Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3628 |
| ensemblid | ENSG00000151689.13 |
| hgncid | 6071 |
| symbol | INPP1 |
| name | inositol polyphosphate-1-phosphatase |
| refseq_nuc | NM_001128928.2 |
| refseq_prot | NP_001122400.1 |
| ensembl_nuc | ENST00000392329.7 |
| ensembl_prot | ENSP00000376142.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 190343589 |
| end | 190371665 |
| strand | + |
| ver | v1.2 |
| region | chr2:190343589-190371665 |
| region5000 | chr2:190338589-190376665 |
| regionname0 | INPP1_chr2_190343589_190371665 |
| regionname5000 | INPP1_chr2_190338589_190376665 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 399 | 393 | 73 | 73 | 194 | 16 | 35 | 148 | INPP1_chr2_190338589_190376665 | INPP1 | MSDIL others(394): Show |
chr2 | 190338589 | 190376665 |
| a0002 | 0/0 | 399 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | MSDIL others(394): Show |
chr2 | 190338589 | 190376665 |
| a0003 | 0/0 | 399 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | MSDIL others(394): Show |
chr2 | 190338589 | 190376665 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1197 | 132 | 19 | 15 | 81 | 5 | 12 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0002 | 0/0 | 1197 | 103 | 11 | 33 | 47 | 6 | 6 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0003 | 0/1 | 1197 | 59 | 0 | 10 | 31 | 4 | 13 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0004 | 0/0 | 1197 | 44 | 33 | 8 | 2 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0005 | 1/0 | 1197 | 42 | 8 | 4 | 27 | 0 | 2 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0007 | 0/0 | 1197 | 10 | 0 | 3 | 6 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0009 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0010 | 0/0 | 1197 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0001c0011 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0002c0006 | 0/0 | 1197 | 16 | 15 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 | ||
| a0003c0008 | 0/0 | 1197 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ATGTC others(1192): Show |
chr2 | 190338589 | 190376665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 2044 | 76 | 11 | 15 | 40 | 5 | 5 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0003 | 0/0 | 2044 | 45 | 7 | 0 | 38 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0004 | 0/0 | 2044 | 3 | 0 | 0 | 0 | 0 | 3 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0006 | 0/0 | 2044 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0007 | 0/0 | 2044 | 2 | 0 | 0 | 1 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0009 | 0/0 | 2044 | 3 | 0 | 0 | 0 | 0 | 3 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0001t0018 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0001 | 0/0 | 2044 | 93 | 5 | 32 | 44 | 6 | 6 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0003 | 0/0 | 2044 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0004 | 0/0 | 2044 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0008 | 0/0 | 2044 | 5 | 4 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0014 | 0/0 | 2044 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0002t0015 | 0/0 | 2044 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0003t0001 | 0/1 | 2044 | 57 | 0 | 10 | 30 | 4 | 12 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0003t0007 | 0/0 | 2044 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0003t0016 | 0/0 | 2044 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0003 | 0/0 | 2044 | 6 | 6 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0004 | 0/0 | 2044 | 22 | 13 | 6 | 2 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0005 | 0/0 | 2044 | 13 | 11 | 2 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0006 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0007 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0004t0017 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0005t0001 | 0/0 | 2044 | 36 | 6 | 4 | 24 | 0 | 2 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0005t0004 | 1/0 | 2044 | 3 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0005t0011 | 0/0 | 2044 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0005t0013 | 0/0 | 2044 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0007t0007 | 0/0 | 2044 | 10 | 0 | 3 | 6 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0009t0004 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0010t0004 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0001c0011t0005 | 0/0 | 2044 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0002c0006t0003 | 0/0 | 2044 | 2 | 1 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0002c0006t0006 | 0/0 | 2044 | 11 | 11 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0002c0006t0010 | 0/0 | 2044 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0002c0006t0012 | 0/0 | 2044 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| a0003c0008t0002 | 0/0 | 2044 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | ACTTG others(2039): Show |
chr2 | 190338589 | 190376665 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0003 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0005 | 0/0 | 10 | 1 | 1 | 3 | 4 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0006 | 0/0 | 9 | 6 | 0 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0029 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0001t0018g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0002 | 0/0 | 18 | 0 | 4 | 14 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0007 | 0/0 | 8 | 0 | 4 | 0 | 4 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0008 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0002t0015g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0001 | 0/0 | 15 | 0 | 2 | 9 | 0 | 4 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0050 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0003t0016g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0004t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0001 | 0/0 | 17 | 0 | 1 | 15 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0004g0039 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0011g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0005t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0007t0007g0015 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0007t0007g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0007t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0007t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0009t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0010t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0001c0011t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0002c0006t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| a0003c0008t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | GBR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0046 | EUR | GBR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0091 | EUR | FIN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | FIN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0178 | EUR | FIN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00438 | hp1 | a0001 | c0002 | t0015 | g0002 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00609 | hp1 | a0001 | c0004 | t0004 | g0150 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00621 | hp2 | a0001 | c0004 | t0004 | g0151 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00639 | hp2 | a0001 | c0004 | t0004 | g0009 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00642 | hp1 | a0002 | c0006 | t0003 | g0132 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00642 | hp2 | a0001 | c0004 | t0004 | g0009 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | CHS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00733 | hp2 | a0001 | c0004 | t0005 | g0147 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00738 | hp2 | a0001 | c0005 | t0001 | g0014 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0186 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01069 | hp1 | a0001 | c0004 | t0004 | g0009 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0162 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01071 | hp1 | a0001 | c0004 | t0004 | g0009 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0050 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01109 | hp2 | a0001 | c0004 | t0004 | g0062 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0189 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01192 | hp2 | a0001 | c0002 | t0008 | g0075 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01255 | hp2 | a0001 | c0005 | t0001 | g0155 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01261 | hp2 | a0001 | c0004 | t0005 | g0136 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0159 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01496 | hp2 | a0001 | c0004 | t0004 | g0146 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0014 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01884 | hp1 | a0001 | c0010 | t0004 | g0069 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01891 | hp1 | a0001 | c0004 | t0005 | g0135 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0084 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01952 | hp2 | a0001 | c0007 | t0007 | g0015 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01981 | hp1 | a0001 | c0007 | t0007 | g0015 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01981 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01993 | hp2 | a0001 | c0007 | t0007 | g0016 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0188 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02055 | hp1 | a0002 | c0006 | t0006 | g0114 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02056 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0082 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02071 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02074 | hp2 | a0001 | c0005 | t0001 | g0187 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0161 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02145 | hp2 | a0001 | c0009 | t0004 | g0056 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CDX | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02258 | hp1 | a0001 | c0004 | t0005 | g0137 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0060 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02280 | hp1 | a0001 | c0004 | t0017 | g0054 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02280 | hp2 | a0001 | c0004 | t0004 | g0057 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02451 | hp1 | a0001 | c0004 | t0005 | g0133 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02523 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02572 | hp1 | a0001 | c0004 | t0007 | g0220 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02602 | hp1 | a0001 | c0003 | t0016 | g0001 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02602 | hp2 | a0001 | c0005 | t0001 | g0156 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0064 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02622 | hp2 | a0002 | c0006 | t0006 | g0038 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02630 | hp1 | a0002 | c0006 | t0012 | g0011 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0140 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02698 | hp2 | a0001 | c0001 | t0009 | g0118 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02717 | hp1 | a0001 | c0004 | t0005 | g0130 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02717 | hp2 | a0002 | c0006 | t0006 | g0011 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02723 | hp1 | a0001 | c0004 | t0005 | g0131 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02723 | hp2 | a0001 | c0002 | t0008 | g0076 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02735 | hp1 | a0001 | c0005 | t0001 | g0001 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0139 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02809 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02818 | hp2 | a0002 | c0006 | t0010 | g0022 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02886 | hp1 | a0001 | c0004 | t0005 | g0040 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02886 | hp2 | a0001 | c0005 | t0004 | g0067 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02896 | hp2 | a0001 | c0004 | t0004 | g0066 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0153 