Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80185 |
| ensemblid | ENSG00000129696.13 |
| hgncid | 26262 |
| symbol | TTI2 |
| name | TELO2 interacting protein 2 |
| refseq_nuc | NM_001102401.4 |
| refseq_prot | NP_001095871.1 |
| ensembl_nuc | ENST00000431156.7 |
| ensembl_prot | ENSP00000411169.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 33498722 |
| end | 33513135 |
| strand | - |
| ver | v1.2 |
| region | chr8:33498722-33513135 |
| region5000 | chr8:33493722-33518135 |
| regionname0 | TTI2_chr8_33498722_33513135 |
| regionname5000 | TTI2_chr8_33493722_33518135 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 508 | 215 | 37 | 29 | 113 | 6 | 29 | 87 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0002 | 1/0 | 508 | 173 | 48 | 28 | 72 | 5 | 19 | 58 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0003 | 0/0 | 508 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0004 | 0/0 | 508 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0005 | 0/0 | 508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0006 | 0/0 | 508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0007 | 0/0 | 508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| a0008 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | MELDS others(503): Show |
chr8 | 33493722 | 33518135 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1524 | 213 | 37 | 28 | 113 | 6 | 28 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0001c0005 | 0/0 | 1524 | 2 | 0 | 1 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0002c0002 | 1/0 | 1524 | 150 | 31 | 26 | 70 | 3 | 19 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0002c0003 | 0/0 | 1524 | 22 | 17 | 2 | 1 | 2 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0002c0010 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0003c0004 | 0/0 | 1524 | 5 | 5 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0004c0007 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0005c0008 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0006c0011 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0007c0009 | 0/0 | 1524 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 | ||
| a0008c0006 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | ATGGA others(1519): Show |
chr8 | 33493722 | 33518135 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2130 | 213 | 37 | 28 | 113 | 6 | 28 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0001c0005t0001 | 0/0 | 2130 | 2 | 0 | 1 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0002c0002t0001 | 0/0 | 2130 | 4 | 4 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0002c0002t0002 | 1/0 | 2131 | 141 | 27 | 26 | 70 | 3 | 14 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0002c0002t0003 | 0/0 | 2131 | 5 | 0 | 0 | 0 | 0 | 5 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0002c0003t0001 | 0/0 | 2130 | 20 | 15 | 2 | 1 | 2 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0002c0003t0002 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0002c0003t0004 | 0/0 | 2131 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0002c0010t0002 | 0/0 | 2131 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0003c0004t0001 | 0/0 | 2130 | 5 | 5 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0004c0007t0001 | 0/0 | 2130 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0005c0008t0001 | 0/0 | 2130 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| a0006c0011t0002 | 0/0 | 2131 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0007c0009t0002 | 0/0 | 2131 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2126): Show |
chr8 | 33493722 | 33518135 |
| a0008c0006t0001 | 0/0 | 2130 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | AATAT others(2125): Show |
chr8 | 33493722 | 33518135 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 1 | 4 | 2 | 3 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0004 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0005 | 0/0 | 8 | 3 | 0 | 4 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0013 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0005t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0001c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0001 | 0/0 | 22 | 1 | 7 | 13 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0002 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0010 | 1/0 | 5 | 0 | 1 | 0 | 1 | 2 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0003g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0003t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0002c0010t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0003c0004t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0003c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0003c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0004c0007t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0005c0008t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0006c0011t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0007c0009t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| a0008c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0033 | EUR | GBR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | GBR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0058 | EUR | GBR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0060 | EUR | FIN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0140 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01070 | hp2 | a0001 | c0005 | t0001 | g0074 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0133 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0143 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0115 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0249 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0116 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0063 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01516 | hp1 | a0004 | c0007 | t0001 | g0172 | EUR | IBS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01928 | hp2 | a0005 | c0008 | t0001 | g0184 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01993 | hp1 | a0006 | c0011 | t0002 | g0253 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0245 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0046 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0056 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02145 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0059 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0067 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0243 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02273 | hp1 | a0007 | c0009 | t0002 | g0097 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0153 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0251 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0026 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02818 | hp2 | a0002 | c0003 | t0001 | g0061 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0068 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0065 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0099 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03041 | hp2 | a0002 | c0003 | t0001 | g0066 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03098 | hp1 | a0002 | c0003 | t0001 | g0054 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0252 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03209 | hp1 | a0002 | c0003 | t0004 | g0078 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0265 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0250 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0062 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ESN | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0121 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0155 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03669 | hp2 | a0002 | c0002 | t0003 | g0018 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03688 | hp1 | a0001 | c0005 | t0001 | g0175 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03831 | hp2 | a0002 | c0002 | t0003 | g0120 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0135 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03927 | hp2 | a0002 | c0002 | t0003 | g0119 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0264 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0142 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04184 | hp2 | a0002 | c0002 | t0003 | g0018 | SAS | BEB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04199 | hp2 | a0002 | c0002 | t0003 | g0018 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0138 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | YRI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | CHB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0240 