Variant report

Variant	nsv608059
Chromosome Location	chr7:102470455-102504773
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102478846-102479241	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102500720-102501319	HepG2	liver:	n/a	n/a
3	ATF2	chr7:102475368-102475893	GM12878	blood:	n/a	n/a
4	ATF2	chr7:102475399-102475848	GM12878	blood:	n/a	n/a
5	ATF2	chr7:102484177-102484790	GM12878	blood:	n/a	n/a
6	ATF2	chr7:102484200-102484713	GM12878	blood:	n/a	n/a
7	ATF2	chr7:102481620-102482163	GM12878	blood:	n/a	n/a
8	BATF	chr7:102481731-102482084	GM12878	blood:	n/a	n/a
9	BATF	chr7:102475444-102475777	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
10	BATF	chr7:102484252-102484610	GM12878	blood:	n/a	n/a
11	BATF	chr7:102475426-102475852	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
12	BATF	chr7:102484259-102484624	GM12878	blood:	n/a	n/a
13	BATF	chr7:102481751-102482055	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:102475417-102475810	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:102475497-102475744	GM12878	blood:	n/a	n/a
16	BCL11A	chr7:102484332-102484641	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:102481679-102482030	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:102484258-102484654	GM12878	blood:	n/a	n/a
19	BCL3	chr7:102484358-102484686	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:102481611-102482122	GM12878	blood:	n/a	n/a
21	BCLAF1	chr7:102484307-102484685	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:102475385-102475792	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:102475416-102475745	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:102484310-102484623	GM12878	blood:	n/a	n/a
25	CBX3	chr7:102475384-102475952	HCT-116	colon:	n/a	n/a
26	CEBPB	chr7:102475352-102475875	HCT-116	colon:	n/a	n/a
27	CEBPB	chr7:102487455-102487714	K562	blood:	n/a	n/a
28	CEBPB	chr7:102476707-102477443	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:102484429-102484624	GM12878	blood:	n/a	n/a
30	CEBPB	chr7:102500896-102501291	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:102487437-102487753	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:102480836-102481048	A549	lung:	n/a	n/a
33	CEBPB	chr7:102487522-102487689	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:102499620-102499901	HepG2	liver:	n/a	chr7:102499752-102499763
35	CEBPB	chr7:102476896-102477453	A549	lung:	n/a	n/a
36	CEBPB	chr7:102487440-102487724	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:102476740-102477413	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr7:102476872-102477326	A549	lung:	n/a	n/a
39	CEBPB	chr7:102480675-102481219	A549	lung:	n/a	n/a
40	CHD1	chr7:102500873-102501370	IMR90	lung:	n/a	n/a
41	CHD2	chr7:102477042-102477313	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr7:102479704-102479749	LNCaP	prostate:	n/a	n/a
43	CTCF	chr7:102500116-102500176	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:102477080-102477230	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:102493152-102493172	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr7:102484023-102484056	GM20000	blood:	n/a	n/a
47	CTCF	chr7:102471580-102471730	GM12871	blood:	n/a	n/a
48	CUX1	chr7:102475438-102475720	GM12878	blood:	n/a	n/a
49	E2F4	chr7:102470411-102470486	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr7:102475513-102475706	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102477205-102477255	HCF	heart:	n/a
2	chr7:102500111-102500161	GM12891	blood:	n/a
3	chr7:102477205-102477255	NHBE	bronchial:	n/a
4	chr7:102477205-102477255	GM12891	blood:	n/a
5	chr7:102500111-102500161	GM12892	blood:	n/a
6	chr7:102477205-102477255	HRE	kidney:	n/a
7	chr7:102477205-102477255	U87	brain:	n/a
