Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 284958 |
| ensemblid | ENSG00000144130.12 |
| hgncid | 27678 |
| symbol | NT5DC4 |
| name | 5'-nucleotidase domain containing 4 |
| refseq_nuc | NM_001393655.1 |
| refseq_prot | NP_001380584.1 |
| ensembl_nuc | ENST00000688554.1 |
| ensembl_prot | ENSP00000509504.1 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 112721020 |
| end | 112739095 |
| strand | + |
| ver | v1.2 |
| region | chr2:112721020-112739095 |
| region5000 | chr2:112716020-112744095 |
| regionname0 | NT5DC4_chr2_112721020_112739095 |
| regionname5000 | NT5DC4_chr2_112716020_112744095 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 455 | 148 | 13 | 32 | 77 | 5 | 20 | 64 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0002 | 0/0 | 455 | 114 | 21 | 24 | 43 | 9 | 17 | 32 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0003 | 0/0 | 455 | 42 | 11 | 16 | 12 | 0 | 3 | 10 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0004 | 1/0 | 455 | 26 | 23 | 1 | 1 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0005 | 0/0 | 455 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0006 | 0/0 | 455 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0007 | 0/0 | 455 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0008 | 0/0 | 455 | 4 | 3 | 0 | 1 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0009 | 0/0 | 455 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0010 | 0/0 | 455 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0011 | 0/0 | 455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0012 | 0/0 | 455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0013 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0014 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0015 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| a0016 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | MASVD others(450): Show |
chr2 | 112716020 | 112744095 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1365 | 147 | 12 | 32 | 77 | 5 | 20 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0001c0020 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0002c0002 | 0/0 | 1365 | 112 | 21 | 24 | 41 | 9 | 17 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0002c0011 | 0/0 | 1365 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0003c0003 | 0/0 | 1365 | 42 | 11 | 16 | 12 | 0 | 3 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0004c0004 | 1/0 | 1365 | 22 | 19 | 1 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0004c0009 | 0/0 | 1365 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0004c0019 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0005c0006 | 0/0 | 1365 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0006c0005 | 0/0 | 1365 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0007c0008 | 0/0 | 1365 | 4 | 4 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0008c0007 | 0/0 | 1365 | 4 | 3 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0009c0012 | 0/0 | 1365 | 2 | 1 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0010c0013 | 0/0 | 1365 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0011c0010 | 0/0 | 1365 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0012c0014 | 0/0 | 1365 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0013c0016 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0014c0017 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0015c0015 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 | ||
| a0016c0018 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ATGGC others(1360): Show |
chr2 | 112716020 | 112744095 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1587 | 138 | 12 | 32 | 71 | 3 | 19 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0001c0001t0003 | 0/0 | 1587 | 6 | 0 | 0 | 6 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0001c0001t0005 | 0/0 | 1587 | 2 | 0 | 0 | 0 | 2 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0001c0001t0006 | 0/0 | 1587 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0001c0020t0001 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0002c0002t0001 | 0/0 | 1587 | 112 | 21 | 24 | 41 | 9 | 17 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0002c0011t0001 | 0/0 | 1587 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0003c0003t0001 | 0/0 | 1587 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0003c0003t0002 | 0/0 | 1587 | 37 | 8 | 14 | 12 | 0 | 3 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0003c0003t0004 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0004c0004t0001 | 1/0 | 1587 | 21 | 18 | 1 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0004c0004t0002 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0004c0009t0001 | 0/0 | 1587 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0004c0019t0001 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0005c0006t0001 | 0/0 | 1587 | 7 | 7 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0006c0005t0001 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0006c0005t0002 | 0/0 | 1587 | 6 | 6 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0007c0008t0001 | 0/0 | 1587 | 4 | 4 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0008c0007t0001 | 0/0 | 1587 | 4 | 3 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0009c0012t0001 | 0/0 | 1587 | 2 | 1 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0010c0013t0001 | 0/0 | 1587 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0011c0010t0001 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0012c0014t0001 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0013c0016t0001 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0014c0017t0001 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0015c0015t0001 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| a0016c0018t0001 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | ACTGA others(1582): Show |
chr2 | 112716020 | 112744095 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 2 | 0 | 2 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0001c0020t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0007 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0011t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0002c0011t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0001 | 0/0 | 13 | 0 | 11 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0003c0003t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0009t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0009t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0009t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0004c0019t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0005c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0006c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0006c0005t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0006c0005t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0006c0005t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0006c0005t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0007c0008t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0007c0008t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0007c0008t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0007c0008t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0008c0007t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0008c0007t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0008c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0009c0012t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0009c0012t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0010c0013t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0010c0013t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0011c0010t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0011c0010t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0012c0014t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0012c0014t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0013c0016t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0014c0017t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0015c0015t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| a0016c0018t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0193 | EUR | GBR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0034 | EUR | GBR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0013 | EUR | GBR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0007 | EUR | FIN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0142 | EUR | FIN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | FIN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00438 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00639 | hp1 | a0009 | c0012 | t0001 | g0071 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0144 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0128 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01168 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0148 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0049 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0058 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01261 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0201 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01433 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01496 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0025 | EUR | IBS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0025 | EUR | IBS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0155 | EUR | IBS | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01884 | hp1 | a0004 | c0004 | t0001 | g0253 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01884 | hp2 | a0007 | c0008 | t0001 | g0250 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01891 | hp2 | a0005 | c0006 | t0001 | g0065 