Variant report

Variant	rs935733
Chromosome Location	chr3:67699674-67699675
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:67692723..67696784-chr3:67696803..67701487,5	K562	blood:
2	chr3:67693746..67699726-chr3:67701571..67705130,8	K562	blood:
3	chr3:67696995..67702204-chr3:67702925..67706326,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241316	Chromatin interaction
ENSG00000172340	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1075642	1.00[EUR][1000 genomes]
rs13319718	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13327007	0.85[ASN][1000 genomes]
rs2076900	1.00[EUR][1000 genomes]
rs2363092	1.00[EUR][1000 genomes]
rs3952242	1.00[EUR][1000 genomes]
rs60697032	1.00[EUR][1000 genomes]
rs61390179	1.00[EUR][1000 genomes]
rs72929314	1.00[EUR][1000 genomes]
rs72929317	1.00[EUR][1000 genomes]
rs9831152	1.00[EUR][1000 genomes]
rs9840770	1.00[EUR][1000 genomes]
rs9851783	1.00[EUR][1000 genomes]
rs9859371	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9883114	1.00[EUR][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	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv460700	chr3:67393629-67712970	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv590560	chr3:67393629-67712970	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv876922	chr3:67635506-67755257	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv428739	chr3:67656829-67730379	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67631400-67700200	Weak transcription	K562	blood
2	chr3:67661200-67704000	Weak transcription	Fetal Kidney	kidney
3	chr3:67661400-67700000	Weak transcription	Ovary	ovary
4	chr3:67661400-67701000	Weak transcription	Fetal Lung	lung
5	chr3:67661400-67704000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr3:67661600-67703600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr3:67670200-67703400	Weak transcription	Aorta	Aorta
8	chr3:67670800-67703200	Weak transcription	Adipose Nuclei	Adipose
9	chr3:67671000-67700600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr3:67673800-67703400	Weak transcription	Fetal Thymus	thymus
11	chr3:67674000-67704000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr3:67681400-67703600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr3:67681800-67704200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr3:67686600-67703600	Weak transcription	Fetal Heart	heart
15	chr3:67686600-67704000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr3:67686800-67703400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:67686800-67703400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr3:67687800-67703400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr3:67688000-67703400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr3:67689400-67700600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr3:67689600-67704000	Weak transcription	Thymus	Thymus
22	chr3:67690800-67700200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:67691800-67700800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:67692800-67699800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr3:67693400-67700000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr3:67693400-67703400	Weak transcription	Brain Substantia Nigra	brain
27	chr3:67694200-67700200	Weak transcription	Primary B cells from peripheral blood	blood
28	chr3:67695800-67703600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr3:67695800-67704000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr3:67696600-67701800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr3:67696800-67702400	Enhancers	Fetal Intestine Large	intestine
32	chr3:67697000-67700000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:67697000-67700800	Enhancers	Osteobl	bone
34	chr3:67697000-67701400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr3:67697200-67699800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr3:67697200-67699800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr3:67697200-67699800	Enhancers	HSMMtube	muscle
38	chr3:67697200-67699800	Enhancers	NHLF	lung
39	chr3:67697200-67700600	Enhancers	Liver	Liver
40	chr3:67697200-67700800	Enhancers	Psoas Muscle	Psoas
41	chr3:67697200-67701000	Enhancers	Stomach Mucosa	stomach
42	chr3:67697200-67702000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr3:67697200-67703600	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr3:67697400-67699800	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr3:67697400-67700200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:67697400-67704200	Enhancers	Small Intestine	intestine
47	chr3:67697600-67699800	Weak transcription	GM12878-XiMat	blood
48	chr3:67697600-67700000	Weak transcription	Colonic Mucosa	Colon
49	chr3:67697600-67700000	Enhancers	HSMM	muscle
50	chr3:67697600-67700400	Enhancers	Placenta Amnion	Placenta Amnion

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