Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27071 |
| ensemblid | ENSG00000070190.13 |
| hgncid | 16500 |
| symbol | DAPP1 |
| name | dual adaptor of phosphotyrosine and 3-phosphoinositides 1 |
| refseq_nuc | NM_014395.3 |
| refseq_prot | NP_055210.2 |
| ensembl_nuc | ENST00000512369.2 |
| ensembl_prot | ENSP00000423602.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 99816827 |
| end | 99870190 |
| strand | + |
| ver | v1.2 |
| region | chr4:99816827-99870190 |
| region5000 | chr4:99811827-99875190 |
| regionname0 | DAPP1_chr4_99816827_99870190 |
| regionname5000 | DAPP1_chr4_99811827_99875190 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 280 | 364 | 86 | 73 | 158 | 12 | 33 | 114 | DAPP1_chr4_99811827_99875190 | DAPP1 | MGRAE others(275): Show |
chr4 | 99811827 | 99875190 |
| a0002 | 0/0 | 280 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | MGRAE others(275): Show |
chr4 | 99811827 | 99875190 |
| a0003 | 0/0 | 280 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | MGRAE others(275): Show |
chr4 | 99811827 | 99875190 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 840 | 272 | 56 | 55 | 123 | 8 | 28 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 | ||
| a0001c0002 | 0/0 | 840 | 90 | 30 | 16 | 35 | 4 | 5 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 | ||
| a0001c0004 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 | ||
| a0001c0005 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 | ||
| a0002c0003 | 0/0 | 840 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 | ||
| a0003c0006 | 0/0 | 840 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | ATGGG others(835): Show |
chr4 | 99811827 | 99875190 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2935 | 145 | 22 | 33 | 68 | 3 | 17 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0002 | 0/0 | 2936 | 56 | 7 | 10 | 36 | 0 | 3 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0005 | 0/0 | 2935 | 18 | 10 | 4 | 3 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0006 | 0/0 | 2935 | 7 | 0 | 2 | 0 | 2 | 3 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0007 | 0/0 | 2935 | 6 | 5 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0008 | 0/0 | 2934 | 5 | 0 | 0 | 5 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2929): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0009 | 0/0 | 2936 | 4 | 0 | 0 | 3 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0010 | 0/0 | 2935 | 4 | 4 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0011 | 0/0 | 2935 | 4 | 0 | 0 | 4 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0013 | 0/0 | 2935 | 3 | 3 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0015 | 0/0 | 2935 | 3 | 3 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0016 | 0/0 | 2935 | 3 | 1 | 1 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0017 | 0/0 | 2936 | 2 | 1 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0018 | 0/0 | 2936 | 2 | 0 | 0 | 0 | 0 | 2 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0019 | 0/0 | 2934 | 2 | 0 | 0 | 0 | 2 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2929): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0020 | 0/0 | 2935 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0021 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0022 | 0/0 | 2935 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0023 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0024 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0025 | 0/0 | 2936 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0001t0028 | 0/0 | 2936 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0003 | 0/0 | 2935 | 52 | 26 | 12 | 6 | 4 | 4 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0004 | 0/0 | 2935 | 29 | 0 | 0 | 29 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0012 | 0/0 | 2936 | 4 | 0 | 4 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2931): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0014 | 0/0 | 2935 | 3 | 2 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0026 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0002t0029 | 0/0 | 2935 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0004t0027 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0001c0005t0001 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0002c0003t0003 | 0/0 | 2935 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| a0003c0006t0003 | 0/0 | 2935 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | GCCAT others(2930): Show |
chr4 | 99811827 | 99875190 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 7 | 2 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0014 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0006g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0007g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0008g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0009g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0010g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0011g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0013g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0015g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0015g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0016g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0016g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0017g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0018g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0018g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0019g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0020g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0021g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0022g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0023g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0024g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0025g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0001t0028g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0005 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0001 | 0/0 | 19 | 0 | 0 | 19 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0012g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0012g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0014g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0014g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0026g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0002t0029g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0004t0027g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0001c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0002c0003t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| a0003c0006t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0019 | g0015 | EUR | GBR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00140 | hp1 | a0001 | c0001 | t0019 | g0015 | EUR | GBR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0043 | EUR | GBR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00408 | hp1 | a0001 | c0001 | t0022 | g0207 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0076 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00558 | hp1 | a0001 | c0001 | t0020 | g0032 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0126 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0075 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0028 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0085 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00673 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00673 | hp2 | a0001 | c0001 | t0028 | g0094 | EAS | CHS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00735 | hp1 | a0001 | c0001 | t0017 | g0048 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00738 | hp1 | a0001 | c0001 | t0024 | g0233 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01070 | hp1 | a0001 | c0002 | t0003 | g0099 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0097 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0100 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0020 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01099 | hp2 | a0002 | c0003 | t0003 | g0011 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0083 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01168 | hp1 | a0001 | c0002 | t0012 | g0001 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01169 | hp2 | a0001 | c0002 | t0012 | g0001 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01192 | hp2 | a0001 | c0005 | t0001 | g0176 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01243 | hp1 | a0001 | c0004 | t0027 | g0055 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01256 | hp2 | a0001 | c0001 | t0016 | g0015 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01257 | hp1 | a0001 | c0001 | t0021 | g0213 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01257 | hp2 | a0001 | c0002 | t0003 | g0077 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0005 | EUR | IBS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0084 | EUR | IBS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0053 | EUR | IBS | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0021 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01891 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01952 | hp1 | a0001 | c0002 | t0012 | g0001 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01981 | hp1 | a0001 | c0001 | t0023 | g0236 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02040 | hp1 | a0001 | c0001 | t0008 | g0125 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0127 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02056 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0031 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0183 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | CDX | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02257 | hp1 | a0001 | c0001 | t0016 | g0054 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0139 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02273 | hp1 | a0001 | c0002 | t0012 | g0071 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0092 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0086 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02523 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02602 | hp1 | a0001 | c0002 | t0014 | g0150 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0121 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0049 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0122 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0034 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0090 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0082 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02809 | hp1 | a0001 | c0001 | t0017 | g0051 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02809 | hp2 | a0001 | c0002 | t0014 | g0228 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0144 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0088 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02897 | hp1 | a0001 | c0002 | t0029 | g0019 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02965 | hp2 | a0001 | c0001 | t0015 | g0191 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0087 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03017 | hp1 | a0001 | c0001 | t0018 | g0146 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0050 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0079 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0078 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0141 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03490 | hp2 | a0001 | c0001 | t0025 | g0208 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0140 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03516 | hp2 | a0001 | c0002 | t0026 | g0158 | AFR | ESN | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03540 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0186 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03831 | hp1 | a0001 | c0001 | t0009 | g0187 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0042 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0027 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0147 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04184 | hp2 | a0003 | c0006 | t0003 | g0020 | SAS | BEB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | STU | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0009 | SAS | STU | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0062 | SAS | STU | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0245 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0098 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | CHB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0019 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18949 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18951 | hp2 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18954 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18956 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18957 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18960 | hp1 | a0001 | c0002 | t0004 | g0091 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0040 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18978 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18991 | hp1 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18994 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18995 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0102 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0069 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19057 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19058 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19062 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19065 | hp1 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19077 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19079 | hp1 | a0001 | c0001 | t0020 | g0032 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19080 | hp1 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19083 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19086 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19088 | hp2 | a0001 | c0001 | t0011 | g0004 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19089 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0041 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | YRI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0244 | AFR | ASW | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ASW | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0009 | EUR | TSI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0005 | EUR | TSI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0080 | EUR | TSI | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02486 | hp1 | a0001 | c0002 | t0003 | g0101 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03471 | hp1 | a0001 | c0002 | t0014 | g0160 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | MSL | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | USA | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0021 | AFR | USA | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | LWK | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0148 | REF | REF | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0201 | REF | REF | DAPP1_chr4_99811827_99875190 | DAPP1 | chr4 | 99811827 | 99875190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99816956 | G | A | 1 | a0002 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.43G>A | p.Asp15Asn | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/9 | 130/2935 | 43/843 | 15/280 | chr4 | 99816956 | |||
| chr4:99840290 | G | T | 1 | a0003 | 1 | HG04184.hp2 | missense_variant&splice_region_variant | MODERATE | c.226G>T | p.Ala76Ser | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/9 | 313/2935 | 226/843 | 76/280 | chr4 | 99840290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99863823 | C | T | 3 | a0001c0002 a0002c0003 a0003c0006 |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
synonymous_variant | LOW | c.654C>T | p.Phe218Phe | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/9 | 741/2935 | 654/843 | 218/280 | chr4 | 99863823 | |||
| chr4:99866076 | C | A | 1 | a0001c0004 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.729C>A | p.Thr243Thr | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/9 | 816/2935 | 729/843 | 243/280 | chr4 | 99866076 | |||
| chr4:99868155 | G | A | 1 | a0001c0005 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.813G>A | p.Thr271Thr | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 900/2935 | 813/843 | 271/280 | chr4 | 99868155 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99816878 | G | T | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(12): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(179): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/9 | 36 | chr4 | 99816878 | ||||||
| chr4:99816908 | G | C | 2 | a0001c0001t0013 a0001c0001t0017 |
5 | HG00735.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-6G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/9 | 6 | chr4 | 99816908 | ||||||
| chr4:99868259 | G | A | 3 | a0001c0001t0016 a0001c0001t0019 a0001c0004t0027 |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*74G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 74 | chr4 | 99868259 | ||||||
| chr4:99868274 | C | T | 1 | a0001c0001t0011 | 4 | HG02056.hp2 NA18957.hp2 NA19080.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 89 | chr4 | 99868274 | ||||||
| chr4:99868341 | C | T | 2 | a0001c0002t0026 a0001c0002t0029 |
2 | HG02897.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*156C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 156 | chr4 | 99868341 | ||||||
| chr4:99868349 | C | T | 2 | a0001c0001t0007 a0001c0001t0010 |
10 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*164C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 164 | chr4 | 99868349 | ||||||
| chr4:99868639 | G | C | 2 | a0001c0002t0004 a0001c0002t0012 |
33 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 454 | chr4 | 99868639 | ||||||
