Variant report

Variant	esv1849077
Chromosome Location	chr7:5409569-5434107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:194)
CpG islands
(count:1464)
Chromatin interactive
region (count:56)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:194 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr7:5420871-5421226	K562	blood:	n/a	n/a
2	CCNT2	chr7:5415752-5415924	K562	blood:	n/a	n/a
3	CCNT2	chr7:5427875-5427877	K562	blood:	n/a	n/a
4	CCNT2	chr7:5428102-5428108	K562	blood:	n/a	n/a
5	CEBPB	chr7:5429206-5429215	HepG2	liver:	n/a	n/a
6	CEBPB	chr7:5422407-5422410	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr7:5434063-5434079	HepG2	liver:	n/a	n/a
8	CTCF	chr7:5409700-5409850	RPTEC	kidney:	n/a	n/a
9	CTCF	chr7:5427607-5427700	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr7:5415555-5415619	Lung_OC	lung:	n/a	n/a
11	CTCF	chr7:5428311-5428362	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr7:5432192-5432249	LNCaP	prostate:	n/a	n/a
13	CTCF	chr7:5429180-5429330	GM12875	blood:	n/a	n/a
14	CTCF	chr7:5422560-5422710	SK-N-SH_RA	brain:	n/a	n/a
15	E2F6	chr7:5428445-5428768	H1-hESC	embryonic stem cell:	n/a	n/a
16	EBF1	chr7:5410225-5410449	GM12878	blood:	n/a	n/a
17	EGR1	chr7:5421797-5422021	K562	blood:	n/a	chr7:5421929-5421939 chr7:5421929-5421942
18	EGR1	chr7:5421852-5422006	K562	blood:	n/a	chr7:5421929-5421939 chr7:5421929-5421942
19	ELF1	chr7:5410086-5410374	GM12878	blood:	n/a	n/a
20	FOXP2	chr7:5421712-5422309	SK-N-MC	brain:	n/a	n/a
21	GABPA	chr7:5427177-5429069	H1-hESC	embryonic stem cell:	n/a	n/a
22	GABPA	chr7:5427270-5429069	H1-hESC	embryonic stem cell:	n/a	n/a
23	GABPA	chr7:5415693-5415971	H1-hESC	embryonic stem cell:	n/a	n/a
24	GTF3C2	chr7:5420902-5421279	K562	blood:	n/a	n/a
25	HMGN3	chr7:5421944-5422128	K562	blood:	n/a	n/a
26	HMGN3	chr7:5427392-5427475	K562	blood:	n/a	n/a
27	MAX	chr7:5428364-5428840	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAX	chr7:5428117-5428810	H1-hESC	embryonic stem cell:	n/a	n/a
29	MAX	chr7:5433896-5434071	NB4	blood:	n/a	n/a
30	MAZ	chr7:5422297-5422301	K562	blood:	n/a	n/a
31	MAZ	chr7:5415355-5415804	IMR90	lung:	n/a	n/a
32	MXI1	chr7:5422085-5422227	K562	blood:	n/a	chr7:5422099-5422114
33	NR3C1	chr7:5414880-5415154	A549	lung:	n/a	n/a
34	PBX3	chr7:5424434-5424626	GM12878	blood:	n/a	n/a
35	POLR2A	chr7:5427850-5428054	HCT-116	colon:	n/a	n/a
36	POLR2A	chr7:5432832-5433134	H1-neurons	neurons:	n/a	n/a
37	POLR2A	chr7:5412136-5412170	HepG2	liver:	n/a	n/a
38	POLR2A	chr7:5433503-5433751	HCT-116	colon:	n/a	n/a
39	POLR2A	chr7:5432835-5432955	MCF-7	breast:	n/a	n/a
40	POLR2A	chr7:5415112-5415146	HepG2	liver:	n/a	n/a
41	POLR2A	chr7:5427355-5427448	A549	lung:	n/a	n/a
42	POLR2A	chr7:5421634-5422802	H1-neurons	neurons:	n/a	n/a
43	POLR2A	chr7:5417588-5417611	HepG2	liver:	n/a	n/a
44	POLR2A	chr7:5410159-5410530	GM12878	blood:	n/a	n/a
45	POLR2A	chr7:5430723-5430786	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr7:5430024-5430904	PANC-1	pancreas:	n/a	n/a
47	POLR2A	chr7:5422377-5422511	MCF-7	breast:	n/a	n/a
48	POLR2A	chr7:5430057-5430938	PANC-1	pancreas:	n/a	n/a
49	POLR2A	chr7:5432866-5433885	PANC-1	pancreas:	n/a	n/a
50	POLR2A	chr7:5431782-5432139	HepG2	liver:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5414016-5414066	GM12891	blood:	n/a
2	chr7:5428633-5428683	RPTEC	kidney:	n/a
3	chr7:5415468-5415518	PrEC	prostate:	n/a
4	chr7:5415468-5415518	Jurkat	blood:	n/a
5	chr7:5410861-5410911	SK-N-SH_RA	brain:	n/a
6	chr7:5429036-5429086	NH-A	brain:	n/a
7	chr7:5413105-5413155	NH-A	brain:	n/a
8	chr7:5413872-5413922	PANC-1	pancreas:	n/a
9	chr7:5410694-5410744	GM12891	blood:	n/a
10	chr7:5413639-5413689	SKMC	muscle:	n/a
11	chr7:5422234-5422284	LNCaP	prostate:	n/a
12	chr7:5411097-5411147	Hepatocyte	liver:	n/a
13	chr7:5417178-5417228	SAEC	small airway:	n/a
14	chr7:5417105-5417155	HCPEpiC	choroid plexus:	n/a
15	chr7:5410988-5411038	HAEpiC	amniotic membrane:	n/a
16	chr7:5413105-5413155	ProgFib	skin:	n/a
17	chr7:5428633-5428683	HIPEpiC	eye:	n/a
18	chr7:5417178-5417228	NH-A	brain:	n/a
19	chr7:5428014-5428064	AG04450	lung:	fetal
20	chr7:5410694-5410744	T-47D	breast:	n/a
21	chr7:5428633-5428683	AoSMC	blood vessel:	n/a
22	chr7:5417105-5417155	LNCaP	prostate:	n/a
23	chr7:5414170-5414220	HMEC	breast:	n/a
24	chr7:5413105-5413155	Caco-2	colon:	n/a
