Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54873 |
| ensemblid | ENSG00000099260.12 |
| hgncid | 15846 |
| symbol | PALMD |
| name | palmdelphin |
| refseq_nuc | NM_017734.5 |
| refseq_prot | NP_060204.1 |
| ensembl_nuc | ENST00000263174.9 |
| ensembl_prot | ENSP00000263174.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 99646113 |
| end | 99694535 |
| strand | + |
| ver | v1.2 |
| region | chr1:99646113-99694535 |
| region5000 | chr1:99641113-99699535 |
| regionname0 | PALMD_chr1_99646113_99694535 |
| regionname5000 | PALMD_chr1_99641113_99699535 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 551 | 356 | 76 | 66 | 162 | 12 | 38 | 122 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0002 | 0/0 | 551 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0003 | 0/0 | 551 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0004 | 0/0 | 551 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0005 | 0/0 | 551 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0006 | 0/0 | 551 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0007 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0008 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0009 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0010 | 0/0 | 551 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| a0011 | 0/0 | 551 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | MEEAE others(546): Show |
chr1 | 99641113 | 99699535 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1653 | 330 | 55 | 65 | 161 | 12 | 35 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0001c0002 | 0/0 | 1653 | 21 | 16 | 1 | 1 | 0 | 3 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0001c0005 | 0/0 | 1653 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0001c0012 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0002c0003 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0002c0008 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0003c0004 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0004c0006 | 0/0 | 1653 | 3 | 2 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0005c0009 | 0/0 | 1653 | 2 | 0 | 1 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0006c0007 | 0/0 | 1653 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0007c0015 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0008c0014 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0009c0010 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0010c0013 | 0/0 | 1653 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 | ||
| a0011c0011 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | ATGGA others(1648): Show |
chr1 | 99641113 | 99699535 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2334 | 321 | 51 | 65 | 157 | 12 | 34 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0002 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2326): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0003 | 0/0 | 2334 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0004 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0006 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0007 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0001t0008 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0002t0001 | 0/0 | 2334 | 10 | 5 | 1 | 1 | 0 | 3 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0002t0002 | 0/0 | 2331 | 11 | 11 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2326): Show |
chr1 | 99641113 | 99699535 |
| a0001c0005t0001 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0001c0012t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0002c0003t0001 | 0/0 | 2334 | 5 | 5 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0002c0008t0001 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0003c0004t0001 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0003c0004t0005 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0004c0006t0001 | 0/0 | 2334 | 3 | 2 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0005c0009t0001 | 0/0 | 2334 | 2 | 0 | 1 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0006c0007t0001 | 0/0 | 2334 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0007c0015t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0008c0014t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0009c0010t0002 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2326): Show |
chr1 | 99641113 | 99699535 |
| a0010c0013t0001 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| a0011c0011t0001 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | ATTAC others(2329): Show |
chr1 | 99641113 | 99699535 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 1 | 3 | 7 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0001c0012t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0002c0008t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0003c0004t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0004c0006t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0005c0009t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0005c0009t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0006c0007t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0006c0007t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0007c0015t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0008c0014t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0009c0010t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0010c0013t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| a0011c0011t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0312 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00735 | hp1 | a0004 | c0006 | t0001 | g0278 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01167 | hp2 | a0005 | c0009 | t0001 | g0028 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01256 | hp1 | a0006 | c0007 | t0001 | g0302 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01258 | hp1 | a0006 | c0007 | t0001 | g0303 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | IBS | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0334 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02145 | hp1 | a0002 | c0008 | t0001 | g0253 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CDX | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02258 | hp1 | a0007 | c0015 | t0001 | g0135 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0272 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | KHV | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02622 | hp2 | a0003 | c0004 | t0005 | g0217 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02630 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02717 | hp2 | a0008 | c0014 | t0001 | g0246 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02723 | hp1 | a0001 | c0012 | t0001 | g0231 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02809 | hp2 | a0003 | c0004 | t0001 | g0008 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02896 | hp1 | a0002 | c0003 | t0001 | g0316 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02897 | hp2 | a0002 | c0003 | t0001 | g0317 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0318 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02970 | hp1 | a0002 | c0003 | t0001 | g0315 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02970 | hp2 | a0001 | c0005 | t0001 | g0273 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02976 | hp1 | a0001 | c0005 | t0001 | g0265 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0237 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0205 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0271 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0276 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0282 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03195 | hp1 | a0002 | c0008 | t0001 | g0238 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0210 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0083 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03516 | hp1 | a0010 | c0013 | t0001 | g0308 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0216 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03654 | hp2 | a0011 | c0011 | t0001 | g0030 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0166 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03927 | hp2 | a0005 | c0009 | t0001 | g0029 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | STU | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19043 | hp1 | a0003 | c0004 | t0001 | g0008 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19240 | hp1 | a0003 | c0004 | t0001 | g0008 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | YRI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0321 | AFR | ASW | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0319 | AFR | ASW | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0281 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02109 | hp2 | a0004 | c0006 | t0001 | g0279 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0325 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG03471 | hp2 | a0009 | c0010 | t0002 | g0329 | AFR | MSL | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0208 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0275 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0203 | REF | REF | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0252 | REF | REF | PALMD_chr1_99641113_99699535 | PALMD | chr1 | 99641113 | 99699535 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99667693 | G | C | 1 | a0006 | 2 | HG01256.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.178G>C | p.Glu60Gln | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/8 | 383/2334 | 178/1656 | 60/551 | chr1 | 99667693 | |||
| chr1:99667734 | C | A | 2 | a0002 a0004 |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
missense_variant | MODERATE | c.219C>A | p.His73Gln | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/8 | 424/2334 | 219/1656 | 73/551 | chr1 | 99667734 | |||
| chr1:99686777 | A | G | 1 | a0007 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.353A>G | p.Glu118Gly | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/8 | 558/2334 | 353/1656 | 118/551 | chr1 | 99686777 | |||
| chr1:99688946 | A | G | 1 | a0008 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.686A>G | p.Asn229Ser | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 891/2334 | 686/1656 | 229/551 | chr1 | 99688946 | |||
| chr1:99688954 | G | A | 1 | a0009 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.694G>A | p.Asp232Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 899/2334 | 694/1656 | 232/551 | chr1 | 99688954 | |||
| chr1:99689087 | C | T | 1 | a0005 | 2 | HG01167.hp2 HG03927.hp2 |
missense_variant | MODERATE | c.827C>T | p.Thr276Met | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1032/2334 | 827/1656 | 276/551 | chr1 | 99689087 | |||
| chr1:99689209 | T | C | 1 | a0010 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.949T>C | p.Phe317Leu | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1154/2334 | 949/1656 | 317/551 | chr1 | 99689209 | |||
| chr1:99689637 | G | T | 2 | a0002 a0003 |
12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
missense_variant | MODERATE | c.1377G>T | p.Glu459Asp | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1582/2334 | 1377/1656 | 459/551 | chr1 | 99689637 | |||
| chr1:99689795 | G | A | 1 | a0011 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1535G>A | p.Ser512Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1740/2334 | 1535/1656 | 512/551 | chr1 | 99689795 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99688911 | G | A | 7 | a0001c0002 a0002c0003 a0002c0008 others(4): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
synonymous_variant | LOW | c.651G>A | p.Val217Val | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 856/2334 | 651/1656 | 217/551 | chr1 | 99688911 | |||
| chr1:99688998 | C | A | 1 | a0001c0012 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.738C>A | p.Ala246Ala | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 943/2334 | 738/1656 | 246/551 | chr1 | 99688998 | |||
| chr1:99689076 | A | T | 1 | a0001c0005 | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.816A>T | p.Pro272Pro | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1021/2334 | 816/1656 | 272/551 | chr1 | 99689076 | |||
| chr1:99689766 | T | C | 1 | a0002c0008 | 2 | HG02145.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1506T>C | p.Asn502Asn | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/8 | 1711/2334 | 1506/1656 | 502/551 | chr1 | 99689766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99646146 | C | A | 1 | a0001c0001t0003 | 3 | NA19010.hp1 NA19012.hp1 NA19056.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-172C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/8 | chr1 | 99646146 | |||||||
| chr1:99646201 | A | G | 1 | a0001c0001t0008 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-117A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/8 | 117 | chr1 | 99646201 | ||||||
| chr1:99694129 | T | C | 1 | a0003c0004t0005 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 67 | chr1 | 99694129 | ||||||
| chr1:99694158 | C | A | 1 | a0001c0001t0006 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 96 | chr1 | 99694158 | ||||||
| chr1:99694481 | T | C | 1 | a0001c0001t0004 | 2 | HG02055.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*419T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 419 | chr1 | 99694481 | ||||||
| chr1:99694499 | T | C | 1 | a0001c0001t0007 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 437 | chr1 | 99694499 | ||||||
| chr1:99694523 | ATCC | A | 3 | a0001c0001t0002 a0001c0002t0002 a0009c0010t0002 |
13 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*468delCCT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 8/8 | 466 | INFO_REALIGN_3_PRIME | chr1 | 99694523 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99646400 | A | G | 70 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(67): Show |
73 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.45+38A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646400 | |||||||
| chr1:99646515 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+153C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646515 | |||||||
| chr1:99646637 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.45+275T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646637 | |||||||
| chr1:99646731 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+369T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646731 | |||||||
| chr1:99646734 | T | G | 1 | a0001c0001t0001g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45+372T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646734 | |||||||
| chr1:99646875 | C | T | 1 | a0001c0002t0002g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+513C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646875 | |||||||
| chr1:99646917 | G | A | 1 | a0001c0002t0001g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+555G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99646917 | |||||||
| chr1:99647063 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0270 a0001c0002t0001g0031 others(3): Show |
7 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+701G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647063 | |||||||
| chr1:99647147 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG03927.hp1 NA18992.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.45+785G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647147 | |||||||
| chr1:99647180 | C | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.45+818C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647180 | |||||||
| chr1:99647188 | T | C | 9 | a0001c0001t0001g0277 a0001c0002t0002g0274 a0001c0002t0002g0275 others(6): Show |
9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+826T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647188 | |||||||
| chr1:99647473 | A | C | 9 | a0001c0001t0001g0277 a0001c0002t0002g0274 a0001c0002t0002g0275 others(6): Show |
9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+1111A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647473 | |||||||
| chr1:99647842 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+1480G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647842 | |||||||
| chr1:99647873 | G | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.45+1511G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647873 | |||||||
| chr1:99647982 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+1620A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99647982 | |||||||
| chr1:99648186 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.45+1824G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648186 | |||||||
| chr1:99648201 | C | T | 2 | a0004c0006t0001g0278 a0004c0006t0001g0279 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.45+1839C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648201 | |||||||
| chr1:99648554 | A | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0270 a0001c0001t0001g0322 others(18): Show |
22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2192A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648554 | |||||||
| chr1:99648555 | G | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0270 a0001c0001t0001g0322 others(18): Show |
22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2193G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648555 | |||||||
| chr1:99648576 | A | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0270 a0001c0001t0001g0322 others(18): Show |
22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2214A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648576 | |||||||
| chr1:99648583 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.45+2221G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648583 | |||||||
| chr1:99648603 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0218 a0001c0001t0001g0219 others(6): Show |
11 | HG02280.hp2 HG02622.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+2241C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648603 | |||||||
| chr1:99648660 | GA | G | 6 | a0001c0001t0001g0010 a0001c0002t0001g0031 a0001c0002t0002g0334 others(3): Show |
7 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+2310delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648660 | ||||||
| chr1:99648752 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.45+2390C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648752 | |||||||
| chr1:99648831 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.45+2469G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648831 | |||||||
| chr1:99648874 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(90): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.45+2512C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648874 | |||||||
| chr1:99648888 | C | CA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.45+2543dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | ||||||
| chr1:99648888 | C | CAA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(57): Show |
69 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.45+2542_45+2543dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | ||||||
| chr1:99648888 | CA | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0213 others(6): Show |
9 | HG00323.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+2543delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99648888 | ||||||
| chr1:99648952 | T | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | NA18983.hp1 NA19066.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.45+2590T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99648952 | |||||||
| chr1:99649076 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.45+2714G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649076 | |||||||
| chr1:99649083 | C | T | 21 | a0001c0001t0001g0010 a0001c0001t0001g0270 a0001c0001t0001g0322 others(18): Show |
22 | HG01167.hp2 HG01515.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+2721C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649083 | |||||||
| chr1:99649111 | T | A | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.45+2749T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649111 | |||||||
| chr1:99649113 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.45+2751G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649113 | |||||||
| chr1:99649470 | GAGAAGAG others(8): Show |
G | 1 | a0001c0002t0001g0282 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45+3114_45+3128del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99649470 | ||||||
| chr1:99649476 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(252): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.45+3114A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649476 | |||||||
| chr1:99649500 | A | C | 9 | a0001c0001t0001g0277 a0001c0002t0002g0274 a0001c0002t0002g0275 others(6): Show |
9 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.45+3138A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649500 | |||||||
| chr1:99649531 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.45+3169C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649531 | |||||||
