Variant report

Variant	nsv887484
Chromosome Location	chr7:7692483-7769363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1294)
CpG islands
(count:368)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1294 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7702363-7702392	K562	blood:	n/a	n/a
2	ARID3A	chr7:7721181-7721479	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:7736088-7736689	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:7721171-7721501	K562	blood:	n/a	n/a
5	ARID3A	chr7:7717765-7718021	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:7747628-7747697	HepG2	liver:	n/a	n/a
7	ATF1	chr7:7760557-7760592	K562	blood:	n/a	n/a
8	ATF1	chr7:7736576-7736728	K562	blood:	n/a	n/a
9	ATF1	chr7:7704145-7704243	K562	blood:	n/a	n/a
10	ATF1	chr7:7693274-7693486	K562	blood:	n/a	n/a
11	ATF2	chr7:7760713-7761199	GM12878	blood:	n/a	n/a
12	ATF2	chr7:7745574-7746340	GM12878	blood:	n/a	n/a
13	ATF2	chr7:7758646-7759422	GM12878	blood:	n/a	n/a
14	ATF2	chr7:7758756-7759422	GM12878	blood:	n/a	n/a
15	ATF2	chr7:7745563-7746490	GM12878	blood:	n/a	n/a
16	ATF3	chr7:7758817-7759402	HCT-116	colon:	n/a	n/a
17	ATF3	chr7:7758872-7759247	K562	blood:	n/a	n/a
18	ATF3	chr7:7758803-7759448	HCT-116	colon:	n/a	n/a
19	BACH1	chr7:7703364-7703366	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr7:7745639-7746151	GM12878	blood:	n/a	chr7:7745675-7745688
21	BATF	chr7:7746233-7746514	GM12878	blood:	n/a	n/a
22	BATF	chr7:7745655-7746200	GM12878	blood:	n/a	chr7:7745675-7745688
23	BATF	chr7:7758917-7759310	GM12878	blood:	n/a	n/a
24	BATF	chr7:7758858-7759333	GM12878	blood:	n/a	n/a
25	BCL11A	chr7:7745649-7746160	GM12878	blood:	n/a	n/a
26	BCL11A	chr7:7758931-7759315	GM12878	blood:	n/a	n/a
27	BCL11A	chr7:7745684-7746120	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:7758799-7759388	GM12878	blood:	n/a	n/a
29	BCLAF1	chr7:7745638-7746216	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:7693238-7693371	K562	blood:	n/a	n/a
31	BHLHE40	chr7:7741586-7741677	GM12878	blood:	n/a	n/a
32	BHLHE40	chr7:7745603-7746215	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:7753124-7753216	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:7758907-7759340	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:7760872-7761205	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:7758959-7759273	K562	blood:	n/a	n/a
37	BHLHE40	chr7:7721000-7721346	GM12878	blood:	n/a	n/a
38	BRCA1	chr7:7720963-7720964	GM12878	blood:	n/a	n/a
39	BRCA1	chr7:7736060-7736936	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr7:7717456-7717943	K562	blood:	n/a	n/a
41	CEBPB	chr7:7758855-7759354	MCF-7	breast:	n/a	chr7:7759133-7759144 chr7:7758864-7758877
42	CEBPB	chr7:7742382-7742728	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:7746267-7746489	MCF-7	breast:	n/a	n/a
44	CEBPB	chr7:7758821-7759307	A549	lung:	n/a	chr7:7759133-7759144 chr7:7758864-7758877
45	CEBPB	chr7:7693194-7693647	MCF-7	breast:	n/a	chr7:7693425-7693436
46	CEBPB	chr7:7758747-7759470	HCT-116	colon:	n/a	chr7:7759133-7759144 chr7:7758864-7758877
47	CEBPB	chr7:7742453-7742643	K562	blood:	n/a	n/a
48	CEBPB	chr7:7733495-7733853	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:7742415-7742708	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:7746183-7746537	K562	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7711168-7711218	GM06990	blood:	n/a
2	chr7:7759286-7759336	ProgFib	skin:	n/a
3	chr7:7711168-7711218	GM06990	blood:	n/a
4	chr7:7759286-7759336	ProgFib	skin:	n/a
5	chr7:7759286-7759336	HMEC	breast:	n/a
6	chr7:7759221-7759271	HCM	heart:	n/a
7	chr7:7726202-7726252	SAEC	small airway:	n/a
8	chr7:7759286-7759336	CMK	blood:	n/a
9	chr7:7747964-7748014	ProgFib	skin:	n/a
10	chr7:7711168-7711218	Hepatocyte	liver:	n/a
11	chr7:7735611-7735661	HepG2	liver:	n/a
12	chr7:7759286-7759336	GM06990	blood:	n/a
13	chr7:7759221-7759271	GM06990	blood:	n/a
14	chr7:7759221-7759271	PFSK-1	brain:	n/a
15	chr7:7726202-7726252	MCF10A-Er-Src	breast:	n/a
16	chr7:7759221-7759271	AG10803	skin:	n/a
17	chr7:7711168-7711218	GM12891	blood:	n/a
18	chr7:7747964-7748014	NH-A	brain:	n/a
19	chr7:7726202-7726252	AG04450	lung:	fetal
20	chr7:7726202-7726252	CMK	blood:	n/a
21	chr7:7735611-7735661	PANC-1	pancreas:	n/a
22	chr7:7747964-7748014	GM06990	blood:	n/a
