Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5664 |
| ensemblid | ENSG00000143801.18 |
| hgncid | 9509 |
| symbol | PSEN2 |
| name | presenilin 2 |
| refseq_nuc | NM_000447.3 |
| refseq_prot | NP_000438.2 |
| ensembl_nuc | ENST00000366783.8 |
| ensembl_prot | ENSP00000355747.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 226870616 |
| end | 226896098 |
| strand | + |
| ver | v1.2 |
| region | chr1:226870616-226896098 |
| region5000 | chr1:226865616-226901098 |
| regionname0 | PSEN2_chr1_226870616_226896098 |
| regionname5000 | PSEN2_chr1_226865616_226901098 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 448 | 410 | 88 | 70 | 192 | 18 | 40 | 153 | PSEN2_chr1_226865616_226901098 | PSEN2 | MLTFM others(443): Show |
chr1 | 226865616 | 226901098 |
| a0002 | 0/0 | 448 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | MLTFM others(443): Show |
chr1 | 226865616 | 226901098 |
| a0003 | 0/0 | 448 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | MLTFM others(443): Show |
chr1 | 226865616 | 226901098 |
| a0004 | 0/0 | 448 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | MLTFM others(443): Show |
chr1 | 226865616 | 226901098 |
| a0005 | 0/0 | 448 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | MLTFM others(443): Show |
chr1 | 226865616 | 226901098 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1344 | 175 | 31 | 34 | 85 | 8 | 16 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0002 | 1/0 | 1344 | 96 | 8 | 22 | 52 | 5 | 8 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0003 | 0/0 | 1344 | 72 | 18 | 7 | 34 | 2 | 11 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0004 | 0/0 | 1344 | 20 | 0 | 4 | 13 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0005 | 0/0 | 1344 | 14 | 12 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0006 | 0/0 | 1344 | 9 | 8 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0007 | 0/0 | 1344 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0008 | 0/0 | 1344 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0009 | 0/0 | 1344 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0012 | 0/0 | 1344 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0013 | 0/0 | 1344 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0015 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0016 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0017 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0018 | 0/0 | 1344 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0019 | 0/0 | 1344 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0021 | 0/0 | 1344 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0001c0022 | 0/0 | 1344 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0002c0010 | 0/0 | 1344 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0003c0011 | 0/0 | 1344 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0004c0014 | 0/0 | 1344 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 | ||
| a0005c0020 | 0/0 | 1344 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | ATGCT others(1339): Show |
chr1 | 226865616 | 226901098 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2249 | 172 | 30 | 34 | 84 | 7 | 16 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0001t0010 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0001t0012 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0001t0014 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0002t0002 | 0/0 | 2249 | 30 | 7 | 6 | 15 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0002t0003 | 0/0 | 2249 | 62 | 0 | 16 | 35 | 5 | 6 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0002t0007 | 1/0 | 2249 | 2 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0002t0011 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0002t0017 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0003t0002 | 0/0 | 2249 | 56 | 8 | 6 | 32 | 2 | 8 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0003t0004 | 0/0 | 2249 | 11 | 9 | 1 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0003t0007 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0003t0008 | 0/0 | 2249 | 3 | 0 | 0 | 0 | 0 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0003t0015 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0004t0004 | 0/0 | 2249 | 19 | 0 | 4 | 13 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0004t0016 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0005t0004 | 0/0 | 2249 | 7 | 7 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0005t0005 | 0/0 | 2249 | 7 | 5 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0006t0002 | 0/0 | 2249 | 9 | 8 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0007t0006 | 0/0 | 2249 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0008t0002 | 0/0 | 2249 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0009t0002 | 0/0 | 2249 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0012t0002 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0013t0001 | 0/0 | 2249 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0015t0004 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0016t0009 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0017t0009 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0018t0001 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0019t0001 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0021t0001 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0001c0022t0002 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0002c0010t0001 | 0/0 | 2249 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0003c0011t0004 | 0/0 | 2249 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0004c0014t0013 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| a0005c0020t0001 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | GCGTA others(2244): Show |
chr1 | 226865616 | 226901098 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 44 | 3 | 7 | 30 | 1 | 3 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0005 | 0/0 | 16 | 0 | 3 | 13 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0007 | 0/0 | 11 | 0 | 4 | 6 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0009 | 0/0 | 8 | 1 | 2 | 0 | 0 | 5 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0010 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0011 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0001t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0004 | 0/0 | 16 | 0 | 5 | 9 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0002 | 0/0 | 27 | 0 | 5 | 17 | 1 | 4 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0008 | 0/0 | 10 | 0 | 7 | 0 | 3 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0007g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0002t0017g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0003 | 0/0 | 20 | 0 | 2 | 13 | 0 | 5 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0006 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0017 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0021 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0008g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0008g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0003t0015g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0013 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0004t0016g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0005t0004g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0005t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0005t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0005t0005g0014 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0005t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0006t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0006t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0006t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0006t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0007t0006g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0007t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0008t0002g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0008t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0009t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0009t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0012t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0013t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0015t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0016t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0017t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0018t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0021t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0001c0022t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0002c0010t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0002c0010t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0003c0011t0004g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0004c0014t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| a0005c0020t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0021 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00280 | hp1 | a0001 | c0002 | t0003 | g0143 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00323 | hp2 | a0001 | c0001 | t0010 | g0113 | EUR | FIN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00423 | hp1 | a0001 | c0008 | t0002 | g0019 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00558 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0039 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01074 | hp2 | a0001 | c0004 | t0004 | g0156 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01106 | hp1 | a0001 | c0003 | t0002 | g0017 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0027 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0014 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01169 | hp1 | a0001 | c0005 | t0005 | g0014 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0039 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0008 | AMR | PUR | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01257 | hp1 | a0001 | c0002 | t0003 | g0130 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01358 | hp1 | a0001 | c0004 | t0004 | g0025 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0136 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0052 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01516 | hp1 | a0001 | c0013 | t0001 | g0012 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0002 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01517 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01517 | hp2 | a0001 | c0013 | t0001 | g0012 | EUR | IBS | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01891 | hp1 | a0001 | c0006 | t0002 | g0024 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01891 | hp2 | a0001 | c0006 | t0002 | g0015 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0051 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01934 | hp2 | a0001 | c0004 | t0004 | g0025 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01952 | hp1 | a0001 | c0004 | t0004 | g0025 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0008 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01993 | hp2 | a0001 | c0018 | t0001 | g0012 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02004 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02027 | hp1 | a0001 | c0004 | t0004 | g0155 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02027 | hp2 | a0002 | c0010 | t0001 | g0159 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02055 | hp1 | a0001 | c0007 | t0006 | g0018 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02071 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02083 | hp2 | a0001 | c0003 | t0015 | g0003 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0169 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02145 | hp2 | a0001 | c0009 | t0002 | g0123 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CDX | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02257 | hp2 | a0001 | c0005 | t0005 | g0066 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02280 | hp1 | a0001 | c0007 | t0006 | g0018 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02451 | hp2 | a0001 | c0005 | t0004 | g0164 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02572 | hp2 | a0001 | c0003 | t0007 | g0071 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02615 | hp2 | a0001 | c0016 | t0009 | g0046 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02622 | hp1 | a0001 | c0005 | t0004 | g0020 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02622 | hp2 | a0001 | c0006 | t0002 | g0015 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02630 | hp1 | a0001 | c0006 | t0002 | g0015 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02647 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02698 | hp1 | a0001 | c0004 | t0004 | g0149 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02717 | hp1 | a0001 | c0005 | t0004 | g0020 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02723 | hp1 | a0001 | c0005 | t0004 | g0042 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02723 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02735 | hp2 | a0001 | c0004 | t0004 | g0150 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02738 | hp2 | a0001 | c0006 | t0002 | g0122 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02809 | hp1 | a0001 | c0005 | t0004 | g0020 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0162 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0165 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02886 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02896 | hp2 | a0003 | c0011 | t0004 | g0041 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02922 | hp2 | a0001 | c0006 | t0002 | g0126 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02965 | hp2 | a0001 | c0009 | t0002 | g0015 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02970 | hp1 | a0001 | c0009 | t0002 | g0015 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02976 | hp1 | a0001 | c0003 | t0004 | g0043 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0062 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0131 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03098 | hp1 | a0001 | c0006 | t0002 | g0024 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03098 | hp2 | a0004 | c0014 | t0013 | g0047 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03130 | hp1 | a0001 | c0007 | t0006 | g0018 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03139 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0166 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0067 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03225 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0043 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0163 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03453 | hp2 | a0001 | c0007 | t0006 | g0100 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0017 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03490 | hp1 | a0001 | c0003 | t0008 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0059 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03516 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | ESN | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03540 | hp1 | a0001 | c0002 | t0017 | g0125 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0161 | AFR | GWD | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03579 | hp2 | a0001 | c0006 | t0002 | g0024 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03654 | hp1 | a0003 | c0011 | t0004 | g0041 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0054 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0144 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03831 | hp1 | a0005 | c0020 | t0001 | g0012 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03834 | hp2 | a0001 | c0004 | t0016 | g0116 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0171 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04184 | hp1 | a0001 | c0003 | t0008 | g0058 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04184 | hp2 | a0001 | c0022 | t0002 | g0004 | SAS | BEB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04204 | hp2 | a0001 | c0003 | t0008 | g0003 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18522 | hp1 | a0001 | c0005 | t0004 | g0042 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0160 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18747 | hp2 | a0001 | c0004 | t0004 | g0152 | EAS | CHB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18906 | hp2 | a0001 | c0005 | t0005 | g0014 | AFR | YRI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18943 | hp1 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18944 | hp1 | a0001 | c0012 | t0002 | g0028 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18944 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18949 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18957 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18959 | hp2 | a0002 | c0010 | t0001 | g0158 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18962 | hp1 | a0001 | c0002 | t0007 | g0114 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18963 | hp2 | a0001 | c0003 | t0004 | g0154 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18966 | hp2 | a0001 | c0008 | t0002 | g0019 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18969 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18971 | hp1 | a0001 | c0008 | t0002 | g0019 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18972 | hp1 | a0001 | c0004 | t0004 | g0147 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18975 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18976 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18976 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0138 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18983 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18992 | hp1 | a0001 | c0008 | t0002 | g0119 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18992 | hp2 | a0001 | c0019 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18995 | hp2 | a0001 | c0004 | t0004 | g0148 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18997 | hp1 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18998 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19002 | hp1 | a0001 | c0004 | t0004 | g0151 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19003 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19005 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19007 | hp1 | a0001 | c0002 | t0011 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19007 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19009 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19012 | hp2 | a0001 | c0004 | t0004 | g0153 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0167 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19056 | hp1 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19057 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19062 | hp1 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0006 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19064 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19067 | hp1 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19072 | hp1 | a0001 | c0003 | t0002 | g0021 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19078 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19078 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19080 | hp2 | a0001 | c0004 | t0004 | g0013 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19083 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19084 | hp1 | a0001 | c0008 | t0002 | g0019 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19088 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19090 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19090 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA19091 | hp2 | a0001 | c0012 | t0002 | g0028 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20752 | hp2 | a0001 | c0021 | t0001 | g0012 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | CLM | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02109 | hp1 | a0001 | c0015 | t0004 | g0168 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0020 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | ACB | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03471 | hp1 | a0001 | c0006 | t0002 | g0015 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG06807 | hp1 | a0001 | c0007 | t0006 | g0018 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20300 | hp1 | a0001 | c0017 | t0009 | g0045 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | USA | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0007 | g0082 | REF | REF | PSEN2_chr1_226865616_226901098 | PSEN2 | chr1 | 226865616 | 226901098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226882007 | G | A | 1 | a0002 | 2 | HG02027.hp2 NA18959.hp2 |
missense_variant | MODERATE | c.100G>A | p.Gly34Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 483/2249 | 100/1347 | 34/448 | chr1 | 226882007 | |||
| chr1:226883725 | G | C | 1 | a0004 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.162G>C | p.Glu54Asp | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 545/2249 | 162/1347 | 54/448 | chr1 | 226883725 | |||
| chr1:226883748 | G | A | 1 | a0003 | 2 | HG02896.hp2 HG03654.hp1 |
missense_variant | MODERATE | c.185G>A | p.Arg62His | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 568/2249 | 185/1347 | 62/448 | chr1 | 226883748 | |||
| chr1:226888112 | A | G | 1 | a0005 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.520A>G | p.Met174Val | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/13 | 903/2249 | 520/1347 | 174/448 | chr1 | 226888112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226881976 | T | C | 17 | a0001c0001 a0001c0003 a0001c0004 others(14): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