| chr1:99649545 | G | C | 5 | a0001c0002t0002g0274 a0001c0002t0002g0275 a0001c0005t0001g0271 others(2): Show |
5 | HG02451.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3183G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649545 | |||||||
| chr1:99649581 | G | A | 1 | a0007c0015t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.45+3219G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649581 | |||||||
| chr1:99649768 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45+3406C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99649768 | |||||||
| chr1:99650004 | A | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(111): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.45+3642A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650004 | |||||||
| chr1:99650048 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45+3686G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650048 | |||||||
| chr1:99650062 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0330 a0001c0001t0001g0331 |
3 | HG02895.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.45+3700A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650062 | |||||||
| chr1:99650094 | G | C | 3 | a0001c0001t0001g0010 a0001c0002t0001g0031 a0011c0011t0001g0030 |
4 | HG01515.hp1 HG01517.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+3732G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650094 | |||||||
| chr1:99650285 | G | GA | 24 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0037 others(21): Show |
26 | HG00408.hp2 HG00544.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.45+3957dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | G | GAA | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0146 others(8): Show |
11 | HG00621.hp1 HG01109.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3956_45+3957dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GA | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0255 others(5): Show |
11 | HG02145.hp1 HG02717.hp1 HG03486.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+3957delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(4): Show |
G | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0256 others(5): Show |
8 | HG01175.hp2 HG02738.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+3947_45+3957del others(11): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(5): Show |
G | 89 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
97 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.45+3946_45+3957del others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.45+3945_45+3957del others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(7): Show |
G | 12 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0270 others(9): Show |
12 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+3944_45+3957del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(11): Show |
G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45+3940_45+3957del others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(12): Show |
G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(40): Show |
51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.45+3939_45+3957del others(19): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650285 | GAAAAAAA others(13): Show |
G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(95): Show |
121 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.45+3938_45+3957del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650285 | ||||||
| chr1:99650482 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+4120G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650482 | |||||||
| chr1:99650486 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(130): Show |
147 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.45+4124G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650486 | |||||||
| chr1:99650533 | T | C | 11 | a0001c0001t0001g0277 a0002c0003t0001g0083 a0002c0003t0001g0205 others(8): Show |
11 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.45+4171T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650533 | |||||||
| chr1:99650562 | CT | C | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.45+4205delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99650562 | ||||||
| chr1:99650689 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.45+4327T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650689 | |||||||
| chr1:99650697 | G | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(169): Show |
203 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.45+4335G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650697 | |||||||
| chr1:99650838 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.45+4476C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650838 | |||||||
| chr1:99650839 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG01934.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+4477G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650839 | |||||||
| chr1:99650841 | T | C | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+4479T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99650841 | |||||||
| chr1:99651086 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.45+4724A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651086 | |||||||
| chr1:99651161 | CCA | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(42): Show |
53 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.45+4802_45+4803del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99651161 | ||||||
| chr1:99651207 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0130 a0001c0001t0001g0136 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.45+4845G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651207 | |||||||
| chr1:99651243 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45+4881G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651243 | |||||||
| chr1:99651294 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.45+4932G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651294 | |||||||
| chr1:99651327 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.45+4965A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651327 | |||||||
| chr1:99651344 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.45+4982T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651344 | |||||||
| chr1:99651488 | G | A | 6 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+5126G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651488 | |||||||
| chr1:99651892 | T | C | 1 | a0001c0001t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45+5530T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651892 | |||||||
| chr1:99651901 | T | C | 18 | a0001c0001t0001g0155 a0001c0001t0001g0213 a0001c0001t0001g0324 others(15): Show |
18 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.45+5539T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651901 | |||||||
| chr1:99651969 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.45+5607C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99651969 | |||||||
| chr1:99652055 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45+5693T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652055 | |||||||
| chr1:99652160 | T | C | 17 | a0001c0001t0001g0155 a0001c0001t0001g0213 a0001c0001t0004g0153 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.45+5798T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652160 | |||||||
| chr1:99652207 | G | A | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+5845G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652207 | |||||||
| chr1:99652321 | T | A | 1 | a0011c0011t0001g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+5959T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652321 | |||||||
| chr1:99652375 | A | G | 4 | a0001c0001t0001g0313 a0001c0001t0001g0324 a0001c0002t0001g0282 others(1): Show |
4 | HG02257.hp2 HG02486.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6013A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652375 | |||||||
| chr1:99652465 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+6103A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652465 | |||||||
| chr1:99652481 | G | C | 1 | a0001c0001t0001g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.45+6119G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652481 | |||||||
| chr1:99652494 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.45+6132C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652494 | |||||||
| chr1:99652551 | C | G | 4 | a0001c0002t0002g0254 a0001c0002t0002g0274 a0001c0002t0002g0275 others(1): Show |
4 | HG02723.hp2 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6189C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652551 | |||||||
| chr1:99652566 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6204T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652566 | |||||||
| chr1:99652587 | G | C | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.45+6225G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652587 | |||||||
| chr1:99652599 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.45+6237G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652599 | |||||||
| chr1:99652618 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.45+6256G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652618 | |||||||
| chr1:99652626 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45+6264A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652626 | |||||||
| chr1:99652659 | A | AGAAAG | 24 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0088 others(21): Show |
25 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+6332_45+6336dup others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | A | AGAAAGGA others(3): Show |
4 | a0001c0001t0001g0090 a0001c0001t0001g0109 a0001c0001t0001g0110 others(1): Show |
4 | HG00408.hp2 HG02083.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6327_45+6336dup others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | A | AGAAAGGA others(8): Show |
3 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 |
3 | HG01346.hp2 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.45+6322_45+6336dup others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | A | AGAAAGGA others(13): Show |
1 | a0001c0002t0001g0237 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.45+6317_45+6336dup others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | AGAAAG | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0022 others(72): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.45+6332_45+6336del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | AGAAAGGA others(3): Show |
A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0077 others(18): Show |
22 | HG01167.hp2 HG01884.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.45+6327_45+6336del others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | AGAAAGGA others(8): Show |
A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(32): Show |
41 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.45+6322_45+6336del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652659 | AGAAAGGA others(13): Show |
A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0070 a0001c0001t0001g0148 others(1): Show |
5 | HG00738.hp2 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+6317_45+6336del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652659 | ||||||
| chr1:99652674 | GGAAAGGA others(18): Show |
G | 1 | a0001c0001t0001g0331 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.45+6317_45+6341del others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652674 | ||||||
| chr1:99652679 | GGAAAGGA others(13): Show |
G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0323 |
2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.45+6322_45+6341del others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652679 | ||||||
| chr1:99652684 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0151 |
2 | HG01261.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.45+6322G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652684 | |||||||
| chr1:99652684 | G | GGAAAAGA others(3): Show |
1 | a0001c0002t0002g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+6326_45+6327ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652684 | ||||||
| chr1:99652684 | GGAAAGGA others(8): Show |
G | 3 | a0002c0003t0001g0316 a0002c0003t0001g0317 a0007c0015t0001g0135 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.45+6327_45+6341del others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652684 | ||||||
| chr1:99652689 | G | A | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0134 others(11): Show |
14 | HG01261.hp2 HG01358.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+6327G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652689 | |||||||
| chr1:99652689 | G | GGAAAAGA others(3): Show |
1 | a0002c0008t0001g0238 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.45+6331_45+6332ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652689 | ||||||
| chr1:99652689 | G | GGAAAAGA others(18): Show |
1 | a0001c0001t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+6331_45+6332ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652689 | ||||||
| chr1:99652694 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
98 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.45+6332G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652694 | |||||||
| chr1:99652694 | G | GGAAAA | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(35): Show |
43 | HG00280.hp1 HG00408.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.45+6377_45+6381dup others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAAGA others(3): Show |
37 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0015 others(34): Show |
38 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.45+6372_45+6381dup others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAAGA others(8): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(15): Show |
18 | HG00280.hp2 HG01358.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.45+6367_45+6381dup others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAAGA others(13): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0043 others(8): Show |
12 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.45+6362_45+6381dup others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAAGA others(18): Show |
4 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0001c0001t0001g0098 others(1): Show |
4 | HG01934.hp2 HG01975.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6357_45+6381dup others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAAGA others(23): Show |
1 | a0001c0001t0001g0018 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.45+6352_45+6381dup others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(3): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0219 a0001c0001t0001g0313 |
3 | HG02886.hp2 HG03540.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.45+6336_45+6337ins others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(8): Show |
1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(13): Show |
1 | a0001c0001t0001g0096 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(18): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0225 |
2 | HG01978.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.45+6336_45+6337ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(33): Show |
1 | a0001c0001t0001g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(23): Show |
1 | a0001c0001t0001g0115 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(13): Show |
1 | a0011c0011t0001g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | G | GGAAAGGA others(18): Show |
1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.45+6336_45+6337ins others(25): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | GGAAAA | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0293 others(2): Show |
5 | HG01884.hp1 HG02735.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6377_45+6381del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652694 | GGAAAAGA others(3): Show |
G | 1 | a0001c0001t0001g0014 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.45+6372_45+6381del others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652694 | ||||||
| chr1:99652699 | A | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0306 a0001c0002t0001g0235 others(1): Show |
4 | HG00140.hp1 HG00544.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+6337A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652699 | |||||||
| chr1:99652704 | A | G | 2 | a0001c0002t0001g0235 a0001c0002t0001g0236 |
2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6342A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652704 | |||||||
| chr1:99652709 | A | G | 2 | a0001c0002t0001g0235 a0001c0002t0001g0236 |
2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6347A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652709 | |||||||
| chr1:99652711 | AAAAGAAA others(22): Show |
A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG03540.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.45+6358_45+6386del others(29): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652711 | ||||||
| chr1:99652714 | A | G | 2 | a0001c0002t0001g0235 a0001c0002t0001g0236 |
2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.45+6352A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652714 | |||||||
| chr1:99652716 | AAAAGAAA others(17): Show |
A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0027 |
2 | HG02886.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.45+6363_45+6386del others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652716 | ||||||
| chr1:99652721 | AAAAGAAA others(12): Show |
A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0114 a0001c0001t0001g0233 others(5): Show |
8 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+6368_45+6386del others(19): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652721 | ||||||
| chr1:99652726 | AAAAGAAA others(7): Show |
A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0033 others(14): Show |
19 | HG00438.hp1 HG00673.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+6373_45+6386del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652726 | ||||||
| chr1:99652731 | AAAAGAAA others(2): Show |
A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(27): Show |
34 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.45+6378_45+6386del others(9): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652731 | ||||||
| chr1:99652736 | AAAAG | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(45): Show |
58 | HG00741.hp1 HG01070.hp2 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.45+6382_45+6385del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652736 | ||||||
| chr1:99652740 | G | GA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(26): Show |
30 | HG00323.hp1 HG00621.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.45+6381dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652740 | G | GAAAAGA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0076 others(10): Show |
13 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652740 | G | GAAAAGAA others(4): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0167 others(7): Show |
10 | HG00597.hp2 HG01099.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(11): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652740 | G | GAAAAGAA others(9): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0176 others(1): Show |
5 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652740 | G | GAAAAGAA others(14): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG00423.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.45+6381_45+6382ins others(21): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652740 | G | GAAAAGAA others(24): Show |
1 | a0001c0001t0001g0172 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.45+6381_45+6382ins others(31): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99652740 | ||||||
| chr1:99652811 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45+6449A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652811 | |||||||
| chr1:99652862 | T | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(34): Show |
42 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.45+6500T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652862 | |||||||
| chr1:99652879 | T | C | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6517T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652879 | |||||||
| chr1:99652922 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6560G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99652922 | |||||||
| chr1:99653017 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45+6655C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653017 | |||||||
| chr1:99653131 | G | A | 2 | a0001c0002t0001g0282 a0001c0002t0001g0325 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6769G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653131 | |||||||
| chr1:99653140 | A | C | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6778A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653140 | |||||||
