Variant report

Variant	rs3769532
Chromosome Location	chr2:33485732-33485733
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:33483858..33485741-chr2:33487136..33490001,2	K562	blood:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11691887	0.82[AFR][1000 genomes]
rs3769535	0.82[ASN][1000 genomes]
rs3769536	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6710501	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs921705	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs963025	0.81[AFR][1000 genomes]
rs9751070	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[ASN][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	nsv998167	chr2:33074313-33541100	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535623	chr2:33074313-33541100	Genic enhancers Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1005435	chr2:33136117-33747159	Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
4	nsv535624	chr2:33136117-33747159	Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:33403800-33489800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:33466400-33497400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:33466600-33500800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:33466800-33491200	Weak transcription	Right Ventricle	heart
5	chr2:33468200-33491000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr2:33469800-33486200	Weak transcription	NHDF-Ad	bronchial
7	chr2:33471800-33491200	Weak transcription	Pancreas	Pancrea
8	chr2:33472000-33489800	Weak transcription	A549	lung
9	chr2:33472000-33491200	Weak transcription	Brain Substantia Nigra	brain
10	chr2:33472000-33516600	Weak transcription	Psoas Muscle	Psoas
11	chr2:33472400-33491000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr2:33472600-33492800	Weak transcription	Colon Smooth Muscle	Colon
13	chr2:33473200-33486600	Weak transcription	Fetal Lung	lung
14	chr2:33473600-33489800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr2:33474000-33491000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr2:33474200-33491200	Weak transcription	Brain Hippocampus Middle	brain
17	chr2:33474400-33489800	Weak transcription	Placenta	Placenta
18	chr2:33474400-33490000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr2:33476200-33490000	Weak transcription	Esophagus	oesophagus
20	chr2:33476200-33490000	Weak transcription	Fetal Intestine Small	intestine
21	chr2:33476200-33491000	Weak transcription	Gastric	stomach
22	chr2:33476400-33487000	Weak transcription	Fetal Muscle Leg	muscle
23	chr2:33476400-33487400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:33476400-33488200	Weak transcription	Ovary	ovary
25	chr2:33476600-33488400	Weak transcription	Fetal Muscle Trunk	muscle
26	chr2:33477400-33491000	Weak transcription	Fetal Stomach	stomach
27	chr2:33477600-33489800	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:33478000-33491000	Weak transcription	Lung	lung
29	chr2:33478800-33487200	Weak transcription	NH-A	brain
30	chr2:33478800-33488000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:33478800-33488200	Weak transcription	Liver	Liver
32	chr2:33478800-33491200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr2:33479600-33487400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr2:33480000-33488000	Weak transcription	HUVEC	blood vessel
35	chr2:33483200-33486600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr2:33483400-33486200	Weak transcription	NHLF	lung
37	chr2:33483600-33488000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr2:33483800-33485800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr2:33483800-33486200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr2:33483800-33486800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr2:33483800-33489800	Weak transcription	Aorta	Aorta
42	chr2:33483800-33491000	Weak transcription	Left Ventricle	heart
43	chr2:33484000-33487800	Weak transcription	Osteobl	bone
44	chr2:33484600-33488000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr2:33485000-33490200	Weak transcription	Fetal Heart	heart
46	chr2:33485400-33487000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr2:33485400-33487800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr2:33485600-33488000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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