Tag | Content |
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EnhancerAtlas ID | HS105-14048 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:48063120-48065020 |
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) |
Arid3b | MA0601.1 | chr11:48063178-48063189 | TTAATTAATAT | - | 6.62 | HES2 | MA0616.2 | chr11:48063318-48063328 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr11:48063318-48063328 | GGCACGTGCC | - | 6.02 | LMX1B | MA0703.2 | chr11:48063175-48063186 | GTTTTAATTAA | + | 6.14 | MAX | MA0058.3 | chr11:48063911-48063921 | AGCACGTGGT | - | 6.02 | RREB1 | MA0073.1 | chr11:48063531-48063551 | GGTGGGGGGTGGGTGGGGGG | - | 6.39 | RREB1 | MA0073.1 | chr11:48063534-48063554 | GGGGGGTGGGTGGGGGGTGG | - | 7.36 | RREB1 | MA0073.1 | chr11:48063530-48063550 | AGGTGGGGGGTGGGTGGGGG | - | 8.36 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_03421 | chr11:48063262-48064768 | Brain_Angular_Gyrus | SE_03421 | chr11:48064774-48067106 | Brain_Angular_Gyrus | SE_04152 | chr11:48062445-48068430 | Brain_Anterior_Caudate | SE_04959 | chr11:48061395-48068282 | Brain_Cingulate_Gyrus | SE_05925 | chr11:48061892-48068498 | Brain_Hippocampus_Middle | SE_06855 | chr11:48062112-48068375 | Brain_Hippocampus_Middle_150 | SE_07812 | chr11:48060464-48067951 | Brain_Inferior_Temporal_Lobe | SE_09330 | chr11:48064727-48067578 | CD14 | SE_18489 | chr11:48063305-48067532 | CD4p_CD25-_Il17-_PMAstim_Th | SE_31537 | chr11:48063135-48063636 | Gastric | SE_31537 | chr11:48064079-48064524 | Gastric | SE_31537 | chr11:48064725-48066595 | Gastric | SE_50361 | chr11:48064716-48067399 | Sigmoid_Colon | SE_53524 | chr11:48064090-48067461 | Spleen | SE_58324 | chr11:48000812-48132698 | Ly1 | SE_58941 | chr11:48001036-48074784 | Ly3 | SE_59630 | chr11:47995176-48103510 | Ly4 | SE_61339 | chr11:48001402-48074705 | HBL1 | SE_62429 | chr11:48001045-48086363 | Tonsil |
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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: 2 | ID | Chromosome | Start | End |
GH11I048042 | chr11 | 48063635 | 48064268 | GH11I048043 | chr11 | 48064753 | 48066952 |
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Enhancer Sequence | AAAGCTGAAA GGCTTTATCC CTGAGACTCA GGGAAATATG ACAATCTTTT ATTTTGTTTT 60 AATTAATATT TTTTGAGTCA GCGTCTTGCT TTGTCACCCA GGCTGGAGTG CAGTGGTGCA 120 ATCATGGCTC GCTGCAGCCT CAACCTCCTG GGTTCTAGCG ATCCTCCCAC CTTAGCCTCC 180 TGAGTAGATG GGACCACAGG CACGTGCCAC CATGCCTGGC TAATTTTTGT ACTTTTTGTA 240 GAGATGGGGT TTTGCTGTGG TCTCAAATTC CTGAGCTCAA GCAATTGGCC TGACTCAGCC 300 TCCCAAAGTG TTGGGATTAC AGGTATGAGC TACCGCACCC AGCCTGACAA TTTTTTAAAC 360 AGAATTTTAG GTGCTTGGGC CCTGGAAGGT TCCCAGTTGT CCAACTCTTG AGGTGGGGGG 420 TGGGTGGGGG GTGGAGAGAG AGAGAGAGAG GAAGGCTTTT CCTTCTCAAA TAGTTTGCAT 480 TTACACGAAG GCCACGGTGT ACTTGTTTAT TGAATCAATA AAGATACAAT CTCTTTGAAT 540 AGTTCAGAAT CTGATATCCC TGTTAGACTG AGTTCACCTT TTGTGAAGGA CACAGGACTG 600 CTGGATAGGG TGTTGCAGCA ATGAGGAGTT ATGTTATAAG GGGTCTCTTC AGTGTCTTTT 660 TGGTCATATG AATTTTATTT GCCCAGTAGA ACATGACTGA TGAGGCTCTG AATAGTCAAA 720 GAAAACATCT CTCTTATGTT CTGCTCATGA ATAGAACACT CTGTGTCCTG AATTGTTGCT 780 CCACTGGGGC CAGCACGTGG TGTATTTTTC TAATGTTTGA ACCAATGGGC TTTTTCATTT 840 TGGGGCAATC AAGGTAAAGA TTTTCTGGTG CTCCTGTGTG ACAGGGAAAG CATGTCTTGT 900 ATTTTCTCTC TCTTTCCCTT CTGTCTTTTG AGTTTGGAAA ATTATATTTT GAGTTACATG 960 ACTAATTACA TGAGTAATTT TAGCAAATTT ACTAGAAATT GATGTTCTGC CAATGATTGG 1020 AAATCCCTTC CTCCCCTCCA CTCTTCTAAA CCAAAACAGT GCTGTGTCCT GAAGCTAGAG 1080 GGGTGAGTAT TCAGTATTGG AGTACAGCGG TTTAGAACAT TGGAGACATT TACAAGGATA 1140 AATCTATGGC CCTGGGTTCT GACTTTCTTT TGCCTGTGTG TGTGTGTAGG GGTGTGTGTG 1200 TGTGTGTGTG TGTGTGTGAG AGAGAGAGAG AGAGAAAGAG AGTAAGAGAG AGCGAGCTGG 1260 GTTTGGGGCT GGGAAGGAAG AATGATTGAT TAGGAAGCTG TTGTGCAGAG TAGAACAGGA 1320 CTTCCTGAAA TGTAAGACCC AAAGAAACAT AGATAGCCAT ATTTTCCAGT CCTGGAATCA 1380 GACTCAAGTC TGATAAAAGG TTTTCTTTTG ATTTGTGATT CTGATAATAT GAAAAGTCTT 1440 ACAAAAGTAT AGAATTGTAG CTGGTAGGCT GCTTTATGAG AAAGAAAATA AACTCCCACA 1500 GAGTGGGCAT TGACCTGGGA GATCTGGAGC CTGGTGCAAG TGCAGACCAT GGTTTTCACA 1560 ATCTTTGATC ACTTTCCTTT TGTGTTGAAC TTTCTCTTTT AGCTCCATAT TTATAAATGG 1620 GGTCATATTT AGCCAGATAT TTTATTTTTA TTTTTATTTT TAAAGAGAGG CAGGATCTTG 1680 CTGTGTTGCC CAGGCTGGAG TGCAGTGCCA TGATCATAGC TCACTGCAGC TTCGAACAGG 1740 GCACAAGCCA TCCTCCCATT TCAGCTTCCT GAGTAGCTGG GATTACAGGC AGGAGCCACA 1800 TTTCCTGGCT TCTAGTTGGG TTTTTTTGTT TCTGGAAGAA CAGAACCATA CTCCTCAGGC 1860 CAGGAAGACC TAGGTAGAGC AAGACCAGCA ACCTCTTGGC 1900
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