Variant report

Variant	rs9296254
Chromosome Location	chr6:38616177-38616178
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:38605341..38608804-chr6:38614063..38616688,3	K562	blood:
2	chr6:38607304..38611528-chr6:38615188..38618189,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DNAH8-8	chr6:38607926-38617146	NONHSAT112318
2	lnc-DNAH8-8	chr6:38615587-38619607	NONHSAT112319

Variant related genes	Relation type
ENSG00000183826	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10947753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4141854	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4631264	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4711552	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4711553	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711554	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4711555	0.83[EUR][1000 genomes]
rs4714171	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4714173	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4714174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58362455	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58648636	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59793635	0.82[AFR][1000 genomes]
rs6905545	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6925790	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6931745	0.84[AFR][1000 genomes]
rs7750482	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7750997	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7752972	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7753374	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7767791	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7775968	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9296255	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9349092	0.93[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9349093	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9349094	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9366965	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9366969	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9369065	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9369069	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9369073	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380757	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9380759	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9380760	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9380762	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9380763	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9394513	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9394514	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9394515	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9394516	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9394519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9462439	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9462441	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9462442	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9462446	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9470901	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9470902	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9470906	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9470908	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9470913	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	esv2758049	chr6:38588969-38711085	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	esv2759421	chr6:38588969-38711085	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv427754	chr6:38588969-38711085	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
6	nsv428144	chr6:38588969-38711085	Enhancers Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 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	chr6:38608800-38618000	Weak transcription	Aorta	Aorta
2	chr6:38609000-38617200	Weak transcription	Small Intestine	intestine
3	chr6:38609000-38618800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:38609000-38623600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:38609000-38624600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:38609000-38625600	Weak transcription	Fetal Stomach	stomach
7	chr6:38609000-38628200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr6:38609000-38634200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr6:38609000-38641200	Weak transcription	Pancreas	Pancrea
10	chr6:38609000-38641200	Weak transcription	Spleen	Spleen
11	chr6:38609000-38642000	Weak transcription	Primary T cells from cord blood	blood
12	chr6:38609000-38645200	Weak transcription	Fetal Intestine Small	intestine
13	chr6:38609000-38645600	Weak transcription	Left Ventricle	heart
14	chr6:38609200-38621000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:38609200-38641200	Weak transcription	Primary B cells from cord blood	blood
16	chr6:38609200-38642400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr6:38609200-38643400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:38609400-38642200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr6:38609600-38642800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr6:38609800-38618000	Weak transcription	Right Atrium	heart
21	chr6:38609800-38624400	Weak transcription	Psoas Muscle	Psoas
22	chr6:38609800-38643000	Weak transcription	Colon Smooth Muscle	Colon
23	chr6:38612800-38623400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr6:38612800-38641600	Weak transcription	Adipose Nuclei	Adipose
25	chr6:38612800-38648400	Weak transcription	Brain Anterior Caudate	brain
26	chr6:38612800-38652800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:38613000-38642400	Weak transcription	Fetal Lung	lung
28	chr6:38613400-38641200	Weak transcription	Liver	Liver
29	chr6:38614600-38617000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr6:38614800-38654800	Weak transcription	Brain Angular Gyrus	brain
31	chr6:38615200-38642400	Weak transcription	Fetal Brain Female	brain
32	chr6:38615200-38645200	Weak transcription	Ovary	ovary
33	chr6:38615200-38649400	Weak transcription	Fetal Brain Male	brain

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