Variant report

Variant	nsv981625
Chromosome Location	chr7:6864047-6874561
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	BATF	chr7:6865157-6865489	GM12878	blood:	n/a	n/a
2	BATF	chr7:6865860-6866054	GM12878	blood:	n/a	n/a
3	BCL11A	chr7:6865814-6866066	GM12878	blood:	n/a	n/a
4	BCL3	chr7:6870972-6871253	GM12878	blood:	n/a	n/a
5	BCL3	chr7:6873151-6873685	GM12878	blood:	n/a	n/a
6	BCL3	chr7:6872794-6873775	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:6865917-6866116	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:6865906-6866108	K562	blood:	n/a	n/a
9	CBX3	chr7:6865692-6866336	K562	blood:	n/a	n/a
10	CBX3	chr7:6864785-6865473	K562	blood:	n/a	n/a
11	CBX3	chr7:6866895-6867260	K562	blood:	n/a	n/a
12	CBX3	chr7:6865752-6866597	K562	blood:	n/a	n/a
13	CHD2	chr7:6865919-6865948	Hela-S3	cervix:	n/a	n/a
14	CHD2	chr7:6865823-6866000	GM12878	blood:	n/a	n/a
15	CHD2	chr7:6865918-6866124	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr7:6866860-6867202	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr7:6865815-6866098	A549	lung:	n/a	n/a
18	CREB1	chr7:6865856-6866080	A549	lung:	n/a	n/a
19	CTCF	chr7:6865880-6866030	HCT-116	colon:	n/a	chr7:6865986-6865995
20	CTCF	chr7:6865900-6866050	GM12869	blood:	n/a	chr7:6865986-6865995
21	CTCF	chr7:6865900-6866050	HUVEC	blood vessel:	n/a	chr7:6865986-6865995
22	CTCF	chr7:6865863-6866114	LNCaP	prostate:	n/a	chr7:6865986-6865995
23	CTCF	chr7:6865900-6866050	HCPEpiC	choroid plexus:	n/a	chr7:6865986-6865995
24	CTCF	chr7:6865900-6866050	HCM	heart:	n/a	chr7:6865986-6865995
25	CTCF	chr7:6865867-6866070	Pancreas_OC	pancreas:	n/a	chr7:6865986-6865995
26	CTCF	chr7:6865900-6866050	HEEpiC	esophagus:	n/a	chr7:6865986-6865995
27	CTCF	chr7:6865887-6866078	Fibrobl	skin:	n/a	chr7:6865986-6865995
28	CTCF	chr7:6865880-6866030	HRPEpiC	eye:	n/a	chr7:6865986-6865995
29	CTCF	chr7:6865867-6866085	NHEK	skin:	n/a	chr7:6865986-6865995
30	CTCF	chr7:6865860-6866098	GM10248	blood:	n/a	chr7:6865986-6865995
31	CTCF	chr7:6865900-6866050	GM12870	blood:	n/a	chr7:6865986-6865995
32	CTCF	chr7:6865778-6866113	A549	lung:	n/a	chr7:6865986-6865995
33	CTCF	chr7:6865920-6866070	GM12866	blood:	n/a	chr7:6865986-6865995
34	CTCF	chr7:6865860-6866010	GM12865	blood:	n/a	chr7:6865986-6865995
35	CTCF	chr7:6866000-6866150	BE2_C	brain:	n/a	n/a
36	CTCF	chr7:6865900-6866050	RPTEC	kidney:	n/a	chr7:6865986-6865995
37	CTCF	chr7:6865893-6866082	MCF-7	breast:	n/a	chr7:6865986-6865995
38	CTCF	chr7:6865866-6866099	GM19240	blood:	n/a	chr7:6865986-6865995
39	CTCF	chr7:6865960-6866110	AG10803	skin:	n/a	chr7:6865986-6865995
40	CTCF	chr7:6865920-6866062	GM20000	blood:	n/a	chr7:6865986-6865995
41	CTCF	chr7:6866136-6866242	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr7:6865940-6866090	HMF	breast:	n/a	chr7:6865986-6865995
43	CTCF	chr7:6865900-6866050	HRPEpiC	eye:	n/a	chr7:6865986-6865995
44	CTCF	chr7:6865889-6866074	Hela-S3	cervix:	n/a	chr7:6865986-6865995
45	CTCF	chr7:6865860-6866010	HMEC	breast:	n/a	chr7:6865986-6865995
46	CTCF	chr7:6865980-6866130	BJ	skin:	n/a	chr7:6865986-6865995
47	CTCF	chr7:6865900-6866050	MCF-7	breast:	n/a	chr7:6865986-6865995
48	CTCF	chr7:6865880-6866030	HBMEC	blood vessel:	n/a	chr7:6865986-6865995
49	CTCF	chr7:6865960-6866110	BJ	skin:	n/a	chr7:6865986-6865995
50	CTCF	chr7:6865940-6866090	HepG2	liver:	n/a	chr7:6865986-6865995

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6865886-6865936	HepG2	liver:	n/a
2	chr7:6865970-6866020	ECC-1	luminal epithelium:	n/a
3	chr7:6865886-6865936	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:6866072-6866122	IMR90	lung:	fetal
5	chr7:6865886-6865936	HepG2	liver:	n/a
6	chr7:6865970-6866020	ECC-1	luminal epithelium:	n/a
7	chr7:6865886-6865936	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:6866072-6866122	IMR90	lung:	fetal
9	chr7:6869135-6869185	Caco-2	colon:	n/a
10	chr7:6865965-6866015	K562	blood:	n/a
11	chr7:6865989-6866039	U87	brain:	n/a
12	chr7:6865886-6865936	CMK	blood:	n/a
13	chr7:6867074-6867124	HL-60	blood:	n/a
14	chr7:6865886-6865936	NB4	blood:	n/a
15	chr7:6867074-6867124	SKMC	muscle:	n/a
16	chr7:6869135-6869185	A549	lung:	n/a
17	chr7:6865970-6866020	GM12878	blood:	n/a
18	chr7:6866040-6866090	HCPEpiC	choroid plexus:	n/a
19	chr7:6865886-6865936	PrEC	prostate:	n/a
20	chr7:6866072-6866122	PrEC	prostate:	n/a
21	chr7:6866072-6866122	HUVEC	blood vessel:	n/a
22	chr7:6864491-6864541	HRE	kidney:	n/a
23	chr7:6865965-6866015	U87	brain:	n/a
24	chr7:6865960-6866010	HEK293	kidney:	embryo
25	chr7:6865915-6865965	A549	lung:	n/a
26	chr7:6866834-6866884	SK-N-SH_RA	brain:	n/a
27	chr7:6867070-6867120	SK-N-MC	brain:	n/a
28	chr7:6865965-6866015	NB4	blood:	n/a
29	chr7:6865970-6866020	HL-60	blood:	n/a
30	chr7:6865965-6866015	HepG2	liver:	n/a
