Variant report

Variant	esv3362647
Chromosome Location	chr3:195661755-195684553
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:788)
CpG islands
(count:549)
Chromatin interactive
region (count:13)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:195681353-195681596	K562	blood:	n/a	n/a
2	ATF2	chr3:195681259-195681587	GM12878	blood:	n/a	n/a
3	ATF3	chr3:195678739-195678871	K562	blood:	n/a	n/a
4	ATF3	chr3:195681303-195681452	K562	blood:	n/a	n/a
5	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
6	BATF	chr3:195682768-195683488	GM12878	blood:	n/a	n/a
7	BATF	chr3:195682771-195683491	GM12878	blood:	n/a	n/a
8	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
9	BATF	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:195682872-195683277	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:195682895-195683356	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:195662910-195663112	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:195681860-195682057	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
15	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
16	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
17	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
18	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
19	BCL11A	chr3:195663537-195663765	GM12878	blood:	n/a	chr3:195663586-195663595
20	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
21	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
22	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
23	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
24	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
25	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
26	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
27	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr3:195679046-195679922	K562	blood:	n/a	n/a
29	CBX3	chr3:195681209-195681715	K562	blood:	n/a	n/a
30	CBX3	chr3:195680129-195680896	K562	blood:	n/a	n/a
31	CBX3	chr3:195681152-195682264	K562	blood:	n/a	n/a
32	CCNT2	chr3:195681222-195681599	K562	blood:	n/a	n/a
33	CCNT2	chr3:195682412-195682541	K562	blood:	n/a	n/a
34	CEBPB	chr3:195681219-195681730	K562	blood:	n/a	n/a
35	CEBPB	chr3:195680276-195680721	K562	blood:	n/a	n/a
36	CEBPB	chr3:195681388-195681580	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:195681244-195681840	GM12878	blood:	n/a	n/a
38	CEBPD	chr3:195681081-195681739	K562	blood:	n/a	n/a
39	CHD1	chr3:195681413-195681628	GM12878	blood:	n/a	n/a
40	CHD2	chr3:195681301-195681610	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr3:195681358-195681608	GM12878	blood:	n/a	n/a
42	CREB1	chr3:195681268-195681489	A549	lung:	n/a	n/a
43	CREB1	chr3:195681296-195681494	K562	blood:	n/a	n/a
44	CREB1	chr3:195681295-195681566	GM12878	blood:	n/a	n/a
45	CREB1	chr3:195681318-195681559	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr3:195681279-195681557	K562	blood:	n/a	n/a
47	CREB1	chr3:195681297-195681526	HepG2	liver:	n/a	n/a
48	CREB1	chr3:195681328-195681466	A549	lung:	n/a	n/a
49	CREB1	chr3:195681317-195681541	HepG2	liver:	n/a	n/a
50	CREB1	chr3:195681284-195681534	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195682326-195682376	GM12891	blood:	n/a
2	chr3:195681400-195681450	HMEC	breast:	n/a
3	chr3:195679450-195679500	LNCaP	prostate:	n/a
4	chr3:195678176-195678226	NB4	blood:	n/a
5	chr3:195682595-195682645	HRPEpiC	eye:	n/a
6	chr3:195683635-195683685	AG09309	skin:	n/a
7	chr3:195679450-195679500	A549	lung:	n/a
8	chr3:195682595-195682645	PrEC	prostate:	n/a
9	chr3:195683635-195683685	BJ	skin:	n/a
10	chr3:195682326-195682376	HRPEpiC	eye:	n/a
11	chr3:195668262-195668312	GM06990	blood:	n/a
12	chr3:195682326-195682376	K562	blood:	n/a
13	chr3:195679450-195679500	AG04450	lung:	fetal
14	chr3:195678176-195678226	AG04450	lung:	fetal
15	chr3:195668262-195668312	ovcar-3	ovarian:	n/a
16	chr3:195678176-195678226	T-47D	breast:	n/a
17	chr3:195679450-195679500	HUVEC	blood vessel:	n/a
18	chr3:195682326-195682376	HNPCEpiC	eye:	n/a
19	chr3:195681400-195681450	HAEpiC	amniotic membrane:	n/a
20	chr3:195682365-195682415	K562	blood:	n/a
21	chr3:195682326-195682376	HL-60	blood:	n/a
22	chr3:195668262-195668312	HepG2	liver:	n/a
23	chr3:195679450-195679500	AG10803	skin:	n/a
24	chr3:195682595-195682645	PANC-1	pancreas:	n/a
25	chr3:195679450-195679500	HCF	heart:	n/a
26	chr3:195668262-195668312	MCF-7	breast:	n/a
27	chr3:195678176-195678226	U87	brain:	n/a
28	chr3:195681400-195681450	SK-N-MC	brain:	n/a
29	chr3:195679450-195679500	HCT-116	colon:	n/a
30	chr3:195682365-195682415	H1-hESC	embryonic stem cell:	embryo
31	chr3:195682595-195682645	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:195678176-195678226	Hepatocyte	liver:	n/a
33	chr3:195681400-195681450	PFSK-1	brain:	n/a
34	chr3:195681091-195681141	AG09319	gingival:	n/a
35	chr3:195681091-195681141	AG10803	skin:	n/a
36	chr3:195678176-195678226	SAEC	small airway:	n/a
37	chr3:195682326-195682376	AG09309	skin:	n/a
38	chr3:195681091-195681141	AG04449	skin:	fetal