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01928 | hp1 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01934 | hp1 | a0010 | c0013 | t0001 | g0086 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01943 | hp1 | a0003 | c0003 | t0002 | g0054 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02004 | hp1 | a0010 | c0013 | t0001 | g0092 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02004 | hp2 | a0003 | c0003 | t0002 | g0001 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02055 | hp2 | a0003 | c0003 | t0002 | g0051 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0083 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | CDX | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | CDX | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02257 | hp1 | a0004 | c0019 | t0001 | g0098 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0040 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02280 | hp1 | a0007 | c0008 | t0001 | g0273 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02280 | hp2 | a0003 | c0003 | t0002 | g0046 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0055 | AMR | PEL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02451 | hp1 | a0003 | c0003 | t0004 | g0080 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02572 | hp1 | a0006 | c0005 | t0002 | g0019 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02615 | hp1 | a0008 | c0007 | t0001 | g0141 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02615 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02622 | hp2 | a0008 | c0007 | t0001 | g0035 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02630 | hp1 | a0013 | c0016 | t0001 | g0183 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02630 | hp2 | a0004 | c0004 | t0001 | g0069 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0039 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02647 | hp2 | a0006 | c0005 | t0002 | g0042 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0157 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02717 | hp1 | a0005 | c0006 | t0001 | g0062 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02723 | hp2 | a0003 | c0003 | t0002 | g0020 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02735 | hp2 | a0003 | c0003 | t0002 | g0053 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02809 | hp1 | a0003 | c0003 | t0002 | g0045 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02818 | hp1 | a0004 | c0004 | t0001 | g0068 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0040 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02896 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02896 | hp2 | a0007 | c0008 | t0001 | g0275 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02897 | hp2 | a0004 | c0004 | t0001 | g0024 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0150 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02922 | hp2 | a0003 | c0003 | t0002 | g0050 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02970 | hp1 | a0006 | c0005 | t0002 | g0019 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02970 | hp2 | a0009 | c0012 | t0001 | g0077 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02976 | hp1 | a0004 | c0009 | t0001 | g0074 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03041 | hp2 | a0014 | c0017 | t0001 | g0140 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0145 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03130 | hp2 | a0004 | c0009 | t0001 | g0133 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03139 | hp1 | a0005 | c0006 | t0001 | g0022 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03139 | hp2 | a0003 | c0003 | t0004 | g0078 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03195 | hp2 | a0008 | c0007 | t0001 | g0035 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03209 | hp2 | a0005 | c0006 | t0001 | g0061 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0020 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0067 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03453 | hp1 | a0004 | c0009 | t0001 | g0075 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0276 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0162 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03516 | hp1 | a0007 | c0008 | t0001 | g0274 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03516 | hp2 | a0004 | c0004 | t0001 | g0079 | AFR | ESN | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03540 | hp2 | a0005 | c0006 | t0001 | g0064 | AFR | GWD | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03579 | hp1 | a0004 | c0004 | t0002 | g0044 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03579 | hp2 | a0003 | c0003 | t0002 | g0048 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0234 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0047 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0137 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0166 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0203 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0032 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0056 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18522 | hp1 | a0004 | c0004 | t0001 | g0023 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18522 | hp2 | a0003 | c0003 | t0002 | g0043 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0198 | EAS | CHB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | CHB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18906 | hp2 | a0005 | c0006 | t0001 | g0063 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18943 | hp2 | a0015 | c0015 | t0001 | g0027 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18944 | hp1 | a0016 | c0018 | t0001 | g0090 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18946 | hp2 | a0003 | c0003 | t0002 | g0052 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18960 | hp1 | a0004 | c0004 | t0001 | g0059 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18977 | hp1 | a0002 | c0011 | t0001 | g0015 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18986 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18993 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19003 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19030 | hp1 | a0006 | c0005 | t0001 | g0076 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19030 | hp2 | a0004 | c0004 | t0001 | g0259 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19043 | hp1 | a0001 | c0020 | t0001 | g0191 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0139 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19064 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19066 | hp2 | a0008 | c0007 | t0001 | g0194 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19070 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19077 | hp1 | a0003 | c0003 | t0002 | g0057 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19086 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19087 | hp2 | a0002 | c0011 | t0001 | g0263 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19240 | hp1 | a0006 | c0005 | t0002 | g0018 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA19240 | hp2 | a0012 | c0014 | t0001 | g0073 | AFR | YRI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ASW | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20129 | hp2 | a0012 | c0014 | t0001 | g0072 | AFR | ASW | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0011 | EUR | TSI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | GIH | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02109 | hp1 | a0003 | c0003 | t0004 | g0081 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02109 | hp2 | a0005 | c0006 | t0001 | g0022 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02486 | hp1 | a0011 | c0010 | t0001 | g0159 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0153 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02559 | hp1 | a0011 | c0010 | t0001 | g0158 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0023 | AFR | ACB | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG06807 | hp1 | a0006 | c0005 | t0002 | g0041 | AFR | USA | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | USA | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20300 | hp1 | a0006 | c0005 | t0002 | g0018 | AFR | USA | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0186 | AFR | USA | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | LWK | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0109 | REF | REF | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0001 | g0060 | REF | REF | NT5DC4_chr2_112716020_112744095 | NT5DC4 | chr2 | 112716020 | 112744095 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112721856 | G | A | 1 | a0015 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.113G>A | p.Arg38His | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 2/17 | 173/1587 | 113/1368 | 38/455 | chr2 | 112721856 | |||
| chr2:112721991 | A | G | 1 | a0005 | 7 | HG01891.hp2 HG02109.hp2 HG02717.hp1 others(4): Show |
missense_variant | MODERATE | c.154A>G | p.Lys52Glu | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 214/1587 | 154/1368 | 52/455 | chr2 | 112721991 | |||
| chr2:112722037 | G | A | 5 | a0002 a0008 a0011 others(2): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
missense_variant | MODERATE | c.200G>A | p.Arg67His | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 260/1587 | 200/1368 | 67/455 | chr2 | 112722037 | |||
| chr2:112722058 | C | T | 2 | a0013 a0014 |
2 | HG02630.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.221C>T | p.Pro74Leu | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 281/1587 | 221/1368 | 74/455 | chr2 | 112722058 | |||
