Tag | Content |
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EnhancerAtlas ID | HS050-06003 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:223935440-223936740 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr1:223936435-223936446 | CTTTCCCGCCC | - | 6.32 | GATA2 | MA0036.3 | chr1:223936005-223936016 | AGAGATAAGAA | - | 6.32 | Gata1 | MA0035.3 | chr1:223936005-223936016 | AGAGATAAGAA | - | 6.32 | RORA(var.2) | MA0072.1 | chr1:223936034-223936048 | AAAATCTAGGTCAG | + | 6.14 | SREBF2 | MA0596.1 | chr1:223935650-223935660 | ATGGGGTGAT | + | 6.02 | Zfx | MA0146.2 | chr1:223936617-223936631 | CAGGCCTCGGCCGC | - | 7.95 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223934158-223937983 | Adipose_Nuclei | SE_01908 | chr1:223935156-223937517 | Aorta | SE_02306 | chr1:223935517-223937238 | Astrocytes | SE_03438 | chr1:223935748-223936798 | Brain_Angular_Gyrus | SE_04026 | chr1:223935516-223937349 | Brain_Anterior_Caudate | SE_05036 | chr1:223934795-223935890 | Brain_Cingulate_Gyrus | SE_05036 | chr1:223935985-223937127 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223934663-223937571 | Brain_Hippocampus_Middle | SE_07159 | chr1:223935466-223937127 | Brain_Hippocampus_Middle_150 | SE_07996 | chr1:223935109-223937042 | Brain_Inferior_Temporal_Lobe | SE_23408 | chr1:223935446-223936989 | Colon_Crypt_1 | SE_24051 | chr1:223935677-223936100 | Colon_Crypt_2 | SE_24051 | chr1:223936159-223937066 | Colon_Crypt_2 | SE_25230 | chr1:223936038-223937178 | Colon_Crypt_3 | SE_26209 | chr1:223934955-223937096 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223935278-223937175 | Esophagus | SE_31491 | chr1:223935283-223937172 | Gastric | SE_33950 | chr1:223935223-223936500 | HCC1954 | SE_34545 | chr1:223936173-223937185 | HCT-116 | SE_37129 | chr1:223934990-223937353 | HSMMtube | SE_38254 | chr1:223934520-223937640 | HUVEC | SE_41495 | chr1:223935110-223937269 | Left_Ventricle | SE_42269 | chr1:223934542-223937274 | Lung | SE_45872 | chr1:223935399-223937657 | Osteoblasts | SE_49408 | chr1:223935446-223937062 | Right_Atrium | SE_50365 | chr1:223934678-223937079 | Sigmoid_Colon | SE_53249 | chr1:223935441-223937088 | Small_Intestine | SE_65644 | chr1:223934516-223937226 | 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 |
GH01I223746 | chr1 | 223934513 | 223937570 |
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Enhancer Sequence | TAGCTTCCTC CTGTGCTTTG GGGGAGAGTG GATCGAGAGA CAGAAGGAAA GGGGAGGTCA 60 GAGAGATCTT GAGGCTTCTT CAGTTTAGCA TTTCAAAGTG CCATCTCTTA GAGGTATTGG 120 TTTCTGAGCA CCCCAGTGTC TACCATTATT GCTCATCACC TGGAAGCCAA GGGTTGCTAG 180 GCAAAAGTCA AGCTGTCTGG GGTGTAATGG ATGGGGTGAT GGTGCCTCCA GCCCTTCTGT 240 CTTCAGTCCA CTTCCCACTC TTAGCCTGCT CTGAATCACC CCCACCCCTC TGACCACAGG 300 TTCCCTGGGA GCCCCTGCCA CCTGCTGCCC CTGCCACCTT CCCCTCCATC TGCAGTGCTG 360 TGCAGCCTTC CCCTGCACTC TTGCAGAGCT AATAGGCCCG TGGGAGACTT CGGAAGGAAG 420 AGGAGGAAAG ATTTCCTCAT AATAGCCTTG CTGGCAACGC TCACCAGGGG ATGGGAGGTG 480 GGCACTGTGC CCAGGAGCCT TGGAGCAAAG GCTGTGCCCA ACCTCTGAGC CCTGTCCCAT 540 CCAGGTTCTG GTCTCTGCGG GGGACAGAGA TAAGAAGCCC TGGCTTTTGG AGCCAAAATC 600 TAGGTCAGAC TCCCTAGGCA GGAATTCTCA AAGTTTATCA GCAGAACACG TTGAGGCAGA 660 AGACCCTTTC TGCTCCAGCC CTTCTTCCCA GGCTCAACCT TCATCAGAAT AGATAGGGGA 720 AAGGAGAGGC TGTGAGGCGT TCTTAAAACA GAAGCAAATT CTGACTCAGA CCGGAATAAA 780 CAACCGTCCT AGTATAAACC CTACAGCTGG GCTGGGCCAG ACCACGGAGC ATGGGCTGGT 840 GGTGGGGCGA GGGTGTGCTC AGTGTCCCTG GGCCACTCAA GGCTGTCTGG GTATCAGCCC 900 TGCGCCATCG AGGACCCCCT CCGGCCCTCT CTCGGCCGTG CGCCCTTTCC CTGCGCCATC 960 GAGGACCCCC TCCAGCCCTC TCTCGGCCGT GCGCCCTTTC CCGCCCTTCC CAGCCTGCAG 1020 AAATCCGTGG ATGCGCTATT CACACGGGAA TGCCTGTGCT CGTTCCGCGA GAGGGTTGCA 1080 TTCCGCCTTT TCTCTGGTAT TCTCGGCGTT CAAGCATTTG AACGGGGTAG GAAAGGTTCT 1140 CCAAGTGCAA GAAAGCGCAG CCCTGAGCCT CCCACCCCAG GCCTCGGCCG CTGCGCTAGT 1200 GCGTCCGGCG GTCCCGCCCG GCAGTAGGAC AGAGGGAGCG AGGGAGTCCG GGAGGAAGGG 1260 AGAGCGGGTG CGGCCAGTCT GACGGTTGCT GTGTTTGCAG 1300
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