Variant report

Variant	nsv1020997
Chromosome Location	chr5:59717732-59773467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:331)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59722961-59722993	K562	blood:	n/a	n/a
2	ARID3A	chr5:59759049-59759883	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59769493-59769923	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:59742744-59743990	HepG2	liver:	n/a	chr5:59743535-59743551
5	ATF3	chr5:59758895-59759556	A549	lung:	n/a	n/a
6	BCL3	chr5:59758809-59759695	A549	lung:	n/a	chr5:59759578-59759587
7	BCL3	chr5:59758832-59759533	A549	lung:	n/a	n/a
8	BHLHE40	chr5:59743262-59743636	HepG2	liver:	n/a	n/a
9	BHLHE40	chr5:59742844-59743730	HepG2	liver:	n/a	n/a
10	BHLHE40	chr5:59758972-59759353	A549	lung:	n/a	n/a
11	BHLHE40	chr5:59743228-59743638	HepG2	liver:	n/a	n/a
12	BHLHE40	chr5:59758956-59759660	HepG2	liver:	n/a	n/a
13	BRCA1	chr5:59773450-59773510	GM12878	blood:	n/a	n/a
14	BRCA1	chr5:59758918-59759295	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr5:59747083-59747168	K562	blood:	n/a	n/a
16	CEBPB	chr5:59740891-59741112	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:59758865-59759496	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758883-59758895
18	CEBPB	chr5:59744444-59744829	Hela-S3	cervix:	n/a	chr5:59744753-59744765
19	CEBPB	chr5:59758954-59759375	A549	lung:	n/a	chr5:59759173-59759184
20	CEBPB	chr5:59759016-59759277	HepG2	liver:	n/a	chr5:59759173-59759184
21	CEBPB	chr5:59758972-59759399	MCF-7	breast:	n/a	chr5:59759173-59759184
22	CEBPB	chr5:59758902-59759356	HepG2	liver:	n/a	chr5:59759173-59759184
23	CEBPB	chr5:59759094-59759253	H1-hESC	embryonic stem cell:	n/a	chr5:59759173-59759184
24	CEBPB	chr5:59758957-59759712	HepG2	liver:	n/a	chr5:59759173-59759184
25	CEBPB	chr5:59761806-59762009	A549	lung:	n/a	n/a
26	CEBPB	chr5:59744195-59744769	A549	lung:	n/a	chr5:59744753-59744765
27	CEBPB	chr5:59758926-59759470	Hela-S3	cervix:	n/a	chr5:59759173-59759184
28	CEBPB	chr5:59758997-59759365	IMR90	lung:	n/a	chr5:59759173-59759184
29	CEBPB	chr5:59738481-59738678	HepG2	liver:	n/a	chr5:59738605-59738616
30	CEBPB	chr5:59758981-59759376	K562	blood:	n/a	chr5:59759173-59759184
31	CEBPB	chr5:59758995-59759301	K562	blood:	n/a	chr5:59759173-59759184
32	CEBPB	chr5:59758780-59759728	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758810-59758822 chr5:59758883-59758895
33	CEBPB	chr5:59758952-59759391	HepG2	liver:	n/a	chr5:59759173-59759184
34	CEBPB	chr5:59759013-59759326	MCF-7	breast:	n/a	chr5:59759173-59759184
35	CHD2	chr5:59759045-59759296	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:59762952-59762973	Fibrobl	skin:	n/a	n/a
37	CTCF	chr5:59754600-59754750	K562	blood:	n/a	n/a
38	CTCF	chr5:59732400-59732550	GM12875	blood:	n/a	n/a
39	CTCF	chr5:59754600-59754750	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr5:59732400-59732550	GM12873	blood:	n/a	n/a
41	CTCF	chr5:59754580-59754730	AG09309	skin:	n/a	n/a
42	CTCF	chr5:59718802-59718835	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr5:59754560-59754710	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:59732460-59732610	GM12871	blood:	n/a	n/a
45	CTCF	chr5:59754620-59754770	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr5:59754600-59754750	A549	lung:	n/a	n/a
47	CTCF	chr5:59755354-59755397	Medullo	brain:	n/a	n/a
48	CTCF	chr5:59732490-59732534	GM12878	blood:	n/a	n/a
49	CTCF	chr5:59755768-59755822	Lung_OC	lung:	n/a	n/a
50	CTCF	chr5:59754560-59754710	AG10803	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59727726-59727776	PANC-1	pancreas:	n/a
2	chr5:59727726-59727776	BJ	skin:	n/a
3	chr5:59727726-59727776	HRE	kidney:	n/a
4	chr5:59727726-59727776	GM06990	blood:	n/a
5	chr5:59727726-59727776	SK-N-SH_RA	brain:	n/a
6	chr5:59727726-59727776	HNPCEpiC	eye:	n/a
7	chr5:59727726-59727776	HCM	heart:	n/a
8	chr5:59727726-59727776	U87	brain:	n/a
9	chr5:59727726-59727776	HCPEpiC	choroid plexus:	n/a
10	chr5:59727726-59727776	SK-N-MC	brain:	n/a
11	chr5:59727726-59727776	HCF	heart:	n/a
12	chr5:59727726-59727776	Hepatocyte	liver:	n/a
13	chr5:59727726-59727776	RPTEC	kidney:	n/a
14	chr5:59727726-59727776	SAEC	small airway:	n/a
15	chr5:59727726-59727776	NHDF-neo	bronchial:	n/a
16	chr5:59727726-59727776	GM19239	blood:	n/a
17	chr5:59727726-59727776	HL-60	blood:	n/a
18	chr5:59727726-59727776	ovcar-3	ovarian:	n/a
19	chr5:59727726-59727776	AG09309	skin:	n/a
20	chr5:59727726-59727776	AG10803	skin:	n/a
21	chr5:59727726-59727776	ProgFib	skin:	n/a
22	chr5:59727726-59727776	AG04449	skin:	fetal
23	chr5:59727726-59727776	GM12892	blood:	n/a
