Variant report

Variant	rs12577422
Chromosome Location	chr11:64161144-64161145
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	chr11:64126652..64130402-chr11:64156162..64161731,4	K562	blood:
2	chr11:64125866..64130028-chr11:64157063..64161519,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000162302	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10128649	0.82[ASN][1000 genomes]
rs10556	0.80[ASN][1000 genomes]
rs10732887	1.00[ASN][1000 genomes]
rs1207462	0.98[ASN][1000 genomes]
rs1213140	0.83[ASN][1000 genomes]
rs12281471	0.87[ASN][1000 genomes]
rs12283639	0.87[ASN][1000 genomes]
rs12284186	1.00[EUR][1000 genomes]
rs12287065	0.80[ASN][1000 genomes]
rs12574188	0.98[ASN][1000 genomes]
rs12575515	0.98[ASN][1000 genomes]
rs12575690	0.89[ASN][1000 genomes]
rs12577425	0.93[ASN][1000 genomes]
rs1468558	0.80[ASN][1000 genomes]
rs17159027	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1783518	1.00[ASN][1000 genomes]
rs2232410	0.82[ASN][1000 genomes]
rs2282548	0.87[ASN][1000 genomes]
rs2289572	0.89[ASN][1000 genomes]
rs2302262	0.80[ASN][1000 genomes]
rs3759056	0.87[ASN][1000 genomes]
rs41294376	0.81[ASN][1000 genomes]
rs473379	0.98[ASN][1000 genomes]
rs474430	0.96[ASN][1000 genomes]
rs490720	0.98[ASN][1000 genomes]
rs4930167	1.00[ASN][1000 genomes]
rs493052	0.81[ASN][1000 genomes]
rs494998	0.98[ASN][1000 genomes]
rs4963221	0.88[ASN][1000 genomes]
rs518698	1.00[ASN][1000 genomes]
rs520277	1.00[ASN][1000 genomes]
rs539008	0.98[ASN][1000 genomes]
rs539250	1.00[ASN][1000 genomes]
rs543767	0.96[ASN][1000 genomes]
rs554812	0.98[ASN][1000 genomes]
rs569741	0.98[ASN][1000 genomes]
rs575081	0.98[ASN][1000 genomes]
rs58010797	0.96[ASN][1000 genomes]
rs58488481	0.98[ASN][1000 genomes]
rs58721876	0.80[ASN][1000 genomes]
rs59283629	0.80[ASN][1000 genomes]
rs60421451	0.82[ASN][1000 genomes]
rs60579179	0.96[ASN][1000 genomes]
rs61431997	0.80[ASN][1000 genomes]
rs621816	0.80[ASN][1000 genomes]
rs7110262	0.80[ASN][1000 genomes]
rs7121001	1.00[ASN][1000 genomes]
rs7950922	0.87[ASN][1000 genomes]
rs7951858	0.82[ASN][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	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases
2	nsv897682	chr11:63999529-64170500	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
3	nsv832187	chr11:64121969-64312300	Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64141200-64162000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:64147800-64162200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:64150600-64163000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:64153800-64163200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:64154000-64167600	Weak transcription	Right Atrium	heart
6	chr11:64156000-64161600	Weak transcription	Fetal Thymus	thymus
7	chr11:64157400-64161600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:64158400-64162200	Weak transcription	Fetal Intestine Large	intestine
9	chr11:64159200-64163200	Weak transcription	Primary B cells from cord blood	blood
10	chr11:64159400-64161600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr11:64159400-64162600	Weak transcription	Adipose Nuclei	Adipose
12	chr11:64159400-64163000	Weak transcription	Colon Smooth Muscle	Colon
13	chr11:64159400-64163200	Weak transcription	Right Ventricle	heart
14	chr11:64159600-64161600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr11:64159600-64162000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr11:64159600-64162000	Weak transcription	Fetal Muscle Leg	muscle
17	chr11:64159600-64163000	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr11:64159600-64163200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr11:64159600-64163200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr11:64159600-64163200	Weak transcription	Spleen	Spleen
21	chr11:64160400-64163000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:64160600-64162600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr11:64160600-64163000	Weak transcription	Placenta Amnion	Placenta Amnion

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