| Tag | Content |
|---|
EnhancerAtlas ID | HS091-19115 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr17:17897730-17898310 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:17897772-17897791 | TGCCCACAAGAGGGCACTG | + | 6.67 |
|
| | 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 |
| GH17I017994 | chr17 | 17897595 | 17898655 |
|
Enhancer Sequence | AGGTACCGTT CCGGCAGGCT GCACGCCCTC GGCCCCCTCA GATGCCCACA AGAGGGCACT 60
GATCAAGTAA AACGGTCCTC AGGGATCCCC AGGCTCTGAA AACACAGAAA TCATGCTCCC 120
TCCACAGGGC CTGATGCCCT CTCCCTTCCT GGCTCATCTG CTGTCTGCCC CAGGGCCAGC 180
TCCGTCTCAG TCCAGACCCT GACCCTACTC CTTACTGGCA TTCCTGCCTC CAGCTGCTGG 240
AGAGAATGTG CTAAAAACAG TCTGTCAGAG GCCCCTTAAG ACCCTTAAGG CAGTTCCCCA 300
TGACATGCCA GGAACGGCTC AGGTCCTGTA GCCATGGCCC TGAATTCATG ACTGGACCCA 360
GTTGGCCTCT TTCCCACCAG TCTCCACCCC TCCTTGCAAC CAGACTGAGA AATGTATAAC 420
ATTCTGGAAA CAGCCTGCAG TTTTATGCCT CTGCACCTCT GCACATGCCA TTCTCTTTGT 480
CTGGAACATG CTCCCTCCTG ACCTGCCTTC CTCATGGGCC TGTGAGATGA TGCAGGGGCC 540
CCTGACAGGA GCCGTCCTAC CTACGTGTGT TTCTGCCTGC 580
|
