Tag | Content |
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EnhancerAtlas ID | HS120-01772 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr13:114301640-114302450 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr13:114302067-114302078 | CTTTCCCGCCC | - | 6.32 | NR2C2 | MA0504.1 | chr13:114301751-114301766 | TCACCTCTGACCTCT | - | 6.88 | NR2C2 | MA0504.1 | chr13:114301758-114301773 | TGACCTCTGACCTTC | - | 7.33 | Nr2f6 | MA0677.1 | chr13:114301758-114301772 | TGACCTCTGACCTT | - | 7.28 | Rxra | MA0512.2 | chr13:114301758-114301772 | TGACCTCTGACCTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41872 | chr13:114301246-114302949 | LNCaP |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I113647 | chr13 | 114301216 | 114302896 |
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Enhancer Sequence | GGCTCTGGGT GGCCATGGGA CACGTGGCAG GCGTGTTGGG TTCCAGCTGG GTTGGCTTTG 60 AGAGTCTGGT GGGATGAACC CTCATGGCTC CACCGTCACT TTGAGGTGGT GTCACCTCTG 120 ACCTCTGACC TTCAGCATGG CATGACCTCG CTGAGGTGAC CCTGGTGTCC CACATATCAC 180 CCTGAGTGTT CTTAATACAC AGTCGAGGGC TGTGTTCATT GGACTATTCT GGTGTCACCG 240 CCCACTTCAT TTCTGTGCCT GGCAGCACTT TTACTCCTGG TTGGGAGCAT GACCGCCTCC 300 CAGTTCAGCT TCCTCCTGCG TCCCAAGTGA GCGGGGCGGC TGTCCTCGAG GACTCCGGGC 360 TCACAGCCAA CCTGCTGGCA CGGCTCGAGG ACTCCGGGCT CACAGCCAAC CTGCTGGCAC 420 GGCCGCCCTT TCCCGCCCTG CCTCGGGTGA GCCAAGGACT TGTCTTCTGC TTCCTGGGTT 480 CCTGAAAGAG CTCTCCTCTG ATTTCTCAAA GGCAAAATAA AACTCAGATT TAAGTCTTTG 540 GTGCGTAGCC CCTAATTTCC TTCCCTTTCT CTGAATCCTC ACTGCCCAGC ATGATGGACC 600 GGCCTGGGCT CAGGACCTGA TTCCACAGGC TCCCAGCCCT CCCACAGGTA CCGTGTCTTC 660 TGTGCTGGTG TCGCACCCGC CGGCCACCGC CACCCTGCGT CTTAGACGTC CCGCCGCAGC 720 TGTGTTTCCA CCTCATCTCC AGCTTGAGTG GCAGCCAGCG GCGCCACCTG CACACGAGCC 780 CCCTCCATTC GAGAAGCACA GACTATGAGT 810
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