Variant report

Variant	nsv934161
Chromosome Location	chr22:33979015-34118621
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:315)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:315 , 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	chr22:34048680-34049001	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:33988518-33988724	HepG2	liver:	n/a	n/a
3	BATF	chr22:34032205-34032459	GM12878	blood:	n/a	chr22:34032362-34032373 chr22:34032367-34032377 chr22:34032363-34032373
4	BATF	chr22:34036603-34036823	GM12878	blood:	n/a	n/a
5	BHLHE40	chr22:34114028-34114321	HepG2	liver:	n/a	n/a
6	CEBPB	chr22:34080182-34080371	HepG2	liver:	n/a	n/a
7	CEBPB	chr22:34027817-34028113	HepG2	liver:	n/a	n/a
8	CEBPB	chr22:33988502-33988764	HepG2	liver:	n/a	n/a
9	CEBPB	chr22:34049638-34049838	HepG2	liver:	n/a	n/a
10	CEBPB	chr22:34048796-34049054	HepG2	liver:	n/a	n/a
11	CEBPB	chr22:34078948-34079234	HepG2	liver:	n/a	n/a
12	CEBPB	chr22:34067486-34067807	HepG2	liver:	n/a	chr22:34067616-34067627 chr22:34067642-34067655 chr22:34067643-34067654 chr22:34067615-34067628
13	CEBPB	chr22:34079121-34079126	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr22:34053142-34053380	A549	lung:	n/a	chr22:34053216-34053227
15	CEBPB	chr22:34053191-34053393	Hela-S3	cervix:	n/a	chr22:34053216-34053227
16	CEBPB	chr22:34078971-34079195	A549	lung:	n/a	n/a
17	CEBPB	chr22:34001203-34001526	HepG2	liver:	n/a	n/a
18	CEBPB	chr22:33993246-33993253	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr22:34005012-34005212	A549	lung:	n/a	chr22:34005098-34005109
20	CEBPB	chr22:34004978-34005268	HepG2	liver:	n/a	chr22:34005098-34005109
21	CEBPB	chr22:34053105-34053301	H1-hESC	embryonic stem cell:	n/a	chr22:34053216-34053227
22	CEBPB	chr22:34053061-34053353	HepG2	liver:	n/a	chr22:34053216-34053227
23	CHD1	chr22:34062434-34062470	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr22:33981265-33981272	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr22:34102300-34102450	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr22:34051120-34051270	GM12864	blood:	n/a	n/a
27	CTCF	chr22:34112658-34112721	GM10248	blood:	n/a	n/a
28	CTCF	chr22:33993920-33994070	AG04449	skin:	n/a	n/a
29	CTCF	chr22:33994712-33994782	GM13976	blood:	n/a	n/a
30	CTCF	chr22:34049798-34049898	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr22:34042253-34042318	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr22:34046419-34046547	Fibrobl	skin:	n/a	n/a
33	CTCF	chr22:33996788-33996841	GM10248	blood:	n/a	n/a
34	CTCF	chr22:34049671-34049916	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr22:34007260-34007410	GM12867	blood:	n/a	n/a
36	CTCF	chr22:34049740-34049890	HEK293	kidney:	n/a	n/a
37	CTCF	chr22:34078560-34078710	NHEK	skin:	n/a	n/a
38	CTCF	chr22:34049660-34049810	GM12873	blood:	n/a	n/a
39	CTCF	chr22:34020860-34021010	GM12864	blood:	n/a	n/a
40	CTCF	chr22:34102257-34102439	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr22:34068200-34068350	GM12865	blood:	n/a	n/a
42	CTCF	chr22:34054343-34054385	ProgFib	skin:	n/a	n/a
43	CTCF	chr22:34078420-34078570	HEK293	kidney:	n/a	chr22:34078508-34078526
44	CTCF	chr22:34067861-34067887	Lung_OC	lung:	n/a	n/a
45	CTCF	chr22:34052237-34052258	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr22:34010560-34010710	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr22:34102228-34102527	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr22:34099177-34099245	Lung_OC	lung:	n/a	n/a
49	CTCF	chr22:34013709-34013727	Lung_OC	lung:	n/a	n/a
50	CTCF	chr22:34038679-34038734	GM13976	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34049875-34049925	AG04450	lung:	fetal
2	chr22:34047559-34047609	SAEC	small airway:	n/a
3	chr22:34046477-34046527	AG09319	gingival:	n/a
4	chr22:34049875-34049925	HCM	heart:	n/a
5	chr22:34046477-34046527	HUVEC	blood vessel:	n/a
6	chr22:34046427-34046477	A549	lung:	n/a
7	chr22:34046427-34046477	HMEC	breast:	n/a
8	chr22:34046427-34046477	HEEpiC	esophagus:	n/a
9	chr22:34046427-34046477	HCPEpiC	choroid plexus:	n/a
10	chr22:34046427-34046477	H1-hESC	embryonic stem cell:	embryo
11	chr22:34049875-34049925	GM12892	blood:	n/a
12	chr22:34046427-34046477	K562	blood:	n/a
13	chr22:34046477-34046527	BJ	skin:	n/a
14	chr22:34046477-34046527	ProgFib	skin:	n/a
15	chr22:34046529-34046579	CMK	blood:	n/a
16	chr22:34049875-34049925	HRCEpiC	kidney:	n/a
17	chr22:34047559-34047609	H1-hESC	embryonic stem cell:	embryo
18	chr22:34047559-34047609	MCF10A-Er-Src	breast:	n/a
19	chr22:34047559-34047609	HUVEC	blood vessel:	n/a
20	chr22:34046427-34046477	NHBE	bronchial:	n/a
21	chr22:34049875-34049925	SK-N-MC	brain:	n/a
22	chr22:34046477-34046527	NHBE	bronchial:	n/a
23	chr22:34047559-34047609	PANC-1	pancreas:	n/a
24	chr22:34046477-34046527	HRPEpiC	eye:	n/a
