| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13289 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:109982290-109984380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr12:109983668-109983681 | AGCAGCTGCCCCC | + | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109544 | chr12 | 109982612 | 109983475 |
|
Enhancer Sequence | ATCAACTGTC AAAACCGAGC CACTGCCACC CCACAAAGCC AGGAAAAGCT TCTAACTGAC 60
AATCTTGGGT AAGTCGGCCC TCAGCCTCTG CATCTCCCAC CACAGACCAA GGCTCCCAGA 120
TCCCCCCAGC CCATGCACTC CATGTGGTCC CCTCTGTGTG CCTGGATACA TCGGGACTCT 180
TGGGTGTCAC TGGGGATTCC TGCCCTGCCA CATGGGGTAA GCTACTGGTA ATTACTCAGC 240
TGTGGGAGCT CCTGGTCATC AGCCTTCAAA CACAGAAACT CAGGTATTTT TCCCAGCAGA 300
CCCTGACCAG CCTCTGTATT TCTCCATAAC GCTGGTCGGC TGGGCACAGC GATCTTGGCA 360
ACAGATTTTG CGAAATAAAC TTGGTCAGTG GATCCCAGTC AACAAAATGT TTTTCCATCT 420
GTTACCCACT TCCTCCTGCC TGTGAAGGGG CAGTGCTCTC TCCTTCTTAT AGGTGAGGCT 480
CTGAGAGGTG GAGTGAGTGA CTTGCCCAGG GACTCAAAGC CAGGATATGA GGAACTGGGA 540
TGTAAGCCCA AGCCTTTGAC CAGGAAGGTG ACCTCACTCA CTCACTTGCC TTCCCTGATC 600
GTCAGAGGCC TGGACAGAAG CCTTCTGTCT CCCAGAGGGG CTAGTCCCAC TGACTCTCCT 660
GACCTGCTCC CATCCCACTA GGGACACTGT CCAGGGGAGG GAGCACACCC CATGTGGGGC 720
TTGGTGTGAA GTCTGCTGGG TGGCTTTGTC ACATTGCAGA TGGTGCCAGA TGAGCCGGGC 780
CCCGCCCAGG AAGCCAGACT GCCAGGGAGT TCAGACTCAG CCAACAAACA GACCCACAGG 840
GCCTCCTGTG CCCCAGGCTG GGTGCTGAGT TACAGCCGTG CACACGGTGG ACGTGATCCC 900
TGCCCTACAG AGCTCACTCT CTGGTGGGAA AGAGTCAGAA CTAATTCAAG GAGGAGGTGT 960
ATGGCCACAT CCTGTGATCA GCGTCCCTGG CATCTAGTGC TGTGCTATTC TGATGCCCAC 1020
TCAAGTGGGG AAAGCTGAGG TCAGGAGCTG GTCATTCCCA TGCCCAAGGC CCCAGAGTCA 1080
GTTAAGTGGC AGAGCCAGGA TTCAAACCCT GGTCTGCCAC ACTCCAGAGC CCTCACTCGG 1140
TTTGAGCAGG CAGAAGAGGG GTGGGAGAAC ATTCTAGGCA AAGGGCTCAG CTTGAGCCAA 1200
GCCCCAGGGG CTGCTCTGTC CCTTATCTGG AGCCCGCTGC CTCCACTGCT TGTCCCACTT 1260
ACCCTTGCCG GGGATGCTGC AAACTGACAG ACACACCCAT TTTGCCAGTG AGTTCCCACA 1320
GCATTTTAAA GGACTTCTTC AGGACCCTAG AGCCCTGGTC TCCCCAAGGC TGCAGAGCAG 1380
CAGCTGCCCC CCAGGCACAG AGCTGAAAGG CAGAGCTGGA TTTCAGGGTG TGCTGAGTAA 1440
AGGGCCGATC TACCCTGCAC TTTGGAAGCT CACCGGGTAG AGGGAGGCCA GAGGAATTTC 1500
AGGGACTCCA CGACTTCCTT AGCTTATCAT TCATGTCCCA ACAGGCTGCA GCCTGTCTCC 1560
CTACCAGCTA AGGCAGAGTT GCAAGTGGGA CAGAATCAGT GCCCACTCCA AACATGGCTC 1620
CTTGGCTGCA TCTGGGAACG GGTTCCATTA GGTGGTGTGT GGAGGGTCTC AAACATCTTA 1680
ACAGTGATGG TGAATGCGCC AGTGCCTCTG CAGCAGGGGC CAGAGTTCCT GTCTCCCCTC 1740
CTGGTTTGCT ATCACAGGGG CCCCTGGTGA ATAGGCTGGG TGGCTCATCC CAGCGAGTGT 1800
TCAAACTCAA AAGCTGGATG GCTAGAAACT GCCCACCTGC ACCAAACCAC CATCAGAAGT 1860
GGTCTTTATC AGCCAGGGCA ACAGAAGCCA GCTCTGCCTC ACTTAGAAAA GAAATGTATT 1920
GGGCAGTATT GAGGGCTGGA AGCCCAGGCC ACAAGCAGAA TGGGAGCCAG GGCAGTTCAG 1980
GGGACCTGTG CAGTTCAGCC TGAAGCTGGG TCTCTTTAGG ATGCTGTGGG CGTGAATGAA 2040
CCAGCTCCAG CCAGCAACCC ATCCTCGCTC AGTGCATGCA GGGGTCTTTA 2090
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