| Tag | Content |
|---|
EnhancerAtlas ID | HS091-25335 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:24275300-24276770 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr5a2 | MA0505.1 | chr2:24275628-24275643 | GAGTTCAAGGCCAAC | + | 7.29 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATGTGTTGA TTCTGTGCAC TTGTTACTCC TTTCCCAAGT GCTATTTCCC AGTATTTTGC 60
TCATCCTTCA AGTCCCAGCT CCAGGGGGCA CCTTCTCCAA GAGGCCATCC TGGACCACTC 120
TGTCTGAAAT GGCCTGTCCC ACTGCATCTC CCTTTAATAC ATCATTGTGT GTATTTTCTT 180
TAGAGTATTC ATCATAATCC ATAATCATTT TGTATATTTA AGTATTGTCT CTGTCCATTA 240
GAATATAAAC TCCAGGGCGG GTTTGGTGGC TCATGCCTAT AATCTCAGCA CTTTGGGAGG 300
TTGAGGTGGG AGAATCTCTT GAGCTCAGGA GTTCAAGGCC AACCTGGACA ACATGTTAAG 360
ACCCTGTCTC TACAAATTTT TTTTAAAAAA ATTAGCTGGG CATGGCAGCA TGCACTTGCA 420
GTACTAGCTA CTCAGAAGGC AGAGGAAGAA AGATTGCTTG AGCCCAGGAA AGGTCAAGGC 480
TGCACAGAGC CGAGATCATG CTGTTGCACT CCAGCCTGGG TGACACACTG AGACCCCTAC 540
TCTTAAAAAA AAAAAGTAAA CTCTAAAAGA ACAGGGATAG AGATCTTGTT TGTAGTGTTC 600
ACTGCTGTAT CCCTGTGATC AGGCACAGGC TTGGCACACC ATAGGTACTC AGTAAATATT 660
TGTGGTTTTG TTTTGTTTTG TTTTGTCTGT TTGTTTATTG TGACAGGGTC TTGCTCTGTC 720
ACCCAGGGTA GAGTGCAGTA GCATGAACAC AGCTCACTGC AGCCTTGACC TCCTGGGCTC 780
AAACAATCCT TCCACTTCAG CTTCTTCAGT AGCTGGGACT ATAGGTATGC GGCACCACAC 840
CCAGCTAATT GAAAAGATTT TTTTTTTTTT TTTTTTTTTT TAGAGATGGG GTCTCCCTAT 900
GTTACCCAGG GTGATCTAGA ACTCCTGAGC TCAAGTGATC CTCCCACCTC AGCCTCCCAA 960
AGTGCTGAGA TTACAGATGT GAGCCACCAT GCCTGGCCTC TCAGCAAATA TTTGTAAATT 1020
ATTGTGTTTA TTCATCTTTG ATGGATGGAT TATAATCTGC ATTGTAATCT GGTATTTGTG 1080
TGTCTGTTTC CCTACCTTCC TCATGAGTTC ATACATTGCT CTGCATGTCT GAAGTCTGGT 1140
CCAGGCCTGG CACATAGGAG GCCAACTGTA AATGTCTGTG GAATGGATGA TGTGAAGTAA 1200
AAGGGGCAAT CAAAGAAAGT GGGGGTGGGG TGGTGGGAAA GCCCAGGAGA CAGCAGAATT 1260
GAGAAAATTG AGGGGGTAAA GTAAATCCAG GCCAGAGAGG TGACGTGATT CATTCTGGCT 1320
CGTACAGGGC CCAGAGCCAG AACTAGGGCC ACAGGCATCT CCATGGCATG GAGGGGAATG 1380
CAGGCTGGAG CTCTTGGTCA GGATCATACT TAATGTCCCA GGTGTTTTTC CAATATCCTA 1440
CTCCTTCATC TGCCCTCATG TCTCCCTGCA 1470
|
