Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55739 |
| ensemblid | ENSG00000213995.12 |
| hgncid | 25576 |
| symbol | NAXD |
| name | NAD(P)HX dehydratase |
| refseq_nuc | NM_001242882.2 |
| refseq_prot | NP_001229811.1 |
| ensembl_nuc | ENST00000680254.1 |
| ensembl_prot | ENSP00000505619.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 110615545 |
| end | 110639996 |
| strand | + |
| ver | v1.2 |
| region | chr13:110615545-110639996 |
| region5000 | chr13:110610545-110644996 |
| regionname0 | NAXD_chr13_110615545_110639996 |
| regionname5000 | NAXD_chr13_110610545_110644996 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 329 | 320 | 78 | 66 | 126 | 13 | 35 | 95 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0002 | 0/0 | 329 | 36 | 2 | 10 | 15 | 3 | 6 | 10 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0003 | 0/0 | 329 | 29 | 7 | 1 | 18 | 0 | 3 | 16 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0004 | 0/0 | 329 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | MAPGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0005 | 0/0 | 329 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0006 | 0/0 | 329 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0007 | 0/0 | 329 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| a0008 | 0/0 | 329 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | MALGP others(324): Show |
chr13 | 110610545 | 110644996 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 987 | 314 | 74 | 66 | 125 | 13 | 34 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0001c0006 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0001c0008 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0001c0009 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0001c0010 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0001c0012 | 0/0 | 987 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0002c0002 | 0/0 | 987 | 35 | 2 | 9 | 15 | 3 | 6 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0002c0013 | 0/0 | 987 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0003c0003 | 0/0 | 987 | 29 | 7 | 1 | 18 | 0 | 3 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0004c0004 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0005c0005 | 0/0 | 987 | 2 | 0 | 0 | 0 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0006c0011 | 0/0 | 987 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0007c0007 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 | ||
| a0008c0014 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | ATGGC others(982): Show |
chr13 | 110610545 | 110644996 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2515 | 162 | 34 | 30 | 67 | 8 | 22 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0002 | 0/1 | 2513 | 35 | 0 | 16 | 10 | 1 | 7 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0003 | 0/0 | 2513 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0004 | 0/0 | 2513 | 28 | 3 | 9 | 12 | 4 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0005 | 0/0 | 2513 | 22 | 12 | 3 | 3 | 0 | 4 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0006 | 0/0 | 2513 | 21 | 0 | 4 | 17 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0007 | 0/0 | 2515 | 11 | 0 | 0 | 11 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0008 | 0/0 | 2513 | 7 | 6 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0009 | 0/0 | 2515 | 3 | 3 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0010 | 0/0 | 2513 | 3 | 3 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0011 | 0/0 | 2513 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0012 | 0/0 | 2515 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0014 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0016 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0017 | 0/0 | 2513 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0018 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0019 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0020 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0022 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0023 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0024 | 0/0 | 2513 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0026 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0027 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0028 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0030 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0032 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0034 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0001t0035 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0006t0001 | 0/0 | 2515 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0008t0001 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0001c0009t0008 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0010t0006 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0001c0012t0001 | 0/0 | 2515 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0002t0001 | 0/0 | 2515 | 30 | 1 | 9 | 11 | 3 | 6 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0002t0013 | 0/0 | 2515 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0002t0015 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0002t0031 | 0/0 | 2515 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0002t0033 | 0/0 | 2515 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0002c0013t0001 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0003c0003t0003 | 0/0 | 2513 | 28 | 7 | 1 | 18 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0003c0003t0029 | 0/0 | 2513 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0004c0004t0008 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0004c0004t0021 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0005c0005t0001 | 0/0 | 2515 | 2 | 0 | 0 | 0 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0006c0011t0001 | 0/0 | 2515 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2510): Show |
chr13 | 110610545 | 110644996 |
| a0007c0007t0025 | 0/0 | 2513 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| a0008c0014t0003 | 0/0 | 2513 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | AATGG others(2508): Show |
chr13 | 110610545 | 110644996 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 39 | 3 | 12 | 15 | 2 | 6 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0006 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 2 | 0 | 3 | 2 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0010 | 0/0 | 6 | 2 | 4 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0003 | 0/0 | 8 | 0 | 0 | 5 | 0 | 3 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0011 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0007 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0005 | 0/0 | 8 | 0 | 2 | 3 | 0 | 3 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0003 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0010g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0010g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0011g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0012g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0016g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0017g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0018g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0020g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0022g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0023g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0024g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0026g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0027g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0028g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0030g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0032g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0034g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0001t0035g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0006t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0009t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0010t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0001c0012t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0015 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0013g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0015g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0031g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0002t0033g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0002c0013t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0002 | 0/0 | 16 | 1 | 1 | 13 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0003c0003t0029g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0004c0004t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0004c0004t0021g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0005c0005t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0006c0011t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0007c0007t0025g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| a0008c0014t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0140 | EUR | GBR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0071 | EUR | FIN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0194 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00438 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00609 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00639 | hp2 | a0003 | c0003 | t0003 | g0002 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00735 | hp2 | a0001 | c0001 | t0034 | g0189 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01099 | hp2 | a0002 | c0013 | t0001 | g0042 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01109 | hp1 | a0001 | c0001 | t0017 | g0069 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0046 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01175 | hp2 | a0006 | c0011 | t0001 | g0203 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0057 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01261 | hp2 | a0001 | c0001 | t0024 | g0003 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0029 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01891 | hp1 | a0001 | c0001 | t0022 | g0075 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0091 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02055 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02056 | hp1 | a0001 | c0001 | t0007 | g0163 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02135 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02155 | hp1 | a0002 | c0002 | t0015 | g0013 | EAS | CDX | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02273 | hp2 | a0001 | c0001 | t0006 | g0106 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02280 | hp1 | a0004 | c0004 | t0021 | g0050 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0002 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02451 | hp2 | a0001 | c0001 | t0014 | g0097 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0206 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0077 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02647 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02698 | hp2 | a0001 | c0001 | t0028 | g0187 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0070 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02809 | hp2 | a0001 | c0001 | t0026 | g0111 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0001 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02897 | hp1 | a0003 | c0003 | t0003 | g0028 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0049 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02922 | hp2 | a0007 | c0007 | t0025 | g0059 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02965 | hp1 | a0001 | c0008 | t0001 | g0123 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0031 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0052 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0076 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0090 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0180 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03516 | hp2 | a0003 | c0003 | t0003 | g0084 | AFR | ESN | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03540 | hp1 | a0003 | c0003 | t0003 | g0081 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0089 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03579 | hp2 | a0004 | c0004 | t0008 | g0058 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03654 | hp2 | a0003 | c0003 | t0003 | g0002 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03669 | hp1 | a0001 | c0012 | t0001 | g0042 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03688 | hp2 | a0005 | c0005 | t0001 | g0035 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0181 | SAS | PJL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03927 | hp1 | a0003 | c0003 | t0003 | g0083 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03942 | hp2 | a0003 | c0003 | t0029 | g0002 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0137 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04204 | hp1 | a0005 | c0005 | t0001 | g0035 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | STU | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | YRI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | CHB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18939 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18941 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18944 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18945 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18951 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18952 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18956 | hp2 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18959 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18967 | hp1 | a0002 | c0002 | t0031 | g0037 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18967 | hp2 | a0001 | c0001 | t0032 | g0088 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18968 | hp1 | a0003 | c0003 | t0003 | g0080 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0082 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18972 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0078 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18980 | hp2 | a0003 | c0003 | t0003 | g0085 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18981 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18985 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18988 | hp2 | a0001 | c0010 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18990 | hp1 | a0008 | c0014 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18993 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19001 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19003 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19004 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19011 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19030 | hp2 | a0001 | c0009 | t0008 | g0056 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19043 | hp1 | a0001 | c0001 | t0027 | g0061 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19057 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19060 | hp2 | a0001 | c0001 | t0030 | g0192 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19064 | hp1 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19065 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19070 | hp2 | a0001 | c0001 | t0023 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19074 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19075 | hp1 | a0002 | c0002 | t0013 | g0185 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19080 | hp2 | a0003 | c0003 | t0003 | g0002 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19085 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19091 | hp1 | a0002 | c0002 | t0013 | g0171 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | YRI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0074 | AFR | ASW | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0062 | EUR | TSI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | GIH | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02109 | hp1 | a0001 | c0001 | t0020 | g0205 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03471 | hp1 | a0002 | c0002 | t0033 | g0174 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | USA | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | USA | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0067 | AFR | USA | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA21309 | hp1 | a0001 | c0001 | t0035 | g0122 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0112 | REF | REF | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NAXD_chr13_110610545_110644996 | NAXD | chr13 | 110610545 | 110644996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110615609 | T | C | 1 | a0004 | 2 | HG02280.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.8T>C | p.Leu3Pro | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/10 | 65/2515 | 8/990 | 3/329 | chr13 | 110615609 | |||
| chr13:110622271 | T | A | 1 | a0007 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.102T>A | p.Asn34Lys | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/10 | 159/2515 | 102/990 | 34/329 | chr13 | 110622271 | |||
| chr13:110625264 | C | G | 1 | a0008 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.318C>G | p.Ile106Met | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/10 | 375/2515 | 318/990 | 106/329 | chr13 | 110625264 | |||
| chr13:110627470 | A | G | 1 | a0002 | 36 | HG00140.hp2 HG00597.hp1 HG01099.hp1 others(33): Show |
missense_variant | MODERATE | c.364A>G | p.Lys122Glu | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/10 | 421/2515 | 364/990 | 122/329 | chr13 | 110627470 | |||
| chr13:110627497 | G | A | 2 | a0003 a0008 |
30 | HG00438.hp2 HG00639.hp2 HG02135.hp2 others(27): Show |
missense_variant | MODERATE | c.391G>A | p.Val131Ile | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/10 | 448/2515 | 391/990 | 131/329 | chr13 | 110627497 | |||
| chr13:110634700 | C | T | 1 | a0006 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.521C>T | p.Pro174Leu | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/10 | 578/2515 | 521/990 | 174/329 | chr13 | 110634700 | |||
| chr13:110635562 | G | A | 1 | a0005 | 2 | HG03688.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.692G>A | p.Arg231His | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/10 | 749/2515 | 692/990 | 231/329 | chr13 | 110635562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110622310 | T | C | 1 | a0001c0008 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.141T>C | p.Ser47Ser | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/10 | 198/2515 | 141/990 | 47/329 | chr13 | 110622310 | |||
| chr13:110634592 | C | T | 2 | a0001c0012 a0002c0013 |
2 | HG01099.hp2 HG03669.hp1 |
synonymous_variant | LOW | c.489C>T | p.Asp163Asp | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 6/10 | 546/2515 | 489/990 | 163/329 | chr13 | 110634592 | |||
| chr13:110634755 | C | T | 1 | a0001c0010 | 1 | NA18988.hp2 | synonymous_variant | LOW | c.576C>T | p.Phe192Phe | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/10 | 633/2515 | 576/990 | 192/329 | chr13 | 110634755 | |||
| chr13:110635578 | C | T | 1 | a0001c0006 | 2 | HG02630.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.708C>T | p.Asn236Asn | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/10 | 765/2515 | 708/990 | 236/329 | chr13 | 110635578 | |||
| chr13:110638477 | C | T | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.939C>T | p.Ser313Ser | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 996/2515 | 939/990 | 313/329 | chr13 | 110638477 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110615573 | G | A | 1 | a0001c0001t0014 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/10 | 29 | chr13 | 110615573 | ||||||
| chr13:110615596 | T | G | 1 | a0002c0002t0015 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-6T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/10 | 6 | chr13 | 110615596 | ||||||
| chr13:110638533 | G | A | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 5 | chr13 | 110638533 | ||||||
| chr13:110638535 | G | A | 1 | a0001c0001t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 7 | chr13 | 110638535 | ||||||
| chr13:110638565 | G | A | 1 | a0001c0001t0027 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 37 | chr13 | 110638565 | ||||||
| chr13:110638569 | G | T | 1 | a0001c0001t0026 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*41G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 41 | chr13 | 110638569 | ||||||
| chr13:110638620 | T | C | 12 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(9): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*92T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 92 | chr13 | 110638620 | ||||||
| chr13:110638697 | T | C | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
154 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 169 | chr13 | 110638697 | ||||||
| chr13:110638735 | G | A | 8 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0019 others(5): Show |
37 | HG00438.hp2 HG00639.hp2 HG02055.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*207G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 207 | chr13 | 110638735 | ||||||
| chr13:110638755 | T | C | 1 | a0001c0001t0030 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 227 | chr13 | 110638755 | ||||||
| chr13:110638818 | T | A | 1 | a0002c0002t0031 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 290 | chr13 | 110638818 | ||||||
| chr13:110638845 | G | A | 9 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(6): Show |
40 | HG00438.hp2 HG00639.hp2 HG01891.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 317 | chr13 | 110638845 | ||||||
| chr13:110638871 | G | T | 1 | a0001c0001t0024 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 343 | chr13 | 110638871 | ||||||
| chr13:110638900 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*372G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 372 | chr13 | 110638900 | ||||||
| chr13:110638909 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*381G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 381 | chr13 | 110638909 | ||||||
| chr13:110638912 | CCT | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
164 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*386_*387delTC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 386 | INFO_REALIGN_3_PRIME | chr13 | 110638912 | |||||
| chr13:110638917 | T | C | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
164 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*389T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 389 | chr13 | 110638917 | ||||||
| chr13:110638919 | T | C | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
143 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*391T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 391 | chr13 | 110638919 | ||||||
| chr13:110638919 | T | G | 4 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0016 others(1): Show |
25 | HG00642.hp2 HG01884.hp1 HG01993.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*391T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 391 | chr13 | 110638919 | ||||||
| chr13:110638969 | C | T | 1 | a0004c0004t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 441 | chr13 | 110638969 | ||||||
| chr13:110638992 | T | G | 1 | a0001c0001t0012 | 2 | NA18951.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*464T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 464 | chr13 | 110638992 | ||||||
| chr13:110639191 | T | C | 3 | a0001c0001t0004 a0001c0001t0017 a0004c0004t0021 |
30 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*663T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 663 | chr13 | 110639191 | ||||||
| chr13:110639275 | G | A | 2 | a0001c0001t0004 a0001c0001t0017 |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*747G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 747 | chr13 | 110639275 | ||||||
| chr13:110639293 | C | T | 1 | a0001c0001t0035 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 765 | chr13 | 110639293 | ||||||
| chr13:110639304 | C | A | 2 | a0001c0001t0006 a0001c0010t0006 |
22 | HG00609.hp1 HG01123.hp1 HG01346.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*776C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 776 | chr13 | 110639304 | ||||||
| chr13:110639310 | C | T | 1 | a0004c0004t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*782C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 782 | chr13 | 110639310 | ||||||
| chr13:110639423 | C | T | 2 | a0001c0001t0016 a0001c0001t0034 |
2 | HG00735.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*895C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 895 | chr13 | 110639423 | ||||||
| chr13:110639424 | G | A | 3 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0020 |
4 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 896 | chr13 | 110639424 | ||||||
| chr13:110639432 | A | T | 1 | a0002c0002t0013 | 2 | NA19075.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*904A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 904 | chr13 | 110639432 | ||||||
| chr13:110639471 | C | T | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0024 others(2): Show |
58 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*943C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 943 | chr13 | 110639471 | ||||||
| chr13:110639472 | G | T | 3 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0016 |