25	chr7:5428014-5428064	HRCEpiC	kidney:	n/a
26	chr7:5413639-5413689	BJ	skin:	n/a
27	chr7:5413639-5413689	GM12892	blood:	n/a
28	chr7:5413872-5413922	Hela-S3	cervix:	n/a
29	chr7:5432820-5432870	AG09319	gingival:	n/a
30	chr7:5426831-5426881	HRE	kidney:	n/a
31	chr7:5428014-5428064	GM19239	blood:	n/a
32	chr7:5414016-5414066	NHDF-neo	bronchial:	n/a
33	chr7:5414174-5414224	AG09319	gingival:	n/a
34	chr7:5410694-5410744	AG10803	skin:	n/a
35	chr7:5414174-5414224	AG10803	skin:	n/a
36	chr7:5414174-5414224	HCM	heart:	n/a
37	chr7:5427244-5427294	HIPEpiC	eye:	n/a
38	chr7:5410861-5410911	T-47D	breast:	n/a
39	chr7:5414016-5414066	PANC-1	pancreas:	n/a
40	chr7:5411097-5411147	ECC-1	luminal epithelium:	n/a
41	chr7:5413639-5413689	BE2_C	brain:	n/a
42	chr7:5410988-5411038	SK-N-MC	brain:	n/a
43	chr7:5410694-5410744	NH-A	brain:	n/a
44	chr7:5414170-5414220	HUVEC	blood vessel:	n/a
45	chr7:5415468-5415518	HepG2	liver:	n/a
46	chr7:5410694-5410744	GM12892	blood:	n/a
47	chr7:5414016-5414066	PFSK-1	brain:	n/a
48	chr7:5413639-5413689	Jurkat	blood:	n/a
49	chr7:5428014-5428064	K562	blood:	n/a
50	chr7:5429036-5429086	A549	lung:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:5407810..5410158-chr7:5453084..5455426,2	MCF-7	breast:
2	chr7:5430820..5432432-chr7:5432742..5434912,2	K562	blood:
3	chr7:5387483..5389970-chr7:5410326..5412582,2	MCF-7	breast:
4	chr7:5404432..5407247-chr7:5409025..5411677,2	K562	blood:
5	chr7:5423295..5425755-chr7:5463506..5465476,2	K562	blood:
6	chr7:5408465..5410922-chr7:5414516..5417131,3	K562	blood:
7	chr7:5422471..5424795-chr7:5463904..5465499,3	K562	blood:
8	chr7:5414064..5415577-chr7:5417568..5419107,2	K562	blood:
9	chr21:43781757..43784363-chr7:5418790..5420733,2	MCF-7	breast:
10	chr7:5414075..5415824-chr7:5461011..5462716,2	MCF-7	breast:
11	chr7:5409222..5410746-chr7:5457782..5460561,2	MCF-7	breast:
12	chr7:5430729..5434402-chr7:5435453..5437686,4	MCF-7	breast:
13	chr7:5419562..5424276-chr7:5462194..5465605,6	MCF-7	breast:
14	chr7:5420196..5424221-chr7:5463874..5468257,7	MCF-7	breast:
15	chr7:5421329..5423129-chr7:5426489..5429179,2	K562	blood:
16	chr7:5412818..5415236-chr7:5460395..5461956,2	MCF-7	breast:
17	chr7:5427166..5429954-chr7:5431918..5434543,3	MCF-7	breast:
18	chr7:5396974..5399179-chr7:5416241..5418171,2	MCF-7	breast:
19	chr7:5408591..5410426-chr7:5492807..5494818,2	K562	blood:
20	chr7:5420732..5423186-chr7:5425259..5427446,2	MCF-7	breast:
21	chr7:5418980..5420716-chr7:5420847..5423992,3	K562	blood:
22	chr7:5415556..5417530-chr7:5418866..5421524,3	MCF-7	breast:
23	chr7:5400868..5403909-chr7:5406532..5410204,3	MCF-7	breast:
24	chr7:5420682..5423339-chr7:5431916..5434654,3	MCF-7	breast:
25	chr7:5416359..5418538-chr7:5463769..5465287,2	MCF-7	breast:
26	chr7:5406566..5411039-chr7:5411257..5413625,4	MCF-7	breast:
27	chr7:5410585..5413099-chr7:5421025..5423584,3	MCF-7	breast:
28	chr7:5406257..5408361-chr7:5427751..5430730,2	MCF-7	breast:
29	chr7:5422026..5424768-chr7:5491088..5492724,2	K562	blood:
30	chr7:5419534..5423325-chr7:5460448..5463513,3	MCF-7	breast:
31	chr7:5420682..5423339-chr7:5431916..5434654,3	MCF-7	breast:
32	chr7:5407651..5410118-chr7:5415216..5418173,2	MCF-7	breast:
33	chr7:5408465..5410922-chr7:5414516..5417131,3	K562	blood:
34	chr7:5428152..5429787-chr7:5466437..5469145,2	K562	blood:
35	chr7:5420460..5423379-chr7:5428515..5430331,2	MCF-7	breast:
36	chr7:5406566..5411039-chr7:5411257..5413625,4	MCF-7	breast:
37	chr7:5417354..5418908-chr7:5419651..5421890,2	MCF-7	breast:
38	chr7:5420732..5423186-chr7:5425259..5427446,2	MCF-7	breast:
39	chr7:5431460..5434900-chr7:5435582..5438933,4	MCF-7	breast:
40	chr7:5415556..5417530-chr7:5418866..5421524,3	MCF-7	breast:
41	chr7:5430820..5432432-chr7:5432742..5434912,2	K562	blood:
42	chr7:5424305..5426249-chr7:5463698..5466479,2	MCF-7	breast:
43	chr7:5427419..5438627-chr7:5461902..5471481,26	MCF-7	breast:
44	chr7:5414064..5415577-chr7:5417568..5419107,2	K562	blood:
45	chr7:5404389..5406016-chr7:5411651..5413603,2	MCF-7	breast:
46	chr7:5420460..5423379-chr7:5428515..5430331,2	MCF-7	breast:
47	chr7:5409422..5411964-chr7:5414870..5417131,2	K562	blood:
48	chr7:5417951..5419476-chr7:5427176..5429581,2	K562	blood:
49	chr7:5418980..5420716-chr7:5420847..5423992,3	K562	blood:
50	chr7:5407651..5410118-chr7:5415216..5418173,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC29A4-3	chr7:5414324-5416320	NONHSAT118913

No data

Variant related genes	Relation type
TNRC18	TF binding region
TNRC18	CpG island
ENSG00000182095	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000188365	chromatin interactions
ENSG00000273084	chromatin interactions
ENSG00000241269	chromatin interactions
ENSG00000234432	chromatin interactions

Extended variants
information (count: 1338 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11976015	chr7:5409569-5409570	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs187544055	chr7:5409587-5409588	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs576457552	chr7:5409588-5409589	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs112474218	chr7:5409590-5409591	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs192292704	chr7:5409611-5409612	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs541646673	chr7:5409616-5409617	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs574504320	chr7:5409617-5409618	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs542008794	chr7:5409630-5409631	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs200047842	chr7:5409643-5409644	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560354199	chr7:5409651-5409652	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs527798766	chr7:5409661-5409662	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs185141114	chr7:5409663-5409664	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs188411117	chr7:5409673-5409674	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs540796718	chr7:5409738-5409739	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs531788890	chr7:5409757-5409758	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs559487217	chr7:5409764-5409765	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs139656693	chr7:5409773-5409774	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs192646042	chr7:5409834-5409835	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs547992801	chr7:5409879-5409880	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs566411513	chr7:5409880-5409881	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs184781296	chr7:5409896-5409897	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs149232899	chr7:5409907-5409908	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs58182076	chr7:5409937-5409938	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs114819957	chr7:5409993-5409994	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs372399028	chr7:5409995-5409996	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs200279443	chr7:5410013-5410014	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs368065450	chr7:5410044-5410045	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs188349737	chr7:5410046-5410047	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs371935752	chr7:5410097-5410098	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs201136741	chr7:5410103-5410104	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561575250	chr7:5410135-5410136	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs79611206	chr7:5410137-5410138	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs180705972	chr7:5410178-5410179	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs530736998	chr7:5410179-5410180	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs531801163	chr7:5410187-5410188	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs200236599	chr7:5410196-5410197	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs543843677	chr7:5410235-5410236	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs562218624	chr7:5410248-5410249	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs139524229	chr7:5410253-5410254	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547812685	chr7:5410273-5410274	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs373532696	chr7:5410286-5410287	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs376686580	chr7:5410307-5410308	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533386033	chr7:5410327-5410328	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368368703	chr7:5410328-5410329	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551812785	chr7:5410339-5410340	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs61745241	chr7:5410365-5410366	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373188558	chr7:5410369-5410370	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376138970	chr7:5410370-5410371	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs370468294	chr7:5410378-5410379	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372684130	chr7:5410390-5410391	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	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
