Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 150472 |
| ensemblid | ENSG00000136682.16 |
| hgncid | 17907 |
| symbol | ZNG1B |
| name | Zn regulated GTPase metalloprotein activator 1B |
| refseq_nuc | NM_172003.3 |
| refseq_prot | NP_742000.1 |
| ensembl_nuc | ENST00000259199.9 |
| ensembl_prot | ENSP00000259199.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 113437691 |
| end | 113496204 |
| strand | + |
| ver | v1.2 |
| region | chr2:113437691-113496204 |
| region5000 | chr2:113432691-113501204 |
| regionname0 | ZNG1B_chr2_113437691_113496204 |
| regionname5000 | ZNG1B_chr2_113432691_113501204 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 395 | 159 | 50 | 34 | 42 | 6 | 25 | 28 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| a0002 | 0/0 | 395 | 94 | 12 | 22 | 48 | 3 | 9 | 29 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| a0003 | 0/0 | 395 | 20 | 20 | 0 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| a0004 | 0/0 | 395 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| a0005 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| a0006 | 0/0 | 395 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | MLPAV others(390): Show |
chr2 | 113432691 | 113501204 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1185 | 154 | 48 | 34 | 42 | 6 | 22 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0001c0004 | 0/0 | 1185 | 5 | 2 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0002c0002 | 0/0 | 1185 | 93 | 12 | 22 | 48 | 3 | 8 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0002c0007 | 0/0 | 1185 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0003c0003 | 0/0 | 1185 | 20 | 20 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0004c0008 | 0/0 | 1185 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0005c0005 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 | ||
| a0006c0006 | 0/0 | 1185 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | ATGTT others(1180): Show |
chr2 | 113432691 | 113501204 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1827 | 150 | 48 | 34 | 41 | 5 | 20 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0001c0001t0004 | 0/0 | 1827 | 3 | 0 | 0 | 0 | 1 | 2 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0001c0001t0008 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0001c0004t0001 | 0/0 | 1827 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0001c0004t0003 | 0/0 | 1828 | 3 | 0 | 0 | 0 | 0 | 3 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1823): Show |
chr2 | 113432691 | 113501204 |
| a0002c0002t0002 | 0/0 | 1827 | 85 | 10 | 21 | 43 | 3 | 8 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0002c0002t0005 | 0/0 | 1826 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1821): Show |
chr2 | 113432691 | 113501204 |
| a0002c0002t0006 | 0/0 | 1826 | 3 | 1 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1821): Show |
chr2 | 113432691 | 113501204 |
| a0002c0002t0007 | 0/0 | 1827 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0002c0002t0009 | 0/0 | 1827 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0002c0007t0002 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0003c0003t0001 | 0/0 | 1827 | 20 | 20 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0004c0008t0001 | 0/0 | 1827 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0005c0005t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| a0006c0006t0002 | 0/0 | 1827 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | AAGGG others(1822): Show |
chr2 | 113432691 | 113501204 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0004 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0001c0004t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0007g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0002t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0002c0007t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0003c0003t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0004c0008t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0005c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| a0006c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00140 | hp1 | a0004 | c0008 | t0001 | g0072 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0198 | EUR | GBR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | FIN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00438 | hp2 | a0005 | c0005 | t0002 | g0002 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0223 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01069 | hp2 | a0002 | c0002 | t0007 | g0019 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0219 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0172 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0017 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0163 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0162 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0186 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0234 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0210 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0213 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0152 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0192 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0229 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0185 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02129 | hp2 | a0002 | c0002 | t0006 | g0205 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0238 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02258 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0216 | AMR | PEL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0239 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02630 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02698 | hp1 | a0001 | c0004 | t0003 | g0224 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0171 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0237 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0009 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0240 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02922 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02965 | hp1 | a0002 | c0002 | t0009 | g0151 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02976 | hp1 | a0003 | c0003 | t0001 | g0235 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0190 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0173 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0024 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0159 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0227 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0232 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0199 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0180 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03516 | hp1 | a0003 | c0003 | t0001 | g0230 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0231 | AFR | ESN | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03540 | hp2 | a0003 | c0003 | t0001 | g0228 | AFR | GWD | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03710 | hp2 | a0001 | c0004 | t0003 | g0226 | SAS | PJL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0209 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0179 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0022 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04184 | hp1 | a0002 | c0007 | t0002 | g0158 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0225 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0208 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | YRI | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18961 | hp2 | a0002 | c0002 | t0005 | g0188 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18964 | hp2 | a0002 | c0002 | t0006 | g0020 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18968 | hp2 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18982 | hp2 | a0006 | c0006 | t0002 | g0177 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19063 | hp2 | a0002 | c0002 | t0005 | g0212 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ASW | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0233 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02559 | hp1 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03471 | hp1 | a0003 | c0003 | t0001 | g0009 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | MSL | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0170 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| NA21309 | hp2 | a0002 | c0002 | t0006 | g0169 | AFR | LWK | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0065 | REF | REF | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | ZNG1B_chr2_113432691_113501204 | ZNG1B | chr2 | 113432691 | 113501204 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113443841 | G | A | 1 | a0005 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.316G>A | p.Gly106Ser | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/15 | 494/1827 | 316/1188 | 106/395 | chr2 | 113443841 | |||
| chr2:113462485 | C | T | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.653C>T | p.Ala218Val | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/15 | 831/1827 | 653/1188 | 218/395 | chr2 | 113462485 | |||
| chr2:113471049 | G | A | 1 | a0003 | 20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
missense_variant | MODERATE | c.724G>A | p.Val242Ile | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/15 | 902/1827 | 724/1188 | 242/395 | chr2 | 113471049 | |||
| chr2:113495715 | A | G | 3 | a0002 a0005 a0006 |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
missense_variant | MODERATE | c.1160A>G | p.His387Arg | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1338/1827 | 1160/1188 | 387/395 | chr2 | 113495715 | |||
| chr2:113495720 | A | C | 2 | a0002 a0005 |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
missense_variant | MODERATE | c.1165A>C | p.Lys389Gln | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1343/1827 | 1165/1188 | 389/395 | chr2 | 113495720 | |||
| chr2:113495724 | A | C | 1 | a0006 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1169A>C | p.Glu390Ala | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 1347/1827 | 1169/1188 | 390/395 | chr2 | 113495724 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113462478 | T | C | 6 | a0001c0004 a0002c0002 a0002c0007 others(3): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
synonymous_variant | LOW | c.646T>C | p.Leu216Leu | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/15 | 824/1827 | 646/1188 | 216/395 | chr2 | 113462478 | |||
| chr2:113465153 | C | T | 1 | a0002c0007 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.687C>T | p.Ile229Ile | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/15 | 865/1827 | 687/1188 | 229/395 | chr2 | 113465153 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113437736 | G | GA | 1 | a0001c0004t0003 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-132dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 131 | INFO_REALIGN_3_PRIME | chr2 | 113437736 | |||||
| chr2:113437766 | A | C | 1 | a0002c0002t0009 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 103 | chr2 | 113437766 | ||||||
| chr2:113437770 | C | G | 1 | a0001c0004t0003 | 3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
5_prime_UTR_variant | MODIFIER | c.-99C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 99 | chr2 | 113437770 | ||||||
| chr2:113437781 | C | T | 1 | a0001c0001t0008 | 1 | NA19002.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-88C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | chr2 | 113437781 | |||||||
| chr2:113437807 | G | A | 1 | a0001c0001t0004 | 3 | HG01515.hp1 HG03710.hp1 HG03831.hp1 |
5_prime_UTR_variant | MODIFIER | c.-62G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/15 | 62 | chr2 | 113437807 | ||||||
| chr2:113495803 | A | G | 1 | a0002c0002t0009 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 60 | chr2 | 113495803 | ||||||
| chr2:113495894 | G | A | 8 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0006 others(5): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 151 | chr2 | 113495894 | ||||||
| chr2:113495970 | G | A | 8 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0006 others(5): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 227 | chr2 | 113495970 | ||||||
| chr2:113496051 | AT | A | 1 | a0002c0002t0005 | 3 | NA18961.hp2 NA18968.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*314delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 314 | INFO_REALIGN_3_PRIME | chr2 | 113496051 | |||||
| chr2:113496058 | C | T | 1 | a0002c0002t0007 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 315 | chr2 | 113496058 | ||||||
| chr2:113496059 | T | C | 1 | a0002c0002t0007 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 316 | chr2 | 113496059 | ||||||
| chr2:113496107 | AT | A | 1 | a0002c0002t0006 | 3 | HG02129.hp2 NA18964.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 15/15 | 371 | INFO_REALIGN_3_PRIME | chr2 | 113496107 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:113438232 | T | C | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+210T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438232 | |||||||
| chr2:113438270 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0027 |
3 | HG01257.hp2 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.154+248T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438270 | |||||||
| chr2:113438348 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+326C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438348 | |||||||
| chr2:113438615 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+593G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438615 | |||||||
| chr2:113438696 | C | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.154+674C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438696 | |||||||
| chr2:113438834 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+812C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438834 | |||||||
| chr2:113438850 | T | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+828T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438850 | |||||||
| chr2:113438876 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.154+854C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113438876 | |||||||
| chr2:113439157 | A | C | 3 | a0003c0003t0001g0238 a0003c0003t0001g0239 a0003c0003t0001g0240 |
3 | HG02145.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.154+1135A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439157 | |||||||
| chr2:113439162 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG02602.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.154+1140T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439162 | |||||||
| chr2:113439236 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.154+1214C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439236 | |||||||
| chr2:113439496 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.154+1474G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439496 | |||||||
| chr2:113439776 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.155-1575T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439776 | |||||||
| chr2:113439874 | A | AT | 90 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(87): Show |
94 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.155-1449dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | ||||||
| chr2:113439874 | A | ATT | 38 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0131 others(35): Show |
43 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.155-1450_155-1449d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | ||||||
| chr2:113439874 | A | ATTT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0148 others(7): Show |
