Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 93034 |
| ensemblid | ENSG00000185013.17 |
| hgncid | 17818 |
| symbol | NT5C1B |
| name | 5'-nucleotidase, cytosolic IB |
| refseq_nuc | NM_033253.4 |
| refseq_prot | NP_150278.2 |
| ensembl_nuc | ENST00000304081.9 |
| ensembl_prot | ENSP00000305979.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 18562871 |
| end | 18589569 |
| strand | - |
| ver | v1.2 |
| region | chr2:18562871-18589569 |
| region5000 | chr2:18557871-18594569 |
| regionname0 | NT5C1B_chr2_18562871_18589569 |
| regionname5000 | NT5C1B_chr2_18557871_18594569 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 550 | 333 | 71 | 61 | 148 | 14 | 38 | 113 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0002 | 0/1 | 115 | 34 | 2 | 10 | 19 | 2 | 0 | 17 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(110): Show |
chr2 | 18557871 | 18594569 |
| a0003 | 0/0 | 550 | 19 | 15 | 4 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0004 | 0/0 | 550 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0005 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0006 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0007 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0008 | 0/0 | 550 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| a0009 | 0/0 | 550 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | MSQTS others(545): Show |
chr2 | 18557871 | 18594569 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1650 | 258 | 38 | 47 | 126 | 13 | 33 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0002 | 0/0 | 1650 | 56 | 27 | 10 | 13 | 1 | 5 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0005 | 0/0 | 1650 | 9 | 0 | 3 | 6 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0006 | 0/0 | 1650 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0007 | 0/0 | 1650 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0008 | 0/0 | 1650 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0012 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0001c0015 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0002c0003 | 0/1 | 1650 | 33 | 1 | 10 | 19 | 2 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0002c0011 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0003c0004 | 0/0 | 1650 | 19 | 15 | 4 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0004c0013 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0005c0009 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0006c0010 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0007c0017 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0008c0016 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 | ||
| a0009c0014 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATGAG others(1645): Show |
chr2 | 18557871 | 18594569 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2679 | 250 | 36 | 46 | 121 | 13 | 33 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0003 | 0/0 | 2680 | 3 | 1 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0004 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0005 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0007 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0008 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0001t0009 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0002t0001 | 0/0 | 2679 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0002t0002 | 0/0 | 2680 | 19 | 12 | 2 | 4 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0001c0002t0003 | 0/0 | 2680 | 32 | 10 | 8 | 9 | 1 | 4 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0001c0002t0006 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0005t0001 | 0/0 | 2679 | 9 | 0 | 3 | 6 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0006t0002 | 0/0 | 2680 | 4 | 4 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0001c0007t0001 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0008t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0008t0003 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0001c0012t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0001c0015t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0002c0003t0002 | 0/1 | 2680 | 33 | 1 | 10 | 19 | 2 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0002c0011t0002 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0003c0004t0002 | 0/0 | 2680 | 19 | 15 | 4 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0004c0013t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0005c0009t0002 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0006c0010t0002 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2675): Show |
chr2 | 18557871 | 18594569 |
| a0007c0017t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0008c0016t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| a0009c0014t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | ATTCT others(2674): Show |
chr2 | 18557871 | 18594569 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0002 | 0/0 | 15 | 14 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0004 | 1/0 | 10 | 0 | 6 | 0 | 2 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 3 | 2 | 1 | 2 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0028 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0008g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0001g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0009 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0054 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0006t0002g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0006t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0006t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0007t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0008t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0008t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0012t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0001c0015t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0003 | 0/0 | 12 | 1 | 9 | 0 | 2 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0011 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0003t0002g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0002c0011t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0016 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0003c0004t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0004c0013t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0005c0009t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0006c0010t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0007c0017t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0008c0016t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| a0009c0014t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00099 | hp2 | a0001 | c0002 | t0003 | g0183 | EUR | GBR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00642 | hp2 | a0004 | c0013 | t0001 | g0077 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0054 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0051 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01192 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01243 | hp1 | a0003 | c0004 | t0002 | g0016 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01255 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01255 | hp2 | a0003 | c0004 | t0002 | g0168 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01256 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01261 | hp2 | a0003 | c0004 | t0002 | g0016 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01433 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01496 | hp1 | a0003 | c0004 | t0002 | g0055 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01517 | hp2 | a0002 | c0003 | t0002 | g0003 | EUR | IBS | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01884 | hp2 | a0003 | c0004 | t0002 | g0032 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0199 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0074 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01975 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0172 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01978 | hp2 | a0001 | c0005 | t0001 | g0024 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01981 | hp1 | a0001 | c0012 | t0001 | g0063 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02004 | hp1 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02055 | hp2 | a0003 | c0004 | t0002 | g0194 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02083 | hp2 | a0005 | c0009 | t0002 | g0203 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02132 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02135 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0009 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02148 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0110 | EAS | CDX | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02257 | hp1 | a0003 | c0004 | t0002 | g0016 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02273 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02300 | hp1 | a0001 | c0005 | t0001 | g0095 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02572 | hp2 | a0003 | c0004 | t0002 | g0195 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02630 | hp2 | a0002 | c0011 | t0002 | g0191 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02717 | hp1 | a0001 | c0002 | t0003 | g0208 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0053 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02886 | hp2 | a0003 | c0004 | t0002 | g0016 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02895 | hp2 | a0001 | c0002 | t0003 | g0202 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02896 | hp1 | a0003 | c0004 | t0002 | g0197 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0182 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02897 | hp2 | a0003 | c0004 | t0002 | g0056 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02922 | hp1 | a0003 | c0004 | t0002 | g0192 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02922 | hp2 | a0001 | c0006 | t0002 | g0059 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0187 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02970 | hp1 | a0001 | c0006 | t0002 | g0211 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0188 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03098 | hp2 | a0003 | c0004 | t0002 | g0032 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03130 | hp2 | a0003 | c0004 | t0002 | g0196 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03139 | hp1 | a0001 | c0006 | t0002 | g0059 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0204 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0176 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03209 | hp2 | a0003 | c0004 | t0002 | g0032 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03486 | hp2 | a0003 | c0004 | t0002 | g0193 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03516 | hp1 | a0003 | c0004 | t0002 | g0055 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0177 | AFR | GWD | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0054 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0180 | SAS | BEB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0053 | SAS | STU | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | CHB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18906 | hp1 | a0003 | c0004 | t0002 | g0056 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18943 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18945 | hp2 | a0001 | c0005 | t0001 | g0024 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18953 | hp1 | a0001 | c0005 | t0001 | g0093 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0185 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18959 | hp2 | a0001 | c0015 | t0001 | g0090 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18963 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0031 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18965 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18965 | hp2 | a0001 | c0005 | t0001 | g0094 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0169 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18975 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18986 | hp2 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18988 | hp2 | a0002 | c0003 | t0002 | g0173 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18990 | hp1 | a0001 | c0005 | t0001 | g0097 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0009 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18994 | hp2 | a0001 | c0008 | t0003 | g0100 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18995 | hp1 | a0007 | c0017 | t0001 | g0092 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19009 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0031 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19056 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19058 | hp1 | a0002 | c0003 | t0002 | g0031 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19058 | hp2 | a0001 | c0005 | t0001 | g0098 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19062 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19064 | hp2 | a0002 | c0003 | t0002 | g0170 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19065 | hp1 | a0002 | c0003 | t0002 | g0171 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19065 | hp2 | a0002 | c0003 | t0002 | g0174 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19076 | hp1 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19082 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19085 | hp1 | a0001 | c0008 | t0001 | g0099 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19087 | hp2 | a0008 | c0016 | t0001 | g0091 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | YRI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20129 | hp1 | a0003 | c0004 | t0002 | g0209 | AFR | ASW | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | ASW | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01123 | hp1 | a0001 | c0005 | t0001 | g0024 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0052 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02486 | hp1 | a0001 | c0007 | t0001 | g0057 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG02559 | hp2 | a0006 | c0010 | t0002 | g0212 | AFR | ACB | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | USA | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20300 | hp1 | a0002 | c0003 | t0002 | g0003 | AFR | USA | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA20300 | hp2 | a0001 | c0006 | t0002 | g0210 | AFR | USA | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| NA21309 | hp2 | a0009 | c0014 | t0001 | g0124 | AFR | LWK | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0002 | g0175 | REF | REF | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | NT5C1B_chr2_18557871_18594569 | NT5C1B | chr2 | 18557871 | 18594569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:18564038 | T | C | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1411A>G | p.Ile471Val | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 1512/2679 | 1411/1653 | 471/550 | chr2 | 18564038 | |||
| chr2:18584248 | G | A | 1 | a0005 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.731C>T | p.Pro244Leu | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/9 | 832/2679 | 731/1653 | 244/550 | chr2 | 18584248 | |||
| chr2:18584642 | G | C | 1 | a0008 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.595C>G | p.Leu199Val | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 696/2679 | 595/1653 | 199/550 | chr2 | 18584642 | |||
| chr2:18584699 | G | A | 1 | a0006 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.538C>T | p.Pro180Ser | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 639/2679 | 538/1653 | 180/550 | chr2 | 18584699 | |||
| chr2:18584857 | C | T | 2 | a0002 a0003 |
52 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(49): Show |
missense_variant | MODERATE | c.380G>A | p.Arg127Gln | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 481/2679 | 380/1653 | 127/550 | chr2 | 18584857 | |||
| chr2:18584890 | G | C | 1 | a0007 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.347C>G | p.Ser116Trp | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 448/2679 | 347/1653 | 116/550 | chr2 | 18584890 | |||
| chr2:18584890 | G | T | 1 | a0002 | 32 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(29): Show |
stop_gained | HIGH | c.347C>A | p.Ser116* | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 448/2679 | 347/1653 | 116/550 | chr2 | 18584890 | |||
| chr2:18586355 | G | A | 1 | a0002 | 1 | HG02630.hp2 | stop_gained | HIGH | c.157C>T | p.Arg53* | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/9 | 258/2679 | 157/1653 | 53/550 | chr2 | 18586355 | |||
| chr2:18586372 | A | G | 1 | a0004 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.140T>C | p.Leu47Pro | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/9 | 241/2679 | 140/1653 | 47/550 | chr2 | 18586372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:18576235 | G | C | 8 | a0001c0002 a0001c0006 a0001c0007 others(5): Show |
116 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(113): Show |
synonymous_variant | LOW | c.1278C>G | p.Leu426Leu | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/9 | 1379/2679 | 1278/1653 | 426/550 | chr2 | 18576235 | |||
| chr2:18582869 | G | A | 1 | a0001c0015 | 1 | NA18959.hp2 | splice_region_variant&synonymous_variant | LOW | c.1020C>T | p.Tyr340Tyr | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/9 | 1121/2679 | 1020/1653 | 340/550 | chr2 | 18582869 | |||
| chr2:18584148 | C | T | 1 | a0001c0007 | 2 | HG02258.hp1 HG02486.hp1 |
synonymous_variant | LOW | c.831G>A | p.Glu277Glu | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/9 | 932/2679 | 831/1653 | 277/550 | chr2 | 18584148 | |||
| chr2:18584907 | C | T | 1 | a0001c0008 | 2 | NA18994.hp2 NA19085.hp1 |
synonymous_variant | LOW | c.330G>A | p.Pro110Pro | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 431/2679 | 330/1653 | 110/550 | chr2 | 18584907 | |||
| chr2:18584925 | A | G | 1 | a0001c0005 | 9 | HG01123.hp1 HG01978.hp2 HG02300.hp1 others(6): Show |
synonymous_variant | LOW | c.312T>C | p.His104His | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 413/2679 | 312/1653 | 104/550 | chr2 | 18584925 | |||
| chr2:18584940 | G | A | 2 | a0001c0006 a0006c0010 |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.297C>T | p.Thr99Thr | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/9 | 398/2679 | 297/1653 | 99/550 | chr2 | 18584940 | |||
| chr2:18587512 | C | T | 1 | a0001c0012 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.111G>A | p.Leu37Leu | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/9 | 212/2679 | 111/1653 | 37/550 | chr2 | 18587512 | |||
| chr2:18587584 | A | G | 8 | a0001c0002 a0001c0006 a0001c0007 others(5): Show |
116 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(113): Show |
