| Tag | Content |
|---|
EnhancerAtlas ID | HS062-00027 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr1:2702940-2704040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:2703362-2703381 | TGCTGCCCCCTGCTGGCTG | - | 7.84 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTGGGGGC GTTTTGTCTC CCCATAGGTG GGGGTCCCAC AGCGGCCAGG GACTGTGTGT 60
CCCCACCTTG GTGCAGAGGA GTAGGTAGGG AGGGGAGTCG TGAGCCCGCT CTGGGCTGCA 120
GTCTGAGCCG CATCTGTCTG CTGATGGCAT TGGTGGGCTG GGACTCTCAG GGTTCCCGAG 180
CCTAGGACTT CTCCATCCCA TGGAGGTGGA GACTCCGCCC CAGTGGGCCC ACTGGAGCAA 240
GGTCCAAATG AGAAGCAGAG GAAGGGGCTT TTAGGTCATG AAGGGTCAAC AGGCGCCAGG 300
GAGTCCTTCA GACGACGCGG AGCAAAAGCC CAGCACGGCC AAGTAGGACC AGGTCGCTGG 360
GCGAGGGGAG ACCTCCACCC CACAACGTCC CCTCTCCGCG ACTCCATCCG AAGGAGGCCC 420
AATGCTGCCC CCTGCTGGCT GCTGGTGGGC ACACGGGTTC CCCAAGCTGA GCAAGAGGAT 480
GCAGGTTCAG GGCATCCGAA CCTGGGCAGG GCAAGGAGAT CAGGACCCAA ACCGGGCCCC 540
AGGGGGAGGA AGACGCGAGA AGGCCCTCAC CCCAGGCCCC AAGGCCTGAA TCCCACCAGA 600
GTGTAACCTT TAGACCCCAG TTCAAACAGG AACCCGGGAT AGCACCTGAG GCAGGTAAGG 660
GTCTGCCTTT CCTGGGAGCA GGGGGTCTTG GAGGCAGGAG GGAAGGTCCC CTCTGCTACC 720
CACCCCAAGG CAGGGTTGCA TCCAAGCCTG GTTTATGTGA GAGACTTGGA GAGAAGCTCG 780
GCCTGCAGTC GGTTCCTGGC CCTTATGCTT CGTAACCACA GTGGAAGCAA GTACGACAAA 840
GCAGCTACGC ATGCAGGGAA ACTGCCGGCC CCGGGGACCT GCCCCAGCCG ATTTCCATGA 900
CAACCCATGG GACCAGGACC CAGATAAGGA GACTGAGGGT CAGGTAGGTG AGGGCCTGCA 960
GCAGGTGCAG AGCTGGGGCT GAATGCAGTC GCCTGGTCCA AAGCCCAGAC TGTGGGGTCC 1020
AGCGCCAGGG CCACGGGAGG CCTGTGCCCT CTTCCCAGCT GGGCCCATTT CCACCTGCCC 1080
TCTGTCACCC CCCAGGCCTC 1100
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