31	chr7:6865989-6866039	IMR90	lung:	fetal
32	chr7:6865989-6866039	GM12891	blood:	n/a
33	chr7:6865970-6866020	U87	brain:	n/a
34	chr7:6865915-6865965	PrEC	prostate:	n/a
35	chr7:6866072-6866122	Hela-S3	cervix:	n/a
36	chr7:6866834-6866884	SKMC	muscle:	n/a
37	chr7:6865915-6865965	PFSK-1	brain:	n/a
38	chr7:6867070-6867120	GM12878	blood:	n/a
39	chr7:6866834-6866884	ECC-1	luminal epithelium:	n/a
40	chr7:6865970-6866020	T-47D	breast:	n/a
41	chr7:6865915-6865965	GM12878	blood:	n/a
42	chr7:6864491-6864541	ProgFib	skin:	n/a
43	chr7:6867074-6867124	PFSK-1	brain:	n/a
44	chr7:6866834-6866884	AG04450	lung:	fetal
45	chr7:6865965-6866015	SAEC	small airway:	n/a
46	chr7:6866834-6866884	HRCEpiC	kidney:	n/a
47	chr7:6865989-6866039	HCPEpiC	choroid plexus:	n/a
48	chr7:6867074-6867124	AoSMC	blood vessel:	n/a
49	chr7:6865960-6866010	HCT-116	colon:	n/a
50	chr7:6865915-6865965	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:6628333..6631201-chr7:6866874..6868650,2	MCF-7	breast:
2	chr7:6865395..6868378-chr7:6875321..6876917,2	MCF-7	breast:
3	chr7:6865923..6867484-chr7:6871034..6873441,2	MCF-7	breast:
4	chr7:6766860..6769459-chr7:6864426..6866111,2	MCF-7	breast:
5	chr7:6487483..6489084-chr7:6871444..6873922,2	MCF-7	breast:

Variant related genes	Relation type
CCZ1B	TF binding region
CCZ1B	CpG island
ENSG00000146576	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000146574	chromatin interactions
ENSG00000273252	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000187953	chromatin interactions

Extended variants
information (count: 422 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:422 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183155978	chr7:6864052-6864053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148069909	chr7:6864068-6864069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375934344	chr7:6864071-6864072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs202055332	chr7:6864074-6864075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs539555796	chr7:6864079-6864080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557722654	chr7:6864091-6864092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369799251	chr7:6864246-6864247	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs544157293	chr7:6864396-6864397	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556458103	chr7:6864433-6864434	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574663147	chr7:6864443-6864444	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs150516080	chr7:6864471-6864472	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369360377	chr7:6864479-6864480	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs560394642	chr7:6864497-6864498	Weak transcription Active TSS Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527338641	chr7:6864531-6864532	Weak transcription Active TSS Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545958706	chr7:6864546-6864547	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4720685	chr7:6864560-6864561	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs201264178	chr7:6864580-6864581	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531361908	chr7:6864592-6864593	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187927347	chr7:6864614-6864615	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148801278	chr7:6864615-6864616	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568702213	chr7:6864620-6864621	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534762830	chr7:6864643-6864644	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529579942	chr7:6864667-6864668	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2711236	chr7:6864689-6864690	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200417252	chr7:6864690-6864691	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2711237	chr7:6864741-6864742	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192573990	chr7:6864777-6864778	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs2528309	chr7:6864790-6864791	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs369294041	chr7:6864800-6864801	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs182591823	chr7:6864802-6864803	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs62442271	chr7:6864806-6864807	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs188159247	chr7:6864868-6864869	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs535339877	chr7:6864871-6864872	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs192738121	chr7:6864908-6864909	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs537421599	chr7:6864929-6864930	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs555501037	