24 | HG00642.hp2 HG01884.hp1 HG01993.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*944G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 944 | chr13 | 110639472 | ||||||
| chr13:110639594 | C | T | 1 | a0002c0002t0033 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1066 | chr13 | 110639594 | ||||||
| chr13:110639602 | C | T | 1 | a0001c0001t0009 | 3 | HG01891.hp2 HG02258.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1074C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1074 | chr13 | 110639602 | ||||||
| chr13:110639651 | C | T | 1 | a0001c0001t0007 | 11 | HG00423.hp1 HG02056.hp1 HG02080.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1123C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1123 | chr13 | 110639651 | ||||||
| chr13:110639697 | A | G | 21 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(18): Show |
140 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1169A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1169 | chr13 | 110639697 | ||||||
| chr13:110639846 | G | C | 1 | a0001c0001t0032 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1318G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1318 | chr13 | 110639846 | ||||||
| chr13:110639884 | T | C | 1 | a0004c0004t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1356 | chr13 | 110639884 | ||||||
| chr13:110639938 | C | T | 2 | a0001c0001t0011 a0001c0001t0020 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1410C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 10/10 | 1410 | chr13 | 110639938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:110615713 | C | T | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.46+66C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615713 | |||||||
| chr13:110615809 | G | A | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.46+162G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615809 | |||||||
| chr13:110615814 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.46+167G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615814 | |||||||
| chr13:110615849 | G | A | 68 | a0001c0001t0001g0060 a0001c0001t0001g0079 a0001c0001t0001g0098 others(65): Show |
109 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.46+202G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615849 | |||||||
| chr13:110615922 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.46+275G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615922 | |||||||
| chr13:110615956 | T | TGACAGAG others(1): Show |
5 | a0001c0001t0006g0008 a0001c0001t0006g0099 a0001c0001t0006g0100 others(2): Show |
10 | HG00609.hp1 NA18940.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+311_46+318dupAC others(6): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110615956 | ||||||
| chr13:110615993 | G | C | 13 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0008g0024 others(10): Show |
14 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.46+346G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110615993 | |||||||
| chr13:110616069 | C | T | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.46+422C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616069 | |||||||
| chr13:110616170 | C | G | 1 | a0001c0001t0009g0031 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.46+523C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616170 | |||||||
| chr13:110616286 | T | C | 100 | a0001c0001t0001g0018 a0001c0001t0001g0060 a0001c0001t0001g0079 others(97): Show |
172 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.46+639T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616286 | |||||||
| chr13:110616345 | C | G | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.46+698C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616345 | |||||||
| chr13:110616388 | C | A | 1 | a0001c0001t0004g0025 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.46+741C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616388 | |||||||
| chr13:110616419 | G | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.46+772G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616419 | |||||||
| chr13:110616645 | G | T | 1 | a0006c0011t0001g0203 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.46+998G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616645 | |||||||
| chr13:110616793 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.46+1146T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616793 | |||||||
| chr13:110616930 | C | T | 65 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(62): Show |
106 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.46+1283C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110616930 | |||||||
| chr13:110617231 | T | G | 1 | a0001c0001t0002g0103 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.46+1584T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617231 | |||||||
| chr13:110617393 | C | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0121 others(3): Show |
14 | HG00738.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.46+1746C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617393 | |||||||
| chr13:110617394 | G | A | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+1747G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617394 | |||||||
| chr13:110617455 | G | A | 1 | a0007c0007t0025g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.46+1808G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617455 | |||||||
| chr13:110617555 | C | T | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+1908C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617555 | |||||||
| chr13:110617657 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.46+2010C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617657 | |||||||
| chr13:110617667 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.46+2020C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617667 | |||||||
| chr13:110617681 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.46+2034A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617681 | |||||||
| chr13:110617703 | A | C | 1 | a0002c0002t0001g0199 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.46+2056A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617703 | |||||||
| chr13:110617727 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+2080C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617727 | |||||||
| chr13:110617736 | G | A | 1 | a0005c0005t0001g0035 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.46+2089G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617736 | |||||||
| chr13:110617845 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.46+2198G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110617845 | |||||||
| chr13:110618016 | T | C | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+2369T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618016 | |||||||
| chr13:110618025 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.46+2378A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618025 | |||||||
| chr13:110618046 | A | G | 2 | a0001c0001t0004g0029 a0001c0001t0004g0087 |
3 | HG00741.hp1 HG01516.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.46+2399A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618046 | |||||||
| chr13:110618271 | G | GC | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+2625dupC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110618271 | ||||||
| chr13:110618309 | G | A | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.46+2662G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618309 | |||||||
| chr13:110618381 | A | C | 1 | a0002c0002t0001g0196 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.46+2734A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618381 | |||||||
| chr13:110618391 | C | T | 14 | a0001c0001t0001g0079 a0003c0003t0003g0002 a0003c0003t0003g0027 others(11): Show |
31 | HG00438.hp2 HG00639.hp2 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+2744C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618391 | |||||||
| chr13:110618415 | G | A | 65 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(62): Show |
106 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.46+2768G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618415 | |||||||
| chr13:110618476 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46+2829A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618476 | |||||||
| chr13:110618477 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.46+2830G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618477 | |||||||
| chr13:110618529 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.46+2882C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618529 | |||||||
| chr13:110618533 | T | C | 14 | a0001c0001t0001g0079 a0003c0003t0003g0002 a0003c0003t0003g0027 others(11): Show |
31 | HG00438.hp2 HG00639.hp2 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.46+2886T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618533 | |||||||
| chr13:110618578 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.46+2931G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618578 | |||||||
| chr13:110618621 | C | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.46+2974C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618621 | |||||||
| chr13:110618688 | T | A | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+3041T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618688 | |||||||
| chr13:110618690 | A | T | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.46+3043A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618690 | |||||||
| chr13:110618724 | A | G | 1 | a0001c0001t0007g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.46+3077A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618724 | |||||||
| chr13:110618753 | CAAA | C | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+3109_46+3111del others(3): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110618753 | ||||||
| chr13:110618792 | C | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0193 |
3 | NA18971.hp2 NA19000.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.46+3145C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618792 | |||||||
| chr13:110618799 | T | A | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+3152T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618799 | |||||||
| chr13:110618817 | C | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.46+3170C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618817 | |||||||
| chr13:110618832 | C | A | 1 | a0003c0003t0003g0078 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.46+3185C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618832 | |||||||
| chr13:110618898 | G | T | 1 | a0001c0001t0030g0192 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.46+3251G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618898 | |||||||
| chr13:110618923 | G | A | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.46+3276G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618923 | |||||||
| chr13:110618930 | G | C | 2 | a0001c0001t0008g0051 a0001c0001t0008g0052 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.46+3283G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110618930 | |||||||
| chr13:110619028 | C | G | 64 | a0001c0001t0001g0079 a0001c0001t0003g0053 a0001c0001t0003g0102 others(61): Show |
105 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.47-3188C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619028 | |||||||
| chr13:110619150 | C | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-3066C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619150 | |||||||
| chr13:110619171 | A | G | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-3045A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619171 | |||||||
| chr13:110619188 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-3028G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619188 | |||||||
| chr13:110619281 | T | C | 2 | a0001c0001t0003g0053 a0001c0001t0003g0102 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.47-2935T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619281 | |||||||
| chr13:110619396 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG01167.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.47-2820A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619396 | |||||||
| chr13:110619432 | C | G | 14 | a0001c0001t0001g0079 a0003c0003t0003g0002 a0003c0003t0003g0027 others(11): Show |
31 | HG00438.hp2 HG00639.hp2 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.47-2784C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619432 | |||||||
