Tag | Content |
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EnhancerAtlas ID | HS185-00127 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:21650560-21651730 |
Target genes | |
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 |
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| Number of super-enhancer constituents: 30 | 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_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: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I021312 | chr1 | 21638973 | 21657659 |
|
Enhancer Sequence | TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT 60 GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG 120 CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT 180 TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT 240 AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA 300 CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT 360 CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT 420 CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA 480 CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG 540 AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA 600 GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT 660 CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG 720 GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT 780 CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC 840 TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA 900 CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA 960 CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA 1020 GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT 1080 GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC 1140 CACCAACCTG GTACCTGATG GCTTGTTTCT 1170
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