| Tag | Content |
|---|
EnhancerAtlas ID | HS184-27208 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:1208840-1210120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:1209683-1209702 | CAGCTCCCCCTGGCGGCAG | - | 6.09 | | INSM1 | MA0155.1 | chr7:1209642-1209654 | CGCCCCCTTGCA | - | 6.02 | | KLF14 | MA0740.1 | chr7:1209637-1209651 | GGCCACGCCCCCTT | + | 8.42 | | KLF16 | MA0741.1 | chr7:1209638-1209649 | GCCACGCCCCC | + | 6.62 | | SP1 | MA0079.4 | chr7:1209635-1209650 | CCGGCCACGCCCCCT | + | 6.19 | | SP3 | MA0746.2 | chr7:1209637-1209650 | GGCCACGCCCCCT | + | 6.82 | | SP4 | MA0685.1 | chr7:1209635-1209652 | CCGGCCACGCCCCCTTG | + | 6.59 | | SP8 | MA0747.1 | chr7:1209638-1209650 | GCCACGCCCCCT | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35540 | chr7:1208673-1210137 | HepG2 |
|
| | 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 |
| GH07I001169 | chr7 | 1208950 | 1210250 |
|
Enhancer Sequence | GTGCACTTCT TACAAATATT TGCTGAGGCT GTGAATTATA ATTGCAAAAG TAGAATCCAC 60
TGTGTCCAAG CAGAAGAGAG GGTGTCATGG GGAGCGGGCA GTGGGGAGTC ACCTGTCTGC 120
CAGGCTGGAC GGGTGAACAC ATTCATCATC TTTAGGCATG CGAGCTTCTC CTACCTCTAT 180
CCATCCTTCC TTCAGCCCAT TTCCCCCGAC TTCTGCCACC ACCTCCGGGA CGTCCTGAAG 240
GCGAACCGGC CTCCCACCTG CTAAGTCCAA CAGACACTTC AGCCTGGCTC TCACCAGCCA 300
TGGCGGGTTG CCCTCCTACC TCTTGACAAC ACGCTCTTCC TCGGCTGCAG AGACACCTCC 360
TCTCCGTATT TTCCTCCCAC ATTAGCAATG ACCACACTCA GGCTATGTCA CTCATGGTAT 420
TTTTGCATCA GAAATGCCAT CCTTGGGCCG GGCGCCATGC CTCATGCCTG TAATCCCAGC 480
GCTTTGAGAG GCCGAGCCGG GTGGATCCCT TGAGGCCAGG AGTTCAAAAA CGGCCTGGGC 540
AACATAGCAA GACCCTGTCT CTACAAAAAG AAACAGTTTT TAAGTCATTC CTGATTTTAC 600
AACGCTACTC TGATCTGAGC CCCTGTGGCC TCGGGATCCC CAGGCGTCTG TTCCCGAGAA 660
CGCGGGGCAG AAAGCCTAGT CCTGCACGCA GTACCAACAA TGCGGAGTCA GCGGGTTGTT 720
TCGACTTTGT TCTGTTTCCT GAGGGGTTCT GAATAAGGGC CACCCCCTTC CTCCTCTGTG 780
CCGCCATGTT CCCTCCCGGC CACGCCCCCT TGCAACCCCT CCAATCTCCG CCCTGCACCC 840
TGGCAGCTCC CCCTGGCGGC AGCAGCGGGT CTTCGTGGAG TCAGCCCCTC CGCTGCTTGG 900
CCGCTGGGTT TGTCCCTTAT TTTAATGGAT GCGCGTTGGC TAGGACTGCA ACATTGTTTC 960
TTTCTTCCAC AAATTTTAGT TTGAAACAGA CAGGAAGTTA ATTTCCCGTC TGGCTGCCAC 1020
ACCTGCTGGT GGCGTGGACT GCGGCCCTTA GGCTGTTCCT TGCTCGATTT AACCCTGGGA 1080
GACATCGAAG CCTTCCCACC CAAGCTGTAG GGAGCTGTTG AAGACCTGGT TCACACGAGA 1140
TCCTTTGCGG GGTGCAGCTG GGGAAAGCAT GATTTCAGCT TGTAAGCTGC ATGGAGAATG 1200
CAAATGTATG TGTGTGTGTA TATATATATG TGTATATATA TATATATATA TATATATATA 1260
TATATATATA TACTTTTTTT 1280
|