synonymous_variant | LOW | c.69T>C | p.Ala23Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 452/2249 | 69/1347 | 23/448 | chr1 | 226881976 | |||
| chr1:226882036 | C | T | 8 | a0001c0001 a0001c0007 a0001c0013 others(5): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
synonymous_variant | LOW | c.129C>T | p.Asn43Asn | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 512/2249 | 129/1347 | 43/448 | chr1 | 226882036 | |||
| chr1:226882039 | T | A | 1 | a0001c0009 | 3 | HG02145.hp2 HG02965.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.132T>A | p.Thr44Thr | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/13 | 515/2249 | 132/1347 | 44/448 | chr1 | 226882039 | |||
| chr1:226883824 | C | T | 8 | a0001c0001 a0001c0007 a0001c0013 others(5): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
synonymous_variant | LOW | c.261C>T | p.His87His | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 644/2249 | 261/1347 | 87/448 | chr1 | 226883824 | |||
| chr1:226883863 | C | T | 1 | a0001c0021 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.300C>T | p.Ile100Ile | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/13 | 683/2249 | 300/1347 | 100/448 | chr1 | 226883863 | |||
| chr1:226885622 | C | T | 2 | a0001c0016 a0001c0017 |
2 | HG02615.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.441C>T | p.Ser147Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/13 | 824/2249 | 441/1347 | 147/448 | chr1 | 226885622 | |||
| chr1:226888901 | A | G | 1 | a0001c0022 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.639A>G | p.Ala213Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1022/2249 | 639/1347 | 213/448 | chr1 | 226888901 | |||
| chr1:226888970 | T | C | 5 | a0001c0006 a0001c0009 a0001c0015 others(2): Show |
15 | HG01891.hp1 HG01891.hp2 HG01993.hp2 others(12): Show |
synonymous_variant | LOW | c.708T>C | p.Ser236Ser | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1091/2249 | 708/1347 | 236/448 | chr1 | 226888970 | |||
| chr1:226889018 | G | C | 1 | a0001c0013 | 2 | HG01516.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.756G>C | p.Ala252Ala | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/13 | 1139/2249 | 756/1347 | 252/448 | chr1 | 226889018 | |||
| chr1:226890039 | C | G | 1 | a0001c0012 | 2 | NA18944.hp1 NA19091.hp2 |
synonymous_variant | LOW | c.792C>G | p.Leu264Leu | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/13 | 1175/2249 | 792/1347 | 264/448 | chr1 | 226890039 | |||
| chr1:226890108 | C | T | 2 | a0001c0004 a0001c0008 |
25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
synonymous_variant | LOW | c.861C>T | p.Pro287Pro | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/13 | 1244/2249 | 861/1347 | 287/448 | chr1 | 226890108 | |||
| chr1:226891294 | G | T | 2 | a0001c0005 a0001c0017 |
15 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(12): Show |
synonymous_variant | LOW | c.903G>T | p.Thr301Thr | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/13 | 1286/2249 | 903/1347 | 301/448 | chr1 | 226891294 | |||
| chr1:226894110 | C | T | 2 | a0001c0007 a0004c0014 |
6 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.1176C>T | p.Phe392Phe | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/13 | 1559/2249 | 1176/1347 | 392/448 | chr1 | 226894110 | |||
| chr1:226895549 | C | T | 1 | a0001c0019 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.1317C>T | p.Asp439Asp | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 1700/2249 | 1317/1347 | 439/448 | chr1 | 226895549 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226870643 | A | G | 21 | a0001c0001t0014 a0001c0002t0002 a0001c0002t0003 others(18): Show |
218 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(215): Show |
5_prime_UTR_variant | MODIFIER | c.-356A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/13 | 11265 | chr1 | 226870643 | ||||||
| chr1:226871273 | A | G | 2 | a0001c0016t0009 a0001c0017t0009 |
2 | HG02615.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-338A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10635 | chr1 | 226871273 | ||||||
| chr1:226871283 | C | G | 1 | a0001c0001t0012 | 1 | NA19067.hp1 | 5_prime_UTR_variant | MODIFIER | c.-328C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10625 | chr1 | 226871283 | ||||||
| chr1:226871314 | A | C | 1 | a0001c0002t0017 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-297A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10594 | chr1 | 226871314 | ||||||
| chr1:226871336 | C | T | 3 | a0001c0002t0003 a0001c0002t0011 a0001c0004t0016 |
64 | HG00280.hp1 HG00621.hp1 HG00738.hp2 others(61): Show |
5_prime_UTR_variant | MODIFIER | c.-275C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/13 | 10572 | chr1 | 226871336 | ||||||
| chr1:226875489 | T | C | 1 | a0001c0001t0010 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6419 | chr1 | 226875489 | ||||||
| chr1:226875507 | A | G | 1 | a0001c0003t0015 | 1 | HG02083.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6401 | chr1 | 226875507 | ||||||
| chr1:226875528 | C | T | 7 | a0001c0003t0004 a0001c0004t0004 a0001c0004t0016 others(4): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/13 | 6380 | chr1 | 226875528 | ||||||
| chr1:226895849 | C | T | 10 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0012 others(7): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 270 | chr1 | 226895849 | ||||||
| chr1:226895984 | G | T | 2 | a0001c0007t0006 a0004c0014t0013 |
6 | HG02055.hp1 HG02280.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*405G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 405 | chr1 | 226895984 | ||||||
| chr1:226896066 | G | C | 1 | a0001c0003t0008 | 3 | HG03490.hp1 HG04184.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*487G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 13/13 | 487 | chr1 | 226896066 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:226870697 | G | T | 1 | a0001c0003t0002g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-350+48G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870697 | |||||||
| chr1:226870717 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-350+68T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870717 | |||||||
| chr1:226870739 | T | G | 23 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0021 others(20): Show |
57 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.-350+90T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870739 | |||||||
| chr1:226870945 | C | T | 1 | a0001c0002t0002g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-350+296C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226870945 | |||||||
| chr1:226871055 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-349-207T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871055 | |||||||
| chr1:226871112 | C | G | 12 | a0001c0003t0002g0162 a0001c0003t0004g0027 a0001c0003t0004g0043 others(9): Show |
19 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-349-150C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871112 | |||||||
| chr1:226871125 | C | T | 3 | a0001c0003t0002g0017 a0001c0003t0002g0160 a0001c0003t0002g0161 |
7 | HG01106.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-349-137C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871125 | |||||||
| chr1:226871176 | G | A | 3 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-349-86G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 1/12 | chr1 | 226871176 | |||||||
| chr1:226871664 | T | G | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-207+260T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871664 | |||||||
| chr1:226871702 | G | A | 2 | a0001c0005t0005g0014 a0001c0005t0005g0066 |
7 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207+298G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871702 | |||||||
| chr1:226871905 | C | G | 106 | a0001c0001t0001g0026 a0001c0001t0001g0157 a0001c0002t0002g0004 others(103): Show |
231 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.-207+501C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226871905 | |||||||
| chr1:226872034 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-207+630C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872034 | |||||||
| chr1:226872038 | G | C | 50 | a0001c0001t0014g0067 a0001c0002t0002g0004 a0001c0002t0002g0036 others(47): Show |
114 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-207+634G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872038 | |||||||
| chr1:226872082 | G | A | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
22 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-207+678G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872082 | |||||||
| chr1:226872083 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-207+679G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872083 | |||||||
| chr1:226872092 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-207+688T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872092 | |||||||
| chr1:226872227 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-207+823G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872227 | |||||||
| chr1:226872329 | A | G | 3 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-207+925A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872329 | |||||||
| chr1:226872641 | C | T | 49 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(46): Show |
113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-207+1237C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872641 | |||||||
| chr1:226872730 | A | T | 1 | a0001c0003t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-207+1326A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872730 | |||||||
| chr1:226872789 | A | C | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-207+1385A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872789 | |||||||
| chr1:226872811 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-207+1407C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872811 | |||||||
| chr1:226872842 | A | G | 1 | a0001c0001t0010g0113 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-207+1438A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872842 | |||||||
| chr1:226872943 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-207+1539C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872943 | |||||||
| chr1:226872975 | T | C | 104 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(101): Show |
227 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.-207+1571T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226872975 | |||||||
| chr1:226873016 | A | T | 1 | a0001c0002t0002g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-207+1612A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873016 | |||||||
| chr1:226873107 | G | A | 1 | a0001c0002t0003g0117 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-207+1703G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873107 | |||||||