| chr2:112722233 | A | G | 1 | a0016 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.317A>G | p.His106Arg | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 4/17 | 377/1587 | 317/1368 | 106/455 | chr2 | 112722233 | |||
| chr2:112723140 | A | G | 1 | a0012 | 2 | NA19240.hp2 NA20129.hp2 |
missense_variant | MODERATE | c.587A>G | p.Asp196Gly | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/17 | 647/1587 | 587/1368 | 196/455 | chr2 | 112723140 | |||
| chr2:112723722 | C | T | 1 | a0010 | 2 | HG01934.hp1 HG02004.hp1 |
missense_variant | MODERATE | c.676C>T | p.Arg226Cys | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/17 | 736/1587 | 676/1368 | 226/455 | chr2 | 112723722 | |||
| chr2:112725202 | A | C | 7 | a0001 a0002 a0003 others(4): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
missense_variant | MODERATE | c.944A>C | p.Tyr315Ser | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 12/17 | 1004/1587 | 944/1368 | 315/455 | chr2 | 112725202 | |||
| chr2:112725234 | T | C | 1 | a0006 | 7 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(4): Show |
missense_variant | MODERATE | c.976T>C | p.Ser326Pro | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 12/17 | 1036/1587 | 976/1368 | 326/455 | chr2 | 112725234 | |||
| chr2:112725460 | A | T | 4 | a0003 a0008 a0009 others(1): Show |
49 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
missense_variant | MODERATE | c.1061A>T | p.Asp354Val | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/17 | 1121/1587 | 1061/1368 | 354/455 | chr2 | 112725460 | |||
| chr2:112726240 | C | T | 1 | a0007 | 4 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.1156C>T | p.Arg386Trp | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 14/17 | 1216/1587 | 1156/1368 | 386/455 | chr2 | 112726240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112722038 | C | T | 2 | a0001c0020 a0004c0019 |
2 | HG02257.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.201C>T | p.Arg67Arg | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 261/1587 | 201/1368 | 67/455 | chr2 | 112722038 | |||
| chr2:112722041 | G | T | 1 | a0002c0011 | 2 | NA18977.hp1 NA19087.hp2 |
synonymous_variant | LOW | c.204G>T | p.Leu68Leu | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 264/1587 | 204/1368 | 68/455 | chr2 | 112722041 | |||
| chr2:112722083 | C | T | 1 | a0004c0009 | 3 | HG02976.hp1 HG03130.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.246C>T | p.Tyr82Tyr | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/17 | 306/1587 | 246/1368 | 82/455 | chr2 | 112722083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112721078 | C | T | 3 | a0003c0003t0002 a0004c0004t0002 a0006c0005t0002 |
44 | HG00438.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-2C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/17 | chr2 | 112721078 | |||||||
| chr2:112738943 | T | A | 1 | a0001c0001t0003 | 6 | NA18941.hp1 NA18957.hp1 NA18963.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 17/17 | 7 | chr2 | 112738943 | ||||||
| chr2:112738977 | C | T | 1 | a0001c0001t0005 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*41C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 17/17 | 41 | chr2 | 112738977 | ||||||
| chr2:112739003 | A | G | 1 | a0003c0003t0004 | 3 | HG02109.hp1 HG02451.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*67A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 17/17 | 67 | chr2 | 112739003 | ||||||
| chr2:112739023 | C | T | 1 | a0001c0001t0006 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 17/17 | 87 | chr2 | 112739023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:112721208 | A | G | 2 | a0004c0004t0001g0040 a0004c0004t0001g0276 |
3 | HG02258.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.74+55A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721208 | |||||||
| chr2:112721222 | C | T | 3 | a0007c0008t0001g0273 a0007c0008t0001g0274 a0007c0008t0001g0275 |
3 | HG02280.hp1 HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.74+69C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721222 | |||||||
| chr2:112721253 | G | A | 23 | a0003c0003t0002g0001 a0003c0003t0002g0004 a0003c0003t0002g0020 others(20): Show |
44 | HG00438.hp2 HG01069.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.74+100G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721253 | |||||||
| chr2:112721294 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.74+141C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721294 | |||||||
| chr2:112721312 | A | G | 256 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.74+159A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721312 | |||||||
| chr2:112721335 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.74+182C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721335 | |||||||
| chr2:112721344 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.74+191C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721344 | |||||||
| chr2:112721345 | G | A | 2 | a0004c0009t0001g0074 a0004c0009t0001g0075 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.74+192G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721345 | |||||||
| chr2:112721738 | G | T | 1 | a0002c0002t0001g0269 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.75-80G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 1/16 | chr2 | 112721738 | |||||||
| chr2:112722145 | A | AC | 13 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0265 others(10): Show |
13 | HG00544.hp1 HG00735.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.267-33dupC | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 112722145 | ||||||
| chr2:112722168 | AC | A | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(247): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.267-9delC | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 112722168 | ||||||
| chr2:112722349 | G | A | 11 | a0001c0001t0001g0082 a0003c0003t0004g0078 a0003c0003t0004g0080 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.362+71G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 4/16 | chr2 | 112722349 | |||||||
| chr2:112722349 | G | T | 1 | a0004c0004t0001g0276 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.362+71G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 4/16 | chr2 | 112722349 | |||||||
| chr2:112722389 | C | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.363-94C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 4/16 | chr2 | 112722389 | |||||||
| chr2:112722656 | C | G | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0004c0004t0001g0039 others(2): Show |
6 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-58C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 5/16 | chr2 | 112722656 | |||||||
| chr2:112722776 | G | A | 14 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
16 | HG00639.hp1 HG02145.hp2 HG02280.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.527+5G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722776 | |||||||
| chr2:112722841 | GGGGCCCC others(4): Show |
G | 1 | a0001c0001t0001g0249 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.527+75_527+85delCC others(9): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 112722841 | ||||||
| chr2:112722891 | G | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
69 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.527+120G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722891 | |||||||
| chr2:112722895 | GA | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(53): Show |
69 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.527+126delA | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 112722895 | ||||||
| chr2:112722914 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(247): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.527+143T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722914 | |||||||
| chr2:112722918 | A | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(247): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.527+147A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722918 | |||||||
| chr2:112722920 | A | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(247): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.527+149A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722920 | |||||||
| chr2:112722921 | C | CAATCCTG others(25): Show |
250 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(247): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.527+151_527+152ins others(32): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 112722921 | ||||||
| chr2:112722955 | G | A | 11 | a0001c0001t0001g0082 a0003c0003t0004g0078 a0003c0003t0004g0080 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.528-126G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | chr2 | 112722955 | |||||||
| chr2:112722979 | GC | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(124): Show |
154 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.528-98delC | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 112722979 | ||||||
| chr2:112723219 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.621+45C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | chr2 | 112723219 | |||||||
| chr2:112723280 | T | G | 1 | a0002c0002t0001g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.621+106T>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | chr2 | 112723280 | |||||||
| chr2:112723361 | G | GCA | 7 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0003c0003t0002g0043 others(4): Show |
9 | HG02572.hp1 HG02970.hp1 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.622-24_622-23dupCA | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACA | 7 | a0001c0001t0001g0135 a0001c0001t0001g0258 a0002c0002t0001g0200 others(4): Show |
7 | HG00735.hp2 HG01109.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.622-26_622-23dupCA others(2): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACA | 40 | a0001c0001t0001g0134 a0001c0001t0001g0251 a0001c0001t0001g0252 others(37): Show |
