Tag | Content |
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EnhancerAtlas ID | HS030-02012 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:196960540-196961770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr1:196961462-196961472 | GGAAATCCCC | - | 6.02 | SP3 | MA0746.2 | chr1:196961302-196961315 | TGTGGGCGTGGTA | - | 6.1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 196961207 | 196961600 | chr1 | 196961084 | 196961378 | chr1 | 196961537 | 196961684 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I196991 | chr1 | 196960982 | 196961565 |
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Enhancer Sequence | GTGAGGAGCT ATGATCCTTT GGAGGAGAAG AGACACTCTG GTTTTTAGAA TTTTCAGTTT 60 TTCTGCTCTG GTTTCTCCCC ATCTTTGTGG TTTTATCTAC CTTTGGTCTT TGATGTTGGT 120 GACCTACAGA TGGGGTTTTG TTGTGGATGT CCTTTTTGTG GATGTTGATG CTATTTCTTT 180 CGTTTTTTAG TTTTCCTTCT AACAATCAGG TCCCTCAGCT GCAGGTCTGT TGGATTTTGC 240 TGGAGGTCCA GTCCAGACCC TGTTTGCCTG GGTATCACCA GCAGAGGCTG CAGAACAGCA 300 AATATTGCAG AACAGCAAAT ATTGCTGCCT GCTCCTTCCT CTGGAAGCTT CATCCCAGCG 360 GGGCACCCAC CTGTATGAGG TGTCAGTTTT CCCCCTACTG GGAGGTGTCT CCCAGTTAGG 420 CTACACGTGG GACGGGGACC CACTTGAGGA GGCAATCTGT CCGTTCTCAG AGCTCAAACA 480 CCATGCTGGG AGAACCACTG CTCTCTTCAG AGCTGTCAGA CAGGGACATT TATGTCTACA 540 GAAGTTTCTG CTGCCTTTTG TTCAGCTATG CCCTGCCCCC AGAGGTGGAG TTTACAGAAG 600 CAGCAGGCCT TGCTGAGCTG CAGTGGTCTC TGCCCAGTTC AAGCTTTTCC AGCTGCTTTG 660 TTTACCTACT CAAGCCTCAG CATTGGCGGA CGCCCCTCCC CCTGCCAGGC TGCTGCCTCA 720 CAGGTCGATC TCAGACTGCC ACACTAGCAG TGAGCAAGGC TCTGTGGGCG TGGTAACTGC 780 CAAGCCAGGC ACAGGATACA GTCTCCTGGT GTGTCCTGGA GACTGGACAC ACCACTAAGA 840 CCACTGGAAA AGTGCAGTAT TTGTGTGTGA GTGTCCCGAT TTTCCAGGTA CAGTCTGTCA 900 CGGGTTTCCT TGGCTAGGAA AGGGAAATCC CCCAACCCCT TGCACTTCTA TTTTTTCTAA 960 GACCACTGGA AAAGTGCAGT ATTTGTGTGT GAGTGTCCCG ATTTTCCAGG TACAGTCTGT 1020 CAGGGCCTCC CTTGGCTAGG AAAGGAAAAT CCCCCAACCC CTTGCACTTC CCAGGGAGGC 1080 AATGCCCTGC TTTGCTTTGG CTCCCCCTCC ATGGACTGCA CCCGCTGTCC AACCAGTCCC 1140 AGTGAGATGA ACCAGATACC TCAGTTGGAA ATGTAGAAAT CACCCATCTT CTGCATCGAT 1200 CACGCTGGGA GCTGCAGACC AGAGCTGTTC 1230
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