Variant report

Variant	nsv1017821
Chromosome Location	chr6:5114609-5213200
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1586)
CpG islands
(count:1101)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:5121891-5122113	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:5190707-5191119	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:5182330-5182406	K562	blood:	n/a	n/a
4	ARID3A	chr6:5206127-5206777	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:5119334-5119631	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:5139558-5139834	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:5115186-5115868	HepG2	liver:	n/a	n/a
8	ATF1	chr6:5211669-5211719	K562	blood:	n/a	n/a
9	ATF2	chr6:5132901-5133409	GM12878	blood:	n/a	n/a
10	ATF2	chr6:5174096-5174925	GM12878	blood:	n/a	n/a
11	ATF2	chr6:5206132-5206459	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:5180186-5180398	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:5180101-5180461	K562	blood:	n/a	n/a
14	BATF	chr6:5132968-5133342	GM12878	blood:	n/a	n/a
15	BATF	chr6:5133033-5133385	GM12878	blood:	n/a	n/a
16	BATF	chr6:5174463-5174847	GM12878	blood:	n/a	n/a
17	BCL3	chr6:5206147-5206487	GM12878	blood:	n/a	n/a
18	BHLHE40	chr6:5119348-5119682	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:5115397-5115822	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:5206103-5206432	HepG2	liver:	n/a	n/a
21	BHLHE40	chr6:5190760-5191019	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:5125414-5125753	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:5206232-5206343	K562	blood:	n/a	n/a
24	BHLHE40	chr6:5143857-5144260	GM12878	blood:	n/a	n/a
25	BRCA1	chr6:5125610-5125688	HepG2	liver:	n/a	n/a
26	BRCA1	chr6:5190793-5191220	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr6:5207611-5207621	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:5190691-5191264	Hela-S3	cervix:	n/a	chr6:5190924-5190935
29	CEBPB	chr6:5190579-5191258	A549	lung:	n/a	chr6:5190924-5190935
30	CEBPB	chr6:5119806-5120167	HepG2	liver:	n/a	chr6:5119973-5119984
31	CEBPB	chr6:5190735-5191141	HepG2	liver:	n/a	chr6:5190924-5190935
32	CEBPB	chr6:5115449-5115673	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:5199589-5199738	HepG2	liver:	n/a	chr6:5199687-5199698
34	CEBPB	chr6:5190817-5191021	HepG2	liver:	n/a	chr6:5190924-5190935
35	CEBPB	chr6:5115391-5115678	A549	lung:	n/a	n/a
36	CEBPB	chr6:5190720-5191186	MCF-7	breast:	n/a	chr6:5190924-5190935
37	CEBPB	chr6:5208776-5209072	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:5159318-5159871	ECC-1	luminal epithelium:	n/a	chr6:5159514-5159525 chr6:5159515-5159526 chr6:5159514-5159527
39	CEBPB	chr6:5188872-5189196	K562	blood:	n/a	chr6:5189053-5189064
40	CEBPB	chr6:5190661-5191140	HepG2	liver:	n/a	chr6:5190924-5190935
41	CEBPB	chr6:5190738-5191109	ECC-1	luminal epithelium:	n/a	chr6:5190924-5190935
42	CEBPB	chr6:5174373-5174584	IMR90	lung:	n/a	n/a
43	CEBPB	chr6:5159363-5159726	ECC-1	luminal epithelium:	n/a	chr6:5159514-5159525 chr6:5159515-5159526 chr6:5159514-5159527
44	CEBPB	chr6:5159307-5159770	HCT-116	colon:	n/a	chr6:5159514-5159525 chr6:5159515-5159526 chr6:5159514-5159527
45	CEBPB	chr6:5127540-5127896	IMR90	lung:	n/a	chr6:5127705-5127714 chr6:5127703-5127714 chr6:5127705-5127714 chr6:5127705-5127714
46	CEBPB	chr6:5121757-5121919	K562	blood:	n/a	chr6:5121764-5121775 chr6:5121766-5121775
47	CEBPB	chr6:5115320-5115748	MCF-7	breast:	n/a	n/a
48	CEBPB	chr6:5190712-5191214	IMR90	lung:	n/a	chr6:5190924-5190935
49	CEBPB	chr6:5184074-5184332	A549	lung:	n/a	chr6:5184208-5184219
50	CEBPB	chr6:5206039-5206443	K562	blood:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5145019-5145069	AoSMC	blood vessel:	n/a
2	chr6:5144078-5144128	Caco-2	colon:	n/a
3	chr6:5136301-5136351	AG04450	lung:	fetal
4	chr6:5145019-5145069	AoSMC	blood vessel:	n/a
5	chr6:5144078-5144128	Caco-2	colon:	n/a
6	chr6:5136301-5136351	AG04450	lung:	fetal
7	chr6:5145532-5145582	NHDF-neo	bronchial:	n/a
8	chr6:5205542-5205592	HEK293	kidney:	embryo
9	chr6:5145161-5145211	HRCEpiC	kidney:	n/a
10	chr6:5139427-5139477	Caco-2	colon:	n/a
11	chr6:5145019-5145069	SK-N-SH	brain:	n/a
12	chr6:5145071-5145121	HCPEpiC	choroid plexus:	n/a
13	chr6:5205542-5205592	AG09309	skin:	n/a
14	chr6:5174647-5174697	HRE	kidney:	n/a
15	chr6:5145614-5145664	GM12892	blood:	n/a
