Variant report

Variant	esv3386832
Chromosome Location	chr3:118944762-118948560
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:23)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:118945708-118945725	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr3:118946780-118946930	GM12872	blood:	n/a	n/a
3	CTCF	chr3:118946400-118946550	A549	lung:	n/a	n/a
4	CUX1	chr3:118945286-118945299	GM12878	blood:	n/a	n/a
5	FOXA1	chr3:118946218-118946731	HepG2	liver:	n/a	chr3:118946573-118946585
6	FOXA1	chr3:118946198-118946675	HepG2	liver:	n/a	chr3:118946573-118946585
7	FOXA2	chr3:118946265-118946782	A549	lung:	n/a	chr3:118946573-118946585
8	FOXA2	chr3:118946204-118946645	HepG2	liver:	n/a	chr3:118946573-118946585
9	FOXA2	chr3:118946156-118946743	A549	lung:	n/a	chr3:118946573-118946585
10	HNF4A	chr3:118945996-118946368	HepG2	liver:	n/a	chr3:118946191-118946205 chr3:118946192-118946205 chr3:118946191-118946204 chr3:118946192-118946204 chr3:118946192-118946204 chr3:118946189-118946207
11	MAFK	chr3:118947350-118947500	IMR90	lung:	n/a	n/a
12	MAZ	chr3:118946317-118946335	HepG2	liver:	n/a	n/a
13	POLR2A	chr3:118946559-118946636	MCF10A-Er-Src	breast:	n/a	n/a
14	POLR2A	chr3:118945758-118945800	GM12878	blood:	n/a	n/a
15	POLR2A	chr3:118947909-118948156	GM12878	blood:	n/a	n/a
16	POLR2A	chr3:118946168-118948435	A549	lung:	n/a	n/a
17	POLR2A	chr3:118946437-118946523	HepG2	liver:	n/a	n/a
18	POLR2A	chr3:118945652-118945753	GM12878	blood:	n/a	n/a
19	POLR2A	chr3:118945640-118945675	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:118947440-118947595	ProgFib	skin:	n/a	n/a
21	SP1	chr3:118946157-118946732	A549	lung:	n/a	n/a
22	STAT3	chr3:118945332-118945525	MCF10A-Er-Src	breast:	n/a	n/a
23	TCF12	chr3:118946142-118946782	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118945807-118945857	GM12891	blood:	n/a
2	chr3:118945807-118945857	MCF-7	breast:	n/a
3	chr3:118945807-118945857	BJ	skin:	n/a
4	chr3:118945807-118945857	AG09309	skin:	n/a
5	chr3:118945807-118945857	IMR90	lung:	fetal
6	chr3:118945807-118945857	HEK293	kidney:	embryo
7	chr3:118945807-118945857	HAEpiC	amniotic membrane:	n/a
8	chr3:118945807-118945857	CMK	blood:	n/a
9	chr3:118945807-118945857	GM12878	blood:	n/a
10	chr3:118945807-118945857	U87	brain:	n/a
11	chr3:118945807-118945857	PrEC	prostate:	n/a
12	chr3:118945807-118945857	Jurkat	blood:	n/a
13	chr3:118945807-118945857	H1-hESC	embryonic stem cell:	embryo
14	chr3:118945807-118945857	RPTEC	kidney:	n/a
15	chr3:118945807-118945857	SK-N-MC	brain:	n/a
16	chr3:118945807-118945857	NHDF-neo	bronchial:	n/a
17	chr3:118945807-118945857	NB4	blood:	n/a
18	chr3:118945807-118945857	SKMC	muscle:	n/a
19	chr3:118945807-118945857	T-47D	breast:	n/a
20	chr3:118945807-118945857	AG10803	skin:	n/a
21	chr3:118945807-118945857	NT2-D1	testis:	n/a
22	chr3:118945807-118945857	HRCEpiC	kidney:	n/a
23	chr3:118945807-118945857	Caco-2	colon:	n/a
24	chr3:118945807-118945857	NHBE	bronchial:	n/a
25	chr3:118945807-118945857	HCT-116	colon:	n/a
26	chr3:118945807-118945857	HepG2	liver:	n/a
27	chr3:118945807-118945857	ECC-1	luminal epithelium:	n/a
28	chr3:118945807-118945857	ovcar-3	ovarian:	n/a
29	chr3:118945807-118945857	HPAEpiC	pulmonary alveolar:	n/a
30	chr3:118945807-118945857	GM12892	blood:	n/a
31	chr3:118945807-118945857	GM19239	blood:	n/a
32	chr3:118945807-118945857	AG04450	lung:	fetal
33	chr3:118945807-118945857	PANC-1	pancreas:	n/a
34	chr3:118945807-118945857	PFSK-1	brain:	n/a
35	chr3:118945807-118945857	HNPCEpiC	eye:	n/a
36	chr3:118945807-118945857	HUVEC	blood vessel:	n/a
37	chr3:118945807-118945857	HCM	heart:	n/a
38	chr3:118945807-118945857	A549	lung:	n/a
39	chr3:118945807-118945857	SAEC	small airway:	n/a
40	chr3:118945807-118945857	SK-N-SH_RA	brain:	n/a
41	chr3:118945807-118945857	AG09319	gingival:	n/a
42	chr3:118945807-118945857	HIPEpiC	eye:	n/a
43	chr3:118945807-118945857	ProgFib	skin:	n/a
44	chr3:118945807-118945857	BE2_C	brain:	n/a
45	chr3:118945807-118945857	Hepatocyte	liver:	n/a
46	chr3:118945807-118945857	HEEpiC	esophagus:	n/a
47	chr3:118945807-118945857	LNCaP	prostate:	n/a
48	chr3:118945807-118945857	HMEC	breast:	n/a
49	chr3:118945807-118945857	SK-N-SH	brain:	n/a
50	chr3:118945807-118945857	K562	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118948409..118952425-chr3:118955700..118962526,10	K562	blood:
2	chr3:118948357..118951865-chr3:118958522..118961643,4	MCF-7	breast:
3	chr3:118941777..118944031-chr3:118945935..118948181,2	K562	blood:
4	chr3:118941692..118943733-chr3:118945853..118947733,2	MCF-7	breast:
5	chr3:118944759..118947412-chr3:118958236..118960502,3	MCF-7	breast:
6	chr3:118943120..118945710-chr3:118958108..118960423,2	K562	blood:
7	chr3:118939426..118941672-chr3:118946174..118948515,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP31-1	chr3:118945333-118945528	ENSG00000240254.1

