Tag | Content |
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EnhancerAtlas ID | HS176-19013 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:39481860-39482510 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:39482062-39482080 | ATCTCCTTCCCTCCTTCC | - | 6.46 | ZNF263 | MA0528.1 | chr19:39482062-39482083 | ATCTCCTTCCCTCCTTCCTCT | - | 6.03 | ZNF263 | MA0528.1 | chr19:39482065-39482086 | TCCTTCCCTCCTTCCTCTTCC | - | 6.88 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TGCCTCCCTT ACTCCCTGGT CCTGCAGAGG ACGCCTGGGA TCTGCAGCAC TGTGGCAATG 60 ACATGTTGGG GAGAAGGGAC CCTCGCAGGC TCCCAGACCT GCTTTGTGAC TTACTGAGTG 120 AGTGCCCGAC CCCTGCCTCA CCAGCCCTGG GCTTCAGAGC CTGAGAATGA AACCCGCCCT 180 TCTTCCACCT CCTCTCCTGC CCATCTCCTT CCCTCCTTCC TCTTCCCAGC TGGTGCCACG 240 AGGAGCTGGC GGACCTCCAA GAGAATTGGC CAAGAATGCA GCCTCTGGAC AGTGACCTGG 300 GTGAGAATCA TCACAGTGGC TCACCCCGGA CCCAGGAATT TCACTTAGTC CTTGTCATCA 360 TCCACCAATG CGGGACAGCT CGGCCCAGAT TGTTCATGGC TCAAGACCCC CACCCCACCC 420 CATTCTGCTT GGTTGGGCTG TGTTGTTTAT TTTATTTAAT GAATTAATTT ATTTATTTGA 480 AACAGAATCT TGCTCTGTTG CCCAGGCTGG AGTGCAATGG CACGATCTCA GTTCACTGCA 540 ACCTCTGTCT CCCGGGTTCA ACTGATTCTC CTTGCCATGG TCCCCTAAGT AGCTAGGATT 600 ACAGGTGCCT GCCACCACAC CCGGCTACTT TTCATGTTTT TAGTAGAGAC 650
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