Tag | Content |
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EnhancerAtlas ID | HS180-04624 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:223935270-223936740 |
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 | CCTGCAGAGC AGACAGTGGT TTGTGACAAG TCTGTCTAGC CATGTTGACA GACTTGTCTT 60 TCTTCCTGCA ATATGAGTTC AGTTCATAAT AACTCATGGA AAGGACCAGA CGTCATTGTT 120 TTCATCTTTG GCAGGTCCAG ACTTTAGGCA GGTGAGGGAA CTTCAGAGAA TAGCTTCCTC 180 CTGTGCTTTG GGGGAGAGTG GATCGAGAGA CAGAAGGAAA GGGGAGGTCA GAGAGATCTT 240 GAGGCTTCTT CAGTTTAGCA TTTCAAAGTG CCATCTCTTA GAGGTATTGG TTTCTGAGCA 300 CCCCAGTGTC TACCATTATT GCTCATCACC TGGAAGCCAA GGGTTGCTAG GCAAAAGTCA 360 AGCTGTCTGG GGTGTAATGG ATGGGGTGAT GGTGCCTCCA GCCCTTCTGT CTTCAGTCCA 420 CTTCCCACTC TTAGCCTGCT CTGAATCACC CCCACCCCTC TGACCACAGG TTCCCTGGGA 480 GCCCCTGCCA CCTGCTGCCC CTGCCACCTT CCCCTCCATC TGCAGTGCTG TGCAGCCTTC 540 CCCTGCACTC TTGCAGAGCT AATAGGCCCG TGGGAGACTT CGGAAGGAAG AGGAGGAAAG 600 ATTTCCTCAT AATAGCCTTG CTGGCAACGC TCACCAGGGG ATGGGAGGTG GGCACTGTGC 660 CCAGGAGCCT TGGAGCAAAG GCTGTGCCCA ACCTCTGAGC CCTGTCCCAT CCAGGTTCTG 720 GTCTCTGCGG GGGACAGAGA TAAGAAGCCC TGGCTTTTGG AGCCAAAATC TAGGTCAGAC 780 TCCCTAGGCA GGAATTCTCA AAGTTTATCA GCAGAACACG TTGAGGCAGA AGACCCTTTC 840 TGCTCCAGCC CTTCTTCCCA GGCTCAACCT TCATCAGAAT AGATAGGGGA AAGGAGAGGC 900 TGTGAGGCGT TCTTAAAACA GAAGCAAATT CTGACTCAGA CCGGAATAAA CAACCGTCCT 960 AGTATAAACC CTACAGCTGG GCTGGGCCAG ACCACGGAGC ATGGGCTGGT GGTGGGGCGA 1020 GGGTGTGCTC AGTGTCCCTG GGCCACTCAA GGCTGTCTGG GTATCAGCCC TGCGCCATCG 1080 AGGACCCCCT CCGGCCCTCT CTCGGCCGTG CGCCCTTTCC CTGCGCCATC GAGGACCCCC 1140 TCCAGCCCTC TCTCGGCCGT GCGCCCTTTC CCGCCCTTCC CAGCCTGCAG AAATCCGTGG 1200 ATGCGCTATT CACACGGGAA TGCCTGTGCT CGTTCCGCGA GAGGGTTGCA TTCCGCCTTT 1260 TCTCTGGTAT TCTCGGCGTT CAAGCATTTG AACGGGGTAG GAAAGGTTCT CCAAGTGCAA 1320 GAAAGCGCAG CCCTGAGCCT CCCACCCCAG GCCTCGGCCG CTGCGCTAGT GCGTCCGGCG 1380 GTCCCGCCCG GCAGTAGGAC AGAGGGAGCG AGGGAGTCCG GGAGGAAGGG AGAGCGGGTG 1440 CGGCCAGTCT GACGGTTGCT GTGTTTGCAG 1470
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