| Tag | Content |
|---|
EnhancerAtlas ID | HS091-02867 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:150527110-150527900 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr1:150527358-150527369 | AAGCACTCAAG | + | 6.02 | | ZNF263 | MA0528.1 | chr1:150527138-150527159 | GGAGGAGGAGGTGTGGGAGAC | + | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGTGGTC TGCAGAAGGG TCGGGGTGGG AGGAGGAGGT GTGGGAGACA CGCTTTGTCC 60
GGACTCCCCT GGGAAGGCCA TCACTGGGGG TCAGGTGGCT GTGACACAAG AGGGCCATGG 120
TGGGAGAGAT CCTGTCCAGC CGTGACAGCC AGGTGGGGGT GTGCCACGCA TCCTGGGCAC 180
TGTCGTATCG GTTGCTCCCA GGTTACCATC CGCTTCATTT TAGGCCTGTG TTAACTTGAC 240
ACCGGGATAA GCACTCAAGA GCTCTGAACA CACAGAATCA TGGGCATCAG GGATTGCTCC 300
TCTCTCAGTT CAGAGTCCCC TTGATGGTCT CGGTGACCTC AACTGACCTG ACCACCTTTT 360
TTTTTTTTTT TCTGAGACAG AGTCTCACTC TGTCACCCAG GCTGGAGTAC AGTGGCACGA 420
TCTCAGCTCA CTGCAACCTC TGCTTCCTGG GTTCAAGCAA TTCTCCTGCC TCAGCCTCCC 480
GAGTAGCTGG GACTACAGGC ATGTGCCACC ACGCCTGGCT AATTTTTGTA TTTGTAGTGG 540
AGATGGGGTT TCACCACGTT GGCCAGGCTG GTCTTGAACT CCTGACCGAA TGATGCACCC 600
ACCTCGGCCT CCCAGAGTGC TGGGATTACA GGCATGAGCC ACTGCGCCCG GCCCTGACCA 660
CCTCAGCTTG TGCTGTTGTC ACATTTCCTT CATCCACAGT GACCTGGGCA ACCTCAAGGT 720
GCCCCCTCTG GGGCCTCTCT CAGCTAACCT CCCACCAGGG AGCCCACTAA CCACCCTTCT 780
ACCCTGTCCC 790
|
