Variant report

Variant	esv1815572
Chromosome Location	chr12:118664823-118685792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr12:118674866-118675185	GM12878	blood:	n/a	chr12:118675058-118675067
2	BCL11A	chr12:118674790-118675224	GM12878	blood:	n/a	chr12:118675058-118675067
3	BCLAF1	chr12:118674680-118675262	GM12878	blood:	n/a	chr12:118675058-118675067
4	CHD2	chr12:118674871-118675269	GM12878	blood:	n/a	n/a
5	CTCF	chr12:118679420-118679570	GM12868	blood:	n/a	n/a
6	CTCF	chr12:118672424-118672429	A549	lung:	n/a	n/a
7	CTCF	chr12:118683178-118683199	GM10266	blood:	n/a	n/a
8	CTCF	chr12:118672389-118672445	MCF-7	breast:	n/a	n/a
9	CTCF	chr12:118677770-118677852	Kidney_OC	kidney:	n/a	n/a
10	CUX1	chr12:118667917-118667921	K562	blood:	n/a	n/a
11	CUX1	chr12:118674721-118674802	K562	blood:	n/a	n/a
12	CUX1	chr12:118674777-118675195	GM12878	blood:	n/a	n/a
13	E2F4	chr12:118668026-118668156	MCF10A-Er-Src	breast:	n/a	n/a
14	E2F4	chr12:118675492-118676320	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr12:118674859-118675144	GM12878	blood:	n/a	n/a
16	EBF1	chr12:118674917-118675153	GM12878	blood:	n/a	n/a
17	EBF1	chr12:118674788-118675232	GM12878	blood:	n/a	n/a
18	EBF1	chr12:118684403-118684612	GM12878	blood:	n/a	n/a
19	ELF1	chr12:118675616-118676203	HCT-116	colon:	n/a	n/a
20	ELF1	chr12:118675680-118676165	SK-N-SH	brain:	n/a	n/a
21	ELF1	chr12:118675796-118676151	MCF-7	breast:	n/a	n/a
22	EP300	chr12:118674826-118675239	GM12878	blood:	n/a	chr12:118675058-118675072
23	EP300	chr12:118664851-118664861	GM12878	blood:	n/a	n/a
24	EP300	chr12:118674836-118675289	GM12878	blood:	n/a	chr12:118675058-118675072
25	EP300	chr12:118674739-118675397	GM12878	blood:	n/a	chr12:118675058-118675072
26	FOS	chr12:118675731-118676105	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr12:118675746-118676105	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:118675687-118676105	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:118675674-118676148	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL1	chr12:118675633-118676197	HCT-116	colon:	n/a	n/a
31	GATA2	chr12:118684366-118684677	K562	blood:	n/a	n/a
32	GATA3	chr12:118675590-118676167	T-47D	breast:	n/a	n/a
33	GATA3	chr12:118675632-118676257	SK-N-SH	brain:	n/a	chr12:118676242-118676250
34	GATA3	chr12:118674998-118675134	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr12:118675688-118676110	MCF-7	breast:	n/a	n/a
36	GATA3	chr12:118675584-118676119	T-47D	breast:	n/a	n/a
37	HEY1	chr12:118683885-118684083	HepG2	liver:	n/a	n/a
38	HEY1	chr12:118683853-118684154	K562	blood:	n/a	n/a
39	HEY1	chr12:118684206-118684704	K562	blood:	n/a	n/a
40	HEY1	chr12:118683805-118684708	K562	blood:	n/a	n/a
41	HEY1	chr12:118684383-118684515	HepG2	liver:	n/a	n/a
42	IKZF1	chr12:118674784-118675487	GM12878	blood:	n/a	n/a
43	IRF1	chr12:118675014-118675175	K562	blood:	n/a	chr12:118675055-118675069 chr12:118675057-118675067 chr12:118675055-118675066
44	IRF4	chr12:118684222-118684515	GM12878	blood:	n/a	n/a
45	IRF4	chr12:118674839-118675222	GM12878	blood:	n/a	n/a
46	JUN	chr12:118683688-118683794	HepG2	liver:	n/a	chr12:118683724-118683737
47	JUND	chr12:118675587-118676183	HCT-116	colon:	n/a	n/a
48	JUND	chr12:118675609-118676141	SK-N-SH	brain:	n/a	n/a
49	JUND	chr12:118675611-118676140	HCT-116	colon:	n/a	n/a
50	MEF2A	chr12:118674753-118675291	GM12878	blood:	n/a	chr12:118674881-118674898 chr12:118674883-118674898

