Tag | Content |
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EnhancerAtlas ID | HS182-17824 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:138271410-138272620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr5:138271634-138271645 | CCACACCCTCC | + | 6.32 | RREB1 | MA0073.1 | chr5:138271621-138271641 | CCACCGCCCACCCCCACACC | + | 6.41 | ZNF263 | MA0528.1 | chr5:138271666-138271687 | TGCCCCTCCCCCCCTTCCTCT | - | 6.53 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_04147 | chr5:138272498-138273420 | Brain_Anterior_Caudate | SE_06001 | chr5:138271827-138274488 | Brain_Hippocampus_Middle | SE_65816 | chr5:138271765-138272478 | Pancreatic_islets |
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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 |
GH05I138936 | chr5 | 138271766 | 138274488 |
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Enhancer Sequence | GGGGGCTCCT TCTCCTTTCC TGGGGCTGAG AGGTTGTGTC TGTGCCCACT CTCCTGAGCT 60 CAGCCAGAAT CTCGCATGTA AAGACATCCA AATGCCGACT TCTTCTCCCC AGAGCCTGGC 120 TTTTATAACT GACTGCCGCC TCACGCTCCA TTCGGATGTC TAATGAATCT CTCAGACTTG 180 ACCTGTCCAA ACTGCTTGCC ACCTCTACTC GCCACCGCCC ACCCCCACAC CCTCCATACC 240 GTTTTCCCCA CGTCACTGCC CCTCCCCCCC TTCCTCTTGC CAAATGCCTA AAAATAAAAA 300 TTCTGAGGTG GATCTGTAGC ACAATGGGCT TCTAGTGACA AATCAAAATT CTGATCTTTA 360 AAATGTATGC ACAATTTACC TGTTACCGCC TGGCCTAAGC CATCCTGCTG TTACTGCTGT 420 GTAGCAAGTT GCAGCCAAAG CGACCTCACA CGGCTCCTGA AGGTCAAGAA TCTGGGAGCA 480 GCTCAGCTGG ATGGCTGTGA CTCGGGGTCT CATGAAGTGG CCAAGATGCC AGCTAAGGCT 540 GCCGTCTCTG AAGGCTTGAC CTGGCGAGGA TTTGCTTCCA GACTCACTCG CGTGGCTATT 600 GACAGAAGGC CTCAGTTCCA TGCCACATGG CCCGTTCCAC AGAGCAGCTC ACAGCTTGGT 660 AGTAGCTGGC TTCCCCAGAG CGGTATCTGC GAGCAGCGTC CAGATGGAAG CCATGGTGTT 720 CCCTTAAAAC CTGATATGGA GGGTGATTCC CCATCATGTC TGTATTCTGT GGGTCACACA 780 GACCAAGGCC GGTCCACTGT GGAAGGCAAG GACGAGGTTG CCAGTGCCCG GCGGTGGGTG 840 GCCACAGCCA GCCTCCCTGC CAGTGTCCCC CACAGACAAG TTGTCCCTGT AAGACAGGTC 900 AGCTCAGGTC ATTCCGAGCT CAGACCTTCC AACGGCGTCC ATGTCCCTCA GTAAAAGCCA 960 GAGTCCTAAA GGCCTCTTGC CTGCTCTGGC CTCCTCTCAC CATTCTCTGC CATCCTCCAT 1020 CTGCCCCTGG TGTCCCTGAA GTCTTGAACA TGCCGAGCAC ATCCTGCCTC GTATGCTTCC 1080 TGGCCTGGAA TGCACTTGCC CCGGGACACC CTGTGCTGGC TTTAGTGTTT CCTTCCTGTC 1140 TCCTCAAGTC ACCTTATTAT CAAAAGGACT CCGACAGGCT AAGTGTGGTG GCTCATGCCT 1200 GTAGTCCCAG 1210
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