Tag | Content |
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EnhancerAtlas ID | HS141-00243 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:21650660-21652700 |
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: 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: 2 | Chromosome | Start | End |
chr1 | 21650806 | 21651685 | chr1 | 21650784 | 21652238 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I021312 | chr1 | 21638973 | 21657659 |
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Enhancer Sequence | GAGTGCGGCC TTGACCATAG CCCATGCAGC CTCGACCATA GCTCATGCAG CCTTGACCTC 60 CTGGGCTCAA GCGATCCTCT TGCCTCAGCC TCCCAAGTAG CTGGGACTAC AGATGTGCAC 120 CACCACACCC GGGCTCATAT AGCTTCTTAA CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG 180 GCCCATCCCC AAGGGAGAAA CCATCCATCA GTGCGGGACT GACAGGGACA CTCCACCCAC 240 TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC TCCAACGGCT GCCACAGCTG TGGTTTACTG 300 ACTTCAGGTC TGACTGCCCT CTCCAGAGCT GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG 360 TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA GAGGACCAGG AGGGGCTCTC CCCACCCCCG 420 CCCCTTTCCC ACATGAAGAG AAACATTTCA GGGTTGAAAA AATGACTCAT TCTCCCCAGA 480 GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA AGGAGCCCGC GGGTCACTTA ATCGGCCTCC 540 CTGCTCTGGC AGAGATGGCT CTGGGCCCCA GGAAGCCAGG GACAAATGGA GGCGGAGGTG 600 GCAGAGATAA GCAGCTAGTG GAGTGTGCCA GCCTCTCCTT CCCCAACCGA GTGTGTCACT 660 GGGCGTCACC CAGCACTGCT CAAGTTGAAC CTGATGCAGA AGAAAAATTC CTCTGGACTT 720 TCCTGAACGA GCTTTATGGC TGACTCACTG CCACCTGGAG CCTGCAAGAA AAGTCACAAA 780 TCACGAAAGA AGGAGAAAAA CAGTTCTCGT TAAGCCATGT CTTCAATGGA GGTATCAGAG 840 GTCGCCAGGA GGAAAGCACA CATGTTTTGT TGTGGGTTTC CTTCTCTAAA GAAACACGTT 900 ACACAATAGA GGGGGGTTGA GACTGGTTGC AAAACTGCAA AATCCAATTT TGTGTACTGG 960 ATTCAATTTC TTCATTAGCT GACACTAAAC ACAGAGACGG GGCCCTTGTG ACTAGATGAA 1020 CCATAAACTG GCTCCAGGAC CACCAACCTG GTACCTGATG GCTTGTTTCT GCTCCCCACT 1080 CTTTCCCTCC ATGCATCTTT CTCTGAGCTT CTGCTCAAGG CAGGTGCCAG GACAAGCCAG 1140 CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG AAGTAACGTC ACAATTAAGG GGCAAGAGGG 1200 GCCAGAGGAC AGAACAGTGC CAGTTCCTCA TCCAGATTGA AATTTGCTTC CAGCTGCCTG 1260 TCCCCACACC AGAAAGGGCA CTCCCTGCTC CCCATGCAGG CTTCTCATCC TCTTTTGCTG 1320 GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT TTTCAGCCAC AAGCAAAACA CACTCAGCCT 1380 TGAAGTCAGA TGCTCTACAG AAGCCTGCAA AAACAGAGTC AGGAGTTGTG TGGCCTTGGC 1440 CGAGTCACCT CACCTCACCA AGCCTCAGCC TCCTCACCTA TTAAATGGGG ACACAATAGG 1500 ACCCACTTCC TTGGAGCTGA CTGAGGTATG AATTGAGTCA ATGCATTCAT TGCTCAGCAC 1560 ACAGCTTAGC TCAAAGTTAA TGCTCAATAA ATTGTGGTTC CCACCTCCTG CTCCACGGAG 1620 CAGACATGAA ACAGGTACGA GAAGCAACGA GAAGGGGCGG CAGCAGAGCA TCAACACACA 1680 GGGAGTCCTG CCTACTGTCC CGACGCCACC CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT 1740 CCGAAGCTGC CGGTGGCACT TTCGCCAGCC ACCTTGTTTC CAAACTTGCT GCCAGCTTCC 1800 CCTAGCGCAG TGATTTCCAC AACGGAGCTC CCGGCTGTGG GAAGGGGGCT TTCTTTGACT 1860 TGTCCTAAAA TGGCCTCACC TGGACCCAGT GGGGTGTGGG GACCAGGGGG CTGGGCCTGG 1920 ACCTATGAGC ATGTTTCCTG CCTCCTCTCA GCCCCCATCC TTCTGCCGCC CCACGTTCTC 1980 AGCCAACAAT AGCTGCTTCC CAGACTCAGC TGCCACACAG CACGAGCTCC CTGAGCAAAA 2040
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