| chr4:99868671 | G | GT | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(6): Show |
76 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*497dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 498 | INFO_REALIGN_3_PRIME | chr4 | 99868671 | |||||
| chr4:99868711 | AG | A | 2 | a0001c0001t0019 a0001c0004t0027 |
3 | HG00099.hp1 HG00140.hp1 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*527delG | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 527 | chr4 | 99868711 | ||||||
| chr4:99868897 | G | A | 1 | a0001c0001t0021 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*712G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 712 | chr4 | 99868897 | ||||||
| chr4:99869057 | C | A | 1 | a0001c0001t0022 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*872C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 872 | chr4 | 99869057 | ||||||
| chr4:99869150 | G | A | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(1): Show |
19 | HG00140.hp2 HG00738.hp2 HG01109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 965 | chr4 | 99869150 | ||||||
| chr4:99869150 | G | T | 1 | a0001c0001t0020 | 2 | HG00558.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*965G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 965 | chr4 | 99869150 | ||||||
| chr4:99869171 | G | A | 8 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0012 others(5): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*986G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 986 | chr4 | 99869171 | ||||||
| chr4:99869344 | C | T | 1 | a0001c0001t0015 | 3 | HG02818.hp1 HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1159C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1159 | chr4 | 99869344 | ||||||
| chr4:99869383 | G | A | 2 | a0001c0001t0006 a0001c0001t0018 |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1198G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1198 | chr4 | 99869383 | ||||||
| chr4:99869407 | C | T | 1 | a0001c0001t0024 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1222C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1222 | chr4 | 99869407 | ||||||
| chr4:99869496 | TTC | T | 1 | a0001c0001t0008 | 5 | HG00558.hp2 HG00597.hp1 HG02040.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1313_*1314delCT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1313 | INFO_REALIGN_3_PRIME | chr4 | 99869496 | |||||
| chr4:99869518 | G | A | 1 | a0001c0001t0022 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1333 | chr4 | 99869518 | ||||||
| chr4:99869657 | C | T | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(2): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1472C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1472 | chr4 | 99869657 | ||||||
| chr4:99869661 | G | C | 1 | a0001c0001t0028 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1476G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1476 | chr4 | 99869661 | ||||||
| chr4:99869924 | C | T | 1 | a0001c0001t0023 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1739C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1739 | chr4 | 99869924 | ||||||
| chr4:99870006 | T | C | 2 | a0001c0001t0019 a0001c0004t0027 |
3 | HG00099.hp1 HG00140.hp1 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1821T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 9/9 | 1821 | chr4 | 99870006 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99817066 | G | T | 2 | a0001c0001t0010g0041 a0001c0001t0010g0245 |
3 | HG02647.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.101+52G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817066 | |||||||
| chr4:99817118 | C | T | 1 | a0001c0002t0003g0244 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101+104C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817118 | |||||||
| chr4:99817240 | T | A | 136 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(133): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.101+226T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817240 | |||||||
| chr4:99817435 | T | C | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
15 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+421T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817435 | |||||||
| chr4:99817608 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.101+594G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817608 | |||||||
| chr4:99817720 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.101+706A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817720 | |||||||
| chr4:99817737 | T | C | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.101+723T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817737 | |||||||
| chr4:99817801 | C | A | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.101+787C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99817801 | |||||||
| chr4:99818024 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.101+1010C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818024 | |||||||
| chr4:99818187 | A | G | 1 | a0001c0001t0001g0241 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.101+1173A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818187 | |||||||
| chr4:99818224 | A | G | 5 | a0001c0001t0013g0049 a0001c0001t0013g0050 a0001c0001t0013g0052 others(2): Show |
5 | HG00735.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+1210A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818224 | |||||||
| chr4:99818303 | A | C | 1 | a0001c0001t0001g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.101+1289A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818303 | |||||||
| chr4:99818391 | G | T | 1 | a0001c0002t0003g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.101+1377G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818391 | |||||||
| chr4:99818736 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.101+1722C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818736 | |||||||
| chr4:99818772 | G | A | 1 | a0001c0001t0002g0057 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.101+1758G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99818772 | |||||||
| chr4:99819023 | C | A | 5 | a0001c0001t0013g0049 a0001c0001t0013g0050 a0001c0001t0013g0052 others(2): Show |
5 | HG00735.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+2009C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819023 | |||||||
| chr4:99819035 | T | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0058 |
4 | NA18956.hp2 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+2021T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819035 | |||||||
| chr4:99819277 | C | T | 135 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(132): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.101+2263C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819277 | |||||||
| chr4:99819376 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+2362C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819376 | |||||||
| chr4:99819407 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG00741.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.101+2393C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819407 | |||||||
| chr4:99819542 | G | A | 1 | a0001c0001t0015g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.101+2528G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819542 | |||||||
| chr4:99819552 | A | C | 133 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(130): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.101+2538A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819552 | |||||||
| chr4:99819554 | G | C | 1 | a0001c0002t0003g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101+2540G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819554 | |||||||
| chr4:99819570 | C | T | 1 | a0001c0001t0013g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101+2556C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819570 | |||||||
| chr4:99819613 | T | G | 117 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(114): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.101+2599T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819613 | |||||||
| chr4:99819679 | C | T | 5 | a0001c0001t0013g0049 a0001c0001t0013g0050 a0001c0001t0013g0052 others(2): Show |
5 | HG00735.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+2665C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819679 | |||||||
| chr4:99819700 | T | TTCAATTA others(302): Show |
10 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(7): Show |
13 | HG00738.hp1 HG02109.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.101+2698_101+2699i others(311): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99819700 | ||||||
| chr4:99819700 | T | TTCAATTA others(303): Show |
3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0023g0236 |
3 | HG01981.hp1 HG03942.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.101+2698_101+2699i others(312): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99819700 | ||||||
| chr4:99819799 | A | G | 2 | a0001c0002t0003g0140 a0001c0002t0003g0141 |
2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101+2785A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819799 | |||||||
| chr4:99819880 | C | T | 1 | a0001c0002t0003g0034 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.101+2866C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819880 | |||||||
| chr4:99819908 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG00741.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.101+2894A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819908 | |||||||
| chr4:99819955 | C | G | 1 | a0001c0002t0014g0228 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.101+2941C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819955 | |||||||
| chr4:99819971 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.101+2957A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99819971 | |||||||
| chr4:99820030 | C | G | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.101+3016C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820030 | |||||||
| chr4:99820084 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+3070G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820084 | |||||||
| chr4:99820339 | C | G | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.101+3325C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820339 | |||||||
| chr4:99820372 | A | G | 66 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(63): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.101+3358A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820372 | |||||||
| chr4:99820402 | A | C | 61 | a0001c0001t0002g0007 a0001c0001t0002g0017 a0001c0001t0002g0064 others(58): Show |
104 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.101+3388A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820402 | |||||||
| chr4:99820417 | C | CAT | 132 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(129): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.101+3404_101+3405i others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99820417 | ||||||
| chr4:99820503 | G | A | 130 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(127): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.101+3489G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820503 | |||||||
| chr4:99820648 | T | G | 125 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(122): Show |
192 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.101+3634T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820648 | |||||||
| chr4:99820770 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.101+3756T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820770 | |||||||
| chr4:99820817 | C | A | 1 | a0001c0001t0007g0022 | 3 | HG02630.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.101+3803C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99820817 | |||||||
| chr4:99821164 | G | A | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.101+4150G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821164 | |||||||
| chr4:99821213 | T | G | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+4199T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821213 | |||||||
| chr4:99821250 | G | C | 1 | a0001c0001t0002g0103 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.101+4236G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821250 | |||||||
| chr4:99821275 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+4261A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821275 | |||||||
| chr4:99821299 | C | T | 59 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(56): Show |
100 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.101+4285C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821299 | |||||||
| chr4:99821330 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.101+4316C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821330 | |||||||
| chr4:99821359 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+4345G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821359 | |||||||
| chr4:99821451 | G | A | 134 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(131): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.101+4437G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821451 | |||||||
| chr4:99821454 | A | G | 1 | a0001c0004t0027g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.101+4440A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821454 | |||||||
| chr4:99821460 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+4446A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821460 | |||||||
| chr4:99821490 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(206): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.101+4476T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821490 | |||||||
| chr4:99821519 | T | G | 1 | a0001c0002t0003g0068 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.101+4505T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821519 | |||||||
| chr4:99821729 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+4715C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821729 | |||||||
| chr4:99821980 | G | A | 1 | a0001c0001t0023g0236 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.101+4966G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821980 | |||||||
| chr4:99821988 | C | A | 129 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(126): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.101+4974C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99821988 | |||||||
| chr4:99822199 | A | G | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.101+5185A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822199 | |||||||
| chr4:99822232 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(16): Show |
24 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.101+5218T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822232 | |||||||
| chr4:99822236 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5222G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822236 | |||||||
| chr4:99822356 | T | G | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.101+5342T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822356 | |||||||
| chr4:99822526 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5512A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822526 | |||||||
| chr4:99822543 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0195 a0001c0001t0001g0196 |
5 | HG02647.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.101+5529A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822543 | |||||||
| chr4:99822647 | T | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5633T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822647 | |||||||
| chr4:99822658 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5644T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822658 | |||||||
| chr4:99822680 | A | T | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.101+5666A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822680 | |||||||
| chr4:99822711 | CA | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5699delA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99822711 | ||||||
| chr4:99822756 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5742T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822756 | |||||||
| chr4:99822844 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5830T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822844 | |||||||
| chr4:99822879 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+5865G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99822879 | |||||||
| chr4:99823049 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+6035G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823049 | |||||||
| chr4:99823164 | G | A | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.101+6150G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823164 | |||||||
| chr4:99823244 | C | A | 116 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(113): Show |
185 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.101+6230C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823244 | |||||||
| chr4:99823297 | T | C | 102 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(99): Show |
166 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.101+6283T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823297 | |||||||
| chr4:99823650 | T | C | 1 | a0001c0001t0007g0117 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.101+6636T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823650 | |||||||
| chr4:99823656 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+6642A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823656 | |||||||
| chr4:99823816 | A | G | 1 | a0001c0002t0003g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.101+6802A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823816 | |||||||
