Variant report

Variant	nsv962565
Chromosome Location	chr20:23956974-23976574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr20:23965266-23965679	GM12878	blood:	n/a	n/a
2	BCL11A	chr20:23959584-23959850	GM12878	blood:	n/a	n/a
3	BCL11A	chr20:23965421-23965603	GM12878	blood:	n/a	n/a
4	BCL11A	chr20:23957003-23957211	GM12878	blood:	n/a	n/a
5	BCL11A	chr20:23965025-23965194	GM12878	blood:	n/a	n/a
6	BCL11A	chr20:23959204-23959390	GM12878	blood:	n/a	chr20:23959323-23959332
7	BCL11A	chr20:23970694-23970943	GM12878	blood:	n/a	n/a
8	BCL3	chr20:23960441-23961293	GM12878	blood:	n/a	chr20:23960654-23960662
9	BCL3	chr20:23960521-23961246	GM12878	blood:	n/a	chr20:23960654-23960662
10	CEBPB	chr20:23961774-23962025	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:23961806-23961982	HepG2	liver:	n/a	n/a
12	CTCF	chr20:23959320-23959470	GM12870	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
13	CTCF	chr20:23965420-23965570	K562	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965421-23965431
14	CTCF	chr20:23965180-23965330	GM12866	blood:	n/a	chr20:23965234-23965243
15	CTCF	chr20:23965200-23965350	A549	lung:	n/a	chr20:23965234-23965243
16	CTCF	chr20:23965220-23965370	SAEC	small airway:	n/a	chr20:23965234-23965243
17	CTCF	chr20:23965760-23965910	GM12873	blood:	n/a	n/a
18	CTCF	chr20:23965200-23965350	GM12865	blood:	n/a	chr20:23965234-23965243
19	CTCF	chr20:23968646-23968738	GM10248	blood:	n/a	n/a
20	CTCF	chr20:23959382-23959452	MCF-7	breast:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
21	CTCF	chr20:23965294-23965540	Fibrobl	skin:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
22	CTCF	chr20:23965265-23965546	GM12878	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
23	CTCF	chr20:23959280-23959430	HL-60	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
24	CTCF	chr20:23960704-23960773	GM19239	blood:	n/a	n/a
25	CTCF	chr20:23965303-23965536	MCF-7	breast:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
26	CTCF	chr20:23965180-23965330	AG09319	gingival:	n/a	chr20:23965234-23965243
27	CTCF	chr20:23965440-23965590	HRE	kidney:	n/a	n/a
28	CTCF	chr20:23965180-23965330	A549	lung:	n/a	chr20:23965234-23965243
29	CTCF	chr20:23975310-23975508	K562	blood:	n/a	n/a
30	CTCF	chr20:23965200-23965350	HCT-116	colon:	n/a	chr20:23965234-23965243
31	CTCF	chr20:23961901-23961919	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr20:23965160-23965310	AoAF	blood vessel:	n/a	chr20:23965234-23965243
33	CTCF	chr20:23959300-23959450	GM12868	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
34	CTCF	chr20:23965280-23965430	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr20:23959353-23959414	GM10266	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
36	CTCF	chr20:23965180-23965330	HCM	heart:	n/a	chr20:23965234-23965243
37	CTCF	chr20:23965149-23965628	K562	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965234-23965243 chr20:23965413-23965434
38	CTCF	chr20:23965271-23965535	NHEK	skin:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
39	CTCF	chr20:23965420-23965570	GM12874	blood:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965421-23965431
40	CTCF	chr20:23959300-23959450	WERI-Rb-1	eye:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
41	CTCF	chr20:23965180-23965330	GM12874	blood:	n/a	chr20:23965234-23965243
42	CTCF	chr20:23965180-23965330	RPTEC	kidney:	n/a	chr20:23965234-23965243
43	CTCF	chr20:23965242-23965620	Spleen_OC	spleen:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
44	CTCF	chr20:23959245-23959449	HepG2	liver:	n/a	chr20:23959276-23959289 chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
45	CTCF	chr20:23959240-23959390	HBMEC	blood vessel:	n/a	chr20:23959276-23959289
46	CTCF	chr20:23965160-23965310	GM12868	blood:	n/a	chr20:23965234-23965243
47	CTCF	chr20:23965300-23965539	MCF-7	breast:	n/a	chr20:23965424-23965433 chr20:23965420-23965433 chr20:23965418-23965436 chr20:23965421-23965431 chr20:23965419-23965435 chr20:23965413-23965434
48	CTCF	chr20:23959280-23959430	K562	blood:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959384-23959402 chr20:23959386-23959407
49	CTCF	chr20:23965200-23965350	HMF	breast:	n/a	chr20:23965234-23965243
50	CTCF	chr20:23959325-23959510	H1-hESC	embryonic stem cell:	n/a	chr20:23959387-23959400 chr20:23959385-23959401 chr20:23959490-23959498 chr20:23959384-23959402 chr20:23959386-23959407

