Tag | Content |
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EnhancerAtlas ID | HS095-17468 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr2:199782590-199783770 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr2:199782644-199782657 | TAAATTTGCATAT | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCCTCCAT CTCTGTACTT TATTCAAAAA AGTTGATAAA TTAAAAATTA CTGCTAAATT 60 TGCATATTCT CTTATTAATA GTTGTTTACT GAGCTTAGAA ATATGCATTA TCTGACTGGG 120 TAGTCTAAAG CAATCAAGCA CGATTAAAGA AAGGGTTGTT CAGCTGGTTA TCAGATAATT 180 CTGAAGCCAG GTGTTGCACA TGATCCTTAC TTGGAGCCAT CTGATCCATT GCCACATAGT 240 TCATTGTCAA GCCAATTTCA CCAGCTTGAC ATATATATGC TGTTAATCAT AAAGAAGATC 300 AAGTGAAAGA AAGTAGTGAT TGCCATCATT AATGGAATAA AACCAGCACT AAAGTCAGGG 360 CACATAGTAA ATTTTTAACA ATCTTGTTTG AGATTTCAAC TGTTGGATGA TCAGATCTTG 420 AGACTGTTTA ACACTTGGCG TATCTGTGAG TTTATTGTTC ATTTGCTCAG TGTTTTCCAT 480 GATGGTATGG AGCTAGATAG GCTTGAAATT GAGGGTAAAA AGAATCAGTT CAGGAAATAA 540 AGTAAATGAC TCAAATTTCA CTTTATGATC TAAGACTGGT TCTCCAACTT CATCGTGCAT 600 CAGAATTAAC TAGAGAGCTT GTTAAAACAT GTTGCTGGGG CCTATCCCCA GAGCTTTCAA 660 TTCAGTAGGT AGAGTAAGGC TTAAAATATG CATTTCCAAC AAGTTCCCAG GTGATGCTGA 720 TGTTGCTGGT CTGAAGATCA CACTTTGAGA AGCACTAATC TAAGAGACTA GGTCATGGGA 780 ACAAAAGCAT TACAGGAAAT CATAAGTTAA TGTCAAATAC TGACCCAGTG CTCAATTAAG 840 GATGCAAGAA GTCAGGACAA CAAATGCGAG GCTGGACAGG AGGGACTGTT ACCAGGGCCA 900 TCACACAACT ATGAGCATGC TGATTCCTCT TAGGAAAATT CTCAGAGGGG CTACAGAGGA 960 TTGGGTTCTG ATTACACAGA GGTAACCCTA CCAGGCTATT TAAATGCATA GGCCAGCACA 1020 TTAAATTTTA CTTATTTTTT GTGAAAGCAG GACACAATTC CTTTTGTACT TGTTAAGGCA 1080 TTACAGAAAA AAATATTTTG AAATATATTC ATTTCTGTTG CTGCTGTAAT AAATTATCGT 1140 AAGAATGACT TAATACAAAG TATTATAGTT CTATAGGTCA 1180
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