Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9683 |
| ensemblid | ENSG00000102921.8 |
| hgncid | 29850 |
| symbol | N4BP1 |
| name | NEDD4 binding protein 1 |
| refseq_nuc | NM_153029.4 |
| refseq_prot | NP_694574.3 |
| ensembl_nuc | ENST00000262384.4 |
| ensembl_prot | ENSP00000262384.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 48538726 |
| end | 48610180 |
| strand | - |
| ver | v1.2 |
| region | chr16:48538726-48610180 |
| region5000 | chr16:48533726-48615180 |
| regionname0 | N4BP1_chr16_48538726_48610180 |
| regionname5000 | N4BP1_chr16_48533726_48615180 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 896 | 317 | 80 | 57 | 133 | 14 | 31 | 109 | N4BP1_chr16_48533726_48615180 | N4BP1 | MAARA others(891): Show |
chr16 | 48533726 | 48615180 |
| a0002 | 0/0 | 896 | 4 | 0 | 1 | 3 | 0 | 0 | 3 | N4BP1_chr16_48533726_48615180 | N4BP1 | MAARA others(891): Show |
chr16 | 48533726 | 48615180 |
| a0003 | 0/0 | 896 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | MAARA others(891): Show |
chr16 | 48533726 | 48615180 |
| a0004 | 0/0 | 896 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | MAARA others(891): Show |
chr16 | 48533726 | 48615180 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2688 | 303 | 67 | 57 | 132 | 14 | 31 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0001c0002 | 0/0 | 2688 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0001c0004 | 0/0 | 2688 | 3 | 3 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0001c0007 | 0/0 | 2688 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0001c0008 | 0/0 | 2688 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0002c0003 | 0/0 | 2688 | 4 | 0 | 1 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0003c0005 | 0/0 | 2688 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 | ||
| a0004c0006 | 0/0 | 2688 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | ATGGC others(2683): Show |
chr16 | 48533726 | 48615180 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7076 | 111 | 22 | 22 | 45 | 5 | 17 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0002 | 0/0 | 7077 | 82 | 2 | 11 | 63 | 2 | 4 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0003 | 1/1 | 7077 | 65 | 12 | 16 | 20 | 7 | 8 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0005 | 0/0 | 7077 | 8 | 8 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0006 | 0/0 | 7076 | 5 | 4 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0007 | 0/0 | 7076 | 5 | 5 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0008 | 0/0 | 7077 | 4 | 0 | 4 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0009 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0010 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0011 | 0/0 | 7077 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0012 | 0/0 | 7076 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0013 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0014 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0015 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0016 | 0/0 | 7077 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0017 | 0/0 | 7077 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0018 | 0/0 | 7077 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0019 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0020 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0021 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0022 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0023 | 0/0 | 7076 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0024 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0025 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0026 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0001t0027 | 0/0 | 7058 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7053): Show |
chr16 | 48533726 | 48615180 |
| a0001c0002t0004 | 0/0 | 7076 | 9 | 9 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0004t0003 | 0/0 | 7077 | 3 | 3 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0001c0007t0001 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0001c0008t0001 | 0/0 | 7076 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| a0002c0003t0002 | 0/0 | 7077 | 4 | 0 | 1 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0003c0005t0003 | 0/0 | 7077 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7072): Show |
chr16 | 48533726 | 48615180 |
| a0004c0006t0001 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | GGAGG others(7071): Show |
chr16 | 48533726 | 48615180 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0016 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0008g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0015g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0016g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0017g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0018g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0019g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0020g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0021g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0023g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0024g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0025g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0026g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0001t0027g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0002t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0004t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0001c0008t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0002c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0002c0003t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0002c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0002c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0003c0005t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| a0004c0006t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0226 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0165 | EUR | FIN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00738 | hp2 | a0002 | c0003 | t0002 | g0277 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0132 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01255 | hp1 | a0001 | c0001 | t0011 | g0133 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0115 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01256 | hp1 | a0001 | c0001 | t0018 | g0146 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0225 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0160 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0162 | EUR | IBS | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CDX | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02300 | hp2 | a0001 | c0001 | t0008 | g0164 | AMR | PEL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02572 | hp2 | a0001 | c0001 | t0019 | g0045 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02602 | hp1 | a0001 | c0001 | t0017 | g0136 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0252 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0037 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0251 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0087 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02886 | hp1 | a0001 | c0001 | t0025 | g0092 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02922 | hp1 | a0003 | c0005 | t0003 | g0015 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0033 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02970 | hp2 | a0003 | c0005 | t0003 | g0015 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0099 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03098 | hp2 | a0001 | c0004 | t0003 | g0271 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0272 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03516 | hp1 | a0001 | c0002 | t0004 | g0238 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0273 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0051 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03834 | hp2 | a0004 | c0006 | t0001 | g0055 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0159 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0137 | SAS | STU | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0028 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | CHB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18906 | hp1 | a0001 | c0001 | t0021 | g0085 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | YRI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0278 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18943 | hp2 | a0001 | c0008 | t0001 | g0275 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18971 | hp2 | a0001 | c0001 | t0027 | g0280 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18975 | hp2 | a0001 | c0001 | t0023 | g0076 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18993 | hp2 | a0001 | c0001 | t0012 | g0141 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18994 | hp1 | a0001 | c0001 | t0012 | g0140 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19011 | hp2 | a0002 | c0003 | t0002 | g0279 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19030 | hp1 | a0001 | c0007 | t0001 | g0274 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0031 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19074 | hp1 | a0002 | c0003 | t0002 | g0276 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ASW | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ASW | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0148 | EUR | TSI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | GIH | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02109 | hp1 | a0001 | c0001 | t0024 | g0110 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0049 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG02559 | hp2 | a0001 | c0001 | t0020 | g0083 | AFR | ACB | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0145 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | USA | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | USA | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0147 | REF | REF | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0016 | REF | REF | N4BP1_chr16_48533726_48615180 | N4BP1 | chr16 | 48533726 | 48615180 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48561439 | C | A | 1 | a0004 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.1204G>T | p.Val402Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 1412/7077 | 1204/2691 | 402/896 | chr16 | 48561439 | |||
| chr16:48561984 | G | T | 1 | a0003 | 2 | HG02922.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.659C>A | p.Ala220Asp | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 867/7077 | 659/2691 | 220/896 | chr16 | 48561984 | |||
| chr16:48609923 | G | A | 1 | a0002 | 4 | HG00738.hp2 NA18939.hp2 NA19011.hp2 others(1): Show |
missense_variant | MODERATE | c.50C>T | p.Ala17Val | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 258/7077 | 50/2691 | 17/896 | chr16 | 48609923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48561005 | T | C | 1 | a0001c0002 | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
synonymous_variant | LOW | c.1638A>G | p.Leu546Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/7 | 1846/7077 | 1638/2691 | 546/896 | chr16 | 48561005 | |||
| chr16:48609808 | G | A | 1 | a0001c0004 | 3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.165C>T | p.Leu55Leu | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 373/7077 | 165/2691 | 55/896 | chr16 | 48609808 | |||
| chr16:48609829 | G | A | 1 | a0001c0007 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.144C>T | p.Pro48Pro | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 352/7077 | 144/2691 | 48/896 | chr16 | 48609829 | |||
| chr16:48609901 | G | A | 1 | a0001c0008 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.72C>T | p.Arg24Arg | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 280/7077 | 72/2691 | 24/896 | chr16 | 48609901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48538782 | G | A | 1 | a0001c0001t0017 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4122C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 4122 | chr16 | 48538782 | ||||||
| chr16:48538805 | A | G | 1 | a0001c0001t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4099T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 4099 | chr16 | 48538805 | ||||||
| chr16:48538906 | G | A | 18 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(15): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*3998C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3998 | chr16 | 48538906 | ||||||
| chr16:48539031 | C | T | 1 | a0001c0001t0020 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3873G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3873 | chr16 | 48539031 | ||||||
| chr16:48539097 | G | A | 1 | a0001c0001t0005 | 8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3807C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3807 | chr16 | 48539097 | ||||||
| chr16:48539166 | T | C | 2 | a0001c0001t0013 a0001c0001t0014 |
2 | HG02615.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3738A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3738 | chr16 | 48539166 | ||||||
| chr16:48539261 | G | A | 1 | a0001c0001t0015 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3643C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3643 | chr16 | 48539261 | ||||||
| chr16:48539378 | G | A | 2 | a0001c0001t0016 a0001c0001t0017 |
2 | HG02602.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3526C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3526 | chr16 | 48539378 | ||||||
| chr16:48539515 | C | T | 1 | a0001c0001t0008 | 4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3389G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3389 | chr16 | 48539515 | ||||||
| chr16:48539517 | A | G | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(13): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3387T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3387 | chr16 | 48539517 | ||||||
| chr16:48539592 | T | C | 1 | a0001c0001t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3312A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3312 | chr16 | 48539592 | ||||||
| chr16:48539670 | C | T | 1 | a0001c0001t0011 | 2 | HG01074.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3234G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3234 | chr16 | 48539670 | ||||||
| chr16:48539806 | G | T | 1 | a0001c0001t0010 | 2 | HG02615.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3098C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 3098 | chr16 | 48539806 | ||||||
| chr16:48540129 | T | G | 18 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(15): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2775A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2775 | chr16 | 48540129 | ||||||
| chr16:48540175 | T | G | 2 | a0001c0001t0006 a0001c0002t0004 |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2729A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2729 | chr16 | 48540175 | ||||||
| chr16:48540348 | G | C | 3 | a0001c0001t0002 a0001c0001t0027 a0002c0003t0002 |
87 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2556C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2556 | chr16 | 48540348 | ||||||
| chr16:48540358 | G | A | 1 | a0001c0001t0023 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2546C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2546 | chr16 | 48540358 | ||||||
