Tag | Content |
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EnhancerAtlas ID | HS067-02630 | Organism | Homo sapiens | Tissue/cell | GM18522 | Coordinate | chr16:1677900-1679250 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr16:1678533-1678544 | CATGAGTCACC | - | 6.62 | Foxd3 | MA0041.1 | chr16:1678258-1678270 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr16:1678533-1678544 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr16:1678473-1678488 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACAATTACTC CTGTGGTGTG GCCCTTCCTC CTTGGCAAGA CTGTAGCCTC TGCAAGAGGG 60 TCTGGGTGCC TGGGAGCAGG AGATGTGGTT GTCCATTAAA GGTAGCAGAG GAGGAGTTCC 120 TTGTTAATGA TCCACCCTTT ACCCTTATTC AAGCAGTTCA GTTCGTGTCC TTCCCATTGG 180 GTTAAGCTGC TCATTAGAGT TTTTCTATCG GGTAGATGCT TTTTGAGGAT TCTGAAATCC 240 TGAATTAGTA ATAATAATTA ATAGTTGGCT GTTCTGATCA TGTAATGCTT TCTGCTGTGG 300 GTTCTCTGTA TCTGAGTTTG TATATGAGAA AGAGCGAGGG CAAGAGAAAG GACTTTTTGT 360 TTGTTTGTTT TGAAACGGAG TTTCGCTCTT GTTGCTCAGG CTGGAGCGCA GTGGCACGAT 420 CTTGGCTAAA TGCAGCCTCC ACCTCCTGGG TTAAAGCGAT TCTCCTGCTT CAGCCTCCTG 480 AGTAGCTGGG ATCACAGGTG CCCGCCACCA CACCCGGCTA ATTTTTGTAT TTTTATTACA 540 GACCGAGTTT CGCCACGTTG GTCAGGCTGG TCTTGAACTC CTGACCTCGG GTGATCCACC 600 TGCCCCAGCC TCCTGAAGTG CTGGGATTAC AGGCATGAGT CACCGCACCT GGCCTAACAC 660 GTTTCATTTC TGCATTGTGT GTCTCATCAA AACTAGGTGG CCTTCTGGTG GGGTCTTGAT 720 GTGTGGCTGA CTGGCCGGTG GCAGGTGTGA CTGTGAACCC TCAAGCTGTG GGGTGACGGT 780 GACTGGGCAC AGGCCTCTGC TCTGAGAAGT GCGGCTTCTG CCATGTTGTC ATGGCCACCG 840 CTGCCTTTTT GATGCCTCCC TGGGAGGGGT GCAGCAAGGC TGGCTGGGGC CTGATTGGAT 900 GCAGGGACCC CACCGCCATC ACTGGGCCTC AGTTGGTCAC TCCTGATCAT GGGCTGAATT 960 CTCTCCTGCT TCAGCTGCTC CTCAGGCGAG AGTGCTGCCC CTGCACACCC TACTTTGGGC 1020 AGTGCTGGGC ATGCTCAGAT TCGCGCCCGT CCAGTTATGG CCCGTCCAGA CTTCTCCCTC 1080 TGGCAGGGCG GGCATTCACC TGTGGCAGGG CACTCGCCTC CTTCCTCTGA ATACCCTTCC 1140 ATTTCTGTGG CAGGTCTGCA CAGACCCAGC CCTGACTTCA TTTCAAGTTC CTGTTCCTGC 1200 TTATATCCGT CCATCATCCA TGCTTGTTTT TGCCATACAG TTCTTGATTT CCTACCTGAC 1260 AGCCACACAG CCAGCGTCCT GTGCTTCCTT CTCCCTCTCT GCATAATGGC TGCGGCCTCA 1320 GCTCTGGCCT CTGTGCTTCG CAGTGTTCCC 1350
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