| Tag | Content |
|---|
EnhancerAtlas ID | HS047-07664 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr12:31398760-31399860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr12:31399705-31399715 | AAACCGCAAA | + | 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 |
| GH12I031245 | chr12 | 31398791 | 31400190 |
| Enhancer Sequence | GATATCCTGT CATTAGTGTT CACAGCCAAC ACGGTCTCAG TTGTGCCTAC CTGGCTTGCA 60
GCATTGGGCT CTGCCCCCCG GCCTCTGTTA TTTCGGGACC CTATCATCCC CATTGCTGGC 120
AGCAAGCCCA GCGCTGTAAC AGCATCTCCT GCCATCAGCC TGCCCTTTGG AATGCTGGGC 180
GGCAACTCCA GGGCTTCTCT GTGATGCTGG TGCCCTCCTC ACCAGGCCAT GACTTAGCAC 240
GCCGGTAAAC GGAGTATGCT CTGGGCCCTC CTAGGGAACA CTGTGGGGGG TGGATTTTCT 300
GGCCTCTATA GTCTAACCAG TTTGGCATGC CCACTGCTCT GGACATCCTG ATTCCTTCCT 360
TCACCATTTG CTGTGGCAGT TCTTCCAATT CTACCTCACT TAACGTGGGT CAATACTTTT 420
CCAGGCCTCT AAGAGGCAAC CTCTTAGAGG TTGTGATGTA GTAGTATGTT GGCGCCATCT 480
CCCGGGGTCC TCGTCAGGGT GTAAATTCCG TACCGTAAAA GAAAGTTCTC CCTTTTCCAA 540
TTTGTATTTT GTTTCCTTTG GTTCAGCACC CTCAAGATCC AGTCCCGTAC ATATTCCCCC 600
AGTTCCTGAT GGTTCACATT GACCAGGCCT ACAACTACTT TTTTTTCTTA GCAGGTTTGT 660
TTTCTTAGCG GGCCCAGCAC TTCTGTGGCT GGGTTATGTT CTAACTTGCC CTTAGCTTCG 720
GGTCTGATGG CCAAGAGAGG AGGCAGAGCT GAATCCTGAG CAGAGCACGA GTTTTCTTGC 780
AAGACACGAT CCTCCACATG ATCTTCAAAT AAGCCGGAGG CTCTAGCCTC TAACAGAGAG 840
GAGTGGATCA CTTCTGCAGG CCCTCTTCCC CACTTATTAC CGGCAGCCTT GCACTCACAG 900
GAATGCCTTT CTTCACAGGC TTCCATTCCA AAGATCTTAT TATCGAAACC GCAAATATGT 960
CGCATACCAA CGTCTGAGCC CTTTTAATTA CTGTCATTGC CTCCTCCCTG ACAGCTGTCT 1020
ACAGCACCCG AATTATTTTC TTTGCACTGT TAGGACAACC TCACTTCACG GCTGTAATTG 1080
TCATCAACAA AAACAACCCC 1100
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