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18972 | hp2 | a0002 | c0010 | t0002 | g0144 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0242 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19030 | hp1 | a0003 | c0004 | t0001 | g0025 | AFR | LWK | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19030 | hp2 | a0002 | c0003 | t0001 | g0069 | AFR | LWK | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19043 | hp1 | a0002 | c0003 | t0002 | g0077 | AFR | LWK | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19055 | hp1 | a0008 | c0006 | t0001 | g0227 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0057 | AFR | YRI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | ASW | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0248 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | USA | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | USA | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0127 | AFR | USA | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0199 | REF | REF | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0010 | REF | REF | TTI2_chr8_33493722_33518135 | TTI2 | chr8 | 33493722 | 33518135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:33500393 | C | T | 1 | a0005 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1357G>A | p.Ala453Thr | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/8 | 1510/2131 | 1357/1527 | 453/508 | chr8 | 33500393 | |||
| chr8:33503498 | C | T | 1 | a0004 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1190G>A | p.Gly397Glu | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/8 | 1343/2131 | 1190/1527 | 397/508 | chr8 | 33503498 | |||
| chr8:33503799 | C | T | 1 | a0008 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.1064G>A | p.Arg355His | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/8 | 1217/2131 | 1064/1527 | 355/508 | chr8 | 33503799 | |||
| chr8:33503832 | C | T | 1 | a0003 | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
missense_variant | MODERATE | c.1031G>A | p.Arg344Gln | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/8 | 1184/2131 | 1031/1527 | 344/508 | chr8 | 33503832 | |||
| chr8:33512033 | C | G | 1 | a0007 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.581G>C | p.Gly194Ala | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/8 | 734/2131 | 581/1527 | 194/508 | chr8 | 33512033 | |||
| chr8:33512286 | C | A | 1 | a0006 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.328G>T | p.Ala110Ser | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/8 | 481/2131 | 328/1527 | 110/508 | chr8 | 33512286 | |||
| chr8:33512426 | T | C | 4 | a0001 a0004 a0005 others(1): Show |
217 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
missense_variant | MODERATE | c.188A>G | p.Glu63Gly | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/8 | 341/2131 | 188/1527 | 63/508 | chr8 | 33512426 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:33503750 | G | A | 1 | a0002c0010 | 1 | NA18972.hp2 | splice_region_variant&synonymous_variant | LOW | c.1113C>T | p.Asn371Asn | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/8 | 1266/2131 | 1113/1527 | 371/508 | chr8 | 33503750 | |||
| chr8:33503762 | C | T | 1 | a0001c0005 | 2 | HG01070.hp2 HG03688.hp1 |
synonymous_variant | LOW | c.1101G>A | p.Pro367Pro | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/8 | 1254/2131 | 1101/1527 | 367/508 | chr8 | 33503762 | |||
| chr8:33509857 | C | T | 1 | a0003c0004 | 5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.723G>A | p.Leu241Leu | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/8 | 876/2131 | 723/1527 | 241/508 | chr8 | 33509857 | |||
| chr8:33512476 | A | G | 7 | a0001c0001 a0001c0005 a0002c0003 others(4): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
synonymous_variant | LOW | c.138T>C | p.Asn46Asn | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/8 | 291/2131 | 138/1527 | 46/508 | chr8 | 33512476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:33498805 | G | A | 1 | a0002c0002t0003 | 5 | HG03669.hp2 HG03831.hp2 HG03927.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*368C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 8/8 | 368 | chr8 | 33498805 | ||||||
| chr8:33499043 | AG | A | 8 | a0001c0001t0001 a0001c0005t0001 a0002c0002t0001 others(5): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*129delC | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 8/8 | 129 | chr8 | 33499043 | ||||||
| chr8:33499076 | A | G | 1 | a0002c0003t0004 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*97T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 8/8 | 97 | chr8 | 33499076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:33499299 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0156 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1423-22C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499299 | |||||||
| chr8:33499305 | A | AT | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423-29dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499305 | |||||||
| chr8:33499307 | A | T | 4 | a0002c0002t0002g0099 a0003c0004t0001g0025 a0003c0004t0001g0026 others(1): Show |
6 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1423-30T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499307 | |||||||
| chr8:33499309 | T | A | 29 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(26): Show |
35 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1423-32A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499309 | |||||||
| chr8:33499311 | T | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1423-34A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499311 | |||||||
| chr8:33499365 | T | C | 1 | a0002c0002t0002g0142 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1423-88A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499365 | |||||||
| chr8:33499382 | T | A | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1423-105A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499382 | |||||||
| chr8:33499457 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1423-180G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499457 | |||||||
| chr8:33499476 | C | T | 1 | a0002c0002t0002g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1423-199G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499476 | |||||||
| chr8:33499525 | G | A | 1 | a0002c0002t0002g0251 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1423-248C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499525 | |||||||
| chr8:33499556 | A | G | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1423-279T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499556 | |||||||
| chr8:33499596 | C | A | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1423-319G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499596 | |||||||
| chr8:33499597 | T | C | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1423-320A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499597 | |||||||
| chr8:33499598 | A | T | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1423-321T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499598 | |||||||
| chr8:33499763 | G | T | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1423-486C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499763 | |||||||
| chr8:33499861 | G | T | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1422+467C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499861 | |||||||
| chr8:33499875 | G | T | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1422+453C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499875 | |||||||
| chr8:33499998 | CT | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(9): Show |
16 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1422+329delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33499998 | |||||||
| chr8:33500245 | C | T | 1 | a0002c0002t0002g0129 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1422+83G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33500245 | |||||||
| chr8:33500252 | A | T | 1 | a0002c0002t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1422+76T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33500252 | |||||||
| chr8:33500300 | A | G | 21 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(18): Show |
23 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.1422+28T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 7/7 | chr8 | 33500300 | |||||||
| chr8:33500625 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1260-135G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33500625 | |||||||
| chr8:33500644 | A | T | 163 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1260-154T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33500644 | |||||||