| chr13:110619542 | C | T | 4 | a0001c0001t0010g0074 a0001c0001t0010g0076 a0001c0001t0010g0077 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-2674C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619542 | |||||||
| chr13:110619693 | C | T | 1 | a0001c0001t0034g0189 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.47-2523C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619693 | |||||||
| chr13:110619769 | C | A | 2 | a0001c0001t0008g0024 a0001c0001t0008g0054 |
3 | HG02486.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.47-2447C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619769 | |||||||
| chr13:110619841 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0200 |
2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.47-2375C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619841 | |||||||
| chr13:110619865 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.47-2351C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619865 | |||||||
| chr13:110619954 | G | A | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-2262G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110619954 | |||||||
| chr13:110620157 | G | C | 4 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(1): Show |
4 | HG01099.hp1 HG01358.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-2059G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620157 | |||||||
| chr13:110620289 | A | G | 95 | a0001c0001t0001g0079 a0001c0001t0002g0003 a0001c0001t0002g0011 others(92): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.47-1927A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620289 | |||||||
| chr13:110620320 | A | G | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-1896A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620320 | |||||||
| chr13:110620528 | C | T | 1 | a0001c0001t0010g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.47-1688C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620528 | |||||||
| chr13:110620537 | A | G | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
165 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.47-1679A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620537 | |||||||
| chr13:110620578 | C | CA | 27 | a0001c0001t0001g0036 a0001c0001t0001g0131 a0001c0001t0001g0132 others(24): Show |
32 | HG00423.hp2 HG00621.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.47-1620dupA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110620578 | ||||||
| chr13:110620578 | C | CAA | 40 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(37): Show |
81 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.47-1621_47-1620dup others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110620578 | ||||||
| chr13:110620578 | CA | C | 27 | a0001c0001t0001g0048 a0001c0001t0001g0124 a0001c0001t0001g0183 others(24): Show |
45 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.47-1620delA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110620578 | ||||||
| chr13:110620606 | T | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.47-1610T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620606 | |||||||
| chr13:110620669 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-1547G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620669 | |||||||
| chr13:110620677 | A | T | 19 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0010g0074 others(16): Show |
36 | HG00438.hp2 HG00639.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.47-1539A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620677 | |||||||
| chr13:110620937 | C | A | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1279C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620937 | |||||||
| chr13:110620940 | T | C | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1276T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620940 | |||||||
| chr13:110620942 | G | T | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1274G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620942 | |||||||
| chr13:110620945 | C | T | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1271C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620945 | |||||||
| chr13:110620946 | A | G | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1270A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620946 | |||||||
| chr13:110620948 | A | T | 1 | a0001c0001t0006g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.47-1268A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620948 | |||||||
| chr13:110620960 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0182 |
9 | HG01257.hp2 HG01258.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.47-1256C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110620960 | |||||||
| chr13:110621028 | A | G | 4 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0057 others(1): Show |
4 | HG01192.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-1188A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621028 | |||||||
| chr13:110621034 | G | T | 4 | a0002c0002t0001g0046 a0002c0002t0001g0137 a0002c0002t0001g0180 others(1): Show |
5 | HG01109.hp2 HG03491.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-1182G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621034 | |||||||
| chr13:110621078 | A | G | 2 | a0001c0001t0003g0053 a0001c0001t0003g0102 |
2 | HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.47-1138A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621078 | |||||||
| chr13:110621157 | G | A | 50 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(47): Show |
78 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-1059G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621157 | |||||||
| chr13:110621165 | A | C | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-1051A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621165 | |||||||
| chr13:110621374 | A | G | 64 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(61): Show |
106 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.47-842A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621374 | |||||||
| chr13:110621416 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0002g0113 a0001c0001t0002g0114 others(3): Show |
10 | HG00738.hp2 HG01069.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-800C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621416 | |||||||
| chr13:110621508 | C | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.47-708C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621508 | |||||||
| chr13:110621716 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.47-500G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621716 | |||||||
| chr13:110621803 | G | A | 3 | a0001c0001t0004g0029 a0001c0001t0004g0038 a0001c0001t0004g0087 |
5 | HG00741.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-413G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621803 | |||||||
| chr13:110621841 | C | T | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.47-375C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621841 | |||||||
| chr13:110621884 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0138 |
2 | HG02293.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.47-332G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621884 | |||||||
| chr13:110621919 | G | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.47-297G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621919 | |||||||
| chr13:110621921 | T | C | 19 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0010g0074 others(16): Show |
36 | HG00438.hp2 HG00639.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.47-295T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621921 | |||||||
| chr13:110621969 | G | T | 6 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0055 others(3): Show |
6 | HG01192.hp2 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-247G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621969 | |||||||
| chr13:110621986 | C | T | 1 | a0001c0001t0008g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47-230C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110621986 | |||||||
| chr13:110622035 | A | G | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.47-181A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110622035 | |||||||
| chr13:110622036 | GAA | G | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-171_47-170delAA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr13 | 110622036 | ||||||
| chr13:110622120 | G | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.47-96G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 1/9 | chr13 | 110622120 | |||||||
| chr13:110622528 | A | G | 1 | a0001c0001t0005g0030 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.197+162A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622528 | |||||||
| chr13:110622565 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.197+199C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622565 | |||||||
| chr13:110622592 | C | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(90): Show |
163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.197+226C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622592 | |||||||
| chr13:110622604 | A | G | 2 | a0002c0002t0001g0190 a0002c0002t0001g0191 |
2 | HG01167.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.197+238A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622604 | |||||||
| chr13:110622684 | A | G | 1 | a0001c0001t0011g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.197+318A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622684 | |||||||
| chr13:110622772 | C | G | 1 | a0001c0001t0028g0187 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.197+406C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622772 | |||||||
| chr13:110622796 | T | G | 4 | a0001c0001t0010g0074 a0001c0001t0010g0076 a0001c0001t0010g0077 others(1): Show |
4 | HG01891.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+430T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622796 | |||||||
| chr13:110622829 | G | T | 3 | a0001c0001t0005g0005 a0001c0001t0005g0095 a0001c0001t0005g0096 |
10 | HG00642.hp2 HG01993.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+463G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622829 | |||||||
| chr13:110622846 | T | G | 1 | a0001c0001t0016g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197+480T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110622846 | |||||||
| chr13:110623022 | G | A | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.197+656G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623022 | |||||||
| chr13:110623106 | G | C | 8 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(5): Show |
9 | HG01192.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+740G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623106 | |||||||
| chr13:110623112 | G | A | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.197+746G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623112 | |||||||
| chr13:110623227 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01943.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.197+861C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623227 | |||||||
| chr13:110623244 | T | C | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.197+878T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623244 | |||||||
| chr13:110623271 | G | T | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.197+905G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623271 | |||||||
| chr13:110623298 | T | C | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.197+932T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623298 | |||||||
| chr13:110623434 | C | G | 4 | a0001c0001t0008g0024 a0001c0001t0008g0054 a0001c0001t0019g0049 others(1): Show |
5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.198-800C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623434 | |||||||
| chr13:110623514 | C | G | 13 | a0003c0003t0003g0002 a0003c0003t0003g0027 a0003c0003t0003g0028 others(10): Show |
30 | HG00438.hp2 HG00639.hp2 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.198-720C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623514 | |||||||
| chr13:110623524 | G | A | 1 | a0005c0005t0001g0035 | 2 | HG03688.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.198-710G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623524 | |||||||
| chr13:110623545 | C | G | 2 | a0003c0003t0003g0085 a0003c0003t0003g0086 |
2 | NA18956.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.198-689C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623545 | |||||||
| chr13:110623726 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0055 others(3): Show |
6 | HG01192.hp2 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-508G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623726 | |||||||
