Variant report

Variant	esv1798220
Chromosome Location	chr3:98894142-99020463
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr3:98930300-98930345	GM12878	blood:	n/a	n/a
2	CEBPB	chr3:98895351-98895574	A549	lung:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
3	CEBPB	chr3:98989685-98989935	IMR90	lung:	n/a	chr3:98989794-98989805 chr3:98989796-98989807 chr3:98989796-98989805
4	CEBPB	chr3:98972518-98972742	A549	lung:	n/a	chr3:98972641-98972652 chr3:98972640-98972653 chr3:98972640-98972651 chr3:98972642-98972651
5	CEBPB	chr3:98976087-98976283	H1-hESC	embryonic stem cell:	n/a	chr3:98976105-98976116 chr3:98976104-98976115
6	CEBPB	chr3:98895292-98895657	IMR90	lung:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
7	CEBPB	chr3:98965180-98965549	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:98976004-98976204	HepG2	liver:	n/a	chr3:98976105-98976116 chr3:98976104-98976115
9	CEBPB	chr3:98927039-98927064	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:98895381-98895526	Hela-S3	cervix:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
11	CEBPB	chr3:98945624-98945864	HepG2	liver:	n/a	chr3:98945722-98945733
12	CEBPB	chr3:98972486-98972780	IMR90	lung:	n/a	chr3:98972641-98972652 chr3:98972640-98972653 chr3:98972640-98972651 chr3:98972642-98972651
13	CEBPB	chr3:98965132-98965584	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr3:98895313-98895658	HepG2	liver:	n/a	chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895481-98895490 chr3:98895481-98895490 chr3:98895479-98895492 chr3:98895480-98895491 chr3:98895479-98895490 chr3:98895479-98895492 chr3:98895479-98895490
15	CEBPB	chr3:98989662-98989844	HepG2	liver:	n/a	chr3:98989794-98989805 chr3:98989796-98989807 chr3:98989796-98989805
16	CEBPB	chr3:98972483-98972748	HepG2	liver:	n/a	chr3:98972641-98972652 chr3:98972640-98972653 chr3:98972640-98972651 chr3:98972642-98972651
17	CEBPB	chr3:98965139-98965653	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr3:98897865-98898056	IMR90	lung:	n/a	n/a
19	CTCF	chr3:98997653-98997756	Spleen_OC	spleen:	n/a	n/a
20	CTCF	chr3:98937475-98937542	HepG2	liver:	n/a	n/a
21	CTCF	chr3:98937460-98937610	RPTEC	kidney:	n/a	n/a
22	CTCF	chr3:98904800-98904950	WI-38	lung:	n/a	n/a
23	CTCF	chr3:98937500-98937650	HVMF	connective:	n/a	n/a
24	CTCF	chr3:98965300-98965450	HVMF	connective:	n/a	n/a
25	CTCF	chr3:98937520-98937670	HCT-116	colon:	n/a	n/a
26	CTCF	chr3:98937480-98937630	A549	lung:	n/a	n/a
27	CTCF	chr3:98979616-98979676	GM20000	blood:	n/a	n/a
28	CTCF	chr3:98957445-98957519	ProgFib	skin:	n/a	n/a
29	CTCF	chr3:98937448-98937572	NHEK	skin:	n/a	n/a
30	CTCF	chr3:98969980-98970130	HPF	lung:	n/a	n/a
31	CTCF	chr3:98943170-98943206	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr3:98927000-98927150	BJ	skin:	n/a	n/a
33	CTCF	chr3:98928620-98928770	GM12871	blood:	n/a	n/a
34	CTCF	chr3:98961240-98961390	AG10803	skin:	n/a	n/a
35	CTCF	chr3:98958060-98958210	AG04449	skin:	n/a	n/a
36	CTCF	chr3:98961260-98961410	AG10803	skin:	n/a	n/a
37	CTCF	chr3:98937409-98937688	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:98937400-98937550	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr3:98937376-98937607	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:98937500-98937650	HMEC	breast:	n/a	n/a
41	CTCF	chr3:98937440-98937590	HCT-116	colon:	n/a	n/a
42	E2F4	chr3:98974826-98974865	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:98964937-98965413	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:98937115-98937150	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:98903417-98903604	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:98968903-98969461	MCF10A-Er-Src	breast:	n/a	chr3:98969283-98969300
47	E2F4	chr3:99019792-99019992	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr3:98969996-98970151	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr3:98895870-98896330	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr3:99000631-99000769	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:99013462-99013512	NT2-D1	testis:	n/a
2	chr3:99013462-99013512	AG09319	gingival:	n/a
3	chr3:99013462-99013512	ProgFib	skin:	n/a
4	chr3:99013462-99013512	AoSMC	blood vessel:	n/a
5	chr3:99013462-99013512	NB4	blood:	n/a
6	chr3:99013462-99013512	Jurkat	blood:	n/a
7	chr3:99013462-99013512	IMR90	lung:	fetal
8	chr3:99013462-99013512	SAEC	small airway:	n/a
9	chr3:99013462-99013512	A549	lung:	n/a
10	chr3:99013462-99013512	AG10803	skin:	n/a
11	chr3:99013462-99013512	H1-hESC	embryonic stem cell:	embryo
12	chr3:99013462-99013512	T-47D	breast:	n/a
13	chr3:99013462-99013512	U87	brain:	n/a
14	chr3:99013462-99013512	HNPCEpiC	eye:	n/a
15	chr3:99013462-99013512	HEK293	kidney:	embryo
16	chr3:99013462-99013512	GM12892	blood:	n/a
17	chr3:99013462-99013512	AG09309	skin:	n/a
18	chr3:99013462-99013512	AG04450	lung:	fetal
19	chr3:99013462-99013512	HRCEpiC	kidney:	n/a
20	chr3:99013462-99013512	HCM	heart:	n/a
21	chr3:99013462-99013512	NHDF-neo	bronchial:	n/a
