| Tag | Content |
|---|
EnhancerAtlas ID | HS116-13646 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr16:58380810-58381660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr16:58380894-58380907 | AGTGACAGCTGCT | - | 6.64 | | Myog | MA0500.1 | chr16:58380897-58380908 | GACAGCTGCTG | + | 6.14 | | NFAT5 | MA0606.1 | chr16:58380862-58380872 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr16:58380862-58380872 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr16:58380862-58380872 | AATGGAAAAT | - | 6.02 | | Tcf12 | MA0521.1 | chr16:58380897-58380908 | GACAGCTGCTG | + | 6.02 |
|
| | 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 |
| GH16I058346 | chr16 | 58380820 | 58380997 |
|
Enhancer Sequence | CCCTGCAGAG TGAGTGATTA GATATAGAAA GGAAATCCAA GGAAGCAAGG AGAATGGAAA 60
ATTACTGACT TGTTAGAACA AAGCAGTGAC AGCTGCTGGC TCTAAAATTA GGAACGGAGA 120
CAAGGAATTT TCAGAGCACC ACCAAACAAA TCACAAAGGC ACAATTCACC CAGCACCTTT 180
CAGAAAGATT TTTAACTCCT AAAAGAATAC AAGGCAAGCG ACCGCCAGGT TGATCATTCA 240
GGGGCTGTGT GCTTCCCTAA ACCTTGCTGC TTACTGAGTC CAGGGTCGTT TCTCTACAGA 300
GGGCTGCCCT TGAATGACAG CTCGGATGAA AACCAAGGGC AGACAGGATG CACCTCTTTA 360
AAGTCTTTTA TGTTTTCTAT GCTTTTCTGA GATTTTGCTG ATTTCACAGA CAGTCTAGAA 420
GTCTAGCACA CACTACTTAC ATTTTCATCA TACTCTTTGA GCTTTTCCAA TCCTAACTCT 480
GGGAATAAAT TGATTACCCA TAGACCTTTA GTTGCCCAGG TACCACACCT TCAGGCACCT 540
GGGTGGCAGA TTCTTTAACG CATCTGAAGA AGAAACTTAG CCAATTATAC TTTTAAAAAT 600
CCCTATGTGA TAATCTGTAA ACACAGCAGT CGTGCCCTCA GGATGAACAA AGGGCAACTT 660
CAACAGCCCA AGATCTGGCT TCTGTTTGGG CCTCTGTCCT GGAGTGACTG AGGACCTCAG 720
ACAGGACACT CAGGCCTTTA GTGTCCTCTC CTAAGAGGGG GTAGCCGTAC TTGCCCTAAG 780
TCACAGGGAG ACCAAGGAAA CAAAACATCA TAAAAACACT CTGAGGCTGG GCATGGTAGC 840
TCATGCTGTA 850
|
