| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29573 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:242129590-242130600 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr2:242130396-242130407 | GCGCCTGCGCA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGCACCCAG GAGACTGTGG TGCGACTTGA GAGGTCCTCC CCTGCCTGGG TCTATGCCCC 60
CACCCTGGGC CCAGAGCCTC TGGGGGTGGA TGGGCATCAC CGTGTTTCTC CTGCATCCCC 120
CGGCAACCCC CAAGCCCTCG CCACCCAGTC CTCAACACAC ACAGTCAGAT CACCGCTCTC 180
CTGGCCTGGC CTGGCTGTGG AGAACCGAGC AGAACCCACT GATGTTCAGA CAGGAGCTCC 240
AGGAGGGTAA GGGGGGCCTG GCCAGGCAAA GGCAAGACCA GGGCGGGGCC CTCCCTGTGG 300
TGTCAGTCCC AGTCAGTGCA GGGCCACAGC AGCACCCAGG GCCATCTGTA GGGCTCCACC 360
TTGTCACTAG GAGGCCATGG ATGCGCTGTG AGCCTGTGGG GAGAGGCTGG GTCCCGGGCC 420
TTCAAGGCCA TGCGGGAGGC CCTGGCCGTG GAGGGCCCTC TTCCTGGTTC TCCTGGGCCA 480
CACGTCTGCC CCAGCAGCCT GCGGGTGGAC ACGGGACCCC TTCCTGCCGC CCCAAGCACA 540
GCTGAGATGA GCCTCCAGGG AGGGCACAGG GCCTCTCACC TCAAGCATCC AGACACTCTC 600
GGTCGCCATG GCCAACTCTG TCCTCAGGGC CCCTTTGGGA GCAGTCCGGC TCCCCTCTGC 660
CCCTGGAGGC CAGCAAGGCA GGCACCCCTG GTCCTGGCCA TGCTTCCCGC CAACCTGACC 720
CTTGCCATGG GCCTGGCCCA AGGAGGAGGG GAGCCGGCTG GAGGCCCAGG GCTGGTGGTG 780
CCCTCTGGCC CTGCCTGCCG CTCCCCGCGC CTGCGCATCC TGTGCCCCCA CACAGCAGAG 840
GGGCTTCCCC CTCCACCCCC TACCCACCCG CCGAACATTC TTCTGTGGTC CTGAGTGTTC 900
TGGGGCAGGG CGGGGACGGG TTGGAGGCGA GGACGGCTTC AGGGTGGGGC GGGGTGGGTG 960
TAGTTGTCGA GGGCAGATGC TGATGCTGAT ATGCTTCTCC ATCCTCCATG 1010
|