24	chr5:59727726-59727776	NB4	blood:	n/a
25	chr5:59727726-59727776	BE2_C	brain:	n/a
26	chr5:59727726-59727776	HRCEpiC	kidney:	n/a
27	chr5:59727726-59727776	MCF10A-Er-Src	breast:	n/a
28	chr5:59727726-59727776	PFSK-1	brain:	n/a
29	chr5:59727726-59727776	HCT-116	colon:	n/a
30	chr5:59727726-59727776	NT2-D1	testis:	n/a
31	chr5:59727726-59727776	NH-A	brain:	n/a
32	chr5:59727726-59727776	LNCaP	prostate:	n/a
33	chr5:59727726-59727776	AoSMC	blood vessel:	n/a
34	chr5:59727726-59727776	Jurkat	blood:	n/a
35	chr5:59727726-59727776	HIPEpiC	eye:	n/a
36	chr5:59727726-59727776	NHBE	bronchial:	n/a
37	chr5:59727726-59727776	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:59727726-59727776	SKMC	muscle:	n/a
39	chr5:59727726-59727776	Caco-2	colon:	n/a
40	chr5:59727726-59727776	SK-N-SH	brain:	n/a
41	chr5:59727726-59727776	A549	lung:	n/a
42	chr5:59727726-59727776	HAEpiC	amniotic membrane:	n/a
43	chr5:59727726-59727776	T-47D	breast:	n/a
44	chr5:59727726-59727776	GM12891	blood:	n/a
45	chr5:59727726-59727776	HRPEpiC	eye:	n/a
46	chr5:59727726-59727776	Hela-S3	cervix:	n/a
47	chr5:59727726-59727776	K562	blood:	n/a
48	chr5:59727726-59727776	PrEC	prostate:	n/a
49	chr5:59727726-59727776	AG09319	gingival:	n/a
50	chr5:59727726-59727776	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59750546..59752966-chr5:59754525..59756849,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213896	TF binding region
ENSG00000224838	TF binding region
SETP21	TF binding region
PDE4D	TF binding region
ENSG00000213896	CpG island
ENSG00000224838	CpG island
SETP21	CpG island
PDE4D	CpG island
ENSG00000214244	chromatin interactions

Extended variants
information (count: 2075 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183307432	chr5:59717740-59717741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574263011	chr5:59717763-59717764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557898528	chr5:59717771-59717772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs148933866	chr5:59717782-59717783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186842595	chr5:59717871-59717872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143165623	chr5:59717895-59717896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544797173	chr5:59717915-59717916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs558946345	chr5:59717955-59717956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs37703	chr5:59717990-59717991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555404318	chr5:59717997-59717998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575567516	chr5:59718044-59718045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191671625	chr5:59718102-59718103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141258288	chr5:59718129-59718130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183759901	chr5:59718150-59718151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540352369	chr5:59718152-59718153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544737251	chr5:59718153-59718154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560685933	chr5:59718167-59718168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529373683	chr5:59718174-59718175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs37702	chr5:59718175-59718176	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562560261	chr5:59718238-59718239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188085658	chr5:59718314-59718315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192617071	chr5:59718374-59718375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530779479	chr5:59718384-59718385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571732556	chr5:59718397-59718398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534446066	chr5:59718415-59718416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146994939	chr5:59718439-59718440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566514972	chr5:59718464-59718465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs37701	chr5:59718489-59718490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535552047	chr5:59718515-59718516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138127801	chr5:59718534-59718535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368923955	chr5:59718535-59718536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575331783	chr5:59718600-59718601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538114570	chr5:59718618-59718619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558063710	