Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83667 |
| ensemblid | ENSG00000130766.5 |
| hgncid | 20746 |
| symbol | SESN2 |
| name | sestrin 2 |
| refseq_nuc | NM_031459.5 |
| refseq_prot | NP_113647.1 |
| ensembl_nuc | ENST00000253063.4 |
| ensembl_prot | ENSP00000253063.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 28259518 |
| end | 28282491 |
| strand | + |
| ver | v1.2 |
| region | chr1:28259518-28282491 |
| region5000 | chr1:28254518-28287491 |
| regionname0 | SESN2_chr1_28259518_28282491 |
| regionname5000 | SESN2_chr1_28254518_28287491 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 480 | 316 | 86 | 66 | 112 | 16 | 36 | 82 | SESN2_chr1_28254518_28287491 | SESN2 | MIVAD others(475): Show |
chr1 | 28254518 | 28287491 |
| a0002 | 0/0 | 480 | 13 | 0 | 0 | 13 | 0 | 0 | 13 | SESN2_chr1_28254518_28287491 | SESN2 | MIVAD others(475): Show |
chr1 | 28254518 | 28287491 |
| a0003 | 0/0 | 480 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SESN2_chr1_28254518_28287491 | SESN2 | MIVAD others(475): Show |
chr1 | 28254518 | 28287491 |
| a0004 | 0/0 | 480 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | MIVAD others(475): Show |
chr1 | 28254518 | 28287491 |
| a0005 | 0/0 | 480 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | MIVAD others(475): Show |
chr1 | 28254518 | 28287491 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1440 | 291 | 80 | 63 | 101 | 16 | 31 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0003 | 0/0 | 1440 | 8 | 0 | 2 | 4 | 0 | 2 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0004 | 0/0 | 1440 | 5 | 0 | 0 | 4 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0006 | 0/0 | 1440 | 4 | 0 | 0 | 3 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0007 | 0/0 | 1440 | 4 | 4 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0009 | 0/0 | 1440 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0010 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0012 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0001c0013 | 0/0 | 1440 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0002c0002 | 0/0 | 1440 | 13 | 0 | 0 | 13 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0003c0005 | 0/0 | 1440 | 5 | 0 | 0 | 5 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0004c0008 | 0/0 | 1440 | 3 | 3 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 | ||
| a0005c0011 | 0/0 | 1440 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | ATGAT others(1435): Show |
chr1 | 28254518 | 28287491 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3462 | 192 | 49 | 38 | 77 | 6 | 22 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0002 | 0/0 | 3463 | 45 | 5 | 8 | 22 | 5 | 5 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3458): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0003 | 0/0 | 3462 | 18 | 16 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0004 | 0/0 | 3462 | 7 | 5 | 0 | 0 | 0 | 2 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0005 | 0/0 | 3462 | 5 | 0 | 4 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0006 | 0/0 | 3462 | 5 | 0 | 1 | 0 | 4 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0007 | 0/0 | 3462 | 5 | 0 | 5 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0008 | 0/0 | 3462 | 3 | 0 | 3 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0009 | 0/0 | 3462 | 3 | 2 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0010 | 0/0 | 3462 | 2 | 1 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0011 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0012 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0013 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0015 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0016 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0001t0017 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0003t0002 | 0/0 | 3463 | 8 | 0 | 2 | 4 | 0 | 2 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3458): Show |
chr1 | 28254518 | 28287491 |
| a0001c0004t0001 | 0/0 | 3462 | 5 | 0 | 0 | 4 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0006t0001 | 0/0 | 3462 | 4 | 0 | 0 | 3 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0007t0001 | 0/0 | 3462 | 4 | 4 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0009t0001 | 0/0 | 3462 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0010t0001 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0012t0001 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0001c0013t0014 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0002c0002t0001 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0002c0002t0002 | 0/0 | 3463 | 12 | 0 | 0 | 12 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3458): Show |
chr1 | 28254518 | 28287491 |
| a0003c0005t0001 | 0/0 | 3462 | 5 | 0 | 0 | 5 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0004c0008t0001 | 0/0 | 3462 | 3 | 3 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| a0005c0011t0001 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | GCTGG others(3457): Show |
chr1 | 28254518 | 28287491 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 5 | 6 | 3 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0002 | 0/0 | 9 | 2 | 0 | 7 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0004 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0003 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0009g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0010g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0011g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0013g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0001t0017g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0004t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0006t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0006t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0007t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0007t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0007t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0010t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0012t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0001c0013t0014g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0003c0005t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0003c0005t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0003c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0003c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0003c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0004c0008t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0004c0008t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| a0005c0011t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0166 | EUR | GBR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | GBR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00140 | hp2 | a0001 | c0001 | t0006 | g0008 | EUR | GBR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0084 | EUR | FIN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0117 | EUR | FIN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00558 | hp1 | a0001 | c0003 | t0002 | g0072 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0200 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0068 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0116 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0008 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01255 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0097 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01258 | hp1 | a0001 | c0001 | t0005 | g0029 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0098 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0094 | EUR | IBS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | IBS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0034 | EUR | IBS | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01891 | hp2 | a0004 | c0008 | t0001 | g0069 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02004 | hp2 | a0001 | c0001 | t0007 | g0149 | AMR | PEL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0173 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02165 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | CDX | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0060 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02523 | hp1 | a0001 | c0006 | t0001 | g0018 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02615 | hp1 | a0001 | c0007 | t0001 | g0061 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02622 | hp1 | a0004 | c0008 | t0001 | g0026 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02630 | hp2 | a0001 | c0012 | t0001 | g0065 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02896 | hp1 | a0001 | c0001 | t0015 | g0213 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02896 | hp2 | a0005 | c0011 | t0001 | g0049 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02970 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0159 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03486 | hp1 | a0001 | c0007 | t0001 | g0025 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03486 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0217 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03516 | hp1 | a0001 | c0010 | t0001 | g0047 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0007 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0083 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0002 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0121 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04184 | hp2 | a0001 | c0006 | t0001 | g0131 | SAS | BEB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0219 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG04228 | hp2 | a0001 | c0013 | t0014 | g0120 | SAS | STU | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18940 | hp1 | a0001 | c0001 | t0016 | g0132 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18943 | hp1 | a0003 | c0005 | t0001 | g0160 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18953 | hp2 | a0003 | c0005 | t0001 | g0184 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18957 | hp2 | a0001 | c0003 | t0002 | g0062 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18966 | hp1 | a0003 | c0005 | t0001 | g0138 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18972 | hp2 | a0001 | c0006 | t0001 | g0113 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18986 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19012 | hp1 | a0003 | c0005 | t0001 | g0004 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19068 | hp2 | a0003 | c0005 | t0001 | g0017 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19085 | hp2 | a0001 | c0006 | t0001 | g0018 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | YRI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20129 | hp2 | a0004 | c0008 | t0001 | g0026 | AFR | ASW | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0099 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0110 | AMR | CLM | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | SESN2_chr1_28254518_28287491 | SESN2 | chr1 | 28254518 | 28287491 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28271776 | C | T | 1 | a0002 | 13 | NA18939.hp1 NA18940.hp2 NA18947.hp2 others(10): Show |
missense_variant | MODERATE | c.259C>T | p.Pro87Ser | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 3/10 | 589/3462 | 259/1443 | 87/480 | chr1 | 28271776 | |||
| chr1:28272596 | G | A | 1 | a0005 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.553G>A | p.Gly185Ser | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 5/10 | 883/3462 | 553/1443 | 185/480 | chr1 | 28272596 | |||
| chr1:28274063 | C | T | 1 | a0004 | 3 | HG01891.hp2 HG02622.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.925C>T | p.His309Tyr | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/10 | 1255/3462 | 925/1443 | 309/480 | chr1 | 28274063 | |||
| chr1:28274096 | A | G | 1 | a0003 | 5 | NA18943.hp1 NA18953.hp2 NA18966.hp1 others(2): Show |
missense_variant | MODERATE | c.958A>G | p.Thr320Ala | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/10 | 1288/3462 | 958/1443 | 320/480 | chr1 | 28274096 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28259865 | C | G | 2 | a0001c0003 a0002c0002 |
21 | HG00558.hp1 HG01346.hp1 HG01361.hp2 others(18): Show |
synonymous_variant | LOW | c.18C>G | p.Ser6Ser | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/10 | 348/3462 | 18/1443 | 6/480 | chr1 | 28259865 | |||
| chr1:28259886 | G | A | 1 | a0001c0004 | 5 | HG00597.hp1 HG02165.hp2 HG03834.hp2 others(2): Show |
synonymous_variant | LOW | c.39G>A | p.Lys13Lys | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/10 | 369/3462 | 39/1443 | 13/480 | chr1 | 28259886 | |||
| chr1:28259937 | G | A | 1 | a0001c0009 | 1 | HG01255.hp1 | splice_region_variant&synonymous_variant | LOW | c.90G>A | p.Glu30Glu | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/10 | 420/3462 | 90/1443 | 30/480 | chr1 | 28259937 | |||
| chr1:28269227 | C | T | 1 | a0001c0013 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/10 | 465/3462 | 135/1443 | 45/480 | chr1 | 28269227 | |||
| chr1:28271718 | G | A | 1 | a0001c0010 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.201G>A | p.Leu67Leu | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 3/10 | 531/3462 | 201/1443 | 67/480 | chr1 | 28271718 | |||
| chr1:28273387 | G | A | 1 | a0001c0006 | 4 | HG02523.hp1 HG04184.hp2 NA18972.hp2 others(1): Show |
synonymous_variant | LOW | c.780G>A | p.Ala260Ala | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/10 | 1110/3462 | 780/1443 | 260/480 | chr1 | 28273387 | |||
| chr1:28273441 | G | A | 1 | a0001c0012 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.834G>A | p.Thr278Thr | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/10 | 1164/3462 | 834/1443 | 278/480 | chr1 | 28273441 | |||
| chr1:28273450 | G | A | 1 | a0001c0007 | 4 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.843G>A | p.Glu281Glu | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/10 | 1173/3462 | 843/1443 | 281/480 | chr1 | 28273450 | |||
| chr1:28274896 | T | C | 1 | a0001c0007 | 4 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.1092T>C | p.Asp364Asp | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/10 | 1422/3462 | 1092/1443 | 364/480 | chr1 | 28274896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28259529 | C | G | 1 | a0001c0001t0017 | 1 | HG03017.hp1 | 5_prime_UTR_variant | MODIFIER | c.-319C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/10 | 319 | chr1 | 28259529 | ||||||
| chr1:28259784 | C | T | 1 | a0001c0001t0016 | 1 | NA18940.hp1 | 5_prime_UTR_variant | MODIFIER | c.-64C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/10 | 64 | chr1 | 28259784 | ||||||
| chr1:28281105 | A | G | 1 | a0001c0001t0007 | 5 | HG00738.hp1 HG01081.hp2 HG01168.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 303 | chr1 | 28281105 | ||||||
| chr1:28281289 | G | C | 1 | a0001c0001t0005 | 5 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*487G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 487 | chr1 | 28281289 | ||||||
| chr1:28281379 | G | T | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0015 |
24 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*577G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 577 | chr1 | 28281379 | ||||||
| chr1:28281450 | T | TA | 3 | a0001c0001t0002 a0001c0003t0002 a0002c0002t0002 |
65 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*661dupA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 662 | INFO_REALIGN_3_PRIME | chr1 | 28281450 | |||||
| chr1:28281518 | G | A | 1 | a0001c0001t0011 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*716G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 716 | chr1 | 28281518 | ||||||
| chr1:28281699 | C | G | 4 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(1): Show |
