Tag | Content |
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EnhancerAtlas ID | HS061-00519 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:27691430-27692740 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:27692118-27692129 | CTTTCCCGCCC | - | 6.32 | KLF16 | MA0741.1 | chr1:27692726-27692737 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692099-27692109 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692425-27692435 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:27692726-27692736 | GCCCCGCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34417 | chr1:27690765-27694847 | HCT-116 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 27691785 | 27692261 | chr1 | 27691800 | 27692047 |
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Enhancer Sequence | TCCCTGAAGC CCAGCTTGAT GGGGAAGGAG CCGGGGTCCA TCCTGGCTTG ACCTGCCTTG 60 CTGTGGGACT CCAGTAGGGT CTGGTTCTGC TTTGGGCTTC AGTCGGCCCT TTTTAGGGTT 120 CCCCTGGCAC TTTCACAGAA CTGATCTCTG TAGTGTTGCA GGAGAGGAGT TGGGCTCACT 180 GGGTTGGGAC CCTCAGGCCA CGGTTCAGAG CCTGTGAGCA CCTGGCATGG GGGAAGGGAG 240 GCTGTGGACC AGTTGAGTCT GTTACGGGCC ATTTAGGAGG TGGGAGTTGC GCAAACATAG 300 AAGTCCCCTC CCTTTGGTCT TCAGCACAGG CTCTTGAAAG GGGCTACCAT CAGTGTGCAT 360 AGACAACGCT GTGCCTAAAT GTATGTATGT GTATATCTGT GACATGTATA GCTTACTATG 420 TCTGACTGTA TCTGTGTGTG TGACAGCGTC TGCTAGGGCC TGCATGAGTC AACATGTATG 480 CGATTTGTGT CTGTCGATAA TTGTATCTTT GTGTCCGAGT GGTCGGGTCA GCCTTCATTT 540 TAGGCTACGA TTTCATGGAC ATCCAGGAAG CACAGCTACT GGACTCTAGC ATAAGCAAGT 600 AAGTATGGGG GCCGAGCATC CGGGCTGGCT GGAGGGAGGA GTGACTCGCG GGGGAATAGC 660 CTCCTTCTGG CCCCGCCCCT GAGCCATCCT TTCCCGCCCA CTTCCCCGCC CCTTCCCCGC 720 CCATTCTTTC TGGGCCGCTG AGGCCACTTA ACCTAAGCTC CCTCACCCAG TATCCAGTCC 780 CGTCGGGCCC CTTCGCTTCT CTTTTTGCCT CTCCTAGCCC GATCCTTGGA AATAGTATGC 840 TAGGACTCCT GAACTCCAGC CTCCCGGCCC CTTTCCCTAA GTCCAAGCTC CTCTCCCAGT 900 AATTGTCCTC AAGAGATCCG CGTGACATTC TCCTGAGGGT GAGGCTGAGT TCTCCAACCC 960 CACCCCTGAG ACACCACAGC CCCGCGCCGC TCCCCGCCCC GCCCCAGAGT TCCAAAGCCC 1020 CTCCCCATCC TTGCCCCGCT GGCTGGGCAC CGCTCCGACT GAAGGGTGCC TAAGCCCCAA 1080 CCTCGAGCCC TAGAGCCGCG CCCGGATCCC TGTCTCGTCC CGAGCCCGGC CGCGCCCCAG 1140 ATCCCCTAAA TCCCACTTTT TTCACGGCCC TGTCCCAAGC CCTTCAGCTT TAGCTCACTT 1200 TAAGTCCCCT AGACCCGGTA CCCCTCTCGG CCCCTCCCTT GAGCCTTCGA GCCCGGCTTG 1260 GTCCCCTCCC AGGACCCTGA GTCCCGCCCG GATCCGGCCC CGCCCCCAGC 1310
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