Variant report

Variant	nsv971490
Chromosome Location	chr7:66192193-66212423
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1084)
CpG islands
(count:978)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1084 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:66205387-66205778	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:66206060-66206127	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:66205424-66205647	K562	blood:	n/a	n/a
4	ATF1	chr7:66205287-66205807	K562	blood:	n/a	n/a
5	ATF2	chr7:66206076-66206368	GM12878	blood:	n/a	n/a
6	ATF2	chr7:66205509-66205864	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:66205081-66205845	GM12878	blood:	n/a	n/a
8	ATF2	chr7:66197387-66197877	GM12878	blood:	n/a	n/a
9	ATF2	chr7:66205229-66205790	GM12878	blood:	n/a	n/a
10	ATF3	chr7:66205242-66205727	K562	blood:	n/a	chr7:66205666-66205675 chr7:66205621-66205632
11	BCL11A	chr7:66206378-66206626	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:66205157-66205563	GM12878	blood:	n/a	chr7:66205371-66205384
13	BCL3	chr7:66205230-66205747	A549	lung:	n/a	chr7:66205614-66205623 chr7:66205371-66205384
14	BCL3	chr7:66205247-66206208	GM12878	blood:	n/a	chr7:66205614-66205623 chr7:66205371-66205384 chr7:66205832-66205845 chr7:66205834-66205843
15	BCL3	chr7:66205350-66205830	A549	lung:	n/a	chr7:66205614-66205623 chr7:66205371-66205384
16	BCLAF1	chr7:66204952-66205904	GM12878	blood:	n/a	chr7:66205614-66205623 chr7:66205371-66205384 chr7:66205832-66205845 chr7:66205834-66205843
17	BCLAF1	chr7:66204826-66205902	GM12878	blood:	n/a	chr7:66205614-66205623 chr7:66205371-66205384 chr7:66205832-66205845 chr7:66205834-66205843
18	BCLAF1	chr7:66197407-66197836	GM12878	blood:	n/a	chr7:66197622-66197631
19	BHLHE40	chr7:66204799-66204999	K562	blood:	n/a	n/a
20	BHLHE40	chr7:66205313-66206296	GM12878	blood:	n/a	chr7:66206234-66206250 chr7:66205657-66205673 chr7:66206236-66206252
21	BHLHE40	chr7:66197553-66197751	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:66205317-66206281	K562	blood:	n/a	chr7:66206234-66206250 chr7:66205657-66205673 chr7:66206236-66206252
23	BRCA1	chr7:66205262-66205697	HepG2	liver:	n/a	n/a
24	BRCA1	chr7:66205291-66206265	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr7:66194449-66194468	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr7:66200893-66201187	K562	blood:	n/a	n/a
27	CBX3	chr7:66204579-66206971	K562	blood:	n/a	n/a
28	CBX3	chr7:66193596-66193906	K562	blood:	n/a	n/a
29	CBX3	chr7:66200842-66201279	K562	blood:	n/a	n/a
30	CBX3	chr7:66204807-66205713	K562	blood:	n/a	n/a
31	CCNT2	chr7:66205229-66206351	K562	blood:	n/a	chr7:66205666-66205675
32	CEBPB	chr7:66206415-66206587	K562	blood:	n/a	n/a
33	CEBPB	chr7:66204555-66205001	MCF-7	breast:	n/a	chr7:66204681-66204692
34	CEBPB	chr7:66204486-66205022	K562	blood:	n/a	chr7:66204681-66204692
35	CEBPB	chr7:66204499-66205013	IMR90	lung:	n/a	chr7:66204681-66204692
36	CEBPB	chr7:66204588-66205020	MCF-7	breast:	n/a	chr7:66204681-66204692
37	CEBPB	chr7:66191924-66192215	K562	blood:	n/a	chr7:66192152-66192163 chr7:66192030-66192041
38	CEBPB	chr7:66191930-66192211	HepG2	liver:	n/a	chr7:66192152-66192163 chr7:66192030-66192041
39	CEBPB	chr7:66204528-66204803	HepG2	liver:	n/a	chr7:66204681-66204692
40	CEBPB	chr7:66206388-66206730	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:66204489-66205670	K562	blood:	n/a	chr7:66204681-66204692
42	CEBPB	chr7:66204582-66204859	ECC-1	luminal epithelium:	n/a	chr7:66204681-66204692
43	CEBPB	chr7:66205292-66205769	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:66205003-66205518	GM12878	blood:	n/a	n/a
45	CEBPB	chr7:66204516-66204856	HepG2	liver:	n/a	chr7:66204681-66204692
46	CEBPB	chr7:66206387-66206580	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr7:66191893-66192215	IMR90	lung:	n/a	chr7:66192152-66192163 chr7:66192030-66192041
48	CEBPB	chr7:66203932-66204123	IMR90	lung:	n/a	chr7:66203993-66204004
49	CEBPB	chr7:66204537-66204997	H1-hESC	embryonic stem cell:	n/a	chr7:66204681-66204692
50	CEBPB	chr7:66204606-66204925	K562	blood:	n/a	chr7:66204681-66204692

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:66206258-66206308	SK-N-SH	brain:	n/a
2	chr7:66202871-66202921	T-47D	breast:	n/a
3	chr7:66206258-66206308	SK-N-SH	brain:	n/a
4	chr7:66202871-66202921	T-47D	breast:	n/a
5	chr7:66205833-66205883	HRPEpiC	eye:	n/a
6	chr7:66205833-66205883	HAEpiC	amniotic membrane:	n/a
7	chr7:66205495-66205545	PANC-1	pancreas:	n/a
8	chr7:66205729-66205779	HCPEpiC	choroid plexus:	n/a
9	chr7:66205334-66205384	MCF-7	breast:	n/a
10	chr7:66202871-66202921	HepG2	liver:	n/a
11	chr7:66205729-66205779	NHBE	bronchial:	n/a
12	chr7:66205729-66205779	SK-N-MC	brain:	n/a
13	chr7:66204797-66204847	MCF-7	breast:	n/a
