Tag | Content |
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EnhancerAtlas ID | HS050-46695 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:42093260-42096010 |
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) |
REL | MA0101.1 | chr3:42094179-42094189 | GGGGATTTCC | + | 6.02 | ZBTB18 | MA0698.1 | chr3:42093373-42093386 | TATCCAGATGTGT | + | 6.52 | ZNF740 | MA0753.2 | chr3:42094869-42094882 | GGGGGGGGGGCGG | - | 6.64 | ZNF740 | MA0753.2 | chr3:42094865-42094878 | GTGGGGGGGGGGG | - | 6.92 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00063 | chr3:42092425-42097420 | Adipose_Nuclei | SE_01171 | chr3:42093532-42095450 | Adrenal_Gland | SE_01796 | chr3:42093170-42096158 | Aorta | SE_02512 | chr3:42093454-42094851 | Astrocytes | SE_10922 | chr3:42092287-42111479 | CD20 | SE_23272 | chr3:42093552-42094870 | Colon_Crypt_1 | SE_23272 | chr3:42094873-42095350 | Colon_Crypt_1 | SE_25861 | chr3:42092606-42095935 | Duodenum_Smooth_Muscle | SE_26989 | chr3:42093342-42095507 | Esophagus | SE_29565 | chr3:42093028-42096170 | Fetal_Muscle | SE_36966 | chr3:42092627-42095822 | HSMMtube | SE_38230 | chr3:42092646-42095313 | HUVEC | SE_40683 | chr3:42092524-42096138 | Left_Ventricle | SE_42248 | chr3:42092644-42096169 | Lung | SE_44342 | chr3:42092481-42096334 | NHDF-Ad | SE_44918 | chr3:42092630-42094832 | NHLF | SE_45733 | chr3:42092534-42097909 | Osteoblasts | SE_48185 | chr3:42092500-42096165 | Psoas_Muscle | SE_48670 | chr3:42092710-42096154 | Right_Atrium | SE_49555 | chr3:42094889-42095394 | Right_Ventricle | SE_50309 | chr3:42092613-42096199 | Sigmoid_Colon | SE_51166 | chr3:42092564-42096576 | Skeletal_Muscle | SE_51885 | chr3:42094060-42094792 | Skeletal_Muscle_Myoblast | SE_52625 | chr3:42092703-42095816 | Small_Intestine | SE_53513 | chr3:42093436-42094956 | Spleen | SE_54717 | chr3:42092721-42096159 | Stomach_Smooth_Muscle | SE_62800 | chr3:42053253-42125059 | Tonsil | SE_63663 | chr3:42093585-42094806 | HSMM | SE_65769 | chr3:42094487-42095477 | Pancreatic_islets | SE_65769 | chr3:42095634-42096112 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 42093341 | 42093564 | chr3 | 42095202 | 42095393 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I042051 | chr3 | 42092628 | 42097539 |
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Enhancer Sequence | ATGGAGAATT CTGAGTGATC TGGGAGACTG AGAGACCTTT ATCTTTTAAG ACATGAAAGA 60 CAATGGAGGT CTGGCTGCTT CACCCCCAAT TCCCAGAATA CAGTCCTGGT GGCTATCCAG 120 ATGTGTGTGG CTGAGATTTT TTTCCTTCTT AAACTTATTC CTCTTTGAGC CCTATCTTCT 180 CTACTACCCA GTGACGTGAC TCATTTGGAA GCCACCCTGT GCCTTTGTGA TATGACAGCT 240 TAGCATGTGA CCAGCTTTTG AATGATTAAA TCTGCAGACT CCATCAGAAG CAAGGAGTAA 300 TCTGTGAAGT CCAAACTCAC AAAGTAGTTA AAGATGATTA TAAATTAAAG AAGCACCACC 360 TGGGCGGGTC TCTAAGGGAC ATGGCATCAG CCCTGTGCTG AACAGTCCAT TGTGTCATAT 