Tag | Content |
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EnhancerAtlas ID | HS043-36402 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr6:34830860-34831770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr6:34831507-34831518 | ATGACCTTGAA | - | 6.62 | Esrrg | MA0643.1 | chr6:34831507-34831517 | ATGACCTTGA | - | 6.02 | PRDM1 | MA0508.2 | chr6:34831233-34831243 | TCACTTTCAC | + | 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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Enhancer Sequence | TTTTGTAGAG ACCAGGTTTT GCCATGTTGC CCAGGCTGGT CTCGAACTCC TGGATTCAAG 60 CCATCTGCCT GCCTTGGCCT CCCAAAGTGC TGGGAATATA GGCGTGAGTC ACTGCGCCCG 120 GCCTGAGTTT TTCTTAATTC TACCTTTAAC TGTAACCTTG GGACAGTTTC TTCATCTGTA 180 AAATGGGAGG GTGGTATTTA AAGGTCCTTA AAGGTTTCTT TTCACTGTGT TAATGCCTTT 240 TTAACTTTAT CTTCCATTGC TCTCCCTGAC AAAACCTATG CTTCAGCTGG GCAGAGCTAT 300 TATTCTTACC AGTTTCTTTT TGTTTCTGGC TGTATGCCTT TGTTTATGCC ATTGCCTATA 360 GAATACCCTC TTCTCACTTT CACAGTCCTT CAAGGACCAC CTCAAATGTT ATTTCTTACC 420 ACAAAGCCAC TCTTGATCCT CTTCTCCTTG TCCTTTTTCC TCTTTGATGT TGTCTAGAAC 480 TGGGGATGTC TTACTCATCA ATTTATCCGT CTCCCACTCC TGCCTAGTGC CTAGTATGGT 540 GCCTTACATA CAGAAGCAAC TAAATACTTA TGGAATGAAT GCAGGTGGCT TCAGGTGCCA 600 TTCATCAGCA CCAGAGCAGT AGGTAGCTGG TCTCTTCTGA GTCTGGGATG ACCTTGAATA 660 AACTTGACAT TTAATGTTGA TATGAGAGCG CTGTCCATGC AGTTAGCGAT GTTGGAATAA 720 AAAGATTCAG AAAGGCCAGT GATTGAAAAA TGACTTGATC TCTTTACAGC CAGTAATAGG 780 TAATGTCAAA GTTGTATGTT CCTAATATTG GGAACTTTAT CCAGTTGTCT GAGCTGAAAG 840 GGATGGGTAT TGTAAGTGGA TGGGAATAAA CATGTCTCCA AAGCCACATT TGTGGTTTTT 900 GTTTTTTTTT 910
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