Tag | Content |
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EnhancerAtlas ID | HS010-00626 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr10:69523120-69524360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HINFP | MA0131.2 | chr10:69523612-69523624 | CCACGTCCGCGG | + | 6.32 | NRF1 | MA0506.1 | chr10:69523394-69523405 | TGCGCATGCGC | - | 6.32 | ZNF263 | MA0528.1 | chr10:69523747-69523768 | GGGGGCGGGCGGGGGGGGGGA | + | 6.33 |
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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 |
GH10I067763 | chr10 | 69522820 | 69525406 |
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Enhancer Sequence | GGGTGTAGAC ACTCAGCACC ATAATTTGGT TTCGAGAAAT GGTATGGAAG GTCTCAAGAA 60 AAGTTACACA CCTTATCAAG TGGAGTCACA ACATAGAGGC TTCCAAAGGT CGAGTTGCCT 120 TCCTGCCTTA TTATGAAATG TACCATTATG AGAAGGGCAG TGGGGTTTCC ATGAACACTC 180 CTAGAAACTT CAACTAGTAA AAGGCCTTCT GTTACTTTTC TCAAATTGCC CATCGACAGA 240 AGTTGGCGCT TCTGTGGCGC TACGTGACAA GGGCTGCGCA TGCGCTCTGG GATCAGCCAG 300 GCCCACCCGC GGCACAACCC CAGGCCTCAG TGCCGTCAGG TGGGCTAAGA CAGAACAGAC 360 CTCGGTTCTC AGGGCTTTAA CGAAATAACG CGGGTAAAGC ACCTAGGGCA GAAGCCACAC 420 AGAACACCAG AAGGCATTAA TGGCATTTAA AGGTATTGAA TGCAGACTAA TGCGCAGAAC 480 TTGGTTCTCA GACCACGTCC GCGGCCACCC CTCTCCTGAG AGAGCAGAGA GCACACTTGC 540 AGCCTGACAT CTCCCAGTTG AGCTCGGCAA TGAAGGGATC ACTGGGGATT TAAAAAATGG 600 GAGACGGCTG CTTGGGCAGA AGCCCGAGGG GGCGGGCGGG GGGGGGGAAG GGACGAGCCC 660 ACAGGCAGCA TCCCGACACC TCACACTTCC TGCCTCAATG CACAGAAGAA AGTGTTCTGA 720 AGGCGACGCC CCCAGTCTTG GCGGGAAACG CCGCGGAAGA CGCTTCTCTC GCAGAAATGC 780 CAAATTTTCG GGAGCGCGGG CTCGCAGCAC GTAACAGAAC AGATCTTTTT GTTTCACGGC 840 CCTCTCGTAG ACCTAATAAG CGCGAGGGCG AAAACCAGGT CAGCGACCAG AAGCCAGGCA 900 AGGTTGCGAT TTTCGGAGCA CAGCGAAGGG GAGAGTTTCT AAGTTCTGAA TGTACCTCTA 960 TTTAGGGTGG TTTCTATTAT TTCTTCGCGT CTACCCTGTA GTTGCCGCAC CCTGAGCCCT 1020 CAGCCCCGCC GCTTCGCACG GAGCGGAGCT CAGAGGGTGC GCGCTCCGCC CTTTCGCGGG 1080 CCTGGCATGA GCGCAGTGGT TGTTACACTA AAGTGTCTCC GCCTGTCGAA TATTCTCGTG 1140 GCAGCGATGG CCGAGTGGTT AAGGCGTTGG ACTTGAAATC CAATGGGGTC TCCCCGCGCA 1200 GGTTCGAACC CTGCTCGCTG CGGAAGCGGG TGCTCTTATT 1240
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