SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs749213 | snp | A/T | 0.371582 | 0.218444 | intron-variant | TINCR | GRCh38.p7 | 19:5564229 | GACGGTACCCTAGGG[A/T]GAGAGAAGCTGCGTG | 257000 |
rs1806964 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | TINCR | GRCh38.p7 | 19:5563732 | ccagcctggccaaca[A/T]ggtgaaacggtctct | 257000 |
rs2288946 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562073 | TTCTCAACTACTACA[A/G]TTACTTACCTGGAGT | 257000 |
rs2288947 | snp | A/G | 0.497641 | 0.0342639 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562104 | GAGATCTAGGCTCCC[A/G]GGAGGCAGGAGAAGT | 257000 |
rs7246801 | snp | C/T | 0.2768 | 0.248559 | intron-variant | TINCR | GRCh38.p7 | 19:5564522 | GTGTGTGGTCAGGGA[C/T]GGGCAAGGGGCAGGG | 257000 |
rs7249815 | snp | C/T | 0 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569907 | atggcacaatctcgg[C/T]tcaccgcaacctccg | 257000 |
rs7250122 | snp | C/T | 0.381503 | 0.21262 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559427 | GCAACCTCTGCCTCC[C/T]GGGTTCCCGCCATTC | 257000 |
rs8105637 | snp | A/G | 0.476487 | 0.105846 | intron-variant | TINCR | GRCh38.p7 | 19:5566221 | aaatgcagagacacc[A/G]gagagataaagagac | 257000 |
rs8113645 | snp | A/G | 0.377187 | 0.215229 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561065 | AAGGTGTGGCTGGGA[A/G]AATGTCCTGGGCAAG | 257000 |
rs10451477 | snp | C/G | 0.298398 | 0.245271 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560801 | CACAGTTGGAGGCCT[C/G]AGAAGGAGCTAGGAT | 257000 |
rs11085142 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557938 | CCCTGGCGGGGAGCG[A/G]GCAGGATTCCCTGAG | 257000 |
rs11670013 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TINCR | GRCh38.p7 | 19:5561893 | ACGGCTCTGGTCCAC[A/G]TGTTAGTCCAAAAAG | 257000 |
rs11880534 | snp | C/T | 0.243633 | 0.249919 | intron-variant | TINCR | GRCh38.p7 | 19:5563331 | ggcTGCGGACCTTGG[C/T]GGGGGGCAACTGGGC | 257000 |
rs12610531 | snp | A/G | 0.342582 | 0.232225 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559819 | AGGCTCTAGATACAC[A/G]CATGTGGCCCAGCTG | 257000 |
rs12610866 | snp | A/C/G | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5563520 | GGGAGAAGGTTTAGT[A/C/G]ATGAAGGGCGTGGCT | 257000 |
rs12980823 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5567627 | AGGGGTccccggccg[C/T]cgcccccgccccacc | 257000 |
rs12983488 | snp | C/T | 0.259397 | 0.249823 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559105 | GTGGTGATTTGCATG[C/T]GATTTGCATGTGATT | 257000 |
rs28594941 | snp | A/C | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568603 | GCCTGGAATCCCAGC[A/C]CTTTGGGAGACTGAG | 257000 |
rs28607963 | snp | A/C | 0.278399 | 0.248382 | intron-variant | TINCR | GRCh38.p7 | 19:5565073 | TCCCACCTCCCTCGG[A/C]GTCAAGGCCCAAGTC | 257000 |
rs34152404 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559056 | ACATTATTATTTCAG[-/G]AACATGCCAGCGCTG | 257000 |
rs34278246 | in-del | -/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559151 | AATGTCAAAACACCC[-/C]TGAAAATGCTTTCTC | 257000 |
rs34526855 | in-del | -/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557804 | AGGTGGGCGGCCAAG[-/T]ACGGGAGGTGGCCCC | 257000 |
rs34657688 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558786 | GCTGTGGGACCTTAG[-/G]CCCATGCCTCAGTTT | 257000 |
rs35571988 | in-del | -/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564237 | TTCTCTCTCCCTAGG[-/G]TACCGTCTGCGCTGA | 257000 |
rs35825675 | in-del | -/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559767 | GACGAGGCATGTCCC[-/C]TGAATATGCACAGGG | 257000 |
rs35974274 | in-del | -/T | 0.392696 | 0.205275 | intron-variant | TINCR | GRCh38.p7 | 19:5564515 | CAGCTGTGTGTGTGG[-/T]CAGGGATGGGCAAGG | 257000 |
rs45500293 | snp | C/T | 0.0119091 | 0.0762411 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560569 | CCGGAATTCCCACAA[C/T]GCACTCCCTGCAATG | 257000 |
rs45575840 | snp | C/G | 0.49703 | 0.0384237 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559889 | CTGCCTCCCCCTGCT[C/G]TGTGTCCCTGACAAC | 257000 |
rs56917160 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | TINCR | GRCh38.p7 | 19:5564894 | AAACTGTCTCCTCTG[A/C]AGGCTTCTGTTCTCT | 257000 |
rs58473504 | snp | A/G | 0.0310518 | 0.120672 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560783 | TTGGGGGTGGAAATG[A/G]GGCACAGTTGGAGGC | 257000 |
rs60466689 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | TINCR | GRCh38.p7 | 19:5567080 | AATGGAGAGAGAGAC[A/G]GAGACAAAGACAAAA | 257000 |
rs60513056 | in-del | -/AAGA | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569203 | AGAAAGAAAGAAAGA[-/AAGA]GGGAGAGAGAGAGAA | 257000 |
rs62637989 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TINCR | GRCh38.p7 | 19:5566367 | AGAGAAACAGAGAGA[C/T]AAAAGAGACACACAG | 257000 |
rs72977062 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5563426 | GCTGAAGGACAGATA[A/G]AGGGGCTTGGGAGGA | 257000 |
rs73920015 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | TINCR | GRCh38.p7 | 19:5561531 | GTGATCTGCAGTCAT[C/T]CCCTCCTGTGGATGT | 257000 |
rs73920016 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | TINCR | GRCh38.p7 | 19:5562298 | CTATTCTGCCCACTG[G/T]CTGGCTGGTGCCTCT | 257000 |
rs73920017 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TINCR | GRCh38.p7 | 19:5564305 | AGCTGAGGCCTCCCC[A/G]GCTGCTGCTGCACCA | 257000 |
rs74173058 | in-del | -/AAA | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568877 | AAAAAAAAAAAAAAA[-/AAA]TGGCCGGGTGTGGTG | 257000 |
rs74174330 | snp | C/T | 0.282105 | 0.24793 | intron-variant | TINCR | GRCh38.p7 | 19:5567590 | AGGCCGCCTTGGGCG[C/T]CCGCCTCCCCCGCCG | 257000 |
rs74411837 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558263 | CGGCCCCAAAGGTAG[C/T]GATGACTCTGCTGGG | 257000 |
rs74795022 | snp | G/T | 0.485187 | 0.0847778 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568593 | GGTGGCTCATGCCTG[G/T]AATCCCAGCACTTTG | 257000 |
rs74896816 | snp | A/G | 0.0349115 | 0.127424 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557888 | AACTCCTCATAGCCC[A/G]GACTTGCTCAGGGTG | 257000 |
rs75239626 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5565045 | CCCTCCTCTGCCCAC[A/C]GCCCTCTATGGCTCC | 257000 |
rs76001042 | snp | C/G/T | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569831 | TTACACAAACATCAC[C/G/T]TTTTTTTTTTTTTTT | 257000 |
rs77608060 | snp | A/C | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567764 | TTGTAGTAGAAGGCG[A/C]GCTTCCAGGAGCTCA | 257000 |
rs78647018 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | TINCR | GRCh38.p7 | 19:5562430 | CCTCTGCTCACGATT[A/G]TGTTAGTGAGACAAT | 257000 |
rs79094586 | snp | G/T | 0.0146672 | 0.084371 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561370 | AGCTGGTCAGGCCAG[G/T]GTTTCATGGTCCACC | 257000 |
rs79327432 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565738 | CCAGACTCCTGCAAC[A/C/G]GGGTGGCATCTGAGG | 257000 |
rs79820213 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569849 | TTTTTTTTTTTTTTT[G/T]TTTGAGACAGAGTTT | 257000 |
rs111235842 | snp | A/G | 0.5 | 0 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560907 | ACAAAGGGCCTGTGG[A/G]GGCCCCAAAGAAGGC | 257000 |
rs111322013 | snp | G/T | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5564514 | CCAGCTGTGTGTGTG[G/T]TCAGGGATGGGCAAG | 257000 |
rs111526643 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569185 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 257000 |
rs111573120 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566820 | GACACACACACAGAG[A/G]AAAAAAGCAGAGACC | 257000 |
rs111780351 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5564273 | CCCAAGTGTTTTTCT[C/T]ATTTCTCACATGGGG | 257000 |
rs112021269 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565034 | TCAGGTCCCGTCCCT[C/T]CTCTGCCCACAGCCC | 257000 |
rs112098968 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | TINCR | GRCh38.p7 | 19:5563802 | CGCCTGTAATCCCAG[C/T]TACTCAGGAGACTGA | 257000 |
rs112164487 | snp | G/T | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5564515 | CAGCTGTGTGTGTGG[G/T]CAGGGATGGGCAAGG | 257000 |
rs112451690 | snp | A/G | 0.5 | 0 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559106 | TGGTGATTTGCATGC[A/G]ATTTGCATGTGATTT | 257000 |
rs114008877 | snp | A/G | 0.0379877 | 0.132479 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559635 | CCACCGCGCCTGGCC[A/G]GCTGTCAATCAAGTG | 257000 |
rs115018845 | snp | A/T | 0.0185938 | 0.0946107 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559653 | TGTCAATCAAGTGAG[A/T]CAGGGCTCCAAAAAG | 257000 |
rs115757604 | snp | A/G | 0.0150606 | 0.0854603 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559226 | CCTCCACCAGCTCCC[A/G]GCATGGGTTGGGGAC | 257000 |
rs115816841 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562115 | TCCCGGGAGGCAGGA[G/T]AAGTGCCTTCCAAAA | 257000 |
rs117012071 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | TINCR | GRCh38.p7 | 19:5564196 | AGAGAGGGCCTGGCA[C/G]GTTTGTCCCGAGCAG | 257000 |
rs117030331 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TINCR | GRCh38.p7 | 19:5565594 | AGAAGGTACGCTGCC[A/G]AGAACACCCTCTCCT | 257000 |
rs117305966 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TINCR | GRCh38.p7 | 19:5565516 | GGCACACAATAAATG[C/T]TGACTCTGTACTGCA | 257000 |
rs117655447 | snp | A/G | 0.0217236 | 0.101931 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557998 | GCCTGGGGTCAACTG[A/G]AGTAACAGTGTCACC | 257000 |
rs137918324 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559358 | TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 257000 |
rs137971419 | in-del | -/AGAG | 0.0479149 | 0.147179 | intron-variant | TINCR | GRCh38.p7 | 19:5567095 | AGAGACAAAGACAAA[-/AGAG]AGAGAGGTGAGGAGA | 257000 |
