Variant report

Variant	nsv887437
Chromosome Location	chr7:6645281-6704332
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1565)
CpG islands
(count:3545)
Chromatin interactive
region (count:115)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6680032-6680221	K562	blood:	n/a	n/a
2	ATF1	chr7:6652571-6652812	K562	blood:	n/a	n/a
3	ATF2	chr7:6676670-6676974	GM12878	blood:	n/a	n/a
4	ATF3	chr7:6676764-6677038	K562	blood:	n/a	n/a
5	ATF3	chr7:6676775-6677020	GM12878	blood:	n/a	n/a
6	ATF3	chr7:6676729-6677016	HepG2	liver:	n/a	n/a
7	ATF3	chr7:6679904-6680092	K562	blood:	n/a	n/a
8	ATF3	chr7:6676663-6677108	GM12878	blood:	n/a	n/a
9	BACH1	chr7:6676690-6676978	K562	blood:	n/a	n/a
10	BACH1	chr7:6677373-6677430	K562	blood:	n/a	n/a
11	BACH1	chr7:6676413-6677735	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr7:6703886-6703996	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr7:6679547-6679737	GM12878	blood:	n/a	n/a
14	BATF	chr7:6659295-6659530	GM12878	blood:	n/a	n/a
15	BCL3	chr7:6662021-6662558	GM12878	blood:	n/a	chr7:6662039-6662052 chr7:6662045-6662058 chr7:6662050-6662059 chr7:6662047-6662056 chr7:6662040-6662053 chr7:6662044-6662053 chr7:6662036-6662049
16	BCL3	chr7:6676620-6677051	GM12878	blood:	n/a	chr7:6676897-6676906
17	BCL3	chr7:6662073-6662402	GM12878	blood:	n/a	n/a
18	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
19	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
20	BCLAF1	chr7:6676612-6677075	GM12878	blood:	n/a	chr7:6676897-6676906
21	BHLHE40	chr7:6698826-6699225	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:6679828-6680319	K562	blood:	n/a	n/a
23	BHLHE40	chr7:6677264-6677647	K562	blood:	n/a	chr7:6677407-6677423
24	BHLHE40	chr7:6679587-6679733	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:6676405-6676427	K562	blood:	n/a	n/a
26	BHLHE40	chr7:6698832-6699007	K562	blood:	n/a	n/a
27	BHLHE40	chr7:6663730-6663805	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:6676722-6677023	K562	blood:	n/a	n/a
29	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
30	BHLHE40	chr7:6676643-6677601	GM12878	blood:	n/a	chr7:6677407-6677423
31	BRCA1	chr7:6698867-6699045	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr7:6652546-6652789	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr7:6677286-6677693	K562	blood:	n/a	n/a
34	CBX3	chr7:6679776-6680216	K562	blood:	n/a	n/a
35	CBX3	chr7:6679531-6680589	K562	blood:	n/a	n/a
36	CBX3	chr7:6676642-6676930	K562	blood:	n/a	n/a
37	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
38	CCNT2	chr7:6676308-6677623	K562	blood:	n/a	n/a
39	CEBPB	chr7:6661168-6661656	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr7:6699089-6699426	H1-hESC	embryonic stem cell:	n/a	chr7:6699226-6699237
41	CEBPB	chr7:6659301-6659458	A549	lung:	n/a	n/a
42	CEBPB	chr7:6698995-6699540	ECC-1	luminal epithelium:	n/a	chr7:6699226-6699237
43	CEBPB	chr7:6698987-6699470	MCF-7	breast:	n/a	chr7:6699226-6699237
44	CEBPB	chr7:6679421-6679645	A549	lung:	n/a	n/a
45	CEBPB	chr7:6698891-6699407	HepG2	liver:	n/a	chr7:6699226-6699237
46	CEBPB	chr7:6658239-6658266	A549	lung:	n/a	n/a
47	CEBPB	chr7:6679441-6679533	K562	blood:	n/a	n/a
48	CEBPB	chr7:6661397-6661453	A549	lung:	n/a	n/a
49	CEBPB	chr7:6699039-6699442	ECC-1	luminal epithelium:	n/a	chr7:6699226-6699237
50	CEBPB	chr7:6679964-6680434	K562	blood:	n/a	n/a

(count:3545 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6703708-6703758	AG09319	gingival:	n/a
2	chr7:6646162-6646212	LNCaP	prostate:	n/a
3	chr7:6655973-6656023	HUVEC	blood vessel:	n/a
4	chr7:6661804-6661854	SK-N-MC	brain:	n/a
5	chr7:6704194-6704244	LNCaP	prostate:	n/a
6	chr7:6646162-6646212	AG09309	skin:	n/a
7	chr7:6655711-6655761	PrEC	prostate:	n/a
8	chr7:6703708-6703758	AG09319	gingival:	n/a
9	chr7:6646162-6646212	LNCaP	prostate:	n/a
10	chr7:6655973-6656023	HUVEC	blood vessel:	n/a
11	chr7:6661804-6661854	SK-N-MC	brain:	n/a
12	chr7:6704194-6704244	LNCaP	prostate:	n/a
13	chr7:6646162-6646212	AG09309	skin:	n/a
14	chr7:6655711-6655761	PrEC	prostate:	n/a
15	chr7:6704074-6704124	AoSMC	blood vessel:	n/a
16	chr7:6651748-6651798	SK-N-SH_RA	brain:	n/a
17	chr7:6647955-6648005	GM19239	blood:	n/a
18	chr7:6692873-6692923	ProgFib	skin:	n/a
19	chr7:6703708-6703758	NT2-D1	testis:	n/a
20	chr7:6695121-6695171	HRE	kidney:	n/a
21	chr7:6699526-6699576	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:6694373-6694423	Jurkat	blood:	n/a
23	chr7:6655711-6655761	HL-60	blood:	n/a
