| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11425 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:18283370-18284210 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr17:18284002-18284017 | TCACCTTTTGACCCC | - | 6.34 | | RARA | MA0729.1 | chr17:18283999-18284017 | CCCTCACCTTTTGACCCC | - | 6.34 | | RARA | MA0729.1 | chr17:18283461-18283479 | GCTTGGCCTTGTGACCTC | - | 6.47 | | ZNF263 | MA0528.1 | chr17:18283786-18283807 | GGAGGAGGTGGGGGTGGGGGG | + | 7.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCAGTTCAAG GCTTCCCCTG CCCCAGGATA ATGATCCCCC ATAAGGCACT GTGCTCATAA 60
GGCTTGGACC AATCTGCCCT CTTTTAGGTC TGCTTGGCCT TGTGACCTCC ACAGAGTGAC 120
TGCATGCACA CAGCAGGTGC TCTATGGAGG CTGCAGGGCG AATGCACAGA AAAAGCCCTG 180
GGGTGGAAGC AAGGTTTCCC CTCCGTCCCT GACCACGTAA CTCAGAGCAA GTTAGGGCAC 240
AATCTGGGCT TTGAACCCTC AACTCTGGAG AATGTTAGGG TGCCCAGCAG TCTCTTGCGC 300
CTGCCCCCGC TCCCCGACTC TGACAGTGTG AGGCTCCTCT AGACGGCTGC TGAAGCCAGC 360
ACTCTGGCAA AGCTCCCTGG GGTGGAGGAG GTATAGGGGA ACACAGGGCT GGAGTGGGAG 420
GAGGTGGGGG TGGGGGGCAT GCTGCTGCCT CCCTGCCCCA GCCAGCCCAA CTGCCCCTCC 480
CAGGGCCCAG CCAGGCTGGC TCAGGTACTA CCGGCTCACA GGGGGGAAGT GGCAGGCAGC 540
TGGGTGGGGT CGGGAACTCA CTGCCAGCAC AGCTGGCTGA GGCTGGGACA CCGAGGCCGC 600
CTGACACCCA GCACCACACA GACCTGAGAC CCTCACCTTT TGACCCCTCA TGTGGCGGGG 660
CAGTGCTAAC ACCCCCAACC AGGTCTAGCT CACAGAGCCT CCTGCAGAGA GAGACCCCAA 720
AGTCAGGGCA GTGTGCTAGG CTGTGGGGGC GGGATGGGGT GGAGAGAGGG CAGGGGACGC 780
CACCTGGATG GGGCACAGAG GGGCCTCTTC CACCGAGCTG CCCACTGTCC CCTCCACCCA 840
|
