Tag | Content |
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EnhancerAtlas ID | HS182-11765 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:8452080-8453540 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_20349 | chr2:8448174-8458311 | CD56 |
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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 |
GH02I008312 | chr2 | 8452320 | 8454331 |
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Enhancer Sequence | TCACTCACCT CTACAGCTGT GGTTTGAGCT ACCATCGCAT CTGCAGGAAT GCGACTCTAT 60 CCTTCTGCTC GGTCTCCCTG CCTCAAAAGC AGTGGCTACT CCTCCCATTG TACCCTGCTT 120 CCAACCCATT CTCCACAGGG TAGCTGTGGG AATCTTTCTA AAAGGCAAAT GTGACCCCAC 180 CATTCCCCTG ATTGAACCCT GTGATGGTTC TCTGTGTTTT TTCATTCTCC CCGTGGTGTG 240 GACCCCTGCC CATGCCCTGA GTCCTCCCAG CCCCACCTCC TGCTCTCTAC ATTCACAGGA 300 CCCCAGGACT CCCCTGCCCC AGATGTCTGG AAGTCCCTTC TCTCATTCTT TATGAGAGGC 360 AAGCTCCTGC CTGTCCTTTC AGATCTTCAC TTAGATTTGA CTTCCCCTGG GAGATACTGG 420 TTGGCCCCTG AGATCAGAGG TGGTGCCTCC TCTGTGTGCT GGTGGGGTCC TGGGCTCTAG 480 CCACAGAAGC ACCTGTCAGC TACATGTTGG TGAGATGGTT TTATGGCACC TGGCTCAGCG 540 CGGGCCCTGA TGCAGACAGT CCAGGTGTGA CCCCTGGCTC TGCCATTCAC TGGCTTTGTG 600 TCCTCTGAAA AGCCACGTCA CACCCCTAAG CCTCTTTCTT TCCCTGTAGA ATGAGGACAG 660 CAGCAGCCTC TCCCTCCTCC CTCGGAGGGT TATTTTGAGC CTTGAATGAT TTCATGTGGA 720 TTGAGTGCCT TGAACATGGG TGTATTGTCA GTGTTAAATA CGAGTTAACT AATACCTGTT 780 TTGTCTCCTG TGTTTGCCCC ATGCCTGATC CCCATGCCGG TGGAGGCTGT TTCCATCTTT 840 TGTCTGTGGT CTCCATAAAT GCAGCCAGTG TTGAACACCC AGTAGAGGAT CAGGCACTGC 900 TGAAATGGAA AATTCAGAGA ATGAGTGGCC CATGGAAGGC AGAAGACGTG GGCCCGCCTG 960 CTGAGGGAGA GCAGGTGAGG AGGCCAGAAA CCTATTCCTC ACAGTTTTGG AGGTTGGAAG 1020 TCCAAAGTCA AAGTCCAGCA GGTTTGGTTT CTGGTGACGG CCACCCGCTG GCTATGTCTC 1080 CACATGGCCA GAAATGTGCA CCTAAACTGA GAGGCAGGGA GCTCTCTGCT ATCTCTTCTT 1140 GTAAAGACAC AAATCCGATT AAGTCAAGGC CCCACCCTTA TGACTCATTT AACCTTAATT 1200 ACTTCCTTAG AGGCCCCATC TCCAAATACA GCCACACAGG CGGTTAGGGC TTTAGCATAG 1260 GAATTGCAGA GACACAGACA TTCAGTCCAT AGCAACCCTC CTGCCCTAGA CCCCCTGGCT 1320 CTGTATACAG AGAGAACAAC ACTGTCCTCC CCACATTCTC TGGTGTGAAG AGGTGAAAGG 1380 GAAAATCATT TCATCAGCAC TCCACCTAAG CCAGCTGCTC TAGCCACGGC TGCTAATGAC 1440 CAGCTAAGCG TGTCCATTGC 1460
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