chr7:6864930-6864931	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs199569203	chr7:6865096-6865097	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs574630717	chr7:6865098-6865099	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs376938545	chr7:6865272-6865273	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs541764945	chr7:6865350-6865351	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553999348	chr7:6865499-6865500	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs572314630	chr7:6865621-6865622	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs545890896	chr7:6865652-6865653	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs564202927	chr7:6865697-6865698	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs71524081	chr7:6865838-6865839	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576071776	chr7:6865849-6865850	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs71524082	chr7:6865853-6865854	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs141173433	chr7:6865862-6865863	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373327925	chr7:6865866-6865867	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs543376063	chr7:6865871-6865872	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6832000-6864600	Weak transcription	Primary T cells from cord blood	blood
2	chr7:6832000-6864800	Weak transcription	Fetal Thymus	thymus
3	chr7:6832400-6864600	Weak transcription	Fetal Lung	lung
4	chr7:6832600-6864600	Weak transcription	NHLF	lung
5	chr7:6833000-6865200	Weak transcription	Left Ventricle	heart
6	chr7:6833000-6865200	Weak transcription	Ovary	ovary
7	chr7:6833200-6865200	Weak transcription	Pancreas	Pancrea
8	chr7:6833600-6864600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr7:6833600-6865200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:6834000-6866000	Weak transcription	Gastric	stomach
11	chr7:6840000-6865200	Weak transcription	Colonic Mucosa	Colon
12	chr7:6846600-6864600	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr7:6847400-6864600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr7:6847800-6864800	Weak transcription	NH-A	brain
15	chr7:6848200-6864600	Weak transcription	Colon Smooth Muscle	Colon
16	chr7:6848400-6864800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:6849000-6864600	Weak transcription	Brain Angular Gyrus	brain
18	chr7:6849800-6864600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr7:6850400-6865200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:6850400-6866000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:6851400-6864600	Weak transcription	GM12878-XiMat	blood
22	chr7:6851400-6864800	Weak transcription	K562	blood
23	chr7:6851600-6864600	Weak transcription	Primary B cells from cord blood	blood
24	chr7:6851600-6864800	Weak transcription	A549	lung
25	chr7:6851800-6864800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr7:6851800-6864800	Weak transcription	Right Ventricle	heart
27	chr7:6852000-6864600	Weak transcription	Brain Cingulate Gyrus	brain
28	chr7:6852800-6864600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:6853200-6865200	Weak transcription	Esophagus	oesophagus
30	chr7:6853400-6864800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr7:6853400-6865200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:6853600-6864600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr7:6853600-6864600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:6854000-6864800	Weak transcription	Fetal Muscle Leg	muscle
35	chr7:6854400-6864800	Weak transcription	Lung	lung
36	chr7:6854400-6864800	Weak transcription	HSMM	muscle
37	chr7:6854400-6865200	Weak transcription	Fetal Kidney	kidney
38	chr7:6855000-6864800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr7:6855200-6864600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:6855200-6866000	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr7:6855600-6864800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:6856400-6864600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr7:6856800-6864600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr7:6857000-6866000	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:6857600-6864600	Weak transcription	Brain Hippocampus Middle	brain
46	chr7:6857600-6864800	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:6858000-6864600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:6858000-6864600	Weak transcription	Fetal Intestine Large	intestine
49	chr7:6858000-6864600	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr7:6858000-6864800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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