| chr16:48540726 | A | C | 18 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(15): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2178T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 2178 | chr16 | 48540726 | ||||||
| chr16:48540958 | C | T | 14 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(11): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1946G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1946 | chr16 | 48540958 | ||||||
| chr16:48541181 | T | G | 1 | a0001c0001t0012 | 2 | NA18993.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1723A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1723 | chr16 | 48541181 | ||||||
| chr16:48541320 | G | C | 1 | a0001c0001t0024 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1584C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1584 | chr16 | 48541320 | ||||||
| chr16:48541454 | G | A | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1450C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1450 | chr16 | 48541454 | ||||||
| chr16:48541582 | C | T | 1 | a0001c0001t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1322G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1322 | chr16 | 48541582 | ||||||
| chr16:48541611 | G | A | 1 | a0001c0001t0025 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1293C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 1293 | chr16 | 48541611 | ||||||
| chr16:48541967 | G | A | 14 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0012 others(11): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*937C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 937 | chr16 | 48541967 | ||||||
| chr16:48542007 | G | A | 1 | a0001c0001t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*897C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 897 | chr16 | 48542007 | ||||||
| chr16:48542027 | C | T | 1 | a0001c0001t0019 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*877G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 877 | chr16 | 48542027 | ||||||
| chr16:48542060 | T | A | 1 | a0001c0001t0006 | 5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*844A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 844 | chr16 | 48542060 | ||||||
| chr16:48542134 | T | C | 2 | a0001c0001t0006 a0001c0002t0004 |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*770A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 770 | chr16 | 48542134 | ||||||
| chr16:48542327 | A | T | 1 | a0001c0001t0009 | 2 | HG02630.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 577 | chr16 | 48542327 | ||||||
| chr16:48542503 | G | A | 1 | a0001c0001t0018 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 401 | chr16 | 48542503 | ||||||
| chr16:48542529 | CT | C | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(13): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*374delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 374 | chr16 | 48542529 | ||||||
| chr16:48542890 | G | A | 1 | a0001c0001t0007 | 5 | HG02486.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 7/7 | 14 | chr16 | 48542890 | ||||||
| chr16:48609989 | CGCGGCGG others(12): Show |
C | 1 | a0001c0001t0027 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36_-18delCGGCCCCC others(11): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/7 | 18 | chr16 | 48609989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48543364 | C | A | 1 | a0001c0002t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2334-103G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543364 | |||||||
| chr16:48543364 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2334-103G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543364 | |||||||
| chr16:48543440 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2334-179C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543440 | |||||||
| chr16:48543497 | G | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2334-236C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543497 | |||||||
| chr16:48543545 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2334-284G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543545 | |||||||
| chr16:48543587 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2334-326C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543587 | |||||||
| chr16:48543596 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2334-335A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543596 | |||||||
| chr16:48543658 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2334-397T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543658 | |||||||
| chr16:48543772 | T | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2334-511A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48543772 | |||||||
| chr16:48544034 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0020g0083 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2334-773C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544034 | |||||||
| chr16:48544065 | C | T | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2334-804G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544065 | |||||||
| chr16:48544190 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.2334-929T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544190 | |||||||
| chr16:48544920 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2333+1227C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48544920 | |||||||
| chr16:48545027 | C | T | 3 | a0001c0001t0002g0178 a0001c0001t0002g0193 a0001c0001t0002g0208 |
3 | HG02738.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2333+1120G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545027 | |||||||
| chr16:48545092 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+1055C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545092 | |||||||
| chr16:48545111 | C | T | 5 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(2): Show |
5 | NA18973.hp1 NA18983.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.2333+1036G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545111 | |||||||
| chr16:48545184 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+963G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545184 | |||||||
| chr16:48545244 | C | T | 1 | a0001c0001t0026g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2333+903G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545244 | |||||||
| chr16:48545295 | C | T | 8 | a0001c0001t0002g0196 a0001c0002t0004g0009 a0001c0002t0004g0031 others(5): Show |
9 | HG02040.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2333+852G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545295 | |||||||
| chr16:48545308 | G | A | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2333+839C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545308 | |||||||
| chr16:48545387 | T | C | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2333+760A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545387 | |||||||
| chr16:48545407 | TA | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(119): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.2333+739delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545407 | |||||||
| chr16:48545446 | C | T | 1 | a0001c0001t0005g0234 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2333+701G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545446 | |||||||
| chr16:48545535 | G | A | 1 | a0001c0007t0001g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2333+612C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545535 | |||||||
| chr16:48545574 | A | G | 1 | a0001c0001t0003g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2333+573T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545574 | |||||||
| chr16:48545893 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2333+254C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545893 | |||||||
| chr16:48545899 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2333+248G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545899 | |||||||
| chr16:48545915 | T | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2333+232A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545915 | |||||||
| chr16:48545941 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0097 others(1): Show |
6 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2333+206G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545941 | |||||||
| chr16:48545967 | G | C | 1 | a0001c0001t0003g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2333+180C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48545967 | |||||||
| chr16:48546027 | C | CA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(111): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2333+119dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546027 | |||||||
| chr16:48546039 | A | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2333+108T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546039 | |||||||
| chr16:48546040 | A | G | 2 | a0001c0001t0016g0137 a0001c0001t0017g0136 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2333+107T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 6/6 | chr16 | 48546040 | |||||||
| chr16:48546290 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2226-36C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546290 | |||||||
| chr16:48546350 | G | A | 1 | a0001c0001t0014g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2226-96C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546350 | |||||||
| chr16:48546549 | C | G | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2226-295G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546549 | |||||||
| chr16:48546623 | G | T | 4 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2226-369C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546623 | |||||||
| chr16:48546744 | G | C | 1 | a0001c0001t0003g0149 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2226-490C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546744 | |||||||
| chr16:48546896 | G | A | 7 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0002g0172 others(4): Show |
7 | HG00738.hp2 NA18939.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.2226-642C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546896 | |||||||
| chr16:48546949 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2226-695G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546949 | |||||||
| chr16:48546953 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2226-699G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48546953 | |||||||
| chr16:48547018 | TCAA | T | 1 | a0001c0001t0001g0006 | 3 | HG01109.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2226-767_2226-765d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547018 | |||||||
| chr16:48547217 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2225+790T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547217 | |||||||
| chr16:48547560 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2225+447T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547560 | |||||||
| chr16:48547737 | A | G | 1 | a0001c0001t0003g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2225+270T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 5/6 | chr16 | 48547737 | |||||||
| chr16:48548508 | C | A | 81 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(78): Show |
87 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.2118-394G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548508 | |||||||
| chr16:48548664 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2118-550A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548664 | |||||||
| chr16:48548677 | T | C | 6 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0232 others(3): Show |
8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2118-563A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548677 | |||||||
| chr16:48548837 | C | CA | 19 | a0001c0001t0001g0102 a0001c0001t0002g0162 a0001c0001t0002g0184 others(16): Show |
20 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2118-724dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548837 | |||||||
| chr16:48548837 | CA | C | 13 | a0001c0001t0001g0044 a0001c0001t0001g0105 a0001c0001t0002g0124 others(10): Show |
15 | HG01070.hp2 HG02155.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.2118-724delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48548837 | |||||||
| chr16:48549208 | A | T | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2118-1094T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48549208 | |||||||
| chr16:48550013 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2117+1373A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550013 | |||||||
| chr16:48550066 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2117+1320G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550066 | |||||||
| chr16:48550212 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2117+1174A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550212 | |||||||
| chr16:48550330 | T | C | 1 | a0001c0001t0003g0227 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2117+1056A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550330 | |||||||
| chr16:48550376 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2117+1010C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550376 | |||||||
| chr16:48550476 | T | C | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2117+910A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550476 | |||||||
| chr16:48550841 | C | A | 7 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0033 others(4): Show |
8 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2117+545G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550841 | |||||||
| chr16:48550894 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2117+492G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48550894 | |||||||
| chr16:48551031 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(118): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.2117+355G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48551031 | |||||||
| chr16:48551160 | A | T | 1 | a0001c0001t0002g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2117+226T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 4/6 | chr16 | 48551160 | |||||||
| chr16:48551522 | C | G | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2021-40G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551522 | |||||||
| chr16:48551626 | G | C | 1 | a0001c0001t0003g0229 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2021-144C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551626 | |||||||
| chr16:48551756 | C | T | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2021-274G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551756 | |||||||
| chr16:48551978 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2021-496C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48551978 | |||||||
| chr16:48552018 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2021-536T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552018 | |||||||
| chr16:48552217 | C | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2021-735G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552217 | |||||||
| chr16:48552426 | G | A | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2021-944C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552426 | |||||||
