Tag | Content |
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EnhancerAtlas ID | HS059-01760 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:59049680-59050920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:59049970-59049981 | TTTCTGGGAAG | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26866 | chr1:59049023-59052890 | Esophagus | SE_34091 | chr1:59048932-59051469 | HCC1954 | SE_36047 | chr1:59048890-59052166 | HMEC | SE_64419 | chr1:59048986-59052077 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I058583 | chr1 | 59048999 | 59052771 |
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Enhancer Sequence | ATTTATTGAT CATCATATTA TAAATTCCTT GTAATTCCCC CAGCAAGCCT ACAAAATAAT 60 TACTCTTGTC CCCATTCACC TGATCAGGAA GCTGAGGCTT AGGGTCACAT AGTTAGAAAT 120 GAGTCCAGGA AGGATCTGAG CCAAGTCTCG TGACTGGGAC ATTTTTCCAT TGCACAGTTT 180 AGTCTCTCGC TGATGGGTCT TGAATAAACG AGAGAGGTCA AAGATGTTCT GCTGGTAAAC 240 TGGGTGTGGT CTGGGTCCTG GCTGCCCAGG GAATGTTTGA TCTTTTCACT TTTCTGGGAA 300 GACAACACGT TTCTGTTTGT GCTTGCTCAT TTGGGTGGGC CCAACTCAGT TTCTTTCAGG 360 AGAAGTTGCC TGTGATGTGT ACAGTTCTGC TTGGTTTTTG TGGTTCATCT GGATTTGAAA 420 AGTGACTGCA GTTTCACCTT ACAAGTGTGT GTCATGGTTT CATTTCAGAA TCCTGCCCAT 480 CATCTTCTTT TCATGGTGTC CTTGTTCTGA ATTGCAAACC ATAAATGGCC TCCTTCTCAT 540 TCTGGTCTCT TCATCTAGGG GCAGTCAGCT TCTCCTGTAA GGGCTTTACA CTCTGGGGAA 600 AGCCAGTAAA ACACTCAGTG ACTTTTAATT TCACTGGGCC CAACAGCTTC CAGACAGATT 660 TGGCAACAAA TAAAGAGAGA TTGGGAAACC TTCTCCCTAC ATTCCTGAGG CAGCCACAAT 720 GCTCGAACCC CACACTGATG AGTCACGGTG CTTCCTTTCC CAGAGCTGGC CCGGCGATGT 780 GTGATGCCCT GTTAAGGGGA TGTGGAGGTG TTTGCTGTTT TTAACCACTT TCAGCTGTCC 840 TTGAGATAAG GGCAGGTGGT GAGAGGTCTT AAGTGGGCTG CTGCTACTGA CAAATTCGTC 900 TGCCTTTCTG GACAGTCCTG ATCCAAGTGA GGCTCCTTAG AGTTATCAAA AGGGGTCTTA 960 GAGGACATGT ATTCCAGTCT CCCACCCAAA GAGAGGTATC TCAGAATGCT AAACAGGTGC 1020 TTGTAGGCTA CCTGTGATAA TGCAACATCC TTACCTCCCC ACAAGACAAC CCATTCCAGT 1080 CCCAAGCAGC TTTACTAAGA AGTTCATCAT AATTAAGGAA ATTCAGTGCC TCTGTAATTT 1140 TCACAAACTG ATCTAAATTT CTACTCTTGG AGCAAGAAAG AGTAAGTAAT GTTCCCCTTT 1200 CACTCCTTGG TTCCTCAGGA ATTTGAAGCC AGTTCTCCTG 1240
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