Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55719 |
| ensemblid | ENSG00000119906.13 |
| hgncid | 17814 |
| symbol | SLF2 |
| name | SMC5-SMC6 complex localization factor 2 |
| refseq_nuc | NM_018121.4 |
| refseq_prot | NP_060591.3 |
| ensembl_nuc | ENST00000238961.9 |
| ensembl_prot | ENSP00000238961.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 100912963 |
| end | 100965134 |
| strand | + |
| ver | v1.2 |
| region | chr10:100912963-100965134 |
| region5000 | chr10:100907963-100970134 |
| regionname0 | SLF2_chr10_100912963_100965134 |
| regionname5000 | SLF2_chr10_100907963_100970134 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1173 | 248 | 69 | 37 | 114 | 7 | 19 | 88 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0002 | 0/0 | 1173 | 70 | 16 | 23 | 9 | 7 | 15 | 8 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0003 | 0/0 | 1173 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0004 | 0/0 | 1173 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0005 | 0/0 | 1173 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0006 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0007 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0008 | 0/0 | 1173 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0009 | 0/0 | 1173 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0010 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| a0011 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | MTRRC others(1168): Show |
chr10 | 100907963 | 100970134 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3519 | 240 | 62 | 37 | 113 | 7 | 19 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0001c0003 | 0/0 | 3519 | 4 | 4 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0001c0005 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0001c0012 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0001c0013 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0002c0002 | 0/0 | 3519 | 68 | 16 | 21 | 9 | 7 | 15 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0002c0004 | 0/0 | 3519 | 2 | 0 | 2 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0003c0006 | 0/0 | 3519 | 2 | 0 | 2 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0004c0007 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0005c0008 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0006c0014 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0007c0009 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0008c0016 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0009c0010 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0010c0015 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 | ||
| a0011c0011 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ATGAC others(3514): Show |
chr10 | 100907963 | 100970134 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6892 | 90 | 11 | 19 | 49 | 2 | 7 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0002 | 0/0 | 6892 | 93 | 29 | 9 | 45 | 3 | 7 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0003 | 0/0 | 6890 | 19 | 12 | 5 | 0 | 1 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0004 | 0/0 | 6892 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0005 | 0/0 | 6891 | 9 | 1 | 0 | 7 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6886): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0006 | 0/0 | 6891 | 9 | 2 | 0 | 7 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6886): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0007 | 0/0 | 6892 | 4 | 3 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0009 | 0/0 | 6892 | 2 | 0 | 0 | 0 | 0 | 2 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0010 | 0/0 | 6894 | 2 | 1 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6889): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0011 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0012 | 0/0 | 6892 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0013 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0014 | 0/0 | 6892 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0015 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0016 | 0/0 | 6890 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0017 | 0/0 | 6891 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6886): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0020 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0025 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0026 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0001t0027 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0003t0008 | 0/0 | 6892 | 4 | 4 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0005t0004 | 0/0 | 6892 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0012t0001 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0001c0013t0002 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0001 | 0/0 | 6892 | 40 | 7 | 16 | 7 | 2 | 8 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0003 | 0/0 | 6890 | 5 | 5 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0004 | 0/0 | 6892 | 12 | 0 | 2 | 1 | 3 | 6 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0005 | 0/0 | 6891 | 6 | 0 | 2 | 1 | 2 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6886): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0018 | 0/0 | 6891 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6886): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0019 | 0/0 | 6894 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6889): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0021 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0023 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0002c0002t0024 | 0/0 | 6890 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0002c0004t0001 | 0/0 | 6892 | 2 | 0 | 2 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0003c0006t0001 | 0/0 | 6892 | 2 | 0 | 2 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0004c0007t0003 | 0/0 | 6890 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0004c0007t0022 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0005c0008t0001 | 0/0 | 6892 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0006c0014t0002 | 0/0 | 6892 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0007c0009t0003 | 0/0 | 6890 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| a0008c0016t0001 | 0/0 | 6892 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0009c0010t0001 | 0/0 | 6892 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0010c0015t0001 | 0/0 | 6892 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6887): Show |
chr10 | 100907963 | 100970134 |
| a0011c0011t0003 | 0/0 | 6890 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | ACTTC others(6885): Show |
chr10 | 100907963 | 100970134 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0010g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0010g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0011g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0012g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0014g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0016g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0017g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0020g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0025g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0026g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0001t0027g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0003t0008g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0003t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0003t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0005t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0005t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0012t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0001c0013t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0001 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0006 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0005g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0018g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0019g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0021g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0023g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0002t0024g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0004t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0002c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0003c0006t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0003c0006t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0004c0007t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0004c0007t0022g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0005c0008t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0005c0008t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0006c0014t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0007c0009t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0008c0016t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0009c0010t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0010c0015t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| a0011c0011t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | GBR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0247 | EUR | GBR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00140 | hp2 | a0002 | c0002 | t0005 | g0268 | EUR | GBR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00280 | hp1 | a0002 | c0002 | t0004 | g0233 | EUR | FIN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00597 | hp1 | a0001 | c0013 | t0002 | g0076 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00621 | hp1 | a0002 | c0002 | t0004 | g0120 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0270 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0214 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00673 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00738 | hp1 | a0002 | c0002 | t0004 | g0238 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01069 | hp2 | a0002 | c0002 | t0018 | g0231 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01070 | hp1 | a0003 | c0006 | t0001 | g0137 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01071 | hp2 | a0003 | c0006 | t0001 | g0138 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0274 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01106 | hp2 | a0001 | c0001 | t0014 | g0091 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0219 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01169 | hp2 | a0002 | c0002 | t0005 | g0278 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0275 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01192 | hp1 | a0002 | c0002 | t0004 | g0006 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0095 | AMR | PUR | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01496 | hp2 | a0002 | c0004 | t0001 | g0008 | AMR | CLM | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01515 | hp1 | a0002 | c0002 | t0005 | g0007 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01515 | hp2 | a0002 | c0002 | t0004 | g0230 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0269 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0075 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0074 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | IBS | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01975 | hp2 | a0002 | c0002 | t0005 | g0284 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0256 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0285 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02015 | hp1 | a0006 | c0014 | t0002 | g0056 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02145 | hp1 | a0001 | c0005 | t0004 | g0212 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02280 | hp2 | a0004 | c0007 | t0022 | g0203 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02572 | hp1 | a0001 | c0003 | t0008 | g0002 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0271 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02615 | hp1 | a0002 | c0002 | t0019 | g0228 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0265 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0218 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0272 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02683 | hp2 | a0002 | c0002 | t0004 | g0234 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02717 | hp1 | a0004 | c0007 | t0003 | g0202 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02886 | hp1 | a0002 | c0002 | t0021 | g0229 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0204 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02970 | hp1 | a0002 | c0002 | t0024 | g0294 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02976 | hp1 | a0001 | c0003 | t0008 | g0002 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03041 | hp1 | a0001 | c0001 | t0026 | g0059 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03130 | hp2 | a0002 | c0002 | t0023 | g0008 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0124 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03209 | hp1 | a0001 | c0003 | t0008 | g0034 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0201 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0249 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03239 | hp2 | a0002 | c0002 | t0005 | g0001 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0223 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03453 | hp2 | a0001 | c0012 | t0001 | g0139 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0264 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03491 | hp1 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03492 | hp2 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03516 | hp2 | a0005 | c0008 | t0001 | g0225 | AFR | ESN | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03669 | hp2 | a0001 | c0001 | t0017 | g0151 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03831 | hp2 | a0002 | c0002 | t0004 | g0236 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0186 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0277 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04184 | hp2 | a0002 | c0002 | t0004 | g0237 | SAS | BEB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04199 | hp1 | a0008 | c0016 | t0001 | g0267 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0261 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04228 | hp1 | a0002 | c0002 | t0004 | g0232 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG04228 | hp2 | a0009 | c0010 | t0001 | g0052 | SAS | STU | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18522 | hp2 | a0010 | c0015 | t0001 | g0140 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18906 | hp1 | a0005 | c0008 | t0001 | g0226 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0123 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18960 | hp2 | a0001 | c0001 | t0025 | g0016 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0115 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18984 | hp1 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18999 | hp1 | a0001 | c0001 | t0027 | g0021 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19066 | hp1 | a0001 | c0001 | t0011 | g0047 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19068 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19074 | hp2 | a0002 | c0002 | t0005 | g0025 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19084 | hp2 | a0001 | c0001 | t0020 | g0171 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | YRI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | ASW | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20805 | hp1 | a0002 | c0002 | t0004 | g0235 | EUR | TSI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0125 | EUR | TSI | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0262 | SAS | GIH | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | GIH | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0216 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02486 | hp2 | a0001 | c0005 | t0004 | g0211 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG02559 | hp2 | a0007 | c0009 | t0003 | g0245 | AFR | ACB | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0281 | AFR | USA | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | USA | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20300 | hp1 | a0011 | c0011 | t0003 | g0250 | AFR | USA | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | USA | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| NA21309 | hp2 | a0001 | c0003 | t0008 | g0012 | AFR | LWK | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0130 | REF | REF | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0133 | REF | REF | SLF2_chr10_100907963_100970134 | SLF2 | chr10 | 100907963 | 100970134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:100916819 | A | G | 1 | a0005 | 2 | HG03516.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.434A>G | p.Lys145Arg | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/20 | 582/6892 | 434/3522 | 145/1173 | chr10 | 100916819 | |||
