Variant report

Variant	rs61943537
Chromosome Location	chr12:118607591-118607592
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:118607204..118610139-chr12:118612001..118614626,2	K562	blood:
2	chr12:118602518..118604035-chr12:118606751..118609682,2	MCF-7	breast:
3	chr12:118606761..118609389-chr12:118613397..118615983,2	MCF-7	breast:

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs10507286	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11068870	0.82[EUR][1000 genomes]
rs16948193	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16948197	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16948204	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16948230	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16948234	0.85[EUR][1000 genomes]
rs17433217	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17440315	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17440336	0.96[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17440364	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17440433	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17440669	0.80[EUR][1000 genomes]
rs17512142	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17512177	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17512198	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17512219	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17512525	0.80[EUR][1000 genomes]
rs2280711	0.82[EUR][1000 genomes]
rs3852531	1.00[ASN][1000 genomes]
rs3852532	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55833534	0.85[EUR][1000 genomes]
rs56033674	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56708462	0.85[EUR][1000 genomes]
rs58113338	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61943364	0.82[EUR][1000 genomes]
rs61943523	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs61943524	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61943525	0.91[AMR][1000 genomes]
rs61943528	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61943535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61943538	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945175	0.83[EUR][1000 genomes]
rs61945176	0.83[EUR][1000 genomes]
rs61945177	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945180	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945181	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945182	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945183	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945184	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945187	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945188	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945189	1.00[ASN][1000 genomes]
rs61945190	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945192	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945206	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945210	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945212	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945216	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945217	1.00[ASN][1000 genomes]
rs61945218	0.85[EUR][1000 genomes]
rs61945220	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945221	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61945226	0.83[EUR][1000 genomes]
rs61945228	0.81[EUR][1000 genomes]
rs61946068	0.80[EUR][1000 genomes]
rs7136216	0.89[EUR][1000 genomes]
rs7301950	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7303417	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7307393	0.80[EUR][1000 genomes]
rs7309671	0.80[EUR][1000 genomes]
rs7314987	1.00[ASN][1000 genomes]
rs73205512	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73205526	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73205531	0.85[EUR][1000 genomes]
rs73220119	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7954330	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7962185	0.83[EUR][1000 genomes]
rs7963353	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7965350	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7970481	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7977403	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9669004	0.83[EUR][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	nsv1053785	chr12:118490955-118874194	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1054703	chr12:118575000-118638613	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv541611	chr12:118575000-118638613	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv1035497	chr12:118599539-118732144	Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv541612	chr12:118599539-118732144	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118576000-118619600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr12:118576000-118624000	Weak transcription	Stomach Mucosa	stomach
3	chr12:118578200-118611600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:118584000-118627600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:118585800-118619000	Weak transcription	HepG2	liver
6	chr12:118586200-118619400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:118586600-118613600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:118587600-118611200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:118587600-118619200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr12:118587800-118620000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr12:118589600-118619000	Weak transcription	A549	lung
12	chr12:118590400-118617000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:118592600-118619400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:118593200-118619200	Strong transcription	Fetal Brain Female	brain
15	chr12:118593200-118619400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:118593200-118619600	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr12:118598200-118620000	Weak transcription	Hela-S3	cervix
18	chr12:118599000-118607800	Weak transcription	Fetal Brain Male	brain
19	chr12:118599200-118608000	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr12:118599800-118607600	Weak transcription	Small Intestine	intestine
21	chr12:118599800-118608000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr12:118599800-118608200	Weak transcription	Colonic Mucosa	Colon
23	chr12:118599800-118608200	Weak transcription	HMEC	breast
24	chr12:118599800-118608400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr12:118599800-118608400	Weak transcription	Colon Smooth Muscle	Colon
26	chr12:118599800-118609800	Weak transcription	Psoas Muscle	Psoas
27	chr12:118599800-118609800	Weak transcription	HUVEC	blood vessel
28	chr12:118599800-118613000	Weak transcription	HSMMtube	muscle
29	chr12:118599800-118625600	Weak transcription	Pancreas	Pancrea
30	chr12:118600000-118607800	Weak transcription	Spleen	Spleen
31	chr12:118600000-118608000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr12:118600000-118608000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr12:118600000-118608800	Weak transcription	Gastric	stomach
34	chr12:118600000-118609400	Weak transcription	Right Ventricle	heart
35	chr12:118600000-118609600	Weak transcription	Fetal Heart	heart
36	chr12:118600000-118610000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:118600200-118608200	Weak transcription	Aorta	Aorta
38	chr12:118600200-118608200	Weak transcription	Rectal Smooth Muscle	rectum
39	chr12:118600200-118613600	Weak transcription	Fetal Kidney	kidney
40	chr12:118600400-118608000	Weak transcription	Ovary	ovary
41	chr12:118600600-118607800	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr12:118600600-118608600	Weak transcription	K562	blood
43	chr12:118600800-118608000	Weak transcription	Osteobl	bone
44	chr12:118600800-118608800	Weak transcription	NHLF	lung
45	chr12:118601000-118608000	Weak transcription	HSMM	muscle
46	chr12:118601000-118608200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr12:118601200-118607800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr12:118601200-118612800	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr12:118602000-118613800	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr12:118602200-118613000	Strong transcription	Primary B cells from peripheral blood	blood

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