Variant report

Variant	nsv976062
Chromosome Location	chr13:76206320-76211659
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:442)
CpG islands
(count:427)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:442 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76208274-76208636	HepG2	liver:	n/a	n/a
2	BACH1	chr13:76210544-76210937	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:76209632-76210184	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr13:76210410-76210755	GM12878	blood:	n/a	chr13:76210665-76210678
5	BHLHE40	chr13:76210644-76210946	K562	blood:	n/a	n/a
6	BHLHE40	chr13:76208407-76208708	HepG2	liver:	n/a	n/a
7	BHLHE40	chr13:76209695-76210786	GM12878	blood:	n/a	chr13:76210232-76210248 chr13:76209876-76209885 chr13:76209876-76209885
8	BHLHE40	chr13:76209286-76211225	HepG2	liver:	n/a	chr13:76210232-76210248 chr13:76209876-76209885 chr13:76209876-76209885
9	BHLHE40	chr13:76209746-76210008	K562	blood:	n/a	chr13:76209876-76209885 chr13:76209876-76209885
10	BRCA1	chr13:76209756-76209956	HepG2	liver:	n/a	n/a
11	BRCA1	chr13:76210832-76210935	GM12878	blood:	n/a	n/a
12	CCNT2	chr13:76210212-76210580	K562	blood:	n/a	n/a
13	CEBPB	chr13:76208282-76208887	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:76208510-76208572	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:76208438-76208565	K562	blood:	n/a	n/a
16	CEBPB	chr13:76210513-76210553	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr13:76208368-76208620	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:76208269-76208635	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:76209805-76210195	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr13:76208351-76208633	IMR90	lung:	n/a	n/a
21	CEBPB	chr13:76208318-76208900	HepG2	liver:	n/a	n/a
22	CEBPD	chr13:76208271-76208662	HepG2	liver:	n/a	n/a
23	CEBPD	chr13:76208350-76208661	HepG2	liver:	n/a	n/a
24	CHD1	chr13:76210947-76210948	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr13:76210863-76211074	GM12878	blood:	n/a	n/a
26	CHD1	chr13:76209769-76213065	IMR90	lung:	n/a	chr13:76211314-76211324 chr13:76210708-76210718
27	CHD2	chr13:76209308-76209928	HepG2	liver:	n/a	chr13:76209566-76209576
28	CHD2	chr13:76211066-76211232	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr13:76209977-76210177	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr13:76210611-76210825	H1-hESC	embryonic stem cell:	n/a	chr13:76210708-76210718
31	CHD2	chr13:76210130-76210396	HepG2	liver:	n/a	n/a
32	CHD2	chr13:76209746-76209973	GM12878	blood:	n/a	n/a
33	CHD2	chr13:76210523-76210961	GM12878	blood:	n/a	chr13:76210708-76210718
34	CHD2	chr13:76209851-76210949	Hela-S3	cervix:	n/a	chr13:76210708-76210718
35	CHD2	chr13:76210660-76211179	HepG2	liver:	n/a	chr13:76210708-76210718
36	CTBP2	chr13:76210449-76211292	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr13:76209655-76210231	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr13:76210580-76210730	GM12871	blood:	n/a	n/a
39	CTCF	chr13:76210760-76210910	AG04449	skin:	n/a	n/a
40	CTCF	chr13:76210260-76210410	GM12875	blood:	n/a	n/a
41	CTCF	chr13:76210880-76211030	GM12868	blood:	n/a	n/a
42	CTCF	chr13:76210826-76210986	GM12892	blood:	n/a	n/a
