Tag | Content |
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EnhancerAtlas ID | HS110-00086 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr1:21650490-21652830 |
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) |
JUN(var.2) | MA0489.1 | chr1:21651121-21651135 | ATGACTCATTCTCC | - | 6.04 | JUN(var.2) | MA0489.1 | chr1:21651116-21651130 | AAAAAATGACTCAT | + | 7.52 | Nkx2-5(var.2) | MA0503.1 | chr1:21652787-21652798 | CTTGAGTGCCT | - | 6.14 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21640019-21654616 | Adipose_Nuclei | SE_00854 | chr1:21648312-21655068 | Adrenal_Gland | SE_01643 | chr1:21650385-21655084 | Aorta | SE_02944 | chr1:21650503-21654392 | Bladder | SE_03598 | chr1:21650640-21651193 | Brain_Angular_Gyrus | SE_03598 | chr1:21651214-21652589 | Brain_Angular_Gyrus | SE_04518 | chr1:21650430-21654343 | Brain_Anterior_Caudate | SE_05710 | chr1:21650819-21652666 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21650172-21654641 | Brain_Hippocampus_Middle | SE_08398 | chr1:21650274-21654628 | Brain_Inferior_Temporal_Lobe | SE_08982 | chr1:21651888-21652526 | Brain_Mid_Frontal_Lobe | SE_26127 | chr1:21650420-21654272 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21650381-21654470 | Esophagus | SE_28486 | chr1:21650385-21652524 | Fetal_Intestine | SE_29337 | chr1:21650482-21652798 | Fetal_Intestine_Large | SE_31433 | chr1:21650314-21655007 | Gastric | SE_39164 | chr1:21650503-21653287 | IMR90 | SE_42174 | chr1:21650278-21654424 | Lung | SE_44380 | chr1:21650380-21654322 | NHDF-Ad | SE_45045 | chr1:21650463-21654349 | NHLF | SE_46660 | chr1:21650609-21653070 | Ovary | SE_47592 | chr1:21650567-21653016 | Pancreas | SE_48583 | chr1:21650390-21654421 | Right_Atrium | SE_50108 | chr1:21650386-21654252 | Sigmoid_Colon | SE_52633 | chr1:21650385-21654180 | Small_Intestine | SE_53334 | chr1:21650242-21653182 | Spleen | SE_54639 | chr1:21650371-21654862 | Stomach_Smooth_Muscle | SE_56171 | chr1:21650384-21653718 | u87 | SE_65263 | chr1:21650278-21654762 | Pancreatic_islets | SE_67931 | chr1:21650384-21653718 | u87 | SE_68932 | chr1:21650478-21654339 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 21650806 | 21651685 | chr1 | 21650784 | 21652238 | chr1 | 21652399 | 21652754 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I021312 | chr1 | 21638973 | 21657659 |
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Enhancer Sequence | TTTTAGTAGA GATGGGTTTT TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA 60 GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC 120 GGCCTGTTTT GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC 180 TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA 240 GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC 300 GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC 360 AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT 420 GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC 480 TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG 540 AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC 600 ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA 660 GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC 720 AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA 780 GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC 840 CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA 900 GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA 960 AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA 1020 GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA 1080 GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC 1140 TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG 1200 GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC 1260 ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC 1320 GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC 1380 AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC 1440 AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC 1500 TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA 1560 TGCTCTACAG AAGCCTGCAA AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT 1620 CACCTCACCA AGCCTCAGCC TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC 1680 TTGGAGCTGA CTGAGGTATG AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC 1740 TCAAAGTTAA TGCTCAATAA ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA 1800 ACAGGTACGA GAAGCAACGA GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG 1860 CCTACTGTCC CGACGCCACC CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC 1920 CGGTGGCACT TTCGCCAGCC ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG 1980 TGATTTCCAC AACGGAGCTC CCGGCTGTGG GAAGGGGGCT TTCTTTGACT TGTCCTAAAA 2040 TGGCCTCACC TGGACCCAGT GGGGTGTGGG GACCAGGGGG CTGGGCCTGG ACCTATGAGC 2100 ATGTTTCCTG CCTCCTCTCA GCCCCCATCC TTCTGCCGCC CCACGTTCTC AGCCAACAAT 2160 AGCTGCTTCC CAGACTCAGC TGCCACACAG CACGAGCTCC CTGAGCAAAA ATACCCATGC 2220 GGGGGAGGGT GGGGAGGTAC AGGAGGGGCC ACAAATGGGG AGGGCTGGGA GAAGGGGTGG 2280 CAGGATCAAG CTTGTCTCTT GAGTGCCTAC TGTGTGTCAA GCTGAGAAGG GTGAAGCCCC 2340
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