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23969832-23969882	IMR90	lung:	fetal
2	chr20:23970065-23970115	HRE	kidney:	n/a
3	chr20:23970065-23970115	HEK293	kidney:	embryo
4	chr20:23969429-23969479	GM12891	blood:	n/a
5	chr20:23965841-23965891	HAEpiC	amniotic membrane:	n/a
6	chr20:23969397-23969447	PANC-1	pancreas:	n/a
7	chr20:23969429-23969479	HepG2	liver:	n/a
8	chr20:23969429-23969479	GM12892	blood:	n/a
9	chr20:23969432-23969482	LNCaP	prostate:	n/a
10	chr20:23965921-23965971	AG04450	lung:	fetal
11	chr20:23968830-23968880	Hepatocyte	liver:	n/a
12	chr20:23970162-23970212	NHDF-neo	bronchial:	n/a
13	chr20:23969429-23969479	HRCEpiC	kidney:	n/a
14	chr20:23970065-23970115	LNCaP	prostate:	n/a
15	chr20:23970162-23970212	HCT-116	colon:	n/a
16	chr20:23965841-23965891	ProgFib	skin:	n/a
17	chr20:23969832-23969882	NHDF-neo	bronchial:	n/a
18	chr20:23969397-23969447	U87	brain:	n/a
19	chr20:23969429-23969479	Hepatocyte	liver:	n/a
20	chr20:23970162-23970212	HepG2	liver:	n/a
21	chr20:23970162-23970212	MCF-7	breast:	n/a
22	chr20:23965841-23965891	NHDF-neo	bronchial:	n/a
23	chr20:23969432-23969482	HL-60	blood:	n/a
24	chr20:23969429-23969479	U87	brain:	n/a
25	chr20:23970162-23970212	GM12891	blood:	n/a
26	chr20:23969397-23969447	T-47D	breast:	n/a
27	chr20:23965921-23965971	IMR90	lung:	fetal
28	chr20:23969432-23969482	SK-N-SH_RA	brain:	n/a
29	chr20:23968830-23968880	HEK293	kidney:	embryo
30	chr20:23970162-23970212	HRCEpiC	kidney:	n/a
31	chr20:23969429-23969479	ovcar-3	ovarian:	n/a
32	chr20:23965841-23965891	AG04449	skin:	fetal
33	chr20:23972451-23972501	Hela-S3	cervix:	n/a
34	chr20:23969237-23969287	SK-N-SH	brain:	n/a
35	chr20:23969432-23969482	HCT-116	colon:	n/a
36	chr20:23970065-23970115	A549	lung:	n/a
37	chr20:23972451-23972501	HCM	heart:	n/a
38	chr20:23972451-23972501	HUVEC	blood vessel:	n/a
39	chr20:23969432-23969482	AG09309	skin:	n/a
40	chr20:23970162-23970212	CMK	blood:	n/a
41	chr20:23969237-23969287	SK-N-MC	brain:	n/a
42	chr20:23970162-23970212	Caco-2	colon:	n/a
43	chr20:23969429-23969479	HUVEC	blood vessel:	n/a
44	chr20:23969432-23969482	PFSK-1	brain:	n/a
45	chr20:23969237-23969287	GM12891	blood:	n/a
46	chr20:23969432-23969482	HPAEpiC	pulmonary alveolar:	n/a
47	chr20:23970162-23970212	U87	brain:	n/a
48	chr20:23972451-23972501	SAEC	small airway:	n/a
49	chr20:23972451-23972501	IMR90	lung:	fetal
50	chr20:23968830-23968880	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:23976507..23978682-chr20:23981230..23983499,2	K562	blood:
2	chr20:23870329..23871235-chr20:23976503..23977926,6	MCF-7	breast:

Variant related genes	Relation type
GGTLC1	TF binding region
ENSG00000236168	TF binding region
POM121L3P	TF binding region
GGTLC1	CpG island
ENSG00000236168	CpG island
POM121L3P	CpG island