24	chr7:6694978-6695028	PANC-1	pancreas:	n/a
25	chr7:6690313-6690363	K562	blood:	n/a
26	chr7:6654422-6654472	U87	brain:	n/a
27	chr7:6698992-6699042	MCF10A-Er-Src	breast:	n/a
28	chr7:6654422-6654472	PFSK-1	brain:	n/a
29	chr7:6704045-6704095	H1-hESC	embryonic stem cell:	embryo
30	chr7:6694373-6694423	A549	lung:	n/a
31	chr7:6648166-6648216	SK-N-MC	brain:	n/a
32	chr7:6693334-6693384	ECC-1	luminal epithelium:	n/a
33	chr7:6703533-6703583	AG09319	gingival:	n/a
34	chr7:6676832-6676882	GM19239	blood:	n/a
35	chr7:6694735-6694785	T-47D	breast:	n/a
36	chr7:6698992-6699042	Hela-S3	cervix:	n/a
37	chr7:6699526-6699576	PANC-1	pancreas:	n/a
38	chr7:6676001-6676051	HPAEpiC	pulmonary alveolar:	n/a
39	chr7:6651748-6651798	HL-60	blood:	n/a
40	chr7:6691949-6691999	Jurkat	blood:	n/a
41	chr7:6704194-6704244	MCF10A-Er-Src	breast:	n/a
42	chr7:6660095-6660145	HepG2	liver:	n/a
43	chr7:6698992-6699042	AG09319	gingival:	n/a
44	chr7:6689218-6689268	U87	brain:	n/a
45	chr7:6682784-6682834	HepG2	liver:	n/a
46	chr7:6655973-6656023	GM12891	blood:	n/a
47	chr7:6695092-6695142	MCF-7	breast:	n/a
48	chr7:6704194-6704244	SAEC	small airway:	n/a
49	chr7:6693838-6693888	Hepatocyte	liver:	n/a
50	chr7:6676630-6676680	PFSK-1	brain:	n/a

(count:115 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:6628238..6630542-chr7:6653702..6656593,2	MCF-7	breast:
2	chr7:6652934..6655791-chr7:6675915..6678392,2	MCF-7	breast:
3	chr7:6675529..6677980-chr7:6768487..6770695,2	K562	blood:
4	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
5	chr7:6661901..6664151-chr7:6670252..6671986,3	MCF-7	breast:
6	chr7:6615800..6617832-chr7:6677563..6680150,2	MCF-7	breast:
7	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
8	chr7:6614762..6617092-chr7:6682142..6684739,2	K562	blood:
9	chr7:6629736..6633407-chr7:6648974..6652007,3	MCF-7	breast:
10	chr7:6668744..6673941-chr7:6674951..6679228,16	MCF-7	breast:
11	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
12	chr7:6654514..6658630-chr7:6675114..6678876,5	MCF-7	breast:
13	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
14	chr7:6674043..6676883-chr7:6677067..6680291,5	K562	blood:
15	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
16	chr7:6649329..6651399-chr7:6652543..6654507,2	MCF-7	breast:
17	chr7:6637338..6640081-chr7:6675258..6678566,5	MCF-7	breast:
18	chr7:6656839..6659879-chr7:6661538..6663786,3	K562	blood:
19	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
20	chr12:56510812..56512603-chr7:6677169..6678802,2	MCF-7	breast:
21	chr7:6626891..6631454-chr7:6676260..6679154,6	K562	blood:
22	chr7:6645718..6648142-chr7:6667020..6668593,2	K562	blood:
23	chr17:41465185..41465700-chr7:6676633..6677215,2	Hela-S3	cervix:
24	chr7:6679487..6682483-chr7:6695124..6696654,2	MCF-7	breast:
25	chr7:6522385..6525546-chr7:6675389..6679461,5	MCF-7	breast:
26	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
27	chr7:6659549..6661363-chr7:6670073..6672008,2	K562	blood:
28	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
29	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:
30	chr7:6541950..6543739-chr7:6677071..6679453,2	K562	blood:
31	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
32	chr7:6652722..6654943-chr7:6655850..6658545,2	K562	blood:
33	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
34	chr7:6696313..6698315-chr7:6745284..6746997,2	K562	blood:
35	chr7:6666282..6668533-chr7:6675191..6678454,4	MCF-7	breast:
36	chr7:6642714..6644762-chr7:6645777..6647383,2	K562	blood:
37	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
38	chr7:6570467..6572933-chr7:6675256..6676794,2	MCF-7	breast:
39	chr7:6669484..6671433-chr7:6744514..6747927,3	MCF-7	breast:
40	chr7:6628726..6630315-chr7:6654459..6656349,2	MCF-7	breast:
41	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
42	chr7:6656631..6659250-chr7:6667009..6671468,4	MCF-7	breast:
43	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
44	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
45	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
46	chr7:6645718..6648142-chr7:6667020..6668593,2	K562	blood:
47	chr7:6644575..6647418-chr7:6652621..6655088,2	K562	blood:
48	chr7:6645170..6647656-chr7:6721647..6723270,2	K562	blood:
49	chr7:6652934..6655791-chr7:6675915..6678392,2	MCF-7	breast:
50	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF853-2	chr7:6679361-6680635	ucscGeneNc_uc003sqr_1
2	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
