Tag | Content |
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EnhancerAtlas ID | HS019-05907 | Organism | Homo sapiens | Tissue/cell | CD20+ | Coordinate | chr16:1677770-1679250 | 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 | ACAGCAAGGA GGCTGGTTTT GTGTAGATTC AAGCCCCAAA TCGTGCCTTT AAGCTGTTTG 60 TTGGTCTTGG AGGACCTGCG ATTCCTGGAA TGTTTTCAGA ATCAGCAACC ATTGCTGATT 120 TTTGCCTGAA ACAATTACTC CTGTGGTGTG GCCCTTCCTC CTTGGCAAGA CTGTAGCCTC 180 TGCAAGAGGG TCTGGGTGCC TGGGAGCAGG AGATGTGGTT GTCCATTAAA GGTAGCAGAG 240 GAGGAGTTCC TTGTTAATGA TCCACCCTTT ACCCTTATTC AAGCAGTTCA GTTCGTGTCC 300 TTCCCATTGG GTTAAGCTGC TCATTAGAGT TTTTCTATCG GGTAGATGCT TTTTGAGGAT 360 TCTGAAATCC TGAATTAGTA ATAATAATTA ATAGTTGGCT GTTCTGATCA TGTAATGCTT 420 TCTGCTGTGG GTTCTCTGTA TCTGAGTTTG TATATGAGAA AGAGCGAGGG CAAGAGAAAG 480 GACTTTTTGT TTGTTTGTTT TGAAACGGAG TTTCGCTCTT GTTGCTCAGG CTGGAGCGCA 540 GTGGCACGAT CTTGGCTAAA TGCAGCCTCC ACCTCCTGGG TTAAAGCGAT TCTCCTGCTT 600 CAGCCTCCTG AGTAGCTGGG ATCACAGGTG CCCGCCACCA CACCCGGCTA ATTTTTGTAT 660 TTTTATTACA GACCGAGTTT CGCCACGTTG GTCAGGCTGG TCTTGAACTC CTGACCTCGG 720 GTGATCCACC TGCCCCAGCC TCCTGAAGTG CTGGGATTAC AGGCATGAGT CACCGCACCT 780 GGCCTAACAC GTTTCATTTC TGCATTGTGT GTCTCATCAA AACTAGGTGG CCTTCTGGTG 840 GGGTCTTGAT GTGTGGCTGA CTGGCCGGTG GCAGGTGTGA CTGTGAACCC TCAAGCTGTG 900 GGGTGACGGT GACTGGGCAC AGGCCTCTGC TCTGAGAAGT GCGGCTTCTG CCATGTTGTC 960 ATGGCCACCG CTGCCTTTTT GATGCCTCCC TGGGAGGGGT GCAGCAAGGC TGGCTGGGGC 1020 CTGATTGGAT GCAGGGACCC CACCGCCATC ACTGGGCCTC AGTTGGTCAC TCCTGATCAT 1080 GGGCTGAATT CTCTCCTGCT TCAGCTGCTC CTCAGGCGAG AGTGCTGCCC CTGCACACCC 1140 TACTTTGGGC AGTGCTGGGC ATGCTCAGAT TCGCGCCCGT CCAGTTATGG CCCGTCCAGA 1200 CTTCTCCCTC TGGCAGGGCG GGCATTCACC TGTGGCAGGG CACTCGCCTC CTTCCTCTGA 1260 ATACCCTTCC ATTTCTGTGG CAGGTCTGCA CAGACCCAGC CCTGACTTCA TTTCAAGTTC 1320 CTGTTCCTGC TTATATCCGT CCATCATCCA TGCTTGTTTT TGCCATACAG TTCTTGATTT 1380 CCTACCTGAC AGCCACACAG CCAGCGTCCT GTGCTTCCTT CTCCCTCTCT GCATAATGGC 1440 TGCGGCCTCA GCTCTGGCCT CTGTGCTTCG CAGTGTTCCC 1480
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