synonymous_variant | LOW | c.39T>C | p.Pro13Pro | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/9 | 140/2679 | 39/1653 | 13/550 | chr2 | 18587584 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:18563058 | C | T | 1 | a0001c0001t0007 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 738 | chr2 | 18563058 | ||||||
| chr2:18563066 | C | CT | 10 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(7): Show |
113 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*729dupA | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 729 | chr2 | 18563066 | ||||||
| chr2:18563216 | A | G | 1 | a0001c0001t0004 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 580 | chr2 | 18563216 | ||||||
| chr2:18563284 | T | C | 1 | a0001c0001t0008 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 512 | chr2 | 18563284 | ||||||
| chr2:18563492 | C | T | 8 | a0001c0002t0002 a0001c0002t0006 a0001c0006t0002 others(5): Show |
78 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*304G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 304 | chr2 | 18563492 | ||||||
| chr2:18563684 | G | A | 1 | a0001c0001t0009 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 112 | chr2 | 18563684 | ||||||
| chr2:18563773 | C | T | 2 | a0001c0001t0004 a0001c0001t0005 |
2 | HG00558.hp1 NA18970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*23G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 9/9 | 23 | chr2 | 18563773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:18564132 | C | T | 2 | a0001c0005t0001g0093 a0001c0005t0001g0094 |
2 | NA18953.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1330-13G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564132 | |||||||
| chr2:18564200 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0044 others(11): Show |
19 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1330-81G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564200 | |||||||
| chr2:18564364 | C | A | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1330-245G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564364 | |||||||
| chr2:18564375 | T | C | 1 | a0003c0004t0002g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1330-256A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564375 | |||||||
| chr2:18564453 | G | T | 7 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0198 others(4): Show |
13 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1330-334C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564453 | |||||||
| chr2:18564470 | C | T | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1330-351G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564470 | |||||||
| chr2:18564737 | C | T | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1330-618G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564737 | |||||||
| chr2:18564925 | C | A | 5 | a0001c0002t0003g0053 a0001c0002t0003g0178 a0001c0002t0003g0179 others(2): Show |
6 | HG01099.hp2 HG01358.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1330-806G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18564925 | |||||||
| chr2:18565116 | A | G | 1 | a0001c0002t0003g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1330-997T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565116 | |||||||
| chr2:18565231 | C | T | 1 | a0001c0002t0003g0052 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1330-1112G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565231 | |||||||
| chr2:18565353 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1330-1234A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565353 | |||||||
| chr2:18565570 | A | G | 5 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(2): Show |
6 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1330-1451T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565570 | |||||||
| chr2:18565624 | A | C | 26 | a0001c0001t0001g0141 a0001c0002t0002g0167 a0001c0002t0002g0201 others(23): Show |
55 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.1330-1505T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565624 | |||||||
| chr2:18565637 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1330-1518C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565637 | |||||||
| chr2:18565659 | C | T | 2 | a0001c0002t0003g0053 a0001c0002t0003g0178 |
3 | HG01358.hp2 HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1330-1540G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565659 | |||||||
| chr2:18565744 | C | T | 45 | a0001c0001t0001g0049 a0001c0002t0001g0058 a0001c0002t0001g0205 others(42): Show |
87 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.1330-1625G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565744 | |||||||
| chr2:18565874 | G | A | 1 | a0003c0004t0002g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1330-1755C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565874 | |||||||
| chr2:18565876 | G | C | 2 | a0003c0004t0002g0032 a0003c0004t0002g0209 |
4 | HG01884.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330-1757C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565876 | |||||||
| chr2:18565915 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1330-1796T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565915 | |||||||
| chr2:18565968 | C | T | 5 | a0001c0001t0001g0145 a0001c0006t0002g0059 a0001c0006t0002g0210 others(2): Show |
6 | HG02300.hp2 HG02559.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1849G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18565968 | |||||||
| chr2:18566159 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1330-2040C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566159 | |||||||
| chr2:18566192 | A | G | 6 | a0001c0001t0001g0141 a0003c0004t0002g0016 a0003c0004t0002g0055 others(3): Show |
10 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1330-2073T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566192 | |||||||
| chr2:18566193 | T | C | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1330-2074A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566193 | |||||||
| chr2:18566206 | T | A | 1 | a0001c0002t0003g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1330-2087A>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566206 | |||||||
| chr2:18566755 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0113 a0001c0001t0001g0116 |
11 | HG00673.hp1 NA18944.hp1 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.1330-2636C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566755 | |||||||
| chr2:18566794 | C | G | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1330-2675G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18566794 | |||||||
| chr2:18567267 | A | G | 1 | a0001c0002t0003g0183 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1330-3148T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567267 | |||||||
| chr2:18567292 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1330-3173G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567292 | |||||||
| chr2:18567366 | A | G | 19 | a0001c0002t0003g0009 a0001c0002t0003g0051 a0001c0002t0003g0052 others(16): Show |
30 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1330-3247T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567366 | |||||||
| chr2:18567491 | G | T | 1 | a0003c0004t0002g0196 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1330-3372C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567491 | |||||||
| chr2:18567520 | G | A | 3 | a0001c0002t0003g0054 a0001c0002t0003g0182 a0001c0002t0003g0184 |
4 | HG00738.hp2 HG01069.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330-3401C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567520 | |||||||
| chr2:18567576 | T | C | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1330-3457A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567576 | |||||||
| chr2:18567893 | T | C | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1330-3774A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18567893 | |||||||
| chr2:18568087 | G | GAC | 26 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0036 others(23): Show |
56 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1330-3970_1330-396 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACAC | 42 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0020 others(39): Show |
66 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330-3972_1330-396 others(8): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACACAC | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
131 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1330-3974_1330-396 others(10): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACACACA others(1): Show |
25 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0035 others(22): Show |
37 | HG00140.hp2 HG00673.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.1330-3976_1330-396 others(12): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACACACA others(3): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0080 others(9): Show |
20 | HG00280.hp2 HG01123.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1330-3978_1330-396 others(14): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACACACA others(5): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0149 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1330-3980_1330-396 others(16): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | G | GACACACA others(7): Show |
