Variant report
Variant | rs5002972 |
---|---|
Chromosome Location | chr6:4428112-4428113 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:6)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:6 , 50 per page) page:
1
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | CEBPB | chr6:4427950-4428239 | HepG2 | liver: | n/a | chr6:4428101-4428112 |
2 | TBP | chr6:4428007-4428363 | H1-hESC | embryonic stem cell: | n/a | n/a |
3 | TEAD4 | chr6:4428055-4428372 | H1-hESC | embryonic stem cell: | n/a | n/a |
4 | CEBPB | chr6:4428066-4428179 | K562 | blood: | n/a | chr6:4428101-4428112 |
5 | TEAD4 | chr6:4428086-4428384 | HepG2 | liver: | n/a | n/a |
6 | SIN3AK20 | chr6:4428111-4428363 | SK-N-SH | brain: | n/a | n/a |
No data |
No data |
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
RNA5SP202 | TF binding region |
rs_ID | r2[population] |
---|---|
rs1010638 | 0.86[ASN][1000 genomes] |
rs10447477 | 0.86[ASN][1000 genomes] |
rs10447478 | 0.85[ASN][1000 genomes] |
rs10458172 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs10458173 | 0.96[ASN][1000 genomes] |
rs10458174 | 0.96[ASN][1000 genomes] |
rs10900958 | 0.96[ASN][1000 genomes] |
rs10900959 | 0.96[ASN][1000 genomes] |
rs10900960 | 0.96[ASN][1000 genomes] |
rs10900961 | 0.96[ASN][1000 genomes] |
rs10900962 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11242933 | 0.96[ASN][1000 genomes] |
rs11242934 | 0.96[ASN][1000 genomes] |
rs11242935 | 0.96[ASN][1000 genomes] |
rs11242936 | 0.96[ASN][1000 genomes] |
rs11242937 | 0.96[ASN][1000 genomes] |
rs11242938 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11242939 | 0.96[ASN][1000 genomes] |
rs11242942 | 0.86[ASN][1000 genomes] |
rs11242943 | 0.87[ASN][1000 genomes] |
rs11242944 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes] |
rs11242945 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs11242946 | 0.96[ASN][1000 genomes] |
rs11242947 | 0.96[ASN][1000 genomes] |
rs11242948 | 0.91[ASN][1000 genomes] |
rs11242950 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs11755069 | 0.96[ASN][1000 genomes] |
rs12190411 | 0.86[CEU][hapmap] |
rs12191559 | 0.96[ASN][1000 genomes] |
rs12200144 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs12203267 | 0.89[ASN][1000 genomes] |
rs12207441 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs12207864 | 0.89[ASN][1000 genomes] |
rs12210818 | 0.96[ASN][1000 genomes] |
rs12211520 | 0.96[ASN][1000 genomes] |
rs12211781 | 0.91[ASN][1000 genomes] |
rs12529480 | 0.96[ASN][1000 genomes] |
rs1265298 | 0.91[ASN][1000 genomes] |
rs1265299 | 0.86[ASN][1000 genomes] |
rs1265303 | 0.92[ASN][1000 genomes] |
rs1265304 | 0.87[ASN][1000 genomes] |
rs1265305 | 0.87[ASN][1000 genomes] |
rs12660869 | 0.96[ASN][1000 genomes] |
rs12663036 | 0.91[ASN][1000 genomes] |
rs12664576 | 0.85[ASN][1000 genomes] |
rs12665814 | 0.91[ASN][1000 genomes] |
rs13213475 | 0.96[ASN][1000 genomes] |
rs13214482 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1330783 | 0.95[ASN][1000 genomes] |
rs1330784 | 0.96[ASN][1000 genomes] |
rs1330786 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1330787 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1330788 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1330789 | 0.96[ASN][1000 genomes] |
rs1330791 | 0.96[ASN][1000 genomes] |
rs1411654 | 0.87[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1411656 | 0.96[ASN][1000 genomes] |
rs1581971 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1581972 | 0.96[ASN][1000 genomes] |
rs1590939 | 0.96[ASN][1000 genomes] |
rs17510496 | 0.91[ASN][1000 genomes] |
rs17510539 | 0.91[ASN][1000 genomes] |
rs17570029 | 0.89[ASN][1000 genomes] |
rs2026183 | 0.90[ASN][1000 genomes] |
rs2026184 | 0.90[ASN][1000 genomes] |
rs2026185 | 1.00[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes] |
rs2150233 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2150234 | 0.91[ASN][1000 genomes] |
rs2183497 | 0.96[ASN][1000 genomes] |
rs2225369 | 0.82[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs2326490 | 0.91[ASN][1000 genomes] |
rs2875944 | 0.91[ASN][1000 genomes] |
rs415338 | 0.84[EUR][1000 genomes] |
rs4286821 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4403297 | 0.91[ASN][1000 genomes] |
rs446293 | 0.85[EUR][1000 genomes] |
rs4481463 | 0.94[ASN][1000 genomes] |
rs4513847 | 0.96[ASN][1000 genomes] |
rs4534025 | 0.94[ASN][1000 genomes] |
rs4621669 | 0.96[ASN][1000 genomes] |
rs4959287 | 0.96[ASN][1000 genomes] |
rs4959288 | 0.97[ASN][1000 genomes] |
rs4959292 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs4959293 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4959294 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4959960 | 0.95[ASN][1000 genomes] |
rs4959961 | 0.92[AFR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4959962 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4959965 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4959966 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4959968 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4959969 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4959970 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4959973 | 0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4959974 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4959976 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4959978 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs59075559 | 0.96[ASN][1000 genomes] |
rs59425532 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs60109220 | 0.91[ASN][1000 genomes] |
rs6597055 | 0.85[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6597060 | 0.92[ASN][1000 genomes] |
rs6597066 | 0.96[ASN][1000 genomes] |
rs6597067 | 0.96[ASN][1000 genomes] |
rs6597068 | 0.96[ASN][1000 genomes] |
rs6597069 | 0.96[ASN][1000 genomes] |
rs66815625 | 0.96[ASN][1000 genomes] |
rs67284074 | 0.96[ASN][1000 genomes] |
rs67655715 | 0.91[ASN][1000 genomes] |
rs6902044 | 0.96[ASN][1000 genomes] |
rs6904462 | 0.96[ASN][1000 genomes] |
rs6908618 | 0.88[ASN][1000 genomes] |
rs6908628 | 0.92[ASN][1000 genomes] |
