Tag | Content |
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EnhancerAtlas ID | HS080-21984 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr20:61983160-61984850 |
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) |
KLF16 | MA0741.1 | chr20:61983894-61983905 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr20:61983895-61983905 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr20:61983893-61983908 | GGGGGGCGGGGCTTT | - | 6.6 | SP2 | MA0516.2 | chr20:61983892-61983909 | CGGGGGGCGGGGCTTTA | - | 6.28 | SP3 | MA0746.2 | chr20:61984232-61984245 | TGCCCCGCCCACC | + | 6.05 | SP4 | MA0685.1 | chr20:61983891-61983908 | GCGGGGGGCGGGGCTTT | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 61983915 | 61984154 | chr20 | 61983415 | 61983758 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I063352 | chr20 | 61983781 | 61983950 |
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Enhancer Sequence | GGAGCGAGGG GCTGATGTCC CTTGAACTCC TCCCGGTAGG CAGAGCTCCC AGCCCCAGCC 60 CCTGGTTCCA TAGACAGCGG CTGGCTGGGT GGGACGCACT GCAGGAGCAC ATTCAGGGCT 120 GAGGCAGCCA GGCTCACGGG GGCAGCAGCC GACCCTCCAC CCCCACCCAC AGAAGTCCCC 180 ACCAATGGGA AGCCTGAGGC CCCATTAAAT CCCCAGCGTT GGCAGGCATG GGGCCAGGCT 240 CAGCTCTGTG GAGGGCGCTG GGGCACGACG CGTCGGGGGG AGCGGCTGCC CAGCCACACA 300 CCTCCTGCTC CACCTCTGCC AAGCTGCCTG GACCCCTGCC CATCCCTCCT CTGCCTCATT 360 CCCTGAGAGC CTGCTCAAAG GCCAGGGCCT CTCCAGGTAC TTGGGCAGAG CTGGCGACTG 420 TTCCCTGAGC TTCCTCTGTG CCTGCCCCCG AGTCCCAGGG CTGGACCTGC ACCTCAACCT 480 CCCTCCCAAC CCTCAGGGAC CCTCCCTTTG TGGAGCCGCC ACTGCTGGAG CTCTGCCCTC 540 CAGGTCGTGG AGACCTGGCC CCCCACGGTC TCAGTCGGTG CTGAGCCTCT GCCCCCCTGA 600 ACTGGTCCTG AGCCAACACC GCCGGCTGGG CTGCCGCTCA GCTGCAGAGG GAGGGAGACC 660 CAGCAAGAGC CACCAGCTGC ATCTCAATGC GGCTCCGGCC CAGCACAGCC TGGCTCCCGA 720 GCGTCCCTCC AGCGGGGGGC GGGGCTTTAC CACCAAGTCA GTCTGGGTGG AATCAGGCTC 780 AAGTTTGCTC CCTCTCCCCA GCCCATCTCT CCAAAAACCA ACGCCCTCCA CCTTCTGAGG 840 CACAAATTAA AAGATTCTCA TATGGCAAGC GGGTGACTAC TCTGTTCAGC ACACACTCTA 900 CAGGGAACGC CAGGGCCATG CTCAGGGAAC AGTGCAGGTC TGCGCCACTC TGGGCAGGGC 960 CCCCCTCCCC CAGGGTCCTC TGCCCGCGCC ACAGGAAACG GGACAAGGTC AGGGCCAGGT 1020 CCCCCAGCCC CCAGGTCCCA CAGCACCCCT GGGCTGCATC ACTGCTGCTC CCTGCCCCGC 1080 CCACCCCTGG CTCCAGCCGC CCTCTGGGGA GCCTTTGAGG AGAACCCCGT TTGGGCTGAA 1140 CCACCCGGCC GTGAGCCGGC TCTGGACTCG CACCATAAAG CTGCACCCTG GGAGCAGACA 1200 GGGTCTGAGG AGCCGCCCAG TCCAGCAGGT CCAGGTTCCT GCTCCAGGGC CCACAGGCTG 1260 GCGTGAGACC CTCTGTCCCC TCCACCCCGA CCCCAGTCCA GGTCAGGGAT TTCTGGGCAC 1320 CTGCCCCAAG TGGACAGCAG GGCCCCCAAC TGGGGGTGGC CAAATCCCAG AGAAGGGCCG 1380 AGGCCTCCCA CCCTGCAGCC TGGCCGGCCA CCAGCCACAG CCACCTGCTG CCCCAGAAAC 1440 AGGCCTCCTC AGCGGGAGCA GACCCAGCAC CAGCGGCCAC TCCAGGAACC CTGGGTCCTG 1500 TCCGGAGAGA GCCTCGGTGA CAATCCCAGC CCCAAAGAGA AAACTGGGGT CACCCCACTA 1560 CATCCCACAG GCCATGGTGA GGAGGAGACA CAGGAGAACA TGGGGTGGCA GCAATCCCTG 1620 CTCTCCTGAG CTGTGGTCCT AGGGGGCTGT GGTCCTAGGG GGGCTGTGGT CCTGGGGGGG 1680 CTGTGGTCCT 1690
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