Variant report

Variant	nsv820015
Chromosome Location	chr3:195770699-195776215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:315)
CpG islands
(count:245)
Chromatin interactive
region (count:12)
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	BACH1	chr3:195775537-195776054	K562	blood:	n/a	n/a
2	BACH1	chr3:195774151-195774768	K562	blood:	n/a	n/a
3	BCL3	chr3:195774148-195775617	GM12878	blood:	n/a	n/a
4	BCL3	chr3:195772562-195772826	K562	blood:	n/a	n/a
5	BCL3	chr3:195775031-195776174	K562	blood:	n/a	n/a
6	BCL3	chr3:195772921-195773868	K562	blood:	n/a	n/a
7	BCL3	chr3:195773958-195776944	K562	blood:	n/a	n/a
8	BCL3	chr3:195774238-195774897	GM12878	blood:	n/a	n/a
9	BCL3	chr3:195774047-195774989	K562	blood:	n/a	n/a
10	BCL3	chr3:195772806-195773634	K562	blood:	n/a	n/a
11	BCLAF1	chr3:195774018-195774942	K562	blood:	n/a	n/a
12	BCLAF1	chr3:195772307-195772767	K562	blood:	n/a	n/a
13	BCLAF1	chr3:195775284-195776103	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:195774136-195774836	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:195775123-195776275	K562	blood:	n/a	n/a
16	BCLAF1	chr3:195774105-195778789	K562	blood:	n/a	n/a
17	BCLAF1	chr3:195774400-195774910	GM12878	blood:	n/a	n/a
18	CBX3	chr3:195772137-195772611	K562	blood:	n/a	n/a
19	CBX3	chr3:195775231-195776155	K562	blood:	n/a	n/a
20	CBX3	chr3:195774332-195774948	K562	blood:	n/a	n/a
21	CCNT2	chr3:195774167-195776092	K562	blood:	n/a	n/a
22	CCNT2	chr3:195772371-195772556	K562	blood:	n/a	n/a
23	CEBPB	chr3:195775891-195776209	K562	blood:	n/a	n/a
24	CEBPB	chr3:195774330-195774761	K562	blood:	n/a	n/a
25	CEBPD	chr3:195774180-195774950	K562	blood:	n/a	chr3:195774466-195774477
26	CEBPD	chr3:195774140-195777172	K562	blood:	n/a	chr3:195774466-195774477
27	CHD2	chr3:195775497-195775683	GM12878	blood:	n/a	n/a
28	CHD2	chr3:195774218-195774823	GM12878	blood:	n/a	n/a
29	CHD2	chr3:195772284-195776154	K562	blood:	n/a	n/a
30	CHD2	chr3:195772409-195772462	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:195774566-195774696	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:195774352-195774676	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr3:195772356-195772391	GM12891	blood:	n/a	n/a
34	CTCF	chr3:195775621-195775635	K562	blood:	n/a	n/a
35	CUX1	chr3:195775349-195775699	K562	blood:	n/a	n/a
36	CUX1	chr3:195774143-195774651	K562	blood:	n/a	n/a
37	CUX1	chr3:195775482-195775576	GM12878	blood:	n/a	n/a
38	EGR1	chr3:195772295-195772570	K562	blood:	n/a	n/a
39	EGR1	chr3:195772332-195772568	K562	blood:	n/a	n/a
40	ELK1	chr3:195775385-195775752	K562	blood:	n/a	n/a
41	EP300	chr3:195776203-195776795	K562	blood:	n/a	n/a
42	EP300	chr3:195775424-195775665	K562	blood:	n/a	n/a
43	ETS1	chr3:195774915-195775859	GM12878	blood:	n/a	n/a
44	FOSL2	chr3:195775209-195775616	HepG2	liver:	n/a	n/a
45	FOSL2	chr3:195774472-195775048	HepG2	liver:	n/a	n/a
46	FOXA1	chr3:195774153-195774433	T-47D	breast:	n/a	n/a
47	FOXA1	chr3:195773035-195773382	T-47D	breast:	n/a	n/a
48	FOXA1	chr3:195774047-195774520	HepG2	liver:	n/a	n/a
49	FOXA1	chr3:195772996-195773421	T-47D	breast:	n/a	n/a
50	FOXA1	chr3:195774154-195774475	HepG2	liver:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195771712-195771762	NB4	blood:	n/a
2	chr3:195771712-195771762	NB4	blood:	n/a
3	chr3:195773232-195773282	GM12892	blood:	n/a
4	chr3:195773232-195773282	AG04450	lung:	fetal
5	chr3:195771573-195771623	K562	blood:	n/a
6	chr3:195771712-195771762	BE2_C	brain:	n/a
7	chr3:195771712-195771762	HCF	heart:	n/a
8	chr3:195773232-195773282	ovcar-3	ovarian:	n/a
9	chr3:195771573-195771623	Hela-S3	cervix:	n/a
10	chr3:195772357-195772407	LNCaP	prostate:	n/a
11	chr3:195771573-195771623	LNCaP	prostate:	n/a
12	chr3:195773232-195773282	HL-60	blood:	n/a
13	chr3:195772357-195772407	PFSK-1	brain:	n/a
14	chr3:195771712-195771762	RPTEC	kidney:	n/a
15	chr3:195771573-195771623	HepG2	liver:	n/a
16	chr3:195771712-195771762	ProgFib	skin:	n/a
17	chr3:195771573-195771623	AG10803	skin:	n/a
18	chr3:195773232-195773282	HUVEC	blood vessel:	n/a
19	chr3:195772357-195772407	AG04450	lung:	fetal
20	chr3:195773232-195773282	HAEpiC	amniotic membrane:	n/a
21	chr3:195772357-195772407	PrEC	prostate:	n/a
22	chr3:195773232-195773282	Caco-2	colon:	n/a
23	chr3:195772357-195772407	GM06990	blood:	n/a
24	chr3:195773232-195773282	CMK	blood:	n/a
25	chr3:195771573-195771623	GM12892	blood:	n/a
26	chr3:195771712-195771762	LNCaP	prostate:	n/a
27	chr3:195772357-195772407	AG09319	gingival:	n/a
28	chr3:195773232-195773282	U87	brain:	n/a
29	chr3:195772357-195772407	HMEC	breast:	n/a
30	chr3:195771573-195771623	GM06990	blood:	n/a
31	chr3:195771573-195771623	PrEC	prostate:	n/a
32	chr3:195772357-195772407	HEK293	kidney:	embryo
33	chr3:195771573-195771623	SK-N-MC	brain:	n/a
34	chr3:195772357-195772407	NT2-D1	testis:	n/a
35	chr3:195772357-195772407	BJ	skin:	n/a
36	chr3:195772357-195772407	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:195773232-195773282	MCF-7	breast:	n/a