58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.622-28_622-23dupCA others(4): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(1): Show |
35 | a0002c0002t0001g0002 a0002c0002t0001g0031 a0002c0002t0001g0157 others(32): Show |
45 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.622-30_622-23dupCA others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(3): Show |
35 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0082 others(32): Show |
39 | HG00140.hp2 HG00673.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.622-32_622-23dupCA others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(5): Show |
32 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0037 others(29): Show |
41 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.622-34_622-23dupCA others(10): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(7): Show |
52 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
71 | HG00280.hp2 HG00544.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.622-36_622-23dupCA others(12): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(9): Show |
14 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(11): Show |
14 | HG01169.hp1 HG01256.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.622-38_622-23dupCA others(14): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(11): Show |
18 | a0001c0001t0001g0008 a0001c0001t0001g0088 a0001c0001t0001g0089 others(15): Show |
21 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.622-40_622-23dupCA others(16): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(13): Show |
5 | a0001c0001t0001g0087 a0001c0001t0001g0207 a0001c0001t0003g0208 others(2): Show |
5 | HG01934.hp1 NA18955.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-42_622-23dupCA others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723361 | G | GCACACAC others(15): Show |
3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG00621.hp1 NA18939.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.622-44_622-23dupCA others(20): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723361 | ||||||
| chr2:112723394 | C | CACACACA others(19): Show |
1 | a0004c0004t0001g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.622-23_622-22insCA others(24): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723394 | ||||||
| chr2:112723394 | C | CACACACA others(13): Show |
1 | a0004c0004t0001g0139 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622-23_622-22insCA others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723394 | ||||||
| chr2:112723394 | C | CACACACA others(3): Show |
4 | a0005c0006t0001g0022 a0005c0006t0001g0061 a0005c0006t0001g0062 others(1): Show |
5 | HG02109.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-23_622-22insCA others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 112723394 | ||||||
| chr2:112723527 | C | T | 1 | a0002c0002t0001g0156 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.672+59C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 8/16 | chr2 | 112723527 | |||||||
| chr2:112723528 | G | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0157 |
3 | HG02698.hp2 HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.672+60G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 8/16 | chr2 | 112723528 | |||||||
| chr2:112723578 | G | A | 7 | a0003c0003t0004g0078 a0003c0003t0004g0080 a0003c0003t0004g0081 others(4): Show |
7 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+110G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 8/16 | chr2 | 112723578 | |||||||
| chr2:112723690 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0097 a0001c0001t0001g0121 others(1): Show |
4 | NA18943.hp2 NA18971.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-29C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 8/16 | chr2 | 112723690 | |||||||
| chr2:112723832 | C | T | 8 | a0003c0003t0004g0078 a0003c0003t0004g0080 a0003c0003t0004g0081 others(5): Show |
9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.756+30C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723832 | |||||||
| chr2:112723842 | C | T | 1 | a0002c0002t0001g0011 | 3 | HG00738.hp1 HG01106.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.756+40C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723842 | |||||||
| chr2:112723862 | T | A | 104 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(101): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.756+60T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723862 | |||||||
| chr2:112723942 | C | A | 2 | a0011c0010t0001g0158 a0011c0010t0001g0159 |
2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.756+140C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723942 | |||||||
| chr2:112723944 | A | G | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.756+142A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723944 | |||||||
| chr2:112723970 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(241): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.757-124A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 9/16 | chr2 | 112723970 | |||||||
| chr2:112724219 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.789+93G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724219 | |||||||
| chr2:112724336 | G | T | 3 | a0003c0003t0004g0078 a0003c0003t0004g0080 a0003c0003t0004g0081 |
3 | HG02109.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.789+210G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724336 | |||||||
| chr2:112724353 | AG | A | 4 | a0001c0001t0001g0082 a0004c0004t0001g0040 a0004c0004t0001g0079 others(1): Show |
5 | HG02258.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+229delG | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 112724353 | ||||||
| chr2:112724367 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0218 others(7): Show |
12 | NA18944.hp2 NA18971.hp2 NA18977.hp2 others(9): Show |
intron_variant | MODIFIER | c.789+241G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724367 | |||||||
| chr2:112724370 | C | T | 1 | a0001c0001t0003g0217 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.789+244C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724370 | |||||||
| chr2:112724458 | G | A | 1 | a0002c0002t0001g0160 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.790-323G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724458 | |||||||
| chr2:112724725 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.790-56T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 10/16 | chr2 | 112724725 | |||||||
| chr2:112725033 | C | T | 4 | a0002c0002t0001g0030 a0002c0002t0001g0145 a0002c0002t0001g0154 others(1): Show |
5 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.915+127C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 11/16 | chr2 | 112725033 | |||||||
| chr2:112725055 | C | G | 1 | a0001c0001t0006g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.916-119C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 11/16 | chr2 | 112725055 | |||||||
| chr2:112725291 | G | A | 1 | a0004c0019t0001g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.982+51G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 12/16 | chr2 | 112725291 | |||||||
| chr2:112725352 | C | T | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-30C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 12/16 | chr2 | 112725352 | |||||||
| chr2:112725353 | G | A | 1 | a0002c0002t0001g0180 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.983-29G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 12/16 | chr2 | 112725353 | |||||||
| chr2:112725576 | G | C | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1153+24G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725576 | |||||||
| chr2:112725633 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1153+81C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725633 | |||||||
| chr2:112725634 | G | A | 1 | a0001c0001t0005g0025 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1153+82G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725634 | |||||||
| chr2:112725731 | C | T | 3 | a0004c0004t0001g0040 a0004c0004t0001g0079 a0004c0004t0001g0276 |
4 | HG02258.hp2 HG02886.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+179C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725731 | |||||||
| chr2:112725864 | A | G | 4 | a0007c0008t0001g0250 a0007c0008t0001g0273 a0007c0008t0001g0274 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153+312A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725864 | |||||||
| chr2:112725882 | GAAGGTAC others(9): Show |
G | 30 | a0003c0003t0001g0127 a0003c0003t0001g0128 a0003c0003t0002g0001 others(27): Show |
50 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1153+332_1154-339d others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 112725882 | ||||||
| chr2:112725992 | G | C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1154-246G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112725992 | |||||||
| chr2:112726202 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1154-36G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 13/16 | chr2 | 112726202 | |||||||
| chr2:112726596 | C | A | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1206-82C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 14/16 | chr2 | 112726596 | |||||||
| chr2:112726742 | G | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(270): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
splice_region_variant&intron_variant | LOW | c.1266+4G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726742 | |||||||
| chr2:112726776 | A | G | 272 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(269): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1266+38A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726776 | |||||||