23	chr7:7747964-7748014	HIPEpiC	eye:	n/a
24	chr7:7747964-7748014	MCF-7	breast:	n/a
25	chr7:7711168-7711218	HMEC	breast:	n/a
26	chr7:7711168-7711218	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:7759286-7759336	NT2-D1	testis:	n/a
28	chr7:7759286-7759336	MCF-7	breast:	n/a
29	chr7:7711168-7711218	NT2-D1	testis:	n/a
30	chr7:7759286-7759336	ovcar-3	ovarian:	n/a
31	chr7:7711168-7711218	SKMC	muscle:	n/a
32	chr7:7735611-7735661	SAEC	small airway:	n/a
33	chr7:7726202-7726252	Jurkat	blood:	n/a
34	chr7:7759221-7759271	SK-N-SH	brain:	n/a
35	chr7:7747964-7748014	GM12891	blood:	n/a
36	chr7:7759221-7759271	HEK293	kidney:	embryo
37	chr7:7759286-7759336	SAEC	small airway:	n/a
38	chr7:7735611-7735661	H1-hESC	embryonic stem cell:	embryo
39	chr7:7735611-7735661	HMEC	breast:	n/a
40	chr7:7747964-7748014	NT2-D1	testis:	n/a
41	chr7:7735611-7735661	IMR90	lung:	fetal
42	chr7:7726202-7726252	NT2-D1	testis:	n/a
43	chr7:7735611-7735661	NH-A	brain:	n/a
44	chr7:7759286-7759336	NB4	blood:	n/a
45	chr7:7711168-7711218	AG09319	gingival:	n/a
46	chr7:7759286-7759336	Hela-S3	cervix:	n/a
47	chr7:7726202-7726252	SK-N-MC	brain:	n/a
48	chr7:7735611-7735661	A549	lung:	n/a
49	chr7:7759221-7759271	HEEpiC	esophagus:	n/a
50	chr7:7711168-7711218	AG04449	skin:	fetal

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7753122..7754929-chr7:7755971..7758600,2	MCF-7	breast:
2	chr7:7704790..7707554-chr7:7715010..7717465,2	K562	blood:
3	chr7:7679155..7682446-chr7:7688919..7692688,4	MCF-7	breast:
4	chr7:7721081..7721703-chr7:7804254..7805179,2	MCF-7	breast:
5	chr7:7742121..7744210-chr7:7768171..7770972,2	MCF-7	breast:
6	chr7:7731035..7732628-chr7:7734421..7736986,2	MCF-7	breast:
7	chr7:7708519..7710790-chr7:7711847..7714046,2	K562	blood:
8	chr7:7731359..7733011-chr7:7740731..7743536,2	MCF-7	breast:
9	chr7:7720780..7722829-chr7:8008432..8010921,2	MCF-7	breast:
10	chr7:7726921..7729917-chr7:7734737..7737606,4	K562	blood:
11	chr7:7705626..7708031-chr7:7715010..7717688,3	K562	blood:
12	chr7:7704790..7707554-chr7:7715010..7717465,2	K562	blood:
13	chr7:7702478..7704915-chr7:7709957..7711916,2	MCF-7	breast:
14	chr7:7726990..7730835-chr7:7733488..7736848,3	K562	blood:
15	chr7:7708519..7710790-chr7:7711847..7714046,2	K562	blood:
16	chr7:7731359..7733011-chr7:7740731..7743536,2	MCF-7	breast:
17	chr7:7737993..7740091-chr7:7743068..7745751,2	K562	blood:
18	chr7:7742121..7744210-chr7:7768171..7770972,2	MCF-7	breast:
19	chr7:7721232..7721744-chr7:8075592..8076157,2	MCF-7	breast:
20	chr7:7676999..7684981-chr7:7684990..7693882,16	K562	blood:
21	chr7:7683722..7685849-chr7:7692076..7694562,2	MCF-7	breast:
22	chr7:7751274..7753371-chr7:7753426..7756190,2	K562	blood:
23	chr7:7751274..7753371-chr7:7753426..7756190,2	K562	blood:
24	chr7:7737993..7740091-chr7:7743068..7745751,2	K562	blood:
25	chr7:7679919..7682368-chr7:7729698..7732128,2	K562	blood:
26	chr7:7713254..7715065-chr7:7752185..7753849,2	K562	blood:
27	chr7:7749070..7751862-chr7:7752531..7755969,3	MCF-7	breast:
28	chr7:7742832..7745558-chr7:7749813..7751585,2	K562	blood:
29	chr20:52277828..52280827-chr7:7693453..7695076,2	MCF-7	breast:
30	chr7:7749070..7751862-chr7:7752531..7755969,3	MCF-7	breast:
31	chr7:7720832..7721819-chr7:7800536..7801542,7	MCF-7	breast:
32	chr7:7720725..7721395-chr7:8256882..8257575,2	MCF-7	breast:
33	chr7:7719627..7722096-chr7:8004642..8007515,2	MCF-7	breast:
34	chr7:7604510..7607346-chr7:7752529..7754039,2	MCF-7	breast:
35	chr7:7737251..7739493-chr7:7744251..7746745,3	K562	blood:
36	chr7:7758694..7760544-chr7:7776223..7777893,2	MCF-7	breast:
37	chr7:7710276..7712409-chr7:7714485..7717060,3	MCF-7	breast:
38	chr7:7742832..7745558-chr7:7749813..7751585,2	K562	blood:
39	chr7:7726921..7729917-chr7:7734737..7737606,4	K562	blood:
40	chr7:7726990..7730835-chr7:7733488..7736848,3	K562	blood:
41	chr7:7710276..7712409-chr7:7714485..7717060,3	MCF-7	breast:
42	chr7:7702478..7704915-chr7:7709957..7711916,2	MCF-7	breast:
43	chr7:7713254..7715065-chr7:7752185..7753849,2	K562	blood:
44	chr7:7679863..7681686-chr7:7702542..7704997,4	K562	blood:
45	chr7:7705626..7708031-chr7:7715010..7717688,3	K562	blood:
46	chr7:7737251..7739493-chr7:7744251..7746745,3	K562	blood:
47	chr7:7731035..7732628-chr7:7734421..7736986,2	MCF-7	breast:
48	chr7:7766237..7767895-chr7:7769478..7771266,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006465.3.1-1	chr7:7760544-7760865	NONHSAT119130
2	lnc-AC006465.3.1-1	chr7:7728976-7729091	NONHSAT119130

No data

Variant related genes	Relation type
RPA3	TF binding region
RPA3	CpG island
ENSG00000106399	chromatin interactions
ENSG00000219545	chromatin interactions
ENSG00000106415	chromatin interactions
ENSG00000270314	chromatin interactions
ENSG00000272894	chromatin interactions
ENSG00000164654	chromatin interactions
ENSG00000233108	chromatin interactions

Extended variants
information (count: 3280 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:3280 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs886724	chr7:7692483-7692484	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186189192	chr7:7692489-7692490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs141262102	chr7:7692522-7692523	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs578147412	chr7:7692527-7692528	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs377201457	chr7:7692545-7692546	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs28916272	chr7:7692546-7692547	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs563888446	chr7:7692596-7692597	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs190906308	chr7:7692597-7692598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs555088138	chr7:7692627-7692628	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs543186625	chr7:7692633-7692634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561460331	chr7:7692687-7692688	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144962252	chr7:7692704-7692705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs6980052	chr7:7692709-7692710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs570865851	chr7:7692713-7692714	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532089141	chr7:7692730-7692731	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs28916271	chr7:7692767-7692768	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568587549	chr7:7692776-7692777	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs536090037	chr7:7692801-7692802	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs560524833	chr7:7692823-7692824	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs565807220	chr7:7692877-7692878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554738376	chr7:7692886-7692887	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs566699848	chr7:7692947-7692948	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs28916270	chr7:7692987-7692988	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs553412090	chr7:7693002-7693003	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536069353	chr7:7693006-7693007	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28916269	chr7:7693053-7693054	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557518416	chr7:7693076-7693077	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs575678795	chr7:7693110-7693111	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542894263	chr7:7693115-7693116	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs28916268	chr7:7693136-7693137	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561531548	chr7:7693147-7693148	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs528788164	chr7:7693160-7693161	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs28992777	chr7:7693201-7693202	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs185874326	chr7:7693210-7693211	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs191219644	chr7:7693213-7693214	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532005084	chr7:7693216-7693217	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs138795892	chr7:7693245-7693246	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370114921	chr7:7693247-7693248	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs28992776	chr7:7693290-7693291	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368388740	chr7:7693301-7693302	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529792441	chr7:7693323-7693324	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs548084448	chr7:7693347-7693348	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs566620595	chr7:7693375-7693376	