Variant report

Variant	esv3402010
Chromosome Location	chr3:195691755-195726353
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	chr3:195717483-195717694	K562	blood:	n/a	n/a
2	ATF3	chr3:195717067-195717371	A549	lung:	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	chr3:195716145-195716590	GM12878	blood:	n/a	n/a
7	BATF	chr3:195717540-195717834	GM12878	blood:	n/a	n/a
8	BATF	chr3:195705475-195705667	GM12878	blood:	n/a	chr3:195705640-195705649 chr3:195705599-195705610
9	BATF	chr3:195715731-195716052	GM12878	blood:	n/a	n/a
10	BATF	chr3:195717279-195717490	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:195711556-195711737	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:195722372-195722606	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:195723014-195723259	GM12878	blood:	n/a	chr3:195723080-195723089
14	BCL11A	chr3:195715512-195715842	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:195717225-195717865	GM12878	blood:	n/a	chr3:195717473-195717482
16	BCL11A	chr3:195717296-195717514	GM12878	blood:	n/a	chr3:195717473-195717482
17	BCL11A	chr3:195716071-195717206	GM12878	blood:	n/a	chr3:195716811-195716824 chr3:195716792-195716801 chr3:195716946-195716959
18	BCL3	chr3:195700608-195700811	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:195717520-195717617	K562	blood:	n/a	n/a
20	BHLHE40	chr3:195717244-195717251	K562	blood:	n/a	n/a
21	CBX3	chr3:195721219-195721517	K562	blood:	n/a	n/a
22	CBX3	chr3:195721166-195721620	K562	blood:	n/a	n/a
23	CBX3	chr3:195717317-195717855	K562	blood:	n/a	n/a
24	CBX3	chr3:195716251-195717942	K562	blood:	n/a	n/a
25	CEBPB	chr3:195719808-195719847	IMR90	lung:	n/a	n/a
26	CEBPB	chr3:195710856-195710881	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:195719811-195719954	A549	lung:	n/a	n/a
28	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
29	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
30	CEBPB	chr3:195719767-195719961	HepG2	liver:	n/a	n/a
31	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
32	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
33	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
34	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
35	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
36	CEBPD	chr3:195716909-195717795	K562	blood:	n/a	n/a
37	CEBPD	chr3:195716979-195717383	HepG2	liver:	n/a	n/a
38	CHD2	chr3:195717301-195717419	GM12878	blood:	n/a	n/a
39	CHD2	chr3:195717521-195717554	K562	blood:	n/a	n/a
40	CHD2	chr3:195717515-195717598	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr3:195721180-195721330	HRE	kidney:	n/a	n/a
42	CTCF	chr3:195721300-195721450	WI-38	lung:	n/a	n/a
43	CTCF	chr3:195717127-195717255	Pancreas_OC	pancreas:	n/a	n/a
44	CTCF	chr3:195721340-195721490	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:195721330-195721519	GM10248	blood:	n/a	n/a
46	CTCF	chr3:195716963-195717762	K562	blood:	n/a	chr3:195717520-195717538
47	CTCF	chr3:195722080-195722230	HMF	breast:	n/a	n/a
48	CTCF	chr3:195721240-195721390	HAc	cerebellar:	n/a	n/a
49	CTCF	chr3:195721394-195721469	HepG2	liver:	n/a	n/a
50	CTCF	chr3:195721300-195721450	GM12868	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195717416-195717466	A549	lung:	n/a
2	chr3:195716632-195716682	ovcar-3	ovarian:	n/a
3	chr3:195717416-195717466	A549	lung:	n/a
4	chr3:195716632-195716682	ovcar-3	ovarian:	n/a
5	chr3:195717366-195717416	HUVEC	blood vessel:	n/a
6	chr3:195700735-195700785	SK-N-SH_RA	brain:	n/a
7	chr3:195709661-195709711	ProgFib	skin:	n/a
8	chr3:195709661-195709711	HIPEpiC	eye:	n/a
9	chr3:195724371-195724421	MCF10A-Er-Src	breast:	n/a
10	chr3:195717962-195718012	GM12878	blood:	n/a
11	chr3:195700735-195700785	NH-A	brain:	n/a
12	chr3:195703920-195703970	GM12892	blood:	n/a
13	chr3:195709698-195709748	ProgFib	skin:	n/a
14	chr3:195719262-195719312	HCT-116	colon:	n/a
15	chr3:195714100-195714150	CMK	blood:	n/a
16	chr3:195701118-195701168	LNCaP	prostate:	n/a
17	chr3:195714100-195714150	HRPEpiC	eye:	n/a
18	chr3:195717416-195717466	NHBE	bronchial:	n/a
19	chr3:195716632-195716682	AG09319	gingival:	n/a
20	chr3:195717574-195717624	GM19239	blood:	n/a
21	chr3:195709715-195709765	AG04450	lung:	fetal
22	chr3:195709715-195709765	HCT-116	colon:	n/a
23	chr3:195709715-195709765	PFSK-1	brain:	n/a
24	chr3:195701118-195701168	SKMC	muscle:	n/a
25	chr3:195701166-195701216	GM06990	blood:	n/a
26	chr3:195719790-195719840	K562	blood:	n/a
27	chr3:195717962-195718012	GM19239	blood:	n/a
28	chr3:195724371-195724421	HEK293	kidney:	embryo
29	chr3:195701118-195701168	ECC-1	luminal epithelium:	n/a
30	chr3:195716626-195716676	SKMC	muscle:	n/a
31	chr3:195716626-195716676	IMR90	lung:	fetal
32	chr3:195701118-195701168	PANC-1	pancreas:	n/a
33	chr3:195717366-195717416	HepG2	liver:	n/a