| chr8:33500726 | C | T | 1 | a0002c0003t0004g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1260-236G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33500726 | |||||||
| chr8:33500752 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1260-262C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33500752 | |||||||
| chr8:33500920 | G | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260-430C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33500920 | |||||||
| chr8:33501212 | C | T | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1260-722G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33501212 | |||||||
| chr8:33501399 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0195 |
2 | HG01255.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1260-909G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33501399 | |||||||
| chr8:33501497 | G | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260-1007C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33501497 | |||||||
| chr8:33501933 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1260-1443A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33501933 | |||||||
| chr8:33501980 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1259+1449C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33501980 | |||||||
| chr8:33502010 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1259+1419A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502010 | |||||||
| chr8:33502058 | T | G | 1 | a0002c0003t0004g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1259+1371A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502058 | |||||||
| chr8:33502091 | G | A | 4 | a0002c0002t0002g0123 a0003c0004t0001g0025 a0003c0004t0001g0026 others(1): Show |
6 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1259+1338C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502091 | |||||||
| chr8:33502093 | G | A | 21 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(18): Show |
23 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.1259+1336C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502093 | |||||||
| chr8:33502234 | G | A | 4 | a0002c0003t0001g0065 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1259+1195C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502234 | |||||||
| chr8:33502319 | T | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+1110A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502319 | |||||||
| chr8:33502457 | A | AT | 22 | a0001c0001t0001g0201 a0002c0002t0001g0153 a0002c0002t0001g0156 others(19): Show |
24 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.1259+971dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502457 | |||||||
| chr8:33502457 | AT | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.1259+971delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502457 | |||||||
| chr8:33502563 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0225 |
2 | NA18992.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1259+866C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502563 | |||||||
| chr8:33502589 | C | CTGAGGAG others(14): Show |
1 | a0001c0001t0001g0082 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1259+819_1259+839d others(23): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502589 | |||||||
| chr8:33502620 | C | T | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+809G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502620 | |||||||
| chr8:33502689 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1259+740C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502689 | |||||||
| chr8:33502824 | T | TCAAAAA | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1259+599_1259+604d others(8): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502824 | |||||||
| chr8:33502847 | AGG | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1259+580_1259+581d others(4): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33502847 | |||||||
| chr8:33503009 | A | G | 4 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259+420T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503009 | |||||||
| chr8:33503085 | C | T | 1 | a0002c0002t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1259+344G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503085 | |||||||
| chr8:33503128 | C | CA | 28 | a0002c0002t0002g0033 a0002c0002t0002g0045 a0002c0002t0002g0101 others(25): Show |
32 | HG00099.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.1259+300dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503128 | |||||||
| chr8:33503140 | A | AC | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
214 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.1259+288_1259+289i others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503140 | |||||||
| chr8:33503140 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1259+289T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503140 | |||||||
| chr8:33503144 | A | AC | 8 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(5): Show |
8 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1259+284_1259+285i others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503144 | |||||||
| chr8:33503149 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1259+280G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503149 | |||||||
| chr8:33503150 | A | T | 11 | a0002c0002t0002g0045 a0002c0002t0002g0072 a0002c0002t0002g0154 others(8): Show |
12 | HG00738.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1259+279T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503150 | |||||||
| chr8:33503189 | C | CAG | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1259+239_1259+240i others(4): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 6/7 | chr8 | 33503189 | |||||||
| chr8:33503594 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1116-22A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/7 | chr8 | 33503594 | |||||||
| chr8:33503595 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0188 |
2 | HG02135.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1116-23C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/7 | chr8 | 33503595 | |||||||
| chr8:33503598 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1116-26C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 5/7 | chr8 | 33503598 | |||||||
| chr8:33504187 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.928-252T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504187 | |||||||
| chr8:33504219 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.928-284A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504219 | |||||||
| chr8:33504221 | T | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.928-286A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504221 | |||||||
| chr8:33504289 | A | AT | 21 | a0001c0001t0001g0168 a0002c0002t0002g0009 a0002c0002t0002g0019 others(18): Show |
27 | HG00597.hp2 HG00639.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.928-355dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATT | 8 | a0002c0002t0001g0153 a0002c0002t0002g0072 a0002c0002t0002g0104 others(5): Show |
8 | HG00738.hp2 HG01243.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.928-356_928-355dup others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATTT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
12 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.928-357_928-355dup others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATTTT | 10 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0216 others(7): Show |
12 | HG02015.hp1 HG02257.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.928-358_928-355dup others(4): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATTTTT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.928-359_928-355dup others(5): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATTTTTT | 45 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(42): Show |
73 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.928-360_928-355dup others(6): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | ATTTTTTT | 18 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0080 others(15): Show |
22 | HG00408.hp2 HG00735.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.928-361_928-355dup others(7): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | A | T | 1 | a0002c0002t0002g0115 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.928-354T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504289 | AT | A | 8 | a0002c0002t0002g0031 a0002c0002t0002g0038 a0002c0002t0002g0045 others(5): Show |
11 | HG02109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-355delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504289 | |||||||