22	chr3:99013462-99013512	SK-N-SH_RA	brain:	n/a
23	chr3:99013462-99013512	K562	blood:	n/a
24	chr3:99013462-99013512	GM19239	blood:	n/a
25	chr3:99013462-99013512	NH-A	brain:	n/a
26	chr3:99013462-99013512	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:99013462-99013512	BE2_C	brain:	n/a
28	chr3:99013462-99013512	HCT-116	colon:	n/a
29	chr3:99013462-99013512	Hepatocyte	liver:	n/a
30	chr3:99013462-99013512	SK-N-MC	brain:	n/a
31	chr3:99013462-99013512	HRPEpiC	eye:	n/a
32	chr3:99013462-99013512	HL-60	blood:	n/a
33	chr3:99013462-99013512	CMK	blood:	n/a
34	chr3:99013462-99013512	MCF-7	breast:	n/a
35	chr3:99013462-99013512	HCF	heart:	n/a
36	chr3:99013462-99013512	RPTEC	kidney:	n/a
37	chr3:99013462-99013512	HIPEpiC	eye:	n/a
38	chr3:99013462-99013512	HEEpiC	esophagus:	n/a
39	chr3:99013462-99013512	GM12878	blood:	n/a
40	chr3:99013462-99013512	SKMC	muscle:	n/a
41	chr3:99013462-99013512	AG04449	skin:	fetal
42	chr3:99013462-99013512	SK-N-SH	brain:	n/a
43	chr3:99013462-99013512	GM06990	blood:	n/a
44	chr3:99013462-99013512	HCPEpiC	choroid plexus:	n/a
45	chr3:99013462-99013512	PANC-1	pancreas:	n/a
46	chr3:99013462-99013512	HepG2	liver:	n/a
47	chr3:99013462-99013512	Caco-2	colon:	n/a
48	chr3:99013462-99013512	PFSK-1	brain:	n/a
49	chr3:99013462-99013512	NHBE	bronchial:	n/a
50	chr3:99013462-99013512	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
2	chr3:98960467..98962608-chr3:98963910..98966387,2	K562	blood:
3	chr3:98898412..98900467-chr3:98901353..98902956,2	MCF-7	breast:
4	chr3:98960467..98962608-chr3:98963910..98966387,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCBLD2-2	chr3:98934068-98935110	NONHSAT090839
2	lnc-ST3GAL6-6	chr3:98904502-98904611	NONHSAT090838
3	lnc-ST3GAL6-6	chr3:98899387-98899480	NONHSAT090838
4	lnc-ST3GAL6-6	chr3:98896222-98896357	NONHSAT090838

Variant related genes	Relation type
ACTG1P13	TF binding region
ACTG1P13	CpG island

Extended variants
information (count: 3585 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3585 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528176045	chr3:98894163-98894164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532254081	chr3:98894169-98894170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146767526	chr3:98894175-98894176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570924769	chr3:98894192-98894193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536679365	chr3:98894224-98894225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs2687671	chr3:98894234-98894235	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114698199	chr3:98894241-98894242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2687670	chr3:98894246-98894247	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139218173	chr3:98894279-98894280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541815437	chr3:98894285-98894286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs572555483	chr3:98894395-98894396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375046276	chr3:98894442-98894443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548368344	chr3:98894449-98894450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183455113	chr3:98894471-98894472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143127851	chr3:98894495-98894496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368802925	chr3:98894564-98894565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111927671	chr3:98894590-98894591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563663936	chr3:98894594-98894595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs61031480	chr3:98894624-98894625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570277407	chr3:98894647-98894648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542858963	chr3:98894660-98894661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148108512	chr3:98894667-98894668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9830015	chr3:98894721-98894722	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs187795259	chr3:98894741-98894742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141864994	chr3:98894747-98894748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191545748	chr3:98894761-98894762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs535137127	chr3:98894782-98894783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372543819	chr3:98894803-98894804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs3914875	chr3:98894806-98894807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376362216	chr3:98894862-98894863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6807227	chr3:98894863-98894864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs374011966	chr3:98894908-98894909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115966049	chr3:98894911-98894912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566159680	chr3:98894915-98894916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183732299	