Tag | Content |
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EnhancerAtlas ID | HS052-00566 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:23865900-23866810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:23866477-23866496 | GGCTGCCACCTAGAGGTGA | - | 6.07 | Nr2f6(var.2) | MA0728.1 | chr1:23865976-23865991 | GAGGTCAAGAGTTCG | + | 6.24 | ZBTB18 | MA0698.1 | chr1:23866634-23866647 | TTTCCAGATGTTT | + | 6.28 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09947 | chr1:23865865-23866650 | CD14 | SE_23782 | chr1:23866175-23866507 | Colon_Crypt_2 | SE_34689 | chr1:23865879-23867213 | HeLa |
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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 |
GH01I023539 | chr1 | 23865911 | 23867050 |
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Enhancer Sequence | AAAGGCCAGG CACAGTGGCT CAATCCCAGC ACCTGTAATC CCAGCACCTT GGAAGGCTGA 60 GGTGGGTGGA TCACTTGAGG TCAAGAGTTC GAGACCAGCC TGGCCAACAT GGTGAAACCA 120 TGTCTCTACT AAAAATACAA TAATTAGCCA GGCATGGTAG CGCATGCCTG TAATCCCAGC 180 TACTTGGGAG GCTGAGGCAG GAGAATTGTA TGAACCCGGG AGGTAGAGGC TGCAGTGAGC 240 CGAGATCACG CCACTGCACT CCAGCCTGGG TGACAGAGCA AGACTCTGTC TCAGGAAAAA 300 AAAAAAGTAG ATTAGTGATT GCTGGGAATG GGTCAGTCTC TGTACAGATG AAGAACATGA 360 GGCTCAGAGA AGCCAATTGC CACCCATCTG TGTGACTTTG GACCAGTGAC TTCACGTCTC 420 TCAGTTGTGA CGTGGAGAGA ATGACGTGCG CCTGAGATGG TGGCTCTGCA GCTCAGTAAA 480 TGTGCCTGCG GCGCCTGGTG GGTCCCCCTG CGTCTTCGTT AGTTCCTTTT CCTTCTCTCA 540 GACCTTTGGC TGGAAGCTGG TGGGGCTGAA AGGTGAAGGC TGCCACCTAG AGGTGAACTC 600 TGGCACCTGC CAAAGCCTGC GAGGCGTCTT ATCTTCTCAT CAAGGTAACT CACCCGCTAT 660 GGGCTTGGGG AGGAGAAACA GGATGTGAAA GAAGCAGCCC CGCTGAGGAC AGGGCTACTA 720 GACTGGCCAG ATTCTTTCCA GATGTTTGTA GGCCCTGGGA ATGCTTTTCA CAGATGTTGG 780 GTCCCGTGGA GGTGATCCCA TGCGGGAAGA GGGACATCCA TGCGGGAGTC AGGTCCCAGC 840 AGAGCTGCTT AGCGTCTCTT GGGGAAATGC CACCTATAAT TCCTTCTTCT TCTTTTTTTT 900 TTTTTTTTTT 910
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