Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26523 |
| ensemblid | ENSG00000092847.14 |
| hgncid | 3262 |
| symbol | AGO1 |
| name | argonaute RISC component 1 |
| refseq_nuc | NM_012199.5 |
| refseq_prot | NP_036331.1 |
| ensembl_nuc | ENST00000373204.6 |
| ensembl_prot | ENSP00000362300.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 35883209 |
| end | 35930532 |
| strand | + |
| ver | v1.2 |
| region | chr1:35883209-35930532 |
| region5000 | chr1:35878209-35935532 |
| regionname0 | AGO1_chr1_35883209_35930532 |
| regionname5000 | AGO1_chr1_35878209_35935532 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2571 | 170 | 57 | 34 | 49 | 7 | 21 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0002 | 0/0 | 2571 | 99 | 28 | 20 | 46 | 1 | 4 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0003 | 0/0 | 2571 | 3 | 0 | 0 | 0 | 0 | 3 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0004 | 0/0 | 2571 | 2 | 1 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0005 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0006 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0007 | 0/0 | 2571 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 | ||
| a0001c0008 | 0/0 | 2571 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ATGGA others(2566): Show |
chr1 | 35878209 | 35935532 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 13712 | 88 | 25 | 20 | 31 | 5 | 6 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0003 | 0/0 | 13713 | 20 | 9 | 3 | 3 | 0 | 5 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0005 | 0/0 | 13711 | 6 | 2 | 1 | 0 | 0 | 3 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13706): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0006 | 0/0 | 13713 | 4 | 4 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0007 | 0/0 | 13713 | 4 | 0 | 0 | 4 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0010 | 0/0 | 13711 | 3 | 0 | 2 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13706): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0011 | 0/0 | 13713 | 3 | 0 | 0 | 3 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0012 | 0/0 | 13713 | 3 | 3 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0014 | 0/0 | 13712 | 3 | 0 | 2 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0015 | 0/0 | 13713 | 3 | 1 | 1 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0017 | 0/0 | 13710 | 2 | 0 | 1 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13705): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0018 | 0/0 | 13716 | 2 | 1 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13711): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0019 | 0/0 | 13712 | 2 | 0 | 0 | 0 | 2 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0020 | 0/0 | 13711 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13706): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0023 | 0/0 | 13710 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13705): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0024 | 0/0 | 13707 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13702): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0025 | 0/0 | 13707 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13702): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0026 | 0/0 | 13708 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13703): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0028 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0029 | 0/0 | 13717 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13712): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0030 | 0/0 | 13712 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0031 | 0/0 | 13712 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0032 | 0/0 | 13712 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0033 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0034 | 0/0 | 13713 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0035 | 0/0 | 13713 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0036 | 0/1 | 13713 | 1 | 0 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0037 | 0/0 | 13712 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0038 | 0/0 | 13713 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0039 | 0/0 | 13712 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0040 | 0/0 | 13711 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13706): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0043 | 0/0 | 13713 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0044 | 0/0 | 13713 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0047 | 0/0 | 13707 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13702): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0048 | 0/0 | 13712 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0049 | 0/0 | 13712 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0052 | 0/0 | 13713 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0055 | 0/0 | 13713 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0001t0063 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0002 | 0/0 | 13709 | 61 | 5 | 12 | 39 | 1 | 4 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0004 | 0/0 | 13712 | 11 | 9 | 2 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0008 | 0/0 | 13710 | 4 | 0 | 2 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13705): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0009 | 0/0 | 13709 | 4 | 3 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0016 | 0/0 | 13713 | 3 | 3 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0021 | 0/0 | 13713 | 2 | 1 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0022 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0041 | 0/0 | 13708 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13703): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0042 | 0/0 | 13709 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0050 | 0/0 | 13709 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0051 | 0/0 | 13709 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0053 | 0/0 | 13709 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0054 | 0/0 | 13709 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0056 | 0/0 | 13712 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0057 | 0/0 | 13677 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13672): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0058 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0059 | 0/0 | 13709 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0060 | 0/0 | 13713 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0061 | 0/0 | 13712 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0002t0062 | 0/0 | 13709 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0003t0013 | 0/0 | 13712 | 3 | 0 | 0 | 0 | 0 | 3 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0004t0045 | 0/0 | 13700 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13695): Show |
chr1 | 35878209 | 35935532 |
| a0001c0004t0046 | 0/0 | 13700 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13695): Show |
chr1 | 35878209 | 35935532 |
| a0001c0005t0027 | 0/0 | 13712 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13707): Show |
chr1 | 35878209 | 35935532 |
| a0001c0006t0006 | 0/0 | 13713 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13708): Show |
chr1 | 35878209 | 35935532 |
| a0001c0007t0002 | 0/0 | 13709 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| a0001c0008t0002 | 0/0 | 13709 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | ACTGG others(13704): Show |
chr1 | 35878209 | 35935532 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 12 | 2 | 2 | 7 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0003 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0007g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0010g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0010g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0010g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0011g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0011g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0012g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0014g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0014g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0015g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0017g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0018g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0019g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0020g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0020g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0023g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0024g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0025g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0026g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0028g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0029g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0030g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0031g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0032g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0033g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0034g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0035g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0036g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0037g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0038g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0039g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0040g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0043g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0044g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0047g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0048g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0049g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0052g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0055g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0001t0063g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0001 | 0/0 | 14 | 1 | 3 | 9 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0008g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0008g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0009g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0016g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0021g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0022g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0041g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0042g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0050g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0051g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0053g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0054g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0056g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0057g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0058g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0059g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0060g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0061g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0002t0062g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0003t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0003t0013g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0003t0013g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0004t0045g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0004t0046g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0005t0027g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0006t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0007t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| a0001c0008t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0148 | EUR | GBR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00280 | hp1 | a0001 | c0001 | t0019 | g0008 | EUR | FIN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0008 | EUR | FIN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00558 | hp2 | a0001 | c0001 | t0035 | g0060 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00609 | hp1 | a0001 | c0001 | t0032 | g0200 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00642 | hp1 | a0001 | c0002 | t0062 | g0176 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01069 | hp1 | a0001 | c0002 | t0009 | g0004 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01074 | hp1 | a0001 | c0001 | t0010 | g0087 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01081 | hp1 | a0001 | c0001 | t0014 | g0101 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0077 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0196 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01168 | hp2 | a0001 | c0001 | t0017 | g0006 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01169 | hp1 | a0001 | c0001 | t0039 | g0006 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01169 | hp2 | a0001 | c0002 | t0004 | g0194 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0120 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01243 | hp1 | a0001 | c0002 | t0060 | g0040 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01243 | hp2 | a0001 | c0002 | t0021 | g0188 | AMR | PUR | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01255 | hp1 | a0001 | c0001 | t0014 | g0009 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01255 | hp2 | a0001 | c0001 | t0018 | g0137 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01257 | hp1 | a0001 | c0001 | t0029 | g0114 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01358 | hp1 | a0001 | c0001 | t0048 | g0084 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01891 | hp1 | a0001 | c0008 | t0002 | g0175 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01891 | hp2 | a0001 | c0006 | t0006 | g0015 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0029 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02027 | hp2 | a0001 | c0002 | t0042 | g0013 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02055 | hp1 | a0001 | c0002 | t0016 | g0185 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02056 | hp1 | a0001 | c0002 | t0050 | g0033 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02129 | hp1 | a0001 | c0004 | t0045 | g0057 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02129 | hp2 | a0001 | c0002 | t0056 | g0043 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02132 | hp2 | a0001 | c0002 | t0008 | g0141 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02145 | hp1 | a0001 | c0001 | t0026 | g0058 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02257 | hp2 | a0001 | c0002 | t0021 | g0007 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02273 | hp1 | a0001 | c0001 | t0015 | g0002 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02273 | hp2 | a0001 | c0002 | t0008 | g0005 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02280 | hp1 | a0001 | c0002 | t0061 | g0041 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02280 | hp2 | a0001 | c0002 | t0051 | g0149 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02572 | hp2 | a0001 | c0002 | t0009 | g0034 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02615 | hp2 | a0001 | c0001 | t0033 | g0025 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0178 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02717 | hp2 | a0001 | c0002 | t0004 | g0007 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02735 | hp1 | a0001 | c0001 | t0049 | g0011 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0145 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02818 | hp1 | a0001 | c0001 | t0047 | g0144 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02886 | hp2 | a0001 | c0001 | t0044 | g0074 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02896 | hp1 | a0001 | c0002 | t0057 | g0004 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02897 | hp1 | a0001 | c0002 | t0016 | g0183 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02922 | hp1 | a0001 | c0001 | t0020 | g0177 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02922 | hp2 | a0001 | c0001 | t0028 | g0015 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0187 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0181 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0036 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0179 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0134 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03098 | hp2 | a0001 | c0001 | t0034 | g0049 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03130 | hp2 | a0001 | c0002 | t0022 | g0189 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03195 | hp2 | a0001 | c0002 | t0058 | g0184 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0182 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03453 | hp1 | a0001 | c0001 | t0025 | g0132 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03490 | hp1 | a0001 | c0001 | t0014 | g0009 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03491 | hp2 | a0001 | c0001 | t0017 | g0035 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03516 | hp2 | a0001 | c0001 | t0063 | g0053 | AFR | ESN | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03540 | hp1 | a0001 | c0001 | t0024 | g0126 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03579 | hp2 | a0001 | c0002 | t0059 | g0004 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03704 | hp1 | a0001 | c0001 | t0037 | g0068 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03704 | hp2 | a0001 | c0001 | t0040 | g0008 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0069 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0138 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03942 | hp1 | a0001 | c0003 | t0013 | g0088 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03942 | hp2 | a0001 | c0001 | t0055 | g0018 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04184 | hp1 | a0001 | c0003 | t0013 | g0102 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | STU | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | STU | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04228 | hp1 | a0001 | c0003 | t0013 | g0090 | SAS | STU | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18906 | hp1 | a0001 | c0002 | t0004 | g0195 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18946 | hp2 | a0001 | c0001 | t0023 | g0191 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18968 | hp2 | a0001 | c0001 | t0031 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18972 | hp1 | a0001 | c0001 | t0011 | g0127 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18975 | hp2 | a0001 | c0002 | t0008 | g0152 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18977 | hp2 | a0001 | c0007 | t0002 | g0160 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18980 | hp2 | a0001 | c0001 | t0015 | g0109 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18982 | hp2 | a0001 | c0005 | t0027 | g0027 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18991 | hp2 | a0001 | c0002 | t0041 | g0150 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18994 | hp1 | a0001 | c0001 | t0011 | g0128 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19005 | hp2 | a0001 | c0001 | t0052 | g0139 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19043 | hp2 | a0001 | c0002 | t0016 | g0007 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19057 | hp1 | a0001 | c0001 | t0038 | g0064 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19060 | hp1 | a0001 | c0002 | t0053 | g0172 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19062 | hp1 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0071 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0042 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | YRI | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | ASW | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | GIH | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0037 | SAS | GIH | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01123 | hp1 | a0001 | c0002 | t0008 | g0147 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0004 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG02559 | hp2 | a0001 | c0002 | t0009 | g0004 | AFR | ACB | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03471 | hp1 | a0001 | c0004 | t0046 | g0059 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0180 | AFR | MSL | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | USA | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| HG06807 | hp2 | a0001 | c0001 | t0043 | g0133 | AFR | USA | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA18955 | hp2 | a0001 | c0001 | t0030 | g0010 | EAS | JPT | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0135 | AFR | USA | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA20300 | hp2 | a0001 | c0002 | t0054 | g0001 | AFR | USA | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0146 | AFR | LWK | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0036 | g0073 | REF | REF | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | AGO1_chr1_35878209_35935532 | AGO1 | chr1 | 35878209 | 35935532 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:35888566 | C | T | 1 | a0001c0003 | 3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.165C>T | p.Tyr55Tyr | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/19 | 378/13712 | 165/2574 | 55/857 | chr1 | 35888566 | |||
| chr1:35888584 | G | A | 1 | a0001c0005 | 1 | NA18982.hp2 | synonymous_variant | LOW | c.183G>A | p.Pro61Pro | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/19 | 396/13712 | 183/2574 | 61/857 | chr1 | 35888584 | |||
| chr1:35888584 | G | C | 1 | a0001c0004 | 2 | HG02129.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.183G>C | p.Pro61Pro | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/19 | 396/13712 | 183/2574 | 61/857 | chr1 | 35888584 | |||
| chr1:35893231 | G | A | 1 | a0001c0006 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.465G>A | p.Glu155Glu | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 4/19 | 678/13712 | 465/2574 | 155/857 | chr1 | 35893231 | |||
| chr1:35894068 | A | G | 3 | a0001c0002 a0001c0007 a0001c0008 |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(98): Show |
synonymous_variant | LOW | c.681A>G | p.Pro227Pro | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 6/19 | 894/13712 | 681/2574 | 227/857 | chr1 | 35894068 | |||
| chr1:35917652 | C | T | 1 | a0001c0008 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.2088C>T | p.Tyr696Tyr | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 16/19 | 2301/13712 | 2088/2574 | 696/857 | chr1 | 35917652 | |||
| chr1:35919195 | C | T | 1 | a0001c0007 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.2406C>T | p.Tyr802Tyr | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 18/19 | 2619/13712 | 2406/2574 | 802/857 | chr1 | 35919195 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:35883247 | C | T | 1 | a0001c0001t0063 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-175C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/19 | 175 | chr1 | 35883247 | ||||||
| chr1:35883265 | C | T | 1 | a0001c0002t0062 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/19 | 157 | chr1 | 35883265 | ||||||
| chr1:35883406 | C | T | 1 | a0001c0002t0061 | 1 | HG02280.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-16C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/19 | chr1 | 35883406 | |||||||
| chr1:35919950 | G | C | 1 | a0001c0002t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*343G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 343 | chr1 | 35919950 | ||||||
| chr1:35920137 | G | A | 1 | a0001c0002t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 530 | chr1 | 35920137 | ||||||
| chr1:35920776 | C | T | 12 | a0001c0001t0020 a0001c0002t0004 a0001c0002t0009 others(9): Show |