| chr4:99823938 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+6924T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823938 | |||||||
| chr4:99823953 | A | G | 7 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
10 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+6939A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99823953 | |||||||
| chr4:99824103 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.101+7089T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824103 | |||||||
| chr4:99824138 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01106.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.101+7124A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824138 | |||||||
| chr4:99824167 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+7153T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824167 | |||||||
| chr4:99824485 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+7471A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824485 | |||||||
| chr4:99824552 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+7538A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824552 | |||||||
| chr4:99824960 | C | T | 3 | a0001c0001t0002g0138 a0001c0001t0007g0117 a0001c0001t0007g0139 |
3 | HG01109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.101+7946C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824960 | |||||||
| chr4:99824992 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.101+7978C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99824992 | |||||||
| chr4:99825036 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.101+8022C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825036 | |||||||
| chr4:99825181 | G | A | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.101+8167G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825181 | |||||||
| chr4:99825189 | C | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
10 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.101+8175C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825189 | |||||||
| chr4:99825296 | C | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.101+8282C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825296 | |||||||
| chr4:99825302 | G | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(113): Show |
185 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.101+8288G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825302 | |||||||
| chr4:99825317 | T | C | 1 | a0001c0001t0013g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101+8303T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825317 | |||||||
| chr4:99825323 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.101+8309C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825323 | |||||||
| chr4:99825340 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(16): Show |
24 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.101+8326T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825340 | |||||||
| chr4:99825650 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+8636G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825650 | |||||||
| chr4:99825860 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.101+8846A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825860 | |||||||
| chr4:99825902 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+8888C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825902 | |||||||
| chr4:99825977 | T | C | 1 | a0001c0002t0014g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.101+8963T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99825977 | |||||||
| chr4:99826007 | C | T | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.101+8993C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826007 | |||||||
| chr4:99826097 | G | A | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.101+9083G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826097 | |||||||
| chr4:99826104 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG03017.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.101+9090C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826104 | |||||||
| chr4:99826106 | C | A | 5 | a0001c0001t0013g0049 a0001c0001t0013g0050 a0001c0001t0013g0052 others(2): Show |
5 | HG00735.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.101+9092C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826106 | |||||||
| chr4:99826147 | A | G | 1 | a0001c0001t0015g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.101+9133A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826147 | |||||||
| chr4:99826479 | A | G | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-9144A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826479 | |||||||
| chr4:99826605 | C | A | 1 | a0001c0002t0003g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.102-9018C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826605 | |||||||
| chr4:99826649 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102-8974C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826649 | |||||||
| chr4:99826691 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-8932G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826691 | |||||||
| chr4:99826782 | C | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-8841C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826782 | |||||||
| chr4:99826815 | C | T | 134 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(131): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.102-8808C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99826815 | |||||||
| chr4:99827147 | G | C | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-8476G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827147 | |||||||
| chr4:99827208 | C | T | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.102-8415C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827208 | |||||||
| chr4:99827325 | G | A | 10 | a0001c0002t0004g0001 a0001c0002t0004g0018 a0001c0002t0004g0070 others(7): Show |
32 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.102-8298G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827325 | |||||||
| chr4:99827327 | G | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-8296G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827327 | |||||||
| chr4:99827335 | C | G | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-8288C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827335 | |||||||
| chr4:99827362 | G | A | 8 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG00099.hp2 HG01168.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-8261G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827362 | |||||||
| chr4:99827392 | G | T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.102-8231G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827392 | |||||||
| chr4:99827532 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0113 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.102-8081_102-8080i others(17): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827532 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0116 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.102-8081_102-8080i others(18): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827532 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0002g0064 a0001c0001t0005g0111 a0001c0001t0005g0112 |
3 | HG01167.hp2 HG01169.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.102-8081_102-8080i others(19): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827532 | C | CAAAAAAA others(11): Show |
6 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0005g0029 others(3): Show |
7 | HG01361.hp2 HG01891.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-8081_102-8080i others(20): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827532 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0105 a0001c0001t0005g0104 |
2 | HG00741.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.102-8081_102-8080i others(21): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827532 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.102-8081_102-8080i others(22): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827532 | ||||||
| chr4:99827542 | AC | A | 2 | a0001c0001t0001g0010 a0001c0001t0010g0060 |
5 | HG01884.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-8080delC | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827542 | |||||||
| chr4:99827543 | C | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0001t0002g0064 others(14): Show |
19 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.102-8080C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827543 | |||||||
| chr4:99827546 | C | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-8077C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827546 | |||||||
| chr4:99827548 | A | C | 1 | a0001c0004t0027g0055 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.102-8075A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827548 | |||||||
| chr4:99827554 | C | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-8069C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827554 | |||||||
| chr4:99827554 | C | CAAA | 105 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(102): Show |
173 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.102-8067_102-8065d others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99827554 | ||||||
| chr4:99827559 | C | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-8064C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827559 | |||||||
| chr4:99827702 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.102-7921C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827702 | |||||||
| chr4:99827786 | G | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0001c0002t0003g0100 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-7837G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827786 | |||||||
| chr4:99827809 | T | C | 136 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(133): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.102-7814T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827809 | |||||||
| chr4:99827879 | G | A | 7 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
10 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.102-7744G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99827879 | |||||||
| chr4:99828014 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-7609A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828014 | |||||||
| chr4:99828193 | G | A | 41 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(38): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.102-7430G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828193 | |||||||
| chr4:99828198 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.102-7425A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828198 | |||||||
| chr4:99828312 | C | A | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.102-7311C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828312 | |||||||
| chr4:99828354 | G | A | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.102-7269G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828354 | |||||||
| chr4:99828374 | T | C | 1 | a0001c0001t0002g0103 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.102-7249T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828374 | |||||||
| chr4:99828376 | G | T | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-7247G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828376 | |||||||
| chr4:99828379 | C | T | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-7244C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828379 | |||||||
| chr4:99828524 | G | C | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-7099G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828524 | |||||||
| chr4:99828538 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-7085G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828538 | |||||||
| chr4:99828555 | G | A | 1 | a0001c0002t0003g0077 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.102-7068G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828555 | |||||||
| chr4:99828555 | G | T | 33 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(30): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.102-7068G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828555 | |||||||
| chr4:99828858 | T | C | 1 | a0001c0002t0003g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.102-6765T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828858 | |||||||
| chr4:99828985 | G | A | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.102-6638G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99828985 | |||||||
| chr4:99829219 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-6404C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829219 | |||||||
| chr4:99829372 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-6251C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829372 | |||||||
| chr4:99829488 | A | C | 1 | a0001c0002t0004g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.102-6135A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829488 | |||||||
| chr4:99829522 | T | A | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.102-6101T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829522 | |||||||
| chr4:99829558 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-6065G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829558 | |||||||
| chr4:99829565 | G | C | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-6058G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829565 | |||||||
| chr4:99829718 | A | G | 6 | a0001c0001t0005g0063 a0001c0001t0016g0015 a0001c0001t0016g0053 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-5905A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829718 | |||||||
| chr4:99829741 | T | A | 32 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(29): Show |
56 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.102-5882T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829741 | |||||||
| chr4:99829770 | C | CT | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5853_102-5852i others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829770 | |||||||
| chr4:99829792 | T | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5831T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829792 | |||||||
| chr4:99829807 | ACAAT | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5812_102-5809d others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99829807 | ||||||
| chr4:99829884 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5739G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829884 | |||||||
| chr4:99829887 | A | T | 6 | a0001c0001t0005g0063 a0001c0001t0016g0015 a0001c0001t0016g0053 others(3): Show |
7 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-5736A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829887 | |||||||
| chr4:99829902 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5721T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829902 | |||||||
| chr4:99829971 | T | A | 2 | a0001c0002t0003g0099 a0001c0002t0003g0100 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.102-5652T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829971 | |||||||
| chr4:99829972 | C | A | 2 | a0001c0002t0003g0099 a0001c0002t0003g0100 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.102-5651C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829972 | |||||||
| chr4:99829973 | T | A | 2 | a0001c0002t0003g0099 a0001c0002t0003g0100 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.102-5650T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99829973 | |||||||
| chr4:99830105 | C | T | 1 | a0001c0001t0016g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.102-5518C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830105 | |||||||
| chr4:99830106 | G | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-5517G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830106 | |||||||
| chr4:99830120 | C | T | 1 | a0001c0001t0005g0123 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.102-5503C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830120 | |||||||
| chr4:99830178 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5445C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830178 | |||||||
| chr4:99830247 | G | A | 97 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(94): Show |
161 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.102-5376G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830247 | |||||||
| chr4:99830287 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.102-5336G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830287 | |||||||
| chr4:99830347 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5276T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830347 | |||||||
| chr4:99830384 | G | GA | 20 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0002g0064 others(17): Show |
26 | HG00558.hp2 HG00642.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.102-5228dupA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99830384 | ||||||
| chr4:99830449 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-5174G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830449 | |||||||
| chr4:99830536 | G | C | 116 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(113): Show |
185 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.102-5087G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830536 | |||||||
| chr4:99830575 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(16): Show |
24 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-5048A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830575 | |||||||
| chr4:99830640 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.102-4983A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830640 | |||||||
| chr4:99830742 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.102-4881A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830742 | |||||||
