Tag | Content |
---|
EnhancerAtlas ID | HS044-00159 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:21650610-21651990 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 |
|
| 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 | GGCCTGTTTT GTTTTTAAAG AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC 60 TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA 120 GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC 180 GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC 240 AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT 300 GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC 360 TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG 420 AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC 480 ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA 540 GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC 600 AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA 660 GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC 720 CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA 780 GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA 840 AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA 900 GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA 960 GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC 1020 TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG 1080 GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC 1140 ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC 1200 GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC 1260 AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC 1320 AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC 1380
|