29 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1169C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 1169 | chr1 | 35920776 | ||||||
| chr1:35921283 | C | CT | 15 | a0001c0001t0015 a0001c0001t0018 a0001c0001t0019 others(12): Show |
84 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1696dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 1697 | INFO_REALIGN_3_PRIME | chr1 | 35921283 | |||||
| chr1:35921283 | CT | C | 8 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0023 others(5): Show |
11 | HG01074.hp1 HG01081.hp2 HG01168.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1696delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 1696 | INFO_REALIGN_3_PRIME | chr1 | 35921283 | |||||
| chr1:35921393 | C | T | 1 | a0001c0001t0049 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1786C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 1786 | chr1 | 35921393 | ||||||
| chr1:35921843 | T | C | 1 | a0001c0001t0023 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2236T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 2236 | chr1 | 35921843 | ||||||
| chr1:35922118 | C | G | 1 | a0001c0001t0048 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2511C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 2511 | chr1 | 35922118 | ||||||
| chr1:35922367 | T | C | 3 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0026 |
3 | HG02145.hp1 HG03453.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2760T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 2760 | chr1 | 35922367 | ||||||
| chr1:35922479 | A | G | 1 | a0001c0001t0014 | 3 | HG01081.hp1 HG01255.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2872A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 2872 | chr1 | 35922479 | ||||||
| chr1:35922597 | G | GGCCT | 2 | a0001c0001t0018 a0001c0001t0029 |
3 | HG01255.hp2 HG01257.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3020_*3023dupCCTG | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3024 | INFO_REALIGN_3_PRIME | chr1 | 35922597 | |||||
| chr1:35922597 | GGCCT | G | 6 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0026 others(3): Show |
6 | HG02129.hp1 HG02145.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3020_*3023delCCTG | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3020 | INFO_REALIGN_3_PRIME | chr1 | 35922597 | |||||
| chr1:35922862 | G | C | 1 | a0001c0001t0030 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3255G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3255 | chr1 | 35922862 | ||||||
| chr1:35922897 | G | T | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3290G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3290 | chr1 | 35922897 | ||||||
| chr1:35923182 | G | T | 1 | a0001c0001t0044 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3575G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3575 | chr1 | 35923182 | ||||||
| chr1:35923246 | T | C | 1 | a0001c0002t0050 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3639T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3639 | chr1 | 35923246 | ||||||
| chr1:35923396 | C | G | 1 | a0001c0001t0055 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3789C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3789 | chr1 | 35923396 | ||||||
| chr1:35923403 | C | T | 1 | a0001c0004t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3796C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 3796 | chr1 | 35923403 | ||||||
| chr1:35923679 | C | T | 1 | a0001c0003t0013 | 3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4072C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 4072 | chr1 | 35923679 | ||||||
| chr1:35923685 | C | G | 4 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0063 others(1): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4078C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 4078 | chr1 | 35923685 | ||||||
| chr1:35923969 | T | A | 1 | a0001c0002t0051 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4362T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 4362 | chr1 | 35923969 | ||||||
| chr1:35924281 | A | C | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4674A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 4674 | chr1 | 35924281 | ||||||
| chr1:35924558 | C | T | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG02145.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4951C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 4951 | chr1 | 35924558 | ||||||
| chr1:35924770 | T | G | 2 | a0001c0002t0056 a0001c0002t0061 |
2 | HG02129.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5163T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 5163 | chr1 | 35924770 | ||||||
| chr1:35924918 | A | G | 23 | a0001c0001t0020 a0001c0002t0002 a0001c0002t0004 others(20): Show |
103 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*5311A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 5311 | chr1 | 35924918 | ||||||
| chr1:35924926 | A | G | 41 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0012 others(38): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*5319A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 5319 | chr1 | 35924926 | ||||||
| chr1:35925216 | A | C | 1 | a0001c0001t0038 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5609A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 5609 | chr1 | 35925216 | ||||||
| chr1:35925267 | C | T | 2 | a0001c0004t0045 a0001c0004t0046 |
2 | HG02129.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5660C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 5660 | chr1 | 35925267 | ||||||
| chr1:35925910 | C | G | 1 | a0001c0002t0054 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6303C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6303 | chr1 | 35925910 | ||||||
| chr1:35926060 | TGAA | T | 11 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0041 others(8): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*6456_*6458delAGA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6456 | INFO_REALIGN_3_PRIME | chr1 | 35926060 | |||||
| chr1:35926097 | T | C | 1 | a0001c0001t0048 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6490T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6490 | chr1 | 35926097 | ||||||
| chr1:35926302 | A | G | 1 | a0001c0001t0037 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6695A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6695 | chr1 | 35926302 | ||||||
| chr1:35926345 | T | C | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6738T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6738 | chr1 | 35926345 | ||||||
| chr1:35926363 | A | G | 2 | a0001c0001t0019 a0001c0001t0040 |
3 | HG00280.hp1 HG00323.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6756A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6756 | chr1 | 35926363 | ||||||
| chr1:35926563 | C | T | 1 | a0001c0004t0046 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6956C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 6956 | chr1 | 35926563 | ||||||
| chr1:35926628 | A | T | 2 | a0001c0004t0045 a0001c0004t0046 |
2 | HG02129.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7021A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 7021 | chr1 | 35926628 | ||||||
| chr1:35926944 | G | GT | 13 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(10): Show |
40 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*7356dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 7357 | INFO_REALIGN_3_PRIME | chr1 | 35926944 | |||||
| chr1:35926944 | GT | G | 28 | a0001c0001t0005 a0001c0001t0017 a0001c0001t0018 others(25): Show |
112 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*7356delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 7356 | INFO_REALIGN_3_PRIME | chr1 | 35926944 | |||||
| chr1:35927000 | G | A | 1 | a0001c0001t0029 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7393G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 7393 | chr1 | 35927000 | ||||||
| chr1:35927127 | G | A | 4 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0063 others(1): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7520G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 7520 | chr1 | 35927127 | ||||||
| chr1:35927856 | C | T | 12 | a0001c0001t0020 a0001c0002t0004 a0001c0002t0009 others(9): Show |
29 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*8249C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8249 | chr1 | 35927856 | ||||||
| chr1:35927901 | TCTACCTT others(25): Show |
T | 1 | a0001c0002t0057 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8295_*8326delCTAC others(28): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8295 | chr1 | 35927901 | ||||||
| chr1:35928246 | T | A | 1 | a0001c0001t0031 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8639T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8639 | chr1 | 35928246 | ||||||
| chr1:35928348 | G | A | 12 | a0001c0001t0020 a0001c0002t0004 a0001c0002t0009 others(9): Show |
29 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*8741G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8741 | chr1 | 35928348 | ||||||
| chr1:35928449 | T | TA | 10 | a0001c0001t0011 a0001c0002t0004 a0001c0002t0016 others(7): Show |
25 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*8852dupA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8853 | INFO_REALIGN_3_PRIME | chr1 | 35928449 | |||||
| chr1:35928459 | A | T | 2 | a0001c0001t0033 a0001c0004t0046 |
2 | HG02615.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8852A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8852 | chr1 | 35928459 | ||||||
| chr1:35928460 | T | A | 2 | a0001c0001t0032 a0001c0002t0053 |
2 | HG00609.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8853T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8853 | chr1 | 35928460 | ||||||
| chr1:35928463 | T | A | 1 | a0001c0001t0031 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8856T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8856 | chr1 | 35928463 | ||||||
| chr1:35928477 | C | T | 1 | a0001c0002t0053 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8870C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8870 | chr1 | 35928477 | ||||||
| chr1:35928565 | TAAGCCAC | T | 2 | a0001c0004t0045 a0001c0004t0046 |
2 | HG02129.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8966_*8972delAAGC others(3): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 8966 | INFO_REALIGN_3_PRIME | chr1 | 35928565 | |||||
| chr1:35928833 | A | G | 1 | a0001c0001t0035 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9226A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 9226 | chr1 | 35928833 | ||||||
| chr1:35929124 | A | C | 12 | a0001c0001t0052 a0001c0002t0002 a0001c0002t0008 others(9): Show |
75 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*9517A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 9517 | chr1 | 35929124 | ||||||
| chr1:35929421 | T | A | 2 | a0001c0004t0045 a0001c0004t0046 |
2 | HG02129.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9814T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 9814 | chr1 | 35929421 | ||||||
| chr1:35929514 | A | C | 17 | a0001c0001t0018 a0001c0001t0024 a0001c0001t0025 others(14): Show |
81 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*9907A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 9907 | chr1 | 35929514 | ||||||
| chr1:35929611 | G | A | 1 | a0001c0002t0059 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10004G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10004 | chr1 | 35929611 | ||||||
| chr1:35929769 | T | A | 12 | a0001c0001t0020 a0001c0002t0004 a0001c0002t0009 others(9): Show |
29 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*10162T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10162 | chr1 | 35929769 | ||||||