| chr2:112726788 | G | A | 2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1266+50G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726788 | |||||||
| chr2:112726864 | T | G | 103 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(100): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1266+126T>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726864 | |||||||
| chr2:112726997 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266+259A>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726997 | |||||||
| chr2:112726999 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1266+261C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112726999 | |||||||
| chr2:112727024 | G | C | 1 | a0005c0006t0001g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1266+286G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727024 | |||||||
| chr2:112727059 | T | C | 3 | a0002c0002t0001g0030 a0002c0002t0001g0145 a0002c0002t0001g0154 |
4 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+321T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727059 | |||||||
| chr2:112727121 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(271): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1266+383G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727121 | |||||||
| chr2:112727178 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(268): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1266+440A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727178 | |||||||
| chr2:112727384 | A | G | 1 | a0002c0002t0001g0174 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1266+646A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727384 | |||||||
| chr2:112727475 | C | T | 2 | a0009c0012t0001g0071 a0014c0017t0001g0140 |
2 | HG00639.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1266+737C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727475 | |||||||
| chr2:112727476 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1266+738G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727476 | |||||||
| chr2:112727584 | G | A | 8 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(5): Show |
9 | HG01891.hp2 HG02109.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+846G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727584 | |||||||
| chr2:112727729 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1266+991G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727729 | |||||||
| chr2:112727799 | A | G | 2 | a0009c0012t0001g0071 a0014c0017t0001g0140 |
2 | HG00639.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1266+1061A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727799 | |||||||
| chr2:112727808 | C | CA | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(135): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1266+1071dupA | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 112727808 | ||||||
| chr2:112727836 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0272 |
2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1266+1098T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727836 | |||||||
| chr2:112727928 | C | T | 274 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(271): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1266+1190C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727928 | |||||||
| chr2:112727930 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1266+1192C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112727930 | |||||||
| chr2:112728056 | G | A | 1 | a0003c0003t0002g0047 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1266+1318G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728056 | |||||||
| chr2:112728057 | C | T | 1 | a0002c0002t0001g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1266+1319C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728057 | |||||||
| chr2:112728123 | T | A | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1266+1385T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728123 | |||||||
| chr2:112728393 | G | C | 1 | a0004c0004t0001g0059 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1267-1234G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728393 | |||||||
| chr2:112728502 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(126): Show |
157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1267-1125C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728502 | |||||||
| chr2:112728523 | GCAT | G | 2 | a0004c0004t0001g0040 a0004c0004t0001g0276 |
3 | HG02258.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1267-1097_1267-109 others(7): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 112728523 | ||||||
| chr2:112728559 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1267-1068C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728559 | |||||||
| chr2:112728615 | C | T | 1 | a0002c0002t0001g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1267-1012C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728615 | |||||||
| chr2:112728642 | G | A | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1267-985G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112728642 | |||||||
| chr2:112729060 | A | C | 1 | a0002c0002t0001g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1267-567A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729060 | |||||||
| chr2:112729060 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(152): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1267-567A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729060 | |||||||
| chr2:112729302 | T | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(113): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1267-325T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729302 | |||||||
| chr2:112729303 | A | G | 1 | a0002c0002t0001g0189 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1267-324A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729303 | |||||||
| chr2:112729364 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1267-263C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729364 | |||||||
| chr2:112729413 | C | T | 1 | a0002c0002t0001g0188 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1267-214C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729413 | |||||||
| chr2:112729487 | C | T | 10 | a0003c0003t0002g0001 a0003c0003t0002g0004 a0003c0003t0002g0021 others(7): Show |
28 | HG00438.hp2 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1267-140C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729487 | |||||||
| chr2:112729488 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1267-139G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 15/16 | chr2 | 112729488 | |||||||
| chr2:112729745 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1344+41C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112729745 | |||||||
| chr2:112729864 | T | C | 3 | a0003c0003t0004g0078 a0003c0003t0004g0080 a0003c0003t0004g0081 |
3 | HG02109.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1344+160T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112729864 | |||||||
| chr2:112729874 | C | G | 8 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(5): Show |
10 | HG02145.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+170C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112729874 | |||||||
| chr2:112730066 | A | G | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+362A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730066 | |||||||
| chr2:112730310 | C | CA | 107 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(104): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1344+627dupA | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112730310 | ||||||
| chr2:112730310 | C | CAA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
144 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1344+626_1344+627d others(4): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112730310 | ||||||
| chr2:112730310 | C | CAAA | 37 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0036 others(34): Show |
45 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.1344+625_1344+627d others(5): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112730310 | ||||||
| chr2:112730310 | C | CAAAA | 7 | a0001c0001t0001g0105 a0002c0002t0001g0153 a0004c0004t0001g0067 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+624_1344+627d others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112730310 | ||||||
| chr2:112730425 | C | G | 7 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(4): Show |
8 | HG01891.hp2 HG02109.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344+721C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730425 | |||||||
| chr2:112730602 | C | T | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+898C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730602 | |||||||
| chr2:112730611 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1344+907G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730611 | |||||||
| chr2:112730643 | C | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(137): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1344+939C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730643 | |||||||
| chr2:112730728 | G | C | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+1024G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730728 | |||||||
| chr2:112730743 | A | G | 1 | a0004c0004t0001g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1344+1039A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112730743 | |||||||
| chr2:112731023 | G | A | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+1319G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731023 | |||||||
