001g0002 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.90-437G>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269763 | |||||||
| chr14:77269780 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.90-454A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269780 | |||||||
| chr14:77269782 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.90-456A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269782 | |||||||
| chr14:77269783 | C | CT | 3 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0069 |
4 | HG01993.hp2 HG02735.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-458_90-457insA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269783 | |||||||
| chr14:77269784 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0031 others(7): Show |
15 | HG00597.hp1 HG00639.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.90-458G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269784 | |||||||
| chr14:77269790 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0095 |
2 | HG03927.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.90-464G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269790 | |||||||
| chr14:77269792 | T | TCTCCTCT others(8): Show |
1 | a0001c0001t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.90-467_90-466insCG others(13): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269792 | |||||||
| chr14:77269794 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.90-468A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269794 | |||||||
| chr14:77269794 | TCCCCCCC others(1): Show |
T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(11): Show |
26 | HG00408.hp2 HG01192.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.90-476_90-469delGG others(6): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269794 | |||||||
| chr14:77269794 | TCCCCCCC others(2): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
63 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.90-477_90-469delGG others(7): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269794 | |||||||
| chr14:77269794 | TCCCCCCC others(3): Show |
T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0019 others(6): Show |
30 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.90-478_90-469delGG others(8): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269794 | |||||||
| chr14:77269797 | C | CT | 2 | a0001c0001t0001g0010 a0001c0001t0001g0032 |
6 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.90-472_90-471insA | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269797 | |||||||
| chr14:77269797 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.90-471G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269797 | |||||||
| chr14:77269798 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0074 others(2): Show |
7 | HG00597.hp1 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.90-472G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269798 | |||||||
| chr14:77269799 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0073 others(1): Show |
8 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.90-473G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269799 | |||||||
| chr14:77269800 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0074 others(3): Show |
8 | HG00597.hp1 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-474G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269800 | |||||||
| chr14:77269801 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0083 |
2 | HG03139.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.90-475G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269801 | |||||||
| chr14:77269801 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(12): Show |
59 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.90-475G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269801 | |||||||
| chr14:77269802 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 others(1): Show |
17 | HG00738.hp1 HG01123.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.90-476G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269802 | |||||||
| chr14:77269803 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.90-477G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269803 | |||||||
| chr14:77269803 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
57 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.90-477G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269803 | |||||||
| chr14:77269804 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | HG01261.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.90-478G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269804 | |||||||
| chr14:77269804 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 |
16 | HG00738.hp1 HG01123.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.90-478G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269804 | |||||||
| chr14:77269805 | C | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0076 others(2): Show |
8 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.90-479G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269805 | |||||||
| chr14:77269806 | C | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0062 others(1): Show |
10 | HG00639.hp1 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.90-480G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269806 | |||||||
| chr14:77269806 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.90-480G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269806 | |||||||
| chr14:77269807 | C | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0102 |
4 | HG01517.hp2 HG02135.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.90-481G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269807 | |||||||
| chr14:77269807 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.90-481G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269807 | |||||||
| chr14:77269808 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0060 a0001c0001t0001g0073 others(6): Show |
13 | HG00597.hp1 HG01106.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.90-482G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269808 | |||||||
| chr14:77269809 | C | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0026 others(12): Show |
33 | HG00408.hp2 HG00597.hp2 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.90-483G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269809 | |||||||
| chr14:77269810 | C | CCCCCCCC others(11): Show |
1 | a0001c0001t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.90-485_90-484insAG others(16): Show |
NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269810 | |||||||
| chr14:77269810 | C | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(36): Show |
203 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.90-484G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269810 | |||||||
| chr14:77269811 | C | A | 2 | a0001c0001t0003g0064 a0001c0001t0004g0065 |
2 | HG02145.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.90-485G>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269811 | |||||||
| chr14:77269811 | C | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(17): Show |
72 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.90-485G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269811 | |||||||
| chr14:77269812 | C | A | 7 | a0001c0001t0003g0014 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
13 | HG00140.hp2 HG01099.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.90-486G>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269812 | |||||||
| chr14:77269812 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.90-486G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269812 | |||||||
| chr14:77269817 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.90-491G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269817 | |||||||
| chr14:77269820 | C | G | 1 | a0001c0001t0001g0031 | 2 | NA19004.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.90-494G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269820 | |||||||
| chr14:77269821 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
324 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.90-495G>A | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269821 | |||||||
| chr14:77269824 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.90-498A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269824 | |||||||
| chr14:77269931 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(18): Show |
94 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.90-605C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269931 | |||||||
| chr14:77269992 | T | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG02809.hp1 HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.90-666A>G | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77269992 | |||||||
| chr14:77270499 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.89+350G>C | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77270499 | |||||||
| chr14:77270567 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89+282C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77270567 | |||||||
| chr14:77270745 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(23): Show |
123 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.89+104C>T | NGB | ENSG00000165553.5 | transcript | ENST00000298352.5 | protein_coding | 1/3 | chr14 | 77270745 |