| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31301 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr9:112279800-112282130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZBTB18 | MA0698.1 | chr9:112280020-112280033 | CATCCAGATGTGC | + | 6.82 |
| | | 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 |
| GH09I109518 | chr9 | 112280381 | 112280550 |
| Enhancer Sequence | AATTAAAATC AGCTGGGGAA ATGTCCTACA ACTATGGATT CCCAAGCCTC ATAGGTATTT 60
GATTTAGGTC TAGTTTGGAG ATAGGTATTT TGATTTAGTA GGTCTGGGTT GGAGCCCAGG 120
AAGTCTGCTT TTGAAACAAG CTCCTGAAAT AGTTCTGATG ACCATGTGAT GGAAACCATA 180
ATTTGGGGAA AGCCTCTGGT GCTGGCTGTT CTCCCTTGCC CATCCAGATG TGCTCTCTAC 240
TTCTAGTCAC TCTGGCCTGT GCCTGCACAG CTGCCTTCTG TGGCCTGGAC CATCTGGGCT 300
TCTTTGGCCT CTGGCTGCCA TTGGGTTCCA TCAGTGGGAG ACCCTAGCAG AAGCTGGGTA 360
GGATGAGAGA GAGGGTGGAC ATTGAGTCTC CTGGCCACTC CCTGCAGGCT GTGGTTTGGC 420
AATGACTGCA TCCATGATGC CTGTCAAGCA GGTCCTCTCT CCTGGCTGCA GCTCTTGCCA 480
AATCCTTCAC CAGCTCCCTT TCTTTTCCCC TGCAGGCCTA GGGGTGGTTA CGGCTTCCTG 540
CAGTGGCTGG TCTCTGGGTG CTTCACTATG GTTTCCTTTA ACCCTGCTCA GGTCTCTCTA 600
AGTAATCCCT TCATTACATA CTCTCCAGTT ACCTCTTTGT TCCCTCTGCT CCTGCCAAGA 660
CAGGAAAACA AAAACATTGA CTGGAAAGAG TCAAGAATTC TGGGCTCAGT TCAATTCAAT 720
TCAGCAAACA TTTACTGAGT GAGGTCCTCT CAGCCAGGCT CTATGCCAGG AGCTGAGGTT 780
ACAGAAAAGA ACTCAGACAT GGCACCCACC TCCTGCAGAG TTCACAGCTT CATGGGATGC 840
TAGAGGGCCC CTGGTGTGGC TGCACTGGAG GTGGAGTAGA GGCTGAGATT GTCATGCCTA 900
GTCCAATTGG AGGCAGAGAG ATGCAGAGAA CCTTTGGCCA TAGGATGCTC CCATTGGACA 960
GGTGCTGATC AGGGTGACCC AGCCTCTAGG TGATCTGTGT GGTCTGGGTG CCTCCTGCCA 1020
TCTCCCAATC ACCGTAATTA AGGCTTCCTT CCTTCTAAAG CAGGTTTAAT TCACCAGCCT 1080
GCCAAGACTC CCCTGCCTCC ATCCAGAGGG GTGTTTGGGA GAAAAGAGGA ACACTTGTTG 1140
GAGTAATGGG CTTGAGGGCC CTGAGGTTAC AACTGAAGTA AAGCTCTGGC TGGTATGTGT 1200
CACAAACCTC CCATTCAGGG CTCATAATTC CACAAACCAT CTCCATTGAC TTTAAAGAAG 1260
GACATGATCT TGAGCAAGTT CCTTCTCTGC CCTGGGCCAC AGTTTCCTCA TTCCTCAAAC 1320
AGGGCTGATA AGGTCAGTGC AGGGAGGCTG ACCAGTGCTG TTCATCCAGA AGACTGAGAA 1380
TAAGAAAAAG CATACTTTAA AGGAGTCTGG CAAACTCCTA TTCATCCTTC AAAAGCCAAC 1440
TGAACATTTT ACTTCCTCCA GGAAGACTTC CTGGAGCCCC CTAACTTCTC CTTCTCTTGT 1500
ATTCATCATA GTCTCCGGTA ACATGACCAC CAGCCTGCCT AGTCCACTTG ACCTCTAGAT 1560
TCCTCAAACA TCTGTCTCTT TCTCTCCAGA ACCCAGCACT GGGCCTAAGG CATATCAGGG 1620
CATCAGAAAA TGTGTTATGA ACTGAGTCAA AAGGAATTCT TCCTGCAACA GAAGAAGTAG 1680
TGCAGAGGGT TCACGTTACA ACTTTCGACT TTACAGTGGT GTGAAAGCAA TACACATTCA 1740
GCTGAACATC AATAAGAGAT ACCAATACTT CATTATAAAA CAAGCTTTGT GTTAGATGAT 1800
TTTGCCCAAC CGTAGGCTAA TGTAAGTGTT TCAAGCATGT TTAAGGGAGA CAGGGCTAAG 1860
CTATGATGTT CAGTAGGTTA GGTGTATTAA ATGTATTTTT GACTTAGTAC GTTTTCAACT 1920
TATGATGGGT TCGCTGGGAT GTAACTGCAT CATAGGTCGA GGAGCATCAG TAGTAATACC 1980
AGTGACCTTA TCAGCCTTGT TTGAAGAATG AGGAAACTGT GGCCCAGGGC AGAGAAGGAA 2040
CTTCCTCAAG GTCACATAGC CTGTAAATGA CATGGTAGCG TTGGGACTTG AAGCCAAACA 2100
AACTTGCTGA CTGCAAGGGC TGGACTCCTC ATGGTGCAGG GAGGCTGACC CGTGCAGGGA 2160
GGCTGACCAG TGCTGTTCAG CCAGGAGATT GAGAATAAGA GGACACTTTG ATGGAGCAAG 2220
TGCTCCTTGC CAGGAACTGT TAAGAGCACA TTTGCATCAA CGCACTTAAC CCTGACAGCC 2280
TTGTGAGGTA TATGTGTGAA CAATGCCCAG TTTGACAGAT TAAGATCCAG 2330
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