rs138458164 | snp | C/T | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559909 | TCCCTGACAACCTCC[C/T]TGGGCCTCAGGCTAC | 257000 |
rs138492500 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TINCR | GRCh38.p7 | 19:5565445 | TGAAGGCGAAATCTG[G/T]TCTCTCTGGGTCACT | 257000 |
rs138533582 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | TINCR | GRCh38.p7 | 19:5564450 | ACAGCAAAGGCAGAT[-/A]GGGGCCCCTGTCTGT | 257000 |
rs138897422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567059 | AGAGGAAAAAACAGA[G/T]ACCAAAATGGAGAGA | 257000 |
rs139157509 | snp | C/T | 0.0341408 | 0.126114 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568844 | ACAGAGCGAGACTTA[C/T]CGCAAAAAAAAAAAA | 257000 |
rs139265480 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TINCR | GRCh38.p7 | 19:5562629 | GGGAAAGAGAGAAAG[C/T]AGGGATGGCGTGAAA | 257000 |
rs139853105 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569743 | TTTCCCAGAGGAAAC[A/C]GAGAGAAAAGTGGCA | 257000 |
rs139980198 | in-del | -/TT | 0.384401 | 0.210799 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559335 | GTGAGGCTGTCAATC[-/TT]TTTTTTTTTTTTTTT | 257000 |
rs140195060 | snp | A/G | 0.00318978 | 0.0398085 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558634 | GTTCCCCTTGGCCCT[A/G]TCAAGCCTATCAGGC | 257000 |
rs141422868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566380 | GACAAAAGAGACACA[C/G]AGAGAGAAAAAGAGC | 257000 |
rs142186312 | snp | A/G | 0.0138799 | 0.0821421 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558250 | CTGGGTGATCCTGCG[A/G]CCCCAAAGGTAGTGA | 257000 |
rs142563466 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TINCR | GRCh38.p7 | 19:5564760 | TGTTTGTATTTTTAG[C/T]AGAGACAGCGTTTCG | 257000 |
rs142848587 | in-del | -/AGAC | 0.00716266 | 0.059414 | intron-variant | TINCR | GRCh38.p7 | 19:5566636 | GACAAATGGACAAAG[-/AGAC]AGAGAGACAGGGAGA | 257000 |
rs142989275 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560073 | GGCACACCCAGGGGC[C/T]AGCAAGACCCAAGTC | 257000 |
rs143214372 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569913 | CAATCTCGGCTCACC[A/G]CAACCTCCGCCTCCC | 257000 |
rs144530222 | snp | A/C | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568817 | TTGTGCCACTGCACT[A/C]CAGCCTGAGCCACAG | 257000 |
rs144595015 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TINCR | GRCh38.p7 | 19:5565014 | GGTTGCCTGTGAGCA[C/T]TGAGTCAGGTCCCGT | 257000 |
rs144964531 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569332 | AATCCCAACACTTTG[A/G]GAGGCCGAGGTGGGC | 257000 |
rs144974663 | in-del | -/A | | | intron-variant | TINCR | GRCh38.p7 | 19:5562246 | AGACACAGGTTGCAG[-/A]AAAAACATAGCCCTT | 257000 |
rs145298912 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557923 | CCAGAGTCTGAGAGG[C/T]CCTGGCGGGGAGCGA | 257000 |
rs145448639 | in-del | -/AG | 0.0260105 | 0.111035 | intron-variant | TINCR | GRCh38.p7 | 19:5566596 | GAGACACAGAGAGAC[-/AG]AGAGAGAAAAACAGC | 257000 |
rs145561914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564242 | TCTCCCTAGGGTACC[A/G]TCTGCGCTGACAGGT | 257000 |
rs145905786 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559802 | GAGGACAGAGGGGAC[C/T]CAGGCTCTAGATACA | 257000 |
rs146114884 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561240 | AACCTCAAAGTCACA[C/T]AGCAGAGCTGAAAGG | 257000 |
rs147245240 | snp | C/T | 0.0267878 | 0.112589 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568604 | CCTGGAATCCCAGCA[C/T]TTTGGGAGACTGAGG | 257000 |
rs147633982 | snp | A/G | 0.0123036 | 0.0774623 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5558026 | ACCTGGAGTAACAGC[A/G]TCACCTGGAGTAACA | 257000 |
rs148109864 | snp | C/T | 0.0422008 | 0.138995 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568138 | GCCCCAGAGTGCGCC[C/T]GGGGGTCTAGAGGCG | 257000 |
rs148336825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561620 | TTTCTTTCTTTTTTT[C/T]GAGACAGAGTCCTGC | 257000 |
rs148492276 | snp | A/G | 0.00755907 | 0.0610114 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557833 | CCTCCCCAGAACGCC[A/G]CGGGCCTTAGCGAGA | 257000 |
rs148951692 | in-del | -/A | 0.031825 | 0.122064 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559124 | TTGCATGTGATTTGC[-/A]TACTGTTTGTTAAAT | 257000 |
rs149921261 | snp | C/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569261 | AGAAAGAAAGAGAGA[C/G]AGAGAGGAAGAGAAG | 257000 |
rs150255652 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5566943 | AGTGGGCAGAGACAC[A/T]GAGTGACAGAGAAAA | 257000 |
rs150308546 | snp | A/C | 0.00159617 | 0.0282053 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558649 | GTCAAGCCTATCAGG[A/C]CTGGAGCTTCCTCAA | 257000 |
rs150786329 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568843 | CACAGAGCGAGACTT[A/G]TCGCAAAAAAAAAAA | 257000 |
rs150838947 | snp | C/T | 0.00438332 | 0.0466095 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562195 | GTCATGGCTCTGCCT[C/T]CTCCAACCCAGACTA | 257000 |
rs150949434 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | TINCR | GRCh38.p7 | 19:5564781 | CAGCGTTTCGCCATG[G/T]TGGCCAGGCTGGTCT | 257000 |
rs151177308 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558345 | GACTGGAAGCAGCAG[C/G]GTCCTTGAGGGAAGT | 257000 |
rs180759742 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558349 | GGAAGCAGCAGGGTC[C/T]TTGAGGGAAGTAGGC | 257000 |
rs181190366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565764 | TGAGGCTCCTGCCCT[C/G]AAAACATCAACCCAG | 257000 |
rs181519676 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569931 | ACCTCCGCCTCCCAG[A/G]TGCAAGCAATTCTCC | 257000 |
rs181530244 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565379 | TGCATCCCCCACAGC[A/G]CCAATTGCGAGTTGA | 257000 |
rs181563237 | snp | C/T | 0.00636936 | 0.0560724 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5570026 | TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT | 257000 |
rs181726638 | snp | A/C | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559004 | AAGGAAAAGGCCGTG[A/C]ACCTCCCGACCCAGG | 257000 |
rs182074465 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560993 | GCAATCCCAGGTGTA[C/T]TGGAGCTGCAGAGAA | 257000 |
rs182551343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5564869 | AGGTGTGAACCATTG[C/T]GCCCAGCCAAAACTG | 257000 |
rs182877343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566915 | AAACAGGGAGGAAAA[C/T]AGCAGAGAGAGAAGT | 257000 |
rs183387683 | snp | A/G | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560247 | AGCAGGAGACCCCGG[A/G]CCAAGTGCTGTCCCC | 257000 |
rs183832742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562064 | CCTTTCTCTTTCTCA[A/G]CTACTACAATTACTT | 257000 |
rs184102146 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557733 | TCTCCTCTGGGAACC[A/G]CCTGGGCTCACTTGC | 257000 |
rs184132778 | snp | A/C | 0.0185938 | 0.0946107 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567975 | GGGCCCCGAGCGCCC[A/C]GCGCACCCGCCCGAC | 257000 |
rs184159389 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5566431 | ACAGAGAAAGAGAGA[C/G]AGAAATGGAGAGACA | 257000 |
rs184256906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562675 | TATTTCTTTAGAGAC[A/G]GAGTTTCACCCTGTC | 257000 |
rs185235984 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565821 | CTGGTGAATGTGACC[C/T]CCATAAAATCCAGGG | 257000 |
rs185366554 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560398 | AGCCTCTGGCGCCTC[C/T]GCCCATGGTGCCTGG | 257000 |
rs185519650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565401 | GCGAGTTGACATTCT[C/T]CTGTGCTATTATTTG | 257000 |
rs185759928 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568790 | GCAGACAGAGGTTGC[A/C]GTGAGCCGAGATTGT | 257000 |
rs186478254 | snp | C/G | 0.00318978 | 0.0398085 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558363 | CCTTGAGGGAAGTAG[C/G]CTCTCCTTGAAGGAT | 257000 |
rs187117653 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5564966 | TCTCCAGCCCTCCCC[A/C]CATCACAGTCTGTTC | 257000 |
rs187152554 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559625 | CAGGCGTGAGCCACC[A/G]CGCCTGGCCGGCTGT | 257000 |
rs187177016 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5567010 | TCATCAGGGAAAGAA[A/C]TAAACAGAGGCAGAG | 257000 |
rs187769157 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561084 | GTCCTGGGCAAGAGC[A/G]GAAGTGCCTCTGAGT | 257000 |
rs187988253 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568221 | GCGCGAATGTCCAGG[G/T]GGTTACATGGTGGAG | 257000 |
rs188394963 | snp | C/T | 0.00914312 | 0.0669923 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5558102 | AGCTCAGCCCAAAAC[C/T]ATAGATGGGGTAGAA | 257000 |
rs188663913 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TINCR | GRCh38.p7 | 19:5566542 | ACACAGAGAGAGATG[A/C]GCGCACACACAGACA | 257000 |
rs188791215 | snp | C/T | 0.00755907 | 0.0610114 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562137 | CTTCCAAAAGTGCCC[C/T]CTACCCCAGCCTATT | 257000 |
rs189151597 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TINCR | GRCh38.p7 | 19:5564282 | TTTTCTCATTTCTCA[C/T]ATGGGGAAGCTGAGG | 257000 |
rs189297333 | snp | G/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558421 | ATTGAAGCTAGGGCT[G/T]TGAAGGATGAATAGG | 257000 |
rs189784154 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560931 | AGAAGGCTAGGTGCT[C/T]TCTGGCTGGGAAGGA | 257000 |
rs189924282 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TINCR | GRCh38.p7 | 19:5565437 | AGGCTCTGTGAAGGC[A/G]AAATCTGGTCTCTCT | 257000 |
rs190234114 | snp | A/C/T | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569912 | ACAATCTCGGCTCAC[A/C/T]GCAACCTCCGCCTCC | 257000 |
rs190331498 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5565187 | CCACACGGGCCTCCT[C/T]GCTGTTCCTCCAACA | 257000 |
