| Tag | Content |
|---|
EnhancerAtlas ID | HS178-14851 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr20:33170380-33172200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr20:33170858-33170873 | GCAGGTCAAAGGTCA | + | 7.16 | | Nr2f6 | MA0677.1 | chr20:33170859-33170873 | CAGGTCAAAGGTCA | + | 7.73 | | PPARG | MA0066.1 | chr20:33170865-33170885 | AAAGGTCAGGGTGACTCAAT | + | 6.26 | | Rxra | MA0512.2 | chr20:33170859-33170873 | CAGGTCAAAGGTCA | + | 7.58 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr20 | 33170652 | 33171022 | | chr20 | 33171562 | 33171703 | | chr20 | 33171368 | 33171418 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH20I034578 | chr20 | 33166405 | 33170385 | | GH20I034582 | chr20 | 33170781 | 33170950 |
|
Enhancer Sequence | GGCTGAGGTG GGAGGGTTGC TGGTGCCAGG AGGTTGAGGC TGCAGTGAGC CATGATCAAC 60
CACTGCACTC CAGCCTGGAT GACACAGTGT GAGACCTTGT CTCAAAAAGA AAAAAAAAAA 120
GTAGGCAATC CTCTCACCTG TACTTCACAG ATGAGGAAAC AGATTCAGAG AAGTGCACTG 180
ACTGAGTAGG TTAGTAAGCG ATGGAGTTGT CTCCAGAGCT CTTAATCACG CCCAATACCA 240
TTCTCCTGAG TGCTGATCAC ACTTCCAAGC TCTGGTCAGG AGAGAGTTGG GGGACAGAGC 300
TCAATCTCGG TGCCCCTCCG AGAGCTGACC AAGTGCTAAA GGGAAGCCAA CAGGGAGAGG 360
CTGGATCTAT ACCCTCCTCA GCTACATTTC AACCACATGC ACATGGCCTA CTTCTGCACA 420
GTACCTAGAT GCCTAGCCCA TGAAGGTTTT CTTCAGAGAT TAATGACCTT TTTGTCTTGC 480
AGGTCAAAGG TCAGGGTGAC TCAATGGGTA TGAATCTGAG ATGTGCAGAC AAACATGTCC 540
ACACCCAGAA TGCTCCAGTG CTGCTGTGCA GCAAGTGCCT CAGAAACGCA GCTTGGCAAA 600
GGCGTGCAGC CCTGTAGCCT CTAAGAAGCG TCCAGCTATA GCTCAGTGTG AACATCTTCC 660
TAAACACAAT CCACATCACT GGCTTCAGGC TTTTCAGGTA GCTGGTAACA ACGGCAACAT 720
TTCTATGAAA AGGCTGGTGA AAATGCGGTG ACAAAAAAAC AGACTACAGC CTCCTGCAGC 780
ACTGCACAGG GACTGGGGTG GCCTGAAGGG CCCTGTTCCT ACAAAGCTGG CACTGGAAAC 840
AAATCTTGCA GGGGGCAGGA GAGCTTAGGT AGAGCTTCAT ACCCAGGCAG AAGAGAAGAC 900
AGCAGGGAGA GCAGGTCTCT TCATATTTTC TGTCCCCACA ACTGTGTGGG CCTGGCTTAG 960
GTCATAAAAT GGTGACATTA TTGCCTAGCC AGGAGCAATG TGTGGCTTTG CATGCAGACA 1020
ATAAAAGCTG CCGGAGAGCT GGCTGCACGG CCAGTGCGGA AAGGTGCCCT GGGATCCCTG 1080
CTCCTCTTCA CCCCATGGCT GGGCCTAACC GGAACAAGGA CAGGGAAGGT GGACCACAGA 1140
CAGCTGGAGA GCTCAGCTGG GCAAGGCTGC CAGAGTTCCG GAGCCTGCCA GGCCATGGAA 1200
GGAGGGTGTT CTGTCAGAAG CCAGGCCAAG GCTGTGTCAT GGGAAGGAAG CATCAGCTTT 1260
TGAGATTTTA CAGAATGGGA ACCACGTGCA TTGGTGCACA GACCATGGAG AATGGCAGGA 1320
AGGTTAGGAC AGAGAACTTG AGCTCTTGAA ACCTAAATCA AACTCTTTCA GGTTCCCCAG 1380
ACCATCTAGG CGTATCTGTA CCTGTCTGTG TCTGTTTTCC CTTATCTGAA GCTAGGATAA 1440
TAGAACCATT TCCGGAGGCT ACTAAAAGCA ATCTCTCCGG AGCTTGGCAT GGTGCAGGGG 1500
GATAAGCATA GATTCTGGAG CCAGACAAAC CTGAGTCTAA ATCCCAGCTC CACTGCTTAC 1560
TAGCTGTGTG ACTGGGAAAA TCATCCCACC TCTCTGAGCA TCGATTTCCT CAACTATAAA 1620
ATGGGAGTGA TAAGAATCTA ACGCCTACCT CCAGGAGTTG CTAGGTTAGG TATGATTATG 1680
TTTCAGAGGG TCTAGAAAGG CACCTGGAAT GGAGCAGGCC TAACATCTAT CAGCTCTCTT 1740
AGACTGCAGA AGAGGACTCC ACACATCCTT TGGAGGGAAA CAGATCAGGA GATTAAACAG 1800
TTGCAGGTGG CCAGCCTCCC 1820
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