Tag | Content |
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EnhancerAtlas ID | HS086-06944 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr19:19619740-19622010 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr19:19621937-19621952 | CAAGCTACGCCCACT | + | 6.12 | SP4 | MA0685.1 | chr19:19621937-19621954 | CAAGCTACGCCCACTCT | + | 6.5 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 19620850 | 19621028 | chr19 | 19621675 | 19621818 |
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Enhancer Sequence | ACTTTTCTTT TGTCCCTTCT GCCCTGGCTT CTCTGTATTG TTTCGTCCTA GCTTCCCAGG 60 CAGGTTGGAG GGAGATGGAG GATGACCCTT AGTTAATGAG AGAAGCAAAG GGCGGGGTGC 120 ATCTGCTGCT GGGGCCTCAC TTACTGTGGG GATGGAGTCC CCACGGCCCC TCTCCTCTGG 180 AGCTTTGTGG CAAACTTACC CCATGGGCTG GGAGAGAGGA ATGAGAATCT CAGTGGGGGC 240 TGGGTTTGGT GGCTCACATT TGTAATCCCA GCACTTTGAG AGGCTGAGGT GGGTGGATCA 300 CCTGAGGTCA GGAGTTCGAT ACCAGCCTGG CCAACATGGT GAAACCCCAT CTCTACTAAA 360 AATACAAAAA TTGGCCGGAT GTGGTGGTGG GTGCCTGTAC CCCAGCTACT TGGGAGGCTG 420 AGGCAGGAGA ATCGCATGAA CCCGGGAGGC AGAGGTTGCA GTGAGCCAAG ATTGCGCCAC 480 TGCACTATAG CCTGGGTAAG AGACCGTGAC TTTCTCAAAA AAAAAAAAAA ATTCTCAGTG 540 GAATTTGCTT GTGTTTGCTG CATCAGCCTT CACGCTAGAG TGGTGGGTTT TCCTGGAGCA 600 ATTTTCAGGC TGGGGGCCTC GATGGTGTCT TTGCTGCAGG ATGTGATATT ACAGATGTGC 660 AATCTAAGCA CAGAGTCACC AACCTGGATC CAAAATGAAC GACGTCCTGG CAAAAATGTT 720 TTCAAGTGTT GATAGTTTCA AGTTTTATTC TTAAGGTGAG ACCTGGGATC ATTTTGCTGA 780 ATTTTAATGT GCATAAAACA TGACCCTGTT TTCCTAGGTG CTATTTATTT GAGGCAGGGT 840 CTCACTCTGT TGCCCAGGCT GGAATGCAGT GGCTTGATCT CAGCTCACTG CAGCCTCAAC 900 CTCCCTAGGC TCAGGTGATC CTCACATCTC AGACTCCTCA GTAGCTGGGA CTATGGGCAT 960 GCACCACCAT GCCCAGCTAA TTTTCGTATT TTTTGCAAAG ACACATTTTT GCCATGTTGC 1020 CCATGGCTGG TCTTGAACTC CTGGACTCAA GCAGTCCTCT CACCTTGGCC TCCCAAAGTG 1080 CTGGGATTAC AGGTGTGAGT CACCACGCTT GGCCGTTTCT TGTCTTTGAA GCATCCTTGC 1140 CTCCGGCCTG GGAGCTCATA CCTTCCCCAC AACTCCCAAG TGCCTGGTCT TATGGGCACA 1200 GAGCTGGTAG AGAACATGGT AGAAACTGAA CCTCAGCCTG TCCAGTAGCG CGATCTTGGC 1260 TCATTGCAAC CTCCGCCTCC CAGGTTCTAG CGATTCTTCT GCCTCAGCCT CCCGAGTAGC 1320 TGGGATTACA GGTGCCGCCA CCAGCACGCC CAGTTAATTT TCAGTAGAGA TGGGGTTTCA 1380 CGTGTTGGCC AGGCTGGTCT CAAACTCCTG ATGTGATCCA CCGGTCTCAG CCTCCCAAAG 1440 TACTGGGATG ACAGGCGTGA GCCACTGCAC CCAGCCACTT TTTTTTTTTT TTTTTTTTGA 1500 GATAGGCTCT CTGTTGCCCA AGCTAGAGTG CCTAGAGGCT CTCTGTTGCC CAGGCTCAGG 1560 CGATCCTCCC ACCTCAGCCT ACCGTGTAGC TGGGGCCAGA GGCTTGCTAC AGGCATTTCT 1620 TGCTTGGCCT GAGAAACATT CCTATGGGGT GCTGTCTCCT GGGCTTGGCT CTTGGTTCCT 1680 CGTGAGGCTC TGCTTCCCTG GATTGGGCAC AGGCTTGTCA GTGCAGTTGG GGCAGATTCA 1740 AGGGGCGGGT CCTGGGTCAT GGTCTCAAAT AGCCTCTCCA GCTGAGAAAA TGGGACACTC 1800 CCCTCGTCCC TGACATCTTG TCCCCGACAT CTCATCCTCT CTGAATTGAG CCTTGGGTCT 1860 GTGGCCACAT GGCAGGCAGA GACCCTGACC CCATCTGCTC CCACAGATTC GTCGGTGGAC 1920 AGATGGCATG CACTATGCCC TGGGCCCCGG AGATGTGGCA GGAGCTATCC AGACAGAAAC 1980 ATATAGCACC TTGAGAGGAG GGCATGGGGT GACATTTTAG GCAAGGCTTG AAGAGGGGAA 2040 AAGTGCCAGG AGTGTGCAAA GGCTTGGAGA TAGGAGCCAG CATGGCAGGT CAAGAACAAA 2100 AAGGGCAATG TGGTGGGACT GGGTGGGAAG ACGGGGCAAG GGCGTGGGTT TTAGCTAAGT 2160 GCAGTGGGAG TCTAGGGAAG GTCCTGGGCC CAGTACTCAA GCTACGCCCA CTCTGAAGCC 2220 ATGCCCACTA CCCCAAGGAT GGGGTTTTGC CCATTTTCCA AGTGGGGAGT 2270
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