| chr10:100916830 | A | T | 1 | a0008 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.445A>T | p.Ile149Phe | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/20 | 593/6892 | 445/3522 | 149/1173 | chr10 | 100916830 | |||
| chr10:100916834 | A | G | 1 | a0004 | 2 | HG02280.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.449A>G | p.Tyr150Cys | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/20 | 597/6892 | 449/3522 | 150/1173 | chr10 | 100916834 | |||
| chr10:100917239 | C | T | 1 | a0003 | 2 | HG01070.hp1 HG01071.hp2 |
missense_variant | MODERATE | c.854C>T | p.Pro285Leu | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/20 | 1002/6892 | 854/3522 | 285/1173 | chr10 | 100917239 | |||
| chr10:100924176 | T | C | 1 | a0007 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1175T>C | p.Ile392Thr | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 1323/6892 | 1175/3522 | 392/1173 | chr10 | 100924176 | |||
| chr10:100924595 | G | C | 1 | a0009 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1594G>C | p.Asp532His | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 1742/6892 | 1594/3522 | 532/1173 | chr10 | 100924595 | |||
| chr10:100924623 | C | A | 2 | a0002 a0008 |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
missense_variant | MODERATE | c.1622C>A | p.Ser541Tyr | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 1770/6892 | 1622/3522 | 541/1173 | chr10 | 100924623 | |||
| chr10:100924901 | C | G | 1 | a0010 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1900C>G | p.Gln634Glu | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 2048/6892 | 1900/3522 | 634/1173 | chr10 | 100924901 | |||
| chr10:100924923 | A | T | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1922A>T | p.Lys641Met | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 2070/6892 | 1922/3522 | 641/1173 | chr10 | 100924923 | |||
| chr10:100924925 | C | A | 1 | a0011 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1924C>A | p.Pro642Thr | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 2072/6892 | 1924/3522 | 642/1173 | chr10 | 100924925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:100923994 | A | G | 1 | a0001c0003 | 4 | HG02572.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.993A>G | p.Lys331Lys | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/20 | 1141/6892 | 993/3522 | 331/1173 | chr10 | 100923994 | |||
| chr10:100929362 | C | T | 1 | a0001c0005 | 2 | HG02145.hp1 HG02486.hp2 |
synonymous_variant | LOW | c.2088C>T | p.Gly696Gly | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 7/20 | 2236/6892 | 2088/3522 | 696/1173 | chr10 | 100929362 | |||
| chr10:100938695 | C | G | 1 | a0001c0013 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.2613C>G | p.Pro871Pro | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/20 | 2761/6892 | 2613/3522 | 871/1173 | chr10 | 100938695 | |||
| chr10:100947769 | A | G | 1 | a0002c0004 | 2 | HG01175.hp2 HG01496.hp2 |
synonymous_variant | LOW | c.3042A>G | p.Arg1014Arg | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/20 | 3190/6892 | 3042/3522 | 1014/1173 | chr10 | 100947769 | |||
| chr10:100959485 | C | A | 1 | a0001c0012 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.3475C>A | p.Arg1159Arg | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/20 | 3623/6892 | 3475/3522 | 1159/1173 | chr10 | 100959485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:100913092 | C | T | 1 | a0001c0001t0027 | 1 | NA18999.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-19C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/20 | chr10 | 100913092 | |||||||
| chr10:100913101 | C | A | 1 | a0001c0001t0011 | 1 | NA19066.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/20 | 10 | chr10 | 100913101 | ||||||
| chr10:100961966 | C | T | 1 | a0001c0003t0008 | 4 | HG02572.hp1 HG02976.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*54C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 54 | chr10 | 100961966 | ||||||
| chr10:100961981 | A | C | 1 | a0001c0001t0026 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*69A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 69 | chr10 | 100961981 | ||||||
| chr10:100962283 | A | G | 1 | a0001c0001t0025 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 371 | chr10 | 100962283 | ||||||
| chr10:100962374 | C | T | 1 | a0002c0002t0024 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*462C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 462 | chr10 | 100962374 | ||||||
| chr10:100962446 | C | G | 1 | a0002c0002t0023 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 534 | chr10 | 100962446 | ||||||
| chr10:100962559 | T | C | 1 | a0001c0001t0012 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 647 | chr10 | 100962559 | ||||||
| chr10:100962671 | G | C | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(10): Show |
117 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*759G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 759 | chr10 | 100962671 | ||||||
| chr10:100962835 | C | A | 1 | a0001c0001t0016 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 923 | chr10 | 100962835 | ||||||
| chr10:100962841 | A | ATG | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(5): Show |
26 | HG00099.hp2 HG00609.hp1 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*956_*957dupTG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 958 | INFO_REALIGN_3_PRIME | chr10 | 100962841 | |||||
| chr10:100962841 | A | ATGTG | 3 | a0001c0001t0003 a0002c0002t0001 a0004c0007t0003 |
3 | HG02683.hp1 HG02717.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*954_*957dupTGTG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 958 | INFO_REALIGN_3_PRIME | chr10 | 100962841 | |||||
| chr10:100962841 | ATG | A | 3 | a0001c0001t0003 a0002c0002t0001 a0002c0002t0005 |
5 | HG00140.hp2 HG01081.hp1 HG01099.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*956_*957delTG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 956 | INFO_REALIGN_3_PRIME | chr10 | 100962841 | |||||
| chr10:100962853 | G | A | 1 | a0001c0001t0017 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*941G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 941 | chr10 | 100962853 | ||||||
| chr10:100962868 | T | C | 5 | a0001c0001t0004 a0001c0001t0007 a0001c0005t0004 others(2): Show |
20 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*956T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 956 | chr10 | 100962868 | ||||||
| chr10:100962868 | T | TGC | 2 | a0001c0001t0010 a0002c0002t0019 |
3 | HG01109.hp2 HG02615.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959_*960dupGC | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 961 | INFO_REALIGN_3_PRIME | chr10 | 100962868 | |||||
| chr10:100962892 | C | T | 6 | a0001c0001t0004 a0001c0001t0010 a0001c0005t0004 others(3): Show |
19 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*980C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 980 | chr10 | 100962892 | ||||||
| chr10:100963159 | G | C | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(11): Show |
116 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 1247 | chr10 | 100963159 | ||||||
| chr10:100963220 | A | G | 2 | a0002c0002t0021 a0004c0007t0022 |
2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1308A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 1308 | chr10 | 100963220 | ||||||
| chr10:100963633 | A | G | 1 | a0001c0001t0015 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 1721 | chr10 | 100963633 | ||||||
| chr10:100963700 | A | T | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1788A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 1788 | chr10 | 100963700 | ||||||
| chr10:100963929 | A | C | 1 | a0004c0007t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2017A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2017 | chr10 | 100963929 | ||||||
| chr10:100963990 | C | G | 1 | a0001c0001t0014 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2078 | chr10 | 100963990 | ||||||
| chr10:100964078 | A | G | 1 | a0001c0001t0013 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2166 | chr10 | 100964078 | ||||||
| chr10:100964588 | G | A | 1 | a0002c0002t0019 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2676G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2676 | chr10 | 100964588 | ||||||
| chr10:100964767 | T | A | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2855T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2855 | chr10 | 100964767 | ||||||
| chr10:100964770 | A | T | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2858A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2858 | chr10 | 100964770 | ||||||
| chr10:100964772 | T | A | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2860 | chr10 | 100964772 | ||||||
| chr10:100964882 | C | T | 1 | a0001c0001t0009 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2970C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 2970 | chr10 | 100964882 | ||||||
| chr10:100964968 | T | G | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3056T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3056 | chr10 | 100964968 | ||||||
| chr10:100964972 | C | A | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3060C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3060 | chr10 | 100964972 | ||||||
| chr10:100965032 | T | C | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3120T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3120 | chr10 | 100965032 | ||||||
| chr10:100965033 | C | T | 1 | a0001c0001t0020 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3121C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3121 | chr10 | 100965033 | ||||||
| chr10:100965038 | CT | C | 5 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0017 others(2): Show |
26 | HG00140.hp2 HG01069.hp2 HG01169.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3140delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3140 | INFO_REALIGN_3_PRIME | chr10 | 100965038 | |||||
| chr10:100965089 | ATG | A | 7 | a0001c0001t0003 a0001c0001t0016 a0002c0002t0003 others(4): Show |
29 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3192_*3193delTG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3192 | INFO_REALIGN_3_PRIME | chr10 | 100965089 | |||||
| chr10:100965104 | T | C | 7 | a0001c0001t0003 a0001c0001t0016 a0002c0002t0003 others(4): Show |
29 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3192T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 20/20 | 3192 | chr10 | 100965104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:100913306 | G | T | 47 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.140+56G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913306 | |||||||
| chr10:100913535 | G | A | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.140+285G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913535 | |||||||
| chr10:100913543 | C | A | 1 | a0002c0002t0004g0120 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140+293C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913543 | |||||||
| chr10:100913693 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.140+443G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913693 | |||||||
| chr10:100913844 | T | G | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.140+594T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913844 | |||||||
| chr10:100913950 | C | G | 49 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
56 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.140+700C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100913950 | |||||||
| chr10:100914077 | A | T | 1 | a0002c0002t0024g0294 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.140+827A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914077 | |||||||
| chr10:100914085 | C | T | 20 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(17): Show |
20 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.140+835C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914085 | |||||||
| chr10:100914311 | TG | T | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.140+1062delG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914311 | |||||||
| chr10:100914314 | T | G | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG01169.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.140+1064T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914314 | |||||||
| chr10:100914349 | AT | A | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.140+1103delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr10 | 100914349 | ||||||
| chr10:100914456 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.140+1206G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914456 | |||||||
| chr10:100914591 | A | G | 47 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.140+1341A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914591 | |||||||
| chr10:100914718 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.141-1281C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914718 | |||||||
| chr10:100914774 | C | T | 11 | a0002c0002t0004g0006 a0002c0002t0004g0120 a0002c0002t0004g0230 others(8): Show |
13 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.141-1225C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914774 | |||||||
| chr10:100914831 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.141-1168A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914831 | |||||||
| chr10:100914879 | T | A | 49 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
56 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.141-1120T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914879 | |||||||
| chr10:100914880 | C | A | 49 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
56 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.141-1119C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100914880 | |||||||
