Variant report

Variant	nsv429772
Chromosome Location	chr7:70250125-70357061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1322)
CpG islands
(count:1590)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1322 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70295432-70295731	HepG2	liver:	n/a	n/a
2	ATF2	chr7:70314491-70315160	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:70258518-70258992	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:70355291-70355733	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70322821-70323622	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr7:70264860-70265281	GM12878	blood:	n/a	n/a
7	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:70314522-70315080	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:70321901-70322317	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:70323194-70323394	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:70264853-70265265	GM12878	blood:	n/a	n/a
14	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
15	BATF	chr7:70264945-70265249	GM12878	blood:	n/a	n/a
16	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:70264916-70265214	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:70264860-70265214	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:70294194-70294616	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:70295491-70295711	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:70349178-70349357	K562	blood:	n/a	n/a
22	BHLHE40	chr7:70250727-70250742	A549	lung:	n/a	n/a
23	BHLHE40	chr7:70346608-70346813	K562	blood:	n/a	n/a
24	BHLHE40	chr7:70294189-70294529	K562	blood:	n/a	n/a
25	BRCA1	chr7:70277589-70277745	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr7:70294156-70294507	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:70294654-70294840	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:70259112-70259395	HepG2	liver:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
29	CEBPB	chr7:70259112-70259411	A549	lung:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
30	CEBPB	chr7:70259155-70259386	K562	blood:	n/a	chr7:70259259-70259270 chr7:70259258-70259271
31	CEBPB	chr7:70258165-70258365	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:70299414-70299733	MCF-7	breast:	n/a	chr7:70299603-70299614
33	CEBPB	chr7:70275646-70275979	HepG2	liver:	n/a	chr7:70275762-70275779
34	CEBPB	chr7:70295315-70295710	HepG2	liver:	n/a	chr7:70295552-70295563
35	CEBPB	chr7:70347542-70347743	HepG2	liver:	n/a	chr7:70347648-70347659
36	CEBPB	chr7:70299453-70299778	A549	lung:	n/a	chr7:70299603-70299614
37	CEBPB	chr7:70250424-70250609	Hela-S3	cervix:	n/a	chr7:70250526-70250537
38	CEBPB	chr7:70257703-70257833	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:70314283-70314959	H1-hESC	embryonic stem cell:	n/a	chr7:70314674-70314686
40	CEBPB	chr7:70311011-70311153	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr7:70250444-70250691	MCF-7	breast:	n/a	chr7:70250526-70250537
42	CEBPB	chr7:70294172-70294801	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr7:70299455-70299763	K562	blood:	n/a	chr7:70299603-70299614
44	CEBPB	chr7:70299422-70299775	IMR90	lung:	n/a	chr7:70299603-70299614
45	CEBPB	chr7:70254214-70254423	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:70250452-70250691	A549	lung:	n/a	chr7:70250526-70250537
47	CEBPB	chr7:70349310-70349766	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:70295452-70295643	HepG2	liver:	n/a	chr7:70295552-70295563
49	CEBPB	chr7:70275675-70275878	K562	blood:	n/a	chr7:70275762-70275779
50	CEBPB	chr7:70250396-70250674	HepG2	liver:	n/a	chr7:70250526-70250537

