Tag | Content |
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EnhancerAtlas ID | HS047-24622 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr3:136499990-136501530 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr3:136500284-136500299 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCAAACATA GTGAAACCCC GTCTCTACTA AAAATATAAA AAATTAGCCA GGCGTGGTGG 60 TGGGCACCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG GAGAATCACT TGAACCTGGG 120 AGGCAAAGGT TACAGTGAGC TGAGATCGTG CCACTGCACT CCAGCCCTGG CTACAATGCG 180 AGACTCCGTC TCAAAAAAAA AAAAAAAAAA AAAAGAAATG AATTGCCTGA CTGGGCACGA 240 TGGCTCAGGC CTGTTATTCC AGCACTTTGG GACGCCAAGG TAGGCAGATC ACTTGAGGTC 300 AGGAGTTCAA GACCAGCCTG ACCAACATGG TGAAACCCTG TCCCTACAAA AAATACAAAA 360 ATTAGCCAGG CATGGTGGCA GGTGCCTGTA ATCCCAGCTA CTGGGGAGGC TGAGGCAGGA 420 GAACTGCTTG AACCTGGAAG GTGGAGGTTG CAATGAGCCT GGATTGTGTC ACTGTATGCC 480 AGTCTGGGCA TGAGACTTCA TGTCTCAAAA AAAAAAAAAA AAATGGATCG CCTGTGACAC 540 TGCTTATCAA TCAGTACTTA GGGTTGGTTA CTTTGTGCTA GCTAATTACG CGCCTCTTCC 600 AACAGTGAGA GAGACTCTTG CCCCTCTCCA CCTACAAGCA GGAACAAAGG AAGAAATGGG 660 GCGGGACCTA GTGATGGCAG GTCAACCCAA ACACTGTCTG GGGGAATGTA CATTATCTAG 720 CACAGTCGGT GTTTTTGCAA GTTTGGAATG TGGAATGATC TCAGGTGTTA CAAAAACAAG 780 CTATGGAATT ACACTGCATC AGAGAGAGAA AAATATTCCT CTTTAAAATA ACTTTCCATT 840 CTCCTAATTA TAGAGAGAAA ATTGTAGTTT GCTGGTGGGT TATTGTTGAT ACTTGTTGAC 900 TTCCTTTTTA ACCCAAAACT AAGTTTTGAC GAGAGGTTCA AGGGACCTTA TTTAGCTAGA 960 ATTTTTTTTT TTTTTTTTAG ACGGAGTCTC CCTCCATGTT GCCCAGGCTG GAGTGCAGTG 1020 GTGGGATCTC GGCTCACTGC AGCCTCTGCC TCCTGGGTTC AAGCGATTCT CCTGTCTCAG 1080 CTTCTCTCAA GTAGCTGAGA TTACAGGTGC ACGCCACCAC ATCCAGCTAA TTTTGTATTT 1140 TTAGTAGAGA CAGGTTTTCA CCATGTTGGC CAGACTGATC TCAAACTTCT GACCTCAGGT 1200 GATCCGCCTG CCTCGGCCTC CCAAAGTGTT GGGATTACAG GGGGGAGCCA CCGTGCCCAG 1260 CCAAGACTGT AACTTTGAGA GAGGTTAATC TCTTTAAATG AGAAAAATCC CTAAAGGGGT 1320 TGGTGATTGA AGACTATCTC TGCCAATACC ACTCCCAGCA GTTGGGGCAA TAATCCTTCA 1380 TTGAAGGGGA TTTGAGTGGC ATATTGCCAC ATCTATGACA GTCACAAAGA AGAAACTCAC 1440 CTGAGCTGGA CAGCCTAGCT GTCTAGATGT GAGGAGATAG CCTTTGGCAT TGTATTTATG 1500 AAAAATGAAA ATTCAGTTGG AAATCCTAAC TTCAAAAATT 1540
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