Tag | Content |
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EnhancerAtlas ID | HS012-14851 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr17:71284640-71285880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:71285859-71285877 | GGGAGGAAGGGAGGGAGG | + | 6.92 | EWSR1-FLI1 | MA0149.1 | chr17:71285855-71285873 | GGAAGGGAGGAAGGGAGG | + | 8.06 | Nr2f6 | MA0677.1 | chr17:71285102-71285116 | TGGGTCATAGGTCA | + | 6.27 | ZNF263 | MA0528.1 | chr17:71284810-71284831 | ACCTCCCTCCTCTCCTCCCCT | - | 6.3 | ZNF263 | MA0528.1 | chr17:71285857-71285878 | AAGGGAGGAAGGGAGGGAGGG | + | 7.27 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00203 | chr17:71281786-71292211 | Adipose_Nuclei | SE_00919 | chr17:71280759-71290474 | Adrenal_Gland | SE_02957 | chr17:71284612-71285820 | Bladder | SE_04533 | chr17:71284556-71288674 | Brain_Anterior_Caudate | SE_06356 | chr17:71277769-71290798 | Brain_Hippocampus_Middle | SE_23373 | chr17:71284593-71285962 | Colon_Crypt_1 | SE_23953 | chr17:71284566-71285818 | Colon_Crypt_2 | SE_24951 | chr17:71284570-71285924 | Colon_Crypt_3 | SE_26142 | chr17:71284616-71290403 | Duodenum_Smooth_Muscle | SE_26892 | chr17:71282261-71285971 | Esophagus | SE_28228 | chr17:71284304-71287350 | Fetal_Intestine | SE_31497 | chr17:71284450-71290426 | Gastric | SE_34727 | chr17:71283787-71290955 | HeLa | SE_40779 | chr17:71281080-71291827 | Left_Ventricle | SE_41738 | chr17:71284580-71285651 | LNCaP | SE_42276 | chr17:71282392-71290554 | Lung | SE_46731 | chr17:71284633-71285420 | Ovary | SE_47498 | chr17:71284561-71285805 | Pancreas | SE_48667 | chr17:71282058-71290313 | Right_Atrium | SE_50297 | chr17:71283561-71288835 | Sigmoid_Colon | SE_52570 | chr17:71282759-71290321 | Small_Intestine | SE_53786 | chr17:71283801-71289650 | Spleen | SE_54836 | chr17:71279223-71290708 | Stomach_Smooth_Muscle | SE_65340 | chr17:71280793-71290305 | 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 |
GH17I073287 | chr17 | 71284034 | 71291744 |
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Enhancer Sequence | ACCCACCTCG GCCTCCCAGT GCTGGGATCA GGACGTGGGA TCAGCGTGAG CCACCGCGCC 60 TGGTCCATCC AGAGGGTTTT AACAGGTCTG TTTACCACCG AGTCTGGTCC AGCAGGGTGT 120 GACACATGGT CCGCCTCCAA CCGCCTCCAA GCACCCACTG GAAGTCCAGC ACCTCCCTCC 180 TCTCCTCCCC TTCTGCCCAC AGCCTGGCTC CAGGGCTCCC AGCCTGACCT CTCTGCATCC 240 TCACCCCCAT CCGCTTCCCT GTTCTCTCAA GCCTCTGCTG CCCAGCCTCA TGGCTTCCCC 300 CACCAGCAAT GTCCCCCCTC CCAGTGCCCA CGCCATACCG CTTATCATTC CAGCAAACAC 360 AAAGTTCTCT CGGGCAGGGA GGGGGAGCCA GGCACCTGGC AGACTTGCCA CACAGTGACG 420 TGGGCGAGGA CGTGAGGGAT GCCTTGAGAT GATACTCTAC TCTGGGTCAT AGGTCAGCTC 480 TCTCTCCTCC CTACCCTTAG GAAAGTGACC TTCCCCTAAC TCTAACTTGG ATTATCTCTG 540 GGCCCCACCC TCCTGCCCCA CCTCAACCTC TAAACAATTA GACATTGAAC CGCTAGACCA 600 AAGGTCAGCA AACACTTTTT GCAAAGGGCC AGAGAGTAAA TATTCTCGGC CTTGTGGCTG 660 ATAGGGTTTT TGTCACAGCT ACTCAACTGT CTTCTTAGTA TAAAACTAGC CGTTGGCCGG 720 GCACAGTGGG TCACAACTGT AATCCCAGCA CTCTGGGAGG CTACGGCAGG AGGATCAGTT 780 GAGCCCAGGA GTTCCAGACC AGCCTGGGCA ACACGGTGAG ACCCCATCTC TACACAAAAT 840 CAAAAAAAGA AAGAAAGGAG CCATAGCAAC ATGTAAACAA GTAGGCATGG CTATGTTCCA 900 ATAACATTTT ATTTACAGAC AACTTCTGGG TTGGTGAGCA GATCGAGGTG CCAGGAAGGT 960 GGTGCGTGCC CTGCCCCCCA CCCCAACACT TGACCCCACG CATCCTCATG CAGCTCTTCC 1020 GTTTGGCTGT TCCTGAGTCG TATCTTTTGT AATAAACCAG TAAAAGAAAA AAAACCACCA 1080 AAAAGCCACA TCTTTATTTA CAAAAGCAAA CGCAGGCTGG GTTTGGCCCA TGGACTGTAG 1140 TTTGCTGACT CCTGAATATC ATATATGACC CTCTTGGCCA GCCATGGGCT CCTAGGCAAA 1200 ACTCTGAAGA AAACAGGAAG GGAGGAAGGG AGGGAGGGAG 1240
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