14	chr7:66205482-66205532	SKMC	muscle:	n/a
15	chr7:66202871-66202921	SK-N-SH_RA	brain:	n/a
16	chr7:66206258-66206308	AG09309	skin:	n/a
17	chr7:66205334-66205384	ECC-1	luminal epithelium:	n/a
18	chr7:66205470-66205520	NHDF-neo	bronchial:	n/a
19	chr7:66205470-66205520	HMEC	breast:	n/a
20	chr7:66207656-66207706	SK-N-MC	brain:	n/a
21	chr7:66205482-66205532	K562	blood:	n/a
22	chr7:66205729-66205779	K562	blood:	n/a
23	chr7:66207656-66207706	HIPEpiC	eye:	n/a
24	chr7:66205833-66205883	ovcar-3	ovarian:	n/a
25	chr7:66205542-66205592	GM12892	blood:	n/a
26	chr7:66202871-66202921	Hepatocyte	liver:	n/a
27	chr7:66204797-66204847	HAEpiC	amniotic membrane:	n/a
28	chr7:66205246-66205296	Hela-S3	cervix:	n/a
29	chr7:66205003-66205053	H1-hESC	embryonic stem cell:	embryo
30	chr7:66207656-66207706	AG09309	skin:	n/a
31	chr7:66205833-66205883	GM06990	blood:	n/a
32	chr7:66205482-66205532	HEK293	kidney:	embryo
33	chr7:66205003-66205053	AG04449	skin:	fetal
34	chr7:66205733-66205783	SK-N-SH	brain:	n/a
35	chr7:66205470-66205520	AG10803	skin:	n/a
36	chr7:66205495-66205545	RPTEC	kidney:	n/a
37	chr7:66206258-66206308	T-47D	breast:	n/a
38	chr7:66202871-66202921	AG04449	skin:	fetal
39	chr7:66205733-66205783	AG09319	gingival:	n/a
40	chr7:66207656-66207706	HMEC	breast:	n/a
41	chr7:66205334-66205384	HCPEpiC	choroid plexus:	n/a
42	chr7:66205729-66205779	GM19239	blood:	n/a
43	chr7:66205729-66205779	HNPCEpiC	eye:	n/a
44	chr7:66205334-66205384	NH-A	brain:	n/a
45	chr7:66204797-66204847	GM12892	blood:	n/a
46	chr7:66205495-66205545	PFSK-1	brain:	n/a
47	chr7:66205334-66205384	H1-hESC	embryonic stem cell:	embryo
48	chr7:66205833-66205883	PrEC	prostate:	n/a
49	chr7:66205455-66205505	U87	brain:	n/a
50	chr7:66207656-66207706	HCF	heart:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:62612068..62612707-chr7:66205545..66206428,2	Hela-S3	cervix:
2	chr7:66204257..66207102-chr7:66209621..66212224,4	MCF-7	breast:
3	chr7:66152724..66154924-chr7:66196549..66198273,2	MCF-7	breast:
4	chr7:66203955..66208659-chr7:66209716..66215353,8	K562	blood:
5	chr7:66119315..66119930-chr7:66205425..66206247,2	NB4	blood:
6	chr10:81964075..81964667-chr7:66203761..66204300,2	Hela-S3	cervix:
7	chr7:66209588..66211104-chr7:66309557..66311367,2	MCF-7	breast:
8	chr7:66195907..66197656-chr7:66213720..66216464,2	MCF-7	breast:
9	chr7:66205946..66208187-chr7:66309676..66311325,2	MCF-7	breast:
10	chr7:66193504..66195252-chr7:66203125..66205739,2	MCF-7	breast:
11	chr7:66118228..66120742-chr7:66209055..66211057,2	MCF-7	breast:
12	chr7:66198882..66201423-chr7:66203889..66205689,3	K562	blood:
13	chr7:66192001..66196955-chr7:66201177..66204851,5	K562	blood:
14	chr7:66205725..66207353-chr7:66207678..66209182,2	MCF-7	breast:
15	chr7:66189119..66192033-chr7:66195349..66197808,2	MCF-7	breast:
16	chr7:66205725..66207353-chr7:66207678..66209182,2	MCF-7	breast:
17	chr7:66204928..66209821-chr7:66213597..66216412,7	MCF-7	breast:
18	chr7:66117717..66119604-chr7:66204829..66207389,2	K562	blood:
19	chr7:66194758..66197486-chr7:66199792..66202230,3	MCF-7	breast:
20	chr7:66118548..66121026-chr7:66205734..66207315,2	MCF-7	breast:
21	chr7:66193552..66195929-chr7:66201268..66203494,2	K562	blood:
22	chr7:66145819..66148736-chr7:66203770..66205462,3	MCF-7	breast:
23	chr7:66194758..66197486-chr7:66199792..66202230,3	MCF-7	breast:
24	chr7:66119236..66121485-chr7:66204940..66206778,2	K562	blood:
25	chr1:28832466..28833159-chr7:66205007..66205858,2	NB4	blood:
26	chr7:66192001..66196955-chr7:66201177..66204851,5	K562	blood:
27	chr1:150551545..150552358-chr7:66205002..66205777,2	Hela-S3	cervix:
28	chr7:66198882..66202892-chr7:66203782..66206309,4	K562	blood:
29	chr7:66197230..66199393-chr7:66204759..66206866,2	MCF-7	breast:
30	chr7:66118921..66119611-chr7:66204868..66205819,2	HCT-116	colon:
31	chr7:66117314..66120062-chr7:66210977..66213938,2	K562	blood:
32	chr3:50378036..50378624-chr7:66205521..66206190,2	Hela-S3	cervix:
33	chr7:66161177..66163221-chr7:66202677..66204246,2	MCF-7	breast:
34	chr7:66211368..66213994-chr7:66217034..66219333,2	MCF-7	breast:
35	chr7:66199744..66203174-chr7:66203641..66207564,4	MCF-7	breast:
36	chr7:66146728..66147607-chr7:66205638..66206158,2	NB4	blood:
37	chr15:78832192..78833048-chr7:66205633..66206174,2	Hela-S3	cervix:
38	chr7:66209147..66212594-chr7:66215527..66217393,3	MCF-7	breast:
39	chr7:66167573..66170177-chr7:66193473..66196391,2	K562	blood:
40	chr7:66021310..66024220-chr7:66204826..66206647,2	MCF-7	breast:
41	chr7:66144717..66148625-chr7:66203954..66207507,5	K562	blood:
42	chr7:66193552..66195929-chr7:66201268..66203494,2	K562	blood:
43	chr7:66203955..66208659-chr7:66209716..66215353,8	K562	blood:
44	chr7:66144687..66148625-chr7:66203954..66207507,6	K562	blood:
45	chr7:66205494..66207120-chr7:66460055..66461810,2	MCF-7	breast:
46	chr7:66204784..66206359-chr7:66385620..66388278,2	MCF-7	breast:
47	chr7:66161961..66163961-chr7:66193287..66195018,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SBDS-15	chr7:66204816-66205372	ENSG00000272831.1

No data

Variant related genes	Relation type
ENSG00000272831	TF binding region
KCTD7	TF binding region
RABGEF1	TF binding region
ENSG00000272831	CpG island
KCTD7	CpG island
RABGEF1	CpG island
ENSG00000068028	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000198874	chromatin interactions
ENSG00000271064	chromatin interactions
ENSG00000235058	chromatin interactions
ENSG00000177418	chromatin interactions
ENSG00000243335	chromatin interactions
ENSG00000230583	chromatin interactions
ENSG00000122359	chromatin interactions
ENSG00000101161	chromatin interactions
ENSG00000154710	chromatin interactions
ENSG00000242125	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000041357	chromatin interactions
ENSG00000106609	chromatin interactions
ENSG00000272831	chromatin interactions
ENSG00000226824	chromatin interactions
ENSG00000126524	chromatin interactions

Extended variants
information (count: 911 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:911 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556851214	chr7:66192210-66192211	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567616875	chr7:66192286-66192287	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553287218	chr7:66192300-66192301	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150223104	chr7:66192330-66192331	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535074105	chr7:66192337-66192338	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs187030546	chr7:66192384-66192385	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546751901	chr7:66192394-66192395	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs62466795	chr7:66192498-66192499	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs540713183	chr7:66192522-66192523	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs563884946	chr7:66192545-66192546	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs138774527	chr7:66192549-66192550	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs543221906	chr7:66192555-66192556	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs563401410	chr7:66192562-66192563	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs529210037	chr7:66192571-66192572	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs549037284	chr7:66192602-66192603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111636104	chr7:66192623-66192624	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529540346	chr7:66192628-66192629	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527726022	chr7:66192656-66192657	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547911478	chr7:66192657-66192658	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549365680	chr7:66192662-66192663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs539999868	chr7:66192673-66192674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550415777	chr7:66192684-66192685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117328880	chr7:66192696-66192697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs537820093	chr7:66192697-66192698	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536130186	chr7:66192728-66192729	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs555823494	chr7:66192733-66192734	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73137978	chr7:66192739-66192740	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534320174	chr7:66192748-66192749	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185081904	chr7:66192775-66192776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189959086	chr7:66192802-66192803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs114986629	chr7:66192813-66192814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78067727	chr7:66192827-66192828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573790875	chr7:66192853-66192854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542897842	chr7:66192870-66192871	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559435648	chr7:66192871-66192872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527640805	chr7:66192880-66192881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374360626	chr7:66192890-66192891	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149510525	chr7:66192923-66192924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182126606	chr7:66192940-66192941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533489127	