| chr4:99830747 | A | T | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-4876A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99830747 | |||||||
| chr4:99831253 | T | C | 61 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(58): Show |
98 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.102-4370T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831253 | |||||||
| chr4:99831266 | A | G | 1 | a0001c0001t0013g0052 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.102-4357A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831266 | |||||||
| chr4:99831343 | A | G | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
69 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.102-4280A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831343 | |||||||
| chr4:99831475 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-4148C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831475 | |||||||
| chr4:99831487 | C | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(16): Show |
24 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-4136C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831487 | |||||||
| chr4:99831495 | A | G | 129 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(126): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.102-4128A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831495 | |||||||
| chr4:99831500 | A | G | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.102-4123A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831500 | |||||||
| chr4:99831601 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.102-4022C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831601 | |||||||
| chr4:99831627 | G | A | 3 | a0001c0002t0003g0026 a0001c0002t0003g0078 a0001c0002t0003g0079 |
4 | HG03195.hp1 HG03225.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-3996G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831627 | |||||||
| chr4:99831634 | C | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-3989C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831634 | |||||||
| chr4:99831647 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.102-3976C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831647 | |||||||
| chr4:99831786 | G | A | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-3837G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831786 | |||||||
| chr4:99831880 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG00741.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.102-3743T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831880 | |||||||
| chr4:99831900 | A | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(16): Show |
24 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.102-3723A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831900 | |||||||
| chr4:99831973 | T | TA | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-3637dupA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99831973 | ||||||
| chr4:99831973 | TA | T | 61 | a0001c0001t0001g0242 a0001c0001t0005g0092 a0001c0001t0005g0093 others(58): Show |
101 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.102-3637delA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99831973 | ||||||
| chr4:99831995 | A | C | 94 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(91): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.102-3628A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99831995 | |||||||
| chr4:99832145 | C | T | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0095 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.102-3478C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832145 | |||||||
| chr4:99832235 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 |
3 | HG00741.hp2 HG01346.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.102-3388G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832235 | |||||||
| chr4:99832370 | A | G | 74 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(71): Show |
116 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.102-3253A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832370 | |||||||
| chr4:99832417 | T | C | 15 | a0001c0001t0002g0064 a0001c0001t0002g0105 a0001c0001t0002g0106 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.102-3206T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832417 | |||||||
| chr4:99832446 | A | C | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-3177A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832446 | |||||||
| chr4:99832505 | C | G | 3 | a0001c0001t0015g0144 a0001c0001t0015g0186 a0001c0001t0015g0191 |
3 | HG02818.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.102-3118C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832505 | |||||||
| chr4:99832656 | T | C | 4 | a0001c0001t0008g0031 a0001c0001t0008g0125 a0001c0001t0008g0126 others(1): Show |
5 | HG00558.hp2 HG00597.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-2967T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832656 | |||||||
| chr4:99832676 | G | A | 80 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(77): Show |
123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.102-2947G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832676 | |||||||
| chr4:99832723 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.102-2900T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832723 | |||||||
| chr4:99832724 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-2899T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832724 | |||||||
| chr4:99832756 | G | A | 2 | a0001c0001t0001g0229 a0001c0002t0003g0080 |
2 | HG04228.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.102-2867G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832756 | |||||||
| chr4:99832874 | A | G | 1 | a0001c0002t0004g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.102-2749A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832874 | |||||||
| chr4:99832951 | C | T | 80 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(77): Show |
123 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.102-2672C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832951 | |||||||
| chr4:99832969 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.102-2654G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832969 | |||||||
| chr4:99832996 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.102-2627G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99832996 | |||||||
| chr4:99833064 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0193 |
2 | HG00639.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.102-2559A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833064 | |||||||
| chr4:99833069 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.102-2554T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833069 | |||||||
| chr4:99833075 | A | G | 2 | a0001c0001t0010g0041 a0001c0001t0010g0245 |
3 | HG02647.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.102-2548A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833075 | |||||||
| chr4:99833303 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102-2320C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833303 | |||||||
| chr4:99833480 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
8 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.102-2143G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833480 | |||||||
| chr4:99833508 | G | T | 93 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0045 others(90): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.102-2115G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833508 | |||||||
| chr4:99833823 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.102-1800C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833823 | |||||||
| chr4:99833824 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.102-1799G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833824 | |||||||
| chr4:99833924 | G | A | 8 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(5): Show |
9 | HG00735.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.102-1699G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833924 | |||||||
| chr4:99833940 | T | G | 14 | a0001c0001t0001g0059 a0001c0001t0002g0105 a0001c0001t0002g0113 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.102-1683T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833940 | |||||||
| chr4:99833950 | C | T | 64 | a0001c0001t0001g0023 a0001c0001t0001g0178 a0001c0001t0001g0179 others(61): Show |
103 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.102-1673C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99833950 | |||||||
| chr4:99834009 | T | A | 1 | a0001c0001t0017g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.102-1614T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834009 | |||||||
| chr4:99834073 | C | A | 5 | a0001c0002t0003g0005 a0001c0002t0003g0027 a0001c0002t0003g0083 others(2): Show |
11 | HG00642.hp1 HG01167.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.102-1550C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834073 | |||||||
| chr4:99834149 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0239 |
2 | NA18978.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.102-1474T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834149 | |||||||
| chr4:99834296 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.102-1327T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834296 | |||||||
| chr4:99834391 | A | AT | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-1219dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99834391 | ||||||
| chr4:99834596 | C | T | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.102-1027C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834596 | |||||||
| chr4:99834597 | G | A | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.102-1026G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834597 | |||||||
| chr4:99834643 | G | T | 1 | a0001c0002t0003g0080 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.102-980G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834643 | |||||||
| chr4:99834918 | C | T | 1 | a0001c0001t0005g0110 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.102-705C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99834918 | |||||||
| chr4:99835012 | AT | A | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.102-597delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99835012 | ||||||
| chr4:99835012 | ATT | A | 6 | a0001c0001t0002g0056 a0001c0001t0005g0063 a0001c0001t0006g0009 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.102-598_102-597del others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 99835012 | ||||||
| chr4:99835094 | C | T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(11): Show |
28 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.102-529C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835094 | |||||||
| chr4:99835133 | C | T | 18 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0059 others(15): Show |
23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.102-490C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835133 | |||||||
| chr4:99835139 | G | T | 14 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(11): Show |
16 | HG00099.hp1 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.102-484G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835139 | |||||||
| chr4:99835223 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102-400G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835223 | |||||||
| chr4:99835265 | T | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0059 others(15): Show |
23 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.102-358T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835265 | |||||||
| chr4:99835349 | A | G | 1 | a0001c0001t0005g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102-274A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835349 | |||||||
| chr4:99835412 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.102-211C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835412 | |||||||
| chr4:99835488 | T | G | 1 | a0001c0002t0004g0070 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.102-135T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 1/8 | chr4 | 99835488 | |||||||
| chr4:99835767 | C | T | 1 | a0001c0002t0003g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.224+22C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99835767 | |||||||
| chr4:99835882 | A | G | 1 | a0001c0001t0006g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.224+137A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99835882 | |||||||
| chr4:99835891 | G | A | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0028g0094 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.224+146G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99835891 | |||||||
| chr4:99836144 | C | T | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+399C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99836144 | |||||||
| chr4:99836268 | C | A | 55 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0028g0094 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.224+523C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99836268 | |||||||
| chr4:99836527 | C | T | 15 | a0001c0001t0001g0059 a0001c0001t0002g0105 a0001c0001t0002g0113 others(12): Show |
16 | HG00642.hp2 HG00741.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.224+782C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99836527 | |||||||
| chr4:99836853 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.224+1108A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99836853 | |||||||
| chr4:99836957 | G | A | 1 | a0001c0001t0010g0041 | 2 | HG02647.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.224+1212G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99836957 | |||||||
| chr4:99837175 | C | T | 3 | a0001c0001t0001g0177 a0001c0002t0014g0150 a0001c0005t0001g0176 |
3 | HG00735.hp2 HG01192.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.224+1430C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837175 | |||||||
| chr4:99837202 | C | T | 7 | a0001c0001t0002g0030 a0001c0001t0002g0064 a0001c0001t0002g0106 others(4): Show |
8 | HG00735.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+1457C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837202 | |||||||
| chr4:99837261 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.224+1516G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837261 | |||||||
| chr4:99837267 | G | T | 38 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(35): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.224+1522G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837267 | |||||||
| chr4:99837349 | A | G | 43 | a0001c0001t0001g0175 a0001c0001t0005g0092 a0001c0001t0005g0093 others(40): Show |
77 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.224+1604A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837349 | |||||||
| chr4:99837400 | G | A | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+1655G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837400 | |||||||
| chr4:99837446 | A | G | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG00140.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.224+1701A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837446 | |||||||
| chr4:99837547 | C | G | 1 | a0001c0002t0003g0244 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224+1802C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837547 | |||||||
| chr4:99837692 | G | A | 3 | a0001c0001t0002g0113 a0001c0001t0002g0115 a0001c0001t0002g0116 |
3 | HG00642.hp2 HG03710.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.224+1947G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837692 | |||||||
| chr4:99837704 | G | A | 35 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(32): Show |
49 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.224+1959G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837704 | |||||||
| chr4:99837712 | T | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(39): Show |
71 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.224+1967T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837712 | |||||||
| chr4:99837844 | T | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(42): Show |
75 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.224+2099T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837844 | |||||||
| chr4:99837991 | T | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
5 | HG01433.hp1 HG01934.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+2246T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99837991 | |||||||
| chr4:99838055 | C | G | 1 | a0001c0002t0003g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.225-2234C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838055 | |||||||
| chr4:99838058 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.225-2231C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838058 | |||||||
| chr4:99838439 | C | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(36): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-1850C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838439 | |||||||
| chr4:99838442 | G | T | 20 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(17): Show |
23 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.225-1847G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838442 | |||||||
| chr4:99838558 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.225-1731G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838558 | |||||||
| chr4:99838765 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.225-1524T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838765 | |||||||
| chr4:99838843 | C | T | 39 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(36): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-1446C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838843 | |||||||
| chr4:99838857 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.225-1432G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838857 | |||||||
