Tag | Content |
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EnhancerAtlas ID | HS060-00584 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:25021810-25023150 |
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) |
Gata1 | MA0035.3 | chr1:25021880-25021891 | TCCTTATCTGT | + | 6.14 | ZNF263 | MA0528.1 | chr1:25022138-25022159 | GGAGGAGGGTGGGCCGGAAGA | + | 6.87 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37045 | chr1:25020011-25023668 | HSMMtube | SE_41323 | chr1:25020136-25023267 | Left_Ventricle |
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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 |
GH01I024693 | chr1 | 25020270 | 25023024 |
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Enhancer Sequence | CACGAACAAA CTCTGAACAC TTACTAATTC TAAGGCCAGG GTAAATCTTT CATCTTGCTC 60 AGCCTCAGTT TCCTTATCTG TAAAATGGGG ATCATAATTT GTCATCCAAA TTGTGAGGAT 120 TGGGTAAAAA CATTTTTAAT AAGGGCATGT ATGTGAGCAT CCCCCATGTA TGGCAAAGAA 180 GTTGTCTAAA TTTAAGAGGT TGTTGTTTTT CTTAATCTCA GAGCAGGAGC CAGGGCAGGA 240 AGTAGGCAGG CTGATTAGGG CGGCCAAGTG TCCCTGCCCA AGAGTGACTA CTTCCGTCCC 300 TGGTGTTCTT CATTAAGTCC CCAGGAAAGG AGGAGGGTGG GCCGGAAGAA AGGGCAAAGC 360 TCTAGGTCCT TATCTAGAAC TCTGCCTCCA TGCAAGAGCC CTCCAAGGGA AGAGAAGTTC 420 TGGATTATCA CCACTGAGCT CCAAGCATGC CAGAGGGCTC AGCAGGGAGA AAGTCTGTCA 480 GCACCTGACC CAGCAACAGC TGGGGAGAGG CCTGGATGGG TAGGTTGCAT GCCTCCCCCT 540 CAGCCTGTGT CATGGCCCTG CCCTGGCCTC ATGGTCCAGG ACTCAGTCCC CATAGCCTGT 600 CCTACCAAGG GGAACACCAG ACTCCAGCAC TGCGATGCAC AAATGCCAAA CCCTCCCAAG 660 GGGCAGCTTT GGCAAGTGAC TGGAACTGGA GTCAGGAGGC GCCGGCTCTT GTTCTGGTTT 720 TGTCCCTTCT CCTCGCTGGG TATCAGCATC CCTACTGTGG AATAAGGGAC ATTCCCTCGA 780 GGGCATTTAC ATAGTGTGGA TCTGGCGTAC CACTTGCTAC CCCTGCCACA AAGTGTTGTT 840 CCTTGTGCCT TCTTCCTGGG CTGCTGGAGA AAAGGCTCAT GCCACATGTG CTGCCCTCTC 900 TGGGTGTGGT CAACAGCTCC CCAGCCCAGG ACACTCAAGT GTGACACCCA GATGACACTC 960 AAGTCATCTG TGTCATTTTC TGTTTCTGGT GCTTCCTGAA TTCCAGTTCT TTCTTGTTCC 1020 CAAGTAGATG GAGAGCTCCC TGAGGACAAG CAACTGGGGT CTCCTTACCC CTCCCCAAGA 1080 ACTAGGGCTT AGCACAGAGT AGACCCTCAG GGCTGGTTAG CAGCTGTGCT GTTGGGCCAT 1140 CCTTGAGGCC CTTGATGAAC ATGGCCTCCA TCACCAGTGC CTGTTGCAGC GTTCTGGCCA 1200 CACAGGGAGG AACCCCAGTT TCTGCTCCTG GTTCTGCTCA ACTCAGTCTG CAGGACTTTA 1260 GGCAAGGCTC TGTCAAAAGC ATCTGTGGTT TTTCAAAATG TGCCAGGTGG AGGCCAGGCG 1320 TGAAGTGGAT AATCCTCAGG 1340
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