16	chr6:5174647-5174697	BJ	skin:	n/a
17	chr6:5145071-5145121	HRE	kidney:	n/a
18	chr6:5145071-5145121	NT2-D1	testis:	n/a
19	chr6:5145532-5145582	PFSK-1	brain:	n/a
20	chr6:5135184-5135234	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:5144078-5144128	Jurkat	blood:	n/a
22	chr6:5139427-5139477	HAEpiC	amniotic membrane:	n/a
23	chr6:5145019-5145069	HepG2	liver:	n/a
24	chr6:5145071-5145121	Hepatocyte	liver:	n/a
25	chr6:5205542-5205592	AG04449	skin:	fetal
26	chr6:5145071-5145121	IMR90	lung:	fetal
27	chr6:5144078-5144128	GM19239	blood:	n/a
28	chr6:5145569-5145619	AG10803	skin:	n/a
29	chr6:5181057-5181107	NH-A	brain:	n/a
30	chr6:5152468-5152518	ovcar-3	ovarian:	n/a
31	chr6:5205542-5205592	SAEC	small airway:	n/a
32	chr6:5136301-5136351	PFSK-1	brain:	n/a
33	chr6:5136301-5136351	HCM	heart:	n/a
34	chr6:5145019-5145069	GM12892	blood:	n/a
35	chr6:5174647-5174697	CMK	blood:	n/a
36	chr6:5205542-5205592	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:5144078-5144128	T-47D	breast:	n/a
38	chr6:5174647-5174697	SK-N-MC	brain:	n/a
39	chr6:5135794-5135844	NHDF-neo	bronchial:	n/a
40	chr6:5139427-5139477	GM12892	blood:	n/a
41	chr6:5133475-5133525	HMEC	breast:	n/a
42	chr6:5145569-5145619	Caco-2	colon:	n/a
43	chr6:5145532-5145582	RPTEC	kidney:	n/a
44	chr6:5181057-5181107	AG04450	lung:	fetal
45	chr6:5135794-5135844	HL-60	blood:	n/a
46	chr6:5132887-5132937	SK-N-SH_RA	brain:	n/a
47	chr6:5145161-5145211	Hela-S3	cervix:	n/a
48	chr6:5145161-5145211	HCPEpiC	choroid plexus:	n/a
49	chr6:5133475-5133525	IMR90	lung:	fetal
50	chr6:5145161-5145211	HCF	heart:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:5145534..5146304-chr8:93741632..93742260,2	MCF-7	breast:
2	chr6:5120935..5125341-chr6:5126554..5131441,5	K562	blood:
3	chr6:5078527..5079328-chr6:5115126..5116009,5	MCF-7	breast:
4	chr6:5143921..5144506-chr6:5398809..5399361,2	MCF-7	breast:
5	chr6:5189281..5191777-chr6:5204127..5205780,2	MCF-7	breast:
6	chr6:5156038..5158677-chr6:5160543..5162347,2	K562	blood:
7	chr6:5143652..5144542-chr6:5175040..5175982,3	MCF-7	breast:
8	chr6:5212097..5214794-chr6:5261245..5262873,2	K562	blood:
9	chr6:5127863..5130262-chr6:5130586..5132719,2	K562	blood:
10	chr6:5056866..5057674-chr6:5135884..5136820,3	MCF-7	breast:
11	chr6:5180084..5182200-chr6:5182677..5184295,2	MCF-7	breast:
12	chr6:5143540..5144964-chr6:5379399..5380247,6	K562	blood:
13	chr6:5143706..5144466-chr6:5167696..5168623,2	MCF-7	breast:
14	chr6:5143322..5144392-chr6:5398327..5399283,4	MCF-7	breast:
15	chr6:5200460..5201968-chr6:5202592..5204399,2	MCF-7	breast:
16	chr6:5003955..5004746-chr6:5115149..5116003,2	MCF-7	breast:
17	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
18	chr6:5191188..5195166-chr6:5259406..5262990,4	K562	blood:
19	chr6:5173898..5177005-chr6:5178469..5180479,3	K562	blood:
20	chr6:5143652..5144542-chr6:5175040..5175982,3	MCF-7	breast:
21	chr6:5143607..5144647-chr6:5402160..5403231,5	MCF-7	breast:
22	chr6:5156022..5159105-chr6:5163033..5165794,3	K562	blood:
23	chr6:5194051..5195705-chr6:5197927..5200504,2	K562	blood:
24	chr6:5120295..5122743-chr6:5128225..5130886,2	K562	blood:
25	chr6:5149373..5152322-chr6:5189165..5191119,2	K562	blood:
26	chr6:5149373..5152322-chr6:5189165..5191119,2	K562	blood:
27	chr6:5120295..5122743-chr6:5128225..5130886,2	K562	blood:
28	chr6:5119211..5120955-chr6:5124804..5127728,2	K562	blood:
29	chr6:5081137..5084088-chr6:5116635..5118182,2	MCF-7	breast:
30	chr6:5122792..5124780-chr6:5175533..5177529,2	K562	blood:
31	chr6:5180084..5182200-chr6:5182677..5184295,2	MCF-7	breast:
32	chr6:5156038..5158677-chr6:5160543..5162347,2	K562	blood:
33	chr6:5139257..5141408-chr6:5217631..5219778,2	MCF-7	breast:
34	chr6:5143546..5144516-chr6:5402052..5403264,7	K562	blood:
35	chr6:5173898..5177005-chr6:5178469..5180479,3	K562	blood:
36	chr6:5057040..5058030-chr6:5115128..5116001,3	MCF-7	breast:
37	chr6:5200460..5201968-chr6:5202592..5204399,2	MCF-7	breast:
38	chr6:5122792..5124780-chr6:5175533..5177529,2	K562	blood:
39	chr6:5127863..5130262-chr6:5130586..5132719,2	K562	blood:
40	chr6:5120935..5125341-chr6:5126554..5131441,5	K562	blood:
41	chr6:5143706..5144466-chr6:5167696..5168623,2	MCF-7	breast:
42	chr6:5203877..5206736-chr6:5207600..5210343,2	MCF-7	breast:
43	chr6:5128862..5130386-chr6:5130746..5132624,2	MCF-7	breast:
