Variant report

Variant	esv3374493
Chromosome Location	chr3:195675655-195681853
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:594)
CpG islands
(count:244)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:594 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	chr3:195680472-195680694	GM12878	blood:	n/a	n/a
6	BATF	chr3:195681129-195681669	GM12878	blood:	n/a	n/a
7	BATF	chr3:195681681-195681957	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:195679579-195679786	GM12878	blood:	n/a	chr3:195679673-195679680
9	BCL11A	chr3:195681171-195681812	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
10	BCL11A	chr3:195681118-195681900	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
11	BCL11A	chr3:195680283-195680924	GM12878	blood:	n/a	chr3:195680659-195680668
12	BCL11A	chr3:195680538-195680860	GM12878	blood:	n/a	chr3:195680659-195680668
13	BCL11A	chr3:195679437-195679731	GM12878	blood:	n/a	chr3:195679673-195679680
14	BCL3	chr3:195681285-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
15	BCLAF1	chr3:195681279-195681563	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
16	BCLAF1	chr3:195681253-195681686	GM12878	blood:	n/a	chr3:195681302-195681315 chr3:195681417-195681426
17	BHLHE40	chr3:195681210-195681587	K562	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
18	BHLHE40	chr3:195681203-195681678	HepG2	liver:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
19	BHLHE40	chr3:195681214-195681663	GM12878	blood:	n/a	chr3:195681296-195681312 chr3:195681304-195681320
20	BRCA1	chr3:195681377-195681604	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr3:195681152-195682264	K562	blood:	n/a	n/a
22	CBX3	chr3:195679046-195679922	K562	blood:	n/a	n/a
23	CBX3	chr3:195680129-195680896	K562	blood:	n/a	n/a
24	CBX3	chr3:195681209-195681715	K562	blood:	n/a	n/a
25	CCNT2	chr3:195681222-195681599	K562	blood:	n/a	n/a
26	CEBPB	chr3:195681244-195681840	GM12878	blood:	n/a	n/a
27	CEBPB	chr3:195680276-195680721	K562	blood:	n/a	n/a
28	CEBPB	chr3:195681219-195681730	K562	blood:	n/a	n/a
29	CEBPB	chr3:195681388-195681580	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr3:195681081-195681739	K562	blood:	n/a	n/a
31	CHD1	chr3:195681413-195681628	GM12878	blood:	n/a	n/a
32	CHD2	chr3:195681358-195681608	GM12878	blood:	n/a	n/a
33	CHD2	chr3:195681301-195681610	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr3:195681296-195681494	K562	blood:	n/a	n/a
35	CREB1	chr3:195681295-195681566	GM12878	blood:	n/a	n/a
36	CREB1	chr3:195681297-195681526	HepG2	liver:	n/a	n/a
37	CREB1	chr3:195681318-195681559	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr3:195681284-195681534	GM12878	blood:	n/a	n/a
39	CREB1	chr3:195681279-195681557	K562	blood:	n/a	n/a
40	CREB1	chr3:195681328-195681466	A549	lung:	n/a	n/a
41	CREB1	chr3:195681317-195681541	HepG2	liver:	n/a	n/a
42	CREB1	chr3:195681268-195681489	A549	lung:	n/a	n/a
