Tag | Content |
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EnhancerAtlas ID | HS183-01355 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr12:120917410-120919310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr12:120918459-120918473 | GGGGCCCAGGCCTG | + | 7.19 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 120917501 | 120917818 | chr12 | 120918817 | 120919260 | chr12 | 120918341 | 120918515 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120479 | chr12 | 120917303 | 120920141 |
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Enhancer Sequence | GAGTGGCTCT TCTAAACTGA GACCTGAAGA ACCAGATGGT GCTAGGCAGG TAAATGAGAG 60 GAGAAGAAAA GCATTCCAGA CAGAAAGAAA GCACTGCAAA GAAAGCTGGG AGGACAGAGG 120 CAAGCTTGGG GCTTTCGGGA AGCTAAATAG TTCAGCACAG TTAGAGCATG GGGTGGAGGT 180 GAGGGCTGTT CTTCCTTGCA CTAGTGCCAC AAGCTACTTA CAGTGAGATG CCCTAATGTA 240 AATCAGAGCC TGGCTGGGTT AGATTACACA TGTCAGTCCT AAGTATTTCA GATGTTCACT 300 GGCAATCAGT ATGAGTTGCC TTTACCATAC AAATGTTTAT TGTATATCCC TGAATAGGAT 360 GATTGTAAAG GGGTGGCATG ATCAGTCTGG GGGAAGGGGC CTTGAGGGGA GTATGGTCTC 420 ACAGTGTCCA AAGGAGAGCT GTGAATAGCA AAAGGATGCT TGTTTGGAAG ACAGAAGGAC 480 AGCAGAAGGG GACAAAGCAA AAATCCAATC ATCCCTCCTT GTGTGAGGAA GATGGGGCTC 540 AGGGGGAGCG GAATTCAAAA TGTGAGGATG TTTATTAAAA CCTATGGTTC CCCCAAAATT 600 AGAGGGGACC TCAATCTGCA TCCAGAGGGG GCTGGTTAAG CAGGAAATGT ACAGTTCTAG 660 TTCTGAATAC TATGCAAACA TTAAAAATAC CACATTCATA TGTGTGGATA TGAAAAGATC 720 TCCAAGATAC TGACATCTAC AGTGTGTACT GTGCTAGATG CTAGGGACAC AGCAGAGGGG 780 ACAAAGTGTC TGCCTCCCTA GAGACAACAC CATCTCCACA CCCTCACCTT GGCCTTCAGG 840 ATGTGCCTGA AGCAGCTTCT CCTCCACTCC TGCTACTCCT GGCAGCTTCT CTGGGATCTG 900 CTGTCTGGAA GCCTGTGTCC CTTTCCTTCC TCCAGGTCTT TGCATGGGCT GGCTCCTCTC 960 CCTGGACACT GTTTTGCTCC CTCTACCTCT GCCTCCCGAG TCTTTGCCTG GCCAAGGCCT 1020 CCTCAGCCTT CAGGTCCTTG ACTTAGTAAG GGGCCCAGGC CTGTGTGACC CAATCTAGAA 1080 CTTTCCTTTG AGTTTATACC TCTGAAAGGC CTTGTTGTCT CCCATTATGC CTTTTGTTCC 1140 ACCTCAAAGC ATTTTTCTTT TTTTTTTTTT TTGAGACGGA GTCTCGCTCT GTTGCCCAGG 1200 CTGGAGTCGT GGCTCCATCT TGGCTCACTG CAAGCTCCGC CTCCCGGGTT CACGTCATTC 1260 TCCTGCCTCA GCCTCCCGAG TAGCTGGGAC TACAGGCGCC CGCCACCATG CCCAGCTAAT 1320 TTTTTGCATT TTTAGTAGAC ATGGGGTTTC ACCATGTTCG CCAGGATGGT CTCGATCTCC 1380 TGACCTCGTG ATCTGCCCAC CTTGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 1440 CATGCCCGGC TCACATATTT CTTAATTTCT TTTTTCCTAT TTGTAGTTTA TGATTCTTAT 1500 ATTTATTGAA GTCTGTATGT ATAACACTGT GCTAATACCA GTGACTTCCT GTGATGTCTT 1560 ATCTTTGACA CTATTTCTGA CACCAAATGT GTGGTGCGGT CTTTATCTCT GGCACCAGAT 1620 ACGTGTCATT TTTCCACATC AATTGTTCAA TTATCTGAGA TCAACTGGAC CTCTGAAAAT 1680 TCTATTCAGT TCTGACACTA ACTACCCAGA GTTAGCACAG ACCCTGAACA AAAGTTAAGG 1740 ACTGAGTCCC ACAAGACCGC CCCCACTTTA GATGCCTGCA CAAATGAGGT GCCCCAGCTA 1800 CCCACATTTT TGTTGGGCCT ACTACAAATT CAGAGGTTCC CACTCACCCC CTTCAGGTTC 1860 AATAATTTAC TAGAGTGACT CACAGAACTC AGGACAGCAC 1900
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