| chr2:112731029 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1344+1325G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731029 | |||||||
| chr2:112731056 | A | G | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+1352A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731056 | |||||||
| chr2:112731132 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0123 |
3 | HG00544.hp2 NA18957.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1344+1428G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731132 | |||||||
| chr2:112731158 | C | T | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+1454C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731158 | |||||||
| chr2:112731195 | C | A | 1 | a0002c0002t0001g0138 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1344+1491C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731195 | |||||||
| chr2:112731356 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1344+1652T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731356 | |||||||
| chr2:112731379 | C | T | 1 | a0007c0008t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1344+1675C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731379 | |||||||
| chr2:112731678 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(150): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1344+1974C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731678 | |||||||
| chr2:112731713 | T | A | 16 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(13): Show |
20 | HG01884.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1344+2009T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731713 | |||||||
| chr2:112731772 | C | T | 1 | a0001c0020t0001g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1344+2068C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731772 | |||||||
| chr2:112731906 | CAG | C | 34 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(31): Show |
40 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1344+2207_1344+220 others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112731906 | ||||||
| chr2:112731917 | C | CT | 34 | a0001c0001t0001g0084 a0001c0001t0001g0119 a0001c0001t0001g0136 others(31): Show |
37 | HG00423.hp1 HG00642.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1344+2236dupT | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112731917 | ||||||
| chr2:112731917 | C | CTT | 6 | a0003c0003t0001g0128 a0003c0003t0002g0050 a0003c0003t0002g0051 others(3): Show |
7 | HG00642.hp2 HG02055.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+2235_1344+223 others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112731917 | ||||||
| chr2:112731917 | CT | C | 7 | a0001c0001t0001g0114 a0001c0001t0001g0129 a0001c0001t0001g0247 others(4): Show |
7 | HG00673.hp1 HG00673.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344+2236delT | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112731917 | ||||||
| chr2:112731919 | T | G | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1344+2215T>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731919 | |||||||
| chr2:112731953 | C | T | 3 | a0004c0009t0001g0133 a0011c0010t0001g0158 a0011c0010t0001g0159 |
3 | HG02486.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1344+2249C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112731953 | |||||||
| chr2:112732035 | C | T | 117 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(114): Show |
166 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1344+2331C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732035 | |||||||
| chr2:112732055 | C | A | 27 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(24): Show |
31 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1344+2351C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732055 | |||||||
| chr2:112732055 | C | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | NA18943.hp1 NA18974.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+2351C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732055 | |||||||
| chr2:112732134 | T | C | 2 | a0004c0004t0001g0040 a0004c0004t0001g0276 |
3 | HG02258.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1344+2430T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732134 | |||||||
| chr2:112732210 | AT | A | 139 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0085 others(136): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1344+2517delT | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112732210 | ||||||
| chr2:112732220 | T | A | 8 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(5): Show |
10 | HG02145.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+2516T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732220 | |||||||
| chr2:112732221 | T | A | 129 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(126): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1344+2517T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732221 | |||||||
| chr2:112732316 | G | GCAGGGGC others(43): Show |
128 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(125): Show |
180 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1344+2763_1344+281 others(54): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112732316 | ||||||
| chr2:112732316 | G | GCAGGGGC others(93): Show |
1 | a0001c0001t0001g0237 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1344+2713_1344+281 others(104): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112732316 | ||||||
| chr2:112732316 | G | GCAGGGGC others(143): Show |
11 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(8): Show |
13 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1344+2663_1344+281 others(154): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112732316 | ||||||
| chr2:112732368 | A | AGGGGCAG others(43): Show |
1 | a0002c0002t0001g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1344+2713_1344+271 others(54): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112732368 | ||||||
| chr2:112732519 | C | T | 9 | a0001c0001t0001g0246 a0001c0001t0001g0266 a0002c0002t0001g0007 others(6): Show |
12 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1344+2815C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732519 | |||||||
| chr2:112732746 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(86): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1344+3042G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732746 | |||||||
| chr2:112732905 | T | C | 8 | a0002c0002t0001g0164 a0004c0004t0001g0023 a0004c0004t0001g0024 others(5): Show |
10 | HG02145.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+3201T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732905 | |||||||
| chr2:112732937 | T | A | 4 | a0007c0008t0001g0250 a0007c0008t0001g0273 a0007c0008t0001g0274 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+3233T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112732937 | |||||||
| chr2:112733041 | T | A | 1 | a0002c0002t0001g0168 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1344+3337T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733041 | |||||||
| chr2:112733160 | A | C | 9 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+3456A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733160 | |||||||
| chr2:112733210 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1344+3506C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733210 | |||||||
| chr2:112733251 | GT | G | 133 | a0001c0001t0001g0066 a0001c0001t0001g0084 a0001c0001t0001g0085 others(130): Show |
186 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.1344+3562delT | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112733251 | ||||||
| chr2:112733251 | GTT | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(120): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1344+3561_1344+356 others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112733251 | ||||||
| chr2:112733374 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(86): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1344+3670G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733374 | |||||||
| chr2:112733529 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1344+3825A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733529 | |||||||
| chr2:112733603 | G | C | 9 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+3899G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733603 | |||||||
| chr2:112733609 | G | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1344+3905G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733609 | |||||||
| chr2:112733729 | G | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1344+4025G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733729 | |||||||
| chr2:112733802 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1344+4098G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733802 | |||||||
| chr2:112733878 | A | T | 1 | a0004c0019t0001g0098 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1344+4174A>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733878 | |||||||
| chr2:112733988 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1344+4284A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733988 | |||||||
| chr2:112733996 | G | T | 3 | a0004c0009t0001g0133 a0011c0010t0001g0158 a0011c0010t0001g0159 |
3 | HG02486.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1344+4292G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112733996 | |||||||
| chr2:112734169 | A | ATATATAT others(9): Show |
1 | a0004c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(20): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATAT others(13): Show |
5 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0075 others(2): Show |
