Variant report

Variant	nsv1040183
Chromosome Location	chr15:34919342-34975424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:573)
CpG islands
(count:0)
Chromatin interactive
region (count:45)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:573 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
2	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
3	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
4	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
5	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
6	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
7	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
8	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
9	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
10	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
11	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
12	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
13	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
14	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
15	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
16	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
17	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
18	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
19	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
20	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
21	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
22	BCL11A	chr15:34942273-34942696	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:34942342-34942649	GM12878	blood:	n/a	n/a
24	BCLAF1	chr15:34949675-34950412	K562	blood:	n/a	n/a
25	BCLAF1	chr15:34946604-34947084	K562	blood:	n/a	chr15:34946703-34946712
26	BHLHE40	chr15:34957939-34958132	K562	blood:	n/a	n/a
27	BHLHE40	chr15:34949672-34950063	K562	blood:	n/a	n/a
28	BHLHE40	chr15:34942322-34942647	K562	blood:	n/a	n/a
29	BHLHE40	chr15:34944964-34945198	K562	blood:	n/a	n/a
30	BHLHE40	chr15:34947721-34947910	K562	blood:	n/a	n/a
31	BHLHE40	chr15:34952400-34952527	K562	blood:	n/a	n/a
32	BRCA1	chr15:34971598-34971907	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr15:34936200-34936568	K562	blood:	n/a	n/a
34	CBX3	chr15:34925387-34926073	K562	blood:	n/a	n/a
35	CBX3	chr15:34936154-34936713	K562	blood:	n/a	n/a
36	CCNT2	chr15:34947583-34947948	K562	blood:	n/a	n/a
37	CCNT2	chr15:34946815-34947164	K562	blood:	n/a	n/a
38	CCNT2	chr15:34949582-34950219	K562	blood:	n/a	n/a
39	CCNT2	chr15:34944905-34945202	K562	blood:	n/a	chr15:34945126-34945135
40	CEBPB	chr15:34936375-34936702	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:34971468-34971933	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr15:34936245-34936728	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:34936361-34936644	K562	blood:	n/a	n/a
44	CEBPB	chr15:34947266-34947909	K562	blood:	n/a	chr15:34947367-34947378 chr15:34947367-34947380
45	CEBPB	chr15:34940084-34940856	K562	blood:	n/a	n/a
46	CEBPB	chr15:34974878-34975174	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:34944749-34945151	K562	blood:	n/a	chr15:34944767-34944778
48	CEBPB	chr15:34949909-34950147	K562	blood:	n/a	n/a
49	CEBPB	chr15:34971617-34971852	K562	blood:	n/a	n/a
50	CEBPB	chr15:34942355-34942966	IMR90	lung:	n/a	n/a

No data

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
2	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
3	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
4	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
5	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
6	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
7	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
8	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
9	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
10	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
11	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
12	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
13	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
14	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
15	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
16	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
17	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
18	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
19	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
20	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
21	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
22	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
23	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
24	chr15:34949750..34952665-chr15:35241317..35244101,2	K562	blood:
25	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
26	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
27	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
28	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
29	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
30	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
31	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
32	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
33	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
34	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
35	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
36	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
37	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
38	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
39	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
40	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
41	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
42	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
43	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
44	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
45	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
2	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
3	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
4	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
5	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
6	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
7	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
8	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
9	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
10	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
11	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000261304	chromatin interactions
NEK7	miRNA target sites
NEK9	miRNA target sites

