| Tag | Content |
|---|
EnhancerAtlas ID | HS105-25117 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr14:75352330-75353800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr14:75352934-75352945 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr14:75352934-75352945 | CAGCAGCTGTC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 75353193 | 75353304 | | chr14 | 75352402 | 75352584 |
| Enhancer Sequence | AGGTTGTGTA AGTATCACTG GGGAGTACAG ATATGTGGCC ACGGGTTATT TATTTAAAGA 60
CATAAAGTTC TAAATTTGAC CATCTGATTT CTTCACTGGC CTCCAGACCT AGAAATTGAG 120
GTGATTATGT TGAGTCCCTA GACTAACCTC AATGTTCACT TTTCCCATGT GATGTTCCTT 180
GAGCATCAGC TCCGTGTCAG GTTTTGGACT GGGAGTGTGC CCACTCTCCA CAGGTGTTTG 240
GATTATAATG AAAGTTAAGT TGGAATCCTC TTTTTATGGG ATATAGAAGG GTGCTCCTAG 300
ATATTCTGTT TGGATGTAAG TGCAGCTGAA AGGCTCGAGG TTACATTTAT TGTGGAGATT 360
GAGAGCATCC TCTCAGTAGC ATAGTTACTC ATTTTTAAAA ACAGTAAAAG CATAAAACTG 420
GTTGAGTCCT GGGACTGACT GACTAGTTTG GAGGGAATGC TGTTATTGCA TAATGCAGAG 480
TTTGGAGAAA GGCTACCCAT GTGTGTTTCA GATTAACTTC TGCGTATGAA TGTTGCTTAA 540
ATGCTGCTTT GCATTCCAAG TGTTTTTGTG GTGGTGCTAA GAGAATGCTC TCTAGTAACC 600
TGTTCAGCAG CTGTCAGGCT GCTTACTCTA CAGGGAGAAT CCTCAAAGTG AAGAGGTCAG 660
CGGATGAGCT TCTTACTTAC TCTACATCAC AATGAGGGTT TTTGTTGTTG TTGTTTTGAG 720
ACAGGATCTT GCTCTGCCAC TTTGGCTGGA GTGCGGTAGC CTGATCTTGG CTCACTGCAT 780
CCTCAGCCTC CTGGGCTCAA GAGATCCTTT CACCTCAGCC TCCTGAGTAG CTGAGACTAC 840
AGGCACATGC CACCATGCCC GGTTGTTTTT TGTATTTTTT GTAGAGATGG GGTTGTTTTG 900
CCATGATACC TGGGCTGGTG TCAAACTCCT GGGCTCAAGC AATCCATCCA CTTGCCTTAG 960
CCTCCCAAAG TGGAGGATAC AGGCGTGAGC TATGGTGCCT GGCTGATTTT TTAAAATTTG 1020
AGTAAATGTT GCACTCAGTA CTAGAAATAT GAATCCCGGT GTTATTTTGG AGGGCAGTTT 1080
GATAGTCATA AGTCTTTGAA GTGTGTGTAC CTTTTCTTTT TTTCTTTTTT TCAAGATGGA 1140
GTCTTGCTCT GTCACCCAGG CTGGAGTGCA GTGGCGCGAT CTCGGCTCAC TGCAGCCTCT 1200
GCCTCTCGGG TTCCAGCAAT TCTCCTGCCT CAGCCTCCTG GGTAGCTGGG ATTACAGGCG 1260
CACGCTACCA CACCTGGCTG ATTTTTGTAT TAGTAGAGAC GGGGTTTCAT CTTGTTGGCC 1320
AGGCTGGTCT CTGAAACTCC TGACATCAGG TGATCCGCCC GACTCAGCCT CCCAAAGTGC 1380
TGGGATTACA AGCATGAGCC ACTGCCCGGC CTGTGTGTTC CTTTTCATCT AGCAATTCCA 1440
TCTCTAGGAA TCTATACTGA AGAACTCCTG 1470
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