Variant report

Variant	nsv970437
Chromosome Location	chr7:4161777-4172782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:854)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:4170503-4171267	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr7:4164261-4164462	A549	lung:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
3	CEBPB	chr7:4170662-4170944	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr7:4164281-4164504	HepG2	liver:	n/a	chr7:4164348-4164359 chr7:4164347-4164358
5	CTCF	chr7:4169540-4169690	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr7:4169380-4169670	HAc	cerebellar:	n/a	n/a
7	CTCF	chr7:4169460-4169610	HepG2	liver:	n/a	n/a
8	CTCF	chr7:4170805-4170916	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr7:4170820-4170970	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr7:4169527-4169703	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:4170726-4170956	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:4169080-4169230	SK-N-SH_RA	brain:	n/a	chr7:4169122-4169130
13	CTCF	chr7:4169457-4169692	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr7:4170780-4170930	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr7:4170760-4170910	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr7:4170802-4170920	Gliobla	brain:	n/a	n/a
17	CTCF	chr7:4170780-4170930	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:4170812-4170900	K562	blood:	n/a	n/a
19	CTCF	chr7:4169540-4169690	K562	blood:	n/a	n/a
20	CTCF	chr7:4169540-4169690	HEK293	kidney:	n/a	n/a
21	CTCF	chr7:4169440-4169590	NHEK	skin:	n/a	n/a
22	CTCF	chr7:4169520-4169670	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr7:4170780-4170930	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr7:4170780-4170930	HCT-116	colon:	n/a	n/a
25	CTCF	chr7:4170817-4170911	MCF-7	breast:	n/a	n/a
26	CTCF	chr7:4170763-4170976	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr7:4170846-4170874	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:4170833-4170921	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:4170900-4171050	K562	blood:	n/a	n/a
30	CTCF	chr7:4170760-4170910	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr7:4170760-4170910	SK-N-SH_RA	brain:	n/a	n/a
32	FOS	chr7:4162868-4163863	HUVEC	blood vessel:	n/a	chr7:4163664-4163675
33	GATA2	chr7:4169052-4169623	SH-SY5Y	brain:	n/a	n/a
34	GATA2	chr7:4163439-4163848	HUVEC	blood vessel:	n/a	n/a
35	GATA3	chr7:4169109-4169481	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr7:4169139-4169365	T-47D	breast:	n/a	n/a
37	GTF2F1	chr7:4170686-4170929	H1-hESC	embryonic stem cell:	n/a	n/a
38	JUND	chr7:4170720-4171009	H1-hESC	embryonic stem cell:	n/a	chr7:4170861-4170869
39	MAFK	chr7:4164315-4164391	HepG2	liver:	n/a	n/a
40	MYC	chr7:4170767-4171018	H1-hESC	embryonic stem cell:	n/a	n/a
41	RAD21	chr7:4170591-4171046	H1-hESC	embryonic stem cell:	n/a	n/a
42	RAD21	chr7:4169511-4169748	H1-hESC	embryonic stem cell:	n/a	n/a
43	RAD21	chr7:4169486-4169801	H1-hESC	embryonic stem cell:	n/a	n/a
44	RAD21	chr7:4170723-4171075	H1-hESC	embryonic stem cell:	n/a	n/a
45	RAD21	chr7:4170649-4171076	H1-hESC	embryonic stem cell:	n/a	n/a
46	REST	chr7:4169017-4169427	SK-N-SH	brain:	n/a	chr7:4169068-4169081
47	TBP	chr7:4170635-4171010	H1-hESC	embryonic stem cell:	n/a	n/a
48	TEAD4	chr7:4170616-4171114	H1-hESC	embryonic stem cell:	n/a	n/a
49	TEAD4	chr7:4170623-4171119	H1-hESC	embryonic stem cell:	n/a	n/a
50	ZNF143	chr7:4170679-4171026	H1-hESC	embryonic stem cell:	n/a	chr7:4170884-4170902

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4167607-4167657	NHBE	bronchial:	n/a
2	chr7:4169485-4169535	AG09319	gingival:	n/a
3	chr7:4169306-4169356	NHDF-neo	bronchial:	n/a
4	chr7:4167809-4167859	SK-N-MC	brain:	n/a
5	chr7:4169314-4169364	Jurkat	blood:	n/a
6	chr7:4167607-4167657	Jurkat	blood:	n/a
7	chr7:4167607-4167657	NT2-D1	testis:	n/a
8	chr7:4167607-4167657	HepG2	liver:	n/a
9	chr7:4169630-4169680	MCF-7	breast:	n/a
10	chr7:4167809-4167859	K562	blood:	n/a
11	chr7:4169314-4169364	HEEpiC	esophagus:	n/a
12	chr7:4172065-4172115	MCF-7	breast:	n/a
13	chr7:4172065-4172115	HRPEpiC	eye:	n/a
14	chr7:4169485-4169535	AoSMC	blood vessel:	n/a
15	chr7:4169306-4169356	Hela-S3	cervix:	n/a
16	chr7:4167943-4167993	GM06990	blood:	n/a
17	chr7:4167943-4167993	Hepatocyte	liver:	n/a
18	chr7:4169485-4169535	PANC-1	pancreas:	n/a
19	chr7:4167607-4167657	K562	blood:	n/a
20	chr7:4169306-4169356	NH-A	brain:	n/a
21	chr7:4170594-4170644	AG09319	gingival:	n/a
22	chr7:4169314-4169364	PFSK-1	brain:	n/a
23	chr7:4170594-4170644	GM12892	blood:	n/a
