Tag | Content |
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EnhancerAtlas ID | HS054-02158 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr13:114301180-114302590 |
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: 2 | Chromosome | Start | End |
chr13 | 114301674 | 114302571 | chr13 | 114301802 | 114302224 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113647 | chr13 | 114301216 | 114302896 |
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Enhancer Sequence | TCACTGAAAA TTCCAATAGA AGACTAGTTT TAGAAGAATC ATTTTTTCCT AATCTTGAAT 60 TACCATAAGC ATATCGAGGG TTGTGGAACT TACATAAAAC TACGGGCAGT CGTGCCTCAG 120 AGGGCTCTGT GTGGGTGCAT GTGCAGCCAG CACCTGCGGG TGCACCGTGG CTTCCCGTGG 180 CGAGCTTCCT GTGCCTGTGT TTCTTCCAGG CCTTGGGGGT TGAAACTCAG GGCTGGTGAT 240 TCTGAAGGGT GGGGCAGGAG CAGCCCCCGG CTTTATCAGG AAGGGGCTCT GATCGGGCAC 300 GGGGGTGCCC CTGTGGGTGG GATTGCTGGA GCCCAGGACA TCAAGGCCAG CCTGGGCAGC 360 ATAGAGAGAC CCTGCCTCTG AAGAAAGAGT GGGGCTCTGG TGTCCATGGA GAGTCTGGGG 420 AGGGAGGAAG AGGCTAGGGT TCTGAGGGCC TGGAGATGGG GGCTCTGGGT GGCCATGGGA 480 CACGTGGCAG GCGTGTTGGG TTCCAGCTGG GTTGGCTTTG AGAGTCTGGT GGGATGAACC 540 CTCATGGCTC CACCGTCACT TTGAGGTGGT GTCACCTCTG ACCTCTGACC TTCAGCATGG 600 CATGACCTCG CTGAGGTGAC CCTGGTGTCC CACATATCAC CCTGAGTGTT CTTAATACAC 660 AGTCGAGGGC TGTGTTCATT GGACTATTCT GGTGTCACCG CCCACTTCAT TTCTGTGCCT 720 GGCAGCACTT TTACTCCTGG TTGGGAGCAT GACCGCCTCC CAGTTCAGCT TCCTCCTGCG 780 TCCCAAGTGA GCGGGGCGGC TGTCCTCGAG GACTCCGGGC TCACAGCCAA CCTGCTGGCA 840 CGGCTCGAGG ACTCCGGGCT CACAGCCAAC CTGCTGGCAC GGCCGCCCTT TCCCGCCCTG 900 CCTCGGGTGA GCCAAGGACT TGTCTTCTGC TTCCTGGGTT CCTGAAAGAG CTCTCCTCTG 960 ATTTCTCAAA GGCAAAATAA AACTCAGATT TAAGTCTTTG GTGCGTAGCC CCTAATTTCC 1020 TTCCCTTTCT CTGAATCCTC ACTGCCCAGC ATGATGGACC GGCCTGGGCT CAGGACCTGA 1080 TTCCACAGGC TCCCAGCCCT CCCACAGGTA CCGTGTCTTC TGTGCTGGTG TCGCACCCGC 1140 CGGCCACCGC CACCCTGCGT CTTAGACGTC CCGCCGCAGC TGTGTTTCCA CCTCATCTCC 1200 AGCTTGAGTG GCAGCCAGCG GCGCCACCTG CACACGAGCC CCCTCCATTC GAGAAGCACA 1260 GACTATGAGT GTGGCCACGC GTCCCATGAC GTGAACTCAC GTCTGCGCCG AGACCTTTGC 1320 CGGCGGTTTT TTACTGACGG AGTAAGCACT GGAGATGCTT GGTACAGCGT CTTCCATCGG 1380 TAAATTGATT TAGTTAACCT TACAACATAT 1410
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