38	chr3:195772357-195772407	CMK	blood:	n/a
39	chr3:195771712-195771762	AG10803	skin:	n/a
40	chr3:195771573-195771623	GM12878	blood:	n/a
41	chr3:195771573-195771623	NH-A	brain:	n/a
42	chr3:195771573-195771623	PANC-1	pancreas:	n/a
43	chr3:195771573-195771623	NHBE	bronchial:	n/a
44	chr3:195771573-195771623	IMR90	lung:	fetal
45	chr3:195773232-195773282	HIPEpiC	eye:	n/a
46	chr3:195772357-195772407	NHDF-neo	bronchial:	n/a
47	chr3:195772357-195772407	HUVEC	blood vessel:	n/a
48	chr3:195773232-195773282	Jurkat	blood:	n/a
49	chr3:195771712-195771762	AG09309	skin:	n/a
50	chr3:195772357-195772407	T-47D	breast:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195774337..195776699-chr3:195790526..195792198,2	K562	blood:
2	chr3:195774699..195776571-chr3:195794634..195796757,3	K562	blood:
3	chr3:195775087..195781112-chr3:195806132..195810328,7	K562	blood:
4	chr3:195751254..195754207-chr3:195773192..195776278,3	K562	blood:
5	chr3:195774978..195780765-chr3:195803293..195810200,8	K562	blood:
6	chr3:195774592..195777044-chr3:195910665..195912937,2	K562	blood:
7	chr3:195771161..195772843-chr3:195786307..195787880,2	K562	blood:
8	chr3:195773121..195775698-chr3:195778391..195781329,2	MCF-7	breast:
9	chr3:195770109..195772936-chr3:195923383..195926412,3	K562	blood:
10	chr3:195774337..195780265-chr3:195790698..195793878,6	K562	blood:
11	chr3:195766788..195768399-chr3:195769156..195771546,2	MCF-7	breast:
12	chr3:195772434..195774325-chr3:195781653..195784506,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228413	TF binding region
ENSG00000228413	CpG island
ENSG00000072274	chromatin interactions
ENSG00000163958	chromatin interactions

Extended variants
information (count: 321 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144491970	chr3:195770736-195770737	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs571328229	chr3:195770792-195770793	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs192448687	chr3:195770796-195770797	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs550929340	chr3:195770815-195770816	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs569164632	chr3:195770865-195770866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536301073	chr3:195770895-195770896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs76433476	chr3:195770898-195770899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566576315	chr3:195770904-195770905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530732534	chr3:195770944-195770945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs62284007	chr3:195770947-195770948	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs113564829	chr3:195771043-195771044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs76126983	chr3:195771061-195771062	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34933234	chr3:195771062-195771063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10557988	chr3:195771063-195771064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs75726353	chr3:195771067-195771068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs78690319	chr3:195771068-195771069	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78275587	chr3:195771069-195771070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373399731	chr3:195771084-195771085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376161365	chr3:195771085-195771086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs13069818	chr3:195771087-195771088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370829593	chr3:195771088-195771089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386670120	chr3:195771094-195771095	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs79433112	chr3:195771111-195771112	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs556483205	chr3:195771154-195771155	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs62284008	chr3:195771155-195771156	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542220273	chr3:195771163-195771164	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs547107536	chr3:195771164-195771165	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11283605	chr3:195771183-195771184	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs60789736	chr3:195771195-195771196	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs183920601	chr3:195771233-195771234	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs149868217	chr3:195771267-195771268	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs73208058	chr3:195771323-195771324	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs568571043	chr3:195771326-195771327	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs376476678	chr3:195771455-195771456	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs375276806	chr3:195771463-195771464	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs546011341	chr3:195771484-195771485	