Variant report

Variant	rs73531419
Chromosome Location	chr6:110009995-110009996
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:109982568..109985653-chr6:110007788..110010480,3	K562	blood:
2	chr6:110006952..110010658-chr6:110010983..110015603,5	K562	blood:
3	chr6:109983707..109985653-chr6:110007788..110010480,2	K562	blood:
4	chr6:110009150..110010856-chr6:110010893..110012924,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155085	Chromatin interaction
ENSG00000112367	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs59662907	0.89[AFR][1000 genomes]
rs59852203	0.89[AFR][1000 genomes]
rs73523063	0.89[AFR][1000 genomes]
rs73531417	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949475	chr6:109907936-110160501	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv933105	chr6:109933270-110064342	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv817322	chr6:109933272-110070574	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv830769	chr6:109944334-110078120	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	nsv604485	chr6:109959269-110054486	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 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	chr6:109978000-110010600	Weak transcription	Brain Germinal Matrix	brain
2	chr6:109980600-110011200	Weak transcription	Fetal Thymus	thymus
3	chr6:109989400-110011400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr6:109990000-110010600	Weak transcription	Fetal Intestine Small	intestine
5	chr6:109991400-110010600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:109992000-110011200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr6:109992400-110011400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:109998400-110010800	Weak transcription	Primary B cells from cord blood	blood
9	chr6:110000400-110011400	Weak transcription	Left Ventricle	heart
10	chr6:110000600-110010800	Weak transcription	Stomach Smooth Muscle	stomach
11	chr6:110001000-110011400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr6:110001200-110011600	Weak transcription	Spleen	Spleen
13	chr6:110006400-110010600	Weak transcription	Fetal Brain Female	brain
14	chr6:110007200-110010000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:110007200-110011000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:110007200-110011400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:110008000-110010800	Weak transcription	Colon Smooth Muscle	Colon
18	chr6:110008200-110010400	Strong transcription	Primary T cells from cord blood	blood
19	chr6:110008400-110011200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr6:110008400-110011200	Weak transcription	Psoas Muscle	Psoas
21	chr6:110008600-110010600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:110008600-110011200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr6:110008600-110011200	Weak transcription	Fetal Muscle Leg	muscle
24	chr6:110008600-110011400	Weak transcription	Brain Angular Gyrus	brain
25	chr6:110008800-110010000	Weak transcription	Aorta	Aorta
26	chr6:110008800-110010600	Weak transcription	Brain Hippocampus Middle	brain
27	chr6:110008800-110010800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:110008800-110011200	Weak transcription	Brain Anterior Caudate	brain
29	chr6:110009000-110010600	Weak transcription	Thymus	Thymus
30	chr6:110009000-110011000	Weak transcription	Hela-S3	cervix
31	chr6:110009000-110011200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:110009000-110011400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:110009000-110011400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr6:110009000-110011400	Weak transcription	Fetal Stomach	stomach
35	chr6:110009000-110011400	Weak transcription	Pancreas	Pancrea
36	chr6:110009200-110011200	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr6:110009200-110011400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:110009200-110011400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr6:110009200-110011400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:110009200-110011400	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr6:110009200-110011400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr6:110009200-110011400	Weak transcription	HSMMtube	muscle
43	chr6:110009200-110011400	Weak transcription	HUVEC	blood vessel
44	chr6:110009200-110011400	Weak transcription	NHDF-Ad	bronchial
45	chr6:110009400-110011200	Weak transcription	NHLF	lung
46	chr6:110009400-110011400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr6:110009400-110011400	Weak transcription	Osteobl	bone
48	chr6:110009800-110011200	Weak transcription	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links