| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19169 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr22:19718020-19719000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:19718333-19718352 | CAGGCACCAGAGGGCGCTC | + | 6.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I019729 | chr22 | 19717312 | 19719321 |
| Enhancer Sequence | TCCAGGCCTG TGTCCCCAAG ACCCATCTGG GGTTCAAGCC ACATCTTGGG CCTATACACA 60
GCCAGCTAGT GAGTGAGCGA GCGAGTGAGT GAGGCCCTGC AAGATGGTCA TCTGTCTTGT 120
CCCGCAAAGG CCAAGACAAA CGCCGTGTCA GCGGCAGCCT CTCCAACCCA GTCTGTGATG 180
GCCAGTGGTG GTCAGTGAGG GCTGGGCCGC GAGGCTCACA GCTCAGGCCG CACCCGCCGG 240
TTTCACAGAC CGGCCAGGAA GCTCCCAGGG CGAGGGCCTA GTCGTGTCCT CCCCATGGGC 300
GAGCAACCCT AGGCAGGCAC CAGAGGGCGC TCGCGGTCTG CAGAAAACGC TGGCTAAGGG 360
GGGAGCGCGG AAAGAGGTGG GCACTGTGGG TGCAGACAGC TGGGGTCCGC GGAGAAACGA 420
AGGCCTGGAG CGGGGGCGCT GGGTTGTCCA GGCTGGCGGC GAGCTGCACC GAGTGGGACG 480
GGCAGGCTGC CCCTAGTGAG GGCGGGGAGG GTGTCGCCGC GTGGCGGCTG ACAGACGGGG 540
CGGGATGAGC GTAGCCCCCG CCCCTGCCCT GGTGCACTGA CAGCCTGTCA GCCGGGAAGA 600
TAAGGGACTT CTTCCGCTGG GCGTGGGGTG GGGGTCAACC CAGGTGCGCT GTCCCCCTCC 660
CGCTGGTGTT TGCTCGGTAA ACACTTATTG GGCCCCGGGC TGTGCACACC GCCGCGGGGG 720
AGGGGCGGGC GACCTGAAGG CCTGGACTCC ATGGCCTCTG CCAGGGATGC CGGGTCCATG 780
GGCCATCAAT GATGCAGGAA AAGAGGCTCT GTCACCTCTG GCCCCGCCTG GAGAGAGTTG 840
CCTGTGGGGT CCTTCGTGGG CCCCCTCCAG CCTGGGGTGG CCCTAGCCTC AGCTTCAGAG 900
CTGGGCTGAC CCCCGACTAG CCGAGGCATT AATGGGGCCC CGTGGAGGAG GTCCTGGGAA 960
GGTCTGGGGA GCTGAAGTCC 980
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