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21525872	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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5372200-5422000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr7:5372200-5424200	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr7:5376800-5411600	Weak transcription	K562	blood
4	chr7:5385000-5418000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:5386600-5418000	Strong transcription	Dnd41	blood
6	chr7:5390400-5421800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:5392400-5420000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:5395000-5418000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr7:5395000-5420400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr7:5395000-5421800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:5395000-5421800	Weak transcription	Psoas Muscle	Psoas
12	chr7:5395000-5421800	Weak transcription	Right Atrium	heart
13	chr7:5395000-5422400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:5395200-5418000	Strong transcription	Fetal Muscle Trunk	muscle
15	chr7:5395200-5419200	Strong transcription	Fetal Muscle Leg	muscle
16	chr7:5395200-5422400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr7:5395600-5421000	Strong transcription	Fetal Intestine Small	intestine
18	chr7:5398200-5420400	Weak transcription	Fetal Heart	heart
19	chr7:5401400-5410000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:5401400-5421800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:5402200-5409600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:5402200-5409600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr7:5402200-5410400	Weak transcription	Small Intestine	intestine
24	chr7:5402200-5412800	Weak transcription	NH-A	brain
25	chr7:5402200-5415200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr7:5402200-5421800	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr7:5402600-5409800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:5402600-5409800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr7:5402600-5412200	Weak transcription	Brain Substantia Nigra	brain
30	chr7:5402800-5409800	Weak transcription	Aorta	Aorta
31	chr7:5402800-5410000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:5403000-5409600	Weak transcription	Stomach Mucosa	stomach
33	chr7:5403000-5424400	Weak transcription	Hela-S3	cervix
34	chr7:5403800-5409600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr7:5403800-5421800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr7:5404000-5412200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:5404200-5409800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:5404200-5416000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr7:5404600-5421800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr7:5405000-5409800	Weak transcription	Right Ventricle	heart
41	chr7:5405000-5416200	Strong transcription	Fetal Lung	lung
42	chr7:5405800-5409800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr7:5406000-5419200	Strong transcription	Fetal Stomach	stomach
44	chr7:5406200-5418000	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr7:5406200-5418000	Strong transcription	Placenta	Placenta
46	chr7:5406200-5418000	Strong transcription	Fetal Thymus	thymus
47	chr7:5406400-5410000	Weak transcription	Ovary	ovary
48	chr7:5406600-5409600	Weak transcription	Brain Cingulate Gyrus	brain
49	chr7:5406600-5409600	Weak transcription	Colon Smooth Muscle	Colon
50	chr7:5406600-5409800	Weak transcription	Brain Hippocampus Middle	brain

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