1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1330-3982_1330-396 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | GAC | G | 11 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0002g0167 others(8): Show |
32 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1330-3970_1330-396 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | GACACACA others(5): Show |
G | 1 | a0001c0001t0001g0083 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1330-3980_1330-396 others(16): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568087 | GACACACA others(7): Show |
G | 7 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0198 others(4): Show |
13 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1330-3982_1330-396 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568087 | |||||||
| chr2:18568089 | C | CACACAT | 3 | a0001c0002t0002g0201 a0003c0004t0002g0195 a0003c0004t0002g0196 |
3 | HG02572.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1330-3971_1330-397 others(10): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568089 | |||||||
| chr2:18568413 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1330-4294G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568413 | |||||||
| chr2:18568442 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1330-4323T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568442 | |||||||
| chr2:18568703 | T | C | 2 | a0001c0002t0001g0205 a0001c0002t0001g0206 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1330-4584A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568703 | |||||||
| chr2:18568789 | G | A | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1330-4670C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568789 | |||||||
| chr2:18568837 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02056.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1330-4718G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18568837 | |||||||
| chr2:18569025 | G | C | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1330-4906C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569025 | |||||||
| chr2:18569215 | G | A | 1 | a0001c0005t0001g0098 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1330-5096C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569215 | |||||||
| chr2:18569311 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1330-5192T>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569311 | |||||||
| chr2:18569336 | G | A | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1330-5217C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569336 | |||||||
| chr2:18569387 | C | T | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-5268G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569387 | |||||||
| chr2:18569548 | A | G | 2 | a0001c0001t0004g0069 a0001c0001t0005g0070 |
2 | HG00558.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1330-5429T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569548 | |||||||
| chr2:18569680 | C | G | 1 | a0001c0002t0003g0052 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1330-5561G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569680 | |||||||
| chr2:18569739 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1330-5620C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569739 | |||||||
| chr2:18569749 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1330-5630G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569749 | |||||||
| chr2:18569800 | G | C | 5 | a0003c0004t0002g0016 a0003c0004t0002g0055 a0003c0004t0002g0192 others(2): Show |
9 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1330-5681C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569800 | |||||||
| chr2:18569867 | G | A | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1330-5748C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18569867 | |||||||
| chr2:18570158 | TA | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0152 a0001c0002t0002g0019 others(4): Show |
10 | HG00597.hp2 HG01934.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329+6025delT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570158 | |||||||
| chr2:18570186 | G | T | 3 | a0003c0004t0002g0055 a0003c0004t0002g0193 a0003c0004t0002g0194 |
4 | HG01496.hp1 HG02055.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+5998C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570186 | |||||||
| chr2:18570202 | G | A | 47 | a0001c0001t0001g0021 a0001c0001t0008g0074 a0001c0002t0001g0058 others(44): Show |
90 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(87): Show |
intron_variant | MODIFIER | c.1329+5982C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570202 | |||||||
| chr2:18570322 | T | C | 25 | a0001c0001t0001g0141 a0001c0002t0002g0167 a0001c0002t0002g0201 others(22): Show |
54 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.1329+5862A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570322 | |||||||
| chr2:18570574 | G | A | 1 | a0001c0002t0003g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1329+5610C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570574 | |||||||
| chr2:18570983 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1329+5201G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18570983 | |||||||
| chr2:18571032 | G | A | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1329+5152C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571032 | |||||||
| chr2:18571105 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(203): Show |
376 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.1329+5079A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571105 | |||||||
| chr2:18571244 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1329+4940A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571244 | |||||||
| chr2:18571283 | A | AT | 6 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(3): Show |
8 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+4900dupA | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571283 | |||||||
| chr2:18571350 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0060 |
3 | NA18954.hp2 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1329+4834A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571350 | |||||||
| chr2:18571377 | C | T | 2 | a0002c0003t0002g0003 a0002c0003t0002g0172 |
13 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1329+4807G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571377 | |||||||
| chr2:18571589 | C | A | 11 | a0001c0002t0003g0009 a0001c0002t0003g0051 a0001c0002t0003g0054 others(8): Show |
20 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1329+4595G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571589 | |||||||
| chr2:18571637 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1329+4547G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571637 | |||||||
| chr2:18571666 | AAAGTGCA others(121): Show |
A | 5 | a0003c0004t0002g0016 a0003c0004t0002g0055 a0003c0004t0002g0192 others(2): Show |
9 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1329+4390_1329+451 others(4): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571666 | |||||||
| chr2:18571708 | C | CTGTG | 3 | a0002c0011t0002g0191 a0003c0004t0002g0032 a0003c0004t0002g0056 |
3 | HG01884.hp2 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1329+4472_1329+447 others(8): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571708 | |||||||
| chr2:18571708 | C | G | 10 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0079 others(7): Show |
15 | HG00597.hp2 HG02027.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.1329+4476G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571708 | |||||||
| chr2:18571710 | G | C | 2 | a0001c0001t0001g0033 a0004c0013t0001g0077 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1329+4474C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571710 | |||||||
| chr2:18571718 | G | GTA | 8 | a0001c0001t0001g0012 a0001c0001t0001g0049 a0001c0001t0001g0050 others(5): Show |
9 | HG01081.hp2 NA18942.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.1329+4464_1329+446 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATA | 5 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0050 others(2): Show |
5 | HG01884.hp1 HG01975.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1329+4462_1329+446 others(8): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATATA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG00621.hp2 HG01358.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1329+4460_1329+446 others(10): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0140 a0001c0005t0001g0094 |
3 | NA18965.hp2 NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1329+4458_1329+446 others(12): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATATAT others(3): Show |
4 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0003g0155 others(1): Show |
4 | HG01952.hp1 HG02155.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+4456_1329+446 others(14): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATATAT others(7): Show |
1 | a0001c0005t0001g0097 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+4452_1329+446 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0006 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1329+4450_1329+446 others(20): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTATAT others(3): Show |
1 | a0001c0002t0002g0019 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1329+4465_1329+446 others(14): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTATAT others(5): Show |
