Variant report

Variant	esv3364452
Chromosome Location	chr10:27385286-27395686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:506)
CpG islands
(count:856)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:27389108-27389628	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:27388661-27388684	K562	blood:	n/a	n/a
3	ATF2	chr10:27388987-27389434	GM12878	blood:	n/a	n/a
4	ATF2	chr10:27388820-27389468	GM12878	blood:	n/a	n/a
5	ATF2	chr10:27390317-27390767	GM12878	blood:	n/a	n/a
6	ATF2	chr10:27390375-27390738	GM12878	blood:	n/a	n/a
7	ATF3	chr10:27389357-27389563	GM12878	blood:	n/a	n/a
8	ATF3	chr10:27389317-27389570	K562	blood:	n/a	n/a
9	ATF3	chr10:27389106-27389746	A549	lung:	n/a	n/a
10	ATF3	chr10:27389292-27389550	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr10:27389224-27389673	GM12878	blood:	n/a	n/a
12	ATF3	chr10:27389125-27389719	A549	lung:	n/a	n/a
13	ATF3	chr10:27389258-27389676	K562	blood:	n/a	n/a
14	BACH1	chr10:27388930-27389912	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr10:27390313-27390663	GM12878	blood:	n/a	n/a
16	BATF	chr10:27390288-27390769	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:27390367-27390761	GM12878	blood:	n/a	n/a
18	BCL3	chr10:27388851-27389750	A549	lung:	n/a	chr10:27389334-27389347
19	BCLAF1	chr10:27388750-27389515	GM12878	blood:	n/a	chr10:27389334-27389347
20	BCLAF1	chr10:27390364-27390731	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:27388892-27389947	K562	blood:	n/a	n/a
22	BHLHE40	chr10:27388974-27389775	GM12878	blood:	n/a	n/a
23	BRCA1	chr10:27389070-27389703	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr10:27389245-27389723	HepG2	liver:	n/a	n/a
25	BRCA1	chr10:27388961-27389663	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr10:27388793-27389805	K562	blood:	n/a	n/a
27	CCNT2	chr10:27388854-27389647	K562	blood:	n/a	n/a
28	CEBPB	chr10:27389972-27390171	HepG2	liver:	n/a	chr10:27390102-27390113
29	CEBPB	chr10:27389297-27389520	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr10:27388982-27389649	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:27389091-27389649	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:27389958-27390218	K562	blood:	n/a	chr10:27390102-27390113
33	CEBPD	chr10:27389168-27389638	HepG2	liver:	n/a	n/a
34	CHD1	chr10:27389321-27389382	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr10:27388880-27389743	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr10:27388863-27389691	K562	blood:	n/a	n/a
37	CHD2	chr10:27388947-27389689	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr10:27388885-27389857	HepG2	liver:	n/a	n/a
39	CHD2	chr10:27388954-27389747	GM12878	blood:	n/a	n/a
40	CREB1	chr10:27389167-27389677	A549	lung:	n/a	n/a
41	CTCF	chr10:27388940-27389090	GM12871	blood:	n/a	n/a
42	CTCF	chr10:27389120-27389270	AG04449	skin:	n/a	n/a
43	CTCF	chr10:27389180-27389330	SAEC	small airway:	n/a	n/a
44	CTCF	chr10:27389080-27389230	BJ	skin:	n/a	n/a
45	CTCF	chr10:27389080-27389230	GM06990	blood:	n/a	n/a
46	CTCF	chr10:27389160-27389390	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr10:27391540-27391571	GM13976	blood:	n/a	n/a
48	CTCF	chr10:27389080-27389230	GM12865	blood:	n/a	n/a
