Tag | Content |
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EnhancerAtlas ID | HS061-03400 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr10:115792660-115793800 |
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) |
JUN | MA0488.1 | chr10:115792981-115792994 | AAAATGAGGTCAT | + | 6.2 | JUND(var.2) | MA0492.1 | chr10:115792980-115792995 | TAAAATGAGGTCATT | + | 6.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 115792753 | 115792856 | chr10 | 115793195 | 115793269 |
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Enhancer Sequence | AAACCCAGTA ACAAAGTGGA CTGTTTCCAC CAGGGCCTGG ATACCATTTA TTTGGGGAGC 60 CACCTTTAGT GTGAGAGACA AGAAGTTGTT CTGTTTGCTC TCTGTGCTGG AAGTCTTGTA 120 ACAATCGTGG CATGCGTGAG ATTACAGATG ACTCAAGATT GTGCAGAAGG AGGCAGCTTT 180 CTTACAGATA GTAACACTTT GTTATAGGTT AAAATGCATC CCTACCCCCC ACCAAAAAAA 240 AGATATGTTG GAGTCCTAAC CCCTAGTATT TCAAAATGTG ACCTCAGTTG GAGATTGGGT 300 CTTTACAGAG GTAATCAAGT TAAAATGAGG TCATTAGCAT AGGCCATGAC CCAATATGAC 360 TGATGTCCTT ATCCAAAGAA GAAATTTGGA CAGGCACACA GACAAGCTTG GGGAAAAGAC 420 AGCCATGTAC AAGCCAAGGA GAGAGGAATG GAACAGATCC TTCCCTCACA GCCCTCAGAA 480 GGAAACAATT CTGCCTACAA CTTGAGGATG GACTTCTAGC AAACGAACTC ACACCTCACT 540 GATCCAGCAC CATTGCAGAA TGAAAAGTCC ATATAAATTC ACTTTCTAGA TAACTCAAGT 600 GTTCTGACAA ATAAGCAGTT CCAAAATTTT CGTTCTACTC TTTTTTAACA AAAATATTTC 660 TAAAACACAC CCTCCACATT CTCAAACCAA AGGCAGCTGA ACCCAATCTA AACCTTTCCT 720 ATTGATGCAG GTTTATCAGT GACTGCAGAG GGACAGAAGA CCCTTTGTTT CTGCAGTAAG 780 TGGCATCACT GGTTTCCCTG TTTTCTCCTC TAATACGAAG TTCCCAGACA GCCCCCTCTG 840 CCTTCTGCAT CATCCTCATT TCCTTGCTTG TCCTAATCTG TTGTGAAAGA ACAGAAACCG 900 GACAAACAAG ACATTAAAAC TGGTTCTCAA ATAAAATTAG TAGTCCCAAG TGAGAGGCTG 960 AAAGACACTC CTAAAGGTTA AACCACGTGA ACTTGAAAAA CTTCTTTTGT TGTCTATTCC 1020 TTTACTCCCT GTTCTCAGGG GGTGAGGATG TCAGATCCCT TATATTAAGG ATACCTCAAG 1080 TGTTGTGCTA CACAGACACA AAGCAGGTCA CAAGAAACTC TTCTGGACTC CTTCGGCTTA 1140
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