| Tag | Content |
|---|
EnhancerAtlas ID | HS085-01666 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr19:41195150-41195940 |
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 | AGGGTCACAA AAGACACAAT CACAGACAAC CACAGTCACA ACCATGCACA CCTCCAAACA 60
CAGACAGACT AAAAAGTACA GGATTCTGCA CAGTGAGCAG CTGTCACACA CACATACACA 120
GTCACACAGA TACTAGGGTC ACAGACACAA TCATAGACAC CACCACAAGC ACACACACAC 180
GACACAGGAT TCCTCAGTCA CCAGCTGCAG CGTACGCGTG CACACACACA CACACATACA 240
CAGCCACAGT CACACAAACA CAGGGCACAC TCCTAGCCAC CTCCCCATCG CTTGCTTCCC 300
CCCTTCCCCC CAGGTACCAC ACACAAAGCC GCCGTCACCG TCACCGCAGA CACTGCAGAC 360
AGACAGGGCT GCACCCGGTC CCTGGGGAGC CGCCCCCAGC CCAGCCTGTA TCCTGGAGCC 420
TGAGGGCCAG GTCCAGGAGG GGGAAGCGGT GCATTGTCTG CGGGTGGGGC CACTCTTGGA 480
CAGCTGGGCA GCCCTGGGGA CAAAGGGGGT GGCCTAGGGA TCCTGTGCCC TGGGACCCAT 540
GACCAAGCCA GGGGGTGGAG GGATTGGGGG TTGCCTGAAA TTGTCCTTAT TTTATTCAGG 600
CTGGGGTGGG GTGGAGTCCC AGGCACAGGG ACCTTGTTTT GAGAAGTGGC TGTGCCTGGG 660
ACTCCGCCCA AGGATTGGGG GGATGCTGTG CCCAGGGTGC CTCTGAGACC TGGGGGCAGG 720
CTGTGCTTGG AGTCCCCCTA GGCCTTGGCG TGGTGGGAAC GCTGTACCCA GTGACCCCAT 780
CCTCGAGACC 790
|