43	CREB1	chr3:195681315-195681561	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr3:195681246-195681450	K562	blood:	n/a	chr3:195681300-195681313
45	CTCF	chr3:195679597-195679901	K562	blood:	n/a	n/a
46	CTCF	chr3:195681406-195681496	GM12878	blood:	n/a	n/a
47	CTCF	chr3:195680720-195680870	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr3:195680865-195680897	LNCaP	prostate:	n/a	n/a
49	CTCF	chr3:195681355-195681484	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr3:195680825-195680912	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195679450-195679500	ProgFib	skin:	n/a
2	chr3:195679450-195679500	ECC-1	luminal epithelium:	n/a
3	chr3:195678176-195678226	HCT-116	colon:	n/a
4	chr3:195678176-195678226	HNPCEpiC	eye:	n/a
5	chr3:195678176-195678226	HepG2	liver:	n/a
6	chr3:195678176-195678226	PrEC	prostate:	n/a
7	chr3:195678176-195678226	HEK293	kidney:	embryo
8	chr3:195681091-195681141	A549	lung:	n/a
9	chr3:195681091-195681141	IMR90	lung:	fetal
10	chr3:195679450-195679500	SKMC	muscle:	n/a
11	chr3:195681091-195681141	SK-N-SH_RA	brain:	n/a
12	chr3:195681400-195681450	BE2_C	brain:	n/a
13	chr3:195678176-195678226	Hepatocyte	liver:	n/a
14	chr3:195678176-195678226	SKMC	muscle:	n/a
15	chr3:195681091-195681141	T-47D	breast:	n/a
16	chr3:195679450-195679500	HEEpiC	esophagus:	n/a
17	chr3:195681400-195681450	HRPEpiC	eye:	n/a
18	chr3:195678176-195678226	HUVEC	blood vessel:	n/a
19	chr3:195681400-195681450	GM12892	blood:	n/a
20	chr3:195678176-195678226	NT2-D1	testis:	n/a
21	chr3:195678176-195678226	NB4	blood:	n/a
22	chr3:195678176-195678226	AoSMC	blood vessel:	n/a
23	chr3:195679450-195679500	K562	blood:	n/a
24	chr3:195681400-195681450	ProgFib	skin:	n/a
25	chr3:195681091-195681141	AG10803	skin:	n/a
26	chr3:195679450-195679500	SK-N-SH_RA	brain:	n/a
27	chr3:195679450-195679500	NHDF-neo	bronchial:	n/a
28	chr3:195681400-195681450	GM06990	blood:	n/a
29	chr3:195679450-195679500	NH-A	brain:	n/a
30	chr3:195678176-195678226	PFSK-1	brain:	n/a
31	chr3:195681400-195681450	Caco-2	colon:	n/a
32	chr3:195681400-195681450	SAEC	small airway:	n/a
33	chr3:195681091-195681141	SAEC	small airway:	n/a
34	chr3:195678176-195678226	BE2_C	brain:	n/a
35	chr3:195679450-195679500	HPAEpiC	pulmonary alveolar:	n/a
36	chr3:195681091-195681141	AoSMC	blood vessel:	n/a
37	chr3:195678176-195678226	GM12878	blood:	n/a
38	chr3:195678176-195678226	AG09319	gingival:	n/a
39	chr3:195679450-195679500	LNCaP	prostate:	n/a
40	chr3:195681091-195681141	ProgFib	skin:	n/a
41	chr3:195678176-195678226	NHBE	bronchial:	n/a
42	chr3:195681400-195681450	HEK293	kidney:	embryo
43	chr3:195681400-195681450	BJ	skin:	n/a
44	chr3:195681091-195681141	ECC-1	luminal epithelium:	n/a
45	chr3:195681091-195681141	SKMC	muscle:	n/a
46	chr3:195678176-195678226	GM12892	blood:	n/a
47	chr3:195681091-195681141	SK-N-MC	brain:	n/a
48	chr3:195678176-195678226	U87	brain:	n/a
49	chr3:195681400-195681450	U87	brain:	n/a
50	chr3:195681091-195681141	HNPCEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

