Tag | Content |
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EnhancerAtlas ID | HS182-11954 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:26989430-26990760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr2:26989795-26989806 | GGAGGGTGTGG | - | 6.32 | Klf1 | MA0493.1 | chr2:26989797-26989808 | AGGGTGTGGCT | - | 6.02 | Lhx3 | MA0135.1 | chr2:26990728-26990741 | TAATTAATTAATA | + | 6.25 | Lhx3 | MA0135.1 | chr2:26990725-26990738 | AAATAATTAATTA | - | 6.71 | POU4F2 | MA0683.1 | chr2:26990723-26990739 | ATAAATAATTAATTAA | + | 6.65 | POU6F1 | MA0628.1 | chr2:26990730-26990740 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr2:26990730-26990740 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27242 | chr2:26986501-26996196 | Esophagus | SE_35222 | chr2:26989420-26996285 | HeLa | SE_40328 | chr2:26989641-26991348 | K562 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26990183 | 26990346 | chr2 | 26990364 | 26990469 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I026766 | chr2 | 26989469 | 26996284 |
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Enhancer Sequence | CCTCCAACCT GGGTGACAGA GTGAGACTCG GTCTCAAAAA AAAAAATAAA AGGAAATCAC 60 ATTTTTGACC CACGATTTCC AGCAGGCACA GACAGACAAG CATGTGCTGA CAACTAGCAG 120 AAGCATCTCA TGCACAAAGA GCACCTCGCA TGCCCCAGGC CCTGCTCTGC CCTTTCATGT 180 GTGAACTCAG GGAATTCTCA TAACCACCCT ATCAGGCAAA GACAGGGGCT GATATTCCTG 240 TATAAGGAAA CTGAGGTAGG AAATGATTAA ATTCCTTGCC CAAGTTCAAC TTAGCTACTA 300 AGTGGCAGAG TTTATAGTTG AGCCAGCATG GTCTGGCTCT AGCATCCATG CTCTTAACCA 360 CCACTGGAGG GTGTGGCTGG GGACTTCTCC AGTCATTTTG GGGTCATTTA GAGTTGTTAA 420 AAGCATAGAA ATCATCCAGT CTAATCCCCA CAATTTACAA AGGAGGCCTC AGGAGAAGTT 480 TCTTTCTGTG ATTCAACTGT TTGGTGTCTG AATGAAGGCT GGAACCCAGG CCTCAGGACT 540 TTAAGTCCTG TTCTTTTATG ACTGTGATAC CCCAGAGTCC CTCCTTCCTG GGAGTTTCCT 600 CTCACAGCTC CCCAGGCCAG GACAGAGAAG CCTGTGCTTG TGGAAGTTGT AAACCTGTAA 660 GTGGCATCTG CGCTCCCAGC CTTTGATGTG CCTCTCTCCA GGACTGGGCT GCCAGCCTCT 720 CAGCCAGCCC AGAGACACTG CTGACAGGGT CCTCCCGCTG GAGTCCAGGC CACTCAAGGT 780 TCAGACTGAC AGCCTGTGGT TGTCTCTGGC AGTTTCTTGG CCTGTGACAA GAGTGATGTT 840 TCCCTTCCCA GGTTCTTGGG AGGATGAAAG GCAGTGGATG AGGAAGCACA TCTGAGCACG 900 TGCTGCCTGC TGTGCTGGGG CGGCAGGTCA GCTTTCCTCT CTGCGGCCCC ATCCCTGGGT 960 CCTGGCAGGG GGCCCCTCCC TGTGAAGTGG CTTCTTCTTT CCCTGGCTGT TTTCTCAAAA 1020 CCTCCTCACT AGCACCTTCT GTCGATCATC TTCTTTAGGC CAAGCCATTT CTGTCTACGT 1080 GAGCCAGTGC CCCATCCACA GGTACTCATT TCAGAACCCC AGTCTCCTGA ATCCAACTGA 1140 GGTTCTACAT ATGAAGAGCC GGGGTCAGCT GGGCACTGTG GCTCCAGCTT GTAATCCCAG 1200 ACTGGAGGCT GAGGTGGGAT GATCATTTGA GCCCAGGAGT TCAAGATCAG CCTGGACAAC 1260 ATAGGGAGAC CTCGTTCTCT ACAAATAATA ATAATAAATA ATTAATTAAT AGAGCCAGGG 1320 TCAAGTAGAT 1330
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