Tag | Content |
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EnhancerAtlas ID | HS053-16382 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr17:17650190-17653830 |
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) |
POU4F2 | MA0683.1 | chr17:17653173-17653189 | CTCATTAAGTATTTAT | - | 6.17 | TEAD1 | MA0090.2 | chr17:17653421-17653431 | CACATTCCAT | + | 6.02 | Zfx | MA0146.2 | chr17:17653795-17653809 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_03155 | chr17:17650193-17651202 | Brain_Angular_Gyrus | SE_03155 | chr17:17651344-17651864 | Brain_Angular_Gyrus | SE_03155 | chr17:17652025-17653687 | Brain_Angular_Gyrus | SE_04718 | chr17:17641708-17653758 | Brain_Anterior_Caudate | SE_05252 | chr17:17638780-17657618 | Brain_Cingulate_Gyrus | SE_06257 | chr17:17638815-17657693 | Brain_Hippocampus_Middle | SE_07567 | chr17:17641461-17653778 | Brain_Hippocampus_Middle_150 | SE_08244 | chr17:17638844-17657613 | Brain_Inferior_Temporal_Lobe | SE_08869 | chr17:17652411-17653233 | Brain_Mid_Frontal_Lobe | SE_13947 | chr17:17650437-17651333 | CD34_Primary_RO01536 | SE_13947 | chr17:17651724-17653325 | CD34_Primary_RO01536 | SE_26567 | chr17:17651984-17653630 | Esophagus | SE_29831 | chr17:17648857-17650822 | Fetal_Muscle | SE_31179 | chr17:17652445-17659633 | Fetal_Thymus | SE_33597 | chr17:17650122-17657535 | H2171 | SE_39763 | chr17:17652369-17653858 | Jurkat | SE_47257 | chr17:17652490-17653415 | Panc1 | SE_50171 | chr17:17652002-17653859 | Sigmoid_Colon | SE_53329 | chr17:17650112-17651189 | Spleen | SE_53329 | chr17:17651945-17653884 | Spleen | SE_54742 | chr17:17650219-17651061 | Stomach_Smooth_Muscle | SE_55326 | chr17:17652779-17653361 | Thymus | SE_58709 | chr17:17640373-17671122 | Ly1 | SE_63051 | chr17:17614295-17670945 | Tonsil | SE_66665 | chr17:17652369-17653858 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 17652032 | 17653314 | chr17 | 17650906 | 17650991 | chr17 | 17652002 | 17653777 |
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| Number: 3 | ID | Chromosome | Start | End |
GH17I017746 | chr17 | 17650310 | 17651005 | GH17I017749 | chr17 | 17651345 | 17651864 | GH17I017748 | chr17 | 17652015 | 17662284 |
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Enhancer Sequence | CGCCTGCCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACCAC GCCCAGCCCC 60 ATGTGTTTTC TGAGGACTCC TTCATTATTT CACACACACA CTAGAGCCAT GTTTTTGAAA 120 GATACGGCTG CCAAACAAAC TGCATTTATT ACATAATGAT TAATTCATCG CCCCCATTTC 180 TTATTAATCA AAGACATCCA TAACTGCCTA TCTGAGCTTT GAGTTGGGGA GAGAACCAGC 240 GGGGCCTCAA GCTGACAGCC TTCCCACCCA GATCAGGGGC ACTGGTAGAT TTGTGTCAGT 300 GGAGCCTCAT TTGGGGTAAA TGCACAGTAC CCCTGAGGTT TCTAGAAGAA ATGGAGACAG 360 CTCACAGACC CCCACACGTC ACCTCCCCAA ACCCCTGGGG CTGCCTGGGA TGTTTTATAA 420 CCCCTTCTCC AGCCAGCCCT GAGCTCAGGC TGGCTGCTTG GCACTTAGCC ACTGGCTGAC 480 TAGTGGCCTG TCAGAGGATG TGGAAGATGG GGTGGGCCAG TCCCTGTTGC TGGAGGCTGC 540 AATTAGTGGC AGCCTGGGAA GGAGACTGAA GCCTGGGCTG AGGTCAGGAC CACTGGGCAG 600 AGCTTGAGGT GAGGGCAACC GACATAGGGC TGTCCTGGCA GCCCATCCTG GGCTGAGAAC 660 GAATTCTAGG GTTCCAGGGG CATTTGACAC GAGGCCGGCC ACACTCTGAG GTTAGGGGCT 720 TTTTCAAAGA TAGTTTGGTG GCAGGGGCCT AGAGTATGGG GAGTGCCGAC TGATTGGGTT 780 GGAGCTGCCC TCTTGTGCTT AGTCGCTTCT AGATGGAGGC CACAGGAGTG CTTGGTAGGT 840 CCAGGTGGAG CCATCAATTG TCAGACATGC AAAAAACTTG AAAAGATATC TCAAAAGGGC 900 CAGTCTGGCT GGGCACAGTG GTGCATGTCT ATAATCCCAG TGCTTTGGGA GGTAGAAGCA 960 GGAGGATCTT TGAGCCCAGG AGTTTGAGAC CATCCTGGGC AACACAGTGA GACCCCATCT 1020 CTACAAAAAA TTTAAAAAAT TAGCTGAGCA TGGTGGAGTG TGCCTGTGGT CCCAGCTACT 1080 TGGAGGCTAA GGCTGGAAGA TCACTTGAGC CTGGGAGGTC GAGGCTACAG TGAGCTGTGA 1140 TCGTGCGACT GCACTCCAGC CTGGGCGACA GAGCAAGACC AGTTCTACCT GGCTAGGGTG 1200 GCCCCAGAGT CATGGCGGAA GGCGAAAGGC ATGTCTTACA TGGTGGCAGG CAAAGAATGA 1260 GGACACCCAA TCTTCTTTAC TCATTCATCT AACACTGACT GTGTGGCCTG GCACCCACCA 1320 GGAATGTCCC TGCCCTCAAA GTCTTTACAG GCTGTTGGAG ATGGGGCAGA TGCCCAAATA 1380 AGTCATTGTT GTCCCAGGTA GTGCCATGCC AGGGGCCATC CAGGGAGCTG AGGGCCCAGT 1440 AAAAAGGCAC TTAAACTCAA ATGCATGGAG AAGGGGACAG CCAGGGTGTG ATTAGGGAAG 1500 ACTTCCTGAA GGAGGTGCTG CTCCGAGAAG GTTGATTGGG TGGTTTTTGT AGGGGTTTTC 1560 TTGTTTCCAC TTTTTAAATA ACTACTTCAT GCCACATGCT ATTAGGTGCT TTTCACATAC 1620 ATCGTCATGT TTAATTTGTA CCAACAACCC TGTGAGATAG GAAATAGCTT CCGTATGTTA 1680 GCAGTGAGTA AGCTAAGGAT CAGAGAGGGG AGGTTGCTTG GACAACTGGC TTAGCCATGA 1740 TTAGAACTCC AATAGGTTCT TAAATGATGA TAGAAAAGGT GTAGGAGGAT GGGAGCCGAG 1800 GCTGGCATAC CTGGCAGAAG AAACAGTGTA CGCACGCGTA TGTCGGTGGG GCACTGTGGT 1860 GTGGAGGGCT GCAGGGCTTG GTAGCACTGG AGTGAGCAGA GGCGAGCCTG AAAGCTGGCG 1920 GCAGGGACCT CAGGGGCCAT GACAGGTATG TGAGTCAAGG GAGTGATGTG GTCCCGCTAC 1980 AAATCACTGG GGGCTTCAGC CCCTAATGGG ACCTCCTCTA GCTGCACCCC CCTCCCTGCC 2040 TGTGCCCTTT TTGGCACCTG GTGGCAGGCA CACCTCAAAG AACTGCTGCA TCTGTTCCTG 2100 CTTCTGACCT CAGGAGACAG CAGCAGGGCT GGCATGGAGC ATCAGGGAAA TGCACAACAA 2160 CACATCAGCC CCTGGGGGCC TCCTGGATCT CCCCACGAAT CCTGCAATAC CCTTCACAAC 2220 CATCCCCGTC CAGAAAGAGG CTGAATGGCG GCCAGCATCT GCCCGTCAGC AGAGAGTTCC 2280 CGCTCTTAGC ACCAGCTCGC CTGAGCTGCC TCCAGGGACA GTCCTGCCCG CCTCCCCAGA 2340 GAGCCAGTGC TTCCGCTGCC GCCTAATAGC TCTCCCGGCT GGAGACGACT CTTGATATTT 2400 AGCCTGCGTG GCAGGAGCCT TAATAGCAGC AACTCTCCCT CCCTGCTCCT GCCTCCTGAG 2460 CCCCAGAGAC AGCTCTGCTC ACCTCCTAGC CGGCATCCTC CACGCACTGC CTAGGCATCA 2520 GGCGGAGGTC TTTCTGCCCA CTCTTGGTAA CATCAAGGAA TGAATGAGCA TCCAGGAGCA 2580 CTTCGAGTGT GCTATTTTCT CCTCTGAGAT TCAGAGATGC CCTTTGAGAG GCTATTAGCA 2640 TGGCCACAAT TTAAATATGA GGAAACTGAA ATTCAGAGAG GGGATGTGAT GGAGATGGCT 2700 CACTTTCGCT TCATCTTCCC CCCCTCTTGG TACCAGGAAG TGGACCATGC TCCTTCAGGC 2760 CTCAGGATCT TTGCCTCTGC TGGTCTTTCT TGCCTGGAAC TCTCTCTCCT CCTTCTCTCT 2820 CATAGATCTC ATCTCAGAGA AGCCTTCCTG CCCTGGTTTA TTTACTAAGG TTGGTCCTTC 2880 TTGCCATACT GTAAGCTCCA TGAAAGTGGG GAGTTCCCCT ACCTTCTGTT GCTCCCCTCT 2940 GTATCCCCAG CACCCAGCAT AGGGCATGTA GCTCCACTAG GGCCTCATTA AGTATTTATT 3000 GAATGAGCAA ATGAGTGAAT GGATAAGCAC ATGCCTGTAC TAGTTAGGGT AAGATCAGCT 3060 GCAGCAACAA ACCAACCTAG CATTTCTAGA TGGAGGTTTG TATTTCCGGA GGATGGTGAG 3120 TATTTCTGGT GGGTGGAGGT TTCCTCCACA TGGCAATGTG GCCGGGGCAT GGTCTGCATC 3180 AAGCTGGCTT AGTGTGGAGG GTCCACCCTG GAAGGAGATA TCACTTGCAT TCACATTCCA 3240 TTGGCTGGAG CACAGTCATG TGACCATGCC CAGCTGCAAG GAAGGCTGGG AAATGTAGTC 3300 CAGCTGTGGC TCCAAGGACG GAGAACAGGT TTTCGTGACT CCAAATCTTC CCATAGGTTG 3360 CTGTATTGGT CTCTCTAATC AGCAGAGCCA ACCGTTACCG AGTCCTTGTC ACTATACCCT 3420 GTTGTAAGCC CTTTTCTCAA ATTAGTCCAT TTTATTCTTA CAACAGCCCT ACAGGAGGGT 3480 ATTATAATTA GCCCAGTTTA CTGATGAGCA GGCAGGGGCT CAAATGACAT GTTAAGGGGA 3540 AAATACCCAT TAGAAACATG ATGGGCCGGG CACGGTGGCT CATGCCTGTA ATCCCAGCAC 3600 TTTGGGAGGC CGAGGCGGGT GGATCACCTG AGGTCGAGAG 3640
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