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118683952-118684002	BJ	skin:	n/a
2	chr12:118683952-118684002	Hepatocyte	liver:	n/a
3	chr12:118683952-118684002	Jurkat	blood:	n/a
4	chr12:118683952-118684002	PANC-1	pancreas:	n/a
5	chr12:118683952-118684002	HepG2	liver:	n/a
6	chr12:118683952-118684002	ovcar-3	ovarian:	n/a
7	chr12:118683952-118684002	HAEpiC	amniotic membrane:	n/a
8	chr12:118683952-118684002	HNPCEpiC	eye:	n/a
9	chr12:118683952-118684002	AG04450	lung:	fetal
10	chr12:118683952-118684002	GM19239	blood:	n/a
11	chr12:118683952-118684002	HCM	heart:	n/a
12	chr12:118683952-118684002	SK-N-SH	brain:	n/a
13	chr12:118683952-118684002	SK-N-MC	brain:	n/a
14	chr12:118683952-118684002	PrEC	prostate:	n/a
15	chr12:118683952-118684002	SKMC	muscle:	n/a
16	chr12:118683952-118684002	RPTEC	kidney:	n/a
17	chr12:118683952-118684002	NB4	blood:	n/a
18	chr12:118683952-118684002	Caco-2	colon:	n/a
19	chr12:118683952-118684002	GM12892	blood:	n/a
20	chr12:118683952-118684002	Hela-S3	cervix:	n/a
21	chr12:118683952-118684002	AoSMC	blood vessel:	n/a
22	chr12:118683952-118684002	HIPEpiC	eye:	n/a
23	chr12:118683952-118684002	GM12891	blood:	n/a
24	chr12:118683952-118684002	H1-hESC	embryonic stem cell:	embryo
25	chr12:118683952-118684002	ProgFib	skin:	n/a
26	chr12:118683952-118684002	AG09319	gingival:	n/a
27	chr12:118683952-118684002	GM06990	blood:	n/a
28	chr12:118683952-118684002	IMR90	lung:	fetal
29	chr12:118683952-118684002	AG09309	skin:	n/a
30	chr12:118683952-118684002	NHBE	bronchial:	n/a
31	chr12:118683952-118684002	MCF10A-Er-Src	breast:	n/a
32	chr12:118683952-118684002	HMEC	breast:	n/a
33	chr12:118683952-118684002	T-47D	breast:	n/a
34	chr12:118683952-118684002	K562	blood:	n/a
35	chr12:118683952-118684002	HL-60	blood:	n/a
36	chr12:118683952-118684002	CMK	blood:	n/a
37	chr12:118683952-118684002	HEK293	kidney:	embryo
38	chr12:118683952-118684002	HUVEC	blood vessel:	n/a
39	chr12:118683952-118684002	NH-A	brain:	n/a
40	chr12:118683952-118684002	GM12878	blood:	n/a
41	chr12:118683952-118684002	HRE	kidney:	n/a
42	chr12:118683952-118684002	MCF-7	breast:	n/a
43	chr12:118683952-118684002	AG10803	skin:	n/a
44	chr12:118683952-118684002	HEEpiC	esophagus:	n/a
45	chr12:118683952-118684002	HCF	heart:	n/a
46	chr12:118683952-118684002	PFSK-1	brain:	n/a
47	chr12:118683952-118684002	U87	brain:	n/a
48	chr12:118683952-118684002	LNCaP	prostate:	n/a
49	chr12:118683952-118684002	SK-N-SH_RA	brain:	n/a
50	chr12:118683952-118684002	HCT-116	colon:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:118673323..118676031-chr12:118677378..118679199,2	MCF-7	breast:
2	chr12:118629722..118631578-chr12:118673558..118677291,3	K562	blood:
3	chr12:118673643..118676401-chr12:118686637..118689650,3	K562	blood:
4	chr12:118666340..118669274-chr12:118811225..118812911,2	MCF-7	breast:
5	chr12:118674498..118676641-chr12:118709744..118711259,2	MCF-7	breast:
6	chr12:118674302..118676883-chr12:118810896..118813058,3	MCF-7	breast:
7	chr12:118670061..118671859-chr12:118680018..118682313,2	K562	blood:
8	chr1:174967586..174968141-chr12:118675636..118676136,2	HCT-116	colon:
9	chr12:118666496..118668871-chr12:118808783..118811137,2	MCF-7	breast:
10	chr12:118676214..118678466-chr12:118707560..118709083,2	MCF-7	breast:
11	chr12:118670146..118671959-chr12:118810899..118813142,2	MCF-7	breast:
12	chr12:118685088..118687913-chr12:118695342..118697547,2	MCF-7	breast:
13	chr12:118670359..118672856-chr12:118680813..118682507,2	K562	blood:
14	chr12:118673323..118676031-chr12:118677378..118679199,2	MCF-7	breast:

No data

Variant related genes	Relation type
RPS2P5	TF binding region
TAOK3	TF binding region
RPS2P5	CpG island
TAOK3	CpG island
ENSG00000135090	chromatin interactions

