Tag | Content |
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EnhancerAtlas ID | HS128-14672 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr22:35746450-35747540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:35746896-35746915 | CGACCACGAGATGGCAGTA | + | 6.69 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59279 | chr22:35740567-35774903 | Ly3 |
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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 |
GH22I035349 | chr22 | 35745344 | 35750273 |
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Enhancer Sequence | CTCAGCACCT GCCATGTAGA CAATGCTCTG TACATGTTGT TATTGTCACG GATGGTTCCC 60 TGCTCCCTTC CAGAATGGCC TCTGCTCCAG ACACCTGGCT CAGAGCCCTG CCCCTCAGAC 120 TCCTCAGTAA TTCTAGGGAC CCCTGCTCTG CCTCTGGTAT TGCCTTCCCA GCTCCAGAAT 180 AACGTCTGTC CCTACTCCCC ACTGGGAGAG AACCAAAGGA CTGTGTCTGT CTTTCCTCCT 240 GGTCTGGGCT GCTAACCCTA AGAGGGTCAG GGCTGTCTTG ATCCTGGCAA CACGGCAGGG 300 TCCCCCTGGC GTTCCTGGAT TGGGCTCTGC GGGCTCTCGG TAGGCGCTTT AGGAAGCCTT 360 TGCCCGCTCC AAGGTGGCTG GAGGTAGGCC CAGTTCTGAG TCCTGAGCAC GGTCTACGGC 420 CCCTGCTCAG GGTCAGTGTT TCAAGGCGAC CACGAGATGG CAGTAGCACT GCATGTACAG 480 GGCTTGCCGG GGCACTAGGG TGGAGTCCAC CGCGGCCAAA TCAGCCCCTC CCGGGTACAG 540 ACACCGGGAG AAAGGGGCGG GTGCTGCCGG CTCCTGCCCG CTCCTGCCCC GCGCGAGCTC 600 ACAGGCGCGC GCGTGCACAC ACACACGCGC ACACGCCCTC TGACTGGTGG GGCTGAGTAA 660 CAATGGTGAT GGGGCTGGGA GCTGGAGTCC GAGGGTCTGG CTTCACCGCC GGGCTCTGCT 720 GTGGGACTAC ACAAGGGATT TCATCTCTGG AAGCCTCAGA TCTTCTTAAA CGTCCCGATT 780 CACAGGGTTG TGGGGAGGAT TTGGTGAGAC AAGCTGGGAG CTCAGCTACG GGAGCTTTGG 840 GTGGGCAAAA GTGAGCCCGG TCCCCTCCCT CTCTTTACAG AGCCCCGGTG TGCCGTTGCT 900 GGGGCCCCCT GCTCCCGCGC CTTCTCAGCC GACACGCTCA GATCCGTGTG CATTGCCGTT 960 TCTGTCTCCA CGTGTAGACA AATCATGAGC TCGCCCAGTA ACTCCAGCTC TACCACAGAT 1020 TCCTTCTCTT TTCCGCCCTT CCCCTATGTC TAATTCCCTT CTCCAGCAGT GAGAAACCTG 1080 CTTCCCGCCG 1090
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