Tag | Content |
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EnhancerAtlas ID | HS095-27960 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:64309430-64310680 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:64309798-64309817 | TTGCCAGGAGGTGGCGCTT | + | 6.26 | NFE2L1 | MA0089.2 | chr7:64310064-64310079 | TCTGCTGTGTCATGC | - | 6.04 | Nfe2l2 | MA0150.2 | chr7:64310066-64310081 | TGCTGTGTCATGCAG | - | 6.19 | STAT3 | MA0144.2 | chr7:64310468-64310479 | CTTCCCAGAAG | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 64309542 | 64310680 | chr7 | 64309728 | 64310374 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I064849 | chr7 | 64309543 | 64310836 |
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Enhancer Sequence | TCTGGTTCCT TCTCATTTGG GTAGGCTATG TCCGAGGGAG TGTCTAAGTG TCAACACTAC 60 TGTTCAGATT ATTTTGTCCC ATGGGGTATT CTCTTGATGT AGTACTCTTC TCATTTTCCT 120 ATCAATGTGG CTTCTTGAGA GCCAAGCTGT AATGATTGTT ATCTTTTTTC TGGATCTAGT 180 CACTAGGCAG GTCTCCAGGC TGGTACTGGG GGTTGTCTGC ACAGAGTCCT GTGATGTGAA 240 TTGTCTGCAG GTCTCTCAGC TGTGGATATT AGCACCTGCT TTGGTGGAGG TAGCAGGTGA 300 TGAATTGGAC TCTGTTAAGG TCCTTAGTTT TGGTTGTTTA ATGCACTATT TTTGTACTCG 360 TTGGCTACTT GCCAGGAGGT GGCGCTTTAA AGGGAGCATC AGCTGTGGTA GTATAGGGAG 420 AATCAGGTGG TGAGTGGGGT CCTAGGACTC CCAAGAATAT ATGATATTTG TTTTCAGCTA 480 CCAGGGTGGG TAGGGAGGGA AGATCATGTG GGGACATGGG TAGGCATGTC TGAGCTTAGC 540 CTCTGCTTGG GCGGGGTTTG CTGCAGCTGC AGTGGGAAGT GGGGGTGTGG TTCTCCGGTC 600 AATAGAGTTA TGTTCCCAAA GGATTATGGC TGCCTCTGCT GTGTCATGCA GGTTGTCAGG 660 GGTGTGGGGG AAAGGGGGAG AGCCAGCAGT TACATGACTC ACCCATCTCT CATGCAACCC 720 CAAAAGCAAG ACTCATTCCC ACCATGCTCC CCACCCCCAA GAGCACCGAG TGTTCTGCCA 780 GGCAGTGAGG GAACAGAGCT AAGAACTTGC CCCTGGCTAC CAGCCTCCCA GCTGCAAAAG 840 CAAGCAGGGC TTTTGTGCCT TGCTGCCTGT GGAGTCTGCT CACCCAATTC ACACCCTTTC 900 CGAATTTCTG GTCAGGAGAC TTCACGTTTG GTTAGAATTG TTAGAAAGTT CAGCTGGAGG 960 TTTCCTTCTC CCTGTGGTCC TTTCCAAGTT CCCCTGGCAG CCCTCCCCAA GGGCCCCTTT 1020 GACGCAAGTC TAAAATGGCT TCCCAGAAGA CTCAGAGCCC ACCGGGCTTT TCCCACTTCT 1080 TCTACCTCTG TATTTAGCTC AGCTCTCTAA ATTGACTCAG CTCCAGGTAA AGTCAGATTT 1140 CTTATTCCAT GTTCTAGACT TTCAGGTTCC CCAGTGAGGG TATGTGTTCA AGGGCAGACT 1200 ATCCCTTTTT CCCACTTTCA CATCTTGAAC ACTATCAATA TTTTGGCTGT 1250
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