Tag | Content |
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EnhancerAtlas ID | HS182-10224 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr18:266320-266970 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr18:266755-266770 | TGAACTCTTGACCTC | - | 7.64 | Nr5a2 | MA0505.1 | chr18:266747-266762 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr18:266752-266770 | CCTTGAACTCTTGACCTC | - | 7.63 | Zfx | MA0146.2 | chr18:266780-266794 | CCCGCCTCGGCCTC | + | 6.01 |
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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 | CTTTGTGCTT CATTTTCGTC ACCAGTTAAA TAAGAGGGTT TTTGTAGATT TTTACTACCA 60 GCAGCAGCTA CAGTGGCATC ACCTAGGAAG CTGGTAGAAA TGCAAAATCT CAGGCTCCCT 120 TCCACACTTA CTGAACAAGA ATCTGCATTT CACAAGAAGC TTGAGAAACA CTGAACTAGA 180 TGATCTCCAA TTTCATGGTC CTTTTCAGGG CTAGTATGAT TTTTTTTTTT TTTTTTGAGA 240 TGGAGTCTCC CTCTGTTGCC CAGGTGTTGT GCACTGGCAT GATCTTGGCT CACTGCAACC 300 TCCGCTGTCC GGGTTCAAGC GATTCTCCTG CCTCAGCCTC CCAAGTAGAT GGGATTACAG 360 CGCCCACCAC CACGCCTGGC TAATTTTCGT ATTTTTAGTA GAGACGGGGC TTTGCCATGT 420 TGGCCAGGCT GGCCTTGAAC TCTTGACCTC AGGTGATCCG CCCGCCTCGG CCTCCCGAAG 480 TACTGCATTT ACAGGCGTGA GCCACTGCGC CCGGCCGCCA ATATGATCTT GGATAGTCCT 540 AACAGTTACT CTTAGCAGGC TTTCAAAGCA CCAGAGATTG CAGCAAAACG CACACAAAGA 600 AAATGATTAT GATGACATAC ACAAAATATA ATCCATTTAA AAAAAACCTC 650
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