34	chr3:195719262-195719312	BE2_C	brain:	n/a
35	chr3:195703920-195703970	GM06990	blood:	n/a
36	chr3:195717574-195717624	HRPEpiC	eye:	n/a
37	chr3:195717366-195717416	Hela-S3	cervix:	n/a
38	chr3:195723614-195723664	PFSK-1	brain:	n/a
39	chr3:195717344-195717394	HRPEpiC	eye:	n/a
40	chr3:195717962-195718012	PrEC	prostate:	n/a
41	chr3:195709698-195709748	K562	blood:	n/a
42	chr3:195716632-195716682	Caco-2	colon:	n/a
43	chr3:195703920-195703970	A549	lung:	n/a
44	chr3:195701166-195701216	AoSMC	blood vessel:	n/a
45	chr3:195717574-195717624	ECC-1	luminal epithelium:	n/a
46	chr3:195719790-195719840	Caco-2	colon:	n/a
47	chr3:195709698-195709748	AG10803	skin:	n/a
48	chr3:195701166-195701216	HIPEpiC	eye:	n/a
49	chr3:195709715-195709765	GM12892	blood:	n/a
50	chr3:195700735-195700785	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:195384346..195385021-chr3:195716746..195717598,2	HCT-116	colon:
2	chr3:195586120..195586802-chr3:195721315..195721912,2	MCF-7	breast:
3	chr3:195384344..195385079-chr3:195717098..195717747,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFRC-1	chr3:195726007-195726255	NONHSAT094273

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

Extended variants
information (count: 1643 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1643 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368671376	chr3:195691764-195691765	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs533193763	chr3:195691770-195691771	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs146534812	chr3:195691784-195691785	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs571674911	chr3:195691785-195691786	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs538761839	chr3:195691792-195691793	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs371833883	chr3:195691801-195691802	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs537309306	chr3:195691810-195691811	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs549284931	chr3:195691820-195691821	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs567282632	chr3:195691834-195691835	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs375218577	chr3:195691844-195691845	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs183451166	chr3:195691848-195691849	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs534321327	chr3:195691900-195691901	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs201904434	chr3:195691908-195691909	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs369380196	chr3:195691955-195691956	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs113232023	chr3:195691976-195691977	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	mRNA abundance
16	rs186081311	chr3:195691982-195691983	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs201097395	chr3:195691994-195691995	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs539227258	chr3:195692007-195692008	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs57651673	chr3:195692049-195692050	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs6776037	chr3:195692069-195692070	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	mRNA abundance
21	rs542946160	chr3:195692086-195692087	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs561221652	chr3:195692121-195692122	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs369721931	chr3:195692129-195692130	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs573232337	chr3:195692131-195692132	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs540256517	chr3:195692132-195692133	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs373240921	chr3:195692139-195692140	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs377693789	chr3:195692161-195692162	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs146932497	chr3:195692171-195692172	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs532452837	chr3:195692180-195692181	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs373596243	chr3:195692181-195692182	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs563510047	chr3:195692183-195692184	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs369978157	chr3:195692188-195692189	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs374086116	chr3:195692213-195692214	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567439815	chr3:195692226-195692227	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534622715	chr3:195692239-195692240	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202015092	chr3:195692242-195692243	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs546233971	chr3:195692254-195692255	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189762094	chr3:195692285-195692286	