| chr4:99838912 | T | C | 51 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(48): Show |
88 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.225-1377T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838912 | |||||||
| chr4:99838967 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | NA18994.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.225-1322G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99838967 | |||||||
| chr4:99839008 | C | T | 61 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(58): Show |
105 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.225-1281C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839008 | |||||||
| chr4:99839040 | G | A | 2 | a0001c0001t0005g0129 a0001c0001t0005g0136 |
2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.225-1249G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839040 | |||||||
| chr4:99839197 | G | GGGTGGA | 59 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(56): Show |
99 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.225-1080_225-1075d others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839197 | ||||||
| chr4:99839357 | A | C | 2 | a0001c0001t0001g0162 a0001c0002t0026g0158 |
2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.225-932A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839357 | |||||||
| chr4:99839367 | ATATAGAT others(3): Show |
A | 23 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(20): Show |
27 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.225-912_225-903del others(10): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839367 | ||||||
| chr4:99839369 | A | ATAGATAT others(8): Show |
2 | a0001c0001t0010g0041 a0001c0001t0010g0245 |
3 | HG02647.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.225-913_225-912ins others(15): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839369 | ||||||
| chr4:99839369 | A | ATAGATAT others(18): Show |
2 | a0001c0001t0002g0007 a0001c0001t0002g0067 |
6 | HG02155.hp2 HG03927.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-913_225-912ins others(25): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839369 | ||||||
| chr4:99839377 | C | A | 89 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(86): Show |
152 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.225-912C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839377 | |||||||
| chr4:99839382 | G | GAT | 4 | a0001c0001t0002g0007 a0001c0001t0002g0067 a0001c0001t0010g0041 others(1): Show |
9 | HG02155.hp2 HG02647.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-899_225-898dup others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839382 | ||||||
| chr4:99839389 | ATAGAT | A | 3 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 |
3 | HG02615.hp1 HG02622.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.225-894_225-890del others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 99839389 | ||||||
| chr4:99839430 | A | G | 1 | a0001c0001t0002g0134 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.225-859A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839430 | |||||||
| chr4:99839449 | C | T | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-840C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839449 | |||||||
| chr4:99839522 | C | T | 39 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(36): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-767C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839522 | |||||||
| chr4:99839559 | C | T | 2 | a0001c0001t0008g0031 a0001c0001t0008g0125 |
3 | HG00558.hp2 HG02040.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.225-730C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839559 | |||||||
| chr4:99839698 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(36): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.225-591A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839698 | |||||||
| chr4:99839769 | T | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
7 | HG02622.hp1 HG02647.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-520T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839769 | |||||||
| chr4:99839828 | G | A | 59 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(56): Show |
99 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.225-461G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839828 | |||||||
| chr4:99839900 | A | G | 1 | a0001c0001t0005g0129 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.225-389A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99839900 | |||||||
| chr4:99840011 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-278T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99840011 | |||||||
| chr4:99840068 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-221G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99840068 | |||||||
| chr4:99840219 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-70G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99840219 | |||||||
| chr4:99840225 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-64A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 2/8 | chr4 | 99840225 | |||||||
| chr4:99840553 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+131A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99840553 | |||||||
| chr4:99840599 | T | C | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.358+177T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99840599 | |||||||
| chr4:99840616 | AT | A | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+197delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99840616 | ||||||
| chr4:99840903 | A | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+481A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99840903 | |||||||
| chr4:99840932 | G | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
18 | HG00738.hp1 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.358+510G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99840932 | |||||||
| chr4:99841322 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+900T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841322 | |||||||
| chr4:99841536 | A | G | 8 | a0001c0001t0001g0156 a0001c0001t0001g0212 a0001c0001t0001g0224 others(5): Show |
8 | HG01074.hp2 HG01106.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+1114A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841536 | |||||||
| chr4:99841626 | A | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0023 others(169): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.358+1204A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841626 | |||||||
| chr4:99841646 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1224G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841646 | |||||||
| chr4:99841843 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1421A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841843 | |||||||
| chr4:99841932 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1510G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841932 | |||||||
| chr4:99841978 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1556G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841978 | |||||||
| chr4:99841987 | A | G | 1 | a0001c0002t0003g0034 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.358+1565A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99841987 | |||||||
| chr4:99842122 | G | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(114): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.358+1700G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842122 | |||||||
| chr4:99842145 | T | C | 8 | a0001c0001t0010g0041 a0001c0001t0010g0060 a0001c0001t0010g0245 others(5): Show |
10 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+1723T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842145 | |||||||
| chr4:99842421 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+1999T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842421 | |||||||
| chr4:99842423 | G | C | 7 | a0001c0001t0001g0059 a0001c0001t0005g0095 a0001c0001t0005g0096 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+2001G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842423 | |||||||
| chr4:99842477 | T | TA | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG00099.hp2 HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.358+2056dupA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99842477 | ||||||
| chr4:99842664 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(36): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.358+2242A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842664 | |||||||
| chr4:99842738 | C | T | 11 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
12 | HG00642.hp2 HG00735.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.358+2316C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842738 | |||||||
| chr4:99842826 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+2404T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842826 | |||||||
| chr4:99842832 | TGAAGTAC others(117): Show |
T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.358+2429_358+2552d others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99842832 | ||||||
| chr4:99842852 | C | CT | 6 | a0001c0001t0001g0223 a0001c0001t0001g0231 a0001c0001t0002g0012 others(3): Show |
6 | HG02622.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+2447dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99842852 | ||||||
| chr4:99842852 | C | CTT | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+2446_358+2447d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99842852 | ||||||
| chr4:99842852 | CT | C | 5 | a0001c0001t0001g0002 a0001c0001t0007g0022 a0001c0002t0003g0005 others(2): Show |
8 | HG01496.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+2447delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99842852 | ||||||
| chr4:99842952 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.358+2530C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99842952 | |||||||
| chr4:99843109 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.358+2687C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843109 | |||||||
| chr4:99843135 | C | T | 1 | a0001c0002t0003g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.358+2713C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843135 | |||||||
| chr4:99843151 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | HG03239.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.358+2729G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843151 | |||||||
| chr4:99843322 | G | A | 1 | a0001c0002t0003g0102 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.358+2900G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843322 | |||||||
| chr4:99843598 | T | C | 4 | a0001c0001t0001g0212 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG01106.hp1 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+3176T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843598 | |||||||
| chr4:99843818 | G | T | 1 | a0001c0001t0005g0129 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.358+3396G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843818 | |||||||
| chr4:99843894 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+3472C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99843894 | |||||||
| chr4:99844131 | G | T | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.358+3709G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99844131 | |||||||
| chr4:99844483 | C | T | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.358+4061C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99844483 | |||||||
| chr4:99844591 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.358+4169A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99844591 | |||||||
| chr4:99844825 | G | C | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+4403G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99844825 | |||||||
| chr4:99845141 | G | C | 1 | a0001c0001t0002g0130 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.358+4719G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845141 | |||||||
| chr4:99845373 | T | C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0134 |
6 | NA18957.hp1 NA18962.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+4951T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845373 | |||||||
| chr4:99845451 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.358+5029C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845451 | |||||||
| chr4:99845458 | G | T | 2 | a0001c0001t0007g0117 a0001c0001t0007g0139 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.358+5036G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845458 | |||||||
| chr4:99845682 | C | A | 1 | a0001c0001t0005g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.358+5260C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845682 | |||||||
| chr4:99845913 | G | A | 1 | a0001c0002t0012g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.358+5491G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99845913 | |||||||
| chr4:99846033 | T | C | 1 | a0001c0001t0002g0105 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.358+5611T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846033 | |||||||
| chr4:99846374 | A | G | 1 | a0001c0001t0007g0022 | 3 | HG02630.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.358+5952A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846374 | |||||||
| chr4:99846487 | G | T | 3 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 |
3 | HG02615.hp1 HG02622.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.358+6065G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846487 | |||||||
| chr4:99846578 | A | T | 1 | a0001c0001t0002g0133 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358+6156A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846578 | |||||||
| chr4:99846597 | C | T | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.358+6175C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846597 | |||||||
| chr4:99846746 | T | C | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.358+6324T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846746 | |||||||
| chr4:99846790 | T | A | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.358+6368T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99846790 | |||||||
| chr4:99847001 | A | T | 2 | a0001c0001t0005g0129 a0001c0001t0005g0136 |
2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.359-6217A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847001 | |||||||
| chr4:99847007 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-6211G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847007 | |||||||
| chr4:99847188 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.359-6030T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847188 | |||||||
| chr4:99847257 | G | A | 52 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(49): Show |
89 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.359-5961G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847257 | |||||||
| chr4:99847396 | A | G | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-5822A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847396 | |||||||
| chr4:99847415 | A | AC | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-5803_359-5802i others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847415 | |||||||
| chr4:99847489 | A | G | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.359-5729A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847489 | |||||||
| chr4:99847496 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-5722C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847496 | |||||||
| chr4:99847799 | A | AGTTT | 18 | a0001c0001t0001g0162 a0001c0001t0002g0007 a0001c0001t0002g0017 others(15): Show |
26 | HG00438.hp2 HG01243.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.359-5390_359-5387d others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99847799 | ||||||
| chr4:99847799 | A | AGTTTGTT others(1): Show |
35 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0012 others(32): Show |
55 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.359-5394_359-5387d others(10): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99847799 | ||||||
| chr4:99847799 | A | AGTTTGTT others(5): Show |
5 | a0001c0001t0002g0057 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG00408.hp2 HG01109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-5398_359-5387d others(14): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99847799 | ||||||
| chr4:99847799 | AGTTTGTT others(1): Show |
A | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-5394_359-5387d others(10): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99847799 | ||||||
| chr4:99847938 | C | T | 119 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(116): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.359-5280C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847938 | |||||||
| chr4:99847976 | G | A | 1 | a0001c0001t0017g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.359-5242G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99847976 | |||||||
| chr4:99848029 | G | C | 1 | a0001c0002t0014g0150 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.359-5189G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848029 | |||||||
| chr4:99848101 | G | A | 11 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
12 | HG00642.hp2 HG00735.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-5117G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848101 | |||||||
| chr4:99848103 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.359-5115G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848103 | |||||||
| chr4:99848160 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.359-5058G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848160 | |||||||
| chr4:99848230 | A | AT | 56 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(53): Show |
