Tag | Content |
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EnhancerAtlas ID | HS052-11969 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr14:89469980-89471080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:89470361-89470382 | TTTCACTTTTTCTTTTACCTT | + | 6.12 | IRF1 | MA0050.2 | chr14:89470355-89470376 | CTTTGATTTCACTTTTTCTTT | + | 6.74 | POU2F2 | MA0507.1 | chr14:89470416-89470429 | AAATGCAAATTAA | - | 6.25 |
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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 |
GH14I089003 | chr14 | 89470073 | 89471095 |
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Enhancer Sequence | AAACCATAGT ACCTACTCTT CCCTCCATTC AGTCTTCTGT GAAGTCCACG ATTCTGCCTG 60 TGAAATAGTA CCCAGATCCA TCCCTACCTT TCTATCCTCA CAGTTCTAGT GCAGGCTCCT 120 GCTCCTCTCA CTGGGACTCC CACAGAGGCC TCCTAAATGG CCTGCTGATC TCCAAGGCCA 180 CAGGCACAGG CACATCCCAC CGCAGCTCAG AGGCTATGCT GGCTTCACAC TCCCCATCTA 240 AACCTCCCCT CAACCCTTGC TCATGGCATC AGGCCCTCCC ATCTCTGGTC TAATCTCTTT 300 TCCTTGCCCT TGTACTCTCT CTAACCATAC CCCACTCAGT GTCTTACACA TGCACATAAA 360 TTCCCACCTT ATTACCTTTG ATTTCACTTT TTCTTTTACC TTTCCATTCC CACACACCTT 420 TATTCTCTCC CTTAACAAAT GCAAATTAAT ACTTCAATGT CTAGCTTTAA AAGCATCTGC 480 TCCATAAAAC CCTTCTCTAT CATTCTGGCT AGAATTAATC CCTCCTTGCC CTATAAGTCC 540 AAAATCCCAT CTCTGGAATC CTCTATAGCA TTTACAATTA GTAGCTTATA TCTGGATAGA 600 ACTTTGTAGC TTATGACCTA TTTCCCAATA ACTTATCTCA TTTGTTTGTA ATGTAGTGAG 660 GCACATGTTT TACAAATGAG GAAACTGGGC TGGGTGAGAA GCAGTGGGAG GGGCTGTTTA 720 ACATTATGGC AGAGACAGCT CTTGATGCAT TTTCCTCCTC TATGATGATA GAAGCTTTTA 780 GCTGGGAACA TGACTACCCA GCAAAAGACT CATTTCCCAG ACTCCTTTGC AGTCAGGTGA 840 CTAAGTTCTA ACCAGTGGGA GGTGGTGGGT GCAATTTCTG AGCCCAGCCC TTAAGGGGTG 900 GGCCTGGCCC TTATTCCCTT CTCTGCTGAC TGGAGTGTAG ACATGAGGAA CCAGAGCACT 960 TGTTTGGGTC ACAAGATGGA AAATGCATTT AAGGATGGAA GAGCAGCAAG TTAGAAGGAG 1020 CCTGGGTCTC TGATGATTGT GGAGCCACTA AACCACCCAC AGACTGCCTC CCTGGACTTC 1080 AAAGTGAGAG AAGAAAAAAA 1100
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