| chr1:99653161 | AAACAAAA others(1): Show |
A | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+6810_45+6817del others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99653161 | ||||||
| chr1:99653211 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.45+6849T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653211 | |||||||
| chr1:99653256 | G | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.45+6894G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653256 | |||||||
| chr1:99653365 | T | G | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+7003T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653365 | |||||||
| chr1:99653592 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.45+7230G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653592 | |||||||
| chr1:99653673 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.45+7311T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653673 | |||||||
| chr1:99653746 | A | C | 1 | a0001c0001t0001g0076 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.45+7384A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653746 | |||||||
| chr1:99653754 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.45+7392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653754 | |||||||
| chr1:99653904 | C | T | 5 | a0001c0002t0002g0254 a0001c0002t0002g0274 a0001c0002t0002g0275 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+7542C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653904 | |||||||
| chr1:99653956 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.45+7594G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99653956 | |||||||
| chr1:99654134 | C | T | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.45+7772C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654134 | |||||||
| chr1:99654140 | C | G | 2 | a0004c0006t0001g0278 a0004c0006t0001g0279 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.45+7778C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654140 | |||||||
| chr1:99654146 | C | T | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.45+7784C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654146 | |||||||
| chr1:99654334 | TTAAA | T | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.45+7974_45+7977del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99654334 | ||||||
| chr1:99654343 | T | C | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7976T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654343 | |||||||
| chr1:99654344 | AGCTATT | A | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7974_46-7969del others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654344 | |||||||
| chr1:99654451 | G | A | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7868G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654451 | |||||||
| chr1:99654453 | C | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.46-7866C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654453 | |||||||
| chr1:99654473 | C | T | 3 | a0001c0001t0001g0324 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG02257.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-7846C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654473 | |||||||
| chr1:99654520 | T | G | 6 | a0002c0008t0001g0238 a0002c0008t0001g0253 a0003c0004t0001g0008 others(3): Show |
8 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.46-7799T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654520 | |||||||
| chr1:99654612 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.46-7707T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654612 | |||||||
| chr1:99654874 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7445C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99654874 | |||||||
| chr1:99655071 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.46-7248C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655071 | |||||||
| chr1:99655168 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46-7151T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655168 | |||||||
| chr1:99655250 | T | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7069T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655250 | |||||||
| chr1:99655260 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7059T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655260 | |||||||
| chr1:99655293 | A | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-7026A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655293 | |||||||
| chr1:99655309 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46-7010T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655309 | |||||||
| chr1:99655444 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-6875C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655444 | |||||||
| chr1:99655516 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6803G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655516 | |||||||
| chr1:99655553 | C | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
5 | HG02257.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-6766C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655553 | |||||||
| chr1:99655715 | G | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6604G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655715 | |||||||
| chr1:99655722 | T | G | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-6597T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655722 | |||||||
| chr1:99655760 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6559G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655760 | |||||||
| chr1:99655787 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6532T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655787 | |||||||
| chr1:99655807 | C | T | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.46-6512C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655807 | |||||||
| chr1:99655837 | A | G | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-6482A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655837 | |||||||
| chr1:99655892 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6427C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655892 | |||||||
| chr1:99655898 | G | A | 1 | a0001c0005t0001g0271 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-6421G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655898 | |||||||
| chr1:99655927 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655927 | |||||||
| chr1:99655933 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.46-6386C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655933 | |||||||
| chr1:99655933 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6386C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99655933 | |||||||
| chr1:99655933 | CGCACACA others(9): Show |
C | 6 | a0001c0001t0001g0311 a0001c0002t0001g0281 a0001c0005t0001g0271 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-6370_46-6355del others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655933 | ||||||
| chr1:99655936 | ACACACAC others(7): Show |
A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.46-6370_46-6357del others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655936 | ||||||
| chr1:99655938 | ACACACAC others(5): Show |
A | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46-6370_46-6359del others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655938 | ||||||
| chr1:99655950 | G | GCA | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-6353_46-6352dup others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99655950 | ||||||
| chr1:99656162 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.46-6157C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656162 | |||||||
| chr1:99656237 | A | G | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG01981.hp2 HG02602.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-6082A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656237 | |||||||
| chr1:99656287 | G | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-6032G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656287 | |||||||
| chr1:99656368 | CTTTTT | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(43): Show |
54 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.46-5947_46-5943del others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99656368 | ||||||
| chr1:99656783 | C | A | 1 | a0001c0002t0002g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.46-5536C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656783 | |||||||
| chr1:99656792 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-5527A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656792 | |||||||
| chr1:99656921 | C | T | 1 | a0001c0001t0001g0322 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46-5398C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99656921 | |||||||
| chr1:99657044 | G | T | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-5275G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657044 | |||||||
| chr1:99657240 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.46-5079T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657240 | |||||||
| chr1:99657267 | C | A | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-5052C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657267 | |||||||
| chr1:99657357 | T | C | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.46-4962T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657357 | |||||||
| chr1:99657515 | CCTAA | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4801_46-4798del others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99657515 | ||||||
| chr1:99657602 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.46-4717C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657602 | |||||||
| chr1:99657731 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4588C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657731 | |||||||
| chr1:99657782 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.46-4537G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657782 | |||||||
| chr1:99657809 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4510T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657809 | |||||||
| chr1:99657939 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-4380C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99657939 | |||||||
| chr1:99658116 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.46-4203C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658116 | |||||||
| chr1:99658303 | C | CA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0084 a0001c0001t0001g0114 others(8): Show |
11 | HG02451.hp2 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-4001dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658303 | ||||||
| chr1:99658303 | CA | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(59): Show |
70 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.46-4001delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658303 | ||||||
| chr1:99658347 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.46-3972A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658347 | |||||||
| chr1:99658519 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.46-3800C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658519 | |||||||
| chr1:99658628 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-3691G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658628 | |||||||
| chr1:99658739 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-3580C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658739 | |||||||
| chr1:99658896 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-3423T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658896 | |||||||
| chr1:99658902 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(56): Show |
67 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.46-3417T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658902 | |||||||
| chr1:99658921 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.46-3398C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99658921 | |||||||
| chr1:99658945 | C | CA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0040 others(4): Show |
7 | HG02015.hp2 HG02055.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-3360dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99658945 | ||||||
| chr1:99659137 | A | G | 2 | a0001c0001t0004g0153 a0001c0001t0004g0156 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-3182A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659137 | |||||||
| chr1:99659510 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-2809T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659510 | |||||||
| chr1:99659565 | C | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(34): Show |
42 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.46-2754C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659565 | |||||||
| chr1:99659711 | A | G | 2 | a0001c0001t0004g0153 a0001c0001t0004g0156 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.46-2608A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659711 | |||||||
| chr1:99659885 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-2434C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99659885 | |||||||
| chr1:99660034 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.46-2285G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660034 | |||||||
| chr1:99660105 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.46-2214T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660105 | |||||||
| chr1:99660149 | C | T | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.46-2170C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660149 | |||||||
| chr1:99660337 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1982C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660337 | |||||||
| chr1:99660343 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1976T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660343 | |||||||
| chr1:99660403 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-1916G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660403 | |||||||
| chr1:99660536 | G | A | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-1783G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660536 | |||||||
| chr1:99660639 | AT | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.46-1670delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 99660639 | ||||||
| chr1:99660690 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.46-1629A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660690 | |||||||
| chr1:99660746 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.46-1573C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660746 | |||||||
| chr1:99660901 | A | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1418A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660901 | |||||||
| chr1:99660981 | T | A | 1 | a0001c0001t0001g0077 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.46-1338T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99660981 | |||||||
| chr1:99661105 | C | T | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-1214C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661105 | |||||||
| chr1:99661291 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.46-1028A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661291 | |||||||
| chr1:99661371 | T | G | 1 | a0001c0002t0002g0334 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.46-948T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661371 | |||||||
| chr1:99661525 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-794G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661525 | |||||||
| chr1:99661678 | G | C | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46-641G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661678 | |||||||
| chr1:99661728 | A | G | 2 | a0006c0007t0001g0302 a0006c0007t0001g0303 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.46-591A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661728 | |||||||
| chr1:99661799 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.46-520A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661799 | |||||||
| chr1:99661833 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-486G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661833 | |||||||
| chr1:99661928 | G | A | 13 | a0001c0001t0001g0155 a0001c0001t0001g0213 a0001c0001t0006g0154 others(10): Show |
13 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-391G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661928 | |||||||
| chr1:99661929 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0102 a0001c0001t0001g0133 |
4 | HG00423.hp1 HG00544.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-390C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661929 | |||||||
| chr1:99661989 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.46-330C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99661989 | |||||||
| chr1:99662062 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(58): Show |
69 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.46-257A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99662062 | |||||||
| chr1:99662285 | A | T | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.46-34A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 1/7 | chr1 | 99662285 | |||||||
| chr1:99662532 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+133T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662532 | |||||||
| chr1:99662563 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.126+164A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662563 | |||||||
| chr1:99662609 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+210T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662609 | |||||||
| chr1:99662779 | G | A | 7 | a0001c0001t0001g0213 a0001c0002t0001g0031 a0001c0002t0001g0039 others(4): Show |
7 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+380G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662779 | |||||||
| chr1:99662819 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.126+420T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662819 | |||||||
| chr1:99662830 | T | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+431T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99662830 | |||||||
| chr1:99663026 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+627G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663026 | |||||||
| chr1:99663036 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+637A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663036 | |||||||
| chr1:99663119 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.126+720C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663119 | |||||||
| chr1:99663150 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.126+751G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663150 | |||||||
| chr1:99663227 | A | G | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.126+828A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663227 | |||||||
| chr1:99663434 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.126+1035A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663434 | |||||||
| chr1:99663520 | C | T | 1 | a0002c0003t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.126+1121C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663520 | |||||||
| chr1:99663654 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1255C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663654 | |||||||
| chr1:99663779 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+1380G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99663779 | |||||||
| chr1:99664018 | G | C | 3 | a0001c0001t0004g0153 a0001c0001t0004g0156 a0010c0013t0001g0308 |
3 | HG02055.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.126+1619G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664018 | |||||||
| chr1:99664151 | A | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1752A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664151 | |||||||
| chr1:99664158 | G | T | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.126+1759G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664158 | |||||||
| chr1:99664251 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.126+1852T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664251 | |||||||
| chr1:99664308 | G | A | 1 | a0010c0013t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.126+1909G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664308 | |||||||
| chr1:99664488 | T | C | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126+2089T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664488 | |||||||
| chr1:99664556 | G | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2157G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664556 | |||||||
| chr1:99664594 | T | G | 15 | a0001c0001t0001g0155 a0001c0001t0001g0213 a0001c0001t0006g0154 others(12): Show |
15 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+2195T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664594 | |||||||
| chr1:99664611 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2212A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664611 | |||||||
