Variant report

Variant	nsv887417
Chromosome Location	chr7:5667645-5760860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2356)
CpG islands
(count:977)
Chromatin interactive
region (count:221)
LncRNA
region (count:3)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2356 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:5733216-5733346	K562	blood:	n/a	n/a
2	ATF1	chr7:5682942-5683270	K562	blood:	n/a	n/a
3	ATF1	chr7:5733174-5733503	K562	blood:	n/a	n/a
4	ATF2	chr7:5732593-5735757	GM12878	blood:	n/a	n/a
5	ATF2	chr7:5740476-5741188	GM12878	blood:	n/a	n/a
6	ATF2	chr7:5719591-5720169	GM12878	blood:	n/a	n/a
7	ATF2	chr7:5678607-5679025	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr7:5738974-5740374	GM12878	blood:	n/a	n/a
9	ATF2	chr7:5732828-5735667	GM12878	blood:	n/a	n/a
10	ATF2	chr7:5739046-5741421	GM12878	blood:	n/a	n/a
11	ATF2	chr7:5678598-5679031	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:5705036-5705355	K562	blood:	n/a	n/a
13	BACH1	chr7:5676117-5676335	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:5743825-5744483	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:5717667-5717963	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr7:5722493-5722849	K562	blood:	n/a	n/a
17	BACH1	chr7:5704998-5705370	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:5740831-5741053	H1-hESC	embryonic stem cell:	n/a	chr7:5740930-5740944
19	BACH1	chr7:5743845-5744457	K562	blood:	n/a	n/a
20	BACH1	chr7:5722464-5722877	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:5706119-5706180	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:5676571-5677031	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr7:5740589-5741297	GM12878	blood:	n/a	chr7:5740929-5740940 chr7:5740930-5740940
24	BATF	chr7:5734904-5735533	GM12878	blood:	n/a	n/a
25	BATF	chr7:5735116-5735510	GM12878	blood:	n/a	n/a
26	BATF	chr7:5739677-5739969	GM12878	blood:	n/a	n/a
27	BATF	chr7:5740767-5741120	GM12878	blood:	n/a	chr7:5740929-5740940 chr7:5740930-5740940
28	BATF	chr7:5730343-5730657	GM12878	blood:	n/a	chr7:5730559-5730569
29	BATF	chr7:5739671-5740018	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:5733149-5733419	GM12878	blood:	n/a	n/a
31	BCL11A	chr7:5740732-5741187	GM12878	blood:	n/a	chr7:5740932-5740941 chr7:5740933-5740942
32	BCL11A	chr7:5732957-5733586	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:5735090-5735442	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:5734858-5735540	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:5740019-5740349	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:5719764-5720011	GM12878	blood:	n/a	n/a
37	BCL11A	chr7:5739609-5740017	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:5739656-5740030	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:5740817-5741202	GM12878	blood:	n/a	chr7:5740932-5740941 chr7:5740933-5740942
40	BCL3	chr7:5672002-5672209	GM12878	blood:	n/a	chr7:5672043-5672051
41	BCL3	chr7:5731506-5732896	A549	lung:	n/a	n/a
42	BCL3	chr7:5736686-5737131	GM12878	blood:	n/a	n/a
43	BCL3	chr7:5731688-5732221	A549	lung:	n/a	n/a
44	BCL3	chr7:5739530-5740089	GM12878	blood:	n/a	n/a
45	BCL3	chr7:5740682-5741206	GM12878	blood:	n/a	chr7:5740932-5740941 chr7:5740933-5740942
46	BCL3	chr7:5730308-5730684	GM12878	blood:	n/a	n/a
47	BCL3	chr7:5734690-5735476	GM12878	blood:	n/a	n/a
48	BCLAF1	chr7:5739102-5740054	GM12878	blood:	n/a	n/a
49	BCLAF1	chr7:5719542-5720080	GM12878	blood:	n/a	n/a
50	BCLAF1	chr7:5744028-5744456	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5678706-5678756	NHDF-neo	bronchial:	n/a
2	chr7:5678706-5678756	NHDF-neo	bronchial:	n/a
3	chr7:5717968-5718018	GM19239	blood:	n/a
4	chr7:5717968-5718018	AG09309	skin:	n/a
5	chr7:5736195-5736245	Caco-2	colon:	n/a
6	chr7:5736195-5736245	PFSK-1	brain:	n/a
7	chr7:5731340-5731390	SK-N-SH	brain:	n/a
8	chr7:5705264-5705314	SAEC	small airway:	n/a
9	chr7:5682666-5682716	HAEpiC	amniotic membrane:	n/a
10	chr7:5678706-5678756	HEK293	kidney:	embryo
11	chr7:5682666-5682716	AG09319	gingival:	n/a
12	chr7:5675839-5675889	AG04450	lung:	fetal
13	chr7:5705264-5705314	HRE	kidney:	n/a
14	chr7:5736195-5736245	HEEpiC	esophagus:	n/a
15	chr7:5731340-5731390	AG09319	gingival:	n/a
16	chr7:5709854-5709904	SK-N-SH_RA	brain:	n/a
17	chr7:5706684-5706734	A549	lung:	n/a
18	chr7:5712269-5712319	AG04450	lung:	fetal
19	chr7:5705264-5705314	HCM	heart:	n/a
20	chr7:5743854-5743904	HNPCEpiC	eye:	n/a
21	chr7:5735129-5735179	GM12891	blood:	n/a
22	chr7:5706684-5706734	CMK	blood:	n/a
