Variant report

Variant	rs4420277
Chromosome Location	chr11:67876650-67876651
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:67874032..67878530-chr11:67886335..67892998,10	MCF-7	breast:
2	chr11:67876263..67879090-chr11:67886261..67888114,2	K562	blood:
3	chr11:67876195..67879063-chr11:67882958..67885886,2	K562	blood:

Variant related genes	Relation type
ENSG00000110721	Chromatin interaction
ENSG00000255236	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10791956	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10791957	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10896293	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10896295	0.84[EUR][1000 genomes]
rs11228131	0.85[ASN][1000 genomes]
rs11228133	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11228136	0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11228137	0.81[ASN][1000 genomes]
rs11535788	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2457179	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2457180	0.81[ASN][1000 genomes]
rs2512608	0.86[EUR][1000 genomes]
rs2512611	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2512612	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3935460	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4073551	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4930557	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61890478	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6591331	0.82[ASN][1000 genomes]
rs6591333	0.81[EUR][1000 genomes]
rs7104982	0.84[EUR][1000 genomes]
rs7123183	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7123668	0.85[EUR][1000 genomes]
rs71480230	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7925022	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7925423	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7940217	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7940501	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7944372	0.87[AMR][1000 genomes];0.85[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	nsv427892	chr11:67451649-67926562	Bivalent Enhancer Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
2	esv2757450	chr11:67472905-67891289	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
3	esv2759835	chr11:67472905-67891289	Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	112 gene(s)	inside rSNPs	diseases
4	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67831400-67884400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr11:67838000-67879200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr11:67839800-67886000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:67848400-67886400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:67849000-67885400	Weak transcription	Fetal Muscle Trunk	muscle
6	chr11:67849400-67887400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:67862400-67877000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:67862400-67881400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:67864400-67883400	Weak transcription	Hela-S3	cervix
10	chr11:67867400-67884200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr11:67867400-67884400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:67867400-67885200	Weak transcription	HSMMtube	muscle
13	chr11:67867400-67885600	Weak transcription	Primary B cells from cord blood	blood
14	chr11:67867400-67886200	Weak transcription	Thymus	Thymus
15	chr11:67867600-67881400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr11:67867600-67884400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr11:67867600-67885400	Weak transcription	HSMM	muscle
18	chr11:67867800-67881400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr11:67868400-67882600	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr11:67868400-67887400	Weak transcription	Primary T cells from cord blood	blood
21	chr11:67868800-67877200	Weak transcription	GM12878-XiMat	blood
22	chr11:67869000-67882600	Weak transcription	Dnd41	blood
23	chr11:67870600-67877400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr11:67873400-67885400	Weak transcription	Fetal Thymus	thymus
25	chr11:67874000-67885600	Weak transcription	Right Ventricle	heart
26	chr11:67874200-67884200	Weak transcription	Fetal Stomach	stomach
27	chr11:67874400-67879200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:67874400-67884000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:67874400-67884400	Weak transcription	Brain Angular Gyrus	brain
30	chr11:67874400-67884400	Weak transcription	Colon Smooth Muscle	Colon
31	chr11:67874400-67884400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr11:67874400-67885600	Weak transcription	Left Ventricle	heart
33	chr11:67874400-67886200	Weak transcription	Brain Germinal Matrix	brain
34	chr11:67875200-67884400	Weak transcription	Right Atrium	heart
35	chr11:67875400-67877600	Genic enhancers	Fetal Intestine Small	intestine
36	chr11:67875400-67881600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr11:67875400-67882200	Weak transcription	Brain Substantia Nigra	brain
38	chr11:67875400-67882600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr11:67875400-67884600	Weak transcription	A549	lung
40	chr11:67875400-67888200	Weak transcription	Spleen	Spleen
41	chr11:67875600-67876800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr11:67875600-67877000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr11:67875600-67877400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:67875600-67877600	Weak transcription	Fetal Heart	heart
45	chr11:67875600-67881400	Weak transcription	Fetal Lung	lung
46	chr11:67875600-67881800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr11:67875600-67881800	Weak transcription	Brain Hippocampus Middle	brain
48	chr11:67875600-67882800	Weak transcription	Brain Cingulate Gyrus	brain
49	chr11:67875600-67882800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:67875600-67883400	Weak transcription	H9 Cell Line	embryonic stem cell

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