10 | HG00735.hp2 HG01517.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-1451_155-1449d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | ||||||
| chr2:113439874 | AT | A | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(19): Show |
25 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.155-1449delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | ||||||
| chr2:113439874 | ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.155-1458_155-1449d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113439874 | ||||||
| chr2:113439953 | C | T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1398C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439953 | |||||||
| chr2:113439975 | G | C | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.155-1376G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113439975 | |||||||
| chr2:113440082 | C | A | 1 | a0001c0001t0001g0011 | 2 | HG02027.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.155-1269C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440082 | |||||||
| chr2:113440095 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.155-1256G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440095 | |||||||
| chr2:113440136 | G | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.155-1215G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440136 | |||||||
| chr2:113440278 | G | A | 1 | a0002c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.155-1073G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440278 | |||||||
| chr2:113440303 | G | T | 64 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0019 others(61): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.155-1048G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440303 | |||||||
| chr2:113440320 | A | G | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1031A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440320 | |||||||
| chr2:113440348 | C | G | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-1003C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440348 | |||||||
| chr2:113440414 | T | C | 1 | a0001c0004t0003g0224 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.155-937T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440414 | |||||||
| chr2:113440467 | C | G | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.155-884C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440467 | |||||||
| chr2:113440538 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.155-813C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440538 | |||||||
| chr2:113440559 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.155-792G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440559 | |||||||
| chr2:113440615 | G | A | 1 | a0002c0002t0002g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.155-736G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440615 | |||||||
| chr2:113440712 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.155-639C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440712 | |||||||
| chr2:113440893 | G | T | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-458G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113440893 | |||||||
| chr2:113441126 | A | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0145 others(2): Show |
5 | HG00099.hp2 HG00280.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-225A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441126 | |||||||
| chr2:113441142 | G | C | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.155-209G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441142 | |||||||
| chr2:113441153 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.155-198T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441153 | |||||||
| chr2:113441319 | ATTT | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.155-27_155-25delTT others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 113441319 | ||||||
| chr2:113441337 | A | T | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.155-14A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 1/14 | chr2 | 113441337 | |||||||
| chr2:113441942 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241+505G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113441942 | |||||||
| chr2:113441990 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.241+553G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113441990 | |||||||
| chr2:113442014 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.241+577C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442014 | |||||||
| chr2:113442197 | C | T | 1 | a0002c0002t0002g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.241+760C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442197 | |||||||
| chr2:113442265 | AATATT | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.241+830_241+834del others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442265 | ||||||
| chr2:113442349 | G | A | 1 | a0003c0003t0001g0233 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.241+912G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442349 | |||||||
| chr2:113442392 | T | C | 13 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(10): Show |
15 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.241+955T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442392 | |||||||
| chr2:113442421 | T | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.241+984T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442421 | |||||||
| chr2:113442561 | TATC | T | 8 | a0002c0002t0002g0001 a0002c0002t0002g0166 a0002c0002t0002g0174 others(5): Show |
11 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.241+1128_241+1130d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442561 | ||||||
| chr2:113442696 | C | A | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.242-1071C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442696 | |||||||
| chr2:113442709 | G | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.242-1058G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442709 | |||||||
| chr2:113442738 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.242-1029T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113442738 | |||||||
| chr2:113442972 | G | GT | 10 | a0001c0001t0004g0126 a0001c0004t0001g0231 a0001c0004t0001g0232 others(7): Show |
12 | HG01361.hp2 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-781dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 113442972 | ||||||
| chr2:113443015 | C | A | 16 | a0003c0003t0001g0009 a0003c0003t0001g0024 a0003c0003t0001g0025 others(13): Show |
20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.242-752C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443015 | |||||||
| chr2:113443067 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.242-700C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443067 | |||||||
| chr2:113443090 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.242-677G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443090 | |||||||
| chr2:113443211 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.242-556G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443211 | |||||||
| chr2:113443229 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.242-538G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443229 | |||||||
| chr2:113443457 | G | A | 2 | a0002c0002t0002g0182 a0002c0002t0002g0209 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.242-310G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443457 | |||||||
| chr2:113443594 | C | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.242-173C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443594 | |||||||
| chr2:113443641 | A | C | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-126A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 2/14 | chr2 | 113443641 | |||||||
| chr2:113443880 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.338+17C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113443880 | |||||||
| chr2:113444118 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.338+255G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444118 | |||||||
| chr2:113444205 | A | AG | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0131 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.338+342_338+343ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444205 | |||||||
| chr2:113444523 | A | G | 1 | a0002c0002t0002g0178 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.339-441A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444523 | |||||||
| chr2:113444783 | A | G | 1 | a0002c0002t0002g0218 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.339-181A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444783 | |||||||
| chr2:113444799 | T | C | 1 | a0002c0002t0002g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.339-165T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444799 | |||||||
| chr2:113444810 | C | T | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.339-154C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | chr2 | 113444810 | |||||||
| chr2:113444859 | AG | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.339-102delG | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 113444859 | ||||||
| chr2:113445072 | TTAA | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+21_430+23delTA others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445072 | ||||||
| chr2:113445236 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.430+181C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445236 | |||||||
| chr2:113445285 | T | C | 1 | a0002c0002t0002g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.430+230T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445285 | |||||||
| chr2:113445300 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+245T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445300 | |||||||
| chr2:113445349 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430+294A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445349 | |||||||
| chr2:113445373 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.430+318G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445373 | |||||||
| chr2:113445398 | T | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.430+343T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445398 | |||||||
| chr2:113445556 | A | G | 5 | a0002c0002t0002g0214 a0002c0002t0002g0215 a0002c0002t0002g0216 others(2): Show |
5 | HG00735.hp2 HG01099.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+501A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445556 | |||||||
| chr2:113445581 | G | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.430+526G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445581 | |||||||
| chr2:113445596 | G | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+541G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445596 | |||||||
| chr2:113445753 | T | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+698T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445753 | |||||||
| chr2:113445763 | TTCTGTGA others(1): Show |
T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.430+721_430+728del others(8): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445763 | ||||||
| chr2:113445796 | A | AT | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(36): Show |
44 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.430+758dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445796 | ||||||
| chr2:113445796 | AT | A | 67 | a0001c0001t0001g0028 a0002c0002t0002g0001 a0002c0002t0002g0002 others(64): Show |
74 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.430+758delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113445796 | ||||||
| chr2:113445798 | T | TA | 16 | a0003c0003t0001g0009 a0003c0003t0001g0024 a0003c0003t0001g0025 others(13): Show |
20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+743_430+744ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445798 | |||||||
| chr2:113445799 | T | A | 22 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0008 others(19): Show |
25 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+744T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445799 | |||||||
| chr2:113445800 | T | A | 65 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0019 others(62): Show |
72 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.430+745T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445800 | |||||||
| chr2:113445801 | T | A | 16 | a0003c0003t0001g0009 a0003c0003t0001g0024 a0003c0003t0001g0025 others(13): Show |
20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+746T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445801 | |||||||
| chr2:113445802 | T | A | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+747T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445802 | |||||||
| chr2:113445843 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.430+788G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445843 | |||||||
| chr2:113445844 | T | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+789T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445844 | |||||||
| chr2:113445879 | A | G | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0120 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+824A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113445879 | |||||||
| chr2:113446212 | C | T | 1 | a0003c0003t0001g0230 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+1157C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446212 | |||||||
| chr2:113446237 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430+1182T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446237 | |||||||
| chr2:113446241 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430+1186G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446241 | |||||||
| chr2:113446289 | A | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1234A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446289 | |||||||
| chr2:113446585 | G | T | 2 | a0002c0002t0002g0173 a0002c0002t0002g0207 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.430+1530G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446585 | |||||||
| chr2:113446645 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430+1590C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446645 | |||||||
| chr2:113446661 | A | G | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+1606A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446661 | |||||||
| chr2:113446665 | C | G | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+1610C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446665 | |||||||
| chr2:113446743 | T | TAC | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1703_430+1704d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446743 | ||||||
| chr2:113446765 | T | C | 1 | a0002c0002t0002g0220 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.430+1710T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446765 | |||||||
| chr2:113446771 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0002c0002t0002g0220 |
4 | HG01257.hp2 HG01258.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1716C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446771 | |||||||
| chr2:113446772 | GCA | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0074 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.430+1736_430+1737d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | ||||||
| chr2:113446772 | GCACA | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1734_430+1737d others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | ||||||
| chr2:113446772 | GCACACA | G | 84 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(81): Show |
94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.430+1732_430+1737d others(8): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446772 | ||||||