23	chr7:5731340-5731390	K562	blood:	n/a
24	chr7:5717968-5718018	HAEpiC	amniotic membrane:	n/a
25	chr7:5736195-5736245	GM12892	blood:	n/a
26	chr7:5717675-5717725	ECC-1	luminal epithelium:	n/a
27	chr7:5705264-5705314	HL-60	blood:	n/a
28	chr7:5743854-5743904	AoSMC	blood vessel:	n/a
29	chr7:5693657-5693707	AG09319	gingival:	n/a
30	chr7:5675839-5675889	HCF	heart:	n/a
31	chr7:5743854-5743904	HEEpiC	esophagus:	n/a
32	chr7:5712269-5712319	Hela-S3	cervix:	n/a
33	chr7:5735129-5735179	SKMC	muscle:	n/a
34	chr7:5678706-5678756	GM12891	blood:	n/a
35	chr7:5693657-5693707	HEK293	kidney:	embryo
36	chr7:5693657-5693707	AG10803	skin:	n/a
37	chr7:5717968-5718018	ovcar-3	ovarian:	n/a
38	chr7:5706684-5706734	PrEC	prostate:	n/a
39	chr7:5706684-5706734	AG09319	gingival:	n/a
40	chr7:5743854-5743904	IMR90	lung:	fetal
41	chr7:5693657-5693707	CMK	blood:	n/a
42	chr7:5735129-5735179	HAEpiC	amniotic membrane:	n/a
43	chr7:5735129-5735179	RPTEC	kidney:	n/a
44	chr7:5692709-5692759	SK-N-SH	brain:	n/a
45	chr7:5709854-5709904	ovcar-3	ovarian:	n/a
46	chr7:5717675-5717725	BE2_C	brain:	n/a
47	chr7:5709854-5709904	HCPEpiC	choroid plexus:	n/a
48	chr7:5735129-5735179	HL-60	blood:	n/a
49	chr7:5693657-5693707	HRE	kidney:	n/a
50	chr7:5712269-5712319	LNCaP	prostate:	n/a

(count:221 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:5708885..5710643-chr7:5716339..5719013,2	K562	blood:
2	chr7:5697370..5699882-chr7:5703729..5706961,3	MCF-7	breast:
3	chr7:5702659..5705852-chr7:5707033..5711502,4	K562	blood:
4	chr7:5598187..5598749-chr7:5704938..5705693,2	K562	blood:
5	chr7:5705152..5706828-chr7:5708642..5710454,2	K562	blood:
6	chr7:5725711..5728589-chr7:5731191..5734129,5	K562	blood:
7	chr7:5694848..5697610-chr7:5699899..5703275,3	K562	blood:
8	chr7:5535386..5537242-chr7:5691957..5693613,2	K562	blood:
9	chr7:5635670..5636537-chr7:5704737..5705483,2	MCF-7	breast:
10	chr7:5734531..5737530-chr7:5742995..5745148,2	K562	blood:
11	chr7:5612887..5615559-chr7:5708216..5710425,2	K562	blood:
12	chr7:5631076..5635641-chr7:5742427..5745815,5	K562	blood:
13	chr7:5697758..5700180-chr7:5700493..5702713,2	MCF-7	breast:
14	chr7:5602877..5603826-chr7:5704704..5705692,6	MCF-7	breast:
15	chr7:5631675..5634644-chr7:5680116..5683516,5	MCF-7	breast:
16	chr7:5533846..5534509-chr7:5743823..5744628,2	MCF-7	breast:
17	chr7:5633680..5635202-chr7:5695155..5698148,2	K562	blood:
18	chr7:5680983..5682807-chr7:5686516..5688646,2	K562	blood:
19	chr7:5665100..5667122-chr7:5668120..5670662,2	K562	blood:
20	chr7:5751218..5753132-chr7:5756274..5759156,2	K562	blood:
21	chr7:5668201..5671136-chr7:5696894..5699870,2	K562	blood:
22	chr7:5560449..5565594-chr7:5704070..5706723,4	K562	blood:
23	chr7:5569883..5572115-chr7:5735560..5738502,2	MCF-7	breast:
24	chr7:5743795..5744628-chr7:5820920..5821459,2	MCF-7	breast:
25	chr7:5597370..5600329-chr7:5734378..5736141,2	MCF-7	breast:
26	chr7:5697370..5699882-chr7:5703729..5706961,3	MCF-7	breast:
27	chr7:5729527..5732207-chr7:5738007..5741204,4	K562	blood:
28	chr7:5734503..5737746-chr7:5737831..5742522,7	MCF-7	breast:
29	chr7:5563689..5568427-chr7:5701312..5705928,6	K562	blood:
30	chr7:5716923..5718931-chr7:5730393..5732059,2	MCF-7	breast:
31	chr7:5740407..5742553-chr7:5742668..5744217,2	K562	blood:
32	chr7:5687349..5689496-chr7:5690114..5692941,3	K562	blood:
33	chr7:5741868..5743994-chr7:5746945..5748590,2	MCF-7	breast:
34	chr7:5645477..5648196-chr7:5732391..5735372,2	K562	blood:
35	chr7:5702659..5705052-chr7:5710002..5711592,2	K562	blood:
36	chr7:5568674..5572164-chr7:5730880..5732613,3	MCF-7	breast:
37	chr7:5744121..5745807-chr7:5745836..5747712,2	MCF-7	breast:
38	chr7:5601679..5603584-chr7:5667818..5670569,2	MCF-7	breast:
39	chr7:5740535..5742233-chr7:5749544..5751969,2	K562	blood:
40	chr7:5744434..5746074-chr7:5746190..5748350,2	K562	blood:
41	chr7:5600355..5603301-chr7:5701063..5703061,2	K562	blood:
42	chr7:5740407..5742553-chr7:5742668..5744217,2	K562	blood:
43	chr7:5726446..5729138-chr7:5729768..5731774,3	MCF-7	breast:
44	chr7:5659044..5660899-chr7:5710392..5712990,2	K562	blood:
45	chr7:5741868..5743994-chr7:5746945..5748590,2	MCF-7	breast:
46	chr7:5279622..5280486-chr7:5743802..5744352,2	K562	blood:
47	chr7:5691115..5694271-chr7:5695445..5698769,3	MCF-7	breast:
48	chr7:5600937..5604507-chr7:5703845..5707460,5	MCF-7	breast:
49	chr7:5736035..5737796-chr7:5742971..5745754,2	K562	blood:
50	chr7:5569849..5571699-chr7:5681727..5683302,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTB-1	chr7:5702063-5702196	ENSG00000237738.1