25	chr22:34046529-34046579	GM12891	blood:	n/a
26	chr22:34049875-34049925	NHBE	bronchial:	n/a
27	chr22:34046477-34046527	H1-hESC	embryonic stem cell:	embryo
28	chr22:34046477-34046527	SAEC	small airway:	n/a
29	chr22:34046427-34046477	PFSK-1	brain:	n/a
30	chr22:34046477-34046527	HEK293	kidney:	embryo
31	chr22:34046529-34046579	HUVEC	blood vessel:	n/a
32	chr22:34049875-34049925	ProgFib	skin:	n/a
33	chr22:34046427-34046477	ECC-1	luminal epithelium:	n/a
34	chr22:34047559-34047609	HRPEpiC	eye:	n/a
35	chr22:34046529-34046579	NH-A	brain:	n/a
36	chr22:34046427-34046477	SAEC	small airway:	n/a
37	chr22:34047559-34047609	SKMC	muscle:	n/a
38	chr22:34046529-34046579	HRCEpiC	kidney:	n/a
39	chr22:34049875-34049925	Hepatocyte	liver:	n/a
40	chr22:34046427-34046477	HCF	heart:	n/a
41	chr22:34046529-34046579	PFSK-1	brain:	n/a
42	chr22:34047559-34047609	HEK293	kidney:	embryo
43	chr22:34046427-34046477	HRE	kidney:	n/a
44	chr22:34046427-34046477	HPAEpiC	pulmonary alveolar:	n/a
45	chr22:34047559-34047609	CMK	blood:	n/a
46	chr22:34047559-34047609	HepG2	liver:	n/a
47	chr22:34046477-34046527	SK-N-MC	brain:	n/a
48	chr22:34047559-34047609	GM06990	blood:	n/a
49	chr22:34046529-34046579	PANC-1	pancreas:	n/a
50	chr22:34047559-34047609	RPTEC	kidney:	n/a

(count:5 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE	TF binding region
ENSG00000253007	TF binding region
LARGE-AS1	CpG island
LARGE	CpG island
ENSG00000253007	CpG island
ENSG00000133424	chromatin interactions

Extended variants
information (count: 6110 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6110 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149773672	chr22:33979019-33979020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376094700	chr22:33979031-33979032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564656777	chr22:33979063-33979064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145693217	chr22:33979134-33979135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577708017	chr22:33979171-33979172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs540273251	chr22:33979189-33979190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553496184	chr22:33979207-33979208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573643851	chr22:33979326-33979327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs80159209	chr22:33979353-33979354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563201355	chr22:33979362-33979363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532027404	chr22:33979375-33979376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190107803	chr22:33979403-33979404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140624202	chr22:33979408-33979409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79797696	chr22:33979467-33979468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547829894	chr22:33979535-33979536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544062315	chr22:33979541-33979542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543683542	chr22:33979550-33979551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567568301	chr22:33979559-33979560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373159732	chr22:33979578-33979579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549744963	chr22:33979583-33979584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs743730	chr22:33979605-33979606	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs73396615	chr22:33979622-33979623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77531988	chr22:33979680-33979681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145723645	chr22:33979845-33979846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533663566	chr22:33979859-33979860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529573317	chr22:33979863-33979864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548954429	chr22:33979898-33979899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138304779	chr22:33979923-33979924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2014025	chr22:33979937-33979938	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528516018	chr22:33979966-33979967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182415349	chr22:33979970-33979971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556186048	chr22:33980010-33980011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571385047	chr22:33980011-33980012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs186701578	chr22:33980089-33980090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs743731	chr22:33980108-33980109	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs531462014	chr22:33980166-33980167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193146787	