Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4676 |
| ensemblid | ENSG00000205531.14 |
| hgncid | 7640 |
| symbol | NAP1L4 |
| name | nucleosome assembly protein 1 like 4 |
| refseq_nuc | NM_005969.4 |
| refseq_prot | NP_005960.1 |
| ensembl_nuc | ENST00000380542.9 |
| ensembl_prot | ENSP00000369915.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 2944437 |
| end | 2992329 |
| strand | - |
| ver | v1.2 |
| region | chr11:2944437-2992329 |
| region5000 | chr11:2939437-2997329 |
| regionname0 | NAP1L4_chr11_2944437_2992329 |
| regionname5000 | NAP1L4_chr11_2939437_2997329 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 375 | 329 | 95 | 51 | 124 | 16 | 42 | 102 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | MADHS others(370): Show |
chr11 | 2939437 | 2997329 |
| a0002 | 0/0 | 375 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | MADHS others(370): Show |
chr11 | 2939437 | 2997329 |
| a0003 | 0/0 | 375 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | MADHS others(370): Show |
chr11 | 2939437 | 2997329 |
| a0004 | 0/0 | 194 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | MADHS others(189): Show |
chr11 | 2939437 | 2997329 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1125 | 312 | 83 | 49 | 123 | 15 | 41 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0001c0002 | 0/0 | 1125 | 10 | 10 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0001c0004 | 0/0 | 1125 | 4 | 0 | 2 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0001c0005 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0001c0006 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0002c0003 | 0/0 | 1125 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0003c0008 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1120): Show |
chr11 | 2939437 | 2997329 | ||
| a0004c0007 | 0/0 | 1135 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | ATGGC others(1130): Show |
chr11 | 2939437 | 2997329 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2463 | 192 | 69 | 29 | 60 | 9 | 25 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0002 | 0/1 | 2463 | 102 | 5 | 19 | 59 | 4 | 14 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0004 | 0/0 | 2463 | 4 | 2 | 0 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0005 | 0/0 | 2463 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0006 | 0/0 | 2463 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0008 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0009 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0010 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0011 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0012 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0013 | 0/0 | 2463 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0001t0014 | 0/0 | 2463 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0002t0003 | 0/0 | 2463 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0002t0007 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0002t0015 | 0/0 | 2452 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2447): Show |
chr11 | 2939437 | 2997329 |
| a0001c0004t0001 | 0/0 | 2463 | 4 | 0 | 2 | 0 | 1 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0005t0001 | 0/0 | 2463 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0001c0006t0001 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0002c0003t0001 | 0/0 | 2463 | 4 | 3 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0003c0008t0002 | 0/0 | 2463 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2458): Show |
chr11 | 2939437 | 2997329 |
| a0004c0007t0001 | 0/0 | 2473 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | GTTGT others(2468): Show |
chr11 | 2939437 | 2997329 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0004 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0011g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0013g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0007g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0002t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0005t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0002c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0003c0008t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| a0004c0007t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0249 | EUR | GBR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0078 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0028 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01358 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0110 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0025 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0206 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02165 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | CDX | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0255 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02280 | hp1 | a0001 | c0002 | t0015 | g0273 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0266 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0267 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02622 | hp1 | a0002 | c0003 | t0001 | g0028 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0017 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02698 | hp2 | a0001 | c0001 | t0010 | g0113 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02886 | hp2 | a0001 | c0002 | t0007 | g0017 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02970 | hp1 | a0001 | c0002 | t0003 | g0111 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0108 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0214 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0109 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | GWD | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0203 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0154 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0231 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18947 | hp1 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18980 | hp1 | a0003 | c0008 | t0002 | g0069 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18987 | hp2 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19076 | hp1 | a0004 | c0007 | t0001 | g0116 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ASW | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0195 | AFR | ASW | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20752 | hp2 | a0001 | c0001 | t0014 | g0187 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | TSI | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0114 | AFR | MSL | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0089 | REF | REF | NAP1L4_chr11_2939437_2997329 | NAP1L4 | chr11 | 2939437 | 2997329 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2959858 | C | T | 1 | a0002 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.658G>A | p.Val220Ile | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/16 | 751/2463 | 658/1128 | 220/375 | chr11 | 2959858 | |||
| chr11:2964706 | T | TCACTTTA others(3): Show |
1 | a0004 | 1 | NA19076.hp1 | frameshift_variant&stop_gained | HIGH | c.570_579dupTATTAAAG others(2): Show |
p.Lys194fs | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/16 | 672/2463 | 579/1128 | 193/375 | chr11 | 2964706 | |||
| chr11:2969894 | G | A | 1 | a0003 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.443C>T | p.Ala148Val | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/16 | 536/2463 | 443/1128 | 148/375 | chr11 | 2969894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2951274 | C | T | 1 | a0001c0006 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.1107G>A | p.Ala369Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/16 | 1200/2463 | 1107/1128 | 369/375 | chr11 | 2951274 | |||
| chr11:2954569 | A | C | 1 | a0002c0003 | 4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
synonymous_variant | LOW | c.993T>G | p.Ala331Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/16 | 1086/2463 | 993/1128 | 331/375 | chr11 | 2954569 | |||
| chr11:2971517 | G | A | 1 | a0001c0002 | 10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
synonymous_variant | LOW | c.333C>T | p.Thr111Thr | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/16 | 426/2463 | 333/1128 | 111/375 | chr11 | 2971517 | |||
| chr11:2972123 | T | C | 1 | a0001c0004 | 4 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
synonymous_variant | LOW | c.294A>G | p.Leu98Leu | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/16 | 387/2463 | 294/1128 | 98/375 | chr11 | 2972123 | |||
| chr11:2978294 | T | G | 1 | a0001c0005 | 2 | HG02055.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.63A>C | p.Ala21Ala | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/16 | 156/2463 | 63/1128 | 21/375 | chr11 | 2978294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2944498 | T | A | 1 | a0001c0001t0004 | 4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1181A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4761 | chr11 | 2944498 | ||||||
| chr11:2944554 | T | G | 1 | a0001c0002t0007 | 2 | HG02630.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1125A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4705 | chr11 | 2944554 | ||||||
| chr11:2944607 | CCCACCCA others(4): Show |
C | 1 | a0001c0002t0015 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1061_*1071delCTGG others(7): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4641 | chr11 | 2944607 | ||||||
| chr11:2944707 | C | T | 1 | a0001c0001t0009 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*972G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4552 | chr11 | 2944707 | ||||||
| chr11:2944791 | G | A | 3 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0015 |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*888C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4468 | chr11 | 2944791 | ||||||
| chr11:2944948 | A | T | 1 | a0001c0001t0008 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*731T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4311 | chr11 | 2944948 | ||||||
| chr11:2945063 | C | G | 3 | a0001c0001t0002 a0001c0001t0012 a0003c0008t0002 |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*616G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 4196 | chr11 | 2945063 | ||||||
| chr11:2945283 | T | C | 1 | a0001c0001t0010 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3976 | chr11 | 2945283 | ||||||
| chr11:2945374 | G | A | 1 | a0001c0001t0011 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*305C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3885 | chr11 | 2945374 | ||||||
| chr11:2945404 | T | C | 1 | a0001c0001t0012 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3855 | chr11 | 2945404 | ||||||
| chr11:2945496 | G | A | 1 | a0001c0001t0013 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3763 | chr11 | 2945496 | ||||||
| chr11:2945592 | C | A | 1 | a0001c0001t0014 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 16/16 | 3667 | chr11 | 2945592 | ||||||
| chr11:2992265 | T | C | 1 | a0001c0001t0006 | 3 | NA18987.hp2 NA18993.hp1 NA19007.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13045 | chr11 | 2992265 | ||||||
| chr11:2992299 | T | C | 1 | a0001c0002t0015 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-63A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13079 | chr11 | 2992299 | ||||||
| chr11:2992315 | G | C | 1 | a0001c0001t0005 | 4 | HG00642.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-79C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/16 | 13095 | chr11 | 2992315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:2945653 | A | G | 1 | a0001c0005t0001g0206 | 1 | HG02055.hp2 | splice_region_variant&intron_variant | LOW | c.*33-7T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945653 | |||||||
| chr11:2945766 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(21): Show |
31 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.*33-120A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945766 | |||||||
| chr11:2945775 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*33-129T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945775 | |||||||
| chr11:2945819 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*33-173G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945819 | |||||||
| chr11:2945834 | AG | A | 3 | a0002c0003t0001g0028 a0002c0003t0001g0266 a0002c0003t0001g0267 |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.*33-189delC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945834 | |||||||
| chr11:2945837 | G | GT | 6 | a0001c0001t0001g0123 a0001c0001t0001g0137 a0001c0001t0001g0141 others(3): Show |
6 | HG03017.hp1 NA18978.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.*33-192dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945837 | |||||||
| chr11:2945937 | C | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.*33-291G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2945937 | |||||||
| chr11:2946018 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*33-372T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946018 | |||||||
| chr11:2946094 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.*33-448C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946094 | |||||||
| chr11:2946114 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*33-468A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946114 | |||||||
| chr11:2946172 | C | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.*33-526G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946172 | |||||||
| chr11:2946213 | A | C | 1 | a0001c0001t0002g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.*33-567T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946213 | |||||||
| chr11:2946223 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.*33-577G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946223 | |||||||
| chr11:2946320 | G | C | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*33-674C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946320 | |||||||
| chr11:2946671 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.*33-1025G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946671 | |||||||
| chr11:2946745 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.*33-1099T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946745 | |||||||
| chr11:2946842 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*33-1196C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946842 | |||||||
| chr11:2946968 | C | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0132 |
4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*33-1322G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2946968 | |||||||
| chr11:2947123 | T | C | 6 | a0001c0002t0003g0016 a0001c0002t0003g0109 a0001c0002t0003g0110 others(3): Show |
8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.*33-1477A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947123 | |||||||
| chr11:2947219 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*33-1573G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947219 | |||||||
| chr11:2947279 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(22): Show |
32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33-1633G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947279 | |||||||
| chr11:2947280 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(22): Show |
32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.*33-1634C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947280 | |||||||
| chr11:2947316 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.*33-1670A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947316 | |||||||
| chr11:2947344 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*33-1698A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947344 | |||||||
| chr11:2947417 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.*33-1771G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947417 | |||||||
| chr11:2947517 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.*32+1710A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947517 | |||||||
| chr11:2947579 | A | G | 90 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0001g0156 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.*32+1648T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947579 | |||||||
