| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19303 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr22:29615910-29617000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr22:29616054-29616066 | CAACATGGCTGC | + | 6.14 |
| | | 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 |
| GH22I029220 | chr22 | 29616341 | 29616490 |
| Enhancer Sequence | GGTGCTAAGT CTGAGCTTTA CTTTGCAGAT TCAGAATCCG AGGGCTAAAC ATTGCAAATC 60
CACCTACATC CACCGCCCAG CCACCCCCAC TCCTGGAAGT CCCAGCAACC CCCACCTCCT 120
GCCAGCCCAT CCTGCACGCC CAGCCAACAT GGCTGCCTCC TCCACTCTCT CAGCCCCTGC 180
CTGCATCCCC TGAACCTCAC CCTCCTTCTG TTTGAACCCC CTGCCCACAC TGGCTTTGTC 240
TCCCATACAC GGCCTTGGCA GTGGCCGGCA AGTCGCTGCT CTGCCTGCAA CCCACTGGGT 300
GCTCCCACCT GGCTAGGTTG ACCCCCATCC TGCCACCATT ACTCCCACAT CCCCAGTGCC 360
TGGCACGGGC CATGTATAAA GTGAGTGCAC AGGAATTGAA TAGGAACTTT GCCTACCCTG 420
AGGAGGAGGC CAGGCCGGAC ATAGACTAAG CCTTCCTGGA GGCTCCTGAT TGGGCTGGAG 480
AGTTTTTGGA GCTCCCAGCC CCAGCTCCGA CCCTAACCCC TGGCTCTGGT CACTGGAAGC 540
AAATATTTAC ATTTGCAAAG TAAATTCCTT GCAGGAGACC TGGACTGGGG CTGGGAAGGC 600
TGCCTCCCTA TGGCCTGTGG TTACTAAACC GAGCAGAGCA GATCTCGGGG GTCGGTTGTG 660
AACGAGGAAG CCCTTTGGCT CCTCTCCAGG GAGAGAATGT CATGAAGGTG GATCCCAGGG 720
ATACCCCCAG CTTTTCACAC CCCGAATCCC CAACTTTTCA CATCTCTAAT CCCCAATTTA 780
GGGCAAGATT GGAATCCCAG CCCCCCTCGT CCCACTGCAA GGACAGAGCG GAAGCCTCTC 840
CTCTCTGGAC CTCAGTGTTC TGTGTCATGA GGTGTCATGA GGGTCCTGAG AAGGGGCACA 900
AAGCTTCTTA GCTCAGGCCT GGCACTGGGC AGAGGGAAGA AGAGCTGCTT ATGGGGCCCA 960
GGGCTAGAAA CTACAGGCAA CACTGGCCGT GTGGAGGTCA AGATGTGGAG GTCAAGACAG 1020
GGAGTGATGA GCTTCGAAGG GGCTTTGACA CTGGGAGGTG TACTGGCCTG TTTGGGAAGG 1080
CTTCCTGGAG 1090
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