Variant report

Variant	rs12720526
Chromosome Location	chr1:186850706-186850707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12720570	1.00[AMR][1000 genomes]
rs12720571	1.00[AMR][1000 genomes]
rs12720594	1.00[AMR][1000 genomes]
rs12720595	1.00[AMR][1000 genomes]
rs12720689	1.00[AMR][1000 genomes]
rs16826260	1.00[AMR][1000 genomes]
rs58303526	1.00[AMR][1000 genomes]
rs74135206	1.00[AMR][1000 genomes]
rs74137541	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv872590	chr1:186557453-187500338	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv947343	chr1:186846236-186851365	Enhancers Weak transcription Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:186839200-186884800	Weak transcription	Duodenum Mucosa	Duodenum
2	chr1:186841000-186853600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:186841000-186853800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr1:186841800-186862400	Weak transcription	Hela-S3	cervix
5	chr1:186843400-186853800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:186844200-186851600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:186845200-186851400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr1:186845200-186856800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:186846600-186851600	Weak transcription	NHDF-Ad	bronchial
10	chr1:186847800-186851200	Enhancers	Rectal Smooth Muscle	rectum
11	chr1:186848000-186856000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr1:186848400-186852600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:186848600-186851600	Enhancers	Colon Smooth Muscle	Colon
14	chr1:186849200-186851200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr1:186849200-186852000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:186849400-186850800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:186849600-186850800	Enhancers	Fetal Stomach	stomach
18	chr1:186850000-186850800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:186850000-186850800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr1:186850000-186851000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:186850000-186851200	Enhancers	Brain Hippocampus Middle	brain
22	chr1:186850200-186850800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr1:186850200-186850800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr1:186850200-186851200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr1:186850400-186851200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr1:186850600-186856400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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