Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2631 |
| ensemblid | ENSG00000146729.10 |
| hgncid | 4179 |
| symbol | NIPSNAP2 |
| name | nipsnap homolog 2 |
| refseq_nuc | NM_001483.3 |
| refseq_prot | NP_001474.1 |
| ensembl_nuc | ENST00000322090.8 |
| ensembl_prot | ENSP00000313050.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 55964585 |
| end | 56000179 |
| strand | + |
| ver | v1.2 |
| region | chr7:55964585-56000179 |
| region5000 | chr7:55959585-56005179 |
| regionname0 | NIPSNAP2_chr7_55964585_56000179 |
| regionname5000 | NIPSNAP2_chr7_55959585_56005179 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 286 | 411 | 91 | 72 | 188 | 16 | 42 | 144 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | MAARV others(281): Show |
chr7 | 55959585 | 56005179 |
| a0002 | 0/0 | 286 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | MAARV others(281): Show |
chr7 | 55959585 | 56005179 |
| a0003 | 0/0 | 286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | MAARV others(281): Show |
chr7 | 55959585 | 56005179 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 858 | 411 | 91 | 72 | 188 | 16 | 42 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | ATGGC others(853): Show |
chr7 | 55959585 | 56005179 | ||
| a0002c0002 | 0/0 | 858 | 4 | 2 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | ATGGC others(853): Show |
chr7 | 55959585 | 56005179 | ||
| a0003c0003 | 0/0 | 858 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | ATGGC others(853): Show |
chr7 | 55959585 | 56005179 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1993 | 142 | 33 | 21 | 70 | 3 | 14 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0002 | 0/0 | 1993 | 113 | 24 | 17 | 57 | 8 | 7 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0003 | 0/1 | 1993 | 75 | 8 | 10 | 49 | 0 | 7 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0004 | 0/0 | 1982 | 54 | 6 | 20 | 11 | 5 | 12 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1977): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0005 | 0/0 | 1993 | 17 | 15 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0006 | 0/0 | 1993 | 3 | 2 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0007 | 0/0 | 1993 | 3 | 3 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0008 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0009 | 0/0 | 1993 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0010 | 0/0 | 1993 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0001c0001t0011 | 0/0 | 1993 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0002c0002t0002 | 0/0 | 1993 | 4 | 2 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| a0003c0003t0002 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | GGTGG others(1988): Show |
chr7 | 55959585 | 56005179 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 8 | 1 | 5 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0007 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0003 | 0/0 | 5 | 1 | 1 | 1 | 0 | 2 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0002c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0002c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| a0003c0003t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | GBR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0247 | EUR | GBR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | GBR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0059 | EUR | GBR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0329 | EUR | FIN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | CHS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0272 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0019 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0273 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0001 | AMR | PUR | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0049 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0052 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0311 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0070 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0060 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0235 | EUR | IBS | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0251 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0290 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0078 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0199 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | CDX | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0289 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0139 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0257 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0296 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0307 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0252 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ESN | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0061 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0246 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0076 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0057 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0054 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0064 | SAS | STU | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | CHB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | YRI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ASW | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | TSI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0058 | EUR | TSI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0063 | EUR | TSI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | GIH | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | GIH | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | MSL | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | USA | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | LWK | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0091 | REF | REF | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | NIPSNAP2_chr7_55959585_56005179 | NIPSNAP2 | chr7 | 55959585 | 56005179 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:55964631 | G | A | 1 | a0002 | 4 | HG01081.hp1 HG01978.hp2 HG02451.hp2 others(1): Show |
missense_variant | MODERATE | c.22G>A | p.Ala8Thr | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/10 | 47/1993 | 22/861 | 8/286 | chr7 | 55964631 | |||
| chr7:55982261 | A | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.425A>G | p.Asn142Ser | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/10 | 450/1993 | 425/861 | 142/286 | chr7 | 55982261 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:55999276 | C | T | 1 | a0001c0001t0011 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 204 | chr7 | 55999276 | ||||||
| chr7:55999296 | G | A | 1 | a0001c0001t0008 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*224G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 224 | chr7 | 55999296 | ||||||
| chr7:55999323 | G | T | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*251G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 251 | chr7 | 55999323 | ||||||
| chr7:55999336 | C | A | 1 | a0001c0001t0010 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*264C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 264 | chr7 | 55999336 | ||||||
| chr7:55999357 | C | T | 2 | a0001c0001t0007 a0001c0001t0009 |
4 | HG01243.hp2 HG01891.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 285 | chr7 | 55999357 | ||||||
| chr7:55999431 | A | C | 1 | a0001c0001t0003 | 74 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*359A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 359 | chr7 | 55999431 | ||||||
| chr7:55999523 | TTTTTCTG others(4): Show |
T | 1 | a0001c0001t0004 | 54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*452_*462delTTTTCT others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 452 | chr7 | 55999523 | ||||||
| chr7:55999948 | A | G | 1 | a0001c0001t0005 | 17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*876A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 876 | chr7 | 55999948 | ||||||
| chr7:56000064 | A | G | 1 | a0001c0001t0006 | 3 | HG01109.hp1 HG02622.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 10/10 | 992 | chr7 | 56000064 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:55964731 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0337 |
3 | HG01884.hp1 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.92+30C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55964731 | |||||||
| chr7:55964778 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.92+77G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55964778 | |||||||
| chr7:55964880 | C | T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.92+179C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55964880 | |||||||
| chr7:55965072 | C | T | 4 | a0001c0001t0002g0042 a0001c0001t0002g0306 a0001c0001t0002g0307 others(1): Show |
5 | HG02723.hp1 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+371C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965072 | |||||||
| chr7:55965095 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.92+394G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965095 | |||||||
| chr7:55965134 | T | C | 40 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(37): Show |
50 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.92+433T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965134 | |||||||
| chr7:55965209 | C | G | 131 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(128): Show |
161 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.92+508C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965209 | |||||||
| chr7:55965214 | G | A | 68 | a0001c0001t0002g0026 a0001c0001t0002g0082 a0001c0001t0002g0138 others(65): Show |
78 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.92+513G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965214 | |||||||
| chr7:55965285 | C | T | 1 | a0001c0001t0003g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.92+584C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965285 | |||||||
| chr7:55965286 | T | C | 1 | a0001c0001t0003g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.92+585T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965286 | |||||||
| chr7:55965287 | A | T | 1 | a0001c0001t0003g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.92+586A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965287 | |||||||
| chr7:55965294 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.92+593C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965294 | |||||||
| chr7:55965340 | CT | C | 52 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0002g0263 others(49): Show |
62 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.92+651delT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55965340 | ||||||
| chr7:55965395 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.92+694C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965395 | |||||||
| chr7:55965440 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.92+739C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965440 | |||||||
| chr7:55965448 | A | C | 133 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.92+747A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965448 | |||||||
| chr7:55965470 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0310 |
4 | NA18971.hp1 NA18981.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+769G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965470 | |||||||
| chr7:55965569 | A | G | 1 | a0001c0001t0005g0014 | 3 | HG02615.hp1 HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.92+868A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965569 | |||||||
| chr7:55965572 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.92+871G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965572 | |||||||
| chr7:55965639 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.92+938G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965639 | |||||||
| chr7:55965661 | ACCT | A | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.92+963_92+965delTC others(1): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55965661 | ||||||
| chr7:55965681 | A | G | 1 | a0001c0001t0002g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92+980A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965681 | |||||||
| chr7:55965731 | C | T | 28 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.92+1030C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965731 | |||||||
| chr7:55965819 | G | A | 3 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 |
3 | HG01256.hp1 HG01258.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.92+1118G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965819 | |||||||
| chr7:55965865 | A | G | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.92+1164A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965865 | |||||||
| chr7:55965887 | T | C | 1 | a0001c0001t0004g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.92+1186T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55965887 | |||||||
| chr7:55966044 | A | G | 1 | a0001c0001t0003g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.92+1343A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966044 | |||||||
