Variant report

Variant	nsv550817
Chromosome Location	chr10:50319387-50328494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:611)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:50323742-50323798	K562	blood:	n/a	n/a
2	ATF3	chr10:50323426-50323778	K562	blood:	n/a	chr10:50323542-50323562
3	BACH1	chr10:50322997-50323317	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:50323658-50323952	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:50324193-50324568	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:50323737-50323937	K562	blood:	n/a	n/a
7	BHLHE40	chr10:50323013-50323326	K562	blood:	n/a	n/a
8	BRCA1	chr10:50323099-50323329	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr10:50323554-50323957	K562	blood:	n/a	n/a
10	CBX3	chr10:50323620-50323895	K562	blood:	n/a	n/a
11	CCNT2	chr10:50323077-50323857	K562	blood:	n/a	chr10:50323655-50323664
12	CEBPB	chr10:50325467-50325766	HepG2	liver:	n/a	chr10:50325613-50325626 chr10:50325613-50325624 chr10:50325634-50325645 chr10:50325613-50325626
13	CEBPB	chr10:50325483-50325774	K562	blood:	n/a	chr10:50325613-50325626 chr10:50325613-50325624 chr10:50325634-50325645 chr10:50325613-50325626
14	CHD1	chr10:50322975-50323188	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr10:50324251-50324451	GM12878	blood:	n/a	n/a
16	CHD2	chr10:50322965-50323427	K562	blood:	n/a	n/a
17	CHD2	chr10:50323045-50323384	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr10:50323123-50323273	HepG2	liver:	n/a	n/a
19	CHD2	chr10:50322314-50322472	K562	blood:	n/a	n/a
20	CTCF	chr10:50323220-50323343	ProgFib	skin:	n/a	n/a
21	CTCF	chr10:50323264-50323334	GM12891	blood:	n/a	n/a
22	CTCF	chr10:50323512-50323630	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr10:50321920-50322070	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr10:50323040-50323190	GM12868	blood:	n/a	n/a
25	CTCF	chr10:50323020-50323170	BJ	skin:	n/a	n/a
26	CTCF	chr10:50323080-50323230	AG09319	gingival:	n/a	n/a
27	CTCF	chr10:50323275-50323371	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr10:50323479-50323600	GM10266	blood:	n/a	n/a
29	CTCF	chr10:50323094-50323802	K562	blood:	n/a	n/a
30	CTCF	chr10:50323020-50323170	HMF	breast:	n/a	n/a
31	CTCF	chr10:50323440-50323590	AG09319	gingival:	n/a	n/a
32	CTCF	chr10:50323511-50323579	ProgFib	skin:	n/a	n/a
33	CTCF	chr10:50322700-50322850	AG04449	skin:	n/a	n/a
34	CTCF	chr10:50323339-50323359	GM12891	blood:	n/a	n/a
35	CTCF	chr10:50323470-50323596	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:50323680-50323830	K562	blood:	n/a	n/a
37	CTCF	chr10:50323000-50323150	HCM	heart:	n/a	n/a
38	CTCF	chr10:50323220-50323370	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr10:50323080-50323230	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr10:50321920-50322070	AG09319	gingival:	n/a	n/a
41	CTCF	chr10:50323244-50323365	A549	lung:	n/a	n/a
42	CTCF	chr10:50323228-50323395	GM19239	blood:	n/a	n/a
43	CTCF	chr10:50323200-50323350	GM12871	blood:	n/a	n/a
44	CTCF	chr10:50323480-50323630	GM12869	blood:	n/a	n/a
45	CTCF	chr10:50323240-50323390	HCM	heart:	n/a	n/a
46	CTCF	chr10:50322980-50323130	K562	blood:	n/a	n/a
47	CTCF	chr10:50323235-50323369	Gliobla	brain:	n/a	n/a
