Variant report

Variant	nsv588935
Chromosome Location	chr22:34008430-34073758
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	ARID3A	chr22:34048680-34049001	HepG2	liver:	n/a	n/a
2	BATF	chr22:34036603-34036823	GM12878	blood:	n/a	n/a
3	BATF	chr22:34032205-34032459	GM12878	blood:	n/a	chr22:34032362-34032373 chr22:34032367-34032377 chr22:34032363-34032373
4	CEBPB	chr22:34049638-34049838	HepG2	liver:	n/a	n/a
5	CEBPB	chr22:34053061-34053353	HepG2	liver:	n/a	chr22:34053216-34053227
6	CEBPB	chr22:34053105-34053301	H1-hESC	embryonic stem cell:	n/a	chr22:34053216-34053227
7	CEBPB	chr22:34027817-34028113	HepG2	liver:	n/a	n/a
8	CEBPB	chr22:34053191-34053393	Hela-S3	cervix:	n/a	chr22:34053216-34053227
9	CEBPB	chr22:34053142-34053380	A549	lung:	n/a	chr22:34053216-34053227
10	CEBPB	chr22:34048796-34049054	HepG2	liver:	n/a	n/a
11	CEBPB	chr22:34067486-34067807	HepG2	liver:	n/a	chr22:34067616-34067627 chr22:34067642-34067655 chr22:34067643-34067654 chr22:34067615-34067628
12	CHD1	chr22:34062434-34062470	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr22:34067861-34067887	Lung_OC	lung:	n/a	n/a
14	CTCF	chr22:34038679-34038734	GM13976	blood:	n/a	n/a
15	CTCF	chr22:34046419-34046547	Fibrobl	skin:	n/a	n/a
16	CTCF	chr22:34049671-34049916	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr22:34051120-34051270	GM12864	blood:	n/a	n/a
18	CTCF	chr22:34049740-34049890	HEK293	kidney:	n/a	n/a
19	CTCF	chr22:34042253-34042318	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr22:34013709-34013727	Lung_OC	lung:	n/a	n/a
21	CTCF	chr22:34010560-34010710	HEEpiC	esophagus:	n/a	n/a
22	CTCF	chr22:34054343-34054385	ProgFib	skin:	n/a	n/a
23	CTCF	chr22:34068200-34068350	GM12865	blood:	n/a	n/a
24	CTCF	chr22:34049660-34049810	GM12873	blood:	n/a	n/a
25	CTCF	chr22:34020860-34021010	GM12864	blood:	n/a	n/a
26	CTCF	chr22:34049798-34049898	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr22:34052237-34052258	Kidney_OC	kidney:	n/a	n/a
28	ELF1	chr22:34062650-34062964	GM12878	blood:	n/a	n/a
29	FAM48A	chr22:34052948-34053017	GM12878	blood:	n/a	n/a
30	FOS	chr22:34032331-34032482	MCF10A-Er-Src	breast:	n/a	chr22:34032364-34032376 chr22:34032366-34032375 chr22:34032365-34032375 chr22:34032366-34032374 chr22:34032365-34032374 chr22:34032366-34032373
31	FOS	chr22:34048801-34048802	MCF10A-Er-Src	breast:	n/a	n/a
32	FOSL2	chr22:34048564-34048966	A549	lung:	n/a	chr22:34048880-34048887 chr22:34048801-34048808 chr22:34048880-34048888 chr22:34048801-34048809 chr22:34048684-34048693 chr22:34048800-34048809
33	FOSL2	chr22:34048520-34048985	HepG2	liver:	n/a	chr22:34048880-34048887 chr22:34048801-34048808 chr22:34048880-34048888 chr22:34048801-34048809 chr22:34048684-34048693 chr22:34048800-34048809
34	FOXA1	chr22:34049123-34049480	HepG2	liver:	n/a	n/a
35	FOXA1	chr22:34027809-34028130	HepG2	liver:	n/a	n/a
36	FOXA1	chr22:34049080-34049482	HepG2	liver:	n/a	n/a
37	FOXA1	chr22:34027741-34028149	HepG2	liver:	n/a	n/a
38	FOXA1	chr22:34016108-34016483	T-47D	breast:	n/a	n/a
39	FOXA1	chr22:34016136-34016341	T-47D	breast:	n/a	n/a
40	FOXA2	chr22:34049169-34049469	HepG2	liver:	n/a	n/a
41	FOXA2	chr22:34050657-34050852	HepG2	liver:	n/a	n/a
42	FOXA2	chr22:34050581-34050902	A549	lung:	n/a	n/a
43	GATA2	chr22:34052835-34053246	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr22:34052638-34053063	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr22:34016088-34016456	T-47D	breast:	n/a	n/a
46	GATA3	chr22:34016209-34016399	SH-SY5Y	brain:	n/a	n/a
47	GTF2F1	chr22:34063887-34063948	H1-hESC	embryonic stem cell:	n/a	n/a
48	HNF4A	chr22:34049160-34049465	HepG2	liver:	n/a	chr22:34049329-34049344 chr22:34049331-34049343 chr22:34049329-34049344 chr22:34049331-34049343 chr22:34049329-34049344 chr22:34049330-34049343 chr22:34049330-34049338 chr22:34049326-34049348 chr22:34049329-34049344 chr22:34049331-34049343 chr22:34049329-34049344
49	JUN	chr22:34013616-34013638	HepG2	liver:	n/a	n/a
50	JUN	chr22:34049609-34049855	HepG2	liver:	n/a	chr22:34049692-34049705 chr22:34049717-34049730 chr22:34049696-34049705

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34047559-34047609	NB4	blood:	n/a
2	chr22:34047559-34047609	SK-N-SH_RA	brain:	n/a
3	chr22:34049875-34049925	GM12878	blood:	n/a
4	chr22:34046427-34046477	SAEC	small airway:	n/a
5	chr22:34049875-34049925	HRE	kidney:	n/a
6	chr22:34047559-34047609	U87	brain:	n/a
7	chr22:34046529-34046579	Caco-2	colon:	n/a
8	chr22:34049875-34049925	PFSK-1	brain:	n/a
9	chr22:34046427-34046477	T-47D	breast:	n/a
10	chr22:34049875-34049925	HL-60	blood:	n/a
11	chr22:34047559-34047609	HRE	kidney:	n/a
12	chr22:34049875-34049925	Jurkat	blood:	n/a
13	chr22:34047559-34047609	HEEpiC	esophagus:	n/a
14	chr22:34049875-34049925	SKMC	muscle:	n/a
15	chr22:34046477-34046527	IMR90	lung:	fetal
16	chr22:34047559-34047609	PFSK-1	brain:	n/a
17	chr22:34049875-34049925	SAEC	small airway:	n/a
18	chr22:34046529-34046579	HEEpiC	esophagus:	n/a
19	chr22:34049875-34049925	GM19239	blood:	n/a