| chr1:99664791 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0111 |
3 | NA18984.hp2 NA18986.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.126+2392C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664791 | |||||||
| chr1:99664992 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+2593A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99664992 | |||||||
| chr1:99665088 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(99): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.127-2554G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665088 | |||||||
| chr1:99665125 | T | C | 7 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0132 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-2517T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665125 | |||||||
| chr1:99665154 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(231): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.127-2488A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665154 | |||||||
| chr1:99665391 | G | A | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-2251G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665391 | |||||||
| chr1:99665404 | T | C | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-2238T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665404 | |||||||
| chr1:99665461 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.127-2181T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665461 | |||||||
| chr1:99665484 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(39): Show |
50 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.127-2158G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665484 | |||||||
| chr1:99665615 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-2027A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665615 | |||||||
| chr1:99665735 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1907G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99665735 | |||||||
| chr1:99666006 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1636A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666006 | |||||||
| chr1:99666143 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1499T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666143 | |||||||
| chr1:99666149 | T | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1493T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666149 | |||||||
| chr1:99666192 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1450T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666192 | |||||||
| chr1:99666243 | GT | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
45 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.127-1389delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 99666243 | ||||||
| chr1:99666355 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.127-1287G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666355 | |||||||
| chr1:99666403 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.127-1239C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666403 | |||||||
| chr1:99666706 | G | C | 2 | a0001c0001t0001g0137 a0007c0015t0001g0135 |
2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.127-936G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666706 | |||||||
| chr1:99666903 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.127-739G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666903 | |||||||
| chr1:99666991 | C | T | 5 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(2): Show |
5 | HG02896.hp1 HG02897.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-651C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666991 | |||||||
| chr1:99666992 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-650G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99666992 | |||||||
| chr1:99667036 | G | A | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-606G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667036 | |||||||
| chr1:99667365 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.127-277G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667365 | |||||||
| chr1:99667435 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.127-207G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667435 | |||||||
| chr1:99667445 | G | A | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.127-197G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667445 | |||||||
| chr1:99667467 | C | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-175C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667467 | |||||||
| chr1:99667521 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.127-121G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667521 | |||||||
| chr1:99667544 | C | T | 3 | a0001c0001t0001g0264 a0004c0006t0001g0278 a0004c0006t0001g0279 |
3 | HG00735.hp1 HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.127-98C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667544 | |||||||
| chr1:99667598 | T | C | 1 | a0001c0002t0002g0319 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-44T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667598 | |||||||
| chr1:99667620 | T | C | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-22T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667620 | |||||||
| chr1:99667625 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-17A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 2/7 | chr1 | 99667625 | |||||||
| chr1:99667882 | CT | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(66): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.251+130delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99667882 | ||||||
| chr1:99667894 | T | C | 1 | a0010c0013t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+128T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667894 | |||||||
| chr1:99667954 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.251+188C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667954 | |||||||
| chr1:99667976 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.251+210T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99667976 | |||||||
| chr1:99668016 | T | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0170 |
2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.251+250T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668016 | |||||||
| chr1:99668127 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.251+361G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668127 | |||||||
| chr1:99668155 | G | A | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.251+389G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668155 | |||||||
| chr1:99668217 | G | A | 1 | a0001c0001t0001g0015 | 2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.251+451G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668217 | |||||||
| chr1:99668222 | G | C | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.251+456G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668222 | |||||||
| chr1:99668418 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.251+652A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668418 | |||||||
| chr1:99668449 | T | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+683T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668449 | |||||||
| chr1:99668714 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.251+948A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668714 | |||||||
| chr1:99668717 | C | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0190 |
3 | HG01123.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.251+951C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668717 | |||||||
| chr1:99668777 | T | C | 9 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(6): Show |
9 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+1011T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668777 | |||||||
| chr1:99668847 | A | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG00639.hp2 HG01261.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.251+1081A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668847 | |||||||
| chr1:99668997 | A | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1231A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99668997 | |||||||
| chr1:99669122 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1356G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669122 | |||||||
| chr1:99669183 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1417A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669183 | |||||||
| chr1:99669213 | AACTG | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1452_251+1455d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99669213 | ||||||
| chr1:99669341 | G | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(91): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.251+1575G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669341 | |||||||
| chr1:99669636 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1870G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669636 | |||||||
| chr1:99669683 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+1917G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669683 | |||||||
| chr1:99669738 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0037 a0001c0001t0001g0049 others(7): Show |
12 | HG00673.hp1 HG01070.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.251+1972C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669738 | |||||||
| chr1:99669752 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.251+1986C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669752 | |||||||
| chr1:99669780 | G | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(260): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.251+2014G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669780 | |||||||
| chr1:99669781 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.251+2015G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669781 | |||||||
| chr1:99669786 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0043 others(5): Show |
9 | HG02129.hp1 HG02135.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.251+2020G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669786 | |||||||
| chr1:99669845 | A | G | 15 | a0001c0001t0001g0155 a0001c0001t0001g0213 a0001c0001t0006g0154 others(12): Show |
15 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+2079A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669845 | |||||||
| chr1:99669850 | G | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2084G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669850 | |||||||
| chr1:99669863 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.251+2097A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669863 | |||||||
| chr1:99669922 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.251+2156G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99669922 | |||||||
| chr1:99670099 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.251+2333T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670099 | |||||||
| chr1:99670107 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2341T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670107 | |||||||
| chr1:99670274 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.251+2508G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670274 | |||||||
| chr1:99670354 | C | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2588C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670354 | |||||||
| chr1:99670361 | C | T | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.251+2595C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670361 | |||||||
| chr1:99670382 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2616C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670382 | |||||||
| chr1:99670473 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.251+2707C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670473 | |||||||
| chr1:99670559 | C | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+2793C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670559 | |||||||
| chr1:99670773 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.251+3007T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670773 | |||||||
| chr1:99670887 | T | TA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0038 others(7): Show |
11 | HG02257.hp1 HG02683.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.251+3129dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99670887 | ||||||
| chr1:99670987 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3221T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99670987 | |||||||
| chr1:99671072 | C | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(39): Show |
50 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.251+3306C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671072 | |||||||
| chr1:99671228 | C | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.251+3462C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671228 | |||||||
| chr1:99671232 | G | A | 1 | a0001c0002t0001g0282 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.251+3466G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671232 | |||||||
| chr1:99671276 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3510C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671276 | |||||||
| chr1:99671311 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3545T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671311 | |||||||
| chr1:99671315 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3549G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671315 | |||||||
| chr1:99671352 | A | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3586A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671352 | |||||||
| chr1:99671364 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.251+3598T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671364 | |||||||
| chr1:99671425 | AG | A | 6 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+3660delG | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671425 | |||||||
| chr1:99671551 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0001g0186 a0001c0001t0001g0192 others(2): Show |
5 | HG00323.hp1 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+3785G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671551 | |||||||
| chr1:99671637 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3871A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671637 | |||||||
| chr1:99671691 | T | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+3925T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671691 | |||||||
| chr1:99671702 | A | G | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.251+3936A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671702 | |||||||
| chr1:99671772 | A | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02027.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.251+4006A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671772 | |||||||
| chr1:99671934 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4168A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671934 | |||||||
| chr1:99671947 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4181T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99671947 | |||||||
| chr1:99672002 | T | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0248 |
2 | HG00673.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.251+4236T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672002 | |||||||
| chr1:99672036 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(35): Show |
43 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.251+4270T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672036 | |||||||
| chr1:99672236 | A | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4470A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672236 | |||||||
| chr1:99672251 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0171 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.251+4485G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672251 | |||||||
| chr1:99672310 | T | C | 3 | a0003c0004t0001g0008 a0003c0004t0001g0216 a0003c0004t0005g0217 |
5 | HG02622.hp2 HG02809.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.251+4544T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672310 | |||||||
| chr1:99672318 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4552G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672318 | |||||||
| chr1:99672337 | T | C | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+4571T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672337 | |||||||
| chr1:99672379 | G | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG00609.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.251+4613G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672379 | |||||||
| chr1:99672399 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.251+4633C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672399 | |||||||
| chr1:99672485 | T | C | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+4719T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672485 | |||||||
| chr1:99672508 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.251+4742T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672508 | |||||||
| chr1:99672554 | T | A | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+4788T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672554 | |||||||
| chr1:99672656 | T | C | 6 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(3): Show |
6 | HG01167.hp2 HG01884.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+4890T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672656 | |||||||
| chr1:99672718 | A | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+4952A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672718 | |||||||
| chr1:99672734 | C | T | 2 | a0004c0006t0001g0278 a0004c0006t0001g0279 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.251+4968C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672734 | |||||||
| chr1:99672735 | G | A | 1 | a0001c0012t0001g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.251+4969G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672735 | |||||||
| chr1:99672773 | C | T | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5007C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672773 | |||||||
| chr1:99672781 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5015G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672781 | |||||||
| chr1:99672794 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.251+5028C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672794 | |||||||
| chr1:99672944 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0171 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.251+5178G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672944 | |||||||
| chr1:99672967 | G | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5201G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99672967 | |||||||
| chr1:99673036 | T | C | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5270T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673036 | |||||||
| chr1:99673103 | G | A | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5337G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673103 | |||||||
| chr1:99673244 | T | C | 2 | a0001c0002t0002g0209 a0001c0002t0002g0318 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.251+5478T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673244 | |||||||
| chr1:99673261 | T | G | 4 | a0001c0001t0001g0324 a0001c0002t0001g0269 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.251+5495T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673261 | |||||||
| chr1:99673271 | AT | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0314 |
5 | HG00741.hp1 HG01106.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+5508delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99673271 | ||||||
| chr1:99673480 | G | GA | 5 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(2): Show |
5 | HG01167.hp2 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+5723dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99673480 | ||||||
| chr1:99673515 | G | T | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+5749G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673515 | |||||||
| chr1:99673586 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(150): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.251+5820T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673586 | |||||||
| chr1:99673587 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(150): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.251+5821C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673587 | |||||||
| chr1:99673588 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(150): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.251+5822G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673588 | |||||||
| chr1:99673702 | A | G | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0001c0005t0001g0273 |
