Variant report

Variant	rs12190363
Chromosome Location	chr6:39180487-39180488
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:39178389..39182010-chr6:39186397..39189185,3	MCF-7	breast:
2	chr6:39176890..39181297-chr6:39193958..39200095,7	K562	blood:
3	chr6:39177427..39182769-chr6:39182785..39188256,10	K562	blood:
4	chr6:39167002..39169864-chr6:39179599..39183167,3	K562	blood:

Variant related genes	Relation type
ENSG00000164626	Chromatin interaction

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

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

rs_ID	r²[population]
rs10807202	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10947786	0.92[CHB][hapmap]
rs10947787	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10947788	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10947789	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12200013	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12202900	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12207689	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2033226	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4711585	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4714223	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4714224	0.86[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55818834	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6918122	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72851851	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830644	chr6:39116530-39325980	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1022974	chr6:39120271-39277553	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:39150600-39193800	Genic enhancers	Fetal Intestine Small	intestine
2	chr6:39156800-39193400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr6:39163800-39192800	Weak transcription	Rectal Smooth Muscle	rectum
4	chr6:39169400-39193600	Enhancers	Liver	Liver
5	chr6:39174200-39195000	Enhancers	Stomach Mucosa	stomach
6	chr6:39177600-39181000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:39177600-39182200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:39177600-39182800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:39177600-39186400	Weak transcription	Primary T cells from cord blood	blood
10	chr6:39177800-39182200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:39177800-39183400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr6:39178000-39180600	Weak transcription	A549	lung
13	chr6:39178000-39181000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr6:39178000-39182000	Weak transcription	Fetal Kidney	kidney
15	chr6:39178000-39183400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:39178000-39193400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:39178200-39180800	Weak transcription	Primary B cells from cord blood	blood
18	chr6:39178200-39181800	Weak transcription	Placenta	Placenta
19	chr6:39178200-39182800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr6:39178200-39183000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr6:39178200-39184400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:39178200-39185000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:39178200-39185000	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr6:39178200-39185200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:39178200-39186600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:39178400-39181800	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr6:39178400-39182000	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr6:39178400-39182600	Weak transcription	Hela-S3	cervix
29	chr6:39178400-39185000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr6:39178400-39185200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:39178600-39181800	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr6:39178600-39182000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:39178600-39193200	Weak transcription	Thymus	Thymus
34	chr6:39178800-39182000	Weak transcription	Colonic Mucosa	Colon
35	chr6:39178800-39184800	Genic enhancers	Fetal Intestine Large	intestine
36	chr6:39179000-39186200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr6:39179000-39186800	Genic enhancers	Fetal Thymus	thymus
38	chr6:39179200-39181200	Weak transcription	Esophagus	oesophagus
39	chr6:39179200-39181800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr6:39179200-39181800	Strong transcription	K562	blood
41	chr6:39179200-39182000	Weak transcription	Lung	lung
42	chr6:39179200-39183000	Weak transcription	GM12878-XiMat	blood
43	chr6:39179200-39183200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr6:39179200-39184400	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr6:39179200-39186200	Weak transcription	Small Intestine	intestine
46	chr6:39179400-39182000	Weak transcription	Gastric	stomach
47	chr6:39179400-39182200	Weak transcription	Fetal Lung	lung
48	chr6:39180000-39181400	Enhancers	Primary hematopoietic stem cells	blood
49	chr6:39180000-39181400	Enhancers	Spleen	Spleen
50	chr6:39180000-39181600	Enhancers	Primary monocytes fromperipheralblood	blood

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