| chr2:113446777 | CACACACA others(13): Show |
C | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1736_430+1755d others(22): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113446777 | ||||||
| chr2:113446778 | A | G | 1 | a0002c0002t0002g0220 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.430+1723A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446778 | |||||||
| chr2:113446838 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+1783A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446838 | |||||||
| chr2:113446860 | A | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+1805A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446860 | |||||||
| chr2:113446958 | C | T | 26 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(23): Show |
27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.430+1903C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113446958 | |||||||
| chr2:113447077 | A | G | 1 | a0002c0002t0002g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.430+2022A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447077 | |||||||
| chr2:113447106 | A | G | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.430+2051A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447106 | |||||||
| chr2:113447154 | G | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0120 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+2099G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447154 | |||||||
| chr2:113447283 | T | TAAAAAAA others(3): Show |
6 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(3): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+2235_430+2244d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(4): Show |
11 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0024 others(8): Show |
13 | HG02486.hp1 HG02559.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+2234_430+2244d others(13): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(5): Show |
2 | a0002c0002t0002g0172 a0003c0003t0001g0234 |
2 | HG01496.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.430+2233_430+2244d others(14): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(6): Show |
60 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0019 others(57): Show |
67 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.430+2232_430+2244d others(15): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(7): Show |
18 | a0002c0002t0002g0008 a0002c0002t0002g0018 a0002c0002t0002g0156 others(15): Show |
21 | HG00544.hp2 HG00609.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+2231_430+2244d others(16): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(8): Show |
6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0002t0002g0152 others(3): Show |
6 | HG01167.hp1 HG01169.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+2230_430+2244d others(17): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(9): Show |
13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.430+2229_430+2244d others(18): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(10): Show |
3 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0141 |
3 | HG02895.hp1 HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.430+2244_430+2245i others(19): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(11): Show |
15 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(12): Show |
16 | HG00639.hp1 HG00642.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(20): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(12): Show |
18 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0090 others(15): Show |
18 | HG00099.hp2 HG01257.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(21): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(13): Show |
5 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0110 others(2): Show |
5 | HG00280.hp2 HG00639.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(22): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(14): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
5 | HG01109.hp1 HG01517.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+2244_430+2245i others(23): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447283 | T | TAAAAAAA others(15): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0130 |
2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.430+2244_430+2245i others(24): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 113447283 | ||||||
| chr2:113447413 | T | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+2358T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447413 | |||||||
| chr2:113447711 | T | C | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+2656T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113447711 | |||||||
| chr2:113448070 | T | C | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3015T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448070 | |||||||
| chr2:113448121 | T | G | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+3066T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448121 | |||||||
| chr2:113448162 | A | G | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+3107A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448162 | |||||||
| chr2:113448239 | C | T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3184C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448239 | |||||||
| chr2:113448356 | C | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3301C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448356 | |||||||
| chr2:113448574 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+3519A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448574 | |||||||
| chr2:113448627 | G | A | 8 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+3572G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448627 | |||||||
| chr2:113448674 | G | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+3619G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448674 | |||||||
| chr2:113448810 | G | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.430+3755G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448810 | |||||||
| chr2:113448845 | T | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.430+3790T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448845 | |||||||
| chr2:113448866 | G | A | 16 | a0003c0003t0001g0009 a0003c0003t0001g0024 a0003c0003t0001g0025 others(13): Show |
20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.430+3811G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448866 | |||||||
| chr2:113448874 | G | T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.430+3819G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113448874 | |||||||
| chr2:113449036 | T | C | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.430+3981T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449036 | |||||||
| chr2:113449129 | C | A | 2 | a0002c0002t0002g0166 a0002c0002t0002g0174 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.431-4010C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449129 | |||||||
| chr2:113449146 | A | G | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-3993A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449146 | |||||||
| chr2:113449351 | G | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-3788G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449351 | |||||||
| chr2:113449381 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-3758C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449381 | |||||||
| chr2:113449547 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-3592A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449547 | |||||||
| chr2:113449565 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-3574T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449565 | |||||||
| chr2:113449582 | C | T | 1 | a0004c0008t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.431-3557C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449582 | |||||||
| chr2:113449829 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-3310T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449829 | |||||||
| chr2:113449938 | G | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-3201G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113449938 | |||||||
| chr2:113450048 | A | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-3091A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450048 | |||||||
| chr2:113450269 | G | A | 117 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(114): Show |
131 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.431-2870G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450269 | |||||||
| chr2:113450351 | C | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.431-2788C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450351 | |||||||
| chr2:113450363 | G | A | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-2776G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450363 | |||||||
| chr2:113450581 | G | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.431-2558G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450581 | |||||||
| chr2:113450686 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-2453G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113450686 | |||||||
| chr2:113451248 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.431-1891G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451248 | |||||||
| chr2:113451255 | G | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-1884G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451255 | |||||||
| chr2:113451575 | T | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.431-1564T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451575 | |||||||
| chr2:113451925 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-1214T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113451925 | |||||||
| chr2:113452068 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0141 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.431-1071G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452068 | |||||||
| chr2:113452406 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0136 |
2 | HG00642.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.431-733C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452406 | |||||||
| chr2:113452443 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.431-696C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452443 | |||||||
| chr2:113452790 | C | A | 166 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.431-349C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 4/14 | chr2 | 113452790 | |||||||
| chr2:113453240 | GT | G | 100 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(97): Show |
114 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.490+53delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453240 | ||||||
| chr2:113453241 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.490+43T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453241 | |||||||
| chr2:113453247 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490+49T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453247 | |||||||
| chr2:113453251 | T | A | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+53T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453251 | |||||||
| chr2:113453344 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.490+146C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453344 | |||||||
| chr2:113453418 | A | T | 51 | a0002c0002t0002g0002 a0002c0002t0002g0019 a0002c0002t0002g0020 others(48): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+220A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453418 | |||||||
| chr2:113453489 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.490+291G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453489 | |||||||
| chr2:113453504 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490+306C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453504 | |||||||
| chr2:113453532 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490+334C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453532 | |||||||
| chr2:113453698 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.490+500T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453698 | |||||||
| chr2:113453754 | T | TA | 89 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 others(86): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.490+566dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453754 | ||||||
| chr2:113453754 | T | TAA | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.490+565_490+566dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 113453754 | ||||||
| chr2:113453843 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.490+645C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453843 | |||||||
| chr2:113453854 | G | T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.490+656G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113453854 | |||||||
| chr2:113454321 | A | G | 1 | a0002c0002t0002g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.491-420A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454321 | |||||||
| chr2:113454331 | T | A | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.491-410T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454331 | |||||||
| chr2:113454455 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.491-286G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454455 | |||||||
| chr2:113454553 | G | A | 18 | a0002c0002t0002g0008 a0002c0002t0002g0018 a0002c0002t0002g0152 others(15): Show |
21 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.491-188G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454553 | |||||||
| chr2:113454573 | T | C | 1 | a0002c0002t0002g0187 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.491-168T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 5/14 | chr2 | 113454573 | |||||||
| chr2:113454882 | A | G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0109 a0001c0001t0001g0110 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.528+104A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113454882 | |||||||
| chr2:113454970 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.528+192C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113454970 | |||||||
| chr2:113455094 | T | C | 1 | a0002c0002t0002g0152 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.528+316T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455094 | |||||||
| chr2:113455180 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(15): Show |
19 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.528+402T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455180 | |||||||
| chr2:113455242 | G | A | 1 | a0002c0002t0002g0156 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.528+464G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455242 | |||||||
| chr2:113455251 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+473T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455251 | |||||||
| chr2:113455291 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.528+513T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455291 | |||||||
| chr2:113455368 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.528+590G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455368 | |||||||
| chr2:113455466 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0137 |
3 | HG02257.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.528+688T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455466 | |||||||
| chr2:113455722 | AT | A | 87 | a0001c0001t0001g0042 a0002c0002t0002g0001 a0002c0002t0002g0002 others(84): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.528+960delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113455722 | ||||||
