Tag | Content |
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EnhancerAtlas ID | HS116-19215 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:121309180-121311060 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr2:121309189-121309201 | ATGTAAACAGAG | + | 6.32 | FOXP2 | MA0593.1 | chr2:121309189-121309200 | ATGTAAACAGA | + | 6.02 | MAX | MA0058.3 | chr2:121309787-121309797 | ACCACGTGCT | + | 6.02 | RREB1 | MA0073.1 | chr2:121309444-121309464 | ACCCAGCCCACCCACTCACC | + | 6.17 | SP2 | MA0516.2 | chr2:121310999-121311016 | GTAAGCTCCGCCCACTC | + | 6.02 | SP8 | MA0747.1 | chr2:121310710-121310722 | GACACGCCCACT | + | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 121309676 | 121310000 | chr2 | 121310053 | 121310600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I120550 | chr2 | 121308041 | 121311056 |
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Enhancer Sequence | GGTTTTGAAA TGTAAACAGA GGCTATTGCA ATAAATGAAA TAAATTCTTG CCAAGACACT 60 AGTGAATTCA TTTCCTCTCA GCCAATGGAT TCTAAGAGGC CGAAAAGGAG AAGTGAAAAT 120 TTTGTTTTAG CACTACATAA GGCTTCTCGT ACTTGCAGCC AAAGAGGTCA GAGATTTGGT 180 CCCAAGACCA ACTTAGAGTC ATGTGTGACA CTGGGATTCA GAGGCTAGTT GTGGGCCACA 240 GGGAGGAAGC TGACCCCTGG GCTCACCCAG CCCACCCACT CACCAGCTCT CCTTTCCTTC 300 CTGGGTCCCT TGGGGAGGAG AAGCCATCCA CCTCATGGAA AGTGCTTTAG AGGCTCCTCT 360 GTGGGTGCCC TACTCTGCAC CCTTTGCGGG GACTCTCTGC TTCAGTTCGC AGGACAACCT 420 TAATAGCTAA CTGCAGAGAG GACTGAATGG TTAAGTAGCT CCTCCAAGGA AGCAGAGCCA 480 AGTATCAGAG GCCGGTTTCC ATCCAGGGAT TGAGAGAAGA ATCAGGAGCA CATAGGCTGT 540 GGCAGTAAAA AGCAGATCCC AAAGACAGTA TAGGGCGGCT CGAAAGGGGC CTTCCTACAT 600 AGCCACCACC ACGTGCTCCG GCGCTACCTC CAGGGGGCTG GGCGCAGCTG GAGGACACAG 660 TTCGGCAGCT TGCTAGAAGC CTCCAGCTCT TCCTTTTCTG TATCCTTCAG GTGACTGTGG 720 AAGGCTGGCC GTGCAGCCTG CCATCAGCCT GGCCTCAGCC GGGGAGGGGG ACCTTTCTCC 780 TGGAGGCCAC AGAAACACTG AGGACCTCTC AGCTGAGAAG GTCAGATGGA GGTGCTGGAT 840 GATTGGAGGA GATCAAACTG ATGAGGAAAA CGCAAATGGC ATCCTTCAGG AGCAAAAGCT 900 GTCTCCTCTT TTACTTCACA TGTCCACCCA GCAGCTCTAT GAGTTCTGAT TCAGCATTGC 960 ACTTACCACC CACCCTCCCC GCCTTTTACA GAAAAGGAAA CTGAGGCTCC GAGGTTGCGG 1020 AGTTGCTTGC TCCAGCTGAT GACAAAGGCA GGTAAAGCCA GGGCTAGAGT CCCTTCCCAG 1080 CCCTCCAAAT GCCGTTAGCG CCATGATCCT ACAGCCTCCT CAAAGTCCAG TCAGGCAAAC 1140 TCTTGCCCTT GTTTCCATTA AACACATATC TTCATCTTTT TCGTACTTTT AATAATAGCA 1200 GGAAGTAAAT CTGGCCATGT AATGTGAGAA AGGTAATAGT CCCAGGTCAG GAAATCCTGT 1260 TGCTTGGAGT CTCTTGGGAA TGTTAACTTT CCCACTCTCA CCCTACCGGG ATCCTGACCT 1320 CCTGCACAGT TGGCTTCCTC AGGCAAAACT GGGCCAGAAA TTCTGGGCCG TTGGCCAGAG 1380 TCAGACCTTC GTCCTCTGGT AGCGTCCGCT GGAAAAGAGG AGGCGAGAGT CACCAGGAGG 1440 CTGGCCCCAC TCGCAGGCCC TGCCCTCTGC CGGTGGGTCC TATGGATGAC ACGAGGCCGC 1500 ACTGGGCTGG AGAAGAAGAG AAGCTCCTGA GACACGCCCA CTCTGCAGAG GGAGGCAACC 1560 GCACAGGTAA TCCATCCTCT CTAGGCTTTT CTGTTCCCGT GCAGTAAGTG AAGTGAAGCA 1620 AGGTGAAGAA GTGAAGTGAG CATTCAGGAC ATGAATTGGC ACGTGGTCGG TGCTAGAGGA 1680 GCTGGCAAGG TAGACTCTGG TCTCTTCTGT GGTGCTGAAG CTGGGGAAAT AAGGAACAAT 1740 CTCATCCACA GGCCAGGCCT CCGGCGTGCT CGGGAGCTAC TGACGGAAAC TCCTAGGGAA 1800 CTTCCCTTGT GGAAAGAACG TAAGCTCCGC CCACTCGGGC AGCTGAGGCC ATTGATTCGT 1860 TCACTCATTC GCTGGACTAT 1880
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