| chr1:226873164 | C | G | 1 | a0001c0002t0002g0145 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-207+1760C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873164 | |||||||
| chr1:226873177 | C | CA | 13 | a0001c0001t0001g0072 a0001c0002t0002g0004 a0001c0002t0002g0036 others(10): Show |
32 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.-207+1786dupA | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 226873177 | ||||||
| chr1:226873177 | CA | C | 14 | a0001c0001t0001g0111 a0001c0003t0004g0027 a0001c0003t0004g0043 others(11): Show |
26 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.-207+1786delA | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 226873177 | ||||||
| chr1:226873425 | T | A | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-206-1940T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873425 | |||||||
| chr1:226873465 | G | A | 2 | a0001c0004t0004g0147 a0001c0004t0004g0148 |
2 | NA18972.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-206-1900G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873465 | |||||||
| chr1:226873513 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-206-1852T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873513 | |||||||
| chr1:226873604 | C | T | 26 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0038 others(23): Show |
64 | HG00280.hp1 HG00621.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.-206-1761C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873604 | |||||||
| chr1:226873721 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0103 others(7): Show |
20 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.-206-1644A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873721 | |||||||
| chr1:226873784 | A | G | 24 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0017 others(21): Show |
62 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-206-1581A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873784 | |||||||
| chr1:226873888 | C | G | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-1477C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873888 | |||||||
| chr1:226873954 | T | A | 49 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(46): Show |
113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-206-1411T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226873954 | |||||||
| chr1:226874007 | C | G | 1 | a0004c0014t0013g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-206-1358C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874007 | |||||||
| chr1:226874011 | A | C | 16 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(13): Show |
38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-206-1354A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874011 | |||||||
| chr1:226874062 | C | A | 14 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(11): Show |
23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-206-1303C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874062 | |||||||
| chr1:226874145 | A | T | 1 | a0001c0006t0002g0024 | 3 | HG01891.hp1 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-206-1220A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874145 | |||||||
| chr1:226874246 | G | A | 11 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0118 others(8): Show |
30 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-206-1119G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874246 | |||||||
| chr1:226874272 | G | A | 1 | a0001c0003t0004g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-206-1093G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874272 | |||||||
| chr1:226874349 | G | A | 5 | a0001c0005t0004g0020 a0001c0005t0004g0042 a0001c0005t0004g0164 others(2): Show |
14 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-206-1016G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874349 | |||||||
| chr1:226874428 | C | A | 104 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(101): Show |
227 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.-206-937C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874428 | |||||||
| chr1:226874436 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-206-929G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874436 | |||||||
| chr1:226874456 | A | G | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-909A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874456 | |||||||
| chr1:226874462 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-206-903A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874462 | |||||||
| chr1:226874627 | T | C | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-738T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874627 | |||||||
| chr1:226874688 | T | C | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-677T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874688 | |||||||
| chr1:226874727 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-206-638G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874727 | |||||||
| chr1:226874784 | C | G | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-206-581C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874784 | |||||||
| chr1:226874834 | A | T | 1 | a0001c0003t0002g0059 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-206-531A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874834 | |||||||
| chr1:226874901 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG01167.hp1 HG01169.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-206-464G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874901 | |||||||
| chr1:226874905 | G | T | 19 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0021 others(16): Show |
53 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-206-460G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874905 | |||||||
| chr1:226874947 | G | A | 1 | a0001c0001t0001g0023 | 3 | NA18906.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-206-418G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226874947 | |||||||
| chr1:226875101 | C | T | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-206-264C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875101 | |||||||
| chr1:226875130 | G | A | 49 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(46): Show |
113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-206-235G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875130 | |||||||
| chr1:226875217 | A | G | 2 | a0001c0002t0002g0120 a0001c0002t0002g0121 |
2 | NA18981.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-206-148A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875217 | |||||||
| chr1:226875308 | G | A | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-206-57G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 2/12 | chr1 | 226875308 | |||||||
| chr1:226875671 | C | T | 1 | a0004c0014t0013g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-21+121C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875671 | |||||||
| chr1:226875699 | C | T | 49 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(46): Show |
113 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-21+149C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875699 | |||||||
| chr1:226875786 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-21+236A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875786 | |||||||
| chr1:226875970 | T | C | 115 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0029 others(112): Show |
250 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-21+420T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226875970 | |||||||
| chr1:226876031 | G | T | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21+481G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876031 | |||||||
| chr1:226876098 | C | T | 1 | a0001c0002t0003g0144 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-21+548C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876098 | |||||||
| chr1:226876105 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-21+555C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876105 | |||||||
| chr1:226876143 | C | T | 1 | a0001c0007t0006g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21+593C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876143 | |||||||
| chr1:226876172 | A | G | 1 | a0001c0002t0003g0143 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-21+622A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876172 | |||||||
| chr1:226876250 | AC | A | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+701delC | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876250 | |||||||
| chr1:226876306 | C | A | 2 | a0001c0004t0004g0149 a0001c0004t0004g0150 |
2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-21+756C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876306 | |||||||
| chr1:226876348 | G | A | 2 | a0001c0004t0004g0151 a0001c0004t0004g0152 |
2 | NA18747.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-21+798G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876348 | |||||||
| chr1:226876483 | G | T | 2 | a0001c0006t0002g0024 a0001c0006t0002g0126 |
4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+933G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876483 | |||||||
| chr1:226876560 | C | A | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1010C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876560 | |||||||
| chr1:226876606 | T | C | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1056T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876606 | |||||||
| chr1:226876629 | C | T | 1 | a0001c0012t0002g0028 | 2 | NA18944.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-21+1079C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876629 | |||||||
| chr1:226876679 | G | A | 1 | a0001c0003t0002g0048 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-21+1129G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876679 | |||||||
| chr1:226876694 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-21+1144C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876694 | |||||||
| chr1:226876926 | T | C | 5 | a0001c0003t0002g0017 a0001c0003t0002g0160 a0001c0003t0002g0161 others(2): Show |
9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+1376T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226876926 | |||||||
| chr1:226877019 | G | A | 14 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(11): Show |
23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-21+1469G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877019 | |||||||
| chr1:226877167 | C | G | 1 | a0001c0003t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-21+1617C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877167 | |||||||
| chr1:226877180 | AG | A | 5 | a0001c0005t0004g0020 a0001c0005t0004g0042 a0001c0005t0004g0164 others(2): Show |
14 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-21+1631delG | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877180 | |||||||
