| Tag | Content |
|---|
EnhancerAtlas ID | HS051-05759 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:9966100-9967240 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:9966645-9966665 | CCCCACAACACCCCACACAC | + | 6.86 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 9966772 | 9967089 | | chr12 | 9966400 | 9966894 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I009813 | chr12 | 9966197 | 9967510 |
|
Enhancer Sequence | TCGCAATTTC GACTCTTTTC ACACATTTCA TGATACGGAG GAAGAAAACA TTTTTCCCCC 60
GAGAGAGGCT TCAGGATGGC TGTCTACAGG CCCTCAGTAC TTTCCTCCAC AAAGAAGAAC 120
CAAAACACCC AGTAGAAAAT CAGACTTGGA ATACAGCATC TAAAAGAACA CATTCGAATT 180
AAGCAGAGAA GCGACAGGAA AGCTCTGAGG CAGGAAAGAG ACAGAGGGGA GGCAGGTAGC 240
TCAGCTGAAA CTGTCTGGGA GCCCAGAGAC TTCTTAGTGC AGGGAAAGTG TGTCCACATT 300
CCCACCGCAG ACTCCTGCAG TCGTAGCCAT GGGAGAGCCC TGGGGGCCCC GAGACTAGGA 360
TGGGGAGCTG CCTGGAGCCT GCACCGCGCA ACAGCACTGT TCCAGGACGG AGCTCAGGCG 420
AGGTCCCACA CACCTCCTGG ACCAGGCTAT TTGGAGCCCA GCCCCAACAA GACTTCATCC 480
TGCCTCGGGT CTCAACAGCT TCCGCATCTC CACATCCCTG GAGCCCCGCA GACATCCTTC 540
ACTTCCCCCA CAACACCCCA CACACCGGGA GGGCTGTAGT GGCACAAGGC TGATTGGTGC 600
CAGCCGTGTG GCTGGGTCCC TGGCACTCTA GCCCCAAAGG TGTTCTACAC CCCGGGGGAA 660
TCGGCAGTGC AGTGCACTGG GGAGGCTGCC TCCAGTCAAA GGGAGCCAAA ACGCAAGCTC 720
CCCAGAGCCT GACAGCCACT TGAGTGAGGT CGCTGCCACT GACAGCCACC CCGACTCCCA 780
ATAGCAAAGC AGCTGCGCAC CGACAGGCTT TCTCCACCCA CTGCCATCTC CACAGCCGGG 840
ACTGCCACCA CCCAAGCACG CCGCTGGGAG GCGCCTGGGG ATTGCCCACT CTGCCAACCA 900
CAGCCTGAGC CCTGAGCACA ACATAGGGGA TTGGGTTGTC TGAGGGTAGG ACCACACCAC 960
CAAGCAAAGC CTCTCCCAGT GCCTGAGCAC ACTGCCCAGG GGCCTGGGGA TCCATGGCCC 1020
TGTCCCACCC GTAGCTCCGC GTATGCTCCT GCACCATCAG GAGGCCTGAC TGAAGACCCA 1080
GCCTGGCTGC TCGCAAGCCC CACCTACCAC AGCCTGTGTG CACCATCAGG AGGCCTGAGG 1140
|