| chr7:55966175 | A | G | 7 | a0001c0001t0001g0229 a0001c0001t0002g0263 a0001c0001t0002g0264 others(4): Show |
7 | HG03654.hp2 HG04228.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.92+1474A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966175 | |||||||
| chr7:55966198 | C | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.92+1497C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966198 | |||||||
| chr7:55966246 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
6 | HG00621.hp1 NA18942.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+1545A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966246 | |||||||
| chr7:55966292 | G | A | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+1591G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966292 | |||||||
| chr7:55966333 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0147 |
6 | HG00738.hp1 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+1632G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966333 | |||||||
| chr7:55966436 | G | T | 1 | a0001c0001t0002g0336 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.92+1735G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966436 | |||||||
| chr7:55966474 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0305 |
2 | HG02922.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.92+1773A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966474 | |||||||
| chr7:55966642 | C | T | 1 | a0001c0001t0002g0297 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.92+1941C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966642 | |||||||
| chr7:55966654 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.92+1953C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966654 | |||||||
| chr7:55966672 | CTTGGTAG others(4): Show |
C | 1 | a0001c0001t0005g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.92+1972_92+1982del others(11): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966672 | |||||||
| chr7:55966727 | A | T | 1 | a0002c0002t0002g0296 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.92+2026A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966727 | |||||||
| chr7:55966741 | C | T | 1 | a0001c0001t0005g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.92+2040C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966741 | |||||||
| chr7:55966866 | T | C | 133 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.92+2165T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966866 | |||||||
| chr7:55966881 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.92+2180C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55966881 | |||||||
| chr7:55967045 | C | T | 69 | a0001c0001t0002g0026 a0001c0001t0002g0082 a0001c0001t0002g0138 others(66): Show |
79 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.92+2344C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967045 | |||||||
| chr7:55967079 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.92+2378G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967079 | |||||||
| chr7:55967172 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0145 others(13): Show |
22 | HG00438.hp1 NA18942.hp1 NA18944.hp2 others(19): Show |
intron_variant | MODIFIER | c.92+2471T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967172 | |||||||
| chr7:55967288 | C | T | 15 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0282 others(12): Show |
17 | HG01081.hp1 HG01978.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.92+2587C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967288 | |||||||
| chr7:55967297 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.92+2596A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967297 | |||||||
| chr7:55967411 | G | A | 1 | a0001c0001t0004g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.92+2710G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967411 | |||||||
| chr7:55967450 | G | C | 61 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(58): Show |
70 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.92+2749G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967450 | |||||||
| chr7:55967555 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.92+2854C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967555 | |||||||
| chr7:55967559 | C | T | 4 | a0001c0001t0002g0256 a0001c0001t0006g0270 a0001c0001t0006g0271 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+2858C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967559 | |||||||
| chr7:55967615 | C | T | 71 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(68): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.92+2914C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967615 | |||||||
| chr7:55967632 | A | ATTAT | 34 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
41 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.92+2962_92+2965dup others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55967632 | ||||||
| chr7:55967632 | A | ATTATTTA others(1): Show |
74 | a0001c0001t0001g0046 a0001c0001t0001g0161 a0001c0001t0001g0162 others(71): Show |
85 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.92+2958_92+2965dup others(8): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55967632 | ||||||
| chr7:55967632 | A | ATTATTTA others(5): Show |
4 | a0001c0001t0003g0083 a0001c0001t0003g0084 a0001c0001t0003g0085 others(1): Show |
4 | HG00639.hp2 HG03017.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.92+2954_92+2965dup others(12): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55967632 | ||||||
| chr7:55967632 | ATTAT | A | 82 | a0001c0001t0001g0222 a0001c0001t0002g0007 a0001c0001t0002g0015 others(79): Show |
102 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.92+2962_92+2965del others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55967632 | ||||||
| chr7:55967657 | T | G | 9 | a0001c0001t0002g0039 a0001c0001t0002g0282 a0001c0001t0002g0283 others(6): Show |
10 | HG02056.hp2 HG02717.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.92+2956T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967657 | |||||||
| chr7:55967706 | T | C | 3 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0272 |
3 | HG01109.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.92+3005T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967706 | |||||||
| chr7:55967846 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.92+3145C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967846 | |||||||
| chr7:55967989 | A | G | 96 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(93): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.92+3288A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55967989 | |||||||
| chr7:55968096 | C | T | 1 | a0001c0001t0004g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.92+3395C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968096 | |||||||
| chr7:55968111 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92+3410C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968111 | |||||||
| chr7:55968331 | G | A | 133 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.92+3630G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968331 | |||||||
| chr7:55968350 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.92+3649C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968350 | |||||||
| chr7:55968384 | C | CT | 6 | a0001c0001t0002g0334 a0001c0001t0002g0335 a0001c0001t0003g0128 others(3): Show |
6 | HG01175.hp1 HG02738.hp2 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.92+3699dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55968384 | ||||||
| chr7:55968384 | CTTT | C | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.92+3697_92+3699del others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55968384 | ||||||
| chr7:55968445 | G | A | 1 | a0001c0001t0002g0318 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.92+3744G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968445 | |||||||
| chr7:55968617 | C | T | 3 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 |
3 | HG00099.hp2 HG00735.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.92+3916C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968617 | |||||||
| chr7:55968620 | C | T | 3 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0272 |
3 | HG01109.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.92+3919C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968620 | |||||||
| chr7:55968621 | G | A | 40 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(37): Show |
50 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.92+3920G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968621 | |||||||
| chr7:55968913 | G | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(63): Show |
82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.92+4212G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55968913 | |||||||
| chr7:55969001 | C | G | 1 | a0001c0001t0002g0333 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.92+4300C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969001 | |||||||
| chr7:55969057 | G | A | 1 | a0001c0001t0004g0055 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92+4356G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969057 | |||||||
| chr7:55969057 | GA | G | 39 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(36): Show |
49 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.92+4363delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55969057 | ||||||
| chr7:55969058 | A | G | 1 | a0001c0001t0004g0055 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.92+4357A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969058 | |||||||
| chr7:55969180 | G | A | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.92+4479G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969180 | |||||||
| chr7:55969290 | G | T | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.92+4589G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969290 | |||||||
| chr7:55969365 | G | GTGC | 58 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(55): Show |
70 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.92+4667_92+4669dup others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55969365 | ||||||
| chr7:55969736 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.92+5035A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969736 | |||||||
| chr7:55969754 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | NA18972.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.92+5053T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969754 | |||||||
| chr7:55969790 | T | A | 1 | a0001c0001t0003g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.92+5089T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969790 | |||||||
| chr7:55969810 | T | C | 2 | a0001c0001t0002g0319 a0001c0001t0004g0056 |
2 | HG03834.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.92+5109T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969810 | |||||||
| chr7:55969821 | A | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.92+5120A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969821 | |||||||
| chr7:55969839 | C | T | 5 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0136 others(2): Show |
5 | HG01123.hp2 HG02257.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+5138C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969839 | |||||||
| chr7:55969856 | G | A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0312 a0001c0001t0002g0313 others(3): Show |
7 | HG02155.hp1 NA18968.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+5155G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969856 | |||||||
| chr7:55969860 | G | A | 6 | a0001c0001t0002g0043 a0001c0001t0002g0312 a0001c0001t0002g0313 others(3): Show |
7 | HG02155.hp1 NA18968.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.92+5159G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969860 | |||||||
| chr7:55969862 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0215 others(7): Show |
12 | HG01981.hp1 HG02015.hp1 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.92+5161A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969862 | |||||||
| chr7:55969863 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.92+5162G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969863 | |||||||
| chr7:55969902 | G | A | 13 | a0001c0001t0005g0014 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.92+5201G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969902 | |||||||
| chr7:55969918 | A | G | 13 | a0001c0001t0005g0014 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.92+5217A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969918 | |||||||
| chr7:55969980 | C | G | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+5279C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55969980 | |||||||
| chr7:55969982 | C | CA | 45 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0147 others(42): Show |
51 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.92+5301dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55969982 | ||||||
| chr7:55969982 | CA | C | 6 | a0001c0001t0001g0212 a0001c0001t0004g0079 a0001c0001t0004g0080 others(3): Show |