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0129 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02970 | hp2 | a0001 | c0004 | t0006 | g0128 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02976 | hp2 | a0001 | c0004 | t0003 | g0126 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0061 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03098 | hp2 | a0001 | c0004 | t0005 | g0143 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03130 | hp1 | a0001 | c0002 | t0008 | g0074 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03130 | hp2 | a0001 | c0004 | t0003 | g0055 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03195 | hp2 | a0002 | c0006 | t0003 | g0113 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03209 | hp1 | a0002 | c0006 | t0006 | g0022 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03209 | hp2 | a0001 | c0004 | t0005 | g0127 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03225 | hp2 | a0001 | c0004 | t0005 | g0112 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0046 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03453 | hp1 | a0001 | c0004 | t0004 | g0194 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03453 | hp2 | a0002 | c0006 | t0006 | g0011 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0073 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03486 | hp2 | a0002 | c0006 | t0006 | g0035 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0167 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0116 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03516 | hp1 | a0002 | c0006 | t0006 | g0111 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03516 | hp2 | a0002 | c0006 | t0006 | g0011 | AFR | ESN | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0065 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03540 | hp2 | a0001 | c0004 | t0004 | g0070 | AFR | GWD | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03579 | hp1 | a0001 | c0004 | t0005 | g0040 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03579 | hp2 | a0001 | c0002 | t0008 | g0077 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0180 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0176 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0043 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0117 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0096 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03834 | hp1 | a0001 | c0007 | t0007 | g0209 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0043 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04184 | hp2 | a0001 | c0011 | t0005 | g0119 | SAS | BEB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0157 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0215 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04228 | hp1 | a0003 | c0008 | t0002 | g0229 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | STU | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18522 | hp1 | a0001 | c0005 | t0004 | g0039 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0141 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | CHB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18906 | hp2 | a0001 | c0004 | t0004 | g0063 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18939 | hp1 | a0001 | c0007 | t0007 | g0016 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18939 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18942 | hp1 | a0001 | c0005 | t0001 | g0049 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18946 | hp1 | a0001 | c0007 | t0007 | g0015 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18947 | hp1 | a0001 | c0005 | t0001 | g0172 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18948 | hp2 | a0001 | c0005 | t0001 | g0049 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18954 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18957 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18960 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18961 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18962 | hp1 | a0001 | c0003 | t0007 | g0197 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18966 | hp1 | a0001 | c0007 | t0007 | g0016 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18967 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18971 | hp1 | a0001 | c0005 | t0013 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18972 | hp1 | a0001 | c0002 | t0004 | g0145 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18978 | hp1 | a0001 | c0005 | t0001 | g0014 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18979 | hp2 | a0001 | c0007 | t0007 | g0212 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18980 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18995 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19002 | hp1 | a0001 | c0005 | t0011 | g0171 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19003 | hp1 | a0001 | c0005 | t0001 | g0160 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19011 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19055 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19056 | hp1 | a0001 | c0005 | t0001 | g0158 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19058 | hp2 | a0001 | c0007 | t0007 | g0015 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19062 | hp2 | a0001 | c0005 | t0001 | g0174 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19063 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19064 | hp1 | a0001 | c0002 | t0014 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19067 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19078 | hp1 | a0001 | c0005 | t0011 | g0170 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19080 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19081 | hp1 | a0001 | c0007 | t0007 | g0016 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19081 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19083 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19091 | hp2 | a0001 | c0005 | t0001 | g0163 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19240 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA19240 | hp2 | a0001 | c0004 | t0005 | g0134 | AFR | YRI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ASW | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ASW | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0168 | EUR | TSI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20752 | hp2 | a0001 | c0004 | t0004 | g0009 | EUR | TSI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | TSI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | TSI | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | GIH | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0183 | SAS | GIH | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG01123 | hp2 | a0001 | c0005 | t0001 | g0014 | AMR | CLM | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02109 | hp1 | a0002 | c0006 | t0006 | g0038 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02109 | hp2 | a0001 | c0001 | t0018 | g0203 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02486 | hp1 | a0001 | c0004 | t0004 | g0059 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02486 | hp2 | a0002 | c0006 | t0010 | g0125 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02559 | hp1 | a0002 | c0006 | t0006 | g0022 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | ACB | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0071 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0177 | AFR | USA | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0058 | AFR | USA | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA18955 | hp2 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20300 | hp1 | a0001 | c0004 | t0003 | g0012 | AFR | USA | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA20300 | hp2 | a0002 | c0006 | t0006 | g0035 | AFR | USA | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| NA21309 | hp2 | a0001 | c0004 | t0003 | g0012 | AFR | LWK | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0050 | REF | REF | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0004 | g0039 | REF | REF | INPP1_chr2_190338589_190376665 | INPP1 | chr2 | 190338589 | 190376665 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190370860 | T | C | 1 | a0003 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.658T>C | p.Tyr220His | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 1239/2044 | 658/1200 | 220/399 | chr2 | 190370860 | |||
| chr2:190370884 | A | G | 1 | a0002 | 16 | HG00642.hp1 HG02055.hp1 HG02109.hp1 others(13): Show |
missense_variant | MODERATE | c.682A>G | p.Thr228Ala | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 1263/2044 | 682/1200 | 228/399 | chr2 | 190370884 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190360201 | C | T | 2 | a0001c0007 a0001c0011 |
11 | HG01952.hp2 HG01981.hp1 HG01993.hp2 others(8): Show |
synonymous_variant | LOW | c.99C>T | p.Ile33Ile | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/7 | 680/2044 | 99/1200 | 33/399 | chr2 | 190360201 | |||
| chr2:190360255 | G | T | 8 | a0001c0001 a0001c0004 a0001c0007 others(5): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
synonymous_variant | LOW | c.153G>T | p.Thr51Thr | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/7 | 734/2044 | 153/1200 | 51/399 | chr2 | 190360255 | |||
| chr2:190366732 | G | A | 8 | a0001c0001 a0001c0002 a0001c0004 others(5): Show |
308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
synonymous_variant | LOW | c.303G>A | p.Glu101Glu | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/7 | 884/2044 | 303/1200 | 101/399 | chr2 | 190366732 | |||
| chr2:190366777 | G | A | 4 | a0001c0001 a0001c0007 a0001c0010 others(1): Show |
144 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(141): Show |
synonymous_variant | LOW | c.348G>A | p.Val116Val | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/7 | 929/2044 | 348/1200 | 116/399 | chr2 | 190366777 | |||
| chr2:190371175 | A | C | 9 | a0001c0001 a0001c0002 a0001c0003 others(6): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
synonymous_variant | LOW | c.973A>C | p.Arg325Arg | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 1554/2044 | 973/1200 | 325/399 | chr2 | 190371175 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190343615 | C | T | 7 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0018 others(4): Show |
92 | HG00323.hp1 HG00673.hp1 HG00733.hp1 others(89): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-555C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/7 | chr2 | 190343615 | |||||||
| chr2:190343621 | G | A | 15 | a0001c0001t0006 a0001c0002t0001 a0001c0002t0014 others(12): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
5_prime_UTR_variant | MODIFIER | c.-549G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/7 | 16482 | chr2 | 190343621 | ||||||
| chr2:190343624 | G | T | 1 | a0001c0002t0008 | 5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-546G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/7 | chr2 | 190343624 | |||||||
| chr2:190343739 | C | G | 1 | a0001c0001t0009 | 3 | HG02698.hp2 HG02738.hp2 HG03491.hp2 |
5_prime_UTR_variant | MODIFIER | c.-431C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/7 | 16364 | chr2 | 190343739 | ||||||
| chr2:190348913 | C | T | 1 | a0001c0003t0016 | 1 | HG02602.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-183C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/7 | chr2 | 190348913 | |||||||
| chr2:190348938 | A | G | 8 | a0001c0002t0001 a0001c0002t0014 a0001c0002t0015 others(5): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
5_prime_UTR_variant | MODIFIER | c.-158A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/7 | 11165 | chr2 | 190348938 | ||||||
| chr2:190348997 | T | C | 1 | a0002c0006t0012 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/7 | 11106 | chr2 | 190348997 | ||||||
| chr2:190349015 | C | T | 2 | a0002c0006t0010 a0002c0006t0012 |
3 | HG02486.hp2 HG02630.hp1 HG02818.hp2 |
5_prime_UTR_variant | MODIFIER | c.-81C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/7 | 11088 | chr2 | 190349015 | ||||||
| chr2:190349024 | A | G | 1 | a0001c0004t0017 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/7 | 11079 | chr2 | 190349024 | ||||||
| chr2:190360044 | G | A | 1 | a0001c0005t0013 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/7 | 59 | chr2 | 190360044 | ||||||
