Tag | Content |
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EnhancerAtlas ID | HS092-29612 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr3:187672280-187673610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr3:187673562-187673582 | CCTCCAACCACCCATCCCCA | + | 6.11 | TCF7L2 | MA0523.1 | chr3:187672531-187672545 | AAAGTTCAAAGGGA | + | 6.78 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_51347 | chr3:187671580-187677656 | Skeletal_Muscle | SE_58285 | chr3:187606861-187725246 | Ly1 | SE_59604 | chr3:187596115-187720147 | Ly4 | SE_60392 | chr3:187615879-187719658 | DHL6 | SE_62680 | chr3:187634828-187719022 | Tonsil |
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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 |
GH03I187954 | chr3 | 187671898 | 187674187 |
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Enhancer Sequence | GGAACCAGCT GGTCGAGCTT TGTGAACTTT GTCTTCATGC CCCGACACCC TACTTCCCAA 60 AGCCTGGACC GGTAAAGTTC TTTTCACCAG AAAGGACAAG GGCAAGTGAG TGCAAGAGAG 120 AAAGTGGCAC ATTTATCACT GAGAACCTGC TTGGGAAATG GGGGAAAGGG GAAGGGAAGA 180 GATCTTATTT TCTAAGACTT GAGAAGGGAA AATGGAAGTG GGAGGGAAAT CATCTGTGGC 240 TTATGTTCTC TAAAGTTCAA AGGGAACTTG CTGCCCCATA CATGATGTTG ATTAGGGAAA 300 GTATCATCTA GTTACACTGA ACCCCACAGA TTGGTAAGCA TGAACTCAGA AGGGTCCCAG 360 CTTTCTGATT CATCTGATCC ACAAGCCTTG GTCAGCAAGC ACGCAGTTGC TTTTGCTTTA 420 AGATGACCTT ATTTGAAATT CCTTATGTAG CTGTCACTGC CAGCACTAAA GCCTGGTCAT 480 TTACAGTAGC TGTCCTTTCT GAATTTAAAT CTGATAAAAC AGGCTGCGCC TGCCCCACAC 540 CTCCTAGGGG TCTAGATCTG AAAGGAGCCC CAGGGATCAT CCCATCTAGT CTAACCCTGG 600 CCCAGAGAGG AAGGGTCACA CCACCAGGCA GTGCTGAAGC CAGGCCTGCA ACACACTTTC 660 CACTACCCCA AGATGCCCCC ACTGGCTGTT CAATTTAAGG ACATAACCCG TGAAGAAAGG 720 AGATTGTGAA ATGCTTCCAC TAGAAGCCCA AGGGTGGCTG AAAGCCCAGA TGCTTCTCTC 780 TTAACCCTCC TAACCTAGTC CCAGTTCAGC AGTTTGCTTC CCACTGTTTC ATGTTAACCC 840 TTTTTCTCCA TGAGGCCAAG GCTTGTCTTC CAATGAGCAG CTCCTTACAA TAACTAAGCC 900 GGCTTCTGCT TGTACCTTCC CAGACACCTC CACTGGCAAA ACCTTTCCAT TGAGCAATCT 960 TCTTGTGAAA ACTGACTCTT CTTTGCCCTT TACAATTACT CAGCAACTCT GCAAAACAGT 1020 AACCCAACTG TTTATTTTGA TTTCAAGCTT GGGGTTAAAG GGCTAGCTTT GTCATTTTTT 1080 TTTTTTTATT CCCCTTGAGG AAGTTACTAG AGACCTCAGG GATTTCTTGT CTTTGACTCT 1140 TGACTACCAG CTTGACATGC CTCCATCTTC CACTAGCCCC CAGTCTGTGC CAGGTGACAC 1200 AGAAGTTTCC AGGAAGGAAA GGGGATACTC CTCCAGAGGA AAGATACTTC CTAAATGGAG 1260 AGCTGGCATT CACTCAACCT TCCCTCCAAC CACCCATCCC CAAGGCACCA ACCTGCCCAT 1320 GTTTTCAATG 1330
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