| Tag | Content |
|---|
EnhancerAtlas ID | HS118-17041 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr7:22904560-22905730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:22905497-22905518 | CTTTTCTTTTTCTTTTTCTTT | + | 6.02 | | IRF1 | MA0050.2 | chr7:22905503-22905524 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_39248 | chr7:22904481-22905692 | IMR90 | | SE_45026 | chr7:22903803-22905832 | NHLF | | SE_46082 | chr7:22902071-22905712 | Osteoblasts |
|
| | 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 |
| GH07I022862 | chr7 | 22902147 | 22908010 |
|
Enhancer Sequence | CTGTATTTGA TTACACTTCA GAAGCAGCCT CCGAACCTAC TGTGTAGGCA TCAAATAGGA 60
CAGAAGTGAG CTGTGGCAAT GACCATGTCC TCACATGACA ACATCTCCCC TGGGGGCTCT 120
AGTGCCTCCT CCCAGGGGAC CCACTCCCAG CTTCTGACTG CCTGATTGGT TTTTCAGCCA 180
GCTGAGCTTC TAGATTCTCC CTGAGATCCA CCTCTGGCCC TGTAAAGGCC TCCTGGTTGC 240
CTCTGTCCTG ATCCCCGCAC TTAGCTCTGG ACTGAAGAAT TATCTGGAGA TAATGTGCTT 300
TGTCCTCCAG TGTCTGCCTT TGCAGAGCAC CAGCCAGGCG TTTTGTTCCA GGCTGCTCCA 360
GCCACCCTGC TGTGGCTTCC ACATGGATGT CCTGATCAGG TCCCCCATCC ACCATCCTCC 420
TGGGCTGTCC TGACCACTCT CGCTGGCCTC TATGTCTCTC TGGGCTTGGC CTGTCAAGGA 480
CCTCGATTCA CTCTGGACTC TGACCCAGAG TTCGCCTGTA AAATCCCCAC ACTTGGCTCT 540
TAGCAAGCAG TGCTTACAAA GTTAGGAAAT ATTTGTAAAA TGCTGCCATG GTATAATGTG 600
AAGCGCTCAA ACAAGTCAGG GCTAATGATG CACTGAGAAT TATTTCTAAA TTGAGGGCAT 660
AAAGAGTTAC AGTTCTTCGA TTTTAAAAAG CAAAGTGACT TTTAATGCAT CAAATCTTAC 720
TGTAGCCAGA GTACTGTAAC TTAGTTTCCA TCAGAATGGA AATAAGTAGT TACTGAGCAA 780
GCAGCTGGAT GAGCCCTATG CTTGATGATA CATATTGAAT TCCAAGGTAG GCCACAGGCC 840
ACTCCTCCCG GGGACAGGAT CCATCATCAC AGCCACCAGG CCCAATAGTG TGAGCCATGC 900
TAAGAAATGA AATGATATAT CATTTAGGGC ACTGGTGCTT TTCTTTTTCT TTTTCTTTTT 960
TTTTTTTTTT TGAGGAGTTT TGCTCTTGTC CCCCAGGCTG GAGTGCAATG GTGTGATCTT 1020
GGCTCACTGC AACCTCTGCA TCCCAGGTTC AAGCCATTCT CCTGCCTCAG CCTCCCAAGT 1080
AGCTACAATT ACAGGTGCCA CCACCACGCG TGGCTAATCT TTTCTTTTTT TTTTTTTTTT 1140
GAGACGGAGT CTCACTCTGT CAGAGTGCAG 1170
|