3 | HG02451.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.251+5936A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673702 | |||||||
| chr1:99673716 | C | T | 6 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(3): Show |
6 | HG02965.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+5950C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673716 | |||||||
| chr1:99673735 | C | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(40): Show |
51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.251+5969C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673735 | |||||||
| chr1:99673768 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.251+6002C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673768 | |||||||
| chr1:99673918 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6152C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99673918 | |||||||
| chr1:99674065 | C | A | 7 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(4): Show |
7 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.251+6299C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674065 | |||||||
| chr1:99674076 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6310T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674076 | |||||||
| chr1:99674174 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0036 others(33): Show |
40 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.251+6408C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674174 | |||||||
| chr1:99674206 | G | C | 1 | a0001c0001t0001g0333 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.251+6440G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674206 | |||||||
| chr1:99674299 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+6533G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674299 | |||||||
| chr1:99674432 | A | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+6666A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674432 | |||||||
| chr1:99674546 | G | A | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+6780G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674546 | |||||||
| chr1:99674607 | C | CA | 8 | a0001c0001t0001g0078 a0001c0001t0001g0107 a0001c0001t0001g0145 others(5): Show |
8 | HG00741.hp2 HG01361.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.251+6855dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99674607 | ||||||
| chr1:99674607 | CA | C | 23 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0137 others(20): Show |
23 | HG00544.hp1 HG01346.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.251+6855delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99674607 | ||||||
| chr1:99674763 | G | T | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+6997G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674763 | |||||||
| chr1:99674858 | T | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(51): Show |
62 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.251+7092T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674858 | |||||||
| chr1:99674920 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.251+7154C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674920 | |||||||
| chr1:99674922 | T | C | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7156T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674922 | |||||||
| chr1:99674931 | G | C | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7165G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674931 | |||||||
| chr1:99674953 | G | A | 14 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+7187G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674953 | |||||||
| chr1:99674999 | C | T | 11 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(8): Show |
11 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.251+7233C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99674999 | |||||||
| chr1:99675000 | G | A | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+7234G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675000 | |||||||
| chr1:99675002 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.251+7236T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675002 | |||||||
| chr1:99675015 | T | C | 1 | a0003c0004t0001g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.251+7249T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675015 | |||||||
| chr1:99675082 | CTA | C | 14 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.251+7318_251+7319d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99675082 | ||||||
| chr1:99675194 | A | G | 3 | a0001c0001t0001g0311 a0001c0001t0001g0324 a0001c0002t0001g0281 |
3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7428A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675194 | |||||||
| chr1:99675213 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.251+7447T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675213 | |||||||
| chr1:99675221 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7455G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675221 | |||||||
| chr1:99675334 | A | C | 1 | a0001c0001t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.251+7568A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675334 | |||||||
| chr1:99675417 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7651T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675417 | |||||||
| chr1:99675527 | C | T | 3 | a0001c0001t0001g0311 a0001c0001t0001g0324 a0001c0002t0001g0281 |
3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+7761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675527 | |||||||
| chr1:99675568 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+7802C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675568 | |||||||
| chr1:99675852 | G | A | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.251+8086G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675852 | |||||||
| chr1:99675880 | T | C | 3 | a0001c0001t0001g0311 a0001c0001t0001g0324 a0001c0002t0001g0281 |
3 | HG02109.hp1 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8114T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675880 | |||||||
| chr1:99675894 | C | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8128C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675894 | |||||||
| chr1:99675901 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+8135T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99675901 | |||||||
| chr1:99676002 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.251+8236G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676002 | |||||||
| chr1:99676057 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+8291T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676057 | |||||||
| chr1:99676321 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.251+8555A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676321 | |||||||
| chr1:99676332 | T | C | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8566T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676332 | |||||||
| chr1:99676359 | C | T | 5 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+8593C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676359 | |||||||
| chr1:99676387 | G | A | 1 | a0010c0013t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.251+8621G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676387 | |||||||
| chr1:99676388 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0184 |
2 | NA18999.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.251+8622C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676388 | |||||||
| chr1:99676401 | T | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.251+8635T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676401 | |||||||
| chr1:99676414 | A | G | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.251+8648A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676414 | |||||||
| chr1:99676439 | T | C | 5 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+8673T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676439 | |||||||
| chr1:99676627 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(47): Show |
58 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.251+8861G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676627 | |||||||
| chr1:99676639 | G | A | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.251+8873G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676639 | |||||||
| chr1:99676782 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0143 others(6): Show |
12 | HG00741.hp1 HG01081.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.251+9016G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676782 | |||||||
| chr1:99676783 | TA | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(45): Show |
56 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.251+9024delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99676783 | ||||||
| chr1:99676824 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.251+9058G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676824 | |||||||
| chr1:99676826 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+9060C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676826 | |||||||
| chr1:99676855 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.251+9089G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676855 | |||||||
| chr1:99676880 | A | G | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9114A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676880 | |||||||
| chr1:99676925 | A | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(44): Show |
55 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.251+9159A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99676925 | |||||||
| chr1:99677030 | G | C | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9264G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677030 | |||||||
| chr1:99677046 | G | A | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9280G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677046 | |||||||
| chr1:99677092 | G | T | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9326G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677092 | |||||||
| chr1:99677111 | T | A | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.251+9345T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677111 | |||||||
| chr1:99677235 | T | TC | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9440dupC | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677235 | ||||||
| chr1:99677248 | G | GA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0040 others(8): Show |
12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-9421dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677248 | ||||||
| chr1:99677248 | GA | G | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9421delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99677248 | ||||||
| chr1:99677443 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.252-9233C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677443 | |||||||
| chr1:99677484 | C | T | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9192C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677484 | |||||||
| chr1:99677506 | A | G | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-9170A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677506 | |||||||
| chr1:99677607 | T | C | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(329): Show |
377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.252-9069T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677607 | |||||||
| chr1:99677693 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.252-8983G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677693 | |||||||
| chr1:99677701 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-8975G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677701 | |||||||
| chr1:99677707 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0040 others(8): Show |
12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-8969T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677707 | |||||||
| chr1:99677734 | C | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0040 others(8): Show |
12 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.252-8942C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677734 | |||||||
| chr1:99677836 | G | A | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-8840G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677836 | |||||||
| chr1:99677841 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.252-8835T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677841 | |||||||
| chr1:99677891 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0242 a0001c0001t0001g0243 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-8785C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677891 | |||||||
| chr1:99677902 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(157): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.252-8774A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99677902 | |||||||
| chr1:99678047 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(141): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.252-8629G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678047 | |||||||
| chr1:99678097 | T | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.252-8579T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678097 | |||||||
| chr1:99678112 | A | AT | 11 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(8): Show |
11 | HG01074.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.252-8548dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678112 | ||||||
| chr1:99678112 | AT | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0134 a0001c0001t0001g0176 others(16): Show |
19 | HG00735.hp1 HG01070.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252-8548delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678112 | ||||||
| chr1:99678116 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.252-8560T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678116 | |||||||
| chr1:99678228 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0201 |
2 | HG02080.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.252-8448C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678228 | |||||||
| chr1:99678236 | G | A | 7 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(4): Show |
7 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-8440G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678236 | |||||||
| chr1:99678237 | G | A | 14 | a0001c0001t0001g0213 a0001c0002t0002g0207 a0001c0002t0002g0208 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.252-8439G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678237 | |||||||
| chr1:99678240 | TTA | T | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-8431_252-8430d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678240 | ||||||
| chr1:99678266 | A | C | 3 | a0001c0001t0004g0153 a0001c0001t0004g0156 a0010c0013t0001g0308 |
3 | HG02055.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-8410A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678266 | |||||||
| chr1:99678314 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.252-8362G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678314 | |||||||
| chr1:99678454 | G | A | 2 | a0005c0009t0001g0028 a0005c0009t0001g0029 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.252-8222G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678454 | |||||||
| chr1:99678491 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8185A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678491 | |||||||
| chr1:99678492 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8184C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678492 | |||||||
| chr1:99678493 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-8183A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678493 | |||||||
| chr1:99678565 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.252-8111G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678565 | |||||||
| chr1:99678597 | T | C | 2 | a0001c0001t0004g0153 a0001c0001t0004g0156 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-8079T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678597 | |||||||
| chr1:99678665 | C | CA | 7 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(4): Show |
7 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-8007dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678665 | ||||||
| chr1:99678670 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.252-8006T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678670 | |||||||
| chr1:99678807 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.252-7869C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99678807 | |||||||
| chr1:99678966 | T | TA | 15 | a0001c0001t0001g0116 a0001c0001t0001g0259 a0001c0001t0001g0311 others(12): Show |
15 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.252-7695dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678966 | ||||||
| chr1:99678966 | TA | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(46): Show |
57 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.252-7695delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99678966 | ||||||
| chr1:99679042 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.252-7634G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679042 | |||||||
| chr1:99679171 | C | T | 20 | a0001c0001t0001g0036 a0001c0001t0001g0213 a0001c0001t0001g0311 others(17): Show |
20 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.252-7505C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679171 | |||||||
| chr1:99679412 | G | T | 7 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0002t0001g0320 others(4): Show |
7 | HG02055.hp2 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-7264G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679412 | |||||||
| chr1:99679472 | C | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(40): Show |
51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.252-7204C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679472 | |||||||
| chr1:99679532 | A | C | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-7144A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679532 | |||||||
| chr1:99679533 | A | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-7143A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679533 | |||||||
| chr1:99679623 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0304 a0001c0001t0001g0305 |
3 | HG02602.hp1 HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.252-7053T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679623 | |||||||
| chr1:99679887 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(64): Show |
75 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.252-6789A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679887 | |||||||
| chr1:99679915 | C | T | 9 | a0001c0001t0001g0027 a0001c0001t0001g0114 a0001c0001t0001g0242 others(6): Show |
9 | HG01891.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.252-6761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679915 | |||||||
| chr1:99679947 | A | G | 19 | a0001c0001t0001g0213 a0001c0001t0001g0311 a0001c0002t0001g0269 others(16): Show |
19 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-6729A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99679947 | |||||||
| chr1:99680179 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.252-6497T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680179 | |||||||
| chr1:99680355 | T | C | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-6321T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680355 | |||||||
| chr1:99680356 | G | A | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-6320G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680356 | |||||||
| chr1:99680614 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-6062T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680614 | |||||||
| chr1:99680705 | C | G | 1 | a0002c0003t0001g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252-5971C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680705 | |||||||
| chr1:99680826 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252-5850A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680826 | |||||||
| chr1:99680842 | A | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5834A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680842 | |||||||
| chr1:99680851 | C | CAT | 17 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0038 others(14): Show |
18 | HG00140.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5812_252-5811d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99680851 | ||||||
| chr1:99680861 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-5815T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680861 | |||||||
| chr1:99680875 | G | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(63): Show |
74 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.252-5801G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680875 | |||||||
| chr1:99680915 | C | T | 10 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0209 others(7): Show |
10 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-5761C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99680915 | |||||||