| chr16:48552570 | T | C | 2 | a0001c0001t0002g0197 a0001c0001t0002g0253 |
2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.2020+969A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552570 | |||||||
| chr16:48552591 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2020+948C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552591 | |||||||
| chr16:48552646 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.2020+893G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552646 | |||||||
| chr16:48552684 | C | T | 1 | a0001c0001t0010g0029 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2020+855G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552684 | |||||||
| chr16:48552685 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2020+854C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552685 | |||||||
| chr16:48552699 | G | GA | 38 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0053 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.2020+839dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAA | 25 | a0001c0001t0001g0047 a0001c0001t0001g0054 a0001c0001t0001g0058 others(22): Show |
25 | HG00280.hp2 HG00323.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2020+838_2020+839d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAA | 41 | a0001c0001t0001g0013 a0001c0001t0001g0088 a0001c0001t0001g0094 others(38): Show |
45 | HG00738.hp2 HG01952.hp1 HG02040.hp2 others(42): Show |
intron_variant | MODIFIER | c.2020+837_2020+839d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAA | 34 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0093 others(31): Show |
37 | HG01258.hp1 HG01934.hp1 HG01993.hp1 others(34): Show |
intron_variant | MODIFIER | c.2020+836_2020+839d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAA | 10 | a0001c0001t0001g0109 a0001c0001t0002g0180 a0001c0001t0002g0198 others(7): Show |
11 | HG00621.hp2 HG01346.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2020+835_2020+839d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(2): Show |
7 | a0001c0001t0002g0020 a0001c0001t0002g0123 a0001c0001t0002g0129 others(4): Show |
8 | HG00639.hp1 HG01243.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.2020+831_2020+839d others(11): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0095 a0001c0001t0002g0199 |
2 | HG01433.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2020+830_2020+839d others(12): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(4): Show |
1 | a0001c0001t0002g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2020+829_2020+839d others(13): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(5): Show |
1 | a0001c0001t0005g0233 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2020+828_2020+839d others(14): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(6): Show |
1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2020+827_2020+839d others(15): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(10): Show |
1 | a0001c0001t0001g0082 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2020+823_2020+839d others(19): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | G | GAAAAAAA others(12): Show |
2 | a0001c0001t0002g0201 a0001c0001t0020g0083 |
2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2020+821_2020+839d others(21): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GA | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(21): Show |
39 | HG00673.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.2020+839delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(6): Show |
G | 5 | a0001c0001t0001g0062 a0001c0001t0002g0204 a0001c0001t0013g0037 others(2): Show |
5 | HG02273.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2020+827_2020+839d others(15): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(7): Show |
G | 10 | a0001c0001t0001g0052 a0001c0001t0001g0091 a0001c0001t0002g0117 others(7): Show |
11 | HG02258.hp2 HG02486.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2020+826_2020+839d others(16): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(9): Show |
G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0096 a0003c0005t0003g0015 |
4 | HG01123.hp1 HG01169.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020+824_2020+839d others(18): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(11): Show |
G | 1 | a0001c0001t0002g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2020+822_2020+839d others(20): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(14): Show |
G | 1 | a0001c0001t0002g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2020+819_2020+839d others(23): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(16): Show |
G | 1 | a0001c0001t0001g0006 | 3 | HG01109.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2020+817_2020+839d others(25): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552699 | GAAAAAAA others(18): Show |
G | 1 | a0001c0001t0003g0148 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2020+815_2020+839d others(27): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552699 | |||||||
| chr16:48552713 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2020+826T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552713 | |||||||
| chr16:48552899 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.2020+640G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48552899 | |||||||
| chr16:48553151 | T | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0262 |
3 | HG03017.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2020+388A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553151 | |||||||
| chr16:48553172 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.2020+367A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553172 | |||||||
| chr16:48553310 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0067 others(4): Show |
7 | HG01993.hp1 HG03239.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.2020+229T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 3/6 | chr16 | 48553310 | |||||||
| chr16:48553968 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0079 others(11): Show |
17 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1890-299C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48553968 | |||||||
| chr16:48554173 | TA | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1890-505delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554173 | |||||||
| chr16:48554320 | G | A | 2 | a0001c0001t0009g0144 a0001c0001t0009g0145 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1890-651C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554320 | |||||||
| chr16:48554369 | G | A | 1 | a0001c0002t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1890-700C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554369 | |||||||
| chr16:48554369 | G | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0265 |
2 | NA18973.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1890-700C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554369 | |||||||
| chr16:48554553 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1890-884T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554553 | |||||||
| chr16:48554610 | T | C | 2 | a0001c0001t0003g0251 a0001c0001t0015g0252 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1890-941A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554610 | |||||||
| chr16:48554703 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1890-1034A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554703 | |||||||
| chr16:48554710 | T | C | 1 | a0001c0001t0001g0010 | 2 | NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1890-1041A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48554710 | |||||||
| chr16:48555135 | G | A | 1 | a0001c0001t0016g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1890-1466C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555135 | |||||||
| chr16:48555141 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1890-1472A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555141 | |||||||
| chr16:48555151 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
263 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1890-1482A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555151 | |||||||
| chr16:48555158 | T | C | 1 | a0001c0002t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1890-1489A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555158 | |||||||
| chr16:48555280 | A | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1890-1611T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555280 | |||||||
| chr16:48555450 | A | T | 1 | a0001c0004t0003g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1890-1781T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555450 | |||||||
| chr16:48555731 | AG | A | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1890-2063delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555731 | |||||||
| chr16:48555962 | G | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1890-2293C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555962 | |||||||
| chr16:48555985 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1890-2316C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48555985 | |||||||
| chr16:48556044 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1890-2375C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556044 | |||||||
| chr16:48556234 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1890-2565T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556234 | |||||||
| chr16:48556313 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
5 | HG02572.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1890-2644G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556313 | |||||||
| chr16:48556416 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(10): Show |
19 | HG01069.hp2 HG01071.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1890-2747C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556416 | |||||||
| chr16:48556561 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0079 others(11): Show |
17 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1890-2892C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556561 | |||||||
| chr16:48556578 | G | T | 1 | a0001c0001t0002g0205 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1890-2909C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556578 | |||||||
| chr16:48556677 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0067 others(4): Show |
7 | HG01993.hp1 HG03239.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1890-3008C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556677 | |||||||
| chr16:48556716 | A | T | 5 | a0001c0001t0002g0018 a0001c0001t0002g0119 a0001c0001t0002g0131 others(2): Show |
6 | NA18945.hp1 NA18952.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.1890-3047T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556716 | |||||||
| chr16:48556745 | G | A | 1 | a0001c0001t0016g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1890-3076C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556745 | |||||||
| chr16:48556788 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1890-3119G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556788 | |||||||
| chr16:48556889 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1890-3220T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556889 | |||||||
| chr16:48556907 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1890-3238T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48556907 | |||||||
| chr16:48557101 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1890-3432A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557101 | |||||||
| chr16:48557690 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1889+3064G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557690 | |||||||
| chr16:48557708 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1889+3046A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557708 | |||||||
| chr16:48557727 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+3027A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557727 | |||||||
| chr16:48557806 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1889+2948T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557806 | |||||||
| chr16:48557837 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1889+2917C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48557837 | |||||||
| chr16:48558293 | C | CA | 6 | a0001c0001t0001g0096 a0001c0001t0002g0200 a0001c0001t0002g0201 others(3): Show |
6 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1889+2460dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558293 | |||||||
| chr16:48558293 | CA | C | 31 | a0001c0001t0001g0061 a0001c0001t0001g0105 a0001c0001t0001g0259 others(28): Show |
33 | HG01070.hp2 HG01106.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.1889+2460delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558293 | |||||||
| chr16:48558317 | TA | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+2436delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558317 | |||||||
| chr16:48558448 | T | C | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1889+2306A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558448 | |||||||
| chr16:48558465 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+2289C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558465 | |||||||
| chr16:48558665 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1889+2089A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558665 | |||||||
| chr16:48558797 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1889+1957C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558797 | |||||||
| chr16:48558931 | AATG | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1889+1820_1889+182 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48558931 | |||||||
| chr16:48559154 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1600G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559154 | |||||||
| chr16:48559164 | ATTATC | A | 6 | a0001c0001t0002g0129 a0001c0001t0002g0202 a0001c0001t0002g0207 others(3): Show |
6 | NA18941.hp2 NA18957.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1889+1585_1889+158 others(9): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559164 | |||||||
| chr16:48559387 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1367A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559387 | |||||||
| chr16:48559476 | A | C | 1 | a0001c0001t0006g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1889+1278T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559476 | |||||||
| chr16:48559722 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1889+1032G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559722 | |||||||
| chr16:48559732 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+1022T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559732 | |||||||
| chr16:48559781 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1889+973G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559781 | |||||||
| chr16:48559868 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+886T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48559868 | |||||||
| chr16:48560103 | G | GA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1889+650dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560103 | |||||||
