Tag | Content |
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EnhancerAtlas ID | HS087-08936 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr17:38646100-38647310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REST | MA0138.2 | chr17:38646613-38646634 | GGAATTGTCCTTGGTGCTGTT | - | 6.41 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_26577 | chr17:38641588-38649349 | Esophagus | SE_33816 | chr17:38646009-38652568 | HCC1954 | SE_34508 | chr17:38646078-38647046 | HCT-116 | SE_34641 | chr17:38639413-38648954 | HeLa | SE_35821 | chr17:38639654-38658761 | HMEC | SE_45551 | chr17:38645995-38647818 | Osteoblasts | SE_54612 | chr17:38645884-38648252 | Stomach_Smooth_Muscle | SE_56976 | chr17:38646190-38647370 | VACO_400 | SE_64249 | chr17:38645980-38648789 | 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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Enhancer Sequence | GATTCTCAAG CTTGGTTACA CACTAGACTC ACCCCAGGCT GCGCCTTGTG CCAATTAGAT 60 TAAACTCTCC AGGGGGTGAA CCCAGGCCTC AGTTTTGTTT GTTTTCCAGT TTTTCAGGTG 120 AGTCCAGTAG ACCATGAATG GCTCAGCAGG ACCACATCAC CTGGGCTCCA CCCCTACAGA 180 AACATAATCT GCATTTTAGC GAGGCCACCC AGGGCATGTG AATATGCAGT GGAGTCTGAG 240 AACCCTGCTT TGGAGCAGGC ACTCCCTGAG CACAGGGCTT GCTGCATTCT TGAGCTATGG 300 ATCTCCTGGG GATGGTAGCT GGTACACAGG GGTCACCCAA CACACCCCAG GCTGCCGACG 360 CGCTCCAGCG CTCTTTCCAC TCCCTGGTCG GGGCATCCAG GACTCTTGGG ATTCTGAGGC 420 CTTGTTCCTC TCCCGAGGTC GGCCTTGCAG TGGGCTGCTC TGAGGTTCTC CCCAAGGTGA 480 GGATGAACAC CCTTCCTCCT GACCTGGGGG AAGGGAATTG TCCTTGGTGC TGTTCCAGCA 540 AAGCTGGAGG AAGGTGGGGG TTAATGAGCC GCTCCTTTCT GAAGAGTGTG AGTCTTGCCT 600 CTAGCTTCCT GGGATGGAGG CTGGGGAAAT TGGGGAGAAC GTGCACCCTC AGCTCCCACC 660 TGCCTGGGGC CCTGGCACAT GCACTGTTCC TCCCCATTAT GACTGTGGAG CCCCAGCCTG 720 CCCCAGCCCG CTCCTGGGTA GGGCCATCTG GCCCTGCTCA CAGTTACTGC CTCTGTCTGA 780 GCTTGCTTGG GCCACGGTGG GGGTGGGGAG TTACATCAGA TGAGCAAGGG CTGGCAGCTG 840 ACTGGGACTT GCTGCTCAGC GGGTGGAGGA AGAGCCTAGC TTTGTAGCAA AACAAACCTG 900 GGGTGAGTCC TGGCTTTGCT GCTTTTCAGC CAAGGGCATT GTGCAACTTT CCTAACCTCT 960 CTGAGCCTCA GTTTCCTTAT CTGCAAAGTG AGGATCTGAA ACCAGTCTTC CAAGGTTGTG 1020 ATGAGGATGA AATACAATAG CCGGGAGCCT GGCCCATGGT GAGGCTCGAG AGAGGAGCAT 1080 TTCCTACCTG CCTGCTTTTT GGGGACAGTA TTGGCCAAAT GGAGCCCTTT TCTGGCTAAG 1140 GTGGGGATCT CTCTGCTTAG AAAGATGACT GCAAGAAGAG AGTGTTTGGG GCACTGCATT 1200 GTGGGCTCTG 1210
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