Variant report

Variant	esv3429984
Chromosome Location	chr3:195683555-195688753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:113)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:113 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
3	CBX3	chr3:195687930-195689486	K562	blood:	n/a	n/a
4	CTCF	chr3:195686747-195686794	Kidney_OC	kidney:	n/a	n/a
5	EBF1	chr3:195685670-195685963	GM12878	blood:	n/a	n/a
6	EGR1	chr3:195687842-195688257	K562	blood:	n/a	n/a
7	EGR1	chr3:195687834-195688183	K562	blood:	n/a	n/a
8	FOSL2	chr3:195686604-195686964	HepG2	liver:	n/a	n/a
9	FOSL2	chr3:195687640-195689431	HepG2	liver:	n/a	n/a
10	FOXA1	chr3:195686597-195686952	HepG2	liver:	n/a	n/a
11	GABPA	chr3:195688689-195689082	Hela-S3	cervix:	n/a	n/a
12	GATA2	chr3:195688610-195688854	K562	blood:	n/a	n/a
13	HEY1	chr3:195686686-195687079	HepG2	liver:	n/a	n/a
14	HEY1	chr3:195688606-195688856	HepG2	liver:	n/a	n/a
15	IRF1	chr3:195688229-195688520	K562	blood:	n/a	n/a
16	JUND	chr3:195688658-195689071	HepG2	liver:	n/a	n/a
17	MAX	chr3:195685786-195685960	NB4	blood:	n/a	n/a
18	NR2F2	chr3:195687758-195688358	K562	blood:	n/a	n/a
19	NR2F2	chr3:195688657-195689446	K562	blood:	n/a	n/a
20	PAX5	chr3:195688072-195688438	GM12878	blood:	n/a	n/a
21	PAX5	chr3:195688591-195688981	GM12878	blood:	n/a	n/a
22	PAX5	chr3:195688478-195689132	GM12878	blood:	n/a	n/a
23	PAX5	chr3:195687790-195687953	GM12878	blood:	n/a	n/a
24	PAX5	chr3:195688612-195688944	GM12878	blood:	n/a	n/a
25	PBX3	chr3:195688647-195689055	GM12878	blood:	n/a	n/a
26	PBX3	chr3:195688671-195688878	GM12878	blood:	n/a	n/a
27	PBX3	chr3:195687744-195687998	GM12878	blood:	n/a	n/a
28	PBX3	chr3:195688309-195688497	GM12878	blood:	n/a	n/a
29	PBX3	chr3:195688141-195688258	GM12878	blood:	n/a	n/a
30	POLR2A	chr3:195687766-195688567	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr3:195688095-195688499	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:195687569-195689515	GM12891	blood:	n/a	n/a
33	POLR2A	chr3:195687782-195687955	A549	lung:	n/a	n/a
34	POLR2A	chr3:195685489-195685700	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr3:195685633-195685931	K562	blood:	n/a	n/a
36	POLR2A	chr3:195686608-195686625	HepG2	liver:	n/a	n/a
37	POLR2A	chr3:195687793-195687938	HepG2	liver:	n/a	n/a
38	POLR2A	chr3:195688219-195689233	GM12878	blood:	n/a	n/a
39	POLR2A	chr3:195687677-195688534	PANC-1	pancreas:	n/a	n/a
40	POLR2A	chr3:195687789-195688602	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr3:195676490-195683654	GM12892	blood:	n/a	n/a
42	POLR2A	chr3:195688740-195688786	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr3:195681108-195683737	SK-N-MC	brain:	n/a	n/a
44	POLR2A	chr3:195687721-195689344	GM12892	blood:	n/a	n/a
45	POLR2A	chr3:195685385-195685964	SK-N-MC	brain:	n/a	n/a
46	POLR2A	chr3:195688063-195688600	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr3:195685369-195685925	GM12892	blood:	n/a	n/a
48	POLR2A	chr3:195687712-195687873	K562	blood:	n/a	n/a
49	POLR2A	chr3:195688632-195689259	GM12878	blood:	n/a	n/a
50	POLR2A	chr3:195687586-195689833	GM12892	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195683635-195683685	MCF10A-Er-Src	breast:	n/a
2	chr3:195683635-195683685	MCF10A-Er-Src	breast:	n/a
3	chr3:195687741-195687791	HCT-116	colon:	n/a
4	chr3:195687741-195687791	HCM	heart:	n/a
5	chr3:195688021-195688071	HCM	heart:	n/a
6	chr3:195687741-195687791	HCPEpiC	choroid plexus:	n/a
7	chr3:195688021-195688071	AG09319	gingival:	n/a
8	chr3:195683635-195683685	NH-A	brain:	n/a
9	chr3:195687741-195687791	IMR90	lung:	fetal
10	chr3:195687741-195687791	MCF-7	breast:	n/a
11	chr3:195687741-195687791	RPTEC	kidney:	n/a
12	chr3:195688021-195688071	SK-N-SH_RA	brain:	n/a
13	chr3:195688021-195688071	HRCEpiC	kidney:	n/a
14	chr3:195688021-195688071	Hela-S3	cervix:	n/a
15	chr3:195683635-195683685	Jurkat	blood:	n/a
16	chr3:195688021-195688071	BJ	skin:	n/a
17	chr3:195688021-195688071	IMR90	lung:	fetal
18	chr3:195687741-195687791	SK-N-SH	brain:	n/a
19	chr3:195687741-195687791	HRE	kidney:	n/a
20	chr3:195688021-195688071	NB4	blood:	n/a
21	chr3:195688021-195688071	NHDF-neo	bronchial:	n/a
22	chr3:195687741-195687791	GM19239	blood:	n/a
23	chr3:195688021-195688071	GM19239	blood:	n/a
24	chr3:195683635-195683685	PANC-1	pancreas:	n/a
25	chr3:195687741-195687791	AoSMC	blood vessel:	n/a
26	chr3:195683635-195683685	A549	lung:	n/a
27	chr3:195688021-195688071	HCT-116	colon:	n/a
28	chr3:195683635-195683685	AG04449	skin:	fetal
29	chr3:195687741-195687791	NHDF-neo	bronchial:	n/a
30	chr3:195687741-195687791	HEEpiC	esophagus:	n/a
31	chr3:195688021-195688071	HNPCEpiC	eye:	n/a
32	chr3:195687741-195687791	U87	brain:	n/a
33	chr3:195687741-195687791	HIPEpiC	eye:	n/a
34	chr3:195688021-195688071	AG09309	skin:	n/a
35	chr3:195683635-195683685	T-47D	breast:	n/a
36	chr3:195687741-195687791	AG04450	lung:	fetal
37	chr3:195688021-195688071	HL-60	blood:	n/a
38	chr3:195687741-195687791	PrEC	prostate:	n/a
39	chr3:195683635-195683685	HEK293	kidney:	embryo
40	chr3:195687741-195687791	Hela-S3	cervix:	n/a
41	chr3:195683635-195683685	ovcar-3	ovarian:	n/a
42	chr3:195683635-195683685	ProgFib	skin:	n/a
43	chr3:195683635-195683685	HMEC	breast:	n/a
44	chr3:195683635-195683685	AG09319	gingival:	n/a
45	chr3:195688021-195688071	HCF	heart:	n/a
46	chr3:195688021-195688071	AG04449	skin:	fetal
47	chr3:195687741-195687791	HAEpiC	amniotic membrane:	n/a
48	chr3:195687741-195687791	HCF	heart:	n/a
49	chr3:195688021-195688071	HUVEC	blood vessel:	n/a
50	chr3:195688021-195688071	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:
2	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNK2-6	chr3:195688656-195689069	expReg_chr3_13675_-