| chr2:113455852 | C | CTG | 121 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(118): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.528+1074_528+1075i others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455852 | |||||||
| chr2:113455970 | G | A | 2 | a0002c0002t0002g0186 a0002c0002t0009g0151 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.528+1192G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113455970 | |||||||
| chr2:113456140 | C | T | 2 | a0002c0002t0002g0020 a0002c0002t0006g0020 |
2 | NA18944.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.528+1362C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456140 | |||||||
| chr2:113456273 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.528+1495G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456273 | |||||||
| chr2:113456454 | G | GT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(11): Show |
14 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.528+1687dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113456454 | ||||||
| chr2:113456454 | GTT | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+1686_528+1687d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113456454 | ||||||
| chr2:113456748 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.528+1970C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113456748 | |||||||
| chr2:113457299 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.528+2521A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457299 | |||||||
| chr2:113457603 | A | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.528+2825A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457603 | |||||||
| chr2:113457652 | A | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.528+2874A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457652 | |||||||
| chr2:113457715 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.528+2937T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457715 | |||||||
| chr2:113457760 | G | GA | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2913_529-2912i others(3): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457760 | |||||||
| chr2:113457908 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.529-2765G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113457908 | |||||||
| chr2:113458154 | A | T | 3 | a0002c0002t0002g0008 a0002c0002t0002g0162 a0002c0002t0002g0163 |
5 | HG01192.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-2519A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458154 | |||||||
| chr2:113458302 | A | G | 2 | a0002c0002t0002g0180 a0002c0002t0002g0181 |
2 | HG02109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.529-2371A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458302 | |||||||
| chr2:113458351 | A | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2322A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458351 | |||||||
| chr2:113458363 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.529-2310A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458363 | |||||||
| chr2:113458385 | G | C | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.529-2288G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458385 | |||||||
| chr2:113458385 | G | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.529-2288G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458385 | |||||||
| chr2:113458386 | G | A | 1 | a0002c0002t0002g0210 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.529-2287G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458386 | |||||||
| chr2:113458405 | A | C | 2 | a0002c0002t0002g0152 a0002c0002t0002g0155 |
2 | HG01167.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.529-2268A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458405 | |||||||
| chr2:113458576 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-2097A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458576 | |||||||
| chr2:113458728 | C | T | 1 | a0002c0002t0002g0204 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.529-1945C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458728 | |||||||
| chr2:113458932 | C | A | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-1741C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113458932 | |||||||
| chr2:113459099 | A | T | 2 | a0002c0002t0002g0162 a0002c0002t0002g0163 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1574A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459099 | |||||||
| chr2:113459403 | T | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.529-1270T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459403 | |||||||
| chr2:113459542 | TA | T | 19 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(16): Show |
19 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.529-1121delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113459542 | ||||||
| chr2:113459817 | G | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.529-856G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459817 | |||||||
| chr2:113459899 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.529-774G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459899 | |||||||
| chr2:113459903 | GA | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.529-760delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 113459903 | ||||||
| chr2:113459904 | A | G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0109 a0001c0001t0001g0110 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-769A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113459904 | |||||||
| chr2:113460238 | T | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.529-435T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113460238 | |||||||
| chr2:113460489 | T | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.529-184T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 6/14 | chr2 | 113460489 | |||||||
| chr2:113460733 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.575+14A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460733 | |||||||
| chr2:113460734 | A | C | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.575+15A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460734 | |||||||
| chr2:113460768 | A | G | 1 | a0002c0002t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.575+49A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460768 | |||||||
| chr2:113460933 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.575+214G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113460933 | |||||||
| chr2:113461027 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.575+308T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461027 | |||||||
| chr2:113461027 | T | TTA | 84 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0097 others(81): Show |
94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.575+324_575+325dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461027 | ||||||
| chr2:113461027 | T | TTATATAT others(3): Show |
1 | a0001c0004t0001g0231 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.575+316_575+325dup others(10): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461027 | ||||||
| chr2:113461058 | A | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.575+339A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461058 | |||||||
| chr2:113461061 | T | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0044 others(17): Show |
23 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.575+342T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461061 | |||||||
| chr2:113461228 | T | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.575+509T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461228 | |||||||
| chr2:113461228 | T | C | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.575+509T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461228 | |||||||
| chr2:113461229 | T | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.575+510T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461229 | |||||||
| chr2:113461230 | T | A | 96 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 others(93): Show |
108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.575+511T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461230 | |||||||
| chr2:113461263 | G | A | 4 | a0002c0002t0002g0008 a0002c0002t0002g0018 a0002c0002t0002g0162 others(1): Show |
7 | HG01192.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+544G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461263 | |||||||
| chr2:113461328 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.575+609C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461328 | |||||||
| chr2:113461467 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.575+748G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461467 | |||||||
| chr2:113461586 | GA | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.576-818delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 113461586 | ||||||
| chr2:113461607 | T | A | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.576-801T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461607 | |||||||
| chr2:113461839 | T | G | 1 | a0002c0002t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.576-569T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113461839 | |||||||
| chr2:113462086 | T | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.576-322T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462086 | |||||||
| chr2:113462136 | G | A | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.576-272G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462136 | |||||||
| chr2:113462228 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.576-180C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462228 | |||||||
| chr2:113462229 | G | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.576-179G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462229 | |||||||
| chr2:113462359 | C | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.576-49C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 7/14 | chr2 | 113462359 | |||||||
| chr2:113462540 | T | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.662+46T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462540 | |||||||
| chr2:113462782 | A | G | 2 | a0001c0001t0001g0094 a0002c0002t0009g0151 |
2 | HG02965.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.662+288A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462782 | |||||||
| chr2:113462901 | GT | G | 47 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0031 others(44): Show |
50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.662+425delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | ||||||
| chr2:113462901 | GTT | G | 90 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(87): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.662+424_662+425del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | ||||||
| chr2:113462901 | GTTT | G | 11 | a0002c0002t0002g0021 a0002c0002t0002g0191 a0003c0003t0001g0009 others(8): Show |
14 | HG01943.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.662+423_662+425del others(3): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113462901 | ||||||
| chr2:113462919 | T | A | 1 | a0002c0002t0002g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.662+425T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462919 | |||||||
| chr2:113462933 | C | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.662+439C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462933 | |||||||
| chr2:113462954 | C | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.662+460C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113462954 | |||||||
| chr2:113463127 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+633C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463127 | |||||||
| chr2:113463335 | G | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.662+841G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463335 | |||||||
| chr2:113463474 | A | T | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.662+980A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463474 | |||||||
| chr2:113463535 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+1041G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463535 | |||||||
| chr2:113463786 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.662+1292A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113463786 | |||||||
| chr2:113464501 | G | GAAAAGAA others(306): Show |
1 | a0002c0002t0002g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.663-609_663-608ins others(313): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | ||||||
| chr2:113464501 | G | GAAAAGAA others(309): Show |
2 | a0002c0002t0002g0172 a0006c0006t0002g0177 |
2 | HG01496.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.663-609_663-608ins others(316): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | ||||||
| chr2:113464501 | G | GAAAAGAA others(310): Show |
77 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(74): Show |
87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.663-609_663-608ins others(317): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | ||||||
| chr2:113464501 | G | GAAAAGAA others(311): Show |
5 | a0002c0002t0002g0203 a0002c0002t0002g0206 a0002c0002t0006g0169 others(2): Show |
5 | HG02074.hp2 HG02965.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.663-609_663-608ins others(318): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | ||||||
| chr2:113464501 | G | GAAAAGAA others(311): Show |
1 | a0002c0002t0002g0211 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.663-609_663-608ins others(318): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr2 | 113464501 | ||||||
| chr2:113464719 | A | G | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.663-410A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464719 | |||||||
| chr2:113464832 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0149 |
2 | HG01517.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.663-297C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464832 | |||||||
| chr2:113464843 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.663-286C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113464843 | |||||||
| chr2:113465056 | T | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.663-73T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 8/14 | chr2 | 113465056 | |||||||
| chr2:113465249 | T | G | 1 | a0002c0002t0005g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.707+76T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465249 | |||||||
| chr2:113465325 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+152T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465325 | |||||||
| chr2:113465381 | A | T | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+208A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465381 | |||||||
| chr2:113465504 | G | GT | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.707+334dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465504 | ||||||
| chr2:113465744 | A | AT | 75 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(72): Show |
83 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.707+597dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | ||||||
| chr2:113465744 | A | ATT | 17 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0104 others(14): Show |
17 | HG00642.hp1 HG00642.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.707+596_707+597dup others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | ||||||
| chr2:113465744 | AT | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
65 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.707+597delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | ||||||
| chr2:113465744 | ATT | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(6): Show |
9 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+596_707+597del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | ||||||