| chr16:48560310 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+444T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560310 | |||||||
| chr16:48560318 | C | T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1889+436G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560318 | |||||||
| chr16:48560334 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1889+420T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560334 | |||||||
| chr16:48560376 | TA | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1889+377delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560376 | |||||||
| chr16:48560456 | A | G | 1 | a0001c0002t0004g0035 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1889+298T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560456 | |||||||
| chr16:48560500 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1889+254C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560500 | |||||||
| chr16:48560602 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0096 |
2 | HG01123.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1889+152T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 2/6 | chr16 | 48560602 | |||||||
| chr16:48562577 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.199-133C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562577 | |||||||
| chr16:48562699 | G | C | 1 | a0001c0001t0003g0160 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.199-255C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562699 | |||||||
| chr16:48562842 | G | A | 1 | a0001c0001t0018g0146 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.199-398C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562842 | |||||||
| chr16:48562984 | A | AT | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-541dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48562984 | |||||||
| chr16:48563081 | G | C | 1 | a0001c0001t0003g0155 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.199-637C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563081 | |||||||
| chr16:48563110 | T | C | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-666A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563110 | |||||||
| chr16:48563141 | T | A | 4 | a0001c0001t0001g0080 a0001c0001t0002g0117 a0001c0001t0002g0203 others(1): Show |
4 | NA18906.hp2 NA18942.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-697A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563141 | |||||||
| chr16:48563175 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0259 others(1): Show |
6 | NA18947.hp1 NA18953.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-731G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563175 | |||||||
| chr16:48563249 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.199-805C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563249 | |||||||
| chr16:48563341 | C | T | 3 | a0001c0001t0008g0017 a0001c0001t0008g0115 a0001c0001t0008g0164 |
4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-897G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563341 | |||||||
| chr16:48563342 | G | A | 1 | a0001c0001t0003g0021 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.199-898C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563342 | |||||||
| chr16:48563347 | C | G | 5 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(2): Show |
6 | HG02451.hp2 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-903G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563347 | |||||||
| chr16:48563364 | A | T | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-920T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563364 | |||||||
| chr16:48563447 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.199-1003T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563447 | |||||||
| chr16:48563757 | G | C | 1 | a0001c0001t0002g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199-1313C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563757 | |||||||
| chr16:48563815 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-1371C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48563815 | |||||||
| chr16:48564004 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-1560C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564004 | |||||||
| chr16:48564109 | C | G | 1 | a0001c0001t0006g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-1665G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564109 | |||||||
| chr16:48564153 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-1709T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564153 | |||||||
| chr16:48564463 | T | C | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-2019A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564463 | |||||||
| chr16:48564606 | C | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-2162G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564606 | |||||||
| chr16:48564704 | G | A | 3 | a0001c0001t0003g0138 a0001c0001t0003g0150 a0001c0001t0003g0159 |
3 | HG00741.hp2 HG01106.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.199-2260C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564704 | |||||||
| chr16:48564782 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.199-2338G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564782 | |||||||
| chr16:48564826 | T | A | 8 | a0001c0001t0002g0128 a0001c0001t0002g0180 a0001c0001t0002g0186 others(5): Show |
8 | HG00621.hp2 HG02132.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-2382A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564826 | |||||||
| chr16:48564826 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-2382A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564826 | |||||||
| chr16:48564878 | C | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2434G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564878 | |||||||
| chr16:48564973 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-2529T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48564973 | |||||||
| chr16:48565073 | G | A | 1 | a0001c0001t0015g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.199-2629C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565073 | |||||||
| chr16:48565539 | T | C | 2 | a0001c0001t0003g0269 a0001c0001t0003g0270 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.199-3095A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565539 | |||||||
| chr16:48565619 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(94): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.199-3175T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565619 | |||||||
| chr16:48565698 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-3254A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565698 | |||||||
| chr16:48565906 | T | C | 19 | a0001c0001t0003g0007 a0001c0001t0003g0138 a0001c0001t0003g0148 others(16): Show |
21 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-3462A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565906 | |||||||
| chr16:48565980 | T | C | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-3536A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48565980 | |||||||
| chr16:48566085 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-3641A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566085 | |||||||
| chr16:48566397 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199-3953C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566397 | |||||||
| chr16:48566421 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-3977C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566421 | |||||||
| chr16:48566465 | C | T | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-4021G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48566465 | |||||||
| chr16:48567377 | C | T | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-4933G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567377 | |||||||
| chr16:48567380 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.199-4936T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567380 | |||||||
| chr16:48567410 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-4966A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567410 | |||||||
| chr16:48567433 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.199-4989A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567433 | |||||||
| chr16:48567449 | C | T | 2 | a0001c0001t0012g0140 a0001c0001t0012g0141 |
2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.199-5005G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567449 | |||||||
| chr16:48567610 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-5166A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567610 | |||||||
| chr16:48567615 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199-5171C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567615 | |||||||
| chr16:48567627 | A | C | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5183T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567627 | |||||||
| chr16:48567739 | CTTATA | C | 2 | a0001c0001t0005g0023 a0001c0001t0005g0024 |
4 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-5300_199-5296d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48567739 | |||||||
| chr16:48568198 | T | C | 1 | a0001c0001t0006g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.199-5754A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568198 | |||||||
| chr16:48568229 | C | T | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-5785G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568229 | |||||||
| chr16:48568332 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-5888C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568332 | |||||||
| chr16:48568348 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.199-5904A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568348 | |||||||
| chr16:48568684 | C | A | 1 | a0001c0001t0003g0157 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.199-6240G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568684 | |||||||
| chr16:48568767 | ATTG | A | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-6326_199-6324d others(5): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568767 | |||||||
| chr16:48568812 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-6368T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568812 | |||||||
| chr16:48568822 | C | T | 100 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(97): Show |
109 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(106): Show |
intron_variant | MODIFIER | c.199-6378G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568822 | |||||||
| chr16:48568850 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-6406C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48568850 | |||||||
| chr16:48569092 | C | T | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(16): Show |
22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-6648G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569092 | |||||||
| chr16:48569163 | A | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-6719T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569163 | |||||||
| chr16:48569187 | C | T | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-6743G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569187 | |||||||
| chr16:48569256 | TG | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0004c0006t0001g0055 |
3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.199-6813delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569256 | |||||||
| chr16:48569281 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-6837G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569281 | |||||||
| chr16:48569415 | AG | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-6972delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569415 | |||||||
| chr16:48569455 | C | T | 1 | a0001c0001t0026g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.199-7011G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569455 | |||||||
| chr16:48569591 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.199-7147G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569591 | |||||||
| chr16:48569822 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0263 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.199-7378G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569822 | |||||||
| chr16:48569853 | T | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-7409A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569853 | |||||||
| chr16:48569860 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.199-7416G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48569860 | |||||||
| chr16:48570185 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.199-7741G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570185 | |||||||
| chr16:48570270 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0212 |
3 | HG02451.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-7826C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570270 | |||||||
| chr16:48570279 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-7835C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570279 | |||||||
| chr16:48570369 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.199-7925C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570369 | |||||||
| chr16:48570611 | C | T | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-8167G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570611 | |||||||
| chr16:48570863 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.199-8419G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570863 | |||||||
| chr16:48570951 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.199-8507C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48570951 | |||||||
| chr16:48571055 | G | A | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-8611C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571055 | |||||||
| chr16:48571109 | C | T | 2 | a0001c0001t0016g0137 a0001c0001t0017g0136 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.199-8665G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571109 | |||||||
| chr16:48571235 | A | T | 4 | a0001c0001t0003g0210 a0001c0001t0003g0236 a0001c0001t0003g0237 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-8791T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571235 | |||||||
| chr16:48571236 | A | G | 4 | a0001c0001t0003g0210 a0001c0001t0003g0236 a0001c0001t0003g0237 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-8792T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571236 | |||||||
| chr16:48571254 | C | T | 1 | a0001c0001t0013g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-8810G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571254 | |||||||
| chr16:48571551 | C | T | 7 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0003g0248 others(4): Show |
7 | HG00738.hp2 NA18939.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-9107G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571551 | |||||||
| chr16:48571687 | C | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-9243G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48571687 | |||||||
| chr16:48572073 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.199-9629C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572073 | |||||||
