Tag | Content |
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EnhancerAtlas ID | HS080-19858 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:152899250-152900000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr2:152899364-152899381 | CAGGTCACAAAGACCTT | + | 6.09 | ESR2 | MA0258.2 | chr2:152899365-152899380 | AGGTCACAAAGACCT | + | 6.63 | PAX5 | MA0014.3 | chr2:152899442-152899454 | GAGCGTGACCTC | + | 6.14 | Pou2f3 | MA0627.1 | chr2:152899473-152899489 | TTATATGCTAATTACA | + | 6.36 | RFX5 | MA0510.2 | chr2:152899538-152899554 | AGATGCCATGGCAACG | - | 6.23 | STAT1 | MA0137.3 | chr2:152899620-152899631 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr2:152899620-152899631 | TTTCCCAGAAA | - | 6.32 | Stat4 | MA0518.1 | chr2:152899617-152899631 | TCCTTTCCCAGAAA | - | 6.27 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 152899361 | 152899600 | chr2 | 152899383 | 152899727 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I152042 | chr2 | 152899381 | 152899610 |
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Enhancer Sequence | AACTCCATCT TGAATAGGAG CTGCGTAAAA TAAGGCCGAG ACCTACTGGG CTGCATTCCC 60 AGGAGATTAA GGCATTCTTA GTTACAGGGT AAGACAGGAG GTCGGCACAA GATACAGGTC 120 ACAAAGACCT TGCTGATAAA ACAGCATGCA GTAACGAAGC CGGCTAAAAC CCACCAAAAC 180 CAAGATGGAG AGGAGCGTGA CCTCTGCTCG GTCTCACAGC TCATTATATG CTAATTACAA 240 TGCATTAGCG TGCTAAAAGA CACACCCACC AGCACCACAA CAGTTTACAG ATGCCATGGC 300 AACGTCAGGA AGTTACCCTG TATGGTCTAA AAAAAGGAGG AACCTTCAGT TCAAGGGAAT 360 TGCCCACTCC TTTCCCAGAA AACTCATGAA TAATCCACCC CTTGTTCAGC ATGTAATCAA 420 GAAGTAACAA TAAGTATAAG CAGCTGAGCA GCCCGTGCCA CTGCTCGCCT ATGGAGCAGA 480 CACTCTTTTA TTCCTTTACT TTCTTAATAC ACTTGCTTTC ACTTTATGGA TTTGCTTCTA 540 ATTATTTCTT GTGCAAGATC CAAGAACGTT CTCTTGGGGT CTGCATTGTG ACCCCTTTCC 600 AATAACAATG AGGTCTCACT TTGTTATCTA GGCTGGAATG CAGTGGCATG ATCATAGCTC 660 ACTGCCACCT CAAATTCCTG GGCTCAGGGA TCCTCCCACC TTAGCCTCCA GAATGGCTGG 720 GACTACAGGC ACACACCACC ATACCTGCAT 750
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