Variant report

Variant	esv3438318
Chromosome Location	chr3:195714755-195719153
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	ATF3	chr3:195717067-195717371	A549	lung:	n/a	n/a
2	ATF3	chr3:195717483-195717694	K562	blood:	n/a	n/a
3	ATF3	chr3:195717164-195717371	K562	blood:	n/a	n/a
4	ATF3	chr3:195717064-195717382	K562	blood:	n/a	n/a
5	BACH1	chr3:195717045-195717538	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:195717540-195717834	GM12878	blood:	n/a	n/a
7	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
8	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
9	BATF	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
11	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
12	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
14	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
15	BHLHE40	chr3:195717520-195717617	K562	blood:	n/a	n/a
16	CBX3	chr3:195717317-195717855	K562	blood:	n/a	n/a
17	CBX3	chr3:195716251-195717942	K562	blood:	n/a	n/a
18	CEBPB	chr3:195715655-195716331	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
19	CEBPB	chr3:195715854-195716146	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
20	CEBPB	chr3:195715847-195716034	HepG2	liver:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
21	CEBPB	chr3:195715851-195716051	A549	lung:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
22	CEBPB	chr3:195715844-195716052	Hela-S3	cervix:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
23	CEBPB	chr3:195715834-195716053	IMR90	lung:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
24	CEBPB	chr3:195715836-195716046	K562	blood:	n/a	chr3:195715997-195716008 chr3:195715997-195716006 chr3:195715997-195716006 chr3:195715995-195716008 chr3:195715997-195716006 chr3:195715997-195716006
25	CEBPD	chr3:195716979-195717383	HepG2	liver:	n/a	n/a
26	CEBPD	chr3:195716909-195717795	K562	blood:	n/a	n/a
27	CHD2	chr3:195717301-195717419	GM12878	blood:	n/a	n/a
28	CHD2	chr3:195717521-195717554	K562	blood:	n/a	n/a
29	CHD2	chr3:195717515-195717598	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:195717440-195717509	GM13976	blood:	n/a	n/a
31	CTCF	chr3:195717460-195717610	Caco-2	colon:	n/a	chr3:195717520-195717538
32	CTCF	chr3:195717460-195717610	K562	blood:	n/a	chr3:195717520-195717538
33	CTCF	chr3:195716963-195717762	K562	blood:	n/a	chr3:195717520-195717538
34	CTCF	chr3:195717123-195717300	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr3:195717366-195717594	K562	blood:	n/a	chr3:195717520-195717538
36	CTCF	chr3:195717200-195717350	GM12866	blood:	n/a	n/a
37	CTCF	chr3:195717119-195717280	Lung_OC	lung:	n/a	n/a
38	CTCF	chr3:195717160-195717310	HMEC	breast:	n/a	n/a
39	CTCF	chr3:195717240-195717390	GM12871	blood:	n/a	n/a
40	CTCF	chr3:195717500-195717650	GM12878	blood:	n/a	chr3:195717520-195717538
41	CTCF	chr3:195717520-195717670	AG04449	skin:	n/a	chr3:195717520-195717538
42	CTCF	chr3:195717351-195717551	K562	blood:	n/a	chr3:195717520-195717538
43	CTCF	chr3:195717460-195717610	GM12872	blood:	n/a	chr3:195717520-195717538
44	CTCF	chr3:195717480-195717630	HAc	cerebellar:	n/a	chr3:195717520-195717538
45	CTCF	chr3:195717140-195717290	GM12874	blood:	n/a	n/a
46	CTCF	chr3:195717460-195717610	BJ	skin:	n/a	chr3:195717520-195717538
47	CTCF	chr3:195717460-195717610	GM06990	blood:	n/a	chr3:195717520-195717538
48	CTCF	chr3:195717480-195717630	AG04450	lung:	n/a	chr3:195717520-195717538
49	CTCF	chr3:195717480-195717630	SK-N-SH_RA	brain:	n/a	chr3:195717520-195717538
50	CTCF	chr3:195717432-195717519	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195717416-195717466	BE2_C	brain:	n/a
2	chr3:195717416-195717466	BE2_C	brain:	n/a
3	chr3:195715851-195715901	LNCaP	prostate:	n/a
4	chr3:195716626-195716676	SK-N-SH	brain:	n/a
5	chr3:195715851-195715901	SK-N-SH	brain:	n/a
6	chr3:195715851-195715901	BE2_C	brain:	n/a
7	chr3:195715851-195715901	HRCEpiC	kidney:	n/a
8	chr3:195717574-195717624	U87	brain:	n/a
9	chr3:195717344-195717394	GM12878	blood:	n/a
10	chr3:195717416-195717466	HIPEpiC	eye:	n/a
11	chr3:195717344-195717394	HRCEpiC	kidney:	n/a
12	chr3:195717962-195718012	HIPEpiC	eye:	n/a
13	chr3:195717574-195717624	AG09309	skin:	n/a
14	chr3:195717574-195717624	HRCEpiC	kidney:	n/a
15	chr3:195717574-195717624	HNPCEpiC	eye:	n/a
16	chr3:195716632-195716682	HCM	heart:	n/a
17	chr3:195716626-195716676	Hepatocyte	liver:	n/a
18	chr3:195717962-195718012	Jurkat	blood:	n/a
19	chr3:195717416-195717466	HAEpiC	amniotic membrane:	n/a
20	chr3:195717344-195717394	GM12892	blood:	n/a
21	chr3:195717962-195718012	HUVEC	blood vessel:	n/a
22	chr3:195715851-195715901	NHDF-neo	bronchial:	n/a
23	chr3:195717344-195717394	CMK	blood:	n/a
24	chr3:195715851-195715901	AoSMC	blood vessel:	n/a
25	chr3:195717574-195717624	GM12878	blood:	n/a
26	chr3:195717366-195717416	AG04449	skin:	fetal
27	chr3:195717366-195717416	HL-60	blood:	n/a
28	chr3:195716632-195716682	AoSMC	blood vessel:	n/a