rs190700418 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569874 | GAGTTTCACTCTTGT[C/T]GCCCAGGGTGGAGTA | 257000 |
rs190715967 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566158 | AGGGAGAGACCAGAG[A/C]AGGAAGAGAGAGACA | 257000 |
rs191455387 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5563911 | CAGAGCAAGACTCCC[A/G]TCTCAAAAATAATAA | 257000 |
rs191525209 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559961 | CAGACTCTGCTCTAG[C/G]AGGAGCTCCAGGGGG | 257000 |
rs191932253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567352 | GAGATGAGAGACAGA[C/G]ACAAAAGAAGAAGAG | 257000 |
rs191937655 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TINCR | GRCh38.p7 | 19:5566734 | AGACAGACACAGAGA[A/G]ACACAAGGAGAAAAA | 257000 |
rs192218804 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568522 | GGTGGGATTATAACC[C/T]TCAGCCACCACGCTC | 257000 |
rs192857226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562458 | AATACATCTCACTAA[C/T]ATTTATTAAGCACCT | 257000 |
rs193301021 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TINCR | GRCh38.p7 | 19:5561932 | CACCAAGGCCATGTC[A/C]CTACCCTAGAGGCCA | 257000 |
rs199587430 | in-del | -/AAAG | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569182 | AAAAAAAAAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 257000 |
rs199623576 | in-del | -/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569509 | AACCCAGGAGGTGGA[-/G]GGTTGTGGTGAGCGG | 257000 |
rs200144293 | in-del | -/AAAGAA | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569198 | AAGAAAGAAAGAAAG[-/AAAGAA]AGAGGGAGAGAGAGA | 257000 |
rs201829803 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569324 | ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCG | 257000 |
rs367552290 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561511 | TAACATCCCTGACAC[A/G]GACAGTGATCTGCAG | 257000 |
rs367828360 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561062 | GCAAAGGTGTGGCTG[C/G]GAAAATGTCCTGGGC | 257000 |
rs368002932 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5563223 | GCCATGGAGGGCTGC[C/T]GGCAGAGGAGGGACA | 257000 |
rs368161804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563088 | AGGCCTGTGTGGCTG[C/G]AGCAGAGTGAGGAAG | 257000 |
rs368555545 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5561670 | GCAATGGCGTGATTT[C/T]GGCTCACTGTAACCT | 257000 |
rs368783791 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562615 | GCTGACAAGTGATGG[A/G]GAAAGAGAGAAAGCA | 257000 |
rs369141157 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566596 | AGAGACACAGAGAGA[C/G]AGAGAGAAAAACAGC | 257000 |
rs369260337 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558821 | ACCTGGAAAATGGGC[C/T]GCAGGAAGCCACTTT | 257000 |
rs369312858 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563245 | GGAGGGACACGCCCC[A/G]ACTCAGGGGCTCACA | 257000 |
rs369911004 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TINCR | GRCh38.p7 | 19:5564217 | TCCCGAGCAGCCCAC[A/G]CAGCTTCTCTCTCCC | 257000 |
rs369944700 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569780 | GGATTCGAACCCAGG[C/T]CACCTAGCATTAGCA | 257000 |
rs370078990 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565028 | ATTGAGTCAGGTCCC[A/G]TCCCTCCTCTGCCCA | 257000 |
rs370850408 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560439 | CGGCCCTCGAGGACA[C/T]GCGTAGCCTCGGCAC | 257000 |
rs370999846 | in-del | -/GA | | | intron-variant | TINCR | GRCh38.p7 | 19:5566597 | AGAGAGACAGAGAGA[-/GA]AAAACAGCAGAGACA | 257000 |
rs371506156 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | TINCR | GRCh38.p7 | 19:5566302 | ACAGAGACAGAGACA[C/G]AGAGAGAGAAATACA | 257000 |
rs371540600 | snp | C/T | 0.000437904 | 0.0147905 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561039 | TCCAGGCAGGGGGCA[C/T]GGCTTGGGCAAAGGT | 257000 |
rs371543088 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569276 | GAGAGAGGAAGAGAA[A/G]GAAAAAAAGAGAAGG | 257000 |
rs371703072 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568816 | ATTGTGCCACTGCAC[C/T]CCAGCCTGAGCCACA | 257000 |
rs371954620 | in-del | -/CT | 0.00478085 | 0.0486577 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559127 | CATGTGATTTGCATA[-/CT]GTTTGTTAAATGTCA | 257000 |
rs372013567 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562720 | GTAATGGCACGATCT[C/T]AGCTCACTGCAACCT | 257000 |
rs372150188 | snp | G/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557840 | AGAACGCCGCGGGCC[G/T]TAGCGAGACGGCAGC | 257000 |
rs372628867 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561929 | AGACACCAAGGCCAT[A/G]TCCCTACCCTAGAGG | 257000 |
rs372679389 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558683 | AGCTCTGACAACTCC[A/G]GCCACTGTCATCTCC | 257000 |
rs372795870 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559019 | CACCTCCCGACCCAG[A/G]TCATCATCAAGGGAC | 257000 |
rs372849687 | snp | A/G | 0 | 0 | intron-variant | TINCR | GRCh38.p7 | 19:5564602 | CTTTTGTTTTGAGAC[A/G]GAGTCTCACTCTGTT | 257000 |
rs373138597 | snp | A/T | 0.000437904 | 0.0147905 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561119 | CTCCTGCCCCTTCTG[A/T]GCTTCTCTTCTTGCG | 257000 |
rs373591879 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565451 | CGAAATCTGGTCTCT[C/T]TGGGTCACTGCTGAA | 257000 |
rs373710542 | in-del | -/GAGA | | | intron-variant | TINCR | GRCh38.p7 | 19:5567337 | GAAAGAAGAGGGAGA[-/GAGA]TGAGAGACAGAGACA | 257000 |
rs374313587 | snp | G/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5567629 | GGGTCCCCGGCCGCC[G/T]CCCCCGCCCCACCCC | 257000 |
rs374329959 | snp | A/C | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559883 | TCTGGGCTGCCTCCC[A/C]CTGCTGTGTGTCCCT | 257000 |
rs374462892 | snp | G/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562554 | AGTTTACAGTCTACT[G/T]CAGGAGACAGGTGAA | 257000 |
rs374909757 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566086 | GGGGACCCAGATATC[C/G]AAGTGTGAGTGTGGG | 257000 |
rs374980355 | snp | G/T | 0.00131314 | 0.0255899 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561058 | TTGGGCAAAGGTGTG[G/T]CTGGGAAAATGTCCT | 257000 |
rs375049123 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562639 | GAAAGCAGGGATGGC[A/G]TGAAATAAAATTTTA | 257000 |
rs375162648 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562766 | AAGCGATTCTCTTGC[C/T]TCAGCCTCCCCAGTA | 257000 |
rs375242818 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562220 | AGACTACCTGAAAGA[A/G]GGAGACAGAAAGACA | 257000 |
rs375611494 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563900 | AGCCTGGGCGACAGA[A/G]CAAGACTCCCGTCTC | 257000 |
rs375978801 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566594 | ACAGAGACACAGAGA[C/G]ACAGAGAGAAAAACA | 257000 |
rs376157995 | in-del | -/GA | | | intron-variant | TINCR | GRCh38.p7 | 19:5566215 | AGAGAAAAATGCAGA[-/GA]CACCAGAGAGATAAA | 257000 |
rs377018412 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565514 | TAGGCACACAATAAA[C/T]GCTGACTCTGTACTG | 257000 |
rs377612792 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TINCR | GRCh38.p7 | 19:5565386 | CCCACAGCGCCAATT[A/G]CGAGTTGACATTCTC | 257000 |
rs527414652 | in-del | -/AA | 0.00318978 | 0.0398085 | intron-variant | TINCR | GRCh38.p7 | 19:5566778 | AATGGGCAGAGACAC[-/AA]AGAGACAAAGGGGAA | 257000 |
rs527449388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5567420 | TGAGAGTGACAGAGA[C/T]AAAAGAGAGAGAGGC | 257000 |
rs527738933 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557829 | GGCCCCTCCCCAGAA[C/T]GCCGCGGGCCTTAGC | 257000 |
rs527815618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565593 | TAGAAGGTACGCTGC[C/T]GAGAACACCCTCTCC | 257000 |
rs527874378 | in-del | -/CA | 0.0023933 | 0.0345097 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560277 | CGAGCTAAGCAAACG[-/CA]CAGTCTGGGCACGGC | 257000 |
rs528314278 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TINCR | GRCh38.p7 | 19:5562254 | GTTGCAGAAAAAACA[C/T]AGCCCTTGCCTTGGC | 257000 |
rs528863301 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568576 | ACTTTTAGGCCAGGT[G/T]CGGTGGCTCATGCCT | 257000 |
rs528989652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561742 | TTTCTGCCACCTGAT[A/G]GCAGTCACAGGAATT | 257000 |
rs529011875 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561033 | AAGTGCTCCAGGCAG[G/T]GGGCACGGCTTGGGC | 257000 |
rs529029216 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569078 | GCTGAGGCAAGAGAA[A/T]GGCGTGAACCTGGGA | 257000 |
rs529162970 | in-del | -/AAAAG | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569577 | GAAACTCCGTCTCAA[-/AAAAG]AAAAGAAAAGAAAAG | 257000 |
rs529242706 | snp | A/G | 0.00279162 | 0.0372561 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560349 | CTGAGTCCTGCAGCC[A/G]ACAGGACTCTTAACT | 257000 |
rs529296033 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559526 | ACTTTTAGTAGAGAC[C/G]GGGTTTCACCGTGTT | 257000 |
rs529910482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5564428 | CCTCGGGACACACAG[C/T]CAGTGAACAGCAAAG | 257000 |
rs529952256 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560821 | GGAGCTAGGATGTCC[A/G]CATCTCCCCGCTTAG | 257000 |
rs530198987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562606 | AAGTCGGCTGCTGAC[A/G]AGTGATGGGGAAAGA | 257000 |
rs530235634 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569975 | CCGAGTAGCTGGGAT[G/T]ACAGGCATGCGCCAC | 257000 |
rs530355133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563582 | CTTCCCAGCTTAATC[C/T]TACTCTGCCTCAGCT | 257000 |
rs530430882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562460 | TACATCTCACTAACA[C/T]TTATTAAGCACCTAC | 257000 |
rs530488418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564774 | GTAGAGACAGCGTTT[C/T]GCCATGTTGGCCAGG | 257000 |
rs531156233 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569950 | AAGCAATTCTCCTGC[C/T]TCAGCCTTCCCGAGT | 257000 |