| chr13:110623745 | G | A | 1 | a0001c0001t0006g0100 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.198-489G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623745 | |||||||
| chr13:110623757 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.198-477T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623757 | |||||||
| chr13:110623776 | G | A | 31 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
60 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.198-458G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623776 | |||||||
| chr13:110623822 | C | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(54): Show |
101 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.198-412C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623822 | |||||||
| chr13:110623861 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.198-373G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623861 | |||||||
| chr13:110623871 | G | GC | 3 | a0001c0001t0010g0076 a0001c0001t0010g0077 a0001c0001t0022g0075 |
3 | HG01891.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.198-362dupC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 110623871 | ||||||
| chr13:110623926 | C | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.198-308C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623926 | |||||||
| chr13:110623975 | C | G | 15 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(12): Show |
29 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.198-259C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110623975 | |||||||
| chr13:110623993 | ACT | A | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.198-238_198-237del others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 110623993 | ||||||
| chr13:110624002 | C | CA | 6 | a0001c0001t0001g0039 a0001c0001t0004g0026 a0001c0001t0007g0039 others(3): Show |
7 | HG00140.hp2 HG01928.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-214dupA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 110624002 | ||||||
| chr13:110624002 | CA | C | 47 | a0001c0001t0001g0177 a0001c0001t0002g0003 a0001c0001t0002g0011 others(44): Show |
75 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.198-214delA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 110624002 | ||||||
| chr13:110624002 | CAA | C | 13 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(10): Show |
27 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.198-215_198-214del others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr13 | 110624002 | ||||||
| chr13:110624047 | G | A | 2 | a0001c0001t0008g0051 a0001c0001t0008g0052 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.198-187G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110624047 | |||||||
| chr13:110624081 | T | C | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.198-153T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 2/9 | chr13 | 110624081 | |||||||
| chr13:110624379 | ATATCT | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.243+103_243+107del others(5): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr13 | 110624379 | ||||||
| chr13:110624380 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.243+101T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624380 | |||||||
| chr13:110624481 | A | G | 129 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0170 others(126): Show |
212 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.243+202A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624481 | |||||||
| chr13:110624488 | C | T | 1 | a0001c0009t0008g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.243+209C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624488 | |||||||
| chr13:110624495 | T | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(54): Show |
101 | HG00609.hp1 HG00621.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.243+216T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624495 | |||||||
| chr13:110624502 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.243+223A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624502 | |||||||
| chr13:110624583 | C | T | 2 | a0001c0001t0004g0063 a0001c0001t0004g0119 |
2 | HG01243.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.243+304C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624583 | |||||||
| chr13:110624674 | C | G | 1 | a0001c0001t0009g0031 | 2 | HG02258.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.243+395C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624674 | |||||||
| chr13:110624686 | T | G | 1 | a0002c0002t0001g0141 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.243+407T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624686 | |||||||
| chr13:110624698 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.243+419G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624698 | |||||||
| chr13:110624721 | C | T | 1 | a0001c0008t0001g0123 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.243+442C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624721 | |||||||
| chr13:110624753 | C | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.244-437C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624753 | |||||||
| chr13:110624765 | A | G | 5 | a0001c0001t0001g0016 a0002c0002t0001g0127 a0002c0002t0001g0128 others(2): Show |
8 | HG00323.hp2 HG01099.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-425A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624765 | |||||||
| chr13:110624844 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.244-346G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624844 | |||||||
| chr13:110624844 | G | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.244-346G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624844 | |||||||
| chr13:110624854 | C | G | 1 | a0001c0001t0016g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-336C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624854 | |||||||
| chr13:110624899 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.244-291C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110624899 | |||||||
| chr13:110625050 | C | G | 1 | a0007c0007t0025g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244-140C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110625050 | |||||||
| chr13:110625150 | G | A | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.244-40G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110625150 | |||||||
| chr13:110625167 | G | A | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.244-23G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 3/9 | chr13 | 110625167 | |||||||
| chr13:110625296 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.332+18G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625296 | |||||||
| chr13:110625313 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.332+35C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625313 | |||||||
| chr13:110625363 | TGATG | T | 15 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(12): Show |
29 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.332+89_332+92delGG others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 110625363 | ||||||
| chr13:110625366 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.332+88T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625366 | |||||||
| chr13:110625401 | T | C | 2 | a0001c0001t0008g0024 a0001c0001t0008g0054 |
3 | HG02486.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.332+123T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625401 | |||||||
| chr13:110625510 | G | A | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.332+232G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625510 | |||||||
| chr13:110625592 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.332+314A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625592 | |||||||
| chr13:110625738 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.332+460G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625738 | |||||||
| chr13:110625851 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0165 |
4 | HG02056.hp2 NA18612.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.332+573C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625851 | |||||||
| chr13:110625921 | G | C | 1 | a0001c0001t0004g0087 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.332+643G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625921 | |||||||
| chr13:110625924 | C | T | 2 | a0001c0001t0005g0096 a0001c0001t0026g0111 |
2 | HG02273.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.332+646C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625924 | |||||||
| chr13:110625963 | A | G | 122 | a0001c0001t0001g0014 a0001c0001t0001g0162 a0001c0001t0001g0164 others(119): Show |
203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.332+685A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625963 | |||||||
| chr13:110625989 | A | G | 1 | a0001c0001t0004g0073 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.332+711A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625989 | |||||||
| chr13:110625990 | C | T | 25 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(22): Show |
35 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.332+712C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110625990 | |||||||
| chr13:110626033 | C | T | 1 | a0001c0001t0004g0072 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.332+755C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626033 | |||||||
| chr13:110626035 | C | T | 2 | a0001c0001t0004g0071 a0001c0001t0004g0073 |
2 | HG00280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.332+757C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626035 | |||||||
| chr13:110626049 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.332+771C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626049 | |||||||
| chr13:110626074 | A | G | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.332+796A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626074 | |||||||
| chr13:110626108 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.332+830G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626108 | |||||||
| chr13:110626153 | G | T | 3 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0004c0004t0008g0058 |
3 | HG02622.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.332+875G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626153 | |||||||
| chr13:110626167 | T | TA | 12 | a0001c0001t0005g0005 a0001c0001t0005g0017 a0001c0001t0005g0030 others(9): Show |
23 | HG00642.hp2 HG01891.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.332+892dupA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 110626167 | ||||||
| chr13:110626179 | C | G | 94 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0020 others(91): Show |
163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.332+901C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626179 | |||||||
| chr13:110626198 | C | G | 1 | a0007c0007t0025g0059 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.332+920C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626198 | |||||||
| chr13:110626254 | GC | G | 45 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(42): Show |
75 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.332+978delC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr13 | 110626254 | ||||||
| chr13:110626324 | G | A | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.332+1046G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626324 | |||||||
| chr13:110626351 | T | G | 65 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(62): Show |
118 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.332+1073T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626351 | |||||||
| chr13:110626410 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333-1029G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626410 | |||||||
| chr13:110626724 | T | C | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333-715T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626724 | |||||||
| chr13:110626859 | C | T | 39 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(36): Show |
68 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.333-580C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626859 | |||||||
| chr13:110626894 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0165 a0001c0001t0019g0049 |
5 | HG02056.hp2 HG02922.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.333-545G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626894 | |||||||
| chr13:110626976 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.333-463T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110626976 | |||||||
| chr13:110627220 | C | T | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.333-219C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110627220 | |||||||