2	lnc-ACTB-1	chr7:5719985-5720092	ENSG00000237738.1
3	lnc-ACTB-1	chr7:5706241-5706335	ENSG00000237738.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6874-5p	chr7:5751514-5751536	MIMAT0027648
hsa-miR-6874-3p	chr7:5751471-5751493	MIMAT0027649

No data

Variant related genes	Relation type
RNF216-IT1	TF binding region
RNF216	TF binding region
RNF216-IT1	CpG island
RNF216	CpG island
ENSG00000228974	chromatin interactions
ENSG00000263900	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000011275	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000272719	chromatin interactions
ENSG00000207973	chromatin interactions
ENSG00000237738	chromatin interactions

Extended variants
information (count: 4360 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4360 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3807572	chr7:5667645-5667646	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182452007	chr7:5667650-5667651	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575875313	chr7:5667657-5667658	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557410663	chr7:5667700-5667701	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186772612	chr7:5667738-5667739	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575628460	chr7:5667772-5667773	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528656193	chr7:5667885-5667886	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs111650998	chr7:5667933-5667934	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559530366	chr7:5667941-5667942	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73676616	chr7:5667984-5667985	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs114293253	chr7:5668002-5668003	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs139499016	chr7:5668064-5668065	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs852454	chr7:5668066-5668067	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs191341150	chr7:5668081-5668082	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182446581	chr7:5668085-5668086	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555295636	chr7:5668088-5668089	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs533283846	chr7:5668089-5668090	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552738212	chr7:5668119-5668120	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549088245	chr7:5668120-5668121	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113652216	chr7:5668127-5668128	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538723305	chr7:5668174-5668175	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs557110332	chr7:5668188-5668189	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575558796	chr7:5668293-5668294	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs7788185	chr7:5668312-5668313	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs11314929	chr7:5668317-5668318	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs398003513	chr7:5668332-5668333	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528127951	chr7:5668342-5668343	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs115133829	chr7:5668389-5668390	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs373758114	chr7:5668394-5668395	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555197380	chr7:5668429-5668430	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189057874	chr7:5668433-5668434	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540875787	chr7:5668438-5668439	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs150965109	chr7:5668460-5668461	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533096027	chr7:5668496-5668497	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551378086	chr7:5668504-5668505	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545056380	chr7:5668515-5668516	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7791135	chr7:5668607-5668608	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530480953	chr7:5668704-5668705	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549020658	chr7:5668799-5668800	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567589083	chr7:5668823-5668824	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs112745079	chr7:5668826-5668827	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs78675897	chr7:5668829-5668830	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs62453427	chr7:5668845-5668846	