| Tag | Content |
|---|
EnhancerAtlas ID | HS034-05423 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:66659520-66660740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr11:66659829-66659840 | TGTGACTCATC | + | 6.14 | | JUND | MA0491.1 | chr11:66659829-66659840 | TGTGACTCATC | + | 6.14 | | Nr2f6(var.2) | MA0728.1 | chr11:66660099-66660114 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr5a2 | MA0505.1 | chr11:66659674-66659689 | ACTGGCCTTGAACTA | - | 6.5 | | ZNF263 | MA0528.1 | chr11:66659566-66659587 | GGAAGAGGAAGGGGAAGGAGT | + | 6.22 | | ZNF263 | MA0528.1 | chr11:66660414-66660435 | AGGGGAGGCAGAGAAGGAAGA | + | 6.64 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_00471 | chr11:66658889-66660128 | Adipose_Nuclei | | SE_34512 | chr11:66658992-66660885 | HCT-116 |
|
| | 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 |
| GH11I066891 | chr11 | 66659143 | 66660981 |
|
Enhancer Sequence | TGTTATACCC ATGGCAGACG CTTGGGAGGA TGTTTAGCAA GTTATAGGAA GAGGAAGGGG 60
AAGGAGTTGA GAGGGAATGA CAAGTTGAAG AAGGAAGGAT GAGAATAAAA GGTGGGGCGA 120
GTCCGGGAAC AAGGCTGCGA GGCTCGGGTG AAAGACTGGC CTTGAACTAG ATGAAGAACA 180
CTTCCCCTGA GACCAGAGTG CCTAAGAGTT CTGGGACAGT CTCAGTTGTA AAACAGCCAG 240
TGCTTGGCCA CAGGTGTCAC CCAATACACT GACTCAGCCA GGGCCTGGGA TGACTAAGAG 300
CTTTTTCAAT GTGACTCATC AAGGCTGACA AGCACAGGCA TCACGTTCCA GAACGCACAA 360
CCAAAAGGGC AAAGCAACAG TCCAGGCAGG TCAGCCTGTA GAGACAAGAC TTCCTACTGA 420
CATCCAAGCT ACTCGTTTGC CACAGCTGCT CCAAGGATGG CAATAATGAG TGCGAGCTGC 480
ATCAGAGATG AGAGATTGAA CTTTAAGAAA AATGTCGCCG GGCGCGGTGG CTCACGCCTG 540
TAGTCCCAGC ACTTTGGGAG GCCAAGGTGG GTGGATCATG AGGTCAGGAG TTCAAGACCA 600
GCCTGGCCAA GATGGTGAAA CCCCGTCTCT ACTAAAAATA CAAAAAAATT AGCCAGGCAC 660
GGTGGCGGGC GCCTATAATC CCAGCTTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC 720
GCTTGAACCC AGGACGTGGA GGTTGCAGTG AGCCAAGATG GCGCCACTGC ATTCTAGCCT 780
GGGTGACAGA GCAAGACTCC ATCTCAAAAA AAAAAAAATT GTTGGCTTTT AGTATTAACT 840
GTGAGTGTTT GGTATTCATG TTGGATCTGC TGCTGATGAT GTGGGGGTGG GTGGAGGGGA 900
GGCAGAGAAG GAAGAATTAG AAGGCCACAG AAGCCCAGGT TGAAGGGCTG GGGCTGCTGC 960
AGTGGAAATA TCTTTTAAGA TGCTACTTGG CAAGCATGAT TCAACCCTGA CAGACCCTTA 1020
GAACAAGTCA GACGACCTGA AAGATGAGAT TCTGCTGTCC AGCTGCACCG TGTCAGTGAG 1080
GACCCCCACT GTGACCCCAG GGCACGACTC ACTCCCACGG GCTTGCCTGA CTCCAGCTCT 1140
GTGCTATGAC ATCACGTTGG TAGCCTGACA CGGGCCACAG TGGGCATATT TATGCCACAG 1200
AAATTGGCAA ACACTATAAT 1220
|