chr22:33980172-33980173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565347491	chr22:33980190-33980191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527852466	chr22:33980212-33980213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567444173	chr22:33980295-33980296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141371797	chr22:33980315-33980316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs117301852	chr22:33980336-33980337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184010910	chr22:33980347-33980348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143340641	chr22:33980382-33980383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148377737	chr22:33980416-33980417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs557110958	chr22:33980436-33980437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572879211	chr22:33980462-33980463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571373391	chr22:33980571-33980572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs141554295	chr22:33980607-33980608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188602269	chr22:33980627-33980628	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:1636 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33960000-33993000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr22:33965200-34045800	Weak transcription	Pancreas	Pancrea
3	chr22:33967600-33981200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr22:33975600-33995200	Weak transcription	Liver	Liver
5	chr22:33976000-33981200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr22:33976000-33981200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr22:33976000-33981200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr22:33976200-33991400	Weak transcription	Left Ventricle	heart
9	chr22:33977400-33979400	Weak transcription	Fetal Heart	heart
10	chr22:33979400-33980400	Enhancers	Fetal Heart	heart
11	chr22:33980400-33989400	Weak transcription	Fetal Heart	heart
12	chr22:33980600-33981800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr22:33980800-33981600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr22:33980800-33981600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr22:33981000-33981600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr22:33981000-33981600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr22:33981000-33982200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr22:33981200-33981400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr22:33981200-33981600	Enhancers	H9 Cell Line	embryonic stem cell
20	chr22:33981200-33981800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr22:33981200-33981800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr22:33981200-33981800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr22:33981200-33981800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr22:33981400-33989200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr22:33981600-33988400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr22:33981800-33982400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr22:33981800-33987200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr22:33981800-33991800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr22:33981800-34006200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr22:33981800-34006800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr22:33982200-33994800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr22:33982600-33982800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr22:33984400-33984800	Weak transcription	Right Ventricle	heart
34	chr22:33984600-33985200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr22:33984800-33985000	Enhancers	Right Ventricle	heart
36	chr22:33985000-33993600	Weak transcription	Right Ventricle	heart
37	chr22:33985200-33993000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr22:33985200-34001800	Weak transcription	Gastric	stomach
39	chr22:33985400-33997400	Weak transcription	Brain Angular Gyrus	brain
40	chr22:33985400-34009400	Weak transcription	GM12878-XiMat	blood
41	chr22:33986400-33986600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr22:33987200-33987400	Enhancers	Aorta	Aorta
43	chr22:33987400-33993000	Weak transcription	Aorta	Aorta
44	chr22:33988400-33988800	Enhancers	HepG2	liver
45	chr22:33988600-33988800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr22:33988600-34019200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr22:33988600-34020800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr22:33989200-33990000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr22:33989200-33995800	Weak transcription	Lung	lung
50	chr22:33989400-33990000	Enhancers	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links