Tag | Content |
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EnhancerAtlas ID | HS131-01362 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr10:119018600-119019970 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr10:119019151-119019165 | TTTCCCTTGGGAGT | - | 6.28 |
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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: 2 | ID | Chromosome | Start | End |
GH10I117259 | chr10 | 119019345 | 119019394 | GH10I117260 | chr10 | 119019428 | 119020930 |
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Enhancer Sequence | GCATTACAGC TTCTTGTTAG ACTGGCATTC AGCACTGACA TTATTGTGAC TGGGTAATTA 60 TTGTTCACAG CTGACTGAGC TATGTAGGGT ACTGTGATTA ATTTCCTTTC TTTTTGCAAA 120 TTTAATTTTC CTGGAGTTAG TCGTTGCCTT GTCCTTTCAT TTTCTTAATG TTTTATGTAG 180 TGTTTATGAA TATATCCACC AAAGTTTCTG GCAAAGATGA AAAATTCTCC AATTGCAGTC 240 AAGTGTTGGC AAACCTGATC TTTCTGTGTA TTTGCTCGTT TGTGGATGTC TGTCCTAGGT 300 CTTCAGTCTA GACTTCCTTC CCCATCACCC CAGCATCTTC TGTGCCTCTC TTCTGTTTCC 360 TGTATTCCTT GCCCTTGACT GACTTCCTCC TTATTGCAGA GCATAGCCTC CCACAGCATA 420 GCCTCCCACA GCTTCCTGAG AGTGTGCGTG GCAGGTAAAG GTCTCTGAGA CCCTGCATAG 480 TTGCAAATAT TTTACCCTTA TCCTACACTT TGTTGACTTT GTCTGCATGT ATAATTCTTG 540 GTTGGAAATC ATTTCCCTTG GGAGTTTTCG GGCCACTGTT CTGTTGTCTT CTAGCATCCA 600 GGGTTGCTGT GGGGGAGGCC AGTGTTGCCC TCATTCCTGA GCCTCTGTAG GAGCCCGAGG 660 GACCTTTACT TCTTCTCTAG GTTATAAAAG TCCATGTTGA TGATTTGCAG TGGGCTCTGT 720 TTTCCTCCTC TGGGCTGAAC ACTTGCTTAA TCAGCCCTTT CACTTGGGGA ACCCCATGTT 780 ACAATTCTGG GGAGACTCTT TGTATTATTA CTTGAATGAA TCCCCCTATT TTCTCTCCTG 840 TTTTACTCCA GTTGGCTGAG CGTTAGGCTC CCTACTTTTA TTCTTCTAAT TTCTTGTCTT 900 TCCCCTTTTC CATTGAGTTA TTCCTGTTCA TCTTTTAAAC TGCTTATTGA GTTTTTAAAA 960 TTGATGCTAT CATATCTTAA ATCTGAAGAG CCTTTTGTGT ATACCCTGAG TGTTTGGGGT 1020 TTTGGTGAGG TTGTTGTTAT TGCAAAAACA CCCTCCCACC ATGTTCCTGT TTCAGCCTCT 1080 TGTGTTGCCC CGGTTGCCAT TCTGGTTAAT TTCTGTGGAG AAACTGTCTC CTGCCAGGGT 1140 GAAGGCTGGA GTGCTAGGGG CCCCACTGCT CTTAACACAG CCTCTCTGCC TGCTTTCATG 1200 TTGACAGCCT CTGCTTTCAG CCCCACCTTC ACAGTACCCG AAGCTTCAGT TCCTTTCTGG 1260 CTGTGAGGCA CAATGGCTCT TGCCTCTTGC TGGCCTCACC ATTTGCAGGT GGAAGATTCC 1320 AGCATTCTCT GCGGTGTCCT CTGCTCACTT CTTCCTCGTA TTGTCCCTTC 1370
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