24	chr7:4169630-4169680	SKMC	muscle:	n/a
25	chr7:4167607-4167657	PrEC	prostate:	n/a
26	chr7:4169306-4169356	CMK	blood:	n/a
27	chr7:4169314-4169364	SK-N-MC	brain:	n/a
28	chr7:4169485-4169535	HPAEpiC	pulmonary alveolar:	n/a
29	chr7:4167943-4167993	ECC-1	luminal epithelium:	n/a
30	chr7:4169314-4169364	HCF	heart:	n/a
31	chr7:4169604-4169654	U87	brain:	n/a
32	chr7:4168039-4168089	BE2_C	brain:	n/a
33	chr7:4169314-4169364	HUVEC	blood vessel:	n/a
34	chr7:4168039-4168089	HRCEpiC	kidney:	n/a
35	chr7:4170594-4170644	NB4	blood:	n/a
36	chr7:4169752-4169802	BE2_C	brain:	n/a
37	chr7:4169752-4169802	HNPCEpiC	eye:	n/a
38	chr7:4172065-4172115	Hepatocyte	liver:	n/a
39	chr7:4167882-4167932	ovcar-3	ovarian:	n/a
40	chr7:4169306-4169356	ProgFib	skin:	n/a
41	chr7:4169314-4169364	NHBE	bronchial:	n/a
42	chr7:4168039-4168089	NHBE	bronchial:	n/a
43	chr7:4167882-4167932	Hepatocyte	liver:	n/a
44	chr7:4167882-4167932	MCF-7	breast:	n/a
45	chr7:4169314-4169364	HNPCEpiC	eye:	n/a
46	chr7:4167943-4167993	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:4167809-4167859	PrEC	prostate:	n/a
48	chr7:4169314-4169364	HCPEpiC	choroid plexus:	n/a
49	chr7:4169752-4169802	SK-N-SH	brain:	n/a
50	chr7:4167809-4167859	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:4159770..4161422-chr7:4162793..4165151,2	K562	blood:
2	chr7:4171607..4173163-chr7:4322084..4324253,2	K562	blood:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island

Extended variants
information (count: 679 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74619452	chr7:4161783-4161784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs8180800	chr7:4161793-4161794	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs574489177	chr7:4161810-4161811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368094798	chr7:4161815-4161816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371983402	chr7:4161820-4161821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528965159	chr7:4161856-4161857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565010825	chr7:4161874-4161875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375744334	chr7:4161883-4161884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527377274	chr7:4161946-4161947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541072478	chr7:4161967-4161968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560529516	chr7:4161995-4161996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529456043	chr7:4162005-4162006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549432948	chr7:4162040-4162041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189471132	chr7:4162082-4162083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143273678	chr7:4162109-4162110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147520664	chr7:4162118-4162119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560229808	chr7:4162140-4162141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148558995	chr7:4162162-4162163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73048305	chr7:4162164-4162165	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs565020359	chr7:4162178-4162179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567368273	chr7:4162179-4162180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536422975	chr7:4162190-4162191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556217121	chr7:4162198-4162199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576393135	chr7:4162212-4162213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538683222	chr7:4162230-4162231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7792741	chr7:4162261-4162262	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs376621125	chr7:4162274-4162275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116561665	chr7:4162306-4162307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540784534	chr7:4162345-4162346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561010399	chr7:4162366-4162367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs574179664	chr7:4162370-4162371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543191051	chr7:4162381-4162382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562885795	chr7:4162391-4162392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150961795	chr7:4162414-4162415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139501401	chr7:4162415-4162416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143169705	chr7:4162481-4162482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527653111	