Tag | Content |
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EnhancerAtlas ID | HS034-28021 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr7:75795470-75796610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLIS3 | MA0737.1 | chr7:75796513-75796527 | CTTTGTAGGGGGTA | - | 6.51 | NRF1 | MA0506.1 | chr7:75796011-75796022 | GCGCATGCGCA | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 75796419 | 75796600 | chr7 | 75795833 | 75796053 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I076162 | chr7 | 75791992 | 75796918 |
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Enhancer Sequence | ACAATTACCA TGTTTTCTTT AAGCGGTCCC TCCCTGTTGC ACACTTGGAT AGTTTATTTT 60 TTTAGACAAG GTTTACTTCA GTCTCGCAGG ATAGAGTGCT GTGATGGGAT CATAGCTCAT 120 TGCAGCCTTG AACCTTGGGG TTCAAGTATC TGGGAAGCTG AGGAGGGACT ACAGAGATGG 180 AGTCGCGCCA TGTTGCCCAG GCCGCTCTTT AACTCCTGGC CTGAAGGGAT CCTTCCGCCT 240 CGGCGGAGCC CGGACATAGT TTTCTAGTTT TGACCCACAG AAACACTGTG CTGGGTCGGA 300 GTTTGTCAAC TACCCTTCTC CAGCCAGCAA CACACAGAAC ATGGCGGGGA AGTCACGGTC 360 ACCAGGCTCC AAACCGAGGA GAAAACAGCC CAGCTCCAGG CACTGTAGCG TCACTGTGAC 420 ATCGCCGAAG GCCGGCGCTA TTACGTCGCC GGAAGGCCCG CGCCTGTGAC GTCAGCGGAG 480 GCGCGCCCCT TCTGTAGAAC CAATCGGAAC TCGAGGCGCG GCGGCTGGGT ATTCCAGGAG 540 AGCGCATGCG CAGACGCGTG GCCACAGACT GCCGGTCAGT GTCAGTAGGC GGCGGGTTAG 600 TGTCCGCAGG CTCCGACTCG GCCGCCGACA CCAATAAGCT ACAAGGACGA GCTTTACCAC 660 TGCCTGTACT ACTGCTACCT GCGCGACTTC CCAGCCTGCG GCGTAGGGCG CAGCAAGGGC 720 CTGACGCTGA GCGAGTAGGC GCTGCGCACC AAGCGGCTGT GGCCCGGAGG GCACTGTCGG 780 GCAGAAGCTC CTCAGTGGCC ACCACAAGCC CGCTAGCTCC GGCTACAGCC CTTGCCGCAC 840 ACTCGCGTCA CCTGAGCCTG TGTAGGTGCG CCCCCCCAAC TCCTCCCCCA GCCAGGTCCC 900 GGGGACACCG GCAGCGTCCC CCACCGCCCG GCGCCGCTCA TTCTGGGCAG GATCGGCCCC 960 GTCTGAGGCT ACACCGCATT AGGGAGCTGC ACCCCTCGGC TTGACCTCTC ATGGCCTTTG 1020 CAACAACATC AAAGCCTTTG GAACTTTGTA GGGGGTACGA GGGGCTAGGA AACCAAGAAA 1080 ACATCTCTTT AAAAATATAA GCGATCGGGC CGGGCACGGT GGCTCACGCC TTTAATCCCA 1140
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