| chr13:110627272 | A | T | 1 | a0001c0001t0002g0104 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.333-167A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 4/9 | chr13 | 110627272 | |||||||
| chr13:110627596 | C | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+49C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627596 | |||||||
| chr13:110627655 | T | C | 43 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(40): Show |
73 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.441+108T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627655 | |||||||
| chr13:110627731 | G | C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.441+184G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627731 | |||||||
| chr13:110627742 | C | T | 1 | a0001c0001t0004g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.441+195C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627742 | |||||||
| chr13:110627937 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.441+390G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627937 | |||||||
| chr13:110627959 | G | A | 12 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(9): Show |
13 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+412G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110627959 | |||||||
| chr13:110628026 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01943.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.441+479C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628026 | |||||||
| chr13:110628032 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.441+485G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628032 | |||||||
| chr13:110628122 | C | T | 1 | a0004c0004t0008g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.441+575C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628122 | |||||||
| chr13:110628156 | G | A | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+609G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628156 | |||||||
| chr13:110628284 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.441+737G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628284 | |||||||
| chr13:110628324 | C | T | 2 | a0002c0002t0001g0175 a0002c0002t0033g0174 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.441+777C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628324 | |||||||
| chr13:110628365 | G | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+818G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628365 | |||||||
| chr13:110628391 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.441+844C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628391 | |||||||
| chr13:110628395 | C | T | 1 | a0001c0001t0007g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.441+848C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628395 | |||||||
| chr13:110628512 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.441+965G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628512 | |||||||
| chr13:110628565 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.441+1018C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628565 | |||||||
| chr13:110628758 | A | G | 97 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(94): Show |
168 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.441+1211A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628758 | |||||||
| chr13:110628836 | C | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+1289C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628836 | |||||||
| chr13:110628905 | C | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+1358C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628905 | |||||||
| chr13:110628944 | G | A | 6 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0055 others(3): Show |
6 | HG01192.hp2 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+1397G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628944 | |||||||
| chr13:110628944 | G | GGCCGGGC others(310): Show |
1 | a0001c0001t0011g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+1397_441+1398i others(319): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628944 | |||||||
| chr13:110628944 | G | GGCCGGGC others(309): Show |
2 | a0001c0001t0011g0204 a0001c0001t0020g0205 |
2 | HG02055.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.441+1397_441+1398i others(318): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628944 | |||||||
| chr13:110628959 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.441+1412G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110628959 | |||||||
| chr13:110629111 | C | T | 2 | a0001c0001t0010g0076 a0001c0001t0022g0075 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.441+1564C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629111 | |||||||
| chr13:110629138 | C | T | 1 | a0001c0001t0005g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441+1591C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629138 | |||||||
| chr13:110629166 | TA | T | 31 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
60 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+1620delA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629166 | |||||||
| chr13:110629169 | G | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+1622G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629169 | |||||||
| chr13:110629253 | C | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+1706C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629253 | |||||||
| chr13:110629258 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.441+1711G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629258 | |||||||
| chr13:110629266 | T | C | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.441+1719T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629266 | |||||||
| chr13:110629267 | G | T | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+1720G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629267 | |||||||
| chr13:110629271 | GC | G | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+1725delC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629271 | |||||||
| chr13:110629407 | A | G | 1 | a0003c0003t0003g0082 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.441+1860A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629407 | |||||||
| chr13:110629571 | G | T | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.441+2024G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629571 | |||||||
| chr13:110629611 | ATATT | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0113 a0001c0001t0002g0115 others(2): Show |
9 | HG00738.hp2 HG01255.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+2067_441+2070d others(6): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 110629611 | ||||||
| chr13:110629644 | A | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+2097A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629644 | |||||||
| chr13:110629873 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0132 a0001c0001t0001g0162 |
5 | NA18947.hp2 NA18973.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+2326G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110629873 | |||||||
| chr13:110630090 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0165 |
4 | HG02056.hp2 NA18612.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2543C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630090 | |||||||
| chr13:110630091 | G | T | 1 | a0001c0001t0019g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+2544G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630091 | |||||||
| chr13:110630215 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.441+2668G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630215 | |||||||
| chr13:110630259 | C | A | 1 | a0001c0001t0018g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441+2712C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630259 | |||||||
| chr13:110630262 | T | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+2715T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630262 | |||||||
| chr13:110630271 | G | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.441+2724G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630271 | |||||||
| chr13:110630287 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+2740C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630287 | |||||||
| chr13:110630307 | C | T | 1 | a0001c0001t0026g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441+2760C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630307 | |||||||
| chr13:110630329 | CTT | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0183 |
3 | HG01346.hp1 HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.441+2784_441+2785d others(4): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 110630329 | ||||||
| chr13:110630402 | T | A | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.441+2855T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630402 | |||||||
| chr13:110630404 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.441+2857T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630404 | |||||||
| chr13:110630462 | C | T | 1 | a0002c0002t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.441+2915C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630462 | |||||||
| chr13:110630522 | A | G | 12 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(9): Show |
13 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+2975A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630522 | |||||||
| chr13:110630524 | C | G | 1 | a0003c0003t0003g0081 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+2977C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630524 | |||||||
| chr13:110630717 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.441+3170G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630717 | |||||||
| chr13:110630787 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.441+3240A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630787 | |||||||
| chr13:110630811 | G | A | 2 | a0001c0001t0006g0099 a0001c0001t0006g0101 |
2 | NA18940.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.441+3264G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110630811 | |||||||
| chr13:110631150 | G | A | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.442-3395G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631150 | |||||||
| chr13:110631189 | C | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
60 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.442-3356C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631189 | |||||||
| chr13:110631201 | G | T | 11 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(8): Show |
12 | HG01192.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-3344G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631201 | |||||||
| chr13:110631244 | G | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0135 others(1): Show |
6 | HG01261.hp1 HG03239.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-3301G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631244 | |||||||
| chr13:110631361 | A | G | 31 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
60 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.442-3184A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631361 | |||||||
| chr13:110631415 | C | T | 1 | a0003c0003t0003g0086 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.442-3130C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631415 | |||||||
| chr13:110631462 | A | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(39): Show |
72 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.442-3083A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631462 | |||||||
| chr13:110631575 | T | C | 2 | a0001c0001t0008g0024 a0001c0001t0008g0054 |
3 | HG02486.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.442-2970T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631575 | |||||||
| chr13:110631613 | A | C | 53 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(50): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.442-2932A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631613 | |||||||
| chr13:110631881 | C | T | 1 | a0001c0001t0004g0025 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.442-2664C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110631881 | |||||||
| chr13:110632020 | G | A | 18 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(15): Show |
28 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-2525G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632020 | |||||||
| chr13:110632021 | G | C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-2524G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632021 | |||||||