| chr8:33504367 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0230 |
2 | NA18982.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.928-432C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504367 | |||||||
| chr8:33504452 | A | AC | 4 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-518dupG | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504452 | |||||||
| chr8:33504464 | C | A | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.928-529G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504464 | |||||||
| chr8:33504464 | CTT | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0075 a0001c0001t0001g0176 others(2): Show |
7 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-531_928-530del others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504464 | |||||||
| chr8:33504488 | A | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.928-553T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504488 | |||||||
| chr8:33504490 | G | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-555C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504490 | |||||||
| chr8:33504546 | A | G | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.928-611T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504546 | |||||||
| chr8:33504557 | G | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.928-622C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504557 | |||||||
| chr8:33504565 | G | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0185 |
2 | NA19063.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.928-630C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504565 | |||||||
| chr8:33504680 | A | C | 1 | a0002c0002t0002g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.928-745T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504680 | |||||||
| chr8:33504808 | C | T | 4 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-873G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504808 | |||||||
| chr8:33504823 | T | C | 3 | a0002c0002t0002g0072 a0002c0002t0002g0154 a0002c0002t0002g0265 |
3 | HG00738.hp2 HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.928-888A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504823 | |||||||
| chr8:33504882 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.928-947C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504882 | |||||||
| chr8:33504999 | G | C | 4 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.928-1064C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33504999 | |||||||
| chr8:33505179 | C | T | 1 | a0002c0002t0002g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.928-1244G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505179 | |||||||
| chr8:33505409 | G | C | 1 | a0002c0003t0001g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.928-1474C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505409 | |||||||
| chr8:33505415 | C | T | 2 | a0002c0003t0001g0054 a0002c0003t0001g0059 |
2 | HG02257.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.928-1480G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505415 | |||||||
| chr8:33505478 | A | C | 1 | a0002c0003t0001g0058 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.928-1543T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505478 | |||||||
| chr8:33505485 | C | CT | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.928-1551dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505485 | |||||||
| chr8:33505485 | CT | C | 11 | a0002c0002t0002g0034 a0002c0002t0002g0036 a0002c0002t0002g0102 others(8): Show |
13 | HG02074.hp1 HG02698.hp1 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.928-1551delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505485 | |||||||
| chr8:33505542 | G | T | 1 | a0002c0002t0002g0149 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.928-1607C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505542 | |||||||
| chr8:33505546 | A | G | 1 | a0002c0002t0002g0149 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.928-1611T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505546 | |||||||
| chr8:33505559 | G | A | 1 | a0002c0002t0002g0149 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.928-1624C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505559 | |||||||
| chr8:33505639 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.927+1590C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505639 | |||||||
| chr8:33505768 | T | C | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+1461A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505768 | |||||||
| chr8:33505815 | G | A | 4 | a0002c0003t0001g0065 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+1414C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505815 | |||||||
| chr8:33505896 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.927+1333C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505896 | |||||||
| chr8:33505974 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.927+1255C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505974 | |||||||
| chr8:33505976 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.927+1253C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33505976 | |||||||
| chr8:33506021 | G | A | 4 | a0002c0003t0001g0065 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+1208C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506021 | |||||||
| chr8:33506075 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.927+1154C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506075 | |||||||
| chr8:33506076 | C | T | 1 | a0002c0002t0002g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+1153G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506076 | |||||||
| chr8:33506102 | G | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.927+1127C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506102 | |||||||
| chr8:33506266 | A | G | 1 | a0002c0002t0002g0251 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.927+963T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506266 | |||||||
| chr8:33506317 | A | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.927+912T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506317 | |||||||
| chr8:33506374 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.927+855G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506374 | |||||||
| chr8:33506386 | G | A | 13 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(10): Show |
15 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.927+843C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506386 | |||||||
| chr8:33506389 | C | CT | 8 | a0002c0002t0002g0103 a0002c0002t0002g0113 a0002c0002t0002g0117 others(5): Show |
8 | HG03710.hp1 NA18940.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+839dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506389 | |||||||
| chr8:33506389 | CT | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
212 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.927+839delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506389 | |||||||
| chr8:33506389 | CTTT | C | 17 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.927+837_927+839del others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506389 | |||||||
| chr8:33506550 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(129): Show |
204 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.927+679G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506550 | |||||||
| chr8:33506551 | C | G | 1 | a0002c0002t0002g0130 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.927+678G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506551 | |||||||
| chr8:33506554 | G | A | 1 | a0002c0002t0002g0130 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.927+675C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506554 | |||||||
| chr8:33506555 | C | T | 1 | a0002c0002t0002g0130 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.927+674G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506555 | |||||||
| chr8:33506586 | T | C | 1 | a0002c0002t0002g0251 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.927+643A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506586 | |||||||
| chr8:33506637 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.927+592G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506637 | |||||||
| chr8:33506690 | C | CT | 8 | a0001c0001t0001g0179 a0001c0001t0001g0207 a0001c0001t0001g0221 others(5): Show |
10 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.927+538dupA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506690 | |||||||
| chr8:33506690 | CT | C | 8 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0259 others(5): Show |
8 | HG01168.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+538delA | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506690 | |||||||
