Tag | Content |
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EnhancerAtlas ID | HS092-24276 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:74966910-74969130 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr2:74968403-74968414 | AGCCTCAGGCA | + | 6.32 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I074739 | chr2 | 74966347 | 74969939 |
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Enhancer Sequence | GTAGGATGTG GCAATCCAGA TCTTTTCATC TGGATGTCAG CAACAGCAAG GCAGGGGCCT 60 GGACAGGATT CAGGTCACAC AGTGTCTAGC TGGCTGGTGG AGCTTTGAGG TCTTTATAGA 120 GAAGCTCTGC ACTGAGATTA TCATGAAGCC TGTGAGTGTT GGGGGTCAGC CTGAAGGCAG 180 CATTCTCTGA GTGCTTCCAG CGGGAACTCC CTGTCGTTCG TGAAGGCAGC CGTGCTTCTA 240 ACACTGGAGT AGCAGCTACC ACTTGTGAGC ACTTACTGCA TGCCAGGCAC TGTGACAGGC 300 ACCTCTGACA AATTATTTCA ATGATTTCAC AACAGCACTA CTGTTTTTAT CCCCATTTCA 360 CAGATGAGGT GACTGAGACT CAAATAGATG CTCAAAGTCA CTGAGCTAGG AAGTGTCAGA 420 CACAACCACA TCCATGTGGA CAGACTCCAG AGCTGGAGAT TCGACCTGAA TCCAAATACT 480 GTTCTCCCCA GAACTCCAGT TGTGAGACTT TTAAGTGGAG CTTGGAGATT AAGGAACAAC 540 CCTTTTGGGG TCATTCTTGC TAGGGCTGTA TGAAGACAGC AGGTGCACGC AGGCTACTGT 600 GAAGTGCGGA ACCACTTGGC TGGCAGCCTG GAATATAGAG GGGCAATCTT CTCAATGGGT 660 TGTCAGGGCT ACCACATTTT GGACTTGCTG CCAGGAGACC CAGGTTCAAG TCCCCACTCT 720 GCTGCTATCT CACATTGTGA CCTTGAGTGG TCACTAATCT CTCACTAGAT ACTGGGCCTC 780 GGTAGCCTCG TCTGTTAAAG GGGATGACTC AACTTGGGTA AGTCTAAAGT TTTCTCAGCT 840 TTAAAACGCA GGGATTCCAT GTGTCACCTC TCCCAGGAAT ATTTGTATCT GTGGAATGAA 900 AGACCTTTTG CTGCTGTCTC AGAGAAGTAT TTATGCAGGT CAGGGGTCCT TTCCCAATGC 960 GTTGGACTCA TCCATCTGGA GGAGCTCTTC TACCGAAGGG CACTACCTTC TCACCAGGCT 1020 GTGGCAGCAG AGGGGTTAAA CAGCATGCCC TGCCCTGCTC CAGGCAGAAG GGTTGTAGGA 1080 CTTAATCACG TTTCAGCTTG GCTGTCGGGC TGTGAGTCAC GGTTGCACTG CGATTATGTA 1140 AGCACGCAGG AATAGGTGGC ATGACATATA TGCTGCCAGC AGCCACGGGC CTCGCCCTTC 1200 CGAGTCACCA CTACTTTTTA AGCCTTTTTT TGGATACAAG TTTCTTTGGG TTCATCTTTG 1260 GAATGGAAAT GGAAGCATGA TTGCAGAATA GGCAGAACAG GAATTATCCA TCAATCAGAG 1320 AGAACCCAGC CCTTTAAGAG AAGCTGGAAT TAGAATATGG AATTCCTGAG CCTTGAGCTG 1380 GCATAGCCGA GCCCTGGTTT ATGCTCTTCC TGCCTCCCTC CTTTTTTCCC TCCTGCCTGT 1440 GTGCTCCACT TCCTCTCCTG AGACTCCCCC AAGGTAGCAT CACTCCCACC AGGAGCCTCA 1500 GGCAGGAAAA ATAAGGCCCA GAGAAGGGAC TGTCCCTGGG GACGTGCACT GAGTGTGTGT 1560 GAGGGTGCGG GGCAGGAATA GGAGTGCCAG GAGTCTACCT CTGGAGCAAT GCCTCCCACA 1620 GTATTTCTGT AGGGGAAAGG ATAGAAACTC ACTTCTTGGG TTCCTCCAAT CACCATGCAC 1680 ATGTCAGTCC TTCAGCTATA AATGCAAAGG AAAGCCAGAA CTGAGATTTG AGCTTTCTCA 1740 CCATCTCCAT GGTCAGATAT CTCCACTGCC AAAGGGTTCA TTCCGCCTCT GGGTTTATCT 1800 CTTTCTTCAT GCTTCTTCCT GGCAGTGTCC TGTTGAAGCT TACCTTCCCA TCTGTGTTTG 1860 CATCCACTCC CTAAAAACCA CAAGACAAAA CAAGAAAATA AAAGCCTCCT CCCCTCACTT 1920 AATCCACGGT TCTTTTTTCT TCCTGCTTAC AAATTTCTTG AACTTGTATG TCTGTCCTTG 1980 CTGCTTCCAC TTCTTCATCT CTCATTTGTG TCTGATGCAA TAGGGCAATG AAGTGTCCTT 2040 GTGGTCCCTG GTGACCTTCT CATCGCTCAA TCCCAAGGCC TTTTTTTAGT CTTCATCCAA 2100 TTTAACCTCT TGGCAACATG TGACATGCTG CCAGCCAGCT GCTCCCTCTT TCTAATGCTC 2160 TCTCCTCTTG GCTTCTGTGA CCCATCTCTT TACTACTCTG TCTGTTTCTC CAATGCCCTC 2220
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