Variant report

Variant	nsv971867
Chromosome Location	chr10:6341441-6353045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:335)
CpG islands
(count:61)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:6341234-6341611	HepG2	liver:	n/a	n/a
2	ATF2	chr10:6341796-6342897	GM12878	blood:	n/a	n/a
3	ATF2	chr10:6341837-6342883	GM12878	blood:	n/a	n/a
4	ATF3	chr10:6341022-6341723	A549	lung:	n/a	n/a
5	ATF3	chr10:6340933-6341776	A549	lung:	n/a	n/a
6	BATF	chr10:6341955-6342434	GM12878	blood:	n/a	n/a
7	BATF	chr10:6352946-6353275	GM12878	blood:	n/a	n/a
8	BATF	chr10:6341929-6342424	GM12878	blood:	n/a	n/a
9	BATF	chr10:6352991-6353227	GM12878	blood:	n/a	n/a
10	BCL11A	chr10:6342012-6342419	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:6341934-6342754	GM12878	blood:	n/a	n/a
12	BCL3	chr10:6341975-6342506	GM12878	blood:	n/a	n/a
13	BCL3	chr10:6340889-6342092	A549	lung:	n/a	chr10:6341456-6341469 chr10:6340963-6340972
14	BCL3	chr10:6340982-6341955	A549	lung:	n/a	chr10:6341456-6341469
15	BCLAF1	chr10:6341568-6342797	GM12878	blood:	n/a	n/a
16	BCLAF1	chr10:6341954-6342775	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:6341176-6341524	HepG2	liver:	n/a	chr10:6341377-6341386 chr10:6341377-6341386
18	BHLHE40	chr10:6341185-6341601	K562	blood:	n/a	chr10:6341377-6341386 chr10:6341377-6341386
19	BHLHE40	chr10:6341091-6341640	HepG2	liver:	n/a	chr10:6341377-6341386 chr10:6341377-6341386
20	BHLHE40	chr10:6341938-6342741	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:6341218-6341615	HepG2	liver:	n/a	chr10:6341377-6341386 chr10:6341377-6341386
22	BHLHE40	chr10:6341170-6341592	A549	lung:	n/a	chr10:6341377-6341386 chr10:6341377-6341386
23	BRCA1	chr10:6342495-6342877	GM12878	blood:	n/a	chr10:6342671-6342680
24	CBX3	chr10:6348903-6349459	HCT-116	colon:	n/a	n/a
25	CEBPB	chr10:6345289-6345488	A549	lung:	n/a	n/a
26	CEBPB	chr10:6340999-6341861	A549	lung:	n/a	n/a
27	CEBPB	chr10:6345178-6345760	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:6341243-6341605	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr10:6341161-6341570	A549	lung:	n/a	n/a
30	CEBPB	chr10:6341108-6341646	A549	lung:	n/a	n/a
31	CHD1	chr10:6341647-6342542	GM12878	blood:	n/a	n/a
32	CHD2	chr10:6341191-6341545	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr10:6341565-6343160	GM12878	blood:	n/a	chr10:6342671-6342680
34	CHD2	chr10:6342502-6342866	K562	blood:	n/a	chr10:6342671-6342680
35	CHD2	chr10:6342503-6342736	HepG2	liver:	n/a	chr10:6342671-6342680
36	CREB1	chr10:6341140-6341552	A549	lung:	n/a	n/a
37	CREB1	chr10:6341291-6341574	A549	lung:	n/a	n/a
38	CREB1	chr10:6341935-6342795	GM12878	blood:	n/a	n/a
39	CTCF	chr10:6342340-6342490	AG10803	skin:	n/a	n/a
40	CTCF	chr10:6342180-6342330	GM12873	blood:	n/a	n/a
41	CTCF	chr10:6342206-6342269	GM12878	blood:	n/a	n/a
42	CTCF	chr10:6342300-6342450	AG10803	skin:	n/a	n/a
43	CTCF	chr10:6342240-6342390	RPTEC	kidney:	n/a	n/a
44	CTCF	chr10:6342060-6342210	AG10803	skin:	n/a	n/a
45	CTCF	chr10:6342340-6342490	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr10:6346858-6346886	GM10248	blood:	n/a	n/a
47	CTCF	chr10:6348075-6348150	GM10248	blood:	n/a	n/a
48	CTCF	chr10:6342300-6342450	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr10:6352170-6352190	GM10248	blood:	n/a	n/a
50	CTCF	chr10:6352105-6352192	LNCaP	prostate:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:6348943-6348993	SKMC	muscle:	n/a
2	chr10:6348943-6348993	SK-N-SH	brain:	n/a
3	chr10:6348943-6348993	Hela-S3	cervix:	n/a
4	chr10:6348943-6348993	T-47D	breast:	n/a
5	chr10:6348943-6348993	SK-N-MC	brain:	n/a
6	chr10:6348943-6348993	NB4	blood:	n/a
7	chr10:6348943-6348993	AG10803	skin:	n/a
8	chr10:6348943-6348993	U87	brain:	n/a
9	chr10:6348943-6348993	HepG2	liver:	n/a
10	chr10:6348943-6348993	HEK293	kidney:	embryo
11	chr10:6348943-6348993	GM19239	blood:	n/a
12	chr10:6348943-6348993	GM12892	blood:	n/a
13	chr10:6348943-6348993	AG04449	skin:	fetal
