| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06153 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:113344620-113345790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr11:113345617-113345632 | CGCCCTCTGCCCCCG | - | 6.01 | | Nkx2-5(var.2) | MA0503.1 | chr11:113344968-113344979 | AAGCACTCAAG | + | 6.02 | | REST | MA0138.2 | chr11:113345220-113345241 | TTCAGGACCAAGGACAGCGGC | + | 9.82 |
|
| | 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 |
| GH11I113474 | chr11 | 113345161 | 113345310 |
|
Enhancer Sequence | AGTGGGGAGA ATCGTTGAAC ATCTAGCTCC CTAAGGAGGA GCAAGGATTG GCCTAAAAGG 60
TTTGTAGCCT GGTCAAAATA CAGAAAGGCT TGGATCTGCA GAAGGATCTG GAGTGGGATC 120
CACAAAGTGC CTTGCACCTC ACTCCCTCAC CCCCTCACCC AACCTCAAGA GCCACCGAAA 180
AAAAAGTAGT GGGGTGTCAG GTGGGGCAAC AGTGACTTGC TCAGACAGCT TCCTTGTGGC 240
TGAGAGCAAG CGCCTGTCCC CACGGAGCTG CACTGCTGTG ACTTGTGTCC ATGGTGAAGC 300
CTGTTATGTA GACGCACACG CACCCTCTTA CCTCTGCTCT TCAAGAGGAA GCACTCAAGG 360
GCTGCCCGCC TCAGACAGGG ATAGGGAAGC GCTCTGTCTG GTGCTTAGAG GTGTCTCTTG 420
TCTCCGCATA CCACCCTAGA GGGGCTCTCG GTCCATCATA GAGCCGGGCC GAGAGCCGGG 480
CGGTCACCCT CCGCTACTGC CGCCACCGTC GCCTGCACTG CCGGGTAGAA ACGGGTCTGG 540
CACCCAAGCC TCCCTCCCCG ACTAGGTGTC AACCCAAGAG AAGGCGAAGG AGAACGAAAG 600
TTCAGGACCA AGGACAGCGG CAACCGTGGG AGCGGGAGAA TCCAGCCAGA ATCTGCCTCT 660
CCCCCATCCT TAGCTTCTGC CTTAGAAACT GAAAAGGGTC AGGTCGCACC AACACAGAGT 720
TGCCAAAAAC AGCCCTTCTT CCTCCGGAAG AAGTCGGAAA CTCTGGCCGC GAGCCCCGGG 780
TCTCGCGCTT GGGTGCTGGG GGAAGTGCCC TCCCGAGATT GTGGGGAGCG GCCTCCCTCC 840
CGCCCTCCGA TGCCGCGGCT CCGCCGTGCT GCCCTGGGCG CCCCGCGGGG AGGCTGCCCC 900
AGCTGCGCCC GCTCGTGCTC GGGGAGAGGA TTCCCTTCTA AGTGGCGAGG AGGCTACTGA 960
GAAGGAGGGA GAGGGGATAG CAGCCGCGGG CTCCAGACGC CCTCTGCCCC CGCCCGACGG 1020
GGAGCCCATG CAGAGCCGGA TCCCAGGCGG GCGCTCCCGA GCAGGCGGCC AGGAGTGGCC 1080
GCACAAACTT CTGGTCCTGG CCTCGCTCCC CTTGGAGGTC CCTCCTCCTC TCCCCGTGAC 1140
ACTGAGTCGC CCGCCGCTCC ATCCGGCCGG 1170
|
