Tag | Content |
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EnhancerAtlas ID | HS177-15786 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr3:127954340-127954920 |
Target genes | |
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 | chr3:127954784-127954796 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954788-127954800 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954792-127954804 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954796-127954808 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954800-127954812 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954804-127954816 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954808-127954820 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr3:127954812-127954824 | GTTTGTTTGTTT | + | 6.32 |
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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 | TTTACTTCCT GGAAGCAAAT TGCTATAACC ATTTTCTTCT AAAGATTCCA AAGACACTTC 60 ATGATTTTTA AGCATGTTCT TTCTCCCACG GATCCTCTAG AAGTGGCAAT ATACTGTGCA 120 CACAGTGAAC ACACCAGCTC CGCTAGAGCT CTATTCAGTG AATAGTTACC GTGGTGTTTT 180 TAAATAGCTG GGTCATGTTC TGTTTTATGT ACATGTCATG GTTTAGTTAA CTACTTCCCT 240 TCCAACAGGC AGTCAGGCTG GTTCTGACCT TTTGCTCTTC CAGACACGTA GCAATGAGTG 300 TCCACATATG TGCCCCATGT GCACGTGGGT CACTGCTAGT CCCCAGGGGT GTTTGACGGC 360 CATTTGCCGT TGTGCTGCTC CTACCCCCAA CCCCACCCCA GTGACAGGCA GGACTATCTG 420 TCTCCCCTGT GTGGATGGGC AAAGGTTTGT TTGTTTGTTT GTTTGTTTGT TTGTTTGTTT 480 GTTTTCAGAC GGAGTCTCAC TTTTTCGCCC AGGCTGGAGT TCAGTGGCGC AATCTCGCCT 540 TACTGCAACC TCCGCCTCCC GGGTTCAAGT GTTTCTCCTG 580
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