| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08806 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr19:45187670-45188800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr19:45188681-45188694 | GAAACTTCTAGAA | - | 6.25 | | ZNF263 | MA0528.1 | chr19:45188201-45188222 | GGTGGAGAGGGTGGGGAAGGA | + | 6.04 | | ZNF263 | MA0528.1 | chr19:45188213-45188234 | GGGGAAGGAGGAAAAGGTGGG | + | 6.16 | | ZNF263 | MA0528.1 | chr19:45188216-45188237 | GAAGGAGGAAAAGGTGGGTGG | + | 6.62 |
|
| | 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 |
| GH19I044683 | chr19 | 45186982 | 45190472 |
|
Enhancer Sequence | GAGGGGGGTC GAGAGTATTG GGGGACTGAG ATTTTTAATT AGGGCACAGA GGTCCTCGCT 60
GAGAAGGTGA CAAATGAGCA AAGACTTGTA GGAGGGGAAG AAAGGAGCCA TGTGGGGCTC 120
TGGAGGAAGA GCATTCCAGA CAGAGGGAAT AGCCAGTGCA AAGGCCCTGG GGCAGAAGCA 180
TGCCTGGCAT ATTCAAGGAG CAGCAAGGGG GCTGGGCATG GTGGCTCACA CCTATAATCC 240
CAGCACTTTG GGAAGCCAAG GCAAGCAGAT CATTTGAGGT CAGGGGTTCA AGACCAGCCT 300
GGCCAACATG GTGAAACCCC TTCTCTATTA AAAATACAAA AATTAGCCGG GCATGGTGGT 360
GGGCACCTGT AATCCCAGCA ACTGGGGAGG CTGAGGCAGG AAAATCACTT GAACCCGGGA 420
GGCGGAGTTT GCAGTGGGCC AAGATCGTGC CCCTGCACTC CAGCCTGGGT GACAGAGCAA 480
GACTCCACCT CAAAAAAAAA AAAAAAAAAG GAGCAGCAAG GAGGCCAGTG TGGTGGAGAG 540
GGTGGGGAAG GAGGAAAAGG TGGGTGGAAG TTGACGTCAG GAGATGGACG GAGGGGCACA 600
TGGCGCAGGG CCAGGTAAGG CACTGCCGAG ACTGTGGCTT TGAGGGGCAG GGTGCTGTGA 660
AAGGCGAATA ACGGCCCCCC AGTGACGTCT ACATCCTAAT CCCCTGTGAA TGTTACGTTA 720
TATGACAAAA GAATGCAGCC ATGATTAAGT TCAGGATCGT GCTTTGGGGA GATTATCCTG 780
GATTGCCCTG GCAGGCTCTT TATGTAATCA CACAGATCCT TATAATCGAG AAGGACACAG 840
GAAGCGTGAG TCAGAGGGGC TGTGACAACA AAGGAAGCAA AGCCCTTTGA AGACGGGAGA 900
AGGAGCTGAA AGTCAAGCAG CACTTCAGAG TCAGAATGAT TGAGTGTGAG AGAGTCCATG 960
GGCCATCGTG AGTGTTGAAG ACGGAAGGGG GCCTTGAGCT AAGGAATGCA AGAAACTTCT 1020
AGAAGCTGGA GGAGGGCCAA GCTCAGTGGC TCACGCCTGC AGTCCCAGCA CTTTGGGAGG 1080
CCAAGGTGGG AGGATCGCTT GAGGCCAGGA GTTGGAGACC AGCCTGGGCA 1130
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