Extended variants
information (count: 816 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:816 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139639427	chr20:23956974-23956975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs573335344	chr20:23956975-23956976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2379307	chr20:23957000-23957001	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76190680	chr20:23957004-23957005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371970146	chr20:23957012-23957013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145314482	chr20:23957044-23957045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560858569	chr20:23957077-23957078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529727590	chr20:23957124-23957125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376912761	chr20:23957142-23957143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1555472	chr20:23957181-23957182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs77217870	chr20:23957223-23957224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79924440	chr20:23957224-23957225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560212258	chr20:23957228-23957229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561165602	chr20:23957238-23957239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180959341	chr20:23957254-23957255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111934170	chr20:23957286-23957287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183595430	chr20:23957298-23957299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147209827	chr20:23957391-23957392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2984255	chr20:23957396-23957397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536679611	chr20:23957408-23957409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576847220	chr20:23957420-23957421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553164573	chr20:23957434-23957435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566973317	chr20:23957462-23957463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539188519	chr20:23957533-23957534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189492910	chr20:23957536-23957537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575949320	chr20:23957537-23957538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182551201	chr20:23957561-23957562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555268927	chr20:23957582-23957583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149759207	chr20:23957591-23957592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4011419	chr20:23957604-23957605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113826109	chr20:23957607-23957608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145704759	chr20:23957661-23957662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532239539	chr20:23957677-23957678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2379308	chr20:23957683-23957684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545543422	chr20:23957695-23957696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187165844	chr20:23957704-23957705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551137062	chr20:23957708-23957709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191986739	chr20:23957709-23957710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4011402	chr20:23957732-23957733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4011403	chr20:23957737-23957738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4011404	chr20:23957775-23957776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373456795	chr20:23957776-23957777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548059994	chr20:23957780-23957781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201241460	chr20:23957801-23957802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568365963	chr20:23957805-23957806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181673124	chr20:23957811-23957812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs202000053	chr20:23957827-23957828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185531847	chr20:23957850-23957851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370227195	chr20:23957870-23957871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189995782	chr20:23957873-23957874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23948800-23959000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23956200-23959000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr20:23956800-23958600	Weak transcription	Dnd41	blood
4	chr20:23958600-23959000	Enhancers	Dnd41	blood
5	chr20:23959000-23959200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr20:23959000-23959200	Enhancers	Fetal Thymus	thymus
7	chr20:23959000-23959200	Enhancers	Lung	lung
8	chr20:23959000-23959200	Flanking Active TSS	Dnd41	blood
9	chr20:23959000-23959400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr20:23959000-23959400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr20:23959000-23959600	Enhancers	Fetal Stomach	stomach
12	chr20:23959000-23963400	Enhancers	Fetal Muscle Trunk	muscle
13	chr20:23959200-23959400	Enhancers	Dnd41	blood
14	chr20:23959200-23959600	Enhancers	A549	lung
15	chr20:23959200-23960400	Enhancers	Primary B cells from cord blood	blood
16	chr20:23959200-23960800	Enhancers	Primary B cells from peripheral blood	blood
17	chr20:23959400-23959600	Flanking Active TSS	Dnd41	blood
18	chr20:23959400-23960000	Weak transcription	Lung	lung
19	chr20:23959400-23960600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr20:23959400-23962200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr20:23959600-23960000	Weak transcription	Fetal Stomach	stomach
22	chr20:23959600-23960000	Weak transcription	A549	lung
23	chr20:23959600-23961000	Enhancers	Dnd41	blood
24	chr20:23960000-23960200	Enhancers	A549	lung
25	chr20:23960000-23960400	ZNF genes & repeats	Fetal Stomach	stomach
26	chr20:23960000-23960800	Enhancers	Pancreas	Pancrea
27	chr20:23960000-23961400	Active TSS	Lung	lung
28	chr20:23960200-23963200	Weak transcription	A549	lung
29	chr20:23960200-23963400	Enhancers	Fetal Muscle Leg	muscle
30	chr20:23960400-23960600	Enhancers	Fetal Kidney	kidney
31	chr20:23960400-23960600	Enhancers	Fetal Lung	lung
32	chr20:23960400-23960800	Enhancers	Esophagus	oesophagus
33	chr20:23960400-23960800	Weak transcription	Fetal Thymus	thymus
34	chr20:23960400-23963400	Enhancers	Fetal Stomach	stomach
35	chr20:23960600-23960800	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr20:23960600-23961200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr20:23960600-23961200	Flanking Active TSS	Fetal Kidney	kidney
38	chr20:23960600-23961200	Flanking Active TSS	Fetal Lung	lung
39	chr20:23960600-23961400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr20:23960600-23961800	Enhancers	Fetal Heart	heart
41	chr20:23960600-23962400	Enhancers	HepG2	liver
42	chr20:23960800-23961200	ZNF genes & repeats	Esophagus	oesophagus
43	chr20:23960800-23961400	Genic enhancers	Pancreas	Pancrea
44	chr20:23960800-23962000	Enhancers	Right Ventricle	heart
45	chr20:23961000-23961200	Flanking Active TSS	Fetal Brain Male	brain
46	chr20:23961000-23961400	Enhancers	Right Atrium	heart
47	chr20:23961000-23961800	Enhancers	Fetal Thymus	thymus
48	chr20:23961000-23962800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr20:23961000-23963000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr20:23961200-23961400	Enhancers	Esophagus	oesophagus

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