Variant report

Variant	esv3373493
Chromosome Location	chr7:150075044-150077892
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:938)
CpG islands
(count:550)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:938 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:150075167-150075634	K562	blood:	n/a	n/a
2	ARID3A	chr7:150075983-150076464	K562	blood:	n/a	n/a
3	ARID3A	chr7:150074970-150075677	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:150076809-150077078	K562	blood:	n/a	n/a
5	ARID3A	chr7:150075995-150076571	HepG2	liver:	n/a	n/a
6	ATF2	chr7:150075152-150076221	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:150077533-150077989	GM12878	blood:	n/a	n/a
8	ATF2	chr7:150074996-150075502	GM12878	blood:	n/a	n/a
9	ATF2	chr7:150075293-150076092	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:150076104-150076400	H1-hESC	embryonic stem cell:	n/a	chr7:150076382-150076391
11	ATF3	chr7:150076161-150076384	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:150075872-150076482	K562	blood:	n/a	chr7:150076382-150076391
13	BCL11A	chr7:150077606-150077893	GM12878	blood:	n/a	n/a
14	BCL3	chr7:150075900-150076590	GM12878	blood:	n/a	chr7:150076205-150076218
15	BCL3	chr7:150075192-150076092	A549	lung:	n/a	n/a
16	BCLAF1	chr7:150075027-150076582	GM12878	blood:	n/a	chr7:150076205-150076218
17	BCLAF1	chr7:150077538-150078018	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:150076913-150077215	K562	blood:	n/a	n/a
19	BHLHE40	chr7:150076922-150078036	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:150075235-150075463	HepG2	liver:	n/a	chr7:150075260-150075276
21	BHLHE40	chr7:150075894-150076678	GM12878	blood:	n/a	chr7:150076270-150076286
22	BHLHE40	chr7:150075291-150076655	K562	blood:	n/a	chr7:150076270-150076286
23	BRCA1	chr7:150075182-150076489	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr7:150076766-150076958	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:150075293-150076113	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr7:150075168-150076621	K562	blood:	n/a	n/a
27	CCNT2	chr7:150075283-150075577	K562	blood:	n/a	chr7:150075484-150075493
28	CCNT2	chr7:150075835-150077110	K562	blood:	n/a	n/a
29	CEBPB	chr7:150075329-150076254	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:150075327-150075792	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr7:150077140-150077232	K562	blood:	n/a	n/a
32	CEBPB	chr7:150076083-150076121	K562	blood:	n/a	n/a
33	CEBPD	chr7:150076331-150076965	HepG2	liver:	n/a	n/a
34	CEBPD	chr7:150075889-150076314	HepG2	liver:	n/a	n/a
35	CEBPD	chr7:150075163-150075455	HepG2	liver:	n/a	n/a
36	CEBPD	chr7:150076002-150076230	HepG2	liver:	n/a	n/a
37	CHD1	chr7:150074574-150078119	GM12878	blood:	n/a	n/a
38	CHD1	chr7:150075389-150076064	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:150075240-150075654	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:150075175-150076628	GM12878	blood:	n/a	n/a
41	CHD2	chr7:150075764-150077171	K562	blood:	n/a	n/a
42	CHD2	chr7:150076937-150077078	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr7:150075328-150075562	HepG2	liver:	n/a	n/a
44	CHD2	chr7:150075940-150076538	HepG2	liver:	n/a	n/a
45	CHD2	chr7:150075240-150076733	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr7:150075891-150076553	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr7:150075374-150075445	K562	blood:	n/a	n/a
48	CHD2	chr7:150077059-150077957	GM12878	blood:	n/a	n/a
49	CREB1	chr7:150075122-150076766	HepG2	liver:	n/a	n/a
50	CREB1	chr7:150075287-150075594	A549	lung:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150076855-150076905	HEEpiC	esophagus:	n/a
2	chr7:150076855-150076905	HEEpiC	esophagus:	n/a
3	chr7:150076338-150076388	HRPEpiC	eye:	n/a
4	chr7:150076495-150076545	AG10803	skin:	n/a
5	chr7:150076435-150076485	CMK	blood:	n/a
6	chr7:150076855-150076905	AG09319	gingival:	n/a
7	chr7:150076495-150076545	HepG2	liver:	n/a
8	chr7:150076435-150076485	ProgFib	skin:	n/a
9	chr7:150076338-150076388	NB4	blood:	n/a
10	chr7:150076495-150076545	K562	blood:	n/a
11	chr7:150076855-150076905	U87	brain:	n/a
12	chr7:150076028-150076078	PrEC	prostate:	n/a
13	chr7:150076338-150076388	A549	lung:	n/a
14	chr7:150076028-150076078	MCF10A-Er-Src	breast:	n/a
15	chr7:150075335-150075385	HEEpiC	esophagus:	n/a
16	chr7:150077602-150077652	ECC-1	luminal epithelium:	n/a
17	chr7:150076495-150076545	U87	brain:	n/a
18	chr7:150076435-150076485	HepG2	liver:	n/a
19	chr7:150076028-150076078	T-47D	breast:	n/a
20	chr7:150076855-150076905	AoSMC	blood vessel:	n/a
21	chr7:150075335-150075385	GM12891	blood:	n/a
22	chr7:150076495-150076545	HCF	heart:	n/a
23	chr7:150076338-150076388	SK-N-SH	brain:	n/a
24	chr7:150075335-150075385	HUVEC	blood vessel:	n/a
25	chr7:150076855-150076905	HUVEC	blood vessel:	n/a
26	chr7:150077602-150077652	ProgFib	skin:	n/a
27	chr7:150076495-150076545	ovcar-3	ovarian:	n/a
28	chr7:150076360-150076410	HRPEpiC	eye:	n/a
29	chr7:150076855-150076905	T-47D	breast:	n/a
30	chr7:150076338-150076388	HepG2	liver:	n/a
31	chr7:150076495-150076545	ProgFib	skin:	n/a
32	chr7:150076855-150076905	Jurkat	blood:	n/a
33	chr7:150076855-150076905	AG10803	skin:	n/a
34	chr7:150076338-150076388	MCF-7	breast:	n/a
35	chr7:150077602-150077652	Hela-S3	cervix:	n/a
36	chr7:150077602-150077652	PFSK-1	brain:	n/a
37	chr7:150077602-150077652	NH-A	brain:	n/a
38	chr7:150077602-150077652	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:150076028-150076078	SAEC	small airway:	n/a
40	chr7:150077602-150077652	AG04450	lung:	fetal