39	chr3:195681400-195681450	ECC-1	luminal epithelium:	n/a
40	chr3:195681091-195681141	BE2_C	brain:	n/a
41	chr3:195678176-195678226	MCF10A-Er-Src	breast:	n/a
42	chr3:195681400-195681450	AoSMC	blood vessel:	n/a
43	chr3:195678176-195678226	Hela-S3	cervix:	n/a
44	chr3:195668262-195668312	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:195678176-195678226	Caco-2	colon:	n/a
46	chr3:195681091-195681141	H1-hESC	embryonic stem cell:	embryo
47	chr3:195681091-195681141	AG04450	lung:	fetal
48	chr3:195682365-195682415	AG04450	lung:	fetal
49	chr3:195682326-195682376	Hepatocyte	liver:	n/a
50	chr3:195681400-195681450	SK-N-SH_RA	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195645901..195648267-chr3:195679890..195681479,3	MCF-7	breast:
2	chr3:195679870..195682569-chr3:197379763..197382610,2	K562	blood:
3	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:
4	chr3:195636473..195638760-chr3:195679951..195681488,2	MCF-7	breast:
5	chr3:195361732..195362263-chr3:195681373..195681896,2	MCF-7	breast:
6	chr3:195655412..195657166-chr3:195660620..195663176,2	K562	blood:
7	chr3:195620748..195623057-chr3:195678515..195681386,2	K562	blood:
8	chr3:195620748..195623055-chr3:195679886..195681403,2	K562	blood:
9	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
10	chr3:195361738..195362245-chr3:195681393..195681916,2	HCT-116	colon:
11	chr3:195639677..195641924-chr3:195679365..195681428,2	MCF-7	breast:
12	chr3:195679874..195682569-chr3:197381110..197382679,2	K562	blood:
13	chr3:195673861..195675995-chr5:278201..279705,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1
2	lnc-TFRC-1	chr3:195666274-195667064	NONHSAT094272
3	lnc-TNK2-2	chr3:195673684-195674350	NONHSAT094275
4	lnc-TFRC-1	chr3:195668449-195672581	NONHSAT094272
5	lnc-TNK2-2	chr3:195665538-195665609	NONHSAT094271
6	lnc-TFRC-1	chr3:195666277-195666553	NONHSAT094273
7	lnc-TNK2-2	chr3:195674206-195674576	NONHSAT094271
8	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275
9	lnc-MUC20-9	chr3:195674996-195675559	NONHSAT094276

No data

Variant related genes	Relation type
ENSG00000260261	TF binding region
ENSG00000231443	TF binding region
ENSG00000260261	CpG island
ENSG00000231443	CpG island
ENSG00000273009	chromatin interactions
ENSG00000061938	chromatin interactions
ENSG00000266730	chromatin interactions
ENSG00000239122	chromatin interactions
ENSG00000242086	chromatin interactions

Extended variants
information (count: 1398 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1398 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9868045	chr3:195661770-195661771	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79267317	chr3:195661794-195661795	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79170631	chr3:195661802-195661803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs80147945	chr3:195661803-195661804	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75792125	chr3:195661805-195661806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs199630645	chr3:195661816-195661817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs371381625	chr3:195661821-195661822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114345101	chr3:195661825-195661826	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375765717	chr3:195661835-195661836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564655459	chr3:195661861-195661862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182006516	chr3:195661888-195661889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540269787	chr3:195661889-195661890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs186215780	chr3:195661890-195661891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs576955643	chr3:195661912-195661913	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544286976	chr3:195661916-195661917	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190741419	chr3:195661923-195661924	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs142593253	chr3:195661941-195661942	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542562766	chr3:195661947-195661948	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs562312730	chr3:195661986-195661987	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561197043	chr3:195662009-195662010	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528386698	chr3:195662030-195662031	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182833496	chr3:195662039-195662040	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs145995577	chr3:195662041-195662042	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs532260401	chr3:195662070-195662071	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186983552	chr3:195662119-195662120	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs190664504	chr3:195662143-195662144	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs138645674	chr3:195662165-195662166	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543564646	chr3:195662187-195662188	