Tag | Content |
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EnhancerAtlas ID | HS088-26793 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr19:11145810-11147280 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:11146769-11146788 | TGTGCACCAGAGGGCGCTG | + | 6.28 | Zfx | MA0146.2 | chr19:11147178-11147192 | CCCGCCTCGGCCTG | + | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_62144 | chr19:11142087-11163834 | Toledo |
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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 |
GH19I011034 | chr19 | 11145132 | 11147747 |
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Enhancer Sequence | ACATGCTGGA GAGGCCCAGC AGCTGCCGCA GGCCAGCGCC AGGCAGGGCT GGGGAGACAA 60 AGGGCCCACC GCCAGGACTC AGGCCTGGGT CCAAAATGCT TTCCTTGGGC CACTCCTGGC 120 CAGGCTCCGC AGGCAGCCGA GAGCCTTCCG ATGTGGGCCA GGGATGGTCA GGTCCTTTTG 180 GCTCTGCCTT GGAATGCAAG AAGGACCCAC GGTTCCTGAG CAGCTCAAAA CCTGCTGCTG 240 GTTATGGTTG GTCTTTCAAG TAAAAGGGTT TACCTCTTCC CGAGGTTAAA AATCATGTTG 300 CTGATCTCAG TGGACTGCTG GCTTTCCCAG TACCTGCCAG GAGGGAGGCA CAAGGGTGAA 360 TCATGGACTA TTGAGGCGCC CTGCAAAGCG TTGCACTGCT GGCTGCAGGC AGCCTCACTT 420 TGGGCAAGTC CCCCCCCATG AGCTGGGGAG ACTCAGTCAT GGGGAGGGAG GAGAGGGCAA 480 GCCCCCAAGG GCCTCTGAAC CTGGCAGGTG CTGCACGGGG CTGGCAGTTG CTTGTGGAGC 540 TGACGTGAGG GCCCGTTCTC AGCAGATGGC AGCTGGCCCT GCAACAGCAG CTGCAGATGT 600 CTTTGAGTCA GTCGTGCGGT GCTCCTGGGG CTTCACCCGA CCCAACTTTC CCAGCCCAAG 660 GCACACTGTG ACAGATGCCT GGCACTGATG TCCTCACTGG GGTTACGGTG ACAGATCAGA 720 CCCCTTCCCA GCTCAGGGGC TCTGAGTTAT AGAGACGATG ATTCAGAATC CATCCCTGAA 780 GTTGTGTCAT AAAAATGTCC TGAAGCAATA ATTCCGAGAA GGCAGGTGGC AGCTTTTGGC 840 TATGCCATGC AAAGTGCCAC ACCCAGGAAA GAGCCATGTG GCCTAGCCCA TGTGGCCAAA 900 CAGCCCCGGT TCCCTCCTGG GACCTCAGCA GCCCAGACTC ATGAGCTTGC CTGCCAAGCT 960 GTGCACCAGA GGGCGCTGTT GAAACACACC AGGAGCCCAG GTGACAGACA GGCCATCCTG 1020 TTCCCCAGCC AGCCTCCCAA GCACAGCGCT CCAGGACCCA GAAGAGAAAC CCTGAAAAGA 1080 CAGTGTGAGC CCTGCCACAG ACCTGTGTGA CAGCAGAGCT GTTTGGCTGC TGTATGAGTG 1140 TCACCGGCCC TGCATTTTTT TCTTTTTTAA TAAAGACAAA GTCTTGCTGT GTTACCCAGG 1200 CTGGCCTCCA GTTCCTGGGG GCTCAAGTGA TCCTCACACC TCAGCCTCCT GAGTAGTTCA 1260 GACTACAGGT ACACACCAAC ACGCCTGGCT AATTTTAAAT TTTTTGTAAA GTGGGGGTCT 1320 CACTGTGTCA CTCAGGCTGG TCTCAAACTC CTGGGCTCAA ACAATCCACC CGCCTCGGCC 1380 TGCAGAGTAG CTGGGATTAC GAGCATGAGC CACGGTGCCC AGCTCAGCCC TGCATATTTG 1440 AGGCAGTGAG TACCTTTTAA ATTTAAGATC 1470
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