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs533859338	chr7:7693376-7693377	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs531770427	chr7:7693393-7693394	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs28992775	chr7:7693408-7693409	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375009577	chr7:7693426-7693427	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570737131	chr7:7693462-7693463	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs28992774	chr7:7693489-7693490	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145667821	chr7:7693520-7693521	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Gastric cancer	17229543	CNVD
Ovarian cancer	21781307	CNVD
Gastric cancer	22014070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1434 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7681600-7703800	Weak transcription	Stomach Mucosa	stomach
2	chr7:7681600-7710200	Weak transcription	Aorta	Aorta
3	chr7:7681800-7692600	Weak transcription	Primary T cells from cord blood	blood
4	chr7:7681800-7696400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr7:7682000-7692600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr7:7682000-7694600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:7682000-7694600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr7:7682000-7694600	Weak transcription	Psoas Muscle	Psoas
9	chr7:7682000-7713800	Weak transcription	Left Ventricle	heart
10	chr7:7682200-7711600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr7:7686600-7701200	Weak transcription	Fetal Stomach	stomach
12	chr7:7687600-7696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:7687800-7717400	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr7:7689400-7693600	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr7:7689600-7694200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr7:7690400-7693600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr7:7690400-7693800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr7:7690600-7713800	Weak transcription	Fetal Intestine Large	intestine
19	chr7:7690800-7693000	Enhancers	NHDF-Ad	bronchial
20	chr7:7691000-7692800	Enhancers	Primary T helper cells fromperipheralblood	blood
21	chr7:7691000-7693200	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr7:7691000-7693400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr7:7691200-7693000	Weak transcription	Gastric	stomach
24	chr7:7691200-7693000	Enhancers	HepG2	liver
25	chr7:7691200-7693600	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr7:7691200-7701200	Weak transcription	Fetal Intestine Small	intestine
27	chr7:7691600-7692600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:7691800-7693000	Enhancers	A549	lung
29	chr7:7691800-7693400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:7691800-7717600	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:7692000-7693000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:7692000-7693200	Weak transcription	K562	blood
33	chr7:7692400-7692800	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr7:7692400-7693000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:7692400-7693200	Weak transcription	Fetal Thymus	thymus
36	chr7:7692400-7693200	Weak transcription	Thymus	Thymus
37	chr7:7692400-7693600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:7692400-7694600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr7:7692400-7717600	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr7:7692600-7692800	Enhancers	Primary T cells from cord blood	blood
41	chr7:7692600-7693000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:7692600-7693000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:7692600-7693800	Enhancers	Hela-S3	cervix
44	chr7:7692800-7700000	Weak transcription	Primary T cells from cord blood	blood
45	chr7:7693000-7693600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:7693000-7693800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:7693000-7693800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr7:7693000-7696800	Weak transcription	A549	lung
49	chr7:7693000-7719200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:7693200-7693600	Enhancers	Fetal Thymus	thymus

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