31 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*897C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 897 | chr1 | 28281699 | ||||||
| chr1:28281827 | A | G | 1 | a0001c0001t0006 | 5 | HG00099.hp2 HG00140.hp2 HG01515.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1025A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1025 | chr1 | 28281827 | ||||||
| chr1:28282089 | C | T | 1 | a0001c0001t0009 | 3 | HG01069.hp1 HG03098.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1287 | chr1 | 28282089 | ||||||
| chr1:28282102 | A | G | 1 | a0001c0013t0014 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1300A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1300 | chr1 | 28282102 | ||||||
| chr1:28282195 | G | A | 1 | a0001c0001t0012 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1393G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1393 | chr1 | 28282195 | ||||||
| chr1:28282210 | G | A | 1 | a0001c0001t0008 | 3 | HG01123.hp1 HG01257.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1408G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1408 | chr1 | 28282210 | ||||||
| chr1:28282263 | G | A | 2 | a0001c0001t0010 a0001c0001t0012 |
3 | HG01109.hp2 HG02717.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1461G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1461 | chr1 | 28282263 | ||||||
| chr1:28282287 | C | A | 3 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0015 |
24 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1485C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1485 | chr1 | 28282287 | ||||||
| chr1:28282381 | G | C | 1 | a0001c0001t0013 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1579G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1579 | chr1 | 28282381 | ||||||
| chr1:28282400 | A | G | 1 | a0001c0001t0015 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1598A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 10/10 | 1598 | chr1 | 28282400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:28260116 | G | T | 16 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(13): Show |
21 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+179G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260116 | |||||||
| chr1:28260133 | T | TTCTCCCC others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.90+208_90+219dupCT others(10): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28260133 | ||||||
| chr1:28260243 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.90+306A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260243 | |||||||
| chr1:28260403 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.90+466C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260403 | |||||||
| chr1:28260473 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(235): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.90+536T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260473 | |||||||
| chr1:28260542 | C | CGCG | 16 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(13): Show |
21 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+614_90+616dupGG others(1): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28260542 | ||||||
| chr1:28260586 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.90+649G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260586 | |||||||
| chr1:28260760 | G | C | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.90+823G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260760 | |||||||
| chr1:28260895 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18963.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.90+958A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260895 | |||||||
| chr1:28260990 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.90+1053C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28260990 | |||||||
| chr1:28261107 | C | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00735.hp1 HG01168.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.90+1170C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28261107 | |||||||
| chr1:28261216 | G | A | 2 | a0001c0001t0001g0048 a0001c0010t0001g0047 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.90+1279G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28261216 | |||||||
| chr1:28261779 | C | CT | 23 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(20): Show |
28 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.90+1861dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28261779 | ||||||
| chr1:28261779 | CT | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(25): Show |
33 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.90+1861delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28261779 | ||||||
| chr1:28261779 | CTT | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0050 others(3): Show |
9 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.90+1860_90+1861del others(2): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28261779 | ||||||
| chr1:28261825 | G | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
13 | HG01069.hp1 HG01123.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.90+1888G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28261825 | |||||||
| chr1:28261964 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00408.hp2 HG00423.hp2 |
intron_variant | MODIFIER | c.90+2027A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28261964 | |||||||
| chr1:28262003 | A | T | 1 | a0001c0001t0001g0042 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.90+2066A>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262003 | |||||||
| chr1:28262112 | G | C | 1 | a0001c0001t0001g0105 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.90+2175G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262112 | |||||||
| chr1:28262272 | G | T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0045 others(10): Show |
16 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.90+2335G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262272 | |||||||
| chr1:28262359 | T | C | 2 | a0001c0001t0001g0048 a0001c0010t0001g0047 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.90+2422T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262359 | |||||||
| chr1:28262406 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | NA19010.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.90+2469G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262406 | |||||||
| chr1:28262415 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.90+2478G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262415 | |||||||
| chr1:28262497 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
14 | HG01069.hp1 HG01123.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+2560G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262497 | |||||||
| chr1:28262503 | C | T | 1 | a0001c0001t0003g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.90+2566C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262503 | |||||||
| chr1:28262597 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.90+2660G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262597 | |||||||
| chr1:28262621 | C | CA | 49 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(46): Show |
60 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.90+2706dupA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAA | 16 | a0001c0001t0001g0045 a0001c0001t0001g0114 a0001c0001t0001g0115 others(13): Show |
17 | HG00738.hp2 HG01123.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.90+2705_90+2706dup others(2): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAAA | 10 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(7): Show |
14 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+2704_90+2706dup others(3): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAAAAA | 39 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0024 others(36): Show |
