| Tag | Content |
|---|
EnhancerAtlas ID | HS076-29595 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:41195040-41195940 |
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 | CACACACAGT CACAACTCCA CCCACGTCCT GTCAGTCACA CGCATGCCCA CCCCCAGACT 60
CAACACATAC TGTCACATAC CCAGTTATAG TTACCGAGGC ATACAAACAC AGGGTCACAA 120
AAGACACAAT CACAGACAAC CACAGTCACA ACCATGCACA CCTCCAAACA CAGACAGACT 180
AAAAAGTACA GGATTCTGCA CAGTGAGCAG CTGTCACACA CACATACACA GTCACACAGA 240
TACTAGGGTC ACAGACACAA TCATAGACAC CACCACAAGC ACACACACAC GACACAGGAT 300
TCCTCAGTCA CCAGCTGCAG CGTACGCGTG CACACACACA CACACATACA CAGCCACAGT 360
CACACAAACA CAGGGCACAC TCCTAGCCAC CTCCCCATCG CTTGCTTCCC CCCTTCCCCC 420
CAGGTACCAC ACACAAAGCC GCCGTCACCG TCACCGCAGA CACTGCAGAC AGACAGGGCT 480
GCACCCGGTC CCTGGGGAGC CGCCCCCAGC CCAGCCTGTA TCCTGGAGCC TGAGGGCCAG 540
GTCCAGGAGG GGGAAGCGGT GCATTGTCTG CGGGTGGGGC CACTCTTGGA CAGCTGGGCA 600
GCCCTGGGGA CAAAGGGGGT GGCCTAGGGA TCCTGTGCCC TGGGACCCAT GACCAAGCCA 660
GGGGGTGGAG GGATTGGGGG TTGCCTGAAA TTGTCCTTAT TTTATTCAGG CTGGGGTGGG 720
GTGGAGTCCC AGGCACAGGG ACCTTGTTTT GAGAAGTGGC TGTGCCTGGG ACTCCGCCCA 780
AGGATTGGGG GGATGCTGTG CCCAGGGTGC CTCTGAGACC TGGGGGCAGG CTGTGCTTGG 840
AGTCCCCCTA GGCCTTGGCG TGGTGGGAAC GCTGTACCCA GTGACCCCAT CCTCGAGACC 900
|