| chr8:33506706 | A | T | 1 | a0002c0002t0002g0247 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.927+523T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506706 | |||||||
| chr8:33506715 | T | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.927+514A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506715 | |||||||
| chr8:33506771 | C | A | 2 | a0002c0003t0002g0077 a0002c0003t0004g0078 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.927+458G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506771 | |||||||
| chr8:33506801 | T | A | 1 | a0002c0002t0002g0124 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.927+428A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506801 | |||||||
| chr8:33506806 | C | A | 2 | a0003c0004t0001g0025 a0003c0004t0001g0026 |
4 | HG02145.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+423G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33506806 | |||||||
| chr8:33507068 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.927+161G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33507068 | |||||||
| chr8:33507144 | T | A | 1 | a0002c0002t0002g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+85A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 4/7 | chr8 | 33507144 | |||||||
| chr8:33507541 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.835-220C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507541 | |||||||
| chr8:33507545 | G | T | 3 | a0002c0002t0002g0029 a0002c0002t0002g0071 a0002c0002t0002g0125 |
4 | HG02572.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-224C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507545 | |||||||
| chr8:33507661 | C | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-340G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507661 | |||||||
| chr8:33507692 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-371A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507692 | |||||||
| chr8:33507950 | C | T | 1 | a0002c0002t0002g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.835-629G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507950 | |||||||
| chr8:33507988 | CA | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.835-668delT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507988 | |||||||
| chr8:33507988 | CAA | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0210 a0001c0001t0001g0215 others(1): Show |
6 | HG02451.hp1 HG02559.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-669_835-668del others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33507988 | |||||||
| chr8:33508073 | G | T | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.835-752C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508073 | |||||||
| chr8:33508087 | T | TA | 80 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(77): Show |
128 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.835-767dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | T | TAA | 70 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
107 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.835-768_835-767dup others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | T | TAAA | 17 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0080 others(14): Show |
19 | HG00423.hp1 HG00438.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.835-769_835-767dup others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | T | TAAAA | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0160 others(4): Show |
7 | HG00673.hp2 HG04204.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-770_835-767dup others(4): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | TA | T | 6 | a0001c0001t0001g0073 a0002c0002t0002g0099 a0002c0002t0002g0100 others(3): Show |
6 | HG02602.hp1 HG02717.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.835-767delT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | TAAA | T | 10 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(7): Show |
10 | HG00738.hp2 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.835-769_835-767del others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | TAAAAAA | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0047 others(3): Show |
9 | HG00597.hp1 HG00609.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-772_835-767del others(6): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | TAAAAAAA others(3): Show |
T | 5 | a0001c0001t0001g0257 a0002c0002t0002g0032 a0002c0002t0002g0108 others(2): Show |
6 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-776_835-767del others(10): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508087 | TAAAAAAA others(7): Show |
T | 1 | a0002c0002t0002g0031 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.835-780_835-767del others(14): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508087 | |||||||
| chr8:33508108 | AAAAAAAA others(5): Show |
A | 10 | a0002c0003t0001g0015 a0002c0003t0001g0058 a0002c0003t0001g0059 others(7): Show |
12 | HG00140.hp2 HG00280.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.835-799_835-788del others(12): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508108 | |||||||
| chr8:33508109 | AAAAAAAA others(4): Show |
A | 7 | a0002c0003t0001g0054 a0002c0003t0001g0055 a0002c0003t0001g0056 others(4): Show |
7 | HG01192.hp2 HG01346.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-799_835-789del others(11): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508109 | |||||||
| chr8:33508120 | G | T | 1 | a0001c0001t0001g0030 | 2 | HG01074.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.835-799C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508120 | |||||||
| chr8:33508145 | T | C | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-824A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508145 | |||||||
| chr8:33508161 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.835-840T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508161 | |||||||
| chr8:33508335 | C | T | 13 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(10): Show |
15 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-1014G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508335 | |||||||
| chr8:33508447 | T | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | NA19005.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.835-1126A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508447 | |||||||
| chr8:33508501 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.835-1180G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508501 | |||||||
| chr8:33508514 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.835-1193G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508514 | |||||||
| chr8:33508526 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.835-1205C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508526 | |||||||
| chr8:33508575 | C | A | 1 | a0002c0002t0002g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.834+1171G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508575 | |||||||
| chr8:33508617 | C | CA | 19 | a0002c0002t0001g0156 a0002c0002t0001g0158 a0002c0002t0002g0107 others(16): Show |
19 | HG01106.hp2 HG01243.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+1128dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508617 | |||||||
| chr8:33508617 | C | CAAA | 14 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0027 others(11): Show |
20 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.834+1126_834+1128d others(5): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508617 | |||||||
| chr8:33508617 | C | CAAAA | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.834+1125_834+1128d others(6): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508617 | |||||||
| chr8:33508617 | C | CAAAAA | 50 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0043 others(47): Show |
55 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.834+1124_834+1128d others(7): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508617 | |||||||
| chr8:33508617 | C | CAAAAAA | 8 | a0001c0001t0001g0161 a0001c0001t0001g0163 a0001c0001t0001g0230 others(5): Show |
8 | HG00741.hp1 HG01346.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+1123_834+1128d others(8): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508617 | |||||||
| chr8:33508646 | G | T | 1 | a0002c0002t0002g0071 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.834+1100C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508646 | |||||||
| chr8:33508657 | T | C | 2 | a0002c0002t0002g0029 a0002c0002t0002g0071 |
3 | HG02572.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.834+1089A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508657 | |||||||