55 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.90+2702_90+2706dup others(5): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAAAAAA | 24 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 others(21): Show |
28 | HG00558.hp1 HG00642.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.90+2701_90+2706dup others(6): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAAAAAAA others(2): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0009g0014 others(1): Show |
6 | HG02572.hp1 HG02622.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.90+2698_90+2706dup others(9): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262621 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.90+2696_90+2706dup others(11): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28262621 | ||||||
| chr1:28262655 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.90+2718G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262655 | |||||||
| chr1:28262724 | T | C | 93 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
120 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.90+2787T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262724 | |||||||
| chr1:28262745 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.90+2808G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262745 | |||||||
| chr1:28262821 | C | G | 93 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
120 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.90+2884C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262821 | |||||||
| chr1:28262822 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.90+2885G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262822 | |||||||
| chr1:28262824 | A | T | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.90+2887A>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262824 | |||||||
| chr1:28262875 | C | T | 16 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(13): Show |
21 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.90+2938C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262875 | |||||||
| chr1:28262895 | T | C | 5 | a0001c0001t0004g0044 a0001c0001t0004g0217 a0001c0001t0004g0218 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.90+2958T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262895 | |||||||
| chr1:28262899 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.90+2962G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262899 | |||||||
| chr1:28262904 | G | C | 3 | a0001c0007t0001g0025 a0001c0007t0001g0060 a0001c0007t0001g0061 |
4 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+2967G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262904 | |||||||
| chr1:28262931 | A | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0067 others(9): Show |
14 | HG01069.hp1 HG01123.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.90+2994A>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28262931 | |||||||
| chr1:28263008 | C | G | 2 | a0001c0001t0001g0048 a0001c0010t0001g0047 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.90+3071C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263008 | |||||||
| chr1:28263067 | T | C | 113 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.90+3130T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263067 | |||||||
| chr1:28263240 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0185 |
3 | HG00280.hp1 HG01081.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.90+3303C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263240 | |||||||
| chr1:28263291 | T | A | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.90+3354T>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263291 | |||||||
| chr1:28263346 | T | A | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.90+3409T>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263346 | |||||||
| chr1:28263351 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.90+3414G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263351 | |||||||
| chr1:28263419 | T | G | 3 | a0001c0007t0001g0025 a0001c0007t0001g0060 a0001c0007t0001g0061 |
4 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.90+3482T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263419 | |||||||
| chr1:28263573 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.90+3636T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263573 | |||||||
| chr1:28263580 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0139 |
3 | HG02074.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.90+3643C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263580 | |||||||
| chr1:28263759 | C | T | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.90+3822C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263759 | |||||||
| chr1:28263808 | T | C | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.90+3871T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263808 | |||||||
| chr1:28263915 | A | G | 1 | a0003c0005t0001g0184 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.90+3978A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28263915 | |||||||
| chr1:28264063 | TA | T | 7 | a0001c0001t0001g0052 a0001c0001t0001g0104 a0001c0001t0001g0142 others(4): Show |
7 | HG00639.hp1 HG00639.hp2 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.90+4144delA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28264063 | ||||||
| chr1:28264180 | T | G | 113 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(110): Show |
143 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.90+4243T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264180 | |||||||
| chr1:28264187 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.90+4250C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264187 | |||||||
| chr1:28264331 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0024 others(14): Show |
22 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.90+4394A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264331 | |||||||
| chr1:28264420 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.90+4483C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264420 | |||||||
| chr1:28264465 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.90+4528T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264465 | |||||||
| chr1:28264562 | CT | C | 77 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.91-4617delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28264562 | ||||||
| chr1:28264585 | ACTGGAAT others(5): Show |
A | 1 | a0001c0001t0001g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.91-4595_91-4584del others(12): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28264585 | ||||||
| chr1:28264697 | T | C | 1 | a0001c0001t0003g0210 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.91-4486T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264697 | |||||||
| chr1:28264902 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.91-4281T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28264902 | |||||||
| chr1:28265350 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0082 |
3 | HG02976.hp1 HG03669.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.91-3833G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265350 | |||||||
| chr1:28265351 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.91-3832C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265351 | |||||||
| chr1:28265460 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91-3723C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265460 | |||||||
| chr1:28265675 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.91-3508G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265675 | |||||||
| chr1:28265687 | G | T | 1 | a0003c0005t0001g0138 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.91-3496G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265687 | |||||||
| chr1:28265794 | G | A | 1 | a0001c0001t0006g0034 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.91-3389G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28265794 | |||||||