6 | HG01070.hp1 HG01891.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+5301delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55969982 | ||||||
| chr7:55970051 | C | T | 1 | a0001c0001t0004g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.92+5350C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970051 | |||||||
| chr7:55970055 | G | A | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.92+5354G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970055 | |||||||
| chr7:55970194 | T | C | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.92+5493T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970194 | |||||||
| chr7:55970252 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.92+5551G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970252 | |||||||
| chr7:55970258 | T | C | 74 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(71): Show |
90 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.92+5557T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970258 | |||||||
| chr7:55970309 | A | AT | 18 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0026 others(15): Show |
19 | HG00597.hp1 HG00597.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.92+5625dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55970309 | ||||||
| chr7:55970331 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92+5630C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970331 | |||||||
| chr7:55970472 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | NA18998.hp1 NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.92+5771C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970472 | |||||||
| chr7:55970564 | G | A | 45 | a0001c0001t0003g0093 a0001c0001t0004g0003 a0001c0001t0004g0008 others(42): Show |
55 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.92+5863G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970564 | |||||||
| chr7:55970672 | C | G | 2 | a0001c0001t0003g0125 a0001c0001t0003g0128 |
2 | HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.92+5971C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970672 | |||||||
| chr7:55970674 | C | G | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.92+5973C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970674 | |||||||
| chr7:55970680 | G | A | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.92+5979G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970680 | |||||||
| chr7:55970723 | C | G | 27 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.92+6022C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970723 | |||||||
| chr7:55970741 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0147 others(3): Show |
9 | HG00323.hp2 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.92+6040T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970741 | |||||||
| chr7:55970761 | C | T | 24 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.92+6060C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970761 | |||||||
| chr7:55970801 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.92+6100C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55970801 | |||||||
| chr7:55971096 | A | C | 2 | a0001c0001t0005g0277 a0001c0001t0005g0278 |
2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.92+6395A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971096 | |||||||
| chr7:55971101 | G | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.92+6400G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971101 | |||||||
| chr7:55971157 | A | C | 69 | a0001c0001t0002g0026 a0001c0001t0002g0082 a0001c0001t0002g0138 others(66): Show |
79 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.92+6456A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971157 | |||||||
| chr7:55971212 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.92+6511T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971212 | |||||||
| chr7:55971506 | C | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0306 a0001c0001t0002g0307 others(3): Show |
7 | HG01928.hp2 HG02004.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.93-6620C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971506 | |||||||
| chr7:55971596 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0138 |
3 | HG02257.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.93-6530A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971596 | |||||||
| chr7:55971915 | T | C | 1 | a0001c0001t0002g0324 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.93-6211T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971915 | |||||||
| chr7:55971919 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.93-6207T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971919 | |||||||
| chr7:55971954 | A | G | 2 | a0001c0001t0004g0049 a0001c0001t0004g0050 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.93-6172A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971954 | |||||||
| chr7:55971975 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.93-6151A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55971975 | |||||||
| chr7:55972288 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.93-5838A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972288 | |||||||
| chr7:55972302 | C | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-5824C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972302 | |||||||
| chr7:55972308 | C | CA | 94 | a0001c0001t0001g0178 a0001c0001t0002g0013 a0001c0001t0002g0026 others(91): Show |
106 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.93-5806dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55972308 | ||||||
| chr7:55972343 | C | A | 1 | a0001c0001t0004g0077 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.93-5783C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972343 | |||||||
| chr7:55972434 | C | CT | 22 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0002g0007 others(19): Show |
26 | HG00544.hp2 HG01358.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.93-5677dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55972434 | ||||||
| chr7:55972457 | A | T | 1 | a0001c0001t0002g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93-5669A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972457 | |||||||
| chr7:55972535 | C | T | 6 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG04228.hp1 NA18944.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-5591C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972535 | |||||||
| chr7:55972620 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.93-5506C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972620 | |||||||
| chr7:55972645 | T | A | 1 | a0001c0001t0003g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.93-5481T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55972645 | |||||||
| chr7:55973108 | A | AG | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-5017dupG | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55973108 | ||||||
| chr7:55973339 | T | C | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-4787T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55973339 | |||||||
| chr7:55973508 | CT | C | 6 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG04228.hp1 NA18944.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-4617delT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55973508 | |||||||
| chr7:55973538 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.93-4588C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55973538 | |||||||
| chr7:55973640 | A | AT | 12 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0002g0247 others(9): Show |
12 | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.93-4471dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55973640 | ||||||
| chr7:55973780 | C | T | 6 | a0001c0001t0003g0025 a0001c0001t0003g0117 a0001c0001t0003g0118 others(3): Show |
7 | HG00423.hp2 HG02132.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.93-4346C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55973780 | |||||||
| chr7:55974022 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.93-4104C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974022 | |||||||
| chr7:55974258 | CAA | C | 30 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0042 others(27): Show |
37 | HG01243.hp1 HG01433.hp2 HG02056.hp2 others(34): Show |
intron_variant | MODIFIER | c.93-3860_93-3859del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974258 | ||||||
| chr7:55974264 | AAAAG | A | 63 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(60): Show |
71 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.93-3842_93-3839del others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974264 | ||||||
| chr7:55974266 | AAG | A | 99 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(96): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.93-3858_93-3857del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974266 | ||||||
| chr7:55974267 | AGAAAG | A | 31 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(28): Show |
34 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.93-3858_93-3854del others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974267 | |||||||
| chr7:55974269 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-3857A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974269 | |||||||
| chr7:55974272 | G | A | 65 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(62): Show |
74 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.93-3854G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974272 | |||||||
| chr7:55974572 | G | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0323 a0001c0001t0002g0331 |
4 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.93-3554G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974572 | |||||||
| chr7:55974704 | C | T | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.93-3422C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974704 | |||||||
| chr7:55974717 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0299 |
3 | NA18939.hp1 NA18940.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.93-3409G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974717 | |||||||
| chr7:55974802 | C | A | 1 | a0001c0001t0003g0083 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.93-3324C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974802 | |||||||
| chr7:55974847 | T | TA | 121 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0002g0013 others(118): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.93-3259dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974847 | ||||||
| chr7:55974847 | T | TAA | 13 | a0001c0001t0002g0047 a0001c0001t0002g0138 a0001c0001t0003g0094 others(10): Show |
13 | HG00609.hp2 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.93-3260_93-3259dup others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974847 | ||||||
| chr7:55974847 | TA | T | 8 | a0001c0001t0001g0145 a0001c0001t0001g0153 a0001c0001t0001g0158 others(5): Show |
8 | HG01074.hp1 HG02896.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-3259delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55974847 | ||||||
| chr7:55974863 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-3263A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974863 | |||||||
| chr7:55974864 | A | AG | 59 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(56): Show |
75 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.93-3262_93-3261ins others(1): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974864 | |||||||
| chr7:55974864 | A | G | 3 | a0001c0001t0002g0329 a0001c0001t0002g0330 a0001c0001t0002g0335 |
3 | HG00323.hp1 HG02135.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.93-3262A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974864 | |||||||
| chr7:55974912 | C | T | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.93-3214C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55974912 | |||||||
| chr7:55975095 | G | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.93-3031G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975095 | |||||||
| chr7:55975192 | A | C | 1 | a0001c0001t0002g0286 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.93-2934A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975192 | |||||||
| chr7:55975214 | A | G | 1 | a0001c0001t0003g0254 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.93-2912A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975214 | |||||||
| chr7:55975217 | G | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.93-2909G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975217 | |||||||
| chr7:55975344 | G | C | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.93-2782G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975344 | |||||||
| chr7:55975558 | G | A | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.93-2568G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975558 | |||||||
| chr7:55975592 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93-2534G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975592 | |||||||
| chr7:55975691 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.93-2435A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975691 | |||||||
| chr7:55975781 | T | C | 32 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0042 others(29): Show |
