| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07320 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr12:31398790-31399940 | 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 | ACGGTCTCAG TTGTGCCTAC CTGGCTTGCA GCATTGGGCT CTGCCCCCCG GCCTCTGTTA 60
TTTCGGGACC CTATCATCCC CATTGCTGGC AGCAAGCCCA GCGCTGTAAC AGCATCTCCT 120
GCCATCAGCC TGCCCTTTGG AATGCTGGGC GGCAACTCCA GGGCTTCTCT GTGATGCTGG 180
TGCCCTCCTC ACCAGGCCAT GACTTAGCAC GCCGGTAAAC GGAGTATGCT CTGGGCCCTC 240
CTAGGGAACA CTGTGGGGGG TGGATTTTCT GGCCTCTATA GTCTAACCAG TTTGGCATGC 300
CCACTGCTCT GGACATCCTG ATTCCTTCCT TCACCATTTG CTGTGGCAGT TCTTCCAATT 360
CTACCTCACT TAACGTGGGT CAATACTTTT CCAGGCCTCT AAGAGGCAAC CTCTTAGAGG 420
TTGTGATGTA GTAGTATGTT GGCGCCATCT CCCGGGGTCC TCGTCAGGGT GTAAATTCCG 480
TACCGTAAAA GAAAGTTCTC CCTTTTCCAA TTTGTATTTT GTTTCCTTTG GTTCAGCACC 540
CTCAAGATCC AGTCCCGTAC ATATTCCCCC AGTTCCTGAT GGTTCACATT GACCAGGCCT 600
ACAACTACTT TTTTTTCTTA GCAGGTTTGT TTTCTTAGCG GGCCCAGCAC TTCTGTGGCT 660
GGGTTATGTT CTAACTTGCC CTTAGCTTCG GGTCTGATGG CCAAGAGAGG AGGCAGAGCT 720
GAATCCTGAG CAGAGCACGA GTTTTCTTGC AAGACACGAT CCTCCACATG ATCTTCAAAT 780
AAGCCGGAGG CTCTAGCCTC TAACAGAGAG GAGTGGATCA CTTCTGCAGG CCCTCTTCCC 840
CACTTATTAC CGGCAGCCTT GCACTCACAG GAATGCCTTT CTTCACAGGC TTCCATTCCA 900
AAGATCTTAT TATCGAAACC GCAAATATGT CGCATACCAA CGTCTGAGCC CTTTTAATTA 960
CTGTCATTGC CTCCTCCCTG ACAGCTGTCT ACAGCACCCG AATTATTTTC TTTGCACTGT 1020
TAGGACAACC TCACTTCACG GCTGTAATTG TCATCAACAA AAACAACCCC TTCCTAATCA 1080
ATTCAATCAA ATGCCTAACA ATTGGTAGTA TTTTTGCTGG ATTTTTAATC TCCAACAATA 1140
TTATTCCAAT 1150
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