| chr11:2947616 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.*32+1611G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947616 | |||||||
| chr11:2947618 | G | GA | 6 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG02258.hp1 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32+1608dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947618 | |||||||
| chr11:2947619 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.*32+1608T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947619 | |||||||
| chr11:2947704 | C | A | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.*32+1523G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947704 | |||||||
| chr11:2947752 | CAACT | C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.*32+1471_*32+1474d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947752 | |||||||
| chr11:2947780 | C | T | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.*32+1447G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947780 | |||||||
| chr11:2947813 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.*32+1414T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947813 | |||||||
| chr11:2947882 | G | A | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.*32+1345C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947882 | |||||||
| chr11:2947892 | C | T | 7 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(4): Show |
9 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.*32+1335G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2947892 | |||||||
| chr11:2948012 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(51): Show |
66 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.*32+1215C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948012 | |||||||
| chr11:2948049 | A | G | 7 | a0001c0001t0002g0013 a0001c0001t0002g0037 a0001c0001t0002g0040 others(4): Show |
8 | HG00621.hp1 HG01123.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.*32+1178T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948049 | |||||||
| chr11:2948121 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*32+1106C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948121 | |||||||
| chr11:2948227 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.*32+1000T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948227 | |||||||
| chr11:2948300 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*32+927T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948300 | |||||||
| chr11:2948463 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.*32+764C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948463 | |||||||
| chr11:2948474 | G | A | 1 | a0001c0001t0002g0015 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.*32+753C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948474 | |||||||
| chr11:2948485 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.*32+742C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948485 | |||||||
| chr11:2948490 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.*32+737C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948490 | |||||||
| chr11:2948541 | G | A | 80 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.*32+686C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948541 | |||||||
| chr11:2948542 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(11): Show |
20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*32+685G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948542 | |||||||
| chr11:2948666 | C | T | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*32+561G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948666 | |||||||
| chr11:2948668 | G | A | 1 | a0001c0005t0001g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*32+559C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948668 | |||||||
| chr11:2948802 | GT | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0132 |
4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*32+424delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948802 | |||||||
| chr11:2948910 | C | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(11): Show |
20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.*32+317G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2948910 | |||||||
| chr11:2949031 | G | A | 2 | a0001c0001t0002g0042 a0001c0001t0002g0060 |
2 | HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.*32+196C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 15/15 | chr11 | 2949031 | |||||||
| chr11:2949290 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1123-26T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949290 | |||||||
| chr11:2949348 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1123-84T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949348 | |||||||
| chr11:2949625 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.1123-361T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949625 | |||||||
| chr11:2949635 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(22): Show |
32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1123-371A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949635 | |||||||
| chr11:2949637 | G | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(22): Show |
32 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.1123-373C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949637 | |||||||
| chr11:2949649 | C | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(8): Show |
12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123-385G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949649 | |||||||
| chr11:2949663 | C | T | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1123-399G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949663 | |||||||
| chr11:2949664 | G | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(23): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1123-400C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949664 | |||||||
| chr11:2949759 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0242 |
2 | NA18946.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1123-495G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949759 | |||||||
| chr11:2949760 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1123-496C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949760 | |||||||
| chr11:2949922 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-658A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2949922 | |||||||
| chr11:2950179 | G | A | 1 | a0001c0001t0011g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1123-915C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950179 | |||||||
| chr11:2950297 | CA | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(11): Show |
20 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1122+961delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950297 | |||||||
| chr11:2950555 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1122+704C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950555 | |||||||
| chr11:2950643 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1122+616A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950643 | |||||||
| chr11:2950848 | T | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1122+411A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950848 | |||||||
| chr11:2950867 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1122+392G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950867 | |||||||
| chr11:2950948 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1122+311A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2950948 | |||||||
| chr11:2951021 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1122+238C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951021 | |||||||
| chr11:2951127 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0115 others(9): Show |
13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+132A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951127 | |||||||
| chr11:2951209 | C | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0136 others(24): Show |
31 | HG01261.hp1 HG02698.hp2 HG02738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1122+50G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951209 | |||||||
| chr11:2951234 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1122+25A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 14/15 | chr11 | 2951234 | |||||||
| chr11:2951357 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1066-42T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951357 | |||||||
| chr11:2951534 | A | T | 5 | a0001c0001t0002g0012 a0001c0001t0002g0035 a0001c0001t0002g0044 others(2): Show |
6 | NA18964.hp1 NA18973.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.1066-219T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951534 | |||||||
| chr11:2951545 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1066-230A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951545 | |||||||
| chr11:2951603 | C | A | 1 | a0001c0001t0002g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1065+177G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951603 | |||||||
| chr11:2951617 | G | C | 1 | a0001c0002t0003g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065+163C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951617 | |||||||
| chr11:2951669 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1065+111C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 13/15 | chr11 | 2951669 | |||||||
| chr11:2951929 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(65): Show |
80 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1036-120C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2951929 | |||||||
| chr11:2951942 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1036-133G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2951942 | |||||||
| chr11:2952014 | G | A | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1036-205C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952014 | |||||||
| chr11:2952094 | CCCTGGCT others(3): Show |
C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0118 a0001c0001t0001g0132 |
4 | HG02145.hp1 HG02257.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1036-295_1036-286d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952094 | |||||||
| chr11:2952188 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1036-379C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952188 | |||||||
| chr11:2952320 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1036-511A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952320 | |||||||
| chr11:2952367 | C | T | 1 | a0001c0001t0002g0015 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1036-558G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952367 | |||||||
| chr11:2952466 | A | G | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1036-657T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952466 | |||||||
| chr11:2952471 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1036-662A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952471 | |||||||
| chr11:2952474 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1036-665A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952474 | |||||||
| chr11:2952510 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1036-701T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952510 | |||||||
| chr11:2952533 | AT | A | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1036-725delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952533 | |||||||
| chr11:2952618 | G | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1036-809C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952618 | |||||||
| chr11:2952650 | G | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1036-841C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952650 | |||||||
| chr11:2952666 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1036-857C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952666 | |||||||
| chr11:2952871 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0083 |
2 | NA18950.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1036-1062C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952871 | |||||||
| chr11:2952958 | C | CTT | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
226 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1036-1151_1036-115 others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2952958 | |||||||
| chr11:2953127 | A | C | 5 | a0001c0001t0001g0253 a0001c0001t0005g0029 a0001c0001t0005g0274 others(2): Show |
6 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1036-1318T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953127 | |||||||
| chr11:2953366 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0134 |
3 | HG00323.hp2 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1035+1161A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953366 | |||||||
| chr11:2953400 | A | G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1035+1127T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953400 | |||||||
| chr11:2953429 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1035+1098T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953429 | |||||||
| chr11:2953581 | C | A | 1 | a0001c0001t0011g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1035+946G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953581 | |||||||
| chr11:2953682 | T | C | 79 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0002g0001 others(76): Show |
102 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1035+845A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2953682 | |||||||
| chr11:2954085 | T | C | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1035+442A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954085 | |||||||
| chr11:2954262 | A | G | 1 | a0001c0001t0014g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1035+265T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954262 | |||||||
| chr11:2954352 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1035+175A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 12/15 | chr11 | 2954352 | |||||||
| chr11:2954757 | A | G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.916-111T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2954757 | |||||||
| chr11:2954818 | T | C | 1 | a0001c0001t0002g0039 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.916-172A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2954818 | |||||||
| chr11:2955102 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-456C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955102 | |||||||
| chr11:2955303 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.915+441A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955303 | |||||||
| chr11:2955322 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.915+422C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955322 | |||||||
| chr11:2955342 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.915+402C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955342 | |||||||
| chr11:2955350 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.915+394G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955350 | |||||||
| chr11:2955354 | T | C | 80 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.915+390A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955354 | |||||||
| chr11:2955362 | A | AT | 26 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0107 others(23): Show |
33 | HG00639.hp2 HG00642.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.915+381dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955362 | |||||||
| chr11:2955481 | C | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(51): Show |
66 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.915+263G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 11/15 | chr11 | 2955481 | |||||||
| chr11:2955875 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-109G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2955875 | |||||||
| chr11:2955938 | A | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.893-172T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2955938 | |||||||
| chr11:2956004 | GC | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(28): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.893-239delG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956004 | |||||||