| chr2:113465744 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0048 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.707+586_707+597del others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113465744 | ||||||
| chr2:113465820 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.707+647C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465820 | |||||||
| chr2:113465899 | C | T | 1 | a0002c0002t0002g0204 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.707+726C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113465899 | |||||||
| chr2:113466050 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.707+877G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466050 | |||||||
| chr2:113466082 | A | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+909A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466082 | |||||||
| chr2:113466103 | A | C | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.707+930A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466103 | |||||||
| chr2:113466327 | G | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.707+1154G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466327 | |||||||
| chr2:113466549 | TTCC | T | 64 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0019 others(61): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.707+1377_707+1379d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466549 | |||||||
| chr2:113466552 | C | T | 43 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(40): Show |
50 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.707+1379C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466552 | |||||||
| chr2:113466636 | T | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+1463T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466636 | |||||||
| chr2:113466793 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.707+1620G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466793 | |||||||
| chr2:113466901 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.707+1728A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466901 | |||||||
| chr2:113466980 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.707+1807C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466980 | |||||||
| chr2:113466981 | G | A | 1 | a0002c0002t0002g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.707+1808G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113466981 | |||||||
| chr2:113467025 | C | T | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.707+1852C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467025 | |||||||
| chr2:113467063 | C | CA | 28 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
30 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.707+1905dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113467063 | ||||||
| chr2:113467063 | C | CAA | 6 | a0001c0001t0001g0128 a0003c0003t0001g0026 a0003c0003t0001g0233 others(3): Show |
6 | HG01175.hp1 HG01891.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.707+1904_707+1905d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113467063 | ||||||
| chr2:113467079 | C | A | 19 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0180 others(16): Show |
23 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.707+1906C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467079 | |||||||
| chr2:113467162 | A | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.707+1989A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467162 | |||||||
| chr2:113467357 | A | T | 1 | a0002c0002t0002g0154 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.707+2184A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467357 | |||||||
| chr2:113467678 | C | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+2505C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467678 | |||||||
| chr2:113467884 | A | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.707+2711A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467884 | |||||||
| chr2:113467911 | C | G | 2 | a0002c0002t0002g0152 a0002c0002t0002g0155 |
2 | HG01167.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.707+2738C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467911 | |||||||
| chr2:113467968 | A | G | 1 | a0002c0002t0002g0223 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.707+2795A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113467968 | |||||||
| chr2:113468121 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0137 |
3 | HG02257.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.708-2912G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468121 | |||||||
| chr2:113468157 | G | A | 1 | a0002c0002t0002g0018 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.708-2876G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468157 | |||||||
| chr2:113468175 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.708-2858T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468175 | |||||||
| chr2:113468201 | T | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-2832T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468201 | |||||||
| chr2:113468238 | G | T | 1 | a0002c0002t0006g0205 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.708-2795G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468238 | |||||||
| chr2:113468455 | A | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0113 a0001c0001t0001g0118 others(2): Show |
5 | HG02559.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.708-2578A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468455 | |||||||
| chr2:113468483 | G | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.708-2550G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468483 | |||||||
| chr2:113468615 | C | CT | 21 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(18): Show |
25 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.708-2406dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113468615 | ||||||
| chr2:113468786 | C | G | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.708-2247C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113468786 | |||||||
| chr2:113469041 | T | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
64 | HG00140.hp1 HG00621.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.708-1992T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469041 | |||||||
| chr2:113469206 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.708-1827C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469206 | |||||||
| chr2:113469269 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.708-1764G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469269 | |||||||
| chr2:113469349 | C | T | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.708-1684C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469349 | |||||||
| chr2:113469458 | A | G | 113 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(110): Show |
127 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.708-1575A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469458 | |||||||
| chr2:113469667 | T | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.708-1366T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469667 | |||||||
| chr2:113469980 | C | T | 1 | a0002c0002t0002g0018 | 2 | HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.708-1053C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113469980 | |||||||
| chr2:113469991 | C | CT | 103 | a0001c0001t0001g0147 a0001c0004t0001g0231 a0001c0004t0001g0232 others(100): Show |
116 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.708-1027dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 113469991 | ||||||
| chr2:113470016 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG02523.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.708-1017C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470016 | |||||||
| chr2:113470107 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.708-926G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470107 | |||||||
| chr2:113470127 | G | C | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0226 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.708-906G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470127 | |||||||
| chr2:113470139 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.708-894G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470139 | |||||||
| chr2:113470273 | C | G | 2 | a0001c0004t0003g0224 a0001c0004t0003g0225 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.708-760C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470273 | |||||||
| chr2:113470515 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.708-518T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470515 | |||||||
| chr2:113470549 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.708-484C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470549 | |||||||
| chr2:113470692 | T | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0200 |
2 | HG00673.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.708-341T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470692 | |||||||
| chr2:113470706 | A | C | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.708-327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470706 | |||||||
| chr2:113470847 | A | G | 1 | a0002c0002t0002g0155 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.708-186A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 9/14 | chr2 | 113470847 | |||||||
| chr2:113471292 | A | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+203A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471292 | |||||||
| chr2:113471327 | G | A | 99 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(96): Show |
109 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.764+238G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471327 | |||||||
| chr2:113471416 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0044 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.764+327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471416 | |||||||
| chr2:113471466 | GT | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+386delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113471466 | ||||||
| chr2:113471480 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+391T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471480 | |||||||
| chr2:113471553 | A | G | 1 | a0002c0002t0002g0153 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.764+464A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471553 | |||||||
| chr2:113471572 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.764+483G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471572 | |||||||
| chr2:113471631 | C | G | 1 | a0002c0002t0006g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.764+542C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471631 | |||||||
| chr2:113471651 | G | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+562G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471651 | |||||||
| chr2:113471761 | T | C | 138 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(135): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.764+672T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471761 | |||||||
| chr2:113471795 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.764+706C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471795 | |||||||
| chr2:113471940 | CAT | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+854_764+855del others(2): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113471940 | ||||||
| chr2:113471955 | G | A | 1 | a0002c0002t0002g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.764+866G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113471955 | |||||||
| chr2:113472036 | G | C | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+947G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472036 | |||||||
| chr2:113472054 | G | A | 2 | a0002c0002t0002g0166 a0002c0002t0002g0174 |
2 | HG00544.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.764+965G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472054 | |||||||
| chr2:113472073 | T | C | 1 | a0002c0002t0002g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.764+984T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472073 | |||||||
| chr2:113472093 | T | C | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+1004T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472093 | |||||||
| chr2:113472096 | G | A | 16 | a0003c0003t0001g0009 a0003c0003t0001g0024 a0003c0003t0001g0025 others(13): Show |
20 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.764+1007G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472096 | |||||||
| chr2:113472176 | C | G | 1 | a0001c0001t0001g0012 | 2 | NA18979.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.764+1087C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472176 | |||||||
| chr2:113472192 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1103A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472192 | |||||||
| chr2:113472304 | G | A | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.764+1215G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472304 | |||||||
| chr2:113472347 | G | A | 1 | a0002c0002t0002g0195 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.764+1258G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472347 | |||||||
| chr2:113472409 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1320C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472409 | |||||||
| chr2:113472424 | A | G | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1335A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472424 | |||||||
| chr2:113472428 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.764+1339T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472428 | |||||||
| chr2:113472445 | C | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+1356C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472445 | |||||||
| chr2:113472445 | C | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.764+1356C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472445 | |||||||
| chr2:113472592 | C | T | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+1503C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472592 | |||||||
| chr2:113472684 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1595G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472684 | |||||||
| chr2:113472801 | T | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1712T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472801 | |||||||
| chr2:113472837 | G | T | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+1748G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472837 | |||||||
| chr2:113472838 | A | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+1749A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472838 | |||||||
| chr2:113472900 | A | T | 2 | a0002c0002t0002g0160 a0002c0002t0002g0164 |
2 | NA18960.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.764+1811A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472900 | |||||||
| chr2:113472987 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+1898A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113472987 | |||||||
| chr2:113473093 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.764+2004C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473093 | |||||||
| chr2:113473190 | G | A | 1 | a0002c0002t0002g0223 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.764+2101G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473190 | |||||||
| chr2:113473325 | T | C | 1 | a0002c0002t0002g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.764+2236T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473325 | |||||||
| chr2:113473389 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.764+2300G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473389 | |||||||