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528365101	chr7:5668855-5668856	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs546415002	chr7:5668879-5668880	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs571092495	chr7:5668887-5668888	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs117438505	chr7:5668888-5668889	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs565015973	chr7:5668934-5668935	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371481169	chr7:5669028-5669029	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs551024155	chr7:5669057-5669058	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	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
Developmental delay	21147756	CNVD
Prostate cancer	18632612	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
Urothelial carcinoma	21177765	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	17440070	CNVD

Chromatin state (count:5368 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5638800-5671000	Weak transcription	Right Atrium	heart
2	chr7:5647600-5673200	Weak transcription	Fetal Brain Male	brain
3	chr7:5650000-5669600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr7:5655600-5673200	Weak transcription	Psoas Muscle	Psoas
5	chr7:5658600-5668600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr7:5659000-5668200	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:5659000-5669800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:5659000-5672800	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr7:5659200-5673400	Strong transcription	Dnd41	blood
10	chr7:5660200-5669200	Strong transcription	Primary T cells from cord blood	blood
11	chr7:5660400-5668000	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr7:5660600-5693800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:5661400-5668000	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr7:5661400-5669800	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr7:5661800-5673600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr7:5663000-5669400	Weak transcription	HUVEC	blood vessel
17	chr7:5663000-5673200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:5663000-5673200	Weak transcription	Stomach Mucosa	stomach
19	chr7:5663600-5669800	Weak transcription	Brain Cingulate Gyrus	brain
20	chr7:5664200-5673600	Weak transcription	Colonic Mucosa	Colon
21	chr7:5664400-5669600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr7:5664600-5667800	Weak transcription	Fetal Intestine Large	intestine
23	chr7:5664600-5669600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr7:5664600-5669600	Weak transcription	Brain Anterior Caudate	brain
25	chr7:5664600-5669800	Weak transcription	Brain Substantia Nigra	brain
26	chr7:5664600-5671400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:5664600-5673200	Weak transcription	Aorta	Aorta
28	chr7:5664600-5673400	Weak transcription	Small Intestine	intestine
29	chr7:5664800-5669600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr7:5664800-5669600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:5664800-5671400	Weak transcription	Pancreas	Pancrea
32	chr7:5665000-5669600	Weak transcription	Fetal Brain Female	brain
33	chr7:5665000-5669600	Weak transcription	Left Ventricle	heart
34	chr7:5665000-5670800	Weak transcription	Fetal Lung	lung
35	chr7:5665000-5671600	Weak transcription	Esophagus	oesophagus
36	chr7:5665000-5673200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:5665200-5669600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr7:5665200-5669600	Weak transcription	Spleen	Spleen
39	chr7:5665200-5671000	Weak transcription	Gastric	stomach
40	chr7:5665200-5671400	Weak transcription	Duodenum Mucosa	Duodenum
41	chr7:5665400-5669600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr7:5665400-5670200	Weak transcription	Brain Angular Gyrus	brain
43	chr7:5665400-5673200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr7:5665600-5669600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:5665600-5670000	Weak transcription	Placenta	Placenta
46	chr7:5665800-5669600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr7:5665800-5670200	Weak transcription	HepG2	liver
48	chr7:5665800-5671400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr7:5666000-5667800	Genic enhancers	Fetal Muscle Trunk	muscle
50	chr7:5666000-5668000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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