rs531280187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562033 | CCCCATCTATGGTCT[C/T]CACAATCTCTAAGGT | 257000 |
rs531371230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5565754 | GGGTGGCATCTGAGG[C/T]TCCTGCCCTCAAAAC | 257000 |
rs531544687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566376 | GAGAGACAAAAGAGA[C/G]ACACAGAGAGAAAAA | 257000 |
rs531905760 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557782 | TGGACCTTCTTGGAG[C/G]ACAAACTAGGTGGGC | 257000 |
rs532034280 | in-del | -/GA | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5561456 | GGACCAGGGAAGGGT[-/GA]AACACCAGTTCTCCA | 257000 |
rs532440092 | snp | G/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558371 | GAAGTAGGCTCTCCT[G/T]GAAGGATAAGCAATG | 257000 |
rs532609010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563626 | ACCGCCAATGATAAC[A/G]GCACCCGGCCAGGCA | 257000 |
rs532713402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564258 | TCTGCGCTGACAGGT[C/T]CCAAGTGTTTTTCTC | 257000 |
rs532993246 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568462 | TGCCCAGGCTGGTTT[C/T]GAACTCCTGACGTCA | 257000 |
rs533094523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567580 | CCGGCCCGGGAGGCC[A/G]CCTTGGGCGCCCGCC | 257000 |
rs533159826 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560496 | GCTGCGCAACGATGA[C/T]GTGGCTGCAGGTCAG | 257000 |
rs533167937 | in-del | -/GGCTGGAGCGC | 0.00399998 | 0.044542 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568288 | ATCTTTTTAAGGACA[-/GGCTGGAGCGC]AGTGGCGCAATCATG | 257000 |
rs533339705 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558459 | CAAACAAAGAAGGTG[A/G]GACATGCAAACCAAG | 257000 |
rs533372437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565664 | AGCCTCCCCGTCCCC[A/G]CTAAGATCTTCCCTC | 257000 |
rs533678313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565904 | CCCAGGCTCTGAGAC[A/G]AGGCCCCACCATCTT | 257000 |
rs533714583 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | TINCR | GRCh38.p7 | 19:5565497 | TGGAGTCTGGCACAC[-/A]GTAGGCACACAATAA | 257000 |
rs533739617 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558721 | GTGTCACGAGGACCA[C/T]GCACTTTGGTGCATG | 257000 |
rs534892898 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568046 | GCCCGGACACGCCCG[C/G]CACGCAGTGGGCAGG | 257000 |
rs535074368 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560604 | GCGATGACCTCCCAC[A/G]GCTAGGCCCAGTTCC | 257000 |
rs535388103 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560706 | CAAGACGAGGCATCC[A/G]GATTTAAGGGGAAGG | 257000 |
rs535446271 | snp | C/T | 0.00159617 | 0.0282053 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567823 | GTCGCTGAGCGTGTC[C/T]CGCGGCCGCACGGTC | 257000 |
rs536035234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566139 | GTGGGAAAGATAAGG[C/T]GGTAGGGAGAGACCA | 257000 |
rs536327481 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559090 | AGGCTTAAGAAATGG[A/G]TGGTGATTTGCATGC | 257000 |
rs536388262 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569436 | AAAAATTAGCCAGGC[A/G]TGGTGGTGGGTGCCT | 257000 |
rs536520766 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567367 | GACAAAAGAAGAAGA[A/G]ACAGAGATGAGAGAC | 257000 |
rs536558558 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565997 | TCCCGTGGCCCCAGC[A/G]CCCTTCTCTGCAGAC | 257000 |
rs537131274 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566254 | AGACACACATGTTGA[A/G]ACACAGCGAGAAAAA | 257000 |
rs537150457 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561088 | TGGGCAAGAGCGGAA[A/G]TGCCTCTGAGTGTCT | 257000 |
rs537231713 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561217 | CAGGGCCCCAAGAGG[A/G]GAGCAACAACCTCAA | 257000 |
rs537656213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565343 | GGCGTCCCCCAGTCA[C/T]TGATCCCTCTCCACC | 257000 |
rs537671851 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560773 | GGGGAGGTATTTGGG[G/T]GTGGAAATGGGGCAC | 257000 |
rs537856867 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5562862 | TCACCATGTTGGCCA[G/T]GCTGGTCTTGAACTC | 257000 |
rs538442256 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5563910 | ACAGAGCAAGACTCC[C/T]GTCTCAAAAATAATA | 257000 |
rs538478267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563948 | AATAAATAAAAGCAT[A/C]CTCGCCAGGGGACAG | 257000 |
rs538678892 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569636 | CTTCTAGGTACTTTA[C/T]TGGGGTGGGGGAAGC | 257000 |
rs538797354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562754 | CCTCCCAGACTCAAG[C/T]GATTCTCTTGCCTCA | 257000 |
rs538812715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564422 | TAGCTGCCTCGGGAC[A/G]CACAGCCAGTGAACA | 257000 |
rs539046991 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5566543 | CACAGAGAGAGATGC[A/G]CGCACACACAGACAG | 257000 |
rs539203487 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559878 | AGGGATCTGGGCTGC[C/T]TCCCCCTGCTGTGTG | 257000 |
rs539440699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566021 | TGCAGACCCCTCCTT[A/G]GGCCAGAAGACGCCC | 257000 |
rs539827670 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557710 | AGTTTCTGGCTAAAC[C/T]GCTGACATCTCCTCT | 257000 |
rs539854467 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557871 | TGCCAAGTCTCACCC[A/G]AAACTCCTCATAGCC | 257000 |
rs540864344 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568385 | AGTAGCTGGGACTAC[A/G]GGCGCTGCCACCAAG | 257000 |
rs540885220 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560906 | CACAAAGGGCCTGTG[A/G]GGGCCCCAAAGAAGG | 257000 |
rs540954284 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564247 | CTAGGGTACCGTCTG[C/T]GCTGACAGGTCCCAA | 257000 |
rs541126123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566226 | CAGAGACACCAGAGA[A/G]ATAAAGAGACACAGA | 257000 |
rs541281162 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568901 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGTA | 257000 |
rs541460122 | in-del | -/AGAG | | | intron-variant | TINCR | GRCh38.p7 | 19:5566424 | GAGAGAGACAGAGAA[-/AGAG]AGACAGAAATGGAGA | 257000 |
rs541622704 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560053 | GATAGGAAGACCCCC[C/T]TCCAGGCACACCCAG | 257000 |
rs541670080 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559315 | GTTATCCTGGCCCCT[G/T]AGCAGTGAGGCTGTC | 257000 |
rs542196696 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559067 | TTCAGAACATGCCAG[C/T]GCTGTCGAGGCTTAA | 257000 |
rs542521136 | in-del | -/AG | 0.00716266 | 0.059414 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568299 | GACAGGCTGGAGCGC[-/AG]TGGCGCAATCATGGT | 257000 |
rs542586608 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560811 | GGCCTGAGAAGGAGC[G/T]AGGATGTCCGCATCT | 257000 |
rs542643257 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569087 | AGAGAATGGCGTGAA[C/T]CTGGGAGGCGGAGCT | 257000 |
rs542661297 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561884 | AGGGGCAACACGGCT[C/G]TGGTCCACGTGTTAG | 257000 |
rs542696129 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569838 | AACATCACTTTTTTT[C/T]TTTTTTTTTTTTTTG | 257000 |
rs542704682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561805 | GCTCAATCCTTTATT[A/G]TAAGGAGACAGGTAA | 257000 |
rs542821084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562992 | CAGGGAGGGCTGCAG[G/T]AAGAGAGGGAGTTGG | 257000 |
rs542857853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562364 | ATTCCCTCCCCTGCA[C/T]CCAGGCACCGCTAGA | 257000 |
rs543022370 | snp | C/T | 0.00597247 | 0.0543191 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560380 | AAAACATTATTTCTT[C/T]CCAGCCTCTGGCGCC | 257000 |
rs543231148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5561671 | CAATGGCGTGATTTC[A/G]GCTCACTGTAACCTC | 257000 |
rs543406817 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560065 | CCCCTCCAGGCACAC[A/C]CAGGGGCCAGCAAGA | 257000 |
rs543594624 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560244 | GCGAGCAGGAGACCC[C/T]GGGCCAAGTGCTGTC | 257000 |
rs543658057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569035 | CCGGGCGTGGTGGCG[A/G]GCGCCTGTAGTCCCA | 257000 |
rs543741651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562269 | TAGCCCTTGCCTTGG[C/T]GTTCAAGGCTTCCCT | 257000 |
rs543778764 | snp | A/G | 0.00199481 | 0.0315187 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559436 | GCCTCCCGGGTTCCC[A/G]CCATTCTCCTGCCTC | 257000 |
rs543818708 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566358 | GAGACACGCAGAGAA[A/T]CAGAGAGACAAAAGA | 257000 |
rs544674575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562447 | GTTAGTGAGACAATA[C/T]ATCTCACTAACATTT | 257000 |
rs545024904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561537 | TGCAGTCATCCCCTC[C/T]TGTGGATGTCCCTTG | 257000 |
rs545046563 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563175 | TTGCAAGCCTCAGGA[A/T]GGACTTGGGCTTTGA | 257000 |
rs545415914 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558206 | ATTCAGTACACTCTC[A/G]AAACAGCATTTCTGT | 257000 |
rs545937164 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569945 | GGTGCAAGCAATTCT[C/T]CTGCCTCAGCCTTCC | 257000 |
rs546045565 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557739 | CTGGGAACCGCCTGG[G/T]CTCACTTGCCCCCTA | 257000 |
rs546149923 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567146 | GAGATAAAAGAGACA[C/G]AGACAAGAGACAGAA | 257000 |
rs546373291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564797 | TGGCCAGGCTGGTCT[C/T]GAACTCTTGACTTCA | 257000 |
rs546646473 | in-del | -/G | 0.00716266 | 0.059414 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568302 | AGGCTGGAGCGCAGT[-/G]GCGCAATCATGGTTC | 257000 |