| chr1:28265838 | T | TA | 38 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0002g0003 others(35): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.91-3344dupA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28265838 | ||||||
| chr1:28266150 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.91-3033A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266150 | |||||||
| chr1:28266198 | G | A | 1 | a0001c0003t0002g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.91-2985G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266198 | |||||||
| chr1:28266213 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.91-2970C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266213 | |||||||
| chr1:28266455 | A | G | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-2728A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266455 | |||||||
| chr1:28266532 | T | C | 1 | a0001c0013t0014g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.91-2651T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266532 | |||||||
| chr1:28266556 | C | CT | 27 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0041 others(24): Show |
32 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.91-2606dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28266556 | ||||||
| chr1:28266556 | C | CTT | 36 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0103 others(33): Show |
49 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.91-2607_91-2606dup others(2): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28266556 | ||||||
| chr1:28266556 | CT | C | 17 | a0001c0001t0001g0108 a0001c0001t0001g0145 a0001c0001t0001g0146 others(14): Show |
18 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.91-2606delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28266556 | ||||||
| chr1:28266712 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.91-2471T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266712 | |||||||
| chr1:28266778 | G | A | 2 | a0001c0001t0007g0149 a0001c0001t0007g0150 |
2 | HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.91-2405G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266778 | |||||||
| chr1:28266858 | A | G | 1 | a0001c0001t0003g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-2325A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28266858 | |||||||
| chr1:28267172 | G | C | 1 | a0001c0001t0001g0035 | 2 | NA18980.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.91-2011G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267172 | |||||||
| chr1:28267211 | T | G | 17 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(14): Show |
22 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.91-1972T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267211 | |||||||
| chr1:28267222 | G | A | 1 | a0001c0001t0007g0149 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.91-1961G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267222 | |||||||
| chr1:28267284 | G | A | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.91-1899G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267284 | |||||||
| chr1:28267492 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.91-1691T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267492 | |||||||
| chr1:28267516 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.91-1667C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267516 | |||||||
| chr1:28267824 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0198 |
2 | NA18975.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.91-1359C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267824 | |||||||
| chr1:28267971 | G | C | 1 | a0001c0012t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-1212G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28267971 | |||||||
| chr1:28268241 | G | A | 1 | a0001c0001t0003g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.91-942G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268241 | |||||||
| chr1:28268317 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.91-866G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268317 | |||||||
| chr1:28268407 | A | G | 1 | a0001c0001t0004g0220 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.91-776A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268407 | |||||||
| chr1:28268469 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91-714C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268469 | |||||||
| chr1:28268597 | A | G | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.91-586A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268597 | |||||||
| chr1:28268660 | C | G | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.91-523C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268660 | |||||||
| chr1:28268665 | C | CA | 7 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.91-507dupA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 28268665 | ||||||
| chr1:28268750 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.91-433G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268750 | |||||||
| chr1:28268995 | G | A | 1 | a0001c0012t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.91-188G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28268995 | |||||||
| chr1:28269014 | C | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0096 a0001c0001t0002g0027 others(4): Show |
8 | HG00639.hp1 HG02723.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.91-169C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28269014 | |||||||
| chr1:28269089 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.91-94T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28269089 | |||||||
| chr1:28269156 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91-27G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 1/9 | chr1 | 28269156 | |||||||
| chr1:28269392 | G | A | 1 | a0001c0001t0013g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.156+144G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269392 | |||||||
| chr1:28269573 | A | G | 98 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.156+325A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269573 | |||||||
| chr1:28269649 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.156+401A>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269649 | |||||||
| chr1:28269722 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.156+474G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269722 | |||||||
| chr1:28269778 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.156+530G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269778 | |||||||
| chr1:28269791 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+543T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269791 | |||||||
| chr1:28269933 | C | G | 7 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+685C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269933 | |||||||
| chr1:28269986 | T | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.156+738T>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28269986 | |||||||
| chr1:28270231 | A | G | 16 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(13): Show |
21 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.156+983A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270231 | |||||||
| chr1:28270282 | C | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
7 | HG00408.hp1 NA18946.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+1034C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270282 | |||||||
| chr1:28270305 | C | T | 1 | a0001c0001t0011g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.156+1057C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270305 | |||||||
| chr1:28270307 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.156+1059C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270307 | |||||||
