Tag | Content |
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EnhancerAtlas ID | HS018-10916 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr19:7871910-7873600 |
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) |
EWSR1-FLI1 | MA0149.1 | chr19:7873257-7873275 | TGCAGGAAGGCAGGAATG | + | 6.11 | FOSL1 | MA0477.1 | chr19:7872594-7872605 | GATGAGTCACC | - | 6.32 | IRF1 | MA0050.2 | chr19:7872805-7872826 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | JUND | MA0491.1 | chr19:7872594-7872605 | GATGAGTCACC | - | 6.62 | RREB1 | MA0073.1 | chr19:7872695-7872715 | CCCCAACTCAAACCAACCCA | + | 6.01 | RREB1 | MA0073.1 | chr19:7872700-7872720 | ACTCAAACCAACCCAAAACC | + | 6.12 |
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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 |
GH19I007807 | chr19 | 7872274 | 7873183 |
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Enhancer Sequence | GGCGCAATCT TTGGCAGTCT CAGCTCACTG CAGCCTCAAC CTGCTGGGCT TGAGGGATTC 60 TCCTGCCTCA GGCTCCTGAG CAGCTGGGAC CACAGGCTCA CGGCACCACA CCCAGCTAAT 120 TTTTTGTCTG TAAAGACAGG GTCTCACTAT GTTTCCTGGG CTGGTCTGGA ACTCCTGGAC 180 TCAAGCGATC CTCCCACCTT GGCCTCCCAA CGTGCTGGGA TTACAGTGGC CGGGTGCAGC 240 GGCTCACGCC TGTAATCCCA GCACATTGGG AGGCCGAGGC AGGTGGATCA CCCGAGGTCA 300 GGAGTTCGAG ACCAGCCTGG CCAACATGGC AAAATCCCAT CTCTACTAAA AATACAAAAA 360 TTAGCCGGGC TTGGTGGCGG GAGCCCGTAA TCCCAGCTAC TTGGGAGCCT GAGGCAGCAG 420 AATCGCTTGA ACCTGGGAGG TGGAGTTTGC AGTGAGCCGA GATCTTGCCA CTGCACCCAG 480 CCTGGGTGAC AGAGCAAGAC TCTGTCTCAA AACAAAACAA ACAGAAAAAC AAAGTGCTGG 540 GATCACAGGC ATAAGCCACC ACACCTGGCC TCTGCATCTC ATGAGCATTT ATTTTGTGCT 600 ATGTGTTTTT TGGATATGAC CTCAAAGAAT CCGGTAACAC AGCCGCCCTC ATTCTCATTT 660 TACCTATGAG CATAGTGGCT CAGAGATGAG TCACCTGCCC ACAGCCCATC AGCTGATAAA 720 CACTGGAGTT GGGTTTGAAA CTGTGAAAGC AATGAGGACC ACATCATTTT CACTTCCCTT 780 CGTGGCCCCA ACTCAAACCA ACCCAAAACC CAAGAAAGAA GATGTGGAGA TTGTGTTGCC 840 TTTCATAACT GGGAAGCGCG GGTGAGTGGA GGGGACCAGA TTCAGGATCT GCTTTTCTTT 900 CTTTCTTTTT TTTTTTTTTT TTTTTTGAGA CGGAGTCTTG CTCTATCGCC CAGTGGAGTG 960 CAGTAGCGCG ATCTCGGCTC ACTGCAACCT CCACCTCCCG GGTTCACACC ATTCTCCTGC 1020 CTCAGCCTCC CGAGTAGCTG GGGCTACAGG TGCCTGCCAC CACGCCCGGC TGATTTTAGC 1080 ATCTGCCTTT CTTTATCTGT CTATGATCTG TTTGCTCCAG AATGTAACCT TCTAGACCAA 1140 AGGTTGGCAA ACATTTGAAA AGGGCCAAAT AGTAAATATT TTTGGGCCTC GAGGGCTCTC 1200 TGCTGCAACT CTGCTATTCT AGCACAAATG CGTCACATAC AATACATAAA TGCATGGGCA 1260 GAAAACAATT TGTTAGCCGG GCACAGTGGC TCACGTCTGT AATCCCAGCA CTTTGGGAGG 1320 CCAAAACAGA TTAGGGTTTT CCAAGGCTGC AGGAAGGCAG GAATGTGGAG TGACTGCTTA 1380 GTAAGTATGG GGGGCTGGGC ATGGTGGCTC ACGTCTGTAA TCCCAGTACC TTGGGAGGCC 1440 AGGGGAGGAA GATTACTTGA GGCCAGGAGT CTGAGACCAG CCTAGGCAAC ATAGCAAGGC 1500 CCCATCTCTA CAAAACATTT GAAAATTAGC TGACCACGGT GGCACATGCC CACGTCCCCA 1560 GCTACTCAGG AGGCAGAGGT GGGAAGATTG CTTGAGCCCA GGAGGCTGAG GCTGCACTCA 1620 ACCATGATTG TGCCACTGCA GTCACCCTGG GTGACAGAAG AAGACCCTCT CTCAACAAAA 1680 ACAAAAATAA 1690
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