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571342952	chr3:195692307-195692308	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62282793	chr3:195692311-195692312	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs267599754	chr3:195692319-195692320	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs62282794	chr3:195692347-195692348	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139762755	chr3:195692349-195692350	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538310463	chr3:195692364-195692365	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556620843	chr3:195692400-195692401	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140005001	chr3:195692418-195692419	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77887672	chr3:195692419-195692420	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182687021	chr3:195692435-195692436	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200169887	chr3:195692438-195692439	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370027567	chr3:195692477-195692478	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1157 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
2	chr3:195677800-195691800	Weak transcription	NHDF-Ad	bronchial
3	chr3:195678000-195696200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr3:195679000-195695800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:195681600-195696200	Weak transcription	Primary B cells from cord blood	blood
6	chr3:195681800-195695600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr3:195681800-195696200	Weak transcription	HepG2	liver
8	chr3:195681800-195696400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:195681800-195696400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:195681800-195696800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr3:195682600-195693400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr3:195682600-195697000	Weak transcription	Fetal Lung	lung
13	chr3:195682600-195715600	Weak transcription	Psoas Muscle	Psoas
14	chr3:195682800-195696200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:195682800-195696400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:195683400-195696600	Weak transcription	HUVEC	blood vessel
17	chr3:195683600-195711800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:195683800-195696400	Weak transcription	Fetal Brain Male	brain
19	chr3:195684200-195711800	Strong transcription	Placenta	Placenta
20	chr3:195685400-195698800	Strong transcription	Dnd41	blood
21	chr3:195685800-195716600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr3:195686000-195691800	Weak transcription	Primary T helper cells fromperipheralblood	blood
23	chr3:195686200-195691800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr3:195686400-195696200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr3:195686400-195710800	Weak transcription	Small Intestine	intestine
26	chr3:195686600-195691800	Weak transcription	HSMM	muscle
27	chr3:195687400-195695600	Weak transcription	Fetal Heart	heart
28	chr3:195687600-195707600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr3:195687800-195693600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr3:195688000-195691800	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr3:195688400-195692200	Weak transcription	K562	blood
32	chr3:195688600-195692600	Strong transcription	Placenta Amnion	Placenta Amnion
33	chr3:195688800-195694000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:195688800-195712200	Strong transcription	Monocytes-CD14+_RO01746	blood
35	chr3:195689000-195691800	Weak transcription	Hela-S3	cervix
36	chr3:195689200-195693400	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr3:195689400-195692800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:195689400-195693400	Strong transcription	Adipose Nuclei	Adipose
39	chr3:195689400-195694200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr3:195689400-195699200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr3:195689600-195697000	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:195689800-195692000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:195690000-195691800	Weak transcription	Fetal Thymus	thymus
44	chr3:195690200-195692200	Weak transcription	NHEK	skin
45	chr3:195690200-195696200	Weak transcription	A549	lung
46	chr3:195690800-195692600	Strong transcription	Brain Substantia Nigra	brain
47	chr3:195690800-195694200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr3:195690800-195707200	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr3:195691000-195692800	Genic enhancers	Fetal Intestine Small	intestine
50	chr3:195691000-195693000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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