| chr1:226877205 | C | T | 1 | a0001c0002t0002g0121 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-21+1655C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877205 | |||||||
| chr1:226877272 | G | T | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-21+1722G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877272 | |||||||
| chr1:226877384 | G | A | 1 | a0001c0003t0002g0049 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-21+1834G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877384 | |||||||
| chr1:226877565 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0070 a0001c0001t0001g0099 |
10 | HG00673.hp2 NA18941.hp2 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.-21+2015G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877565 | |||||||
| chr1:226877673 | G | A | 1 | a0001c0005t0004g0042 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-21+2123G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877673 | |||||||
| chr1:226877777 | G | A | 18 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0021 others(15): Show |
52 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-21+2227G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226877777 | |||||||
| chr1:226878040 | A | G | 1 | a0001c0003t0002g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-21+2490A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878040 | |||||||
| chr1:226878153 | C | T | 16 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(13): Show |
38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.-21+2603C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878153 | |||||||
| chr1:226878154 | A | G | 1 | a0001c0001t0001g0035 | 2 | NA19002.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-21+2604A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878154 | |||||||
| chr1:226878211 | C | A | 1 | a0001c0003t0004g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-21+2661C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878211 | |||||||
| chr1:226878241 | A | C | 2 | a0001c0004t0004g0025 a0001c0004t0004g0156 |
4 | HG01074.hp2 HG01358.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+2691A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878241 | |||||||
| chr1:226878328 | C | T | 2 | a0001c0002t0003g0040 a0001c0002t0003g0142 |
3 | NA18950.hp1 NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-21+2778C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878328 | |||||||
| chr1:226878355 | A | T | 1 | a0002c0010t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-21+2805A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878355 | |||||||
| chr1:226878440 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG02056.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-21+2890C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878440 | |||||||
| chr1:226878509 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-21+2959T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878509 | |||||||
| chr1:226878546 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-21+2996A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878546 | |||||||
| chr1:226878673 | A | T | 1 | a0001c0002t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-21+3123A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878673 | |||||||
| chr1:226878675 | A | G | 1 | a0002c0010t0001g0158 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-21+3125A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878675 | |||||||
| chr1:226878881 | T | C | 4 | a0001c0002t0002g0146 a0001c0003t0004g0027 a0001c0003t0004g0169 others(1): Show |
6 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-20-3007T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226878881 | |||||||
| chr1:226879172 | C | T | 4 | a0001c0002t0003g0138 a0001c0002t0003g0139 a0001c0002t0003g0140 others(1): Show |
4 | HG02145.hp2 NA18976.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-2716C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879172 | |||||||
| chr1:226879195 | C | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0072 others(4): Show |
23 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20-2693C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879195 | |||||||
| chr1:226879288 | T | A | 1 | a0001c0002t0002g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-2600T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879288 | |||||||
| chr1:226879289 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-20-2599C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879289 | |||||||
| chr1:226879571 | C | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-20-2317C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879571 | |||||||
| chr1:226879641 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0102 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-2247C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879641 | |||||||
| chr1:226879758 | C | T | 14 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(11): Show |
23 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.-20-2130C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879758 | |||||||
| chr1:226879955 | G | A | 7 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0069 others(4): Show |
11 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.-20-1933G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226879955 | |||||||
| chr1:226880000 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-20-1888A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880000 | |||||||
| chr1:226880042 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-20-1846T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880042 | |||||||
| chr1:226880074 | T | G | 1 | a0001c0002t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1814T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880074 | |||||||
| chr1:226880075 | G | T | 1 | a0001c0002t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1813G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880075 | |||||||
| chr1:226880076 | T | G | 1 | a0001c0002t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-1812T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880076 | |||||||
| chr1:226880213 | A | G | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1675A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880213 | |||||||
| chr1:226880245 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-20-1643C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880245 | |||||||
| chr1:226880348 | A | G | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-1540A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880348 | |||||||
| chr1:226880350 | G | A | 1 | a0001c0003t0002g0050 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-20-1538G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880350 | |||||||
| chr1:226880526 | G | A | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-20-1362G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880526 | |||||||
| chr1:226880545 | A | AGACAGCG others(15): Show |
120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-20-1289_-20-1268d others(24): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | ||||||
| chr1:226880545 | A | AGACAGCG others(37): Show |
1 | a0001c0001t0001g0009 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-20-1311_-20-1268d others(46): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | ||||||
| chr1:226880545 | AGACAGCG others(15): Show |
A | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1289_-20-1268d others(24): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr1 | 226880545 | ||||||
| chr1:226880621 | A | C | 2 | a0001c0001t0001g0032 a0001c0003t0002g0056 |
3 | HG02004.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-20-1267A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880621 | |||||||
| chr1:226880633 | G | T | 1 | a0001c0002t0003g0039 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-20-1255G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880633 | |||||||
| chr1:226880697 | G | T | 27 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(24): Show |
48 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.-20-1191G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880697 | |||||||
| chr1:226880771 | G | A | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-1117G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226880771 | |||||||
| chr1:226881169 | A | G | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-20-719A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881169 | |||||||
| chr1:226881293 | C | T | 1 | a0001c0002t0003g0137 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-20-595C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881293 | |||||||
| chr1:226881544 | C | G | 7 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(4): Show |
11 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-20-344C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881544 | |||||||
| chr1:226881566 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(73): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.-20-322A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881566 | |||||||
| chr1:226881636 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-20-252C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881636 | |||||||
| chr1:226881656 | C | T | 2 | a0001c0006t0002g0024 a0001c0006t0002g0126 |
4 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-232C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881656 | |||||||
| chr1:226881658 | T | A | 1 | a0001c0002t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-20-230T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881658 | |||||||
| chr1:226881714 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-20-174A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 3/12 | chr1 | 226881714 | |||||||
| chr1:226882078 | A | G | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+30A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882078 | |||||||
| chr1:226882102 | C | G | 1 | a0001c0004t0004g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.141+54C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882102 | |||||||
| chr1:226882106 | A | G | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.141+58A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882106 | |||||||
| chr1:226882173 | C | G | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+125C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882173 | |||||||
| chr1:226882238 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.141+190A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882238 | |||||||
| chr1:226882417 | G | C | 5 | a0001c0002t0003g0038 a0001c0002t0003g0127 a0001c0002t0003g0128 others(2): Show |
6 | HG02040.hp2 HG02056.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+369G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882417 | |||||||