| chr11:2956024 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.893-258G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956024 | |||||||
| chr11:2956032 | G | A | 1 | a0001c0001t0011g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.893-266C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956032 | |||||||
| chr11:2956086 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0106 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.893-320C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956086 | |||||||
| chr11:2956223 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.893-457C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956223 | |||||||
| chr11:2956324 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.893-558C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956324 | |||||||
| chr11:2956403 | A | C | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.893-637T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956403 | |||||||
| chr11:2956447 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893-681T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956447 | |||||||
| chr11:2956608 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.893-842A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956608 | |||||||
| chr11:2956787 | T | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(9): Show |
13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.893-1021A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956787 | |||||||
| chr11:2956822 | G | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0215 a0001c0001t0013g0214 |
3 | HG02922.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.893-1056C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956822 | |||||||
| chr11:2956877 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.893-1111A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956877 | |||||||
| chr11:2956980 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(25): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.893-1214G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956980 | |||||||
| chr11:2956982 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.893-1216A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2956982 | |||||||
| chr11:2957076 | T | TA | 9 | a0001c0001t0001g0211 a0001c0002t0003g0016 a0001c0002t0003g0108 others(6): Show |
11 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.893-1311dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957076 | |||||||
| chr11:2957173 | A | G | 10 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG00099.hp2 HG01258.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.892+1226T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957173 | |||||||
| chr11:2957316 | A | G | 13 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0115 others(10): Show |
14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.892+1083T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957316 | |||||||
| chr11:2957320 | C | T | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(53): Show |
68 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.892+1079G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957320 | |||||||
| chr11:2957479 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.892+920C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957479 | |||||||
| chr11:2957481 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(10): Show |
19 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.892+918G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957481 | |||||||
| chr11:2957501 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.892+898G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957501 | |||||||
| chr11:2957542 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
12 | HG02083.hp1 NA18939.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.892+857A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957542 | |||||||
| chr11:2957630 | G | A | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.892+769C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957630 | |||||||
| chr11:2957750 | A | C | 1 | a0001c0001t0002g0081 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.892+649T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957750 | |||||||
| chr11:2957979 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.892+420G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957979 | |||||||
| chr11:2957999 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.892+400C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2957999 | |||||||
| chr11:2958219 | G | T | 1 | a0001c0001t0002g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.892+180C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958219 | |||||||
| chr11:2958229 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.892+170T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958229 | |||||||
| chr11:2958331 | G | A | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.892+68C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 10/15 | chr11 | 2958331 | |||||||
| chr11:2958557 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.747-13C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958557 | |||||||
| chr11:2958568 | G | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.747-24C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958568 | |||||||
| chr11:2958715 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.747-171C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958715 | |||||||
| chr11:2958891 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.747-347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958891 | |||||||
| chr11:2958989 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(9): Show |
13 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.747-445T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2958989 | |||||||
| chr11:2959006 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02145.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.747-462G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959006 | |||||||
| chr11:2959136 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.747-592A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959136 | |||||||
| chr11:2959150 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.747-606G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959150 | |||||||
| chr11:2959201 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.746+569A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959201 | |||||||
| chr11:2959264 | T | A | 1 | a0001c0001t0002g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.746+506A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959264 | |||||||
| chr11:2959393 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.746+377A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959393 | |||||||
| chr11:2959492 | T | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.746+278A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959492 | |||||||
| chr11:2959601 | T | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
112 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.746+169A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959601 | |||||||
| chr11:2959614 | A | T | 1 | a0001c0002t0003g0016 | 2 | HG02451.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.746+156T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959614 | |||||||
| chr11:2959674 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.746+96G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 9/15 | chr11 | 2959674 | |||||||
| chr11:2959939 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.607-30C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2959939 | |||||||
| chr11:2960055 | A | G | 1 | a0001c0002t0003g0109 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.607-146T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960055 | |||||||
| chr11:2960161 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.607-252C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960161 | |||||||
| chr11:2960164 | G | A | 1 | a0001c0001t0010g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.607-255C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960164 | |||||||
| chr11:2960367 | C | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(64): Show |
79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.607-458G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960367 | |||||||
| chr11:2960483 | G | A | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-574C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960483 | |||||||
| chr11:2960486 | A | C | 7 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(4): Show |
9 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.607-577T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960486 | |||||||
| chr11:2960552 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(28): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.607-643G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960552 | |||||||
| chr11:2960637 | T | TG | 14 | a0001c0001t0001g0137 a0001c0001t0001g0173 a0001c0001t0001g0182 others(11): Show |
14 | HG00438.hp2 HG01243.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.607-729dupC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960637 | |||||||
| chr11:2960666 | G | A | 110 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0150 others(107): Show |
136 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.607-757C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960666 | |||||||
| chr11:2960677 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0174 |
3 | HG00639.hp1 HG00735.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.607-768A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960677 | |||||||
| chr11:2960792 | C | T | 5 | a0001c0001t0001g0253 a0001c0001t0005g0029 a0001c0001t0005g0274 others(2): Show |
6 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.607-883G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960792 | |||||||
| chr11:2960851 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0178 a0001c0001t0001g0179 others(6): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.607-942C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960851 | |||||||
| chr11:2960862 | T | C | 80 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.607-953A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960862 | |||||||
| chr11:2960921 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.607-1012T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2960921 | |||||||
| chr11:2961022 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.607-1113T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961022 | |||||||
| chr11:2961110 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.607-1201A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961110 | |||||||
| chr11:2961125 | C | CG | 154 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(151): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.607-1217dupC | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961125 | |||||||
| chr11:2961125 | C | CGG | 13 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0194 others(10): Show |
19 | HG00639.hp2 HG01496.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.607-1218_607-1217d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961125 | |||||||
| chr11:2961217 | C | T | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
87 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.607-1308G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961217 | |||||||
| chr11:2961233 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.607-1324C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961233 | |||||||
| chr11:2961253 | T | C | 1 | a0001c0001t0002g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.607-1344A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961253 | |||||||
| chr11:2961343 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.607-1434G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961343 | |||||||
| chr11:2961361 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0179 a0001c0001t0001g0188 |
4 | HG01109.hp1 HG02486.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.607-1452T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961361 | |||||||
| chr11:2961497 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02723.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.607-1588C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961497 | |||||||
| chr11:2961501 | T | TA | 75 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(72): Show |
98 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.607-1593dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961501 | |||||||
| chr11:2961501 | TA | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(53): Show |
63 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.607-1593delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2961501 | |||||||
| chr11:2962110 | AACG | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
106 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.607-2204_607-2202d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962110 | |||||||
| chr11:2962170 | C | T | 198 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.607-2261G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962170 | |||||||
| chr11:2962171 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(29): Show |
42 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.607-2262G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962171 | |||||||
| chr11:2962241 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.607-2332T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962241 | |||||||
| chr11:2962264 | G | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.607-2355C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962264 | |||||||
| chr11:2962523 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.606+2157G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962523 | |||||||
| chr11:2962545 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.606+2135C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962545 | |||||||
| chr11:2962557 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.606+2123A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962557 | |||||||
| chr11:2962563 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.606+2117T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962563 | |||||||
| chr11:2962707 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0078 |
2 | HG00280.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.606+1973T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962707 | |||||||
| chr11:2962756 | G | A | 1 | a0001c0001t0014g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.606+1924C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962756 | |||||||
| chr11:2962937 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.606+1743A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962937 | |||||||
| chr11:2962960 | C | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.606+1720G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2962960 | |||||||
| chr11:2963074 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(75): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.606+1606A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963074 | |||||||
| chr11:2963092 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0227 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.606+1588G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963092 | |||||||
| chr11:2963098 | CA | C | 170 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0020 others(167): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.606+1581delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963098 | |||||||
| chr11:2963098 | CAA | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0009 others(56): Show |
75 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.606+1580_606+1581d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963098 | |||||||
| chr11:2963105 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0001g0198 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.606+1557_606+1574d others(20): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963105 | |||||||