39 | HG01081.hp1 HG01243.hp1 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.93-2345T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975781 | |||||||
| chr7:55975805 | A | C | 1 | a0001c0001t0003g0112 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.93-2321A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975805 | |||||||
| chr7:55975913 | T | C | 96 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(93): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.93-2213T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975913 | |||||||
| chr7:55975942 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.93-2184C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975942 | |||||||
| chr7:55975952 | G | T | 1 | a0001c0001t0004g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.93-2174G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55975952 | |||||||
| chr7:55976039 | AGT | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(116): Show |
156 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.93-2056_93-2055del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976039 | ||||||
| chr7:55976039 | AGTGT | A | 61 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(58): Show |
68 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.93-2058_93-2055del others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976039 | ||||||
| chr7:55976039 | AGTGTGT | A | 12 | a0001c0001t0001g0211 a0001c0001t0002g0047 a0001c0001t0002g0230 others(9): Show |
12 | HG00099.hp2 HG00735.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.93-2060_93-2055del others(6): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976039 | ||||||
| chr7:55976039 | AGTGTGTG others(1): Show |
A | 46 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(43): Show |
60 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.93-2062_93-2055del others(8): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976039 | ||||||
| chr7:55976039 | AGTGTGTG others(3): Show |
A | 85 | a0001c0001t0001g0305 a0001c0001t0002g0039 a0001c0001t0002g0040 others(82): Show |
101 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.93-2064_93-2055del others(10): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976039 | ||||||
| chr7:55976127 | C | G | 71 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(68): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.93-1999C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976127 | |||||||
| chr7:55976182 | CTG | C | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.93-1942_93-1941del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976182 | ||||||
| chr7:55976256 | T | C | 5 | a0001c0001t0002g0237 a0001c0001t0002g0247 a0001c0001t0002g0248 others(2): Show |
5 | HG00099.hp2 HG00735.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-1870T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976256 | |||||||
| chr7:55976285 | C | T | 16 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0256 others(13): Show |
20 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.93-1841C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976285 | |||||||
| chr7:55976324 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0003g0137 |
2 | HG01123.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.93-1802C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976324 | |||||||
| chr7:55976457 | G | A | 1 | a0001c0001t0005g0277 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.93-1669G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976457 | |||||||
| chr7:55976481 | T | G | 1 | a0001c0001t0004g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.93-1645T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976481 | |||||||
| chr7:55976697 | G | A | 1 | a0001c0001t0002g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93-1429G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976697 | |||||||
| chr7:55976743 | C | T | 2 | a0001c0001t0004g0259 a0001c0001t0004g0262 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.93-1383C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976743 | |||||||
| chr7:55976756 | C | T | 96 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(93): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.93-1370C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976756 | |||||||
| chr7:55976782 | G | A | 1 | a0001c0001t0002g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.93-1344G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976782 | |||||||
| chr7:55976811 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.93-1315C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55976811 | |||||||
| chr7:55976906 | G | GA | 3 | a0001c0001t0002g0026 a0001c0001t0002g0138 a0003c0003t0002g0139 |
4 | HG02257.hp1 HG02572.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-1214dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55976906 | ||||||
| chr7:55977014 | A | G | 24 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.93-1112A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977014 | |||||||
| chr7:55977029 | T | C | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.93-1097T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977029 | |||||||
| chr7:55977098 | AT | A | 229 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0013 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.93-1018delT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 55977098 | ||||||
| chr7:55977140 | T | C | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-986T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977140 | |||||||
| chr7:55977193 | C | T | 71 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(68): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.93-933C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977193 | |||||||
| chr7:55977399 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.93-727T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977399 | |||||||
| chr7:55977453 | G | A | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.93-673G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977453 | |||||||
| chr7:55977663 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.93-463A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977663 | |||||||
| chr7:55977730 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.93-396C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977730 | |||||||
| chr7:55977734 | T | C | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.93-392T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977734 | |||||||
| chr7:55977755 | T | C | 230 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0013 others(227): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.93-371T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55977755 | |||||||
| chr7:55978003 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.93-123G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55978003 | |||||||
| chr7:55978028 | G | A | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.93-98G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55978028 | |||||||
| chr7:55978075 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.93-51T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 1/9 | chr7 | 55978075 | |||||||
| chr7:55978441 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.278+46T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55978441 | |||||||
| chr7:55978691 | C | T | 6 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG04228.hp1 NA18944.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.278+296C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55978691 | |||||||
| chr7:55978728 | A | G | 66 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(63): Show |
82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.278+333A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55978728 | |||||||
| chr7:55978893 | G | C | 1 | a0001c0001t0003g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.278+498G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55978893 | |||||||
| chr7:55978901 | TC | T | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.278+508delC | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 55978901 | ||||||
| chr7:55979048 | T | A | 133 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.278+653T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979048 | |||||||
| chr7:55979214 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.278+819G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979214 | |||||||
| chr7:55979345 | C | T | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.278+950C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979345 | |||||||
| chr7:55979522 | T | C | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.278+1127T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979522 | |||||||
| chr7:55979645 | A | C | 1 | a0001c0001t0001g0204 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.278+1250A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979645 | |||||||
| chr7:55979674 | A | G | 2 | a0001c0001t0003g0130 a0001c0001t0003g0133 |
2 | NA18943.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.278+1279A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979674 | |||||||
| chr7:55979831 | G | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.278+1436G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979831 | |||||||
| chr7:55979836 | A | G | 1 | a0001c0001t0004g0079 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.278+1441A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979836 | |||||||
| chr7:55979879 | C | T | 94 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0082 others(91): Show |
105 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.278+1484C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979879 | |||||||
| chr7:55979919 | G | A | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.278+1524G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55979919 | |||||||
| chr7:55980119 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.279-1354C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980119 | |||||||
| chr7:55980139 | C | T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.279-1334C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980139 | |||||||
| chr7:55980183 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.279-1290T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980183 | |||||||
| chr7:55980207 | A | C | 1 | a0001c0001t0002g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.279-1266A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980207 | |||||||
| chr7:55980258 | G | A | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.279-1215G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980258 | |||||||
| chr7:55980719 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.279-754G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980719 | |||||||
| chr7:55980757 | A | G | 1 | a0001c0001t0011g0246 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.279-716A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980757 | |||||||
| chr7:55980781 | C | T | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.279-692C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980781 | |||||||
| chr7:55980796 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.279-677C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980796 | |||||||
| chr7:55980913 | G | A | 1 | a0001c0001t0003g0117 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.279-560G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55980913 | |||||||
| chr7:55980988 | T | TA | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.279-484dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 55980988 | ||||||
| chr7:55981044 | C | T | 9 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0298 others(6): Show |
13 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.279-429C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55981044 | |||||||
| chr7:55981293 | G | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
5 | HG02280.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.279-180G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55981293 | |||||||
| chr7:55981326 | A | G | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.279-147A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55981326 | |||||||
| chr7:55981424 | T | C | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.279-49T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 3/9 | chr7 | 55981424 | |||||||
| chr7:55981655 | T | C | 1 | a0001c0001t0004g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.373+88T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55981655 | |||||||
| chr7:55981720 | C | T | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.373+153C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55981720 | |||||||
| chr7:55981746 | A | G | 2 | a0001c0001t0004g0259 a0001c0001t0004g0262 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.373+179A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55981746 | |||||||
| chr7:55981852 | C | G | 1 | a0001c0001t0002g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.373+285C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55981852 | |||||||
