| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08887 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr19:50507320-50508190 |
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 | CTGAAGGAAT GGATGACTCA CACAGGCTGG GCACTGGGGT TTGCTATTTT TATCAAACAA 60
CCTGAGTCAT ATAAGGGAAA ACCAAAACCA CATTGGCCCA GAGTAGCTCC TCCTGTGCTT 120
CCACTGTGGG TTTCTGGGGG AGGTCAAGCG TGGTTTCTTC TCTCAGGAGC TCCTGGCTCT 180
GTGTGTTTTC CTCTCCTTCT CCCTCTTCCT TCCCCGCCCT CCTGCCCTCT CCCCACCCTG 240
CTCTCTCACC TCAATCTCTT TCTTACTGTT GGTTTTCATC CTTCTCCCTT TCTCCTCCCT 300
CTGTGCTCCT CGGCCCCTCA TTCCTTCTCA TCATGATCCC TTCTCGCTCT TTCTCCCTGC 360
CCTCTCCTTC TCCTTTCTCT CCCTTTCTTG GGAGAAGCCA GAGTGCCTGC GTTCAAATCC 420
CAGCTCTACT ACTTCCAGGC TGTGTGCCCT TGGGCAAGTA GCTTCCTCTC TCTGTACCCC 480
AGTTGCAGGA TGGGGTAATA TGGGTGCCTA TCTCACAGTG TGGCTGGCAG CATTACATGG 540
GTAAGACACA GAGAGTTCCC AAAGTGTCTG GCATGGGATC CTGCCTGTAA TCCCAGCACT 600
TTAGGAGGCT GAGGCGGGAG GATCGCTTGA GCCCAGGAGT TTGGGACCAG CCTGGGCAAC 660
ACAGTGAGAC TGTCTCTATT TAAAAAAAAT TAAAAAATTA GCCTGGCGTG GTGGCGCCTG 720
CCTGTAGTCC AAGCTACTCG GGAGGCTGAG GGGGGAGAAT CACTTGAGCC TGGGAGGTTG 780
AGGCTGCAGT GAGCCGTGAT TGCACAACCG CACTCCAGCC TGGGTGATGG AGCGAGACTC 840
CATCTCTTAA AAATAAAAGT GCTGGCACAG 870
|
