Tag | Content |
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EnhancerAtlas ID | HS159-00521 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:223925470-223928060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr1:223927699-223927711 | GAAATCACTGCA | + | 6.74 | Nkx2-5(var.2) | MA0503.1 | chr1:223926788-223926799 | AGGCACTCAAG | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr1:223927104-223927119 | TGAACTCCTGACCTC | - | 6.22 | RORA | MA0071.1 | chr1:223927759-223927769 | TGACCTTGAT | - | 6.02 | STAT3 | MA0144.2 | chr1:223926464-223926475 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223925520-223928901 | Adipose_Nuclei | SE_01908 | chr1:223926095-223926935 | Aorta | SE_01908 | chr1:223927075-223928148 | Aorta | SE_09681 | chr1:223926086-223926867 | CD14 | SE_23408 | chr1:223925806-223926930 | Colon_Crypt_1 | SE_23408 | chr1:223927008-223928133 | Colon_Crypt_1 | SE_24051 | chr1:223926231-223926878 | Colon_Crypt_2 | SE_24051 | chr1:223927084-223928100 | Colon_Crypt_2 | SE_25230 | chr1:223926296-223926903 | Colon_Crypt_3 | SE_25230 | chr1:223927114-223928239 | Colon_Crypt_3 | SE_26209 | chr1:223926103-223928290 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223926095-223928145 | Esophagus | SE_31491 | chr1:223923671-223928232 | Gastric | SE_33950 | chr1:223925357-223926983 | HCC1954 | SE_33950 | chr1:223927048-223928269 | HCC1954 | SE_34545 | chr1:223926186-223927072 | HCT-116 | SE_36294 | chr1:223927044-223927974 | HMEC | SE_37129 | chr1:223924560-223926499 | HSMMtube | SE_37129 | chr1:223926584-223928521 | HSMMtube | SE_38254 | chr1:223923616-223925758 | HUVEC | SE_41495 | chr1:223927102-223928062 | Left_Ventricle | SE_42269 | chr1:223925796-223927012 | Lung | SE_42269 | chr1:223927049-223928176 | Lung | SE_50365 | chr1:223925795-223926977 | Sigmoid_Colon | SE_50365 | chr1:223927008-223928158 | Sigmoid_Colon | SE_53249 | chr1:223926157-223926979 | Small_Intestine | SE_53249 | chr1:223927086-223928250 | Small_Intestine | SE_64794 | chr1:223926064-223928210 | NHEK | SE_65644 | chr1:223924602-223925734 | Pancreatic_islets | SE_65644 | chr1:223925909-223927309 | 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: 1 | ID | Chromosome | Start | End |
GH01I223736 | chr1 | 223924574 | 223930136 |
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Enhancer Sequence | AAAAGAAAAA CAACCCAGAA AGAAGGGAAT GTGTCAAAAC CGGGAGAGGG GAAAAAAAAA 60 GGCATGCATG CTTTCAAAAG CACCTTAGGG GCTACAGATG GGCCCTATAC TTAGTGTTGA 120 CACCCAACAG CCATAAAAGA ATCTCACTGT GCCCCCAGGG GAGCACAGGG AAGGTCTGAT 180 TCTAGATTTT TTCTGTGCCA TTTATTTATC TATATCCTCA TGCACAAGTT CTATACTGTT 240 TTAATTGCTG TAGCTTTTTA TGTGTTTAAA CATCTAATAG AGGTAGACTT CCTTCTCTTA 300 GATTTTTTTC TAGCTATGCT TCATATTTAA TTTTTAAATA AACTTATCAG AATCAGCTAA 360 