20	chr22:34046427-34046477	HepG2	liver:	n/a
21	chr22:34046529-34046579	SKMC	muscle:	n/a
22	chr22:34046477-34046527	HepG2	liver:	n/a
23	chr22:34046529-34046579	GM12892	blood:	n/a
24	chr22:34046477-34046527	GM06990	blood:	n/a
25	chr22:34047559-34047609	IMR90	lung:	fetal
26	chr22:34046477-34046527	GM12878	blood:	n/a
27	chr22:34049875-34049925	K562	blood:	n/a
28	chr22:34047559-34047609	GM12891	blood:	n/a
29	chr22:34047559-34047609	RPTEC	kidney:	n/a
30	chr22:34046529-34046579	ProgFib	skin:	n/a
31	chr22:34047559-34047609	HNPCEpiC	eye:	n/a
32	chr22:34047559-34047609	HPAEpiC	pulmonary alveolar:	n/a
33	chr22:34047559-34047609	CMK	blood:	n/a
34	chr22:34047559-34047609	HMEC	breast:	n/a
35	chr22:34047559-34047609	BE2_C	brain:	n/a
36	chr22:34046477-34046527	HRPEpiC	eye:	n/a
37	chr22:34047559-34047609	NHBE	bronchial:	n/a
38	chr22:34046529-34046579	LNCaP	prostate:	n/a
39	chr22:34047559-34047609	GM06990	blood:	n/a
40	chr22:34046529-34046579	IMR90	lung:	fetal
41	chr22:34046529-34046579	K562	blood:	n/a
42	chr22:34049875-34049925	AoSMC	blood vessel:	n/a
43	chr22:34046427-34046477	A549	lung:	n/a
44	chr22:34046427-34046477	Caco-2	colon:	n/a
45	chr22:34049875-34049925	PANC-1	pancreas:	n/a
46	chr22:34049875-34049925	AG10803	skin:	n/a
47	chr22:34049875-34049925	AG04449	skin:	fetal
48	chr22:34046529-34046579	SK-N-SH	brain:	n/a
49	chr22:34049875-34049925	ovcar-3	ovarian:	n/a
50	chr22:34047559-34047609	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:34017891..34021270-chr22:34021737..34025602,3	MCF-7	breast:
2	chr22:34017891..34021270-chr22:34021737..34025602,3	MCF-7	breast:
3	chr22:34052912..34055684-chr22:34057448..34059597,2	MCF-7	breast:
4	chr22:33994236..33996382-chr22:34011754..34014539,2	MCF-7	breast:

Variant related genes	Relation type
LARGE	TF binding region
LARGE	CpG island
ENSG00000133424	chromatin interactions

Extended variants
information (count: 2818 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2818 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4239873	chr22:34008430-34008431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183312073	chr22:34008464-34008465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187803638	chr22:34008478-34008479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554893073	chr22:34008509-34008510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575024711	chr22:34008533-34008534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544031577	chr22:34008538-34008539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191523942	chr22:34008655-34008656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111305443	chr22:34008727-34008728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7288655	chr22:34008740-34008741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563712451	chr22:34008745-34008746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532713152	chr22:34008805-34008806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555040546	chr22:34008849-34008850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140575119	chr22:34008948-34008949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10483173	chr22:34009001-34009002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs528497858	chr22:34009026-34009027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544500160	chr22:34009071-34009072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548591393	chr22:34009146-34009147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534046111	chr22:34009150-34009151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111598511	chr22:34009151-34009152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564378737	chr22:34009164-34009165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs115167709	chr22:34009167-34009168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs145816450	chr22:34009178-34009179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183674056	chr22:34009222-34009223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145321766	chr22:34009231-34009232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs5999033	chr22:34009297-34009298	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs576987935	chr22:34009372-34009373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558232114	chr22:34009432-34009433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143411411	chr22:34009457-34009458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs5999034	chr22:34009465-34009466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554130727	chr22:34009469-34009470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539277385	chr22:34009500-34009501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575107997	chr22:34009526-34009527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185359271	chr22:34009528-34009529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557599009	chr22:34009540-34009541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190208367	