8	chr7:102500111-102500161	Caco-2	colon:	n/a
9	chr7:102477205-102477255	BE2_C	brain:	n/a
10	chr7:102477205-102477255	HL-60	blood:	n/a
11	chr7:102477205-102477255	SAEC	small airway:	n/a
12	chr7:102500111-102500161	SK-N-MC	brain:	n/a
13	chr7:102500111-102500161	HEK293	kidney:	embryo
14	chr7:102500111-102500161	HRPEpiC	eye:	n/a
15	chr7:102477205-102477255	ECC-1	luminal epithelium:	n/a
16	chr7:102500111-102500161	NB4	blood:	n/a
17	chr7:102500111-102500161	GM06990	blood:	n/a
18	chr7:102500111-102500161	NT2-D1	testis:	n/a
19	chr7:102477205-102477255	GM19239	blood:	n/a
20	chr7:102477205-102477255	SKMC	muscle:	n/a
21	chr7:102500111-102500161	NHBE	bronchial:	n/a
22	chr7:102500111-102500161	AG09319	gingival:	n/a
23	chr7:102500111-102500161	SKMC	muscle:	n/a
24	chr7:102500111-102500161	RPTEC	kidney:	n/a
25	chr7:102477205-102477255	NB4	blood:	n/a
26	chr7:102500111-102500161	HCT-116	colon:	n/a
27	chr7:102477205-102477255	NT2-D1	testis:	n/a
28	chr7:102477205-102477255	GM12892	blood:	n/a
29	chr7:102500111-102500161	CMK	blood:	n/a
30	chr7:102500111-102500161	BE2_C	brain:	n/a
31	chr7:102500111-102500161	MCF-7	breast:	n/a
32	chr7:102477205-102477255	HNPCEpiC	eye:	n/a
33	chr7:102500111-102500161	HCF	heart:	n/a
34	chr7:102500111-102500161	AG04450	lung:	fetal
35	chr7:102477205-102477255	T-47D	breast:	n/a
36	chr7:102477205-102477255	HPAEpiC	pulmonary alveolar:	n/a
37	chr7:102500111-102500161	AG09309	skin:	n/a
38	chr7:102477205-102477255	Caco-2	colon:	n/a
39	chr7:102477205-102477255	A549	lung:	n/a
40	chr7:102477205-102477255	LNCaP	prostate:	n/a
41	chr7:102500111-102500161	H1-hESC	embryonic stem cell:	embryo
42	chr7:102500111-102500161	HUVEC	blood vessel:	n/a
43	chr7:102500111-102500161	PFSK-1	brain:	n/a
44	chr7:102500111-102500161	NH-A	brain:	n/a
45	chr7:102477205-102477255	ovcar-3	ovarian:	n/a
46	chr7:102500111-102500161	LNCaP	prostate:	n/a
47	chr7:102477205-102477255	AoSMC	blood vessel:	n/a
48	chr7:102477205-102477255	SK-N-SH_RA	brain:	n/a
49	chr7:102477205-102477255	AG04449	skin:	fetal
50	chr7:102500111-102500161	NHDF-neo	bronchial:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
2	chr7:102473090..102475084-chr7:102477070..102479073,2	K562	blood:
3	chr20:52596990..52599653-chr7:102503790..102506770,2	MCF-7	breast:
4	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
5	chr7:102489665..102492498-chr7:102495300..102497224,2	K562	blood:
6	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
7	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
8	chr7:102473443..102475589-chr7:102480022..102482918,2	K562	blood:
9	chr7:102470809..102472496-chr7:102473289..102475572,2	MCF-7	breast:
10	chr7:102497049..102499033-chr7:102503041..102505939,2	K562	blood:
11	chr7:102483542..102485503-chr7:102492215..102494195,2	K562	blood:
12	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
13	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
14	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
15	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
16	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
17	chr7:102459530..102461153-chr7:102484743..102487140,2	K562	blood:
18	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
19	chr7:102471265..102473661-chr7:102474795..102476825,2	K562	blood:
20	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
21	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
22	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
23	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
24	chr7:102483542..102485503-chr7:102492215..102494195,2	K562	blood:
25	chr7:102489665..102492498-chr7:102495300..102497224,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM185A-1	chr7:102497897-102498202	NONHSAT122525