| chr16:48572166 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-9722G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572166 | |||||||
| chr16:48572180 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-9736A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572180 | |||||||
| chr16:48572445 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.199-10001G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572445 | |||||||
| chr16:48572518 | G | A | 6 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0225 others(3): Show |
6 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-10074C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572518 | |||||||
| chr16:48572552 | T | C | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-10108A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572552 | |||||||
| chr16:48572587 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.199-10143T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572587 | |||||||
| chr16:48572746 | T | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.199-10302A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572746 | |||||||
| chr16:48572819 | A | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.199-10375T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48572819 | |||||||
| chr16:48573108 | CA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.199-10665delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573108 | |||||||
| chr16:48573170 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.199-10726G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573170 | |||||||
| chr16:48573185 | C | T | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-10741G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573185 | |||||||
| chr16:48573318 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-10874T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573318 | |||||||
| chr16:48573482 | A | T | 1 | a0001c0001t0019g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-11038T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573482 | |||||||
| chr16:48573891 | T | C | 1 | a0001c0001t0007g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199-11447A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48573891 | |||||||
| chr16:48574055 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-11611A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574055 | |||||||
| chr16:48574062 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.199-11618A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574062 | |||||||
| chr16:48574169 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0257 a0001c0001t0001g0262 |
3 | HG03017.hp2 HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.199-11725T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574169 | |||||||
| chr16:48574252 | A | T | 1 | a0001c0001t0002g0187 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.199-11808T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574252 | |||||||
| chr16:48574345 | T | G | 5 | a0001c0001t0002g0114 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | HG01934.hp1 HG02083.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-11901A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574345 | |||||||
| chr16:48574377 | T | C | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-11933A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574377 | |||||||
| chr16:48574444 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199-12000A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574444 | |||||||
| chr16:48574608 | G | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-12164C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574608 | |||||||
| chr16:48574748 | C | G | 1 | a0001c0001t0003g0211 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-12304G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48574748 | |||||||
| chr16:48575244 | A | C | 103 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(100): Show |
112 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(109): Show |
intron_variant | MODIFIER | c.199-12800T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575244 | |||||||
| chr16:48575484 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(31): Show |
53 | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.199-13040G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575484 | |||||||
| chr16:48575559 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.199-13115C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575559 | |||||||
| chr16:48575646 | A | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0088 others(1): Show |
4 | HG00323.hp1 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-13202T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575646 | |||||||
| chr16:48575748 | A | G | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0176 |
3 | HG01074.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.199-13304T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575748 | |||||||
| chr16:48575919 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.199-13475G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48575919 | |||||||
| chr16:48576381 | G | A | 1 | a0001c0001t0011g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.199-13937C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576381 | |||||||
| chr16:48576861 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.199-14417A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576861 | |||||||
| chr16:48576900 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.199-14456A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576900 | |||||||
| chr16:48576953 | C | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0053 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.199-14509G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48576953 | |||||||
| chr16:48577022 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-14578A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577022 | |||||||
| chr16:48577129 | C | T | 1 | a0001c0001t0013g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.199-14685G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577129 | |||||||
| chr16:48577315 | G | GT | 6 | a0001c0001t0001g0261 a0001c0001t0002g0116 a0001c0001t0016g0137 others(3): Show |
6 | HG03098.hp2 HG03130.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-14872dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577315 | |||||||
| chr16:48577315 | G | GTT | 6 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0232 others(3): Show |
8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-14873_199-1487 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577315 | |||||||
| chr16:48577394 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0245 |
2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.199-14950A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577394 | |||||||
| chr16:48577647 | G | A | 1 | a0001c0001t0003g0222 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.199-15203C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577647 | |||||||
| chr16:48577825 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0212 |
3 | HG02451.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.199-15381G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577825 | |||||||
| chr16:48577992 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.199-15548C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577992 | |||||||
| chr16:48577997 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.199-15553G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577997 | |||||||
| chr16:48577998 | G | A | 20 | a0001c0001t0002g0169 a0001c0001t0003g0004 a0001c0001t0003g0130 others(17): Show |
23 | HG00621.hp1 HG01069.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-15554C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48577998 | |||||||
| chr16:48578450 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-16006T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578450 | |||||||
| chr16:48578497 | C | T | 5 | a0001c0001t0002g0114 a0001c0001t0002g0120 a0001c0001t0002g0121 others(2): Show |
5 | HG01934.hp1 HG02083.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-16053G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578497 | |||||||
| chr16:48578692 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.199-16248G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578692 | |||||||
| chr16:48578996 | GCATTTGA others(13): Show |
G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-16572_199-1655 others(24): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48578996 | |||||||
| chr16:48579039 | T | C | 6 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(3): Show |
6 | HG01106.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-16595A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579039 | |||||||
| chr16:48579173 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.199-16729C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579173 | |||||||
| chr16:48579338 | T | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-16894A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579338 | |||||||
| chr16:48579410 | C | G | 1 | a0001c0001t0003g0269 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199-16966G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579410 | |||||||
| chr16:48579427 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.199-16983T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579427 | |||||||
| chr16:48579911 | T | A | 1 | a0001c0002t0004g0034 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199-17467A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579911 | |||||||
| chr16:48579926 | CAT | C | 7 | a0001c0001t0001g0077 a0001c0001t0006g0039 a0001c0001t0006g0040 others(4): Show |
7 | HG01106.hp2 HG01891.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-17484_199-1748 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48579926 | |||||||
| chr16:48580039 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.199-17595T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580039 | |||||||
| chr16:48580168 | T | C | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.199-17724A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580168 | |||||||
| chr16:48580172 | G | A | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-17728C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580172 | |||||||
| chr16:48580312 | C | T | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-17868G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580312 | |||||||
| chr16:48580382 | G | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-17938C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580382 | |||||||
| chr16:48580752 | C | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-18308G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580752 | |||||||
| chr16:48580794 | T | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(16): Show |
22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-18350A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580794 | |||||||
| chr16:48580926 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.199-18482T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580926 | |||||||
| chr16:48580935 | G | A | 3 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0235 |
5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-18491C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48580935 | |||||||
| chr16:48581136 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.199-18692A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581136 | |||||||
| chr16:48581248 | T | TA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.199-18805dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581248 | |||||||
| chr16:48581375 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.199-18931G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581375 | |||||||
| chr16:48581812 | A | G | 4 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
4 | NA18983.hp2 NA18988.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-19368T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581812 | |||||||
| chr16:48581897 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-19453T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48581897 | |||||||
| chr16:48582220 | C | A | 2 | a0001c0001t0009g0144 a0001c0001t0009g0145 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.199-19776G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582220 | |||||||
| chr16:48582367 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-19923C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582367 | |||||||
| chr16:48582458 | T | TA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-20015dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582458 | |||||||
| chr16:48582694 | GA | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-20251delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582694 | |||||||
| chr16:48582722 | G | A | 4 | a0001c0001t0002g0240 a0001c0001t0002g0242 a0001c0001t0002g0243 others(1): Show |
4 | HG02523.hp1 NA18949.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-20278C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582722 | |||||||
| chr16:48582782 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.199-20338C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582782 | |||||||
| chr16:48582878 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.199-20434T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582878 | |||||||
| chr16:48582946 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.199-20502A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48582946 | |||||||
| chr16:48583065 | G | A | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-20621C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583065 | |||||||
| chr16:48583151 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.199-20707G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583151 | |||||||
| chr16:48583413 | T | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-20969A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583413 | |||||||
| chr16:48583421 | A | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0212 a0001c0001t0003g0269 others(1): Show |
5 | HG02451.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-20977T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583421 | |||||||
| chr16:48583636 | T | A | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-21192A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583636 | |||||||
| chr16:48583699 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0084 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-21255A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583699 | |||||||
| chr16:48583843 | T | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-21399A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583843 | |||||||
| chr16:48583871 | T | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.199-21427A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583871 | |||||||
| chr16:48583939 | G | A | 1 | a0001c0001t0010g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.199-21495C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48583939 | |||||||
| chr16:48584457 | T | G | 1 | a0001c0001t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.199-22013A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584457 | |||||||
