Tag | Content |
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EnhancerAtlas ID | HS060-29436 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:30784570-30785940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:30785079-30785100 | CTTCAGTTTCTCTTTCTGTAA | + | 6.4 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_18824 | chr6:30784605-30789008 | CD4p_CD25-_Il17-_PMAstim_Th | SE_33790 | chr6:30785165-30789035 | HCC1954 | SE_34510 | chr6:30777025-30788930 | HCT-116 | SE_64605 | chr6:30784621-30788804 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 30784962 | 30785406 | chr6 | 30785034 | 30785335 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I030816 | chr6 | 30784419 | 30790976 |
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Enhancer Sequence | CCCAGGCAGA GGAGGCGCCC AGAGCGAGTG AGAGCTGTGA GGACTGCTAG CAGGCTGTCA 60 CCTCTCAAGC TCACTGCAAC CTCTGCCTCC CAGGTTCAAG TGATTCTCCT GCCTCAGCCT 120 CCTGAGTAGG TAGGATTACA GGCGTGTGCC ACCACACCCG GCTAATTTTT GTACTTTTAG 180 TGGAGACAGG GTTTCACCAT GTTCGCCAGG CTGGTCTCAA ACTCCTGACT TCAGGTGATT 240 CACCCACCTT GGCCTCCCAA AATGCTGGGA TTACAGGCAT CAGCCACTGC TCCTGGCCTC 300 TGTGTAGTTT TGTTTGGAGC TGCAGTAAAT AGTGTCTAAT CTTTTCCTTC CTTACAGGCT 360 ATTTCTCCAT ATTGCTTCCC AGATACAAAA TTCATAAATG TATACAAGCC ATACCCATGT 420 TACCCACTCC CTCAGGCCCT GCCAAGGCCT TGAGAAACTA GACTCAGACT GTGTCTCCAT 480 GTAGGGGGAT TGCACATAGC ATCTTTGAAC TTCAGTTTCT CTTTCTGTAA AATGGGGAAT 540 TTTGACTACT TAGCATGCGT CATGTGTTAA AACCCTAACC TCGTTAGCAA TTATAACCAC 600 TATCAGTATC CCATACTCTG GTTTTTTTAG GGCTTTCCCA AGGCAAATGG GAAGATTTGC 660 TGCCAAGCTC ACTTCGGGAG GTCACCAGGC CCAGAACATT CTTGTCCTCA CAAATTTTCA 720 CTTCCTTCAT TTAAGAACAA GGACTAGAGT GTTCTCACTT AATTACAACT GGGATAGGTG 780 GGAGGGAGTT ACCCATGTGG GCAACATTAG GGAAACTTTT TCTTTGAGAC AGGGTCTTGC 840 TCTGTTGCCC AGGCTGGAGT ACAGTGGTGT GATCATGGCT CACTGCAGCC TCGACTTCCT 900 GGGCTCAAGC AATCCTCCTG TCTTAGCCTC CTAAGTTCTG ACAGCCCTTA GGGACTACAG 960 GCGCACACCA CCACACCCCA TTCATTTTTG CATTTCTTGT GGAGATGCGT TTTTTCCATG 1020 TTTCTCAGGC TGGTCTTGAA TTCCTGGGCT CAAGAGATCC TTAGGGAAAC ATTCTACCAA 1080 ACCAGAAGTG ATGGATCAAC TCCCAGCAAG CCTTTAGTGG GCATTGTTCT TTTCAGGGAG 1140 CTGGATAGAA GAGGGGTCTC GGAGCCACAA CACCCGTGCT GCCCATGATG GTAGAAAAGG 1200 GAAGTCTAAA AAGAGTTTGG GTCTGAACTG GGGCCTAGGA AAAGTTAATG GGGCAGTGAT 1260 TTTGGCCTTT TCTACCCACC TCCTTGTAAT AATATTATTT TAACAATCTG GCTGGGTATG 1320 TGGCTCATAC CTATAATCCC AGCACTTTGG GAGGCCAAGG TGAATGGATC 1370
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