| chr13:110632057 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0142 a0001c0001t0001g0201 |
9 | HG00280.hp2 HG01192.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-2488C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632057 | |||||||
| chr13:110632065 | CTCGCGGT others(122): Show |
C | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-2452_442-2324d others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 110632065 | ||||||
| chr13:110632070 | G | A | 57 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(54): Show |
98 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.442-2475G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632070 | |||||||
| chr13:110632099 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.442-2446G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632099 | |||||||
| chr13:110632110 | G | A | 1 | a0002c0002t0001g0173 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.442-2435G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632110 | |||||||
| chr13:110632183 | G | A | 1 | a0001c0001t0014g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-2362G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632183 | |||||||
| chr13:110632187 | A | G | 1 | a0001c0001t0014g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.442-2358A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632187 | |||||||
| chr13:110632222 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442-2323C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632222 | |||||||
| chr13:110632228 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.442-2317G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632228 | |||||||
| chr13:110632246 | C | T | 1 | a0001c0001t0017g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442-2299C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632246 | |||||||
| chr13:110632252 | G | A | 1 | a0001c0001t0017g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442-2293G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632252 | |||||||
| chr13:110632298 | C | T | 3 | a0001c0001t0008g0024 a0001c0001t0008g0054 a0004c0004t0021g0050 |
4 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-2247C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632298 | |||||||
| chr13:110632299 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442-2246G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632299 | |||||||
| chr13:110632395 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.442-2150G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632395 | |||||||
| chr13:110632412 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(26): Show |
58 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.442-2133C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632412 | |||||||
| chr13:110632465 | G | A | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-2080G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632465 | |||||||
| chr13:110632492 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.442-2053G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632492 | |||||||
| chr13:110632551 | A | G | 1 | a0001c0001t0005g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442-1994A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632551 | |||||||
| chr13:110632594 | C | G | 56 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(53): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.442-1951C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632594 | |||||||
| chr13:110632595 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.442-1950G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632595 | |||||||
| chr13:110632620 | C | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0193 |
3 | NA18971.hp2 NA19000.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.442-1925C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632620 | |||||||
| chr13:110632645 | G | A | 16 | a0001c0001t0003g0053 a0001c0001t0004g0070 a0001c0001t0005g0005 others(13): Show |
30 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.442-1900G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632645 | |||||||
| chr13:110632726 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.442-1819C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632726 | |||||||
| chr13:110632751 | C | G | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-1794C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632751 | |||||||
| chr13:110632751 | C | T | 1 | a0001c0001t0010g0077 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.442-1794C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632751 | |||||||
| chr13:110632755 | GA | G | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-1789delA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632755 | |||||||
| chr13:110632807 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442-1738T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632807 | |||||||
| chr13:110632815 | TTCACAAA others(34): Show |
T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(26): Show |
58 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.442-1712_442-1672d others(43): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 110632815 | ||||||
| chr13:110632844 | C | G | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.442-1701C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632844 | |||||||
| chr13:110632933 | A | C | 2 | a0001c0012t0001g0042 a0002c0013t0001g0042 |
2 | HG01099.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.442-1612A>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632933 | |||||||
| chr13:110632940 | C | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(11): Show |
28 | HG00642.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.442-1605C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632940 | |||||||
| chr13:110632969 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.442-1576C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632969 | |||||||
| chr13:110632979 | C | T | 55 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(52): Show |
95 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.442-1566C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110632979 | |||||||
| chr13:110633016 | G | A | 4 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0019g0049 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1529G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633016 | |||||||
| chr13:110633020 | C | T | 8 | a0001c0001t0008g0024 a0001c0001t0008g0051 a0001c0001t0008g0052 others(5): Show |
9 | HG01192.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-1525C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633020 | |||||||
| chr13:110633028 | C | T | 1 | a0001c0001t0006g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442-1517C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633028 | |||||||
| chr13:110633052 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.442-1493C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633052 | |||||||
| chr13:110633054 | A | T | 1 | a0001c0001t0002g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.442-1491A>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633054 | |||||||
| chr13:110633090 | G | C | 1 | a0001c0001t0020g0205 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442-1455G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633090 | |||||||
| chr13:110633102 | C | T | 3 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0020g0205 |
3 | HG02055.hp2 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.442-1443C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633102 | |||||||
| chr13:110633108 | G | A | 1 | a0002c0002t0001g0190 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.442-1437G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633108 | |||||||
| chr13:110633112 | A | G | 2 | a0001c0001t0008g0024 a0001c0001t0008g0054 |
3 | HG02486.hp1 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.442-1433A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633112 | |||||||
| chr13:110633126 | G | T | 1 | a0001c0001t0027g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-1419G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633126 | |||||||
| chr13:110633149 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.442-1396G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633149 | |||||||
| chr13:110633155 | CA | C | 1 | a0002c0002t0001g0015 | 4 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-1389delA | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633155 | |||||||
| chr13:110633162 | C | T | 52 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(49): Show |
93 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.442-1383C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633162 | |||||||
| chr13:110633211 | A | G | 97 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(94): Show |
168 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.442-1334A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633211 | |||||||
| chr13:110633218 | C | T | 1 | a0001c0001t0010g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-1327C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633218 | |||||||
| chr13:110633256 | T | C | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.442-1289T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633256 | |||||||
| chr13:110633281 | T | G | 1 | a0001c0001t0022g0075 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.442-1264T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633281 | |||||||
| chr13:110633312 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.442-1233C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633312 | |||||||
| chr13:110633370 | C | T | 53 | a0001c0001t0001g0200 a0001c0001t0003g0053 a0001c0001t0003g0102 others(50): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.442-1175C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633370 | |||||||
| chr13:110633379 | T | C | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-1166T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633379 | |||||||
| chr13:110633460 | G | T | 56 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(53): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.442-1085G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633460 | |||||||
| chr13:110633470 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-1075G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633470 | |||||||
| chr13:110633490 | T | C | 31 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
60 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.442-1055T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633490 | |||||||
| chr13:110633510 | A | G | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.442-1035A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633510 | |||||||
| chr13:110633632 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.442-913T>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633632 | |||||||
| chr13:110633642 | G | A | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-903G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633642 | |||||||
| chr13:110633698 | TGGCTCAT others(1): Show |
T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-846_442-839del others(8): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633698 | |||||||
| chr13:110633758 | GT | G | 74 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(71): Show |
135 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(132): Show |
intron_variant | MODIFIER | c.442-775delT | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr13 | 110633758 | ||||||
| chr13:110633836 | G | A | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-709G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633836 | |||||||
| chr13:110633852 | G | A | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-693G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633852 | |||||||
| chr13:110633938 | C | G | 1 | a0004c0004t0008g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-607C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633938 | |||||||
| chr13:110633971 | T | C | 96 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(93): Show |
167 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.442-574T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110633971 | |||||||
| chr13:110634049 | T | G | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.442-496T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634049 | |||||||
| chr13:110634199 | G | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.442-346G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634199 | |||||||
| chr13:110634234 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.442-311G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634234 | |||||||
