| Tag | Content |
|---|
EnhancerAtlas ID | HS139-10707 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:111998870-112000210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr11:112000118-112000129 | ATATTAATTAT | + | 6.02 | | FOXC1 | MA0032.2 | chr11:112000128-112000139 | TATGTAAACAT | + | 6.32 | | Foxq1 | MA0040.1 | chr11:112000095-112000106 | AATAAACAATG | - | 6.02 | | Tcf12 | MA0521.1 | chr11:111999705-111999716 | CAGCAGCTGTT | - | 6.32 |
|
| | 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 |
| GH11I112128 | chr11 | 111998729 | 112000881 |
|
Enhancer Sequence | TGGCAAACAT GGCAAAACCC CATCTCTACT AAAAATACAA AAAATTAGAG GGGTTTGGTG 60
GCATGTGCCT GTAGTCCCAG CTACCCCAGA GGCTGAGGCA GGAGAATCGC TTGAACCCCA 120
GAGGTGGAGG TTGCAGTGAG CCCAGACTGT ACCACTGCAC TCTAACCTGG GCCACACCAC 180
GAGACACTCG GTCTAAAAAA AAAAAAAGAA AAAAAAATTA GTTTGTCTTC TTCTACCTAA 240
GGGTGAAAAT AACATGTGAG CTTCAAGATT CAATGCATGG CTTCCAACCC TGATGGGCTA 300
GCTGGAGAGT GGTGGAGTGA GAAGACAAGG TGGCAGACCC AAGGTGGATT GTCAGATGGC 360
AGAGATGGGA AGACACCAGG AAACCAGGCT CATATTTTCA TGGAACCACT GGCTGCTGAA 420
GCCTGTGACT TTGGCAGGCA GCCCAGGGTG AATCACTACT TAGATGAATG AGGAGATTCT 480
GCTTTGTCCC TGACACTTCA AATTGTTATT CCTTCCTTAA GCAATTTATG GGCACTCCCA 540
TAGACTCTCT AGCCTTTGGA GCCTTTGCAT TAGGAGCTTG ATTTATGGAT ATCTGTATAG 600
TTACAGGAAA TAATGTCGTA TAAAAGGCAT TTAATATGGA GGGGCTTTAT GACCCCTTGC 660
TTGGGTGTAA CCATCCCTGT CAGGGTGCCA GGAGAGAAGG GTGGAGCCTT TTTGGATGCT 720
GGGAAGTGAG GGTGTGAGGT GTTATCCAGG TGGGAAAGGC ATGCTGAGAG GGAGGGCCCC 780
TGTGTGGTTC TGAACACTGT GCTCCATCCA CACAGCCCTC CTCGGGGGCT GGGTGCAGCA 840
GCTGTTGGAG TTCTTTCTTC ACAGTAAATA TTTAACCACG TAAGATGCCC AGGCTACCAG 900
CCACTGCTAA GTGACAGGCA AAATCCTAAG CCACAGATGT TGCCCTCTGG CTCTCAGCTC 960
AGAGAGCTGA GGCTGTTGAC TGGAGTCCTC AGAACTTCAG AGAGCTTGGA AGTTTGTGCA 1020
TTTCATCAAC TGACTTGCTT TGTCTGCCAG AAAGCATTAA GCCTCAGAAT TTATACCTTC 1080
CCTTCTTCAT TCATTTGTGT ATATTCATAC ATTGAGCACC TGCTCTGGTC CGGGTTCTGC 1140
GCTTAGGTGA TTGGGATACA TCAGTGAATA AAACAGACAA AGGTCTCTGC CTCTGGGACC 1200
CAACGTTCTA CCAAGGAAGA GGGACAATAA ACAATGAGCA TACTATATAT ATTAATTATA 1260
TGTAAACATT ATATATTATA AGGTGATGGG CCTATAGATG AAAAATAATG TGGTGTAAAG 1320
GGAACTAGAA TGTGTGGAGG 1340
|
