Variant report

Variant	rs6583792
Chromosome Location	chr10:93651632-93651633
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:93651466..93653343-chr10:93668717..93670774,2	K562	blood:
2	chr10:93648930..93651665-chr10:93666944..93669498,2	MCF-7	breast:
3	chr10:93649585..93651720-chr10:93654975..93657870,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272817	Chromatin interaction
ENSG00000174721	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10736066	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417256	0.81[CEU][hapmap]
rs1417257	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1538832	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17347260	1.00[ASN][1000 genomes]
rs17433251	1.00[ASN][1000 genomes]
rs1772181	1.00[ASN][1000 genomes]
rs1772186	1.00[ASN][1000 genomes]
rs1772188	1.00[CHB][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2258946	1.00[CHB][hapmap];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2421705	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2421706	1.00[CHB][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61743258	0.81[ASN][1000 genomes]
rs61874701	1.00[ASN][1000 genomes]
rs61874749	0.81[ASN][1000 genomes]
rs61876142	0.81[ASN][1000 genomes]
rs61876148	0.81[ASN][1000 genomes]
rs61876151	0.81[ASN][1000 genomes]
rs6583790	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7089495	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7093658	0.90[ASN][1000 genomes]
rs72823110	0.81[ASN][1000 genomes]
rs72823162	1.00[ASN][1000 genomes]
rs7912830	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7917198	0.81[ASN][1000 genomes]
rs7917450	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv7491	chr10:93626192-93671694	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv1842657	chr10:93634155-93668663	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3329479	chr10:93651472-93653420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6583792	TNKS2-AS1	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93647400-93667800	Weak transcription	Spleen	Spleen
2	chr10:93649800-93652200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:93649800-93656200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr10:93650200-93652200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:93650200-93653400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr10:93650400-93652000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:93650400-93652000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr10:93650400-93652000	Enhancers	Hela-S3	cervix
9	chr10:93650400-93652000	Enhancers	HepG2	liver
10	chr10:93650400-93652000	Enhancers	NHDF-Ad	bronchial
11	chr10:93650400-93652200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:93650600-93651800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:93650600-93651800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:93650600-93651800	Enhancers	HUVEC	blood vessel
15	chr10:93650600-93652000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr10:93650600-93652000	Enhancers	Muscle Satellite Cultured Cells	--
17	chr10:93650600-93652000	Enhancers	A549	lung
18	chr10:93650800-93652000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:93651200-93652000	Enhancers	NHLF	lung
20	chr10:93651400-93651800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr10:93651400-93651800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:93651400-93652000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr10:93651600-93651800	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr10:93651600-93651800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:93651600-93651800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr10:93651600-93652000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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