3	lnc-ZNF853-2	chr7:6670130-6670199	ucscGeneNc_uc003sqr_1
4	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119055
5	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1
6	lnc-ZNF853-2	chr7:6671200-6671264	ucscGeneNc_uc003sqr_1
7	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
8	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119056
9	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1

No data

Variant related genes	Relation type
ZNF853	TF binding region
ZNF316	TF binding region
ENSG00000260054	TF binding region
ENSG00000228010	TF binding region
ZNF853	CpG island
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000228010	CpG island
ENSG00000205903	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000228010	chromatin interactions
ENSG00000198580	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2673 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2673 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4724827	chr7:6645281-6645282	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541197592	chr7:6645300-6645301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73346973	chr7:6645319-6645320	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs550325163	chr7:6645328-6645329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141147946	chr7:6645355-6645356	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551840161	chr7:6645361-6645362	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs144990621	chr7:6645385-6645386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530910113	chr7:6645452-6645453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549430819	chr7:6645454-6645455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562420960	chr7:6645457-6645458	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373563082	chr7:6645527-6645528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568335714	chr7:6645549-6645550	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533079178	chr7:6645552-6645553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563802222	chr7:6645556-6645557	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs185972153	chr7:6645571-6645572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs189097531	chr7:6645621-6645622	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565858022	chr7:6645641-6645642	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs539303975	chr7:6645644-6645645	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531504701	chr7:6645650-6645651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs61121531	chr7:6645680-6645681	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs536617855	chr7:6645705-6645706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs554962902	chr7:6645725-6645726	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs115633673	chr7:6645736-6645737	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182234173	chr7:6645747-6645748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543155767	chr7:6645762-6645763	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs60161508	chr7:6645786-6645787	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs578121191	chr7:6645788-6645789	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs187159132	chr7:6645802-6645803	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs56678265	chr7:6645810-6645811	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs563785926	chr7:6645869-6645870	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs114735146	chr7:6645895-6645896	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs374815292	chr7:6645900-6645901	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs542998539	chr7:6645968-6645969	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs561277251	chr7:6645979-6645980	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs61068758	chr7:6646002-6646003	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs192509961	chr7:6646005-6646006	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs66748789	chr7:6646017-6646018	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs71010905	chr7:6646019-6646020	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs60466263	chr7:6646034-6646035	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs571486961	chr7:6646044-6646045	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs533136584	chr7:6646048-6646049	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551304529	