Tag | Content |
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EnhancerAtlas ID | HS194-03037 | Organism | Homo sapiens | Tissue/cell | Urothelial_cell | Coordinate | chr2:74967500-74969030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr2:74968403-74968414 | AGCCTCAGGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 74967600 | 74968600 | chr2 | 74968770 | 74968998 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I074739 | chr2 | 74966347 | 74969939 |
| Enhancer Sequence | AGGCTACTGT GAAGTGCGGA ACCACTTGGC TGGCAGCCTG GAATATAGAG GGGCAATCTT 60 CTCAATGGGT TGTCAGGGCT ACCACATTTT GGACTTGCTG CCAGGAGACC CAGGTTCAAG 120 TCCCCACTCT GCTGCTATCT CACATTGTGA CCTTGAGTGG TCACTAATCT CTCACTAGAT 180 ACTGGGCCTC GGTAGCCTCG TCTGTTAAAG GGGATGACTC AACTTGGGTA AGTCTAAAGT 240 TTTCTCAGCT TTAAAACGCA GGGATTCCAT GTGTCACCTC TCCCAGGAAT ATTTGTATCT 300 GTGGAATGAA AGACCTTTTG CTGCTGTCTC AGAGAAGTAT TTATGCAGGT CAGGGGTCCT 360 TTCCCAATGC GTTGGACTCA TCCATCTGGA GGAGCTCTTC TACCGAAGGG CACTACCTTC 420 TCACCAGGCT GTGGCAGCAG AGGGGTTAAA CAGCATGCCC TGCCCTGCTC CAGGCAGAAG 480 GGTTGTAGGA CTTAATCACG TTTCAGCTTG GCTGTCGGGC TGTGAGTCAC GGTTGCACTG 540 CGATTATGTA AGCACGCAGG AATAGGTGGC ATGACATATA TGCTGCCAGC AGCCACGGGC 600 CTCGCCCTTC CGAGTCACCA CTACTTTTTA AGCCTTTTTT TGGATACAAG TTTCTTTGGG 660 TTCATCTTTG GAATGGAAAT GGAAGCATGA TTGCAGAATA GGCAGAACAG GAATTATCCA 720 TCAATCAGAG AGAACCCAGC CCTTTAAGAG AAGCTGGAAT TAGAATATGG AATTCCTGAG 780 CCTTGAGCTG GCATAGCCGA GCCCTGGTTT ATGCTCTTCC TGCCTCCCTC CTTTTTTCCC 840 TCCTGCCTGT GTGCTCCACT TCCTCTCCTG AGACTCCCCC AAGGTAGCAT CACTCCCACC 900 AGGAGCCTCA GGCAGGAAAA ATAAGGCCCA GAGAAGGGAC TGTCCCTGGG GACGTGCACT 960 GAGTGTGTGT GAGGGTGCGG GGCAGGAATA GGAGTGCCAG GAGTCTACCT CTGGAGCAAT 1020 GCCTCCCACA GTATTTCTGT AGGGGAAAGG ATAGAAACTC ACTTCTTGGG TTCCTCCAAT 1080 CACCATGCAC ATGTCAGTCC TTCAGCTATA AATGCAAAGG AAAGCCAGAA CTGAGATTTG 1140 AGCTTTCTCA CCATCTCCAT GGTCAGATAT CTCCACTGCC AAAGGGTTCA TTCCGCCTCT 1200 GGGTTTATCT CTTTCTTCAT GCTTCTTCCT GGCAGTGTCC TGTTGAAGCT TACCTTCCCA 1260 TCTGTGTTTG CATCCACTCC CTAAAAACCA CAAGACAAAA CAAGAAAATA AAAGCCTCCT 1320 CCCCTCACTT AATCCACGGT TCTTTTTTCT TCCTGCTTAC AAATTTCTTG AACTTGTATG 1380 TCTGTCCTTG CTGCTTCCAC TTCTTCATCT CTCATTTGTG TCTGATGCAA TAGGGCAATG 1440 AAGTGTCCTT GTGGTCCCTG GTGACCTTCT CATCGCTCAA TCCCAAGGCC TTTTTTTAGT 1500 CTTCATCCAA TTTAACCTCT TGGCAACATG 1530
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