chr3:98894954-98894955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188431130	chr3:98894985-98894986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34291508	chr3:98895021-98895022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs578177989	chr3:98895023-98895024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1851066	chr3:98895124-98895125	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs150612675	chr3:98895129-98895130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573949794	chr3:98895141-98895142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78645911	chr3:98895155-98895156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576407222	chr3:98895173-98895174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559630973	chr3:98895190-98895191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573028953	chr3:98895249-98895250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117912354	chr3:98895321-98895322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192702803	chr3:98895334-98895335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12636065	chr3:98895386-98895387	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558538773	chr3:98895397-98895398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11720946	chr3:98895407-98895408	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	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
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98879200-98899200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:98892400-98895200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr3:98894200-98894600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:98894200-98894600	Enhancers	HUVEC	blood vessel
5	chr3:98895200-98895400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:98895200-98895600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr3:98899200-98899600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:98899200-98899600	Enhancers	NHEK	skin
9	chr3:98899200-98900200	Enhancers	HMEC	breast
10	chr3:98901800-98912400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr3:98904600-98906000	Weak transcription	Aorta	Aorta
12	chr3:98906000-98906200	ZNF genes & repeats	Aorta	Aorta
13	chr3:98910000-98910200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:98910000-98910200	Enhancers	HSMMtube	muscle
15	chr3:98910000-98910800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr3:98911000-98911400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:98915200-98918000	Active TSS	Fetal Thymus	thymus
18	chr3:98918000-98918400	Enhancers	Fetal Thymus	thymus
19	chr3:98925800-98939600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr3:98928400-98928800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:98931000-98932400	Enhancers	Fetal Kidney	kidney
22	chr3:98932000-98932400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:98934400-98935000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr3:98945400-98945600	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr3:98945400-98946600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr3:98945600-98945800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr3:98945600-98946200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:98945600-98946800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr3:98945600-98946800	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr3:98945800-98946000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:98945800-98946400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:98945800-98946600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr3:98945800-98946800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:98946000-98946200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr3:98946000-98946600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:98946000-98946800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr3:98946200-98946800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr3:98946800-98947800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr3:98947800-98948000	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:98951400-98952800	Enhancers	Osteobl	bone
41	chr3:98951800-98952200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:98951800-98952200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr3:98952200-98959000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:98952200-98959200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr3:98952800-98959200	Weak transcription	Osteobl	bone
46	chr3:98955600-98955800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:98957400-98959600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:98959000-98959400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:98959000-98960600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr3:98959200-98960400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links