chr7:6646058-6646059	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs182491705	chr7:6646062-6646063	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs114007331	chr7:6646065-6646066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs554899599	chr7:6646072-6646073	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs56906567	chr7:6646086-6646087	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs534362906	chr7:6646087-6646088	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs185212033	chr7:6646103-6646104	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs550350993	chr7:6646122-6646123	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs568836565	chr7:6646126-6646127	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2670 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6631000-6646200	Strong transcription	Brain Anterior Caudate	brain
2	chr7:6631000-6646800	Strong transcription	Fetal Intestine Large	intestine
3	chr7:6631200-6648200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:6631200-6648400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:6631200-6648400	Strong transcription	Placenta	Placenta
6	chr7:6631200-6648600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:6631200-6649200	Strong transcription	Fetal Muscle Leg	muscle
8	chr7:6631200-6649200	Strong transcription	Fetal Thymus	thymus
9	chr7:6631200-6649400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:6631200-6649400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr7:6631200-6649400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:6631200-6649400	Strong transcription	Fetal Muscle Trunk	muscle
13	chr7:6631400-6647600	Weak transcription	Stomach Mucosa	stomach
14	chr7:6631400-6648400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:6631400-6649000	Strong transcription	Brain Inferior Temporal Lobe	brain
16	chr7:6631400-6649400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr7:6631400-6649400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr7:6631400-6649600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:6631400-6649600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr7:6631400-6649800	Strong transcription	Fetal Intestine Small	intestine
21	chr7:6631400-6649800	Strong transcription	Fetal Stomach	stomach
22	chr7:6631600-6647200	Strong transcription	Primary B cells from peripheral blood	blood
23	chr7:6631600-6648400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr7:6631600-6648800	Strong transcription	Lung	lung
25	chr7:6631600-6649400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr7:6631600-6649400	Strong transcription	Liver	Liver
27	chr7:6631600-6650800	Strong transcription	Thymus	Thymus
28	chr7:6631800-6648800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:6631800-6649200	Strong transcription	Dnd41	blood
30	chr7:6632000-6646200	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr7:6632000-6648800	Strong transcription	Sigmoid Colon	Sigmoid Colon
32	chr7:6632000-6649400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr7:6632000-6649400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr7:6632000-6649600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr7:6632000-6650600	Strong transcription	Brain Germinal Matrix	brain
36	chr7:6632200-6648400	Strong transcription	Primary T cells from cord blood	blood
37	chr7:6632200-6648400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr7:6632200-6648600	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr7:6632200-6648800	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr7:6632400-6646400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:6632400-6648400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr7:6632400-6648800	Strong transcription	Skeletal Muscle Female	skeletal muscle
43	chr7:6632400-6649400	Strong transcription	Stomach Smooth Muscle	stomach
44	chr7:6632400-6649400	Strong transcription	Spleen	Spleen
45	chr7:6632400-6649600	Strong transcription	Adipose Nuclei	Adipose
46	chr7:6632600-6649400	Strong transcription	Fetal Brain Female	brain
47	chr7:6632800-6649400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
48	chr7:6633200-6648600	Strong transcription	Esophagus	oesophagus
49	chr7:6634400-6648400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:6635400-6646400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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