| Tag | Content |
|---|
EnhancerAtlas ID | HS074-08007 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr19:50507020-50507930 |
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 | TTTGCTCTGG GGCGATGTCA CCCAATGGTG GTGTGTCCCC AAATGCAAGC TCCGCATCAG 60
CAGGGCCTTC ACCAGCCCCG CTCTCCCTGC ACTGTCTGTG CTGGCACCGC GGCCAGACAC 120
ATGAAATGGT AGGTGCTGCT TAAGGATCCA CTGAGCAACC GGGCACAGTG CTCACGCCTA 180
TAATCCCAAC ACTTTGGGAG GCAGAGGCAG GAGGATGGCT TGAGGCCAAG AGTTTGAGAC 240
CAGCCTGGCC AACATAGTGA GATCGTCTCT ACTTTAAAAA ATAAATAAAT AAAGGGACTG 300
CTGAAGGAAT GGATGACTCA CACAGGCTGG GCACTGGGGT TTGCTATTTT TATCAAACAA 360
CCTGAGTCAT ATAAGGGAAA ACCAAAACCA CATTGGCCCA GAGTAGCTCC TCCTGTGCTT 420
CCACTGTGGG TTTCTGGGGG AGGTCAAGCG TGGTTTCTTC TCTCAGGAGC TCCTGGCTCT 480
GTGTGTTTTC CTCTCCTTCT CCCTCTTCCT TCCCCGCCCT CCTGCCCTCT CCCCACCCTG 540
CTCTCTCACC TCAATCTCTT TCTTACTGTT GGTTTTCATC CTTCTCCCTT TCTCCTCCCT 600
CTGTGCTCCT CGGCCCCTCA TTCCTTCTCA TCATGATCCC TTCTCGCTCT TTCTCCCTGC 660
CCTCTCCTTC TCCTTTCTCT CCCTTTCTTG GGAGAAGCCA GAGTGCCTGC GTTCAAATCC 720
CAGCTCTACT ACTTCCAGGC TGTGTGCCCT TGGGCAAGTA GCTTCCTCTC TCTGTACCCC 780
AGTTGCAGGA TGGGGTAATA TGGGTGCCTA TCTCACAGTG TGGCTGGCAG CATTACATGG 840
GTAAGACACA GAGAGTTCCC AAAGTGTCTG GCATGGGATC CTGCCTGTAA TCCCAGCACT 900
TTAGGAGGCT 910
|