41	chr7:150075335-150075385	NH-A	brain:	n/a
42	chr7:150076646-150076696	HCF	heart:	n/a
43	chr7:150077602-150077652	GM12878	blood:	n/a
44	chr7:150075335-150075385	ECC-1	luminal epithelium:	n/a
45	chr7:150076646-150076696	ovcar-3	ovarian:	n/a
46	chr7:150076360-150076410	HCM	heart:	n/a
47	chr7:150076646-150076696	AG09309	skin:	n/a
48	chr7:150076646-150076696	SK-N-SH	brain:	n/a
49	chr7:150077602-150077652	MCF10A-Er-Src	breast:	n/a
50	chr7:150076338-150076388	NHDF-neo	bronchial:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:43121396..43121896-chr7:150076079..150076580,2	Hela-S3	cervix:
2	chr7:150076049..150078828-chr7:151216255..151218028,2	K562	blood:
3	chr7:150053678..150054204-chr7:150075015..150075784,3	MCF-7	breast:
4	chr7:150018539..150023441-chr7:150073756..150077036,7	MCF-7	breast:
5	chr7:150054220..150054841-chr7:150074964..150075932,2	K562	blood:
6	chr7:150074371..150076020-chr7:150114930..150116474,2	MCF-7	breast:
7	chr7:150065873..150066638-chr7:150075580..150076156,2	NB4	blood:
8	chr16:88869570..88870304-chr7:150076110..150076610,2	Hela-S3	cervix:
9	chr7:150074289..150079503-chr7:150100156..150104408,10	MCF-7	breast:
10	chr7:150073288..150077950-chr7:150093880..150099928,8	MCF-7	breast:
11	chr11:910973..911787-chr7:150076009..150076583,2	NB4	blood:
12	chr7:150076502..150077064-chr7:150117931..150118573,2	MCF-7	breast:
13	chr7:150075531..150076123-chrX:100662734..100663410,2	Hela-S3	cervix:
14	chr7:150017073..150026383-chr7:150074145..150079980,13	MCF-7	breast:
15	chr7:150017819..150020177-chr7:150077421..150080084,2	MCF-7	breast:
16	chr7:150077875..150079475-chr7:150112498..150114188,2	MCF-7	breast:
17	chr11:9482102..9482787-chr7:150075710..150076563,2	Hela-S3	cervix:
18	chr7:150063876..150080670-chr7:150093696..150109118,65	MCF-7	breast:
19	chr7:150026422..150030526-chr7:150071487..150075243,4	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REPIN1-1	chr7:150076418-150076481	NONHSAT124127
2	lnc-RARRES2-3	chr7:150076943-150077277	ENSG00000239377.1
3	lnc-RARRES2-3	chr7:150076838-150077277	NONHSAT124128

No data

Variant related genes	Relation type
ZNF775	TF binding region
ZNF775	CpG island
ENSG00000106615	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000177830	chromatin interactions
ENSG00000188707	chromatin interactions
ENSG00000126945	chromatin interactions
ENSG00000102393	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000127399	chromatin interactions
ENSG00000214022	chromatin interactions
ENSG00000106526	chromatin interactions
ENSG00000167513	chromatin interactions
ENSG00000172262	chromatin interactions

Extended variants
information (count: 102 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:102 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538416408	chr7:150075075-150075076	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs558305944	chr7:150075090-150075091	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs138133130	chr7:150075138-150075139	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs79198823	chr7:150075156-150075157	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs557478785	chr7:150075160-150075161	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs149571771	chr7:150075166-150075167	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs557786476	chr7:150075203-150075204	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs543020143	chr7:150075227-150075228	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs572757598	chr7:150075229-150075230	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs187376773	chr7:150075243-150075244	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs201392992	chr7:150075274-150075275	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs559573624	chr7:150075286-150075287	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs144281910	chr7:150075288-150075289	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs533580931	chr7:150075314-150075315	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs528816591	chr7:150075335-150075336	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs148756278	chr7:150075369-150075370	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs565463928	chr7:150075409-150075410	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs73172708	chr7:150075440-150075441	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs531172074	chr7:150075441-150075442	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs550357035	chr7:150075459-150075460	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs113325829	chr7:150075515-150075516	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs529623715	chr7:150075537-150075538	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs11773825	chr7:150075576-150075577	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs566155400	chr7:150075646-150075647	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs529639648	chr7:150075649-150075650	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs544914961	chr7:150075685-150075686	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs191992905	chr7:150075711-150075712	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs558461897	chr7:150075724-150075725	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs573041225	chr7:150075743-150075744	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs143697573	chr7:150075750-150075751	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs370849768	chr7:150075838-150075839	