Tag | Content |
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EnhancerAtlas ID | HS182-20060 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:97746110-97747120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:97747062-97747077 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr7:97746562-97746583 | TCTTCCTCTTCCCCTTCCCTT | - | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I098116 | chr7 | 97746026 | 97747210 |
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Enhancer Sequence | CATTACATTT AGTAGTTATG CCCCTTGGGC TCCCCCAGTC CATTCCTTGT TTAGAGTGAC 60 CTGGACAGCT TTGAGGAGTA CTGACTGGTC AGATATTTTG TAGAATGTCC CTCAACTGGG 120 ATTTGTCTGA TGTTTTTCTC ACGATTAGAC TGGGGGTGTG GGTTTCTGGG AGGAAGACCA 180 CAGAGTTAAA GTGCCATTCT CATCACATCA CATCAAGGGT GTGTGCACAC AACATCACAC 240 AGCATGACTT GTCACTTGAT CACCTGGCTG AGTAGTGTTT GTCAGCTTTC ACCCTGTAAA 300 GTTACTCTGT CCTCCCCTCC CCATGGTGTA CGAGTGCAGG GTCAACACTT AATGAGTGGC 360 AAGCTGTGCT CCACCTCTTT GCAAGGAAGT GTCTGTAGAC ATTCTTTGGA GTTCTGTTGA 420 AGAGACTCGC GTATTCTCTT CTTTTCTTTT TTTCTTCCTC TTCCCCTTCC CTTTCCTTGA 480 CAGGTCTTGC TCTGTAGTCC AAACTGGAGT GCAGTAGCAC AGTCATGACT CACTGCAGCC 540 TTGAACTCCC GGGCCCATGC GATCCTCTGT TTATTTCTTT ATTCAAGCAT TTACTTATGT 600 CAGTGTGGAT GCATGGATAT TTATTTTATA CTTCGAGTTG ATTCCACAGT GTTGTTTATT 660 TGTTCTTACA TTGTACCAGC TTTGGCCATC GAGAGCTCTT TCAGTTAGCT CCTGGGTGCC 720 CCGCTGACAT ATCCTCATTT TTTTTTTAAG CATTTCCTTA TTTTCTGGCA TTTCAAGAAG 780 CTACAGGTTC ATCTTGTATA TTCCCTGCCC CAGTCCTAGA ATCAGCCTTT TCTTCAAGGA 840 GCTCTGGTTC CTCTGATTGG AGAGTGATAT GAGAAACCAA GATCTGGGCC AGGCGCAGTG 900 GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGTG GGCGGATCAC TTGAGGTCAG 960 GAGTTCAAGA CTAGCCTGAC CAACGTGGTA AAACCTCGTC TCTACTAACA 1010
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