43	CTCF	chr13:76210903-76210978	GM13977	blood:	n/a	n/a
44	CTCF	chr13:76210080-76210230	GM12874	blood:	n/a	n/a
45	CTCF	chr13:76210842-76210994	MCF-7	breast:	n/a	n/a
46	CTCF	chr13:76209980-76210130	GM12867	blood:	n/a	n/a
47	CTCF	chr13:76210160-76210310	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr13:76209900-76210050	GM12866	blood:	n/a	n/a
49	CTCF	chr13:76209720-76209870	GM12865	blood:	n/a	n/a
50	CTCF	chr13:76209820-76209970	GM12872	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76209457-76209507	HPAEpiC	pulmonary alveolar:	n/a
2	chr13:76211051-76211101	NB4	blood:	n/a
3	chr13:76211051-76211101	RPTEC	kidney:	n/a
4	chr13:76211251-76211301	HEK293	kidney:	embryo
5	chr13:76210054-76210104	MCF-7	breast:	n/a
6	chr13:76211051-76211101	HAEpiC	amniotic membrane:	n/a
7	chr13:76209457-76209507	MCF-7	breast:	n/a
8	chr13:76209457-76209507	MCF10A-Er-Src	breast:	n/a
9	chr13:76209541-76209591	PFSK-1	brain:	n/a
10	chr13:76209541-76209591	AG04450	lung:	fetal
11	chr13:76209457-76209507	SK-N-SH	brain:	n/a
12	chr13:76207486-76207536	GM19239	blood:	n/a
13	chr13:76209541-76209591	GM12892	blood:	n/a
14	chr13:76210054-76210104	NHBE	bronchial:	n/a
15	chr13:76210054-76210104	HRE	kidney:	n/a
16	chr13:76207486-76207536	AG04449	skin:	fetal
17	chr13:76211051-76211101	SK-N-MC	brain:	n/a
18	chr13:76209541-76209591	Jurkat	blood:	n/a
19	chr13:76209541-76209591	K562	blood:	n/a
20	chr13:76211051-76211101	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:76209541-76209591	HRE	kidney:	n/a
22	chr13:76209457-76209507	HRCEpiC	kidney:	n/a
23	chr13:76207486-76207536	PANC-1	pancreas:	n/a
24	chr13:76209541-76209591	NT2-D1	testis:	n/a
25	chr13:76210838-76210888	Hela-S3	cervix:	n/a
26	chr13:76211251-76211301	NT2-D1	testis:	n/a
27	chr13:76209457-76209507	HAEpiC	amniotic membrane:	n/a
28	chr13:76210838-76210888	HAEpiC	amniotic membrane:	n/a
29	chr13:76209457-76209507	A549	lung:	n/a
30	chr13:76209457-76209507	H1-hESC	embryonic stem cell:	embryo
31	chr13:76207486-76207536	GM12892	blood:	n/a
32	chr13:76207486-76207536	GM12878	blood:	n/a
33	chr13:76210838-76210888	AG09309	skin:	n/a
34	chr13:76209457-76209507	RPTEC	kidney:	n/a
35	chr13:76209541-76209591	NHBE	bronchial:	n/a
36	chr13:76211251-76211301	HIPEpiC	eye:	n/a
37	chr13:76207486-76207536	IMR90	lung:	fetal
38	chr13:76209541-76209591	SK-N-SH	brain:	n/a
39	chr13:76207486-76207536	NHDF-neo	bronchial:	n/a
40	chr13:76211251-76211301	ECC-1	luminal epithelium:	n/a
41	chr13:76211251-76211301	HEEpiC	esophagus:	n/a
42	chr13:76210838-76210888	Caco-2	colon:	n/a
43	chr13:76207486-76207536	U87	brain:	n/a
44	chr13:76211251-76211301	K562	blood:	n/a
45	chr13:76209541-76209591	AG04449	skin:	fetal
46	chr13:76207486-76207536	NB4	blood:	n/a
47	chr13:76207486-76207536	HNPCEpiC	eye:	n/a
48	chr13:76209541-76209591	HEEpiC	esophagus:	n/a
49	chr13:76210838-76210888	NH-A	brain:	n/a
50	chr13:76209541-76209591	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:76194856..76197534-chr13:76208958..76210482,2	MCF-7	breast:
2	chr13:76210811..76212641-chr13:76212952..76214964,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD6-2	chr13:76209965-76210130	ENSG00000261105.1
2	lnc-COMMD6-2	chr13:76209965-76210130	ENSG00000261105.1