| chr1:99681022 | G | C | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5654G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681022 | |||||||
| chr1:99681097 | G | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG01081.hp2 HG01192.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-5579G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681097 | |||||||
| chr1:99681101 | A | G | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5575A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681101 | |||||||
| chr1:99681103 | A | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5573A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681103 | |||||||
| chr1:99681105 | A | ATG | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-5541_252-5540d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | ||||||
| chr1:99681105 | A | G | 2 | a0001c0001t0001g0311 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.252-5571A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681105 | |||||||
| chr1:99681105 | ATG | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(205): Show |
242 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.252-5541_252-5540d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | ||||||
| chr1:99681105 | ATGTG | A | 22 | a0001c0001t0001g0128 a0001c0001t0001g0251 a0001c0001t0001g0301 others(19): Show |
22 | HG00544.hp1 HG00735.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.252-5543_252-5540d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | ||||||
| chr1:99681105 | ATGTGTG | A | 29 | a0001c0001t0001g0100 a0001c0001t0001g0131 a0001c0001t0001g0137 others(26): Show |
29 | HG00738.hp1 HG01167.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.252-5545_252-5540d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681105 | ||||||
| chr1:99681107 | G | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0075 a0001c0001t0001g0155 others(4): Show |
7 | HG02258.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.252-5569G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681107 | |||||||
| chr1:99681109 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.252-5567G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681109 | |||||||
| chr1:99681111 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0251 a0001c0001t0001g0301 |
3 | HG01175.hp1 HG03453.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.252-5565G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681111 | |||||||
| chr1:99681127 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.252-5545_252-5536d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681127 | ||||||
| chr1:99681129 | G | A | 16 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5547G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681129 | |||||||
| chr1:99681131 | GTGTGTA | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(33): Show |
42 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.252-5541_252-5536d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681131 | ||||||
| chr1:99681133 | G | A | 16 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5543G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681133 | |||||||
| chr1:99681135 | G | A | 17 | a0001c0001t0002g0309 a0001c0002t0001g0269 a0001c0002t0001g0282 others(14): Show |
17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5541G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681135 | |||||||
| chr1:99681135 | GTATGTA | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
8 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-5537_252-5532d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681135 | ||||||
| chr1:99681137 | A | G | 2 | a0001c0001t0002g0309 a0001c0002t0001g0281 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.252-5539A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681137 | |||||||
| chr1:99681139 | G | A | 17 | a0001c0001t0002g0309 a0001c0002t0001g0269 a0001c0002t0001g0282 others(14): Show |
17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5537G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681139 | |||||||
| chr1:99681142 | T | G | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5534T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681142 | |||||||
| chr1:99681143 | A | G | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5533A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681143 | |||||||
| chr1:99681144 | T | G | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5532T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681144 | |||||||
| chr1:99681146 | T | G | 12 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(9): Show |
12 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-5530T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681146 | |||||||
| chr1:99681148 | T | G | 16 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5528T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681148 | |||||||
| chr1:99681150 | T | G | 16 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5526T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681150 | |||||||
| chr1:99681152 | T | G | 16 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 others(13): Show |
16 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-5524T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681152 | |||||||
| chr1:99681153 | G | A | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5523G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681153 | |||||||
| chr1:99681154 | T | G | 17 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0282 others(14): Show |
17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5522T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681154 | |||||||
| chr1:99681156 | T | G | 17 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0282 others(14): Show |
17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-5520T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681156 | |||||||
| chr1:99681156 | T | TAGAGAGA others(5): Show |
1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-5516_252-5515i others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99681156 | ||||||
| chr1:99681220 | A | G | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-5456A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681220 | |||||||
| chr1:99681228 | A | T | 1 | a0001c0001t0001g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.252-5448A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681228 | |||||||
| chr1:99681248 | T | A | 6 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(3): Show |
6 | HG00544.hp1 HG01346.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-5428T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681248 | |||||||
| chr1:99681287 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.252-5389G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681287 | |||||||
| chr1:99681384 | C | T | 1 | a0004c0006t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252-5292C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681384 | |||||||
| chr1:99681605 | G | A | 1 | a0002c0003t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-5071G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681605 | |||||||
| chr1:99681731 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.252-4945A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681731 | |||||||
| chr1:99681780 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.252-4896G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681780 | |||||||
| chr1:99681834 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(64): Show |
75 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.252-4842A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681834 | |||||||
| chr1:99681835 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(96): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.252-4841C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681835 | |||||||
| chr1:99681865 | C | G | 17 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(14): Show |
17 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.252-4811C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681865 | |||||||
| chr1:99681964 | C | G | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-4712C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681964 | |||||||
| chr1:99681967 | G | C | 18 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(15): Show |
18 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.252-4709G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99681967 | |||||||
| chr1:99682010 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.252-4666T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682010 | |||||||
| chr1:99682027 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252-4649G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682027 | |||||||
| chr1:99682031 | G | A | 10 | a0001c0001t0001g0311 a0002c0003t0001g0083 a0002c0003t0001g0205 others(7): Show |
10 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-4645G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682031 | |||||||
| chr1:99682053 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.252-4623G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682053 | |||||||
| chr1:99682425 | C | T | 27 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(24): Show |
27 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.252-4251C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682425 | |||||||
| chr1:99682431 | C | T | 27 | a0001c0001t0001g0311 a0001c0002t0001g0269 a0001c0002t0001g0281 others(24): Show |
27 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.252-4245C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682431 | |||||||
| chr1:99682444 | C | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-4232C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682444 | |||||||
| chr1:99682539 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-4137T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682539 | |||||||
| chr1:99682585 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-4091C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682585 | |||||||
| chr1:99682647 | G | A | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-4029G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682647 | |||||||
| chr1:99682723 | A | G | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3953A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682723 | |||||||
| chr1:99682735 | C | T | 4 | a0001c0005t0001g0265 a0001c0005t0001g0271 a0001c0005t0001g0272 others(1): Show |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3941C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682735 | |||||||
| chr1:99682736 | G | A | 2 | a0001c0001t0004g0153 a0001c0001t0004g0156 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.252-3940G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682736 | |||||||
| chr1:99682742 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.252-3934A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682742 | |||||||
| chr1:99682817 | T | C | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3859T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682817 | |||||||
| chr1:99682824 | G | A | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3852G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682824 | |||||||
| chr1:99682942 | G | T | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3734G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682942 | |||||||
| chr1:99682945 | A | G | 33 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(30): Show |
33 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3731A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682945 | |||||||
| chr1:99682948 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.252-3728G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682948 | |||||||
| chr1:99682955 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.252-3721G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99682955 | |||||||
| chr1:99683003 | CTCCAAAA others(1): Show |
C | 9 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(6): Show |
9 | HG00544.hp1 HG01346.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.252-3672_252-3665d others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | |||||||
| chr1:99683003 | CTCCAAAA others(13): Show |
C | 1 | a0002c0003t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-3672_252-3653d others(22): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | |||||||
| chr1:99683003 | CTCCAAAA others(17): Show |
C | 3 | a0001c0002t0001g0269 a0001c0002t0001g0282 a0001c0002t0001g0325 |
3 | HG01884.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-3672_252-3649d others(26): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | |||||||
| chr1:99683003 | CTCCAAAA others(21): Show |
C | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-3672_252-3645d others(30): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | |||||||
| chr1:99683003 | CTCCAAAA others(79): Show |
C | 9 | a0002c0003t0001g0205 a0002c0003t0001g0315 a0002c0003t0001g0316 others(6): Show |
11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3672_252-3587d others(88): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683003 | |||||||
| chr1:99683004 | T | G | 11 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(8): Show |
11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3672T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683004 | |||||||
| chr1:99683005 | C | A | 11 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(8): Show |
11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3671C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683005 | |||||||
| chr1:99683006 | C | A | 11 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(8): Show |
11 | HG01167.hp2 HG02965.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3670C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683006 | |||||||
| chr1:99683008 | A | G | 13 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(10): Show |
13 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3668A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683008 | |||||||
| chr1:99683019 | G | A | 22 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(19): Show |
22 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.252-3657G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683019 | |||||||
| chr1:99683019 | G | GGAAA | 3 | a0001c0001t0001g0016 a0001c0001t0001g0107 a0001c0001t0001g0109 |
3 | HG02056.hp2 HG02165.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.252-3622_252-3619d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | ||||||
| chr1:99683019 | G | GGAAAGAA others(5): Show |
1 | a0001c0001t0001g0133 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.252-3630_252-3619d others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | ||||||
| chr1:99683019 | GGA | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0245 a0001c0001t0001g0288 |
3 | HG02735.hp1 HG03540.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.252-3656_252-3655d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683019 | |||||||
| chr1:99683019 | GGAAAGAA others(63): Show |
G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(13): Show |
16 | HG00639.hp2 HG00735.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.252-3618_252-3549d others(72): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | ||||||
| chr1:99683019 | GGAAAGAA others(67): Show |
G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0063 others(2): Show |
5 | HG01361.hp1 HG01928.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3618_252-3545d others(76): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | ||||||
| chr1:99683019 | GGAAAGAA others(71): Show |
G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0060 others(2): Show |
5 | HG00280.hp2 HG00438.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3618_252-3541d others(80): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683019 | ||||||
| chr1:99683021 | AAAGAAAG others(56): Show |
A | 1 | a0001c0001t0001g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.252-3653_252-3591d others(65): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683021 | ||||||
| chr1:99683022 | AAGAAAGA others(59): Show |
A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0066 others(16): Show |
19 | HG00140.hp1 HG00423.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.252-3618_252-3553d others(68): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683022 | ||||||
| chr1:99683023 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(16): Show |
21 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.252-3653A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683023 | |||||||
| chr1:99683026 | AAGAAAGA others(55): Show |
A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(19): Show |
22 | HG00323.hp1 HG01099.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.252-3618_252-3557d others(64): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683026 | ||||||
| chr1:99683029 | AAAGAAAG others(66): Show |
A | 1 | a0001c0001t0001g0314 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.252-3644_252-3572d others(75): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683029 | ||||||
| chr1:99683030 | AAGAAAGA others(51): Show |
A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(24): Show |
30 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.252-3618_252-3561d others(60): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683030 | ||||||
| chr1:99683033 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-3643A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683033 | |||||||
| chr1:99683034 | AAGAAAGA others(47): Show |
A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(38): Show |
41 | HG00408.hp1 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.252-3618_252-3565d others(56): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683034 | ||||||
| chr1:99683038 | AAGAAAGA others(43): Show |
A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(32): Show |
38 | HG00438.hp1 HG00735.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.252-3618_252-3569d others(52): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683038 | ||||||
| chr1:99683040 | GAAAGAAA others(44): Show |
G | 1 | a0001c0001t0001g0058 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.252-3633_252-3583d others(53): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683040 | ||||||
| chr1:99683042 | AAGAAAGA others(39): Show |
A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0021 others(18): Show |
21 | HG00621.hp1 HG01070.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.252-3618_252-3573d others(48): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683042 | ||||||
| chr1:99683046 | AAGAAAGA others(3): Show |
A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0098 |
2 | NA18954.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.252-3626_252-3617d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683046 | ||||||
| chr1:99683046 | AAGAAAGA others(35): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(13): Show |
16 | HG00140.hp2 HG00597.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.252-3618_252-3577d others(44): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683046 | ||||||
| chr1:99683048 | GAAAGAA | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0141 |
3 | HG02135.hp1 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.252-3626_252-3621d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683048 | ||||||
| chr1:99683050 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.252-3626A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683050 | |||||||
| chr1:99683050 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0258 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.252-3622_252-3613d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683050 | ||||||
| chr1:99683050 | AAGAAAGA others(31): Show |
A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(3): Show |
7 | HG00673.hp2 HG03098.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-3618_252-3581d others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683050 | ||||||
| chr1:99683053 | AAAG | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0298 a0006c0007t0001g0303 |
3 | HG01258.hp1 HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.252-3621_252-3619d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683053 | ||||||
| chr1:99683054 | A | AAGAAGAG others(6): Show |
1 | a0001c0001t0001g0016 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.252-3619_252-3618i others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | ||||||
| chr1:99683054 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0042 others(9): Show |
14 | HG00323.hp2 HG00738.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.252-3622A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683054 | |||||||
| chr1:99683054 | AAGAGAGA others(15): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.252-3606_252-3585d others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | ||||||
| chr1:99683054 | AAGAGAGA others(19): Show |