Extended variants
information (count: 716 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:716 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17586463	chr12:118664823-118664824	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112540973	chr12:118664841-118664842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1277175	chr12:118664855-118664856	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562116486	chr12:118664900-118664901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs16948193	chr12:118664920-118664921	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs370578284	chr12:118664973-118664974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2668264	chr12:118664977-118664978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs564777621	chr12:118664995-118664996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201066796	chr12:118665071-118665072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146436683	chr12:118665075-118665076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1092854	chr12:118665184-118665185	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs559822696	chr12:118665222-118665223	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528909335	chr12:118665506-118665507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549182234	chr12:118665538-118665539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551359531	chr12:118665641-118665642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199644036	chr12:118665730-118665731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182267261	chr12:118665741-118665742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565933417	chr12:118665855-118665856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538027801	chr12:118665856-118665857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551435233	chr12:118665900-118665901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138921175	chr12:118665940-118665941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539852337	chr12:118665942-118665943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376705017	chr12:118665953-118665954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369936605	chr12:118666006-118666007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371324877	chr12:118666039-118666040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553356695	chr12:118666042-118666043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536177951	chr12:118666132-118666133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573399233	chr12:118666154-118666155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141490013	chr12:118666248-118666249	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536834655	chr12:118666249-118666250	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555816789	chr12:118666255-118666256	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557029441	chr12:118666402-118666403	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs445926	chr12:118666427-118666428	Strong transcription ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs117743056	chr12:118666539-118666540	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs535899647	chr12:118666562-118666563	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143526396	chr12:118666587-118666588	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559690966	chr12:118666588-118666589	Strong transcription ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188581162	chr12:118666752-118666753	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148036820	chr12:118666754-118666755	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562580458	chr12:118666755-118666756	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs61945187	chr12:118666794-118666795	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551513773	chr12:118666847-118666848	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371746036	chr12:118666899-118666900	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs55705124	chr12:118666908-118666909	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114554346	chr12:118666918-118666919	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs643270	chr12:118666919-118666920	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547034668	chr12:118666921-118666922	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs61945188	chr12:118666974-118666975	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs535820912	chr12:118667031-118667032	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575926158	chr12:118667051-118667052	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic cancer	17952125	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118621000-118682600	Weak transcription	A549	lung
2	chr12:118628400-118697200	Weak transcription	Psoas Muscle	Psoas
3	chr12:118628800-118672600	Weak transcription	Colon Smooth Muscle	Colon
4	chr12:118628800-118673000	Weak transcription	NH-A	brain
5	chr12:118636800-118695000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:118637200-118700600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr12:118637200-118700800	Weak transcription	Fetal Muscle Leg	muscle
8	chr12:118637400-118671400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr12:118637400-118672400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:118637400-118684200	Weak transcription	Pancreas	Pancrea
11	chr12:118637400-118694200	Weak transcription	Brain Angular Gyrus	brain
12	chr12:118637400-118701400	Weak transcription	Spleen	Spleen
13	chr12:118637400-118703800	Weak transcription	Esophagus	oesophagus
14	chr12:118637400-118724000	Weak transcription	Aorta	Aorta
15	chr12:118637600-118673000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr12:118638800-118687800	Weak transcription	Gastric	stomach
17	chr12:118639000-118672200	Weak transcription	Placenta	Placenta
18	chr12:118639000-118672200	Weak transcription	Left Ventricle	heart
19	chr12:118639000-118672800	Weak transcription	Small Intestine	intestine
20	chr12:118639400-118674800	Weak transcription	HMEC	breast
21	chr12:118639800-118672600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:118643000-118672200	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr12:118644200-118665600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:118644800-118666400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr12:118647800-118666400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr12:118648000-118666400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr12:118649800-118666600	Weak transcription	Thymus	Thymus
28	chr12:118650400-118690400	Weak transcription	Stomach Mucosa	stomach
29	chr12:118650600-118671400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr12:118650600-118672400	Weak transcription	Rectal Smooth Muscle	rectum
31	chr12:118650600-118679400	Weak transcription	HUVEC	blood vessel
32	chr12:118650800-118672200	Weak transcription	HSMM	muscle
33	chr12:118651800-118672200	Weak transcription	Lung	lung
34	chr12:118651800-118672400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:118652000-118666400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:118652000-118666400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:118652000-118666600	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr12:118652000-118672200	Weak transcription	Fetal Thymus	thymus
39	chr12:118652000-118672600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr12:118652000-118673000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:118652200-118666400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr12:118652200-118666400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr12:118652200-118666600	Weak transcription	Fetal Lung	lung
44	chr12:118652200-118666600	Weak transcription	Osteobl	bone
45	chr12:118652200-118672600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
46	chr12:118652200-118727800	Weak transcription	NHLF	lung
47	chr12:118652400-118666400	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr12:118654000-118674000	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:118657600-118666600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
50	chr12:118658000-118666800	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links