49	CTCF	chr10:27389060-27389210	AG09309	skin:	n/a	n/a
50	CTCF	chr10:27389115-27389210	NHEK	skin:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:27392722-27392772	HCT-116	colon:	n/a
2	chr10:27389522-27389572	T-47D	breast:	n/a
3	chr10:27392722-27392772	HCT-116	colon:	n/a
4	chr10:27389522-27389572	T-47D	breast:	n/a
5	chr10:27389408-27389458	A549	lung:	n/a
6	chr10:27389522-27389572	RPTEC	kidney:	n/a
7	chr10:27389392-27389442	SK-N-SH_RA	brain:	n/a
8	chr10:27389534-27389584	HMEC	breast:	n/a
9	chr10:27392722-27392772	HMEC	breast:	n/a
10	chr10:27389408-27389458	H1-hESC	embryonic stem cell:	embryo
11	chr10:27389522-27389572	Caco-2	colon:	n/a
12	chr10:27389600-27389650	HRE	kidney:	n/a
13	chr10:27389534-27389584	HRE	kidney:	n/a
14	chr10:27389534-27389584	RPTEC	kidney:	n/a
15	chr10:27389908-27389958	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:27388890-27388940	AG04449	skin:	fetal
17	chr10:27389621-27389671	ovcar-3	ovarian:	n/a
18	chr10:27385809-27385859	HCPEpiC	choroid plexus:	n/a
19	chr10:27389392-27389442	Caco-2	colon:	n/a
20	chr10:27389408-27389458	HNPCEpiC	eye:	n/a
21	chr10:27389600-27389650	HCPEpiC	choroid plexus:	n/a
22	chr10:27389408-27389458	AoSMC	blood vessel:	n/a
23	chr10:27388890-27388940	HepG2	liver:	n/a
24	chr10:27389572-27389622	H1-hESC	embryonic stem cell:	embryo
25	chr10:27389879-27389929	AG09319	gingival:	n/a
26	chr10:27385809-27385859	NT2-D1	testis:	n/a
27	chr10:27388890-27388940	AG09319	gingival:	n/a
28	chr10:27389600-27389650	HEEpiC	esophagus:	n/a
29	chr10:27389392-27389442	SKMC	muscle:	n/a
30	chr10:27389621-27389671	AG10803	skin:	n/a
31	chr10:27389666-27389716	HCPEpiC	choroid plexus:	n/a
32	chr10:27389392-27389442	GM12891	blood:	n/a
33	chr10:27389076-27389126	HCM	heart:	n/a
34	chr10:27388890-27388940	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:27389879-27389929	HRPEpiC	eye:	n/a
36	chr10:27389408-27389458	HPAEpiC	pulmonary alveolar:	n/a
37	chr10:27389408-27389458	HCM	heart:	n/a
38	chr10:27389879-27389929	GM12891	blood:	n/a
39	chr10:27389908-27389958	SK-N-SH_RA	brain:	n/a
40	chr10:27389879-27389929	NB4	blood:	n/a
41	chr10:27389621-27389671	GM12892	blood:	n/a
42	chr10:27389666-27389716	T-47D	breast:	n/a
43	chr10:27389600-27389650	A549	lung:	n/a
44	chr10:27389666-27389716	IMR90	lung:	fetal
45	chr10:27392722-27392772	NHDF-neo	bronchial:	n/a
46	chr10:27389392-27389442	GM12892	blood:	n/a
47	chr10:27389392-27389442	HIPEpiC	eye:	n/a
48	chr10:27389522-27389572	LNCaP	prostate:	n/a
49	chr10:27389076-27389126	HCT-116	colon:	n/a
50	chr10:27389666-27389716	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:27390343..27392480-chr10:27398264..27400217,2	K562	blood:
2	chr10:27395462..27398841-chr10:27442023..27446304,5	K562	blood:
3	chr10:27389620..27391351-chr10:27392502..27395276,2	MCF-7	breast:
4	chr10:27392451..27395279-chr10:27423684..27425871,2	K562	blood:
5	chr10:27387680..27390568-chr10:27529145..27530975,2	K562	blood:
6	chr10:27385400..27386918-chr10:27442592..27445370,2	K562	blood:
7	chr10:27389620..27391351-chr10:27392502..27395276,2	MCF-7	breast:
8	chr10:27387641..27389495-chr10:27392433..27394066,2	K562	blood:

