Variant report
Variant | rs6742943 |
---|---|
Chromosome Location | chr2:187168809-187168810 |
allele | A/C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:187168079..187170910-chr2:187226806..187228664,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10172511 | 0.93[ASN][1000 genomes] |
rs10188807 | 0.96[ASN][1000 genomes] |
rs10189971 | 0.92[ASN][1000 genomes] |
rs10193268 | 0.93[ASN][1000 genomes] |
rs10194541 | 0.93[ASN][1000 genomes] |
rs10194719 | 0.93[ASN][1000 genomes] |
rs10196208 | 0.89[ASN][1000 genomes] |
rs10201768 | 0.85[ASN][1000 genomes] |
rs10201874 | 0.90[ASN][1000 genomes] |
rs10203879 | 0.93[ASN][1000 genomes] |
rs10205506 | 0.92[ASN][1000 genomes] |
rs10205705 | 0.92[ASN][1000 genomes] |
rs10210844 | 0.85[ASN][1000 genomes] |
rs1026118 | 0.90[ASN][1000 genomes] |
rs10439308 | 0.95[ASN][1000 genomes] |
rs10804003 | 0.80[ASN][1000 genomes] |
rs10804004 | 0.87[ASN][1000 genomes] |
rs10931239 | 0.93[ASN][1000 genomes] |
rs10931242 | 0.90[ASN][1000 genomes] |
rs11676936 | 0.92[ASN][1000 genomes] |
rs11683595 | 0.91[ASN][1000 genomes] |
rs11693737 | 0.89[ASN][1000 genomes] |
rs11884786 | 0.88[ASN][1000 genomes] |
rs11889909 | 0.92[ASN][1000 genomes] |
rs12052331 | 0.96[ASN][1000 genomes] |
rs12053380 | 0.89[ASN][1000 genomes] |
rs12463831 | 0.96[ASN][1000 genomes] |
rs12467212 | 0.89[ASN][1000 genomes] |
rs12467891 | 0.87[ASN][1000 genomes] |
rs12469301 | 0.91[ASN][1000 genomes] |
rs12473542 | 0.93[ASN][1000 genomes] |
rs12475522 | 0.89[ASN][1000 genomes] |
rs12477683 | 0.93[ASN][1000 genomes] |
rs12478370 | 0.86[ASN][1000 genomes] |
rs12611673 | 0.87[ASN][1000 genomes] |
rs12615503 | 0.96[ASN][1000 genomes] |
rs12615675 | 0.82[ASN][1000 genomes] |
rs12619990 | 0.90[ASN][1000 genomes] |
rs12620626 | 0.96[ASN][1000 genomes] |
rs12623611 | 0.87[ASN][1000 genomes] |
rs12693440 | 0.88[ASN][1000 genomes] |
rs12693444 | 0.92[ASN][1000 genomes] |
rs12693447 | 0.90[ASN][1000 genomes] |
rs12693448 | 0.92[ASN][1000 genomes] |
rs12693449 | 0.90[ASN][1000 genomes] |
rs13009502 | 0.83[ASN][1000 genomes] |
rs13015996 | 0.87[ASN][1000 genomes] |
rs13016181 | 0.87[ASN][1000 genomes] |
rs13016273 | 0.84[ASN][1000 genomes] |
rs13017706 | 0.82[ASN][1000 genomes] |
rs13018467 | 0.87[ASN][1000 genomes] |
rs13023992 | 0.91[ASN][1000 genomes] |
rs13024310 | 0.87[ASN][1000 genomes] |
rs13027135 | 0.93[ASN][1000 genomes] |
rs13029473 | 0.86[ASN][1000 genomes] |
rs13029980 | 0.83[ASN][1000 genomes] |
rs13403118 | 0.88[ASN][1000 genomes] |
rs13409734 | 0.96[ASN][1000 genomes] |
rs13421394 | 0.91[ASN][1000 genomes] |
rs13421948 | 0.96[ASN][1000 genomes] |
rs13426333 | 0.94[ASN][1000 genomes] |
rs1349154 | 0.92[ASN][1000 genomes] |
rs1375321 | 0.92[ASN][1000 genomes] |