| chr7:55981861 | A | C | 4 | a0001c0001t0002g0042 a0001c0001t0002g0306 a0001c0001t0002g0307 others(1): Show |
5 | HG02723.hp1 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.373+294A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55981861 | |||||||
| chr7:55982027 | G | A | 24 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.374-183G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55982027 | |||||||
| chr7:55982120 | G | A | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.374-90G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55982120 | |||||||
| chr7:55982164 | T | C | 1 | a0001c0001t0004g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.374-46T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 4/9 | chr7 | 55982164 | |||||||
| chr7:55982297 | A | G | 27 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+17A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982297 | |||||||
| chr7:55982477 | G | A | 27 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.444+197G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982477 | |||||||
| chr7:55982516 | A | G | 1 | a0001c0001t0002g0297 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.444+236A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982516 | |||||||
| chr7:55982592 | A | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.444+312A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982592 | |||||||
| chr7:55982613 | T | A | 1 | a0001c0001t0003g0116 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.444+333T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982613 | |||||||
| chr7:55982676 | C | T | 10 | a0001c0001t0001g0175 a0001c0001t0002g0007 a0001c0001t0002g0041 others(7): Show |
14 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.444+396C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982676 | |||||||
| chr7:55982677 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.444+397G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982677 | |||||||
| chr7:55982691 | G | T | 1 | a0001c0001t0003g0136 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.444+411G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982691 | |||||||
| chr7:55982708 | C | T | 5 | a0001c0001t0005g0014 a0001c0001t0005g0038 a0001c0001t0005g0275 others(2): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+428C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982708 | |||||||
| chr7:55982751 | CA | C | 67 | a0001c0001t0001g0212 a0001c0001t0001g0219 a0001c0001t0002g0007 others(64): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.444+487delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 55982751 | ||||||
| chr7:55982832 | C | T | 227 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(224): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.444+552C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982832 | |||||||
| chr7:55982979 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.444+699C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55982979 | |||||||
| chr7:55983135 | C | CA | 20 | a0001c0001t0001g0171 a0001c0001t0001g0175 a0001c0001t0001g0219 others(17): Show |
24 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.445-585dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 55983135 | ||||||
| chr7:55983136 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.445-592A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983136 | |||||||
| chr7:55983222 | T | G | 1 | a0001c0001t0007g0251 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.445-506T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983222 | |||||||
| chr7:55983406 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.445-322G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983406 | |||||||
| chr7:55983421 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0166 |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.445-307C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983421 | |||||||
| chr7:55983510 | C | T | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0055 others(1): Show |
6 | NA18957.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-218C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983510 | |||||||
| chr7:55983656 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.445-72C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983656 | |||||||
| chr7:55983712 | T | C | 5 | a0001c0001t0005g0014 a0001c0001t0005g0038 a0001c0001t0005g0275 others(2): Show |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-16T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 5/9 | chr7 | 55983712 | |||||||
| chr7:55983979 | T | TTATATGT others(3): Show |
229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.585+121_585+130dup others(10): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55983979 | ||||||
| chr7:55984016 | TCA | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0138 |
3 | HG02257.hp1 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.585+152_585+153del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55984016 | ||||||
| chr7:55984121 | CCT | C | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.585+254_585+255del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984121 | |||||||
| chr7:55984359 | T | G | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.586-488T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984359 | |||||||
| chr7:55984390 | A | G | 32 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0042 others(29): Show |
39 | HG01081.hp1 HG01243.hp1 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.586-457A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984390 | |||||||
| chr7:55984421 | AAAAGT | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.586-420_586-416del others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55984421 | ||||||
| chr7:55984425 | G | C | 66 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(63): Show |
82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.586-422G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984425 | |||||||
| chr7:55984450 | C | G | 2 | a0001c0001t0005g0274 a0001c0001t0005g0281 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.586-397C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984450 | |||||||
| chr7:55984584 | T | A | 1 | a0001c0001t0002g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.586-263T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984584 | |||||||
| chr7:55984594 | C | G | 1 | a0001c0001t0004g0074 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.586-253C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984594 | |||||||
| chr7:55984641 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.586-206C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984641 | |||||||
| chr7:55984717 | C | CA | 6 | a0001c0001t0001g0178 a0001c0001t0001g0227 a0001c0001t0002g0232 others(3): Show |
6 | HG00642.hp1 HG01891.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-112dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55984717 | ||||||
| chr7:55984717 | CA | C | 121 | a0001c0001t0001g0157 a0001c0001t0001g0305 a0001c0001t0002g0007 others(118): Show |
142 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.586-112delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55984717 | ||||||
| chr7:55984717 | CAA | C | 45 | a0001c0001t0002g0269 a0001c0001t0003g0144 a0001c0001t0004g0003 others(42): Show |
55 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.586-113_586-112del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 55984717 | ||||||
| chr7:55984772 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.586-75T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984772 | |||||||
| chr7:55984784 | T | G | 1 | a0001c0001t0002g0287 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.586-63T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 6/9 | chr7 | 55984784 | |||||||
| chr7:55984986 | A | G | 1 | a0001c0001t0002g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.617+108A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55984986 | |||||||
| chr7:55985090 | A | G | 1 | a0001c0001t0002g0313 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.617+212A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985090 | |||||||
| chr7:55985203 | A | G | 4 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0126 others(1): Show |
4 | HG00597.hp2 NA18979.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+325A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985203 | |||||||
| chr7:55985279 | A | G | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.617+401A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985279 | |||||||
| chr7:55985285 | T | G | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.617+407T>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985285 | |||||||
| chr7:55985310 | A | G | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.617+432A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985310 | |||||||
| chr7:55985390 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0172 a0001c0001t0001g0212 |
4 | NA18954.hp1 NA18961.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+512T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985390 | |||||||
| chr7:55985425 | C | T | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.617+547C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985425 | |||||||
| chr7:55985583 | A | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.617+705A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985583 | |||||||
| chr7:55985636 | A | G | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.617+758A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985636 | |||||||
| chr7:55985642 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG03710.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.617+764G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985642 | |||||||
| chr7:55985686 | C | T | 2 | a0001c0001t0003g0110 a0001c0001t0003g0121 |
2 | HG02080.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.617+808C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985686 | |||||||
| chr7:55985729 | G | C | 1 | a0001c0001t0002g0294 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.617+851G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985729 | |||||||
| chr7:55985745 | C | CA | 9 | a0001c0001t0001g0227 a0001c0001t0002g0256 a0001c0001t0002g0263 others(6): Show |
9 | HG01109.hp1 HG01433.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+887dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55985745 | ||||||
| chr7:55985745 | CA | C | 95 | a0001c0001t0001g0146 a0001c0001t0002g0013 a0001c0001t0002g0026 others(92): Show |
107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.617+887delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55985745 | ||||||
| chr7:55985845 | C | T | 1 | a0001c0001t0002g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.617+967C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985845 | |||||||
| chr7:55985905 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0318 a0001c0001t0002g0324 others(2): Show |
6 | HG00099.hp1 HG00323.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+1027G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55985905 | |||||||
| chr7:55986031 | G | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0268 |
2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.617+1153G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986031 | |||||||
| chr7:55986095 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+1217T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986095 | |||||||
| chr7:55986187 | C | T | 13 | a0001c0001t0005g0014 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+1309C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986187 | |||||||
| chr7:55986340 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0151 a0001c0001t0001g0157 others(1): Show |
7 | NA18942.hp1 NA18947.hp2 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+1462G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986340 | |||||||
| chr7:55986469 | C | A | 1 | a0001c0001t0002g0282 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.617+1591C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986469 | |||||||
| chr7:55986539 | G | C | 1 | a0001c0001t0002g0318 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.617+1661G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986539 | |||||||
| chr7:55986720 | C | CA | 71 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(68): Show |
87 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.617+1844dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55986720 | ||||||
| chr7:55986883 | A | T | 61 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(58): Show |
70 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.617+2005A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986883 | |||||||
| chr7:55986922 | GGAT | G | 6 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG04228.hp1 NA18944.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.617+2045_617+2047d others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986922 | |||||||
| chr7:55986982 | A | AT | 45 | a0001c0001t0002g0282 a0001c0001t0004g0003 a0001c0001t0004g0008 others(42): Show |
