| Tag | Content |
|---|
EnhancerAtlas ID | HS041-02278 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:182668190-182669760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HEY2 | MA0649.1 | chr1:182668684-182668694 | GACACGTGCC | + | 6.02 | | Npas2 | MA0626.1 | chr1:182668684-182668694 | GACACGTGCC | - | 6.02 |
|
| | 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 |
| GH01I182698 | chr1 | 182668125 | 182669832 |
|
Enhancer Sequence | AAGGTTAAGG CAGAAGATAG GTGGCTGCGT AGAGGGAGTT ATGACTTGCG CATTTTGATT 60
CATCTTTTCT TATTAAAAGC CGCCTCTCCA GCTGCTGTAC TTTCATCACC CTGCATGCCT 120
CCATCCCTGG GCCAGAGGGG TTTCCACATC ACCACAGAGG CAGGCCTTCC TTCATTTTAT 180
TTATTCCATT TGGGATTAAA CACATTGAAA GGGGGCCATG GCTAAATGGG TGTTTCTCGC 240
CTGGCTCGGT ACTTAGAAAT CAAAGAAGGA GCTTCATGGT GTATGTGGAA GGGGATGGAG 300
TGTAGAGAGG AGGAGGTGGT TTCTGCAGAC AGGCAGCTCT TCCCATCTTC CCAGGAGCAA 360
AGATTAGTTC CCTGGGCCCA GGCCTCAGTG GCAGGGGGCC AAGGAAAGCA GGCCCAAGGC 420
CTTTCCTAAC TCTTAGCCCC CAGGGATTGG CACATGCCAC GGGGAAAGTG AAAAACATTT 480
TACAAAACAG GCTAGACACG TGCCACATAG CTGTGTCCTT AGAAACTTCC ACACAGATCC 540
CTGTTGGAGG CTCTTCTCCC TGTGCTGTGG CTCCCCAAAG CCTGCTTCGT TGCTGCAGGG 600
ACCTTAAGAA TCCGAGGGGA TTCACAGAGC CCTGGGGATT GCAACGGGAT TACCGGGGAG 660
GGATACAGGC AAAATCCCCT GAGAGGCCTG CAATGTGCTG CAGGCCTGGG GCCTTCCTGG 720
CAGGATGGAT ATCTCTATTC CTGGAGCCAA AAGTTCTGGG ATCTGCAGAA AGGGATCCCT 780
CGGGGACTAT AATGAATGCC GTGTTCCAGC AGTGCCAGCT CGGTTCAGCT GCTTGATTAA 840
TGACATATGA GAGGTCTCAC GGCAAATTTA ACAGGAGGGC GCACCCTCAC ACAGTGCCTG 900
CCCTGGATAA GATCCGGCAC CTCACACCCT GCAGGAGACT GGAGGGGCTC ACAGAACTCC 960
TTCCCGAGCT CGGGATCCAG GGCGAAGCCT GTGAAGAGCC CGCCTGGGTC TCAGGTTCTG 1020
AGTCTTGAGT GCATAACAAT GCGCCCCAGA GCCCGCCGAG GGGAGAACTA GCTCCATCTG 1080
CTCCTTCCCA ATTCTCGGCT CCGGCGAGGG GGAGGGGGAT CCCTCGGCGG TTAGGCCGGG 1140
TCCTGCACGG TTATTGGCTG ACACATTTTC AAAGCTACTC TCAAAGGCTT TTATGAAAAT 1200
GCTGTTGCCG GGCAGCAGCT GAAGCCATTT GCCCTAGAAA ATGGATGGAA GCAGGTGTAA 1260
CCACTCACCC CAACATGACC CCCAAAACAT TCCCCGCGAC ACACACGCTA GTCTACAGTG 1320
TGTTACTTTG TCCCTGTATA TTTCAATAAG CGCACCAATC TGACACCTCA GCATTCCTCC 1380
CCGAAAACGT AACCATGAGC ATTGTTCTTC CTGGTTTCTC TTTCAAGAGA AAGGAGGTGC 1440
CAGTCCAGGG TGGTATTCCA AGAGACACCC CAGGTTCAGC CTCGGGCTGC CTCTGGCGGC 1500
AGAAGACACA GGGTGCATCT TCCGTCTTCT AATTCCCATA GCTTTCAGGA GATAGCAGAA 1560
TTGCTGGAAG 1570
|
