| Tag | Content |
|---|
EnhancerAtlas ID | HS003-40726 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr7:1209010-1210010 |
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 | CTACCTCTAT CCATCCTTCC TTCAGCCCAT TTCCCCCGAC TTCTGCCACC ACCTCCGGGA 60
CGTCCTGAAG GCGAACCGGC CTCCCACCTG CTAAGTCCAA CAGACACTTC AGCCTGGCTC 120
TCACCAGCCA TGGCGGGTTG CCCTCCTACC TCTTGACAAC ACGCTCTTCC TCGGCTGCAG 180
AGACACCTCC TCTCCGTATT TTCCTCCCAC ATTAGCAATG ACCACACTCA GGCTATGTCA 240
CTCATGGTAT TTTTGCATCA GAAATGCCAT CCTTGGGCCG GGCGCCATGC CTCATGCCTG 300
TAATCCCAGC GCTTTGAGAG GCCGAGCCGG GTGGATCCCT TGAGGCCAGG AGTTCAAAAA 360
CGGCCTGGGC AACATAGCAA GACCCTGTCT CTACAAAAAG AAACAGTTTT TAAGTCATTC 420
CTGATTTTAC AACGCTACTC TGATCTGAGC CCCTGTGGCC TCGGGATCCC CAGGCGTCTG 480
TTCCCGAGAA CGCGGGGCAG AAAGCCTAGT CCTGCACGCA GTACCAACAA TGCGGAGTCA 540
GCGGGTTGTT TCGACTTTGT TCTGTTTCCT GAGGGGTTCT GAATAAGGGC CACCCCCTTC 600
CTCCTCTGTG CCGCCATGTT CCCTCCCGGC CACGCCCCCT TGCAACCCCT CCAATCTCCG 660
CCCTGCACCC TGGCAGCTCC CCCTGGCGGC AGCAGCGGGT CTTCGTGGAG TCAGCCCCTC 720
CGCTGCTTGG CCGCTGGGTT TGTCCCTTAT TTTAATGGAT GCGCGTTGGC TAGGACTGCA 780
ACATTGTTTC TTTCTTCCAC AAATTTTAGT TTGAAACAGA CAGGAAGTTA ATTTCCCGTC 840
TGGCTGCCAC ACCTGCTGGT GGCGTGGACT GCGGCCCTTA GGCTGTTCCT TGCTCGATTT 900
AACCCTGGGA GACATCGAAG CCTTCCCACC CAAGCTGTAG GGAGCTGTTG AAGACCTGGT 960
TCACACGAGA TCCTTTGCGG GGTGCAGCTG GGGAAAGCAT 1000
|