29	chr3:195717416-195717466	U87	brain:	n/a
30	chr3:195717574-195717624	BJ	skin:	n/a
31	chr3:195716626-195716676	Jurkat	blood:	n/a
32	chr3:195717366-195717416	MCF10A-Er-Src	breast:	n/a
33	chr3:195717366-195717416	ECC-1	luminal epithelium:	n/a
34	chr3:195717416-195717466	ECC-1	luminal epithelium:	n/a
35	chr3:195716632-195716682	LNCaP	prostate:	n/a
36	chr3:195717962-195718012	GM12892	blood:	n/a
37	chr3:195717344-195717394	BJ	skin:	n/a
38	chr3:195717344-195717394	Hela-S3	cervix:	n/a
39	chr3:195717416-195717466	HMEC	breast:	n/a
40	chr3:195717366-195717416	HCM	heart:	n/a
41	chr3:195717416-195717466	HUVEC	blood vessel:	n/a
42	chr3:195717366-195717416	NHBE	bronchial:	n/a
43	chr3:195716626-195716676	HMEC	breast:	n/a
44	chr3:195717962-195718012	SAEC	small airway:	n/a
45	chr3:195717344-195717394	AG09309	skin:	n/a
46	chr3:195717344-195717394	PANC-1	pancreas:	n/a
47	chr3:195717344-195717394	BE2_C	brain:	n/a
48	chr3:195716632-195716682	Hela-S3	cervix:	n/a
49	chr3:195717416-195717466	H1-hESC	embryonic stem cell:	embryo
50	chr3:195716632-195716682	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:
2	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:

Variant related genes	Relation type
SDHAP1	TF binding region
ENSG00000231464	TF binding region
SDHAP1	CpG island
ENSG00000231464	CpG island
ENSG00000242086	chromatin interactions
ENSG00000215837	chromatin interactions
ENSG00000229178	chromatin interactions

Extended variants
information (count: 171 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:171 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529416954	chr3:195714787-195714788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs369951604	chr3:195714791-195714792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368870637	chr3:195714814-195714815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547561999	chr3:195714824-195714825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs375326398	chr3:195714826-195714827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs202114954	chr3:195714829-195714830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs530414000	chr3:195714841-195714842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112910218	chr3:195714858-195714859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201903923	chr3:195714860-195714861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370900645	chr3:195714861-195714862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375502680	chr3:195714891-195714892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368845943	chr3:195714899-195714900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542324032	chr3:195714919-195714920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560601757	chr3:195714925-195714926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372242088	chr3:195714930-195714931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs143209743	chr3:195714938-195714939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369428744	chr3:195714965-195714966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559054274	chr3:195715060-195715061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376120013	chr3:195715061-195715062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547133888	chr3:195715175-195715176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200229871	chr3:195715212-195715213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201446151	chr3:195715214-195715215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550831679	chr3:195715226-195715227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550991629	chr3:195715241-195715242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs200545916	chr3:195715326-195715327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569317070	chr3:195715501-195715502	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs536611818	chr3:195715565-195715566	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113487910	chr3:195715570-195715571	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555106076	chr3:195715599-195715600	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566944151	chr3:195715661-195715662	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2638943	chr3:195715768-195715769	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534533599	chr3:195715778-195715779	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375984170	chr3:195715782-195715783	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553167875	chr3:195715851-195715852	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs368828393	chr3:195715854-195715855	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372567682	chr3:195715861-195715862	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs79302584	chr3:195715868-195715869	