| Tag | Content |
|---|
EnhancerAtlas ID | HS095-04826 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:2223330-2224650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:2223672-2223693 | TTCCCTCCTCGCCCCTCCCCC | - | 6.32 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_56724 | chr11:2222752-2227371 | VACO_400 | | SE_57716 | chr11:2222825-2224599 | VACO_503 | | SE_65606 | chr11:2222980-2227005 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 2223839 | 2223970 | | chr11 | 2224165 | 2224215 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I002201 | chr11 | 2223156 | 2226663 |
|
Enhancer Sequence | CCAGACCCCA CCCTCATCCA TGCCTGGAAC CTGCATCCAC GTGGCAACCC CTCCCTCCAA 60
ACCCAGCTCA TGCCAGGGCT CAGAGCATGG TGGAGAGGGT AGCCCTGGGC ACCTGGGGCA 120
TGGCAGGACT GCCCTGCCTG CCCCGCCTGC CCCGCCCTGG CCCGTGCCTG CAAGAGCCAC 180
CTAGGGAAGG CTCCTTCACC TGGCCCTGGG CCTACACTCC ACCCAGGAAT GTCCTGCACC 240
CCTGGAGTGT GGAGATGAAG GTTACGGGGT CCAGCCTCTG GGCACCGGGA CATCTGGGGT 300
AGGGGCTGAA GGCCATTCAA AGCCCCTGCC CCGAAGTCTA CCTTCCCTCC TCGCCCCTCC 360
CCCACCCACC CTGGGGGAGG TTTGTAATCT TCAGTGTCAT AACCTGTCAG GCCTGTTTGG 420
AAGGGAAGGG CCGCCAGCTT CCTACCAGGG AGCAGGGAGC TCAGGCGTTG GTTAGAGAAG 480
AGGTGAAGCG TGCACAGGAA GCGTGCGGGG CCCCCCTGGG CATGGGGGAG GGGCGCCGGC 540
CGACGGGAGC TTGGGCACGT GCTCACACAC GGGACTGGAC CGTGTGTCAC AGCAAGCCTG 600
GGTAGGTGCA GACAGGTCCG CGCGTGTCAC CTGCGCAGTG CACAGGGGCC TCTGCTGCGG 660
ACGCAGGGCC TGCCGGAGTG ACTGCCTGGC TGCCCAAGAT TCCAGGGGTT CCACTCCATC 720
CGGTGCTGAG TGGTGCCCCC CACCCCAGAG ACCTGGGACA GCCGAGAAAT GGAGGAGAGG 780
AACCCACCCA CCCAGCCCTG TGGCCTCCAG GCTTGACTTG GGTGCAGCTG GCAGAGGCCC 840
TGCCCCTCTG GCTGTCTCCC TCCTAGAGGG GTCTAGGAGT TTCAGGAACT GGGGACCGAG 900
GGAGGTCTTC TGCAGAGACA AGAGGGCGCA GGGCGCAGGC CAGGAAACCC CTTCACCTGC 960
AGAGCCATCG GTGTGGGGAG GTCAGCCACG GGGTGTCTTG GTGTCTCAAG GGGGCCTTAG 1020
GTAGAGCTGT TCACTCCCTC CTTGTGGCCC CCCGAGGCCC AGGAGGGACC TGGAGCCCAT 1080
GTCCCAGGAG TGCCCTTGGG AAGGTCAACT CCAGGAACCC TTGCAGCCCG AGGCTAGGGC 1140
TCTGAAGCTG GGATGGGCAG CGGGGGCCCT GCAGGGCCCC ACAGGCACAG AAATCTCTGT 1200
AATCCTGAAC CATAAAGGGG CCGCCTTCCC TTTTGATTCT AAATTTTAAT AGCAAAATGA 1260
AGAGATAAGT CAGCTTTGAT CTGAGTTTTA TTAGCCTATG CCTTTGTTCC CTCTCTCCTT 1320
|
