Variant report

Variant	rs9844793
Chromosome Location	chr3:155564699-155564700
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:155563464-155565338	K562	blood:	n/a	n/a
2	POLR2A	chr3:155564462-155564700	K562	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:155564204..155569110-chr3:155569153..155573660,11	K562	blood:
2	chr3:155562568..155565221-chr3:155570394..155575178,4	MCF-7	breast:
3	chr3:155558812..155562150-chr3:155562255..155568620,8	K562	blood:
4	chr3:155563365..155564979-chr3:155565910..155569268,3	K562	blood:
5	chr3:155559420..155561024-chr3:155562363..155565076,2	MCF-7	breast:
6	chr3:155563365..155564970-chr3:155565910..155568625,2	K562	blood:

No data

Variant related genes	Relation type
SLC33A1	TF binding region
ENSG00000169359	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11915601	1.00[EUR][1000 genomes]
rs11927594	1.00[EUR][1000 genomes]
rs16825395	1.00[EUR][1000 genomes]
rs1991546	1.00[EUR][1000 genomes]
rs4621291	1.00[EUR][1000 genomes]
rs6762067	1.00[EUR][1000 genomes]
rs6790239	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6790610	1.00[EUR][1000 genomes]
rs6792780	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6808062	1.00[EUR][1000 genomes]
rs7617114	1.00[EUR][1000 genomes]
rs7617813	1.00[EUR][1000 genomes]
rs7637292	1.00[EUR][1000 genomes]
rs7640763	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9814868	0.86[AFR][1000 genomes]
rs9842049	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9869777	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9876902	0.82[AFR][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	nsv877680	chr3:155438022-155723064	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2753744	chr3:155487298-155707298	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv877681	chr3:155535670-155654017	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155524400-155565800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr3:155524400-155567400	Weak transcription	Lung	lung
3	chr3:155524400-155569400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr3:155524600-155568000	Weak transcription	HUVEC	blood vessel
5	chr3:155530600-155569800	Weak transcription	Aorta	Aorta
6	chr3:155533400-155565800	Weak transcription	HepG2	liver
7	chr3:155533400-155569400	Weak transcription	Brain Substantia Nigra	brain
8	chr3:155535000-155568000	Weak transcription	Right Ventricle	heart
9	chr3:155535400-155568800	Weak transcription	Osteobl	bone
10	chr3:155535600-155568000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr3:155536800-155568200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr3:155537200-155565600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr3:155540000-155569400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:155540200-155568000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:155541000-155568000	Weak transcription	Psoas Muscle	Psoas
16	chr3:155541200-155567400	Weak transcription	Ovary	ovary
17	chr3:155541600-155567800	Weak transcription	Colonic Mucosa	Colon
18	chr3:155541800-155565800	Weak transcription	NHDF-Ad	bronchial
19	chr3:155541800-155566000	Weak transcription	Small Intestine	intestine
20	chr3:155542800-155569600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr3:155543000-155566000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr3:155543000-155569400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr3:155543000-155569400	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr3:155543000-155569400	Weak transcription	NHLF	lung
25	chr3:155543000-155570200	Weak transcription	Esophagus	oesophagus
26	chr3:155543200-155569400	Weak transcription	A549	lung
27	chr3:155544200-155569000	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:155544800-155565800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr3:155545600-155567200	Weak transcription	Colon Smooth Muscle	Colon
30	chr3:155545600-155568000	Weak transcription	Fetal Kidney	kidney
31	chr3:155547600-155565800	Weak transcription	Thymus	Thymus
32	chr3:155547600-155567200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:155547800-155565800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr3:155547800-155565800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr3:155547800-155567000	Weak transcription	Hela-S3	cervix
36	chr3:155547800-155567200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr3:155547800-155568000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:155547800-155569000	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr3:155547800-155569400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr3:155547800-155569600	Weak transcription	HSMMtube	muscle
41	chr3:155548400-155565400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:155551800-155565800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:155551800-155565800	Weak transcription	Fetal Intestine Large	intestine
44	chr3:155551800-155566200	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr3:155551800-155567200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr3:155551800-155568200	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr3:155551800-155568200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr3:155551800-155569600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr3:155552000-155565800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr3:155552000-155568000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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