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs545326387	chr3:195716023-195716024	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs2451783	chr3:195716027-195716028	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs533035168	chr3:195716048-195716049	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs370854258	chr3:195716049-195716050	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs556796572	chr3:195716052-195716053	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574896858	chr3:195716068-195716069	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542187791	chr3:195716082-195716083	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs376643695	chr3:195716093-195716094	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs372856860	chr3:195716094-195716095	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs371184398	chr3:195716208-195716209	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560663023	chr3:195716229-195716230	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528203412	chr3:195716568-195716569	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76754665	chr3:195716652-195716653	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD

Chromatin state (count:406 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195682600-195715600	Weak transcription	Psoas Muscle	Psoas
2	chr3:195685800-195716600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:195697400-195717600	Weak transcription	Fetal Heart	heart
4	chr3:195697600-195716600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr3:195698000-195715400	Weak transcription	Hela-S3	cervix
6	chr3:195698000-195715800	Weak transcription	Fetal Lung	lung
7	chr3:195698000-195715800	Weak transcription	HUVEC	blood vessel
8	chr3:195698000-195716400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:195698000-195716400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:195698000-195716400	Weak transcription	Primary B cells from cord blood	blood
11	chr3:195698000-195716400	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr3:195698000-195717400	Weak transcription	Fetal Brain Male	brain
13	chr3:195698000-195717400	Weak transcription	Stomach Mucosa	stomach
14	chr3:195698200-195716400	Weak transcription	Primary hematopoietic stem cells	blood
15	chr3:195698400-195715800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr3:195698600-195717200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr3:195699000-195716600	Weak transcription	NHDF-Ad	bronchial
18	chr3:195703000-195715600	Weak transcription	A549	lung
19	chr3:195703000-195716400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr3:195703000-195716400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr3:195703000-195716400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr3:195703000-195716600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr3:195703200-195715400	Weak transcription	Primary T cells from cord blood	blood
24	chr3:195703200-195715600	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr3:195703200-195715600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr3:195703400-195715800	Weak transcription	HMEC	breast
27	chr3:195703600-195715600	Weak transcription	Colonic Mucosa	Colon
28	chr3:195703800-195715800	Weak transcription	HSMM	muscle
29	chr3:195705200-195716400	Weak transcription	Brain Angular Gyrus	brain
30	chr3:195707000-195715800	Weak transcription	NH-A	brain
31	chr3:195709200-195716400	Weak transcription	HSMMtube	muscle
32	chr3:195710000-195715000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr3:195710000-195715200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr3:195710000-195715400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:195710000-195715400	Weak transcription	Fetal Brain Female	brain
36	chr3:195710000-195715600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:195710000-195715600	Weak transcription	NHEK	skin
38	chr3:195710000-195715800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr3:195710000-195716400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr3:195710000-195716400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:195710000-195716600	Weak transcription	GM12878-XiMat	blood
42	chr3:195710200-195715400	Weak transcription	Brain Anterior Caudate	brain
43	chr3:195710200-195715600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:195710200-195715600	Weak transcription	K562	blood
45	chr3:195710400-195715600	Weak transcription	HepG2	liver
46	chr3:195710400-195716400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr3:195711000-195715600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:195711000-195715600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr3:195711200-195716400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr3:195711200-195716400	Weak transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links