Variant report

Variant	rs10191232
Chromosome Location	chr2:73227186-73227187
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:73225489..73227470-chr2:73297396..73299459,2	K562	blood:
2	chr2:73227183..73229213-chr2:73231275..73232943,2	K562	blood:
3	chr2:73218918..73222719-chr2:73226745..73229455,3	K562	blood:

Variant related genes	Relation type
ENSG00000144040	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10169188	0.95[AFR][1000 genomes]
rs10184684	0.95[AFR][1000 genomes]
rs10186042	0.91[AFR][1000 genomes]
rs10194871	1.00[ASW][hapmap];0.92[LWK][hapmap];1.00[MKK][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10201147	0.86[AFR][1000 genomes]
rs10211218	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs13392698	1.00[ASW][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes]
rs13401894	1.00[MEX][hapmap]
rs13403043	1.00[ASW][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes]
rs13406318	1.00[ASW][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes]
rs13412451	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13414995	0.93[YRI][hapmap];0.95[AFR][1000 genomes]
rs13428265	0.87[AFR][1000 genomes]
rs9808477	0.91[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002295	chr2:73216155-73350391	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73176600-73227400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:73183200-73228200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:73190600-73234400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:73194200-73248800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:73207800-73263200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr2:73208000-73247600	Weak transcription	Primary B cells from cord blood	blood
7	chr2:73208400-73227400	Weak transcription	A549	lung
8	chr2:73208400-73227600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr2:73208600-73227200	Weak transcription	Colon Smooth Muscle	Colon
10	chr2:73209000-73227200	Weak transcription	HSMM	muscle
11	chr2:73210400-73227200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:73211000-73258400	Weak transcription	Colonic Mucosa	Colon
13	chr2:73211600-73235800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr2:73212200-73247400	Weak transcription	HSMMtube	muscle
15	chr2:73212400-73227400	Weak transcription	Adipose Nuclei	Adipose
16	chr2:73212400-73236000	Weak transcription	Esophagus	oesophagus
17	chr2:73212800-73238800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:73213800-73227400	Weak transcription	Gastric	stomach
19	chr2:73213800-73236200	Weak transcription	Pancreas	Pancrea
20	chr2:73214000-73232000	Weak transcription	Aorta	Aorta
21	chr2:73214000-73238400	Weak transcription	Fetal Lung	lung
22	chr2:73214200-73247800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr2:73214200-73286400	Weak transcription	Psoas Muscle	Psoas
24	chr2:73215200-73228400	Weak transcription	Placenta	Placenta
25	chr2:73215400-73236000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr2:73215800-73235600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr2:73215800-73247400	Weak transcription	Thymus	Thymus
28	chr2:73215800-73263000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr2:73216000-73236000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr2:73216200-73227600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr2:73216200-73248800	Weak transcription	Primary hematopoietic stem cells	blood
32	chr2:73216800-73234400	Weak transcription	Primary T cells from cord blood	blood
33	chr2:73217400-73228000	Weak transcription	Left Ventricle	heart
34	chr2:73217400-73231800	Weak transcription	Fetal Heart	heart
35	chr2:73217400-73236200	Weak transcription	Fetal Muscle Leg	muscle
36	chr2:73217400-73249000	Weak transcription	Ovary	ovary
37	chr2:73217600-73227200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:73217600-73227400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr2:73217800-73237400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr2:73218000-73227400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr2:73220600-73227200	Strong transcription	Fetal Intestine Small	intestine
42	chr2:73220600-73227400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr2:73220600-73227400	Weak transcription	K562	blood
44	chr2:73220600-73227600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr2:73220600-73249000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr2:73220600-73263200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr2:73220800-73228800	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr2:73221200-73231400	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr2:73221200-73263000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr2:73222200-73229000	Strong transcription	Primary monocytes fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links