Tag | Content |
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EnhancerAtlas ID | HS080-18333 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:29513100-29514150 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr2:29513599-29513612 | ATATGCAAATTAA | - | 7.34 | Pou2f3 | MA0627.1 | chr2:29513597-29513613 | AGATATGCAAATTAAA | + | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 29513258 | 29513860 | chr2 | 29513926 | 29514013 | chr2 | 29513200 | 29513828 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I029290 | chr2 | 29513321 | 29513855 |
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Enhancer Sequence | GGGAATGACA TCTACCCTAG CTGCTCAGAT GCGAGCCTGA GTGAGAACCT TGTGTTGTGA 60 AGGAGCCAAG CACCCTGGAA GGGGGCACAG GGCTGCCGTG GATGGGGAGA TGTGGGCAGA 120 GTGAGGAGGC GCAGGAGCTG CTGGGACTGT CAGCCAGCTT GTCCAGCAGA GGGTCAGTAG 180 GCGAGTGATG TCTGCTCCTC CTCATAGGCA TCCCTTTTTC CTGAGGTGGA GTTAGAGGCG 240 GAGCAGTTAC AGATGAAAAT GCTCCTAGGA GGGGCAGACA GGCAGGAGGA CAAGAGCAGA 300 TGTGGGGGGC ACCCCTGGGC CATGTGCTCC TAAAGATGAA GCAGGGCTCT ATTTAGCACA 360 GTGTACCAAC CTTGTGGCTG GGGTCTCCTG TTGATCCTTA CAGCAGTGAA CTTTATTCTC 420 AATGAAAGGG CGATTTGTTA AATGTACAGT ATAACTAAAG GTTATTTTTA TGCCTTGGTT 480 AGACTTGGTA CATGAATAGA TATGCAAATT AAAAATGCCT ATCAGAGACT GTGCTCCAGT 540 GCTGGGGAGG AAACACATGG TGTGGGGATA GTCAAAGGCA TGCCGGAGTG GGAGGCACCT 600 GGAGAGGGGA CACAATGGCC TGGAAGGATA AGGGGAGACT CCAGCTGTGA GCCTGAGAGG 660 AGAGGCAGGC AGGCAGGGGC CGTGCGGGGA ATGGTCTGCA GCAGGAGGTG GTGGTGGGAA 720 TTGCTAGGAT GAATTTCAGG AGCTGGTTGA AGCAAAGGGA AAGCAGTAAA CTAATGTGAA 780 ATGGATAAGA GATGTGGCCT AAAAATAACC AAGAACCTAA ATATTTTGTT AGTAACAATG 840 GCTATTGACC AGGTGCGATG GCTCCTGCCT GTTATCCCAG CAGTTTGGGA GGCCCAGGCA 900 AGAGGATCAC TTGAGGCCAG GAGTTCAAGA TCAGCCTAGG CAACATAGCA AGACCCTGTC 960 TGTACAATTT TTTTTTTTAA TTAGCTGGGC ATGGTGGTGC ACGCCTGTAG TTCTAGCTAC 1020 TAGGGAGGCT GTGGCAGGAG GATTGCTTGA 1050
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