| chr10:100915122 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.141-877A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100915122 | |||||||
| chr10:100915392 | C | T | 300 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(297): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.141-607C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100915392 | |||||||
| chr10:100915598 | A | T | 1 | a0001c0001t0006g0117 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141-401A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100915598 | |||||||
| chr10:100915667 | T | C | 1 | a0002c0002t0001g0259 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.141-332T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100915667 | |||||||
| chr10:100915710 | C | A | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.141-289C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 1/19 | chr10 | 100915710 | |||||||
| chr10:100916399 | A | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG01169.hp1 HG01346.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.185-171A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 2/19 | chr10 | 100916399 | |||||||
| chr10:100916512 | ATAAATAT | A | 3 | a0001c0001t0002g0114 a0001c0001t0002g0116 a0001c0001t0006g0115 |
3 | NA18974.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.185-49_185-43delAA others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr10 | 100916512 | ||||||
| chr10:100917327 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.915+27A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917327 | |||||||
| chr10:100917384 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.915+84A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917384 | |||||||
| chr10:100917396 | C | T | 2 | a0005c0008t0001g0225 a0005c0008t0001g0226 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915+96C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917396 | |||||||
| chr10:100917430 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.915+130G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917430 | |||||||
| chr10:100917619 | C | T | 22 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(19): Show |
22 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.915+319C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917619 | |||||||
| chr10:100917638 | G | A | 1 | a0002c0002t0001g0260 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.915+338G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917638 | |||||||
| chr10:100917709 | C | T | 2 | a0005c0008t0001g0225 a0005c0008t0001g0226 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915+409C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917709 | |||||||
| chr10:100917777 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.915+477A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917777 | |||||||
| chr10:100917903 | G | A | 1 | a0002c0002t0019g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.916-481G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917903 | |||||||
| chr10:100917919 | C | CAAAT | 11 | a0002c0002t0004g0006 a0002c0002t0004g0120 a0002c0002t0004g0230 others(8): Show |
13 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.916-446_916-443dup others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr10 | 100917919 | ||||||
| chr10:100917919 | CAAAT | C | 3 | a0001c0001t0002g0112 a0002c0002t0001g0292 a0002c0002t0001g0293 |
3 | HG01952.hp2 HG02257.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.916-446_916-443del others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr10 | 100917919 | ||||||
| chr10:100917921 | A | T | 1 | a0001c0001t0002g0220 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.916-463A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100917921 | |||||||
| chr10:100918008 | G | T | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.916-376G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100918008 | |||||||
| chr10:100918170 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.916-214A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100918170 | |||||||
| chr10:100918318 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.916-66G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100918318 | |||||||
| chr10:100918377 | C | T | 5 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 others(2): Show |
5 | HG01109.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.916-7C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 3/19 | chr10 | 100918377 | |||||||
| chr10:100918455 | T | G | 2 | a0003c0006t0001g0137 a0003c0006t0001g0138 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.973+14T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100918455 | |||||||
| chr10:100918582 | G | T | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.973+141G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100918582 | |||||||
| chr10:100918591 | A | G | 2 | a0002c0002t0019g0228 a0002c0002t0021g0229 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.973+150A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100918591 | |||||||
| chr10:100918591 | A | T | 1 | a0002c0002t0001g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.973+150A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100918591 | |||||||
| chr10:100919001 | C | CT | 27 | a0001c0001t0001g0136 a0001c0001t0001g0205 a0001c0001t0001g0206 others(24): Show |
29 | HG00280.hp1 HG00621.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.973+589dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919001 | C | CTT | 88 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(85): Show |
97 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.973+588_973+589dup others(2): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919001 | C | CTTT | 23 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0002g0004 others(20): Show |
26 | HG00621.hp2 HG00735.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.973+587_973+589dup others(3): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919001 | CT | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG00738.hp2 HG01346.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.973+589delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919001 | CTTTTTTT others(7): Show |
C | 22 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(19): Show |
22 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.973+576_973+589del others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919001 | CTTTTTTT others(9): Show |
C | 49 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
56 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.973+574_973+589del others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919001 | ||||||
| chr10:100919159 | C | T | 3 | a0001c0001t0004g0214 a0004c0007t0003g0202 a0004c0007t0022g0203 |
3 | HG00639.hp2 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.973+718C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100919159 | |||||||
| chr10:100919331 | T | A | 212 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(209): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.973+890T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100919331 | |||||||
| chr10:100919512 | GA | G | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.973+1078delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100919512 | ||||||
| chr10:100919666 | C | T | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.973+1225C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100919666 | |||||||
| chr10:100919881 | T | A | 1 | a0001c0001t0002g0093 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.973+1440T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100919881 | |||||||
| chr10:100919950 | C | T | 2 | a0002c0002t0001g0289 a0002c0002t0001g0290 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.973+1509C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100919950 | |||||||
| chr10:100920215 | G | A | 2 | a0001c0001t0001g0146 a0001c0012t0001g0139 |
2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.973+1774G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920215 | |||||||
| chr10:100920402 | G | T | 1 | a0002c0002t0001g0288 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.973+1961G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920402 | |||||||
| chr10:100920554 | C | T | 2 | a0005c0008t0001g0225 a0005c0008t0001g0226 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.973+2113C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920554 | |||||||
| chr10:100920682 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.973+2241G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920682 | |||||||
| chr10:100920739 | C | T | 10 | a0001c0001t0004g0214 a0001c0001t0007g0215 a0001c0001t0007g0216 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.973+2298C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920739 | |||||||
| chr10:100920743 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0002g0110 a0001c0001t0014g0091 |
3 | HG01106.hp2 HG02273.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.973+2302A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100920743 | |||||||
| chr10:100921113 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.973+2672G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921113 | |||||||
| chr10:100921179 | C | A | 1 | a0002c0002t0019g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.973+2738C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921179 | |||||||
| chr10:100921525 | A | G | 3 | a0002c0002t0001g0259 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG01934.hp1 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.974-2450A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921525 | |||||||
| chr10:100921637 | A | G | 2 | a0005c0008t0001g0225 a0005c0008t0001g0226 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.974-2338A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921637 | |||||||
| chr10:100921802 | A | G | 3 | a0002c0002t0001g0283 a0002c0002t0001g0285 a0002c0002t0005g0284 |
3 | HG01975.hp2 HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.974-2173A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921802 | |||||||
| chr10:100921849 | A | G | 7 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(4): Show |
7 | HG01109.hp2 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-2126A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100921849 | |||||||
| chr10:100922105 | T | A | 212 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(209): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.974-1870T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922105 | |||||||
| chr10:100922193 | C | A | 1 | a0001c0012t0001g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.974-1782C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922193 | |||||||
| chr10:100922297 | A | G | 2 | a0001c0001t0002g0089 a0001c0001t0006g0090 |
2 | HG02055.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.974-1678A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922297 | |||||||
| chr10:100922400 | C | T | 5 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-1575C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922400 | |||||||
| chr10:100922629 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.974-1346T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922629 | |||||||
| chr10:100922776 | A | AT | 32 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0106 others(29): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.974-1182dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100922776 | ||||||
| chr10:100922776 | AT | A | 7 | a0001c0001t0001g0149 a0001c0001t0004g0214 a0002c0002t0001g0261 others(4): Show |
7 | HG00639.hp2 HG04199.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-1182delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr10 | 100922776 | ||||||
| chr10:100922802 | G | A | 2 | a0001c0005t0004g0211 a0001c0005t0004g0212 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.974-1173G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922802 | |||||||
| chr10:100922866 | C | T | 2 | a0002c0002t0001g0281 a0002c0002t0001g0282 |
2 | HG01081.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.974-1109C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100922866 | |||||||
| chr10:100923572 | C | T | 10 | a0001c0001t0004g0214 a0001c0001t0007g0215 a0001c0001t0007g0216 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.974-403C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100923572 | |||||||
| chr10:100923659 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.974-316A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 4/19 | chr10 | 100923659 | |||||||
| chr10:100925088 | G | A | 3 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1971+116G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/19 | chr10 | 100925088 | |||||||
| chr10:100925284 | A | C | 11 | a0002c0002t0004g0006 a0002c0002t0004g0120 a0002c0002t0004g0230 others(8): Show |
13 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1971+312A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/19 | chr10 | 100925284 | |||||||
| chr10:100925827 | G | A | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1972-122G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 5/19 | chr10 | 100925827 | |||||||
| chr10:100926187 | C | T | 7 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042+168C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926187 | |||||||
| chr10:100926215 | G | C | 3 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2042+196G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926215 | |||||||
| chr10:100926316 | A | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0074 a0001c0001t0002g0075 |
4 | HG01069.hp1 HG01071.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042+297A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926316 | |||||||
| chr10:100926460 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2042+441C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926460 | |||||||
| chr10:100926471 | C | A | 1 | a0001c0001t0002g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2042+452C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926471 | |||||||
| chr10:100926605 | CA | C | 8 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(5): Show |
8 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2042+599delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100926605 | ||||||
| chr10:100926834 | C | T | 63 | a0001c0001t0001g0128 a0002c0002t0001g0001 a0002c0002t0001g0007 others(60): Show |
72 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.2042+815C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926834 | |||||||
| chr10:100926842 | G | A | 41 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0121 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.2042+823G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926842 | |||||||
| chr10:100926866 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2042+847C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926866 | |||||||
| chr10:100926928 | A | G | 1 | a0002c0002t0001g0290 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2042+909A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100926928 | |||||||
| chr10:100927081 | GT | G | 47 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.2042+1069delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100927081 | ||||||