| chr1:35930013 | A | C | 1 | a0001c0002t0060 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10406A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10406 | chr1 | 35930013 | ||||||
| chr1:35930234 | T | C | 1 | a0001c0002t0058 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10627T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10627 | chr1 | 35930234 | ||||||
| chr1:35930257 | G | A | 1 | a0001c0001t0047 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10650G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10650 | chr1 | 35930257 | ||||||
| chr1:35930419 | C | A | 1 | a0001c0001t0034 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10812C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10812 | chr1 | 35930419 | ||||||
| chr1:35930504 | G | A | 1 | a0001c0001t0007 | 4 | HG00673.hp1 NA18977.hp1 NA19063.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10897G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10897 | chr1 | 35930504 | ||||||
| chr1:35930505 | C | A | 1 | a0001c0001t0007 | 4 | HG00673.hp1 NA18977.hp1 NA19063.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10898C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10898 | chr1 | 35930505 | ||||||
| chr1:35930517 | GTT | G | 3 | a0001c0002t0009 a0001c0002t0057 a0001c0002t0059 |
6 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*10913_*10914delTT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 19/19 | 10913 | INFO_REALIGN_3_PRIME | chr1 | 35930517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:35883533 | G | A | 1 | a0001c0002t0050g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.25+87G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883533 | |||||||
| chr1:35883684 | T | C | 1 | a0001c0002t0009g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.25+238T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883684 | |||||||
| chr1:35883761 | G | T | 1 | a0001c0001t0012g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.25+315G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883761 | |||||||
| chr1:35883827 | C | G | 1 | a0001c0001t0032g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.25+381C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883827 | |||||||
| chr1:35883843 | G | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG01884.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.25+397G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883843 | |||||||
| chr1:35883959 | G | A | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+513G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35883959 | |||||||
| chr1:35884092 | C | CCCCCG | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.25+657_25+661dupCC others(3): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 35884092 | ||||||
| chr1:35884114 | T | A | 4 | a0001c0002t0004g0042 a0001c0002t0056g0043 a0001c0002t0060g0040 others(1): Show |
4 | HG01243.hp1 HG02129.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.25+668T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35884114 | |||||||
| chr1:35884287 | A | AGACTGGG others(14): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
5 | HG02145.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+842_25+862dupGA others(19): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 35884287 | ||||||
| chr1:35884296 | C | T | 3 | a0001c0002t0004g0194 a0001c0002t0004g0195 a0001c0002t0004g0196 |
3 | HG01167.hp2 HG01169.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.25+850C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35884296 | |||||||
| chr1:35884301 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.25+855G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35884301 | |||||||
| chr1:35884409 | G | C | 4 | a0001c0002t0009g0004 a0001c0002t0009g0034 a0001c0002t0057g0004 others(1): Show |
6 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+963G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35884409 | |||||||
| chr1:35884443 | A | C | 1 | a0001c0001t0001g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+997A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35884443 | |||||||
| chr1:35885365 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0034g0049 |
2 | HG01109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.25+1919T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35885365 | |||||||
| chr1:35885429 | T | C | 1 | a0001c0002t0002g0050 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.25+1983T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35885429 | |||||||
| chr1:35885474 | A | G | 1 | a0001c0002t0002g0192 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.25+2028A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35885474 | |||||||
| chr1:35885914 | C | A | 1 | a0001c0002t0002g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.25+2468C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35885914 | |||||||
| chr1:35886072 | C | T | 1 | a0001c0001t0023g0191 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.26-2355C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35886072 | |||||||
| chr1:35886742 | T | A | 7 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.26-1685T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35886742 | |||||||
| chr1:35886781 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.26-1646A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35886781 | |||||||
| chr1:35887444 | GGGTAAAG others(5): Show |
G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.26-980_26-969delTA others(10): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 35887444 | ||||||
| chr1:35887525 | G | A | 1 | a0001c0001t0026g0058 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.26-902G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35887525 | |||||||
| chr1:35887660 | C | CT | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.26-757dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 35887660 | ||||||
| chr1:35887670 | T | A | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.26-757T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35887670 | |||||||
| chr1:35888235 | TAAAAAAG | T | 3 | a0001c0002t0004g0187 a0001c0002t0021g0188 a0001c0002t0022g0189 |
3 | HG01243.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.26-183_26-177delAA others(5): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 35888235 | ||||||
| chr1:35888260 | C | T | 1 | a0001c0001t0005g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.26-167C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 1/18 | chr1 | 35888260 | |||||||
| chr1:35888741 | A | T | 1 | a0001c0002t0002g0186 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.209+131A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35888741 | |||||||
| chr1:35888743 | G | A | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.209+133G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35888743 | |||||||
| chr1:35888768 | C | T | 24 | a0001c0002t0004g0007 a0001c0002t0004g0042 a0001c0002t0004g0179 others(21): Show |
27 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.209+158C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35888768 | |||||||
| chr1:35888791 | A | G | 1 | a0001c0001t0005g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.209+181A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35888791 | |||||||
| chr1:35888924 | G | T | 2 | a0001c0001t0020g0177 a0001c0001t0020g0178 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.209+314G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35888924 | |||||||
| chr1:35888992 | GGGACAGA others(37): Show |
G | 84 | a0001c0001t0001g0140 a0001c0001t0018g0137 a0001c0001t0018g0145 others(81): Show |
109 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.209+475_209+518del others(44): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 35888992 | ||||||
| chr1:35889183 | C | CT | 15 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0003g0131 others(12): Show |
15 | HG00741.hp1 HG02080.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.209+593dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 35889183 | ||||||
| chr1:35889183 | CT | C | 11 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
12 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.209+593delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 35889183 | ||||||
| chr1:35889223 | G | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.209+613G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35889223 | |||||||
| chr1:35889224 | T | C | 13 | a0001c0002t0004g0007 a0001c0002t0004g0179 a0001c0002t0004g0180 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.209+614T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35889224 | |||||||
| chr1:35889691 | C | G | 2 | a0001c0002t0021g0188 a0001c0002t0022g0189 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.209+1081C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35889691 | |||||||
| chr1:35889705 | C | T | 2 | a0001c0002t0021g0188 a0001c0002t0022g0189 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.209+1095C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35889705 | |||||||
| chr1:35889894 | T | G | 1 | a0001c0001t0018g0137 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.209+1284T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35889894 | |||||||
| chr1:35890149 | A | G | 2 | a0001c0001t0019g0008 a0001c0001t0040g0008 |
3 | HG00280.hp1 HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.209+1539A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890149 | |||||||
| chr1:35890198 | T | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.209+1588T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890198 | |||||||
| chr1:35890410 | A | T | 4 | a0001c0001t0012g0134 a0001c0001t0012g0135 a0001c0001t0012g0201 others(1): Show |
4 | HG03098.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1800A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890410 | |||||||
| chr1:35890432 | G | A | 4 | a0001c0001t0011g0027 a0001c0001t0011g0127 a0001c0001t0011g0128 others(1): Show |
4 | NA18972.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+1822G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890432 | |||||||
| chr1:35890444 | G | A | 2 | a0001c0002t0002g0050 a0001c0002t0002g0138 |
2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.209+1834G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890444 | |||||||
| chr1:35890586 | C | T | 1 | a0001c0001t0001g0012 | 3 | HG01928.hp2 HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.210-1971C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890586 | |||||||
| chr1:35890624 | T | G | 1 | a0001c0001t0001g0016 | 2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.210-1933T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890624 | |||||||
| chr1:35890718 | C | T | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210-1839C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890718 | |||||||
| chr1:35890856 | A | G | 94 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(91): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.210-1701A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890856 | |||||||
| chr1:35890875 | AGTT | A | 5 | a0001c0002t0002g0013 a0001c0002t0002g0142 a0001c0002t0002g0143 others(2): Show |
6 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.210-1680_210-1678d others(5): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 35890875 | ||||||
| chr1:35890946 | A | G | 2 | a0001c0002t0021g0188 a0001c0002t0022g0189 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.210-1611A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35890946 | |||||||
| chr1:35891011 | G | T | 51 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(48): Show |
73 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.210-1546G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891011 | |||||||
| chr1:35891191 | C | G | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210-1366C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891191 | |||||||
