Variant report

Variant	nsv527321
Chromosome Location	chr7:116635048-116660803
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:428)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:116652878-116653024	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:116651749-116652155	K562	blood:	n/a	n/a
3	ARID3A	chr7:116659634-116660310	K562	blood:	n/a	n/a
4	ARID3A	chr7:116652471-116653072	K562	blood:	n/a	n/a
5	ARID3A	chr7:116654055-116657700	K562	blood:	n/a	chr7:116656765-116656781
6	ATF1	chr7:116654267-116654570	K562	blood:	n/a	n/a
7	ATF1	chr7:116657117-116657522	K562	blood:	n/a	n/a
8	ATF1	chr7:116654776-116655066	K562	blood:	n/a	n/a
9	ATF1	chr7:116659690-116660449	K562	blood:	n/a	chr7:116660233-116660247
10	ATF2	chr7:116651069-116652631	GM12878	blood:	n/a	n/a
11	ATF2	chr7:116650241-116651016	GM12878	blood:	n/a	n/a
12	ATF2	chr7:116650286-116651137	GM12878	blood:	n/a	n/a
13	ATF2	chr7:116651239-116653173	GM12878	blood:	n/a	n/a
14	ATF3	chr7:116654248-116654679	K562	blood:	n/a	n/a
15	ATF3	chr7:116659983-116660435	K562	blood:	n/a	n/a
16	ATF3	chr7:116654811-116655067	K562	blood:	n/a	chr7:116654927-116654941
17	ATF3	chr7:116660080-116660389	K562	blood:	n/a	n/a
18	BACH1	chr7:116658055-116658062	K562	blood:	n/a	n/a
19	BATF	chr7:116650312-116652479	GM12878	blood:	n/a	n/a
20	BATF	chr7:116651672-116652373	GM12878	blood:	n/a	n/a
21	BATF	chr7:116650467-116650798	GM12878	blood:	n/a	n/a
22	BATF	chr7:116647011-116647328	GM12878	blood:	n/a	n/a
23	BATF	chr7:116655589-116655819	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:116650314-116650900	GM12878	blood:	n/a	chr7:116650709-116650718
25	BCL11A	chr7:116651673-116652382	GM12878	blood:	n/a	chr7:116652039-116652048
26	BCL11A	chr7:116651970-116652230	GM12878	blood:	n/a	chr7:116652039-116652048
27	BCL3	chr7:116650436-116650863	GM12878	blood:	n/a	chr7:116650709-116650718
28	BCL3	chr7:116651669-116652362	GM12878	blood:	n/a	chr7:116652039-116652048
29	BCL3	chr7:116654186-116654584	GM12878	blood:	n/a	n/a
30	BCL3	chr7:116650332-116650902	GM12878	blood:	n/a	chr7:116650709-116650718
31	BCLAF1	chr7:116649838-116650807	GM12878	blood:	n/a	chr7:116650709-116650718
32	BCLAF1	chr7:116649184-116649684	GM12878	blood:	n/a	n/a
33	BCLAF1	chr7:116650265-116651392	GM12878	blood:	n/a	chr7:116650709-116650718
34	BCLAF1	chr7:116651436-116652694	GM12878	blood:	n/a	chr7:116652039-116652048
35	BCLAF1	chr7:116650823-116652481	GM12878	blood:	n/a	chr7:116652039-116652048
36	BHLHE40	chr7:116651418-116652496	GM12878	blood:	n/a	n/a
37	BHLHE40	chr7:116656986-116657432	GM12878	blood:	n/a	n/a
38	BHLHE40	chr7:116649284-116649526	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:116657087-116657501	K562	blood:	n/a	n/a
40	BHLHE40	chr7:116654747-116655105	K562	blood:	n/a	n/a
41	BHLHE40	chr7:116650316-116651130	GM12878	blood:	n/a	n/a
42	BHLHE40	chr7:116651350-116651408	K562	blood:	n/a	n/a
43	BHLHE40	chr7:116660055-116660522	K562	blood:	n/a	n/a
44	BHLHE40	chr7:116659533-116659560	K562	blood:	n/a	n/a
45	BRCA1	chr7:116644441-116644451	H1-hESC	embryonic stem cell:	n/a	n/a
46	CBX3	chr7:116654665-116655195	K562	blood:	n/a	chr7:116655085-116655096
47	CBX3	chr7:116659992-116660611	K562	blood:	n/a	n/a
48	CCNT2	chr7:116657036-116657474	K562	blood:	n/a	n/a
49	CCNT2	chr7:116655507-116655946	K562	blood:	n/a	n/a
50	CCNT2	chr7:116660082-116660464	K562	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:116660172-116660222	HCM	heart:	n/a
2	chr7:116660172-116660222	HCM	heart:	n/a
3	chr7:116660213-116660263	HEK293	kidney:	embryo
4	chr7:116660213-116660263	HEEpiC	esophagus:	n/a
5	chr7:116660172-116660222	RPTEC	kidney:	n/a
6	chr7:116659986-116660036	MCF10A-Er-Src	breast:	n/a
7	chr7:116638247-116638297	AG04449	skin:	fetal
8	chr7:116659986-116660036	HRE	kidney:	n/a
9	chr7:116660240-116660290	NB4	blood:	n/a
10	chr7:116660240-116660290	SK-N-MC	brain:	n/a
11	chr7:116659609-116659659	RPTEC	kidney:	n/a
12	chr7:116638247-116638297	AG09309	skin:	n/a
13	chr7:116659986-116660036	CMK	blood:	n/a
14	chr7:116660172-116660222	ovcar-3	ovarian:	n/a
15	chr7:116660172-116660222	SAEC	small airway:	n/a
16	chr7:116660240-116660290	GM12878	blood:	n/a
17	chr7:116660172-116660222	LNCaP	prostate:	n/a
18	chr7:116660213-116660263	HRCEpiC	kidney:	n/a
19	chr7:116638247-116638297	CMK	blood:	n/a
20	chr7:116659609-116659659	NHBE	bronchial:	n/a
21	chr7:116660213-116660263	Jurkat	blood:	n/a
