| Tag | Content |
|---|
EnhancerAtlas ID | HS102-02493 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:223841110-223842030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | ERG | MA0474.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | ETS1 | MA0098.3 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | FEV | MA0156.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | FLI1 | MA0475.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | Myod1 | MA0499.1 | chr1:223841275-223841288 | TGCAGCTGTCACT | + | 6.78 |
|
| | 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 |
| GH01I223654 | chr1 | 223841653 | 223843699 |
|
Enhancer Sequence | TCTTGGCTGC AATAAGAAAG AATGAGAAAA AGAGAAAACC TCCTGAAAAA AAAGTGGCGG 60
GGGGTGGTGA TGGGGTCCAT GTGATGCTGA GGTTTCTGTT TGTTTTGCTG ATTTTCAGTA 120
AGCAGGATTT GTTTCTTTTT CACCTTCACT TCCGGTTCTG TATTTTGCAG CTGTCACTGG 180
ATGGTGGTTT GGAAGCCCCT CAAATTCAAT TCAGAGCCAT GTTGCCCATA AAATGTAAGG 240
ATTGTCCAAT TCAACGCAGA AACTCCCATC TGTGAAGCCT TGGTATCGGG AGGGCTTATG 300
AAATCAATAA AGCTCATCTG CCACCAAGGA GAGCCTCAGT TTCTGACAAT GGAGGCTAGA 360
ACTTACAAAA CTAAATGAAA TTATTTCTTA AAAACTCAAC TGCCCCTAAT TTAAAAGGAA 420
TATGATAAGT TCAGAAATGA AGGTTTTTGA TTACAGGATC CCAGGCCTAT GAAAGAATGT 480
CTGGCTACAA AAATAAGATT CCTGTTTTCT TACTAATTAT AAAAGCACTT ATTATGACAG 540
CCCATAATTA CTTAGATATG GCCATTCCAA AGGACAAATT ATGTCTACTT AAAGGTAACT 600
ACAACAAAAA CACAGTATAG CACAGATATC TACTCTACGC CTGTAATCCT GGCTCCTTGC 660
TCTAGCATTA AAGTGGTTAA ATGAACTGGC AAAATCTCTC ATTAGGGGGA GCCAAGAGGT 720
AGTTCCAGCA TTTGGACCTA CAGTGAAGTT CCAGCATTTG GACTCACAGT GAAGAATGCA 780
GTCTCAGAAA CACAAACCCA GACGGACACA TCAGGTACCT AATTCACTCG GTGAAGTCTC 840
ACAGCTTCAT CTGATGTTTA CTCATGACAC ATACACACCC GCCCTCTCCC AAAACAAATA 900
AGACTCTCCC CAGTTACTCA 920
|