14	chr10:6348943-6348993	NT2-D1	testis:	n/a
15	chr10:6348943-6348993	HCPEpiC	choroid plexus:	n/a
16	chr10:6348943-6348993	HIPEpiC	eye:	n/a
17	chr10:6348943-6348993	MCF-7	breast:	n/a
18	chr10:6348943-6348993	HRPEpiC	eye:	n/a
19	chr10:6348943-6348993	CMK	blood:	n/a
20	chr10:6348943-6348993	HEEpiC	esophagus:	n/a
21	chr10:6348943-6348993	ProgFib	skin:	n/a
22	chr10:6348943-6348993	A549	lung:	n/a
23	chr10:6348943-6348993	HCM	heart:	n/a
24	chr10:6348943-6348993	Hepatocyte	liver:	n/a
25	chr10:6348943-6348993	HCF	heart:	n/a
26	chr10:6348943-6348993	BE2_C	brain:	n/a
27	chr10:6348943-6348993	PFSK-1	brain:	n/a
28	chr10:6348943-6348993	HCT-116	colon:	n/a
29	chr10:6348943-6348993	LNCaP	prostate:	n/a
30	chr10:6348943-6348993	PANC-1	pancreas:	n/a
31	chr10:6348943-6348993	HMEC	breast:	n/a
32	chr10:6348943-6348993	HUVEC	blood vessel:	n/a
33	chr10:6348943-6348993	IMR90	lung:	fetal
34	chr10:6348943-6348993	ovcar-3	ovarian:	n/a
35	chr10:6348943-6348993	AG09309	skin:	n/a
36	chr10:6348943-6348993	GM12878	blood:	n/a
37	chr10:6348943-6348993	AG04450	lung:	fetal
38	chr10:6348943-6348993	K562	blood:	n/a
39	chr10:6348943-6348993	HRE	kidney:	n/a
40	chr10:6348943-6348993	HNPCEpiC	eye:	n/a
41	chr10:6348943-6348993	HPAEpiC	pulmonary alveolar:	n/a
42	chr10:6348943-6348993	MCF10A-Er-Src	breast:	n/a
43	chr10:6348943-6348993	RPTEC	kidney:	n/a
44	chr10:6348943-6348993	H1-hESC	embryonic stem cell:	embryo
45	chr10:6348943-6348993	SAEC	small airway:	n/a
46	chr10:6348943-6348993	NH-A	brain:	n/a
47	chr10:6348943-6348993	GM12891	blood:	n/a
48	chr10:6348943-6348993	Jurkat	blood:	n/a
49	chr10:6348943-6348993	Caco-2	colon:	n/a
50	chr10:6348943-6348993	SK-N-SH_RA	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:6245398..6245952-chr10:6348848..6349696,2	K562	blood:
2	chr10:6327503..6329352-chr10:6339746..6341603,2	MCF-7	breast:
3	chr10:6351716..6354358-chr10:6354404..6356505,2	MCF-7	breast:
4	chr10:6336971..6341697-chr10:6441247..6445868,11	MCF-7	breast:
5	chr10:6342449..6344753-chr10:6350540..6352238,2	K562	blood:
6	chr10:6339890..6341669-chr10:6345172..6346790,2	MCF-7	breast:
7	chr10:6339981..6341771-chr10:6430124..6433037,2	MCF-7	breast:
8	chr10:6316454..6323166-chr10:6337458..6343783,14	MCF-7	breast:
9	chr10:6243246..6245035-chr10:6341115..6343745,2	K562	blood:
10	chr10:6301955..6304716-chr10:6339271..6341993,2	MCF-7	breast:
11	chr10:6243492..6246409-chr10:6345954..6348805,3	MCF-7	breast:
12	chr10:6338433..6344348-chr10:6402915..6408706,10	MCF-7	breast:
13	chr10:6306983..6309812-chr10:6338962..6341584,2	MCF-7	breast:
14	chr10:6338687..6345306-chr10:6353335..6358938,10	MCF-7	breast:
15	chr10:6342449..6344753-chr10:6350540..6352238,2	K562	blood:
16	chr10:6204469..6207295-chr10:6338789..6342054,3	MCF-7	breast:
17	chr10:6339999..6343004-chr10:6366040..6368957,3	MCF-7	breast:
18	chr10:6240895..6249179-chr10:6337425..6345825,48	MCF-7	breast:
19	chr10:6339437..6341250-chr10:6341763..6343524,3	MCF-7	breast:
20	chr10:6341160..6345288-chr10:6356730..6359741,4	MCF-7	breast:
21	chr10:6279091..6282826-chr10:6339063..6342558,5	MCF-7	breast:
22	chr10:6319975..6324028-chr10:6337597..6341506,5	MCF-7	breast:
23	chr10:6339890..6341669-chr10:6345172..6346790,2	MCF-7	breast:
24	chr10:6148853..6150588-chr10:6340669..6343232,2	MCF-7	breast:
25	chr10:6242967..6247217-chr10:6336875..6343685,22	MCF-7	breast:
26	chr10:6348091..6350506-chr10:6353125..6355879,3	MCF-7	breast:
27	chr10:6339849..6343647-chr10:6369137..6372590,4	MCF-7	breast:
28	chr10:6249507..6251896-chr10:6339799..6342783,2	MCF-7	breast:

No data

Variant related genes	Relation type
SDCBPP1	TF binding region
SDCBPP1	CpG island
ENSG00000213994	chromatin interactions
ENSG00000134453	chromatin interactions
ENSG00000215244	chromatin interactions
ENSG00000170525	chromatin interactions

Extended variants