48	CTCF	chr10:50323000-50323150	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr10:50322980-50323130	AG10803	skin:	n/a	n/a
50	CTCF	chr10:50323140-50323290	NHDF-neo	bronchial:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:50323369-50323419	T-47D	breast:	n/a
2	chr10:50323369-50323419	T-47D	breast:	n/a
3	chr10:50323706-50323756	LNCaP	prostate:	n/a
4	chr10:50321116-50321166	MCF-7	breast:	n/a
5	chr10:50323825-50323875	HCT-116	colon:	n/a
6	chr10:50326783-50326833	K562	blood:	n/a
7	chr10:50323369-50323419	SK-N-SH_RA	brain:	n/a
8	chr10:50321116-50321166	AG04449	skin:	fetal
9	chr10:50323706-50323756	RPTEC	kidney:	n/a
10	chr10:50323706-50323756	CMK	blood:	n/a
11	chr10:50323127-50323177	IMR90	lung:	fetal
12	chr10:50323829-50323879	GM12878	blood:	n/a
13	chr10:50323708-50323758	GM19239	blood:	n/a
14	chr10:50323708-50323758	Hepatocyte	liver:	n/a
15	chr10:50323244-50323294	SAEC	small airway:	n/a
16	chr10:50323369-50323419	GM12891	blood:	n/a
17	chr10:50323127-50323177	Caco-2	colon:	n/a
18	chr10:50323244-50323294	HEEpiC	esophagus:	n/a
19	chr10:50326783-50326833	NHBE	bronchial:	n/a
20	chr10:50323708-50323758	HCPEpiC	choroid plexus:	n/a
21	chr10:50323369-50323419	A549	lung:	n/a
22	chr10:50321116-50321166	HCF	heart:	n/a
23	chr10:50323706-50323756	GM06990	blood:	n/a
24	chr10:50321116-50321166	PFSK-1	brain:	n/a
25	chr10:50323369-50323419	GM12892	blood:	n/a
26	chr10:50323825-50323875	GM06990	blood:	n/a
27	chr10:50326783-50326833	H1-hESC	embryonic stem cell:	embryo
28	chr10:50326783-50326833	MCF10A-Er-Src	breast:	n/a
29	chr10:50323706-50323756	PANC-1	pancreas:	n/a
30	chr10:50323127-50323177	GM19239	blood:	n/a
31	chr10:50323244-50323294	HRCEpiC	kidney:	n/a
32	chr10:50326783-50326833	U87	brain:	n/a
33	chr10:50323244-50323294	NH-A	brain:	n/a
34	chr10:50321116-50321166	GM12878	blood:	n/a
35	chr10:50323369-50323419	ECC-1	luminal epithelium:	n/a
36	chr10:50326783-50326833	ProgFib	skin:	n/a
37	chr10:50323832-50323882	U87	brain:	n/a
38	chr10:50323832-50323882	HNPCEpiC	eye:	n/a
39	chr10:50323708-50323758	GM12892	blood:	n/a
40	chr10:50323832-50323882	IMR90	lung:	fetal
41	chr10:50323706-50323756	GM12878	blood:	n/a
42	chr10:50323832-50323882	AG10803	skin:	n/a
43	chr10:50323369-50323419	HUVEC	blood vessel:	n/a
44	chr10:50323708-50323758	BJ	skin:	n/a
45	chr10:50323127-50323177	ovcar-3	ovarian:	n/a
46	chr10:50323832-50323882	HEEpiC	esophagus:	n/a
47	chr10:50323706-50323756	HNPCEpiC	eye:	n/a
48	chr10:50323244-50323294	MCF10A-Er-Src	breast:	n/a
49	chr10:50321116-50321166	HAEpiC	amniotic membrane:	n/a
50	chr10:50323832-50323882	NB4	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:50281055..50283973-chr10:50326395..50329291,2	K562	blood:
2	chr10:50322533..50324257-chr10:50507150..50509486,2	K562	blood:
3	chr10:50314500..50318570-chr10:50326499..50328270,3	K562	blood:
4	chr10:50322609..50324135-chr10:50326068..50328008,2	K562	blood:
5	chr10:50318764..50321622-chr10:50328764..50331472,2	K562	blood:
6	chr10:50321527..50324998-chr10:50325157..50328658,6	K562	blood:
7	chr10:50322283..50325786-chr10:50341748..50344745,3	K562	blood:
8	chr10:50327680..50329332-chr10:50338988..50341061,2	K562	blood:

No data

Variant related genes	Relation type
FAM170B-AS1	TF binding region
VSTM4	TF binding region
FAM170B-AS1	CpG island
VSTM4	CpG island
ENSG00000177354	chromatin interactions
ENSG00000234736	chromatin interactions
ENSG00000165633	chromatin interactions
ENSG00000172538	chromatin interactions

Extended variants
information (count: 306 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7072243	chr10:50319387-50319388	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539422858	chr10:50319437-50319438	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552168156	chr10:50319441-50319442	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563911629	chr10:50319455-50319456	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs553130380	chr10:50319461-50319462	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs191450171	chr10:50319489-50319490	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs78365172	chr10:50319607-50319608	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144239065	chr10:50319611-50319612	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs17782733	chr10:50319628-50319629	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs535233290	chr10:50319641-50319642	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548325665	chr10:50319667-50319668	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566843903	chr10:50319675-50319676	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs148705643	chr10:50319691-50319692	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144974666	chr10:50319695-50319696	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs574974800	chr10:50319698-50319699	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs114485793	chr10:50319699-50319700	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34605156	chr10:50319708-50319709	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs538382827	chr10:50319709-50319710	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543804080	chr10:50319733-50319734	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556705635	chr10:50319765-50319766	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs77566760	chr10:50319785-50319786	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542068892	chr10:50319817-50319818	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs77793719	chr10:50319876-50319877	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs371646224	chr10:50319916-50319917	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7077339	chr10:50319928-50319929	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183158966	chr10:50319938-50319939	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs564158749	chr10:50319949-50319950	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200144168	chr10:50319965-50319966	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs147534463	chr10:50319984-50319985	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561448313	chr10:50320024-50320025	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76785027	chr10:50320040-50320041	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188935268	chr10:50320136-50320137	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs193112147	chr10:50320141-50320142	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551523952	chr10:50320150-50320151	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185107580	chr10:50320229-50320230	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552590921	chr10:50320239-50320240	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs79051490	chr10:50320255-50320256	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs11100986	chr10:50320281-50320282	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs556571226	chr10:50320360-50320361	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188388169	chr10:50320400-50320401	Bivalent Enhancer Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs4364979	chr10:50320511-50320512	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs374819513	chr10:50320526-50320527	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191770149	chr10:50320594-50320595	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs184315145	chr10:50320635-50320636	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557774681	chr10:50320647-50320648	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs145577680	chr10:50320686-50320687	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543034165	chr10:50320688-50320689	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188220008	chr10:50320699-50320700	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs528988089	chr10:50320710-50320711	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs4559606	chr10:50320723-50320724	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Schizophrenia	23813976	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Hypotonia	21948486	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50312200-50320400	Enhancers	Colon Smooth Muscle	Colon
2	chr10:50312600-50322800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:50314400-50321400	Genic enhancers	Fetal Stomach	stomach
4	chr10:50314600-50319800	Enhancers	Lung	lung
5	chr10:50314600-50320200	Enhancers	Right Atrium	heart
6	chr10:50314600-50321000	Genic enhancers	Fetal Muscle Leg	muscle
7	chr10:50315000-50322600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:50315400-50319400	Weak transcription	Aorta	Aorta
9	chr10:50315400-50319600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr10:50315400-50323000	Weak transcription	Pancreas	Pancrea
11	chr10:50315600-50323000	Weak transcription	Spleen	Spleen
12	chr10:50315800-50320600	Enhancers	Fetal Lung	lung
13	chr10:50315800-50322200	Enhancers	Left Ventricle	heart
14	chr10:50315800-50322600	Weak transcription	Liver	Liver
15	chr10:50316000-50321200	Enhancers	Right Ventricle	heart
16	chr10:50316000-50321600	Enhancers	Ovary	ovary
17	chr10:50316600-50320200	Weak transcription	Fetal Thymus	thymus
18	chr10:50317000-50320400	Enhancers	NHDF-Ad	bronchial
19	chr10:50317200-50319400	Enhancers	Brain Angular Gyrus	brain
20	chr10:50317200-50320600	Enhancers	NHLF	lung
21	chr10:50317200-50321000	Enhancers	Adipose Nuclei	Adipose
22	chr10:50317200-50321600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:50317200-50321600	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr10:50317400-50322000	Weak transcription	K562	blood
25	chr10:50318000-50320600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr10:50318000-50321800	Enhancers	HSMMtube	muscle
27	chr10:50318000-50322200	Weak transcription	Brain Anterior Caudate	brain
28	chr10:50318200-50319800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:50318200-50322800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:50318400-50319600	Enhancers	Brain Hippocampus Middle	brain
31	chr10:50318600-50320000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr10:50318600-50320400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
33	chr10:50318600-50321000	Genic enhancers	Fetal Muscle Trunk	muscle
34	chr10:50318600-50321400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr10:50318600-50321400	Weak transcription	Osteobl	bone
36	chr10:50318600-50321800	Weak transcription	Fetal Heart	heart
37	chr10:50318600-50322200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:50318800-50319600	Enhancers	Psoas Muscle	Psoas
39	chr10:50318800-50319800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr10:50318800-50321000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr10:50319000-50320400	Enhancers	Placenta	Placenta
42	chr10:50319000-50320800	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr10:50319000-50321400	Weak transcription	HSMM	muscle
44	chr10:50319000-50322000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr10:50319000-50322800	Weak transcription	Esophagus	oesophagus
46	chr10:50319200-50319600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr10:50319200-50319600	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr10:50319200-50321800	Weak transcription	Brain Substantia Nigra	brain
49	chr10:50319400-50320400	Enhancers	Aorta	Aorta
50	chr10:50319400-50321600	Weak transcription	Brain Angular Gyrus	brain

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