No data

Variant related genes	Relation type
ENSG00000260261	TF binding region
ENSG00000260261	CpG island
ENSG00000242086	chromatin interactions

Extended variants
information (count: 376 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572597584	chr3:195683577-195683578	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374004595	chr3:195683581-195683582	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs558681780	chr3:195683603-195683604	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577491286	chr3:195683665-195683666	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374246475	chr3:195683683-195683684	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs563026365	chr3:195683687-195683688	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs9839111	chr3:195683691-195683692	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs9812261	chr3:195683703-195683704	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150735999	chr3:195683706-195683707	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs527745441	chr3:195683708-195683709	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs182076700	chr3:195683757-195683758	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190187753	chr3:195683760-195683761	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs565043945	chr3:195683843-195683844	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372194391	chr3:195683864-195683865	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374630024	chr3:195683881-195683882	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182311031	chr3:195683883-195683884	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201294962	chr3:195683905-195683906	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs372298906	chr3:195683912-195683913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569032403	chr3:195683932-195683933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190803882	chr3:195683937-195683938	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs180704458	chr3:195683943-195683944	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566235171	chr3:195683944-195683945	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs533616880	chr3:195683951-195683952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558744217	chr3:195683952-195683953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs577403762	chr3:195683957-195683958	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs538034368	chr3:195683992-195683993	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs556864587	chr3:195683999-195684000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575022724	chr3:195684009-195684010	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs542254164	chr3:195684011-195684012	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs113679302	chr3:195684015-195684016	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs111721628	chr3:195684037-195684038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs545238464	chr3:195684039-195684040	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111808743	chr3:195684073-195684074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs149608438	chr3:195684076-195684077	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572594109	chr3:195684083-195684084	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113488782	chr3:195684121-195684122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564553963	chr3:195684131-195684132	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532362854	chr3:195684135-195684136	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185763152	chr3:195684136-195684137	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs190139230	chr3:195684170-195684171	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs111857020	chr3:195684226-195684227	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529902871	chr3:195684256-195684257	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs201729854	chr3:195684257-195684258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547806973	chr3:195684262-195684263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114506538	chr3:195684285-195684286	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs533531142	chr3:195684290-195684291	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs4927814	chr3:195684297-195684298	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182599622	chr3:195684310-195684311	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188534265	chr3:195684339-195684340	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs556441125	chr3:195684346-195684347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	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:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
2	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
3	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
4	chr3:195667400-195684200	Weak transcription	Spleen	Spleen
5	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr3:195677800-195691800	Weak transcription	NHDF-Ad	bronchial
7	chr3:195678000-195696200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr3:195679000-195691600	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr3:195679000-195695800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr3:195681600-195685600	Weak transcription	Gastric	stomach
11	chr3:195681600-195691600	Weak transcription	Primary T cells from cord blood	blood
12	chr3:195681600-195696200	Weak transcription	Primary B cells from cord blood	blood
13	chr3:195681800-195684200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr3:195681800-195684200	Weak transcription	NHEK	skin
15	chr3:195681800-195685200	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr3:195681800-195685400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:195681800-195685400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:195681800-195685400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr3:195681800-195685400	Weak transcription	Brain Anterior Caudate	brain
20	chr3:195681800-195685400	Weak transcription	Brain Substantia Nigra	brain
21	chr3:195681800-195685600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:195681800-195685600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr3:195681800-195685600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr3:195681800-195685600	Weak transcription	Brain Cingulate Gyrus	brain
25	chr3:195681800-195685600	Weak transcription	Left Ventricle	heart
26	chr3:195681800-195685600	Weak transcription	Pancreas	Pancrea
27	chr3:195681800-195685600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr3:195681800-195685600	Weak transcription	GM12878-XiMat	blood
29	chr3:195681800-195685800	Weak transcription	Colon Smooth Muscle	Colon
30	chr3:195681800-195685800	Weak transcription	NH-A	brain
31	chr3:195681800-195686000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr3:195681800-195686000	Weak transcription	HSMM	muscle
33	chr3:195681800-195686200	Weak transcription	Thymus	Thymus
34	chr3:195681800-195688200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:195681800-195688600	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr3:195681800-195688800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr3:195681800-195689400	Weak transcription	A549	lung
38	chr3:195681800-195691600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr3:195681800-195691600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:195681800-195691600	Weak transcription	Stomach Mucosa	stomach
41	chr3:195681800-195695600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr3:195681800-195696200	Weak transcription	HepG2	liver
43	chr3:195681800-195696400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:195681800-195696400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr3:195681800-195696800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr3:195682000-195683600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:195682000-195685200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:195682000-195685600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr3:195682000-195685600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr3:195682000-195691600	Weak transcription	HMEC	breast

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