96 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.359-4973dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99848230 | ||||||
| chr4:99848230 | A | ATT | 20 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(17): Show |
24 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.359-4974_359-4973d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99848230 | ||||||
| chr4:99848283 | A | G | 11 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
12 | HG00642.hp2 HG00735.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-4935A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848283 | |||||||
| chr4:99848283 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0210 a0001c0001t0001g0211 |
4 | HG02165.hp1 NA18947.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-4935A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848283 | |||||||
| chr4:99848320 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.359-4898C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848320 | |||||||
| chr4:99848431 | G | A | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.359-4787G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848431 | |||||||
| chr4:99848521 | G | A | 1 | a0001c0001t0018g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.359-4697G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848521 | |||||||
| chr4:99848545 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.359-4673T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848545 | |||||||
| chr4:99848611 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.359-4607G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848611 | |||||||
| chr4:99848674 | T | A | 1 | a0001c0001t0007g0120 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.359-4544T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848674 | |||||||
| chr4:99848678 | C | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-4540C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99848678 | |||||||
| chr4:99849100 | ATTTAG | A | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 others(1): Show |
4 | HG00735.hp2 HG01515.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-4112_359-4108d others(7): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99849100 | ||||||
| chr4:99849257 | G | A | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.359-3961G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849257 | |||||||
| chr4:99849277 | C | T | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.359-3941C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849277 | |||||||
| chr4:99849297 | C | T | 42 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(39): Show |
76 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.359-3921C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849297 | |||||||
| chr4:99849342 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.359-3876G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849342 | |||||||
| chr4:99849470 | G | A | 9 | a0001c0002t0003g0019 a0001c0002t0003g0081 a0001c0002t0003g0082 others(6): Show |
10 | HG02451.hp1 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.359-3748G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849470 | |||||||
| chr4:99849513 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.359-3705G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849513 | |||||||
| chr4:99849539 | G | A | 117 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(114): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.359-3679G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849539 | |||||||
| chr4:99849593 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.359-3625G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849593 | |||||||
| chr4:99849665 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-3553G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849665 | |||||||
| chr4:99849801 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.359-3417G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849801 | |||||||
| chr4:99849849 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.359-3369C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99849849 | |||||||
| chr4:99850147 | C | T | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.359-3071C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850147 | |||||||
| chr4:99850238 | C | T | 54 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(51): Show |
88 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.359-2980C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850238 | |||||||
| chr4:99850267 | C | T | 11 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
12 | HG00642.hp2 HG00735.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.359-2951C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850267 | |||||||
| chr4:99850325 | G | A | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.359-2893G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850325 | |||||||
| chr4:99850364 | C | T | 3 | a0001c0002t0003g0020 a0001c0002t0003g0102 a0003c0006t0003g0020 |
4 | HG01074.hp1 HG04184.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-2854C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850364 | |||||||
| chr4:99850431 | G | T | 6 | a0001c0001t0001g0149 a0001c0001t0001g0151 a0001c0001t0001g0152 others(3): Show |
6 | HG00099.hp2 HG01168.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-2787G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850431 | |||||||
| chr4:99850587 | A | G | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.359-2631A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850587 | |||||||
| chr4:99850738 | C | T | 36 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(33): Show |
61 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.359-2480C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850738 | |||||||
| chr4:99850844 | ATATGT | A | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-2370_359-2366d others(7): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99850844 | ||||||
| chr4:99850952 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.359-2266G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99850952 | |||||||
| chr4:99851227 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.359-1991T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851227 | |||||||
| chr4:99851252 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.359-1966G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851252 | |||||||
| chr4:99851363 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-1855C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851363 | |||||||
| chr4:99851399 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.359-1819C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851399 | |||||||
| chr4:99851446 | T | C | 8 | a0001c0001t0010g0041 a0001c0001t0010g0060 a0001c0001t0010g0245 others(5): Show |
10 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.359-1772T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851446 | |||||||
| chr4:99851527 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.359-1691T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851527 | |||||||
| chr4:99851534 | G | GT | 53 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0059 others(50): Show |
84 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(81): Show |
intron_variant | MODIFIER | c.359-1660dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99851534 | ||||||
| chr4:99851534 | G | GTT | 13 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(10): Show |
21 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.359-1661_359-1660d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99851534 | ||||||
| chr4:99851534 | G | GTTT | 5 | a0001c0001t0006g0044 a0001c0001t0016g0015 a0001c0001t0016g0053 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-1662_359-1660d others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99851534 | ||||||
| chr4:99851534 | GT | G | 28 | a0001c0001t0001g0038 a0001c0001t0001g0167 a0001c0001t0001g0169 others(25): Show |
43 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.359-1660delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99851534 | ||||||
| chr4:99851534 | GTT | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(5): Show |
18 | HG01884.hp2 HG01975.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.359-1661_359-1660d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 99851534 | ||||||
| chr4:99851618 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-1600G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851618 | |||||||
| chr4:99851626 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.359-1592C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851626 | |||||||
| chr4:99851664 | C | T | 1 | a0001c0001t0021g0213 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.359-1554C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99851664 | |||||||
| chr4:99852136 | A | G | 1 | a0001c0002t0004g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.359-1082A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852136 | |||||||
| chr4:99852139 | A | G | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-1079A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852139 | |||||||
| chr4:99852191 | A | G | 4 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG00099.hp2 HG02258.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-1027A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852191 | |||||||
| chr4:99852351 | A | T | 1 | a0001c0001t0017g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.359-867A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852351 | |||||||
| chr4:99852405 | T | A | 8 | a0001c0001t0010g0041 a0001c0001t0010g0060 a0001c0001t0010g0245 others(5): Show |
10 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.359-813T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852405 | |||||||
| chr4:99852493 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.359-725C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852493 | |||||||
| chr4:99852517 | C | A | 53 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(50): Show |
90 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.359-701C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852517 | |||||||
| chr4:99852593 | A | G | 51 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(48): Show |
87 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.359-625A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99852593 | |||||||
| chr4:99853129 | C | G | 1 | a0001c0001t0002g0033 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.359-89C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 3/8 | chr4 | 99853129 | |||||||
| chr4:99853375 | GCT | G | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+33_489+34delTC | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99853375 | ||||||
| chr4:99853420 | A | G | 1 | a0001c0002t0003g0244 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+72A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99853420 | |||||||
| chr4:99853481 | G | A | 11 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(8): Show |
12 | HG00642.hp2 HG00735.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+133G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99853481 | |||||||
| chr4:99853687 | C | T | 4 | a0001c0001t0002g0030 a0001c0001t0002g0064 a0001c0001t0002g0106 others(1): Show |
5 | HG02818.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+339C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99853687 | |||||||
| chr4:99853959 | A | C | 1 | a0001c0001t0010g0245 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.489+611A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99853959 | |||||||
| chr4:99854005 | T | A | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.489+657T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854005 | |||||||
| chr4:99854023 | A | G | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.489+675A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854023 | |||||||
| chr4:99854633 | CTG | C | 29 | a0001c0001t0002g0030 a0001c0001t0002g0056 a0001c0001t0002g0064 others(26): Show |
37 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.489+1288_489+1289d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99854633 | ||||||
| chr4:99854643 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.489+1295T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854643 | |||||||
| chr4:99854910 | T | A | 1 | a0001c0001t0005g0108 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+1562T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854910 | |||||||
| chr4:99854968 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.489+1620A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854968 | |||||||
| chr4:99854970 | A | G | 120 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(117): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.489+1622A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99854970 | |||||||
| chr4:99855060 | G | A | 3 | a0001c0001t0015g0144 a0001c0001t0015g0186 a0001c0001t0015g0191 |
3 | HG02818.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.489+1712G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855060 | |||||||
| chr4:99855095 | G | A | 55 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.489+1747G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855095 | |||||||
| chr4:99855233 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.489+1885C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855233 | |||||||
| chr4:99855359 | G | A | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.489+2011G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855359 | |||||||
| chr4:99855671 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.489+2323A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855671 | |||||||
| chr4:99855683 | T | C | 1 | a0001c0001t0002g0058 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.489+2335T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855683 | |||||||
| chr4:99855778 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.489+2430G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855778 | |||||||
| chr4:99855827 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.489+2479G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99855827 | |||||||
| chr4:99856107 | T | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
7 | HG02155.hp1 NA18953.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+2759T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856107 | |||||||
| chr4:99856301 | G | A | 1 | a0001c0001t0002g0030 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.489+2953G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856301 | |||||||
| chr4:99856314 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0205 others(6): Show |
15 | HG00408.hp1 HG02056.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2966G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856314 | |||||||
| chr4:99856320 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.489+2972G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856320 | |||||||
| chr4:99856466 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.489+3118G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856466 | |||||||
| chr4:99856576 | G | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.489+3228G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856576 | |||||||
| chr4:99856588 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.489+3240A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856588 | |||||||
| chr4:99856617 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.489+3269C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856617 | |||||||
| chr4:99856717 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.489+3369A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856717 | |||||||
| chr4:99856800 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(115): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.489+3452A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856800 | |||||||
| chr4:99856806 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(115): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.489+3458A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99856806 | |||||||
| chr4:99857061 | A | G | 1 | a0001c0002t0003g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.489+3713A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857061 | |||||||
| chr4:99857078 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0138 |
2 | HG01975.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.489+3730A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857078 | |||||||
| chr4:99857236 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.489+3888G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857236 | |||||||
| chr4:99857254 | G | A | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.489+3906G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857254 | |||||||
| chr4:99857479 | A | T | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.490-4099A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857479 | |||||||
| chr4:99857699 | TATACACA others(3): Show |
T | 2 | a0001c0001t0018g0146 a0001c0001t0018g0147 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.490-3877_490-3868d others(12): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857699 | ||||||
| chr4:99857701 | T | C | 19 | a0001c0001t0001g0024 a0001c0001t0001g0195 a0001c0001t0001g0196 others(16): Show |
39 | HG00140.hp2 HG00423.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.490-3877T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857701 | |||||||
| chr4:99857701 | T | TAC | 24 | a0001c0001t0001g0003 a0001c0001t0001g0059 a0001c0001t0001g0151 others(21): Show |
26 | HG00099.hp2 HG00609.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-3843_490-3842d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | T | TACAC | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0232 others(1): Show |
