Variant report

Variant	nsv526945
Chromosome Location	chr15:45935755-45941689
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45940982-45941313	HepG2	liver:	n/a	n/a
2	BCL3	chr15:45937705-45938213	A549	lung:	n/a	n/a
3	CEBPB	chr15:45937591-45937846	K562	blood:	n/a	n/a
4	CEBPB	chr15:45941177-45941419	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:45937520-45938135	A549	lung:	n/a	n/a
6	CEBPB	chr15:45937509-45938117	IMR90	lung:	n/a	n/a
7	CEBPB	chr15:45937522-45937851	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr15:45937505-45937794	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:45937676-45937806	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:45937523-45937860	K562	blood:	n/a	n/a
11	CEBPB	chr15:45937526-45937900	HepG2	liver:	n/a	n/a
12	CEBPB	chr15:45937508-45937921	MCF-7	breast:	n/a	n/a
13	CEBPB	chr15:45937488-45937887	MCF-7	breast:	n/a	n/a
14	CEBPB	chr15:45937532-45937896	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr15:45937569-45937878	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr15:45937522-45937881	K562	blood:	n/a	n/a
17	CEBPB	chr15:45937525-45937983	A549	lung:	n/a	n/a
18	CEBPB	chr15:45937370-45938276	A549	lung:	n/a	n/a
19	CHD2	chr15:45938592-45938633	H1-hESC	embryonic stem cell:	n/a	n/a
20	E2F4	chr15:45940812-45941443	MCF10A-Er-Src	breast:	n/a	n/a
21	ELF1	chr15:45941196-45941447	HepG2	liver:	n/a	n/a
22	EP300	chr15:45937714-45938295	A549	lung:	n/a	chr15:45938001-45938011
23	EP300	chr15:45937683-45938279	A549	lung:	n/a	chr15:45938001-45938011
24	ESR1	chr15:45941088-45941460	T-47D	breast:	n/a	n/a
25	FOS	chr15:45937212-45938733	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr15:45937413-45938795	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr15:45941017-45941453	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr15:45936663-45936923	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr15:45941037-45941432	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr15:45936638-45936973	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr15:45940979-45941443	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr15:45940929-45941453	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr15:45936757-45936857	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr15:45937825-45938248	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr15:45937261-45938155	MCF10A-Er-Src	breast:	n/a	n/a
36	FOSL1	chr15:45940916-45941499	HCT-116	colon:	n/a	n/a
37	FOSL2	chr15:45937672-45938278	A549	lung:	n/a	n/a
38	FOSL2	chr15:45940909-45941488	SK-N-SH	brain:	n/a	n/a
39	FOSL2	chr15:45937834-45938092	A549	lung:	n/a	n/a
40	FOSL2	chr15:45940936-45941377	A549	lung:	n/a	n/a
41	FOXA1	chr15:45940663-45941356	HepG2	liver:	n/a	n/a
42	FOXA1	chr15:45937767-45938186	T-47D	breast:	n/a	n/a
43	FOXA1	chr15:45940761-45941009	HepG2	liver:	n/a	n/a
44	FOXA1	chr15:45940722-45941061	T-47D	breast:	n/a	n/a
45	FOXA1	chr15:45940754-45941022	HepG2	liver:	n/a	n/a
46	FOXA1	chr15:45937801-45938174	T-47D	breast:	n/a	n/a
47	FOXA2	chr15:45937689-45938315	A549	lung:	n/a	n/a
48	FOXA2	chr15:45940593-45941032	A549	lung:	n/a	n/a
49	FOXA2	chr15:45937708-45938296	A549	lung:	n/a	n/a