rs546788157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563583 | TTCCCAGCTTAATCT[G/T]ACTCTGCCTCAGCTT | 257000 |
rs546887175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564352 | GCTCTGCCTCTAGAG[A/G]TCTGGGAGTGGTCTG | 257000 |
rs547147781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566476 | AGCAGAGACCAAAAT[A/G]GGCAGAGACACAGAG | 257000 |
rs547183851 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560442 | CCCTCGAGGACATGC[A/G]TAGCCTCGGCACCCC | 257000 |
rs547603563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567452 | GAAAAACAGCAGAGA[A/C]AGAAACAGGCAGAGA | 257000 |
rs547694373 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560671 | TCAGAACCCCTTCCC[C/T]GCTGCCCCAAGACCC | 257000 |
rs547808078 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557834 | CTCCCCAGAACGCCG[C/T]GGGCCTTAGCGAGAC | 257000 |
rs547844299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565059 | CAGCCCTCTATGGCT[C/T]CCACCTCCCTCGGAG | 257000 |
rs548136764 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559537 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 257000 |
rs548295718 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560856 | TGGAGAGTTCGGACA[C/T]GACTGGCTGCACCCC | 257000 |
rs548318043 | in-del | -/AG | 0.00398564 | 0.0444627 | intron-variant | TINCR | GRCh38.p7 | 19:5566212 | AGCAGAGAAAAATGC[-/AG]AGACACCAGAGAGAT | 257000 |
rs548354743 | in-del | -/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5564490 | CAAAGCTGGACTCTG[-/C]CATCAACCCCAGCTG | 257000 |
rs548510831 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557806 | GGTGGGCGGCCAAGA[C/T]GGGAGGTGGCCCCTC | 257000 |
rs548628137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563760 | TCTACTAAAAATACA[A/T]AAAAATTAGCCAGGC | 257000 |
rs548996873 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561063 | CAAAGGTGTGGCTGG[A/G]AAAATGTCCTGGGCA | 257000 |
rs549033744 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560639 | CCCCAGATCCTCGTC[C/T]TCTTGGCCAGAGTTC | 257000 |
rs549035966 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568577 | CTTTTAGGCCAGGTG[C/T]GGTGGCTCATGCCTG | 257000 |
rs549565782 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560555 | CTGAGGGTCTCCACC[C/T]GGAATTCCCACAACG | 257000 |
rs549670505 | snp | C/G | 0.00398564 | 0.0444627 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567946 | CGCCCGGCTCCGGCT[C/G]CAGCTCTGGCCCCGG | 257000 |
rs549923802 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558522 | TGGATGGAGTAGCAG[C/G]AGAAAAACAGACTGG | 257000 |
rs549967122 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560972 | GAAGACTTCCTGGAG[A/G]AGACTGCAATCCCAG | 257000 |
rs550751233 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569953 | CAATTCTCCTGCCTC[A/G]GCCTTCCCGAGTAGC | 257000 |
rs550789978 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569339 | ACACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 257000 |
rs551206981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562556 | TTTACAGTCTACTGC[A/G]GGAGACAGGTGAAAA | 257000 |
rs551390797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561952 | CCTAGAGGCCAGAAG[C/G]ATAAGTGTATGGAGG | 257000 |
rs551795439 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568665 | GACCAACCTGGCCAA[C/T]ATGGTGAAACCCCGT | 257000 |
rs552020379 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569284 | AAGAGAAGGAAAAAA[A/G]GAGAAGGGCTGGGTG | 257000 |
rs552340333 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565222 | AGGTGCAGTCCTGCC[G/T]CAGGGCCTTTGCACA | 257000 |
rs552529425 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564268 | CAGGTCCCAAGTGTT[G/T]TTCTCATTTCTCACA | 257000 |
rs552596283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563637 | TAACGGCACCCGGCC[A/G]GGCACGGTGGCTCAC | 257000 |
rs552676892 | snp | G/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569677 | TTTCTCATGACACTA[G/T]GACTTCCCATTTTAC | 257000 |
rs553057841 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561389 | TCATGGTCCACCTGG[C/G]AGCCCAGACCCTGGA | 257000 |
rs553250929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563079 | GCAGCGAGGAGGCCT[G/T]TGTGGCTGGAGCAGA | 257000 |
rs553312524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563839 | AGAATCGCTTGAACC[C/T]GGGAGGCAGAGGTTG | 257000 |
rs553366839 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568990 | ACGCGGTGAAACCCC[C/T]CCGTCTCTACCAAAA | 257000 |
rs553423568 | snp | A/G | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558825 | GGAAAATGGGCTGCA[A/G]GAAGCCACTTTTGCA | 257000 |
rs553531252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5565402 | CGAGTTGACATTCTC[C/T]TGTGCTATTATTTGG | 257000 |
rs553724915 | in-del | -/GCG | 0.00716266 | 0.059414 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568295 | TAAGGACAGGCTGGA[-/GCG]CAGTGGCGCAATCAT | 257000 |
rs553837789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565941 | CTCTCGGCCATCCTC[A/G]ACCCATTTCCCAGAG | 257000 |
rs554037943 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559558 | GCCAGGATGGTCTCC[A/G]TCTCCTGACCTCATG | 257000 |
rs554218724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565377 | CCTGCATCCCCCACA[A/G]CGCCAATTGCGAGTT | 257000 |
rs554257404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564530 | TCAGGGATGGGCAAG[A/G]GGCAGGGCATTAGGA | 257000 |
rs554476603 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562270 | AGCCCTTGCCTTGGC[A/G]TTCAAGGCTTCCCTA | 257000 |
rs554504245 | snp | C/G | 0.00199481 | 0.0315187 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557973 | ACAGCCCAGATATGG[C/G]AGGGGGCTGGCCTGG | 257000 |
rs554614160 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564680 | GCCTCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 257000 |
rs554709357 | in-del | -/AGAGAA | | | intron-variant | TINCR | GRCh38.p7 | 19:5566187 | CAGAGCTTCAGAGAC[-/AGAGAA]AAACAGCAGAGAAAA | 257000 |
rs554746354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563448 | TTGGGAGGAAGAGAG[C/G]AATAGACTGATGTCA | 257000 |
rs555226944 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568227 | ATGTCCAGGGGGTTA[C/T]ATGGTGGAGGCTCCA | 257000 |
rs555952489 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560871 | CGACTGGCTGCACCC[C/T]CAGCCAGGGCTGTTC | 257000 |
rs556545204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566052 | CACTTGAGGGTCGTC[C/T]TGGCCAGGGGACCTC | 257000 |
rs556811366 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559295 | AGCCATCTGTAAAAT[A/G]GGCTGTTATCCTGGC | 257000 |
rs557035857 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568155 | GGGGTCTAGAGGCGG[A/G]GTGGCCACTCAGCAC | 257000 |
rs557184732 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562863 | CACCATGTTGGCCAG[A/G]CTGGTCTTGAACTCC | 257000 |
rs557772602 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568927 | CAGTACTTTGGGAGG[C/T]CCAGGTGGGCAGATC | 257000 |
rs557939525 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5567043 | GGAGAGAGACACACA[G/T]AGAGGAAAAAACAGA | 257000 |
rs557997774 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569680 | CTCATGACACTATGA[C/G]TTCCCATTTTACAAG | 257000 |
rs558360434 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568094 | GGGCGGGTGCCACGG[G/T]CCCCTCAGGCGTCCG | 257000 |
rs558376166 | snp | G/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560739 | GAAACAGCCCAGGGG[G/T]TGGGCACAGGTGCCT | 257000 |
rs558586587 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TINCR | GRCh38.p7 | 19:5563951 | AAATAAAAGCATCCT[C/T]GCCAGGGGACAGCGG | 257000 |
rs558670845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562813 | TGCGCCATCATGCCC[A/G]GCTAATTTTTGTAGT | 257000 |
rs558778255 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568549 | GCTCAGCCTACATTA[A/G]AAAAAAAATTTACTT | 257000 |
rs559045685 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566323 | GAGAAATACACAGCG[A/G]GAAGAGACAGAAATG | 257000 |
rs559203921 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569869 | AGACAGAGTTTCACT[C/G]TTGTTGCCCAGGGTG | 257000 |
rs559343448 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569255 | AATGAAAGAAAGAAA[A/G]AGAGAGAGAGAGGAA | 257000 |
rs559365995 | snp | A/G | 0.00119737 | 0.0244387 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560844 | CCGCTTAGTCATTGG[A/G]GAGTTCGGACACGAC | 257000 |
rs559474783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562426 | CTTGCCTCTGCTCAC[A/G]ATTATGTTAGTGAGA | 257000 |
rs559745715 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557732 | ATCTCCTCTGGGAAC[C/T]GCCTGGGCTCACTTG | 257000 |
rs559777929 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5562379 | TCCAGGCACCGCTAG[A/C]GCTCCAGAAAAATAT | 257000 |
rs559786050 | in-del | -/AGAGACAGAGACAAA | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5566492 | GGCAGAGACACAGAG[-/AGAGACAGAGACAAA]AGAGACAGAGACTCA | 257000 |
rs560357617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5563613 | TCTCCACCTGTAAAC[C/T]GCCAATGATAACGGC | 257000 |
rs560370815 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558712 | CCCCTCTTTGTGTCA[C/T]GAGGACCATGCACTT | 257000 |
rs560597448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564209 | CAGGTTTGTCCCGAG[C/T]AGCCCACGCAGCTTC | 257000 |
rs561088156 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559822 | CTCTAGATACACGCA[C/T]GTGGCCCAGCTGTTA | 257000 |
rs561104530 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569955 | ATTCTCCTGCCTCAG[A/C]CTTCCCGAGTAGCTG | 257000 |
rs561502682 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566427 | AGAGACAGAGAAAGA[C/G]AGACAGAAATGGAGA | 257000 |
rs561632097 | snp | C/T | 0.0023933 | 0.0345097 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560392 | CTTCCCAGCCTCTGG[C/T]GCCTCCGCCCATGGT | 257000 |
