Variant report

Variant	rs9386246
Chromosome Location	chr6:149449027-149449028
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149440205..149443227-chr6:149446390..149449238,3	K562	blood:
2	chr6:149433670..149435558-chr6:149447633..149449437,2	MCF-7	breast:
3	chr6:149447328..149451282-chr6:149451738..149453433,3	K562	blood:

Variant related genes	Relation type
ENSG00000219487	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs11155625	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11756915	0.97[EUR][1000 genomes]
rs12191264	0.93[JPT][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12191441	0.81[CHB][hapmap];0.92[JPT][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12196468	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196841	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12197043	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12198786	0.97[EUR][1000 genomes]
rs12200486	0.96[EUR][1000 genomes]
rs12210293	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210437	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210478	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12212173	0.96[EUR][1000 genomes]
rs12212622	0.96[EUR][1000 genomes]
rs12216302	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2069314	0.97[EUR][1000 genomes]
rs28641142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35030564	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs35372633	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35426452	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3934770	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3935038	0.97[EUR][1000 genomes]
rs4243485	0.97[EUR][1000 genomes]
rs4243486	0.97[EUR][1000 genomes]
rs4243487	0.86[JPT][hapmap]
rs4243488	0.86[JPT][hapmap]
rs4283906	0.97[EUR][1000 genomes]
rs4355632	0.97[EUR][1000 genomes]
rs4385337	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4415179	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4495293	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4544932	0.97[EUR][1000 genomes]
rs4624897	0.97[EUR][1000 genomes]
rs4895779	0.97[EUR][1000 genomes]
rs4897081	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4897082	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4897083	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4897084	0.87[CEU][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4897087	0.97[EUR][1000 genomes]
rs5013008	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55794530	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55855829	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55953746	0.97[EUR][1000 genomes]
rs55991942	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56260426	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs56328446	0.97[EUR][1000 genomes]
rs56396328	0.97[EUR][1000 genomes]
rs56883363	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56924759	0.97[EUR][1000 genomes]
rs57292049	0.98[EUR][1000 genomes]
rs57478974	0.97[EUR][1000 genomes]
rs57596511	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57937779	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs58571272	0.97[EUR][1000 genomes]
rs61228112	0.97[EUR][1000 genomes]
rs61462811	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61660880	0.98[EUR][1000 genomes]
rs62425896	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6570941	0.86[AMR][1000 genomes]
rs6570942	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6570943	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6909824	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.97[EUR][1000 genomes]
rs6934263	0.97[EUR][1000 genomes]
rs7741894	0.97[EUR][1000 genomes]
rs7743161	0.96[EUR][1000 genomes]
rs7749723	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7749728	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7767040	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9377192	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390658	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9688704	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9766171	0.97[EUR][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	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149445400-149449400	Weak transcription	GM12878-XiMat	blood
2	chr6:149446800-149449400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:149447600-149449400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:149447600-149449600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr6:149447600-149449600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:149447600-149454400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:149447800-149449600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr6:149447800-149454200	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr6:149448000-149449600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:149448000-149452600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:149448200-149449400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr6:149448200-149452200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr6:149448400-149449400	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr6:149448400-149449400	Enhancers	K562	blood
15	chr6:149448400-149451200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr6:149448400-149452400	Enhancers	Primary hematopoietic stem cells	blood
17	chr6:149448400-149452400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr6:149448600-149449400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr6:149448600-149450400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr6:149448600-149450600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:149448800-149449800	Weak transcription	Hela-S3	cervix
22	chr6:149448800-149450200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:149448800-149450400	Weak transcription	Osteobl	bone
24	chr6:149448800-149452000	Enhancers	Primary T cells from cord blood	blood
25	chr6:149448800-149453600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr6:149448800-149454200	Enhancers	Placenta	Placenta
27	chr6:149449000-149449400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr6:149449000-149450200	Flanking Active TSS	Dnd41	blood
29	chr6:149449000-149450600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr6:149449000-149452000	Enhancers	NHLF	lung

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