| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00367 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:11953260-11954450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:11954170-11954189 | CAGCGCCACCTGCTGGAGA | - | 7.38 | | HSF1 | MA0486.2 | chr1:11953533-11953546 | TTCTGGAACTTTC | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCAGCCTC AGCCTCCCAA GTAGCTAAGC TTACAGATGT GTGTCACTGT GCCTGGCTTT 60
GTTGTTTTGT TTTTTTAATC CCTGATGCAT GGTAACATGA TGAGGTTTTA CCTGCCAGGC 120
TTTTCCTAGC AAAGCAATTA TTTTTTAGGT AGAATTATCC CTCCAGCCTA TTGTGAAAGA 180
AGCAGAAGTT ACTGGAAAGT TGGAGTGATT GCCCAAGTCC CCAGAAGGAG GGGGCAGCTA 240
TTAGTGCAGC TGTCTGTGGG CTTGAGAAGC AGTTTCTGGA ACTTTCCTCA CCCCACCCTT 300
CAGTCCTGTC TTATTAGAAG CCCAATTCTG TCCTTGTTCA GGAACAGTGT AGCCATGAAT 360
ACAGCCCCAT GCTGGGCTCT GACAGCTGAC AGGACCACCA ACATGAGGCC CGTGGATGGT 420
GGAGGGAACC TGCACTCACT GACCACCTAT CATGATTTGG TGCCGACCCG TTTAACCCTT 480
ATGTTGACCT GACAATAGGC ATTATTACCA CATTTTACTG GTAAGCAACC TGAGGCCCAG 540
AGAGACAGAG CAACTTGGCC AAGATCACAC AGCCTTTAAG AGGCAGAGCT GAGATTTGAA 600
CTGAGGTCTG TGTATTTGCA AAGTCTATGC CTGGGCAAAA ATCTCAGGAG AGATGGAGTG 660
AGTTGACTCA AACCACCGCG TACTGGTCCC AGACCAAATG GGGGACAGGC CTCCTGCACA 720
GCCAGGAGCA CCCACCCAAG GACCAAGATC TCATCTGAGA GTTCTGTGTC TCACCTACCA 780
CCTGGGGTGT GGAGTGGGGA AGAACCCAGC CTGGCCTTGG GCTGGGCCAC CACCCTGTCT 840
TCCCACACCT GGTCAGCCTG CTCCTTCCCA AATCAAGCAT GCAGTGTCGC CCAGGTAAGG 900
AGAGAGCCTC CAGCGCCACC TGCTGGAGAT GCAGTAGCAG CGCCCTCCAG GGGACCCTGC 960
ATCCCCAGAG TGTCTGGGGA GAGTGGGGTG AGATATAATG GGGGAAAGGG AGGGGGTCAG 1020
TGCGTCTCGC AGGCAATTAT CTCCTATACT TGACCCCATG AACAGGGGTG AGTATTCCTC 1080
CTTCTAGAAC CTCAGAAAGT TGCAGCTGGA AGGCTCAAAG CAGGGAACTG ATCTTGCAAG 1140
GATGGATGGG TGGATGGGTG GGTGGGTGGG TGGATGGATG AATGGGTGGG 1190
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