1 | a0001c0002t0002g0019 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1329+4465_1329+446 others(16): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTATAT others(7): Show |
1 | a0001c0002t0002g0019 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1329+4465_1329+446 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTGTGT others(3): Show |
3 | a0001c0002t0002g0190 a0001c0006t0002g0211 a0003c0004t0002g0032 |
3 | HG02970.hp1 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1329+4465_1329+446 others(14): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTGTGT others(5): Show |
2 | a0001c0006t0002g0059 a0006c0010t0002g0212 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1329+4465_1329+446 others(16): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTGTGT others(7): Show |
2 | a0001c0006t0002g0059 a0003c0004t0002g0209 |
2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1329+4465_1329+446 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | G | GTGTGTGT others(13): Show |
1 | a0003c0004t0002g0032 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1329+4465_1329+446 others(24): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTA | G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0023 others(18): Show |
28 | HG01106.hp1 HG01175.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.1329+4464_1329+446 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATA | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(17): Show |
42 | HG00558.hp1 HG00733.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1329+4462_1329+446 others(8): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATA | G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(13): Show |
23 | HG00140.hp1 HG00140.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1329+4460_1329+446 others(10): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(1): Show |
G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(7): Show |
23 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1329+4458_1329+446 others(12): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(3): Show |
G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(21): Show |
34 | HG00733.hp1 HG01099.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1329+4456_1329+446 others(14): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(5): Show |
G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(20): Show |
24 | HG00408.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1329+4454_1329+446 others(16): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(7): Show |
G | 19 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(16): Show |
33 | HG00673.hp1 HG01106.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1329+4452_1329+446 others(18): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(9): Show |
G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0027 others(10): Show |
18 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(15): Show |
intron_variant | MODIFIER | c.1329+4450_1329+446 others(20): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(11): Show |
G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0102 |
3 | HG02145.hp2 HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1329+4448_1329+446 others(22): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(17): Show |
G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
32 | HG00558.hp2 HG00673.hp2 HG02074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1329+4442_1329+446 others(28): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(19): Show |
G | 1 | a0001c0001t0001g0043 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1329+4440_1329+446 others(30): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(21): Show |
G | 1 | a0001c0001t0001g0012 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1329+4438_1329+446 others(32): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(23): Show |
G | 13 | a0001c0001t0001g0037 a0001c0002t0001g0058 a0001c0002t0001g0205 others(10): Show |
20 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+4436_1329+446 others(34): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571718 | GTATATAT others(27): Show |
G | 19 | a0001c0002t0003g0009 a0001c0002t0003g0051 a0001c0002t0003g0052 others(16): Show |
30 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1329+4432_1329+446 others(38): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571718 | |||||||
| chr2:18571720 | A | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0002c0003t0002g0011 others(4): Show |
8 | HG01516.hp1 HG01517.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329+4464T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571720 | |||||||
| chr2:18571720 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0025 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1329+4451_1329+446 others(17): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571720 | |||||||
| chr2:18571722 | A | G | 13 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0165 others(10): Show |
20 | HG01106.hp1 HG01175.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+4462T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571722 | |||||||
| chr2:18571724 | A | G | 16 | a0001c0001t0001g0045 a0001c0001t0001g0101 a0001c0001t0001g0139 others(13): Show |
39 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.1329+4460T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571724 | |||||||
| chr2:18571726 | A | G | 12 | a0001c0002t0002g0167 a0001c0002t0002g0201 a0002c0003t0002g0003 others(9): Show |
33 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.1329+4458T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571726 | |||||||
| chr2:18571728 | A | G | 9 | a0001c0002t0002g0167 a0001c0002t0002g0201 a0002c0003t0002g0003 others(6): Show |
23 | HG01256.hp2 HG01433.hp2 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.1329+4456T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571728 | |||||||
| chr2:18571730 | A | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0073 others(5): Show |
8 | HG01123.hp2 HG02572.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+4454T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571730 | |||||||
| chr2:18571732 | A | G | 3 | a0001c0002t0002g0167 a0003c0004t0002g0195 a0003c0004t0002g0196 |
3 | HG02572.hp2 HG03130.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1329+4452T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571732 | |||||||
| chr2:18571734 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0003c0004t0002g0195 |
3 | HG02572.hp2 HG04115.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1329+4450T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571734 | |||||||
| chr2:18571744 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1329+4440T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571744 | |||||||
| chr2:18571750 | A | G | 12 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(9): Show |
19 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1329+4434T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571750 | |||||||
| chr2:18571754 | A | G | 19 | a0001c0002t0003g0009 a0001c0002t0003g0051 a0001c0002t0003g0052 others(16): Show |
30 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.1329+4430T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18571754 | |||||||
| chr2:18572063 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0136 |
4 | NA18948.hp2 NA18955.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+4121C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572063 | |||||||
| chr2:18572069 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1329+4115C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572069 | |||||||
| chr2:18572083 | CA | C | 56 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0045 others(53): Show |
100 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(97): Show |
intron_variant | MODIFIER | c.1329+4100delT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572083 | |||||||
| chr2:18572083 | CAA | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(81): Show |
168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.1329+4099_1329+410 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572083 | |||||||
| chr2:18572205 | T | C | 1 | a0001c0002t0002g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1329+3979A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572205 | |||||||
| chr2:18572247 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1329+3937T>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572247 | |||||||
| chr2:18572324 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(16): Show |
50 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1329+3860G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572324 | |||||||
| chr2:18572640 | A | G | 46 | a0001c0001t0001g0141 a0001c0002t0001g0058 a0001c0002t0001g0205 others(43): Show |
87 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(84): Show |
intron_variant | MODIFIER | c.1329+3544T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572640 | |||||||
| chr2:18572712 | G | T | 2 | a0003c0004t0002g0032 a0003c0004t0002g0209 |
4 | HG01884.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+3472C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572712 | |||||||
| chr2:18572799 | T | C | 1 | a0001c0002t0003g0202 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1329+3385A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572799 | |||||||