| chr10:100927124 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2042+1105A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927124 | |||||||
| chr10:100927144 | G | C | 67 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(64): Show |
76 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.2042+1125G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927144 | |||||||
| chr10:100927175 | C | T | 7 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042+1156C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927175 | |||||||
| chr10:100927286 | T | G | 5 | a0001c0001t0004g0214 a0001c0005t0004g0211 a0001c0005t0004g0212 others(2): Show |
5 | HG00639.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2042+1267T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927286 | |||||||
| chr10:100927311 | CTG | C | 62 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(59): Show |
71 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.2042+1296_2042+129 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100927311 | ||||||
| chr10:100927808 | TC | T | 5 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 others(2): Show |
5 | HG01109.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2043-1508delC | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927808 | |||||||
| chr10:100927918 | G | A | 5 | a0001c0001t0004g0214 a0001c0005t0004g0211 a0001c0005t0004g0212 others(2): Show |
5 | HG00639.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043-1399G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927918 | |||||||
| chr10:100927969 | A | G | 40 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0121 others(37): Show |
40 | HG00099.hp2 HG00639.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.2043-1348A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100927969 | |||||||
| chr10:100928031 | A | AC | 19 | a0001c0001t0001g0072 a0001c0001t0001g0134 a0001c0001t0001g0147 others(16): Show |
19 | HG00140.hp1 HG00408.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.2043-1271dupC | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928031 | ||||||
| chr10:100928031 | AC | A | 43 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0154 others(40): Show |
44 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2043-1271delC | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928031 | ||||||
| chr10:100928037 | C | A | 1 | a0002c0002t0001g0283 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2043-1280C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928037 | |||||||
| chr10:100928039 | C | A | 2 | a0001c0001t0002g0114 a0002c0002t0001g0283 |
2 | HG01978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2043-1278C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928039 | |||||||
| chr10:100928041 | C | A | 4 | a0001c0001t0001g0213 a0001c0001t0002g0114 a0001c0001t0002g0116 others(1): Show |
4 | HG00597.hp2 HG01978.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043-1276C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928041 | |||||||
| chr10:100928041 | C | CA | 5 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0002g0094 others(2): Show |
5 | HG03209.hp1 HG03654.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043-1276_2043-127 others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928041 | |||||||
| chr10:100928043 | C | A | 62 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0092 others(59): Show |
65 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2043-1274C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928043 | |||||||
| chr10:100928043 | C | CA | 16 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0193 others(13): Show |
16 | HG01975.hp2 HG02004.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.2043-1274_2043-127 others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928043 | |||||||
| chr10:100928045 | C | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(162): Show |
177 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.2043-1272C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928045 | |||||||
| chr10:100928045 | C | CA | 39 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0107 others(36): Show |
40 | HG00408.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.2043-1272_2043-127 others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928045 | |||||||
| chr10:100928046 | CACA | C | 6 | a0001c0001t0003g0249 a0001c0001t0003g0251 a0001c0001t0003g0252 others(3): Show |
6 | HG01258.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043-1270_2043-126 others(7): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928046 | |||||||
| chr10:100928047 | A | C | 14 | a0001c0001t0001g0167 a0001c0001t0003g0244 a0001c0001t0003g0246 others(11): Show |
14 | HG00099.hp2 HG00639.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.2043-1270A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928047 | |||||||
| chr10:100928049 | A | C | 3 | a0001c0001t0003g0255 a0001c0001t0003g0256 a0002c0002t0005g0278 |
3 | HG01169.hp2 HG01978.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2043-1268A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928049 | |||||||
| chr10:100928051 | A | C | 6 | a0001c0001t0003g0249 a0001c0001t0003g0251 a0001c0001t0003g0252 others(3): Show |
6 | HG01258.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043-1266A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928051 | |||||||
| chr10:100928053 | A | C | 2 | a0001c0001t0003g0253 a0001c0001t0003g0254 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2043-1264A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928053 | |||||||
| chr10:100928064 | C | G | 1 | a0001c0001t0003g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2043-1253C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928064 | |||||||
| chr10:100928065 | A | G | 6 | a0001c0001t0003g0244 a0001c0001t0003g0246 a0001c0001t0003g0247 others(3): Show |
6 | HG00099.hp2 HG01109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2043-1252A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928065 | |||||||
| chr10:100928066 | C | A | 6 | a0001c0001t0003g0244 a0001c0001t0003g0246 a0001c0001t0003g0247 others(3): Show |
6 | HG00099.hp2 HG01109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2043-1251C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928066 | |||||||
| chr10:100928066 | C | G | 1 | a0001c0001t0003g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2043-1251C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928066 | |||||||
| chr10:100928067 | A | G | 9 | a0001c0001t0003g0244 a0001c0001t0003g0246 a0001c0001t0003g0247 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043-1250A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928067 | |||||||
| chr10:100928068 | C | A | 9 | a0001c0001t0003g0244 a0001c0001t0003g0246 a0001c0001t0003g0247 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043-1249C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928068 | |||||||
| chr10:100928069 | G | A | 66 | a0001c0001t0002g0145 a0001c0001t0006g0204 a0002c0002t0001g0001 others(63): Show |
75 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2043-1248G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928069 | |||||||
| chr10:100928070 | A | C | 8 | a0001c0001t0002g0145 a0001c0001t0006g0204 a0002c0002t0001g0260 others(5): Show |
8 | HG01175.hp2 HG01261.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2043-1247A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928070 | |||||||
| chr10:100928071 | G | A | 6 | a0002c0002t0001g0260 a0002c0002t0001g0263 a0002c0002t0001g0276 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043-1246G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928071 | |||||||
| chr10:100928073 | G | C | 1 | a0001c0001t0003g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2043-1244G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928073 | |||||||
| chr10:100928073 | G | GAC | 4 | a0001c0001t0003g0244 a0001c0001t0003g0246 a0001c0001t0003g0258 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043-1243_2043-124 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928073 | ||||||
| chr10:100928073 | GAGAGAC | G | 6 | a0002c0002t0001g0260 a0002c0002t0001g0263 a0002c0002t0001g0276 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043-1238_2043-123 others(10): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928073 | ||||||
| chr10:100928079 | C | CAGAG | 7 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0003g0224 others(4): Show |
7 | HG02109.hp2 HG02647.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043-1216_2043-121 others(8): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928079 | C | CAGAGAG | 11 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(8): Show |
11 | HG01081.hp1 HG01109.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2043-1218_2043-121 others(10): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928079 | C | CAGAGAGA others(3): Show |
2 | a0001c0005t0004g0211 a0001c0005t0004g0212 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2043-1222_2043-121 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928079 | C | CAGAGAGA others(9): Show |
2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2043-1228_2043-121 others(20): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928079 | C | G | 12 | a0001c0001t0002g0145 a0001c0001t0003g0244 a0001c0001t0003g0246 others(9): Show |
12 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2043-1238C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928079 | |||||||
| chr10:100928079 | CAG | C | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0220 |
3 | HG02922.hp1 HG02965.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2043-1214_2043-121 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928079 | CAGAGAGA others(1): Show |
C | 58 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(55): Show |
67 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2043-1220_2043-121 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928079 | ||||||
| chr10:100928081 | G | C | 2 | a0001c0001t0002g0145 a0001c0001t0006g0204 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2043-1236G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928081 | |||||||
| chr10:100928087 | G | C | 6 | a0002c0002t0001g0260 a0002c0002t0001g0263 a0002c0002t0001g0276 others(3): Show |
6 | HG01175.hp2 HG01261.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.2043-1230G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928087 | |||||||
| chr10:100928120 | AATG | A | 5 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 others(2): Show |
5 | HG01109.hp2 HG02109.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2043-1194_2043-119 others(7): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr10 | 100928120 | ||||||
| chr10:100928168 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2043-1149A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928168 | |||||||
| chr10:100928335 | A | G | 4 | a0002c0002t0001g0269 a0002c0002t0001g0274 a0002c0002t0005g0268 others(1): Show |
4 | HG00140.hp2 HG01099.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043-982A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928335 | |||||||
| chr10:100928399 | T | G | 2 | a0001c0001t0002g0078 a0001c0001t0002g0105 |
2 | NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2043-918T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928399 | |||||||
| chr10:100928605 | A | G | 31 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0084 others(28): Show |
33 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2043-712A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928605 | |||||||
| chr10:100928658 | T | C | 64 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(61): Show |
73 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2043-659T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928658 | |||||||
| chr10:100928684 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2043-633A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928684 | |||||||
| chr10:100928744 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2043-573C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928744 | |||||||
| chr10:100928760 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2043-557A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928760 | |||||||
| chr10:100928834 | C | T | 1 | a0001c0001t0005g0196 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2043-483C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928834 | |||||||
| chr10:100928859 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2043-458T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928859 | |||||||
| chr10:100928880 | C | T | 1 | a0001c0001t0010g0219 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2043-437C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100928880 | |||||||
| chr10:100929276 | T | C | 1 | a0002c0002t0004g0236 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2043-41T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 6/19 | chr10 | 100929276 | |||||||
| chr10:100929460 | T | C | 49 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
56 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.2165+21T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 7/19 | chr10 | 100929460 | |||||||
| chr10:100929747 | G | A | 64 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(61): Show |
73 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2166-83G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 7/19 | chr10 | 100929747 | |||||||
| chr10:100930017 | T | C | 1 | a0001c0001t0005g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2333+20T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930017 | |||||||
| chr10:100930123 | T | C | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2333+126T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930123 | |||||||
| chr10:100930365 | G | A | 11 | a0002c0002t0004g0006 a0002c0002t0004g0120 a0002c0002t0004g0230 others(8): Show |
13 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.2333+368G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930365 | |||||||
| chr10:100930559 | G | A | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2334-417G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930559 | |||||||
| chr10:100930726 | A | G | 1 | a0002c0002t0001g0260 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2334-250A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930726 | |||||||
| chr10:100930752 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2334-224T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930752 | |||||||
| chr10:100930857 | A | G | 1 | a0001c0001t0016g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2334-119A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 8/19 | chr10 | 100930857 | |||||||
| chr10:100931352 | T | G | 1 | a0001c0001t0002g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2436+274T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100931352 | |||||||
| chr10:100931460 | A | G | 1 | a0001c0012t0001g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2436+382A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100931460 | |||||||
| chr10:100931467 | GT | G | 12 | a0001c0001t0001g0019 a0001c0001t0001g0141 a0001c0001t0001g0154 others(9): Show |
13 | HG00733.hp2 HG00738.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2436+399delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100931467 | ||||||
