Tag | Content |
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EnhancerAtlas ID | HS003-00230 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:9399530-9402600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr1:9399763-9399780 | AGGGTCGCCCTGACCTC | - | 6.14 | ESR1 | MA0112.3 | chr1:9399763-9399780 | AGGGTCGCCCTGACCTC | + | 6.48 | MAFF | MA0495.3 | chr1:9400530-9400545 | TTGCTGCCTCAGCAG | + | 6.18 | MAFF | MA0495.3 | chr1:9400530-9400545 | TTGCTGCCTCAGCAG | - | 6.21 | MAFG | MA0659.1 | chr1:9400527-9400548 | GTCTTGCTGCCTCAGCAGAAA | + | 6.26 | MAFG | MA0659.1 | chr1:9400527-9400548 | GTCTTGCTGCCTCAGCAGAAA | - | 6.46 | MAFK | MA0496.2 | chr1:9400528-9400547 | TCTTGCTGCCTCAGCAGAA | - | 6.26 | RARA(var.2) | MA0730.1 | chr1:9400078-9400095 | AGGTCACCCAGAGGTCT | + | 6.71 | RREB1 | MA0073.1 | chr1:9401289-9401309 | ACACACACCACTCCCCACCA | + | 6.11 | SPI1 | MA0080.4 | chr1:9401151-9401165 | CACTTCCCCTTTCT | - | 6.22 | SPIB | MA0081.2 | chr1:9401151-9401163 | CACTTCCCCTTT | - | 6.07 | ZNF263 | MA0528.1 | chr1:9401356-9401377 | GAGGGAGGCAGTGGGGGAGAG | + | 6.08 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_00563 | chr1:9398014-9401867 | Adipose_Nuclei | SE_01570 | chr1:9396605-9401557 | Aorta | SE_04130 | chr1:9399267-9401741 | Brain_Anterior_Caudate | SE_05868 | chr1:9397588-9401442 | Brain_Hippocampus_Middle | SE_23818 | chr1:9397648-9399972 | Colon_Crypt_2 | SE_24876 | chr1:9397269-9400977 | Colon_Crypt_3 | SE_26667 | chr1:9397116-9401645 | Esophagus | SE_26667 | chr1:9401990-9403019 | Esophagus | SE_32227 | chr1:9398097-9400869 | Gastric | SE_46801 | chr1:9399337-9399973 | Ovary | SE_46801 | chr1:9400573-9401182 | Ovary | SE_50208 | chr1:9399747-9401626 | Sigmoid_Colon | SE_52461 | chr1:9397815-9401627 | Small_Intestine | SE_65576 | chr1:9397177-9400464 | Pancreatic_islets | SE_65576 | chr1:9400475-9401380 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I009337 | chr1 | 9397919 | 9401060 | GH01I009341 | chr1 | 9401991 | 9403019 |
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Enhancer Sequence | GGGAAGGCTC CGTGGAGGAG GGGCCCCTGG AAGATCCCAC ACAGATGGGA TTCCTGTCAG 60 ATGGGGTTGT TTGAAGTGAA AAGAACATCG TTATAACTCA TGTGGTTCTT AAGGACTAGC 120 AGGGCTGGTG TGGCCACTGG TGTCTAAGGG ACCTTTGGAG AAGCTGAGAG GGCCTGTCAG 180 GGGCTTGGAA GGTGGAGAGC AGGGACCCTG TGAGGAGGGG AGGGGCCTCC AGCAGGGTCG 240 CCCTGACCTC TGTCTTCCCA GACCCCGAGT GACTGATGGC TTCTACAGGG TCTGGGCAAG 300 GGGATCGGCA GCCTGTTTAT GTGCCCTGCC CCCCATTCTT GTGGACCTGG TGGCAGGACA 360 GGGGAAGCTG CCTGCTCCTT CCGTGGCACA GGTCGGCCTC TAGATGTGGC TGGTTCAGGT 420 CAGTTGTATT TTAGGATTGG CTTGGAGAGG GATGGGAGCC CCTCCACCTT TTCCTTCTGA 480 TGTGTGTTTC CTCCAGCCCC CCACCTCGGG AGGACCCCCA CCGACAGCCC TGAACCACCT 540 GGGCATGCAG GTCACCCAGA GGTCTGGGGC TAGTGCCATT CAGGGGCAGT AGCCCGAGAC 600 TCTGCATTTC CAGCAAGCTC CTGGGTGATG GTCTGTGGGC CGCCCTAGGG TCACCGGGTG 660 CAGGGCACGC AGGGTGACCA GTTCCCTCGC CCCTGTAGGA