rs561667443 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5567377 | GAAGAGACAGAGATG[A/G]GAGACAGAGACGAGA | 257000 |
rs561705432 | in-del | -/GGCTGG | 0.999987 | 0.00021574 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568288 | ATCTTTTTAAGGACA[-/GGCTGG]AGCGCAGTGGCGCAA | 257000 |
rs561798407 | in-del | -/CT | 0.0023933 | 0.0345097 | intron-variant | TINCR | GRCh38.p7 | 19:5564574 | CAGAGGAGGTTGAAA[-/CT]CTCTCTTTTTTCTTT | 257000 |
rs562052331 | in-del | -/GAAA | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569242 | GAGGAAAGAAAGAAT[-/GAAA]GAAAGAAAGAAAGAG | 257000 |
rs562146556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565547 | TAATTACAGTCTGGA[C/T]GTCTGAGGGTCGTCC | 257000 |
rs562977090 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5564271 | GTCCCAAGTGTTTTT[C/T]TCATTTCTCACATGG | 257000 |
rs562978747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5564821 | GACTTCAGGTGATCC[A/G]CCCACCTTGGCCCCC | 257000 |
rs563042883 | snp | A/G | 0.00318978 | 0.0398085 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557779 | CCTTGGACCTTCTTG[A/G]AGCACAAACTAGGTG | 257000 |
rs563159441 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558237 | ATCTAGTTCCAAGCT[A/G]GGTGATCCTGCGGCC | 257000 |
rs563359952 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569037 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 257000 |
rs563381424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567163 | GACAAGAGACAGAAA[C/G]AAGAGGGAGACAGAG | 257000 |
rs563394858 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568575 | TACTTTTAGGCCAGG[C/T]GCGGTGGCTCATGCC | 257000 |
rs563546892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561674 | TGGCGTGATTTCGGC[C/T]CACTGTAACCTCTGA | 257000 |
rs563580311 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559495 | GCCCGCCACCAGGCC[C/T]GGCTATTTTTTTTGT | 257000 |
rs563977959 | snp | A/G | 0.0107246 | 0.0724382 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560465 | GGCACCCCCTCCCCA[A/G]AGACCCTCCCCAGGG | 257000 |
rs564003226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567567 | TGGGAAAGCAGTGCC[A/G]GCCCGGGAGGCCGCC | 257000 |
rs564193449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5561563 | CCTTGTGTCCTTTAA[C/G]AGGAACAGGGATGGC | 257000 |
rs564347028 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568442 | GAGATGGGGCCTGGC[C/T]GTGTTGCCCAGGCTG | 257000 |
rs564363923 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5565626 | GCCCCAAGCTCTGAA[A/C]CTCCATCCCTCATCA | 257000 |
rs564410439 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560927 | CCAAAGAAGGCTAGG[G/T]GCTCTCTGGCTGGGA | 257000 |
rs564537554 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559377 | TCTCGCTCTGTCGCC[C/T]AGGCTGGAGTGCAGT | 257000 |
rs564607673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566234 | CCAGAGAGATAAAGA[A/G]ACACAGACACACATG | 257000 |
rs564832146 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TINCR | GRCh38.p7 | 19:5563264 | CAGGGGCTCACAGGC[A/G]CCCTCTGGCACCTGC | 257000 |
rs565291107 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560454 | TGCGTAGCCTCGGCA[A/C]CCCCTCCCCAAAGAC | 257000 |
rs565720482 | snp | A/G | 0.0310518 | 0.120672 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561064 | AAAGGTGTGGCTGGG[A/G]AAATGTCCTGGGCAA | 257000 |
rs565900402 | snp | A/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558939 | AAAGGAAGGGGGCGA[A/T]GGAAGGGAGAACAGA | 257000 |
rs565987665 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565981 | GCCGGCAGTGAGCTG[C/T]TCCCGTGGCCCCAGC | 257000 |
rs566356339 | snp | A/G | 0.0023933 | 0.0345097 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560648 | CTCGTCCTCTTGGCC[A/G]GAGTTCTTCAGAACC | 257000 |
rs566642137 | snp | C/G | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562170 | TTCAGCCAGTACCCA[C/G]GTCCCCTTGGTCATG | 257000 |
rs566667395 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564400 | TTGATGCCCAGAGAG[C/G]GTGGGTTAGCTGCCT | 257000 |
rs566812483 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569574 | AGGGAAACTCCGTCT[C/T]AAAAAAGAAAAGAAA | 257000 |
rs567416975 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569402 | ACACAGAGAAACCCC[A/G]TCTCTACAAAAAATA | 257000 |
rs567455571 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568832 | CCAGCCTGAGCCACA[C/G]AGCGAGACTTATCGC | 257000 |
rs567561394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5563784 | GCCAGGCATGGTGGC[A/G]GGCGCCTGTAATCCC | 257000 |
rs567639720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562584 | AAAAAATAAGTAAAA[C/T]GTAGAGAAGTCGGCT | 257000 |
rs567733381 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5567321 | TCAGAGACAAGAGAC[A/C]GAAAGAAGAGGGAGA | 257000 |
rs567811220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565837 | CCATAAAATCCAGGG[C/T]AATTCACATGGCCCC | 257000 |
rs568049243 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569543 | TCTGCCATTGCACTC[C/T]AGCCTGGGCAACAAG | 257000 |
rs568423652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564292 | TCTCACATGGGGAAG[C/T]TGAGGCCTCCCCGGC | 257000 |
rs568918245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565323 | ACATGTCACCTTTCC[A/G]GAGAGGCGTCCCCCA | 257000 |
rs569041859 | in-del | -/TGGA | 0.0023933 | 0.0345097 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569882 | TCTTGTTGCCCAGGG[-/TGGA]TGGAGTACAATGGCA | 257000 |
rs569117682 | snp | A/C | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558584 | CAGATCCAAAATCAG[A/C]AGCCTGTCATTCAAG | 257000 |
rs569156604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565752 | CGGGGTGGCATCTGA[A/G]GCTCCTGCCCTCAAA | 257000 |
rs569192180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562856 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGGTCTT | 257000 |
rs569275626 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TINCR | GRCh38.p7 | 19:5563652 | AGGCACGGTGGCTCA[C/G]GCGTGTAATCCCAGC | 257000 |
rs569666644 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TINCR | GRCh38.p7 | 19:5562938 | ATTGCGGGTGTGAGC[C/T]GCTGCGCCTCGCTGG | 257000 |
rs570227079 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558903 | GGAAGAAGAGAAAAA[C/T]GGAAGATAGGGAGGG | 257000 |
rs570302749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565996 | TTCCCGTGGCCCCAG[A/C]GCCCTTCTCTGCAGA | 257000 |
rs570330390 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565025 | AGCATTGAGTCAGGT[C/T]CCGTCCCTCCTCTGC | 257000 |
rs570362185 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TINCR | GRCh38.p7 | 19:5566878 | GAGACAGAAAAGAGA[C/G]AGGGAGACAGAGATG | 257000 |
rs570443859 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5561936 | AAGGCCATGTCCCTA[A/C]CCTAGAGGCCAGAAG | 257000 |
rs570536026 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | TINCR | GRCh38.p7 | 19:5566360 | GACACGCAGAGAAAC[-/AG]AGAGACAAAAGAGAC | 257000 |
rs570900100 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557845 | GCCGCGGGCCTTAGC[A/G]AGACGGCAGCTGCCA | 257000 |
rs571649897 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568131 | ACTGCTGGCCCCAGA[A/G]TGCGCCCGGGGGTCT | 257000 |
rs571764387 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568774 | AGAATCGCTTGAACC[C/T]GCAGACAGAGGTTGC | 257000 |
rs571826260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5562003 | CTGTCTCTTCTCCTC[G/T]CTGGGCCTCAGTTTC | 257000 |
rs571860492 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569299 | AGAGAAGGGCTGGGT[A/G]CAGGGGCTAACGCCT | 257000 |
rs571998338 | snp | A/C | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560881 | CACCCCCAGCCAGGG[A/C]TGTTCACTGCACAAA | 257000 |
rs572042073 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561812 | CCTTTATTGTAAGGA[C/G]ACAGGTAACAGAGCC | 257000 |
rs572236255 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568884 | AAAAAAAAAAATGGC[C/T]GGGTGTGGTGGCTCA | 257000 |
rs572288360 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5562643 | GCAGGGATGGCGTGA[A/C]ATAAAATTTTATTAT | 257000 |
rs572327376 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559733 | AGATTATTAAATGCC[C/G]CATTTTCTTGCCAAA | 257000 |
rs572332501 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568322 | AATCATGGTTCGTTG[C/T]AGCCTTGACCTCCCG | 257000 |
rs572341826 | in-del | -/GAGA | 0.00398564 | 0.0444627 | intron-variant | TINCR | GRCh38.p7 | 19:5567333 | GACAGAAAGAAGAGG[-/GAGA]GAGATGAGAGACAGA | 257000 |
rs572625668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566988 | GAGACAATCACAGGC[A/G]ACCAAATCATCAGGG | 257000 |
rs572760145 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569911 | CACAATCTCGGCTCA[C/T]CGCAACCTCCGCCTC | 257000 |
rs572795209 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560007 | TGGGGACAAAGTCCT[C/G]GGTTAGGCACCAAGG | 257000 |
rs573667655 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568163 | GAGGCGGAGTGGCCA[C/T]TCAGCACAGAGCCAT | 257000 |
rs573706105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5567328 | CAAGAGACAGAAAGA[A/C]GAGGGAGAGAGATGA | 257000 |
rs573773587 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569835 | ACAAACATCACTTTT[G/T]TTTTTTTTTTTTTTT | 257000 |
rs573835112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562355 | GACCCAGAAATTCCC[A/T]CCCCTGCATCCAGGC | 257000 |
rs574043680 | snp | A/C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561272 | TCAAGGCTCCCTCCC[A/C/G]ATAGGCTGGGCAGGA | 257000 |
rs574463703 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557709 | CAGTTTCTGGCTAAA[C/T]CGCTGACATCTCCTC | 257000 |
rs574793173 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568724 | GCGTGGTGGCACATG[C/T]CTGTAGTTCCAGCTA | 257000 |
rs574908053 | in-del | -/GAAA | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569243 | GAGGAAAGAAAGAAT[-/GAAA]GAAAGAAAGAGAGAG | 257000 |
