| Tag | Content |
|---|
EnhancerAtlas ID | HS026-05375 | Organism | Homo sapiens | Tissue/cell | CNCC | Coordinate | chr11:1369870-1370840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr11:1370059-1370074 | GGTCGTGGGTGGGCC | - | 6.12 | | Nr2f6(var.2) | MA0728.1 | chr11:1370340-1370355 | TGACCTTGTGACCTG | - | 6.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCTACGTCA CCCTCTCTCT GTATCACAGG GCCCCTCTCT GGTCCTCAGA CACTGTGGGA 60
GGCTGGAGGG ATCAACCCCA GCCCTCTCTT CCCTACCCAC CTTCTGAACT AAATGAAAAG 120
CAAGACTCTG CATGAGCACA GGGGGCCAAG CTGGGTCCTA CATGTGGATC AGGCTGGGCG 180
GCCGACCCTG GTCGTGGGTG GGCCGACCCG TGTGGGGAGC TTGGGGAGGG CGGCATCCTT 240
CCGCCCGGGA GGGGAGATTA ACTCACACAC ACAAAGCACT AGCTGGTGGC AAAGGACATG 300
CTTTATCATA TACGGCAGAG CCATGTGGGC ACCGAGAACC CGAGAAAAAC CCAGCTCCCC 360
ATGAGAAGTG TGTCTGTCCA GCGTCTGGGG GAGGGGCGTG TGGTCCTCAG GAAGGCCATG 420
CAGGGCGCCC ACCCGGAGCT CCCCGGGGAT GGCCTCTGCG TGCGGCCTCA TGACCTTGTG 480
ACCTGGGTCT GGCTCTCAGG AGCACCAGGC AGGCAGGGAG GGCATGCCCT GGAGGAGCCC 540
TGCCTGTGGC CGCATTGCCG TTAGAATTTC AATGAGGGGC ACTCAGTTTG ATGGATGACT 600
CCTGCGGCCC TGGAGGCCTG AGGCCCCACC TGCTCCGTCT GCTCGGGAGA CACAACGTCT 660
TGACTCGGCC TCTGTCCCTT TGTCCTCCCT GCCAGGCCTG CCAGCCCTGC GCTGTGACTC 720
TGCCCTGCAG GCCGGGGGGC CGGGTAGACA CCCCTCAGGA AGAAAAGCCT CTGCCTGGAG 780
CCGCTAGCCT GTGCTGGGGG GGGCTTGGAG ACCCCAGGGT GTGGGCTTCG GGGCTGCAGA 840
TGGCCCAGGC GCTGACCCAA ATTCAGTGCT CTCGGGGGTG GGTCTGTGTG TCCCTCCACT 900
GGGCCTCTGG ACCAGAACCT TCCGGGGACT CCAGCTTCCC TCTGAGACGT CTCGGCCGAC 960
CCAGCCCCTC 970
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