| Tag | Content |
|---|
EnhancerAtlas ID | HS060-00315 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr1:12069780-12071550 | 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 | chr1:12071102-12071115 | GGGGACAGCTGCT | - | 7.04 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGTGAGGC TGGCCCGTGT GGCCAAAGGT TAGGGCTCCA GGGTGCAGCC CAGGCACACT 60
GGGGCTCAGC TGCTGGGCTT GCGTCTTGGG TGTGGACACA AATTTTTCTG GTGGGGATTT 120
AGCTCATTCG TGTTAGATGT GTACCATGGG CTGGGCACGG TGGCTGACGC CTATAATCCC 180
AGCACTTTGG GAGGCTGAGG CAGGTAGATC ACCTGAGGTC AGGAGTTTGA GACTAGCCTG 240
ACCAACATGG TGAAACCCCG TCTCTACTAA AAATACAAAG ATTAGCTGGT CGTGGTGGTG 300
TGTGCTTGTA ATCCCAGCCA CTCGACAGGC TGAGGCAGGA GAATGGCTTG AACCCAGAAG 360
GCGGAGGTTG CAGTGAGCCG AGATTATGCC ATTGCACTCC AGCCTGGGCG ACAAGAGCAA 420
AACTCTGTCT CAAAAAGAAA AAAAAAATGG ATGTGTACCA CGTACCTCAT GGATGCCAGA 480
TGGTGCTGGA GGCTCAACAA GACACAGCGT CGCTGCCTTC AAGGCACTTG CAGTTGAAGG 540
CATGATGGCA TCACAGTACT GCGAGACTGC AGTTCACAGC GCCCTGTGCT GAACCGCAGG 600
GCCTACAGCG CTTAACATGT GCTATTTCAC TCAGTCTTCC CTATTTCTCC ATTTTCTACA 660
TAGAAATGTT GGGGAACTTG TCTGGCATCT CAAAAAATGG CCAGGCTAGG AGGGGAGCCC 720
AGGTGTACTT GGCTCCAGCA GCCCCCGCAC TCTGATTCTC CTTACCTGCC ACTCTTTGGA 780
CCCATGAAGA GGGCATAGCC CCCCATTTAC CCACAGAGAA GCTGGTTACT TGGCTGGGGA 840
CTGGCAGAGC TGGGATTGGA ACTCAGATCT CCATGGGGTC TCTGTGGAGC TTTCATTAAT 900
AATTTGCTGG AAAGAACATC AGTCTGAGGA GTCTGGAGTC CTGGGTTCTC TCCAGCCACT 960
CATGTTTGGC CCAAGCTCTT AACTCTCCTG TGTCTCATTA TTTTCATCTG TAAAATGGGA 1020
GTAAGATTTC ATGACACAGC TGCATGACTG AATGTAAAAG TGCCCTGCAA AAGTCCTCGG 1080
CCTGCCCAGC TCATGATAAC ATCAGCACAC GGGGACCCTG CAGAAGTCCT CGGCCTGCCT 1140
AGCCCATGAT AGCATCAGCA CACGGGGACC CTGCACTTCC TGCCCTCGCC CCTGACGTCA 1200
GAGTCTGCAG GGTGGCAGAG CCAGAGGGGA GATGGATCAG AGGGTGTCAG CTCCAACCCT 1260
CACCGGATCA CTGGGCTTTC CCTGCCCTCG ACTGCGGATG TGCCCCCCCC GCACCCCCAC 1320
CTGGGGACAG CTGCTTCCTA GGGACACACT GCTTGCCCTC TGGGGACTCT CAGAAAGGGG 1380
GAATGGGGGG AACTGCTGCT TGTCAGCCAC AGTGACACAG CTGAACCTGG AAAGGGTCTC 1440
CTGTCAGCAC CTCAACCCCT TGCTTGGCAA GCAGGGAAAC TGAGTTCCCG ACAGCTCAGG 1500
GACTTGCACA TGGTCCTGGG TGAAGGAAAC ACAGGGCTTG AGAATCAGAA AAGCCTAACT 1560
TGTAGCTCCC TGGCTTATTA GCCGTGTGGC CTTGGGAAGT TATTTAACCC CTCTGGGCCT 1620
CCTTTTCCCC ATCTGTGAGA CAGGGATAAA CACGATTGTT GGAGGATGAT GTAAGGGTGT 1680
GTGTCAAGCG TCCTTAGGAT GGTGCCTGGC GGGTAGTCCT AATACTGCCT ATCATCAGCT 1740
ATCATGGTTA CAAAAGAACC ATTTCTTTGC 1770
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