| chr10:100931655 | T | G | 71 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(68): Show |
80 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2436+577T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100931655 | |||||||
| chr10:100931991 | CA | C | 65 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(62): Show |
74 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2436+925delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100931991 | ||||||
| chr10:100932257 | TA | T | 67 | a0001c0001t0001g0161 a0002c0002t0001g0001 a0002c0002t0001g0007 others(64): Show |
76 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.2436+1192delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932257 | ||||||
| chr10:100932564 | G | A | 1 | a0002c0002t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2436+1486G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932564 | |||||||
| chr10:100932692 | AGT | A | 27 | a0001c0001t0001g0129 a0001c0001t0001g0135 a0001c0001t0001g0136 others(24): Show |
27 | HG00738.hp2 HG01081.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.2436+1642_2436+164 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932692 | AGTGT | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(48): Show |
54 | HG00099.hp2 HG00733.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.2436+1640_2436+164 others(8): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932692 | AGTGTGT | A | 16 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0002g0035 others(13): Show |
16 | HG00673.hp2 HG01192.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2436+1638_2436+164 others(10): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932692 | AGTGTGTG others(1): Show |
A | 7 | a0001c0001t0002g0026 a0001c0001t0002g0042 a0001c0001t0002g0043 others(4): Show |
7 | HG00639.hp2 HG02109.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2436+1636_2436+164 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932692 | AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0007g0215 a0001c0005t0004g0212 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2436+1634_2436+164 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932692 | AGTGTGTG others(5): Show |
A | 1 | a0001c0005t0004g0211 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2436+1632_2436+164 others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932692 | ||||||
| chr10:100932708 | TGTGTGTG others(7): Show |
T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2436+1632_2436+164 others(18): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932708 | ||||||
| chr10:100932710 | TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0007g0216 a0001c0001t0007g0217 |
2 | HG02109.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2436+1634_2436+164 others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932710 | ||||||
| chr10:100932710 | TGTGTGTG others(7): Show |
T | 2 | a0001c0001t0010g0218 a0001c0001t0010g0219 |
2 | HG01109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2436+1634_2436+164 others(18): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932710 | ||||||
| chr10:100932712 | TGTGTGTG others(3): Show |
T | 10 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0037 others(7): Show |
12 | HG00609.hp2 HG00673.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2436+1636_2436+164 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932712 | ||||||
| chr10:100932712 | TGTGTGTG others(5): Show |
T | 38 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(35): Show |
44 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.2436+1636_2436+164 others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932712 | ||||||
| chr10:100932712 | TGTGTGTG others(7): Show |
T | 1 | a0004c0007t0003g0202 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2436+1636_2436+164 others(18): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932712 | ||||||
| chr10:100932714 | T | C | 2 | a0001c0001t0001g0221 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2436+1636T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932714 | |||||||
| chr10:100932714 | TGTGTGTG others(1): Show |
T | 74 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(71): Show |
81 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2436+1638_2436+164 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932714 | ||||||
| chr10:100932714 | TGTGTGTG others(3): Show |
T | 8 | a0002c0002t0001g0025 a0002c0002t0001g0259 a0002c0002t0001g0261 others(5): Show |
8 | HG01099.hp1 HG01934.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.2436+1638_2436+164 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932714 | ||||||
| chr10:100932716 | T | C | 2 | a0001c0001t0001g0221 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2436+1638T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932716 | |||||||
| chr10:100932716 | TGTGTGC | T | 12 | a0001c0001t0001g0113 a0001c0001t0002g0011 a0001c0001t0002g0046 others(9): Show |
14 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.2436+1640_2436+164 others(10): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932716 | ||||||
| chr10:100932716 | TGTGTGCG others(1): Show |
T | 4 | a0001c0001t0002g0109 a0002c0002t0001g0001 a0002c0002t0001g0266 others(1): Show |
4 | HG01981.hp2 NA18952.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.2436+1640_2436+164 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932716 | ||||||
| chr10:100932718 | T | C | 11 | a0001c0001t0001g0128 a0001c0001t0001g0181 a0001c0001t0001g0188 others(8): Show |
11 | HG00408.hp1 HG01099.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2436+1640T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932718 | |||||||
| chr10:100932720 | T | C | 45 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(42): Show |
46 | HG00408.hp1 HG00544.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.2436+1642T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932720 | |||||||
| chr10:100932720 | T | TGC | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0194 |
3 | HG01433.hp2 HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2436+1659_2436+166 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932720 | ||||||
| chr10:100932720 | T | TGTGTGCG others(1): Show |
3 | a0002c0002t0004g0006 a0002c0002t0004g0232 a0002c0002t0004g0233 |
4 | HG00280.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2436+1643_2436+164 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932720 | ||||||
| chr10:100932720 | T | TGTGTGTG others(3): Show |
1 | a0002c0002t0004g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2436+1643_2436+164 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932720 | ||||||
| chr10:100932720 | T | TGTGTGTG others(5): Show |
1 | a0002c0002t0004g0235 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2436+1643_2436+164 others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932720 | ||||||
| chr10:100932722 | C | T | 1 | a0001c0001t0005g0023 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2436+1644C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932722 | |||||||
| chr10:100932725 | G | A | 1 | a0002c0002t0004g0232 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2436+1647G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932725 | |||||||
| chr10:100932726 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2436+1648C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932726 | |||||||
| chr10:100932727 | G | A | 1 | a0002c0002t0004g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2436+1649G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932727 | |||||||
| chr10:100932728 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2436+1650C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932728 | |||||||
| chr10:100932729 | G | A | 2 | a0001c0001t0001g0142 a0002c0002t0019g0228 |
2 | HG02615.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2436+1651G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932729 | |||||||
| chr10:100932730 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2436+1652C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932730 | |||||||
| chr10:100932731 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2436+1653G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932731 | |||||||
| chr10:100932734 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2436+1656C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932734 | |||||||
| chr10:100932736 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2436+1658C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932736 | |||||||
| chr10:100932737 | G | T | 5 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2436+1659G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932737 | |||||||
| chr10:100932847 | T | C | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2436+1769T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932847 | |||||||
| chr10:100932873 | AG | A | 51 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
58 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2436+1797delG | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100932873 | ||||||
| chr10:100932886 | G | A | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2436+1808G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100932886 | |||||||
| chr10:100933146 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2436+2068C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933146 | |||||||
| chr10:100933213 | A | G | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2436+2135A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933213 | |||||||
| chr10:100933357 | C | G | 3 | a0001c0001t0001g0210 a0001c0001t0005g0178 a0001c0001t0005g0196 |
3 | NA18959.hp1 NA19000.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2436+2279C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933357 | |||||||
| chr10:100933457 | C | G | 2 | a0001c0001t0007g0215 a0001c0001t0007g0217 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2436+2379C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933457 | |||||||
| chr10:100933841 | G | A | 1 | a0001c0001t0009g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2436+2763G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933841 | |||||||
| chr10:100933940 | A | G | 1 | a0001c0001t0002g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2436+2862A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933940 | |||||||
| chr10:100933959 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2436+2881G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100933959 | |||||||
| chr10:100934057 | G | A | 1 | a0001c0001t0016g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2436+2979G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934057 | |||||||
| chr10:100934311 | T | G | 1 | a0001c0001t0002g0046 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2437-3091T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934311 | |||||||
| chr10:100934514 | A | C | 2 | a0001c0001t0002g0044 a0001c0001t0002g0065 |
2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2437-2888A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934514 | |||||||
| chr10:100934674 | A | G | 212 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(209): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2437-2728A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934674 | |||||||
| chr10:100934792 | T | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2437-2610T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934792 | |||||||
| chr10:100934874 | G | A | 1 | a0001c0001t0011g0047 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2437-2528G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934874 | |||||||
| chr10:100934967 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2437-2435A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100934967 | |||||||
| chr10:100935055 | A | T | 1 | a0001c0001t0006g0087 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2437-2347A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935055 | |||||||
| chr10:100935109 | T | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2437-2293T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935109 | |||||||
| chr10:100935209 | C | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2437-2193C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935209 | |||||||
| chr10:100935213 | G | A | 3 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2437-2189G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935213 | |||||||
| chr10:100935334 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2437-2068G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935334 | |||||||
| chr10:100935436 | T | C | 212 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(209): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2437-1966T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935436 | |||||||
| chr10:100935448 | C | T | 1 | a0001c0001t0005g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2437-1954C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935448 | |||||||
| chr10:100935578 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2437-1824G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935578 | |||||||
| chr10:100935607 | G | A | 5 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(2): Show |
5 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2437-1795G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935607 | |||||||
| chr10:100935829 | GTT | G | 5 | a0001c0001t0003g0246 a0001c0001t0003g0249 a0001c0001t0003g0255 others(2): Show |
5 | HG02486.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2437-1570_2437-156 others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100935829 | ||||||
| chr10:100935846 | T | G | 71 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0001c0001t0002g0145 others(68): Show |
80 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2437-1556T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935846 | |||||||
| chr10:100935859 | C | CT | 6 | a0001c0001t0001g0023 a0001c0001t0001g0163 a0001c0001t0001g0169 others(3): Show |
6 | HG01109.hp1 HG01261.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.2437-1526dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100935859 | ||||||
| chr10:100935859 | CTTT | C | 57 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(54): Show |
66 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.2437-1528_2437-152 others(7): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100935859 | ||||||
| chr10:100935859 | CTTTTTTT | C | 7 | a0001c0001t0004g0214 a0001c0001t0007g0215 a0001c0001t0007g0216 others(4): Show |
7 | HG00639.hp2 HG01109.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2437-1532_2437-152 others(11): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100935859 | ||||||
| chr10:100935860 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2437-1542T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935860 | |||||||
| chr10:100935861 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2437-1541T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935861 | |||||||
| chr10:100935862 | T | C | 5 | a0002c0002t0001g0274 a0002c0002t0004g0236 a0002c0002t0019g0228 others(2): Show |
5 | HG01099.hp1 HG02615.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2437-1540T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935862 | |||||||