| chr8:33508671 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.834+1075C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508671 | |||||||
| chr8:33508686 | G | A | 4 | a0002c0003t0001g0065 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+1060C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508686 | |||||||
| chr8:33508761 | A | T | 2 | a0003c0004t0001g0025 a0003c0004t0001g0026 |
4 | HG02145.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+985T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508761 | |||||||
| chr8:33508847 | A | G | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+899T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508847 | |||||||
| chr8:33508898 | A | T | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+848T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33508898 | |||||||
| chr8:33509006 | G | A | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+740C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509006 | |||||||
| chr8:33509132 | C | CA | 25 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
29 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.834+613dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509132 | |||||||
| chr8:33509132 | C | CAA | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
188 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.834+612_834+613dup others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509132 | |||||||
| chr8:33509132 | C | CAAA | 7 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(4): Show |
7 | HG01978.hp2 HG03710.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+611_834+613dup others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509132 | |||||||
| chr8:33509132 | CAAA | C | 16 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(13): Show |
18 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.834+611_834+613del others(3): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509132 | |||||||
| chr8:33509148 | A | G | 1 | a0002c0002t0002g0239 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.834+598T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509148 | |||||||
| chr8:33509162 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+584T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509162 | |||||||
| chr8:33509163 | AGGAAGTA others(3): Show |
A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+573_834+582del others(10): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509163 | |||||||
| chr8:33509176 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+570C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509176 | |||||||
| chr8:33509178 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+568A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509178 | |||||||
| chr8:33509188 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+558G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509188 | |||||||
| chr8:33509189 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+557T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509189 | |||||||
| chr8:33509190 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+556G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509190 | |||||||
| chr8:33509191 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+555C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509191 | |||||||
| chr8:33509192 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+554G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509192 | |||||||
| chr8:33509207 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+539G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509207 | |||||||
| chr8:33509218 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+528A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509218 | |||||||
| chr8:33509241 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
391 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(388): Show |
intron_variant | MODIFIER | c.834+505T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509241 | |||||||
| chr8:33509254 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+492C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509254 | |||||||
| chr8:33509255 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+491T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509255 | |||||||
| chr8:33509259 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+487G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509259 | |||||||
| chr8:33509261 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+485C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509261 | |||||||
| chr8:33509262 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+484C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509262 | |||||||
| chr8:33509267 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+479C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509267 | |||||||
| chr8:33509268 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+478G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509268 | |||||||
| chr8:33509272 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+474C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509272 | |||||||
| chr8:33509279 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+467T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509279 | |||||||
| chr8:33509285 | C | T | 18 | a0001c0001t0001g0198 a0002c0003t0001g0015 a0002c0003t0001g0054 others(15): Show |
20 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.834+461G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509285 | |||||||
| chr8:33509286 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+460T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509286 | |||||||
| chr8:33509291 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+455A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509291 | |||||||
| chr8:33509312 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+434A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509312 | |||||||
| chr8:33509313 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+433A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509313 | |||||||
| chr8:33509314 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+432C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509314 | |||||||
| chr8:33509323 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+423C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509323 | |||||||
| chr8:33509325 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+421G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509325 | |||||||
| chr8:33509326 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+420T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509326 | |||||||
| chr8:33509328 | G | A | 3 | a0001c0001t0001g0198 a0002c0003t0002g0077 a0002c0003t0004g0078 |
3 | HG03209.hp1 NA18990.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.834+418C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509328 | |||||||
| chr8:33509329 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+417G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509329 | |||||||
| chr8:33509331 | C | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
202 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.834+415G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509331 | |||||||
| chr8:33509340 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+406G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509340 | |||||||
| chr8:33509341 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+405G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509341 | |||||||
| chr8:33509350 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+396C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509350 | |||||||
| chr8:33509357 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+389T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509357 | |||||||
| chr8:33509362 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.834+384G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509362 | |||||||
| chr8:33509375 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+371T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509375 | |||||||
| chr8:33509377 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+369T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509377 | |||||||
| chr8:33509380 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+366A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509380 | |||||||
| chr8:33509382 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+364T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509382 | |||||||
| chr8:33509384 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+362T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509384 | |||||||