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

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-2	chr3:195676113-195676284	NONHSAT094275
2	lnc-TNK2-2	chr3:195676059-195679566	ENSG00000260261.1

No data

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

Extended variants
information (count: 258 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75915648	chr3:195675664-195675665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572875673	chr3:195675672-195675673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540508465	chr3:195675675-195675676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565105105	chr3:195675708-195675709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62285306	chr3:195675729-195675730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147709623	chr3:195675752-195675753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56133758	chr3:195675761-195675762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs562831195	chr3:195675835-195675836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530085696	chr3:195675841-195675842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548539248	chr3:195675869-195675870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566886889	chr3:195675884-195675885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369203772	chr3:195675885-195675886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534263398	chr3:195675891-195675892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200930141	chr3:195675960-195675961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546839758	chr3:195675975-195675976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77331356	chr3:195676051-195676052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150437051	chr3:195676054-195676055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138213397	chr3:195676057-195676058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557334702	chr3:195676059-195676060	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs190461683	chr3:195676067-195676068	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs1048562	chr3:195676122-195676123	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs535898133	chr3:195676136-195676137	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs376501650	chr3:195676137-195676138	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs183441266	chr3:195676167-195676168	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs565067896	chr3:195676170-195676171	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs2448522	chr3:195676175-195676176	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs547322271	chr3:195676178-195676179	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs141789999	chr3:195676214-195676215	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs539892245	chr3:195676217-195676218	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs565144306	chr3:195676250-195676251	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs201876511	chr3:195676264-195676265	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs577062350	chr3:195676273-195676274	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs544396756	chr3:195676449-195676450	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs12107374	chr3:195676458-195676459	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs189741770	chr3:195676484-195676485	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs28589448	chr3:195676497-195676498	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs201694796	chr3:195676518-195676519	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs28413663	chr3:195676538-195676539	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs7619101	chr3:195676561-195676562	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs11714495	chr3:195676564-195676565	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs200402998	chr3:195676577-195676578	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs201394523	chr3:195676581-195676582	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs188338810	chr3:195676604-195676605	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs75862535	chr3:195676608-195676609	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	mRNA abundance
45	rs112202664	chr3:195676612-195676613	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs2448523	chr3:195676656-195676657	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs11713007	chr3:195676661-195676662	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs7619268	chr3:195676676-195676677	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs114796663	chr3:195676682-195676683	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs553301772	chr3:195676683-195676684	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195647200-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:195648600-195680600	Weak transcription	Pancreas	Pancrea
3	chr3:195656600-195681000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:195656800-195676400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:195656800-195679400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:195657800-195681400	Weak transcription	GM12878-XiMat	blood
7	chr3:195659000-195676400	Weak transcription	Hela-S3	cervix
8	chr3:195659600-195681200	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
10	chr3:195660000-195681200	Weak transcription	Colonic Mucosa	Colon
11	chr3:195660400-195680600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr3:195660600-195681200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr3:195661200-195681000	Weak transcription	Ovary	ovary
14	chr3:195661800-195681200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:195663400-195681200	Weak transcription	Left Ventricle	heart
16	chr3:195663600-195681000	Weak transcription	Fetal Brain Female	brain
17	chr3:195663600-195681200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:195663600-195681200	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr3:195663800-195682000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr3:195664400-195681200	Weak transcription	Osteobl	bone
21	chr3:195665000-195681200	Weak transcription	Placenta	Placenta
22	chr3:195665200-195677800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
24	chr3:195665400-195681400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
26	chr3:195666000-195677200	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr3:195666000-195677800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr3:195667200-195681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr3:195667400-195677200	Weak transcription	Gastric	stomach
30	chr3:195667400-195677200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr3:195667400-195680800	Weak transcription	Right Ventricle	heart
32	chr3:195667400-195681200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr3:195667400-195681200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:195667400-195681200	Weak transcription	Brain Anterior Caudate	brain
35	chr3:195667400-195681200	Weak transcription	Brain Cingulate Gyrus	brain
36	chr3:195667400-195681200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr3:195667400-195681200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr3:195667400-195681400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr3:195667400-195681400	Weak transcription	Brain Substantia Nigra	brain
40	chr3:195667400-195684200	Weak transcription	Spleen	Spleen
41	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr3:195667600-195677600	Weak transcription	Primary T cells from cord blood	blood
43	chr3:195667600-195680200	Weak transcription	Fetal Stomach	stomach
44	chr3:195667600-195681200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr3:195667600-195681200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:195667600-195681200	Weak transcription	Esophagus	oesophagus
47	chr3:195667600-195681400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr3:195667600-195681600	Weak transcription	Fetal Intestine Large	intestine
49	chr3:195667800-195681200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr3:195668000-195681200	Weak transcription	Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links