GTTCAAAAAC AATTTTTAAT CTTATTACCT TTTTTTTTCT TTTTTGTGAG ACGGGGTCTT 420 GTTCTGTCAC CCAGGCTGGA GTACAGTGGT ACAATCATAG CTCACTGCAG CCTTGACCTC 480 CCAGGTTCAA AGTGATTCTC CTGCCTCAGC CTCCCAAGTT GCTGGGACGA TAGAAGCATG 540 ACACCACACC TGGCTAATTT TTTAAAAATA ATTTTTATAG AGACAGGGTC TCACAGTATA 600 GTGAGATTTC AGGGTGGTCT TGAAATCCTG AGGGCTCAAG AAATCCTCCA GCCCTGGCCT 660 CCCAAGAGCT AGAATTACAG GCATGAGCCA CCGTACCTAG CCCTATTGCT ATTTTTATTA 720 GCATTACATT AAGTTTATAG GCTAACTTAA GAGGACATGG CATTTTTATG ATAATGAGTT 780 TTTGCAGTCA AGAACGCAGG CCAGTTTTTT TTAAATGGGG TAAATGATTG TCCAAGCGCC 840 TCCAGGCAGG CTCACGTGCA CACTCTGGAG TCAGTGAAGA AGGTGAACAG CTGACAGGAG 900 CAGCCTCCCA GTCAGAGAAG CCCTGCACAC TGTTGCAAAC AGACAGCTTG CATCTGGAGT 960 CTTCTGTGAT CCGAGGAGGA AGCGTGGCTG AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT 1020 GAGTTGGGGA CAATTGTCAG ATTCTAGCAG TGAAAGTGGT TCATGTGCAG GTGCAACCTG 1080 CCCCGCAGTC ACGGGACACA GCCACATGGA GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG 1140 GGAAGAAACA CCCTAACTGC ACTCCTCCCT TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG 1200 GGCCCCCGGT GAGATACCCA TAGAGATCAG CTCCCAGGCA GCAGGATGGA GGGTGTAGAC 1260 TGGACATGAA GAGGCAGCTG GAATGTATCG GGCACTCAGC TCCAGCTCAC CACGATCCAG 1320 GCACTCAAGT TCCCAAGACA ATAGTTTCTG CTCTCAGATA AATGGAATAA TTAAGGATCA 1380 AAAGGTTATC AACAGGTAAC CAAGCATAAA CAGATTTTTT TTTTTTTTTT TTTTAGACAG 1440 AGTCTCACTC TGTGCCCCAG GCTGGAATGC AGTGGTGCAA TCTGGGCTCA CTGCAACCTC 1500 CACCTCCCAG GTTCAAGTGA TTCTCATGCC TCAGCCTCTC CAGTAGCTGG GACTACAGGC 1560 GCGTGCCAAC ATGCCTGGCT AATTTTTGTA TTTTTAGTAA AGATGGAGTT TCACCATGTT 1620 GGCCAGGCTA GTCTTGAACT CCTGACCTCA TGTGATCTGC CCACCTCGGC CTCCCAAAGT 1680 GATGGGATTA CAGGTGTGAG TCACCATGCC TGGCCCATAA GCAGATTTTG TACCTGAGCA 1740 GGAAGGCTAA GAGCTTGTAA CAACTGAACA TTCCCCCCGG AGAGGAAGGC AGGAGTTTTG 1800 CTTGTGCCAA GTGCACTGTT CAGACAGTCC TCTGAGGTAC ACCAAGGTCT GAGTAGCCAT 1860 CCCACCCTCC CCTCTGCCAA AATTTTTGTG TGACTGGAGA GCAGAGCCCT CCTCCAAAAA 1920 TAAAATGAGC ACAAGGAAAA TACTATTTGC AGATACATAA TATTAAAACC ATAGGTCTTT 1980 CTTTTTCTAG TCCCATCCAT ATGGCAACAT TCCAGGAGAG GCCTCCGTCA CTGGAAGGCA 2040 CCCTCAGGGG CTTTCCTGGA GCTAAAAACA GTTTAAGCCA AAAGTTATTT GTAGCATCTG 2100 AGTTAAACTC TTCGTCTCAC CCTTCTCGAG CTAGCTGGCT TATTTTATCC GGACCAGGAT 2160 ATAACAGCTC TAAACAGGCT TTGCCAGGAA GAGACGTCAT GGACTTCAAC CAGGGCACCT 2220 GACCAGGAAG AAATCACTGC AGGATGATCT GAAAGAGTTT TCATAAATTA TTTTACGTAA 2280 GGTAGATTCT GACCTTGATG GGGACAGCCA AGGTTCTGGA CCCTCAGCTG GGAAAGATGG 2340 GACTAAGTCT ACAACTGCTG AGGTTGTAGA ACAGGCTTCT TGTTGGGAGG AACCCTCTTG 2400 TGGACATGGG CCGTCGAGGT GGAGTGAGAG AACACCGTGC CACCTGGACG CTGAAACACC 2460 ATTGAGTCAC CTCTGTTTGA AATGCTTGTT CCCTGGTGCC GTAAAGAAAT AGCACTTGAA 2520 CATAAATTTA ATTTACTCAG CAAGGACATT TTTATACTTT CTGTGAAAGG GTACACTCAC 2580 CAGGAGTTTT 2590
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