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70294511-70294561	AG10803	skin:	n/a
2	chr7:70257926-70257976	Hela-S3	cervix:	n/a
3	chr7:70252953-70253003	T-47D	breast:	n/a
4	chr7:70252335-70252385	BE2_C	brain:	n/a
5	chr7:70294511-70294561	AG10803	skin:	n/a
6	chr7:70257926-70257976	Hela-S3	cervix:	n/a
7	chr7:70252953-70253003	T-47D	breast:	n/a
8	chr7:70252335-70252385	BE2_C	brain:	n/a
9	chr7:70252571-70252621	NHBE	bronchial:	n/a
10	chr7:70256003-70256053	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:70255332-70255382	ovcar-3	ovarian:	n/a
12	chr7:70252448-70252498	SK-N-SH	brain:	n/a
13	chr7:70252335-70252385	HIPEpiC	eye:	n/a
14	chr7:70252953-70253003	AG04449	skin:	fetal
15	chr7:70255804-70255854	HMEC	breast:	n/a
16	chr7:70252953-70253003	ECC-1	luminal epithelium:	n/a
17	chr7:70258726-70258776	SKMC	muscle:	n/a
18	chr7:70294511-70294561	HMEC	breast:	n/a
19	chr7:70311321-70311371	NB4	blood:	n/a
20	chr7:70255985-70256035	GM12878	blood:	n/a
21	chr7:70254810-70254860	K562	blood:	n/a
22	chr7:70258726-70258776	HL-60	blood:	n/a
23	chr7:70256003-70256053	CMK	blood:	n/a
24	chr7:70311532-70311582	SAEC	small airway:	n/a
25	chr7:70257960-70258010	MCF-7	breast:	n/a
26	chr7:70257960-70258010	HNPCEpiC	eye:	n/a
27	chr7:70322401-70322451	HRPEpiC	eye:	n/a
28	chr7:70257960-70258010	NB4	blood:	n/a
29	chr7:70254810-70254860	T-47D	breast:	n/a
30	chr7:70255210-70255260	HRPEpiC	eye:	n/a
31	chr7:70252335-70252385	HEK293	kidney:	embryo
32	chr7:70255332-70255382	ProgFib	skin:	n/a
33	chr7:70252571-70252621	T-47D	breast:	n/a
34	chr7:70311532-70311582	GM19239	blood:	n/a
35	chr7:70252662-70252712	BJ	skin:	n/a
36	chr7:70252335-70252385	GM19239	blood:	n/a
37	chr7:70255416-70255466	AG09319	gingival:	n/a
38	chr7:70257926-70257976	PrEC	prostate:	n/a
39	chr7:70252953-70253003	PFSK-1	brain:	n/a
40	chr7:70252662-70252712	ProgFib	skin:	n/a
41	chr7:70256003-70256053	HEK293	kidney:	embryo
42	chr7:70258649-70258699	NH-A	brain:	n/a
43	chr7:70256003-70256053	HCT-116	colon:	n/a
44	chr7:70258649-70258699	NHDF-neo	bronchial:	n/a
45	chr7:70322401-70322451	Caco-2	colon:	n/a
46	chr7:70311532-70311582	HUVEC	blood vessel:	n/a
47	chr7:70258726-70258776	SK-N-SH	brain:	n/a
48	chr7:70258010-70258060	ECC-1	luminal epithelium:	n/a
49	chr7:70252953-70253003	Jurkat	blood:	n/a
50	chr7:70294525-70294575	HRPEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70319996..70320657-chr7:71198026..71198561,2	MCF-7	breast:
2	chr7:70321684..70322394-chr7:70659915..70660431,2	MCF-7	breast:
3	chr7:70321614..70322798-chr7:71200589..71201582,5	MCF-7	breast:
4	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
5	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
6	chr7:70321651..70322570-chr7:71197952..71198877,7	K562	blood:
7	chr7:70321665..70322892-chr7:71197945..71198934,7	MCF-7	breast:
8	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
9	chr7:70321514..70322440-chr7:71198003..71198947,6	MCF-7	breast:
10	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
11	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
12	chr7:70321617..70322562-chr7:70976561..70977221,2	MCF-7	breast:
13	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
14	chr7:70295507..70296249-chr7:71198004..71198896,2	MCF-7	breast:
15	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
16	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
17	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
18	chr7:70321682..70322568-chr7:71200885..71201597,2	K562	blood:
19	chr7:70309809..70312680-chr7:70313436..70316301,3	K562	blood:
20	chr7:70316123..70316992-chr7:71197861..71198674,2	K562	blood:
21	chr7:69997760..70000305-chr7:70252452..70255075,2	MCF-7	breast:
22	chr5:126205511..126206011-chr7:70301812..70302369,2	MCF-7	breast:
23	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
24	chr7:70320133..70320969-chr7:71200768..71201606,2	MCF-7	breast:
25	chr7:70244569..70247076-chr7:70250539..70253250,4	K562	blood:
26	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AUTS2-3	chr7:70302724-70302999	NONHSAT121342