| chr2:113473414 | T | C | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+2325T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473414 | |||||||
| chr2:113473445 | G | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2356G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473445 | |||||||
| chr2:113473466 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2377A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473466 | |||||||
| chr2:113473490 | C | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+2401C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473490 | |||||||
| chr2:113473515 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+2426A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473515 | |||||||
| chr2:113473696 | T | C | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+2607T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473696 | |||||||
| chr2:113473779 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.764+2690T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473779 | |||||||
| chr2:113473781 | G | C | 1 | a0001c0004t0003g0226 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.764+2692G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473781 | |||||||
| chr2:113473821 | G | A | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.764+2732G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473821 | |||||||
| chr2:113473835 | G | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.764+2746G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473835 | |||||||
| chr2:113473858 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.764+2769G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473858 | |||||||
| chr2:113473881 | C | T | 88 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 others(85): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.764+2792C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473881 | |||||||
| chr2:113473899 | C | T | 108 | a0001c0001t0001g0050 a0001c0004t0001g0231 a0001c0004t0001g0232 others(105): Show |
122 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.764+2810C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473899 | |||||||
| chr2:113473917 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.764+2828A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113473917 | |||||||
| chr2:113474034 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764+2945A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474034 | |||||||
| chr2:113474061 | C | G | 2 | a0001c0001t0001g0039 a0002c0002t0002g0172 |
2 | HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+2972C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474061 | |||||||
| chr2:113474263 | G | A | 1 | a0002c0002t0002g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+3174G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474263 | |||||||
| chr2:113474267 | A | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+3178A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474267 | |||||||
| chr2:113474272 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.764+3183C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474272 | |||||||
| chr2:113474356 | C | T | 1 | a0003c0003t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.764+3267C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474356 | |||||||
| chr2:113474359 | C | T | 1 | a0002c0002t0002g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.764+3270C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474359 | |||||||
| chr2:113474403 | G | A | 1 | a0002c0002t0002g0156 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.764+3314G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474403 | |||||||
| chr2:113474474 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.764+3385G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474474 | |||||||
| chr2:113474599 | C | T | 13 | a0002c0002t0002g0023 a0002c0002t0002g0182 a0002c0002t0002g0185 others(10): Show |
14 | HG00738.hp1 HG00741.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.764+3510C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474599 | |||||||
| chr2:113474613 | G | C | 166 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.764+3524G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474613 | |||||||
| chr2:113474647 | T | C | 39 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(36): Show |
40 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.764+3558T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474647 | |||||||
| chr2:113474663 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.764+3574C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474663 | |||||||
| chr2:113474676 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+3587C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474676 | |||||||
| chr2:113474753 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.764+3664A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474753 | |||||||
| chr2:113474765 | G | A | 4 | a0002c0002t0002g0008 a0002c0002t0002g0018 a0002c0002t0002g0162 others(1): Show |
7 | HG01192.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.764+3676G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474765 | |||||||
| chr2:113474909 | G | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.764+3820G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113474909 | |||||||
| chr2:113475118 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.764+4029G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475118 | |||||||
| chr2:113475202 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764+4113G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475202 | |||||||
| chr2:113475234 | C | T | 1 | a0002c0002t0002g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+4145C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475234 | |||||||
| chr2:113475364 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.764+4275A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475364 | |||||||
| chr2:113475371 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.764+4282G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475371 | |||||||
| chr2:113475381 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.764+4292G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475381 | |||||||
| chr2:113475406 | T | C | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+4317T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475406 | |||||||
| chr2:113475412 | C | T | 1 | a0002c0002t0002g0184 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.764+4323C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475412 | |||||||
| chr2:113475445 | T | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4356T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475445 | |||||||
| chr2:113475459 | T | C | 1 | a0002c0002t0002g0194 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.764+4370T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475459 | |||||||
| chr2:113475509 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+4420C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475509 | |||||||
| chr2:113475592 | C | A | 1 | a0002c0002t0002g0179 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.764+4503C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475592 | |||||||
| chr2:113475597 | C | T | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.764+4508C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475597 | |||||||
| chr2:113475618 | T | C | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.764+4529T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475618 | |||||||
| chr2:113475720 | A | G | 1 | a0002c0002t0002g0166 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.764+4631A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475720 | |||||||
| chr2:113475773 | T | A | 3 | a0003c0003t0001g0238 a0003c0003t0001g0239 a0003c0003t0001g0240 |
3 | HG02145.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.764+4684T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475773 | |||||||
| chr2:113475782 | G | A | 1 | a0002c0002t0002g0211 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.764+4693G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475782 | |||||||
| chr2:113475816 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4727C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475816 | |||||||
| chr2:113475861 | T | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+4772T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113475861 | |||||||
| chr2:113476028 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.764+4939C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476028 | |||||||
| chr2:113476278 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.764+5189G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476278 | |||||||
| chr2:113476318 | T | C | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.764+5229T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476318 | |||||||
| chr2:113476448 | G | C | 1 | a0002c0002t0002g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.764+5359G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476448 | |||||||
| chr2:113476490 | C | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0093 |
5 | HG02622.hp2 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.764+5401C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476490 | |||||||
| chr2:113476532 | A | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.764+5443A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476532 | |||||||
| chr2:113476535 | AGCTGCGT others(20): Show |
A | 1 | a0002c0002t0002g0185 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.764+5459_764+5485d others(29): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113476535 | ||||||
| chr2:113476548 | C | T | 120 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(117): Show |
134 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.764+5459C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476548 | |||||||
| chr2:113476552 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.764+5463G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476552 | |||||||
| chr2:113476688 | C | G | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.765-5489C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476688 | |||||||
| chr2:113476688 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.765-5489C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476688 | |||||||
| chr2:113476713 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.765-5464T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476713 | |||||||
| chr2:113476848 | T | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.765-5329T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113476848 | |||||||
| chr2:113477105 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-5072C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477105 | |||||||
| chr2:113477180 | C | T | 1 | a0001c0001t0004g0126 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.765-4997C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477180 | |||||||
| chr2:113477181 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-4996G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477181 | |||||||
| chr2:113477186 | A | AC | 2 | a0001c0001t0001g0010 a0001c0001t0001g0027 |
3 | HG01257.hp2 HG01258.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.765-4988dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113477186 | ||||||
| chr2:113477242 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.765-4935C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477242 | |||||||
| chr2:113477251 | G | A | 1 | a0002c0002t0005g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.765-4926G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477251 | |||||||
| chr2:113477278 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-4899C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477278 | |||||||
| chr2:113477284 | G | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4893G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477284 | |||||||
| chr2:113477327 | C | T | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-4850C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477327 | |||||||
| chr2:113477340 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 |
3 | HG00280.hp1 HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.765-4837G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477340 | |||||||
| chr2:113477363 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4814C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477363 | |||||||
| chr2:113477379 | G | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(12): Show |
16 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.765-4798G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477379 | |||||||
| chr2:113477408 | G | A | 1 | a0002c0007t0002g0158 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.765-4769G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477408 | |||||||
| chr2:113477442 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-4735C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477442 | |||||||
| chr2:113477897 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.765-4280G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477897 | |||||||
| chr2:113477901 | G | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4276G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477901 | |||||||
| chr2:113477911 | G | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4266G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477911 | |||||||
| chr2:113477991 | A | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-4186A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477991 | |||||||
| chr2:113477993 | T | G | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.765-4184T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113477993 | |||||||
| chr2:113478289 | A | AT | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-3881dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478289 | ||||||
| chr2:113478377 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-3800G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478377 | |||||||
| chr2:113478423 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.765-3754G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478423 | |||||||
| chr2:113478644 | G | GT | 102 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 others(99): Show |
116 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.765-3522dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478644 | ||||||
| chr2:113478789 | T | TA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(4): Show |
11 | HG01952.hp2 HG02040.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-3378dupA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113478789 | ||||||
| chr2:113478866 | G | A | 19 | a0001c0001t0001g0114 a0001c0004t0001g0231 a0001c0004t0001g0232 others(16): Show |
23 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.765-3311G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478866 | |||||||
| chr2:113478978 | G | A | 1 | a0002c0002t0002g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.765-3199G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113478978 | |||||||
| chr2:113479036 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.765-3141G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479036 | |||||||
| chr2:113479191 | C | A | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.765-2986C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479191 | |||||||
| chr2:113479344 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.765-2833A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479344 | |||||||