22	chr7:116659609-116659659	GM12892	blood:	n/a
23	chr7:116660240-116660290	NHDF-neo	bronchial:	n/a
24	chr7:116638247-116638297	LNCaP	prostate:	n/a
25	chr7:116638122-116638172	AG04449	skin:	fetal
26	chr7:116660213-116660263	IMR90	lung:	fetal
27	chr7:116659609-116659659	HUVEC	blood vessel:	n/a
28	chr7:116659986-116660036	AG04450	lung:	fetal
29	chr7:116660213-116660263	ProgFib	skin:	n/a
30	chr7:116660172-116660222	NHDF-neo	bronchial:	n/a
31	chr7:116660172-116660222	NH-A	brain:	n/a
32	chr7:116660240-116660290	Caco-2	colon:	n/a
33	chr7:116660213-116660263	ovcar-3	ovarian:	n/a
34	chr7:116660172-116660222	HNPCEpiC	eye:	n/a
35	chr7:116660213-116660263	BE2_C	brain:	n/a
36	chr7:116638122-116638172	SK-N-SH	brain:	n/a
37	chr7:116660240-116660290	HCM	heart:	n/a
38	chr7:116660172-116660222	NT2-D1	testis:	n/a
39	chr7:116660240-116660290	NT2-D1	testis:	n/a
40	chr7:116660240-116660290	CMK	blood:	n/a
41	chr7:116660172-116660222	IMR90	lung:	fetal
42	chr7:116638247-116638297	PANC-1	pancreas:	n/a
43	chr7:116638122-116638172	NHBE	bronchial:	n/a
44	chr7:116660213-116660263	U87	brain:	n/a
45	chr7:116659609-116659659	T-47D	breast:	n/a
46	chr7:116660240-116660290	BE2_C	brain:	n/a
47	chr7:116659986-116660036	Hepatocyte	liver:	n/a
48	chr7:116659609-116659659	SK-N-SH_RA	brain:	n/a
49	chr7:116659986-116660036	HEK293	kidney:	embryo
50	chr7:116660172-116660222	GM12878	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:116639946-116640697..7:116957165-116964911	H1-hESC	embryonic stem cell:	embryo
2	chr7:116591145..116594307-chr7:116639573..116642649,3	K562	blood:
3	chr7:116593241..116595466-chr7:116660192..116661837,2	K562	blood:
4	chr7:116655560..116657072-chr7:116673244..116674855,2	K562	blood:
5	chr7:116640801..116642552-chr7:116652189..116653977,2	K562	blood:
6	7:116657331-116659879..7:116754962-116765597	GM12878	blood:
7	chr7:116628482..116629108-chr7:116652523..116653032,2	MCF-7	breast:
8	7:116641011-116646266..7:116754962-116765597	GM12878	blood:
9	chr7:116591034..116595853-chr7:116650615..116657201,10	K562	blood:
10	chr7:116625923..116629048-chr7:116633177..116636894,3	K562	blood:
11	chr7:116638342..116641684-chr7:116649141..116651622,3	K562	blood:
12	chr7:116640801..116642552-chr7:116652189..116653977,2	K562	blood:
13	chr7:116637852..116640358-chr7:116641000..116643196,2	MCF-7	breast:
14	7:116657331-116659879..7:116957165-116964911	H1-hESC	embryonic stem cell:	embryo
15	chr7:116570499..116571103-chr7:116652412..116652980,2	MCF-7	breast:
16	7:115847372-115857098..7:116641011-116646266	GM12878	blood:
17	chr7:116639159..116641684-chr7:116649141..116652754,4	K562	blood:
18	chr7:116628542..116629513-chr7:116652715..116653338,2	MCF-7	breast:
19	chr7:116500946..116504332-chr7:116654661..116656841,4	K562	blood:
20	chr7:116500369..116502943-chr7:116652939..116655757,2	K562	blood:
21	7:116651084-116657331..7:117341506-117356953	Hela-S3	cervix:
22	chr7:116633872..116635793-chr7:116756393..116758415,2	K562	blood:
23	chr7:116591145..116593929-chr7:116638139..116641073,2	K562	blood:
24	chr7:116639114..116641911-chr7:116644148..116646393,2	K562	blood:
25	chr7:116589849..116592788-chr7:116643834..116645467,2	K562	blood:
26	chr7:116570171..116571182-chr7:116652604..116653376,5	K562	blood:
27	7:115861595-115870968..7:116641011-116646266	GM12878	blood:
28	chr7:116639114..116641911-chr7:116644148..116646393,2	K562	blood:
29	chr7:116593412..116595040-chr7:116633936..116636108,2	MCF-7	breast:
30	chr7:116591200..116595164-chr7:116659811..116663168,5	K562	blood:
31	7:116610596-116619447..7:116651084-116657331	H1-hESC	embryonic stem cell:	embryo
32	7:115847372-115857098..7:116657331-116659879	Hela-S3	cervix:
33	chr7:116638342..116641684-chr7:116649141..116651622,3	K562	blood:
34	chr7:116611251..116613447-chr7:116648555..116650654,2	K562	blood:
35	chr7:116637852..116640358-chr7:116641000..116643196,2	MCF-7	breast:
36	chr7:116639159..116641684-chr7:116649141..116652754,4	K562	blood:
37	chr7:116589691..116599368-chr7:116647062..116658963,30	K562	blood:
38	chr7:116592302..116594663-chr7:116658883..116661789,2	MCF-7	breast:
39	chr7:116657348..116659036-chr7:116675681..116678662,2	K562	blood:
40	7:116649468-116651024..7:116754962-116765597	GM12878	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CAPZA2-2	chr7:116660313-116660683	NONHSAT122921
