| Tag | Content |
|---|
EnhancerAtlas ID | HS113-34812 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr7:114429340-114430500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA(var.2) | MA0072.1 | chr7:114429724-114429738 | TTGACCTAGTTAAA | - | 7.01 |
|
| | 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 |
| GH07I114789 | chr7 | 114429487 | 114430810 |
|
Enhancer Sequence | CATTTTTCTA TTCAATTGTT AGTCATCTGC CTGTGATATG AGTTGCAAAT ATTTTCCCCC 60
CAGCATGTCG CTTGTCCTTT GACTTTGCAT ATTATTGTGT GTGTGTATTT TCTTTTTATC 120
ATAACTTGAA AGTTCATTTC CTCCTCTGCT CCGTTGTCTA AAGATAATTT TGATGATCAC 180
AACTGGGTAC AACTTATTAG TATCTAGTGG ATAGAGGCCA GAAATGCCAC TAAATATGCT 240
ACAATGCACA GGAAAGCATC TTACAACAAG GAATTATCCA GCCAAACATG TCAGCAGTGC 300
TGAGGTTGAG AAACCCAGGT GTAAAGGAAC CAGCCCATGT TTTTTCTAAC AATTTAGAAC 360
ATTTCATATT TTACATTGAA ATTTTTGACC TAGTTAAAAT TTGTCCTGTT CAACAGTATA 420
AAGTATGTAT CCAGTGTTAT ATTTTTTCAG ATGAGTACCT AGTTGTACTA ACATCAATTA 480
TTACCCCATG TACTAATTAT CTATTGCTGT GTAATAAAAT TCCTCCAAAT CTTAGCAGCC 540
TAAAACACAC ACATTTATGA TGTCACACAG TTTCTGAAGG TCAGAATCTG AGAGTGGCTT 600
TTCTGGGTGG TTCTGGCTCA GCCTTGCTCG TAAAGTTCCA ATTATGCTAT TGGCCAGGAA 660
CGCAGCCATC TGGAGGCTCA GTGATGGGCT ACCAAGATCA TCCCCATGGT TCTTACCAGG 720
CTTTAGTTTC TTATTGGCTG TTGGCTGGAG GCCTCTGTTG CTTACTTTGT GGGCCTCTCA 780
GTAGGTGCCT AAGTGTCTTC ATGATATAGC ATCTGGCTTC TGCCAAAGCA AGTGATCTAA 840
GCCAAAAAGA GAACCCACAA AGACAAAAGC TGGGGTGTTT TTAATGGCAT AATTTCAGAA 900
GGGACATACT ATTGCTTCCG CAACATCTTA CTCACTAGAA GTGAGTCACT AAGTCCAGTC 960
CTCACCCAAG GGCAGGAGAA TCAACCTCTA GCTCTTGAAA GGAGAAATAC CAAAGAATTT 1020
GTGAACATAT TTTAAAACTA TCTTGCCCTA CTTAGTTGTG ATGTCTCCTT TATCATATAT 1080
TAAATTCCCA TATGGATTGG GCTAATTTCT ATAATTAATG TGCATTGCTT CTAACAAGTT 1140
TTTACAAGGT AATTTAAAAA 1160
|
