Tag | Content |
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EnhancerAtlas ID | HS182-03561 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:17184550-17185320 |
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) |
Foxd3 | MA0041.1 | chr11:17184868-17184880 | AAACAAACAAAC | - | 6.32 | SOX10 | MA0442.2 | chr11:17184951-17184962 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr11:17184952-17184962 | CCTTTGTTTT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 17184566 | 17184636 | chr11 | 17184981 | 17185156 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I017161 | chr11 | 17183349 | 17187450 |
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Enhancer Sequence | ATAAACAAAT AGGACTTGTT TGGCCAGGCA CGGTGGCCAC GCCTATAATC CCAGCACTTG 60 GGGGGACTGA GGCGGGTGGA TCACTTGAGG TCAGGAGCTC GAGACCAGCC TAGTCAACAT 120 GGTGTAACCC CAACTCTACT AAAAATACAA AAATTAGCAG GGCATGGTGG CATGCACCTG 180 TAGTCCCAGC TACTCGGGAA GCTGAGCCAG GAGAATCACT TGAACCTGGG AGGTGGAGGT 240 TGCAGTGTGC CGAGATCACG CCACTGCACT CCAGAGCCTG GGTGACAGAG CGAGACCCTG 300 TTTCAAAAAA ACAAACAAAA ACAAACAAAC AAATAGGACT TGTTTAATTT TAAGTTTTTC 360 TATGCAATGT ATTTTAACTT TCAGCCCTTA CTATCAGTTA TTCCTTTGTT TTTTAGACAC 420 AGGGTCTCAT TCTGTAGCCT TGGCTGGAGT ACAAGGGCCT TATCATCATA GCTCATTGCA 480 GCCTCAAACT CCTGGGCTTG AGATCCTCCT ACTGCAGCTT CTTGAGTAGC TGGGACTACA 540 GAATAGCTGT AGTCCCAGCG TGCATCACCA CACACAGCTA TTTTTTTTTT CTATAGACAC 600 GGGTCTCCCT ACATTCCCCA GATTGGTCTC GAATTCTTGG CCTCAAGCAA TCCTCCCACC 660 TCGGCCTCCC AAAGCACTGG GTTTACAGGC ATGAGCCACC AAACCCACCA TTCTACCAGT 720 TGTTTCTATT ATAATCTAGC ACAGATTGTC ATCTAATGTA ACACAAAGTA 770
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