| chr2:18572883 | T | G | 12 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(9): Show |
34 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1329+3301A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572883 | |||||||
| chr2:18572930 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1329+3254G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572930 | |||||||
| chr2:18572949 | G | A | 1 | a0001c0002t0002g0017 | 4 | HG01346.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+3235C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18572949 | |||||||
| chr2:18573024 | A | G | 1 | a0001c0002t0003g0177 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1329+3160T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573024 | |||||||
| chr2:18573059 | CA | C | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+3124delT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573059 | |||||||
| chr2:18573075 | G | T | 7 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0198 others(4): Show |
13 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1329+3109C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573075 | |||||||
| chr2:18573384 | T | C | 47 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0002t0001g0058 others(44): Show |
89 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(86): Show |
intron_variant | MODIFIER | c.1329+2800A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573384 | |||||||
| chr2:18573445 | TAC | T | 43 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(40): Show |
84 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(81): Show |
intron_variant | MODIFIER | c.1329+2737_1329+273 others(6): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573445 | |||||||
| chr2:18573563 | T | C | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1329+2621A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573563 | |||||||
| chr2:18573736 | C | T | 7 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0198 others(4): Show |
13 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1329+2448G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573736 | |||||||
| chr2:18573837 | T | C | 1 | a0001c0002t0002g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1329+2347A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573837 | |||||||
| chr2:18573838 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1329+2346C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573838 | |||||||
| chr2:18573938 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1329+2246C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573938 | |||||||
| chr2:18573940 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1329+2244C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18573940 | |||||||
| chr2:18574169 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1329+2015A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574169 | |||||||
| chr2:18574183 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1329+2001T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574183 | |||||||
| chr2:18574248 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1329+1936G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574248 | |||||||
| chr2:18574298 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1329+1886A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574298 | |||||||
| chr2:18574327 | C | T | 2 | a0001c0002t0002g0198 a0001c0002t0006g0199 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1329+1857G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574327 | |||||||
| chr2:18574344 | T | G | 3 | a0002c0003t0002g0015 a0002c0003t0002g0173 a0002c0003t0002g0174 |
6 | HG02132.hp1 NA18984.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.1329+1840A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574344 | |||||||
| chr2:18574386 | C | A | 66 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0002t0001g0058 others(63): Show |
119 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.1329+1798G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574386 | |||||||
| chr2:18574429 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0101 |
3 | HG01516.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1329+1755T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574429 | |||||||
| chr2:18574440 | A | G | 1 | a0003c0004t0002g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1329+1744T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574440 | |||||||
| chr2:18574616 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1329+1568C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574616 | |||||||
| chr2:18574745 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1329+1439T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574745 | |||||||
| chr2:18574830 | C | T | 26 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0002t0002g0167 others(23): Show |
56 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.1329+1354G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574830 | |||||||
| chr2:18574985 | GA | G | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+1198delT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18574985 | |||||||
| chr2:18575048 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1329+1136T>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575048 | |||||||
| chr2:18575415 | A | G | 5 | a0003c0004t0002g0016 a0003c0004t0002g0055 a0003c0004t0002g0192 others(2): Show |
9 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1329+769T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575415 | |||||||
| chr2:18575472 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0075 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1329+712T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575472 | |||||||
| chr2:18575550 | T | C | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1329+634A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575550 | |||||||
| chr2:18575595 | C | T | 3 | a0003c0004t0002g0055 a0003c0004t0002g0193 a0003c0004t0002g0194 |
4 | HG01496.hp1 HG02055.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1329+589G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575595 | |||||||
| chr2:18575705 | G | T | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1329+479C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575705 | |||||||
| chr2:18575909 | G | T | 44 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(41): Show |
85 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(82): Show |
intron_variant | MODIFIER | c.1329+275C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575909 | |||||||
| chr2:18575937 | A | C | 20 | a0001c0002t0002g0201 a0001c0002t0003g0009 a0001c0002t0003g0051 others(17): Show |
31 | HG00099.hp2 HG00408.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1329+247T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18575937 | |||||||
| chr2:18576095 | A | G | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1329+89T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 8/8 | chr2 | 18576095 | |||||||
| chr2:18576396 | C | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01516.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1145-28G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 7/8 | chr2 | 18576396 | |||||||
| chr2:18576576 | T | C | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144+197A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 7/8 | chr2 | 18576576 | |||||||
| chr2:18576900 | T | C | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1022-5A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18576900 | |||||||
| chr2:18577007 | C | T | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-112G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577007 | |||||||
| chr2:18577021 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0138 a0001c0001t0001g0165 |
4 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1022-126G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577021 | |||||||
| chr2:18577228 | T | A | 12 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(9): Show |
34 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1022-333A>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577228 | |||||||
| chr2:18577259 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1022-364G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577259 | |||||||
| chr2:18577273 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1022-378C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577273 | |||||||
| chr2:18577346 | G | A | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-451C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577346 | |||||||
| chr2:18577351 | G | C | 1 | a0001c0001t0001g0050 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1022-456C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577351 | |||||||
| chr2:18577367 | G | C | 1 | a0001c0008t0001g0099 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1022-472C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577367 | |||||||
| chr2:18577373 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1022-478C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577373 | |||||||
| chr2:18577422 | C | CA | 9 | a0001c0001t0001g0075 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG00621.hp1 HG02055.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.1022-528dupT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577422 | |||||||
