| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18642 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:61700910-61701810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr20:61701380-61701401 | GGCCCTCTCCAAGGTGCTGAC | - | 8.87 | | RREB1 | MA0073.1 | chr20:61701608-61701628 | CCCCACCCCACCCTCCCTCC | + | 6.21 | | ZNF263 | MA0528.1 | chr20:61701606-61701627 | CTCCCCACCCCACCCTCCCTC | - | 6.42 | | ZNF263 | MA0528.1 | chr20:61701592-61701613 | TTCCCCTGCTCCTCCTCCCCA | - | 6.84 | | ZNF263 | MA0528.1 | chr20:61701589-61701610 | TTCTTCCCCTGCTCCTCCTCC | - | 7.68 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGCAGAGCC AGCACCATCC AAGGAGATGC TGCGGGGTTG GGAGGGAGGA CCGGGTCCAT 60
GCTCCCCAGT GGAGGTGCCG GCTCTGGGAG ACACAGGGCC CCTCGCCCTG CATGCATGCA 120
CATGCGGCTT CTCAGGGCAG CTGGACTTGC TCTGTTCATG AGCTCTTGGC CTTCTGAAAC 180
TGCTAGTTAG AGGCCAGTTA GAATGCTTGG CCTAGAGAGG CCCCTGTTCC CCCATCGGAG 240
CTGAGCTGCC ATCTCTCATC AGAGGCTCGT GTCAGAAAGC CCTGGTGGAG GAAAGCCAAC 300
ACTTGGGAAG CACAGGGAGG CAGGCTGGAC CCGGCGTCCT TGCGGGCTGT TGGCAACACC 360
GTCTGGAGAG GGACCGGGCC CTGTGCCCGC CAGTCCCCAG GGCGGGGCGG CCTGAGCTGG 420
CCTGGTCTGC TGTCCTTGGG ATCAGGCCAG GACTCAGCTC TGTGCCTGGG GGCCCTCTCC 480
AAGGTGCTGA CGACACCATG TTCCAGCCTT CACTCCTGCC AGCCTGGGAG ACCTTCGAGC 540
GGCTTTAACA AACCCCATCG CAACTGGGCT TGCCTTGAAC ACAGCCCTGG ACAATGGCTC 600
TGTCTGGGTG TCTTTGGGAA TACACGTCTT TTTACTAACT TCAGTCAGAC CTTCAGCCTT 660
CCTTGATCCA GCCTCTCTGT TCTTCCCCTG CTCCTCCTCC CCACCCCACC CTCCCTCCCA 720
CAGCAATTCC CCAAAGGAGC AGAGGCAGAG GGAGAGCCTT CCTCTGCTTG TCCCTTGAGA 780
AGAGGATGTG GAAACGTCAG AGATTCTCCT GAGAGTTGCA GGCAGGCAGG GAGGACAGAC 840
GTACTTGGGA CACTTCCTGC TGTGATTCCA AACTCTGCTG ACCCAAGGAG GAGGTCTGCA 900
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