Variant report

Variant	rs7950327
Chromosome Location	chr11:65844283-65844284
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:65822840..65824603-chr11:65843148..65845154,2	MCF-7	breast:
2	chr11:65818986..65821722-chr11:65843087..65845750,3	K562	blood:
3	chr11:65837300..65840343-chr11:65840812..65845835,6	K562	blood:
4	chr11:65843731..65845242-chr11:65847002..65849986,2	K562	blood:
5	chr11:65818921..65820486-chr11:65841745..65844587,2	K562	blood:

Variant related genes	Relation type
ENSG00000175115	Chromatin interaction
ENSG00000087365	Chromatin interaction
ENSG00000238752	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1211863	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2452683	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4930174	0.93[EUR][1000 genomes]
rs4930341	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs540943	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57287207	1.00[ASN][1000 genomes]
rs57720880	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58583648	0.93[EUR][1000 genomes]
rs59807152	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59827057	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60095752	1.00[ASN][1000 genomes]
rs60415795	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6591205	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6591206	1.00[ASN][1000 genomes]
rs7103495	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72932629	1.00[ASN][1000 genomes]
rs72932698	1.00[ASN][1000 genomes]
rs72934614	0.93[EUR][1000 genomes]
rs72934624	0.93[EUR][1000 genomes]
rs72934632	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934636	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934642	0.93[EUR][1000 genomes]
rs72934655	0.93[EUR][1000 genomes]
rs72934666	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934668	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934673	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72934677	0.93[EUR][1000 genomes]
rs72936625	0.89[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	nsv948711	chr11:65692760-65949674	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
2	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	esv1819302	chr11:65787660-66007018	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	esv3407551	chr11:65794503-66158322	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65839000-65849800	Weak transcription	Psoas Muscle	Psoas
2	chr11:65839200-65846800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:65839200-65847600	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:65839200-65847800	Weak transcription	Colonic Mucosa	Colon
5	chr11:65839400-65847200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr11:65839400-65847200	Weak transcription	Right Atrium	heart
7	chr11:65839400-65847600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr11:65839400-65847600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr11:65839400-65847600	Weak transcription	Small Intestine	intestine
10	chr11:65839400-65847800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:65839400-65848800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:65839400-65850400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:65839400-65850400	Weak transcription	Fetal Intestine Large	intestine
14	chr11:65839400-65850800	Weak transcription	Liver	Liver
15	chr11:65839400-65850800	Weak transcription	Fetal Kidney	kidney
16	chr11:65839400-65850800	Weak transcription	Right Ventricle	heart
17	chr11:65839600-65850400	Weak transcription	Brain Substantia Nigra	brain
18	chr11:65839600-65854600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:65839800-65845200	Strong transcription	Fetal Muscle Trunk	muscle
20	chr11:65840000-65844800	Strong transcription	Stomach Smooth Muscle	stomach
21	chr11:65840000-65846600	Strong transcription	Fetal Muscle Leg	muscle
22	chr11:65840000-65847400	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr11:65840000-65847600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:65840000-65847600	Weak transcription	Colon Smooth Muscle	Colon
25	chr11:65840200-65846200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
26	chr11:65840200-65848000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:65840200-65848200	Strong transcription	Fetal Stomach	stomach
28	chr11:65840400-65844400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:65840400-65844600	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr11:65840400-65845000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
31	chr11:65840400-65845400	Genic enhancers	Primary T cells fromperipheralblood	blood
32	chr11:65840400-65847600	Weak transcription	HUVEC	blood vessel
33	chr11:65840600-65844400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr11:65840600-65844400	Weak transcription	K562	blood
35	chr11:65840600-65845800	Strong transcription	Fetal Thymus	thymus
36	chr11:65840600-65850800	Weak transcription	Brain Germinal Matrix	brain
37	chr11:65840600-65870600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:65840800-65847200	Weak transcription	Lung	lung
39	chr11:65840800-65850400	Weak transcription	Fetal Brain Male	brain
40	chr11:65840800-65850800	Weak transcription	Brain Angular Gyrus	brain
41	chr11:65841000-65844800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr11:65841000-65845400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:65841000-65845800	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr11:65841000-65846400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:65841000-65847000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:65841000-65847200	Weak transcription	HepG2	liver
47	chr11:65841000-65847800	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
48	chr11:65841200-65844800	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr11:65841200-65844800	Strong transcription	Fetal Intestine Small	intestine
50	chr11:65841400-65844800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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