| chr2:18577422 | C | CAAAAA | 10 | a0001c0002t0002g0201 a0001c0006t0002g0059 a0001c0006t0002g0211 others(7): Show |
18 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-532_1022-528d others(7): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577422 | |||||||
| chr2:18577422 | C | CAAAAAA | 12 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(9): Show |
34 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.1022-533_1022-528d others(8): Show |
NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577422 | |||||||
| chr2:18577422 | CA | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(12): Show |
19 | HG00597.hp2 HG01070.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1022-528delT | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577422 | |||||||
| chr2:18577499 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1022-604G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577499 | |||||||
| chr2:18577547 | T | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(14): Show |
24 | HG00558.hp1 HG01928.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.1022-652A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577547 | |||||||
| chr2:18577647 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0076 |
5 | NA18955.hp2 NA18997.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-752A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577647 | |||||||
| chr2:18577674 | C | T | 9 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(6): Show |
18 | HG00597.hp2 HG00639.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1022-779G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577674 | |||||||
| chr2:18577684 | T | C | 1 | a0003c0004t0002g0168 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1022-789A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577684 | |||||||
| chr2:18577882 | C | A | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1022-987G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18577882 | |||||||
| chr2:18578086 | C | A | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1022-1191G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578086 | |||||||
| chr2:18578169 | C | T | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-1274G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578169 | |||||||
| chr2:18578182 | T | C | 64 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(61): Show |
116 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1022-1287A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578182 | |||||||
| chr2:18578381 | C | G | 5 | a0002c0011t0002g0191 a0003c0004t0002g0032 a0003c0004t0002g0056 others(2): Show |
8 | HG01884.hp2 HG02630.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-1486G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578381 | |||||||
| chr2:18578419 | T | C | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1022-1524A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578419 | |||||||
| chr2:18578627 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1022-1732T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578627 | |||||||
| chr2:18578985 | A | G | 1 | a0003c0004t0002g0195 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1022-2090T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18578985 | |||||||
| chr2:18579231 | T | G | 1 | a0001c0002t0003g0176 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1022-2336A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579231 | |||||||
| chr2:18579262 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0159 |
3 | NA18971.hp2 NA19066.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1022-2367G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579262 | |||||||
| chr2:18579274 | A | C | 1 | a0001c0002t0003g0176 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1022-2379T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579274 | |||||||
| chr2:18579338 | A | C | 45 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(42): Show |
86 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(83): Show |
intron_variant | MODIFIER | c.1022-2443T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579338 | |||||||
| chr2:18579415 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1022-2520G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579415 | |||||||
| chr2:18579524 | A | G | 25 | a0001c0002t0002g0167 a0001c0002t0002g0201 a0002c0003t0002g0003 others(22): Show |
54 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.1022-2629T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579524 | |||||||
| chr2:18579647 | G | T | 2 | a0001c0002t0002g0198 a0001c0002t0006g0199 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1022-2752C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579647 | |||||||
| chr2:18579669 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0025 others(18): Show |
40 | HG00408.hp1 HG00438.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1022-2774G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579669 | |||||||
| chr2:18579676 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1022-2781G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579676 | |||||||
| chr2:18579706 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1022-2811G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579706 | |||||||
| chr2:18579952 | C | G | 1 | a0001c0002t0002g0017 | 4 | HG01346.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+2916G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579952 | |||||||
| chr2:18579955 | A | C | 3 | a0001c0002t0002g0019 a0001c0002t0002g0190 a0005c0009t0002g0203 |
6 | HG00597.hp2 HG02027.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021+2913T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18579955 | |||||||
| chr2:18580008 | T | G | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1021+2860A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18580008 | |||||||
| chr2:18580026 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1021+2842C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18580026 | |||||||
| chr2:18580143 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1021+2725C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18580143 | |||||||
| chr2:18580512 | G | A | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1021+2356C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18580512 | |||||||
| chr2:18580956 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1021+1912G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18580956 | |||||||
| chr2:18581053 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1021+1815T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581053 | |||||||
| chr2:18581071 | A | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
162 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.1021+1797T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581071 | |||||||
| chr2:18581161 | A | G | 1 | a0001c0001t0001g0040 | 2 | NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1021+1707T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581161 | |||||||
| chr2:18581312 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1021+1556T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581312 | |||||||
| chr2:18581322 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1021+1546G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581322 | |||||||
| chr2:18581431 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1021+1437G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581431 | |||||||
| chr2:18581745 | A | G | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1021+1123T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581745 | |||||||
| chr2:18581806 | C | T | 1 | a0001c0007t0001g0057 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1021+1062G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581806 | |||||||
| chr2:18581919 | A | G | 1 | a0007c0017t0001g0092 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1021+949T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18581919 | |||||||
| chr2:18582052 | G | A | 2 | a0003c0004t0002g0056 a0003c0004t0002g0197 |
3 | HG02896.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1021+816C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582052 | |||||||
| chr2:18582228 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1021+640G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582228 | |||||||
| chr2:18582306 | G | A | 38 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(35): Show |
77 | HG00597.hp2 HG00639.hp2 HG01106.hp1 others(74): Show |
intron_variant | MODIFIER | c.1021+562C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582306 | |||||||
| chr2:18582651 | C | T | 2 | a0003c0004t0002g0056 a0003c0004t0002g0197 |
3 | HG02896.hp1 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1021+217G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582651 | |||||||
| chr2:18582704 | A | G | 24 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(21): Show |
53 | HG01106.hp1 HG01192.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.1021+164T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582704 | |||||||
| chr2:18582747 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1021+121C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 6/8 | chr2 | 18582747 | |||||||
| chr2:18583196 | C | G | 1 | a0001c0002t0003g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-199G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583196 | |||||||