| chr13:110634245 | C | T | 19 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(16): Show |
29 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-300C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634245 | |||||||
| chr13:110634260 | G | A | 53 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(50): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.442-285G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634260 | |||||||
| chr13:110634411 | C | T | 1 | a0001c0001t0006g0106 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.442-134C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 5/9 | chr13 | 110634411 | |||||||
| chr13:110634643 | C | T | 2 | a0002c0002t0001g0137 a0002c0002t0001g0181 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.493-29C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 6/9 | chr13 | 110634643 | |||||||
| chr13:110634665 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.493-7T>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 6/9 | chr13 | 110634665 | |||||||
| chr13:110634874 | G | GAC | 26 | a0001c0001t0001g0170 a0002c0002t0001g0013 a0002c0002t0001g0015 others(23): Show |
33 | HG00597.hp1 HG01099.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.597+103_597+104dup others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 110634874 | ||||||
| chr13:110634905 | C | G | 2 | a0001c0001t0010g0076 a0001c0001t0022g0075 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.597+129C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634905 | |||||||
| chr13:110634909 | C | T | 1 | a0001c0001t0001g0044 | 2 | HG01261.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.597+133C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634909 | |||||||
| chr13:110634910 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.597+134G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634910 | |||||||
| chr13:110634916 | C | T | 1 | a0001c0001t0016g0089 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.597+140C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634916 | |||||||
| chr13:110634918 | C | T | 1 | a0002c0002t0013g0171 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.597+142C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634918 | |||||||
| chr13:110634957 | T | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.597+181T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634957 | |||||||
| chr13:110634997 | C | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.597+221C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110634997 | |||||||
| chr13:110635029 | TTGTC | T | 1 | a0002c0002t0001g0015 | 4 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.597+257_597+260del others(4): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 110635029 | ||||||
| chr13:110635033 | CTG | C | 52 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(49): Show |
93 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.597+261_597+262del others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr13 | 110635033 | ||||||
| chr13:110635120 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0149 a0001c0001t0001g0164 others(1): Show |
15 | HG02155.hp2 NA18944.hp1 NA18951.hp2 others(12): Show |
intron_variant | MODIFIER | c.597+344C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110635120 | |||||||
| chr13:110635196 | C | T | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598-272C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110635196 | |||||||
| chr13:110635205 | C | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(26): Show |
58 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.598-263C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110635205 | |||||||
| chr13:110635413 | C | T | 1 | a0001c0001t0035g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.598-55C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 7/9 | chr13 | 110635413 | |||||||
| chr13:110635598 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0153 |
2 | HG01952.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.718+10G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110635598 | |||||||
| chr13:110635685 | C | T | 2 | a0002c0002t0001g0175 a0002c0002t0033g0174 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.718+97C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110635685 | |||||||
| chr13:110635744 | G | C | 1 | a0003c0003t0003g0027 | 2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.718+156G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110635744 | |||||||
| chr13:110635773 | G | GC | 13 | a0001c0001t0005g0005 a0001c0001t0005g0012 a0001c0001t0005g0017 others(10): Show |
27 | HG00642.hp2 HG01884.hp1 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.718+187dupC | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr13 | 110635773 | ||||||
| chr13:110635853 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.718+265T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110635853 | |||||||
| chr13:110635908 | C | T | 1 | a0001c0001t0005g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.718+320C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110635908 | |||||||
| chr13:110636092 | G | A | 2 | a0002c0002t0013g0171 a0002c0002t0013g0185 |
2 | NA19075.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.718+504G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636092 | |||||||
| chr13:110636114 | A | G | 55 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(52): Show |
96 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.718+526A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636114 | |||||||
| chr13:110636260 | T | C | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.718+672T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636260 | |||||||
| chr13:110636369 | G | A | 32 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(29): Show |
61 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.719-760G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636369 | |||||||
| chr13:110636375 | A | ACTT | 95 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(92): Show |
166 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.719-754_719-753ins others(3): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636375 | |||||||
| chr13:110636396 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.719-733G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636396 | |||||||
| chr13:110636410 | G | A | 4 | a0001c0001t0011g0204 a0001c0001t0011g0206 a0001c0001t0019g0049 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-719G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636410 | |||||||
| chr13:110636540 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.719-589A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636540 | |||||||
| chr13:110636671 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0155 a0001c0001t0004g0073 |
4 | HG02451.hp1 HG02886.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.719-458C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636671 | |||||||
| chr13:110636782 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0105 |
4 | HG01167.hp1 HG01169.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.719-347G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636782 | |||||||
| chr13:110636837 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.719-292G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636837 | |||||||
| chr13:110636844 | G | A | 1 | a0001c0001t0010g0076 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.719-285G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636844 | |||||||
| chr13:110636846 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.719-283G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110636846 | |||||||
| chr13:110637032 | T | C | 6 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0055 others(3): Show |
6 | HG01192.hp2 HG02622.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.719-97T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110637032 | |||||||
| chr13:110637045 | C | T | 36 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0005g0005 others(33): Show |
67 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.719-84C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 8/9 | chr13 | 110637045 | |||||||
| chr13:110637351 | A | G | 41 | a0001c0001t0001g0154 a0001c0001t0002g0003 a0001c0001t0002g0011 others(38): Show |
71 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.839+102A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637351 | |||||||
| chr13:110637397 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.839+148C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637397 | |||||||
| chr13:110637458 | G | T | 1 | a0001c0001t0004g0067 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.839+209G>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637458 | |||||||
| chr13:110637530 | G | C | 1 | a0001c0001t0008g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.839+281G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637530 | |||||||
| chr13:110637548 | G | A | 1 | a0002c0002t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.839+299G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637548 | |||||||
| chr13:110637568 | A | G | 18 | a0001c0001t0001g0147 a0001c0001t0004g0066 a0001c0001t0005g0005 others(15): Show |
32 | HG00423.hp1 HG00642.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.839+319A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637568 | |||||||
| chr13:110637715 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.839+466T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637715 | |||||||
| chr13:110637812 | G | A | 1 | a0004c0004t0021g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.839+563G>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637812 | |||||||
| chr13:110637823 | A | G | 1 | a0001c0001t0005g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.840-555A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637823 | |||||||
| chr13:110637873 | A | G | 39 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(36): Show |
69 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.840-505A>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637873 | |||||||
| chr13:110637883 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.840-495C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637883 | |||||||
| chr13:110637911 | C | T | 30 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0019 others(27): Show |
59 | HG00609.hp1 HG00621.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.840-467C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637911 | |||||||
| chr13:110637964 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.840-414T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637964 | |||||||
| chr13:110637969 | T | C | 1 | a0001c0001t0001g0040 | 2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.840-409T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110637969 | |||||||
| chr13:110637977 | A | ACC | 6 | a0001c0001t0002g0011 a0001c0001t0002g0113 a0001c0001t0002g0114 others(3): Show |
10 | HG00738.hp2 HG01069.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.840-398_840-397dup others(2): Show |
NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr13 | 110637977 | ||||||
| chr13:110638017 | C | A | 50 | a0001c0001t0003g0053 a0001c0001t0003g0102 a0001c0001t0004g0007 others(47): Show |
90 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.840-361C>A | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638017 | |||||||
| chr13:110638162 | C | G | 1 | a0002c0002t0001g0120 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.840-216C>G | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638162 | |||||||
| chr13:110638281 | G | C | 1 | a0001c0001t0004g0025 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.840-97G>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638281 | |||||||
| chr13:110638283 | T | C | 20 | a0001c0001t0004g0007 a0001c0001t0004g0025 a0001c0001t0004g0026 others(17): Show |
30 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.840-95T>C | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638283 | |||||||
| chr13:110638320 | C | T | 1 | a0001c0001t0005g0012 | 4 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.840-58C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638320 | |||||||
| chr13:110638334 | C | T | 1 | a0003c0003t0003g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.840-44C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638334 | |||||||
| chr13:110638368 | C | T | 1 | a0003c0003t0003g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.840-10C>T | NAXD | ENSG00000213995.12 | transcript | ENST00000680254.1 | protein_coding | 9/9 | chr13 | 110638368 |