| chr1:28270350 | C | CA | 7 | a0001c0001t0001g0055 a0001c0001t0001g0122 a0001c0001t0001g0153 others(4): Show |
7 | HG01243.hp2 HG02738.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+1119dupA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28270350 | ||||||
| chr1:28270420 | C | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.156+1172C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270420 | |||||||
| chr1:28270540 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.157-1134C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270540 | |||||||
| chr1:28270698 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0036 a0001c0001t0001g0119 others(2): Show |
8 | HG01106.hp1 HG01358.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.157-976G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270698 | |||||||
| chr1:28270820 | C | G | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157-854C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270820 | |||||||
| chr1:28270830 | A | G | 38 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0002g0003 others(35): Show |
51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-844A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270830 | |||||||
| chr1:28270939 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0064 |
2 | HG01243.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157-735T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270939 | |||||||
| chr1:28270979 | C | T | 7 | a0001c0001t0002g0015 a0001c0001t0002g0031 a0001c0001t0002g0032 others(4): Show |
11 | HG00558.hp2 HG01934.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-695C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28270979 | |||||||
| chr1:28271077 | C | T | 16 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(13): Show |
21 | HG01069.hp2 HG01071.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.157-597C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271077 | |||||||
| chr1:28271167 | T | G | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.157-507T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271167 | |||||||
| chr1:28271200 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0003g0043 a0001c0001t0003g0215 |
4 | HG01069.hp2 HG01071.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-474C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271200 | |||||||
| chr1:28271324 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0050 others(3): Show |
9 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-350G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271324 | |||||||
| chr1:28271451 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.157-223A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271451 | |||||||
| chr1:28271487 | T | C | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0186 |
3 | HG01891.hp1 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.157-187T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271487 | |||||||
| chr1:28271509 | T | C | 98 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
125 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.157-165T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271509 | |||||||
| chr1:28271538 | CTCCCCAT others(4): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.157-133_157-123del others(11): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr1 | 28271538 | ||||||
| chr1:28271542 | C | G | 4 | a0001c0001t0003g0109 a0001c0001t0005g0110 a0001c0001t0005g0116 others(1): Show |
4 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-132C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271542 | |||||||
| chr1:28271599 | C | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0082 |
3 | HG02976.hp1 HG03669.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157-75C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 2/9 | chr1 | 28271599 | |||||||
| chr1:28272219 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
8 | HG02083.hp2 HG02135.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.355-65G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 3/9 | chr1 | 28272219 | |||||||
| chr1:28272246 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.355-38G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 3/9 | chr1 | 28272246 | |||||||
| chr1:28272803 | G | A | 1 | a0001c0013t0014g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.750+10G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 5/9 | chr1 | 28272803 | |||||||
| chr1:28273187 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.751-171G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 5/9 | chr1 | 28273187 | |||||||
| chr1:28273636 | T | G | 5 | a0001c0001t0004g0044 a0001c0001t0004g0217 a0001c0001t0004g0218 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.901+128T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273636 | |||||||
| chr1:28273742 | A | G | 1 | a0001c0007t0001g0061 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.901+234A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273742 | |||||||
| chr1:28273777 | G | A | 1 | a0001c0001t0007g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.902-263G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273777 | |||||||
| chr1:28273843 | G | A | 1 | a0001c0003t0002g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.902-197G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273843 | |||||||
| chr1:28273935 | T | A | 7 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.902-105T>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273935 | |||||||
| chr1:28273962 | C | A | 1 | a0001c0001t0003g0111 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.902-78C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 6/9 | chr1 | 28273962 | |||||||
| chr1:28274274 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1020+116G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274274 | |||||||
| chr1:28274342 | G | A | 1 | a0002c0002t0002g0073 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1020+184G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274342 | |||||||
| chr1:28274353 | G | T | 1 | a0001c0007t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1020+195G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274353 | |||||||
| chr1:28274400 | C | T | 3 | a0001c0001t0008g0097 a0001c0001t0008g0098 a0001c0001t0008g0099 |
3 | HG01123.hp1 HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1020+242C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274400 | |||||||
| chr1:28274423 | T | C | 1 | a0001c0007t0001g0025 | 2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1020+265T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274423 | |||||||
| chr1:28274477 | G | C | 5 | a0001c0001t0004g0044 a0001c0001t0004g0217 a0001c0001t0004g0218 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+319G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274477 | |||||||
| chr1:28274486 | G | C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0158 a0001c0001t0001g0192 others(2): Show |
5 | HG02602.hp1 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1020+328G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274486 | |||||||
| chr1:28274496 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1021-329G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274496 | |||||||
| chr1:28274526 | C | G | 1 | a0001c0010t0001g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1021-299C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274526 | |||||||
| chr1:28274528 | CA | C | 19 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(16): Show |
23 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.1021-284delA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 28274528 | ||||||
| chr1:28274555 | G | A | 1 | a0003c0005t0001g0160 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1021-270G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274555 | |||||||
