| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01029 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr13:111123560-111124530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:111124412-111124430 | GCTGCCTTCCCTCCATCC | - | 6.38 |
|
| | 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 |
| GH13I110470 | chr13 | 111123251 | 111125025 |
|
Enhancer Sequence | GTGCGTGAAC GCCACACGGG GCTCCCCTGT AGGGGGGAAT GGATGGGATG CACCCATTAT 60
CAGGTGATTT GGACAGTTGC CCACGTGAGT TGGGAGCCTG TTCCACCATC AAATGTGAGC 120
CCTTACGTCA TGAACAGGGA GGCTGGGGCA GGCTGGGGGT GGGTGGTGAT TGAGGAACTG 180
ATCAGTTTCT GAAACGCATG TCACTTTTTA TGGTGCTGAA ATATACTGCC CTTCTGTCGC 240
CACATGCAGA AGAGGATAAA ATGCCCAATT CAAGGATTGC AAAAATCAGA GAGTCTATTC 300
CAGATCTAAG ACCCACACAT GCAAACCCAA GTGCATGGCT CCCTGGGTAC AGTTTGTAAC 360
ATTGCCAGTG AAAGTCATGT CTCTTCATTG TGAGTAAATC ACACCGTTAA AACTCTGAGT 420
ACGGTCTAGC TGATTAACGT CAGGTTAATC CAGATCCTTT ATTCTGTATT CCAGTTACTC 480
CCAGCTCCCA GGCAGTGATG GCTTTACCGG CCCAGGAGGT CCCCGGGCCC TGCTCATTGG 540
ATCTTTTTGG TGGGATACAC CCCACAGAAC ACAGAAAACA TTCCCTTTTC CGTATCCATA 600
CATAGGAGTG CCGAGCCTGC CGTGTACTTG ATCTTGTCCC ACAGAATCAC CTGCCAGTCT 660
CATCGTTGCA GGCTTCTCTC CTGCATGCAC AGCGGGGGTG GTGGTGACCT CAGAAGCCTT 720
TCCTTCTGAG CACTGCGTGA CTGTCAGCTG TGGGAGTTCA TTCTGAGGCC ATGTCAGGGC 780
TGACTGCACC GAAAAAGGAA GTGACCTGAT GAGATCATTT TATCCAGTGG CACCCACAAA 840
AGACACAGGA CAGCTGCCTT CCCTCCATCC GCAGATGGGA CTTGATGATT TTCTTTTTTC 900
TTTTTATTTT TTTCTCTTTT GAGATGGAAT CTCACTCTGT CGCCCAGGCT GGAGTGCAGT 960
GGTGCGATCT 970
|
