| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12605 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:50507200-50508010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr19:50507361-50507376 | TGCTATTTTTATCAA | - | 6.33 | | ZNF263 | MA0528.1 | chr19:50507600-50507621 | CTTCTCCCTTTCTCCTCCCTC | - | 6.08 | | ZNF263 | MA0528.1 | chr19:50507514-50507535 | CCTTCTCCCTCTTCCTTCCCC | - | 6.82 | | ZNF263 | MA0528.1 | chr19:50507508-50507529 | TCCTCTCCTTCTCCCTCTTCC | - | 6.85 | | ZNF263 | MA0528.1 | chr19:50507511-50507532 | TCTCCTTCTCCCTCTTCCTTC | - | 7.37 |
|
| | 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 |
| GH19I050003 | chr19 | 50506683 | 50508541 |
|
Enhancer Sequence | TAATCCCAAC ACTTTGGGAG GCAGAGGCAG GAGGATGGCT TGAGGCCAAG AGTTTGAGAC 60
CAGCCTGGCC AACATAGTGA GATCGTCTCT ACTTTAAAAA ATAAATAAAT AAAGGGACTG 120
CTGAAGGAAT GGATGACTCA CACAGGCTGG GCACTGGGGT TTGCTATTTT TATCAAACAA 180
CCTGAGTCAT ATAAGGGAAA ACCAAAACCA CATTGGCCCA GAGTAGCTCC TCCTGTGCTT 240
CCACTGTGGG TTTCTGGGGG AGGTCAAGCG TGGTTTCTTC TCTCAGGAGC TCCTGGCTCT 300
GTGTGTTTTC CTCTCCTTCT CCCTCTTCCT TCCCCGCCCT CCTGCCCTCT CCCCACCCTG 360
CTCTCTCACC TCAATCTCTT TCTTACTGTT GGTTTTCATC CTTCTCCCTT TCTCCTCCCT 420
CTGTGCTCCT CGGCCCCTCA TTCCTTCTCA TCATGATCCC TTCTCGCTCT TTCTCCCTGC 480
CCTCTCCTTC TCCTTTCTCT CCCTTTCTTG GGAGAAGCCA GAGTGCCTGC GTTCAAATCC 540
CAGCTCTACT ACTTCCAGGC TGTGTGCCCT TGGGCAAGTA GCTTCCTCTC TCTGTACCCC 600
AGTTGCAGGA TGGGGTAATA TGGGTGCCTA TCTCACAGTG TGGCTGGCAG CATTACATGG 660
GTAAGACACA GAGAGTTCCC AAAGTGTCTG GCATGGGATC CTGCCTGTAA TCCCAGCACT 720
TTAGGAGGCT GAGGCGGGAG GATCGCTTGA GCCCAGGAGT TTGGGACCAG CCTGGGCAAC 780
ACAGTGAGAC TGTCTCTATT TAAAAAAAAT 810
|