| chr2:190371404 | G | A | 1 | a0001c0002t0014 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 2 | chr2 | 190371404 | ||||||
| chr2:190371453 | C | T | 1 | a0001c0001t0018 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 51 | chr2 | 190371453 | ||||||
| chr2:190371589 | T | C | 1 | a0001c0002t0015 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*187T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 187 | chr2 | 190371589 | ||||||
| chr2:190371653 | A | G | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(10): Show |
152 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*251A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 7/7 | 251 | chr2 | 190371653 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:190344069 | C | T | 50 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(47): Show |
95 | HG00323.hp1 HG00544.hp2 HG00673.hp1 others(92): Show |
intron_variant | MODIFIER | c.-209+108C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344069 | |||||||
| chr2:190344137 | G | T | 1 | a0001c0003t0001g0050 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-209+176G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344137 | |||||||
| chr2:190344139 | C | A | 2 | a0001c0004t0003g0055 a0001c0004t0017g0054 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-209+178C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344139 | |||||||
| chr2:190344168 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-209+207C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344168 | |||||||
| chr2:190344302 | T | A | 14 | a0001c0001t0003g0068 a0001c0004t0004g0009 a0001c0004t0004g0057 others(11): Show |
18 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.-209+341T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344302 | |||||||
| chr2:190344351 | T | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-209+390T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344351 | |||||||
| chr2:190344702 | G | A | 8 | a0001c0002t0001g0072 a0001c0004t0004g0057 a0001c0004t0004g0058 others(5): Show |
8 | HG01346.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-209+741G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344702 | |||||||
| chr2:190344724 | C | T | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-209+763C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344724 | |||||||
| chr2:190344922 | G | A | 7 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0004g0070 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-209+961G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344922 | |||||||
| chr2:190344992 | C | T | 56 | a0001c0001t0002g0030 a0001c0002t0001g0007 a0001c0002t0001g0026 others(53): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-209+1031C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190344992 | |||||||
| chr2:190345218 | A | G | 1 | a0001c0001t0003g0152 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-209+1257A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345218 | |||||||
| chr2:190345556 | G | A | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-209+1595G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345556 | |||||||
| chr2:190345628 | T | C | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-209+1667T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345628 | |||||||
| chr2:190345718 | G | T | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
4 | HG02080.hp2 NA18947.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-209+1757G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345718 | |||||||
| chr2:190345777 | T | C | 1 | a0001c0005t0001g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-209+1816T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345777 | |||||||
| chr2:190345778 | G | A | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-209+1817G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345778 | |||||||
| chr2:190345855 | G | GTTACCAC others(13): Show |
1 | a0001c0001t0002g0228 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-209+1895_-209+189 others(24): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 190345855 | ||||||
| chr2:190345857 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-209+1896G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345857 | |||||||
| chr2:190345858 | G | T | 1 | a0001c0001t0002g0228 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-209+1897G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345858 | |||||||
| chr2:190345904 | G | A | 1 | a0001c0004t0003g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-209+1943G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345904 | |||||||
| chr2:190345908 | C | A | 1 | a0001c0004t0003g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-209+1947C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190345908 | |||||||
| chr2:190346043 | G | A | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-209+2082G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346043 | |||||||
| chr2:190346136 | T | C | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-209+2175T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346136 | |||||||
| chr2:190346384 | G | T | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-209+2423G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346384 | |||||||
| chr2:190346531 | T | G | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-208-2357T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346531 | |||||||
| chr2:190346887 | G | A | 104 | a0001c0001t0006g0081 a0001c0001t0006g0082 a0001c0002t0001g0002 others(101): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-208-2001G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346887 | |||||||
| chr2:190346975 | C | T | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-208-1913C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190346975 | |||||||
| chr2:190347007 | C | CT | 39 | a0001c0001t0002g0029 a0001c0001t0002g0225 a0001c0001t0002g0226 others(36): Show |
54 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-208-1859dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 190347007 | ||||||
| chr2:190347007 | CT | C | 8 | a0001c0001t0002g0193 a0001c0001t0003g0110 a0001c0002t0001g0078 others(5): Show |
8 | HG01169.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-208-1859delT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 190347007 | ||||||
| chr2:190347072 | T | C | 1 | a0001c0005t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-208-1816T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347072 | |||||||
| chr2:190347075 | G | A | 5 | a0001c0004t0005g0112 a0002c0006t0003g0113 a0002c0006t0006g0035 others(2): Show |
6 | HG02055.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-208-1813G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347075 | |||||||
| chr2:190347137 | G | A | 1 | a0001c0005t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-208-1751G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347137 | |||||||
| chr2:190347160 | C | T | 1 | a0001c0001t0007g0223 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-208-1728C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347160 | |||||||
| chr2:190347301 | A | G | 5 | a0001c0002t0001g0008 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
11 | HG01257.hp1 HG01258.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-208-1587A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347301 | |||||||
| chr2:190347329 | A | T | 1 | a0001c0005t0001g0049 | 2 | NA18942.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-208-1559A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347329 | |||||||
| chr2:190347505 | C | T | 104 | a0001c0001t0006g0081 a0001c0001t0006g0082 a0001c0002t0001g0002 others(101): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-208-1383C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347505 | |||||||
| chr2:190347694 | G | A | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-208-1194G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347694 | |||||||
| chr2:190347709 | C | T | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-208-1179C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347709 | |||||||
| chr2:190347751 | T | G | 1 | a0001c0004t0003g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-208-1137T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347751 | |||||||
| chr2:190347779 | A | T | 1 | a0001c0001t0003g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-208-1109A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347779 | |||||||
| chr2:190347811 | A | C | 1 | a0001c0001t0002g0222 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-208-1077A>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347811 | |||||||
| chr2:190347943 | G | C | 1 | a0001c0004t0004g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-208-945G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347943 | |||||||
| chr2:190347974 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-208-914C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190347974 | |||||||
| chr2:190348008 | C | T | 1 | a0001c0002t0001g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-208-880C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348008 | |||||||
| chr2:190348036 | G | T | 1 | a0001c0001t0009g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-208-852G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348036 | |||||||
| chr2:190348037 | C | T | 1 | a0001c0001t0003g0110 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-208-851C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348037 | |||||||
| chr2:190348052 | C | T | 1 | a0001c0003t0001g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-208-836C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348052 | |||||||
| chr2:190348070 | G | A | 1 | a0001c0004t0004g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-208-818G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348070 | |||||||
| chr2:190348101 | G | A | 4 | a0001c0001t0003g0115 a0001c0001t0003g0195 a0001c0001t0003g0196 others(1): Show |
4 | HG00544.hp2 NA18747.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-208-787G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348101 | |||||||
| chr2:190348143 | C | T | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-208-745C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348143 | |||||||
| chr2:190348175 | G | A | 1 | a0001c0003t0001g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-208-713G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348175 | |||||||
| chr2:190348263 | A | T | 104 | a0001c0001t0006g0081 a0001c0001t0006g0082 a0001c0002t0001g0002 others(101): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-208-625A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348263 | |||||||
| chr2:190348358 | G | GT | 13 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0025 others(10): Show |
20 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-208-521dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 190348358 | ||||||
| chr2:190348422 | C | T | 6 | a0001c0004t0005g0040 a0001c0004t0005g0134 a0001c0004t0005g0135 others(3): Show |
7 | HG01261.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-208-466C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348422 | |||||||
| chr2:190348423 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-208-465G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348423 | |||||||
| chr2:190348499 | T | C | 236 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(233): Show |
407 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.-208-389T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348499 | |||||||
| chr2:190348587 | T | C | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-208-301T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348587 | |||||||
| chr2:190348765 | GAGA | G | 3 | a0001c0002t0001g0185 a0001c0003t0001g0048 a0001c0003t0001g0184 |
4 | HG00408.hp1 NA18974.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-208-120_-208-118d others(5): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 190348765 | ||||||
| chr2:190348835 | T | C | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-208-53T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348835 | |||||||