Extended variants
information (count: 1774 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559566963	chr15:34919376-34919377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533313809	chr15:34919451-34919452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186909139	chr15:34919457-34919458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550163726	chr15:34919492-34919493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs191373448	chr15:34919560-34919561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183452912	chr15:34919561-34919562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548826812	chr15:34919581-34919582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574424425	chr15:34919600-34919601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs8023728	chr15:34919625-34919626	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534395611	chr15:34919626-34919627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553176455	chr15:34919635-34919636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571502050	chr15:34919656-34919657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369619599	chr15:34919755-34919756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187795171	chr15:34919757-34919758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557588651	chr15:34919782-34919783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575574058	chr15:34919801-34919802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs558068260	chr15:34919812-34919813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs193157895	chr15:34919846-34919847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185012933	chr15:34919847-34919848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573403328	chr15:34919865-34919866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7495020	chr15:34919872-34919873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs188626968	chr15:34919881-34919882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559629552	chr15:34919905-34919906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192800638	chr15:34919945-34919946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113921019	chr15:34919953-34919954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112888332	chr15:34919968-34919969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568834627	chr15:34919974-34919975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112226967	chr15:34919978-34919979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113148540	chr15:34919981-34919982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544976970	chr15:34920003-34920004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs143290598	chr15:34920054-34920055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555552992	chr15:34920065-34920066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs556218112	chr15:34920067-34920068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183895283	chr15:34920081-34920082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574061768	chr15:34920160-34920161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544660438	chr15:34920195-34920196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7495027	chr15:34920204-34920205	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117104664	chr15:34920214-34920215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528217058	chr15:34920219-34920220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546251071	chr15:34920230-34920231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188278717	chr15:34920252-34920253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs180714037	chr15:34920366-34920367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551010097	chr15:34920369-34920370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569568335	chr15:34920421-34920422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536523847	chr15:34920517-34920518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184768292	chr15:34920530-34920531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7497584	chr15:34920531-34920532	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs151263148	chr15:34920534-34920535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7180587	chr15:34920640-34920641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6495695	chr15:34920758-34920759	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:169 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34917600-34920000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr15:34917600-34920000	Weak transcription	NHEK	skin
3	chr15:34917800-34920200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr15:34918600-34920000	Weak transcription	HUVEC	blood vessel
5	chr15:34919200-34920200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr15:34920000-34920400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:34920000-34921600	Enhancers	NHEK	skin
8	chr15:34920000-34922200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:34920000-34922400	Enhancers	HUVEC	blood vessel
10	chr15:34920200-34921000	Enhancers	HMEC	breast
11	chr15:34920200-34921200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:34920200-34921600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr15:34920200-34921600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr15:34920400-34921200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr15:34920800-34921400	Enhancers	A549	lung
16	chr15:34920800-34921400	Enhancers	NHLF	lung
17	chr15:34921200-34921400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:34921200-34923000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr15:34921400-34923200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr15:34922200-34923200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:34923200-34923400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr15:34923200-34923400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr15:34923200-34923400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr15:34923200-34923400	Enhancers	NHEK	skin
25	chr15:34929000-34929400	Enhancers	K562	blood
26	chr15:34929400-34931400	Weak transcription	K562	blood
27	chr15:34931400-34932800	Enhancers	K562	blood
28	chr15:34932600-34932800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr15:34932800-34934400	Weak transcription	K562	blood
30	chr15:34932800-34936200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:34934400-34934600	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr15:34934400-34935200	Enhancers	K562	blood
33	chr15:34934600-34934800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
34	chr15:34935200-34935800	Weak transcription	K562	blood
35	chr15:34935800-34937400	ZNF genes & repeats	K562	blood
36	chr15:34936000-34936200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:34936000-34937000	Enhancers	HSMM	muscle
38	chr15:34936200-34936600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr15:34936200-34936600	Enhancers	HUVEC	blood vessel
40	chr15:34936200-34937200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:34936200-34937200	Enhancers	Muscle Satellite Cultured Cells	--
42	chr15:34936200-34942200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:34936400-34936600	Enhancers	NHLF	lung
44	chr15:34936400-34936800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:34936600-34936800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr15:34936600-34936800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:34936600-34937200	Enhancers	NH-A	brain
48	chr15:34936600-34937600	Enhancers	HSMMtube	muscle
49	chr15:34936600-34942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr15:34936600-34944200	Weak transcription	HUVEC	blood vessel

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