chr5:59718661-59718662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563035538	chr5:59718682-59718683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546886913	chr5:59718712-59718713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560102327	chr5:59718713-59718714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9885184	chr5:59718734-59718735	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542737478	chr5:59718832-59718833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185441899	chr5:59718837-59718838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531630995	chr5:59718857-59718858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73108651	chr5:59718955-59718956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114896090	chr5:59718956-59718957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527979507	chr5:59718972-59718973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375987907	chr5:59718998-59718999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368513752	chr5:59719008-59719009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4700374	chr5:59719013-59719014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs535513008	chr5:59719017-59719018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190290854	chr5:59719036-59719037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571244254	chr5:59719037-59719038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59717000-59730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:59727200-59766600	Weak transcription	Primary B cells from cord blood	blood
3	chr5:59730000-59730400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:59730400-59731000	Enhancers	Colon Smooth Muscle	Colon
5	chr5:59730400-59731800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:59730400-59733200	Enhancers	HepG2	liver
7	chr5:59731800-59732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr5:59732000-59732400	Enhancers	GM12878-XiMat	blood
9	chr5:59732400-59733000	Enhancers	Primary B cells from peripheral blood	blood
10	chr5:59732400-59733400	Flanking Active TSS	GM12878-XiMat	blood
11	chr5:59732800-59733000	Enhancers	Aorta	Aorta
12	chr5:59733000-59742600	Weak transcription	Aorta	Aorta
13	chr5:59733200-59738800	Weak transcription	HepG2	liver
14	chr5:59733400-59733800	Enhancers	GM12878-XiMat	blood
15	chr5:59734000-59734400	Enhancers	Fetal Kidney	kidney
16	chr5:59738800-59742800	Enhancers	HepG2	liver
17	chr5:59740000-59741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:59740000-59741600	Enhancers	Fetal Brain Male	brain
19	chr5:59740200-59740600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr5:59740400-59741000	Enhancers	Fetal Brain Female	brain
21	chr5:59740400-59741000	Enhancers	Hela-S3	cervix
22	chr5:59740600-59740800	Enhancers	Gastric	stomach
23	chr5:59741000-59744200	Weak transcription	Hela-S3	cervix
24	chr5:59741200-59741600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:59741600-59741800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:59741600-59743200	Enhancers	Stomach Mucosa	stomach
27	chr5:59741600-59744800	Weak transcription	Fetal Brain Male	brain
28	chr5:59741800-59783200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:59742600-59743000	Enhancers	Aorta	Aorta
30	chr5:59742600-59743000	Enhancers	A549	lung
31	chr5:59742600-59744400	Enhancers	Gastric	stomach
32	chr5:59742800-59743200	Flanking Active TSS	HepG2	liver
33	chr5:59743000-59743600	Flanking Active TSS	A549	lung
34	chr5:59743000-59743800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:59743200-59744400	Weak transcription	Stomach Mucosa	stomach
36	chr5:59743200-59745200	Enhancers	HepG2	liver
37	chr5:59743400-59743800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr5:59743600-59744000	Active TSS	A549	lung
39	chr5:59743800-59747600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:59744000-59744200	Enhancers	A549	lung
41	chr5:59744200-59744400	Flanking Active TSS	A549	lung
42	chr5:59744200-59744600	Enhancers	Brain Angular Gyrus	brain
43	chr5:59744200-59744600	Active TSS	Hela-S3	cervix
44	chr5:59744400-59744600	Enhancers	Stomach Mucosa	stomach
45	chr5:59744400-59744800	Enhancers	A549	lung
46	chr5:59745200-59747400	Weak transcription	HepG2	liver
47	chr5:59747400-59750000	Enhancers	HepG2	liver
48	chr5:59747600-59748800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:59749200-59749400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:59749400-59751400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links