| Tag | Content |
|---|
EnhancerAtlas ID | HS087-11154 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr19:41195060-41195940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr19:41195439-41195457 | GCTTGCTTCCCCCCTTCC | - | 6.44 | | PLAG1 | MA0163.1 | chr19:41195645-41195659 | GGGGACAAAGGGGG | + | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCACGTCCT GTCAGTCACA CGCATGCCCA CCCCCAGACT CAACACATAC TGTCACATAC 60
CCAGTTATAG TTACCGAGGC ATACAAACAC AGGGTCACAA AAGACACAAT CACAGACAAC 120
CACAGTCACA ACCATGCACA CCTCCAAACA CAGACAGACT AAAAAGTACA GGATTCTGCA 180
CAGTGAGCAG CTGTCACACA CACATACACA GTCACACAGA TACTAGGGTC ACAGACACAA 240
TCATAGACAC CACCACAAGC ACACACACAC GACACAGGAT TCCTCAGTCA CCAGCTGCAG 300
CGTACGCGTG CACACACACA CACACATACA CAGCCACAGT CACACAAACA CAGGGCACAC 360
TCCTAGCCAC CTCCCCATCG CTTGCTTCCC CCCTTCCCCC CAGGTACCAC ACACAAAGCC 420
GCCGTCACCG TCACCGCAGA CACTGCAGAC AGACAGGGCT GCACCCGGTC CCTGGGGAGC 480
CGCCCCCAGC CCAGCCTGTA TCCTGGAGCC TGAGGGCCAG GTCCAGGAGG GGGAAGCGGT 540
GCATTGTCTG CGGGTGGGGC CACTCTTGGA CAGCTGGGCA GCCCTGGGGA CAAAGGGGGT 600
GGCCTAGGGA TCCTGTGCCC TGGGACCCAT GACCAAGCCA GGGGGTGGAG GGATTGGGGG 660
TTGCCTGAAA TTGTCCTTAT TTTATTCAGG CTGGGGTGGG GTGGAGTCCC AGGCACAGGG 720
ACCTTGTTTT GAGAAGTGGC TGTGCCTGGG ACTCCGCCCA AGGATTGGGG GGATGCTGTG 780
CCCAGGGTGC CTCTGAGACC TGGGGGCAGG CTGTGCTTGG AGTCCCCCTA GGCCTTGGCG 840
TGGTGGGAAC GCTGTACCCA GTGACCCCAT CCTCGAGACC 880
|
