Variant report

Variant	rs7304234
Chromosome Location	chr12:123332323-123332324
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123329734..123338030-chr12:123339120..123345153,11	MCF-7	breast:
2	chr12:123330610..123333935-chr12:123339820..123343037,3	MCF-7	breast:
3	chr12:123331521..123333381-chr12:123337742..123339712,2	K562	blood:
4	chr12:123327852..123329476-chr12:123331474..123333275,2	K562	blood:
5	chr12:123331248..123334066-chr12:123346925..123349387,2	K562	blood:
6	chr12:123331465..123333467-chr13:94634904..94637688,2	MCF-7	breast:
7	chr12:123329055..123330600-chr12:123330820..123333817,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000130787	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1671677	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs1671680	0.85[AMR][1000 genomes]
rs1696324	0.85[AMR][1000 genomes]
rs1798568	0.85[AMR][1000 genomes]
rs59499651	0.85[AMR][1000 genomes]
rs7138206	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7312620	0.85[AMR][1000 genomes]
rs7314233	1.00[AMR][1000 genomes]
rs7966607	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899571	chr12:123215734-123363562	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv899572	chr12:123292503-123477311	Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv899573	chr12:123312051-123528405	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv517200	chr12:123312051-123654498	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
6	nsv899574	chr12:123316566-123360151	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv560490	chr12:123326374-123346971	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv899575	chr12:123326374-123360151	Weak transcription Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123321600-123332800	Weak transcription	Ovary	ovary
2	chr12:123321600-123333000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr12:123321800-123336800	Weak transcription	Aorta	Aorta
4	chr12:123322000-123332400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr12:123322600-123332600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:123322800-123334000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr12:123322800-123334400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:123322800-123339600	Weak transcription	Dnd41	blood
9	chr12:123322800-123353000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr12:123323200-123340800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr12:123323200-123352000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr12:123323400-123335200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:123323600-123332400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr12:123323600-123340800	Weak transcription	Rectal Smooth Muscle	rectum
15	chr12:123324600-123344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
16	chr12:123324600-123352800	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:123324800-123332400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr12:123324800-123351600	Weak transcription	Small Intestine	intestine
19	chr12:123325000-123338400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:123325200-123335400	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr12:123325400-123332600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr12:123325800-123333000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr12:123326600-123335600	Weak transcription	NHLF	lung
24	chr12:123326600-123336800	Weak transcription	Psoas Muscle	Psoas
25	chr12:123326600-123345000	Weak transcription	A549	lung
26	chr12:123326800-123335400	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr12:123327200-123333000	Weak transcription	Liver	Liver
28	chr12:123327200-123333000	Enhancers	Brain Substantia Nigra	brain
29	chr12:123327200-123337000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr12:123327200-123340000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr12:123327200-123344200	Weak transcription	Hela-S3	cervix
32	chr12:123327400-123336400	Weak transcription	Stomach Smooth Muscle	stomach
33	chr12:123327400-123352600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:123327600-123334200	Weak transcription	Adipose Nuclei	Adipose
35	chr12:123327600-123335400	Weak transcription	HUVEC	blood vessel
36	chr12:123327600-123337000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:123327600-123353400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr12:123327800-123332600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr12:123328200-123332400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:123328200-123336800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:123328400-123336200	Weak transcription	Placenta	Placenta
42	chr12:123328600-123332400	Weak transcription	Fetal Intestine Large	intestine
43	chr12:123329200-123335600	Weak transcription	Primary T cells from cord blood	blood
44	chr12:123329200-123337600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr12:123329200-123355000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:123329400-123341800	Weak transcription	HepG2	liver
47	chr12:123329600-123336600	Strong transcription	Fetal Stomach	stomach
48	chr12:123329600-123344600	Strong transcription	Fetal Intestine Small	intestine
49	chr12:123329800-123333000	Enhancers	Brain Angular Gyrus	brain
50	chr12:123330000-123335400	Weak transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links