| chr2:113479347 | T | C | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-2830T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479347 | |||||||
| chr2:113479461 | C | T | 26 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(23): Show |
27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.765-2716C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479461 | |||||||
| chr2:113479812 | C | T | 1 | a0001c0004t0001g0231 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.765-2365C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479812 | |||||||
| chr2:113479832 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.765-2345T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479832 | |||||||
| chr2:113479871 | G | C | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-2306G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479871 | |||||||
| chr2:113479930 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-2247T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113479930 | |||||||
| chr2:113480021 | A | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-2156A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480021 | |||||||
| chr2:113480052 | C | T | 1 | a0003c0003t0001g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.765-2125C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480052 | |||||||
| chr2:113480223 | C | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-1954C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480223 | |||||||
| chr2:113480406 | A | C | 10 | a0001c0001t0001g0096 a0003c0003t0001g0024 a0003c0003t0001g0025 others(7): Show |
12 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.765-1771A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480406 | |||||||
| chr2:113480574 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.765-1603C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480574 | |||||||
| chr2:113480915 | A | G | 1 | a0002c0002t0002g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.765-1262A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480915 | |||||||
| chr2:113480948 | C | T | 4 | a0002c0002t0002g0185 a0002c0002t0002g0206 a0002c0002t0002g0222 others(1): Show |
4 | HG02056.hp1 HG02074.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.765-1229C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113480948 | |||||||
| chr2:113481085 | AT | A | 5 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 others(2): Show |
5 | HG01978.hp2 HG02698.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.765-1072delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | ||||||
| chr2:113481085 | ATT | A | 77 | a0001c0001t0001g0096 a0002c0002t0002g0001 a0002c0002t0002g0002 others(74): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.765-1073_765-1072d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | ||||||
| chr2:113481085 | ATTT | A | 26 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0008 others(23): Show |
31 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.765-1074_765-1072d others(5): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481085 | ||||||
| chr2:113481110 | C | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-1067C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481110 | |||||||
| chr2:113481139 | A | G | 2 | a0001c0001t0001g0061 a0001c0001t0001g0067 |
2 | HG01099.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.765-1038A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481139 | |||||||
| chr2:113481181 | T | TC | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.765-995dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 113481181 | ||||||
| chr2:113481299 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.765-878A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481299 | |||||||
| chr2:113481325 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.765-852C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481325 | |||||||
| chr2:113481344 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.765-833C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481344 | |||||||
| chr2:113481353 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.765-824C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481353 | |||||||
| chr2:113481397 | C | T | 91 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0096 others(88): Show |
102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.765-780C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481397 | |||||||
| chr2:113481636 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-541C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481636 | |||||||
| chr2:113481666 | A | G | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(13): Show |
16 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.765-511A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481666 | |||||||
| chr2:113481674 | A | G | 1 | a0003c0003t0001g0233 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.765-503A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481674 | |||||||
| chr2:113481714 | A | G | 1 | a0002c0002t0002g0204 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.765-463A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481714 | |||||||
| chr2:113481757 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-420C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481757 | |||||||
| chr2:113481955 | G | A | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-222G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481955 | |||||||
| chr2:113481976 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.765-201T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113481976 | |||||||
| chr2:113482007 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.765-170C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482007 | |||||||
| chr2:113482035 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.765-142G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482035 | |||||||
| chr2:113482119 | C | T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.765-58C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482119 | |||||||
| chr2:113482147 | A | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.765-30A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 10/14 | chr2 | 113482147 | |||||||
| chr2:113482391 | GTCTAAT | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+168_816+173del others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113482391 | ||||||
| chr2:113482693 | A | C | 1 | a0001c0001t0001g0050 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.816+465A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482693 | |||||||
| chr2:113482763 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.816+535G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482763 | |||||||
| chr2:113482781 | A | G | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+553A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113482781 | |||||||
| chr2:113482944 | C | CT | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+717dupT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113482944 | ||||||
| chr2:113483151 | T | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+923T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483151 | |||||||
| chr2:113483241 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0105 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.816+1013C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483241 | |||||||
| chr2:113483276 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+1048T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483276 | |||||||
| chr2:113483315 | G | A | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+1087G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483315 | |||||||
| chr2:113483510 | C | T | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
6 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+1282C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483510 | |||||||
| chr2:113483565 | A | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+1337A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483565 | |||||||
| chr2:113483735 | A | T | 64 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0019 others(61): Show |
71 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.816+1507A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483735 | |||||||
| chr2:113483747 | T | A | 1 | a0002c0002t0002g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.816+1519T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113483747 | |||||||
| chr2:113484023 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+1795G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484023 | |||||||
| chr2:113484289 | C | A | 1 | a0002c0002t0002g0176 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.816+2061C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484289 | |||||||
| chr2:113484294 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.816+2066A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484294 | |||||||
| chr2:113484619 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.816+2391G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484619 | |||||||
| chr2:113484648 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(15): Show |
19 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+2420G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484648 | |||||||
| chr2:113484663 | G | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.816+2435G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484663 | |||||||
| chr2:113484811 | T | C | 26 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0038 others(23): Show |
27 | HG00639.hp2 HG01884.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.816+2583T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484811 | |||||||
| chr2:113484837 | AT | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0089 others(7): Show |
10 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+2625delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113484837 | ||||||
| chr2:113484954 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.816+2726T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113484954 | |||||||
| chr2:113485174 | C | T | 1 | a0002c0002t0002g0216 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.816+2946C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485174 | |||||||
| chr2:113485193 | C | G | 166 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.816+2965C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485193 | |||||||
| chr2:113485337 | A | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+3109A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485337 | |||||||
| chr2:113485552 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.816+3324G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485552 | |||||||
| chr2:113485571 | G | A | 3 | a0002c0002t0002g0170 a0002c0002t0002g0173 a0002c0002t0002g0207 |
3 | HG02572.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+3343G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485571 | |||||||
| chr2:113485880 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0141 |
2 | HG03239.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.816+3652G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485880 | |||||||
| chr2:113485982 | G | A | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+3754G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113485982 | |||||||
| chr2:113486008 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.816+3780A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486008 | |||||||
| chr2:113486024 | A | C | 4 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(1): Show |
6 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+3796A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486024 | |||||||
| chr2:113486283 | G | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+4055G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486283 | |||||||
| chr2:113486442 | T | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.816+4214T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486442 | |||||||
| chr2:113486505 | A | G | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.816+4277A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486505 | |||||||
| chr2:113486551 | T | A | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0120 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.816+4323T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486551 | |||||||
| chr2:113486746 | A | AC | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+4522dupC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113486746 | ||||||
| chr2:113486805 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+4577G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486805 | |||||||
| chr2:113486813 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.816+4585C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486813 | |||||||
| chr2:113486890 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0113 a0001c0001t0001g0118 others(2): Show |
5 | HG02559.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+4662T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486890 | |||||||
| chr2:113486901 | T | C | 1 | a0002c0002t0002g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.816+4673T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486901 | |||||||
| chr2:113486919 | C | T | 1 | a0002c0002t0002g0222 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.816+4691C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113486919 | |||||||
| chr2:113487001 | AG | A | 121 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0078 others(118): Show |
135 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.816+4774delG | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487001 | |||||||
| chr2:113487217 | G | A | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+4989G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487217 | |||||||
| chr2:113487235 | A | C | 1 | a0003c0003t0001g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+5007A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487235 | |||||||
| chr2:113487238 | A | T | 1 | a0003c0003t0001g0240 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+5010A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487238 | |||||||
| chr2:113487431 | C | A | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.816+5203C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487431 | |||||||
| chr2:113487524 | C | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.816+5296C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487524 | |||||||
| chr2:113487696 | TATATGAC others(3): Show |
T | 9 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 others(6): Show |
11 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.816+5471_816+5480d others(12): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113487696 | ||||||
| chr2:113487716 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.816+5488A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487716 | |||||||
| chr2:113487776 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816+5548C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487776 | |||||||
| chr2:113487791 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.816+5563G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487791 | |||||||
| chr2:113487876 | C | T | 1 | a0002c0002t0002g0189 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.816+5648C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487876 | |||||||
| chr2:113487922 | T | C | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.816+5694T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487922 | |||||||
| chr2:113487932 | G | A | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0080 others(10): Show |
