Tag | Content |
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EnhancerAtlas ID | HS182-04218 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:76884420-76885800 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:76885050-76885068 | CCTGCCTCCCTTGCCTCC | - | 6.09 | EWSR1-FLI1 | MA0149.1 | chr11:76884720-76884738 | GGAGGGAAGGAAGGCCGG | + | 6.96 |
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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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Enhancer Sequence | GTTGGGATAT CCTCATTCTT GACTTTTCTG AATAACATTT GTTGGGCCCT TTCTGTGTGC 60 CCAGCATAGG CTGGATGGTC AGTCCACAGC CTCCTTCAAC CTTCTCAAAC AGCCCGTGAG 120 AAAGGGACTG TGCTGGTCCC AGGTTAGAGA TGCGGGACTG GGGGCTCAGG GAGGTTAAGG 180 GGCTCAGGCT GGGGCCACCT CGCTGCGAGC CCTCTCCTTT CGCAGCACAG GCTCTGGGAG 240 GGTTGTTTAC CCAGAGGCCT GCAGGGAGGC ACAGGGGGAA GCTGGGGCCT CGGGATCTGG 300 GGAGGGAAGG AAGGCCGGGG AAAGTGGCCC GGAGAGAGAG GAAACAGTCT CCGGAAGCTG 360 ACAGGCTGCA AGACCGTCCC CTCCTGCTGC CTCCTGCCTG GAAAACATGT CCCAGAGTGG 420 ATGAGGCCTG TCCCCTTTAG GACTCAGGTC TGCAGGGGCC TGAGGGTCGC AGAGGGCTCC 480 AGTGAGCTCT CCCTCTAATG CAGGGGGTGC AGGGGACTGA CACCAGGGCA GTCGGGCACA 540 GTCTTCCCTG GCTCTGAAGT GGGACCCTTC CCTCGGCCCA GTCCTCAGCA TCTGTGGACT 600 GGGCCTTGGC AATAGCCTCC TCAAGGGTCT CCTGCCTCCC TTGCCTCCTG TCCTGCCTCC 660 CCTGGCCCCC AGTGACATTG TTCTCAAATG CAGACCTGGC CCAGTCTCTC CCTGCTCTAA 720 AACTTCCCTG GCTTCCAGCA TCCATGGATG AGGCCCTCAC AGAGCCCCAC AGCCTCACAG 780 CCCAGCACCT GCCTTCTACT CTTTCTCCCC AGCCCCTCCA CCAACCAAAC CCCAGGGCCC 840 TTTGAAAAAT GTGCCTCTTC CTTAAGGCAG CTAGAAAGTT GTCTGAATAA CCGCAGATCT 900 ACAATACCTG CAACGTGAAA GGTCCTCCCT GGGGCTGTGC AGAGCACCCC TCACCTGCAC 960 AGCCATAACT TGGCCTGGAC GAGCCTCTCT AGCTCCCTCA AGATTCCCAG CAAAGTCCTG 1020 CGCTTTCAGG CTTCCAAACC TTTGCACAGG CTCACCCCCT CCAGCCTTGG AATACTCCCC 1080 CTCCTGTCAG GGTTAGGGTG ATAAAGACGC CTCCTCCATG AAGCTCCCCA CTTGGGTGTC 1140 CCAAGGGGAA TTAATCTGTC TTCTCTGTGC TCCCAAAGCA CACAGCTCCA CCACGACAGG 1200 CCTCACTTTA TGCTCTTTTG TGGATTTGAG CTGCAGATCC CGGTGCCTGT CCCAGCTTTG 1260 CTCCTCCCAT GCCGTGTGGA CTTGGCCTTT CTGAGCCTTT GTCTGGGTTG GTCAAGTGCA 1320 CAGCAGGGCT GCCTCCCAGC AGGAGCCTTG GCCCTGATGC CCTTGGCTGT GTGCCTGGCA 1380
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