information (count: 484 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:484 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532401828	chr10:6341446-6341447	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs547652359	chr10:6341466-6341467	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs17153314	chr10:6341486-6341487	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs76223710	chr10:6341487-6341488	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs548286793	chr10:6341524-6341525	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs17153320	chr10:6341537-6341538	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536655186	chr10:6341548-6341549	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs558081173	chr10:6341606-6341607	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs181508559	chr10:6341622-6341623	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs142316482	chr10:6341657-6341658	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs370188335	chr10:6341660-6341661	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs146333880	chr10:6341661-6341662	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs139472560	chr10:6341671-6341672	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs185254058	chr10:6341683-6341684	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs190181038	chr10:6341692-6341693	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs529010800	chr10:6341801-6341802	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs144229622	chr10:6341830-6341831	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs548804625	chr10:6341834-6341835	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs181220359	chr10:6341870-6341871	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs79818271	chr10:6341930-6341931	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs5782889	chr10:6341949-6341950	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs12778005	chr10:6341962-6341963	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs113734816	chr10:6341992-6341993	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs541309813	chr10:6341999-6342000	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs140017633	chr10:6342026-6342027	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs149821472	chr10:6342043-6342044	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs548037017	chr10:6342069-6342070	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs185607686	chr10:6342087-6342088	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs530516480	chr10:6342115-6342116	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs567231853	chr10:6342118-6342119	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs942195	chr10:6342123-6342124	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs569127868	chr10:6342137-6342138	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189582019	chr10:6342270-6342271	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs547296457	chr10:6342296-6342297	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs180923739	chr10:6342311-6342312	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs536056412	chr10:6342335-6342336	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs550798968	chr10:6342377-6342378	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs186072999	chr10:6342411-6342412	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs537884701	chr10:6342417-6342418	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs192327342	chr10:6342419-6342420	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs539923262	chr10:6342437-6342438	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs77787412	chr10:6342494-6342495	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs556151425	chr10:6342495-6342496	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs115650821	chr10:6342546-6342547	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs559140828	chr10:6342550-6342551	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs540227667	chr10:6342581-6342582	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs17153333	chr10:6342584-6342585	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs574596238	chr10:6342590-6342591	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs542052113	chr10:6342598-6342599	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs76624424	chr10:6342609-6342610	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6333000-6341800	Weak transcription	NHDF-Ad	bronchial