ACTGTTCTCA AGAGAGGAGA 720 CAGACTCTCC TTGGGCAGGC TTTCTCTCCT GTCTGGTTTT CCATTTGGGG GCCTAGAGAA 780 GGGGTGCTGT CAATCAGCAG AGGAGGGGCC TGGGGGGGAA GGCAGGGACA CTGGTGTTTG 840 GGGACTGGCC GGAGCCCCGC GGTCTGACTT TCACACGGAT TCCTGCCACC AGCCCAGCTG 900 CCGATACAAT TAAACCTCAG TGATTCACTG TAGTGCATGT CAAGGCAAGG CGTTGTGTTA 960 TGAAAACGTG GGTCCCAGAG GTTTGTTTTG TTGGCAGGTC TTGCTGCCTC AGCAGAAAAG 1020 AGGCGCTTTT GATATGGGAA CGGAAACTTG GGACCATGTT AGAAATAGTG TGTTCGGCAG 1080 AGAGGACCTT GGTCCTCCTC CAGCTGTGGA AACTCCACGC CTGGCGGGAA GATGGCAGCC 1140 TGTGGGGCTG GGGAGGGTCC CCGCAGCACC TGGGTCTGCG GTCTGAGCCG CCTGTGCTGT 1200 GATGTGGCCG GCCTTCCCTG CCACCGAGGG GCGTGGGATG CACCCGTCCC CTGCTCGCCC 1260 CTCTGCCTGC AAAGGTAACA TGCTGCTGTT TTTTATTTTA TGGAAAGTCC AGCTTGCAGA 1320 GGAAATACCT TTCTCAACGC AGCCTGTCTG ATGTCGCGGA GCAGCTCTGC CCAGCAAGGC 1380 GAGCACATGA AACGCACATT TGTAGTCCTC CTGTGTACCT GGCTGCGGTG CGGGGAGGCA 1440 GAGTGGGAAG GGGAGAAGAC TGGTCTAGCT CAAAAGGCCA GTCCTGGGCT TCAATTTCCA 1500 ACACTGGGCT GACTCTGCTG GGACAAGCAA CTGCCTCTGT TCTTGTCTCT TCCTCCTCGG 1560 GCCCTGATTG CTGGCCTGGA CTAGCCCATT CAATGGATAT TGGGCCAATT TCCCTTTTTT 1620 CCACTTCCCC TTTCTTCCCC TTGTGTTCTC AAAATGTGAT AAATGGAATA GGCACACCCC 1680 AGATCCAAGT TGCTTTTCTG AGAAACTTCC CGCAGTACTT AGGTCCTGGC CCCCCGGCCT 1740 CAGAACAGAG AGGCACGGTA CACACACCAC TCCCCACCAG GGCACTGCAG ACCTATGTCC 1800 AGGCTGCCAC CCCTTCCCAA GGGCATGAGG GAGGCAGTGG GGGAGAGTTC GGAGATGCAG 1860 GTAGAACCTC CGCCAGCAGC CCCTTCCCCT GAAGCTTGCA CTCATTGTTC AGATGATTGG 1920 GTGTTGCCTG CCTCCCCCCA CTAGACTGAG CTCCCTGAGG GCAGCAAGTT CTGCCTGTTC 1980 TGTGTATCCA GTAGGTGCTT AATACTTTTG GAATGAATTC CAGCCCTGAG GCACATTATT 2040 TGGACTTGGG TGTTTTCCCA CTGTTCACCA GCTGAACATT GCCAGACCAT CTCTCTGGTT 2100 GGGTCACTTC TGCCGGTGAC ATCTTGTCCA TGTTGTTTGT TCTTTCCAGT TTCCTCTTGG 2160 GAGAGATGTT TTCTAGCAGT TCGGAGGAAG GCCTGTTCTC CCTTCCTGAA CGGTGACCAC 2220 GCTGGCCTGT GTTTTTGTTT GTTTTTTTGA GACGGGGTTT CACTCTTGTT GCCCAGGCTG 2280 GAGTACAATA GCGCGATCTC GTCTCACCGC AATCTCCACC TCCCGGGTTC AAGCGATTCT 2340 CCTGCCTCAG CCTCCTGAGT AGCTGGAATT ACAGGCATGC ACCACCACGC CCAGCTAATT 2400 TTGTATTTTT AGTAGAGATG GGGTTTCTCC ATGTTGGTCA GGCTGGTCTC GAACTCCCGA 2460 CCTCAGGTGA TCTGCCCGCC TCAGGGTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC 2520 ACGCCCAGCC TAGTTGGCCT GTGTTTTGAA TTGGCCACCT TGTTGAGGCA CTCAGGGACT 2580 GAGAAACAAA GCAAGGTCTT GAGAAGCTCA TTCTAACCTG TCTTAGGGGC TTAGCAGATA 2640 CTTGTGGGGT GGGTGAGCAA GCGACTCAGA GCACAGGCCT CAGATGGTGG AGTTCTCGGC 2700 CGACTTCCCA TGTTCCATGT GAGTGAGCCT GGCCAGGAGA GGATCCGTGG GCAGTGGCAG 2760 CACCTGGCAT GAGACACCTG GGCTGTGCCA GGCCTGTGAG TGACGATCCC TCCGTGAGAA 2820 TGAAGAAATG CAACCCATGA GAAGAGGTTT GCGTAGTGAC AAGTCCAGAA ACTGTGTGCA 2880 TCAGCCTGGG GCACCCCTAG CTGTGGGCAG AAGCTCCATG GTGCAGCTCA TAGTGGCAGT 2940 CAGGCCCCAG CGTCAACCGT GGGAGAGCAC GGAGGATCCC AGTGGCTTGT CAATTCGCTG 3000 ATAGCAGAAG GTAGGGCCTT TGCCAGTTTG GAGCTGCCTC AGGGTGTTGA CCTGCTCAGT 3060 GAGAAAGTAG 3070
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