55 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.617+2105dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55986982 | ||||||
| chr7:55986983 | T | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.617+2105T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986983 | |||||||
| chr7:55986983 | T | TA | 78 | a0001c0001t0001g0046 a0001c0001t0001g0147 a0001c0001t0001g0161 others(75): Show |
88 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.617+2132dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55986983 | ||||||
| chr7:55986983 | T | TAA | 18 | a0001c0001t0001g0167 a0001c0001t0002g0082 a0001c0001t0002g0232 others(15): Show |
19 | HG00423.hp2 HG00597.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.617+2131_617+2132d others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55986983 | ||||||
| chr7:55986983 | T | TTA | 3 | a0001c0001t0004g0057 a0001c0001t0004g0076 a0002c0002t0002g0290 |
3 | HG01978.hp2 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.617+2105_617+2106i others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986983 | |||||||
| chr7:55986983 | T | TTAAA | 30 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(27): Show |
39 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.617+2105_617+2106i others(6): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986983 | |||||||
| chr7:55986983 | T | TTAAAA | 3 | a0001c0001t0002g0314 a0001c0001t0002g0320 a0001c0001t0002g0334 |
3 | HG02071.hp2 NA19000.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.617+2105_617+2106i others(7): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986983 | |||||||
| chr7:55986983 | TAAAAAAA | T | 13 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0264 others(10): Show |
17 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+2126_617+2132d others(9): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55986983 | ||||||
| chr7:55986984 | A | T | 33 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0042 others(30): Show |
40 | HG01109.hp1 HG01243.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.617+2106A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986984 | |||||||
| chr7:55986990 | A | T | 1 | a0001c0001t0002g0300 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.617+2112A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986990 | |||||||
| chr7:55986991 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.617+2113A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986991 | |||||||
| chr7:55986991 | A | T | 13 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0264 others(10): Show |
17 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.617+2113A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986991 | |||||||
| chr7:55986992 | A | T | 1 | a0001c0001t0002g0263 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.617+2114A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986992 | |||||||
| chr7:55986998 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.617+2120A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986998 | |||||||
| chr7:55986999 | A | C | 1 | a0001c0001t0002g0039 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.617+2121A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55986999 | |||||||
| chr7:55987004 | A | AC | 4 | a0001c0001t0001g0149 a0001c0001t0001g0154 a0001c0001t0001g0158 others(1): Show |
4 | HG00438.hp1 NA19012.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+2126_617+2127i others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987004 | |||||||
| chr7:55987004 | A | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(23): Show |
35 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.617+2126A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987004 | |||||||
| chr7:55987006 | A | C | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.617+2128A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987006 | |||||||
| chr7:55987021 | G | A | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.617+2143G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987021 | |||||||
| chr7:55987056 | A | G | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.617+2178A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987056 | |||||||
| chr7:55987177 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+2299G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987177 | |||||||
| chr7:55987297 | A | G | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.617+2419A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987297 | |||||||
| chr7:55987300 | A | G | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+2422A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987300 | |||||||
| chr7:55987320 | A | G | 1 | a0001c0001t0002g0039 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.617+2442A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987320 | |||||||
| chr7:55987352 | G | A | 1 | a0001c0001t0002g0325 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.617+2474G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987352 | |||||||
| chr7:55987552 | C | T | 1 | a0001c0001t0004g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.617+2674C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987552 | |||||||
| chr7:55987593 | C | A | 325 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(322): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.617+2715C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987593 | |||||||
| chr7:55987634 | C | T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.617+2756C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987634 | |||||||
| chr7:55987766 | G | A | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.617+2888G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987766 | |||||||
| chr7:55987798 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+2920C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987798 | |||||||
| chr7:55987886 | A | G | 1 | a0001c0001t0004g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.617+3008A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55987886 | |||||||
| chr7:55988016 | C | G | 1 | a0001c0001t0004g0063 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.617+3138C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988016 | |||||||
| chr7:55988051 | C | A | 1 | a0001c0001t0003g0096 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.617+3173C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988051 | |||||||
| chr7:55988170 | G | A | 24 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.617+3292G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988170 | |||||||
| chr7:55988266 | T | A | 1 | a0001c0001t0004g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.617+3388T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988266 | |||||||
| chr7:55988452 | A | C | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.617+3574A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988452 | |||||||
| chr7:55988492 | T | C | 9 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0298 others(6): Show |
13 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.617+3614T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988492 | |||||||
| chr7:55988632 | G | A | 1 | a0001c0001t0008g0199 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.617+3754G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988632 | |||||||
| chr7:55988633 | C | T | 1 | a0001c0001t0001g0004 | 5 | HG02615.hp2 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+3755C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988633 | |||||||
| chr7:55988659 | G | A | 1 | a0003c0003t0002g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.617+3781G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988659 | |||||||
| chr7:55988665 | C | T | 66 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(63): Show |
82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.617+3787C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988665 | |||||||
| chr7:55988715 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.617+3837C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988715 | |||||||
| chr7:55988788 | C | T | 23 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0084 others(20): Show |
28 | HG00609.hp2 HG01099.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.617+3910C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988788 | |||||||
| chr7:55988878 | A | G | 230 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0013 others(227): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.617+4000A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55988878 | |||||||
| chr7:55989049 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.617+4171C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989049 | |||||||
| chr7:55989281 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0166 |
3 | HG02055.hp1 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.617+4403C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989281 | |||||||
| chr7:55989383 | G | A | 3 | a0001c0001t0003g0097 a0001c0001t0003g0113 a0001c0001t0003g0141 |
3 | NA18612.hp2 NA19068.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.617+4505G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989383 | |||||||
| chr7:55989387 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.617+4509G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989387 | |||||||
| chr7:55989479 | C | A | 1 | a0001c0001t0001g0004 | 5 | HG02615.hp2 HG02886.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+4601C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989479 | |||||||
| chr7:55989639 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.617+4761A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989639 | |||||||
| chr7:55989926 | G | A | 1 | a0001c0001t0007g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.618-4968G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989926 | |||||||
| chr7:55989942 | T | C | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-4952T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55989942 | |||||||
| chr7:55989950 | C | CA | 18 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(15): Show |
18 | HG01109.hp2 HG01261.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.618-4926dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55989950 | ||||||
| chr7:55989950 | CA | C | 108 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(105): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.618-4926delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55989950 | ||||||
| chr7:55990062 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-4832G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990062 | |||||||
| chr7:55990118 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.618-4776A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990118 | |||||||
| chr7:55990149 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | NA18998.hp1 NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.618-4745A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990149 | |||||||
| chr7:55990200 | A | G | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.618-4694A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990200 | |||||||
| chr7:55990231 | C | CT | 28 | a0001c0001t0001g0178 a0001c0001t0002g0013 a0001c0001t0002g0047 others(25): Show |
31 | HG00642.hp1 HG01175.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.618-4648dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55990231 | ||||||
| chr7:55990231 | C | CTT | 6 | a0001c0001t0002g0237 a0001c0001t0002g0243 a0001c0001t0002g0247 others(3): Show |
6 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-4649_618-4648d others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55990231 | ||||||
| chr7:55990247 | G | A | 96 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(93): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.618-4647G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990247 | |||||||
| chr7:55990298 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0229 |
2 | HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.618-4596G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990298 | |||||||
| chr7:55990307 | C | A | 1 | a0001c0001t0004g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.618-4587C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990307 | |||||||
| chr7:55990319 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.618-4575C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990319 | |||||||
| chr7:55990390 | G | A | 1 | a0001c0001t0004g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.618-4504G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990390 | |||||||
| chr7:55990490 | C | T | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.618-4404C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990490 | |||||||
| chr7:55990500 | G | T | 1 | a0001c0001t0005g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.618-4394G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990500 | |||||||
| chr7:55990507 | A | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0138 a0003c0003t0002g0139 |
4 | HG02257.hp1 HG02572.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-4387A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990507 | |||||||