| chr11:2963161 | G | GA | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.606+1518dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963161 | |||||||
| chr11:2963172 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(8): Show |
12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+1508C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963172 | |||||||
| chr11:2963228 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.606+1452T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963228 | |||||||
| chr11:2963234 | TACAAAGA others(6): Show |
T | 1 | a0001c0001t0002g0015 | 2 | NA18947.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.606+1433_606+1445d others(15): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963234 | |||||||
| chr11:2963399 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.606+1281A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963399 | |||||||
| chr11:2963414 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.606+1266C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963414 | |||||||
| chr11:2963415 | C | G | 80 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.606+1265G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963415 | |||||||
| chr11:2963440 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.606+1240C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963440 | |||||||
| chr11:2963485 | G | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.606+1195C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963485 | |||||||
| chr11:2963579 | C | A | 1 | a0001c0001t0002g0065 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.606+1101G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963579 | |||||||
| chr11:2963843 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(8): Show |
12 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.606+837C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963843 | |||||||
| chr11:2963907 | G | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.606+773C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2963907 | |||||||
| chr11:2964123 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.606+557G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964123 | |||||||
| chr11:2964148 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.606+532T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964148 | |||||||
| chr11:2964176 | G | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | NA18946.hp2 NA18948.hp1 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.606+504C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964176 | |||||||
| chr11:2964246 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0115 others(10): Show |
14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.606+434C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964246 | |||||||
| chr11:2964311 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.606+369T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964311 | |||||||
| chr11:2964315 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.606+365G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964315 | |||||||
| chr11:2964632 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.606+48A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964632 | |||||||
| chr11:2964671 | A | C | 1 | a0004c0007t0001g0116 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.606+9T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964671 | |||||||
| chr11:2964673 | T | TA | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.606+6dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 8/15 | chr11 | 2964673 | |||||||
| chr11:2964814 | G | C | 3 | a0001c0004t0001g0025 a0001c0004t0001g0231 a0001c0004t0001g0249 |
4 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-63C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964814 | |||||||
| chr11:2964819 | A | G | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-68T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964819 | |||||||
| chr11:2964926 | G | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(64): Show |
79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.535-175C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964926 | |||||||
| chr11:2964955 | C | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-204G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2964955 | |||||||
| chr11:2965226 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.535-475T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965226 | |||||||
| chr11:2965470 | C | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(64): Show |
79 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.535-719G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965470 | |||||||
| chr11:2965546 | A | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.535-795T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965546 | |||||||
| chr11:2965611 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.535-860A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965611 | |||||||
| chr11:2965692 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(24): Show |
36 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.535-941C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965692 | |||||||
| chr11:2965760 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-1009C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965760 | |||||||
| chr11:2965776 | C | A | 1 | a0001c0001t0002g0066 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.535-1025G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965776 | |||||||
| chr11:2965823 | C | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG02818.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.535-1072G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965823 | |||||||
| chr11:2965859 | C | A | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-1108G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965859 | |||||||
| chr11:2965867 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.535-1116C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2965867 | |||||||
| chr11:2966005 | C | T | 4 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0004g0153 others(1): Show |
4 | HG01516.hp1 HG02965.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1254G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966005 | |||||||
| chr11:2966013 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.535-1262C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966013 | |||||||
| chr11:2966056 | A | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.535-1305T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966056 | |||||||
| chr11:2966073 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.535-1322T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966073 | |||||||
| chr11:2966080 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.535-1329A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966080 | |||||||
| chr11:2966088 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-1337A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966088 | |||||||
| chr11:2966191 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.535-1440A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966191 | |||||||
| chr11:2966413 | T | TAACAGAC others(5): Show |
238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.535-1674_535-1663d others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966413 | |||||||
| chr11:2966649 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.535-1898C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966649 | |||||||
| chr11:2966798 | A | G | 4 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0111 others(1): Show |
6 | HG02451.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-2047T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2966798 | |||||||
| chr11:2967009 | A | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.535-2258T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967009 | |||||||
| chr11:2967093 | C | T | 44 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0107 others(41): Show |
46 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.535-2342G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967093 | |||||||
| chr11:2967138 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.535-2387C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967138 | |||||||
| chr11:2967201 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.535-2450A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967201 | |||||||
| chr11:2967357 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(52): Show |
67 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.534+2446T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967357 | |||||||
| chr11:2967369 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.534+2434A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967369 | |||||||
| chr11:2967391 | T | C | 6 | a0001c0002t0003g0016 a0001c0002t0003g0109 a0001c0002t0003g0110 others(3): Show |
8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+2412A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967391 | |||||||
| chr11:2967415 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0218 others(8): Show |
15 | NA18942.hp1 NA18950.hp1 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.534+2388T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967415 | |||||||
| chr11:2967447 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(15): Show |
25 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.534+2356G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967447 | |||||||
| chr11:2967582 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.534+2221C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967582 | |||||||
| chr11:2967608 | T | TA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0194 a0001c0001t0001g0208 others(17): Show |
27 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.534+2194dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967608 | |||||||
| chr11:2967616 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
12 | HG02083.hp1 NA18939.hp2 NA18952.hp2 others(9): Show |
intron_variant | MODIFIER | c.534+2187T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967616 | |||||||
| chr11:2967636 | TA | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0136 others(18): Show |
28 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.534+2166delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967636 | |||||||
| chr11:2967728 | A | G | 1 | a0001c0005t0001g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.534+2075T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967728 | |||||||
| chr11:2967817 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0135 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.534+1986G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967817 | |||||||
| chr11:2967912 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.534+1891T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2967912 | |||||||
| chr11:2968202 | A | G | 3 | a0002c0003t0001g0028 a0002c0003t0001g0266 a0002c0003t0001g0267 |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1601T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968202 | |||||||
| chr11:2968219 | G | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0115 a0001c0001t0001g0194 others(15): Show |
25 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.534+1584C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968219 | |||||||
| chr11:2968313 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.534+1490G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968313 | |||||||
| chr11:2968394 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.534+1409C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968394 | |||||||
| chr11:2968483 | T | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.534+1320A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968483 | |||||||
| chr11:2968539 | C | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.534+1264G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968539 | |||||||
| chr11:2968680 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG01433.hp1 HG02723.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1123G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968680 | |||||||
| chr11:2968770 | G | A | 3 | a0001c0001t0002g0068 a0001c0001t0002g0080 a0001c0001t0002g0095 |
3 | HG01361.hp1 HG02055.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.534+1033C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968770 | |||||||
| chr11:2968806 | G | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.534+997C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968806 | |||||||
| chr11:2968810 | A | G | 3 | a0001c0002t0003g0109 a0001c0002t0003g0110 a0001c0002t0003g0112 |
3 | HG01884.hp1 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.534+993T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968810 | |||||||
| chr11:2968820 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.534+983A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968820 | |||||||
| chr11:2968914 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.534+889G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968914 | |||||||
| chr11:2968953 | AATCAGAA others(7): Show |
A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+836_534+849del others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968953 | |||||||
| chr11:2968985 | G | A | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.534+818C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968985 | |||||||
| chr11:2968988 | G | GT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0140 a0001c0001t0001g0141 others(14): Show |
19 | HG00423.hp1 HG00642.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.534+814dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968988 | |||||||
| chr11:2968988 | GT | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.534+814delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968988 | |||||||
| chr11:2968994 | T | TG | 76 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0002g0001 others(73): Show |
100 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.534+808_534+809ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968994 | |||||||
| chr11:2968995 | T | G | 31 | a0001c0001t0001g0020 a0001c0001t0001g0150 a0001c0001t0001g0176 others(28): Show |
33 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.534+808A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968995 | |||||||
| chr11:2968996 | T | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.534+807A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968996 | |||||||
| chr11:2968997 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.534+806A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2968997 | |||||||
| chr11:2969023 | C | CT | 239 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.534+779_534+780ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969023 | |||||||
| chr11:2969148 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+655C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969148 | |||||||
| chr11:2969188 | G | A | 2 | a0001c0001t0004g0151 a0001c0001t0004g0154 |
2 | HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.534+615C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969188 | |||||||
| chr11:2969215 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0168 |
2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.534+588C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969215 | |||||||
| chr11:2969296 | G | A | 81 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0002g0001 others(78): Show |
104 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.534+507C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969296 | |||||||
| chr11:2969316 | G | T | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.534+487C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969316 | |||||||
| chr11:2969365 | T | TAC | 2 | a0001c0001t0001g0150 a0001c0002t0007g0017 |
3 | HG01433.hp1 HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.534+436_534+437dup others(2): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969365 | |||||||