| chr1:226882446 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.141+398G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882446 | |||||||
| chr1:226882502 | C | G | 5 | a0001c0003t0002g0017 a0001c0003t0002g0160 a0001c0003t0002g0161 others(2): Show |
9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+454C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882502 | |||||||
| chr1:226882531 | C | T | 1 | a0001c0003t0004g0169 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+483C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882531 | |||||||
| chr1:226882551 | C | T | 2 | a0001c0003t0002g0006 a0001c0003t0002g0055 |
13 | NA18942.hp1 NA18946.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+503C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882551 | |||||||
| chr1:226882677 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(73): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.141+629C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882677 | |||||||
| chr1:226882899 | G | A | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-806G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882899 | |||||||
| chr1:226882994 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(73): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.142-711C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226882994 | |||||||
| chr1:226883099 | ACCT | A | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-601_142-599del others(3): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr1 | 226883099 | ||||||
| chr1:226883253 | T | C | 3 | a0001c0002t0002g0037 a0001c0002t0002g0124 a0001c0002t0017g0125 |
4 | HG02280.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-452T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883253 | |||||||
| chr1:226883307 | G | A | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.142-398G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883307 | |||||||
| chr1:226883335 | C | T | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-370C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883335 | |||||||
| chr1:226883347 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(144): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.142-358T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883347 | |||||||
| chr1:226883423 | C | A | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-282C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883423 | |||||||
| chr1:226883483 | A | C | 1 | a0001c0002t0003g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.142-222A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883483 | |||||||
| chr1:226883493 | T | C | 1 | a0001c0003t0002g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.142-212T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883493 | |||||||
| chr1:226883570 | G | T | 1 | a0001c0002t0002g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-135G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883570 | |||||||
| chr1:226883584 | G | A | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-121G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883584 | |||||||
| chr1:226883585 | C | T | 1 | a0001c0004t0004g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.142-120C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883585 | |||||||
| chr1:226883663 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(73): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.142-42G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883663 | |||||||
| chr1:226883676 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.142-29T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883676 | |||||||
| chr1:226883678 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0098 |
3 | HG02132.hp2 HG02155.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.142-27C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883678 | |||||||
| chr1:226883682 | C | T | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.142-23C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883682 | |||||||
| chr1:226883683 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.142-22C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 4/12 | chr1 | 226883683 | |||||||
| chr1:226883983 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.356+64G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226883983 | |||||||
| chr1:226884002 | A | C | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.356+83A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884002 | |||||||
| chr1:226884065 | T | C | 26 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0017 others(23): Show |
64 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.356+146T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884065 | |||||||
| chr1:226884300 | C | T | 26 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0017 others(23): Show |
64 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.356+381C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884300 | |||||||
| chr1:226884447 | G | A | 2 | a0001c0016t0009g0046 a0001c0017t0009g0045 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.356+528G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884447 | |||||||
| chr1:226884538 | C | CT | 21 | a0001c0001t0001g0108 a0001c0003t0002g0003 a0001c0003t0002g0006 others(18): Show |
57 | HG00597.hp1 HG00733.hp2 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.356+635dupT | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 226884538 | ||||||
| chr1:226884538 | CT | C | 29 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0084 others(26): Show |
41 | HG01109.hp2 HG01167.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.356+635delT | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 226884538 | ||||||
| chr1:226884554 | T | A | 3 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.356+635T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884554 | |||||||
| chr1:226884566 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.356+647T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884566 | |||||||
| chr1:226884600 | G | T | 2 | a0001c0001t0001g0007 a0001c0002t0003g0135 |
2 | HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.356+681G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884600 | |||||||
| chr1:226884610 | T | C | 16 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(13): Show |
38 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.356+691T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884610 | |||||||
| chr1:226884700 | G | A | 1 | a0001c0002t0002g0170 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.356+781G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884700 | |||||||
| chr1:226884787 | G | A | 1 | a0001c0002t0003g0127 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.357-751G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884787 | |||||||
| chr1:226884923 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.357-615A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884923 | |||||||
| chr1:226884985 | C | T | 1 | a0004c0014t0013g0047 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.357-553C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226884985 | |||||||
| chr1:226885130 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.357-408A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885130 | |||||||
| chr1:226885139 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0083 a0001c0001t0001g0085 others(2): Show |
15 | HG01261.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.357-399G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885139 | |||||||
| chr1:226885239 | G | A | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.357-299G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885239 | |||||||
| chr1:226885287 | A | C | 2 | a0001c0016t0009g0046 a0001c0017t0009g0045 |
2 | HG02615.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.357-251A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885287 | |||||||
| chr1:226885408 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.357-130C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885408 | |||||||
| chr1:226885410 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.357-128A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885410 | |||||||
| chr1:226885504 | G | C | 1 | a0001c0002t0003g0139 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.357-34G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 5/12 | chr1 | 226885504 | |||||||
| chr1:226885694 | C | T | 1 | a0001c0002t0003g0129 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.498+15C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885694 | |||||||
| chr1:226885709 | G | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.498+30G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885709 | |||||||
| chr1:226885747 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.498+68C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885747 | |||||||
| chr1:226885824 | C | T | 1 | a0001c0002t0003g0135 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.498+145C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885824 | |||||||
| chr1:226885958 | C | T | 1 | a0001c0004t0004g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.498+279C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885958 | |||||||
| chr1:226885964 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0157 |
4 | NA18945.hp2 NA18984.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+285G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885964 | |||||||
| chr1:226885968 | C | CAAG | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.498+290_498+292dup others(3): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr1 | 226885968 | ||||||
| chr1:226885976 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.498+297C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226885976 | |||||||
| chr1:226886011 | T | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.498+332T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886011 | |||||||
| chr1:226886040 | A | T | 55 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0017 others(52): Show |
114 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.498+361A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886040 | |||||||
| chr1:226886210 | A | G | 1 | a0001c0005t0004g0042 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.498+531A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886210 | |||||||
| chr1:226886246 | A | T | 1 | a0001c0002t0003g0139 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.498+567A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886246 | |||||||
| chr1:226886301 | C | T | 25 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0154 others(22): Show |
45 | HG00558.hp2 HG01074.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.498+622C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886301 | |||||||