| chr1:35891241 | G | T | 94 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(91): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.210-1316G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891241 | |||||||
| chr1:35891461 | CT | C | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.210-1090delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 35891461 | ||||||
| chr1:35891534 | T | C | 1 | a0001c0001t0003g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.210-1023T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891534 | |||||||
| chr1:35891572 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.210-985A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891572 | |||||||
| chr1:35891627 | T | C | 1 | a0001c0001t0003g0066 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.210-930T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891627 | |||||||
| chr1:35891633 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.210-924C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891633 | |||||||
| chr1:35891798 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00280.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.210-759C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35891798 | |||||||
| chr1:35892028 | C | G | 1 | a0001c0002t0004g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.210-529C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35892028 | |||||||
| chr1:35892078 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.210-479G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35892078 | |||||||
| chr1:35892454 | A | C | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
18 | HG01109.hp1 HG01934.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.210-103A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 2/18 | chr1 | 35892454 | |||||||
| chr1:35892717 | G | A | 1 | a0001c0002t0008g0147 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.330+40G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 3/18 | chr1 | 35892717 | |||||||
| chr1:35892933 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.331-164C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 3/18 | chr1 | 35892933 | |||||||
| chr1:35892956 | C | T | 1 | a0001c0001t0005g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331-141C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 3/18 | chr1 | 35892956 | |||||||
| chr1:35893554 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0003g0021 |
2 | NA18969.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.513-120C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 4/18 | chr1 | 35893554 | |||||||
| chr1:35894201 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0003g0117 a0001c0001t0003g0118 others(4): Show |
7 | HG01175.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.784+30C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 6/18 | chr1 | 35894201 | |||||||
| chr1:35894297 | G | A | 1 | a0001c0001t0037g0068 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.785-18G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 6/18 | chr1 | 35894297 | |||||||
| chr1:35894536 | G | A | 1 | a0001c0002t0004g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.872+134G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 7/18 | chr1 | 35894536 | |||||||
| chr1:35894605 | T | G | 1 | a0001c0001t0010g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.872+203T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 7/18 | chr1 | 35894605 | |||||||
| chr1:35894721 | A | G | 10 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
12 | HG01109.hp1 HG01934.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.872+319A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 7/18 | chr1 | 35894721 | |||||||
| chr1:35894994 | C | G | 1 | a0001c0001t0003g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.873-128C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 7/18 | chr1 | 35894994 | |||||||
| chr1:35896188 | G | A | 20 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0075 others(17): Show |
25 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1020+919G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896188 | |||||||
| chr1:35896265 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1020+996C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896265 | |||||||
| chr1:35896355 | T | A | 1 | a0001c0002t0002g0148 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1020+1086T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896355 | |||||||
| chr1:35896561 | T | C | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1020+1292T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896561 | |||||||
| chr1:35896596 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1020+1327T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896596 | |||||||
| chr1:35896658 | T | C | 1 | a0001c0002t0051g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1020+1389T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896658 | |||||||
| chr1:35896659 | A | T | 1 | a0001c0002t0051g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1020+1390A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896659 | |||||||
| chr1:35896720 | G | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0010g0077 others(1): Show |
4 | HG01081.hp2 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+1451G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896720 | |||||||
| chr1:35896849 | A | G | 2 | a0001c0001t0020g0177 a0001c0001t0020g0178 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1020+1580A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896849 | |||||||
| chr1:35896905 | T | C | 1 | a0001c0001t0047g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1020+1636T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35896905 | |||||||
| chr1:35897082 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1020+1813A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897082 | |||||||
| chr1:35897403 | A | T | 1 | a0001c0001t0003g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1020+2134A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897403 | |||||||
| chr1:35897571 | C | T | 86 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(83): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1020+2302C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897571 | |||||||
| chr1:35897756 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1020+2487G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897756 | |||||||
| chr1:35897874 | G | A | 94 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(91): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1020+2605G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897874 | |||||||
| chr1:35897912 | C | T | 1 | a0001c0002t0016g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1020+2643C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897912 | |||||||
| chr1:35897971 | TATTTTGG others(16): Show |
T | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2704_1020+272 others(27): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr1 | 35897971 | ||||||
| chr1:35897996 | A | G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2727A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897996 | |||||||
| chr1:35897997 | A | G | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1020+2728A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897997 | |||||||
| chr1:35897998 | T | G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2729T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35897998 | |||||||
| chr1:35898000 | A | C | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2731A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898000 | |||||||
| chr1:35898002 | A | G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2733A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898002 | |||||||
| chr1:35898003 | C | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1020+2734C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898003 | |||||||
| chr1:35898279 | C | T | 3 | a0001c0002t0002g0032 a0001c0002t0008g0147 a0001c0002t0062g0176 |
4 | HG00642.hp1 HG01123.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020+3010C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898279 | |||||||
| chr1:35898381 | G | C | 94 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(91): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1021-3093G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898381 | |||||||
| chr1:35898424 | T | C | 2 | a0001c0001t0024g0126 a0001c0001t0025g0132 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1021-3050T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898424 | |||||||
| chr1:35898430 | G | A | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-3044G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898430 | |||||||
| chr1:35898469 | A | T | 4 | a0001c0002t0009g0004 a0001c0002t0009g0034 a0001c0002t0057g0004 others(1): Show |
6 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-3005A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898469 | |||||||
| chr1:35898477 | C | T | 5 | a0001c0001t0001g0075 a0001c0001t0003g0017 a0001c0001t0003g0066 others(2): Show |
6 | HG00544.hp1 HG01192.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1021-2997C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898477 | |||||||
| chr1:35898493 | G | A | 24 | a0001c0002t0004g0007 a0001c0002t0004g0042 a0001c0002t0004g0179 others(21): Show |
27 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1021-2981G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898493 | |||||||
| chr1:35898497 | C | T | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-2977C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898497 | |||||||
| chr1:35898498 | G | A | 1 | a0001c0002t0041g0150 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1021-2976G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898498 | |||||||
| chr1:35898521 | C | T | 52 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1021-2953C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898521 | |||||||
| chr1:35898946 | T | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1021-2528T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35898946 | |||||||
| chr1:35899115 | A | G | 94 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(91): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1021-2359A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35899115 | |||||||
| chr1:35899151 | C | T | 4 | a0001c0001t0026g0058 a0001c0001t0047g0144 a0001c0004t0045g0057 others(1): Show |
4 | HG02129.hp1 HG02145.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1021-2323C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35899151 | |||||||
| chr1:35899180 | A | G | 9 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
11 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021-2294A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35899180 | |||||||
| chr1:35899372 | A | G | 1 | a0001c0002t0002g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1021-2102A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35899372 | |||||||
| chr1:35899972 | C | G | 2 | a0001c0004t0045g0057 a0001c0004t0046g0059 |
2 | HG02129.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1021-1502C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35899972 | |||||||
| chr1:35900093 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0049g0011 |
5 | HG01168.hp1 HG01433.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-1381C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900093 | |||||||
| chr1:35900454 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1021-1020A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900454 | |||||||
| chr1:35900492 | C | T | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-982C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900492 | |||||||