6 | HG02109.hp2 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(24): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATAT others(21): Show |
1 | a0005c0006t0001g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(32): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(3): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0221 a0001c0001t0005g0025 |
4 | HG01515.hp1 HG01517.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(14): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(5): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0107 others(8): Show |
15 | HG00280.hp2 HG00544.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(16): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(7): Show |
62 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(59): Show |
79 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(9): Show |
28 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0027 others(25): Show |
34 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(20): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(11): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0115 a0001c0001t0001g0241 others(1): Show |
4 | HG01074.hp2 HG01261.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(22): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(13): Show |
1 | a0001c0001t0001g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(24): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(21): Show |
1 | a0012c0014t0001g0073 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(32): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(23): Show |
1 | a0012c0014t0001g0072 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(34): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATATGT others(25): Show |
1 | a0004c0004t0001g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(36): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATG | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTG | 56 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0126 others(53): Show |
76 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(10): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(1): Show |
20 | a0001c0001t0001g0100 a0001c0001t0001g0251 a0002c0002t0001g0007 others(17): Show |
45 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(12): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(3): Show |
17 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0002c0002t0001g0033 others(14): Show |
21 | HG00639.hp1 HG00642.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(14): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(5): Show |
18 | a0001c0001t0001g0113 a0001c0001t0001g0223 a0002c0002t0001g0028 others(15): Show |
20 | HG00323.hp1 HG01169.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(16): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(7): Show |
19 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0095 others(16): Show |
19 | HG01109.hp1 HG01243.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(9): Show |
7 | a0001c0001t0001g0125 a0001c0001t0001g0220 a0001c0001t0001g0242 others(4): Show |
8 | HG01884.hp2 HG01978.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(20): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(11): Show |
4 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0002c0002t0001g0187 others(1): Show |
4 | HG01175.hp1 HG02615.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+4466_1344+446 others(22): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATATGTGT others(13): Show |
1 | a0001c0001t0001g0266 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1344+4466_1344+446 others(24): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(3): Show |
1 | a0004c0004t0001g0039 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1344+4489_1344+449 others(14): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0099 a0002c0002t0001g0029 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1344+4487_1344+449 others(16): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(7): Show |
2 | a0001c0001t0001g0122 a0002c0002t0001g0171 |
2 | HG02293.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1344+4485_1344+449 others(18): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(9): Show |
1 | a0003c0003t0004g0078 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1344+4483_1344+449 others(20): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(11): Show |
1 | a0003c0003t0004g0080 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1344+4481_1344+449 others(22): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734169 | A | ATGTGTGT others(13): Show |
1 | a0003c0003t0004g0081 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344+4479_1344+449 others(24): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112734169 | ||||||
| chr2:112734195 | G | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1344+4491G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734195 | |||||||
| chr2:112734423 | C | T | 1 | a0001c0020t0001g0191 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1345-4490C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734423 | |||||||
| chr2:112734619 | G | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-4294G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734619 | |||||||
| chr2:112734652 | T | C | 10 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(7): Show |
11 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1345-4261T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734652 | |||||||
| chr2:112734686 | G | C | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-4227G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734686 | |||||||
| chr2:112734769 | A | C | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-4144A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734769 | |||||||
| chr2:112734837 | A | G | 1 | a0004c0009t0001g0074 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1345-4076A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112734837 | |||||||
| chr2:112735038 | A | AT | 59 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(56): Show |
74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1345-3852dupT | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | A | ATT | 13 | a0001c0001t0001g0085 a0001c0001t0001g0266 a0002c0002t0001g0172 others(10): Show |
26 | HG00639.hp1 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1345-3853_1345-385 others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | A | ATTT | 37 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0104 others(34): Show |
60 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1345-3854_1345-385 others(7): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | A | ATTTT | 15 | a0001c0001t0001g0136 a0002c0002t0001g0147 a0002c0002t0001g0156 others(12): Show |
15 | HG00423.hp2 HG00642.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1345-3855_1345-385 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | ATT | A | 17 | a0001c0001t0001g0027 a0001c0001t0001g0097 a0001c0001t0001g0106 others(14): Show |
18 | HG01515.hp1 HG01517.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1345-3853_1345-385 others(6): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | ATTT | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(102): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1345-3854_1345-385 others(7): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735038 | ATTTT | A | 13 | a0004c0004t0001g0059 a0004c0004t0001g0139 a0004c0004t0001g0253 others(10): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1345-3855_1345-385 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735038 | ||||||
| chr2:112735049 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1345-3864T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735049 | |||||||
| chr2:112735275 | A | G | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-3638A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735275 | |||||||
| chr2:112735296 | G | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-3617G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735296 | |||||||
| chr2:112735362 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1345-3551A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735362 | |||||||
| chr2:112735395 | A | G | 1 | a0002c0002t0001g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1345-3518A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735395 | |||||||
| chr2:112735480 | C | T | 2 | a0001c0001t0001g0100 a0003c0003t0002g0053 |
2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1345-3433C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735480 | |||||||
| chr2:112735482 | T | TC | 12 | a0003c0003t0001g0127 a0003c0003t0001g0128 a0003c0003t0002g0020 others(9): Show |
14 | HG00642.hp2 HG01074.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1345-3423dupC | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735482 | ||||||
| chr2:112735482 | TC | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-3423delC | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735482 | ||||||
| chr2:112735494 | TTTTC | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(116): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1345-3411_1345-340 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112735494 | ||||||
| chr2:112735619 | C | A | 9 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-3294C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735619 | |||||||
| chr2:112735768 | A | G | 2 | a0002c0002t0001g0202 a0002c0002t0001g0203 |
2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1345-3145A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735768 | |||||||
| chr2:112735770 | A | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0002c0002t0001g0029 |
4 | HG01069.hp2 HG01071.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-3143A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735770 | |||||||