No data

Variant related genes	Relation type
ANKRD26	TF binding region
ANKRD26	CpG island
ENSG00000107890	chromatin interactions
ENSG00000120539	chromatin interactions
ENSG00000107897	chromatin interactions
ENSG00000136758	chromatin interactions

Extended variants
information (count: 468 )
Associated
traits (count: 47 )

Variant overlapped rSNPs/rCNVs (count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575196358	chr10:27385300-27385301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113501004	chr10:27385353-27385354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190222438	chr10:27385401-27385402	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs532744815	chr10:27385417-27385418	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs7922043	chr10:27385444-27385445	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs569173724	chr10:27385465-27385466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs12767796	chr10:27385490-27385491	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs181367679	chr10:27385498-27385499	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7923079	chr10:27385519-27385520	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577835133	chr10:27385521-27385522	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs12762717	chr10:27385546-27385547	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs186437071	chr10:27385561-27385562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs570889449	chr10:27385602-27385603	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs146661646	chr10:27385607-27385608	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113990083	chr10:27385608-27385609	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs556516167	chr10:27385682-27385683	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs111764848	chr10:27385711-27385712	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576367043	chr10:27385719-27385720	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190836018	chr10:27385733-27385734	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs555585166	chr10:27385741-27385742	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112555231	chr10:27385751-27385752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182104138	chr10:27385798-27385799	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs186258694	chr10:27385809-27385810	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190743294	chr10:27385838-27385839	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs183213705	chr10:27385859-27385860	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188570093	chr10:27385906-27385907	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs148910797	chr10:27385954-27385955	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71483828	chr10:27386021-27386022	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10829179	chr10:27386024-27386025	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs548589739	chr10:27386044-27386045	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs373386720	chr10:27386047-27386048	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528921861	chr10:27386079-27386080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs368430556	chr10:27386089-27386090	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs561798938	chr10:27386106-27386107	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542605580	chr10:27386130-27386131	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562781266	chr10:27386154-27386155	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547935935	chr10:27386158-27386159	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191758189	chr10:27386171-27386172	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs140835266	chr10:27386213-27386214	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs11347521	chr10:27386249-27386250	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs397795190	chr10:27386263-27386264	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs551374952	chr10:27386282-27386283	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564904834	chr10:27386286-27386287	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs1627919	chr10:27386304-27386305	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs139191861	chr10:27386375-27386376	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs118004492	chr10:27386382-27386383	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs183142726	chr10:27386389-27386390	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs73596354	chr10:27386402-27386403	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs557441015	chr10:27386441-27386442	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375729149	chr10:27386451-27386452	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:47)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21525872	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:805 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27283200-27388400	Weak transcription	Psoas Muscle	Psoas
2	chr10:27291600-27388000	Weak transcription	Small Intestine	intestine
3	chr10:27313200-27388200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr10:27313200-27388600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:27313400-27388400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr10:27314600-27388800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr10:27323400-27388600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr10:27326800-27388200	Weak transcription	Brain Substantia Nigra	brain
9	chr10:27328000-27388200	Weak transcription	K562	blood
10	chr10:27350200-27387800	Weak transcription	HMEC	breast
11	chr10:27358600-27388400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr10:27361600-27388200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr10:27362200-27388400	Weak transcription	Colonic Mucosa	Colon
14	chr10:27362400-27388000	Weak transcription	Right Ventricle	heart
15	chr10:27362400-27388200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr10:27362400-27388400	Weak transcription	Pancreas	Pancrea
17	chr10:27362600-27388400	Weak transcription	Esophagus	oesophagus
18	chr10:27362600-27388400	Weak transcription	Spleen	Spleen
19	chr10:27362600-27388800	Weak transcription	Gastric	stomach
20	chr10:27362800-27388600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr10:27365000-27388000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr10:27366600-27388000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr10:27366600-27388600	Weak transcription	Fetal Kidney	kidney
24	chr10:27367400-27388200	Weak transcription	Primary B cells from peripheral blood	blood
25	chr10:27367600-27388400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr10:27367800-27387800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr10:27369800-27388200	Weak transcription	NHDF-Ad	bronchial
28	chr10:27370000-27388600	Weak transcription	Aorta	Aorta
29	chr10:27377200-27388200	Weak transcription	NHLF	lung
30	chr10:27378000-27387800	Weak transcription	Brain Hippocampus Middle	brain
31	chr10:27378000-27388400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr10:27378200-27387800	Weak transcription	Primary T cells fromperipheralblood	blood
33	chr10:27378200-27388000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr10:27378200-27388000	Weak transcription	Fetal Brain Male	brain
35	chr10:27378200-27388200	Weak transcription	Rectal Smooth Muscle	rectum
36	chr10:27378200-27388400	Weak transcription	Primary B cells from cord blood	blood
37	chr10:27378200-27388400	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr10:27378400-27387800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr10:27378400-27387800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr10:27378400-27387800	Weak transcription	HepG2	liver
41	chr10:27378600-27388000	Weak transcription	Thymus	Thymus
42	chr10:27378600-27388200	Weak transcription	HUVEC	blood vessel
43	chr10:27378800-27386600	Weak transcription	Lung	lung
44	chr10:27378800-27388000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:27378800-27388000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr10:27378800-27388000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr10:27378800-27388600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr10:27378800-27388800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:27378800-27388800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr10:27379000-27388400	Weak transcription	Fetal Thymus	thymus

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