Tag | Content |
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EnhancerAtlas ID | HS147-00653 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:21650330-21652970 |
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 | GACATAGTTT CACTCCATTG CCCAGGCTGG AGTGCAATGG TGCAATCTCG GCTCACTGCA 60 ACCTCCACCA CCCGGGTTTC AAGCTATTTT CCTGCCTCAG CCTCCTTGAG TAGCTGGGAT 120 TACAGGTATG CACCACCATG CCCGGCTAAT TTTTTTGTAT TTTTAGTAGA GATGGGTTTT 180 TGCCATGTTG GTCTGGCTGA CCTCAAACTC CTGACCTCAA GTGATCCACC TGCCTCAGCC 240 TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACTTCACCC GGCCTGTTTT GTTTTTAAAG 300 AGACAAGGTC TCACTCTGTT GCCCAAGCTG GAGTGCGGCC TTGACCATAG CCCATGCAGC 360 CTCGACCATA GCTCATGCAG CCTTGACCTC CTGGGCTCAA GCGATCCTCT TGCCTCAGCC 420 TCCCAAGTAG CTGGGACTAC AGATGTGCAC CACCACACCC GGGCTCATAT AGCTTCTTAA 480 CTGGGTGGGC AGAGGAAGCA GGGGGCAGAG GCCCATCCCC AAGGGAGAAA CCATCCATCA 540 GTGCGGGACT GACAGGGACA CTCCACCCAC TCAGCCCAGT GTGCTTCTGT CCAGGGAGAC 600 TCCAACGGCT GCCACAGCTG TGGTTTACTG ACTTCAGGTC TGACTGCCCT CTCCAGAGCT 660 GCCCTAGAAT CCCTTTGTCT GTGGCTGAAG TGTCCCTCAG AGCTGAGGAA CAAGTTTGGA 720 GAGGACCAGG AGGGGCTCTC CCCACCCCCG CCCCTTTCCC ACATGAAGAG AAACATTTCA 780 GGGTTGAAAA AATGACTCAT TCTCCCCAGA GAGGGCTGGA GCTGAGCTGA GTCAGGCAGA 840 AGGAGCCCGC GGGTCACTTA ATCGGCCTCC CTGCTCTGGC AGAGATGGCT CTGGGCCCCA 900 GGAAGCCAGG GACAAATGGA GGCGGAGGTG GCAGAGATAA GCAGCTAGTG GAGTGTGCCA 960 GCCTCTCCTT CCCCAACCGA GTGTGTCACT GGGCGTCACC CAGCACTGCT CAAGTTGAAC 1020 CTGATGCAGA AGAAAAATTC CTCTGGACTT TCCTGAACGA GCTTTATGGC TGACTCACTG 1080 CCACCTGGAG CCTGCAAGAA AAGTCACAAA TCACGAAAGA AGGAGAAAAA CAGTTCTCGT 1140 TAAGCCATGT CTTCAATGGA GGTATCAGAG GTCGCCAGGA GGAAAGCACA CATGTTTTGT 1200 TGTGGGTTTC CTTCTCTAAA GAAACACGTT ACACAATAGA GGGGGGTTGA GACTGGTTGC 1260 AAAACTGCAA AATCCAATTT TGTGTACTGG ATTCAATTTC TTCATTAGCT GACACTAAAC 1320 ACAGAGACGG GGCCCTTGTG ACTAGATGAA CCATAAACTG GCTCCAGGAC CACCAACCTG 1380 GTACCTGATG GCTTGTTTCT GCTCCCCACT CTTTCCCTCC ATGCATCTTT CTCTGAGCTT 1440 CTGCTCAAGG CAGGTGCCAG GACAAGCCAG CGTCTCGAGC GGTTCCCCTT CAGCGGTGAG 1500 AAGTAACGTC ACAATTAAGG GGCAAGAGGG GCCAGAGGAC AGAACAGTGC CAGTTCCTCA 1560 TCCAGATTGA AATTTGCTTC CAGCTGCCTG TCCCCACACC AGAAAGGGCA CTCCCTGCTC 1620 CCCATGCAGG CTTCTCATCC TCTTTTGCTG GCCTCCTCCC TCCTCGCTGT CCCTGGTCTT 1680 TTTCAGCCAC AAGCAAAACA CACTCAGCCT TGAAGTCAGA TGCTCTACAG AAGCCTGCAA 1740 AAACAGAGTC AGGAGTTGTG TGGCCTTGGC CGAGTCACCT CACCTCACCA AGCCTCAGCC 1800 TCCTCACCTA TTAAATGGGG ACACAATAGG ACCCACTTCC TTGGAGCTGA CTGAGGTATG 1860 AATTGAGTCA ATGCATTCAT TGCTCAGCAC ACAGCTTAGC TCAAAGTTAA TGCTCAATAA 1920 ATTGTGGTTC CCACCTCCTG CTCCACGGAG CAGACATGAA ACAGGTACGA GAAGCAACGA 1980 GAAGGGGCGG CAGCAGAGCA TCAACACACA GGGAGTCCTG CCTACTGTCC CGACGCCACC 2040 CAGAGGCTCA AGGGGTGCCC CGGCTGCTCT CCGAAGCTGC CGGTGGCACT TTCGCCAGCC 2100 ACCTTGTTTC CAAACTTGCT GCCAGCTTCC CCTAGCGCAG TGATTTCCAC AACGGAGCTC 2160 CCGGCTGTGG GAAGGGGGCT TTCTTTGACT TGTCCTAAAA TGGCCTCACC TGGACCCAGT 2220 GGGGTGTGGG GACCAGGGGG CTGGGCCTGG ACCTATGAGC ATGTTTCCTG CCTCCTCTCA 2280 GCCCCCATCC TTCTGCCGCC CCACGTTCTC AGCCAACAAT AGCTGCTTCC CAGACTCAGC 2340 TGCCACACAG CACGAGCTCC CTGAGCAAAA ATACCCATGC GGGGGAGGGT GGGGAGGTAC 2400 AGGAGGGGCC ACAAATGGGG AGGGCTGGGA GAAGGGGTGG CAGGATCAAG CTTGTCTCTT 2460 GAGTGCCTAC TGTGTGTCAA GCTGAGAAGG GTGAAGCCCC TGGGGGTTAG AGAAACCTGG 2520 GAGACCGTGG GGTGTGTGTG TCGGGGGTGC TGGTCTCTAA GACAGCAGAG CCTCCAGTCC 2580 CCAGAGAGGG ATCAGACCCA GGTCCAGGGT CTAAGGGTGA AGAAGGGGTC CAGGGAGAAG 2640
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