| chr11:2969365 | T | TACAC | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.534+434_534+437dup others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969365 | |||||||
| chr11:2969463 | G | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.534+340C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969463 | |||||||
| chr11:2969483 | G | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.534+320C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969483 | |||||||
| chr11:2969545 | T | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.534+258A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969545 | |||||||
| chr11:2969582 | T | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.534+221A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969582 | |||||||
| chr11:2969622 | T | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(25): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.534+181A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969622 | |||||||
| chr11:2969755 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.534+48C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969755 | |||||||
| chr11:2969790 | G | A | 1 | a0001c0001t0002g0014 | 2 | NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.534+13C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 7/15 | chr11 | 2969790 | |||||||
| chr11:2969989 | C | G | 90 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0001g0156 others(87): Show |
115 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.403-55G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2969989 | |||||||
| chr11:2970160 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.403-226T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970160 | |||||||
| chr11:2970240 | C | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.403-306G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970240 | |||||||
| chr11:2970280 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.403-346T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970280 | |||||||
| chr11:2970301 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0237 a0001c0006t0001g0236 |
3 | HG00438.hp1 HG00558.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.403-367C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970301 | |||||||
| chr11:2970333 | T | C | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.403-399A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970333 | |||||||
| chr11:2970438 | A | T | 205 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.403-504T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970438 | |||||||
| chr11:2970443 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.403-509G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970443 | |||||||
| chr11:2970662 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.403-728C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970662 | |||||||
| chr11:2970848 | AC | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.402+599delG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970848 | |||||||
| chr11:2970848 | ACCC | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(52): Show |
66 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.402+597_402+599del others(3): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970848 | |||||||
| chr11:2970856 | CCCA | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(64): Show |
80 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.402+589_402+591del others(3): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970856 | |||||||
| chr11:2970857 | C | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0035 a0001c0001t0002g0044 others(2): Show |
5 | NA18964.hp1 NA19002.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+591G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970857 | |||||||
| chr11:2970857 | C | CA | 72 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0002g0001 others(69): Show |
93 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.402+590_402+591ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970857 | |||||||
| chr11:2970858 | C | A | 78 | a0001c0001t0001g0043 a0001c0001t0001g0156 a0001c0001t0002g0001 others(75): Show |
100 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.402+590G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970858 | |||||||
| chr11:2970858 | C | CA | 9 | a0001c0001t0001g0150 a0001c0001t0002g0007 a0001c0002t0003g0016 others(6): Show |
11 | HG01433.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+589dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970858 | |||||||
| chr11:2970887 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.402+561T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970887 | |||||||
| chr11:2970888 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.402+560C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970888 | |||||||
| chr11:2970923 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.402+525C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970923 | |||||||
| chr11:2970930 | A | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.402+518T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2970930 | |||||||
| chr11:2971124 | A | G | 31 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(28): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.402+324T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2971124 | |||||||
| chr11:2971297 | A | G | 1 | a0001c0001t0014g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.402+151T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 6/15 | chr11 | 2971297 | |||||||
| chr11:2971841 | CCTCT | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(29): Show |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.315+257_315+260del others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/15 | chr11 | 2971841 | |||||||
| chr11:2971967 | G | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.315+135C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 5/15 | chr11 | 2971967 | |||||||
| chr11:2972502 | G | C | 1 | a0001c0001t0010g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.174-259C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972502 | |||||||
| chr11:2972543 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.174-300A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972543 | |||||||
| chr11:2972644 | A | C | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.174-401T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972644 | |||||||
| chr11:2972697 | C | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0070 |
2 | NA18956.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.174-454G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972697 | |||||||
| chr11:2972707 | C | T | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.174-464G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972707 | |||||||
| chr11:2972827 | A | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(211): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.174-584T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972827 | |||||||
| chr11:2972898 | G | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.174-655C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972898 | |||||||
| chr11:2972928 | G | C | 1 | a0001c0001t0002g0070 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.174-685C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972928 | |||||||
| chr11:2972962 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.174-719G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972962 | |||||||
| chr11:2972991 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174-748A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972991 | |||||||
| chr11:2972991 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174-748A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2972991 | |||||||
| chr11:2973271 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.174-1028T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973271 | |||||||
| chr11:2973681 | T | C | 1 | a0001c0002t0003g0112 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.174-1438A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973681 | |||||||
| chr11:2973711 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.174-1468C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973711 | |||||||
| chr11:2973748 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.174-1505T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973748 | |||||||
| chr11:2973832 | G | A | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.174-1589C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973832 | |||||||
| chr11:2973837 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.174-1594G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973837 | |||||||
| chr11:2973917 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.174-1674T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973917 | |||||||
| chr11:2973955 | T | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174-1712A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973955 | |||||||
| chr11:2973956 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.174-1713T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2973956 | |||||||
| chr11:2974022 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.174-1779G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974022 | |||||||
| chr11:2974085 | T | A | 3 | a0002c0003t0001g0028 a0002c0003t0001g0266 a0002c0003t0001g0267 |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.174-1842A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974085 | |||||||
| chr11:2974111 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.174-1868G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974111 | |||||||
| chr11:2974237 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.173+1787G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974237 | |||||||
| chr11:2974238 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.173+1786C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974238 | |||||||
| chr11:2974546 | C | T | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+1478G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974546 | |||||||
| chr11:2974654 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.173+1370C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974654 | |||||||
| chr11:2974659 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.173+1365C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974659 | |||||||
| chr11:2974742 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.173+1272_173+1281d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974742 | |||||||
| chr11:2974884 | T | C | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.173+1140A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974884 | |||||||
| chr11:2974969 | A | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(31): Show |
44 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.173+1055T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2974969 | |||||||
| chr11:2975049 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01081.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.173+975G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975049 | |||||||
| chr11:2975106 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.173+918C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975106 | |||||||
| chr11:2975152 | T | A | 1 | a0001c0001t0001g0247 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.173+872A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | |||||||
| chr11:2975152 | T | TA | 31 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(28): Show |
34 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.173+871dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | |||||||
| chr11:2975152 | T | TAA | 82 | a0001c0001t0001g0043 a0001c0001t0001g0115 a0001c0001t0001g0144 others(79): Show |
105 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.173+870_173+871dup others(2): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | |||||||
| chr11:2975152 | TA | T | 23 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0159 others(20): Show |
29 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.173+871delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975152 | |||||||
| chr11:2975245 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
7 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+779C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975245 | |||||||
| chr11:2975302 | G | A | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | NA18946.hp2 NA18955.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.173+722C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975302 | |||||||
| chr11:2975392 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+632A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975392 | |||||||
| chr11:2975459 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.173+565T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975459 | |||||||
| chr11:2975479 | C | T | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.173+545G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975479 | |||||||
| chr11:2975557 | C | T | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.173+467G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975557 | |||||||
| chr11:2975817 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.173+207C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975817 | |||||||
| chr11:2975856 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.173+168C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975856 | |||||||
| chr11:2975859 | C | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.173+165G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975859 | |||||||
| chr11:2975902 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.173+122A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 4/15 | chr11 | 2975902 | |||||||
| chr11:2976156 | T | C | 1 | a0001c0001t0002g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.74-33A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976156 | |||||||
| chr11:2976255 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.74-132C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976255 | |||||||
| chr11:2976374 | GCTCTCAC others(5): Show |
G | 1 | a0001c0001t0002g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74-263_74-252delTC others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976374 | |||||||
| chr11:2976456 | C | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.74-333G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976456 | |||||||
| chr11:2976457 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74-334G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976457 | |||||||
| chr11:2976468 | G | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(25): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.74-345C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976468 | |||||||
| chr11:2976616 | G | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.74-493C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976616 | |||||||
| chr11:2976623 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0194 a0001c0001t0001g0208 others(9): Show |
18 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.74-500A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976623 | |||||||
| chr11:2976716 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.74-593G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976716 | |||||||
| chr11:2976920 | C | T | 2 | a0001c0001t0004g0152 a0001c0001t0004g0153 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74-797G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976920 | |||||||
| chr11:2976946 | C | T | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(65): Show |
81 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.74-823G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976946 | |||||||
| chr11:2976949 | ACCCGAGT others(10): Show |
A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02647.hp1 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.74-843_74-827delAT others(15): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976949 | |||||||