| chr2:190348867 | T | C | 1 | a0001c0004t0004g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-208-21T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 1/6 | chr2 | 190348867 | |||||||
| chr2:190349249 | C | T | 102 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(99): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-65+218C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190349249 | |||||||
| chr2:190349694 | CTT | C | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-65+664_-65+665del others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190349694 | |||||||
| chr2:190349741 | A | AT | 153 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(150): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-65+710_-65+711ins others(1): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190349741 | |||||||
| chr2:190349906 | G | A | 1 | a0001c0009t0004g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-65+875G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190349906 | |||||||
| chr2:190350002 | G | A | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-65+971G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350002 | |||||||
| chr2:190350034 | G | A | 1 | a0001c0004t0004g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-65+1003G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350034 | |||||||
| chr2:190350081 | G | T | 1 | a0001c0003t0001g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-65+1050G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350081 | |||||||
| chr2:190350103 | C | T | 1 | a0001c0002t0003g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-65+1072C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350103 | |||||||
| chr2:190350309 | A | G | 37 | a0001c0004t0003g0012 a0001c0004t0003g0055 a0001c0004t0003g0126 others(34): Show |
50 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.-65+1278A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350309 | |||||||
| chr2:190350371 | T | C | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-65+1340T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350371 | |||||||
| chr2:190350395 | T | G | 2 | a0001c0002t0008g0073 a0001c0002t0008g0074 |
2 | HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-65+1364T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350395 | |||||||
| chr2:190350636 | T | C | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-65+1605T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350636 | |||||||
| chr2:190350768 | A | G | 25 | a0001c0002t0001g0002 a0001c0002t0001g0019 a0001c0002t0001g0020 others(22): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-65+1737A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350768 | |||||||
| chr2:190350816 | G | A | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-65+1785G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350816 | |||||||
| chr2:190350836 | G | T | 1 | a0001c0004t0004g0059 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-65+1805G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350836 | |||||||
| chr2:190350861 | A | T | 2 | a0001c0003t0001g0047 a0001c0003t0001g0182 |
3 | NA18997.hp2 NA19010.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-65+1830A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350861 | |||||||
| chr2:190350932 | C | T | 27 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0004g0129 others(24): Show |
36 | HG00642.hp1 HG01261.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-65+1901C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190350932 | |||||||
| chr2:190351132 | G | C | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-65+2101G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351132 | |||||||
| chr2:190351219 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-65+2188C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351219 | |||||||
| chr2:190351226 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-65+2195C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351226 | |||||||
| chr2:190351258 | G | T | 1 | a0001c0004t0004g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-65+2227G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351258 | |||||||
| chr2:190351383 | T | A | 154 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(151): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.-65+2352T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351383 | |||||||
| chr2:190351415 | T | C | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+2384T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351415 | |||||||
| chr2:190351604 | T | A | 1 | a0001c0003t0001g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-65+2573T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351604 | |||||||
| chr2:190351686 | A | G | 15 | a0001c0001t0002g0053 a0001c0001t0002g0218 a0001c0001t0002g0219 others(12): Show |
31 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-65+2655A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351686 | |||||||
| chr2:190351738 | A | G | 1 | a0001c0005t0004g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-65+2707A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351738 | |||||||
| chr2:190351798 | A | G | 4 | a0001c0004t0004g0063 a0001c0004t0004g0064 a0001c0004t0004g0065 others(1): Show |
4 | HG02615.hp1 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-65+2767A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351798 | |||||||
| chr2:190351986 | T | C | 27 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0004g0129 others(24): Show |
36 | HG00642.hp1 HG01261.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.-65+2955T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190351986 | |||||||
| chr2:190352081 | T | C | 1 | a0001c0001t0002g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-65+3050T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352081 | |||||||
| chr2:190352116 | A | G | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | HG00280.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.-65+3085A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352116 | |||||||
| chr2:190352131 | C | T | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | NA18612.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-65+3100C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352131 | |||||||
| chr2:190352190 | G | A | 1 | a0001c0002t0003g0141 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-65+3159G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352190 | |||||||
| chr2:190352225 | A | T | 1 | a0001c0004t0003g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-65+3194A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352225 | |||||||
| chr2:190352323 | C | A | 1 | a0001c0010t0004g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-65+3292C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352323 | |||||||
| chr2:190352348 | G | A | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+3317G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352348 | |||||||
| chr2:190352388 | T | C | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+3357T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352388 | |||||||
| chr2:190352426 | A | G | 1 | a0001c0009t0004g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-65+3395A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352426 | |||||||
| chr2:190352496 | G | C | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+3465G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352496 | |||||||
| chr2:190352531 | A | G | 141 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(138): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-65+3500A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352531 | |||||||
| chr2:190352638 | C | T | 5 | a0001c0003t0001g0046 a0001c0003t0001g0178 a0001c0003t0001g0179 others(2): Show |
6 | HG00140.hp2 HG00323.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.-65+3607C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352638 | |||||||
| chr2:190352706 | A | G | 2 | a0001c0004t0004g0009 a0001c0004t0004g0062 |
6 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.-65+3675A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352706 | |||||||
| chr2:190352965 | G | T | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-65+3934G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352965 | |||||||
| chr2:190352985 | C | T | 1 | a0001c0001t0007g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-65+3954C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352985 | |||||||
| chr2:190352986 | G | A | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-65+3955G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190352986 | |||||||
| chr2:190353509 | T | C | 1 | a0001c0004t0003g0055 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-65+4478T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353509 | |||||||
| chr2:190353645 | A | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(56): Show |
119 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.-65+4614A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353645 | |||||||
| chr2:190353657 | A | G | 1 | a0001c0004t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-65+4626A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353657 | |||||||
| chr2:190353720 | C | T | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+4689C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353720 | |||||||
| chr2:190353875 | G | A | 1 | a0001c0001t0003g0144 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-65+4844G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353875 | |||||||
| chr2:190353914 | T | A | 1 | a0001c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-65+4883T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353914 | |||||||
| chr2:190353968 | C | T | 1 | a0001c0003t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-65+4937C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353968 | |||||||
| chr2:190353969 | A | G | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-65+4938A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190353969 | |||||||
| chr2:190354042 | C | A | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-65+5011C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354042 | |||||||
| chr2:190354042 | C | G | 1 | a0001c0002t0001g0080 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-65+5011C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354042 | |||||||
| chr2:190354043 | G | A | 2 | a0001c0004t0004g0070 a0001c0004t0004g0071 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-65+5012G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354043 | |||||||
| chr2:190354118 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-65+5087T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354118 | |||||||
| chr2:190354191 | T | C | 113 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(110): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.-65+5160T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354191 | |||||||
| chr2:190354246 | G | A | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-65+5215G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354246 | |||||||
| chr2:190354338 | C | A | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.-65+5307C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354338 | |||||||
| chr2:190354360 | T | G | 6 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0004t0004g0057 others(3): Show |
6 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-65+5329T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354360 | |||||||
| chr2:190354389 | T | TTCA | 86 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(83): Show |
154 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-65+5359_-65+5361d others(5): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354389 | ||||||
| chr2:190354486 | T | A | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-65+5455T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354486 | |||||||
| chr2:190354546 | G | A | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-64-5493G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354546 | |||||||
| chr2:190354547 | A | G | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.-64-5492A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354547 | |||||||
| chr2:190354571 | A | G | 8 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(5): Show |