| chr10:100935866 | T | C | 1 | a0001c0005t0004g0211 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2437-1536T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100935866 | |||||||
| chr10:100936152 | C | T | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2437-1250C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936152 | |||||||
| chr10:100936166 | G | C | 7 | a0001c0001t0002g0042 a0001c0001t0002g0048 a0001c0001t0002g0049 others(4): Show |
7 | NA18994.hp2 NA19000.hp2 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.2437-1236G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936166 | |||||||
| chr10:100936187 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2437-1215C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936187 | |||||||
| chr10:100936303 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2437-1099A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936303 | |||||||
| chr10:100936317 | TTTTTG | T | 175 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(172): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2437-1054_2437-105 others(9): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936317 | ||||||
| chr10:100936317 | TTTTTGTT others(3): Show |
T | 1 | a0001c0005t0004g0211 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2437-1059_2437-105 others(14): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936317 | ||||||
| chr10:100936317 | TTTTTGTT others(8): Show |
T | 1 | a0001c0001t0002g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2437-1064_2437-105 others(19): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936317 | ||||||
| chr10:100936508 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2437-894T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936508 | |||||||
| chr10:100936551 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2437-851G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936551 | |||||||
| chr10:100936624 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0098 others(1): Show |
5 | HG00558.hp2 HG00609.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2437-778G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936624 | |||||||
| chr10:100936865 | T | TA | 6 | a0001c0001t0001g0169 a0001c0001t0001g0190 a0001c0001t0001g0200 others(3): Show |
6 | HG02647.hp2 HG02723.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2437-524dupA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936865 | ||||||
| chr10:100936865 | TA | T | 7 | a0001c0001t0001g0072 a0001c0001t0001g0149 a0001c0001t0001g0160 others(4): Show |
7 | HG01516.hp2 HG01517.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2437-524delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936865 | ||||||
| chr10:100936865 | TAA | T | 64 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(61): Show |
73 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2437-525_2437-524d others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr10 | 100936865 | ||||||
| chr10:100936945 | A | G | 1 | a0002c0002t0001g0273 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2437-457A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 9/19 | chr10 | 100936945 | |||||||
| chr10:100937618 | G | GT | 8 | a0001c0001t0001g0127 a0001c0001t0001g0206 a0001c0001t0002g0050 others(5): Show |
8 | HG01361.hp1 HG02886.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.2512+151dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 100937618 | ||||||
| chr10:100937619 | T | G | 22 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(19): Show |
22 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2512+142T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100937619 | |||||||
| chr10:100937651 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2512+174C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100937651 | |||||||
| chr10:100937843 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2512+366C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100937843 | |||||||
| chr10:100937844 | G | A | 1 | a0001c0001t0003g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2512+367G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100937844 | |||||||
| chr10:100938137 | G | A | 1 | a0002c0002t0004g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2513-458G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100938137 | |||||||
| chr10:100938309 | A | AT | 12 | a0002c0002t0001g0272 a0002c0002t0004g0006 a0002c0002t0004g0120 others(9): Show |
14 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.2513-282dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr10 | 100938309 | ||||||
| chr10:100938316 | C | T | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2513-279C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100938316 | |||||||
| chr10:100938524 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2513-71A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 10/19 | chr10 | 100938524 | |||||||
| chr10:100938802 | T | G | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2654+66T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100938802 | |||||||
| chr10:100938872 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2654+136A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100938872 | |||||||
| chr10:100939275 | T | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(51): Show |
58 | HG00408.hp1 HG00673.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.2654+539T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100939275 | |||||||
| chr10:100939348 | A | C | 1 | a0001c0001t0002g0116 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2654+612A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100939348 | |||||||
| chr10:100939603 | G | A | 22 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(19): Show |
22 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2654+867G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100939603 | |||||||
| chr10:100939788 | A | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0220 a0001c0001t0006g0204 |
3 | HG02895.hp2 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2654+1052A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100939788 | |||||||
| chr10:100940372 | T | G | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2654+1636T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100940372 | |||||||
| chr10:100940511 | C | G | 3 | a0001c0001t0007g0215 a0001c0001t0007g0216 a0001c0001t0007g0217 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2654+1775C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100940511 | |||||||
| chr10:100940722 | TCCTTCCC others(2): Show |
T | 109 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(106): Show |
121 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.2654+2003_2654+201 others(13): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940722 | ||||||
| chr10:100940754 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0143 |
3 | NA18941.hp1 NA19010.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.2654+2018C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100940754 | |||||||
| chr10:100940820 | C | CTCCT | 3 | a0001c0001t0001g0187 a0001c0001t0007g0186 a0002c0002t0001g0291 |
3 | HG03834.hp1 NA18980.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.2654+2112_2654+211 others(8): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(1): Show |
43 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(40): Show |
48 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2654+2108_2654+211 others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(5): Show |
5 | a0002c0002t0001g0009 a0002c0002t0001g0269 a0002c0002t0001g0277 others(2): Show |
7 | HG01256.hp2 HG01258.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2654+2104_2654+211 others(16): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(9): Show |
2 | a0002c0002t0001g0123 a0002c0002t0021g0229 |
2 | HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2654+2100_2654+211 others(20): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(13): Show |
1 | a0002c0002t0019g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2654+2096_2654+211 others(24): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(17): Show |
10 | a0002c0002t0001g0124 a0002c0002t0004g0006 a0002c0002t0004g0120 others(7): Show |
12 | HG00280.hp1 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2654+2092_2654+211 others(28): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940820 | C | CTCCTTCC others(21): Show |
2 | a0002c0002t0004g0232 a0002c0002t0004g0237 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2654+2088_2654+211 others(32): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr10 | 100940820 | ||||||
| chr10:100940920 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2654+2184C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100940920 | |||||||
| chr10:100940986 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2654+2250G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100940986 | |||||||
| chr10:100941427 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2655-2599C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100941427 | |||||||
| chr10:100941655 | G | A | 22 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(19): Show |
22 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2655-2371G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100941655 | |||||||
| chr10:100942053 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2655-1973C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942053 | |||||||
| chr10:100942178 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2655-1848G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942178 | |||||||
| chr10:100942438 | A | G | 1 | a0001c0001t0016g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2655-1588A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942438 | |||||||
| chr10:100942601 | C | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0144 |
2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2655-1425C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942601 | |||||||
| chr10:100942667 | C | T | 1 | a0001c0001t0006g0117 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2655-1359C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942667 | |||||||
| chr10:100942738 | C | T | 64 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(61): Show |
73 | HG00140.hp2 HG00280.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2655-1288C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942738 | |||||||
| chr10:100942798 | C | T | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2655-1228C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942798 | |||||||
| chr10:100942871 | C | T | 13 | a0001c0001t0002g0014 a0001c0001t0002g0026 a0001c0001t0002g0031 others(10): Show |
14 | HG02109.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.2655-1155C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100942871 | |||||||
| chr10:100943028 | T | A | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2655-998T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943028 | |||||||
| chr10:100943246 | T | C | 2 | a0002c0002t0001g0263 a0002c0002t0001g0291 |
2 | NA18984.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2655-780T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943246 | |||||||
| chr10:100943376 | G | T | 51 | a0002c0002t0001g0001 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
58 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.2655-650G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943376 | |||||||
| chr10:100943419 | C | T | 2 | a0002c0002t0004g0232 a0002c0002t0004g0237 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2655-607C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943419 | |||||||
| chr10:100943526 | C | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(51): Show |
58 | HG00408.hp1 HG00673.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.2655-500C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943526 | |||||||
| chr10:100943677 | T | C | 110 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(107): Show |
122 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.2655-349T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943677 | |||||||
| chr10:100943799 | T | G | 1 | a0001c0001t0004g0214 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2655-227T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943799 | |||||||
| chr10:100943824 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2655-202A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100943824 | |||||||
| chr10:100944006 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2655-20C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 11/19 | chr10 | 100944006 | |||||||
| chr10:100944217 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2757+89C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944217 | |||||||
| chr10:100944221 | C | T | 197 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2757+93C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944221 | |||||||
| chr10:100944224 | G | A | 196 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(193): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2757+96G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944224 | |||||||
| chr10:100944288 | G | A | 186 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(183): Show |
204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2757+160G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944288 | |||||||
| chr10:100944291 | C | T | 1 | a0002c0002t0019g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2757+163C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944291 | |||||||
| chr10:100944319 | A | C | 14 | a0001c0001t0002g0061 a0001c0001t0003g0241 a0001c0001t0003g0244 others(11): Show |
14 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2757+191A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944319 | |||||||
| chr10:100944339 | C | CA | 6 | a0001c0001t0003g0246 a0001c0001t0003g0249 a0001c0001t0003g0253 others(3): Show |
6 | HG02486.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2757+217dupA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr10 | 100944339 | ||||||
| chr10:100944352 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+224A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944352 | |||||||
| chr10:100944356 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+228A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944356 | |||||||
| chr10:100944358 | G | A | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+230G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944358 | |||||||
| chr10:100944360 | C | T | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+232C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944360 | |||||||
| chr10:100944361 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+233A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944361 | |||||||
| chr10:100944367 | T | C | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+239T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944367 | |||||||
| chr10:100944368 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+240A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944368 | |||||||
| chr10:100944385 | T | C | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+257T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944385 | |||||||