A | 1 | a0001c0001t0001g0075 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.252-3610_252-3585d others(28): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | ||||||
| chr1:99683054 | AAGAGAGA others(23): Show |
A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18978.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.252-3614_252-3585d others(32): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | ||||||
| chr1:99683054 | AAGAGAGA others(27): Show |
A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0120 a0001c0001t0001g0123 others(7): Show |
12 | HG00673.hp1 HG02165.hp2 NA18948.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-3618_252-3585d others(36): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683054 | ||||||
| chr1:99683056 | G | GAAAGAAA others(3): Show |
2 | a0001c0001t0001g0305 a0001c0005t0001g0273 |
2 | HG02698.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.252-3619_252-3618i others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | ||||||
| chr1:99683056 | G | GAAAGAAA others(7): Show |
1 | a0001c0005t0001g0272 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252-3619_252-3618i others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | ||||||
| chr1:99683056 | G | GAAAGAAA others(11): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0259 |
2 | HG02602.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.252-3619_252-3618i others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | ||||||
| chr1:99683056 | G | GAAAGAAA others(19): Show |
1 | a0001c0005t0001g0265 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252-3619_252-3618i others(28): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683056 | ||||||
| chr1:99683058 | G | A | 50 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0040 others(47): Show |
51 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.252-3618G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683058 | |||||||
| chr1:99683060 | G | A | 6 | a0001c0001t0001g0259 a0001c0001t0001g0305 a0001c0005t0001g0265 others(3): Show |
6 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3616G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683060 | |||||||
| chr1:99683062 | G | A | 33 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0041 others(30): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.252-3614G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683062 | |||||||
| chr1:99683064 | G | A | 6 | a0001c0001t0001g0259 a0001c0001t0001g0305 a0001c0005t0001g0265 others(3): Show |
6 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3612G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683064 | |||||||
| chr1:99683065 | A | AAAGAAAG others(4): Show |
1 | a0001c0001t0001g0018 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.252-3611_252-3610i others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683065 | |||||||
| chr1:99683066 | G | A | 14 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0089 others(11): Show |
14 | HG00544.hp2 HG00609.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.252-3610G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683066 | |||||||
| chr1:99683068 | G | A | 5 | a0001c0001t0001g0259 a0001c0005t0001g0265 a0001c0005t0001g0271 others(2): Show |
5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3608G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683068 | |||||||
| chr1:99683070 | G | A | 3 | a0001c0001t0001g0142 a0001c0002t0002g0319 a0005c0009t0001g0029 |
3 | HG03927.hp2 NA18960.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3606G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683070 | |||||||
| chr1:99683072 | G | A | 5 | a0001c0001t0001g0259 a0001c0005t0001g0265 a0001c0005t0001g0271 others(2): Show |
5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3604G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683072 | |||||||
| chr1:99683074 | G | A | 1 | a0005c0009t0001g0029 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.252-3602G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683074 | |||||||
| chr1:99683074 | GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0001g0099 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.252-3598_252-3577d others(24): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683074 | ||||||
| chr1:99683074 | GAGAGAGA others(55): Show |
G | 1 | a0002c0003t0001g0083 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.252-3598_252-3537d others(64): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683074 | ||||||
| chr1:99683076 | G | A | 5 | a0001c0001t0001g0259 a0001c0005t0001g0265 a0001c0005t0001g0271 others(2): Show |
5 | HG02451.hp2 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3600G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683076 | |||||||
| chr1:99683076 | GAGAGAGA others(25): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.252-3596_252-3565d others(34): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683076 | ||||||
| chr1:99683078 | GAGAGAGA others(31): Show |
G | 1 | a0001c0001t0001g0327 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.252-3594_252-3557d others(40): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683078 | ||||||
| chr1:99683078 | GAGAGAGA others(51): Show |
G | 1 | a0001c0002t0001g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.252-3594_252-3537d others(60): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683078 | ||||||
| chr1:99683080 | G | A | 6 | a0001c0001t0001g0035 a0001c0001t0001g0259 a0001c0005t0001g0265 others(3): Show |
6 | HG02451.hp2 HG02683.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252-3596G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683080 | |||||||
| chr1:99683080 | GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0001g0015 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.252-3592_252-3573d others(22): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683080 | ||||||
| chr1:99683080 | GAGAGAGA others(49): Show |
G | 2 | a0001c0002t0001g0282 a0001c0002t0001g0325 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.252-3592_252-3537d others(58): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683080 | ||||||
| chr1:99683082 | GAGAGAGA others(7): Show |
G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0139 |
3 | HG01934.hp1 NA19055.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.252-3590_252-3577d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | ||||||
| chr1:99683082 | GAGAGAGA others(11): Show |
G | 1 | a0001c0001t0001g0122 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.252-3590_252-3573d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | ||||||
| chr1:99683082 | GAGAGAGA others(47): Show |
G | 1 | a0001c0002t0001g0281 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.252-3590_252-3537d others(56): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683082 | ||||||
| chr1:99683084 | G | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0075 a0001c0001t0001g0259 others(4): Show |
7 | HG02451.hp2 HG02683.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.252-3592G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683084 | |||||||
| chr1:99683084 | GAGAGAGA others(8): Show |
G | 1 | a0001c0001t0001g0015 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.252-3590_252-3576d others(17): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683084 | ||||||
| chr1:99683084 | GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0101 a0001c0001t0001g0158 |
3 | HG00323.hp2 HG02300.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.252-3588_252-3573d others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683084 | ||||||
| chr1:99683086 | GAGAGAAA others(3): Show |
G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0310 |
2 | HG01069.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.252-3586_252-3577d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | ||||||
| chr1:99683086 | GAGAGAAA others(6): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.252-3588_252-3576d others(15): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | ||||||
| chr1:99683086 | GAGAGAAA others(7): Show |
G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0332 |
2 | HG00280.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.252-3586_252-3573d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | ||||||
| chr1:99683086 | GAGAGAAA others(11): Show |
G | 1 | a0001c0001t0001g0296 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.252-3586_252-3569d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | ||||||
| chr1:99683086 | GAGAGAAA others(30): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.252-3588_252-3552d others(39): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683086 | ||||||
| chr1:99683088 | G | A | 10 | a0001c0001t0001g0035 a0001c0001t0001g0075 a0001c0001t0001g0124 others(7): Show |
10 | HG01943.hp2 HG02451.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.252-3588G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683088 | |||||||
| chr1:99683088 | GAGAA | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0095 others(2): Show |
5 | HG01167.hp1 HG02015.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-3510_252-3507d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | ||||||
| chr1:99683088 | GAGAAAGA others(1): Show |
G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0089 a0001c0001t0001g0093 others(5): Show |
8 | HG00408.hp2 HG01934.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.252-3514_252-3507d others(10): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | ||||||
| chr1:99683088 | GAGAAAGA others(5): Show |
G | 5 | a0001c0001t0001g0081 a0001c0001t0001g0086 a0001c0001t0001g0097 others(2): Show |
5 | HG00738.hp1 HG01975.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3518_252-3507d others(14): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | ||||||
| chr1:99683088 | GAGAAAGA others(9): Show |
G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0300 |
2 | HG00639.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.252-3522_252-3507d others(18): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683088 | ||||||
| chr1:99683089 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0134 a0001c0001t0001g0225 |
3 | HG04184.hp1 NA19058.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.252-3587A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683089 | |||||||
| chr1:99683090 | GAA | G | 6 | a0001c0001t0001g0088 a0001c0001t0001g0102 a0001c0001t0001g0108 others(3): Show |
6 | HG00423.hp1 HG00609.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-3584_252-3583d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683090 | GAAAGAA | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0082 others(6): Show |
9 | HG01081.hp2 HG01175.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.252-3584_252-3579d others(8): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683090 | GAAAGAAA others(3): Show |
G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0046 others(11): Show |
15 | HG01978.hp1 HG01981.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.252-3584_252-3575d others(12): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683090 | GAAAGAAA others(7): Show |
G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0090 |
2 | HG02738.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.252-3584_252-3571d others(16): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683090 | GAAAGAAA others(11): Show |
G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0284 a0006c0007t0001g0303 |
3 | HG01258.hp1 HG01361.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.252-3584_252-3567d others(20): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683090 | GAAAGAAA others(14): Show |
G | 1 | a0006c0007t0001g0302 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.252-3583_252-3563d others(23): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683090 | ||||||
| chr1:99683091 | AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.252-3582_252-3572d others(13): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683091 | ||||||
| chr1:99683092 | A | G | 39 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0041 others(36): Show |
40 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.252-3584A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683092 | |||||||
| chr1:99683093 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(7): Show |
10 | HG00639.hp2 HG01261.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.252-3583A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683093 | |||||||
| chr1:99683096 | A | G | 42 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0025 others(39): Show |
42 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.252-3580A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683096 | |||||||
| chr1:99683097 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0063 |
3 | HG01928.hp2 NA18986.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.252-3579A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683097 | |||||||
| chr1:99683099 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0003g0215 |
2 | HG01169.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.252-3577A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683099 | |||||||
| chr1:99683100 | A | G | 43 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0026 others(40): Show |
44 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-3576A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683100 | |||||||
| chr1:99683101 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0060 others(1): Show |
4 | HG00280.hp2 HG00438.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3575A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683101 | |||||||
| chr1:99683103 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.252-3573A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683103 | |||||||
| chr1:99683103 | AAAGAAAG others(40): Show |
A | 3 | a0001c0002t0001g0237 a0001c0002t0002g0274 a0005c0009t0001g0028 |
3 | HG01167.hp2 HG02723.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.252-3570_252-3524d others(49): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683103 | ||||||
| chr1:99683104 | A | AAG | 3 | a0001c0005t0001g0265 a0001c0005t0001g0271 a0001c0005t0001g0273 |
3 | HG02970.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.252-3570_252-3569d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683104 | ||||||
| chr1:99683104 | A | G | 32 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0042 others(29): Show |
33 | HG00408.hp2 HG01081.hp2 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.252-3572A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683104 | |||||||
| chr1:99683107 | AAAGAAAG others(36): Show |
A | 3 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0235 |
3 | HG00544.hp1 HG02486.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.252-3566_252-3524d others(45): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683107 | ||||||
| chr1:99683108 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0001g0256 a0001c0001t0001g0297 others(8): Show |
11 | HG01192.hp2 HG01346.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3568A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683108 | |||||||
| chr1:99683111 | AAAGAAAG others(32): Show |
A | 5 | a0001c0002t0002g0254 a0001c0002t0002g0334 a0005c0009t0001g0029 others(2): Show |
5 | HG01884.hp1 HG03471.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3562_252-3524d others(41): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683111 | ||||||
| chr1:99683112 | A | G | 6 | a0001c0001t0001g0092 a0001c0002t0001g0039 a0001c0002t0001g0320 others(3): Show |
6 | HG01346.hp2 HG02976.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.252-3564A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683112 | |||||||
| chr1:99683115 | AAAGAAAG others(28): Show |
A | 4 | a0001c0002t0001g0236 a0001c0002t0002g0210 a0001c0002t0002g0275 others(1): Show |
4 | HG03209.hp2 HG04199.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.252-3558_252-3524d others(37): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683115 | ||||||
| chr1:99683116 | A | G | 3 | a0001c0002t0001g0039 a0001c0002t0001g0320 a0001c0002t0002g0319 |
3 | HG01346.hp2 HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252-3560A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683116 | |||||||
| chr1:99683119 | AAAGAAAG others(24): Show |
A | 2 | a0001c0002t0002g0209 a0001c0002t0002g0318 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.252-3554_252-3524d others(33): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683119 | ||||||
| chr1:99683120 | A | G | 11 | a0001c0002t0001g0320 a0001c0002t0002g0319 a0002c0003t0001g0205 others(8): Show |
13 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3556A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683120 | |||||||
| chr1:99683123 | AAAGAAAG others(20): Show |
A | 3 | a0001c0002t0001g0039 a0001c0002t0002g0207 a0001c0002t0002g0208 |
3 | HG01346.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.252-3550_252-3524d others(29): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683123 | ||||||
| chr1:99683124 | A | G | 11 | a0001c0002t0001g0320 a0001c0002t0002g0319 a0002c0003t0001g0205 others(8): Show |
13 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.252-3552A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683124 | |||||||
| chr1:99683128 | A | G | 10 | a0001c0002t0002g0319 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.252-3548A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683128 | |||||||
| chr1:99683132 | A | G | 9 | a0002c0003t0001g0205 a0002c0003t0001g0315 a0002c0003t0001g0316 others(6): Show |
11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3544A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683132 | |||||||
| chr1:99683136 | A | G | 9 | a0002c0003t0001g0205 a0002c0003t0001g0315 a0002c0003t0001g0316 others(6): Show |
11 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.252-3540A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683136 | |||||||
| chr1:99683144 | AAG | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0249 |
3 | NA18948.hp2 NA18993.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.252-3530_252-3529d others(4): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683144 | ||||||
| chr1:99683147 | AAAG | A | 15 | a0001c0002t0001g0269 a0001c0002t0001g0281 a0001c0002t0001g0282 others(12): Show |
17 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.252-3526_252-3524d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683147 | ||||||
| chr1:99683161 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.252-3515A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683161 | |||||||
| chr1:99683162 | GAAA | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(31): Show |
38 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3513_252-3511d others(5): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683162 | |||||||
| chr1:99683165 | A | AG | 5 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(2): Show |
5 | HG00673.hp1 NA18970.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.252-3510dupG | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683165 | ||||||
| chr1:99683165 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.252-3511A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683165 | |||||||
| chr1:99683170 | C | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.252-3506C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683170 | |||||||
| chr1:99683180 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.252-3496A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683180 | |||||||
| chr1:99683312 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(30): Show |
40 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.252-3364A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683312 | |||||||
| chr1:99683325 | C | A | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-3351C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683325 | |||||||
| chr1:99683327 | G | C | 4 | a0001c0002t0001g0269 a0001c0002t0001g0281 a0001c0002t0001g0282 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-3349G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683327 | |||||||
| chr1:99683453 | A | AT | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3221dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99683453 | ||||||
| chr1:99683560 | G | C | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3116G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683560 | |||||||
| chr1:99683621 | A | G | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3055A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683621 | |||||||
| chr1:99683648 | A | G | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(41): Show |
51 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.252-3028A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683648 | |||||||
| chr1:99683649 | T | C | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-3027T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683649 | |||||||
| chr1:99683752 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.252-2924G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683752 | |||||||
| chr1:99683899 | G | A | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2777G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683899 | |||||||
| chr1:99683917 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.252-2759G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683917 | |||||||
| chr1:99683924 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.252-2752C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683924 | |||||||
| chr1:99683953 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.252-2723T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99683953 | |||||||
| chr1:99684046 | A | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0170 |
2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.252-2630A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684046 | |||||||
| chr1:99684077 | T | G | 2 | a0001c0002t0001g0235 a0001c0002t0001g0237 |
2 | HG00544.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.252-2599T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684077 | |||||||
| chr1:99684096 | A | G | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2580A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684096 | |||||||
| chr1:99684103 | T | C | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2573T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684103 | |||||||
| chr1:99684259 | G | A | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2417G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684259 | |||||||
| chr1:99684275 | A | G | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2401A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684275 | |||||||
| chr1:99684314 | C | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2362C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684314 | |||||||
| chr1:99684331 | G | A | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2345G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684331 | |||||||
| chr1:99684337 | C | T | 37 | a0001c0001t0001g0026 a0001c0001t0001g0311 a0001c0002t0001g0031 others(34): Show |
39 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.252-2339C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684337 | |||||||
| chr1:99684362 | A | G | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2314A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684362 | |||||||
| chr1:99684396 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2280C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684396 | |||||||
| chr1:99684422 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.252-2254T>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684422 | |||||||
| chr1:99684466 | T | C | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-2210T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684466 | |||||||
| chr1:99684471 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.252-2205G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684471 | |||||||
| chr1:99684521 | T | C | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2155T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684521 | |||||||
| chr1:99684541 | T | TTTTG | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2135_252-2134i others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684541 | |||||||
| chr1:99684544 | C | A | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2132C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684544 | |||||||
| chr1:99684565 | C | T | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-2111C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684565 | |||||||
| chr1:99684616 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.252-2060G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684616 | |||||||
| chr1:99684721 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0142 |
2 | HG01496.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.252-1955T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684721 | |||||||
| chr1:99684751 | A | G | 4 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0004g0153 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-1925A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684751 | |||||||
| chr1:99684804 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0285 a0001c0001t0001g0286 others(1): Show |
5 | HG02257.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.252-1872C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684804 | |||||||
| chr1:99684943 | A | C | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1733A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684943 | |||||||
| chr1:99684980 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.252-1696G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99684980 | |||||||
| chr1:99685031 | G | C | 13 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(10): Show |
13 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.252-1645G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685031 | |||||||
| chr1:99685166 | ATCTG | A | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1504_252-1501d others(6): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 99685166 | ||||||
| chr1:99685268 | A | G | 36 | a0001c0001t0001g0311 a0001c0002t0001g0031 a0001c0002t0001g0039 others(33): Show |
38 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.252-1408A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685268 | |||||||
| chr1:99685336 | T | C | 4 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0004g0153 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-1340T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685336 | |||||||
| chr1:99685452 | A | G | 13 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(10): Show |
13 | HG01884.hp1 HG02723.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.252-1224A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685452 | |||||||
| chr1:99685481 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-1195A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685481 | |||||||
| chr1:99685532 | G | A | 2 | a0004c0006t0001g0278 a0004c0006t0001g0279 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.252-1144G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685532 | |||||||
| chr1:99685547 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-1129C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685547 | |||||||
| chr1:99685616 | A | G | 2 | a0001c0002t0002g0209 a0001c0002t0002g0318 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.252-1060A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685616 | |||||||
| chr1:99685660 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.252-1016A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685660 | |||||||
| chr1:99685841 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-835G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685841 | |||||||
| chr1:99685920 | C | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-756C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685920 | |||||||
| chr1:99685928 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.252-748T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99685928 | |||||||
| chr1:99686030 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-646A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686030 | |||||||
| chr1:99686034 | C | A | 4 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0004g0153 others(1): Show |
4 | HG02055.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.252-642C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686034 | |||||||
| chr1:99686135 | C | G | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-541C>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686135 | |||||||
| chr1:99686279 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0158 |
2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.252-397G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686279 | |||||||
| chr1:99686400 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0170 |
2 | HG00741.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.252-276C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686400 | |||||||
| chr1:99686422 | G | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(115): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.252-254G>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686422 | |||||||
| chr1:99686476 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(37): Show |
44 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.252-200G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686476 | |||||||
| chr1:99686515 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-161A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686515 | |||||||
| chr1:99686524 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-152A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686524 | |||||||
| chr1:99686536 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-140A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686536 | |||||||
| chr1:99686549 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-127A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686549 | |||||||
| chr1:99686612 | C | T | 1 | a0001c0001t0001g0015 | 2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.252-64C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686612 | |||||||
| chr1:99686627 | C | T | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-49C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686627 | |||||||
| chr1:99686650 | T | C | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.252-26T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 3/7 | chr1 | 99686650 | |||||||
| chr1:99686853 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.366+63A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686853 | |||||||
| chr1:99686887 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(116): Show |
144 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.367-43T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686887 | |||||||
| chr1:99686916 | C | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0197 |
2 | HG02155.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.367-14C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 4/7 | chr1 | 99686916 | |||||||
| chr1:99687020 | T | C | 2 | a0004c0006t0001g0278 a0004c0006t0001g0279 |
2 | HG00735.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.401-56T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 5/7 | chr1 | 99687020 | |||||||
| chr1:99687210 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.514+21G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687210 | |||||||
| chr1:99687243 | G | A | 6 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(3): Show |
6 | HG01934.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.514+54G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687243 | |||||||
| chr1:99687349 | T | C | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0132 others(2): Show |
5 | HG00408.hp2 HG00609.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.514+160T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687349 | |||||||
| chr1:99687368 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.514+179T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687368 | |||||||
| chr1:99687431 | G | C | 1 | a0001c0001t0001g0296 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.514+242G>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687431 | |||||||
| chr1:99687585 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.514+396A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687585 | |||||||
| chr1:99687649 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.514+460A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687649 | |||||||
| chr1:99687687 | ACT | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(64): Show |
73 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.514+501_514+502del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99687687 | ||||||
| chr1:99687707 | A | G | 1 | a0001c0001t0008g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.514+518A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687707 | |||||||
| chr1:99687866 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.514+677C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687866 | |||||||
| chr1:99687897 | G | GA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(113): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.514+710dupA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99687897 | ||||||
| chr1:99687935 | G | A | 2 | a0001c0002t0002g0209 a0001c0002t0002g0318 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.514+746G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99687935 | |||||||
| chr1:99688060 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0163 |
5 | HG00423.hp2 HG00621.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.515-715T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688060 | |||||||
| chr1:99688118 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0019 others(98): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.515-657C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688118 | |||||||
| chr1:99688460 | A | G | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.515-315A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688460 | |||||||
| chr1:99688469 | CTT | C | 35 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(32): Show |
37 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.515-302_515-301del others(2): Show |
PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 99688469 | ||||||
| chr1:99688498 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0212 |
2 | HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.515-277C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688498 | |||||||
| chr1:99688499 | T | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.515-276T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688499 | |||||||
| chr1:99688530 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.515-245C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688530 | |||||||
| chr1:99688561 | CA | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0085 a0001c0001t0001g0099 others(2): Show |
6 | NA18999.hp1 NA19002.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.515-213delA | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688561 | |||||||
| chr1:99688573 | C | A | 15 | a0001c0002t0001g0320 a0001c0002t0002g0207 a0001c0002t0002g0208 others(12): Show |
15 | HG01167.hp2 HG01884.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.515-202C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688573 | |||||||
| chr1:99688677 | T | C | 21 | a0001c0002t0001g0031 a0001c0002t0001g0039 a0001c0002t0001g0235 others(18): Show |
21 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.515-98T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 6/7 | chr1 | 99688677 | |||||||
| chr1:99690253 | T | G | 38 | a0001c0001t0002g0309 a0001c0001t0004g0153 a0001c0001t0004g0156 others(35): Show |
40 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.1612+381T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690253 | |||||||
| chr1:99690292 | A | C | 14 | a0001c0001t0002g0309 a0001c0002t0001g0320 a0001c0002t0002g0207 others(11): Show |
14 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.1612+420A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690292 | |||||||
| chr1:99690345 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1612+473T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690345 | |||||||
| chr1:99690421 | AT | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(49): Show |
56 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1612+553delT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 99690421 | ||||||
| chr1:99690498 | A | G | 22 | a0001c0001t0002g0309 a0001c0002t0001g0031 a0001c0002t0001g0039 others(19): Show |
22 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1612+626A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690498 | |||||||
| chr1:99690517 | T | C | 1 | a0001c0001t0006g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1612+645T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690517 | |||||||
| chr1:99690633 | A | G | 53 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(50): Show |
57 | HG00673.hp1 HG00735.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1612+761A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690633 | |||||||
| chr1:99690702 | G | A | 10 | a0002c0003t0001g0083 a0002c0003t0001g0205 a0002c0003t0001g0315 others(7): Show |
12 | HG02145.hp1 HG02622.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.1612+830G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690702 | |||||||
| chr1:99690772 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1612+900A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690772 | |||||||
| chr1:99690867 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1612+995A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99690867 | |||||||
| chr1:99691102 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.1612+1230T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691102 | |||||||
| chr1:99691145 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1612+1273G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691145 | |||||||
| chr1:99691160 | A | G | 2 | a0001c0002t0001g0031 a0011c0011t0001g0030 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1612+1288A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691160 | |||||||
| chr1:99691261 | T | C | 6 | a0001c0001t0002g0309 a0001c0002t0002g0254 a0001c0002t0002g0274 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1612+1389T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691261 | |||||||
| chr1:99691640 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1612+1768A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691640 | |||||||
| chr1:99691767 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1612+1895A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99691767 | |||||||
| chr1:99692160 | A | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1859A>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692160 | |||||||
| chr1:99692326 | C | A | 38 | a0001c0001t0002g0309 a0001c0001t0004g0153 a0001c0001t0004g0156 others(35): Show |
40 | HG00544.hp1 HG01167.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.1613-1693C>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692326 | |||||||
| chr1:99692632 | C | T | 10 | a0001c0001t0001g0027 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1387C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692632 | |||||||
| chr1:99692901 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(87): Show |
96 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1613-1118T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692901 | |||||||
| chr1:99692994 | A | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG01891.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1613-1025A>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99692994 | |||||||
| chr1:99693356 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1613-663C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693356 | |||||||
| chr1:99693473 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1613-546A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693473 | |||||||
| chr1:99693536 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1613-483G>A | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693536 | |||||||
| chr1:99693744 | T | C | 80 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(77): Show |
86 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.1613-275T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693744 | |||||||
| chr1:99693750 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1613-269C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693750 | |||||||
| chr1:99693828 | C | T | 1 | a0001c0001t0001g0020 | 2 | NA18955.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1613-191C>T | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693828 | |||||||
| chr1:99693833 | T | G | 2 | a0001c0001t0004g0153 a0001c0001t0004g0156 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1613-186T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693833 | |||||||
| chr1:99693862 | T | C | 64 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(61): Show |
68 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.1613-157T>C | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693862 | |||||||
| chr1:99693910 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1613-109A>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693910 | |||||||
| chr1:99693981 | T | G | 1 | a0010c0013t0001g0308 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1613-38T>G | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | chr1 | 99693981 | |||||||
| chr1:99693996 | C | CT | 74 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(71): Show |
78 | HG00544.hp1 HG00673.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.1613-14dupT | PALMD | ENSG00000099260.12 | transcript | ENST00000263174.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 99693996 |