| chr2:112735809 | G | T | 1 | a0002c0002t0001g0034 | 2 | HG00099.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1345-3104G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735809 | |||||||
| chr2:112735815 | C | T | 1 | a0002c0002t0001g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1345-3098C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735815 | |||||||
| chr2:112735869 | C | T | 1 | a0007c0008t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1345-3044C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735869 | |||||||
| chr2:112735906 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1345-3007G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112735906 | |||||||
| chr2:112736036 | G | A | 5 | a0004c0004t0001g0024 a0004c0004t0001g0067 a0004c0004t0001g0068 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-2877G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736036 | |||||||
| chr2:112736039 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1345-2874T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736039 | |||||||
| chr2:112736098 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1345-2815A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736098 | |||||||
| chr2:112736188 | A | G | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-2725A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736188 | |||||||
| chr2:112736327 | A | G | 1 | a0002c0002t0001g0260 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1345-2586A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736327 | |||||||
| chr2:112736330 | GTTAACTC others(11): Show |
G | 4 | a0004c0009t0001g0133 a0011c0010t0001g0158 a0011c0010t0001g0159 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-2580_1345-256 others(22): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112736330 | ||||||
| chr2:112736412 | A | G | 1 | a0013c0016t0001g0183 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1345-2501A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736412 | |||||||
| chr2:112736446 | GATTAAC | G | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-2462_1345-245 others(10): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112736446 | ||||||
| chr2:112736482 | G | T | 1 | a0004c0004t0001g0069 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1345-2431G>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736482 | |||||||
| chr2:112736493 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1345-2420C>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736493 | |||||||
| chr2:112736538 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1345-2375C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736538 | |||||||
| chr2:112736554 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1345-2359G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736554 | |||||||
| chr2:112736563 | A | T | 1 | a0002c0002t0001g0186 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1345-2350A>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736563 | |||||||
| chr2:112736673 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1345-2240T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736673 | |||||||
| chr2:112736800 | C | T | 4 | a0004c0009t0001g0133 a0011c0010t0001g0158 a0011c0010t0001g0159 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-2113C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736800 | |||||||
| chr2:112736818 | TTTTC | T | 5 | a0001c0001t0001g0088 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | NA18946.hp1 NA18948.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-2091_1345-208 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112736818 | ||||||
| chr2:112736897 | T | G | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-2016T>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736897 | |||||||
| chr2:112736932 | C | CTTCT | 9 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-1979_1345-197 others(8): Show |
NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112736932 | ||||||
| chr2:112736943 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(114): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1345-1970T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736943 | |||||||
| chr2:112736952 | A | C | 112 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(109): Show |
161 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1345-1961A>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112736952 | |||||||
| chr2:112737039 | G | A | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-1874G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737039 | |||||||
| chr2:112737295 | A | G | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1618A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737295 | |||||||
| chr2:112737314 | A | G | 16 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(13): Show |
19 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1345-1599A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737314 | |||||||
| chr2:112737336 | C | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-1577C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737336 | |||||||
| chr2:112737337 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1345-1576G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737337 | |||||||
| chr2:112737407 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1345-1506T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737407 | |||||||
| chr2:112737543 | C | T | 9 | a0004c0004t0001g0139 a0004c0004t0001g0259 a0004c0009t0001g0074 others(6): Show |
10 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-1370C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737543 | |||||||
| chr2:112737592 | G | C | 1 | a0002c0002t0001g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1345-1321G>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737592 | |||||||
| chr2:112737650 | G | A | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1263G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737650 | |||||||
| chr2:112737723 | T | C | 1 | a0005c0006t0001g0065 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1345-1190T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737723 | |||||||
| chr2:112737739 | G | A | 3 | a0004c0004t0001g0253 a0012c0014t0001g0072 a0012c0014t0001g0073 |
3 | HG01884.hp1 NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1345-1174G>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737739 | |||||||
| chr2:112737757 | T | A | 1 | a0003c0003t0002g0043 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1345-1156T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737757 | |||||||
| chr2:112737868 | A | G | 2 | a0009c0012t0001g0071 a0014c0017t0001g0140 |
2 | HG00639.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1345-1045A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112737868 | |||||||
| chr2:112737959 | CA | C | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-952delA | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 112737959 | ||||||
| chr2:112738002 | T | C | 4 | a0007c0008t0001g0250 a0007c0008t0001g0273 a0007c0008t0001g0274 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-911T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738002 | |||||||
| chr2:112738029 | C | T | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1345-884C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738029 | |||||||
| chr2:112738126 | T | A | 3 | a0003c0003t0004g0078 a0003c0003t0004g0080 a0003c0003t0004g0081 |
3 | HG02109.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1345-787T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738126 | |||||||
| chr2:112738136 | C | A | 2 | a0004c0019t0001g0098 a0006c0005t0002g0041 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345-777C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738136 | |||||||
| chr2:112738137 | C | A | 2 | a0004c0019t0001g0098 a0006c0005t0002g0041 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1345-776C>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738137 | |||||||
| chr2:112738208 | T | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(267): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1345-705T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738208 | |||||||
| chr2:112738319 | T | C | 1 | a0002c0002t0001g0196 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1345-594T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738319 | |||||||
| chr2:112738554 | A | T | 12 | a0004c0004t0001g0139 a0004c0004t0001g0253 a0004c0004t0001g0259 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1345-359A>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738554 | |||||||
| chr2:112738609 | A | G | 4 | a0006c0005t0001g0076 a0006c0005t0002g0018 a0006c0005t0002g0019 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-304A>G | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738609 | |||||||
| chr2:112738611 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1345-302T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738611 | |||||||
| chr2:112738745 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0117 |
2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1345-168T>C | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738745 | |||||||
| chr2:112738767 | T | A | 2 | a0001c0001t0001g0136 a0002c0002t0001g0156 |
2 | NA19000.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1345-146T>A | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738767 | |||||||
| chr2:112738875 | C | T | 1 | a0004c0004t0001g0039 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1345-38C>T | NT5DC4 | ENSG00000144130.12 | transcript | ENST00000688554.1 | protein_coding | 16/16 | chr2 | 112738875 |