| Tag | Content |
|---|
EnhancerAtlas ID | HS116-11409 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr14:103893560-103894610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr14:103894216-103894231 | GGGTCTTTGTGACCT | - | 6.34 | | IRF1 | MA0050.2 | chr14:103893839-103893860 | AAAAAAAAAAAGAAACAAAAG | - | 6.21 | | RARA(var.2) | MA0730.1 | chr14:103894132-103894149 | AGGACAACCAGAGGTCA | + | 6.62 | | STAT1 | MA0137.3 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr14:103893964-103893975 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr14:103893964-103893978 | TTTCTGGGAAAAGG | + | 6.15 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09869 | chr14:103893831-103896534 | CD14 |
|
| | 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 |
| GH14I103426 | chr14 | 103893282 | 103895765 |
|
Enhancer Sequence | GCGCTGTGGC TCACACGTGT AATCCTAGCA CATTGGGAGG CCGAGGCAGG TGGATCACCT 60
GGGGTCAGGA GTTCGAGACC AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT 120
ACAAAATTAG CCAGTCGTGG TGGTGCGCAC CTGTAATCCC AGCTACTCCA GAGGCTGAGG 180
GAGTAGAAAC TATGAAAACT TGGGAGATGG AGGTTGCAAT GAGCCGAGAT CATGTCACTG 240
CTCTCCAGCC TAGGCAACAG AGGGAGACTG TTTCAAAAAA AAAAAAAAAA GAAACAAAAG 300
AATGGCTGCT CCATAGACAG AGCAGCAGTA TCAGCTGCTT GACTGAGTCT ACTTATAGTT 360
ATTTCTTGAT TATATGCTAA ACAAGGGGTG AATTATTCAT GAGCTTTCTG GGAAAAGGGC 420
AGAGATTTCC TGGAACTGAA GGTCCCTCCC CTTTTAGGGG ACTATTTAGG GTAACTTCCC 480
AAGGTTGCCG TGGCATTTGT AAACTGTCAT GGTGGTGGTG GGAGTGTCTT TTAGCATGCT 540
GATGCATTAT AATTAGCTTA TAATGAGCAG TGAGGACAAC CAGAGGTCAC TTTCATCGCC 600
ATCTTGGTTT TGGTGGGTTT TGGCCTGCTT CTTTACCACA TCCTGTTCTA TCAGCAGGGT 660
CTTTGTGACC TGTATCTTCT GCCAAGCTCC TCCTATCTCA CCCTGTGACT AAGAATGCCT 720
GACTTCCTGG GAATGCAGCC CAGTAGGTCT CAGGCTTATT TTACCCAGCC CCTTTTCAAG 780
ATGGAGTTGC TCTGGTTCAA ACACTTCTGA CATATTTCCC CCCTCCCTTT TACAGGGGGA 840
CCCTTAATCC TTAAGAATTG TAGCGGGACA AAGATCATCT GTAACTTCTT CAAGCCAAAT 900
AGGGGTGATG ATATTCCTGC CTATTAGGGT CTCTTGTATT TAGGGTAGGG AGAAGTTTAG 960
TTAGAAAGCA TTGTTATAGA AGCCCTTATT TTCAGTTACA CAATTTTATA AAGTTACAAT 1020
TGCTTATTGT AACCAGCTGA GTTTTAGGTT 1050
|