| chr10:100944387 | C | T | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+259C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944387 | |||||||
| chr10:100944388 | A | G | 2 | a0004c0007t0003g0202 a0004c0007t0022g0203 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2757+260A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944388 | |||||||
| chr10:100944444 | G | A | 2 | a0001c0001t0002g0116 a0001c0001t0003g0244 |
2 | HG02723.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2757+316G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944444 | |||||||
| chr10:100944494 | C | CA | 147 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0083 others(144): Show |
165 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.2757+386dupA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr10 | 100944494 | ||||||
| chr10:100944494 | C | CAA | 19 | a0001c0001t0002g0038 a0001c0001t0002g0085 a0001c0001t0002g0088 others(16): Show |
19 | HG00735.hp1 HG01106.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.2757+385_2757+386d others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr10 | 100944494 | ||||||
| chr10:100944677 | T | C | 1 | a0002c0002t0005g0278 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2757+549T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944677 | |||||||
| chr10:100944740 | A | G | 1 | a0001c0001t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2758-590A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944740 | |||||||
| chr10:100944954 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2758-376C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944954 | |||||||
| chr10:100944957 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2758-373G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100944957 | |||||||
| chr10:100945103 | A | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2758-227A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | chr10 | 100945103 | |||||||
| chr10:100945301 | A | AT | 106 | a0001c0001t0001g0149 a0001c0001t0002g0002 a0001c0001t0002g0003 others(103): Show |
118 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.2758-24dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr10 | 100945301 | ||||||
| chr10:100945944 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2934+438G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100945944 | |||||||
| chr10:100945948 | G | T | 1 | a0001c0001t0009g0010 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2934+442G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100945948 | |||||||
| chr10:100946087 | T | C | 1 | a0001c0001t0012g0095 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2934+581T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946087 | |||||||
| chr10:100946156 | A | G | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2934+650A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946156 | |||||||
| chr10:100946159 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2934+653A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946159 | |||||||
| chr10:100946167 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0005g0201 a0010c0015t0001g0140 |
3 | HG02723.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2934+661C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946167 | |||||||
| chr10:100946191 | T | A | 2 | a0002c0002t0001g0025 a0002c0002t0005g0025 |
2 | NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2934+685T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946191 | |||||||
| chr10:100946325 | C | CT | 27 | a0001c0001t0001g0128 a0001c0001t0001g0210 a0001c0001t0001g0221 others(24): Show |
29 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.2935-696dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr10 | 100946325 | ||||||
| chr10:100946519 | G | T | 1 | a0002c0002t0001g0288 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2935-520G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946519 | |||||||
| chr10:100946841 | A | G | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(48): Show |
57 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.2935-198A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 13/19 | chr10 | 100946841 | |||||||
| chr10:100948041 | C | T | 2 | a0002c0002t0001g0269 a0002c0002t0005g0268 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3120+194C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948041 | |||||||
| chr10:100948357 | C | G | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3120+510C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948357 | |||||||
| chr10:100948391 | G | A | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(48): Show |
57 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3120+544G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948391 | |||||||
| chr10:100948394 | G | A | 7 | a0002c0002t0004g0006 a0002c0002t0004g0230 a0002c0002t0004g0233 others(4): Show |
9 | HG00280.hp1 HG00738.hp1 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.3120+547G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948394 | |||||||
| chr10:100948491 | A | T | 18 | a0001c0001t0004g0214 a0001c0001t0010g0218 a0001c0001t0010g0219 others(15): Show |
20 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.3120+644A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948491 | |||||||
| chr10:100948712 | C | G | 1 | a0004c0007t0022g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3120+865C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948712 | |||||||
| chr10:100948793 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3120+946G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100948793 | |||||||
| chr10:100949018 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3121-1058A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100949018 | |||||||
| chr10:100949187 | A | G | 1 | a0002c0002t0004g0235 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3121-889A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100949187 | |||||||
| chr10:100949539 | G | A | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3121-537G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100949539 | |||||||
| chr10:100949619 | G | A | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(48): Show |
57 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3121-457G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100949619 | |||||||
| chr10:100950066 | C | A | 1 | a0001c0001t0001g0181 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3121-10C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 15/19 | chr10 | 100950066 | |||||||
| chr10:100950346 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3252+139A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 16/19 | chr10 | 100950346 | |||||||
| chr10:100950414 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0144 |
2 | HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.3252+207G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 16/19 | chr10 | 100950414 | |||||||
| chr10:100950469 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3253-207C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 16/19 | chr10 | 100950469 | |||||||
| chr10:100950650 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0100 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3253-26G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 16/19 | chr10 | 100950650 | |||||||
| chr10:100951013 | C | T | 1 | a0001c0001t0013g0030 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3330+260C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951013 | |||||||
| chr10:100951063 | A | C | 2 | a0001c0001t0007g0215 a0001c0001t0007g0217 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3330+310A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951063 | |||||||
| chr10:100951104 | G | A | 14 | a0001c0001t0002g0014 a0001c0001t0002g0026 a0001c0001t0002g0031 others(11): Show |
15 | HG02109.hp1 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.3330+351G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951104 | |||||||
| chr10:100951185 | G | A | 1 | a0002c0002t0004g0235 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3330+432G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951185 | |||||||
| chr10:100951191 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3330+438C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951191 | |||||||
| chr10:100951273 | ATGTTAAT others(14): Show |
A | 1 | a0002c0002t0001g0286 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3330+523_3330+543d others(23): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100951273 | ||||||
| chr10:100951752 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3330+999C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100951752 | |||||||
| chr10:100952005 | A | G | 20 | a0001c0001t0003g0239 a0001c0001t0003g0240 a0001c0001t0003g0241 others(17): Show |
20 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.3330+1252A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952005 | |||||||
| chr10:100952053 | G | C | 1 | a0001c0001t0002g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3330+1300G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952053 | |||||||
| chr10:100952058 | G | A | 301 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0020 others(298): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.3330+1305G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952058 | |||||||
| chr10:100952075 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3330+1322C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952075 | |||||||
| chr10:100952132 | C | T | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3330+1379C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952132 | |||||||
| chr10:100952198 | C | T | 2 | a0001c0001t0001g0146 a0001c0012t0001g0139 |
2 | HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3330+1445C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952198 | |||||||
| chr10:100952317 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0170 others(1): Show |
5 | NA18951.hp1 NA18968.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3330+1564G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952317 | |||||||
| chr10:100952489 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3330+1736G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952489 | |||||||
| chr10:100952709 | C | T | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3330+1956C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952709 | |||||||
| chr10:100952737 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3330+1984G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100952737 | |||||||
| chr10:100953001 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0005g0199 |
2 | NA18971.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3330+2248C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100953001 | |||||||
| chr10:100953271 | C | T | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3330+2518C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100953271 | |||||||
| chr10:100953461 | T | TA | 15 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0157 others(12): Show |
15 | HG00544.hp1 HG00735.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.3330+2722dupA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100953461 | ||||||
| chr10:100953657 | A | T | 1 | a0001c0001t0002g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3331-2794A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100953657 | |||||||
| chr10:100953918 | C | G | 1 | a0001c0001t0005g0159 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3331-2533C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100953918 | |||||||
| chr10:100954093 | CA | C | 207 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(204): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.3331-2344delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100954093 | ||||||
| chr10:100954101 | A | C | 1 | a0002c0002t0001g0262 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3331-2350A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954101 | |||||||
| chr10:100954194 | G | A | 1 | a0001c0001t0007g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3331-2257G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954194 | |||||||
| chr10:100954405 | A | C | 2 | a0001c0005t0004g0211 a0001c0005t0004g0212 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3331-2046A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954405 | |||||||
| chr10:100954488 | C | A | 3 | a0001c0001t0002g0121 a0001c0001t0002g0122 a0002c0002t0021g0229 |
3 | HG02886.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3331-1963C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954488 | |||||||
| chr10:100954535 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3331-1916C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954535 | |||||||
| chr10:100954890 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3331-1561G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100954890 | |||||||
| chr10:100954941 | C | CT | 101 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(98): Show |
113 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.3331-1494dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100954941 | ||||||
| chr10:100954941 | CT | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0166 a0001c0001t0001g0221 others(5): Show |
8 | HG01516.hp1 HG01943.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3331-1494delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100954941 | ||||||
| chr10:100955041 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3331-1410G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955041 | |||||||
| chr10:100955060 | C | T | 1 | a0002c0002t0001g0261 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3331-1391C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955060 | |||||||
| chr10:100955130 | C | T | 103 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(100): Show |
115 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.3331-1321C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955130 | |||||||
| chr10:100955426 | T | C | 105 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(102): Show |
117 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.3331-1025T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955426 | |||||||
| chr10:100955487 | G | A | 1 | a0004c0007t0022g0203 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3331-964G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955487 | |||||||
| chr10:100955633 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3331-818C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955633 | |||||||
| chr10:100955713 | G | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0006g0036 |
3 | NA18944.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.3331-738G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955713 | |||||||
| chr10:100955905 | CA | C | 204 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(201): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.3331-531delA | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr10 | 100955905 | ||||||
| chr10:100955906 | A | G | 1 | a0002c0002t0019g0228 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3331-545A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955906 | |||||||
| chr10:100955907 | A | G | 17 | a0001c0001t0004g0214 a0001c0001t0010g0218 a0001c0001t0010g0219 others(14): Show |