chr7:4162503-4162504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547599831	chr7:4162528-4162529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181495762	chr7:4162542-4162543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536096047	chr7:4162556-4162557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115929558	chr7:4162596-4162597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569819048	chr7:4162607-4162608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538943287	chr7:4162608-4162609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558856944	chr7:4162610-4162611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs77118325	chr7:4162624-4162625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146653266	chr7:4162625-4162626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554402357	chr7:4162630-4162631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374712802	chr7:4162637-4162638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185882412	chr7:4162663-4162664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530049486	chr7:4162683-4162684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4132400-4180200	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:4152000-4162400	Weak transcription	Left Ventricle	heart
3	chr7:4154600-4191600	Weak transcription	Gastric	stomach
4	chr7:4155200-4163600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:4156600-4174000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:4156800-4167000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:4157400-4167400	Weak transcription	Pancreas	Pancrea
8	chr7:4157400-4169200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:4157600-4163400	Weak transcription	Spleen	Spleen
10	chr7:4157600-4165600	Weak transcription	Aorta	Aorta
11	chr7:4162000-4162400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:4162200-4167800	Weak transcription	Fetal Intestine Small	intestine
13	chr7:4162200-4170200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr7:4162600-4163400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:4162600-4164800	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:4162800-4164800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr7:4163000-4164200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:4163000-4164200	Enhancers	HSMM	muscle
19	chr7:4163400-4163800	Active TSS	Spleen	Spleen
20	chr7:4163400-4164600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr7:4163400-4164600	Enhancers	HSMMtube	muscle
22	chr7:4163600-4164000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr7:4163600-4164000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr7:4163600-4164200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:4163800-4167200	Weak transcription	Spleen	Spleen
26	chr7:4164000-4184000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr7:4164200-4165200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:4164600-4166400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:4164800-4165200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr7:4164800-4165200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr7:4165200-4165400	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:4165200-4168400	Enhancers	Primary hematopoietic stem cells	blood
33	chr7:4165200-4169600	Weak transcription	Fetal Intestine Large	intestine
34	chr7:4165400-4166600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:4165400-4167200	Weak transcription	Fetal Stomach	stomach
36	chr7:4165600-4165800	Strong transcription	Aorta	Aorta
37	chr7:4165600-4166800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:4165600-4174400	Weak transcription	Fetal Brain Female	brain
39	chr7:4165600-4185800	Weak transcription	Primary neutrophils fromperipheralblood	blood
40	chr7:4165800-4167000	Weak transcription	Aorta	Aorta
41	chr7:4165800-4169000	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr7:4166400-4167200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr7:4166600-4167000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:4166600-4167600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:4167000-4167600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:4167000-4168000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr7:4167000-4176600	Strong transcription	Aorta	Aorta
48	chr7:4167000-4177200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:4167200-4167600	Genic enhancers	Spleen	Spleen
50	chr7:4167200-4168000	Strong transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links