| chr1:226886346 | C | T | 1 | a0001c0005t0004g0164 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498+667C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886346 | |||||||
| chr1:226886424 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.498+745G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886424 | |||||||
| chr1:226886451 | C | G | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.498+772C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886451 | |||||||
| chr1:226886539 | G | T | 1 | a0001c0005t0005g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.498+860G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886539 | |||||||
| chr1:226886559 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.498+880C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886559 | |||||||
| chr1:226886642 | G | A | 13 | a0001c0003t0004g0154 a0001c0004t0004g0013 a0001c0004t0004g0025 others(10): Show |
21 | HG00558.hp2 HG01074.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.498+963G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886642 | |||||||
| chr1:226886739 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0081 |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+1060C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886739 | |||||||
| chr1:226886837 | C | T | 1 | a0001c0002t0003g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.498+1158C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886837 | |||||||
| chr1:226886909 | C | T | 1 | a0001c0002t0003g0139 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.499-1182C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886909 | |||||||
| chr1:226886910 | T | G | 1 | a0001c0002t0003g0139 | 1 | NA18976.hp2 | intron_variant | MODIFIER | c.499-1181T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886910 | |||||||
| chr1:226886924 | C | A | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.499-1167C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886924 | |||||||
| chr1:226886972 | A | G | 1 | a0001c0004t0004g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.499-1119A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886972 | |||||||
| chr1:226886981 | G | C | 1 | a0001c0003t0002g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.499-1110G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226886981 | |||||||
| chr1:226887125 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.499-966G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887125 | |||||||
| chr1:226887210 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.499-881C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887210 | |||||||
| chr1:226887318 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.499-773G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887318 | |||||||
| chr1:226887663 | C | A | 1 | a0001c0002t0002g0036 | 2 | NA18955.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.499-428C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887663 | |||||||
| chr1:226887681 | T | C | 1 | a0001c0001t0001g0023 | 3 | NA18906.hp1 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.499-410T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887681 | |||||||
| chr1:226887701 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(75): Show |
190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.499-390G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887701 | |||||||
| chr1:226887757 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.499-334C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887757 | |||||||
| chr1:226887970 | G | A | 1 | a0001c0003t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.499-121G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 6/12 | chr1 | 226887970 | |||||||
| chr1:226888215 | G | A | 5 | a0001c0003t0002g0052 a0001c0006t0002g0015 a0001c0006t0002g0122 others(2): Show |
9 | HG01515.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.566+57G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888215 | |||||||
| chr1:226888238 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0080 |
3 | HG01109.hp1 HG01243.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.566+80C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888238 | |||||||
| chr1:226888283 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0069 others(5): Show |
12 | HG00099.hp2 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.566+125G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888283 | |||||||
| chr1:226888359 | A | G | 14 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0037 others(11): Show |
31 | HG00558.hp1 HG01099.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.566+201A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888359 | |||||||
| chr1:226888447 | A | G | 1 | a0001c0003t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.566+289A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888447 | |||||||
| chr1:226888448 | A | G | 1 | a0001c0003t0004g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.566+290A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888448 | |||||||
| chr1:226888522 | C | G | 31 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(28): Show |
72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.567-307C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888522 | |||||||
| chr1:226888579 | A | G | 3 | a0001c0003t0004g0163 a0001c0003t0004g0165 a0001c0003t0004g0166 |
3 | HG02886.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.567-250A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888579 | |||||||
| chr1:226888608 | C | T | 2 | a0001c0002t0003g0132 a0001c0002t0003g0133 |
2 | NA18965.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.567-221C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 7/12 | chr1 | 226888608 | |||||||
| chr1:226889073 | G | C | 1 | a0001c0007t0006g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.787+24G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889073 | |||||||
| chr1:226889115 | C | A | 8 | a0001c0003t0004g0027 a0001c0003t0004g0169 a0001c0005t0004g0020 others(5): Show |
19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.787+66C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889115 | |||||||
| chr1:226889164 | G | A | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.787+115G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889164 | |||||||
| chr1:226889254 | C | T | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.787+205C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889254 | |||||||
| chr1:226889338 | G | A | 1 | a0001c0003t0002g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.787+289G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889338 | |||||||
| chr1:226889629 | G | A | 1 | a0001c0002t0002g0146 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.788-406G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889629 | |||||||
| chr1:226889841 | T | G | 1 | a0001c0003t0002g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.788-194T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889841 | |||||||
| chr1:226889931 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-104G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889931 | |||||||
| chr1:226889945 | G | C | 7 | a0001c0006t0002g0015 a0001c0006t0002g0024 a0001c0006t0002g0122 others(4): Show |
13 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.788-90G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 8/12 | chr1 | 226889945 | |||||||
| chr1:226890148 | C | T | 1 | a0001c0002t0003g0128 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.886+15C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890148 | |||||||
| chr1:226890366 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0083 a0001c0001t0001g0085 others(1): Show |
11 | HG01261.hp2 HG01884.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.886+233C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890366 | |||||||
| chr1:226890417 | G | A | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.886+284G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890417 | |||||||
| chr1:226890677 | G | T | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.886+544G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890677 | |||||||
| chr1:226890798 | G | A | 1 | a0001c0003t0004g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.887-480G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890798 | |||||||
| chr1:226890808 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.887-470T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890808 | |||||||
| chr1:226890873 | G | A | 3 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.887-405G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890873 | |||||||
| chr1:226890891 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(102): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.887-387C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890891 | |||||||
| chr1:226890900 | C | T | 1 | a0001c0002t0002g0145 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.887-378C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890900 | |||||||
| chr1:226890936 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.887-342C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890936 | |||||||
| chr1:226890982 | C | T | 1 | a0001c0006t0002g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.887-296C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226890982 | |||||||
| chr1:226891020 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.887-258T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891020 | |||||||
| chr1:226891127 | A | G | 1 | a0001c0006t0002g0126 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.887-151A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891127 | |||||||
| chr1:226891254 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.887-24T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891254 | |||||||
| chr1:226891254 | T | G | 2 | a0001c0003t0004g0027 a0001c0003t0004g0169 |
4 | HG01109.hp2 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.887-24T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 9/12 | chr1 | 226891254 | |||||||
| chr1:226891521 | C | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.970+160C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/12 | chr1 | 226891521 | |||||||
| chr1:226891600 | G | C | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.971-143G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 10/12 | chr1 | 226891600 | |||||||
| chr1:226891942 | G | A | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1072+98G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891942 | |||||||
| chr1:226891972 | C | T | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1072+128C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891972 | |||||||
