Variant report

Variant	rs10911479
Chromosome Location	chr1:183954126-183954127
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:183954011..183955861-chr1:184020180..184021943,2	K562	blood:
2	chr1:183950977..183955895-chr1:183999343..184002420,4	K562	blood:
3	chr1:183952222..183954901-chr1:183961001..183962966,2	K562	blood:

Variant related genes	Relation type
ENSG00000198860	Chromatin interaction

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs13373873	0.92[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55658841	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56279195	1.00[EUR][1000 genomes]
rs56905396	1.00[EUR][1000 genomes]
rs59041291	1.00[EUR][1000 genomes]
rs59809579	1.00[EUR][1000 genomes]
rs60817535	1.00[EUR][1000 genomes]
rs6689337	1.00[EUR][1000 genomes]
rs6689360	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6696380	1.00[EUR][1000 genomes]
rs74130493	1.00[EUR][1000 genomes]
rs74130494	1.00[EUR][1000 genomes]
rs74130497	1.00[EUR][1000 genomes]
rs74130498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74130979	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74130983	1.00[EUR][1000 genomes]
rs74130984	1.00[EUR][1000 genomes]
rs74130991	1.00[EUR][1000 genomes]
rs7518746	1.00[EUR][1000 genomes]
rs7534028	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832026	chr1:183785065-183961847	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv530079	chr1:183797938-184639971	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv533206	chr1:183861204-184091272	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1006655	chr1:183922288-184186677	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:183902600-183965200	Weak transcription	Left Ventricle	heart
2	chr1:183923200-183961000	Weak transcription	Pancreas	Pancrea
3	chr1:183950800-183954800	Weak transcription	Right Atrium	heart
4	chr1:183951400-183955000	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr1:183952000-183958800	Enhancers	NHDF-Ad	bronchial
6	chr1:183952200-183954200	Enhancers	NHLF	lung
7	chr1:183952400-183955200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:183952800-183954400	Enhancers	Brain Substantia Nigra	brain
9	chr1:183953000-183954200	Enhancers	Brain Cingulate Gyrus	brain
10	chr1:183953000-183959000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:183953000-183965200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr1:183953200-183954200	Enhancers	Brain Hippocampus Middle	brain
13	chr1:183953200-183954200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr1:183953200-183957400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr1:183953600-183954200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr1:183953600-183957600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr1:183953800-183954800	Weak transcription	K562	blood
18	chr1:183953800-183956600	Weak transcription	Brain Anterior Caudate	brain
19	chr1:183953800-183965200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:183954000-183954200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:183954000-183954600	Weak transcription	Lung	lung
22	chr1:183954000-183956000	Weak transcription	Fetal Heart	heart
23	chr1:183954000-183956400	Weak transcription	Brain Angular Gyrus	brain
24	chr1:183954000-183958400	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr1:183954000-183965600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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