2	lnc-CAPZA2-2	chr7:116660272-116660683	NONHSAT122920

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6132	chr7:116660285-116660303	MIMAT0024616

No data

Variant related genes	Relation type
ST7	TF binding region
ST7	CpG island
ENSG00000135269	chromatin interactions
ENSG00000214188	chromatin interactions
ENSG00000105989	chromatin interactions
ENSG00000213050	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000227199	chromatin interactions
ENSG00000198898	chromatin interactions
ENSG00000004866	chromatin interactions

Extended variants
information (count: 786 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12706135	chr7:116635048-116635049	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs556715247	chr7:116635061-116635062	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575141257	chr7:116635142-116635143	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs60985897	chr7:116635146-116635147	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs145785834	chr7:116635151-116635152	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs554525046	chr7:116635167-116635168	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs192077074	chr7:116635168-116635169	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs79572121	chr7:116635199-116635200	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs368212800	chr7:116635208-116635209	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs564891704	chr7:116635307-116635308	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532232165	chr7:116635351-116635352	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs182534134	chr7:116635361-116635362	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs187811730	chr7:116635382-116635383	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557517972	chr7:116635401-116635402	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs375193650	chr7:116635452-116635453	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs549564719	chr7:116635479-116635480	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs138701403	chr7:116635487-116635488	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs192743788	chr7:116635524-116635525	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs184181213	chr7:116635594-116635595	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs577040048	chr7:116635612-116635613	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs189360774	chr7:116635687-116635688	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs11771917	chr7:116635705-116635706	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs193137841	chr7:116635707-116635708	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs184890357	chr7:116635721-116635722	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs564832412	chr7:116635793-116635794	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs569397125	chr7:116635821-116635822	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs11982484	chr7:116635872-116635873	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs569341353	chr7:116635883-116635884	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs536011433	chr7:116635988-116635989	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs530485109	chr7:116636038-116636039	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs573018241	chr7:116636073-116636074	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540557380	chr7:116636097-116636098	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs189264503	chr7:116636135-116636136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572741692	chr7:116636136-116636137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs72227239	chr7:116636137-116636138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76374801	chr7:116636152-116636153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs71148355	chr7:116636153-116636154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181448541	chr7:116636197-116636198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185743518	chr7:116636221-116636222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35057858	chr7:116636223-116636224	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs529800732	chr7:116636245-116636246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189434364	chr7:116636259-116636260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575108667	