| Tag | Content |
|---|
EnhancerAtlas ID | HS041-18652 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr7:149192890-149194010 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr7:149193133-149193143 | GTCACGTGAT | - | 6.02 | | Nr5a2 | MA0505.1 | chr7:149193455-149193470 | GCTGTCCTTGGACTC | - | 6.15 | | TFEB | MA0692.1 | chr7:149193133-149193143 | GTCACGTGAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATCTATTTG GAAGGAAGCA GGACCCAAAG AAGGTAGGAC TCTAAGGGGT CTTCAAGGCT 60
GGGAGATTCT GGACAAGCTG AACTGTTTCT AGGCGAAAAC CCCAATGCGG GTGGGAGTCT 120
TGCTCTCAAG GAGTAGGTGG TCCTACAGCA CCTGGGTGGG CCAGCGTGGT TCTGGGCTTG 180
AGTCCACCCT CCACCTAAGG CCACTGTTCC TTCCCTCACC TCTCCTTTCT CAGATCAATC 240
CCTGTCACGT GATCCCAGAC GCCAAGAGTT TACTCCAGAA GCTTCCTTTC AACTGGTCAC 300
CAGCTCCTTA TCCACTGAAA TCCTACCCAT CCTCCACGTG CATTATTATG GGCTTTGTGT 360
GGCATGAAAG GGACCTCTGC TAAACTACTT TATTAAGAAA ATATTAGTCT TTTACTCATG 420
GACAACAAGG TGCATGGTTT TCTTACAGTT CTGATGGGGC CAGGAAACCC TGTGTAAGGT 480
CTTCACACTA TGTGGTGGGA GGTGGCGACT GTGCGCTGCT CACTCCAGCC CAGCTTCTTA 540
CTGACAAGTG GCTGGAATAT GTGGGGCTGT CCTTGGACTC CTGCCAGGGG AGCTGAAACT 600
CTTTGCTTGA GAGGAGCTGA TGGTAAGAGG AGCCGGATCC CTCATCCACT GCCCACCCGC 660
AGGATGAAGT CCAGGCATGC AAACCCCTTC TTAGTCTCTC TCTGCAGACT CCTTTCCCAC 720
TGCCTCCAAA CCAAAACCAT CTTCTCCAGG CTCATGGACT CCTTTCTGTG CCTGCACACG 780
CCCTGCACTG TCCCGTCTCT CTGCGCCTTT GCCCAGGCAC TCCTCCCTCC CTGAAAGCAC 840
CACCGGTCTA GCTGGGCCTG AAATCCTAGC CTTCCCTAAA AGCCCGGCTC AAATCACAGA 900
GGCGCAGAGC ATCAGGCCAG GAGGGGTGGA CAGCGGTACC AAGAGGCCCC CTGACACTCC 960
TTCCCCCGGA GCCCACCGCA AGCTTCCACC TGGGCGCCAG CACTCACCCC TTTCTGTTTT 1020
GCACGATTAT TGCCCGCGTA CCTGCCTGCC TGGTCCTTGA ACACACAGCC ACTGTGTGTC 1080
TTTTCACACT TTCCAGCTGG GTAAGCCTGG GCAAGTTAAG 1120
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