| chr2:18583308 | A | G | 1 | a0001c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.892-311T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583308 | |||||||
| chr2:18583337 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.892-340C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583337 | |||||||
| chr2:18583435 | T | G | 1 | a0001c0002t0003g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.892-438A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583435 | |||||||
| chr2:18583560 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0103 |
3 | HG01109.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.891+528T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583560 | |||||||
| chr2:18583670 | C | A | 1 | a0001c0002t0002g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.891+418G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583670 | |||||||
| chr2:18583903 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0078 |
3 | HG01070.hp1 HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.891+185G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583903 | |||||||
| chr2:18583915 | A | G | 12 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(9): Show |
34 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.891+173T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583915 | |||||||
| chr2:18583956 | G | A | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.891+132C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583956 | |||||||
| chr2:18583990 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA19057.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.891+98C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583990 | |||||||
| chr2:18583991 | G | C | 2 | a0001c0002t0003g0187 a0001c0002t0003g0188 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.891+97C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18583991 | |||||||
| chr2:18584026 | TG | T | 7 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0198 others(4): Show |
13 | HG00639.hp2 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.891+61delC | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 5/8 | chr2 | 18584026 | |||||||
| chr2:18584336 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.724-81C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/8 | chr2 | 18584336 | |||||||
| chr2:18584341 | G | C | 1 | a0001c0002t0002g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.724-86C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/8 | chr2 | 18584341 | |||||||
| chr2:18584462 | A | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0101 a0001c0001t0001g0102 |
4 | HG01516.hp1 HG01517.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.723+52T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 4/8 | chr2 | 18584462 | |||||||
| chr2:18585030 | G | A | 2 | a0001c0002t0003g0187 a0001c0002t0003g0188 |
2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.259-52C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18585030 | |||||||
| chr2:18585386 | A | C | 1 | a0002c0003t0002g0169 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.259-408T>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18585386 | |||||||
| chr2:18585611 | G | C | 10 | a0002c0003t0002g0003 a0002c0003t0002g0011 a0002c0003t0002g0015 others(7): Show |
32 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.259-633C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18585611 | |||||||
| chr2:18585849 | T | C | 1 | a0001c0002t0003g0189 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.258+405A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18585849 | |||||||
| chr2:18586006 | CT | C | 3 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+247delA | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18586006 | |||||||
| chr2:18586109 | C | T | 1 | a0003c0004t0002g0196 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.258+145G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18586109 | |||||||
| chr2:18586118 | G | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(24): Show |
65 | HG00140.hp2 HG00438.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.258+136C>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18586118 | |||||||
| chr2:18586185 | A | G | 12 | a0001c0002t0002g0167 a0002c0003t0002g0003 a0002c0003t0002g0011 others(9): Show |
34 | HG01106.hp1 HG01192.hp1 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.258+69T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18586185 | |||||||
| chr2:18586221 | T | C | 1 | a0001c0002t0002g0207 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+33A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 3/8 | chr2 | 18586221 | |||||||
| chr2:18586416 | C | T | 1 | a0003c0004t0002g0195 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.121-25G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586416 | |||||||
| chr2:18586617 | A | G | 5 | a0003c0004t0002g0016 a0003c0004t0002g0055 a0003c0004t0002g0192 others(2): Show |
9 | HG01243.hp1 HG01261.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-226T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586617 | |||||||
| chr2:18586673 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.121-282A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586673 | |||||||
| chr2:18586742 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0021 others(12): Show |
22 | HG00558.hp1 HG01928.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-351G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586742 | |||||||
| chr2:18586898 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.121-507T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586898 | |||||||
| chr2:18586925 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0145 |
2 | HG00735.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.121-534G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18586925 | |||||||
| chr2:18587052 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0163 |
2 | HG00099.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.120+451G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18587052 | |||||||
| chr2:18587155 | G | C | 1 | a0001c0002t0003g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.120+348C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18587155 | |||||||
| chr2:18587227 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.120+276G>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18587227 | |||||||
| chr2:18587272 | A | T | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+231T>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 2/8 | chr2 | 18587272 | |||||||
| chr2:18587720 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-128G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18587720 | |||||||
| chr2:18587795 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-203T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18587795 | |||||||
| chr2:18587819 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.31-227A>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18587819 | |||||||
| chr2:18587911 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.31-319T>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18587911 | |||||||
| chr2:18587917 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.31-325A>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18587917 | |||||||
| chr2:18588009 | A | G | 1 | a0002c0011t0002g0191 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.31-417T>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588009 | |||||||
| chr2:18588092 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31-500A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588092 | |||||||
| chr2:18588144 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.31-552C>T | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588144 | |||||||
| chr2:18588276 | T | C | 2 | a0003c0004t0002g0032 a0003c0004t0002g0209 |
4 | HG01884.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-684A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588276 | |||||||
| chr2:18588414 | GCT | G | 4 | a0001c0006t0002g0059 a0001c0006t0002g0210 a0001c0006t0002g0211 others(1): Show |
5 | HG02559.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-824_31-823delAG | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588414 | |||||||
| chr2:18588827 | C | G | 1 | a0001c0002t0002g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30+612G>C | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588827 | |||||||
| chr2:18588910 | C | T | 1 | a0001c0002t0002g0167 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.30+529G>A | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18588910 | |||||||
| chr2:18589052 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.30+387A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18589052 | |||||||
| chr2:18589066 | T | C | 33 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(30): Show |
52 | HG00597.hp2 HG00639.hp2 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.30+373A>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18589066 | |||||||
| chr2:18589274 | G | C | 64 | a0001c0002t0001g0058 a0001c0002t0001g0205 a0001c0002t0001g0206 others(61): Show |
116 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.30+165C>G | NT5C1B | ENSG00000185013.17 | transcript | ENST00000304081.9 | protein_coding | 1/8 | chr2 | 18589274 |