19 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3331-544A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955907 | |||||||
| chr10:100955931 | C | T | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3331-520C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955931 | |||||||
| chr10:100955932 | G | A | 1 | a0001c0001t0005g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3331-519G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100955932 | |||||||
| chr10:100956088 | T | C | 1 | a0002c0002t0001g0281 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3331-363T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956088 | |||||||
| chr10:100956096 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0197 |
2 | NA18960.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.3331-355T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956096 | |||||||
| chr10:100956131 | C | A | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3331-320C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956131 | |||||||
| chr10:100956307 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3331-144A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956307 | |||||||
| chr10:100956365 | T | C | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3331-86T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956365 | |||||||
| chr10:100956372 | G | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0188 a0001c0001t0005g0023 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.3331-79G>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 17/19 | chr10 | 100956372 | |||||||
| chr10:100956588 | G | A | 1 | a0001c0001t0003g0251 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3417+51G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100956588 | |||||||
| chr10:100956639 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3417+102A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100956639 | |||||||
| chr10:100956795 | A | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0057 |
3 | NA18947.hp2 NA18951.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.3417+258A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100956795 | |||||||
| chr10:100956882 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3417+345C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100956882 | |||||||
| chr10:100956943 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0098 others(1): Show |
5 | HG00558.hp2 HG00609.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3417+406G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100956943 | |||||||
| chr10:100957319 | A | G | 18 | a0001c0001t0004g0214 a0001c0001t0010g0218 a0001c0001t0010g0219 others(15): Show |
20 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.3417+782A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957319 | |||||||
| chr10:100957330 | A | AT | 15 | a0001c0001t0001g0023 a0001c0001t0001g0126 a0001c0001t0001g0128 others(12): Show |
15 | HG00140.hp1 HG00597.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.3417+830dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | A | ATT | 11 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0129 others(8): Show |
12 | HG01346.hp1 HG01346.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.3417+829_3417+830d others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | A | ATTT | 11 | a0001c0001t0001g0068 a0001c0001t0001g0141 a0001c0001t0001g0147 others(8): Show |
11 | HG00733.hp2 HG00738.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.3417+828_3417+830d others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | AT | A | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0161 others(12): Show |
16 | HG00408.hp1 HG00673.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.3417+830delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATT | A | 8 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0003g0224 others(5): Show |
8 | HG01106.hp1 HG01192.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3417+829_3417+830d others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTT | A | 16 | a0001c0001t0001g0198 a0001c0001t0002g0017 a0001c0001t0002g0049 others(13): Show |
17 | HG01258.hp2 HG02132.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.3417+828_3417+830d others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTT | A | 50 | a0001c0001t0001g0221 a0001c0001t0002g0014 a0001c0001t0002g0015 others(47): Show |
54 | HG00099.hp2 HG00408.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.3417+827_3417+830d others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTT | A | 69 | a0001c0001t0001g0222 a0001c0001t0002g0002 a0001c0001t0002g0003 others(66): Show |
77 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.3417+826_3417+830d others(7): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTT | A | 6 | a0001c0001t0002g0032 a0001c0001t0002g0145 a0001c0001t0007g0215 others(3): Show |
6 | HG02109.hp2 HG02630.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3417+825_3417+830d others(8): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTTT | A | 11 | a0001c0001t0004g0214 a0002c0002t0004g0006 a0002c0002t0004g0120 others(8): Show |
13 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.3417+824_3417+830d others(9): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3417+821_3417+830d others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTTT others(10): Show |
A | 3 | a0002c0002t0001g0260 a0002c0002t0001g0266 a0009c0010t0001g0052 |
3 | HG04228.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3417+814_3417+830d others(19): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTTT others(11): Show |
A | 47 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(44): Show |
53 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3417+813_3417+830d others(20): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957330 | ATTTTTTT others(12): Show |
A | 1 | a0002c0002t0001g0269 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3417+812_3417+830d others(21): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr10 | 100957330 | ||||||
| chr10:100957349 | T | A | 3 | a0002c0002t0001g0260 a0002c0002t0001g0266 a0009c0010t0001g0052 |
3 | HG04228.hp2 NA18991.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.3417+812T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957349 | |||||||
| chr10:100957350 | T | A | 47 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(44): Show |
53 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3417+813T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957350 | |||||||
| chr10:100957351 | T | A | 1 | a0002c0002t0001g0269 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3417+814T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957351 | |||||||
| chr10:100957432 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0206 |
2 | NA18975.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.3417+895C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957432 | |||||||
| chr10:100957443 | C | T | 1 | a0001c0001t0017g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3417+906C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957443 | |||||||
| chr10:100957589 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3417+1052G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957589 | |||||||
| chr10:100957976 | G | A | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(48): Show |
57 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3417+1439G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957976 | |||||||
| chr10:100957988 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0014g0091 |
2 | HG01106.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3418-1440G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100957988 | |||||||
| chr10:100958040 | C | G | 5 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0001g0191 others(2): Show |
5 | HG02040.hp2 HG02056.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.3418-1388C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958040 | |||||||
| chr10:100958185 | C | T | 1 | a0002c0002t0001g0285 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3418-1243C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958185 | |||||||
| chr10:100958433 | C | G | 2 | a0001c0001t0003g0243 a0001c0001t0003g0248 |
2 | HG01081.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3418-995C>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958433 | |||||||
| chr10:100958704 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3418-724A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958704 | |||||||
| chr10:100958962 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3418-466G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958962 | |||||||
| chr10:100958996 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3418-432G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100958996 | |||||||
| chr10:100959042 | AGGCACAG others(26): Show |
A | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3418-385_3418-353d others(35): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 18/19 | chr10 | 100959042 | |||||||
| chr10:100959735 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3486+239G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100959735 | |||||||
| chr10:100959999 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0155 a0001c0001t0001g0167 others(8): Show |
12 | HG00673.hp2 HG02132.hp1 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.3486+503T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100959999 | |||||||
| chr10:100960000 | G | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0155 a0001c0001t0001g0167 others(8): Show |
12 | HG00673.hp2 HG02132.hp1 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.3486+504G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960000 | |||||||
| chr10:100960006 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3486+510A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960006 | |||||||
| chr10:100960029 | C | T | 1 | a0002c0002t0021g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3486+533C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960029 | |||||||
| chr10:100960083 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3486+587T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960083 | |||||||
| chr10:100960145 | T | C | 51 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0113 others(48): Show |
57 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3486+649T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960145 | |||||||
| chr10:100960157 | T | A | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3486+661T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960157 | |||||||
| chr10:100960548 | T | C | 1 | a0001c0001t0005g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3486+1052T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960548 | |||||||
| chr10:100960552 | T | G | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3486+1056T>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960552 | |||||||
| chr10:100960720 | C | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0141 a0001c0001t0001g0144 others(4): Show |
8 | HG00733.hp2 HG00738.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.3487-1157C>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960720 | |||||||
| chr10:100960813 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3487-1064G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960813 | |||||||
| chr10:100960914 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3487-963T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960914 | |||||||
| chr10:100960976 | A | G | 2 | a0002c0002t0001g0292 a0002c0002t0001g0293 |
2 | HG01952.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3487-901A>G | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960976 | |||||||
| chr10:100960997 | T | A | 28 | a0001c0001t0003g0224 a0001c0001t0003g0239 a0001c0001t0003g0240 others(25): Show |
29 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.3487-880T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100960997 | |||||||
| chr10:100960998 | C | CT | 92 | a0001c0001t0001g0068 a0001c0001t0001g0107 a0001c0001t0001g0136 others(89): Show |
104 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.3487-850dupT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | C | CTT | 57 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0131 others(54): Show |
63 | HG00597.hp1 HG00733.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.3487-851_3487-850d others(4): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | C | CTTT | 20 | a0001c0001t0002g0027 a0001c0001t0002g0073 a0001c0001t0002g0116 others(17): Show |
22 | HG00639.hp1 HG00738.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.3487-852_3487-850d others(5): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | C | CTTTT | 8 | a0001c0001t0002g0061 a0001c0001t0006g0115 a0001c0005t0004g0211 others(5): Show |
8 | HG00280.hp1 HG00621.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3487-853_3487-850d others(6): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | CT | C | 6 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0184 others(3): Show |
6 | HG01934.hp2 HG02896.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3487-850delT | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0045 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3487-859_3487-850d others(12): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3487-865_3487-850d others(18): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100960998 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0017g0151 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3487-867_3487-850d others(20): Show |
SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr10 | 100960998 | ||||||
| chr10:100961071 | G | A | 2 | a0003c0006t0001g0137 a0003c0006t0001g0138 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3487-806G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961071 | |||||||
| chr10:100961078 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3487-799C>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961078 | |||||||
| chr10:100961137 | G | T | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3487-740G>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961137 | |||||||
| chr10:100961262 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0098 others(1): Show |
5 | HG00558.hp2 HG00609.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.3487-615G>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961262 | |||||||
| chr10:100961490 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3487-387T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961490 | |||||||
| chr10:100961709 | A | C | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3487-168A>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961709 | |||||||
| chr10:100961728 | T | C | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3487-149T>C | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961728 | |||||||
| chr10:100961756 | T | A | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3487-121T>A | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961756 | |||||||
| chr10:100961757 | A | T | 1 | a0001c0001t0020g0171 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3487-120A>T | SLF2 | ENSG00000119906.13 | transcript | ENST00000238961.9 | protein_coding | 19/19 | chr10 | 100961757 |