No data

Variant related genes	Relation type
ENSG00000261105	TF binding region
LMO7	TF binding region
ENSG00000261105	CpG island
LMO7	CpG island
ENSG00000136153	chromatin interactions

Extended variants
information (count: 208 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:208 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76171199	chr13:76206394-76206395	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs41286116	chr13:76206411-76206412	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74510440	chr13:76206466-76206467	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532120923	chr13:76206484-76206485	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527238135	chr13:76206528-76206529	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs375102233	chr13:76206533-76206534	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191199622	chr13:76206558-76206559	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs201037975	chr13:76206559-76206560	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs561010935	chr13:76206561-76206562	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201314170	chr13:76206564-76206565	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371166426	chr13:76206574-76206575	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531530206	chr13:76206590-76206591	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370637277	chr13:76206626-76206627	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140509912	chr13:76206671-76206672	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs183747264	chr13:76206692-76206693	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs9573594	chr13:76206727-76206728	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558280907	chr13:76206742-76206743	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs9573595	chr13:76206775-76206776	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs12020000	chr13:76206779-76206780	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs9565178	chr13:76206788-76206789	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536217717	chr13:76206797-76206798	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs555815984	chr13:76206830-76206831	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs574249614	chr13:76206837-76206838	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs12020007	chr13:76206859-76206860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs199939950	chr13:76206860-76206861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12020008	chr13:76206874-76206875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538137593	chr13:76206911-76206912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556854412	chr13:76206938-76206939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548931514	chr13:76206984-76206985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375132994	chr13:76206998-76206999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10690832	chr13:76206999-76207000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72116132	chr13:76207010-76207011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201266152	chr13:76207015-76207016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373236241	chr13:76207017-76207018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578105420	chr13:76207027-76207028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545197793	chr13:76207057-76207058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs567146213	chr13:76207096-76207097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142790538	chr13:76207105-76207106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370550932	chr13:76207146-76207147	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147277498	chr13:76207163-76207164	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs202038018	chr13:76207190-76207191	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549798912	chr13:76207192-76207193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs565230546	chr13:76207206-76207207	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs187621047	chr13:76207237-76207238	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs547624111	chr13:76207239-76207240	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs566938234	chr13:76207257-76207258	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372933238	chr13:76207263-76207264	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549529411	chr13:76207264-76207265	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs9544012	chr13:76207286-76207287	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs34317046	chr13:76207296-76207297	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76125000-76209600	Weak transcription	Right Ventricle	heart
2	chr13:76148200-76209600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr13:76149800-76209600	Weak transcription	Lung	lung
4	chr13:76159000-76209600	Weak transcription	Brain Hippocampus Middle	brain
5	chr13:76164600-76209400	Weak transcription	Esophagus	oesophagus
6	chr13:76165200-76209200	Weak transcription	Fetal Muscle Leg	muscle
7	chr13:76170800-76209600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr13:76177600-76209400	Weak transcription	Left Ventricle	heart
9	chr13:76177600-76209600	Weak transcription	Fetal Stomach	stomach
10	chr13:76180000-76209600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr13:76180800-76209200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr13:76180800-76209200	Weak transcription	Adipose Nuclei	Adipose
13	chr13:76180800-76209600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr13:76181000-76209400	Weak transcription	Fetal Thymus	thymus
15	chr13:76181000-76209600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr13:76181000-76209600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr13:76181200-76209400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr13:76181200-76209600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr13:76181600-76207400	Weak transcription	HMEC	breast
20	chr13:76182800-76209400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr13:76189600-76209400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr13:76190600-76209600	Weak transcription	Brain Angular Gyrus	brain
23	chr13:76192000-76209600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr13:76192200-76209400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr13:76192600-76209600	Weak transcription	Fetal Intestine Small	intestine
26	chr13:76193400-76209400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:76196200-76207600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr13:76197000-76209600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr13:76197800-76209600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr13:76198800-76209400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr13:76199800-76209600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr13:76200200-76208200	Weak transcription	Placenta	Placenta
33	chr13:76200200-76209400	Weak transcription	Primary T cells from cord blood	blood
34	chr13:76200200-76209400	Weak transcription	Aorta	Aorta
35	chr13:76200200-76209600	Weak transcription	Primary B cells from cord blood	blood
36	chr13:76200200-76209600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr13:76200200-76209600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr13:76200400-76209400	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr13:76201800-76207200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr13:76202400-76209400	Weak transcription	Fetal Lung	lung
41	chr13:76203200-76209600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr13:76203400-76207600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr13:76203800-76207200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr13:76203800-76209400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr13:76203800-76209400	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr13:76204000-76206800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr13:76204000-76207200	Weak transcription	NH-A	brain
48	chr13:76204800-76209200	Weak transcription	HSMMtube	muscle
49	chr13:76205400-76209400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr13:76205600-76206600	Genic enhancers	NHDF-Ad	bronchial

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