rs575280126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5564100 | AATGTTGTCACTACT[A/G]CATTTCACAGAGTGT | 257000 |
rs575296301 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5564460 | CAGATAGGGGCCCCT[A/G]TCTGTTGGGGAAGAC | 257000 |
rs575335106 | snp | C/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569771 | GCAGAGCTGGGATTC[C/G]AACCCAGGCCACCTA | 257000 |
rs576087557 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5563662 | GCTCACGCGTGTAAT[A/C]CCAGCACTTTGGGAG | 257000 |
rs576209222 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561985 | GATGATGGTCAATAA[C/G]ATCTGTCTCTTCTCC | 257000 |
rs576382676 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558186 | TTTCAAACATGTAAT[C/T]TTTTATTCAGTACAC | 257000 |
rs576531770 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TINCR | GRCh38.p7 | 19:5565487 | GTGTCCAGCATGGAG[G/T]CTGGCACACAGTAGG | 257000 |
rs576668790 | snp | A/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559045 | GGGACAGGTCCAACA[A/T]TATTATTTCAGAACA | 257000 |
rs576696047 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558249 | GCTGGGTGATCCTGC[A/G]GCCCCAAAGGTAGTG | 257000 |
rs576842598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5566098 | ATCCAAGTGTGAGTG[C/T]GGGTAACGGACACTG | 257000 |
rs577454082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5565403 | GAGTTGACATTCTCC[A/T]GTGCTATTATTTGGC | 257000 |
rs577739963 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568976 | GACCATCCTGGCTAA[C/T]GCGGTGAAACCCCCC | 257000 |
rs577856366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TINCR | GRCh38.p7 | 19:5562259 | AGAAAAAACATAGCC[C/T]TTGCCTTGGCGTTCA | 257000 |
rs577896854 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569728 | AGAGAAGAAAAGAGA[C/T]TTCCCAGAGGAAACA | 257000 |
rs578047633 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560166 | CCTCCTTCTCCCCCT[C/T]CTCTCAGCCAAGCGG | 257000 |
rs578074725 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560770 | CCTGGGGAGGTATTT[G/T]GGGGTGGAAATGGGG | 257000 |
rs578131999 | in-del | -/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568094 | GGGCGGGTGCCACGG[-/T]CCCCTCAGGCGTCCG | 257000 |
rs578146620 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559366 | TTGAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 257000 |
rs745518867 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560958 | AGGAGGGAATCTGAG[A/G]AGACTTCCTGGAGGA | 257000 |
rs745579957 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562585 | AAAAATAAGTAAAAC[A/G]TAGAGAAGTCGGCTG | 257000 |
rs745779519 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5567915 | ACAGCCCCCGCCGCA[-/G]CCCCTCCATGGCGCC | 257000 |
rs746069403 | snp | A/C | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568399 | CAGGCGCTGCCACCA[A/C]GCCCAGCTCACTTTT | 257000 |
rs746347696 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565609 | GAGAACACCCTCTCC[C/T]AGCCCCAAGCTCTGA | 257000 |
rs746429519 | in-del | -/GGGAA | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558956 | GAAGGGAGAACAGAT[-/GGGAA]GGGAAGGGAAGGGAA | 257000 |
rs746650756 | snp | A/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5563672 | GTAATCCCAGCACTT[A/T]GGGAGGCTGAGGTAG | 257000 |
rs746929794 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558695 | TCCAGCCACTGTCAT[C/G]TCCCCTCTTTGTGTC | 257000 |
rs747248944 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559113 | TTGCATGCGATTTGC[A/G]TGTGATTTGCATACT | 257000 |
rs747311057 | in-del | -/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564514 | CAGCTGTGTGTGTGG[-/T]TCAGGGATGGGCAAG | 257000 |
rs747506292 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567464 | AGACAGAAACAGGCA[C/G]AGAAACAGGCACAGA | 257000 |
rs747561370 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566499 | ACACAGAGAGAGACA[A/G]AGACAAAAGAGACAG | 257000 |
rs748393733 | in-del | -/TT | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559336 | TGAGGCTGTCAATCT[-/TT]TTTTTTTTTTTTTTT | 257000 |
rs748479512 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566650 | GAGACAGAGAGACAG[A/G]GAGAGAGAGACACAC | 257000 |
rs749488906 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562595 | AAAACGTAGAGAAGT[C/T]GGCTGCTGACAAGTG | 257000 |
rs750326962 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564987 | CAGTCTGTTCTCCCC[A/G]CTGCAGCCAGGGGTT | 257000 |
rs750755300 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559073 | ACATGCCAGCGCTGT[C/T]GAGGCTTAAGAAATG | 257000 |
rs750995111 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559925 | TGGGCCTCAGGCTAC[C/G]CTCTGCAGAACAGAC | 257000 |
rs751202761 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558606 | TCATTCAAGGCCAAG[A/G]CATTCCACAATAGTT | 257000 |
rs751571482 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566188 | AGAGCTTCAGAGACA[A/G]AGAAAAACAGCAGAG | 257000 |
rs752205250 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559854 | CAGAGGCCCAAACCA[C/T]GCATGAGCAGGGATC | 257000 |
rs752289047 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566247 | GAGACACAGACACAC[A/G]TGTTGAGACACAGCG | 257000 |
rs752477951 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566950 | AGAGACACAGAGTGA[C/T]AGAGAAAAGAGAGAC | 257000 |
rs753262601 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560358 | GCAGCCAACAGGACT[A/C]TTAACTAAAACATTA | 257000 |
rs753358196 | snp | C/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557893 | CTCATAGCCCAGACT[C/T]GCTCAGGGTGGAGCC | 257000 |
rs753508678 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5567127 | GACAAAGATGAGAGA[C/T]GCAGAGATAAAAGAG | 257000 |
rs753832754 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567546 | GGCCGGGCGGGCAGC[A/G]CGAGGTGGGAAAGCA | 257000 |
rs753855920 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563357 | TGGGCTGGGCCAGGG[A/G]TTGAGAAGTGGGAGG | 257000 |
rs754118621 | in-del | -/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561368 | CAGCTGGTCAGGCCA[-/G]GGGTTTCATGGTCCA | 257000 |
rs754337827 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558920 | GAAGATAGGGAGGGA[A/G]AGGAAAGGAAGGGGG | 257000 |
rs754853630 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565307 | TCCACATCATAGCCT[A/G]ACATGTCACCTTTCC | 257000 |
rs755359727 | in-del | -/AGAGACAGAGATG | | | intron-variant | TINCR | GRCh38.p7 | 19:5567364 | AGAGACAAAAGAAGA[-/AGAGACAGAGATG]AGAGACAGAGACGAG | 257000 |
rs755376608 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562042 | TGGTCTCCACAATCT[C/G]TAAGGTCCTTTCTCT | 257000 |
rs755424024 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5567505 | GAAAGCAAGACCTGA[C/T]ACCGGCAAGGCCGGG | 257000 |
rs755852504 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566321 | GAGAGAAATACACAG[C/T]GGGAAGAGACAGAAA | 257000 |
rs756116106 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564777 | GAGACAGCGTTTCGC[C/T]ATGTTGGCCAGGCTG | 257000 |
rs756203567 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5562182 | CCAGGTCCCCTTGGT[C/G]ATGGCTCTGCCTCCT | 257000 |
rs756218986 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560746 | CCCAGGGGGTGGGCA[A/C]AGGTGCCTCCTGGGG | 257000 |
rs756735745 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567200 | GATGGAGATGAGACA[A/G]CCACAAAAGAGATGA | 257000 |
rs756790857 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566374 | CAGAGAGACAAAAGA[A/G]ACACACAGAGAGAAA | 257000 |
rs757373413 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567547 | GCCGGGCGGGCAGCG[C/G]GAGGTGGGAAAGCAG | 257000 |
rs757428633 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565357 | ACTGATCCCTCTCCA[C/T]CTTCCCTGCATCCCC | 257000 |
rs757470127 | in-del | -/GAGA | | | intron-variant | TINCR | GRCh38.p7 | 19:5567069 | ACAGAGACCAAAATG[-/GAGA]GAGAGACAGAGACAA | 257000 |
rs758102336 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563530 | TTAGTGATGAAGGGC[A/G]TGGCTTTAAAGCTGG | 257000 |
rs758154234 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558348 | TGGAAGCAGCAGGGT[C/T]CTTGAGGGAAGTAGG | 257000 |
rs758423986 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565022 | GTGAGCATTGAGTCA[A/G]GTCCCGTCCCTCCTC | 257000 |
rs758564833 | in-del | -/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569830 | TTACACAAACATCAC[-/T]TTTTTTTTTTTTTTT | 257000 |
rs758834894 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559104 | GGTGGTGATTTGCAT[A/G]CGATTTGCATGTGAT | 257000 |
rs759105419 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569092 | ATGGCGTGAACCTGG[A/G]AGGCGGAGCTTGCAG | 257000 |
rs759510965 | in-del | -/GAAAG | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569185 | AAAAAAAAAAAAAAA[-/GAAAG]AAAGAAAGAAAGAAA | 257000 |
rs759615627 | snp | G/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566863 | CAGAGACCAGAGAGG[G/T]AGACAGAAAAGAGAG | 257000 |
rs759771595 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563042 | TCCAGGCTGAAGGAA[C/G]AGCCTGTCCAGAGGC | 257000 |
rs760453910 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569512 | CCCAGGAGGTGGAGG[C/T]TGTGGTGAGCGGAGA | 257000 |
rs760468271 | snp | G/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5570032 | TAGTAGAGACGGGGT[G/T]TCTCCATGTTAGTCA | 257000 |
rs761235496 | in-del | -/AG | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569256 | ATGAAAGAAAGAAAG[-/AG]AGAGAGAGAGGAAGA | 257000 |
rs761402209 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562923 | TCCCAAAGTGCTGGG[A/G]TTGCGGGTGTGAGCC | 257000 |
rs762094280 | snp | G/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5561335 | GGGCTCCAGCAGGAG[G/T]GTCTGAAGCAGTGTG | 257000 |
rs762131548 | snp | G/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565907 | AGGCTCTGAGACGAG[G/T]CCCCACCATCTTCAC | 257000 |
rs762591141 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564205 | CTGGCAGGTTTGTCC[C/G]GAGCAGCCCACGCAG | 257000 |