4 | HG01192.hp2 HG01515.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-3845_490-3842d others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | T | TATACAC | 3 | a0001c0001t0002g0033 a0001c0001t0002g0118 a0001c0001t0002g0124 |
3 | HG01123.hp1 HG01952.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.490-3876_490-3875i others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | T | TATACACA others(3): Show |
1 | a0001c0001t0002g0033 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.490-3876_490-3875i others(12): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | TAC | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0165 others(12): Show |
20 | HG00738.hp1 HG01255.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.490-3843_490-3842d others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | TACAC | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0025 others(19): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.490-3845_490-3842d others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | TACACAC | T | 4 | a0001c0001t0007g0022 a0001c0001t0007g0117 a0001c0001t0007g0120 others(1): Show |
6 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3847_490-3842d others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | TACACACA others(3): Show |
T | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3851_490-3842d others(12): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857701 | TACACACA others(7): Show |
T | 3 | a0001c0002t0003g0028 a0001c0002t0003g0068 a0001c0002t0003g0244 |
3 | NA18978.hp2 NA18979.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.490-3855_490-3842d others(16): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99857701 | ||||||
| chr4:99857703 | C | T | 34 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(31): Show |
56 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.490-3875C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857703 | |||||||
| chr4:99857705 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0002g0128 |
2 | HG03209.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.490-3873C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857705 | |||||||
| chr4:99857707 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(1): Show |
7 | HG00642.hp2 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-3871C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857707 | |||||||
| chr4:99857709 | C | T | 4 | a0001c0001t0007g0022 a0001c0001t0007g0117 a0001c0001t0007g0120 others(1): Show |
6 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3869C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857709 | |||||||
| chr4:99857713 | C | T | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3865C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857713 | |||||||
| chr4:99857871 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.490-3707T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857871 | |||||||
| chr4:99857913 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-3665G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857913 | |||||||
| chr4:99857960 | T | C | 1 | a0001c0001t0005g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.490-3618T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99857960 | |||||||
| chr4:99858139 | A | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0001c0002t0003g0100 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-3439A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858139 | |||||||
| chr4:99858237 | G | T | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-3341G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858237 | |||||||
| chr4:99858388 | C | G | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-3190C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858388 | |||||||
| chr4:99858503 | CAGG | C | 2 | a0001c0001t0007g0022 a0001c0001t0007g0120 |
4 | HG02630.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-3074_490-3072d others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858503 | |||||||
| chr4:99858896 | AT | A | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2670delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 99858896 | ||||||
| chr4:99858897 | T | A | 2 | a0001c0002t0004g0001 a0001c0002t0004g0018 |
4 | HG00673.hp1 HG02523.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.490-2681T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858897 | |||||||
| chr4:99858968 | C | T | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.490-2610C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858968 | |||||||
| chr4:99858983 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.490-2595C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99858983 | |||||||
| chr4:99859079 | A | G | 55 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.490-2499A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859079 | |||||||
| chr4:99859086 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.490-2492T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859086 | |||||||
| chr4:99859177 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.490-2401A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859177 | |||||||
| chr4:99859509 | G | A | 5 | a0001c0001t0016g0015 a0001c0001t0016g0053 a0001c0001t0016g0054 others(2): Show |
6 | HG00099.hp1 HG00140.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.490-2069G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859509 | |||||||
| chr4:99859600 | T | C | 1 | a0001c0002t0003g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-1978T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859600 | |||||||
| chr4:99859616 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.490-1962G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859616 | |||||||
| chr4:99859955 | C | A | 3 | a0001c0001t0015g0144 a0001c0001t0015g0186 a0001c0001t0015g0191 |
3 | HG02818.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.490-1623C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99859955 | |||||||
| chr4:99860023 | C | G | 46 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(43): Show |
72 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.490-1555C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860023 | |||||||
| chr4:99860061 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0170 |
3 | HG01261.hp2 HG01433.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.490-1517T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860061 | |||||||
| chr4:99860394 | G | A | 5 | a0001c0001t0002g0105 a0001c0001t0002g0114 a0001c0001t0005g0029 others(2): Show |
6 | HG00741.hp1 HG01106.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-1184G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860394 | |||||||
| chr4:99860440 | C | T | 118 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(115): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.490-1138C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860440 | |||||||
| chr4:99860515 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-1063A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860515 | |||||||
| chr4:99860680 | G | T | 1 | a0001c0001t0005g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.490-898G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860680 | |||||||
| chr4:99860880 | T | C | 55 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.490-698T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860880 | |||||||
| chr4:99860886 | C | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0035 others(26): Show |
42 | HG00609.hp1 HG01071.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.490-692C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860886 | |||||||
| chr4:99860887 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.490-691C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860887 | |||||||
| chr4:99860898 | G | A | 3 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0014g0160 |
3 | HG03453.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-680G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99860898 | |||||||
| chr4:99861005 | G | T | 4 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(1): Show |
7 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-573G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99861005 | |||||||
| chr4:99861020 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.490-558C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99861020 | |||||||
| chr4:99861518 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.490-60G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99861518 | |||||||
| chr4:99861524 | A | G | 40 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
64 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.490-54A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 4/8 | chr4 | 99861524 | |||||||
| chr4:99861931 | C | T | 1 | a0001c0001t0007g0117 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+306C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99861931 | |||||||
| chr4:99862185 | C | T | 1 | a0001c0001t0008g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.537+560C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862185 | |||||||
| chr4:99862211 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.537+586A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862211 | |||||||
| chr4:99862376 | T | C | 1 | a0001c0002t0003g0083 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.538-634T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862376 | |||||||
| chr4:99862442 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.538-568A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862442 | |||||||
| chr4:99862564 | A | C | 1 | a0001c0001t0005g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.538-446A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862564 | |||||||
| chr4:99862744 | A | ATTATT | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(239): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.538-263_538-262ins others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 99862744 | ||||||
| chr4:99862845 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.538-165G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862845 | |||||||
| chr4:99862874 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.538-136G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862874 | |||||||
| chr4:99862961 | T | G | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-49T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99862961 | |||||||
| chr4:99863006 | T | G | 6 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(3): Show |
9 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.538-4T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 5/8 | chr4 | 99863006 | |||||||
| chr4:99863185 | A | C | 1 | a0001c0002t0003g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.600+113A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | chr4 | 99863185 | |||||||
| chr4:99863199 | T | C | 1 | a0001c0002t0003g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.600+127T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | chr4 | 99863199 | |||||||
| chr4:99863495 | ATGAGAGA others(40): Show |
A | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.601-274_601-228del others(47): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | chr4 | 99863495 | |||||||
| chr4:99863633 | T | C | 4 | a0001c0002t0003g0140 a0001c0002t0003g0141 a0001c0002t0014g0160 others(1): Show |
4 | HG02809.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-137T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | chr4 | 99863633 | |||||||
| chr4:99863718 | G | GT | 35 | a0001c0001t0001g0198 a0001c0001t0001g0230 a0001c0001t0002g0006 others(32): Show |
51 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.601-35dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 99863718 | ||||||
| chr4:99863718 | G | GTT | 8 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0017 others(5): Show |
16 | HG00438.hp2 HG00735.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-36_601-35dupTT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 99863718 | ||||||
| chr4:99863718 | GT | G | 16 | a0001c0001t0001g0047 a0001c0001t0010g0041 a0001c0001t0010g0060 others(13): Show |
18 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.601-35delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 99863718 | ||||||
| chr4:99864060 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.686+205T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864060 | |||||||
| chr4:99864070 | T | C | 7 | a0001c0001t0007g0022 a0001c0001t0007g0117 a0001c0001t0007g0120 others(4): Show |
10 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.686+215T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864070 | |||||||
| chr4:99864238 | A | T | 55 | a0001c0002t0003g0005 a0001c0002t0003g0011 a0001c0002t0003g0019 others(52): Show |
92 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.686+383A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864238 | |||||||
| chr4:99864408 | C | T | 1 | a0001c0001t0025g0208 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.686+553C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864408 | |||||||
| chr4:99864420 | A | C | 1 | a0001c0002t0003g0085 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.686+565A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864420 | |||||||
| chr4:99864823 | C | T | 1 | a0001c0001t0009g0040 | 2 | NA18945.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.686+968C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99864823 | |||||||
| chr4:99865217 | C | A | 1 | a0001c0001t0017g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.687-817C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865217 | |||||||
| chr4:99865285 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.687-749G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865285 | |||||||
| chr4:99865447 | A | G | 1 | a0001c0001t0001g0010 | 4 | HG01884.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.687-587A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865447 | |||||||
| chr4:99865542 | G | A | 1 | a0001c0001t0005g0121 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.687-492G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865542 | |||||||
| chr4:99865805 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-229A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865805 | |||||||
| chr4:99865810 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-224T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865810 | |||||||
| chr4:99865811 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-223A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865811 | |||||||
| chr4:99865814 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-220T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865814 | |||||||
| chr4:99865817 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-217A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865817 | |||||||
| chr4:99865820 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-214T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865820 | |||||||
| chr4:99865828 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-206C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865828 | |||||||
| chr4:99865835 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-199A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865835 | |||||||
| chr4:99865840 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-194C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865840 | |||||||
| chr4:99865842 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-192T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865842 | |||||||
| chr4:99865845 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-189C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865845 | |||||||
| chr4:99865851 | C | CTGTAGAG others(7): Show |
1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-183_687-182ins others(14): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865851 | |||||||
| chr4:99865855 | T | A | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-179T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865855 | |||||||
| chr4:99865856 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-178A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865856 | |||||||
| chr4:99865858 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-176C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865858 | |||||||
| chr4:99865859 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-175A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865859 | |||||||
| chr4:99865860 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-174A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865860 | |||||||
| chr4:99865862 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-172T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865862 | |||||||
| chr4:99865865 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-169T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865865 | |||||||
| chr4:99865867 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-167T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865867 | |||||||
| chr4:99865869 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-165T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865869 | |||||||
| chr4:99865870 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-164C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865870 | |||||||
| chr4:99865871 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-163C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865871 | |||||||
| chr4:99865872 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-162C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865872 | |||||||
| chr4:99865873 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-161T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865873 | |||||||
