Tag | Content |
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EnhancerAtlas ID | HS041-12214 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr2:191081590-191082200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:191081993-191082008 | GAGGTCAAGAGTTCA | + | 7.64 | RARA | MA0729.1 | chr2:191081993-191082011 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I190214 | chr2 | 191079126 | 191082404 |
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Enhancer Sequence | ACTAAGTCCC CTCCCAGAGC GGGACAAACC AGAGACCCTT TGCAGTTGCT GGGTCACCAG 60 CAGGGGTGGT GTGGAATACA AACAGTACAG CTCTCCGCCT GCCAGGGAGA GGAATGGTGT 120 CTTCAAAGCA AACAATGAGG AAGTGAGGGT GGAGCCAGGG ATGCTTTTGC TAATGAAAGT 180 GCCCCTCAGG AAAGGTGCCA CAGGCTGTTA GCTCTTCAAA CCAGCAGCTC TTGGCCCAGT 240 GCCAGACCCA GCAGGGCCCG ACCAAAGGCA CCCTGGGAAG CCAGCTGGTC AGTCCCTTGC 300 CTCCCCAAGT TCCTCCAGGG GTCAGTGGAC CCTGGGGAAG TGCCTCACCT AACTCCAGCC 360 TGTAATCCCA ACACTTTCTG AGACTGAGGC AGGTGGATCA CCTGAGGTCA AGAGTTCAAG 420 ACCAGCCTGG CCAACATGGT GAAACCCTGT CTCCACTAAA ACTACAAAAA TCAGCTGGGT 480 GTGGTGACAC ATGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATAGCTTGA 540 ACCCAGGAGA TGGAGGTTGC AGTGAGTTGA GATCACACAC TGCACTCCAG CCTGGGCGAC 600 AGAACGAGAT 610
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