Variant report

Variant	rs10068664
Chromosome Location	chr5:96530356-96530357
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:96518600..96520567-chr5:96529112..96530644,2	MCF-7	breast:
2	chr5:96529786..96532537-chr5:96535359..96538183,3	K562	blood:
3	chr5:96521334..96524159-chr5:96530024..96533344,3	K562	blood:

Variant related genes	Relation type
ENSG00000248758	Chromatin interaction
ENSG00000058729	Chromatin interaction
ENSG00000251513	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1000082	0.96[ASN][1000 genomes]
rs1000083	0.96[ASN][1000 genomes]
rs10463199	0.89[ASN][1000 genomes]
rs10866776	0.86[ASN][1000 genomes]
rs11135499	0.86[ASN][1000 genomes]
rs1406325	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1406326	0.89[ASN][1000 genomes]
rs1528592	0.86[ASN][1000 genomes]
rs1528594	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1609326	0.89[ASN][1000 genomes]
rs1609327	0.86[ASN][1000 genomes]
rs1830366	0.89[ASN][1000 genomes]
rs1830368	0.86[ASN][1000 genomes]
rs183410	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1852739	0.89[ASN][1000 genomes]
rs1862592	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1919244	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1919245	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1997296	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2081139	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2081140	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2081142	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2351504	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2351506	0.89[ASN][1000 genomes]
rs2548412	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2548422	0.95[EUR][1000 genomes]
rs2548423	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2643465	0.89[ASN][1000 genomes]
rs2643496	0.82[ASN][1000 genomes]
rs2643503	0.82[ASN][1000 genomes]
rs2643577	0.89[ASN][1000 genomes]
rs2697598	0.86[ASN][1000 genomes]
rs2697637	0.89[ASN][1000 genomes]
rs3108540	0.85[ASN][1000 genomes]
rs317112	0.96[ASN][1000 genomes]
rs4869152	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4869153	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4869156	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6556953	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6874040	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6899065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7723203	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9314193	0.89[ASN][1000 genomes]
rs9686259	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9687077	0.86[ASN][1000 genomes]
rs972717	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv830412	chr5:96427305-96606619	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1019790	chr5:96471680-96980633	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	nsv537812	chr5:96471680-96980633	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv882391	chr5:96496189-96533469	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv882392	chr5:96496189-96546238	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
8	nsv882393	chr5:96496189-96567950	Flanking Bivalent TSS/Enh Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96520000-96531600	Weak transcription	HSMM	muscle
2	chr5:96520000-96534800	Weak transcription	Left Ventricle	heart
3	chr5:96528200-96531800	Flanking Active TSS	Dnd41	blood
4	chr5:96528800-96530800	Enhancers	GM12878-XiMat	blood
5	chr5:96529400-96530400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr5:96529400-96530600	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr5:96529400-96530600	Genic enhancers	Primary B cells from cord blood	blood
8	chr5:96529400-96530600	Enhancers	Primary B cells from peripheral blood	blood
9	chr5:96529400-96531400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:96529400-96533000	Weak transcription	Adipose Nuclei	Adipose
11	chr5:96529600-96530600	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr5:96529800-96530400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr5:96529800-96530600	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr5:96529800-96530600	Enhancers	Primary T cells from cord blood	blood
15	chr5:96529800-96530600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr5:96530000-96530400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr5:96530000-96530400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:96530000-96530400	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr5:96530000-96530400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:96530000-96530400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr5:96530000-96530400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr5:96530000-96530600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:96530000-96530600	Enhancers	Primary T cells fromperipheralblood	blood
24	chr5:96530000-96530600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr5:96530000-96530600	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr5:96530000-96530600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr5:96530000-96530600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr5:96530200-96530400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr5:96530200-96530400	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr5:96530200-96530600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:96530200-96530600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
32	chr5:96530200-96530600	Enhancers	Right Ventricle	heart
33	chr5:96530200-96531000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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