No data

Variant related genes	Relation type
RNU6-1136P	TF binding region
RN7SKP198	TF binding region
RNU6-1136P	CpG island
RN7SKP198	CpG island
ENSG00000252643	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000238324	chromatin interactions

Extended variants
information (count: 1153 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17136087	chr7:102470455-102470456	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370761888	chr7:102470477-102470478	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs531550055	chr7:102470478-102470479	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs141231770	chr7:102470520-102470521	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs201045193	chr7:102470529-102470530	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs76761058	chr7:102470542-102470543	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs191607019	chr7:102470622-102470623	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566599802	chr7:102470658-102470659	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534973775	chr7:102470660-102470661	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs534012345	chr7:102470664-102470665	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs555517342	chr7:102470708-102470709	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs183750996	chr7:102470712-102470713	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs189293811	chr7:102470793-102470794	Enhancers Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556772822	chr7:102470820-102470821	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs368784667	chr7:102470838-102470839	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146985636	chr7:102470850-102470851	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs192712929	chr7:102470872-102470873	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs560648460	chr7:102470887-102470888	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs138368403	chr7:102470906-102470907	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542701167	chr7:102470965-102470966	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs34422377	chr7:102470980-102470981	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560771870	chr7:102471051-102471052	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs143929719	chr7:102471063-102471064	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184772359	chr7:102471122-102471123	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs190047008	chr7:102471136-102471137	Enhancers Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs10487283	chr7:102471213-102471214	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs78081667	chr7:102471217-102471218	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371810533	chr7:102471234-102471235	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs534072819	chr7:102471239-102471240	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549411212	chr7:102471252-102471253	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567558589	chr7:102471286-102471287	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs552418190	chr7:102471312-102471313	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12669668	chr7:102471345-102471346	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs181759843	chr7:102471398-102471399	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147241982	chr7:102471430-102471431	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs78515005	chr7:102471435-102471436	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554448866	chr7:102471542-102471543	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75264223	chr7:102471585-102471586	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs542364162	chr7:102471620-102471621	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs560998284	chr7:102471623-102471624	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575964497	chr7:102471652-102471653	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147908712	chr7:102471661-102471662	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543379803	chr7:102471750-102471751	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs564518518	chr7:102471773-102471774	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs727175	chr7:102471780-102471781	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs545895548	chr7:102471842-102471843	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs3045618	chr7:102471873-102471874	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs62484940	chr7:102471878-102471879	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs62484941	chr7:102471879-102471880	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559125727	chr7:102471880-102471881	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102421600-102475600	Weak transcription	Fetal Thymus	thymus
2	chr7:102422000-102474800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:102422000-102476000	Weak transcription	Fetal Muscle Trunk	muscle
4	chr7:102447400-102477200	Weak transcription	Psoas Muscle	Psoas
5	chr7:102447800-102473000	Weak transcription	Placenta	Placenta
6	chr7:102448000-102479000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:102448200-102470800	Weak transcription	Small Intestine	intestine
8	chr7:102448400-102471800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr7:102450000-102475000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:102450200-102475600	Weak transcription	Esophagus	oesophagus
11	chr7:102452000-102480000	Weak transcription	Colon Smooth Muscle	Colon
12	chr7:102452200-102472800	Weak transcription	HSMMtube	muscle
13	chr7:102454200-102484600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:102454400-102475000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:102454600-102475000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:102454600-102475600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr7:102454800-102473200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:102455000-102475000	Weak transcription	NHLF	lung
19	chr7:102455000-102475000	Weak transcription	Osteobl	bone
20	chr7:102455200-102472800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:102455600-102473200	Weak transcription	HSMM	muscle
22	chr7:102459800-102481800	Weak transcription	Brain Substantia Nigra	brain
23	chr7:102460000-102474800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:102460000-102475000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr7:102460200-102475200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr7:102460400-102474600	Weak transcription	HUVEC	blood vessel
27	chr7:102460400-102477000	Weak transcription	Stomach Mucosa	stomach
28	chr7:102460400-102480800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:102460800-102480800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:102463200-102475000	Weak transcription	A549	lung
31	chr7:102466200-102473800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr7:102466400-102472200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:102466400-102475000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
34	chr7:102467400-102472000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:102467600-102473000	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr7:102467800-102471400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:102468000-102474600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr7:102468000-102475000	Weak transcription	HMEC	breast
39	chr7:102468000-102484600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr7:102468200-102471600	Weak transcription	Thymus	Thymus
41	chr7:102468200-102481000	Weak transcription	Brain Germinal Matrix	brain
42	chr7:102468800-102470600	Strong transcription	Monocytes-CD14+_RO01746	blood
43	chr7:102468800-102471800	Enhancers	Placenta Amnion	Placenta Amnion
44	chr7:102469000-102470800	Strong transcription	Primary T cells from cord blood	blood
45	chr7:102469000-102470800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr7:102469000-102471400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr7:102469000-102471600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:102469000-102471600	Strong transcription	Liver	Liver
49	chr7:102469000-102473400	Strong transcription	K562	blood
50	chr7:102469200-102470600	Strong transcription	Sigmoid Colon	Sigmoid Colon

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