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs557137126	chr7:150075840-150075841	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs145987286	chr7:150075862-150075863	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs551455173	chr7:150075922-150075923	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs542630508	chr7:150075933-150075934	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs375620014	chr7:150075964-150075965	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs573310101	chr7:150076021-150076022	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs113565794	chr7:150076028-150076029	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs545707593	chr7:150076029-150076030	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs565628272	chr7:150076141-150076142	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs531085251	chr7:150076145-150076146	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs77166832	chr7:150076149-150076150	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs57274670	chr7:150076156-150076157	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs371433588	chr7:150076164-150076165	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs529771876	chr7:150076176-150076177	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs546409738	chr7:150076184-150076185	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs566120281	chr7:150076188-150076189	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs532024956	chr7:150076192-150076193	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs373736569	chr7:150076193-150076194	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs114875396	chr7:150076198-150076199	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Congenital long qt syndrome	19214780	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:656 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150068200-150075400	Weak transcription	HMEC	breast
2	chr7:150068800-150075200	Weak transcription	NH-A	brain
3	chr7:150069000-150075200	Weak transcription	Fetal Brain Male	brain
4	chr7:150070000-150075400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:150070000-150075400	Weak transcription	Aorta	Aorta
6	chr7:150070400-150075200	Weak transcription	Psoas Muscle	Psoas
7	chr7:150070400-150075600	Weak transcription	Ovary	ovary
8	chr7:150070600-150075200	Weak transcription	Small Intestine	intestine
9	chr7:150070600-150075600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:150070800-150075200	Weak transcription	NHEK	skin
11	chr7:150071400-150075200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:150071400-150075400	Weak transcription	Right Ventricle	heart
13	chr7:150071600-150075200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr7:150071600-150075200	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr7:150071600-150075200	Weak transcription	Colon Smooth Muscle	Colon
16	chr7:150071800-150075200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr7:150071800-150075200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:150071800-150075200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:150071800-150075200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr7:150071800-150075200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr7:150071800-150075200	Weak transcription	Right Atrium	heart
22	chr7:150071800-150075200	Weak transcription	NHDF-Ad	bronchial
23	chr7:150071800-150075400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr7:150071800-150075400	Weak transcription	Brain Angular Gyrus	brain
25	chr7:150071800-150075400	Weak transcription	Fetal Brain Female	brain
26	chr7:150071800-150075600	Weak transcription	Esophagus	oesophagus
27	chr7:150071800-150076000	Weak transcription	Gastric	stomach
28	chr7:150072000-150075200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr7:150072000-150075200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr7:150072000-150075200	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:150072000-150075200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr7:150072000-150075200	Weak transcription	Brain Substantia Nigra	brain
33	chr7:150072000-150075400	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:150072000-150075400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:150072000-150075400	Weak transcription	NHLF	lung
36	chr7:150072400-150075200	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr7:150072400-150075400	Enhancers	Primary B cells from peripheral blood	blood
38	chr7:150072600-150075200	Weak transcription	Fetal Stomach	stomach
39	chr7:150072600-150075600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:150072800-150075200	Enhancers	Primary T cells fromperipheralblood	blood
41	chr7:150072800-150075200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr7:150072800-150075200	Enhancers	Duodenum Mucosa	Duodenum
43	chr7:150072800-150075200	Enhancers	Fetal Intestine Large	intestine
44	chr7:150072800-150075200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr7:150072800-150075200	Enhancers	HSMMtube	muscle
46	chr7:150072800-150075400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr7:150072800-150075600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr7:150073000-150075200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:150073000-150075200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr7:150073000-150075200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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