Tag | Content |
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EnhancerAtlas ID | HS037-02438 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr1:161585500-161586980 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:161585721-161585736 | TGTACTTTTGACCTC | - | 6.25 | STAT3 | MA0144.2 | chr1:161586307-161586318 | CTTCCCAGAAG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATAGTGAAAC CGCATCTCTA CTAAAAATTA GGTGGGTGTG GCGGCATGCA CCTGTAGTCC 60 CCAGGAGGCT GAGGTGGGAG AATCGCTTGA ACCGGGAAGG TGGAGATTGC AGTGAGCCAA 120 GATGCTACCA CTGCACTCCA GCCTGGGTGA CAGAGACTCT GTCCACCCAC CCTCCAAAAA 180 AAAATAGCTG ATATATTTGA ATTTATTTCA CCACCTCGTT TTGTACTTTT GACCTCAATT 240 ATTCTTTTAT TTTTATTTTT TTTTAATTGA TCATTCTTGG GTGTTTCTCA CAGAGGGGGA 300 TTTGGCAGGG TCATAGGACA ATGGTGGAGG GAGGGTCAGC AGATAAACAA GTGAACAAAG 360 GTCTCTGGTT TTCCTAGGCA GAGGACCCTG CGGCCTTCCG CAGTGTTTGT GTCCCTGGGT 420 ACTTGAGATT AGGGAGTGGC GATGACTCTT AACGAGCATG CTGCCTTCAA GCATCTGTTT 480 AACAAAGCAC ATCTTCCACT GCCCTTAATC CATTTAACCC TGAGTGGACA CAGCACATGT 540 TTCAGAGAGC ACAGGGTTGG GGGTAAGGTC ATACATAGAT CAACAGCATC CCAAGGCAGA 600 AGAATTTTTC TTAGTACAGA ACAAAATGGA GTTTCCCATG TCTACTTCTT TCTACACAGA 660 CACAGCAACA ATCTGATTTC TCTATCTTTT CCCCACATTT CCCCCTTTTC TATTCCACAA 720 AACCGCCATC GTCATCATGG CCCGTTCTCA ACGAGCTGTT GGGTATAGCT CACAGACGGG 780 GTGGCGGCTG GGCAGAGGGG CTCCTCACTT CCCAGAAGGG GCAGACGGGC AGAGGCACCC 840 CCCACCTCCC GGACGGGGCG GTGGCAGGGC AGAGTCGCCC CCCATCTCCC TCCCAGATGG 900 GGTGGCTGCC GGGCAGAGGC GCTCCTCACT TCCCAGACGG GGCGGCTGCC GGGCGGAGGG 960 GCTCCTCACT TCTCAGACGG GGCGGCTGGG CAGAGACGCT CCTCACCTCC CAGACGGGGT 1020 CGCGGCCGGG CAGAGGTGCT CCTCACATCC CAGACGTGGC GGCGGGGCAG AGGCGCTCCC 1080 CACATCTCAG ACGATGGGCA GCCGGGCAGA GATGCTCCTC ACTTCCTAGA TGGGATGGAG 1140 GCCAGGAAGA GGCTCTCCTC ACTTCCCAGA CTGGGCAGCC GGGCAGAGGG GCTCCTCACA 1200 TCCCAGACGA TGGGAGGCCA GGCAGAGACG CTCCTCACTT CCCAGACGGG GTGGCAGCCG 1260 GGCAGAGGCT GCAATCTCGG CACTTTGGGA GGCCAAGTCA GGCGGCTGGG AGGTGGAGGT 1320 TGTAGCTAGC CGAGACCACG CCACTGCACT CCAGCCTGGG CAACATTGAG CACTGAGTGA 1380 ACGAGACTCC GTCTGCAATC CCGGCACCTT GGGAGGCCGA GGCTGGCAGA TCACTCGCGG 1440 TTAGGAGCTG GAGACCAGCA CGGCCAACAC GGCGAAACCC 1480
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