Tag | Content |
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EnhancerAtlas ID | HS034-15932 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:10905290-10906330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:10906046-10906064 | GGCAGGAAGGAAGGAGGG | + | 8.01 | ZBTB18 | MA0698.1 | chr2:10906079-10906092 | ATTCCAGATGTGC | + | 6.03 |
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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 |
GH02I010764 | chr2 | 10904898 | 10906118 |
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Enhancer Sequence | GAGGCAGTGA GTGTCCTGAC AGTCCTCTGT CCTGTTCAGC AATGGCCTCC ACTCCACTTG 60 ATAAAATGAA CACCCTGTGA CTCGAGTCCC AGGGGATGCT ATGGGCACCT GGAGCTGGGT 120 GACTTCTCTG TATCATCACT GAAGGTGAGG GTGACAAGGA CTGTGAGACT GAGGCTGATG 180 GTTTCTGATG GCCTGGCCCT CCCTTCTGCC ACAAAACACT GAGCCCCTAA TGTGTCCCCT 240 CTCCTGCTGG CCCCCATGGC TGTGGGAGAG TCTCGGCCTG GGCCAGGAAC AAAGGCACCC 300 GGTTTTCTAC TGTGACTGTG GCCAAGGGTC AGAGTGGAGC TGGGCCTCTC ACCTGTCCTC 360 TGGCAGCTCC TGCAGGTCTC CTGGAAAGTA GGGTGGGGCC AGAAAGCTCG GGAATCTGGG 420 TGGGGCACCT CGGGTGCTGC TTACATCAGA GAGGCTCAGG CCCCTGCTGG GACGATCAGG 480 CAGTGATTCT GGAAGGCCCT TCAAGGAGGG TGTGCCCAGA GCACCTGTGC CAGGTGTGCC 540 TTTCAGAGGG CGCTGTGCAT GTCCACCAAG GAACTGGAAG CACATGATGG CTGGTGGGGC 600 TGGCCCTTCC CTGCCTCACC ATGTGCCAAT TTGGGATTCT CTCAGTCCCA GGGATGCCAG 660 ACTCAGTGGG AAGGGCCCCC TGGAGCACAT GGAGGGAGCA GAGGGGCTGT CGGGAGACCT 720 GGCTTCTCCA GTCCAGAGCA CCCCTAGAGT GCCTTTGGCA GGAAGGAAGG AGGGCACTGG 780 TTTGGTGGCA TTCCAGATGT GCCCGAGACT GTGCTGGGCT CTCTTACTGT CCGCCTCATG 840 CCATGGGGTG GACATCACTT TCCTCTGAGT GCAGAAGAGG AAGCTGAGGG GTTGAGCGAG 900 CGATCCAGGA CCTGCAGCGG TTGGAGTATT ATGCCGGGAT GGGGATGCAG GTCTTGGGGA 960 CCAGAGCCTG CGGATTGTGC TGTGTGCATG ACACCACTTC CCAAGGAAGC CCTGGACTGG 1020 CCCAACCACA GGGAAGCAGC 1040
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