Tag | Content |
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EnhancerAtlas ID | HS154-20235 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr7:75795480-75796600 |
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 | TGTTTTCTTT AAGCGGTCCC TCCCTGTTGC ACACTTGGAT AGTTTATTTT TTTAGACAAG 60 GTTTACTTCA GTCTCGCAGG ATAGAGTGCT GTGATGGGAT CATAGCTCAT TGCAGCCTTG 120 AACCTTGGGG TTCAAGTATC TGGGAAGCTG AGGAGGGACT ACAGAGATGG AGTCGCGCCA 180 TGTTGCCCAG GCCGCTCTTT AACTCCTGGC CTGAAGGGAT CCTTCCGCCT CGGCGGAGCC 240 CGGACATAGT TTTCTAGTTT TGACCCACAG AAACACTGTG CTGGGTCGGA GTTTGTCAAC 300 TACCCTTCTC CAGCCAGCAA CACACAGAAC ATGGCGGGGA AGTCACGGTC ACCAGGCTCC 360 AAACCGAGGA GAAAACAGCC CAGCTCCAGG CACTGTAGCG TCACTGTGAC ATCGCCGAAG 420 GCCGGCGCTA TTACGTCGCC GGAAGGCCCG CGCCTGTGAC GTCAGCGGAG GCGCGCCCCT 480 TCTGTAGAAC CAATCGGAAC TCGAGGCGCG GCGGCTGGGT ATTCCAGGAG AGCGCATGCG 540 CAGACGCGTG GCCACAGACT GCCGGTCAGT GTCAGTAGGC GGCGGGTTAG TGTCCGCAGG 600 CTCCGACTCG GCCGCCGACA CCAATAAGCT ACAAGGACGA GCTTTACCAC TGCCTGTACT 660 ACTGCTACCT GCGCGACTTC CCAGCCTGCG GCGTAGGGCG CAGCAAGGGC CTGACGCTGA 720 GCGAGTAGGC GCTGCGCACC AAGCGGCTGT GGCCCGGAGG GCACTGTCGG GCAGAAGCTC 780 CTCAGTGGCC ACCACAAGCC CGCTAGCTCC GGCTACAGCC CTTGCCGCAC ACTCGCGTCA 840 CCTGAGCCTG TGTAGGTGCG CCCCCCCAAC TCCTCCCCCA GCCAGGTCCC GGGGACACCG 900 GCAGCGTCCC CCACCGCCCG GCGCCGCTCA TTCTGGGCAG GATCGGCCCC GTCTGAGGCT 960 ACACCGCATT AGGGAGCTGC ACCCCTCGGC TTGACCTCTC ATGGCCTTTG CAACAACATC 1020 AAAGCCTTTG GAACTTTGTA GGGGGTACGA GGGGCTAGGA AACCAAGAAA ACATCTCTTT 1080 AAAAATATAA GCGATCGGGC CGGGCACGGT GGCTCACGCC 1120
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