| chr16:48584610 | C | CAA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-22168_199-2216 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584610 | |||||||
| chr16:48584662 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.199-22218G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584662 | |||||||
| chr16:48584827 | T | G | 3 | a0001c0001t0003g0210 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG03041.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.199-22383A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584827 | |||||||
| chr16:48584867 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.199-22423A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48584867 | |||||||
| chr16:48585183 | T | A | 2 | a0001c0001t0003g0251 a0001c0001t0015g0252 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.199-22739A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585183 | |||||||
| chr16:48585202 | G | A | 1 | a0001c0001t0003g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.199-22758C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585202 | |||||||
| chr16:48585262 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.199-22818T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585262 | |||||||
| chr16:48585397 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0104 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-22953C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585397 | |||||||
| chr16:48585413 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.199-22969C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585413 | |||||||
| chr16:48585415 | T | C | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.199-22971A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585415 | |||||||
| chr16:48585462 | C | A | 1 | a0001c0001t0003g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-23018G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585462 | |||||||
| chr16:48585608 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.199-23164C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585608 | |||||||
| chr16:48585702 | C | CT | 7 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(4): Show |
7 | HG00621.hp2 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-23259dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585702 | |||||||
| chr16:48585916 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.199-23472G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48585916 | |||||||
| chr16:48586030 | G | A | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(81): Show |
90 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.199-23586C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586030 | |||||||
| chr16:48586292 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+23483C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586292 | |||||||
| chr16:48586454 | A | G | 1 | a0001c0001t0019g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+23321T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586454 | |||||||
| chr16:48586484 | C | T | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+23291G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586484 | |||||||
| chr16:48586598 | G | A | 6 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0232 others(3): Show |
8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+23177C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586598 | |||||||
| chr16:48586603 | A | C | 1 | a0001c0001t0013g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+23172T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586603 | |||||||
| chr16:48586867 | A | T | 2 | a0001c0001t0009g0144 a0001c0001t0009g0145 |
2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.198+22908T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586867 | |||||||
| chr16:48586869 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22906T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586869 | |||||||
| chr16:48586921 | C | T | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+22854G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586921 | |||||||
| chr16:48586987 | G | A | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+22788C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48586987 | |||||||
| chr16:48587053 | C | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22722G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587053 | |||||||
| chr16:48587059 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.198+22716T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587059 | |||||||
| chr16:48587141 | T | A | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+22634A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587141 | |||||||
| chr16:48587260 | T | G | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+22515A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587260 | |||||||
| chr16:48587286 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.198+22489A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587286 | |||||||
| chr16:48587301 | G | A | 1 | a0001c0001t0003g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.198+22474C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587301 | |||||||
| chr16:48587433 | A | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+22342T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587433 | |||||||
| chr16:48587491 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+22284A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587491 | |||||||
| chr16:48587561 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0104 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+22214G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587561 | |||||||
| chr16:48587800 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.198+21975T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587800 | |||||||
| chr16:48587909 | G | A | 2 | a0001c0001t0001g0054 a0004c0006t0001g0055 |
2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.198+21866C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587909 | |||||||
| chr16:48587963 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+21812A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48587963 | |||||||
| chr16:48588215 | A | G | 1 | a0001c0001t0013g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+21560T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588215 | |||||||
| chr16:48588246 | AAGGTAAA others(4226): Show |
A | 1 | a0001c0001t0021g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17296_198+2152 others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588246 | |||||||
| chr16:48588294 | CT | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.198+21480delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588294 | |||||||
| chr16:48588333 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+21442G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588333 | |||||||
| chr16:48588370 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.198+21405A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588370 | |||||||
| chr16:48588389 | G | A | 3 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0235 |
5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+21386C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588389 | |||||||
| chr16:48588440 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198+21335T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588440 | |||||||
| chr16:48588483 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+21292G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588483 | |||||||
| chr16:48588671 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+21104A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588671 | |||||||
| chr16:48588672 | C | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+21103G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588672 | |||||||
| chr16:48588842 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.198+20933G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48588842 | |||||||
| chr16:48589020 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+20755T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589020 | |||||||
| chr16:48589267 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198+20508C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589267 | |||||||
| chr16:48589284 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+20491C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589284 | |||||||
| chr16:48589306 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20469A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589306 | |||||||
| chr16:48589315 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0104 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+20460G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589315 | |||||||
| chr16:48589316 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20459A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589316 | |||||||
| chr16:48589411 | G | T | 1 | a0001c0001t0002g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.198+20364C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589411 | |||||||
| chr16:48589436 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198+20339A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589436 | |||||||
| chr16:48589536 | A | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+20239T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589536 | |||||||
| chr16:48589628 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+20147G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589628 | |||||||
| chr16:48589710 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.198+20065A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589710 | |||||||
| chr16:48589863 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.198+19912C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589863 | |||||||
| chr16:48589884 | G | A | 1 | a0001c0001t0026g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.198+19891C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589884 | |||||||
| chr16:48589917 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0097 |
3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+19858A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589917 | |||||||
| chr16:48589953 | G | A | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(30): Show |
52 | HG00140.hp2 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.198+19822C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48589953 | |||||||
| chr16:48590084 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.198+19691G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590084 | |||||||
| chr16:48590153 | A | G | 1 | a0001c0001t0010g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+19622T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590153 | |||||||
| chr16:48590173 | C | A | 1 | a0001c0001t0026g0087 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.198+19602G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590173 | |||||||
| chr16:48590340 | C | T | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+19435G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590340 | |||||||
| chr16:48590486 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198+19289C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590486 | |||||||
| chr16:48590510 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0097 |
3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+19265C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590510 | |||||||
| chr16:48590551 | C | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0084 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+19224G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590551 | |||||||
| chr16:48590634 | G | A | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+19141C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590634 | |||||||
| chr16:48590893 | CTTAG | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(16): Show |
22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+18878_198+1888 others(8): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48590893 | |||||||
| chr16:48591036 | G | C | 1 | a0001c0001t0003g0154 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.198+18739C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591036 | |||||||
| chr16:48591101 | G | C | 3 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0235 |
5 | HG02451.hp1 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+18674C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591101 | |||||||
| chr16:48591547 | A | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.198+18228T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591547 | |||||||
| chr16:48591632 | GT | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.198+18142delA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591632 | |||||||
| chr16:48591741 | A | T | 1 | a0001c0001t0001g0003 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198+18034T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591741 | |||||||
| chr16:48591832 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.198+17943A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591832 | |||||||
| chr16:48591885 | CG | C | 3 | a0001c0001t0003g0007 a0001c0001t0003g0151 a0001c0001t0003g0231 |
3 | HG00099.hp2 HG01109.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.198+17889delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591885 | |||||||
| chr16:48591886 | G | GT | 102 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(99): Show |
110 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(107): Show |
intron_variant | MODIFIER | c.198+17888dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | |||||||
| chr16:48591886 | G | GTT | 8 | a0001c0001t0002g0008 a0001c0001t0002g0116 a0001c0001t0002g0202 others(5): Show |
9 | HG02148.hp1 HG02451.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+17887_198+1788 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | |||||||
| chr16:48591886 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0256 |
2 | HG01952.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.198+17889C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591886 | |||||||
| chr16:48591898 | T | TTTC | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.198+17876_198+1787 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591898 | |||||||
| chr16:48591993 | T | A | 1 | a0001c0001t0002g0191 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.198+17782A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48591993 | |||||||
| chr16:48592024 | C | A | 1 | a0001c0001t0002g0190 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.198+17751G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592024 | |||||||
| chr16:48592112 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.198+17663A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592112 | |||||||
| chr16:48592115 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.198+17660G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592115 | |||||||
| chr16:48592254 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.198+17521G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592254 | |||||||
| chr16:48592255 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.198+17520C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592255 | |||||||
