| Tag | Content |
|---|
EnhancerAtlas ID | HS154-12064 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:25351840-25352570 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr2:25352212-25352223 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr2:25352213-25352223 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr2:25352214-25352234 | GGGCGGGGCGTGGGGTGGGG | - | 6.03 | | RREB1 | MA0073.1 | chr2:25352226-25352246 | GGGTGGGGCGTGGGGTGGGG | - | 6.62 | | RREB1 | MA0073.1 | chr2:25352231-25352251 | GGGCGTGGGGTGGGGTGGGG | - | 6.86 |
|
| | 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 |
| GH02I025128 | chr2 | 25351786 | 25352750 |
|
Enhancer Sequence | AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA GATGCCTTTC ATGGCTCCGA TCACTGCGGA 60
CTTTCCATCT GGACCTTCCT TCCTCTGTTG CTTCCTGATG CTATTTCAGG CCCTGAAAAC 120
GTGCATGCTT GACCAGCCCG CAGCCACTCA GTAAGAGCTT GCAGATACTG GGTTTTAATC 180
CTGGATCCCC TAAGCATGGG ATTCATTCCT GTCCCTGCAC CCTCATTTTT CCCCTCGGTG 240
AAATGGAATG GGGAGAAAGG CCCACGTTGC TGTCCCACCT GGGCTATCTG TGCACTAGGC 300
TAGTTAGGTC GGTTGATCCC AGGCTACTAG AGCTAGACTC GGGTCGACGG GGGCGGGGGC 360
GGGGGCGGGG GCGGGGGCGG GGCGTGGGGT GGGGCGTGGG GTGGGGTGGG GTTCGTATGC 420
CATCTGGTGG CTGTTTCTGG AATAGCATCT CACTGACAAG CTGCTGTGGT CTCTGGGCTG 480
GGAGTCCTCC GGCTCCTGTT CTGTCCAGAT GTGGGCCCAC TCCCTGTGAC TTGAGTATCA 540
TTGACTCTTG CCTGAGCCAA CCACTGTGCC TTTCCTTTTC CCTCCCTCTC TTTCCTCTCC 600
TTTCTTCCAC TTCTGTTTTG TTTTTTGCCT CCCTTTCCTA TCTTCATCTC CCATCTCCTT 660
TTCCTTCTGA AGTCTTAGGT GCATCAAGAC ACACATGTTC TACACCTCAC CTGGCCCATG 720
GGGCTCAGAG 730
|