| chr11:2976969 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.74-846G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976969 | |||||||
| chr11:2976984 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.74-861G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2976984 | |||||||
| chr11:2977049 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.74-926G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977049 | |||||||
| chr11:2977132 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.74-1009A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977132 | |||||||
| chr11:2977152 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0196 |
3 | HG02109.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.74-1029T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977152 | |||||||
| chr11:2977194 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-1071G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977194 | |||||||
| chr11:2977231 | C | T | 80 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(77): Show |
103 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.73+1053G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977231 | |||||||
| chr11:2977237 | G | T | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+1047C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977237 | |||||||
| chr11:2977324 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.73+960A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977324 | |||||||
| chr11:2977392 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
7 | HG00741.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+892C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977392 | |||||||
| chr11:2977640 | A | G | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(76): Show |
92 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.73+644T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977640 | |||||||
| chr11:2977679 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+605T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977679 | |||||||
| chr11:2977682 | G | A | 5 | a0001c0001t0001g0107 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG01346.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+602C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977682 | |||||||
| chr11:2977703 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0194 a0001c0001t0001g0208 others(12): Show |
22 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.73+581C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977703 | |||||||
| chr11:2977708 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.73+576A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977708 | |||||||
| chr11:2977718 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.73+566G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977718 | |||||||
| chr11:2977762 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.73+522A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977762 | |||||||
| chr11:2977772 | T | A | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.73+512A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977772 | |||||||
| chr11:2977788 | T | C | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.73+496A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977788 | |||||||
| chr11:2977866 | T | TA | 78 | a0001c0001t0001g0043 a0001c0001t0001g0191 a0001c0001t0001g0192 others(75): Show |
101 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.73+417dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | |||||||
| chr11:2977866 | TA | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.73+417delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | |||||||
| chr11:2977866 | TAA | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG01261.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+416_73+417delTT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977866 | |||||||
| chr11:2977914 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.73+370G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2977914 | |||||||
| chr11:2978019 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.73+265A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978019 | |||||||
| chr11:2978049 | C | G | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.73+235G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978049 | |||||||
| chr11:2978257 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73+27G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978257 | |||||||
| chr11:2978277 | G | T | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
splice_region_variant&intron_variant | LOW | c.73+7C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 3/15 | chr11 | 2978277 | |||||||
| chr11:2978355 | T | A | 9 | a0001c0001t0001g0253 a0001c0001t0002g0254 a0001c0001t0005g0029 others(6): Show |
11 | HG00642.hp1 HG01243.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.15-13A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978355 | |||||||
| chr11:2978370 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-28A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978370 | |||||||
| chr11:2978371 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.15-29A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978371 | |||||||
| chr11:2978418 | T | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.15-76A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978418 | |||||||
| chr11:2978441 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.15-99A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978441 | |||||||
| chr11:2978683 | G | C | 1 | a0001c0001t0006g0271 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15-341C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978683 | |||||||
| chr11:2978689 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(31): Show |
43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.15-347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978689 | |||||||
| chr11:2978907 | C | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(29): Show |
42 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.14+300G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978907 | |||||||
| chr11:2978949 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.14+258T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978949 | |||||||
| chr11:2978968 | T | TA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.14+238dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2978968 | |||||||
| chr11:2979056 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.14+151A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979056 | |||||||
| chr11:2979100 | G | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.14+107C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979100 | |||||||
| chr11:2979165 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.14+42G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 2/15 | chr11 | 2979165 | |||||||
| chr11:2979254 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0183 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-17C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979254 | |||||||
| chr11:2979299 | T | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0183 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-17-62A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979299 | |||||||
| chr11:2979339 | A | C | 1 | a0001c0001t0001g0217 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-17-102T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979339 | |||||||
| chr11:2979512 | C | T | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-275G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979512 | |||||||
| chr11:2979526 | A | T | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG00733.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-17-289T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979526 | |||||||
| chr11:2979528 | T | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-291A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979528 | |||||||
| chr11:2979771 | T | TA | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
104 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-17-535dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979771 | |||||||
| chr11:2979778 | A | AT | 14 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0194 others(11): Show |
15 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-17-542_-17-541ins others(1): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979778 | |||||||
| chr11:2979783 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-17-546A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979783 | |||||||
| chr11:2979870 | C | T | 9 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-633G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979870 | |||||||
| chr11:2979875 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-17-638C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979875 | |||||||
| chr11:2979890 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.-17-653G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2979890 | |||||||
| chr11:2980164 | A | G | 1 | a0001c0001t0006g0272 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-17-927T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980164 | |||||||
| chr11:2980383 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-1146G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980383 | |||||||
| chr11:2980477 | C | A | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-17-1240G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980477 | |||||||
| chr11:2980477 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-1240G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980477 | |||||||
| chr11:2980478 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-17-1241C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980478 | |||||||
| chr11:2980584 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-1347C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980584 | |||||||
| chr11:2980621 | G | T | 1 | a0001c0001t0011g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-1384C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980621 | |||||||
| chr11:2980777 | A | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-1540T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980777 | |||||||
| chr11:2980837 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(31): Show |
43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.-17-1600G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980837 | |||||||
| chr11:2980934 | G | GA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-1698dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980934 | |||||||
| chr11:2980934 | GA | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-1698delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980934 | |||||||
| chr11:2980957 | A | AGT | 6 | a0001c0002t0003g0016 a0001c0002t0003g0109 a0001c0002t0003g0110 others(3): Show |
8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-1722_-17-1721d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980957 | |||||||
| chr11:2980997 | A | G | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-1760T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2980997 | |||||||
| chr11:2981058 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-17-1821G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981058 | |||||||
| chr11:2981068 | AAAAC | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-1835_-17-1832d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981068 | |||||||
| chr11:2981102 | C | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-17-1865G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981102 | |||||||
| chr11:2981246 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-2009C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981246 | |||||||
| chr11:2981246 | G | GA | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(72): Show |
88 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-17-2010dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981246 | |||||||
| chr11:2981248 | A | T | 1 | a0001c0001t0002g0087 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-2011T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981248 | |||||||
| chr11:2981278 | C | T | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
250 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.-17-2041G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981278 | |||||||
| chr11:2981364 | C | G | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-2127G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981364 | |||||||
| chr11:2981368 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-17-2131A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981368 | |||||||
| chr11:2981369 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-17-2132C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981369 | |||||||
| chr11:2981373 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0208 a0001c0001t0001g0243 others(2): Show |
10 | HG00639.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-2136C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981373 | |||||||
| chr11:2981374 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-2137G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981374 | |||||||
| chr11:2981417 | T | TC | 12 | a0001c0001t0001g0026 a0001c0001t0001g0138 a0001c0001t0001g0229 others(9): Show |
13 | HG02056.hp2 HG02738.hp2 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-2181dupG | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981417 | |||||||
| chr11:2981418 | C | CA | 10 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0134 others(7): Show |
10 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2182dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | C | CAAAAAA | 8 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0082 others(5): Show |
11 | HG01071.hp1 HG01993.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-2187_-17-2182d others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | C | CAAAAAAA | 25 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0013 others(22): Show |
35 | HG00438.hp2 HG01081.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.-17-2188_-17-2182d others(9): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | C | CAAAAAAA others(1): Show |
26 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0002g0036 others(23): Show |
36 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-17-2189_-17-2182d others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | C | CAAAAAAA others(2): Show |
13 | a0001c0001t0001g0043 a0001c0001t0002g0042 a0001c0001t0002g0071 others(10): Show |
13 | HG00621.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-2190_-17-2182d others(11): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0033 a0001c0001t0002g0078 a0001c0001t0002g0079 others(4): Show |
7 | HG00280.hp2 HG01168.hp1 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-2191_-17-2182d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | CA | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0021 others(46): Show |
60 | HG00099.hp1 HG00639.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.-17-2182delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | CAA | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0194 a0001c0001t0001g0207 others(3): Show |
7 | HG01243.hp1 HG01516.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-2183_-17-2182d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | CAAAAAAA | C | 9 | a0001c0001t0001g0115 a0001c0001t0001g0144 a0001c0001t0001g0177 others(6): Show |
9 | HG00099.hp2 HG01258.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-2188_-17-2182d others(9): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0178 others(10): Show |
14 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17-2189_-17-2182d others(10): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981418 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0010g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-2193_-17-2182d others(14): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981418 | |||||||
| chr11:2981419 | A | C | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(40): Show |