| chr4:99865876 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-158C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865876 | |||||||
| chr4:99865877 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-157A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865877 | |||||||
| chr4:99865878 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-156A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865878 | |||||||
| chr4:99865879 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-155T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865879 | |||||||
| chr4:99865880 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-154A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865880 | |||||||
| chr4:99865881 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-153C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865881 | |||||||
| chr4:99865883 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-151C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865883 | |||||||
| chr4:99865885 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-149A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865885 | |||||||
| chr4:99865886 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-148A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865886 | |||||||
| chr4:99865888 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-146T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865888 | |||||||
| chr4:99865895 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-139C>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865895 | |||||||
| chr4:99865896 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-138A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865896 | |||||||
| chr4:99865897 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-137A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865897 | |||||||
| chr4:99865898 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-136C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865898 | |||||||
| chr4:99865899 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-135T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865899 | |||||||
| chr4:99865900 | A | AAT | 3 | a0001c0001t0001g0178 a0001c0001t0001g0189 a0001c0001t0001g0220 |
3 | HG00621.hp1 HG03669.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.687-110_687-109dup others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865900 | A | AATAT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0035 others(17): Show |
33 | HG00609.hp1 HG01071.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.687-112_687-109dup others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865900 | A | AATATAT | 3 | a0001c0001t0001g0143 a0001c0001t0001g0172 a0001c0001t0001g0243 |
3 | HG01175.hp1 HG02071.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.687-114_687-109dup others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865900 | A | AATATATA others(1): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG01934.hp1 NA19077.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.687-116_687-109dup others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865900 | AAT | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
91 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.687-110_687-109del others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865900 | AATAT | A | 40 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
64 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.687-112_687-109del others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865900 | ||||||
| chr4:99865914 | TA | T | 7 | a0001c0001t0001g0059 a0001c0001t0005g0095 a0001c0001t0005g0096 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.687-119delA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865914 | |||||||
| chr4:99865916 | T | TATA | 63 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(60): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.687-117_687-115dup others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865916 | ||||||
| chr4:99865917 | A | AT | 2 | a0001c0001t0010g0041 a0001c0001t0010g0245 |
3 | HG02647.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.687-116dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865917 | ||||||
| chr4:99865917 | A | ATAATATA others(15): Show |
7 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(4): Show |
12 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-115_687-114ins others(22): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865917 | ||||||
| chr4:99865917 | A | ATATATAA others(40): Show |
1 | a0001c0001t0022g0207 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.687-111_687-110ins others(47): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865917 | ||||||
| chr4:99865921 | A | T | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-113A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865921 | |||||||
| chr4:99865924 | T | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0195 a0001c0001t0007g0117 others(2): Show |
5 | HG00735.hp1 HG01109.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.687-110T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865924 | |||||||
| chr4:99865925 | A | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(5): Show |
13 | HG01192.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.687-109A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865925 | |||||||
| chr4:99865928 | A | ATAT | 63 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(60): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.687-105_687-103dup others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865928 | ||||||
| chr4:99865933 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-101T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865933 | |||||||
| chr4:99865934 | A | T | 64 | a0001c0001t0001g0163 a0001c0001t0002g0064 a0001c0001t0002g0106 others(61): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.687-100A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865934 | |||||||
| chr4:99865940 | T | TATATAA | 7 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(4): Show |
12 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-94_687-93insAT others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865940 | |||||||
| chr4:99865940 | TTATATTA others(25): Show |
T | 1 | a0001c0001t0002g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.687-88_687-57delTA others(30): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865940 | ||||||
| chr4:99865945 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-89T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865945 | |||||||
| chr4:99865945 | T | TATATAA | 3 | a0001c0001t0006g0009 a0001c0001t0006g0043 a0001c0001t0006g0044 |
6 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-89_687-88insAT others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865945 | |||||||
| chr4:99865945 | T | TATATAAT others(3): Show |
58 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(55): Show |
95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.687-89_687-88insAT others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865945 | |||||||
| chr4:99865946 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(4): Show |
12 | HG01884.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.687-88T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865946 | |||||||
| chr4:99865952 | T | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 others(64): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.687-82T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865952 | |||||||
| chr4:99865952 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-82T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865952 | |||||||
| chr4:99865952 | T | TA | 3 | a0001c0001t0006g0009 a0001c0001t0006g0043 a0001c0001t0006g0044 |
6 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-82_687-81insA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865952 | |||||||
| chr4:99865953 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.687-81T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865953 | |||||||
| chr4:99865957 | T | TATATAA | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.687-77_687-76insAT others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865957 | |||||||
| chr4:99865957 | T | TATATAAT others(1): Show |
2 | a0001c0001t0010g0041 a0001c0001t0010g0245 |
3 | HG02647.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.687-77_687-76insAT others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865957 | |||||||
| chr4:99865957 | T | TATATAAT others(3): Show |
1 | a0001c0001t0006g0042 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.687-77_687-76insAT others(8): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865957 | |||||||
| chr4:99865957 | T | TATATATA | 2 | a0001c0001t0007g0022 a0001c0001t0007g0120 |
4 | HG02630.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-77_687-76insAT others(5): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865957 | |||||||
| chr4:99865958 | T | A | 61 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(58): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.687-76T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865958 | |||||||
| chr4:99865960 | T | TATA | 58 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(55): Show |
95 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.687-73_687-71dupAT others(1): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865960 | ||||||
| chr4:99865962 | T | TA | 3 | a0001c0001t0006g0009 a0001c0001t0006g0043 a0001c0001t0006g0044 |
6 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.687-71dupA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865962 | ||||||
| chr4:99865966 | T | A | 11 | a0001c0001t0006g0042 a0001c0001t0007g0022 a0001c0001t0007g0117 others(8): Show |
14 | HG01109.hp1 HG02040.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.687-68T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865966 | |||||||
| chr4:99865966 | T | TTA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0192 a0001c0001t0001g0222 others(5): Show |
8 | HG00408.hp1 HG01167.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-47_687-46dupTA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865966 | ||||||
| chr4:99865966 | T | TTATA | 24 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0143 others(21): Show |
34 | HG00609.hp1 HG00621.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.687-49_687-46dupTA others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865966 | ||||||
| chr4:99865966 | T | TTATATA | 6 | a0001c0001t0001g0023 a0001c0001t0001g0180 a0001c0001t0001g0182 others(3): Show |
8 | NA18953.hp2 NA18972.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.687-51_687-46dupTA others(4): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865966 | ||||||
| chr4:99865966 | TTA | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0061 a0001c0002t0003g0034 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-47_687-46delTA | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865966 | ||||||
| chr4:99865967 | T | A | 44 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0002g0006 others(41): Show |
71 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.687-67T>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865967 | |||||||
| chr4:99865968 | A | T | 5 | a0001c0001t0001g0162 a0001c0001t0001g0166 a0001c0001t0006g0009 others(2): Show |
8 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.687-66A>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | chr4 | 99865968 | |||||||
| chr4:99865970 | A | AT | 4 | a0001c0001t0007g0022 a0001c0001t0007g0117 a0001c0001t0007g0120 others(1): Show |
6 | HG01109.hp1 HG02257.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.687-63dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865970 | ||||||
| chr4:99865970 | A | ATAATATA others(15): Show |
1 | a0001c0001t0008g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.687-62_687-61insAT others(20): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865970 | ||||||
| chr4:99865970 | A | ATAATATA others(1): Show |
3 | a0001c0001t0010g0041 a0001c0001t0010g0060 a0001c0001t0010g0245 |
4 | HG02451.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-62_687-61insAT others(6): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865970 | ||||||
| chr4:99865970 | A | ATATAATA others(17): Show |
39 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(36): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.687-60_687-59insAT others(22): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865970 | ||||||
| chr4:99865970 | A | ATATAT | 59 | a0001c0001t0002g0064 a0001c0001t0002g0106 a0001c0001t0002g0107 others(56): Show |
96 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.687-63_687-59dupTA others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 99865970 | ||||||
| chr4:99866309 | A | G | 3 | a0001c0001t0002g0016 a0001c0001t0002g0058 a0001c0001t0002g0131 |
5 | NA18956.hp2 NA18960.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+188A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866309 | |||||||
| chr4:99866508 | T | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.774+387T>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866508 | |||||||
| chr4:99866512 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.774+391A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866512 | |||||||
| chr4:99866513 | G | T | 44 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.774+392G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866513 | |||||||
| chr4:99866514 | A | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.774+393A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866514 | |||||||
| chr4:99866538 | T | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0058 |
4 | NA18956.hp2 NA18961.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+417T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866538 | |||||||
| chr4:99866756 | C | A | 1 | a0001c0002t0003g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.774+635C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866756 | |||||||
| chr4:99866766 | A | AT | 7 | a0001c0001t0001g0159 a0001c0001t0001g0177 a0001c0001t0001g0180 others(4): Show |
7 | HG00735.hp2 HG02647.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.774+666dupT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 99866766 | ||||||
| chr4:99866766 | AT | A | 64 | a0001c0001t0001g0143 a0001c0001t0001g0173 a0001c0001t0001g0212 others(61): Show |
103 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.774+666delT | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 99866766 | ||||||
| chr4:99866766 | ATT | A | 10 | a0001c0001t0006g0009 a0001c0001t0006g0042 a0001c0001t0006g0043 others(7): Show |
15 | HG00140.hp2 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.774+665_774+666del others(2): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 99866766 | ||||||
| chr4:99866766 | ATTT | A | 42 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(39): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.774+664_774+666del others(3): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 99866766 | ||||||
| chr4:99866766 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.774+657_774+666del others(10): Show |
DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 99866766 | ||||||
| chr4:99866843 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.774+722C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866843 | |||||||
| chr4:99866903 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.774+782G>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866903 | |||||||
| chr4:99866982 | G | T | 3 | a0001c0001t0010g0041 a0001c0001t0010g0060 a0001c0001t0010g0245 |
4 | HG02451.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+861G>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99866982 | |||||||
| chr4:99867065 | C | T | 4 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0001c0002t0003g0100 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+944C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867065 | |||||||
| chr4:99867085 | A | G | 3 | a0001c0001t0005g0121 a0001c0001t0005g0122 a0001c0001t0005g0123 |
3 | HG02615.hp1 HG02622.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.774+964A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867085 | |||||||
| chr4:99867328 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0061 |
7 | HG01884.hp2 HG02258.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-789A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867328 | |||||||
| chr4:99867387 | T | C | 4 | a0001c0002t0003g0021 a0001c0002t0003g0099 a0001c0002t0003g0100 others(1): Show |
6 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-730T>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867387 | |||||||
| chr4:99867400 | A | C | 1 | a0001c0002t0003g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.775-717A>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867400 | |||||||
| chr4:99867642 | A | G | 44 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(41): Show |
68 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.775-475A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867642 | |||||||
| chr4:99867747 | G | C | 6 | a0001c0001t0002g0030 a0001c0001t0002g0064 a0001c0001t0002g0105 others(3): Show |
7 | HG00741.hp1 HG01106.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-370G>C | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867747 | |||||||
| chr4:99867805 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.775-312C>A | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867805 | |||||||
| chr4:99867926 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.775-191C>T | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867926 | |||||||
| chr4:99867943 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.775-174A>G | DAPP1 | ENSG00000070190.13 | transcript | ENST00000512369.2 | protein_coding | 8/8 | chr4 | 99867943 |