| Tag | Content |
|---|
EnhancerAtlas ID | HS002-09317 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr8:22604810-22606270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr8:22605839-22605849 | ATGGAATGTG | - | 6.02 | | ZNF263 | MA0528.1 | chr8:22606178-22606199 | GAGGGAGGGTGGGGAGGTGGG | + | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 22605286 | 22605400 | | chr8 | 22606038 | 22606156 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022741 | chr8 | 22599459 | 22607261 |
|
Enhancer Sequence | CCTTGTTCAG GCTCTGTCCC TTCCTCAAGT GCCACTGTGT AGATCCAGGG TCTCTGCTGT 60
GCCCAGCCTC CTGTACAGCA CCCGAGAGAG GCCACAGACG ACTGGGTTCT GGACTTGAAC 120
CTGGGTGACC TTGGGCAAGT CACCAGATCT GTGGGTCTCT GTGGCCTCTT CAGTAAAATA 180
ATGAAGATGA TTTATTGCAA GCCTCAAGGT TTGTGTTTCT TTGGGCAGGA GCCTACTGTG 240
ATCAGAGCTG GGGGAGCCAG TGTGAGCAGC AGGGTGAGTG GGGTGTGCAT GGGTGTGCAC 300
GCTCAGGGGG GTGGGGGGCT TGAGGGGTGG CAGGGGGACC CTACGGGATG TTGCTTTTCA 360
GCCTGGCGCT GCCTCGCTGA GTAGCCTGAG ACTAGGAAAA GGCTTAAAGA ATTCACAGTG 420
GGAAGGCTGC AGCCTGACTC TGCTCCTGGC CGGCGTTTGC CCGCTGCCTG GCCCTGGCTG 480
TTCCAACGAT GGACTTCCTT CCTCTTTGGC CATAAAAGTC TCCCGGAAAG CCTTCCCACA 540
GAGGCCCCGG GGGCTTTCTC AGGGAATGTG TGAGTGTGTG CTCACACAAG CACTGTGGAG 600
CAGGAGCCCA GGGCCGCGTG CAGGCTCTCC CACAGAGCTG TGGGTCCTGG CGCTGGAGGA 660
GAGGTTCGTC CCAGCCTGGG TGGAGAGCGG AGGAAAGGCT GGCCCTTGCC TGGACTTGGG 720
CCCTGGCTTA TGCAATGCTC AGACTCTTAG TCAACTTCAG CAACTGGGGC ACATCCACAC 780
GCATGTGCAC ACACGTGCAG GCACACACCC GGGCAGGGAG GTGTGAGGAA GGGAGACCAA 840
TGAGCCTGTG CCAAGCTCTG CTTACAGATC TCCCCAGATC TGGAGAGAAA AGGGGAGCCC 900
TTCTCCAAGA GGGGGCTGCG CTCAGGCTGC TAGGGTATGA TGATGGCTCC AAGCCTGTGG 960
CTGAGGTTGG ATGGACCATT GAGAGGAGCC CTCCAGGGTG AGGGGACAGA AGCCCATCAG 1020
TCCGTATTGA TGGAATGTGG CTACAGTGTG GAGAGAAGAA GATACTTTCT CTTCCTGCCC 1080
CAGAAGGTAC CCAAGCCTCC GGGATGCTGG GTCACAGAAC CCGCCTGGCA GAGAGTTGCA 1140
TCAGAGCGAA ACTGCATGCT AGATGCCTGA GGGGAGAGGG CACTGAGGAC TTGTGATCCT 1200
AATTTCCCAA CCTTCAGCTG CTCAGGGTCA AGTCCTTAGG CTCCACTTGC TCTTCTCCCC 1260
TCCCCAGCAT TCTTCTGTAC TAGGTTGCAC ATGATGAGGG TGGTCTGAGG GGAGAACAAG 1320
GAGGGGGTGT GACTCAGAGT TCACCCGGCT GTCAGCAGCC CTGAGTCAGA GGGAGGGTGG 1380
GGAGGTGGGT GGAACAGCTT TTGGTAGTCT TGGGGTTCCC TATAAGCAAG AGCATCCCAG 1440
AAAAATAGAA GAGAGCCCCC 1460
|