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs111256967	chr3:195771494-195771495	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs189414847	chr3:195771561-195771562	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs35588786	chr3:195771564-195771565	Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs9876236	chr3:195771574-195771575	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs149052603	chr3:195771577-195771578	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs529980222	chr3:195771585-195771586	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548189859	chr3:195771595-195771596	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566372389	chr3:195771602-195771603	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113671186	chr3:195771605-195771606	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs181453813	chr3:195771610-195771611	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558406170	chr3:195771615-195771616	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs9823320	chr3:195771629-195771630	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538049914	chr3:195771661-195771662	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs4927706	chr3:195771722-195771723	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195762800-195780200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:195763000-195774600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:195765000-195775200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr3:195767200-195775400	Weak transcription	Fetal Brain Female	brain
5	chr3:195768400-195773000	Weak transcription	Dnd41	blood
6	chr3:195768400-195775200	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr3:195768400-195781600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:195768600-195771600	Weak transcription	Esophagus	oesophagus
9	chr3:195768600-195775400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr3:195768600-195778800	Weak transcription	Fetal Stomach	stomach
11	chr3:195769000-195771400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:195769000-195771400	Weak transcription	Thymus	Thymus
13	chr3:195769000-195773600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr3:195769000-195774600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr3:195769200-195776000	Weak transcription	K562	blood
16	chr3:195769400-195774400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr3:195769400-195775400	Weak transcription	Primary neutrophils fromperipheralblood	blood
18	chr3:195769600-195771400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:195769600-195773000	Weak transcription	Primary T cells from cord blood	blood
20	chr3:195769600-195774400	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr3:195769600-195775400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:195769600-195775400	Weak transcription	Small Intestine	intestine
23	chr3:195769800-195771400	Weak transcription	Colonic Mucosa	Colon
24	chr3:195769800-195771400	Weak transcription	Pancreas	Pancrea
25	chr3:195769800-195775000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr3:195769800-195775000	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr3:195769800-195775400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr3:195769800-195775800	Weak transcription	Aorta	Aorta
29	chr3:195769800-195776400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr3:195770000-195774200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr3:195770000-195774200	Weak transcription	A549	lung
32	chr3:195770000-195774800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr3:195770000-195775800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr3:195770000-195778800	Weak transcription	Gastric	stomach
35	chr3:195770200-195773200	Weak transcription	Left Ventricle	heart
36	chr3:195770200-195774600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr3:195770200-195775200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr3:195770200-195775400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr3:195770200-195775400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:195770200-195778000	Weak transcription	Ovary	ovary
41	chr3:195770200-195778800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:195770400-195772200	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr3:195770400-195773400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr3:195770400-195776800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr3:195770400-195778200	Weak transcription	Fetal Kidney	kidney
46	chr3:195770600-195775800	Weak transcription	GM12878-XiMat	blood
47	chr3:195770800-195774400	Weak transcription	Duodenum Mucosa	Duodenum
48	chr3:195770800-195774600	Weak transcription	HMEC	breast
49	chr3:195770800-195776000	Weak transcription	Brain Germinal Matrix	brain
50	chr3:195771000-195771400	Weak transcription	Fetal Intestine Small	intestine

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