No data

Variant related genes	Relation type
B4GALT4-AS1	TF binding region
B4GALT4-AS1	CpG island
ENSG00000121578	chromatin interactions

Extended variants
information (count: 153 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:153 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563665400	chr3:118944819-118944820	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530832451	chr3:118944829-118944830	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs549387022	chr3:118944831-118944832	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs111596711	chr3:118944833-118944834	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559120175	chr3:118944837-118944838	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546815469	chr3:118944851-118944852	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571473195	chr3:118944948-118944949	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs9881379	chr3:118944950-118944951	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557105924	chr3:118944951-118944952	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34519805	chr3:118944971-118944972	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs568803939	chr3:118945025-118945026	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs372768274	chr3:118945055-118945056	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs12488261	chr3:118945121-118945122	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535848330	chr3:118945126-118945127	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs9881947	chr3:118945128-118945129	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187767950	chr3:118945156-118945157	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs6778091	chr3:118945159-118945160	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs553104607	chr3:118945181-118945182	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577825770	chr3:118945217-118945218	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545071135	chr3:118945236-118945237	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563609158	chr3:118945261-118945262	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531070355	chr3:118945267-118945268	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs193066859	chr3:118945325-118945326	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs561383361	chr3:118945335-118945336	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs528350015	chr3:118945345-118945346	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs114902823	chr3:118945369-118945370	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs571436698	chr3:118945370-118945371	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs184584775	chr3:118945391-118945392	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs374532036	chr3:118945446-118945447	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs189149176	chr3:118945452-118945453	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs527541689	chr3:118945526-118945527	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs111847958	chr3:118945535-118945536	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs568841170	chr3:118945551-118945552	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs3752377	chr3:118945578-118945579	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548550314	chr3:118945583-118945584	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs192991616	chr3:118945606-118945607	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs3752376	chr3:118945614-118945615	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs372837689	chr3:118945616-118945617	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534945299	chr3:118945617-118945618	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs72655934	chr3:118945623-118945624	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370906725	chr3:118945624-118945625	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201535886	chr3:118945644-118945645	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538832333	chr3:118945647-118945648	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375222901	chr3:118945649-118945650	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533134962	chr3:118945650-118945651	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148499432	chr3:118945658-118945659	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs374995502	chr3:118945671-118945672	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138372481	chr3:118945760-118945761	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs369127511	chr3:118945764-118945765	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146077977	chr3:118945770-118945771	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118924400-118959000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:118924600-118945600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:118927000-118952600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:118927000-118953800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:118927000-118953800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:118927200-118953800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:118927200-118955200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr3:118927400-118950200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr3:118927400-118953000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:118927600-118952400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr3:118927800-118956400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr3:118928000-118955600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr3:118928200-118951000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:118928800-118950000	Strong transcription	Primary monocytes fromperipheralblood	blood
15	chr3:118929200-118956200	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr3:118929200-118956200	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr3:118929200-118956400	Strong transcription	H1 Cell Line	embryonic stem cell
18	chr3:118929200-118956600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
19	chr3:118930000-118949800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr3:118930000-118955400	Strong transcription	Primary B cells from peripheral blood	blood
21	chr3:118930200-118955800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:118930200-118958400	Weak transcription	Hela-S3	cervix
23	chr3:118931600-118957400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr3:118931800-118946400	Genic enhancers	A549	lung
25	chr3:118932600-118955800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:118935800-118947600	Weak transcription	HUVEC	blood vessel
27	chr3:118936400-118945000	Weak transcription	NH-A	brain
28	chr3:118937200-118952600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr3:118938400-118947200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr3:118938400-118951200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr3:118938600-118945600	Weak transcription	Small Intestine	intestine
32	chr3:118938600-118947200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr3:118938600-118947800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr3:118939200-118947800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr3:118939400-118945200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr3:118940200-118950000	Strong transcription	Dnd41	blood
37	chr3:118940200-118950000	Strong transcription	GM12878-XiMat	blood
38	chr3:118941000-118944800	Weak transcription	Stomach Mucosa	stomach
39	chr3:118941000-118953000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:118941800-118944800	Weak transcription	Fetal Lung	lung
41	chr3:118941800-118952400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:118942000-118949800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr3:118942200-118945600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:118942400-118945000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr3:118942400-118945000	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr3:118942400-118945400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr3:118942400-118946200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr3:118942400-118947200	Weak transcription	Fetal Brain Male	brain
49	chr3:118942800-118944800	Weak transcription	Brain Angular Gyrus	brain
50	chr3:118942800-118944800	Weak transcription	Brain Germinal Matrix	brain

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