Tag | Content |
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EnhancerAtlas ID | HS043-02368 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:114928530-114930000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:114929784-114929802 | GGAAGCAAGGAAGCAATC | + | 6.32 | Sox3 | MA0514.1 | chr1:114929286-114929296 | CCTTTGTTTT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I114386 | chr1 | 114929581 | 114929730 |
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Enhancer Sequence | GGTGTGCACC ACCACGCTAA TTTTTGTATT TTTAGTAGAA ATGGGGTTTC CCCATGTTGG 60 CCAGGCTGGT CTCAAACTCC TATCCTCAAG GGATCCACCC ACCTTGGCTT CCCAAAGTGC 120 TGGGATTACA GGCATGGGCC CCACACCTGG CCTCATAGTC ACTGTTTTGT TCCTTGCTTT 180 ATTTCTAGTG TATAAGTTGT ACTTTCCTGT CTCTGCATGC TTTTGTATTT GTTACAGACT 240 GGATATTTTA AATATGTTGT AGCAACTCTG GATACCAGTC GTTCCCTTCT CATATCCCTG 300 GGGTTTGTCA CTGCTTAGTG ACTGGCTATT TTAGTGTAGC CCCTCCCATC CACCAGTATT 360 AAGCCTCTGT TGTTGCTCCT CAGGTTGTCA TGACTGGGTA TGCCCAGTCT CCTTGGGATG 420 ACAGTGTTTT TTTCTAGGCC CAGCTTACTC TATTCACGAC CATGTCTAGC TGTTGATCTC 480 CAGTAATTGC CAGCTCTACT GTTTTCAACA ATGTTCTGAG TCATAAATTG CTCTACAAGC 540 TAATTCTATC ATATTGTGAC TCCTTTGAAG AAAAGGTTTC ACATTTGTTC TAATCCCAGG 600 AGAGGTCCTG TGAGCTGTCT TATTCCCTGG TTCTCCTGCA AACTAGCTGG TCTACAGTTT 660 ATACAGATGT TGAATCTCTT CAGTTGCTTT TTACCACAAC CTCTAGTGGT ATGTCCTGAG 720 ATTTGAAATT ATCTGTGCTG TGTTACAAAT GAAGTCCCTT TGTTTTGGAA GACATTAGGG 780 GTTATTTCAT CTGGTTCAGT TCCCAGGTAA AATCTCTAAA CCAGGGCATT GGAACTGTAA 840 CAATGGCAAG CTTCTGTGTG ACACACCACC ACCTCTATCT CCACCCTAGA AACTGAGTGC 900 TTAGTGGAGG GGGTTGGGCA GCAGCCTGAA GCCTTCTCAG CTTAACTCTT CTGGCACAGA 960 ACTATCACCT CATGAGCCAG GGGAAAGATC ATCTGTGTCC CAGTATTCTA AACATGCCAC 1020 ACCCAACGTA AAGCCTCTGG TGGCAAAGTG GGAGCTGAGT GGAAGATGTG AACCCATAAT 1080 GTTCAACTGC ACTCCCCTGG GTTTTAACCT CAGCAAAAGC AGCTGGGGGC AGACCAAGAA 1140 TTGTTAACAT CCTGCTTTTC CCAAGAAGAG GGTTCTCCAA CTGGGAGGTG AGGAAAAGGG 1200 AGCCCTGTGT TCTTGGCTGC AGCAGTCTGG AGTCTCCACA TTAATAAGCA TAGAGGAAGC 1260 AAGGAAGCAA TCTAGGTTTA AATATCACAA ACTCCCATTT CCTACACAAT TTTCGCATTT 1320 CCTTGAATAG CTGTTTTTCT CATCTGCTGT TTGCTCACAG GATCATTTAC AGAGGCTTTA 1380 CATAAATAAA TAGCTTTATT TTACATGGTT ATATTTTATT TTACATATAT TTTGTTTTAC 1440 ATAAATAACT GGTGAAAATA ATTATCACCA 1470
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