| chr16:48592346 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0097 |
3 | HG02622.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.198+17429C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592346 | |||||||
| chr16:48592480 | C | T | 1 | a0001c0001t0021g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17295G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592480 | |||||||
| chr16:48592483 | C | G | 1 | a0001c0001t0021g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+17292G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592483 | |||||||
| chr16:48592603 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+17172T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592603 | |||||||
| chr16:48592668 | T | A | 6 | a0001c0001t0003g0210 a0001c0001t0003g0211 a0001c0001t0003g0236 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+17107A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48592668 | |||||||
| chr16:48593150 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.198+16625A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593150 | |||||||
| chr16:48593274 | C | T | 1 | a0002c0003t0002g0277 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.198+16501G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593274 | |||||||
| chr16:48593395 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.198+16380C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593395 | |||||||
| chr16:48593398 | A | G | 1 | a0001c0001t0003g0167 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.198+16377T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593398 | |||||||
| chr16:48593813 | T | C | 2 | a0001c0001t0012g0140 a0001c0001t0012g0141 |
2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.198+15962A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593813 | |||||||
| chr16:48593997 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.198+15778C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48593997 | |||||||
| chr16:48594001 | C | CA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0056 others(31): Show |
38 | HG00621.hp2 HG01175.hp1 HG01516.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+15773dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | |||||||
| chr16:48594001 | C | CAA | 6 | a0001c0001t0001g0069 a0001c0002t0004g0009 a0001c0002t0004g0032 others(3): Show |
7 | HG02055.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+15772_198+1577 others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | |||||||
| chr16:48594001 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0013g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.198+15760_198+1577 others(18): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | |||||||
| chr16:48594001 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0014g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.198+15773_198+1577 others(22): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594001 | |||||||
| chr16:48594018 | AC | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.198+15756delG | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594018 | |||||||
| chr16:48594019 | C | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(63): Show |
87 | HG00140.hp2 HG00639.hp2 HG00741.hp1 others(84): Show |
intron_variant | MODIFIER | c.198+15756G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594019 | |||||||
| chr16:48594104 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+15671G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594104 | |||||||
| chr16:48594124 | C | T | 2 | a0001c0001t0016g0137 a0001c0001t0017g0136 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.198+15651G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594124 | |||||||
| chr16:48594169 | C | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0082 a0001c0001t0001g0084 others(3): Show |
6 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+15606G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594169 | |||||||
| chr16:48594382 | T | A | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+15393A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594382 | |||||||
| chr16:48594544 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+15231G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594544 | |||||||
| chr16:48594575 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.198+15200A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594575 | |||||||
| chr16:48594608 | G | A | 1 | a0001c0001t0002g0245 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+15167C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48594608 | |||||||
| chr16:48595170 | G | A | 1 | a0001c0002t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+14605C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595170 | |||||||
| chr16:48595277 | C | G | 1 | a0001c0001t0006g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198+14498G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595277 | |||||||
| chr16:48595289 | C | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+14486G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595289 | |||||||
| chr16:48595397 | T | C | 3 | a0001c0001t0008g0017 a0001c0001t0008g0115 a0001c0001t0008g0164 |
4 | HG01070.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+14378A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595397 | |||||||
| chr16:48595438 | T | C | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+14337A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595438 | |||||||
| chr16:48595456 | C | CA | 17 | a0001c0001t0002g0022 a0001c0001t0002g0173 a0001c0001t0002g0177 others(14): Show |
19 | HG01106.hp1 HG01256.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+14318dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595456 | C | CAAA | 9 | a0001c0001t0001g0081 a0001c0001t0006g0042 a0001c0001t0006g0043 others(6): Show |
10 | HG01106.hp2 HG01169.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+14316_198+1431 others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595456 | C | CAAAA | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(64): Show |
90 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.198+14315_198+1431 others(8): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595456 | C | CAAAAA | 30 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0046 others(27): Show |
33 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+14314_198+1431 others(9): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595456 | CA | C | 6 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(3): Show |
6 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+14318delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595456 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+14311_198+1431 others(12): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595456 | |||||||
| chr16:48595975 | A | G | 1 | a0001c0001t0002g0241 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.198+13800T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48595975 | |||||||
| chr16:48596023 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+13752G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596023 | |||||||
| chr16:48596329 | C | T | 1 | a0001c0001t0003g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+13446G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596329 | |||||||
| chr16:48596555 | G | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+13220C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596555 | |||||||
| chr16:48596735 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.198+13040A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596735 | |||||||
| chr16:48596789 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.198+12986T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596789 | |||||||
| chr16:48596861 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.198+12914A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596861 | |||||||
| chr16:48596874 | A | T | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+12901T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596874 | |||||||
| chr16:48596883 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
4 | HG02818.hp2 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+12892A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596883 | |||||||
| chr16:48596980 | C | T | 2 | a0001c0001t0005g0232 a0001c0001t0005g0233 |
2 | HG01891.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.198+12795G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48596980 | |||||||
| chr16:48597118 | A | G | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.198+12657T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597118 | |||||||
| chr16:48597242 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.198+12533G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597242 | |||||||
| chr16:48597243 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+12532T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597243 | |||||||
| chr16:48597268 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0245 |
2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.198+12507C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597268 | |||||||
| chr16:48597296 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+12479T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597296 | |||||||
| chr16:48597434 | C | G | 3 | a0002c0003t0002g0276 a0002c0003t0002g0278 a0002c0003t0002g0279 |
3 | NA18939.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.198+12341G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597434 | |||||||
| chr16:48597438 | T | A | 3 | a0002c0003t0002g0276 a0002c0003t0002g0278 a0002c0003t0002g0279 |
3 | NA18939.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.198+12337A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597438 | |||||||
| chr16:48597451 | C | T | 2 | a0001c0001t0002g0178 a0001c0001t0003g0143 |
2 | HG02132.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.198+12324G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48597451 | |||||||
| chr16:48598567 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.198+11208G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598567 | |||||||
| chr16:48598613 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.198+11162T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598613 | |||||||
| chr16:48598637 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.198+11138T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598637 | |||||||
| chr16:48598847 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(121): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.198+10928T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48598847 | |||||||
| chr16:48599194 | C | T | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0003g0248 |
3 | NA18955.hp2 NA19001.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+10581G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599194 | |||||||
| chr16:48599248 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198+10527T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599248 | |||||||
| chr16:48599369 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+10406A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599369 | |||||||
| chr16:48599814 | T | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0004c0006t0001g0055 |
3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+9961A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599814 | |||||||
| chr16:48599858 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.198+9917C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599858 | |||||||
| chr16:48599859 | T | G | 1 | a0001c0001t0010g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+9916A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48599859 | |||||||
| chr16:48600067 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.198+9708T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600067 | |||||||
| chr16:48600156 | G | C | 3 | a0001c0001t0003g0174 a0001c0001t0003g0175 a0001c0001t0003g0176 |
3 | HG01074.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.198+9619C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600156 | |||||||
| chr16:48600163 | A | G | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+9612T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600163 | |||||||
| chr16:48600228 | C | T | 2 | a0001c0001t0016g0137 a0001c0001t0017g0136 |
2 | HG02602.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.198+9547G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600228 | |||||||
| chr16:48600327 | C | T | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9448G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600327 | |||||||
| chr16:48600534 | A | G | 1 | a0001c0001t0003g0224 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.198+9241T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600534 | |||||||
| chr16:48600600 | A | T | 1 | a0001c0001t0003g0223 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.198+9175T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600600 | |||||||
| chr16:48600848 | T | A | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+8927A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600848 | |||||||
| chr16:48600858 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.198+8917C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48600858 | |||||||
| chr16:48601363 | T | A | 1 | a0001c0001t0023g0076 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.198+8412A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601363 | |||||||
| chr16:48601427 | A | G | 1 | a0001c0001t0003g0135 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.198+8348T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601427 | |||||||
| chr16:48601708 | TG | T | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.198+8066delC | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601708 | |||||||
| chr16:48601710 | G | T | 106 | a0001c0001t0001g0254 a0001c0001t0002g0008 a0001c0001t0002g0018 others(103): Show |
116 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.198+8065C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601710 | |||||||
| chr16:48601781 | C | T | 1 | a0001c0007t0001g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.198+7994G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601781 | |||||||
| chr16:48601818 | T | G | 6 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0232 others(3): Show |
8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+7957A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601818 | |||||||
| chr16:48601858 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.198+7917G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48601858 | |||||||
| chr16:48602057 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.198+7718A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602057 | |||||||
| chr16:48602173 | G | A | 1 | a0001c0001t0008g0115 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.198+7602C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602173 | |||||||
| chr16:48602255 | AAC | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+7518_198+7519d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602255 | |||||||
| chr16:48602606 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.198+7169A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602606 | |||||||