8 | HG01192.hp2 HG01884.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-64-5468A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354571 | |||||||
| chr2:190354758 | T | C | 1 | a0001c0001t0002g0216 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-64-5281T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354758 | |||||||
| chr2:190354786 | T | G | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5253T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354786 | |||||||
| chr2:190354888 | G | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(78): Show |
149 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-64-5151G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354888 | |||||||
| chr2:190354925 | G | GGT | 2 | a0001c0003t0001g0027 a0001c0003t0001g0045 |
5 | NA18941.hp2 NA18942.hp2 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5094_-64-5093d others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354925 | ||||||
| chr2:190354925 | G | GTGTGTGT others(10): Show |
1 | a0002c0006t0006g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-64-5114_-64-5113i others(19): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354925 | |||||||
| chr2:190354939 | T | TGC | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5099_-64-5098i others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354939 | ||||||
| chr2:190354947 | C | T | 123 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(120): Show |
204 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.-64-5092C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354947 | |||||||
| chr2:190354948 | A | AT | 12 | a0001c0002t0001g0008 a0001c0002t0001g0101 a0001c0002t0001g0102 others(9): Show |
18 | HG00423.hp1 HG01169.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-64-5077dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354948 | ||||||
| chr2:190354948 | A | G | 123 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(120): Show |
204 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.-64-5091A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354948 | |||||||
| chr2:190354948 | AT | A | 6 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0002t0001g0094 others(3): Show |
6 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-64-5077delT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354948 | ||||||
| chr2:190354948 | ATT | A | 7 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-64-5078_-64-5077d others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190354948 | ||||||
| chr2:190354949 | T | TGCA | 72 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(69): Show |
139 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(5): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGC | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(6): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGCA | 7 | a0001c0001t0002g0214 a0001c0001t0002g0219 a0001c0001t0004g0036 others(4): Show |
8 | HG02683.hp2 HG02698.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(7): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGTGTG others(3): Show |
8 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0002c0006t0006g0011 others(5): Show |
14 | HG02257.hp2 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(12): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGTGTG others(7): Show |
10 | a0001c0004t0004g0129 a0001c0004t0005g0040 a0001c0004t0005g0112 others(7): Show |
13 | HG01261.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(16): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGTGTG others(9): Show |
2 | a0001c0004t0005g0137 a0002c0006t0003g0132 |
2 | HG00642.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-64-5090_-64-5089i others(18): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354949 | T | TGTGTGTG others(11): Show |
1 | a0001c0004t0005g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-64-5090_-64-5089i others(20): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354949 | |||||||
| chr2:190354950 | T | A | 26 | a0001c0001t0007g0215 a0001c0004t0003g0012 a0001c0004t0003g0126 others(23): Show |
35 | HG00642.hp1 HG01261.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-64-5089T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354950 | |||||||
| chr2:190354950 | T | G | 18 | a0001c0004t0003g0055 a0001c0004t0004g0009 a0001c0004t0004g0057 others(15): Show |
22 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.-64-5089T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354950 | |||||||
| chr2:190354951 | T | TGCA | 10 | a0001c0004t0003g0055 a0001c0004t0004g0009 a0001c0004t0004g0057 others(7): Show |
14 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-64-5088_-64-5087i others(5): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354951 | |||||||
| chr2:190354951 | T | TGTGTGTG others(4): Show |
1 | a0001c0004t0005g0127 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-64-5088_-64-5087i others(13): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354951 | |||||||
| chr2:190354951 | T | TGTGTGTG others(8): Show |
3 | a0001c0004t0005g0130 a0001c0004t0005g0131 a0001c0004t0007g0220 |
3 | HG02572.hp1 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-64-5088_-64-5087i others(17): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354951 | |||||||
| chr2:190354951 | T | TGTGTGTG others(10): Show |
1 | a0001c0004t0005g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-64-5088_-64-5087i others(19): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190354951 | |||||||
| chr2:190355021 | A | AT | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-5014dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190355021 | ||||||
| chr2:190355124 | G | T | 42 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(39): Show |
55 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-64-4915G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355124 | |||||||
| chr2:190355471 | T | TCA | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-4568_-64-4567i others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355471 | |||||||
| chr2:190355491 | T | A | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-4548T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355491 | |||||||
| chr2:190355612 | C | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(78): Show |
149 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-64-4427C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355612 | |||||||
| chr2:190355627 | T | C | 5 | a0002c0006t0006g0011 a0002c0006t0006g0022 a0002c0006t0010g0022 others(2): Show |
8 | HG02486.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-64-4412T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355627 | |||||||
| chr2:190355750 | G | T | 1 | a0001c0002t0001g0089 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-64-4289G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355750 | |||||||
| chr2:190355811 | C | T | 1 | a0002c0006t0006g0038 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-64-4228C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355811 | |||||||
| chr2:190355847 | G | T | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-4192G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355847 | |||||||
| chr2:190355941 | A | T | 1 | a0001c0005t0001g0172 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-64-4098A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355941 | |||||||
| chr2:190355945 | T | A | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-4094T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355945 | |||||||
| chr2:190355971 | T | C | 5 | a0001c0001t0004g0036 a0001c0001t0004g0117 a0001c0001t0009g0116 others(2): Show |
6 | HG02683.hp2 HG02698.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-64-4068T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190355971 | |||||||
| chr2:190355987 | T | TA | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.-64-4049dupA | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190355987 | ||||||
| chr2:190356152 | A | G | 1 | a0001c0001t0004g0036 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-64-3887A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356152 | |||||||
| chr2:190356396 | A | G | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3643A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356396 | |||||||
| chr2:190356466 | G | C | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-64-3573G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356466 | |||||||
| chr2:190356574 | G | A | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-3465G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356574 | |||||||
| chr2:190356584 | G | A | 1 | a0001c0009t0004g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-64-3455G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356584 | |||||||
| chr2:190356601 | C | T | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3438C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356601 | |||||||
| chr2:190356640 | A | C | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.-64-3399A>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356640 | |||||||
| chr2:190356688 | G | T | 1 | a0001c0001t0002g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-64-3351G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356688 | |||||||
| chr2:190356691 | T | C | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3348T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356691 | |||||||
| chr2:190356743 | T | C | 1 | a0001c0003t0001g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-64-3296T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356743 | |||||||
| chr2:190356750 | ATTGT | A | 2 | a0001c0004t0003g0012 a0001c0004t0003g0126 |
5 | HG02257.hp2 HG02976.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-3286_-64-3283d others(6): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190356750 | ||||||
| chr2:190356796 | C | T | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3243C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356796 | |||||||
| chr2:190356814 | G | A | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3225G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356814 | |||||||
| chr2:190356858 | A | G | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-3181A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190356858 | |||||||
| chr2:190357045 | G | A | 1 | a0001c0004t0005g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-64-2994G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357045 | |||||||
| chr2:190357051 | G | A | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-64-2988G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357051 | |||||||
| chr2:190357202 | C | T | 121 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(118): Show |
202 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.-64-2837C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357202 | |||||||
| chr2:190357203 | G | A | 1 | a0001c0003t0001g0043 | 2 | HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-64-2836G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357203 | |||||||
| chr2:190357232 | C | T | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-64-2807C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357232 | |||||||
| chr2:190357387 | T | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-2652T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357387 | |||||||
| chr2:190357549 | T | C | 1 | a0001c0002t0008g0075 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-64-2490T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357549 | |||||||
| chr2:190357605 | C | A | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-2434C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357605 | |||||||
| chr2:190357784 | G | A | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.-64-2255G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357784 | |||||||
| chr2:190357801 | A | T | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-64-2238A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357801 | |||||||
| chr2:190357989 | T | C | 2 | a0001c0004t0004g0146 a0001c0004t0005g0147 |
2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-64-2050T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190357989 | |||||||
