| Tag | Content |
|---|
EnhancerAtlas ID | HS116-04087 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr10:35283070-35284420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | + | 7.07 | | RFX1 | MA0509.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | - | 7.08 | | RFX2 | MA0600.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | - | 6.76 | | RFX2 | MA0600.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | + | 6.89 | | RFX5 | MA0510.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | - | 6.43 | | RFX5 | MA0510.2 | chr10:35283636-35283652 | AGTTGCCATGACAACA | + | 6.61 |
|
| | 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 |
| GH10I034993 | chr10 | 35282890 | 35284330 |
|
Enhancer Sequence | TTGCTCTGGG CTTCTTACTG CTGGTCCCAC CCCCAGCCTG CTTCAGTCAT TCCTGTTGGT 60
TGAACAGGAG GCACCAAGCT TCACCTGCCT GATGGCCACA GCTTTAGCTG CACTCAGGAA 120
GGGGAGTTAA GCTGGTGGTT GAAATAGATG TAGGAAGAGA AACTTGCCAT TGTGTCTCAT 180
TGGTTTAGGG ATGCAGAACC ATGGCAACTT CCATGAAAGG CTGCAGAGAG AAAATGAGAA 240
ATATTTAGAG CAGTAATTTT TTATTGCTGC CTGTAGAGTC TGAATCAATG GGAAGGCAAA 300
TATTATTTAT CAAACACTTA AAATAGTATG TCAGGCATGG CGCTAGGAAC TTCAGATAAG 360
TTATCTCATA CAATCTTCAC AACACTATAG TTTTTGTTCG TTAAGAGATG GAAGGAGCTT 420
GCTCGGGGTC ACCTTGGCAA GCTATTCAAT GGACTAGAAT GATTCATCTT CCAAATGTCT 480
ACAGTTCCCC ATTGAGCTGG AGAGAGAGGG CAGCCTCCCT AACGAGCCAG CTCTACAGCT 540
TCAGCTCCCA AAGCTTGCAG AGTACCAGTT GCCATGACAA CAGGACAAAA TGCAGAGACC 600
CTAGCTGCTG GGAGGAAATG ACATGAGCCA AAAGAGTAAA AACTCACCCC GGTACTGGAA 660
TGTATGAGTC ACTTACAAAG AACACCTGTA ATTTTGAGAG CTTAAACCAC CAGAGGGAGA 720
CAGAGATTGC CACAGGCGGG GGAATCTGTC TGTATTCCAA ATGCTGCTGC CTCCCAGCGC 780
TCCCGCCTTT TCCCCACACT AAGGGCCTCT GCCCAGTCTC CCAGGCTGAC CCTTCCTCTT 840
TCAGAGCTCC TCAAACTATC TCCTCCCAAC TGGAGCTCAG GACTTGGGAC CTGGCCCCTT 900
GAGGGTGACA GAAAGGTGAC TTGCATCTTC TGGGGGAAAA AGCAGAGGCA TTCAGAAACG 960
AGAGCCCTTC CAGAAAACCA GTTTGCACAA TGACCAGGAA CTCTGACACC TTAAGCCCAT 1020
GCGAATCTTG AATAGAGAAA TCTTGGACAC TGAGGTAAGG GTGGTGCTCG GAAAGTGTCT 1080
TGGTCCAGAT TTTTCCAGAC CCTTTGATTC ACAGTGGCAT AGATGCTGGC AACCTGCTTG 1140
CTAATCGCCC AAGCGATTCC AGCCTGGTGT CAGGGAGGAA GATGCCCTCC GTCCTCTTTC 1200
ATCTGGAAAA AGCAGGGTAG CATGTGTTAA CTCTTACATA TCAAATTCCT CTAGGAATTC 1260
TGGGGATTCC TTTTATTTGG CTCAGAGAGG AAACACCTAG AACATTTATA CTCTAACCCA 1320
GAGAACTGAG GTGGTTTCCT GGGTATTTCT 1350
|