420 CTTAGGGATT ATGTGGCTTG ACATTACTTG CTCTTTCAGC AGTAGCCCTC ACTATAGTCC 480 CCAACCAGTA CCGTCAGCAT CACTGGGAGC TTGTCAGAAA TGCAAATTCT TGGGTCTTCA 540 GACCTCAGAA ACTCAGGCAT GGGGGCCCAG CAATCTGTGT TCTAACAAGC CCTTCAGGAG 600 ATTCTGATGC TCTTTACTGG TTTAGATGAT CTTGTAGACT GGTGCAAAAG TCAGTCCTTC 660 TGGGTTTGGG GGTTGCTCCC ACATAGCCTG GAAGGAGGGA ACAGTAGTCT TATCTGAGGC 720 TTCCTCAGGG AAATAACCCT CCAGCTTAAG GCCTCTTATG CTATTGTTGA GCAGATTCAG 780 CCTCTGATTT AGGAAAGTAG CCAATTGGAG CAAAAAGCAT GATTCAGTCT TGAAGGAAAA 840 AAATAACTTG GGCTACTCTG CGTCATGTGA AGAAGTAACT GGGTCTCGTG TGGATGCCAG 900 TGATAACAGT TGGCATACTG GGGATTTCCT TCTAATCTTT ATTCTGTGTG CATGCAGGAT 960 GTGCATTTAA TCTAGTTGGG ATCCCATTGT ATGCATTGTT CTGTATTGCC CCCTCCCCCA 1020 TTATGAAAGA GTCCCGTGAC ACCACAGTGT TAAGGACTGA GGTGGTAAGG GCTCCAGGAT 1080 GTCAGTGGCT ATCAGAGGTC CCCAGCTCTG AGAAAACTGG TGGCTGAATG CGTAGTCCCC 1140 GAAGAAGTCA TTTTCCCAAG GCATTTGGAG TTGTTGGTGC TACTGGCACA TTTTGGACCT 1200 CTGTTAAGGG GAAAGACAGG GGGAGCTGAC TGACTGGGCT ACTCCATTGC CATTTAGATT 1260 TCCTGACTCT GCAAGCTGGC TGAATGTTGC TTTTTCATGT GCTGCCTGGA CTAAAGCTGT 1320 CTGATTCTTT CCTTCTGAAC AATGGCTGTT TTTATGAGAT CTTGCTTCTC CCAGGCAGTG 1380 GCCCACACAG TGAAGTCTTT TCTTTCCCGT TTGTGTAAGC TAGTGGACCT TATGGACTCT 1440 GTCTGGCTGA CTTTTCTCTA ATGTTTACAG TTCGTGTAGT GTGATAGCCG AGCTCATTTT 1500 CCGTGTGAAG AAAAAGAAAA GGTGGATAAT GGACCGCCTC CCCCTCCCTG CCTCCAGAAA 1560 AAAAGGCACT CAGAGAGAAA AGACTGCAGT CCCATTCAGA GTCGGGTGGG GGGGGGGGGC 1620 GGGGGATGGC AAAGGGGGAG GGTAAAAGAG GACCCTTAGG GCAAATGACT GTTCTGGGGA 1680 TGGGGTGGGG AGTCAGCCTT CTTGGGGGAG CTGGGGATAC TTTGTGTAGG GCCCCATTCT 1740 GTGGTATGGG CTTCTTTCCT CCTGGACCCT GGTGTAGGCT GGAGAAATCA GTATTATGGA 1800 AGCCACTGCC TCCTCACCCC GCCCCCAGGA TCTAGGCCCA GAGGACCTGG CAAAAGCTGG 1860 GTTGGCACCC ACACCCAGGA CCTGCCCGAG CCAAGTCCAC GCTGCCCCTG CCTGACCTGG 1920 GCTGGTCAAG TAGAGTAGGC CTGAACTGCC CGGGTGAAGG AGTATCCCAA GTCCATCATA 1980 CCGCCTTTCC CCTCCCTCAC CAAGGGAAAA TGAAACCCCA CGTGCCGAGG GCTACCTTTG 2040 CTTTTTCTGT TACCTTTGAT GGATTGACTG CTCATCCCAC ACAATTGGGA CCAAAATCTC 2100 TGGCCCTGCA ATCAGTCTGC CCTACTCTGA TGCTTGCTTA AGCTGTGACA AAAGATACTT 2160 GGATGCACAA AGGTCTCTTT TGAGTTTAAT TGGAATTTCT CTAAACACTC TGACTCTCCC 2220 TGAATCTTCC CTGTTTCCTA AGACCAACAT CGTGGAGTCA GTAGATTTAG TGAGCACCTG 2280 CTAATTACCA CTGGGGTGTT GAGGATTCAG GGTAGACAGC GACCTGTCCT TATAAAGCAA 2340 GCTAACATTT GAGTATGTAT CTGTGCATAC TCAATGAAAA ATGAATTTCA TTATTTACCT 2400 GAATAACGAA ATATTCAGGG CTCCTTATGT GCTAAGTACT GTGCTAAGCA CTTTGTCAAC 2460 ATAATCAATA AATACTTTTG AAGTGAGTGA CCTCCTTCAG CACCCCCTTT GGCTGGAGAG 2520 TCAGGCCTGG CTGGTTTCAT GGTCCACCCT GCTGTCCTTC CTCATCTGGT GCCCCAGCCT 2580 GGTAGGCAGA GGCAAGGAGA GGCAGGTACA GGGTGCACCT TGAGAGCCTT GCAAGCCAGA 2640 ATCAGGAGCT TGGGTTTTAT TTTAGCAATG ATAGGAAGCC GTAGGTGAGT TTAAGCAGGA 2700 GAATCATAAA TAACTCACCC CAGGTCACCT CACCAGCAAA TCAGTTATAT 2750
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