No data

Variant related genes	Relation type
AUTS2	TF binding region
ENSG00000236978	TF binding region
AUTS2	CpG island
ENSG00000236978	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 4062 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4062 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2293503	chr7:70250125-70250126	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs561398631	chr7:70250128-70250129	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576360033	chr7:70250169-70250170	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs543731021	chr7:70250179-70250180	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566478345	chr7:70250198-70250199	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs565092896	chr7:70250208-70250209	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149336761	chr7:70250227-70250228	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs551180576	chr7:70250234-70250235	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144577131	chr7:70250284-70250285	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs527272593	chr7:70250300-70250301	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs548997811	chr7:70250302-70250303	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs535322463	chr7:70250333-70250334	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs577630704	chr7:70250376-70250377	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148458016	chr7:70250377-70250378	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs555272426	chr7:70250395-70250396	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs575366825	chr7:70250432-70250433	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs538108692	chr7:70250433-70250434	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200665763	chr7:70250435-70250436	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550101579	chr7:70250442-70250443	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146269802	chr7:70250469-70250470	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs142600901	chr7:70250480-70250481	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185142496	chr7:70250497-70250498	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553970346	chr7:70250621-70250622	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572528317	chr7:70250651-70250652	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536233708	chr7:70250657-70250658	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554923560	chr7:70250665-70250666	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs576034349	chr7:70250669-70250670	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543670517	chr7:70250685-70250686	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs565280339	chr7:70250698-70250699	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs28538425	chr7:70250713-70250714	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs190470224	chr7:70250716-70250717	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146479801	chr7:70250725-70250726	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577790023	chr7:70250812-70250813	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527346448	chr7:70250825-70250826	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139882942	chr7:70250832-70250833	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs531341157	chr7:70250838-70250839	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143258284	chr7:70250846-70250847	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571612853	chr7:70250865-70250866	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs2293502	chr7:70250866-70250867	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547601327	chr7:70250869-70250870	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10233246	chr7:70250874-70250875	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs149192549	chr7:70250950-70250951	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143340591	chr7:70250957-70250958	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372998593	chr7:70250967-70250968	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201229021	chr7:70250992-70250993	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs147968085	chr7:70251002-70251003	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529622990	chr7:70251020-70251021	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs193205868	chr7:70251079-70251080	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35360940	chr7:70251116-70251117	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs369078387	chr7:70251117-70251118	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70222000-70258000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:70226400-70254800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:70227400-70253000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:70228400-70257400	Weak transcription	Right Atrium	heart
5	chr7:70229400-70259600	Strong transcription	Fetal Muscle Trunk	muscle
6	chr7:70229400-70259600	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr7:70230200-70254000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr7:70230200-70257400	Strong transcription	Rectal Mucosa Donor 31	rectum
9	chr7:70233400-70250200	Weak transcription	Colonic Mucosa	Colon
10	chr7:70234600-70259600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:70235200-70258200	Strong transcription	HSMMtube	muscle
12	chr7:70236400-70257000	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr7:70236800-70258200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:70238600-70259600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr7:70238800-70259600	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:70239200-70259400	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr7:70239800-70259400	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr7:70240200-70257000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
19	chr7:70240200-70258000	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr7:70240800-70259200	Strong transcription	Fetal Intestine Small	intestine
21	chr7:70241000-70259200	Strong transcription	Aorta	Aorta
22	chr7:70241200-70257200	Strong transcription	Skeletal Muscle Female	skeletal muscle
23	chr7:70241400-70256400	Strong transcription	Stomach Smooth Muscle	stomach
24	chr7:70241400-70257400	Strong transcription	HSMM	muscle
25	chr7:70241800-70257200	Strong transcription	H9 Cell Line	embryonic stem cell
26	chr7:70241800-70259400	Strong transcription	Duodenum Mucosa	Duodenum
27	chr7:70242000-70252600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:70242000-70257200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:70242200-70259600	Strong transcription	Dnd41	blood
30	chr7:70242200-70259600	Weak transcription	NHDF-Ad	bronchial
31	chr7:70242600-70250400	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr7:70243200-70259600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:70243600-70259600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr7:70243800-70258200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:70243800-70258200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr7:70244200-70256000	Strong transcription	Lung	lung
37	chr7:70244200-70256400	Strong transcription	Ovary	ovary
38	chr7:70244400-70251000	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr7:70244800-70259200	Strong transcription	GM12878-XiMat	blood
40	chr7:70245200-70251600	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:70245400-70250600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr7:70245400-70256800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
43	chr7:70245400-70258600	Strong transcription	Fetal Thymus	thymus
44	chr7:70246000-70250200	Strong transcription	Primary T cells from cord blood	blood
45	chr7:70246000-70250600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr7:70246200-70253000	Strong transcription	Adipose Nuclei	Adipose
47	chr7:70246200-70254400	Strong transcription	NH-A	brain
48	chr7:70246200-70257200	Strong transcription	Thymus	Thymus
49	chr7:70246200-70258400	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr7:70246400-70253000	Strong transcription	Left Ventricle	heart

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