| chr2:190358021 | T | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-2018T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358021 | |||||||
| chr2:190358072 | A | AT | 17 | a0001c0002t0001g0034 a0001c0002t0001g0042 a0001c0002t0001g0091 others(14): Show |
21 | HG00280.hp1 HG00738.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-64-1942dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190358072 | ||||||
| chr2:190358072 | AT | A | 15 | a0001c0002t0001g0080 a0001c0002t0001g0092 a0001c0002t0001g0095 others(12): Show |
15 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.-64-1942delT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190358072 | ||||||
| chr2:190358072 | ATTTTT | A | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(62): Show |
129 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.-64-1946_-64-1942d others(7): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190358072 | ||||||
| chr2:190358072 | ATTTTTT | A | 53 | a0001c0001t0003g0013 a0001c0001t0003g0138 a0001c0001t0003g0144 others(50): Show |
70 | HG00438.hp2 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-64-1947_-64-1942d others(8): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190358072 | ||||||
| chr2:190358133 | G | A | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-64-1906G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358133 | |||||||
| chr2:190358183 | G | C | 1 | a0001c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-64-1856G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358183 | |||||||
| chr2:190358223 | C | T | 2 | a0001c0001t0009g0118 a0001c0001t0009g0139 |
2 | HG02698.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-64-1816C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358223 | |||||||
| chr2:190358283 | G | A | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-64-1756G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358283 | |||||||
| chr2:190358325 | C | G | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-64-1714C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358325 | |||||||
| chr2:190358355 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-64-1684G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358355 | |||||||
| chr2:190358671 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-64-1368A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358671 | |||||||
| chr2:190358806 | T | C | 1 | a0001c0003t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-64-1233T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190358806 | |||||||
| chr2:190359066 | G | A | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-64-973G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359066 | |||||||
| chr2:190359324 | G | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-715G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359324 | |||||||
| chr2:190359482 | G | A | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(61): Show |
124 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-64-557G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359482 | |||||||
| chr2:190359504 | C | G | 1 | a0001c0003t0001g0027 | 3 | NA18941.hp2 NA18942.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-64-535C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359504 | |||||||
| chr2:190359504 | C | T | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-64-535C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359504 | |||||||
| chr2:190359512 | G | A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0068 |
7 | HG01891.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-527G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359512 | |||||||
| chr2:190359556 | C | CA | 16 | a0001c0002t0001g0008 a0001c0002t0001g0019 a0001c0002t0001g0083 others(13): Show |
24 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.-64-467dupA | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190359556 | ||||||
| chr2:190359570 | AAAG | A | 45 | a0001c0001t0002g0051 a0001c0004t0003g0012 a0001c0004t0003g0055 others(42): Show |
59 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-64-466_-64-464del others(3): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190359570 | ||||||
| chr2:190359571 | AAG | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-64-466_-64-465del others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 190359571 | ||||||
| chr2:190359573 | G | A | 7 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0008g0073 others(4): Show |
7 | HG01192.hp2 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-64-466G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359573 | |||||||
| chr2:190359640 | C | T | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-64-399C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359640 | |||||||
| chr2:190359671 | T | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-368T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359671 | |||||||
| chr2:190359682 | C | CCT | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-357_-64-356ins others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359682 | |||||||
| chr2:190359685 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-64-354A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359685 | |||||||
| chr2:190359882 | A | G | 1 | a0001c0004t0004g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-64-157A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190359882 | |||||||
| chr2:190360026 | T | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(78): Show |
149 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-64-13T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190360026 | |||||||
| chr2:190360027 | G | T | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-64-12G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 2/6 | chr2 | 190360027 | |||||||
| chr2:190360471 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+165A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360471 | |||||||
| chr2:190360512 | G | C | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.204+206G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360512 | |||||||
| chr2:190360551 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+245A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360551 | |||||||
| chr2:190360580 | C | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+274C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360580 | |||||||
| chr2:190360676 | C | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+370C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360676 | |||||||
| chr2:190360777 | T | C | 1 | a0003c0008t0002g0229 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.204+471T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360777 | |||||||
| chr2:190360780 | C | A | 27 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0004g0129 others(24): Show |
36 | HG00642.hp1 HG01261.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.204+474C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360780 | |||||||
| chr2:190360783 | G | GT | 96 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(93): Show |
164 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.204+487dupT | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 190360783 | ||||||
| chr2:190360783 | G | GTT | 38 | a0001c0002t0001g0092 a0001c0004t0003g0012 a0001c0004t0003g0055 others(35): Show |
51 | HG00639.hp2 HG00642.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.204+486_204+487dup others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 190360783 | ||||||
| chr2:190360961 | C | T | 65 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(62): Show |
125 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.204+655C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360961 | |||||||
| chr2:190360985 | G | A | 3 | a0001c0004t0004g0070 a0001c0004t0004g0071 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.204+679G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190360985 | |||||||
| chr2:190361022 | G | A | 3 | a0001c0004t0005g0134 a0001c0004t0005g0137 a0001c0004t0005g0143 |
3 | HG02258.hp1 HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.204+716G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361022 | |||||||
| chr2:190361028 | A | G | 4 | a0001c0004t0004g0146 a0001c0004t0004g0150 a0001c0004t0004g0151 others(1): Show |
4 | HG00609.hp1 HG00621.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+722A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361028 | |||||||
| chr2:190361056 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+750A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361056 | |||||||
| chr2:190361140 | AG | A | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+837delG | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 190361140 | ||||||
| chr2:190361214 | C | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+908C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361214 | |||||||
| chr2:190361223 | T | G | 2 | a0001c0002t0001g0095 a0001c0002t0001g0101 |
2 | HG00423.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.204+917T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361223 | |||||||
| chr2:190361262 | T | C | 3 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0009t0004g0056 |
3 | HG02145.hp2 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.204+956T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361262 | |||||||
| chr2:190361753 | C | A | 1 | a0001c0002t0001g0031 | 2 | HG01109.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.205-874C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361753 | |||||||
| chr2:190361757 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.205-870G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361757 | |||||||
| chr2:190361886 | C | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.205-741C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361886 | |||||||
| chr2:190361970 | C | A | 3 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0006g0128 |
6 | HG02257.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-657C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190361970 | |||||||
| chr2:190362016 | A | G | 132 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(129): Show |
213 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.205-611A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362016 | |||||||
| chr2:190362160 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.205-467A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362160 | |||||||
| chr2:190362189 | T | C | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | HG00280.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.205-438T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362189 | |||||||
| chr2:190362206 | T | C | 64 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(61): Show |
124 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.205-421T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362206 | |||||||
| chr2:190362235 | A | C | 1 | a0001c0002t0001g0026 | 3 | HG01496.hp1 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.205-392A>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362235 | |||||||
| chr2:190362249 | G | A | 1 | a0001c0001t0018g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.205-378G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362249 | |||||||
| chr2:190362347 | A | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(60): Show |
123 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.205-280A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362347 | |||||||
| chr2:190362464 | T | A | 1 | a0001c0001t0002g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.205-163T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362464 | |||||||
| chr2:190362471 | G | A | 121 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(118): Show |
202 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.205-156G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362471 | |||||||
| chr2:190362509 | T | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.205-118T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362509 | |||||||
| chr2:190362604 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.205-23T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 3/6 | chr2 | 190362604 | |||||||
