Tag | Content |
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EnhancerAtlas ID | HS108-18033 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:79074810-79077210 |
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) |
HSF1 | MA0486.2 | chr17:79075266-79075279 | GAACATTCTGGAA | - | 6.54 | Zfx | MA0146.2 | chr17:79075540-79075554 | CCGGCCTGGGCCTG | + | 6.71 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25200 | chr17:79075306-79076154 | Colon_Crypt_3 | SE_34261 | chr17:79065007-79076982 | HCT-116 | SE_65309 | chr17:79074020-79076638 | 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 |
GH17I081101 | chr17 | 79074967 | 79075961 |
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Enhancer Sequence | GGTAGACTCT TGGCCCTGTG TTTCCCGCTA GGCGTCCCCC GGCACAGTCC TGCGGCCCTG 60 TGTCTCCCGC TAGGTGTCCC CCGGCACAGT CCTGCGGCCC TGTGTCTCCC GCTAGGCGTC 120 CCCCAGCACA GTCCTGCAGC CCTGTGTTTC CGGCATCCCC AGCCTTGTCG TTCCTTGTGG 180 GGGAATCCCG CCCTGGGATC CGCCATGTCC CAGGACCAAG CCTGGCCCTG CTGAACCAGG 240 AGCGAGTTCC TCAGGGACGG GCTGCAGCAG CCCCCTCCAT GGATATCCTG AGCCCCGATG 300 TGAGCAAGGG GATCCCCTCC TAGGAGGCTG ACTTAGCCCC CAGAGCAGGC AAGGCCCAGA 360 GGCCAGACTC CCCACCGGGA ACAGGCAGGG CCAGCAGGCC CCTGTTCACC CATAGTCCAT 420 GGGTAGGAGT TGGGATGGGA TCACATGTGT CCCCTGGAAC ATTCTGGAAC ATTTCAAGAG 480 TTTCGAAGAT GTAGTTCCGG AGCCAAGCCC ACCAGGGAGG CCCTGGTCAT GTCTTTCTAA 540 AATAAAGGGT TGCAGGGATC CACGGGCTAT ACCTTGACAC TTGTTCCCCC CACCCACCAC 600 ACTCTCATGT ACGTGCGCGT GCGTGCACAC ACACACACAC GCACGTGATA CAGAACCAGT 660 GCTCCAGTCC CCACAGCCTG GGGACAGCCA GGAGACAAGT GCTCTTCCCT CCCTGGAGAG 720 GCCCCTCCTG CCGGCCTGGG CCTGCTGGGC ACTGTGGGCA GGTGCAGGCA AGGACAGCAG 780 CAGCACCTTT GACCCCTGGA GGCAGCCTCG CTGCTGAAGG ACTCAGCGGT GACAGGCTGT 840 GCTGCCACAG CTGCCAGGCA GGGAGCGCTG TGGAGCGCAG GCCTCCCGCC TGCTAGACCC 900 AGGACAGTGG CGGGCGTCTG CGCCCTCTGG CGGGGGCCAG GCCCCATGAC GGGGCCAGGG 960 AGTGAGAGCG GGGCTGTCAG TGGCTGGGGT GCTGCCTGCA GGGATGGAGG GCGGGGAAGC 1020 CAGGCTGCTT GCCGCAGGTC TCCCAGGAGG GGTTGCGGGA TGTGCCTGCG GTGGCAGCAG 1080 CTGACCTCCT GGGCTCGTGG GCCCCCGGGC GTGTGTGGAA GAGGCCTGTG TCCCACAGAC 1140 CCACTTAGAG ACGAGCCTCT GGGCTGGGGG CCAGGGTGTG AGGGCAGCCT CCCAGGGCAG 1200 TTCGTAGTAG CTCCCTGGTG CTTGGGTTTG GGCCTGCCTC GGGGCTCTCA GGGTGCGGGG 1260 GTGACGCTGG CTCGTGGCCG CTGTGTCAGG GCCGTGCCGC TGCGAGGTCG GTGTCCCTCG 1320 GCCGTCTGCC CTAGTGCTGG TCCCTGCTGG CCTCTCCGCG CCACCCAAGA CTCACTCCTC 1380 TACCACTGAT CTCAGCCAGG GCTCGGCAGA CGTTCTGAAG GGCCACAAAG TTTGTGCTTT 1440 TGGCTCTGTG GGCCGTGCCG TCTCCAGCTC TGTTACTGCA ATGTGAGGGC AGCCATGAAT 1500 GAATGATTCA CAAATCGATG CACAGCTGTG TTGCAATAAA ACTTTATTTA CAAAACAGGA 1560 AGCCAGCCCT CGGGCTGTGG TTTGCTGACC CCTGGTCTGA GCCAGCAGCA GAGGGGTAGG 1620 GGTGGCATGG GGAGGACTTG CTCAGAATGG CTGTCGTCCA ACATCCTCCG TGGGTCCCCA 1680 GCGTGGGTGC CCAGCCACAT GTAGAAGGGA ACGGGGATGA GTTGGGGGGA GCAGTGAAAG 1740 CCGGAGAGGC CCCCAGAGGT GCCAGAGACA TAGCAGTTCT GGCCCACAGC TTAAGGGTCT 1800 GGGGGTCCCG GGAATCCAGG CCCTGCAGCC TGCTTAGGCC AAATGGCCAG GAGGGGCAGG 1860 GGTTACTTGA TTAGCTCCCA GGACCCAGGC CCGGCCGGCT CCCAGTCCCA GAACCTTTCT 1920 CCATGCCTGT GGCTTCCTCC TCCTTTGTCC CCACTGTGCT CAGCTGGTCT GTGTCCAGCA 1980 GGCCGCAGAG TACGCCCGAG GGAGCGCGGG CTCTTGGGCC CAAGGGCAGT GGTTGGAGCA 2040 GTGAGCCTCA GTGTGTCTGA CGGGGCTGCC TTCCTGCCCT CGGCAGCCAG GCCTGACCCC 2100 CACTGGGCAG CACCACCCCC TCCCCCGGCC ATCTGGGGCG CCTTCCTGGC ACTTTGGGGT 2160 TTGCCCACCG GAGTTTGACC TTGTGCGTCC CTGTCCGTTC CTCCTTCCTC CAGGCCCTGA 2220 TGGGCCCCGC GGGCGTTGAG CCTGGGTTTG CTCTCATCCC TGGAGGTCCC CCGACTGCAT 2280 GGCTTGTGGT CCATCCCCGG CCCTTTACCG GCAGCCGCTT CTGTGGGTTG GGGTCAGAGG 2340 CTCACGGGTG GCCTGTCTCG CCGAGAGGTA CCACCTGGTG AAGAGCAGCC TCCAGCCCCA 2400
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