Tag | Content |
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EnhancerAtlas ID | HS060-18826 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:25382180-25383720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TEAD1 | MA0090.2 | chr2:25382236-25382246 | CACATTCCAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 25383403 | 25383666 | chr2 | 25382980 | 25383000 | chr2 | 25383036 | 25383220 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I025159 | chr2 | 25382580 | 25383616 | GH02I025160 | chr2 | 25383624 | 25385019 |
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Enhancer Sequence | CAGCATGCCC AGCATGGGAG CATCCTCAGG AAGGCCTAGG CCATTATTCA TTCTAGCACA 60 TTCCATGTAA GCCATACTGG GGAACACCTT GTCTTAAGAA TCTGGCTTTC TGGCCAGGCG 120 CAGTGGCTCA AGCCTGTAAC CCCAGCACTT TGGGAGGCCA AGGTGGGCAG ATCACCTGGG 180 GTCAGGAGTT CAAGACCAGC CTGGCCAACT TGGTGAAACC CCATCTCTAC TAAAAATACA 240 AAAGTTAGCC GGGCGTGGTG GCGCACTCTT GTAATCCCAG CTATTTGGAA GGTTGAGGCA 300 GGAGAATTGC TTGAACCCAG GAGGCGGAGG TTGAAGTGAG ATGAGATCAC ACCATTGCAC 360 TCCAGCCTGG GTGACAGAGC GAGATTCCAT CTCAAAAACA ACAACAATGA CAACAAAATG 420 GCAGGGGAAG GTGGGGGGTT CCAGGCAGAG GGTATAGGAG GATGCGAGAC CTGTGAGGAG 480 ACCAACGAGT GTGAGGCAGC GCCTTCATCC GGGGAAACTT GGGAAGCAGG GTTTGGTAAG 540 GAGAGAGTGC CCGTCTACAA GGGCCCTGCC CACCATGCTT AGTAGTTTGG AATTGACAGA 600 AATTGGGGTG GGGGCACTGT TTTGACTCTT GAGCCTGGGA CTGTGGGAAA AAGCAAGATT 660 TTGTGTAAAC TAACGTGAAG AATTCGTATA TGATGGGCTG GGGAGAGCAG CTGGAAACTA 720 GGAGACCAGT TGGTTGGGAA GCTGTTATCA GAGAGGCCTG GGGGAAGTAC TAAGGATGAG 780 AAGGGCTGGA GCTGAAACAC GCGGGGAGGG AGGAGCCTGG GCACGGCAGG AGGGGTCAGA 840 GGGCCTGAGT CAGGGCTTAA GCCCTAGGGG CTGGAAGAAG CAACTGCGTA GAGTATGTTG 900 TATTAAACAG ATGTGTGTCT CCATGAGTGT GTGTGTGTGA GAGAGACCGT ATGTCTGAGC 960 GTATCTGTGA GTAGCCTGGG AGTGAAATTG GAACTGATAC TAACCCTCAG CTCTCACACT 1020 TAGCTTCTAT GATAAAAAGA AGATTATGTC CATTTTCTCC TTTAATCTTC ACAATAACCC 1080 TCATACTGGG AAGGGAGGGG TAGATGAAAG AACTAAATTT TGGAGAAGTT CAGAGACTTG 1140 CCTAAGGTCC CATGGATTGC TACGAGCAGT TCCCCGGAGA CATTACCAAG ACTTCTCACC 1200 TGACAGTCCA GAGCACTCCC AGGCGTGGGT AGGCCTCAAC CTGTCCAACT GGCTTTTGGA 1260 GGTGGACCGG AGCCGGGGAG CCCCTGAGCG CCCGGGGTCA CTCTTGCAGG AATCCTGCCT 1320 TTACACGTGT GCTAGCTGAG CAGTCTCCCA CTCAGTGGAG TGTGTGGAAA ATACGGCCAT 1380 CCTAGAGGTG CTGGAGCCAC CCTGTGCCTT CACCCAAACT ATCTGATCCC TCGAAGATCC 1440 ATTTGGGGGT GGGGGCAGGA AGCACATTTT CCTTTCACGC TCACTAAGTC CTGTGAAATA 1500 TCCTACCGCA TGGAAACCAC TGTGCTCCTC CGATCCATGC 1540
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