| chr8:33509389 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+357C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509389 | |||||||
| chr8:33509392 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+354C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509392 | |||||||
| chr8:33509401 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+345C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509401 | |||||||
| chr8:33509403 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+343T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509403 | |||||||
| chr8:33509410 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+336G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509410 | |||||||
| chr8:33509411 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+335T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509411 | |||||||
| chr8:33509412 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+334G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509412 | |||||||
| chr8:33509413 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+333T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509413 | |||||||
| chr8:33509420 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+326G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509420 | |||||||
| chr8:33509425 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+321A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509425 | |||||||
| chr8:33509434 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+312A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509434 | |||||||
| chr8:33509435 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+311C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509435 | |||||||
| chr8:33509437 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+309A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509437 | |||||||
| chr8:33509442 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+304A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509442 | |||||||
| chr8:33509451 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+295G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509451 | |||||||
| chr8:33509454 | T | TTAAAAAA others(11): Show |
1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+291_834+292ins others(18): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509454 | |||||||
| chr8:33509455 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.834+291G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509455 | |||||||
| chr8:33509455 | C | CA | 5 | a0001c0001t0001g0052 a0001c0001t0001g0076 a0002c0002t0002g0141 others(2): Show |
6 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.834+290dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509455 | |||||||
| chr8:33509455 | CA | C | 11 | a0002c0002t0002g0099 a0002c0002t0002g0100 a0002c0002t0002g0101 others(8): Show |
11 | HG02273.hp1 HG02602.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.834+290delT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509455 | |||||||
| chr8:33509463 | AAAAAAAA others(7): Show |
A | 2 | a0002c0002t0002g0249 a0002c0002t0002g0251 |
2 | HG01243.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.834+269_834+282del others(14): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509463 | |||||||
| chr8:33509464 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.834+269_834+281del others(13): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509464 | |||||||
| chr8:33509473 | A | G | 3 | a0002c0002t0003g0018 a0002c0002t0003g0119 a0002c0002t0003g0120 |
5 | HG03669.hp2 HG03831.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+273T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509473 | |||||||
| chr8:33509475 | AAG | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0075 others(4): Show |
8 | HG01993.hp2 HG02451.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+269_834+270del others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509475 | |||||||
| chr8:33509476 | AG | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.834+269delC | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509476 | |||||||
| chr8:33509477 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(44): Show |
53 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.834+269C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509477 | |||||||
| chr8:33509660 | T | C | 1 | a0002c0002t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.834+86A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509660 | |||||||
| chr8:33509735 | A | C | 4 | a0002c0002t0001g0153 a0002c0002t0001g0156 a0002c0002t0001g0157 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+11T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 3/7 | chr8 | 33509735 | |||||||
| chr8:33509979 | C | CA | 18 | a0001c0001t0001g0095 a0002c0002t0001g0153 a0002c0002t0001g0156 others(15): Show |
20 | HG01109.hp1 HG01346.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.648-48dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33509979 | |||||||
| chr8:33509979 | CA | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
193 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.648-48delT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33509979 | |||||||
| chr8:33509979 | CAA | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(25): Show |
34 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.648-49_648-48delTT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33509979 | |||||||
| chr8:33510083 | A | G | 2 | a0002c0002t0002g0098 a0002c0002t0002g0238 |
2 | NA18961.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.648-151T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510083 | |||||||
| chr8:33510135 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.648-203A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510135 | |||||||
| chr8:33510147 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.648-215C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510147 | |||||||
| chr8:33510178 | A | G | 2 | a0002c0002t0002g0072 a0002c0002t0002g0154 |
2 | HG00738.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.648-246T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510178 | |||||||
| chr8:33510274 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.648-342G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510274 | |||||||
| chr8:33510330 | G | A | 1 | a0002c0002t0002g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.648-398C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510330 | |||||||
| chr8:33510442 | T | C | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.648-510A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510442 | |||||||
| chr8:33510449 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.648-517A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510449 | |||||||
| chr8:33510537 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0079 a0001c0001t0001g0080 |
5 | HG02258.hp2 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.648-605G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510537 | |||||||
| chr8:33510615 | G | C | 1 | a0002c0002t0002g0148 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.648-683C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510615 | |||||||
| chr8:33510674 | G | A | 2 | a0002c0002t0002g0149 a0002c0002t0002g0150 |
2 | NA18957.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.648-742C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510674 | |||||||
| chr8:33510785 | TCC | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.648-855_648-854del others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510785 | |||||||
| chr8:33510810 | T | C | 2 | a0002c0002t0002g0151 a0002c0002t0002g0152 |
2 | NA18939.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.648-878A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510810 | |||||||
| chr8:33510941 | T | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.648-1009A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33510941 | |||||||
| chr8:33511152 | A | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.647+815T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511152 | |||||||
| chr8:33511293 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.647+674A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511293 | |||||||
| chr8:33511360 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG00673.hp2 HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.647+607T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511360 | |||||||
| chr8:33511401 | G | A | 2 | a0002c0003t0002g0077 a0002c0003t0004g0078 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.647+566C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511401 | |||||||