rs762697235 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559648 | CCGGCTGTCAATCAA[A/G]TGAGACAGGGCTCCA | 257000 |
rs763132056 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566093 | CAGATATCCAAGTGT[A/G]AGTGTGGGTAACGGA | 257000 |
rs763664932 | snp | A/G | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557835 | TCCCCAGAACGCCGC[A/G]GGCCTTAGCGAGACG | 257000 |
rs764036853 | in-del | -/AA | | | intron-variant | TINCR | GRCh38.p7 | 19:5567421 | GAGAGTGACAGAGAC[-/AA]AAGAGAGAGAGGCAG | 257000 |
rs764143412 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5563354 | AACTGGGCTGGGCCA[A/G]GGGTTGAGAAGTGGG | 257000 |
rs764233135 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564601 | TCTTTTGTTTTGAGA[C/T]GGAGTCTCACTCTGT | 257000 |
rs764635289 | in-del | -/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564060 | ACAACCTGTCTCCCT[-/G]CAACGCTGCTGCCTC | 257000 |
rs764833871 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560591 | CCTGCAATGCCCCGC[A/G]ATGACCTCCCACAGC | 257000 |
rs765221983 | snp | G/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565986 | CAGTGAGCTGTTCCC[G/T]TGGCCCCAGCGCCCT | 257000 |
rs765404363 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564848 | CCCCCAAAGTGCTGG[C/G]ATTGCAGGTGTGAAC | 257000 |
rs765901301 | in-del | -/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5566258 | ACACATGTTGAGACA[-/C]AGCGAGAAAAAGAGC | 257000 |
rs765950274 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558546 | AGACTGGGGGAGCAG[A/G]AAGAGTCAGTGTGAG | 257000 |
rs766361186 | in-del | -/TTT | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559335 | GTGAGGCTGTCAATC[-/TTT]TTTTTTTTTTTTTTT | 257000 |
rs766382774 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566106 | GTGAGTGTGGGTAAC[A/G]GACACTGGAGTGGGG | 257000 |
rs766617079 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566741 | CACAGAGAGACACAA[A/G]GAGAAAAACAGCAGA | 257000 |
rs766730680 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562931 | TGCTGGGATTGCGGG[C/T]GTGAGCCGCTGCGCC | 257000 |
rs766755621 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561843 | CAGAGAGGAGAAGCA[A/G]TTTTCCCAAGGTCAC | 257000 |
rs766984892 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558765 | GGGGCTGCTTTCCTC[A/G]GTGTGGCTGTGGGAC | 257000 |
rs767460334 | snp | A/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566245 | AAGAGACACAGACAC[A/T]CATGTTGAGACACAG | 257000 |
rs767974281 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5563068 | GAGGCTCTGAGGCAG[C/T]GAGGAGGCCTGTGTG | 257000 |
rs768279014 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568845 | CAGAGCGAGACTTAT[C/T]GCAAAAAAAAAAAAA | 257000 |
rs768280417 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562755 | CTCCCAGACTCAAGC[A/G]ATTCTCTTGCCTCAG | 257000 |
rs768645173 | snp | G/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5558018 | ACAGTGTCACCTGGA[G/T]TAACAGCGTCACCTG | 257000 |
rs768753207 | snp | G/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559182 | CCACCTCCACCCCCA[G/T]TGGAGAAGCGGGAAA | 257000 |
rs769028597 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565899 | GTGGTCCCAGGCTCT[C/G]AGACGAGGCCCCACC | 257000 |
rs769156330 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565383 | TCCCCCACAGCGCCA[A/G]TTGCGAGTTGACATT | 257000 |
rs769318456 | in-del | -/TG | | | intron-variant | TINCR | GRCh38.p7 | 19:5565522 | AATAAATGCTGACTC[-/TG]TGTACTGCATAATTA | 257000 |
rs769321237 | in-del | -/A | | | intron-variant | TINCR | GRCh38.p7 | 19:5566236 | GAGAGATAAAGAGAC[-/A]ACAGACACACATGTT | 257000 |
rs769370411 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5563975 | ACAGCGGTAAGGCCA[C/T]GTGAAAAGCCCCTAG | 257000 |
rs769575250 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558183 | TGTTTTCAAACATGT[A/C]ATCTTTTATTCAGTA | 257000 |
rs769918924 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559266 | CAGAGGGTGGTGACC[C/T]TGGGCAAGCCAAAAG | 257000 |
rs769994681 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566659 | AGACAGGGAGAGAGA[C/G]ACACACACATACACA | 257000 |
rs770080190 | snp | C/T | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568570 | AAATTTACTTTTAGG[C/T]CAGGTGCGGTGGCTC | 257000 |
rs770726767 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560830 | ATGTCCGCATCTCCC[C/T]GCTTAGTCATTGGAG | 257000 |
rs770735613 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559682 | AGATGTGCACAAGTC[C/T]TGGCATGGAGTAAGG | 257000 |
rs771015517 | in-del | -/CAAA | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558444 | TGAATAGGAGCTTGC[-/CAAA]CAAAGAAGGTGGGAC | 257000 |
rs771472380 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5564473 | CTGTCTGTTGGGGAA[A/G]ACAAAGCTGGACTCT | 257000 |
rs771505638 | in-del | -/AC | | | intron-variant | TINCR | GRCh38.p7 | 19:5566805 | GGAAGAGAGACAGAG[-/AC]ACACACACACAGAGG | 257000 |
rs771928512 | snp | A/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562630 | GGAAAGAGAGAAAGC[A/T]GGGATGGCGTGAAAT | 257000 |
rs772275593 | snp | A/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566070 | GCCAGGGGACCTCTT[A/T]GGGGACCCAGATATC | 257000 |
rs772508778 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5565655 | CATCCTCTCAGCCTC[C/T]CCGTCCCCGCTAAGA | 257000 |
rs772645357 | in-del | -/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569185 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAGAAA | 257000 |
rs773051488 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5558248 | AGCTGGGTGATCCTG[C/T]GGCCCCAAAGGTAGT | 257000 |
rs773262278 | snp | A/C | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559310 | GGGCTGTTATCCTGG[A/C]CCCTGAGCAGTGAGG | 257000 |
rs773341185 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5566678 | CACACATACACAGAC[A/C]CAGAGAAAAACAGAG | 257000 |
rs773445073 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5564173 | GGGGCCCTATCTACC[C/T]GGAAGTGAGAGAGGG | 257000 |
rs773890342 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569038 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 257000 |
rs774031870 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559756 | TTGCCAAACCCTGAC[A/G]AGGCATGTCCCTGAA | 257000 |
rs774079278 | snp | C/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560870 | ACGACTGGCTGCACC[C/G]CCAGCCAGGGCTGTT | 257000 |
rs774283975 | in-del | -/ACAG | | | intron-variant | TINCR | GRCh38.p7 | 19:5566551 | GAGATGCGCGCACAC[-/ACAG]ACAGAACTGGACAGG | 257000 |
rs774399666 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566861 | GACAGAGACCAGAGA[A/G]GGAGACAGAAAAGAG | 257000 |
rs774954648 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562979 | TAAACAGGATGGTCA[A/G]GGAGGGCTGCAGGAA | 257000 |
rs775229583 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562738 | CTCACTGCAACCTCC[A/G]CCTCCCAGACTCAAG | 257000 |
rs775771074 | in-del | -/TCA | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559020 | ACCTCCCGACCCAGG[-/TCA]TCATCAAGGGACAGG | 257000 |
rs775976902 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566074 | GGGGACCTCTTTGGG[A/G]ACCCAGATATCCAAG | 257000 |
rs776342321 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5562812 | ATGCGCCATCATGCC[C/T]GGCTAATTTTTGTAG | 257000 |
rs777114753 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5566635 | AGACAAATGGACAAA[C/G]AGACAGAGAGACAGG | 257000 |
rs777133491 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566220 | AAAATGCAGAGACAC[C/T]AGAGAGATAAAGAGA | 257000 |
rs777303719 | snp | C/T | | | intron-variant | TINCR | GRCh38.p7 | 19:5566349 | AAATGGACAGAGACA[C/T]GCAGAGAAACAGAGA | 257000 |
rs777870837 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5562273 | CCTTGCCTTGGCGTT[C/G]AAGGCTTCCCTATTC | 257000 |
rs777999924 | in-del | -/G | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557814 | GCCAAGACGGGAGGT[-/G]GCCCCTCCCCAGAAC | 257000 |
rs778430016 | snp | C/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5567371 | AAAGAAGAAGAGACA[C/G]AGATGAGAGACAGAG | 257000 |
rs778900418 | in-del | -/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5563159 | CAGGTCATCCAGGGT[-/C]TTGCAAGCCTCAGGA | 257000 |
rs779404475 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559012 | GGCCGTGCACCTCCC[A/G]ACCCAGGTCATCATC | 257000 |
rs779458585 | snp | A/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557754 | GCTCACTTGCCCCCT[A/T]GGAGAATTCCCTTGG | 257000 |
rs779954812 | in-del | -/AGAG | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5569254 | GAATGAAAGAAAGAA[-/AGAG]AGAGAGAGAGGAAGA | 257000 |
rs780156481 | snp | A/C | | | intron-variant | TINCR | GRCh38.p7 | 19:5565061 | GCCCTCTATGGCTCC[A/C]ACCTCCCTCGGAGTC | 257000 |
rs780326603 | snp | A/G | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5560180 | TCCTCTCAGCCAAGC[A/G]GGAATTGCAGGGTAG | 257000 |
rs780434296 | snp | C/T | | | downstream-variant-500B | TINCR | GRCh38.p7 | 19:5557970 | TTCACAGCCCAGATA[C/T]GGGAGGGGGCTGGCC | 257000 |
rs780691844 | in-del | -/AAA | | | intron-variant | TINCR | GRCh38.p7 | 19:5567205 | AGATGAGACAGCCAC[-/AAA]AGAGATGAGAGAGAC | 257000 |
rs780921470 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5561853 | AAGCAATTTTCCCAA[A/G]GTCACCCAGCAAGTC | 257000 |
rs780945442 | snp | A/G | | | intron-variant | TINCR | GRCh38.p7 | 19:5565331 | CCTTTCCGGAGAGGC[A/G]TCCCCCAGTCACTGA | 257000 |
rs781198159 | snp | C/T | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559225 | TCCTCCACCAGCTCC[C/T]GGCATGGGTTGGGGA | 257000 |
rs781316093 | in-del | -/GGT | | | nc-transcript-variant | TINCR | GRCh38.p7 | 19:5559089 | GAGGCTTAAGAAATG[-/GGT]GGTGATTTGCATGCG | 257000 |
rs796225844 | snp | A/G | | | upstream-variant-2KB | TINCR | GRCh38.p7 | 19:5568139 | CCCCAGAGTGCGCCC[A/G]GGGGTCTAGAGGCGG | 257000 |