| chr2:190362757 | C | T | 1 | a0001c0002t0008g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.265+70C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190362757 | |||||||
| chr2:190362766 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+79A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190362766 | |||||||
| chr2:190362790 | A | G | 1 | a0001c0001t0007g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.265+103A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190362790 | |||||||
| chr2:190362851 | A | G | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.265+164A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190362851 | |||||||
| chr2:190363008 | A | G | 121 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(118): Show |
202 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(199): Show |
intron_variant | MODIFIER | c.265+321A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363008 | |||||||
| chr2:190363029 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+342A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363029 | |||||||
| chr2:190363113 | T | C | 2 | a0001c0002t0001g0090 a0001c0002t0001g0091 |
2 | HG00280.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.265+426T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363113 | |||||||
| chr2:190363152 | T | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+465T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363152 | |||||||
| chr2:190363154 | A | C | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+467A>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363154 | |||||||
| chr2:190363350 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+663A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363350 | |||||||
| chr2:190363476 | T | C | 1 | a0001c0003t0001g0176 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.265+789T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363476 | |||||||
| chr2:190363526 | A | T | 1 | a0001c0002t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.265+839A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363526 | |||||||
| chr2:190363613 | G | A | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+926G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363613 | |||||||
| chr2:190363639 | TTA | T | 1 | a0001c0001t0002g0028 | 3 | HG01169.hp1 HG01257.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.265+953_265+954del others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363639 | |||||||
| chr2:190363657 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.265+970C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363657 | |||||||
| chr2:190363694 | C | A | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+1007C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363694 | |||||||
| chr2:190363701 | G | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+1014G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363701 | |||||||
| chr2:190363704 | A | G | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.265+1017A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363704 | |||||||
| chr2:190363799 | C | T | 125 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
206 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.265+1112C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363799 | |||||||
| chr2:190363924 | G | T | 1 | a0001c0001t0002g0052 | 2 | NA18986.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.265+1237G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190363924 | |||||||
| chr2:190364157 | T | G | 1 | a0001c0005t0001g0177 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.265+1470T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364157 | |||||||
| chr2:190364321 | C | A | 9 | a0001c0004t0004g0009 a0001c0004t0004g0059 a0001c0004t0004g0060 others(6): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+1634C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364321 | |||||||
| chr2:190364321 | C | T | 1 | a0001c0005t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.265+1634C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364321 | |||||||
| chr2:190364322 | A | G | 183 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(180): Show |
310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.265+1635A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364322 | |||||||
| chr2:190364385 | C | CA | 4 | a0001c0004t0004g0057 a0001c0004t0004g0058 a0001c0004t0017g0054 others(1): Show |
4 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1705dupA | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190364385 | ||||||
| chr2:190364410 | C | T | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1723C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364410 | |||||||
| chr2:190364458 | C | T | 4 | a0001c0001t0002g0210 a0001c0001t0003g0021 a0001c0001t0003g0037 others(1): Show |
7 | HG00423.hp2 HG00609.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+1771C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364458 | |||||||
| chr2:190364474 | G | A | 50 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0198 others(47): Show |
87 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.265+1787G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364474 | |||||||
| chr2:190364499 | A | G | 6 | a0001c0001t0004g0036 a0001c0001t0004g0117 a0001c0001t0009g0116 others(3): Show |
7 | HG02683.hp2 HG02698.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.265+1812A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364499 | |||||||
| chr2:190364541 | CA | C | 56 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0003t0001g0001 others(53): Show |
100 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.265+1868delA | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190364541 | ||||||
| chr2:190364553 | A | T | 63 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(60): Show |
123 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.265+1866A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364553 | |||||||
| chr2:190364554 | A | T | 170 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(167): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.265+1867A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364554 | |||||||
| chr2:190364555 | A | T | 173 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(170): Show |
300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.265+1868A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364555 | |||||||
| chr2:190364604 | T | G | 4 | a0001c0003t0001g0044 a0001c0003t0001g0048 a0001c0003t0001g0097 others(1): Show |
6 | HG00408.hp1 HG02027.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1917T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364604 | |||||||
| chr2:190364606 | T | G | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+1919T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(1): Show |
5 | a0001c0004t0004g0058 a0001c0004t0005g0112 a0001c0004t0005g0134 others(2): Show |
6 | HG03225.hp2 HG03486.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.265+1919_265+1920i others(10): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(2): Show |
19 | a0001c0001t0002g0198 a0001c0001t0002g0201 a0001c0002t0003g0140 others(16): Show |
25 | HG01070.hp2 HG01261.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.265+1919_265+1920i others(11): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(3): Show |
71 | a0001c0001t0002g0005 a0001c0001t0002g0030 a0001c0001t0002g0051 others(68): Show |
147 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.265+1919_265+1920i others(12): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(4): Show |
60 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0029 others(57): Show |
93 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.265+1919_265+1920i others(13): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(5): Show |
14 | a0001c0001t0002g0006 a0001c0001t0002g0221 a0001c0001t0002g0226 others(11): Show |
24 | HG00438.hp2 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.265+1919_265+1920i others(14): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(6): Show |
3 | a0001c0001t0002g0193 a0001c0004t0004g0064 a0001c0010t0004g0069 |
3 | HG01884.hp1 HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.265+1919_265+1920i others(15): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364606 | T | TTTTTTTT others(7): Show |
2 | a0001c0004t0004g0070 a0001c0004t0004g0071 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.265+1919_265+1920i others(16): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364606 | |||||||
| chr2:190364727 | A | G | 1 | a0001c0004t0004g0066 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.266-1968A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364727 | |||||||
| chr2:190364749 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.266-1946T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364749 | |||||||
| chr2:190364793 | G | A | 2 | a0001c0004t0004g0070 a0001c0004t0004g0071 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.266-1902G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364793 | |||||||
| chr2:190364809 | G | T | 173 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(170): Show |
300 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.266-1886G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364809 | |||||||
| chr2:190364811 | C | G | 5 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0198 others(2): Show |
5 | HG00741.hp2 HG01074.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-1884C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190364811 | |||||||
| chr2:190365254 | A | G | 1 | a0001c0004t0017g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.266-1441A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190365254 | |||||||
| chr2:190365331 | A | G | 1 | a0001c0004t0003g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.266-1364A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190365331 | |||||||
| chr2:190365452 | C | T | 3 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0006g0128 |
6 | HG02257.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-1243C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190365452 | |||||||
| chr2:190365620 | T | C | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-1075T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190365620 | |||||||
| chr2:190365857 | CGCTCTCT others(9): Show |
C | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-832_266-817del others(16): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190365857 | ||||||
| chr2:190365918 | T | C | 1 | a0001c0003t0001g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.266-777T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190365918 | |||||||
| chr2:190365959 | TGCTCTCT others(21): Show |
T | 4 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0004t0004g0070 others(1): Show |
4 | HG02630.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-693_266-666del others(28): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190365959 | ||||||
| chr2:190365967 | CTCGCTCT others(37): Show |
C | 176 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(173): Show |
303 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.266-725_266-682del others(44): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190365967 | ||||||
| chr2:190365968 | TCGCTCTC others(41): Show |
T | 1 | a0001c0001t0002g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.266-725_266-678del others(48): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190365968 | ||||||
| chr2:190366020 | T | G | 1 | a0001c0001t0002g0207 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.266-675T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366020 | |||||||
| chr2:190366051 | CTCTCTCT others(1): Show |
C | 6 | a0001c0001t0004g0036 a0001c0001t0004g0117 a0001c0001t0009g0116 others(3): Show |
7 | HG02683.hp2 HG02698.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-630_266-623del others(8): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366051 | ||||||
| chr2:190366059 | GTCTC | G | 171 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(168): Show |
297 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.266-632_266-629del others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366059 | ||||||
| chr2:190366103 | A | T | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-592A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366103 | |||||||
