Tag | Content |
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EnhancerAtlas ID | HS187-21540 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:106347430-106348860 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr6:106348083-106348104 | GGGGGAGGGGGTGCTGGAGAA | + | 6.2 | ZNF263 | MA0528.1 | chr6:106347703-106347724 | CTTACCTCCTTTCCCTCCTCT | - | 6.47 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61807 | chr6:106309470-106360339 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I105900 | chr6 | 106347876 | 106349190 |
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Enhancer Sequence | TGATCCACTC ACCTCGGCCT CCCAAACTGC TGGGATTATA GGCATGAGGC ACTGCGTCCA 60 GCCTAAAATA AGAGGGAGTT CTACTAGCCA ACTCATGCAT TGCTCTGCTC CAGGGTACCT 120 AAGTAACCAA CTGCTCTAAT GGTTTCTCTC CAGATGGACA GACCTGCCAG GTTGATACCT 180 TTGCCAGCCC CTCTGGAATT CCAGTGAATA AAATTTTCCC TAACAGATCA CTTGTTTAGT 240 GTAGCACTTA GCGCCTAGCC TCACCACTGT TTACTTACCT CCTTTCCCTC CTCTGTGAGC 300 TCTCTGCATG TAAGAACTAC ACTCTTTATA ACAGTTTTGT TGGTGGCCAT GCACAGTGGC 360 TGACTTATAG TAGATGCTCT ATGGAGTGAC TGTTTGCAAA CAACCTTCCA AATAAGATAA 420 GAATAACAAA ATTGAGCCTG GTTAGTCTGC ATCCAGATAG AATGGAATTT TTTAAATGGC 480 AGCAAGGGGA GCAAAGCACA TTGTTAAGTA ATGCTAAATG AAAACAGGCA GCAACCCTCA 540 AAGGTGAGCT TCAAAAGTCA GATCAACCTT CACTCAGCCC TAGAACATTT CTAACTAAAT 600 CCCACCTCTC ACTAGAAGTG TCACCATTTT TCTTTTCTTT GAAAAAGCAT GATGGGGGAG 660 GGGGTGCTGG AGAACGACAA ATGAGAGGGT GACTCCCATA TAAGTCAGCT TCCTCTTCCC 720 CAAATCAGTT TCCAGAAACT CTGCCATATC ATGCAACGAG AACCCCCAGC TCCTAATTCA 780 AAGGAAAGTC TCAGAGGTCT TGGGTAAAGA CGATAACACC TCTCCTTTGG TGGCTTTCAG 840 TGATAAACAG CTTCCTGCCT GAGCACTCAT AAACCTGAAC TCGTGGAAAA GAATTACTAC 900 ACGGAAAACA GAACCCAGGC AGGGTTCGTA AACGGTACCC GGCATGGGTT TCTCACATCT 960 TCGTTGATAA ACGTCCTGTT GCCTCCTGAG GAATCTGTGA GACTCCTTGG GTACAGCTGT 1020 GGTCAGGAAC ACACCATGCA ACAACTAGAC CTGAGAAGTG TCCATCTTTC TGCCATCGAG 1080 ACCTGCCCTA GAAGAAAAAC AGAAACAACA CAGATGGAGC TGCCTGTTCA AATCCTTGTG 1140 GATGTCATAA GATTAGCAGC TTTCCTCTGA GTCGGCCTCA AAGACTTCCT TTGCAATTGT 1200 TCCTAAGCTA GCTCAAGGGA TAGGCAGTGA AGTTCACTAA AACAAAAACA TAACCTCAAA 1260 CATCCAAAAC AGCTGGTGGA AATTGTGACT GTTTTAGAGG AGCTGACTTA TCTAGCTGAG 1320 TCAAAACAAG TGTGAGCGCT TCAAACAGGC ACAAGATCAG AAACAAAATT AGGTGTTTAT 1380 TGAGTGCTGT CCTCTTGATT TTTTTTTTCT CCTTTGCTTA GGCATGAATC 1430
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