| chr7:55990615 | A | G | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-4279A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990615 | |||||||
| chr7:55990661 | G | A | 61 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(58): Show |
70 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.618-4233G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990661 | |||||||
| chr7:55990791 | CT | C | 19 | a0001c0001t0001g0171 a0001c0001t0002g0007 a0001c0001t0002g0026 others(16): Show |
24 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.618-4089delT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55990791 | ||||||
| chr7:55990995 | T | C | 1 | a0001c0001t0002g0326 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.618-3899T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55990995 | |||||||
| chr7:55991110 | G | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.618-3784G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991110 | |||||||
| chr7:55991190 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.618-3704T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991190 | |||||||
| chr7:55991273 | A | G | 69 | a0001c0001t0002g0026 a0001c0001t0002g0082 a0001c0001t0002g0138 others(66): Show |
79 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.618-3621A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991273 | |||||||
| chr7:55991354 | C | T | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.618-3540C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991354 | |||||||
| chr7:55991405 | C | T | 1 | a0001c0001t0005g0037 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.618-3489C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991405 | |||||||
| chr7:55991410 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.618-3484G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991410 | |||||||
| chr7:55991489 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.618-3405G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991489 | |||||||
| chr7:55991537 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.618-3357A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991537 | |||||||
| chr7:55991606 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.618-3288A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991606 | |||||||
| chr7:55991721 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.618-3173G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991721 | |||||||
| chr7:55991748 | CA | C | 31 | a0001c0001t0001g0156 a0001c0001t0001g0163 a0001c0001t0001g0189 others(28): Show |
35 | HG01081.hp1 HG01243.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.618-3128delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55991748 | ||||||
| chr7:55991757 | A | T | 1 | a0001c0001t0003g0126 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.618-3137A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991757 | |||||||
| chr7:55991759 | A | AAT | 14 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0088 others(11): Show |
19 | HG00609.hp2 HG01099.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-3134_618-3133i others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55991759 | ||||||
| chr7:55991759 | A | AATAT | 27 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 others(24): Show |
30 | HG00423.hp2 HG00673.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.618-3134_618-3133i others(6): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55991759 | ||||||
| chr7:55991759 | A | T | 14 | a0001c0001t0002g0026 a0001c0001t0002g0138 a0001c0001t0003g0089 others(11): Show |
15 | HG00597.hp2 HG01123.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.618-3135A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991759 | |||||||
| chr7:55991761 | A | AATAT | 6 | a0001c0001t0003g0022 a0001c0001t0003g0084 a0001c0001t0003g0096 others(3): Show |
7 | HG03704.hp2 HG04199.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.618-3132_618-3131i others(6): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55991761 | ||||||
| chr7:55991761 | A | AT | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.618-3133_618-3132i others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991761 | |||||||
| chr7:55991761 | A | ATAT | 8 | a0001c0001t0004g0052 a0001c0001t0004g0053 a0001c0001t0004g0059 others(5): Show |
8 | HG00140.hp2 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.618-3133_618-3132i others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991761 | |||||||
| chr7:55991761 | A | ATATATAT others(8): Show |
1 | a0001c0001t0010g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.618-3133_618-3132i others(17): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991761 | |||||||
| chr7:55991761 | A | T | 71 | a0001c0001t0001g0165 a0001c0001t0002g0026 a0001c0001t0002g0082 others(68): Show |
83 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.618-3133A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991761 | |||||||
| chr7:55991763 | A | AATATATA others(7): Show |
2 | a0001c0001t0002g0264 a0001c0001t0002g0268 |
2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.618-3130_618-3129i others(16): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55991763 | ||||||
| chr7:55991763 | A | AT | 6 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0001c0001t0002g0324 others(3): Show |
6 | HG01106.hp1 HG01109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-3131_618-3130i others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991763 | |||||||
| chr7:55991763 | A | ATAT | 23 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0019 others(20): Show |
32 | HG00639.hp1 HG00738.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.618-3131_618-3130i others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991763 | |||||||
| chr7:55991763 | A | ATATATAT others(2): Show |
6 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0298 others(3): Show |
10 | HG00544.hp2 HG01981.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-3131_618-3130i others(11): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991763 | |||||||
| chr7:55991763 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0304 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.618-3131_618-3130i others(15): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991763 | |||||||
| chr7:55991763 | A | T | 116 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0165 others(113): Show |
133 | HG00140.hp2 HG00423.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.618-3131A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991763 | |||||||
| chr7:55991765 | A | AT | 7 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0305 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-3129_618-3128i others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991765 | |||||||
| chr7:55991765 | A | ATAT | 4 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0050 others(1): Show |
5 | HG00408.hp2 HG01070.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3129_618-3128i others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991765 | |||||||
| chr7:55991765 | A | ATATATAT others(6): Show |
4 | a0001c0001t0002g0263 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | HG04228.hp1 NA18944.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-3129_618-3128i others(15): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991765 | |||||||
| chr7:55991765 | A | T | 221 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0031 others(218): Show |
266 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.618-3129A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991765 | |||||||
| chr7:55991767 | T | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0172 a0001c0001t0001g0207 others(1): Show |
5 | HG03710.hp2 NA18954.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-3127T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991767 | |||||||
| chr7:55991808 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.618-3086A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991808 | |||||||
| chr7:55991840 | G | A | 1 | a0001c0001t0002g0265 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.618-3054G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991840 | |||||||
| chr7:55991898 | G | C | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.618-2996G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991898 | |||||||
| chr7:55991944 | A | C | 3 | a0001c0001t0006g0270 a0001c0001t0006g0271 a0001c0001t0006g0272 |
3 | HG01109.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.618-2950A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55991944 | |||||||
| chr7:55992043 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.618-2851A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992043 | |||||||
| chr7:55992091 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.618-2803A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992091 | |||||||
| chr7:55992408 | C | T | 40 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(37): Show |
50 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.618-2486C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992408 | |||||||
| chr7:55992433 | TCAG | T | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-2459_618-2457d others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55992433 | ||||||
| chr7:55992672 | A | G | 1 | a0001c0001t0004g0064 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.618-2222A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992672 | |||||||
| chr7:55992862 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0280 a0001c0001t0005g0295 |
4 | HG02280.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.618-2032C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992862 | |||||||
| chr7:55992976 | T | A | 1 | a0001c0001t0006g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.618-1918T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55992976 | |||||||
| chr7:55993059 | G | A | 3 | a0001c0001t0004g0051 a0001c0001t0004g0058 a0001c0001t0004g0063 |
3 | HG03669.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.618-1835G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993059 | |||||||
| chr7:55993095 | T | TC | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.618-1798dupC | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55993095 | ||||||
| chr7:55993255 | C | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.618-1639C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993255 | |||||||
| chr7:55993293 | T | TA | 5 | a0001c0001t0002g0042 a0001c0001t0002g0306 a0001c0001t0002g0307 others(2): Show |
6 | HG02723.hp1 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.618-1589dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55993293 | ||||||
| chr7:55993375 | C | T | 2 | a0001c0001t0004g0019 a0001c0001t0004g0067 |
3 | HG00738.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.618-1519C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993375 | |||||||
| chr7:55993380 | C | A | 1 | a0001c0001t0004g0081 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.618-1514C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993380 | |||||||
| chr7:55993408 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.618-1486T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993408 | |||||||
| chr7:55993448 | G | A | 1 | a0001c0001t0003g0101 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.618-1446G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993448 | |||||||
| chr7:55993575 | TA | T | 210 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(207): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.618-1301delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55993575 | ||||||
| chr7:55993699 | C | T | 13 | a0001c0001t0005g0014 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.618-1195C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55993699 | |||||||
| chr7:55993927 | G | GA | 15 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0263 others(12): Show |
19 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.618-954dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55993927 | ||||||
| chr7:55993927 | GA | G | 61 | a0001c0001t0002g0286 a0001c0001t0003g0002 a0001c0001t0003g0022 others(58): Show |
70 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.618-954delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55993927 | ||||||
| chr7:55994126 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0003g0106 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.618-768G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994126 | |||||||
| chr7:55994142 | G | T | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.618-752G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994142 | |||||||
| chr7:55994153 | C | A | 5 | a0001c0001t0002g0256 a0001c0001t0002g0269 a0001c0001t0006g0270 others(2): Show |
5 | HG01109.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.618-741C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994153 | |||||||
| chr7:55994442 | G | A | 66 | a0001c0001t0002g0082 a0001c0001t0003g0002 a0001c0001t0003g0022 others(63): Show |
75 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.618-452G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994442 | |||||||
| chr7:55994516 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.618-378A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994516 | |||||||
| chr7:55994596 | C | A | 27 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.618-298C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994596 | |||||||
| chr7:55994649 | G | A | 4 | a0001c0001t0004g0020 a0001c0001t0004g0021 a0001c0001t0004g0055 others(1): Show |
6 | NA18957.hp1 NA18959.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-245G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994649 | |||||||
| chr7:55994739 | CTT | C | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.618-152_618-151del others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 55994739 | ||||||
| chr7:55994869 | A | C | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.618-25A>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 7/9 | chr7 | 55994869 | |||||||
| chr7:55995104 | C | T | 1 | a0001c0001t0007g0253 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.712+116C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995104 | |||||||
| chr7:55995125 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.712+137G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995125 | |||||||
| chr7:55995142 | C | T | 1 | a0001c0001t0003g0107 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.712+154C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995142 | |||||||
| chr7:55995222 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.712+234G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995222 | |||||||
| chr7:55995244 | GA | G | 133 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0016 others(130): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.712+258delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 55995244 | ||||||
| chr7:55995322 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.712+334C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995322 | |||||||
| chr7:55995323 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0211 a0001c0001t0001g0216 others(4): Show |
8 | HG03139.hp1 NA18966.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+335G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995323 | |||||||
| chr7:55995503 | C | A | 2 | a0001c0001t0002g0082 a0001c0001t0003g0106 |
2 | HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.712+515C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995503 | |||||||
| chr7:55995508 | G | C | 230 | a0001c0001t0001g0305 a0001c0001t0002g0007 a0001c0001t0002g0013 others(227): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.712+520G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995508 | |||||||
| chr7:55995517 | A | G | 2 | a0001c0001t0003g0109 a0001c0001t0003g0114 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.712+529A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995517 | |||||||
| chr7:55995529 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0241 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.712+541C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995529 | |||||||
| chr7:55995572 | C | G | 2 | a0001c0001t0004g0066 a0001c0001t0004g0068 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.712+584C>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995572 | |||||||
| chr7:55995607 | G | C | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.712+619G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995607 | |||||||
| chr7:55995684 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0168 |
6 | HG02615.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.712+696C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995684 | |||||||
| chr7:55995813 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.712+825G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995813 | |||||||
| chr7:55995847 | G | A | 13 | a0001c0001t0005g0014 a0001c0001t0005g0037 a0001c0001t0005g0038 others(10): Show |
17 | HG01243.hp1 HG01433.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.712+859G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995847 | |||||||
| chr7:55995921 | T | C | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.712+933T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995921 | |||||||
| chr7:55995947 | C | A | 4 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0127 others(1): Show |
4 | NA18939.hp2 NA18961.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+959C>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995947 | |||||||
| chr7:55995948 | A | G | 4 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0127 others(1): Show |
4 | NA18939.hp2 NA18961.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.712+960A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55995948 | |||||||
| chr7:55996085 | A | G | 3 | a0001c0001t0002g0327 a0001c0001t0002g0330 a0001c0001t0002g0336 |
3 | HG02135.hp1 NA18988.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.712+1097A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996085 | |||||||
| chr7:55996235 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.713-1131G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996235 | |||||||
| chr7:55996243 | ACCACTGC others(4): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.713-1121_713-1111d others(13): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 55996243 | ||||||
| chr7:55996285 | C | CA | 71 | a0001c0001t0002g0026 a0001c0001t0002g0082 a0001c0001t0002g0138 others(68): Show |
81 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.713-1065dupA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 55996285 | ||||||
| chr7:55996285 | C | CAA | 23 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(20): Show |
25 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.713-1066_713-1065d others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 55996285 | ||||||
| chr7:55996303 | A | T | 9 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0298 others(6): Show |
13 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.713-1063A>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996303 | |||||||
| chr7:55996362 | C | T | 1 | a0001c0001t0002g0269 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.713-1004C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996362 | |||||||
| chr7:55996378 | G | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.713-988G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996378 | |||||||
| chr7:55996479 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.713-887C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996479 | |||||||
| chr7:55996569 | G | A | 229 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0015 others(226): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.713-797G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996569 | |||||||
| chr7:55996581 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.713-785G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996581 | |||||||
| chr7:55996639 | G | A | 5 | a0001c0001t0001g0033 a0001c0001t0001g0178 a0001c0001t0001g0202 others(2): Show |
6 | HG02280.hp2 HG02559.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.713-727G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996639 | |||||||
| chr7:55996740 | A | G | 24 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(21): Show |
26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.713-626A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996740 | |||||||
| chr7:55996849 | G | C | 1 | a0001c0001t0002g0284 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.713-517G>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996849 | |||||||
| chr7:55996960 | G | T | 1 | a0001c0001t0002g0313 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.713-406G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55996960 | |||||||
| chr7:55997127 | C | T | 3 | a0001c0001t0004g0048 a0001c0001t0004g0049 a0001c0001t0004g0050 |
3 | HG01256.hp1 HG01258.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.713-239C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55997127 | |||||||
| chr7:55997135 | G | A | 3 | a0001c0001t0007g0251 a0001c0001t0007g0252 a0001c0001t0007g0253 |
3 | HG01891.hp1 HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.713-231G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | chr7 | 55997135 | |||||||
| chr7:55997158 | GA | G | 13 | a0001c0001t0001g0200 a0001c0001t0002g0007 a0001c0001t0002g0026 others(10): Show |
18 | HG00544.hp2 HG01358.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.713-192delA | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 55997158 | ||||||
| chr7:55997552 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.796+103G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55997552 | |||||||
| chr7:55997687 | T | A | 44 | a0001c0001t0004g0003 a0001c0001t0004g0008 a0001c0001t0004g0018 others(41): Show |
54 | HG00140.hp2 HG00408.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.796+238T>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55997687 | |||||||
| chr7:55998013 | C | T | 4 | a0001c0001t0005g0014 a0001c0001t0005g0038 a0001c0001t0005g0275 others(1): Show |
7 | HG02109.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+564C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998013 | |||||||
| chr7:55998042 | G | A | 27 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0230 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.796+593G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998042 | |||||||
| chr7:55998231 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.797-777A>G | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998231 | |||||||
| chr7:55998386 | G | A | 95 | a0001c0001t0002g0013 a0001c0001t0002g0026 a0001c0001t0002g0047 others(92): Show |
107 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.797-622G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998386 | |||||||
| chr7:55998406 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.797-602C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998406 | |||||||
| chr7:55998409 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.797-599G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998409 | |||||||
| chr7:55998483 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.797-525G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998483 | |||||||
| chr7:55998493 | G | GT | 68 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0030 others(65): Show |
78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.797-489dupT | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTT | 60 | a0001c0001t0001g0222 a0001c0001t0002g0026 a0001c0001t0002g0042 others(57): Show |
70 | HG00423.hp1 HG00673.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.797-490_797-489dup others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTTT | 24 | a0001c0001t0001g0213 a0001c0001t0003g0022 a0001c0001t0003g0085 others(21): Show |
25 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.797-491_797-489dup others(3): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTTTT | 27 | a0001c0001t0002g0082 a0001c0001t0003g0084 a0001c0001t0003g0093 others(24): Show |
29 | HG00140.hp2 HG00408.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.797-492_797-489dup others(4): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTTTTT | 15 | a0001c0001t0004g0003 a0001c0001t0004g0019 a0001c0001t0004g0021 others(12): Show |
21 | HG01071.hp2 HG01192.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.797-493_797-489dup others(5): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0002g0292 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.797-499_797-489dup others(11): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998493 | G | GTTTTTTT others(6): Show |
2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.797-501_797-489dup others(13): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998493 | ||||||
| chr7:55998503 | T | TTG | 13 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0283 others(10): Show |
15 | HG01081.hp1 HG02056.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.797-504_797-503ins others(2): Show |
NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 55998503 | ||||||
| chr7:55998525 | G | A | 66 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(63): Show |
82 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.797-483G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998525 | |||||||
| chr7:55998603 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
5 | HG02280.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.797-405C>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998603 | |||||||
| chr7:55998712 | G | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG01891.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.797-296G>T | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998712 | |||||||
| chr7:55998799 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.797-209G>A | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998799 | |||||||
| chr7:55998968 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.797-40T>C | NIPSNAP2 | ENSG00000146729.10 | transcript | ENST00000322090.8 | protein_coding | 9/9 | chr7 | 55998968 |