50	FOXA2	chr15:45940726-45941086	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45937757-45937807	PFSK-1	brain:	n/a
2	chr15:45937757-45937807	Hela-S3	cervix:	n/a
3	chr15:45937757-45937807	BJ	skin:	n/a
4	chr15:45937757-45937807	PrEC	prostate:	n/a
5	chr15:45937757-45937807	HMEC	breast:	n/a
6	chr15:45937757-45937807	GM06990	blood:	n/a
7	chr15:45937757-45937807	ovcar-3	ovarian:	n/a
8	chr15:45937757-45937807	GM12892	blood:	n/a
9	chr15:45937757-45937807	SAEC	small airway:	n/a
10	chr15:45937757-45937807	SK-N-SH_RA	brain:	n/a
11	chr15:45937757-45937807	K562	blood:	n/a
12	chr15:45937757-45937807	RPTEC	kidney:	n/a
13	chr15:45937757-45937807	HRE	kidney:	n/a
14	chr15:45937757-45937807	AG04450	lung:	fetal
15	chr15:45937757-45937807	NT2-D1	testis:	n/a
16	chr15:45937757-45937807	MCF-7	breast:	n/a
17	chr15:45937757-45937807	LNCaP	prostate:	n/a
18	chr15:45937757-45937807	NHBE	bronchial:	n/a
19	chr15:45937757-45937807	BE2_C	brain:	n/a
20	chr15:45937757-45937807	SK-N-SH	brain:	n/a
21	chr15:45937757-45937807	T-47D	breast:	n/a
22	chr15:45937757-45937807	HCPEpiC	choroid plexus:	n/a
23	chr15:45937757-45937807	CMK	blood:	n/a
24	chr15:45937757-45937807	HEEpiC	esophagus:	n/a
25	chr15:45937757-45937807	HUVEC	blood vessel:	n/a
26	chr15:45937757-45937807	HEK293	kidney:	embryo
27	chr15:45937757-45937807	MCF10A-Er-Src	breast:	n/a
28	chr15:45937757-45937807	HRCEpiC	kidney:	n/a
29	chr15:45937757-45937807	HCM	heart:	n/a
30	chr15:45937757-45937807	ProgFib	skin:	n/a
31	chr15:45937757-45937807	HCF	heart:	n/a
32	chr15:45937757-45937807	HNPCEpiC	eye:	n/a
33	chr15:45937757-45937807	PANC-1	pancreas:	n/a
34	chr15:45937757-45937807	Caco-2	colon:	n/a
35	chr15:45937757-45937807	A549	lung:	n/a
36	chr15:45937757-45937807	H1-hESC	embryonic stem cell:	embryo
37	chr15:45937757-45937807	AG04449	skin:	fetal
38	chr15:45937757-45937807	HAEpiC	amniotic membrane:	n/a
39	chr15:45937757-45937807	HPAEpiC	pulmonary alveolar:	n/a
40	chr15:45937757-45937807	ECC-1	luminal epithelium:	n/a
41	chr15:45937757-45937807	Hepatocyte	liver:	n/a
42	chr15:45937757-45937807	SKMC	muscle:	n/a
43	chr15:45937757-45937807	NB4	blood:	n/a
44	chr15:45937757-45937807	NH-A	brain:	n/a
45	chr15:45937757-45937807	AG10803	skin:	n/a
46	chr15:45937757-45937807	AoSMC	blood vessel:	n/a
47	chr15:45937757-45937807	U87	brain:	n/a
48	chr15:45937757-45937807	GM12878	blood:	n/a
49	chr15:45937757-45937807	HL-60	blood:	n/a
50	chr15:45937757-45937807	GM19239	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45931592..45934146-chr15:45938709..45942844,4	MCF-7	breast:
2	chr15:45936300..45938060-chr15:45941234..45942847,2	MCF-7	breast:
3	chr15:45934455..45936874-chr15:45938212..45940753,2	MCF-7	breast:
4	chr15:45936300..45938060-chr15:45941234..45942847,2	MCF-7	breast:
5	chr15:45933273..45936098-chr15:48986463..48988127,2	MCF-7	breast:
6	chr15:45931689..45934379-chr15:45936432..45937938,2	MCF-7	breast:
7	chr15:45931549..45933106-chr15:45935286..45937099,2	K562	blood:
8	chr15:45927181..45929961-chr15:45939240..45941307,2	MCF-7	breast:
9	chr15:45934455..45936874-chr15:45938212..45940753,2	MCF-7	breast:
10	chr15:45940658..45942644-chr15:45946028..45948330,2	MCF-7	breast:

No data

Variant related genes	Relation type
SQRDL	TF binding region
SQRDL	CpG island

Extended variants
information (count: 239 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:239 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1816804	chr15:45935755-45935756	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs593126	chr15:45935777-45935778	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs572683134	chr15:45935803-45935804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs644493	chr15:45935816-45935817	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566772195	chr15:45935849-45935850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533875305	chr15:45935947-45935948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368555637	chr15:45936075-45936076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs77751058	chr15:45936093-45936094	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149349793	chr15:45936094-45936095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563573281	chr15:45936114-45936115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560903399	chr15:45936118-45936119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529747278	chr15:45936119-45936120	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs688967	chr15:45936127-45936128	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375420232	chr15:45936208-45936209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144700975	chr15:45936216-45936217	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4270120	chr15:45936234-45936235	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs4271550	chr15:45936266-45936267	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565341388	chr15:45936277-45936278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531007290	chr15:45936279-45936280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs673208	chr15:45936292-45936293	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs567306208	chr15:45936320-45936321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs673555	chr15:45936345-45936346	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs546490224	chr15:45936346-45936347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs566472059	chr15:45936348-45936349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538568773	chr15:45936354-45936355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs673596	chr15:45936371-45936372	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs35377056	chr15:45936389-45936390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs375239577	chr15:45936390-45936391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537927642	chr15:45936499-45936500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543193531	chr15:45936503-45936504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540616499	chr15:45936535-45936536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540272355	chr15:45936536-45936537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560199309	chr15:45936573-45936574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs181355216	chr15:45936580-45936581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs36097479	chr15:45936582-45936583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386783642	chr15:45936587-45936588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200720329	chr15:45936589-45936590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531047189	chr15:45936615-45936616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs55913172	chr15:45936632-45936633	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561094495	chr15:45936713-45936714	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs535462143	chr15:45936722-45936723	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs675413	chr15:45936745-45936746	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs550648374	chr15:45936785-45936786	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562591862	chr15:45936818-45936819	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs675876	chr15:45936856-45936857	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs386783643	chr15:45936862-45936863	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs675890	chr15:45936864-45936865	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs537689519	chr15:45936884-45936885	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs674953	chr15:45936932-45936933	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs574542443	chr15:45936940-45936941	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45929000-45939000	Enhancers	Stomach Mucosa	stomach
2	chr15:45930000-45937800	Weak transcription	Right Ventricle	heart
3	chr15:45930200-45935800	Enhancers	Fetal Intestine Large	intestine
4	chr15:45930400-45936800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr15:45930400-45940800	Weak transcription	Fetal Thymus	thymus
6	chr15:45930600-45940800	Weak transcription	Thymus	Thymus
7	chr15:45930800-45936800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr15:45931000-45936600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr15:45931000-45938800	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr15:45931600-45936600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr15:45932800-45936600	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr15:45933200-45936400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:45933200-45936600	Weak transcription	Primary T cells from cord blood	blood
14	chr15:45933600-45936000	Enhancers	HMEC	breast
15	chr15:45933800-45936000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:45933800-45951200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr15:45934200-45936800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr15:45934200-45937200	Enhancers	Lung	lung
19	chr15:45934200-45938600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr15:45934200-45961600	Weak transcription	Fetal Kidney	kidney
21	chr15:45934400-45936800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr15:45934400-45938800	Enhancers	NHLF	lung
23	chr15:45934600-45935800	Enhancers	NHDF-Ad	bronchial
24	chr15:45934600-45936000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr15:45934600-45936400	Weak transcription	Esophagus	oesophagus
26	chr15:45934600-45936600	Weak transcription	Spleen	Spleen
27	chr15:45934600-45936600	Weak transcription	GM12878-XiMat	blood
28	chr15:45934600-45936800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr15:45934600-45936800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr15:45934600-45937000	Weak transcription	Placenta	Placenta
31	chr15:45934600-45937400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr15:45934600-45937400	Enhancers	A549	lung
33	chr15:45934600-45937600	Weak transcription	Ovary	ovary
34	chr15:45934800-45936200	Enhancers	Liver	Liver
35	chr15:45934800-45936600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr15:45934800-45936600	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr15:45934800-45936800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr15:45934800-45936800	Weak transcription	Right Atrium	heart
39	chr15:45934800-45936800	Weak transcription	Small Intestine	intestine
40	chr15:45934800-45937000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr15:45934800-45937000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr15:45934800-45937000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:45934800-45937800	Weak transcription	Brain Hippocampus Middle	brain
44	chr15:45934800-45937800	Weak transcription	Gastric	stomach
45	chr15:45934800-45937800	Weak transcription	Left Ventricle	heart
46	chr15:45934800-45945800	Weak transcription	Primary hematopoietic stem cells	blood
47	chr15:45935000-45935800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr15:45935000-45936800	Weak transcription	Duodenum Mucosa	Duodenum
49	chr15:45935000-45937000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr15:45935000-45937000	Weak transcription	Adipose Nuclei	Adipose

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