| Tag | Content |
|---|
EnhancerAtlas ID | HS187-03158 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:35283080-35284320 |
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 | CTTCTTACTG CTGGTCCCAC CCCCAGCCTG CTTCAGTCAT TCCTGTTGGT TGAACAGGAG 60
GCACCAAGCT TCACCTGCCT GATGGCCACA GCTTTAGCTG CACTCAGGAA GGGGAGTTAA 120
GCTGGTGGTT GAAATAGATG TAGGAAGAGA AACTTGCCAT TGTGTCTCAT TGGTTTAGGG 180
ATGCAGAACC ATGGCAACTT CCATGAAAGG CTGCAGAGAG AAAATGAGAA ATATTTAGAG 240
CAGTAATTTT TTATTGCTGC CTGTAGAGTC TGAATCAATG GGAAGGCAAA TATTATTTAT 300
CAAACACTTA AAATAGTATG TCAGGCATGG CGCTAGGAAC TTCAGATAAG TTATCTCATA 360
CAATCTTCAC AACACTATAG TTTTTGTTCG TTAAGAGATG GAAGGAGCTT GCTCGGGGTC 420
ACCTTGGCAA GCTATTCAAT GGACTAGAAT GATTCATCTT CCAAATGTCT ACAGTTCCCC 480
ATTGAGCTGG AGAGAGAGGG CAGCCTCCCT AACGAGCCAG CTCTACAGCT TCAGCTCCCA 540
AAGCTTGCAG AGTACCAGTT GCCATGACAA CAGGACAAAA TGCAGAGACC CTAGCTGCTG 600
GGAGGAAATG ACATGAGCCA AAAGAGTAAA AACTCACCCC GGTACTGGAA TGTATGAGTC 660
ACTTACAAAG AACACCTGTA ATTTTGAGAG CTTAAACCAC CAGAGGGAGA CAGAGATTGC 720
CACAGGCGGG GGAATCTGTC TGTATTCCAA ATGCTGCTGC CTCCCAGCGC TCCCGCCTTT 780
TCCCCACACT AAGGGCCTCT GCCCAGTCTC CCAGGCTGAC CCTTCCTCTT TCAGAGCTCC 840
TCAAACTATC TCCTCCCAAC TGGAGCTCAG GACTTGGGAC CTGGCCCCTT GAGGGTGACA 900
GAAAGGTGAC TTGCATCTTC TGGGGGAAAA AGCAGAGGCA TTCAGAAACG AGAGCCCTTC 960
CAGAAAACCA GTTTGCACAA TGACCAGGAA CTCTGACACC TTAAGCCCAT GCGAATCTTG 1020
AATAGAGAAA TCTTGGACAC TGAGGTAAGG GTGGTGCTCG GAAAGTGTCT TGGTCCAGAT 1080
TTTTCCAGAC CCTTTGATTC ACAGTGGCAT AGATGCTGGC AACCTGCTTG CTAATCGCCC 1140
AAGCGATTCC AGCCTGGTGT CAGGGAGGAA GATGCCCTCC GTCCTCTTTC ATCTGGAAAA 1200
AGCAGGGTAG CATGTGTTAA CTCTTACATA TCAAATTCCT 1240
|
