| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00465 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:20692190-20694350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:20692610-20692621 | CCGCAGCTGTC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:20693611-20693632 | AGGGGAGGGGGAAGAGAGAGA | + | 6.88 | | ZNF263 | MA0528.1 | chr1:20692537-20692558 | CCCCTCACCCCTCCTTCCTCC | - | 6.97 | | ZNF263 | MA0528.1 | chr1:20692533-20692554 | CCCTCCCCTCACCCCTCCTTC | - | 7.95 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 20692247 | 20693635 | | chr1 | 20693127 | 20693202 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I020367 | chr1 | 20692601 | 20692750 | | GH01I020366 | chr1 | 20693127 | 20693202 |
|
Enhancer Sequence | CAGTACCCAC AGTACCAGTA ATAAAATTAA ACGAATCAGT GTTCTCAAGT TAGCCGCTCT 60
CCTAATCACA ACGGCTGCCT AGAGTGGGGC AGTGCTAATG CATGGGGCAT GGGTGGTCCC 120
GGCAACAGGG GTGAGGGGTG AGGGCCTCCA CCAGGCAGGA GGCAGAAGCC AGCGTGGCAG 180
GATCCCGCTC CCTTCTGGGT CTTTCCAGCC TACAGCTGGC TTCTGGCTTT GCTGGGCTAT 240
ATTTTATGTC CCTCTTCATC TGCTTCTCTG TCCCAATAGG TCGCCCACCC CTGGCTTTGT 300
CCCATCTCTC CACGCTCCTC CAGGGTCTCT CAGTCTGTTT TCCCCCTCCC CTCACCCCTC 360
CTTCCTCCAA CGAGCACCCT CCCCAACCCC TGCGCGCGCG CTCCTCCAAA CCCCGCAAAG 420
CCGCAGCTGT CCTTAACCCA CAATCCTGCC AATTAAACCG CTCCCTCCGG CTCTGGCTGC 480
GGCTGCTGAC GTCGGAAGAT CCAGGCGAGG CGAGGCCGCC GCCTACGCGG GTGGGGTTGG 540
GAGAGGCGAC GGCCCCCTCC TCGGGCCCCG CGGCCGTCGG TCAGTCAGCC GGCGGCAACA 600
CGAGCCCGCA CTAGACCCAA GCGCCGCCCG TCGGTCCCCA CTCCCGACGG GCCTCGCATT 660
CCTGGTCCTC CACCTTCTGC CAAGACCCTG CCCACGCTTC CCGCACCAGC CTTAGGTCCC 720
GAGGTCCCCA ACTTTGGCGA AGATCCCGCC TGGGCTCCCC GCATCTTCCC TTGGTCCCAA 780
GGTCCCCAAC TTGTCGCCAA GACCCCGCCT GGGCTCCCAG CACCGCCCCT CGCGCTCGGG 840
GTCTCCCGCC CCACGCCAAG TCAGCAAATG CACCCCAGGT TCTGCCTCTC GCGCTGCCGC 900
TCCGCGACCC CCACTCCGAG TTCCCCGCGT CCCAGCATCC CAAGTGCGCT CCCAGCACCC 960
TCCGCGCCCC GACCGCGCAC GCCCCGCGGA CGCCGCGCCG CGACCCCGCT GGGTCCCCCG 1020
CCCTCCCGGC AGCCTCCGCG CGCTCGGTCC TCGGTTTCCC CTCTCCGAGC GTCGCTGGCT 1080
CTGTCTCCAC GAAGGCGTCG CAGTGGGAAC CGGGAGGGGG CACATTAAGA GCAATTAGCC 1140
TGCGCACACT TGGCAGCGAT ACCTTAATAA ATAATAGTCT GAAAGTCATG TAAATAAATA 1200
TTAGAGCGCA TTACGCGGGC AGGAGGCGCG GCACGGGGCC CGCGAGCTGG TGGCGAGACA 1260
CCGCCGCCTC TCGGGATTGG CACGTGCAGG CGGGGGCCCG AGATCCCCGC GCCCCGGCGG 1320
CCTGCGACCC GCTGCCAGGG GCCGGGCAGG CAGGGGTGGA GGGAGAGGCC CGGGGAAGGA 1380
GCCCCAGGGA GACAGAGAAA GCCACAGAAA GAAATAGGGA GAGGGGAGGG GGAAGAGAGA 1440
GAGAGATGGA GGGTGTGAGG ATGCAGCAGG GAAGTGGAAG AGGCAGAATT TGGTCCCCTA 1500
AGGCTCTGGG AGATTCCTCC CTGCTCCTGG CCAGGCTTCT TTTCCTTGGC CGGGCTCTCC 1560
TCCTCTGCCT CTCTGACTGC CCCTTCCCAG TCTCCTTTGC TGGTCTCCCT ACATCTCCCC 1620
AGTCCCACCG CTGGAGGCGC AGGGCTCAGA CCTTGAATCT CGTGGCTCCT AGCCTCATTC 1680
ATTCACTCGA AGAGCACAGC CCGCCTAGGT GCTTCCCAGT CATCCGCCTG TCAGGGGCTC 1740
CCACCTGCAG ACCTCCAGCC AGATCGGTCT CCTCTGACCC ACAGGCTGAC AGCTCCCTTG 1800
GACGTTGGAC CTCAACTGGC CGGACACTGA ACGCCTGCCC TCCCCTCTAG AACCTGTTTC 1860
ACCCATGCTG TGCCCCAGTT CAGGAAACAG CTCTAGCTTT CTACTTGTGG AGGCCAAAAA 1920
CCTTCGTGCC ATTCTTGAGA CCTCTCTCTG ACACCTCATA TGTAGCCCCT CAGAGAGTCC 1980
TGCCATGTCC ACCTCGAACA TGTTTCCAGA TTCCTCCCAC TGCCACCTGC TCCGCGCTGC 2040
CGCTTAGCCC AAGCCTCCCC ACTCTCTCAC TGGGACTGCA GCCACAGCTC CTCCTCCCTG 2100
GGCTCCTGCC CCCCTTAACC CTCACCATCA CTGTGGACAG AGTGGAGGCT ATAAAAGTAC 2160
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