| Tag | Content |
|---|
EnhancerAtlas ID | HS091-48915 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr9:136646820-136648150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:136647450-136647469 | CGACCACGAGAGGGCAGTA | + | 6.9 | | FOXC1 | MA0032.2 | chr9:136647374-136647385 | TAAGTAAACAT | + | 6.02 | | Gfi1b | MA0483.1 | chr9:136647685-136647696 | AAATCACAGCT | + | 6.14 | | KLF16 | MA0741.1 | chr9:136647222-136647233 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr9:136647223-136647233 | GGGGCGGGGC | - | 6.02 |
|
| | 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 |
| GH09I133782 | chr9 | 136647361 | 136648946 |
|
Enhancer Sequence | TGGATCAGAG GGAAGGCAGC TTGGACACTG TTAAGGGAAA AATGGCTACA AGTGGCAAGG 60
ACGGCGTCCC CCAGCAGAGG GATGAGGAGG GGGGCAAGGA CACAGGCCCC TGGGGAGAAT 120
GGAGCTGGTG CCAGCCAGGG CGCTGCCAGG ACATGGGAGA ATGCAGACAG CAATGCTGGC 180
TTCCAAAAGA CCTGCAGTTC CAACTACACA TACTAAGAAA AATTCAAAAC CATACAGAGA 240
TGGGGTGGGC GGGTGTGCGC GTCTGCAGAA AGCAGGACAG TGCTTGGGGC CTCGTGGCAG 300
CTGGCTTTGC CTGGGGATAG GAGGAGTAGT TTTTCTCTCC TCCTTTACAC TTCTCTACAT 360
TTTCCAAATT TTCTACGGAA AATCAGTAAT TAATAATCCG GCGGGGGCGG GGCGGGGGAG 420
GAACAGAAAG ATTACAAAAA AAGAAAACTT GGAAGGAAAT ATACCGAAAC ATTGCCTTTC 480
ATCATTTCTA GGTAAGTTCA CGGGTGATAC TTTCTTTAAA ATTTCATTTC TTTTTTTTTC 540
CTCCAAATTT TTGATAAGTA AACATTACCT TTAGAATCAG AGAAAGCAAA AAAAGATTCT 600
AAGTAGCTGC AGCCATCGTC TGGGGACATG CGACCACGAG AGGGCAGTAT TGATGGGCAC 660
AGCTGAAAAG CTGCGTTCAG GCCACAGGCT GCCTGCGGAA TCCTCCAGCA CTAACTCCAG 720
GGGCTGCGGG ATCCTGTGCA CAGCTAGGGG GCTGCATTGG GCCTGTGATG GGGACAAGGG 780
GGTCTGGGCT GACCTTCTGG CCCTCTCCCC AGGTTAGGGT ACTGGGCTGG CACTCACAGT 840
AAATGGTGAA TTAACCATTG ATCTAAAATC ACAGCTCAAA ATGTATTCTG GGCAATGGCG 900
TCTCTGGGTG ACAATCTCTG GGTGACAAGC TGGCCTGACT TGTTTTTCTG CCTTAAGACA 960
CCTTCAGGAG GCTCAAGGAG ACAAGACCCA GAGACTCGGC CTGGGGCCAC CGGGGGCTCT 1020
TTGTTGAATA GAAGCTCTGC TAATAAGTGT AGACAAATTG CTGAAAGTTT CAAGCCTCAG 1080
TTTCTGGGGC TGATGATGGA GGTGACATCC TGATGTCTGA AACCTCTCAG GAGAGAACTG 1140
TCTCAGGCTT TGCACTGCTG TCCAGCTGCC CTGAGCAGGG CACAACCCCA AAGGTATGCC 1200
CCCGACCCAA GGTGCTTCAG AGGAGCCTCC AGGGCGCATC CCTGCCTCTG CCCACTGCCA 1260
GCCTGGCTCA ATCCTCTCCC CTCCCTGAGC CTCAAGCTTC CCTAAATGGG CATGAACAGA 1320
AGGGAACCAC 1330
|