44	chr6:5109410..5110934-chr6:5113324..5116153,2	K562	blood:
45	chr6:5143614..5144581-chr6:5379550..5380557,6	MCF-7	breast:
46	chr6:5119211..5120955-chr6:5124804..5127728,2	K562	blood:
47	chr6:5196236..5198103-chr6:5221332..5223439,2	K562	blood:
48	chr6:5135691..5136262-chr6:5402310..5402817,2	K562	blood:
49	chr6:5156022..5159105-chr6:5163033..5165794,3	K562	blood:
50	chr6:5183663..5185555-chr6:5194773..5196690,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3691-5p	chr6:5148520-5148542	MIMAT0018120
hsa-miR-3691-3p	chr6:5148480-5148501	MIMAT0019224

No data

Variant related genes	Relation type
MIR3691	TF binding region
LYRM4	TF binding region
MIR3691	CpG island
LYRM4	CpG island
ENSG00000214113	chromatin interactions
ENSG00000145982	chromatin interactions
ENSG00000124787	chromatin interactions
CSPG5	Mature miRNA region

Extended variants
information (count: 4011 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:4011 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75075478	chr6:5114674-5114675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs72809833	chr6:5114709-5114710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536427672	chr6:5114715-5114716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548287273	chr6:5114729-5114730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569744324	chr6:5114737-5114738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553199070	chr6:5114744-5114745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190630278	chr6:5114803-5114804	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530899242	chr6:5114876-5114877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs368980779	chr6:5114880-5114881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs552271913	chr6:5114909-5114910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs376343810	chr6:5114919-5114920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570685331	chr6:5114928-5114929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201424296	chr6:5114980-5114981	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182807268	chr6:5115014-5115015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553570192	chr6:5115035-5115036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs72809834	chr6:5115087-5115088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536171451	chr6:5115117-5115118	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145867766	chr6:5115131-5115132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs72809836	chr6:5115146-5115147	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs576121881	chr6:5115203-5115204	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs374956534	chr6:5115215-5115216	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35415538	chr6:5115282-5115283	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs543513921	chr6:5115303-5115304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369363626	chr6:5115327-5115328	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs372879787	chr6:5115339-5115340	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558687634	chr6:5115378-5115379	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs148973839	chr6:5115445-5115446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs540860327	chr6:5115541-5115542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs457759	chr6:5115596-5115597	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs529925401	chr6:5115610-5115611	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs541759111	chr6:5115657-5115658	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs563311527	chr6:5115670-5115671	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs142932065	chr6:5115671-5115672	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370826501	chr6:5115711-5115712	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs373428644	chr6:5115747-5115748	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs552208559	chr6:5115814-5115815	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs570600868	chr6:5115822-5115823	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528631440	chr6:5115899-5115900	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372328761	chr6:5115946-5115947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs9392655	