Tag | Content |
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EnhancerAtlas ID | HS141-00329 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:27691510-27692740 |
Target genes | Number: 21 | 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 | CTGGTTCTGC TTTGGGCTTC AGTCGGCCCT TTTTAGGGTT CCCCTGGCAC TTTCACAGAA 60 CTGATCTCTG TAGTGTTGCA GGAGAGGAGT TGGGCTCACT GGGTTGGGAC CCTCAGGCCA 120 CGGTTCAGAG CCTGTGAGCA CCTGGCATGG GGGAAGGGAG GCTGTGGACC AGTTGAGTCT 180 GTTACGGGCC ATTTAGGAGG TGGGAGTTGC GCAAACATAG AAGTCCCCTC CCTTTGGTCT 240 TCAGCACAGG CTCTTGAAAG GGGCTACCAT CAGTGTGCAT AGACAACGCT GTGCCTAAAT 300 GTATGTATGT GTATATCTGT GACATGTATA GCTTACTATG TCTGACTGTA TCTGTGTGTG 360 TGACAGCGTC TGCTAGGGCC TGCATGAGTC AACATGTATG CGATTTGTGT CTGTCGATAA 420 TTGTATCTTT GTGTCCGAGT GGTCGGGTCA GCCTTCATTT TAGGCTACGA TTTCATGGAC 480 ATCCAGGAAG CACAGCTACT GGACTCTAGC ATAAGCAAGT AAGTATGGGG GCCGAGCATC 540 CGGGCTGGCT GGAGGGAGGA GTGACTCGCG GGGGAATAGC CTCCTTCTGG CCCCGCCCCT 600 GAGCCATCCT TTCCCGCCCA CTTCCCCGCC CCTTCCCCGC CCATTCTTTC TGGGCCGCTG 660 AGGCCACTTA ACCTAAGCTC CCTCACCCAG TATCCAGTCC CGTCGGGCCC CTTCGCTTCT 720 CTTTTTGCCT CTCCTAGCCC GATCCTTGGA AATAGTATGC TAGGACTCCT GAACTCCAGC 780 CTCCCGGCCC CTTTCCCTAA GTCCAAGCTC CTCTCCCAGT AATTGTCCTC AAGAGATCCG 840 CGTGACATTC TCCTGAGGGT GAGGCTGAGT TCTCCAACCC CACCCCTGAG ACACCACAGC 900 CCCGCGCCGC TCCCCGCCCC GCCCCAGAGT TCCAAAGCCC CTCCCCATCC TTGCCCCGCT 960 GGCTGGGCAC CGCTCCGACT GAAGGGTGCC TAAGCCCCAA CCTCGAGCCC TAGAGCCGCG 1020 CCCGGATCCC TGTCTCGTCC CGAGCCCGGC CGCGCCCCAG ATCCCCTAAA TCCCACTTTT 1080 TTCACGGCCC TGTCCCAAGC CCTTCAGCTT TAGCTCACTT TAAGTCCCCT AGACCCGGTA 1140 CCCCTCTCGG CCCCTCCCTT GAGCCTTCGA GCCCGGCTTG GTCCCCTCCC AGGACCCTGA 1200 GTCCCGCCCG GATCCGGCCC CGCCCCCAGC 1230
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