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149330613	chr3:195662197-195662198	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs182922011	chr3:195662198-195662199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564823132	chr3:195662200-195662201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs534196981	chr3:195662209-195662210	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558566160	chr3:195662215-195662216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576795580	chr3:195662221-195662222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537977410	chr3:195662253-195662254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554162859	chr3:195662269-195662270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188874965	chr3:195662289-195662290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369095600	chr3:195662308-195662309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373281591	chr3:195662332-195662333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560923640	chr3:195662337-195662338	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs144578309	chr3:195662358-195662359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs540498936	chr3:195662386-195662387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564895548	chr3:195662394-195662395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532095815	chr3:195662398-195662399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs550412187	chr3:195662399-195662400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs562641233	chr3:195662468-195662469	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs193283168	chr3:195662472-195662473	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs548789428	chr3:195662476-195662477	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566710740	chr3:195662505-195662506	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534239396	chr3:195662519-195662520	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195666600	Weak transcription	Lung	lung
3	chr3:195648600-195666600	Weak transcription	Spleen	Spleen
4	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
5	chr3:195648800-195666600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr3:195648800-195666800	Weak transcription	Esophagus	oesophagus
7	chr3:195651200-195671200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:195651800-195673800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr3:195653000-195666800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr3:195656800-195666600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr3:195656800-195666600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr3:195656800-195669200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:195656800-195671200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:195657000-195666800	Weak transcription	Primary T cells from cord blood	blood
18	chr3:195657200-195666800	Weak transcription	Thymus	Thymus
19	chr3:195657400-195670000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
21	chr3:195658400-195666800	Weak transcription	Gastric	stomach
22	chr3:195658800-195666800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr3:195659000-195667200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
25	chr3:195659600-195666600	Weak transcription	Brain Anterior Caudate	brain
26	chr3:195659600-195666800	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
29	chr3:195660000-195666600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:195660000-195666600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr3:195660000-195666600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr3:195660000-195666600	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:195660000-195666800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:195660000-195666800	Weak transcription	Brain Substantia Nigra	brain
35	chr3:195660000-195666800	Weak transcription	Fetal Intestine Large	intestine
36	chr3:195660000-195666800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr3:195660000-195669800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
39	chr3:195660200-195666600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:195660400-195666600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr3:195660400-195666800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:195660400-195666800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr3:195660600-195666400	Weak transcription	Fetal Intestine Small	intestine
45	chr3:195660600-195666800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr3:195660600-195669600	Weak transcription	A549	lung
47	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr3:195660800-195666800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr3:195660800-195667000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:195660800-195669400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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