13 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+5704G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487932 | |||||||
| chr2:113487968 | G | A | 2 | a0002c0002t0002g0173 a0002c0002t0002g0207 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.816+5740G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487968 | |||||||
| chr2:113487985 | A | G | 84 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(81): Show |
94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.816+5757A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113487985 | |||||||
| chr2:113488001 | C | T | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.817-5756C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488001 | |||||||
| chr2:113488038 | C | A | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-5719C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488038 | |||||||
| chr2:113488102 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5655A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488102 | |||||||
| chr2:113488183 | T | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-5574T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488183 | |||||||
| chr2:113488208 | C | A | 7 | a0002c0002t0002g0019 a0002c0002t0002g0172 a0002c0002t0002g0187 others(4): Show |
7 | HG00423.hp1 HG01069.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-5549C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488208 | |||||||
| chr2:113488241 | G | A | 8 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-5516G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488241 | |||||||
| chr2:113488303 | C | T | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5454C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488303 | |||||||
| chr2:113488384 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0097 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.817-5373C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488384 | |||||||
| chr2:113488603 | TA | T | 94 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(91): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.817-5141delA | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113488603 | ||||||
| chr2:113488605 | A | T | 11 | a0001c0001t0001g0112 a0002c0002t0002g0194 a0002c0002t0002g0195 others(8): Show |
13 | HG00140.hp2 HG01071.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.817-5152A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488605 | |||||||
| chr2:113488714 | T | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-5043T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488714 | |||||||
| chr2:113488870 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0112 |
2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.817-4887G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488870 | |||||||
| chr2:113488897 | G | A | 9 | a0002c0002t0002g0002 a0002c0002t0002g0176 a0002c0002t0002g0193 others(6): Show |
10 | HG00438.hp2 HG00673.hp1 HG04204.hp1 others(7): Show |
intron_variant | MODIFIER | c.817-4860G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488897 | |||||||
| chr2:113488928 | G | A | 1 | a0002c0002t0006g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-4829G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488928 | |||||||
| chr2:113488933 | T | C | 1 | a0002c0002t0002g0208 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.817-4824T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488933 | |||||||
| chr2:113488993 | G | C | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-4764G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113488993 | |||||||
| chr2:113489139 | C | G | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.817-4618C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489139 | |||||||
| chr2:113489232 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-4525C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489232 | |||||||
| chr2:113489369 | C | T | 8 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG00639.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-4388C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489369 | |||||||
| chr2:113489494 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.817-4263G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489494 | |||||||
| chr2:113489647 | C | T | 1 | a0002c0002t0002g0189 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.817-4110C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489647 | |||||||
| chr2:113489746 | C | A | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-4011C>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489746 | |||||||
| chr2:113489851 | C | T | 1 | a0002c0002t0006g0205 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.817-3906C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113489851 | |||||||
| chr2:113490082 | A | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-3675A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490082 | |||||||
| chr2:113490412 | C | CACAG | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-3342_817-3341i others(6): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113490412 | ||||||
| chr2:113490477 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.817-3280C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490477 | |||||||
| chr2:113490484 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0114 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-3273G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490484 | |||||||
| chr2:113490549 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.817-3208G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490549 | |||||||
| chr2:113490935 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-2822C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113490935 | |||||||
| chr2:113491003 | A | C | 1 | a0002c0002t0002g0171 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.817-2754A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491003 | |||||||
| chr2:113491183 | G | T | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-2574G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491183 | |||||||
| chr2:113491384 | C | T | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.817-2373C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491384 | |||||||
| chr2:113491708 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-2049T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491708 | |||||||
| chr2:113491845 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1912T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491845 | |||||||
| chr2:113491866 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.817-1891G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113491866 | |||||||
| chr2:113492017 | G | A | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-1740G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492017 | |||||||
| chr2:113492052 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-1705A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492052 | |||||||
| chr2:113492072 | CAG | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1684_817-1683d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492072 | |||||||
| chr2:113492110 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1647T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492110 | |||||||
| chr2:113492188 | C | T | 1 | a0002c0002t0006g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-1569C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492188 | |||||||
| chr2:113492211 | C | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1546C>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492211 | |||||||
| chr2:113492232 | G | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1525G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492232 | |||||||
| chr2:113492242 | T | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1515T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492242 | |||||||
| chr2:113492276 | GAT | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1471_817-1470d others(4): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113492276 | ||||||
| chr2:113492287 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-1470A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492287 | |||||||
| chr2:113492301 | A | G | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-1456A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492301 | |||||||
| chr2:113492305 | C | T | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1452C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492305 | |||||||
| chr2:113492331 | T | C | 1 | a0002c0002t0002g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.817-1426T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492331 | |||||||
| chr2:113492338 | C | T | 1 | a0002c0002t0009g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.817-1419C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492338 | |||||||
| chr2:113492541 | G | A | 18 | a0002c0002t0002g0008 a0002c0002t0002g0018 a0002c0002t0002g0152 others(15): Show |
21 | HG00544.hp2 HG01167.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.817-1216G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492541 | |||||||
| chr2:113492604 | A | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-1153A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492604 | |||||||
| chr2:113492629 | A | G | 3 | a0001c0004t0003g0224 a0001c0004t0003g0225 a0001c0004t0003g0226 |
3 | HG02698.hp1 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.817-1128A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492629 | |||||||
| chr2:113492707 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1050A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492707 | |||||||
| chr2:113492708 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.817-1049T>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492708 | |||||||
| chr2:113492879 | G | A | 166 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(163): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.817-878G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113492879 | |||||||
| chr2:113493083 | G | A | 87 | a0001c0001t0001g0049 a0002c0002t0002g0001 a0002c0002t0002g0002 others(84): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.817-674G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493083 | |||||||
| chr2:113493111 | A | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-646A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493111 | |||||||
| chr2:113493154 | C | T | 1 | a0002c0002t0002g0217 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.817-603C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493154 | |||||||
| chr2:113493155 | G | A | 18 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0003c0003t0001g0009 others(15): Show |
22 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-602G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493155 | |||||||
| chr2:113493221 | AT | A | 86 | a0001c0001t0001g0124 a0002c0002t0002g0001 a0002c0002t0002g0002 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-526delT | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 113493221 | ||||||
| chr2:113493241 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-516A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493241 | |||||||
| chr2:113493273 | C | T | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.817-484C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493273 | |||||||
| chr2:113493388 | A | G | 2 | a0001c0004t0001g0231 a0001c0004t0001g0232 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.817-369A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493388 | |||||||
| chr2:113493461 | G | A | 10 | a0001c0001t0001g0118 a0003c0003t0001g0024 a0003c0003t0001g0025 others(7): Show |
12 | HG01891.hp2 HG02486.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.817-296G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493461 | |||||||
| chr2:113493489 | T | C | 84 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(81): Show |
94 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.817-268T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493489 | |||||||
| chr2:113493523 | AC | A | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.817-233delC | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 11/14 | chr2 | 113493523 | |||||||
| chr2:113493835 | A | T | 1 | a0002c0002t0002g0200 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.885+10A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 12/14 | chr2 | 113493835 | |||||||
| chr2:113493848 | A | T | 107 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0003g0224 others(104): Show |
121 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.885+23A>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 12/14 | chr2 | 113493848 | |||||||
| chr2:113494130 | A | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.951+136A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494130 | |||||||
| chr2:113494302 | T | G | 1 | a0002c0002t0006g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.951+308T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494302 | |||||||
| chr2:113494469 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.951+475A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494469 | |||||||
| chr2:113494599 | A | G | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.952-521A>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494599 | |||||||
| chr2:113494603 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-517T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494603 | |||||||
| chr2:113494619 | A | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-501A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494619 | |||||||
| chr2:113494721 | T | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-399T>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494721 | |||||||
| chr2:113494753 | T | G | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.952-367T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494753 | |||||||
| chr2:113494793 | A | C | 7 | a0003c0003t0001g0009 a0003c0003t0001g0228 a0003c0003t0001g0229 others(4): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-327A>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494793 | |||||||
| chr2:113494909 | A | AT | 85 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(82): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.952-211_952-210ins others(1): Show |
ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494909 | |||||||
| chr2:113494991 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.952-129T>G | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113494991 | |||||||
| chr2:113495031 | G | T | 2 | a0002c0002t0002g0185 a0002c0002t0006g0205 |
2 | HG02056.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.952-89G>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 13/14 | chr2 | 113495031 | |||||||
| chr2:113495258 | G | C | 86 | a0002c0002t0002g0001 a0002c0002t0002g0002 a0002c0002t0002g0008 others(83): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1081+9G>C | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495258 | |||||||
| chr2:113495321 | C | T | 104 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0002c0002t0002g0001 others(101): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.1081+72C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495321 | |||||||
| chr2:113495613 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1082-24C>T | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495613 | |||||||
| chr2:113495633 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.1082-4G>A | ZNG1B | ENSG00000136682.16 | transcript | ENST00000259199.9 | protein_coding | 14/14 | chr2 | 113495633 |