chr7:116636287-116636288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs180990757	chr7:116636296-116636297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186087851	chr7:116636311-116636312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546935639	chr7:116636382-116636383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs113131210	chr7:116636383-116636384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147388953	chr7:116636397-116636398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138026388	chr7:116636426-116636427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569221431	chr7:116636427-116636428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Squamous cell cancer	20885788	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116597000-116641600	Weak transcription	Ovary	ovary
2	chr7:116610600-116638800	Weak transcription	Hela-S3	cervix
3	chr7:116613600-116635600	Weak transcription	Pancreas	Pancrea
4	chr7:116613600-116647000	Weak transcription	Right Atrium	heart
5	chr7:116627600-116639000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:116627800-116638000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr7:116627800-116648200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr7:116627800-116648800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:116631200-116636800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:116631600-116640600	Weak transcription	K562	blood
11	chr7:116632600-116635400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:116632600-116638000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr7:116632600-116638000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:116632600-116649000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:116632800-116638000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:116634400-116635600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:116634800-116637000	Enhancers	Placenta Amnion	Placenta Amnion
18	chr7:116635000-116635200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:116635000-116635600	Enhancers	Psoas Muscle	Psoas
20	chr7:116635000-116635800	Enhancers	Fetal Heart	heart
21	chr7:116635000-116635800	Enhancers	Left Ventricle	heart
22	chr7:116635000-116635800	Enhancers	Right Ventricle	heart
23	chr7:116635200-116635600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr7:116635400-116635800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:116635600-116635800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:116635600-116635800	Enhancers	Pancreas	Pancrea
27	chr7:116635600-116639000	Weak transcription	Colon Smooth Muscle	Colon
28	chr7:116635600-116654800	Weak transcription	Psoas Muscle	Psoas
29	chr7:116635800-116638000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:116635800-116638000	Weak transcription	Right Ventricle	heart
31	chr7:116635800-116640600	Weak transcription	Fetal Heart	heart
32	chr7:116635800-116640600	Weak transcription	Pancreas	Pancrea
33	chr7:116635800-116660200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr7:116637000-116638200	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:116638000-116638600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr7:116638000-116638600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr7:116638000-116638600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:116638000-116638600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:116638000-116638600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:116638000-116639200	Enhancers	Right Ventricle	heart
41	chr7:116638200-116638400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr7:116638200-116638600	ZNF genes & repeats	Fetal Stomach	stomach
43	chr7:116638400-116639000	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr7:116638600-116639000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr7:116638600-116644000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:116638600-116647400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:116638800-116639400	Enhancers	NH-A	brain
48	chr7:116638800-116639800	Enhancers	Hela-S3	cervix
49	chr7:116639000-116639600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:116639000-116639600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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