| chr16:48602796 | A | AAAAT | 5 | a0001c0001t0003g0111 a0001c0001t0003g0134 a0001c0001t0011g0132 others(2): Show |
6 | HG01074.hp1 HG01255.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+6975_198+6978d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | |||||||
| chr16:48602796 | AAAAT | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
153 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(150): Show |
intron_variant | MODIFIER | c.198+6975_198+6978d others(6): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | |||||||
| chr16:48602796 | AAAATAAA others(1): Show |
A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.198+6971_198+6978d others(10): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48602796 | |||||||
| chr16:48603003 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198+6772G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603003 | |||||||
| chr16:48603004 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198+6771C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603004 | |||||||
| chr16:48603042 | T | A | 1 | a0001c0001t0001g0103 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.198+6733A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603042 | |||||||
| chr16:48603132 | T | C | 1 | a0001c0001t0002g0245 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+6643A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603132 | |||||||
| chr16:48603161 | C | T | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+6614G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603161 | |||||||
| chr16:48603267 | C | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
257 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.198+6508G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603267 | |||||||
| chr16:48603276 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.198+6499C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603276 | |||||||
| chr16:48603462 | C | T | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+6313G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603462 | |||||||
| chr16:48603560 | A | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0004c0006t0001g0055 |
3 | HG03239.hp1 HG03710.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.198+6215T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603560 | |||||||
| chr16:48603767 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.198+6008G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603767 | |||||||
| chr16:48603969 | C | T | 6 | a0001c0001t0007g0048 a0001c0001t0007g0049 a0001c0001t0007g0050 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+5806G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48603969 | |||||||
| chr16:48604015 | A | T | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0003g0248 |
3 | NA18955.hp2 NA19001.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.198+5760T>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604015 | |||||||
| chr16:48604096 | T | G | 2 | a0001c0001t0002g0169 a0001c0001t0003g0168 |
2 | HG00621.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.198+5679A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604096 | |||||||
| chr16:48604257 | T | C | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+5518A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604257 | |||||||
| chr16:48604363 | C | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+5412G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604363 | |||||||
| chr16:48604436 | C | T | 2 | a0001c0001t0011g0132 a0001c0001t0011g0133 |
2 | HG01074.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.198+5339G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604436 | |||||||
| chr16:48604515 | T | G | 1 | a0003c0005t0003g0015 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198+5260A>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604515 | |||||||
| chr16:48604548 | CCAAAGCT others(91): Show |
C | 8 | a0001c0002t0004g0009 a0001c0002t0004g0031 a0001c0002t0004g0032 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+5129_198+5226d others(100): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604548 | |||||||
| chr16:48604582 | C | CA | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+5192dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604582 | |||||||
| chr16:48604586 | A | C | 1 | a0001c0001t0021g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.198+5189T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604586 | |||||||
| chr16:48604591 | A | C | 1 | a0001c0001t0003g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.198+5184T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604591 | |||||||
| chr16:48604602 | T | TA | 14 | a0001c0001t0002g0243 a0001c0001t0006g0039 a0001c0001t0006g0040 others(11): Show |
15 | HG01106.hp2 HG01891.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+5172dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604602 | |||||||
| chr16:48604602 | T | TAA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(95): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.198+5171_198+5172d others(4): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604602 | |||||||
| chr16:48604870 | C | G | 1 | a0001c0001t0002g0170 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.198+4905G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48604870 | |||||||
| chr16:48605193 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+4582A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605193 | |||||||
| chr16:48605251 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0019 others(99): Show |
111 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(108): Show |
intron_variant | MODIFIER | c.198+4524C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605251 | |||||||
| chr16:48605365 | G | A | 15 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(12): Show |
16 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+4410C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605365 | |||||||
| chr16:48605565 | C | T | 1 | a0001c0002t0004g0009 | 2 | HG02486.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+4210G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605565 | |||||||
| chr16:48605593 | A | G | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+4182T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605593 | |||||||
| chr16:48605812 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+3963A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605812 | |||||||
| chr16:48605872 | T | A | 6 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0225 others(3): Show |
6 | HG00280.hp1 HG00738.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+3903A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605872 | |||||||
| chr16:48605956 | A | G | 15 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(12): Show |
16 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+3819T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48605956 | |||||||
| chr16:48606002 | T | C | 2 | a0001c0001t0003g0229 a0001c0001t0003g0230 |
2 | NA18984.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.198+3773A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606002 | |||||||
| chr16:48606011 | T | C | 1 | a0001c0001t0003g0231 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198+3764A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606011 | |||||||
| chr16:48606062 | C | T | 1 | a0001c0002t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198+3713G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606062 | |||||||
| chr16:48606076 | C | T | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+3699G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606076 | |||||||
| chr16:48606114 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+3661G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606114 | |||||||
| chr16:48606175 | G | A | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+3600C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606175 | |||||||
| chr16:48606286 | C | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0104 others(4): Show |
7 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+3489G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606286 | |||||||
| chr16:48606373 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.198+3402G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606373 | |||||||
| chr16:48606535 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198+3240A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606535 | |||||||
| chr16:48606721 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+3054A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606721 | |||||||
| chr16:48606787 | T | C | 6 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0232 others(3): Show |
8 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+2988A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606787 | |||||||
| chr16:48606830 | A | G | 1 | a0001c0001t0003g0130 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.198+2945T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606830 | |||||||
| chr16:48606949 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.198+2826A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48606949 | |||||||
| chr16:48607350 | A | C | 1 | a0001c0001t0002g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.198+2425T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607350 | |||||||
| chr16:48607563 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.198+2212T>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607563 | |||||||
| chr16:48607860 | ATTTGT | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+1910_198+1914d others(7): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607860 | |||||||
| chr16:48607917 | G | A | 2 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.198+1858C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48607917 | |||||||
| chr16:48608027 | A | C | 9 | a0001c0001t0002g0114 a0001c0001t0002g0120 a0001c0001t0002g0121 others(6): Show |
9 | HG01934.hp1 HG02083.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1748T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608027 | |||||||
| chr16:48608170 | G | GT | 4 | a0001c0001t0001g0266 a0001c0001t0001g0268 a0001c0001t0002g0240 others(1): Show |
4 | NA18963.hp2 NA18988.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1604dupA | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608170 | |||||||
| chr16:48608180 | G | T | 13 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(10): Show |
14 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+1595C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608180 | |||||||
| chr16:48608219 | A | C | 1 | a0001c0001t0002g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.198+1556T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608219 | |||||||
| chr16:48608275 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | NA18962.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.198+1500A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608275 | |||||||
| chr16:48608324 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(112): Show |
142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.198+1451A>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608324 | |||||||
| chr16:48608568 | T | A | 1 | a0001c0001t0003g0239 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+1207A>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608568 | |||||||
| chr16:48608659 | G | T | 1 | a0001c0001t0010g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.198+1116C>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608659 | |||||||
| chr16:48608682 | G | C | 3 | a0001c0004t0003g0271 a0001c0004t0003g0272 a0001c0004t0003g0273 |
3 | HG03098.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198+1093C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608682 | |||||||
| chr16:48608688 | G | A | 2 | a0001c0001t0013g0037 a0001c0001t0014g0038 |
2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.198+1087C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608688 | |||||||
| chr16:48608755 | T | TA | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
130 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.198+1019dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608755 | |||||||
| chr16:48608755 | TA | T | 6 | a0001c0001t0002g0114 a0001c0001t0002g0116 a0001c0001t0002g0117 others(3): Show |
6 | HG01255.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1019delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608755 | |||||||
| chr16:48608773 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.198+1002G>C | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608773 | |||||||
| chr16:48608790 | G | A | 2 | a0001c0001t0003g0269 a0001c0001t0003g0270 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+985C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608790 | |||||||
| chr16:48608814 | C | A | 1 | a0001c0001t0002g0245 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.198+961G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608814 | |||||||
| chr16:48608981 | G | A | 5 | a0001c0001t0006g0039 a0001c0001t0006g0040 a0001c0001t0006g0041 others(2): Show |
5 | HG01106.hp2 HG01891.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+794C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48608981 | |||||||
| chr16:48609007 | G | C | 1 | a0001c0001t0024g0110 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+768C>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609007 | |||||||
| chr16:48609017 | C | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(97): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.198+758G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609017 | |||||||
| chr16:48609048 | C | CA | 8 | a0001c0001t0002g0249 a0001c0001t0002g0250 a0001c0001t0002g0253 others(5): Show |
8 | HG02074.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+726dupT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | |||||||
| chr16:48609048 | CA | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0268 a0001c0001t0003g0111 others(4): Show |
8 | HG02615.hp1 HG02896.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+726delT | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | |||||||
| chr16:48609048 | CAA | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(108): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.198+725_198+726del others(2): Show |
N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609048 | |||||||
| chr16:48609366 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.198+409T>G | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609366 | |||||||
| chr16:48609524 | C | A | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(16): Show |
22 | HG00673.hp1 HG01952.hp2 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+251G>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609524 | |||||||
| chr16:48609699 | G | A | 2 | a0001c0001t0003g0269 a0001c0001t0003g0270 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+76C>T | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609699 | |||||||
| chr16:48609751 | C | T | 2 | a0001c0001t0010g0028 a0001c0001t0010g0029 |
2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.198+24G>A | N4BP1 | ENSG00000102921.8 | transcript | ENST00000262384.4 | protein_coding | 1/6 | chr16 | 48609751 |