rs6911222 | 0.94[ASN][1000 genomes] |
rs6912116 | 0.94[ASN][1000 genomes] |
rs6912489 | 0.94[ASN][1000 genomes] |
rs6912741 | 0.96[ASN][1000 genomes] |
rs6913210 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6914316 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6917196 | 0.94[ASN][1000 genomes] |
rs6920549 | 0.96[ASN][1000 genomes] |
rs6923978 | 0.96[ASN][1000 genomes] |
rs6924842 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6926926 | 0.94[ASN][1000 genomes] |
rs6927710 | 0.96[ASN][1000 genomes] |
rs6929358 | 0.96[ASN][1000 genomes] |
rs6930889 | 0.90[ASN][1000 genomes] |
rs6931444 | 0.94[ASN][1000 genomes] |
rs6934676 | 0.94[ASN][1000 genomes] |
rs6937848 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7450619 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7453615 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7454057 | 0.96[ASN][1000 genomes] |
rs7750156 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes] |
rs7752768 | 0.96[ASN][1000 genomes] |
rs7754765 | 0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7756945 | 0.92[ASN][1000 genomes] |
rs7760765 | 0.90[ASN][1000 genomes] |
rs7765880 | 0.94[ASN][1000 genomes] |
rs7766314 | 0.94[ASN][1000 genomes] |
rs911568 | 0.92[ASN][1000 genomes] |
rs911569 | 0.92[ASN][1000 genomes] |
rs9328251 | 0.90[ASN][1000 genomes] |
rs9328252 | 0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9378400 | 0.94[ASN][1000 genomes] |
rs9378872 | 0.94[ASN][1000 genomes] |
rs9378873 | 0.95[ASN][1000 genomes] |
rs9378874 | 0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9378875 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9378876 | 0.96[ASN][1000 genomes] |
rs9378877 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9392046 | 0.96[ASN][1000 genomes] |
rs9392047 | 0.96[ASN][1000 genomes] |
rs9392594 | 0.94[ASN][1000 genomes] |
rs9392596 | 0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9392597 | 0.94[ASN][1000 genomes] |
rs9392598 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs9392599 | 0.94[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs9405243 | 0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9405731 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9405738 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9405742 | 0.82[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs9504074 | 0.86[AFR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9504076 | 0.92[ASN][1000 genomes] |
rs9504089 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap] |
rs9504090 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9504091 | 0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9504093 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9504094 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs9504096 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv600861 | chr6:4238488-4469641 | Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
2 | nsv462618 | chr6:4238488-4472587 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
3 | nsv600862 | chr6:4238488-4472587 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
4 | nsv949364 | chr6:4253413-4466981 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv600863 | chr6:4255387-4472587 | Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
6 | nsv1027498 | chr6:4255640-4471635 | Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
7 | esv2763995 | chr6:4255640-4474114 | Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
8 | nsv1020205 | chr6:4255640-4474114 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
9 | nsv600864 | chr6:4255708-4464630 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
10 | nsv516402 | chr6:4255708-4472587 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
11 | nsv462619 | chr6:4255708-4472587 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
12 | nsv600865 | chr6:4255708-4472587 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
13 | nsv462620 | chr6:4255708-4481421 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
14 | nsv600866 | chr6:4255708-4481421 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
15 | nsv600867 | chr6:4255725-4464630 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
16 | nsv462621 | chr6:4255725-4472587 | Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
17 | nsv600868 | chr6:4255725-4472587 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
18 | nsv1029501 | chr6:4255745-4471635 | Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
19 | nsv432845 | chr6:4255905-4471472 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
20 | nsv1030655 | chr6:4257190-4473701 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
21 | nsv538108 | chr6:4257190-4473701 | Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
22 | nsv1030840 | chr6:4257390-4473562 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
23 | nsv538109 | chr6:4257390-4473562 | Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
24 | nsv1026890 | chr6:4259075-4471635 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
25 | nsv1030588 | chr6:4264933-4455210 | Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
26 | nsv1021257 | chr6:4264933-4473384 | Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
27 | nsv538110 | chr6:4264933-4473384 | Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
28 | nsv916553 | chr6:4269714-4437920 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
29 | nsv1016621 | chr6:4277411-4473384 | Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
30 | nsv600869 | chr6:4294450-4430623 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
31 | nsv883413 | chr6:4371622-4474114 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
32 | nsv1021743 | chr6:4382308-4494308 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
33 | nsv538111 | chr6:4382308-4494308 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
34 | nsv600870 | chr6:4391872-4429310 | Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:4426800-4428200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |