Tag | Content |
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EnhancerAtlas ID | HS179-14954 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr17:73868380-73870240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr17:73869769-73869780 | AGCCACACCCT | + | 6.02 | MEF2A | MA0052.3 | chr17:73869060-73869072 | GCTATTTTTAGC | - | 6.44 | MEF2B | MA0660.1 | chr17:73869060-73869072 | GCTATTTTTAGC | - | 6.92 | MEF2C | MA0497.1 | chr17:73869952-73869967 | AAGATAAAAATAGCT | + | 6.21 | MEF2C | MA0497.1 | chr17:73869059-73869074 | GGCTATTTTTAGCTG | - | 6.35 | Nr5a2 | MA0505.1 | chr17:73869140-73869155 | CCTGACCTTGAGCTG | - | 6.62 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_02036 | chr17:73868308-73875346 | Aorta | SE_13675 | chr17:73868413-73869841 | CD34_Primary_RO01536 | SE_14576 | chr17:73868064-73869645 | CD4_Memory_Primary_7pool | SE_17725 | chr17:73868491-73869641 | CD4p_CD25-_CD45RAp_Naive | SE_18950 | chr17:73868506-73869606 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20394 | chr17:73868388-73869217 | CD56 | SE_20964 | chr17:73868437-73869557 | CD8_Memory_7pool | SE_26317 | chr17:73868161-73870861 | Duodenum_Smooth_Muscle | SE_27397 | chr17:73868303-73875310 | Esophagus | SE_32219 | chr17:73868312-73875271 | Gastric | SE_34314 | chr17:73868073-73875593 | HCT-116 | SE_38319 | chr17:73868191-73870770 | HUVEC | SE_41448 | chr17:73868267-73875286 | Left_Ventricle | SE_43010 | chr17:73868258-73875306 | Lung | SE_44121 | chr17:73868299-73869835 | MM1S | SE_49759 | chr17:73868501-73869563 | Right_Ventricle | SE_49759 | chr17:73869606-73870216 | Right_Ventricle | SE_50595 | chr17:73868295-73875348 | Sigmoid_Colon | SE_54339 | chr17:73868298-73875519 | Spleen | SE_54896 | chr17:73868161-73875333 | Stomach_Smooth_Muscle | SE_58075 | chr17:73869095-73869360 | VACO_9m | SE_62999 | chr17:73844393-73875248 | Tonsil | SE_67410 | chr17:73868299-73869835 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 73868569 | 73869385 | chr17 | 73869726 | 73870061 | chr17 | 73868951 | 73869202 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I075872 | chr17 | 73868226 | 73870570 |
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Enhancer Sequence | GCCACCGCGC CTGGCCCCAA TTTTTTTTTT ATTTTTGTTT TTTGTAGCGA TGAGGTCTCA 60 CCATGTTGGC CATACTGATC TCAAACTCCT GGGCTTGAGT GATCCTCCCA CCTCAGCCTC 120 CCAAAGTGCT GGGATTACAG GTGTGAGCCA TCATGCCCAG CCTCAATATT TTTTTAAAGA 180 GATGTTTGTT TCCCAAACTT CCACGCAAGA CTCTGGAGCT ACAGGCCACT CTGCAGATGG 240 CATGCTTGCT GAGTGGCTGT GTCTGTGGCC ACAGGTGTGA CTAGTCATGC CTGAATTCCA 300 CCAAGAAAGC ACCAGGCCTG TCTAGCTCAC ATTCCAGGAC ATGCCAACAC TTCCTGCAGG 360 GTCAGAGACC AGAAGGTTCC CTGGCGAGGG GCGCCTGTGG GGTAGGGAGT GCCAAGTTGG 420 GGGACAAGAT GAGACAGCAG GTGGCCTGAG GGGTGGGAGC GGTCCTCTGC AAGGTAGGAG 480 GCTTGTAGTA GGTGGTCCAA GGAGCATCCA AGGGGACAGC GGGGCAGCCT TCTCCACCAG 540 CCCCTTCACT GCCGGGTGAG CTGGGGACCC ATGGCTGCCA AGGGAACGAT GTTGAAAACA 600 CAAAGCACCA GGGGCAAGGA GGCCCCGCCC GGAAAAACAA CATCCTGGCT GCTAGAGCCC 660 AGGCAGGCTC TATGGGAGGG GCTATTTTTA GCTGCTGAGG CTGCTGGGGC TGGACTTGTA 720 TGGCCTTGCT GTCTGGCTGC ATAACTCACC CATTATCCCG CCTGACCTTG AGCTGGGCGT 780 CTGTCTGAGA GGCCTCTCTG TCTGCCCTTG CCCTCGGCCA CAGCCCCTCT CTGGGGTGCA 840 CCTGGGCCAC ACAGAACCCA GGCAGGAGTG AGCTGGCCTG GGCCTGGAAA CACACTGGAC 900 TGTAGCCTCA GGGCGCCCCA GGCCTGGCTC AGGTTCTAGG GCAGCAGAGG GCACTGGGCC 960 CTCCCAGAAG AGAGGCAGAG GCTCTCCTGG GGCACAGGTC ACAGGTGTCC CCAGCATGGA 1020 GGGCAAGAAG ATTCCAGAGG GGGACATAAG TCCTTTTATT TTTTGAGATG GAGTCTTGCT 1080 CTGTCGCCCA GGCTGGAGTG CAGTGGTATA ATTGATCTCG GCTCACTGCA ACCTCTGCCT 1140 TCCGGGTTCA AGTGATTCTC CTGCCTCAGG CCCCTGAGTA GCTGGGAGTA CAGGCACCCA 1200 CAACCATGCC CGGCTAATTT TTGTATTTTT AGTAGAGACG AGGGTTTCAC CATGTTGCCT 1260 AGGCTGGTCT CGAACTCCTG ACCTCAAGTG ATCTGCCTGC CTTGGCCTCC CAAAGTGCTG 1320 GGATAACAGG CATGAGCCAC CGCGCCCGGC CAGGACATAA GTTCTCTTAT TGTAGATGTT 1380 CTGGGCTCCA GCCACACCCT GGGCCGGCTC TGTGGGCTGA GGGCTATGTG TGAAGGAAGC 1440 TCCAGGTCTC AAAACTCTCT TGCCCACGCC CAGGGGTCCT GCCCTGTTCC TGGAGGGGTG 1500 ATGCCTGCAT TTAATGCTGG GCACAAACAG TACAAACAGC AAAGGCAGGT CCAGAACTAG 1560 GCTGCGGCAT GAAAGATAAA AATAGCTGGT GGGAGTCAGG CCATCCCAAG TAAACACTCA 1620 AGCAGCCAGG ACGGCAGTGG GGCTGGAGAA GCCACCTCTG GCTGCCCGTG CTGGGAAAAA 1680 GGGAGTGGGG GTGCCCCAAA GGGCAGGTAC CCTGTTCCAG CCCCCTTCTC CCAGGCCAGG 1740 GCTCCCTCTC AACAGGAATC CTGGGACGAG GGGCTCCGGC CCCTCTCCTG CCTGCCCACT 1800 CAGCCAGCTT ACAAATGAGA GCGGTTCTGG GAATCCTTGG GTAGAGAGGA TGGAAAAGGA 1860
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