| Tag | Content |
|---|
EnhancerAtlas ID | HS043-42546 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr8:139205830-139206980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr8:139206459-139206476 | CCAAGTCCCACCCCTTC | + | 6 |
| | | 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 |
| GH08I138194 | chr8 | 139206401 | 139206550 |
| Enhancer Sequence | TTTACAGAGT AAAGCAGTTT CCCCTTGGGA TGCTGAGCTG CACCTCCACA GGTACGTGGC 60
TCCGGCCAGG CCCTCAGGGG ATGGAGCCTG AGGCAGCCCG AGCCAGCCCT GGAAGGAGAG 120
GCCATCTCAC CAGAGAAGAG CAGACCCCAT GAGCAGAGCA CTTAGGAGGG TCCTTGCGTG 180
AGCTCTCTAG CGGTCCCCTC AGAACAAACC TACTATGTAG ATGAGGAATC CCAGGCCCCA 240
GAGGGTGAGC CCATTGTCTC AGGTCCCACA GCTGCTCCAA GGAGAAGCTC AGAGCCTGGA 300
TTTAAACCCA CGCCAGCATG GCTTTGACGC TTCTGGCCCC TGCCTAACAC AGTGGCTGCC 360
TTGAGGCTCA CTCGGGGAAG GATGAGAGCT GTAGCCATCT AGAGCCCAGG GCCTCCTGTC 420
TACCCAGCTG CCCGCTCATC CACACACCGT CAATGCTGCA GCAGAGTCGG AGCATATGAG 480
CCCCCAAGTG TGGACATTAG GCCTTTGACT CGTCTCAGTG GCCTTTACAC ACTCTCTAAA 540
TGGACTCCTG TGTTGCCCTC CTACAGTCTG CTGGCCCTGC ATTTTTGATA ATCAGTGCTT 600
GGCATGTGTT TCCCTGTTAT CGCTACAAGC CAAGTCCCAC CCCTTCTCCC AGGCTGCCGT 660
CCAACAGCCC CTCCCCAAAG GCCCTCCAGC TCTAGGCTCC CAACACCCTC CTCTGTCTCT 720
GCCTCCGCAT TCCGCCCTCT CCAGGGATCT CCTCTGCATT CACTGTGAGA CTGGATTTTA 780
CTAACTTTGT AACATGCCCT AAAGCAGGGG TGCTCAACCC TGGCTGCACA TAATATTCAT 840
CTGGGGAGCT TTGAATAAAA ACACAGTATC TGAACTCCAA TCCCAGATAC TCTGTTTCAG 900
CCAGTTTGTA TGCCCAGGCT CAGGCAAAGA TGCATCATTA AAGTTCCAAG GATGATTCTA 960
ATGTACAGAC AAAGTTGAGA AACACTGGTT TAACAGACAG AGGTGTCAGT TTGGGGGATG 1020
AGACTTTGAG TCCTGCTTCT AGTACTGATT AGCTGTGTTA GTCACCCTGG TATAGACTTC 1080
TTTCCAATCT TGATTTGCCT CTTCTTCATA GAGAAATAAG AGTACCCACC CAGATATCTA 1140
ACACAAGGGG 1150
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