chr22:34009555-34009556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546374322	chr22:34009564-34009565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371815670	chr22:34009581-34009582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192819978	chr22:34009584-34009585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528579807	chr22:34009593-34009594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146163309	chr22:34009622-34009623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs374808011	chr22:34009640-34009641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556024404	chr22:34009754-34009755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9607066	chr22:34009806-34009807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200940116	chr22:34009819-34009820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561959605	chr22:34009834-34009835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530897833	chr22:34009857-34009858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184893631	chr22:34009909-34009910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116592658	chr22:34009910-34009911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2283922	chr22:34009972-34009973	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs188434445	chr22:34010049-34010050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33965200-34045800	Weak transcription	Pancreas	Pancrea
2	chr22:33985400-34009400	Weak transcription	GM12878-XiMat	blood
3	chr22:33988600-34019200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr22:33988600-34020800	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr22:33989600-34020400	Weak transcription	Fetal Intestine Large	intestine
6	chr22:33994000-34029600	Weak transcription	Aorta	Aorta
7	chr22:33994200-34010600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr22:33994200-34020600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr22:33994200-34050600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr22:33995800-34049800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr22:34000600-34014600	Weak transcription	Liver	Liver
12	chr22:34000600-34014800	Weak transcription	Ovary	ovary
13	chr22:34000600-34015200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr22:34000600-34017800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr22:34001800-34017600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr22:34003000-34062400	Weak transcription	Gastric	stomach
17	chr22:34003800-34009200	Weak transcription	Fetal Heart	heart
18	chr22:34005400-34013000	Weak transcription	Right Atrium	heart
19	chr22:34007000-34009000	Weak transcription	Left Ventricle	heart
20	chr22:34007200-34050400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr22:34007400-34013600	Weak transcription	Right Ventricle	heart
22	chr22:34007400-34014400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr22:34007400-34018200	Weak transcription	Fetal Stomach	stomach
24	chr22:34007400-34020400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr22:34007400-34020600	Weak transcription	Lung	lung
26	chr22:34007800-34014000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr22:34007800-34020400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr22:34008000-34014800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr22:34008000-34019200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr22:34008000-34021200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr22:34008000-34031000	Weak transcription	Fetal Intestine Small	intestine
32	chr22:34008000-34039400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr22:34008200-34010200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr22:34009000-34011000	Enhancers	Left Ventricle	heart
35	chr22:34009200-34009400	Enhancers	Fetal Heart	heart
36	chr22:34009400-34009600	Enhancers	GM12878-XiMat	blood
37	chr22:34009600-34010000	Weak transcription	GM12878-XiMat	blood
38	chr22:34010000-34010200	Enhancers	GM12878-XiMat	blood
39	chr22:34010000-34025200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr22:34010200-34010400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr22:34010200-34029800	Weak transcription	GM12878-XiMat	blood
42	chr22:34010400-34010600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr22:34010400-34010800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr22:34010600-34011200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr22:34010800-34011000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr22:34010800-34011000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr22:34010800-34012400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr22:34011000-34013000	Weak transcription	Left Ventricle	heart
49	chr22:34011000-34019200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr22:34011400-34011800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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