| chr1:28274733 | A | G | 7 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021-92A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274733 | |||||||
| chr1:28274808 | C | T | 1 | a0001c0001t0013g0121 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1021-17C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 7/9 | chr1 | 28274808 | |||||||
| chr1:28275296 | T | TAC | 7 | a0001c0001t0001g0037 a0001c0001t0001g0128 a0001c0001t0001g0147 others(4): Show |
8 | HG01168.hp1 HG01168.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211+302_1211+303d others(4): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28275296 | ||||||
| chr1:28275296 | TAC | T | 14 | a0001c0001t0003g0043 a0001c0001t0003g0111 a0001c0001t0003g0112 others(11): Show |
16 | HG01069.hp2 HG01071.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1211+302_1211+303d others(4): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28275296 | ||||||
| chr1:28275296 | TACACAC | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0001g0055 others(4): Show |
9 | HG01243.hp1 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1211+298_1211+303d others(8): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28275296 | ||||||
| chr1:28275296 | TACACACA others(1): Show |
T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0041 a0001c0001t0001g0045 others(10): Show |
16 | HG00099.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1211+296_1211+303d others(10): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28275296 | ||||||
| chr1:28275300 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1211+285C>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275300 | |||||||
| chr1:28275317 | A | T | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0186 |
3 | HG01891.hp1 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1211+302A>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275317 | |||||||
| chr1:28275318 | C | A | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0186 |
3 | HG01891.hp1 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1211+303C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275318 | |||||||
| chr1:28275468 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1211+453C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275468 | |||||||
| chr1:28275529 | C | T | 1 | a0001c0010t0001g0047 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1211+514C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275529 | |||||||
| chr1:28275542 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1211+527T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275542 | |||||||
| chr1:28275642 | C | A | 1 | a0001c0001t0015g0213 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1211+627C>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275642 | |||||||
| chr1:28275706 | C | T | 43 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0002g0003 others(40): Show |
57 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1211+691C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275706 | |||||||
| chr1:28275846 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1211+831G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28275846 | |||||||
| chr1:28275866 | CA | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0134 others(1): Show |
7 | HG02129.hp1 NA18942.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1211+853delA | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28275866 | ||||||
| chr1:28276020 | G | C | 1 | a0001c0001t0004g0044 | 2 | HG02257.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1211+1005G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276020 | |||||||
| chr1:28276115 | CCAGCCTG others(4): Show |
C | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1211+1101_1211+111 others(15): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276115 | |||||||
| chr1:28276129 | AGAGCAAG | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1211+1115_1211+112 others(11): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276129 | |||||||
| chr1:28276210 | G | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1211+1195G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276210 | |||||||
| chr1:28276215 | A | G | 7 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
7 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.1211+1200A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276215 | |||||||
| chr1:28276435 | C | T | 3 | a0001c0007t0001g0025 a0001c0007t0001g0060 a0001c0007t0001g0061 |
4 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1211+1420C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276435 | |||||||
| chr1:28276466 | G | A | 5 | a0001c0001t0004g0044 a0001c0001t0004g0217 a0001c0001t0004g0218 others(2): Show |
6 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1211+1451G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276466 | |||||||
| chr1:28276570 | C | CT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(57): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1211+1581dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276570 | ||||||
| chr1:28276570 | C | CTT | 8 | a0001c0001t0001g0059 a0001c0001t0001g0128 a0001c0001t0001g0133 others(5): Show |
8 | HG01123.hp1 HG01496.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1211+1580_1211+158 others(6): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276570 | ||||||
| chr1:28276570 | C | CTTT | 4 | a0001c0001t0003g0011 a0001c0001t0003g0216 a0001c0001t0003g0221 others(1): Show |
7 | HG02717.hp1 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1211+1579_1211+158 others(7): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276570 | ||||||
| chr1:28276570 | C | CTTTT | 6 | a0001c0001t0001g0124 a0001c0001t0003g0210 a0001c0001t0003g0211 others(3): Show |
6 | HG02257.hp1 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1211+1578_1211+158 others(8): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276570 | ||||||
| chr1:28276570 | CT | C | 12 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0108 others(9): Show |
13 | HG00639.hp1 HG01069.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1211+1581delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276570 | ||||||
| chr1:28276596 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0091 |
2 | NA18999.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1211+1581T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276596 | |||||||
| chr1:28276679 | G | A | 24 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0109 others(21): Show |
29 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1211+1664G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276679 | |||||||
| chr1:28276683 | G | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1211+1668G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276683 | |||||||
| chr1:28276878 | C | CT | 21 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0037 others(18): Show |
27 | HG00140.hp2 HG01070.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1211+1882dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276878 | ||||||
| chr1:28276878 | CT | C | 39 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0066 others(36): Show |
47 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.1211+1882delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28276878 | ||||||
| chr1:28276902 | T | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0182 a0001c0001t0001g0202 others(7): Show |
12 | HG00323.hp2 HG00438.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1211+1887T>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276902 | |||||||
| chr1:28276911 | A | C | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1211+1896A>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276911 | |||||||
| chr1:28276934 | T | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1211+1919T>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276934 | |||||||
