Tag | Content |
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EnhancerAtlas ID | HS183-04233 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr4:1073470-1075200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr4:1074998-1075009 | TCTGATTGGCC | - | 6.02 |
| | 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 |
GH04I001081 | chr4 | 1075078 | 1076890 |
| Enhancer Sequence | TCCAGTCTGT TAAACACATA GTGAAAGGCT TTGAGTGAGC CCAGGACTTA CCTCTAACAA 60 CGTCAGTTGA AATACACACA TGACGAGATG ATGTGTAAAT GTCTAAATCT TCCTCTAGCT 120 TCATGCTGCG GCCAGAGTTT AGCCACTTAG GCATCTGATC ACTGCCATTT TCCTCCCTCT 180 TTAGGGCCAC CCGCCGTCTG TACTGGGATG TAGCCTCTCC AGGACAGAGG CCGCTGGCCG 240 GCCCGCCCTG GTTGGGCTCT CCCTGGCATT CCTCTCTTGC ACCTCTGCAC ACTCAGCTTC 300 TCCCTCCAGA CAACCCCTTC TCTTCTCTCT GCCAACACCT GCCTGGAGCC TGCTGGACTA 360 GGACGTTCTG AGAGTGGGAT CCCGAATTGA CTTCTGTGAT CACTCACTGC CTGGCCACAC 420 ATACCACACC GTGCACGCTC GGTACGCACT AGTTCCTTCA TTTGCCAAAG GCAGACAGGA 480 AAACATCATA GGATTCATTT TGCGTTGGCC CCCTCCTAGC CCTGCCATCC TTATGGCTCG 540 TGATCTCTGC GGAAAGAGGC TCACTCTTTT CCAACAGCTC CAGCAAGAGT CCCAGGGGTG 600 ACTCCAATTA GTCCAGCCTG GCTGGAGTGA ATTCTAATTT TAGGTGGCCT CAGCACTCAT 660 TTTGAAGACA GGTTTAACTT TCTCATACCA GAGGCAGGGC TCAGTCACCT TCAACAGTTT 720 CCAGTTCTCC ACCCGCTCCC AGTGTCTCAG AGTGGTCCAT CCGGACACTT GCCTCCCAGT 780 GGCCACCTCC CTGTGGGAGG GTGGACAAAA CCCACTTGGC TGGCCCCGCT GACCCCTCAC 840 CCTTCATTGA CCGTACAGAT GTACCACAGT GATGCCCTCA GTCACAGCGG GACCCCGTGG 900 AGCTTGTGCC TGCCTGCTCT AAACCCACCA ATTAAAACTC CTCACGGGAA ACCTGCCTGG 960 ATGACGCCCT GAGCCCCAAT AAAGGTGCTG GCCCACGAGA CCCCTCTCTG CCTGAGCCTT 1020 CTTTCCTGCC TCTTGCTACC TGTGGACAGA GCACTGTCCT CCCCACAGGC GCCCTCCCTG 1080 TCCAGGACCT GTAAGTAATA AATCTGAATG TGTTTCCTAT CACAGGGGTG GACTGAATTT 1140 GTGCCTTCCA TCTGAAGAGC TAGGAGCTAC CCCAGGCCGG GTTTTCTCTG GGATGCTGGA 1200 GGGAACATGA GGTTGGGCTC CCTGTGCCAG AGTGATGGCC AGGCAGGCAT AGCCTGGAGA 1260 TGGGGCAGAC ACAAGCCACA GGACATGTGC CAGTATGAAC GTTTCCTGTG TGAGGGACCC 1320 CCAGCCATGG GTTGGGTAAT GGGTTCAGGC CATCCCCCAG GTGAAAGAAG GATTCCATAT 1380 AAGGCACACC AGGTCAGCCC CTTAATTTCC TGTTAGGGCA GGGCTGTCAG CTGCCGGGCA 1440 CTGGAACGCC AGTTGAGCGG GGGGCACGCA GAACACTGGG TCACATGATC ATTCCCAAAC 1500 CAATCACTGT CGCTGCAGGA TGGAGTGCTC TGATTGGCCA CCTGGATCAC ACACTTAGTT 1560 TGGGACCTGA GCCTCGCAGG GAGATGAAAT AAGTACCAAA ATGAGTTCAT GTCCAGTCAA 1620 CTGTATGGAT TAGCAAAATC TGGGGGCTTG GAGAGGGGGT GGGGTTGGGA TGGGAAGGCA 1680 GGTGCAGAAT CGGAAAGACC TGCAGGTCCT GTGATTTCTG CAAGCAACCC 1730
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