| chr1:226891980 | A | G | 1 | a0001c0004t0004g0156 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1072+136A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891980 | |||||||
| chr1:226891999 | C | T | 24 | a0001c0003t0002g0003 a0001c0003t0002g0006 a0001c0003t0002g0017 others(21): Show |
62 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1072+155C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226891999 | |||||||
| chr1:226892013 | C | G | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1072+169C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892013 | |||||||
| chr1:226892058 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1072+214C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892058 | |||||||
| chr1:226892077 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1072+233G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892077 | |||||||
| chr1:226892103 | C | T | 15 | a0001c0004t0004g0013 a0001c0004t0004g0025 a0001c0004t0004g0147 others(12): Show |
27 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1072+259C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892103 | |||||||
| chr1:226892118 | C | T | 1 | a0001c0003t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1072+274C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892118 | |||||||
| chr1:226892120 | G | A | 31 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(28): Show |
72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1072+276G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892120 | |||||||
| chr1:226892465 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(130): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1072+621C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892465 | |||||||
| chr1:226892561 | G | A | 1 | a0001c0002t0002g0037 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1072+717G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892561 | |||||||
| chr1:226892584 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1072+740T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892584 | |||||||
| chr1:226892606 | C | T | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1072+762C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892606 | |||||||
| chr1:226892751 | G | A | 31 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(28): Show |
72 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.1072+907G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892751 | |||||||
| chr1:226892758 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1072+914G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892758 | |||||||
| chr1:226892808 | A | T | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1072+964A>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892808 | |||||||
| chr1:226892860 | T | C | 5 | a0001c0003t0004g0043 a0001c0003t0004g0163 a0001c0003t0004g0165 others(2): Show |
6 | HG02886.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1072+1016T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892860 | |||||||
| chr1:226892868 | A | G | 3 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 |
3 | HG01884.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1072+1024A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892868 | |||||||
| chr1:226892889 | C | A | 1 | a0001c0002t0003g0128 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1072+1045C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892889 | |||||||
| chr1:226892964 | G | T | 1 | a0001c0002t0017g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073-1043G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226892964 | |||||||
| chr1:226893099 | A | ATT | 13 | a0001c0003t0004g0027 a0001c0003t0004g0043 a0001c0003t0004g0163 others(10): Show |
25 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1073-906_1073-905d others(4): Show |
PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 226893099 | ||||||
| chr1:226893140 | G | T | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1073-867G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893140 | |||||||
| chr1:226893226 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(117): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1073-781C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893226 | |||||||
| chr1:226893281 | G | C | 1 | a0001c0002t0003g0132 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1073-726G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893281 | |||||||
| chr1:226893283 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1073-724C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893283 | |||||||
| chr1:226893312 | C | T | 1 | a0001c0003t0002g0049 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1073-695C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893312 | |||||||
| chr1:226893327 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1073-680A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893327 | |||||||
| chr1:226893491 | C | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(173): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.1073-516C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893491 | |||||||
| chr1:226893576 | T | G | 4 | a0001c0007t0006g0018 a0001c0007t0006g0100 a0003c0011t0004g0041 others(1): Show |
8 | HG02055.hp1 HG02280.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1073-431T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893576 | |||||||
| chr1:226893604 | A | G | 28 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(25): Show |
66 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1073-403A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893604 | |||||||
| chr1:226893660 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1073-347T>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893660 | |||||||
| chr1:226893840 | T | A | 14 | a0001c0004t0004g0013 a0001c0004t0004g0025 a0001c0004t0004g0147 others(11): Show |
25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1073-167T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893840 | |||||||
| chr1:226893866 | A | C | 1 | a0001c0003t0002g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1073-141A>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893866 | |||||||
| chr1:226893921 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(116): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1073-86A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893921 | |||||||
| chr1:226893969 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1073-38C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 11/12 | chr1 | 226893969 | |||||||
| chr1:226894149 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.1191+24G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894149 | |||||||
| chr1:226894229 | C | T | 4 | a0001c0006t0002g0015 a0001c0006t0002g0122 a0001c0009t0002g0015 others(1): Show |
8 | HG01891.hp2 HG02145.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+104C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894229 | |||||||
| chr1:226894308 | G | A | 5 | a0001c0003t0002g0017 a0001c0003t0002g0160 a0001c0003t0002g0161 others(2): Show |
9 | HG01106.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1191+183G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894308 | |||||||
| chr1:226894366 | G | T | 14 | a0001c0004t0004g0013 a0001c0004t0004g0025 a0001c0004t0004g0147 others(11): Show |
25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1191+241G>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894366 | |||||||
| chr1:226894404 | G | C | 28 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(25): Show |
66 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1191+279G>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894404 | |||||||
| chr1:226894490 | G | A | 14 | a0001c0004t0004g0013 a0001c0004t0004g0025 a0001c0004t0004g0147 others(11): Show |
25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1191+365G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894490 | |||||||
| chr1:226894499 | A | G | 1 | a0001c0007t0006g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1191+374A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894499 | |||||||
| chr1:226894633 | T | C | 2 | a0001c0002t0003g0138 a0001c0002t0003g0140 |
2 | NA18982.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1191+508T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894633 | |||||||
| chr1:226894645 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(151): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1191+520A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894645 | |||||||
| chr1:226894733 | G | A | 1 | a0001c0002t0003g0039 | 2 | HG01071.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1191+608G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894733 | |||||||
| chr1:226894737 | G | A | 10 | a0001c0002t0002g0004 a0001c0002t0002g0036 a0001c0002t0002g0118 others(7): Show |
26 | HG00558.hp1 HG01099.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.1191+612G>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894737 | |||||||
| chr1:226894744 | A | G | 42 | a0001c0002t0002g0062 a0001c0002t0002g0063 a0001c0002t0002g0064 others(39): Show |
93 | HG00099.hp1 HG00597.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.1191+619A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894744 | |||||||
| chr1:226894751 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1191+626C>T | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894751 | |||||||
| chr1:226894858 | T | C | 14 | a0001c0004t0004g0013 a0001c0004t0004g0025 a0001c0004t0004g0147 others(11): Show |
25 | HG00423.hp1 HG00558.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1192-566T>C | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894858 | |||||||
| chr1:226894882 | C | A | 6 | a0001c0005t0004g0020 a0001c0005t0004g0042 a0001c0005t0004g0164 others(3): Show |
15 | HG01168.hp2 HG01169.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1192-542C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894882 | |||||||
| chr1:226894984 | C | A | 1 | a0003c0011t0004g0041 | 2 | HG02896.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1192-440C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894984 | |||||||
| chr1:226894992 | C | G | 8 | a0001c0003t0004g0027 a0001c0003t0004g0169 a0001c0005t0004g0020 others(5): Show |
19 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1192-432C>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226894992 | |||||||
| chr1:226895025 | T | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.1192-399T>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895025 | |||||||
| chr1:226895156 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1192-268A>G | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895156 | |||||||
| chr1:226895266 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1192-158C>A | PSEN2 | ENSG00000143801.18 | transcript | ENST00000366783.8 | protein_coding | 12/12 | chr1 | 226895266 |