rs1375324 | 0.93[ASN][1000 genomes] |
rs1375325 | 0.93[ASN][1000 genomes] |
rs1375327 | 0.93[ASN][1000 genomes] |
rs1375328 | 0.93[ASN][1000 genomes] |
rs1448851 | 0.92[ASN][1000 genomes] |
rs1448852 | 0.92[ASN][1000 genomes] |
rs1448854 | 0.92[ASN][1000 genomes] |
rs1448856 | 0.87[ASN][1000 genomes] |
rs1448858 | 0.87[ASN][1000 genomes] |
rs1448860 | 0.92[ASN][1000 genomes] |
rs1448861 | 0.93[ASN][1000 genomes] |
rs1448863 | 0.85[ASN][1000 genomes] |
rs1562646 | 0.90[ASN][1000 genomes] |
rs1562647 | 0.90[ASN][1000 genomes] |
rs16827561 | 0.86[ASN][1000 genomes] |
rs1839193 | 0.82[ASN][1000 genomes] |
rs1900835 | 0.87[ASN][1000 genomes] |
rs1992930 | 0.88[ASN][1000 genomes] |
rs2197816 | 0.92[ASN][1000 genomes] |
rs2370667 | 0.93[ASN][1000 genomes] |
rs2370675 | 0.86[ASN][1000 genomes] |
rs2370691 | 0.92[ASN][1000 genomes] |
rs2370692 | 0.90[ASN][1000 genomes] |
rs28498768 | 0.96[ASN][1000 genomes] |
rs2887819 | 0.93[ASN][1000 genomes] |
rs3107167 | 0.96[ASN][1000 genomes] |
rs3107177 | 0.92[ASN][1000 genomes] |
rs3107406 | 0.94[ASN][1000 genomes] |
rs3107414 | 0.95[ASN][1000 genomes] |
rs3112322 | 0.88[ASN][1000 genomes] |
rs34229945 | 0.93[ASN][1000 genomes] |
rs35076657 | 0.82[ASN][1000 genomes] |
rs35437667 | 0.86[ASN][1000 genomes] |
rs4016824 | 0.89[ASN][1000 genomes] |
rs4130801 | 0.93[ASN][1000 genomes] |
rs4144824 | 0.88[ASN][1000 genomes] |
rs4271735 | 0.84[ASN][1000 genomes] |
rs4341896 | 0.87[ASN][1000 genomes] |
rs4363995 | 0.81[ASN][1000 genomes] |
rs4430906 | 0.91[ASN][1000 genomes] |
rs4522568 | 0.94[ASN][1000 genomes] |
rs4530331 | 0.95[ASN][1000 genomes] |
rs4535008 | 0.91[ASN][1000 genomes] |
rs4569437 | 0.91[ASN][1000 genomes] |
rs4608482 | 0.83[ASN][1000 genomes] |
rs4637073 | 0.92[ASN][1000 genomes] |
rs4666701 | 0.93[ASN][1000 genomes] |
rs4667079 | 0.96[ASN][1000 genomes] |
rs4667080 | 0.96[ASN][1000 genomes] |
rs4667081 | 0.90[ASN][1000 genomes] |
rs4667086 | 0.90[ASN][1000 genomes] |
rs4667089 | 0.88[ASN][1000 genomes] |
rs4667090 | 0.82[ASN][1000 genomes] |
rs5008098 | 0.95[ASN][1000 genomes] |
rs56347348 | 0.89[ASN][1000 genomes] |
rs56393956 | 0.96[ASN][1000 genomes] |
rs56681734 | 0.96[ASN][1000 genomes] |
rs56718299 | 0.96[ASN][1000 genomes] |
rs56786415 | 0.95[ASN][1000 genomes] |
rs57289110 | 0.96[ASN][1000 genomes] |
rs58244659 | 0.96[ASN][1000 genomes] |
rs58488407 | 0.95[ASN][1000 genomes] |
rs58579412 | 0.96[ASN][1000 genomes] |
rs58783284 | 0.96[ASN][1000 genomes] |
rs59087873 | 0.95[ASN][1000 genomes] |
rs59224241 | 0.96[ASN][1000 genomes] |
rs59276018 | 0.96[ASN][1000 genomes] |
rs59360834 | 0.93[ASN][1000 genomes] |
rs60859807 | 0.96[ASN][1000 genomes] |
rs61083860 | 0.95[ASN][1000 genomes] |
rs61253791 | 0.96[ASN][1000 genomes] |
rs6434170 | 0.93[ASN][1000 genomes] |