| chr1:35900499 | G | A | 52 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1021-975G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900499 | |||||||
| chr1:35900682 | G | A | 1 | a0001c0002t0002g0151 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1021-792G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900682 | |||||||
| chr1:35900834 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1021-640C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900834 | |||||||
| chr1:35900888 | A | C | 53 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(50): Show |
75 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1021-586A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900888 | |||||||
| chr1:35900894 | C | T | 1 | a0001c0001t0012g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1021-580C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900894 | |||||||
| chr1:35900915 | T | A | 77 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(74): Show |
102 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1021-559T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900915 | |||||||
| chr1:35900919 | T | A | 1 | a0001c0002t0004g0195 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1021-555T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35900919 | |||||||
| chr1:35900983 | C | CT | 5 | a0001c0001t0001g0061 a0001c0001t0001g0112 a0001c0001t0001g0199 others(2): Show |
5 | HG01175.hp1 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1021-475dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr1 | 35900983 | ||||||
| chr1:35901131 | C | T | 52 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1021-343C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35901131 | |||||||
| chr1:35901160 | T | C | 1 | a0001c0001t0043g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1021-314T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35901160 | |||||||
| chr1:35901276 | C | T | 2 | a0001c0001t0020g0177 a0001c0001t0020g0178 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1021-198C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35901276 | |||||||
| chr1:35901444 | C | T | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-30C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 8/18 | chr1 | 35901444 | |||||||
| chr1:35901776 | A | G | 53 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(50): Show |
75 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-172A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 9/18 | chr1 | 35901776 | |||||||
| chr1:35902155 | A | C | 1 | a0001c0001t0047g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1264-49A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 10/18 | chr1 | 35902155 | |||||||
| chr1:35902179 | A | G | 153 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0022 others(150): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1264-25A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 10/18 | chr1 | 35902179 | |||||||
| chr1:35902573 | G | A | 2 | a0001c0004t0045g0057 a0001c0004t0046g0059 |
2 | HG02129.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1397+236G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902573 | |||||||
| chr1:35902694 | T | C | 3 | a0001c0002t0002g0153 a0001c0002t0002g0154 a0001c0002t0008g0152 |
3 | NA18967.hp1 NA18975.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1397+357T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902694 | |||||||
| chr1:35902840 | T | C | 6 | a0001c0001t0018g0137 a0001c0001t0018g0145 a0001c0001t0024g0126 others(3): Show |
6 | HG01255.hp2 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+503T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902840 | |||||||
| chr1:35902883 | C | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0015g0109 others(1): Show |
4 | NA18973.hp1 NA18980.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1397+546C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902883 | |||||||
| chr1:35902991 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1397+654C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902991 | |||||||
| chr1:35902997 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0079 |
2 | NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1397+660G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35902997 | |||||||
| chr1:35902999 | C | CT | 18 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
19 | HG01175.hp1 HG02027.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1397+686dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35902999 | ||||||
| chr1:35902999 | CT | C | 10 | a0001c0001t0001g0080 a0001c0001t0001g0110 a0001c0001t0005g0036 others(7): Show |
11 | HG01167.hp1 HG01261.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1397+686delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35902999 | ||||||
| chr1:35903026 | G | A | 1 | a0001c0002t0002g0051 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1397+689G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903026 | |||||||
| chr1:35903155 | C | T | 1 | a0001c0001t0014g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1397+818C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903155 | |||||||
| chr1:35903164 | G | C | 6 | a0001c0001t0001g0044 a0001c0001t0003g0117 a0001c0001t0003g0118 others(3): Show |
6 | HG01175.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1397+827G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903164 | |||||||
| chr1:35903167 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1397+830C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903167 | |||||||
| chr1:35903258 | G | A | 1 | a0001c0002t0002g0157 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1397+921G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903258 | |||||||
| chr1:35903302 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1397+965G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903302 | |||||||
| chr1:35903305 | CT | C | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1397+981delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35903305 | ||||||
| chr1:35903349 | C | T | 2 | a0001c0004t0045g0057 a0001c0004t0046g0059 |
2 | HG02129.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1397+1012C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903349 | |||||||
| chr1:35903410 | G | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1397+1073G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903410 | |||||||
| chr1:35903423 | T | C | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1397+1086T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903423 | |||||||
| chr1:35903431 | C | T | 1 | a0001c0002t0058g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1397+1094C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903431 | |||||||
| chr1:35903481 | T | C | 2 | a0001c0001t0024g0126 a0001c0001t0025g0132 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1397+1144T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903481 | |||||||
| chr1:35903545 | C | T | 2 | a0001c0001t0012g0134 a0001c0001t0012g0135 |
2 | HG03098.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1397+1208C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903545 | |||||||
| chr1:35903588 | G | C | 1 | a0001c0002t0002g0158 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1397+1251G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903588 | |||||||
| chr1:35903664 | A | C | 7 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1397+1327A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35903664 | |||||||
| chr1:35903961 | CA | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0105 others(2): Show |
6 | HG01891.hp1 NA18955.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+1637delA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35903961 | ||||||
| chr1:35904108 | C | CT | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG00642.hp2 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1397+1792dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35904108 | ||||||
| chr1:35904108 | CT | C | 99 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0044 others(96): Show |
129 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1397+1792delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35904108 | ||||||
| chr1:35904108 | CTT | C | 6 | a0001c0001t0018g0137 a0001c0001t0018g0145 a0001c0001t0024g0126 others(3): Show |
6 | HG01255.hp2 HG02145.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1397+1791_1397+179 others(6): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35904108 | ||||||
| chr1:35904198 | C | T | 3 | a0001c0001t0018g0137 a0001c0001t0018g0145 a0001c0001t0043g0133 |
3 | HG01255.hp2 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1397+1861C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904198 | |||||||
| chr1:35904255 | G | A | 1 | a0001c0002t0061g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1397+1918G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904255 | |||||||
| chr1:35904328 | A | G | 2 | a0001c0001t0005g0037 a0001c0001t0017g0035 |
2 | HG03491.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1397+1991A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904328 | |||||||
| chr1:35904379 | A | C | 3 | a0001c0001t0001g0108 a0001c0001t0015g0109 a0001c0001t0038g0064 |
3 | NA18980.hp2 NA19000.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1397+2042A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904379 | |||||||
| chr1:35904405 | T | A | 1 | a0001c0001t0048g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1397+2068T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904405 | |||||||
| chr1:35904486 | A | G | 1 | a0001c0002t0051g0149 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1397+2149A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904486 | |||||||
| chr1:35904656 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0049g0011 |
5 | HG01168.hp1 HG01433.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-2279G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904656 | |||||||
| chr1:35904765 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1398-2170T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904765 | |||||||
| chr1:35904911 | G | A | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1398-2024G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904911 | |||||||
| chr1:35904931 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1398-2004A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904931 | |||||||
| chr1:35904994 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1398-1941A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35904994 | |||||||
| chr1:35905004 | G | A | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1398-1931G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905004 | |||||||
| chr1:35905150 | G | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
7 | HG02145.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1398-1785G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905150 | |||||||
| chr1:35905184 | A | C | 2 | a0001c0001t0020g0177 a0001c0001t0020g0178 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1398-1751A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905184 | |||||||
| chr1:35905198 | G | A | 1 | a0001c0002t0002g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1398-1737G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905198 | |||||||
| chr1:35905361 | A | G | 4 | a0001c0001t0011g0027 a0001c0001t0011g0127 a0001c0001t0011g0128 others(1): Show |
4 | NA18972.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-1574A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905361 | |||||||
| chr1:35905501 | G | A | 1 | a0001c0002t0053g0172 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1398-1434G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905501 | |||||||