| chr8:33511474 | T | TA | 17 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.647+492dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511474 | |||||||
| chr8:33511480 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+487C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511480 | |||||||
| chr8:33511482 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+485A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511482 | |||||||
| chr8:33511483 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+484T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511483 | |||||||
| chr8:33511484 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+483A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511484 | |||||||
| chr8:33511489 | T | C | 2 | a0002c0003t0002g0077 a0002c0003t0004g0078 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.647+478A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511489 | |||||||
| chr8:33511499 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+468T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511499 | |||||||
| chr8:33511501 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+466G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511501 | |||||||
| chr8:33511503 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+464G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511503 | |||||||
| chr8:33511509 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+458A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511509 | |||||||
| chr8:33511511 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+456G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511511 | |||||||
| chr8:33511512 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+455A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511512 | |||||||
| chr8:33511520 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+447T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511520 | |||||||
| chr8:33511523 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+444T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511523 | |||||||
| chr8:33511524 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+443C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511524 | |||||||
| chr8:33511525 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+442T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511525 | |||||||
| chr8:33511527 | CCGTGGTT others(4): Show |
C | 1 | a0001c0001t0001g0237 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.647+429_647+439del others(11): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511527 | |||||||
| chr8:33511529 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+438C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511529 | |||||||
| chr8:33511531 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+436C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511531 | |||||||
| chr8:33511532 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+435C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511532 | |||||||
| chr8:33511535 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+432T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511535 | |||||||
| chr8:33511540 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+427T>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511540 | |||||||
| chr8:33511542 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+425G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511542 | |||||||
| chr8:33511543 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+424G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511543 | |||||||
| chr8:33511545 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+422A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511545 | |||||||
| chr8:33511546 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+421T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511546 | |||||||
| chr8:33511547 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+420A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511547 | |||||||
| chr8:33511548 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+419A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511548 | |||||||
| chr8:33511549 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+418A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511549 | |||||||
| chr8:33511550 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+417A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511550 | |||||||
| chr8:33511564 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.647+403A>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511564 | |||||||
| chr8:33511566 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+401C>G | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511566 | |||||||
| chr8:33511567 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+400T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511567 | |||||||
| chr8:33511576 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+391A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511576 | |||||||
| chr8:33511580 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+387C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511580 | |||||||
| chr8:33511587 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+380C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511587 | |||||||
| chr8:33511599 | T | A | 5 | a0002c0002t0002g0045 a0002c0002t0002g0247 a0002c0002t0002g0248 others(2): Show |
6 | HG02486.hp1 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+368A>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511599 | |||||||
| chr8:33511608 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+359C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511608 | |||||||
| chr8:33511610 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+357T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511610 | |||||||
| chr8:33511626 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+341C>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511626 | |||||||
| chr8:33511629 | T | G | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.647+338A>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511629 | |||||||
| chr8:33511633 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+334T>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511633 | |||||||
| chr8:33511672 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.647+295C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511672 | |||||||
| chr8:33511757 | C | A | 1 | a0002c0002t0001g0158 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.647+210G>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511757 | |||||||
| chr8:33511942 | G | A | 17 | a0002c0003t0001g0015 a0002c0003t0001g0054 a0002c0003t0001g0055 others(14): Show |
19 | HG00140.hp2 HG00280.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.647+25C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 2/7 | chr8 | 33511942 | |||||||
| chr8:33512734 | CAG | C | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-99-24_-99-23delCT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512734 | |||||||
| chr8:33512743 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(58): Show |
97 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-99-31C>T | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512743 | |||||||
| chr8:33512778 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
15 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.-99-66T>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512778 | |||||||
| chr8:33512877 | T | TA | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(62): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-99-166dupT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512877 | |||||||
| chr8:33512877 | T | TAA | 9 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(6): Show |
9 | HG02615.hp2 HG02809.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99-167_-99-166dup others(2): Show |
TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512877 | |||||||
| chr8:33512877 | TA | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0028 others(31): Show |
41 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.-99-166delT | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33512877 | |||||||
| chr8:33513073 | C | G | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-100+9G>C | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33513073 | |||||||
| chr8:33513081 | C | T | 3 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0046 |
5 | HG02055.hp1 HG02145.hp2 HG02818.hp1 others(2): Show |
splice_donor_variant&intron_variant | HIGH | c.-100+1G>A | TTI2 | ENSG00000129696.13 | transcript | ENST00000431156.7 | protein_coding | 1/7 | chr8 | 33513081 |