| Tag | Content |
|---|
EnhancerAtlas ID | HS109-00251 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:21650530-21652170 |
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: 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 |
|
| | 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 | CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC 60
AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG AGACAAGGTC TCACTCTGTT 120
GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG 180
CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC 240
AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA 300
GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA 360
CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG 420
TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT 480
GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC 540
CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT 600
TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA 660
ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA 720
GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA 780
GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC 840
CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA 900
AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA 960
GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA 1020
GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT 1080
TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG 1140
ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT 1200
GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG 1260
GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG 1320
GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC 1380
CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC 1440
TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC AAGCAAAACA 1500
CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA AAACAGAGTC AGGAGTTGTG 1560
TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC TCCTCACCTA TTAAATGGGG 1620
ACACAATAGG ACCCACTTCC 1640
|