| chr1:35905529 | G | A | 1 | a0001c0002t0008g0141 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1398-1406G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905529 | |||||||
| chr1:35905567 | T | C | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1398-1368T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905567 | |||||||
| chr1:35905818 | G | C | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1398-1117G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905818 | |||||||
| chr1:35905871 | A | G | 1 | a0001c0002t0002g0136 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1398-1064A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905871 | |||||||
| chr1:35905958 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0094 a0001c0001t0001g0095 |
4 | HG00323.hp2 NA18981.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398-977A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35905958 | |||||||
| chr1:35906320 | G | C | 1 | a0001c0001t0047g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1398-615G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906320 | |||||||
| chr1:35906513 | A | G | 1 | a0001c0002t0002g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1398-422A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906513 | |||||||
| chr1:35906558 | C | T | 1 | a0001c0001t0043g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1398-377C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906558 | |||||||
| chr1:35906744 | G | A | 6 | a0001c0002t0002g0030 a0001c0002t0002g0051 a0001c0002t0002g0155 others(3): Show |
7 | NA18946.hp1 NA18973.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1398-191G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906744 | |||||||
| chr1:35906808 | G | GA | 20 | a0001c0001t0001g0020 a0001c0001t0001g0048 a0001c0001t0001g0081 others(17): Show |
21 | HG00673.hp1 HG01109.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1398-110dupA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 35906808 | ||||||
| chr1:35906819 | A | C | 2 | a0001c0001t0018g0137 a0001c0001t0018g0145 |
2 | HG01255.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1398-116A>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906819 | |||||||
| chr1:35906919 | C | T | 1 | a0001c0001t0047g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1398-16C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906919 | |||||||
| chr1:35906925 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1398-10G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 11/18 | chr1 | 35906925 | |||||||
| chr1:35907130 | C | G | 1 | a0001c0007t0002g0160 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1582+11C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907130 | |||||||
| chr1:35907340 | C | A | 1 | a0001c0001t0003g0072 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1582+221C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907340 | |||||||
| chr1:35907585 | A | G | 1 | a0001c0001t0044g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1582+466A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907585 | |||||||
| chr1:35907743 | C | T | 1 | a0001c0001t0048g0084 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1582+624C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907743 | |||||||
| chr1:35907788 | A | G | 1 | a0001c0001t0005g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1582+669A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907788 | |||||||
| chr1:35907820 | A | T | 26 | a0001c0001t0020g0177 a0001c0001t0020g0178 a0001c0002t0004g0007 others(23): Show |
29 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1582+701A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907820 | |||||||
| chr1:35907953 | C | T | 6 | a0001c0001t0020g0177 a0001c0001t0020g0178 a0001c0002t0009g0004 others(3): Show |
8 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+834C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35907953 | |||||||
| chr1:35908023 | G | A | 1 | a0001c0002t0002g0142 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1582+904G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908023 | |||||||
| chr1:35908075 | G | A | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1582+956G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908075 | |||||||
| chr1:35908222 | C | G | 63 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(60): Show |
87 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.1582+1103C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908222 | |||||||
| chr1:35908243 | A | G | 1 | a0001c0001t0043g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1582+1124A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908243 | |||||||
| chr1:35908469 | G | A | 5 | a0001c0001t0024g0126 a0001c0001t0025g0132 a0001c0001t0026g0058 others(2): Show |
5 | HG02129.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1582+1350G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908469 | |||||||
| chr1:35908500 | C | T | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1582+1381C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908500 | |||||||
| chr1:35908520 | C | T | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1582+1401C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908520 | |||||||
| chr1:35908729 | C | T | 2 | a0001c0001t0020g0177 a0001c0001t0020g0178 |
2 | HG02647.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1582+1610C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35908729 | |||||||
| chr1:35908791 | A | ACTTCTCA others(342): Show |
1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1582+1689_1582+169 others(353): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35908791 | ||||||
| chr1:35908816 | C | CT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0103 a0001c0001t0018g0137 others(8): Show |
11 | HG01243.hp1 HG01255.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1582+1717dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35908816 | ||||||
| chr1:35908816 | CT | C | 19 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0005g0006 others(16): Show |
21 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.1582+1717delT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35908816 | ||||||
| chr1:35909019 | T | C | 3 | a0001c0001t0024g0126 a0001c0001t0025g0132 a0001c0001t0026g0058 |
3 | HG02145.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1582+1900T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909019 | |||||||
| chr1:35909069 | C | T | 13 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(10): Show |
17 | HG00544.hp2 HG00609.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1582+1950C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909069 | |||||||
| chr1:35909134 | T | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0113 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1582+2015T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909134 | |||||||
| chr1:35909280 | T | G | 3 | a0001c0001t0024g0126 a0001c0001t0025g0132 a0001c0001t0026g0058 |
3 | HG02145.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1582+2161T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909280 | |||||||
| chr1:35909361 | C | T | 1 | a0001c0001t0005g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1582+2242C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909361 | |||||||
| chr1:35909478 | T | C | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1582+2359T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909478 | |||||||
| chr1:35909509 | C | T | 95 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(92): Show |
122 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1582+2390C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909509 | |||||||
| chr1:35909822 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1582+2703C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909822 | |||||||
| chr1:35909850 | A | G | 1 | a0001c0002t0002g0146 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1582+2731A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909850 | |||||||
| chr1:35909925 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0092 others(5): Show |
9 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1582+2806A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35909925 | |||||||
| chr1:35910135 | A | G | 1 | a0001c0002t0002g0171 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1582+3016A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910135 | |||||||
| chr1:35910203 | C | G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1582+3084C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910203 | |||||||
| chr1:35910267 | A | G | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1582+3148A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910267 | |||||||
| chr1:35910290 | G | T | 1 | a0001c0001t0032g0200 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1582+3171G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910290 | |||||||
| chr1:35910442 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0140 |
2 | NA18990.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1582+3323A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910442 | |||||||
| chr1:35910469 | G | A | 6 | a0001c0001t0020g0177 a0001c0001t0020g0178 a0001c0002t0009g0004 others(3): Show |
8 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1582+3350G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910469 | |||||||
| chr1:35910671 | G | A | 2 | a0001c0001t0019g0008 a0001c0001t0040g0008 |
3 | HG00280.hp1 HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1583-3171G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910671 | |||||||
| chr1:35910967 | G | A | 1 | a0001c0001t0043g0133 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1583-2875G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35910967 | |||||||
| chr1:35911070 | GA | G | 13 | a0001c0002t0004g0007 a0001c0002t0004g0179 a0001c0002t0004g0180 others(10): Show |
14 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1583-2762delA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35911070 | ||||||
| chr1:35911078 | A | T | 2 | a0001c0001t0001g0129 a0001c0002t0041g0150 |
2 | HG02080.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1583-2764A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911078 | |||||||
| chr1:35911225 | A | T | 3 | a0001c0001t0012g0134 a0001c0001t0012g0135 a0001c0001t0012g0201 |
3 | HG03098.hp1 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1583-2617A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911225 | |||||||
| chr1:35911247 | G | A | 1 | a0001c0003t0013g0088 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1583-2595G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911247 | |||||||
| chr1:35911295 | C | T | 1 | a0001c0002t0060g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1583-2547C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911295 | |||||||
| chr1:35911494 | A | AT | 5 | a0001c0001t0003g0119 a0001c0001t0012g0135 a0001c0002t0002g0156 others(2): Show |
5 | HG01261.hp2 HG01361.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1583-2337dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35911494 | ||||||
| chr1:35911888 | C | G | 4 | a0001c0001t0012g0134 a0001c0001t0012g0135 a0001c0001t0012g0201 others(1): Show |
4 | HG03098.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1583-1954C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911888 | |||||||
| chr1:35911919 | A | G | 3 | a0001c0001t0024g0126 a0001c0001t0025g0132 a0001c0001t0026g0058 |
3 | HG02145.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1583-1923A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911919 | |||||||
| chr1:35911975 | T | A | 1 | a0001c0002t0004g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1583-1867T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35911975 | |||||||
| chr1:35912096 | G | A | 3 | a0001c0001t0024g0126 a0001c0001t0025g0132 a0001c0001t0026g0058 |
