| Tag | Content |
|---|
EnhancerAtlas ID | HS034-05436 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:66845260-66846580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:66845719-66845740 | CTATTCTCCTCCTCCTTCTCC | - | 6.41 | | ZNF263 | MA0528.1 | chr11:66845722-66845743 | TTCTCCTCCTCCTTCTCCCCC | - | 8.06 | | ZNF740 | MA0753.2 | chr11:66845480-66845493 | GTGGGGGGGGCGG | - | 7.82 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27125 | chr11:66844558-66847331 | Esophagus | | SE_59331 | chr11:66840537-66890130 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 66845907 | 66846062 | | chr11 | 66845381 | 66845631 | | chr11 | 66845748 | 66846170 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I067077 | chr11 | 66844554 | 66847070 |
|
Enhancer Sequence | GGTCTGGTGG TGGGACCAGG TGGGCTATCT GGGAGGAGGG AGGCGGGAGC CTGGAGACCA 60
GCTGGGGAGC TGCAGATGTC CAGACACAAG AAACAAGCCA CTACAAGTCA AGGCTTGGTG 120
ACTTCTGGGC TGGAAGCTGT AGCACCAAGG GTGGACTTTG GGAAGGGTGG GGACGTTGGG 180
AGGGAGGGAA GAATGCAGGC CTCTCCCACC TGGGGTCGGG GTGGGGGGGG CGGGAGGAAT 240
GTGGGGAGGG CGAGCACTTC TCCCAGACCC GGCACTGGGA GAGGCGGGGA CCTTAGTTGG 300
GTGGCCGCTT TCTCACTCTG GCCTCTCCCT CTGCCCCGCC TGTTTCAGGC CCCATCCTGC 360
CTAGCCCGCC ACACACAGCT CTCCAAAGTG TCCAAGGAGG GCACGGGGGC GGGGGGCAGG 420
GGGGTCCTTG GAGACGCCTG TGAGGAGCCA GAGTTATTAC TATTCTCCTC CTCCTTCTCC 480
CCCCAACAAT CCCCTCTTTC AATTCCTCAC TACCCAGCCT GGTAGGGCAG GCACGGCCAG 540
ACGGATGGGA GCTGGGGAAG GCCCAGCCTG GAGGCCAGCG CAAGCCAAGA GCCACAAACC 600
ACCGTCTTCG TTTCCCCATG CCGCCTCCGC CCAGCCTTGG GGTTGTCTGC TGGGAAGGCA 660
GAGGGCAGGG GTGGGGACCT CAAGTCATCT CCTCCAGGAC AGGCCACTCC CTGACACCCT 720
CAGGGTGAGG AGGAGGGTGG GGCGCACACT GTCTGTGAGT CACAGAGCTT CCCTCTCCCC 780
TGTGCCGGGG CAGCACTCTG GGCCCCATCC CATGTCTAGA CACAGGGAGA GGATGGTGGC 840
CAGCAGATCA CCCTACTCCA GGCCACCCTC TGCTCTCCAG CCTCCTTTTC CTCCTGGGGT 900
CCTGTCCTTT GGAGGATAAC CACTCACAGC CCCCAGGAAG TCATCGCTCA GCCGCTGGTT 960
AGGAAACCAA CAAAGCATAT GGCCAGGCTG AGGGCAGTAA GCGTCGAATG AGTGGAACGG 1020
CTGACCGCCC ACCCATGCAT TCAAGGGCGT AATCTCCACG GTAATGCTGC TGATTAATAG 1080
GTCCAGATTG CTGGGCGTGG TGACTCACGC CTGTAATCCC AGCACTTTGG AAGGCCAAGG 1140
TGGGCGGATC ACCTGAGGTC AGGAGTTTGA GACCTGCCTG ACCAACATGG TAAAATCTGT 1200
CTCTACTAAA AATACAAAAA ATTAGCCAGG CATGGTGGCA GACGCCTGTA ATCCCAGCTA 1260
CTCAGGAGGC TGAGGCAGGA GAATCGCTTG AAACAAGAAG ACAGAGATTG CACTGAACCA 1320
|