54 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-17-2182T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981419 | |||||||
| chr11:2981420 | A | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0030 others(31): Show |
41 | HG00639.hp2 HG01346.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.-17-2183T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981420 | |||||||
| chr11:2981421 | A | C | 5 | a0001c0001t0001g0194 a0001c0001t0001g0207 a0002c0003t0001g0028 others(2): Show |
6 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-17-2184T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981421 | |||||||
| chr11:2981431 | A | C | 1 | a0001c0001t0010g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-17-2194T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981431 | |||||||
| chr11:2981571 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(75): Show |
91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.-17-2334C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981571 | |||||||
| chr11:2981587 | C | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-17-2350G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981587 | |||||||
| chr11:2981610 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-2373G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981610 | |||||||
| chr11:2981688 | A | G | 89 | a0001c0001t0001g0043 a0001c0001t0001g0150 a0001c0001t0002g0001 others(86): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-17-2451T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981688 | |||||||
| chr11:2981699 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-17-2462G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981699 | |||||||
| chr11:2981735 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17-2498C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981735 | |||||||
| chr11:2981823 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-2586C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981823 | |||||||
| chr11:2981861 | G | A | 4 | a0001c0001t0002g0254 a0002c0003t0001g0028 a0002c0003t0001g0266 others(1): Show |
5 | HG01243.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-2624C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981861 | |||||||
| chr11:2981870 | T | A | 1 | a0001c0005t0001g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-17-2633A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981870 | |||||||
| chr11:2981912 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.-17-2675G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2981912 | |||||||
| chr11:2982026 | A | G | 1 | a0001c0001t0002g0014 | 2 | NA19058.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-17-2789T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982026 | |||||||
| chr11:2982107 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-17-2870T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982107 | |||||||
| chr11:2982170 | C | T | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2933G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982170 | |||||||
| chr11:2982172 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(7): Show |
10 | HG01891.hp2 HG02647.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-2935A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982172 | |||||||
| chr11:2982256 | C | T | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-17-3019G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982256 | |||||||
| chr11:2982432 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0133 a0001c0001t0001g0135 |
5 | HG01099.hp1 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-3195A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982432 | |||||||
| chr11:2982571 | C | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-3334G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982571 | |||||||
| chr11:2982589 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-17-3352G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982589 | |||||||
| chr11:2982716 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-17-3479G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982716 | |||||||
| chr11:2982775 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-3538G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2982775 | |||||||
| chr11:2983035 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-17-3798T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983035 | |||||||
| chr11:2983211 | A | T | 1 | a0002c0003t0001g0266 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17-3974T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983211 | |||||||
| chr11:2983296 | C | G | 81 | a0001c0001t0001g0043 a0001c0001t0001g0147 a0001c0001t0001g0150 others(78): Show |
104 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-17-4059G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983296 | |||||||
| chr11:2983388 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-17-4151C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983388 | |||||||
| chr11:2983550 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(69): Show |
85 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-17-4313T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983550 | |||||||
| chr11:2983583 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-17-4346C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983583 | |||||||
| chr11:2983592 | G | GA | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-17-4356dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983592 | |||||||
| chr11:2983592 | GA | G | 9 | a0001c0001t0001g0156 a0001c0001t0006g0270 a0001c0002t0003g0016 others(6): Show |
11 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-4356delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983592 | |||||||
| chr11:2983611 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-17-4374T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983611 | |||||||
| chr11:2983695 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-17-4458T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983695 | |||||||
| chr11:2983750 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-4513T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983750 | |||||||
| chr11:2983796 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-17-4559G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983796 | |||||||
| chr11:2983804 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-17-4567T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983804 | |||||||
| chr11:2983891 | C | CAGG | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-17-4657_-17-4655d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983891 | |||||||
| chr11:2983923 | T | C | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-4686A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983923 | |||||||
| chr11:2983957 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-17-4720C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983957 | |||||||
| chr11:2983994 | GA | G | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(135): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-17-4758delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2983994 | |||||||
| chr11:2984042 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17-4805G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984042 | |||||||
| chr11:2984096 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-17-4859G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984096 | |||||||
| chr11:2984121 | T | C | 1 | a0002c0003t0001g0267 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-17-4884A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984121 | |||||||
| chr11:2984124 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-4887C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984124 | |||||||
| chr11:2984166 | C | CA | 31 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0031 others(28): Show |
33 | HG00438.hp1 HG00558.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-4930dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | |||||||
| chr11:2984166 | CA | C | 15 | a0001c0001t0001g0115 a0001c0001t0001g0150 a0001c0001t0001g0172 others(12): Show |
16 | HG00642.hp1 HG01433.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17-4930delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | |||||||
| chr11:2984166 | CAA | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0129 a0001c0001t0001g0146 others(30): Show |
38 | HG00099.hp2 HG01109.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-17-4931_-17-4930d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | |||||||
| chr11:2984166 | CAAA | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(101): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-17-4932_-17-4930d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984166 | |||||||
| chr11:2984190 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-17-4953C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984190 | |||||||
| chr11:2984236 | A | G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0002g0042 |
3 | HG00733.hp1 HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-17-4999T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984236 | |||||||
| chr11:2984287 | CA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-5051delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984287 | |||||||
| chr11:2984349 | G | A | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-17-5112C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984349 | |||||||
| chr11:2984440 | G | A | 94 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0137 others(91): Show |
119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-17-5203C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984440 | |||||||
| chr11:2984513 | G | A | 1 | a0001c0001t0002g0087 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17-5276C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984513 | |||||||
| chr11:2984692 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0133 a0001c0001t0001g0135 |
5 | HG01099.hp1 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-5455C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984692 | |||||||
| chr11:2984797 | ACAG | A | 85 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0137 others(82): Show |
108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-17-5563_-17-5561d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984797 | |||||||
| chr11:2984870 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-17-5633G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2984870 | |||||||
| chr11:2985397 | ATC | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(63): Show |
78 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-17-6162_-17-6161d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985397 | |||||||
| chr11:2985417 | A | T | 1 | a0001c0002t0003g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-17-6180T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985417 | |||||||
| chr11:2985434 | A | AGTCTTAT others(30): Show |
1 | a0001c0001t0001g0175 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-17-6234_-17-6198d others(39): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985434 | |||||||
| chr11:2985703 | T | C | 1 | a0001c0001t0002g0254 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-17-6466A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985703 | |||||||
| chr11:2985719 | ACAAT | A | 6 | a0001c0002t0003g0016 a0001c0002t0003g0109 a0001c0002t0003g0110 others(3): Show |
8 | HG01884.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-6486_-17-6483d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985719 | |||||||
| chr11:2985752 | CA | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0021 others(61): Show |
77 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.-18+6501delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985752 | |||||||
| chr11:2985863 | T | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-18+6391A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985863 | |||||||
| chr11:2985905 | A | G | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+6349T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985905 | |||||||
| chr11:2985914 | CT | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 |
3 | HG02258.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18+6339delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2985914 | |||||||
| chr11:2986252 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-18+6002T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986252 | |||||||
| chr11:2986263 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18+5991T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986263 | |||||||
| chr11:2986311 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
5 | HG02145.hp1 HG02257.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+5943A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986311 | |||||||
| chr11:2986318 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+5936C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986318 | |||||||
| chr11:2986344 | A | C | 1 | a0001c0001t0002g0041 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18+5910T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986344 | |||||||
| chr11:2986352 | C | T | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+5902G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986352 | |||||||
| chr11:2986355 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+5899G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986355 | |||||||
| chr11:2986372 | T | C | 1 | a0001c0001t0002g0088 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-18+5882A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986372 | |||||||
| chr11:2986373 | C | CA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+5880dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986373 | |||||||
| chr11:2986373 | CA | C | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
93 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18+5880delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986373 | |||||||
| chr11:2986377 | AAAAAAAA others(4): Show |
A | 9 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
9 | HG01891.hp2 HG02809.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+5866_-18+5876d others(13): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986377 | |||||||
| chr11:2986382 | AAAAAAG | A | 92 | a0001c0001t0001g0043 a0001c0001t0001g0137 a0001c0001t0001g0138 others(89): Show |
116 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-18+5866_-18+5871d others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986382 | |||||||
| chr11:2986383 | AAAAAGAA others(4): Show |
A | 1 | a0001c0001t0001g0246 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18+5860_-18+5870d others(13): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986383 | |||||||
| chr11:2986417 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-18+5837G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986417 | |||||||
| chr11:2986468 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+5786T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986468 | |||||||
| chr11:2986592 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18+5662G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986592 | |||||||
| chr11:2986626 | A | AT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.-18+5627dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | |||||||
| chr11:2986626 | A | ATT | 11 | a0001c0001t0001g0120 a0001c0001t0001g0247 a0001c0001t0002g0040 others(8): Show |
13 | HG01884.hp1 HG02056.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18+5626_-18+5627d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | |||||||
| chr11:2986626 | A | ATTTT | 17 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(14): Show |
18 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+5624_-18+5627d others(6): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | |||||||
| chr11:2986626 | A | T | 1 | a0001c0001t0002g0092 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18+5628T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986626 | |||||||