chr6:5115987-5115988	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568669907	chr6:5115988-5115989	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs535739866	chr6:5115995-5115996	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs557708042	chr6:5115996-5115997	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs117443973	chr6:5116050-5116051	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574295409	chr6:5116069-5116070	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs193077829	chr6:5116080-5116081	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558628083	chr6:5116095-5116096	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576863372	chr6:5116122-5116123	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533783568	chr6:5116179-5116180	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541149795	chr6:5116255-5116256	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5098600-5117000	Weak transcription	Fetal Brain Female	brain
2	chr6:5099000-5130000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr6:5101800-5132200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:5103200-5132800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr6:5105200-5115800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:5105200-5131400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:5105800-5125600	Weak transcription	Ovary	ovary
8	chr6:5105800-5128200	Weak transcription	Primary B cells from cord blood	blood
9	chr6:5107800-5132000	Weak transcription	Pancreas	Pancrea
10	chr6:5109000-5116400	Weak transcription	Brain Germinal Matrix	brain
11	chr6:5109200-5118600	Weak transcription	Esophagus	oesophagus
12	chr6:5109200-5121800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr6:5109200-5130200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr6:5109400-5121600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr6:5110200-5121800	Weak transcription	Brain Anterior Caudate	brain
16	chr6:5110400-5121600	Weak transcription	Adipose Nuclei	Adipose
17	chr6:5111200-5119200	Weak transcription	Fetal Intestine Large	intestine
18	chr6:5112200-5128600	Weak transcription	Primary T cells from cord blood	blood
19	chr6:5112600-5115600	Weak transcription	Lung	lung
20	chr6:5112600-5122800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:5112600-5123400	Weak transcription	Fetal Lung	lung
22	chr6:5112800-5117200	Weak transcription	Placenta	Placenta
23	chr6:5112800-5121600	Weak transcription	Spleen	Spleen
24	chr6:5112800-5122800	Weak transcription	Right Ventricle	heart
25	chr6:5112800-5124800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr6:5112800-5125400	Weak transcription	Right Atrium	heart
27	chr6:5112800-5132600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:5113000-5116800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:5113000-5119000	Weak transcription	A549	lung
30	chr6:5113000-5130400	Weak transcription	Gastric	stomach
31	chr6:5113200-5115000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:5113200-5115000	Weak transcription	HepG2	liver
33	chr6:5113200-5115600	Weak transcription	Left Ventricle	heart
34	chr6:5113200-5118600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:5113200-5122200	Weak transcription	Fetal Stomach	stomach
36	chr6:5113200-5122800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr6:5113200-5122800	Weak transcription	Fetal Muscle Leg	muscle
38	chr6:5113200-5124800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:5113200-5130400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr6:5113400-5122800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:5113400-5132400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr6:5113600-5115800	Weak transcription	Fetal Intestine Small	intestine
43	chr6:5113600-5117000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr6:5113600-5122800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:5113800-5116800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:5113800-5125400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr6:5114200-5116000	Enhancers	Fetal Heart	heart
48	chr6:5115000-5116000	Enhancers	HepG2	liver
49	chr6:5115000-5117600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:5115600-5115800	Enhancers	Liver	Liver

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