3 | HG02145.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1583-1746G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912096 | |||||||
| chr1:35912127 | G | A | 1 | a0001c0002t0002g0028 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1583-1715G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912127 | |||||||
| chr1:35912158 | C | G | 1 | a0001c0002t0002g0169 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1583-1684C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912158 | |||||||
| chr1:35912163 | C | T | 3 | a0001c0003t0013g0088 a0001c0003t0013g0090 a0001c0003t0013g0102 |
3 | HG03942.hp1 HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1583-1679C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912163 | |||||||
| chr1:35912227 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0094 |
3 | NA18981.hp2 NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1583-1615C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912227 | |||||||
| chr1:35912228 | G | A | 1 | a0001c0002t0002g0164 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1583-1614G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912228 | |||||||
| chr1:35912258 | C | T | 6 | a0001c0001t0020g0177 a0001c0001t0020g0178 a0001c0002t0009g0004 others(3): Show |
8 | HG01069.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1583-1584C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912258 | |||||||
| chr1:35912360 | G | GA | 29 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0045 others(26): Show |
30 | HG00673.hp1 HG00741.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1583-1459dupA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35912360 | ||||||
| chr1:35912360 | GA | G | 62 | a0001c0001t0001g0198 a0001c0002t0002g0001 a0001c0002t0002g0013 others(59): Show |
82 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.1583-1459delA | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35912360 | ||||||
| chr1:35912360 | GAA | G | 9 | a0001c0001t0005g0038 a0001c0001t0018g0137 a0001c0001t0020g0177 others(6): Show |
11 | HG01069.hp1 HG01255.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1583-1460_1583-145 others(6): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35912360 | ||||||
| chr1:35912360 | GAAA | G | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1583-1461_1583-145 others(7): Show |
AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr1 | 35912360 | ||||||
| chr1:35912361 | A | G | 1 | a0001c0001t0001g0022 | 2 | HG02486.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1583-1481A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912361 | |||||||
| chr1:35912401 | A | G | 1 | a0001c0001t0018g0137 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1583-1441A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912401 | |||||||
| chr1:35912465 | C | A | 1 | a0001c0002t0004g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1583-1377C>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912465 | |||||||
| chr1:35912573 | T | G | 6 | a0001c0001t0001g0044 a0001c0001t0003g0117 a0001c0001t0003g0118 others(3): Show |
6 | HG01175.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583-1269T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912573 | |||||||
| chr1:35912807 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1583-1035C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912807 | |||||||
| chr1:35912862 | G | A | 1 | a0001c0002t0002g0166 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1583-980G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35912862 | |||||||
| chr1:35913089 | G | A | 1 | a0001c0004t0046g0059 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1583-753G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35913089 | |||||||
| chr1:35913108 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1583-734C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35913108 | |||||||
| chr1:35913145 | A | G | 7 | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0055 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1583-697A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35913145 | |||||||
| chr1:35913169 | G | A | 3 | a0001c0001t0018g0137 a0001c0001t0018g0145 a0001c0001t0047g0144 |
3 | HG01255.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1583-673G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35913169 | |||||||
| chr1:35913265 | C | T | 3 | a0001c0001t0018g0137 a0001c0001t0018g0145 a0001c0001t0047g0144 |
3 | HG01255.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1583-577C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 12/18 | chr1 | 35913265 | |||||||
| chr1:35914065 | G | C | 1 | a0001c0002t0002g0169 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1742+64G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 13/18 | chr1 | 35914065 | |||||||
| chr1:35914532 | T | C | 138 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0044 others(135): Show |
171 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1833+258T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 14/18 | chr1 | 35914532 | |||||||
| chr1:35914689 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0003g0089 |
2 | HG02080.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1833+415T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 14/18 | chr1 | 35914689 | |||||||
| chr1:35915272 | A | T | 1 | a0001c0002t0060g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1834-76A>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 14/18 | chr1 | 35915272 | |||||||
| chr1:35915293 | G | C | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1834-55G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 14/18 | chr1 | 35915293 | |||||||
| chr1:35915625 | T | C | 1 | a0001c0001t0005g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2028+83T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35915625 | |||||||
| chr1:35915680 | A | G | 1 | a0001c0001t0010g0077 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2028+138A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35915680 | |||||||
| chr1:35915946 | T | C | 1 | a0001c0001t0012g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2028+404T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35915946 | |||||||
| chr1:35916021 | C | T | 53 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(50): Show |
75 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2028+479C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916021 | |||||||
| chr1:35916029 | A | AT | 77 | a0001c0001t0020g0177 a0001c0001t0020g0178 a0001c0001t0052g0139 others(74): Show |
102 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.2028+499dupT | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 35916029 | ||||||
| chr1:35916067 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0015g0023 |
2 | NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2028+525T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916067 | |||||||
| chr1:35916202 | A | G | 1 | a0001c0002t0004g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2028+660A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916202 | |||||||
| chr1:35916307 | G | A | 1 | a0001c0002t0002g0031 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2028+765G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916307 | |||||||
| chr1:35916383 | T | G | 1 | a0001c0002t0004g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2028+841T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916383 | |||||||
| chr1:35916385 | G | C | 4 | a0001c0001t0011g0027 a0001c0001t0011g0127 a0001c0001t0011g0128 others(1): Show |
4 | NA18972.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.2028+843G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916385 | |||||||
| chr1:35916420 | C | T | 6 | a0001c0002t0002g0013 a0001c0002t0002g0142 a0001c0002t0002g0143 others(3): Show |
7 | HG00544.hp2 HG00609.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2028+878C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916420 | |||||||
| chr1:35916671 | A | G | 2 | a0001c0001t0018g0137 a0001c0001t0018g0145 |
2 | HG01255.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2029-922A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916671 | |||||||
| chr1:35916849 | T | A | 52 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2029-744T>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916849 | |||||||
| chr1:35916882 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0048 others(2): Show |
6 | HG01109.hp1 HG01934.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2029-711A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916882 | |||||||
| chr1:35916941 | G | C | 1 | a0001c0004t0045g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2029-652G>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35916941 | |||||||
| chr1:35917044 | C | T | 1 | a0001c0001t0012g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2029-549C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35917044 | |||||||
| chr1:35917101 | C | T | 10 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2029-492C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35917101 | |||||||
| chr1:35917210 | T | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0105 others(1): Show |
5 | NA18955.hp2 NA18989.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-383T>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35917210 | |||||||
| chr1:35917469 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2029-124G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 15/18 | chr1 | 35917469 | |||||||
| chr1:35917985 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0003g0117 a0001c0001t0003g0118 others(3): Show |
6 | HG01175.hp2 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2163+258A>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 16/18 | chr1 | 35917985 | |||||||
| chr1:35918115 | C | T | 52 | a0001c0001t0052g0139 a0001c0002t0002g0001 a0001c0002t0002g0005 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2164-207C>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 16/18 | chr1 | 35918115 | |||||||
| chr1:35918427 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0130 |
2 | HG00741.hp1 HG01071.hp2 |
splice_region_variant&intron_variant | LOW | c.2265+4G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 17/18 | chr1 | 35918427 | |||||||
| chr1:35918457 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2265+34C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 17/18 | chr1 | 35918457 | |||||||
| chr1:35918614 | T | C | 99 | a0001c0001t0005g0006 a0001c0001t0005g0036 a0001c0001t0005g0037 others(96): Show |
126 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.2265+191T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 17/18 | chr1 | 35918614 | |||||||
| chr1:35918810 | C | G | 1 | a0001c0001t0003g0118 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2266-245C>G | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 17/18 | chr1 | 35918810 | |||||||
| chr1:35918894 | G | A | 1 | a0001c0002t0002g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2266-161G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 17/18 | chr1 | 35918894 | |||||||
| chr1:35919362 | T | C | 1 | a0001c0002t0002g0168 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2465+108T>C | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 18/18 | chr1 | 35919362 | |||||||
| chr1:35919390 | G | T | 1 | a0001c0002t0002g0157 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2466-109G>T | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 18/18 | chr1 | 35919390 | |||||||
| chr1:35919460 | G | A | 52 | a0001c0002t0002g0001 a0001c0002t0002g0005 a0001c0002t0002g0013 others(49): Show |
74 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2466-39G>A | AGO1 | ENSG00000092847.14 | transcript | ENST00000373204.6 | protein_coding | 18/18 | chr1 | 35919460 |