Tag | Content |
---|
EnhancerAtlas ID | HS043-19226 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr18:13100730-13103270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP4 | MA0691.1 | chr18:13101180-13101190 | AACAGCTGAT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGTTTTATT TGATGGTCAG AACCTTTCCT GTGCAACTGT CACCAGATCT TGACCAGAAT 60 TGTTAATAAG TTAGCAGATG AAGAAGACAG GACAGTGGGT GGAGCCTGGC TTCATCACTT 120 ACTCACGTGA CATTGAGGCT CCAGACAGGT CCAATAGACT TGCTCAGTTT CCCCATTTGT 180 AAAATGGCCT TTGGAATGAA CTTCTTCCAC AGAGGGCTTC AAGGATAAAT TTAGTAATTC 240 CTGTATGGGC AGACCCTGAC TTACGGTGGC TTGACTTACC ATTTTTTGAC CTGGTGATGG 300 TGTGAAAGCC ACGTGCATTC AGTGAAAATC GTATTTTGAT TTTTGACCTT GCCCTGGGTA 360 GCGAGCGACA CAGGGTGCTG CACCCTCTTG TGATTCTGGG CGGCGGCAGC CCTGAGCCAC 420 AGCTTCTAGT CAGCCGCAAT CACAAGGGTG AACAGCTGAT ACTGTATTCT GCAGTGCACT 480 GTCTTCAGTA AATGACATGA GATATTCAAC CCCTTGTTAT AAAATGAACT TTGTGTTAGA 540 GGATTTGCTC AACTGTGGGC TCAGGTAGGT GTTCTCAGCA CTTTTAAGGC AGGCTCGGCT 600 TAGGGTAGGT TAGGTGGATT AAATGCATTT TCCACTTAGG GTAATTTCAA CTTAGGATGG 660 GTTTACTGGG ACGTGAGGAG CATTCGTGTT CAGTAATGGT GATATATGTA CAGCAGTTAG 720 CATGGTGTTT GTTGTCTATT AGGCACTCTG TATTGCTCAC ATTCCTCGAG AGTCCTGCGA 780 TCATTTATTT TTGTCCCTGT CTGTCTCCCT CACTGCTGGC TCAGGCTAAA TGAGCAGTGT 840 TGTCGGGGGA CCTGTTAGAG AGGATATGGG TGCATCTCTC ACCTGCCCTC TAGCTCCTTG 900 CCTCTCCATT GATTTTGTCT ATCCCCAGCC TCAGCCTCCT GCTTCCATGG TCTCCCTCCT 960 GGACCTTGTT GTTCAGCCCT GAAGCTCCCC GCTCTGAGCC TGGCACTTGC TGACTGTCGC 1020 CCATCTCTTC AGCTCACCCA CTGAGGGCTC ACAGCAGTTC TCTGGCCTCC CTGAGACCCC 1080 CTGCCTGCTG GCACTGCCTG TTTTGTGCTC TCTCCCAGCC CGCCCATGCC CCTCTCCTCT 1140 TGTCACTTCT GGACTCCTGA GTCTGTCCTT ATAGTTGCTG TTTCACAGGC TTCCATGACT 1200 GCCGGGTGTT CCTCTCCCTC TCTGTTCCTG CCTGGCAAGA TCCCAACCCT GGCTTGTCCC 1260 AGGAGCCTAG CTCCTCCTGC CTCCACCCTT GCAGTGAAAC CACACTGGAA GGAGCTACTC 1320 CACCCTTCTG GGGGTTCCTG GTGCCCCTCC ACATGAGGCT TTGCTGCCTC TGCTCCTCTG 1380 TGTGTGTCCT GCAGCTCCTG CCACCCCCCA CAGCTGGGGG CCCTTCTTTC CTCTGGGAGC 1440 TCCTGCCACC TCCCCTGCTC CTGCTGTCAC TCTTCCTAAC TCTTGACTTT GCCTTACACG 1500 TGAAAAATAG ACAGGCCCTG AGACTCAGTG AAAGGCTTCT GTTTCCATCA CAGATGAACC 1560 CTCTGCCTGG AACCAGGCCT GTCCATTCTC GCCTCTCGGG GGGCTTCCTG TGGTCCCCTC 1620 TCGCTCCAGA GCCATCAGCT TCTCCCTCCT TGTTGATTCG TCTCCACCAG CACCCAGTAC 1680 ACTCCACCAT CACCAGGTTA AGAAGCATCT TCCTCGGCCC CCACACCCTT TCCTTGTGGC 1740 TACCCCTGTC TCAGCAGCCC CCTGCCCTCA CTTCCTTAGG CCATGGCTGC TGTCACCTCA 1800 TGCCCGGAAC CCCGTCCTGT GAAGGTCACT TAAGAGCTCC ATGTGCCAAA TCCAGGGTCC 1860 GTTTTGTGTC TTGGTTGACT TGATCTCCCA GCACTGTCGA CTGCTCTTCC ACTTTGGAGG 1920 ACTTCTCCGT GCAGCTGCTA TGCGCCAGGG CTCAAGTTTT CCTGCCTCAC CTGCTCCTGC 1980 TCGGATCCCT TGCTGACTCC TCTCCCTGGT TTCTAAAGAC TGGCAGGGTC CCGGCCCAGC 2040 CTGCCTGTGC CTTTCCTTCT CTCTGTGTTC TCCTGCGCGA TGATGGCCTG TAGCCTGTGA 2100 CTCTCATGAC TTCCCGTGTG CTCGGGCCCA GGCATCACAC CCTGGCGCCT GCTTGGCTTC 2160 CACATGTGGG CATCTCATGG GCACATCAGA TGTGATATGC CCAAGAGAGG CCCTACGCCT 2220 CCTCCAGGCT CAGCCTCATG TCAGTAAGTG GCACCACTAT CTGTTCATTG GTTGTTATTT 2280 CTGATTTATC TTCTTCCTCC CTCCTGCCAC TCTGTCCATC AGCAAGTCCT TTGAAGCCTG 2340 TCTTCAAAGT AGAGGCCACA CATGCGCATG TCTTTTTCTC CCCTTTGCCA CTGTCCAAGC 2400 TGGAGGCAGT CACCCTGTGC ATCATCTCAT AGCCAAACTG CTGCAGCCCT GACTTACCTG 2460 GGCTTCCTCG TCCCCTTCAA TGCCTTGCAG TCTCTTTTTT ACAGAGCAGT CTGTAACGCT 2520 TTAAAAATGT AAATCATCTT 2540
|
| |
|
|
|