| chr2:190366165 | C | T | 1 | a0001c0010t0004g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.266-530C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366165 | |||||||
| chr2:190366173 | G | GTC | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-518_266-517dup others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366173 | ||||||
| chr2:190366180 | G | GCTCT | 175 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(172): Show |
302 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.266-512_266-509dup others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366180 | ||||||
| chr2:190366194 | G | GCTCT | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-500_266-497dup others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366194 | ||||||
| chr2:190366228 | G | C | 26 | a0001c0004t0003g0012 a0001c0004t0003g0126 a0001c0004t0005g0040 others(23): Show |
35 | HG00642.hp1 HG01261.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.266-467G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366228 | |||||||
| chr2:190366253 | CTCTG | C | 12 | a0001c0004t0005g0040 a0001c0004t0005g0112 a0001c0004t0005g0127 others(9): Show |
13 | HG01261.hp2 HG01891.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.266-438_266-435del others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366253 | ||||||
| chr2:190366275 | G | GTCTC | 176 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(173): Show |
303 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.266-413_266-410dup others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366275 | ||||||
| chr2:190366275 | G | T | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-420G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366275 | |||||||
| chr2:190366283 | CTCGCTCT others(3): Show |
C | 1 | a0001c0004t0004g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-409_266-400del others(10): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366283 | ||||||
| chr2:190366300 | T | G | 1 | a0001c0004t0004g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-395T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366300 | |||||||
| chr2:190366302 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.266-393G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366302 | |||||||
| chr2:190366302 | G | T | 1 | a0001c0004t0004g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-393G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366302 | |||||||
| chr2:190366312 | A | T | 1 | a0001c0004t0004g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-383A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366312 | |||||||
| chr2:190366316 | T | G | 1 | a0001c0004t0004g0146 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.266-379T>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366316 | |||||||
| chr2:190366333 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.266-362C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366333 | |||||||
| chr2:190366334 | G | A | 1 | a0001c0004t0004g0194 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.266-361G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366334 | |||||||
| chr2:190366389 | C | T | 1 | a0001c0001t0002g0227 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.266-306C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366389 | |||||||
| chr2:190366409 | CTCTCACT others(3): Show |
C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(162): Show |
284 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.266-256_266-247del others(10): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366409 | ||||||
| chr2:190366409 | CTCTCACT others(13): Show |
C | 13 | a0001c0001t0003g0013 a0001c0001t0003g0024 a0001c0001t0003g0025 others(10): Show |
21 | HG00438.hp2 HG00673.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.266-266_266-247del others(20): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366409 | ||||||
| chr2:190366458 | GCT | G | 6 | a0001c0004t0004g0060 a0001c0004t0004g0061 a0001c0004t0004g0063 others(3): Show |
6 | HG02258.hp2 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.266-230_266-229del others(2): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 190366458 | ||||||
| chr2:190366481 | T | C | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-214T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366481 | |||||||
| chr2:190366547 | C | A | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.266-148C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366547 | |||||||
| chr2:190366558 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.266-137G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366558 | |||||||
| chr2:190366635 | C | G | 1 | a0001c0002t0008g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.266-60C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 4/6 | chr2 | 190366635 | |||||||
| chr2:190367128 | T | C | 32 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0154 others(29): Show |
50 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.466+233T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367128 | |||||||
| chr2:190367179 | C | A | 182 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(179): Show |
309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.466+284C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367179 | |||||||
| chr2:190367261 | A | G | 178 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(175): Show |
305 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.466+366A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367261 | |||||||
| chr2:190367307 | G | T | 2 | a0001c0002t0001g0032 a0001c0002t0001g0086 |
3 | HG01346.hp2 HG02273.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.466+412G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367307 | |||||||
| chr2:190367405 | G | C | 178 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(175): Show |
305 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.466+510G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367405 | |||||||
| chr2:190367562 | T | A | 2 | a0001c0004t0004g0070 a0001c0004t0004g0071 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.466+667T>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367562 | |||||||
| chr2:190367563 | T | C | 3 | a0001c0003t0001g0050 a0001c0003t0001g0164 a0001c0003t0001g0180 |
3 | HG00639.hp1 HG01099.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.466+668T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367563 | |||||||
| chr2:190367619 | C | G | 3 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0068 |
7 | HG01891.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+724C>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367619 | |||||||
| chr2:190367623 | C | A | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.466+728C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367623 | |||||||
| chr2:190367655 | A | G | 183 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(180): Show |
310 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.466+760A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367655 | |||||||
| chr2:190367666 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.466+771C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367666 | |||||||
| chr2:190367675 | C | T | 1 | a0002c0006t0006g0038 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.466+780C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367675 | |||||||
| chr2:190367885 | G | T | 1 | a0001c0003t0001g0181 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.466+990G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190367885 | |||||||
| chr2:190368005 | C | A | 1 | a0002c0006t0010g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.467-1098C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368005 | |||||||
| chr2:190368198 | T | C | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.467-905T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368198 | |||||||
| chr2:190368292 | A | C | 29 | a0001c0002t0001g0007 a0001c0002t0001g0026 a0001c0002t0001g0154 others(26): Show |
47 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.467-811A>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368292 | |||||||
| chr2:190368449 | G | A | 176 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(173): Show |
303 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.467-654G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368449 | |||||||
| chr2:190368451 | G | A | 1 | a0001c0009t0004g0056 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.467-652G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368451 | |||||||
| chr2:190368526 | G | C | 177 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(174): Show |
304 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.467-577G>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368526 | |||||||
| chr2:190368650 | T | C | 180 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(177): Show |
307 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.467-453T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 5/6 | chr2 | 190368650 | |||||||
| chr2:190369408 | C | T | 1 | a0001c0003t0001g0166 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.641+131C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190369408 | |||||||
| chr2:190369451 | A | G | 1 | a0001c0003t0001g0168 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.641+174A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190369451 | |||||||
| chr2:190369464 | C | A | 53 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0017 others(50): Show |
90 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.641+187C>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190369464 | |||||||
| chr2:190369710 | T | C | 1 | a0001c0004t0004g0064 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.641+433T>C | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190369710 | |||||||
| chr2:190370015 | G | A | 56 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0017 others(53): Show |
99 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.641+738G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370015 | |||||||
| chr2:190370237 | A | G | 1 | a0001c0003t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.642-607A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370237 | |||||||
| chr2:190370243 | CTACT | C | 15 | a0001c0001t0002g0206 a0001c0004t0003g0012 a0001c0004t0003g0126 others(12): Show |
23 | HG00642.hp1 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.642-595_642-592del others(4): Show |
INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 190370243 | ||||||
| chr2:190370269 | C | T | 72 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(69): Show |
125 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.642-575C>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370269 | |||||||
| chr2:190370438 | G | T | 1 | a0001c0004t0004g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.642-406G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370438 | |||||||
| chr2:190370473 | G | T | 1 | a0001c0002t0001g0033 | 2 | NA18955.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.642-371G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370473 | |||||||
| chr2:190370531 | A | G | 1 | a0001c0002t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.642-313A>G | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370531 | |||||||
| chr2:190370659 | G | T | 5 | a0001c0002t0008g0073 a0001c0002t0008g0074 a0001c0002t0008g0075 others(2): Show |
5 | HG01192.hp2 HG02723.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-185G>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370659 | |||||||
| chr2:190370764 | G | A | 2 | a0001c0002t0001g0017 a0001c0002t0001g0078 |
4 | HG02451.hp2 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-80G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370764 | |||||||
| chr2:190370774 | G | A | 1 | a0001c0004t0004g0071 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.642-70G>A | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370774 | |||||||
| chr2:190370810 | A | T | 1 | a0001c0004t0004g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-34A>T | INPP1 | ENSG00000151689.13 | transcript | ENST00000392329.7 | protein_coding | 6/6 | chr2 | 190370810 |