Tag | Content |
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EnhancerAtlas ID | HS076-08891 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr10:129239490-129240800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr10:129239931-129239945 | ATTCCCTGGGGACA | + | 6.01 | Gfi1b | MA0483.1 | chr10:129240136-129240147 | GGCTGTGATTT | - | 6.02 | RREB1 | MA0073.1 | chr10:129239956-129239976 | CCCCCCACCACCCCCACTGT | + | 6.58 | RREB1 | MA0073.1 | chr10:129239945-129239965 | ACACCAGCCACCCCCCCACC | + | 6.59 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 129240040 | 129240200 | chr10 | 129240200 | 129240600 |
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| Number: 2 | ID | Chromosome | Start | End |
GH10I127440 | chr10 | 129239181 | 129239973 | GH10I127441 | chr10 | 129240041 | 129240230 |
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Enhancer Sequence | TCTTCTGTCC CTGCCCTTGG TGGCCCAAGC ATCCTTCTAG GGTCCTTGCA AGCAGCAGGG 60 CTAGGGGCAG CCCCACGAGG GCTGCCTCCC CACGGCTGGC CCTAGCACCC TCAGCAAATC 120 CACAGGAACT CACCAAGGTC AGAGCACAGA ACCTTGGCGG TGCTTCTCAG CATCTGGCCC 180 AGTGTCAGCT TGAACCTTCC AGCACCAGGA GGCGGAGAAT CCGAACCTCC CACTGGGGGA 240 CAGGCTTACT ATTCTTGGTC CAGCCCAGCA ACCTGTCTGT CTACGCAGAG GGCACCTCCT 300 CCAGGGGACG GGTGCCGGCA AGGTCTGTGA GGACAGTCAG ACACCTGAAG TTTCCTAGCA 360 GGCGGCTGCG TGCCAGTGAC CAGCCATGCG CAGGAGGGGA GGTGCGGGGG AGGAGGTTCA 420 CAGGAACAGA AGCAGCAACC CATTCCCTGG GGACAACACC AGCCACCCCC CCACCACCCC 480 CACTGTAGTG TCCTCCTTGC CCTTCCCCCC TGCGGGCCTC CCCTGCACCC CAGCTTCTGC 540 AAAGGTTTTC CCTCCTCACC CCTGTGGCTG GGTTCGGTTT CCTACTTGAT TTGCATCATC 600 AACAATTTCC TGACCTTTAG CTGAGCCTCT CCAGCCAGAG CCTCCAGGCT GTGATTTGCA 660 TCTCAGCAGT CCAGCCTCCT CAGCTCTCTG AGTCAGAATG TGCCCTCCCT GGGATGCAGG 720 GAGGCCAGGA GAAGCACCTT AGGAGACCCC AAATCTCTCT TGCCAGCACA TTCACCTTCA 780 GAGAGCCCAG CGCTTCACCC GGCCTTTCCT GACTTCCCAC AGCAGTTTTG CTGCCTGGAA 840 CAAGGCCATT TCTTCAGAGG AGGTGCAGCT CCTGGGCGCT TGGCTCCCCC GACAGCACAG 900 GACAGTTCTG GAAATAGACC TGTTGGCCTG GCTCTGTCAC TCATTTACCA GAGGGCCTGA 960 ATCTTCCTCC CAAGCCTAGT TCCCATTTCC TCCTTCCAGC CTCAGTAACC TCCAGACTGG 1020 CCCTGGCACA GCTGACTCCT CCTGGGGCAG ACATTGAAGC CTATGTGCTC TGTTGCTCAC 1080 CCAAACCAGC ACAGCGCATC CACCAGGCCC CCAGACCCAG CCGCAGCCCC AAGCCCAGAG 1140 CTGCCCACTC ACCTGCCTGC CCTTCCTTGG GGGAGAACGT TGACCCCTCC TTTTTGGCTG 1200 GGTTAATACG TTTTCTAATT ACTCCTGCGT CAGAGTATTT TGTAACTGCT CCTGTTCCCC 1260 AAAGCCTGAT GATCTGAGAC CAACCTGTAA GAAATATGTA AATACAACTT 1310
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