| chr1:28276947 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1211+1932C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276947 | |||||||
| chr1:28276989 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0074 |
2 | HG01106.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1211+1974C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28276989 | |||||||
| chr1:28277149 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0002g0030 a0001c0001t0002g0084 |
3 | HG00140.hp1 HG00323.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1212-1948C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28277149 | |||||||
| chr1:28277180 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1212-1917C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28277180 | |||||||
| chr1:28277205 | CT | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1212-1877delT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28277205 | ||||||
| chr1:28277539 | G | GT | 6 | a0001c0001t0004g0044 a0001c0001t0004g0053 a0001c0001t0004g0217 others(3): Show |
7 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212-1557dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28277539 | ||||||
| chr1:28277673 | C | T | 11 | a0001c0001t0003g0011 a0001c0001t0003g0043 a0001c0001t0003g0210 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1212-1424C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28277673 | |||||||
| chr1:28277902 | G | A | 4 | a0001c0001t0003g0043 a0001c0007t0001g0025 a0001c0007t0001g0060 others(1): Show |
6 | HG01069.hp2 HG01071.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212-1195G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28277902 | |||||||
| chr1:28277952 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1212-1145C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28277952 | |||||||
| chr1:28278123 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1212-974C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278123 | |||||||
| chr1:28278162 | A | T | 90 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0024 others(87): Show |
115 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1212-935A>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278162 | |||||||
| chr1:28278344 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA18980.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1212-753G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278344 | |||||||
| chr1:28278364 | C | T | 8 | a0001c0001t0003g0109 a0001c0001t0003g0111 a0001c0001t0003g0112 others(5): Show |
9 | HG00323.hp2 HG01109.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1212-733C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278364 | |||||||
| chr1:28278507 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1212-590C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278507 | |||||||
| chr1:28278523 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0087 |
3 | HG01256.hp1 HG01258.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1212-574C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278523 | |||||||
| chr1:28278524 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1212-573G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278524 | |||||||
| chr1:28278554 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1212-543G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278554 | |||||||
| chr1:28278785 | T | C | 2 | a0001c0001t0001g0056 a0001c0012t0001g0065 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1212-312T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278785 | |||||||
| chr1:28278808 | G | A | 90 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0024 others(87): Show |
115 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1212-289G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278808 | |||||||
| chr1:28278812 | T | C | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0186 |
3 | HG01891.hp1 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1212-285T>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278812 | |||||||
| chr1:28278824 | TGTAGA | T | 3 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0186 |
3 | HG01891.hp1 HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1212-268_1212-264d others(7): Show |
SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 28278824 | ||||||
| chr1:28278859 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0189 |
3 | HG00099.hp1 HG01192.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1212-238G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278859 | |||||||
| chr1:28278916 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1212-181A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28278916 | |||||||
| chr1:28279003 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1212-94C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28279003 | |||||||
| chr1:28279059 | G | A | 2 | a0001c0001t0003g0111 a0001c0001t0003g0112 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1212-38G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28279059 | |||||||
| chr1:28279081 | G | C | 1 | a0001c0001t0002g0164 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1212-16G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 8/9 | chr1 | 28279081 | |||||||
| chr1:28279376 | G | C | 1 | a0001c0012t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1356+135G>C | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28279376 | |||||||
| chr1:28279421 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1356+180A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28279421 | |||||||
| chr1:28279553 | G | GT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0050 others(4): Show |
10 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1356+323dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28279553 | ||||||
| chr1:28279832 | G | A | 1 | a0001c0001t0006g0166 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1356+591G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28279832 | |||||||
| chr1:28279861 | G | GT | 6 | a0001c0001t0001g0167 a0001c0001t0001g0188 a0001c0001t0001g0192 others(3): Show |
6 | HG01074.hp2 HG02630.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1356+630dupT | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28279861 | ||||||
| chr1:28279974 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1356+733C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28279974 | |||||||
| chr1:28280219 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0182 a0001c0001t0001g0202 |
5 | HG00438.hp2 HG02015.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1357-497G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280219 | |||||||
| chr1:28280233 | G | A | 1 | a0001c0012t0001g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1357-483G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280233 | |||||||
| chr1:28280276 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG00673.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1357-440A>G | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280276 | |||||||
| chr1:28280300 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1357-416G>A | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280300 | |||||||
| chr1:28280495 | C | T | 2 | a0004c0008t0001g0026 a0004c0008t0001g0069 |
3 | HG01891.hp2 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1357-221C>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280495 | |||||||
| chr1:28280593 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1357-123G>T | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | chr1 | 28280593 | |||||||
| chr1:28280665 | T | TG | 8 | a0001c0001t0001g0142 a0001c0001t0004g0044 a0001c0001t0004g0053 others(5): Show |
9 | HG02109.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1357-46dupG | SESN2 | ENSG00000130766.5 | transcript | ENST00000253063.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 28280665 |