| Tag | Content |
|---|
EnhancerAtlas ID | HS184-01849 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr1:175559740-175560950 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:175559891-175559912 | AGGTGAAAAGTGAAAGCAAAG | - | 6.3 | | IRF2 | MA0051.1 | chr1:175559895-175559913 | GAAAAGTGAAAGCAAAGC | + | 7.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGACAGTGTT GGCACAAAGG AGGGGGGGAT CCACTCAGTT GAGGTGGGTG GCCAGCAGTG 60
AGGAGGGGAA GGGCATTCTA GGCCAAAGGA CAGCGTGGGC TAAGGTGAGG AGAACTGCAA 120
TGGCAAGATG AGTGGTTCAT TCCAACCAGC AAGGTGAAAA GTGAAAGCAA AGCAGGTAAT 180
AGCAGGAGGT AAGCTCAGAG AGGTAGTCAG GTGCCAGGGG CTGCAAACAC TAATTGAATA 240
CCTTGTATGT GTGCAGTGTT CTGAGCGTCC CCACAAAGCA TCAGTCATAA TATGAGCGCT 300
GAGGATCTCA CGCTAGTTAT AGCAGACAGG GCAAGTCATA CAGGAAAAAC AAACAATAAA 360
ACCAGGTAAC AACAAGGAGT GCAGGGACAG ACTGAGAGGA CAGCAGTTCC AAGGAAGGCA 420
CAGTCAGATC TCTGAACTGG GGAGGGGAGA TCACAGAAGA AATAGCTTTT AGGCTTAGCT 480
CTAAGGGAAT AAGCAAGGTC TCAAGATGCC ACATCCTCCT GGCCACCTCC TCTCTGATGT 540
GTGTGTCTGC ATCTTTGTAA CTAAATAGCC TCCATTCACT CCTCTGTATG AATGCAGACT 600
GGGAGCTGGC TGAGGAGGAA GAGCCCTCAA CAGCCCTAGC TTGGATGGCA GCCAGGGCTC 660
TGTGTCCCTG GGACATAATC CCAACTGACT CTCCTTGCTG GATGAGCACA GCAAAAGGTA 720
TAAATAACAG CAGAAATGAA CCCCTCCCAG GACTGCTGTG GGATTAATAA GCCCTTGAGA 780
CCCTGGCACT TCAAACCCTG TGGAAACTAG TGCTTCAATT GCTATTATGA GCAGACTCCC 840
AGCCATGGCT CCTTCAGCAC ATGCTGCTAG ATAATCTCTC CCCAACCACT GCCGGGAGCT 900
ATCAATCACC CAGTGCCTAT CTCTTAACCC ACAGCCTGAG AAGGGAAGGG AAGAGGCTGC 960
AAGGACAGTG TGGGGTGGTG ACATGAAGGG GCCAGAGATT ATCAGCTGGT TGATCTCTTC 1020
CAGAAGTGTG AGAATAGTGC ACAGGCTCTG AAGTCAGCCA ATGTGGTTTT GAAACTTGGT 1080
TTTCCCACCT ATTACATCTG TGAAGCTAGG TGGCCAGTAA CAGGGCTGTT GACAAATATT 1140
CCCATTCTCT AACTGGGTTC ATGGTAGAAT TATACTTATC TGCCCCCTCT GGAGTTAGGT 1200
GTGGCCATGT 1210
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