Tag | Content |
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EnhancerAtlas ID | HS092-07408 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:99291100-99292060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROG1 | MA0623.2 | chr10:99291307-99291317 | GACATATGTC | + | 6.02 | NEUROG1 | MA0623.2 | chr10:99291307-99291317 | GACATATGTC | - | 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 |
chr10 | 99291234 | 99291788 | chr10 | 99291800 | 99292039 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I097531 | chr10 | 99291481 | 99291650 |
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Enhancer Sequence | GGGATTACAG GCGTGCACCA CCACGCCTGG CTAATTTTTG TATTTTCGTA GAGGTGAGGT 60 TTCCGCCCAG CTAATTTTTG TACTTTATGT AGAGACGAGG TTTCACCATG TTGGCCAGGC 120 AGGTCTCAAA CTCCTGACCT CAAGTGATCT GCCTGCCTCA GCCTCTCAAA GTGCTGGAAT 180 TCCAAGCGTG AGTCACCAAG CCCGGCCGAC ATATGTCATC TTTTAAATGT AAAAAATAAG 240 AAAAGTGGTT GGACCAGAGA CTCCTGACTG TGCTTGGGAT CACTGGGTCA TGGAGCCAGT 300 CCCTGAGCTT CAGCCTTTGG TTAGTCCCCC AGGGGCGATT CTAGGTATCG GGTCCATTCC 360 TGACCCTCTG GCCCTTTCTG AGCACCAGCA TCCTGGTGCT CCGAGAAACT GTCTCGTGCC 420 CTTGGAAACT GTGATAAACA GTTCCTAGGC CCACAACAGT CTCCCCTGTG GTTTCCAGGT 480 CCCCAGGTGA GGGCGGAGCA TGAGGAATGT GACAGGCCAT GGTGTAATGG GATTTTGCTA 540 AGAATTTACC ACCAGGAGGT AGTCTCCAAA TGGGTCCCAG AATAGAAAAA CTGGCCTGTG 600 GTGTGATGAG GAGTGGGACC ACAGACCTGG GGGCCAAGAC CAGCAGGAAG ACTCAGCAAC 660 AAGGCATTGT GATCCTGGGG GCTGGGTAGT TGGCCATCCT GGCAGGCAGT TGGAGGTGGG 720 CAGGGACAGC CAGGTGGGAC ACTGAGGGTT AGAAAGGTGA GAGAGTCAAG GAGTAGATAG 780 TGGGGGGCTG ACTGGGCCGG GAGAGCAGCC AGTGGAGGGA GCACCTTGGG TCAAGGCGCT 840 CTCAGTCTGC CATCTCTTGG CCCTGGAGCA AACCAAGCAG TTGGAGTTGT CTGCAGGGAG 900 ATTTGTAAGT TCACTTGTTT GCTGTTTCAT GCCATCTTCC TCCCAAAGCC TTTCCTGAGT 960
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