| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33068 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:37888810-37890090 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr22:37889186-37889206 | CCCCACACCACCAGCCTCCA | + | 6.8 | | TFAP2C | MA0524.2 | chr22:37889244-37889256 | TGCCCTGGGGCT | - | 6.11 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33401 | chr22:37878298-37890078 | H2171 | | SE_34331 | chr22:37889648-37890281 | HCT-116 | | SE_67129 | chr22:37878298-37890078 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I037492 | chr22 | 37888901 | 37889170 | | GH22I037493 | chr22 | 37889649 | 37890281 |
|
Enhancer Sequence | TGTGGCAGGG GAGGGGCGCA AAAGAGATAA GGGCACAGGC AGGCAGCATA CCAGCTCGTC 60
GATACCCCAA AACCCACCCC GCCACCCATC CCTTCCTAAG TCCTGCTGCT GCTCCTCCTA 120
CACATGCACA CACACACACC CTTAGTAGGA CCGACGGTGG CAGTAGGCTC CTCCCTGATT 180
CTCTGCCTCA TCCCTGCCCC CTACGGGTCA TTCTCCATCC AGCAGCCAGA GAGGCTTTAA 240
AAAGCAAATC AGATCATGTT AACTCCCCTG CTTTCAACAC ACCAGTGACT TCCCAGATTC 300
TCAGGAATAA AAGCCACATC CCCCACGTGG GTGACACAGT CCTGCCTGAG AGCCTGGGGA 360
GGCTGCCAGC CACTGACCCC ACACCACCAG CCTCCACTCT CCCTTCAGCT GCGTCCAACC 420
ACAGGGCCTT TGCATGCCCT GGGGCTGCCC AAAGCCCCAG CCCTGCACCA CTCAGCCCAG 480
TTAACCCTTG CCCTCCCTTC AGAGCCTAGG TCACACCTTC CCTGGTCCCC AGACATCAGG 540
GCCCCTGGCA TGTGCCCCAC GGCCCCCAGT TCTCCACTGC ACACCTCACA CTCTCTCATT 600
GTGTTCATAG GTGGGATTAT CTGACTCTCT ACCCCCTAAT TAGACAGCAA GCTCCATGAG 660
GGCAGGGACA GTCACGTCCC CAATGCCTGA CAGAGCTGGT ACTCAATACT CACCTGCTGT 720
CCCCAACACC CTCCAAGCAC ACCACACACA GCCATGCCTC TGTGCCTTCT GCCTGGAACG 780
AACTCCTCTT TAACTTTGAA GGCCCCCGCG GAAACTCCCT CTCTTCCAGG AAGTCTTCCC 840
TAACTACCCG CTCCTCTTGC CCCAGATTTG CTACTCCCTC ATCTGAGCTC CCCCAGCCCC 900
TTCTACCTGT CTGGCCTAAG GCCTCACCCT ACTGCCTCCG GGAACCCCCC TGGGTCCTCA 960
CAGCACCTGC CACCACACAC GTGTGAGAAG CACCACTACA CACACTCTGC CAGAAAAGAA 1020
CAAGCCAGTA TGTGTGCAAA CCCACAGTCA CAGCCACGTC TGCATGCACC TCCCCGCAGG 1080
GTCTCCCTCA ACCTTGGCAA TCACCATGGC AGGTGGGGTG GTCTTGTCTC TCAGGCCCCC 1140
AGCATGACCC CCACTCCTGT TGGAACCCTC ACAACAGGCC CTTCCAGGCC AAAGAGGCCA 1200
CCCAAGCTAA AGGACACTCA GCTGCACACA TCCCTGGACA ATGGGAGCAA CACGGGATAC 1260
AGCTTTGCCC CCGCGCACTC 1280
|