chr7:66192946-66192947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145986239	chr7:66192948-66192949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138779271	chr7:66192969-66192970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529506926	chr7:66192982-66192983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs549605588	chr7:66193000-66193001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566252801	chr7:66193011-66193012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534284164	chr7:66193020-66193021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184627933	chr7:66193037-66193038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371072745	chr7:66193064-66193065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs2707839	chr7:66193084-66193085	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs78949927	chr7:66193117-66193118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
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
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
Hodgkin''s lymphoma	18641027	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
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	21346763	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:66149000-66199600	Weak transcription	Thymus	Thymus
2	chr7:66162600-66192400	Weak transcription	NH-A	brain
3	chr7:66162600-66196800	Weak transcription	Right Ventricle	heart
4	chr7:66165400-66204600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr7:66165800-66197000	Weak transcription	Right Atrium	heart
6	chr7:66176400-66204600	Weak transcription	Colonic Mucosa	Colon
7	chr7:66177600-66193600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr7:66178600-66200400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr7:66178800-66193600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr7:66178800-66197000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr7:66179000-66197200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr7:66179200-66200600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr7:66179400-66199800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:66179600-66204600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr7:66180800-66193600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:66181600-66193600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr7:66181600-66196000	Weak transcription	Ovary	ovary
18	chr7:66181600-66202000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:66182600-66199800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr7:66182800-66205000	Weak transcription	Gastric	stomach
21	chr7:66184000-66192200	Weak transcription	Fetal Brain Female	brain
22	chr7:66184400-66192200	Weak transcription	Stomach Smooth Muscle	stomach
23	chr7:66185400-66197600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:66188400-66196800	Weak transcription	Adipose Nuclei	Adipose
25	chr7:66188400-66201800	Weak transcription	Fetal Brain Male	brain
26	chr7:66189400-66197000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr7:66189600-66193600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:66189800-66196800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:66190000-66193800	Strong transcription	Fetal Intestine Small	intestine
30	chr7:66190000-66194000	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr7:66190000-66200400	Weak transcription	HepG2	liver
32	chr7:66190000-66201200	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr7:66190200-66198800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr7:66190400-66196200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:66190400-66197600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:66190400-66204600	Weak transcription	Stomach Mucosa	stomach
37	chr7:66190600-66193600	Strong transcription	Fetal Stomach	stomach
38	chr7:66190600-66200200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr7:66190600-66201200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr7:66190800-66194200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr7:66190800-66200200	Weak transcription	Brain Anterior Caudate	brain
42	chr7:66190800-66200400	Weak transcription	Primary hematopoietic stem cells	blood
43	chr7:66190800-66200600	Weak transcription	HSMM	muscle
44	chr7:66190800-66204400	Weak transcription	Fetal Heart	heart
45	chr7:66190800-66204600	Weak transcription	NHEK	skin
46	chr7:66191000-66192200	Weak transcription	HMEC	breast
47	chr7:66191000-66193400	Weak transcription	Fetal Kidney	kidney
48	chr7:66191000-66193600	Weak transcription	Spleen	Spleen
49	chr7:66191000-66197200	Weak transcription	GM12878-XiMat	blood
50	chr7:66191000-66197200	Weak transcription	HSMMtube	muscle

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