2	chr10:6333800-6341800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr10:6334000-6341600	Weak transcription	Primary T cells from cord blood	blood
4	chr10:6334000-6341600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr10:6334200-6341600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr10:6334600-6341600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr10:6334600-6341600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:6338200-6342200	Enhancers	Duodenum Mucosa	Duodenum
9	chr10:6338400-6344000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:6338600-6343000	Enhancers	HMEC	breast
11	chr10:6338600-6343800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr10:6338800-6342200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:6338800-6342200	Enhancers	Hela-S3	cervix
14	chr10:6338800-6342800	Enhancers	Aorta	Aorta
15	chr10:6338800-6343800	Enhancers	Stomach Mucosa	stomach
16	chr10:6338800-6345000	Enhancers	Fetal Intestine Small	intestine
17	chr10:6339000-6343800	Enhancers	Lung	lung
18	chr10:6339200-6345200	Enhancers	Fetal Intestine Large	intestine
19	chr10:6339400-6342000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr10:6339400-6342200	Weak transcription	HSMM	muscle
21	chr10:6339400-6342600	Weak transcription	Colonic Mucosa	Colon
22	chr10:6339400-6342800	Weak transcription	Spleen	Spleen
23	chr10:6339600-6342200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:6339600-6342200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr10:6339600-6342200	Weak transcription	Fetal Muscle Leg	muscle
26	chr10:6339600-6342600	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr10:6339600-6343800	Enhancers	Primary B cells from peripheral blood	blood
28	chr10:6339600-6346400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr10:6339800-6341600	Weak transcription	Small Intestine	intestine
30	chr10:6339800-6341600	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr10:6339800-6342800	Enhancers	Brain Substantia Nigra	brain
32	chr10:6339800-6343000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr10:6340200-6341800	Enhancers	Pancreas	Pancrea
34	chr10:6340200-6341800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr10:6340200-6342600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr10:6340200-6343400	Weak transcription	Fetal Kidney	kidney
37	chr10:6340200-6349000	Weak transcription	Adipose Nuclei	Adipose
38	chr10:6340400-6341600	Weak transcription	Fetal Thymus	thymus
39	chr10:6340400-6341800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr10:6340400-6341800	Flanking Active TSS	A549	lung
41	chr10:6340400-6342000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:6340400-6342000	Weak transcription	Fetal Lung	lung
43	chr10:6340400-6342200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr10:6340600-6342000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr10:6340600-6343200	Enhancers	Brain Anterior Caudate	brain
46	chr10:6340800-6341800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr10:6340800-6342800	Weak transcription	Brain Hippocampus Middle	brain
48	chr10:6340800-6343000	Enhancers	Gastric	stomach
49	chr10:6341000-6341600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr10:6341000-6341600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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