| chr11:2986656 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18+5598G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986656 | |||||||
| chr11:2986661 | T | G | 4 | a0001c0001t0005g0029 a0001c0001t0005g0274 a0001c0001t0005g0275 others(1): Show |
5 | HG00642.hp1 HG02258.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-18+5593A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986661 | |||||||
| chr11:2986696 | G | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0022 others(47): Show |
62 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-18+5558C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986696 | |||||||
| chr11:2986784 | AT | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(226): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-18+5469delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986784 | |||||||
| chr11:2986920 | C | CACCCAG | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.-18+5333_-18+5334i others(8): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2986920 | |||||||
| chr11:2987099 | C | T | 1 | a0001c0001t0006g0270 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-18+5155G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987099 | |||||||
| chr11:2987174 | G | A | 85 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0137 others(82): Show |
108 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.-18+5080C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987174 | |||||||
| chr11:2987199 | T | TGCCCAGG others(3): Show |
1 | a0001c0001t0001g0172 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-18+5045_-18+5054d others(12): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987199 | |||||||
| chr11:2987280 | A | G | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+4974T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987280 | |||||||
| chr11:2987464 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-18+4790C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987464 | |||||||
| chr11:2987502 | T | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02723.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-18+4752A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987502 | |||||||
| chr11:2987662 | CAGG | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0194 a0001c0001t0001g0208 others(9): Show |
18 | HG00639.hp2 HG00642.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18+4589_-18+4591d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987662 | |||||||
| chr11:2987700 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-18+4554A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987700 | |||||||
| chr11:2987712 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+4542C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987712 | |||||||
| chr11:2987744 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-18+4510C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987744 | |||||||
| chr11:2987753 | C | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18+4501G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987753 | |||||||
| chr11:2987756 | C | CA | 16 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0146 others(13): Show |
16 | HG00140.hp2 HG01109.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+4497dupT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | |||||||
| chr11:2987756 | C | CAAA | 16 | a0001c0001t0001g0020 a0001c0001t0001g0179 a0001c0001t0001g0180 others(13): Show |
17 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+4495_-18+4497d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | |||||||
| chr11:2987756 | CA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0043 others(99): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-18+4497delT | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | |||||||
| chr11:2987756 | CAA | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
7 | HG01168.hp1 HG02145.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+4496_-18+4497d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987756 | |||||||
| chr11:2987794 | G | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+4460C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987794 | |||||||
| chr11:2987907 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-18+4347A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987907 | |||||||
| chr11:2987982 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+4272A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987982 | |||||||
| chr11:2987990 | C | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+4264G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2987990 | |||||||
| chr11:2988040 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-18+4214T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988040 | |||||||
| chr11:2988116 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(22): Show |
34 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.-18+4138C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988116 | |||||||
| chr11:2988134 | T | C | 6 | a0001c0001t0001g0253 a0001c0001t0002g0254 a0001c0001t0005g0029 others(3): Show |
7 | HG00642.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+4120A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988134 | |||||||
| chr11:2988161 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-18+4093G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988161 | |||||||
| chr11:2988197 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(25): Show |
38 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.-18+4057C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988197 | |||||||
| chr11:2988203 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18+4051C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988203 | |||||||
| chr11:2988208 | T | C | 112 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18+4046A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988208 | |||||||
| chr11:2988311 | GTCATCTT others(30): Show |
G | 1 | a0001c0001t0001g0175 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-18+3906_-18+3942d others(39): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988311 | |||||||
| chr11:2988330 | A | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+3924T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988330 | |||||||
| chr11:2988351 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
7 | HG02109.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+3903T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988351 | |||||||
| chr11:2988410 | A | G | 87 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0137 others(84): Show |
110 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-18+3844T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988410 | |||||||
| chr11:2988540 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18+3714T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988540 | |||||||
| chr11:2988579 | G | C | 1 | a0001c0001t0009g0195 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18+3675C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988579 | |||||||
| chr11:2988691 | A | G | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-18+3563T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988691 | |||||||
| chr11:2988819 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-18+3435A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988819 | |||||||
| chr11:2988824 | A | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.-18+3430T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988824 | |||||||
| chr11:2988854 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3400G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988854 | |||||||
| chr11:2988862 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+3392T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988862 | |||||||
| chr11:2988868 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+3386A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988868 | |||||||
| chr11:2988998 | T | A | 1 | a0001c0001t0001g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-18+3256A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2988998 | |||||||
| chr11:2989083 | A | G | 13 | a0001c0001t0001g0021 a0001c0001t0001g0107 a0001c0001t0001g0196 others(10): Show |
14 | HG01346.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-18+3171T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989083 | |||||||
| chr11:2989160 | C | T | 88 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0137 others(85): Show |
111 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-18+3094G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989160 | |||||||
| chr11:2989200 | A | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+3054T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989200 | |||||||
| chr11:2989273 | T | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+2981A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989273 | |||||||
| chr11:2989276 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18+2978T>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989276 | |||||||
| chr11:2989410 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-18+2844G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989410 | |||||||
| chr11:2989573 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18+2681T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989573 | |||||||
| chr11:2989581 | CTA | C | 4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | NA18952.hp2 NA18955.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2671_-18+2672d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989581 | |||||||
| chr11:2989594 | C | T | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
108 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18+2660G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989594 | |||||||
| chr11:2989611 | C | G | 9 | a0001c0001t0009g0195 a0001c0002t0003g0016 a0001c0002t0003g0108 others(6): Show |
11 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+2643G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989611 | |||||||
| chr11:2989631 | T | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0176 a0001c0001t0001g0177 others(17): Show |
21 | HG00099.hp2 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+2623A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989631 | |||||||
| chr11:2989756 | G | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
115 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-18+2498C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989756 | |||||||
| chr11:2989873 | G | C | 1 | a0001c0001t0001g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-18+2381C>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989873 | |||||||
| chr11:2989958 | CAT | C | 3 | a0002c0003t0001g0028 a0002c0003t0001g0266 a0002c0003t0001g0267 |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2294_-18+2295d others(4): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2989958 | |||||||
| chr11:2990043 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-18+2211T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990043 | |||||||
| chr11:2990114 | AT | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18+2139delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990114 | |||||||
| chr11:2990121 | A | G | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(26): Show |
39 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18+2133T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990121 | |||||||
| chr11:2990129 | AT | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2124delA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990129 | |||||||
| chr11:2990132 | T | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2122A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990132 | |||||||
| chr11:2990133 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2121C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990133 | |||||||
| chr11:2990135 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2119C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990135 | |||||||
| chr11:2990136 | CCTA | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
111 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-18+2115_-18+2117d others(5): Show |
NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990136 | |||||||
| chr11:2990138 | T | G | 3 | a0002c0003t0001g0028 a0002c0003t0001g0266 a0002c0003t0001g0267 |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+2116A>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990138 | |||||||
| chr11:2990149 | T | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
110 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-18+2105A>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990149 | |||||||
| chr11:2990245 | G | T | 2 | a0001c0001t0001g0115 a0001c0001t0011g0114 |
2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-18+2009C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990245 | |||||||
| chr11:2990291 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18+1963G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990291 | |||||||
| chr11:2990636 | C | A | 1 | a0001c0001t0001g0261 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-18+1618G>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990636 | |||||||
| chr11:2990819 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-18+1435C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990819 | |||||||
| chr11:2990841 | A | T | 1 | a0001c0002t0015g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18+1413T>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990841 | |||||||
| chr11:2990892 | A | G | 1 | a0001c0001t0010g0113 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+1362T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990892 | |||||||
| chr11:2990909 | C | G | 8 | a0001c0002t0003g0016 a0001c0002t0003g0108 a0001c0002t0003g0109 others(5): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-18+1345G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990909 | |||||||
| chr11:2990956 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18+1298T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990956 | |||||||
| chr11:2990994 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-18+1260A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2990994 | |||||||
| chr11:2991331 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-18+923A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991331 | |||||||
| chr11:2991411 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-18+843A>G | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991411 | |||||||
| chr11:2991439 | A | AT | 8 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
9 | HG01243.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+814dupA | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991439 | |||||||
| chr11:2991674 | A | G | 1 | a0001c0001t0002g0007 | 3 | NA18939.hp1 NA19001.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-18+580T>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991674 | |||||||
| chr11:2991928 | G | A | 1 | a0001c0001t0002g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18+326C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2991928 | |||||||
| chr11:2992057 | C | G | 79 | a0001c0001t0001g0043 a0001c0001t0002g0001 a0001c0001t0002g0003 others(76): Show |
102 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-18+197G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992057 | |||||||
| chr11:2992084 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-18+170C>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992084 | |||||||
| chr11:2992086 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-18+168G>A | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992086 | |||||||
| chr11:2992098 | C | G | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+156G>C | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992098 | |||||||
| chr11:2992162 | G | A | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0268 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+92C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992162 | |||||||
| chr11:2992177 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-18+77C>T | NAP1L4 | ENSG00000205531.14 | transcript | ENST00000380542.9 | protein_coding | 1/15 | chr11 | 2992177 |