Tag | Content |
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EnhancerAtlas ID | HS091-43723 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:44961000-44962400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:44961876-44961895 | TCGCGCCCCCTGGTGGCCG | - | 8.35 | RREB1 | MA0073.1 | chr7:44961724-44961744 | TGGTTGGGGGTGGTGGTGGG | - | 6.67 | RREB1 | MA0073.1 | chr7:44961727-44961747 | TTGGGGGTGGTGGTGGGGGG | - | 7.18 | SOX10 | MA0442.2 | chr7:44961151-44961162 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr7:44961151-44961161 | AAAACAAAGG | - | 6.02 | ZNF263 | MA0528.1 | chr7:44961665-44961686 | CCCTCCTCCCCTTCCTCACCA | - | 6.75 |
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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: 4 | ID | Chromosome | Start | End |
GH07I044921 | chr7 | 44961301 | 44961450 | GH07I044923 | chr7 | 44961599 | 44961800 | GH07I044924 | chr7 | 44961801 | 44961970 | GH07I044922 | chr7 | 44961999 | 44962199 |
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Enhancer Sequence | AGCGATTCTG GAGGTTGAGG CAGGAGAATC ACTTGAACCT GGGAGGCAGC AGTTGCAGTG 60 ACCTGAGATC ATGCCACTGC TTTCCAGCAT GGACAGCAGA GCAAGACTCC ATCTATAAGT 120 AAATAAATAA ATAAAATTCC CTAGGTGCTT AAAAACAAAG GAAGAGGAAA AAAAAGGAGG 180 TGCATCTAAC ATCTAGGAAG AGCACCTGGG GGAGCACCTA CTGGGAGCAC CTGAAGGAGC 240 AACTCAAGGG CCACTGGCAG GAACCTCCGG GAAGCGCAGA AGGCATGTGT GGGGAGAGAT 300 TGGTGGGGGT TGGGTGTTCT TACCTACTGA ATGGGCGGGC TAGATCAAGA GGTGACAACC 360 TGGAAGAGAA ATGGGGCTAG AGACAGGCTG GCTGTAAACC AGTGGTTGTC GAGGAGATAG 420 CATCAGTGAG GGAGGTGCCC CAGTGGGAGA GCCGCCCTGA AAAGGGAGGA GGGTGTCTCT 480 CCACTGTTGA GCCAGAGCCA CAAAGAGGGT TGACTCTGCC ATAGAGCGGC CTTTCTTCCC 540 AGCTATTATG TCGGCTCTGC AGGGACCCTC ACACTTGATG AGTCAAGGGG CTTGTGCCTT 600 ACTGAGCAGC CAGAGGGATC CCTCTCTGAG ACCCTCAGAC CTGCTCCTTG CCTGACCAGT 660 GCCAGCCCTC CTCCCCTTCC TCACCAGGGG ATGGCTGAAG CATGGAAAAG TGGCCGGCAG 720 CAGATGGTTG GGGGTGGTGG TGGGGGGCAT GGGGACTCAA CGCCCTGGGT TGCTGAGTCC 780 TGTGAGACCT GTGGCCCCGG GACACCCCAC CCCAGGCCTG GGCTCTCAGC AAGAATGCCA 840 TGTGGAGCCT GTCAACTAGC CCGTCAACTA GCACTCTCGC GCCCCCTGGT GGCCGTCCCT 900 GATGAGGTGG GTATAGGACA TGGTCCCAGT GAGAACTTGT GGCAATCCAC AGTTCATGCC 960 TACGTTCATT CATTCATTCA TTCTTGAAAT ATTTGGGGAG TACCTGCAGG CCTCCGAAGC 1020 TCTATGCTGT CCACTCTGGC ACCCACACGT GCTCTGAGCA CTTGAAGTGC AGCGAGTCCA 1080 CTGGAGAAGT ACAGTAAGTG TAAAGAGTAC ACTGGCCGTC AAAGACATAG TGCACACAAT 1140 GTAAAATGTA GTATCGATCA TTTTCATATT GATGATACAT TGAAATTATA ATGTTTTAGA 1200 TCAACCATTT TAAATAAAAT ATGATTACAA TCAATTTCAC CTGTTTCTTT TTTACCGAGA 1260 CCAGCTGGGT CGGGGAGACC CTAACCTAGT GGTGCTAGAG GAATTAAAGA CACACACACA 1320 GAAATATAGA GGTGTAAAGT GGGAAATCAG GGGTCTCACA GCCTTCAGAG CTGAGAGCCC 1380 CGAACAGAGA TTTACCCACA 1400
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