rs6434171 | 0.92[ASN][1000 genomes] |
rs66593320 | 0.96[ASN][1000 genomes] |
rs6704957 | 0.89[ASN][1000 genomes] |
rs6715735 | 0.91[ASN][1000 genomes] |
rs6717965 | 0.93[ASN][1000 genomes] |
rs6726048 | 0.87[ASN][1000 genomes] |
rs6728734 | 0.93[ASN][1000 genomes] |
rs6741525 | 0.96[ASN][1000 genomes] |
rs6743356 | 0.91[ASN][1000 genomes] |
rs6744814 | 0.96[ASN][1000 genomes] |
rs6745187 | 0.96[ASN][1000 genomes] |
rs6745873 | 0.93[ASN][1000 genomes] |
rs6752407 | 0.85[ASN][1000 genomes] |
rs6754898 | 0.96[ASN][1000 genomes] |
rs6755955 | 0.93[ASN][1000 genomes] |
rs6759502 | 0.85[ASN][1000 genomes] |
rs6760230 | 0.96[ASN][1000 genomes] |
rs67917059 | 0.95[ASN][1000 genomes] |
rs716130 | 0.93[ASN][1000 genomes] |
rs72907565 | 0.96[ASN][1000 genomes] |
rs73035230 | 0.95[ASN][1000 genomes] |
rs73035235 | 0.96[ASN][1000 genomes] |
rs73035261 | 0.96[ASN][1000 genomes] |
rs7558599 | 0.90[ASN][1000 genomes] |
rs7560019 | 0.96[ASN][1000 genomes] |
rs7571191 | 0.96[ASN][1000 genomes] |
rs7571408 | 0.96[ASN][1000 genomes] |
rs7579391 | 0.91[ASN][1000 genomes] |
rs7580038 | 0.87[ASN][1000 genomes] |
rs7586291 | 0.85[ASN][1000 genomes] |
rs7586995 | 0.81[ASN][1000 genomes] |
rs7587077 | 0.93[ASN][1000 genomes] |
rs7587079 | 0.93[ASN][1000 genomes] |
rs7599277 | 0.85[ASN][1000 genomes] |
rs7602918 | 0.93[ASN][1000 genomes] |
rs7606494 | 0.92[ASN][1000 genomes] |
rs980540 | 0.92[ASN][1000 genomes] |
rs9807987 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv875545 | chr2:186566024-187280164 | Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv817325 | chr2:186625679-187200841 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv868949 | chr2:186657142-187327560 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
4 | nsv932296 | chr2:186737443-187265790 | Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
5 | nsv1014726 | chr2:187036909-187213113 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
6 | nsv536078 | chr2:187036909-187213113 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | nsv1006411 | chr2:187150025-187291081 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv536079 | chr2:187150025-187291081 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:187163600-187170600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
2 | chr2:187168000-187172400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr2:187168000-187173000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr2:187168400-187169600 | Enhancers | HepG2 | liver |
5 | chr2:187168400-187172400 | Weak transcription | NHEK | skin |
6 | chr2:187168800-187169000 | Enhancers | Fetal Intestine Large | intestine |
7 | chr2:187168800-187170400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |