| Tag | Content |
|---|
EnhancerAtlas ID | HS051-12870 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr18:12236820-12237840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr18:12237374-12237393 | GCCTGCCCCCTGGTGGCCG | - | 7.29 | | ZEB1 | MA0103.3 | chr18:12237023-12237034 | CGCACCTGCGC | + | 6.32 |
|
| | 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 |
| GH18I012237 | chr18 | 12237301 | 12237490 |
|
Enhancer Sequence | AGTGAGGTGA AGATTCGCCC TGGCCTATGA CAAAAAAGGG TCCTTCTGAG GCTGGGGGGA 60
TGTGCAGGCC CATCCTATCT CAGGAGTGGG GAATCTGGAA GCCATGTTCA TAGCCTCCCT 120
AGCTAAGTAG CTGCGAGTTC AGCTGAGCTG AGCTTCACGC TCTCCCCTGG GCTTGTAGGG 180
CATTGTTCAG GGACACAGGA AGCCGCACCT GCGCTGGGGC GTACGCAGGG CAGGCAAAAA 240
TGACATAACT GTTACCATGG GCTCTGAAAG CCCTACGCTT GGGCTGCACT GGCCACAGCT 300
CACCTCCTCT AGAGCTTCAT AGAACGCACA CGCTTGCAAA CCCACAGGCG CGCTGATAAA 360
CCTCAGGGCT TCCCCCAGGG TCTCACCAAT CCTCTATTGA CAGCTGTGGC TGGAGAACCT 420
CCACGCAAGC CAGAATGTGG GAAGATGGCC CGGTGGGTGG AGTGGGGGTG AGGACAGCAG 480
GGGAGCCAGT CCAGGGGTGC TTTGTCTCAG CGGGAACTGT GCGGAGTTTG TCAGTGCCCG 540
GTAACTGTCG TGTCGCCTGC CCCCTGGTGG CCGCGGGCGC ACACCGCTCT CCCCAGGCCT 600
TCCTGCACCG CCTCCTGATA GAGATGGGGC CATCTGGGGA GCAAACCGTG CCGGGAGCCA 660
GTGTTGCCTG CAGAAACCAC TGGGCACGAG AGCCTCCTCC CTGGACAGTG CAGAGGGTCT 720
TGCCCCTGGA AACGCACAGG AGACGACCTT TGCTGTCTTT TGGCTTGAAA TAACCTCCGG 780
CTGTATTTCT ACATTGGCTC CAAAGACACA CGTTTCAGCC TCTGGAAAAG CAGGAGCGTT 840
TGCTTACCCA GGGTCACTGT CGGATTCAGT GCTGGTCATG GGTGTCGTCC TCTGTTCCTG 900
TGCTGGCCTC TGAACAATGC AGAAAAGGAA GGAAAAAGTG ACCAGACAGT CAATCTTTGC 960
TGCCCTAGTT TTTCATTTTT AAAAATTATG ATGCCATATT TGCACACCCA CGTTCATAGC 1020
|
