| Tag | Content |
|---|
EnhancerAtlas ID | HS148-03594 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr11:113344400-113345790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr11:113344550-113344560 | TTCAAGTGGT | - | 6.02 | | 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 | CACTAAGGAG GGAAGTCCAA GGCAGGGACT GAAACCCAGG AAAGCAGCTT GCTGATTTTC 60
TTGAAACTGG TCATGCTGAC CACAGTCTCT CTATCTGGCC ACCCTCATCA AACAGCTGCA 120
TGAGGGAAAG ACGATAAGCA TGATTTCTTT TTCAAGTGGT CCTAATGCTG CAGGATGAAT 180
CAGAGATAAG CATGCATATT TGCATTTGAA GCAGGGTGGG AGTGGGGAGA ATCGTTGAAC 240
ATCTAGCTCC CTAAGGAGGA GCAAGGATTG GCCTAAAAGG TTTGTAGCCT GGTCAAAATA 300
CAGAAAGGCT TGGATCTGCA GAAGGATCTG GAGTGGGATC CACAAAGTGC CTTGCACCTC 360
ACTCCCTCAC CCCCTCACCC AACCTCAAGA GCCACCGAAA AAAAAGTAGT GGGGTGTCAG 420
GTGGGGCAAC AGTGACTTGC TCAGACAGCT TCCTTGTGGC TGAGAGCAAG CGCCTGTCCC 480
CACGGAGCTG CACTGCTGTG ACTTGTGTCC ATGGTGAAGC CTGTTATGTA GACGCACACG 540
CACCCTCTTA CCTCTGCTCT TCAAGAGGAA GCACTCAAGG GCTGCCCGCC TCAGACAGGG 600
ATAGGGAAGC GCTCTGTCTG GTGCTTAGAG GTGTCTCTTG TCTCCGCATA CCACCCTAGA 660
GGGGCTCTCG GTCCATCATA GAGCCGGGCC GAGAGCCGGG CGGTCACCCT CCGCTACTGC 720
CGCCACCGTC GCCTGCACTG CCGGGTAGAA ACGGGTCTGG CACCCAAGCC TCCCTCCCCG 780
ACTAGGTGTC AACCCAAGAG AAGGCGAAGG AGAACGAAAG TTCAGGACCA AGGACAGCGG 840
CAACCGTGGG AGCGGGAGAA TCCAGCCAGA ATCTGCCTCT CCCCCATCCT TAGCTTCTGC 900
CTTAGAAACT GAAAAGGGTC AGGTCGCACC AACACAGAGT TGCCAAAAAC AGCCCTTCTT 960
CCTCCGGAAG AAGTCGGAAA CTCTGGCCGC GAGCCCCGGG TCTCGCGCTT GGGTGCTGGG 1020
GGAAGTGCCC TCCCGAGATT GTGGGGAGCG GCCTCCCTCC CGCCCTCCGA TGCCGCGGCT 1080
CCGCCGTGCT GCCCTGGGCG CCCCGCGGGG AGGCTGCCCC AGCTGCGCCC GCTCGTGCTC 1140
GGGGAGAGGA TTCCCTTCTA AGTGGCGAGG AGGCTACTGA GAAGGAGGGA GAGGGGATAG 1200
CAGCCGCGGG CTCCAGACGC CCTCTGCCCC CGCCCGACGG GGAGCCCATG CAGAGCCGGA 1260
TCCCAGGCGG GCGCTCCCGA GCAGGCGGCC AGGAGTGGCC GCACAAACTT CTGGTCCTGG 1320
CCTCGCTCCC CTTGGAGGTC CCTCCTCCTC TCCCCGTGAC ACTGAGTCGC CCGCCGCTCC 1380
ATCCGGCCGG 1390
|
