Tag | Content |
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EnhancerAtlas ID | HS007-01609 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr1:245181380-245182590 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUND(var.2) | MA0492.1 | chr1:245182100-245182115 | GATTACCTCATTTTA | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAGCCGGGCA CGATGGCAGG CACCTGTAAT CCCAGCTACT TTGGAGGCTG AGGCAGAAGA 60 ATCACTTGTA CCCGGGAGGC AGAGGTTGCA GTGAGCTGAG ATCATGCCAC TGCACTCCAG 120 CCTGGGCGAC AGAGCGAGAC TCTGTCTCAA AAAAAAAAAA AAAAAAAAAG GCAATGAAAC 180 CATCCTTTCA GGAGGCCGGG CTAAATGAGG GTTATTTGAT GAGATTGCAA TCTCAAGACC 240 AGAACCTAGT AGAGAGGCCA GCAAAGCAGT GGGAAGTGGT TTGAAAATGG TTCTGGAAAG 300 GAACTGTTTG ATGCTTATAA ACCAGTGCCA TCAGAGCTGC AGCACCATAC AGCTCCGGTG 360 GCTGTGGTCA CATTGCATTC TGTGGGAATG ACATTGTGGA ACACCAGGCC TTCCTGTGGG 420 TATCCCAGTA GGAAATGAGT GGGCAGGGTG CTGGTGGTGG TGGTAGGGTT AGGGAGGGGG 480 TGCAGCAGGC AGCCCGGCCT GCAATTTGAA TAACTAACTA CATGAATGAC AAGTGCCTTG 540 ACCTCAGACC TCTCCTTGAA GGGTTCTCCT CCTGGGGGCG GGGGACAGAG GTATTGTTAG 600 AGAAGTCAGG GAAAGTATGG CATTATGAGA GAGAGGGAAA AGAGAGAAAA GAAACCAGCA 660 TCTGCTTGAG GCTTGTCATC TAACACACTA CGTGTAGTTG GGTGCCAGAG GCTTCACGTG 720 GATTACCTCA TTTTAATCTT TTTATTTATG GGTTAAGGGT TGGCATCTCC GGTTTCCAGA 780 GACAAGGAGA AGGTAAATCG TTTGCTCCAT GTCACACCAG GTTTCTCTAA CGCCAAGTCT 840 CTTGCTACAC TGTGGGCATG CCACACTGCC CACACTCCCA CTCCTACTCT TTAGAGACAT 900 CAGGGGCTTC TCTTCTGCCT TCAGGCTTCC TGACAGTAGC AGTGAAAAGA AAATCTCCCG 960 ATCACTGACA GCAATGATGC CAGGCCTTTT TTGGTAAAAG GGCCAATTCA GTAAAAGAAA 1020 ACGTGTTTAT GGGCTGAATC TTTTTTTCCA TTGAAAGTTA AAATAACTTT ACCGAGGCCC 1080 TGAGGGAAAG TGGATGTTCT TACAACCTAA AGAGTCTGCT TTGTTAATTA AAGATGGTTA 1140 CTAAGAAAAT TGTTATTGTT TTTAGCATTA AAATATTGCT GCTGAGTATA TTTGAGGAAT 1200 AACAACATGG 1210
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