Variant report

Variant	nsv889411
Chromosome Location	chr7:149465674-149539138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2565)
CpG islands
(count:3239)
Chromatin interactive
region (count:145)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2565 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:149534971-149535569	K562	blood:	n/a	n/a
2	ARID3A	chr7:149535841-149535998	K562	blood:	n/a	n/a
3	ARID3A	chr7:149535139-149535495	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:149468988-149469116	K562	blood:	n/a	n/a
5	ARID3A	chr7:149497005-149497192	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:149487148-149487379	K562	blood:	n/a	n/a
7	ATF1	chr7:149535083-149535603	K562	blood:	n/a	n/a
8	ATF2	chr7:149535204-149535758	GM12878	blood:	n/a	n/a
9	ATF3	chr7:149535238-149535658	HepG2	liver:	n/a	n/a
10	ATF3	chr7:149535169-149535747	HepG2	liver:	n/a	n/a
11	ATF3	chr7:149535278-149535707	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:149487245-149487558	K562	blood:	n/a	n/a
13	ATF3	chr7:149535189-149535637	GM12878	blood:	n/a	n/a
14	ATF3	chr7:149535296-149535599	GM12878	blood:	n/a	n/a
15	ATF3	chr7:149535201-149535664	K562	blood:	n/a	n/a
16	ATF3	chr7:149535244-149535639	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:149536416-149536466	K562	blood:	n/a	n/a
18	BACH1	chr7:149468291-149468689	K562	blood:	n/a	n/a
19	BACH1	chr7:149471378-149471536	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:149470146-149470517	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:149484599-149484951	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr7:149470828-149470909	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr7:149487050-149487759	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr7:149522460-149522788	K562	blood:	n/a	n/a
25	BACH1	chr7:149534875-149535446	K562	blood:	n/a	n/a
26	BCLAF1	chr7:149535237-149535739	GM12878	blood:	n/a	chr7:149535443-149535456 chr7:149535653-149535666 chr7:149535657-149535670 chr7:149535352-149535365
27	BCLAF1	chr7:149468749-149469265	K562	blood:	n/a	chr7:149468998-149469007
28	BCLAF1	chr7:149535230-149535768	GM12878	blood:	n/a	chr7:149535443-149535456 chr7:149535653-149535666 chr7:149535657-149535670 chr7:149535352-149535365
29	BHLHE40	chr7:149538185-149538369	K562	blood:	n/a	n/a
30	BHLHE40	chr7:149485581-149486169	HepG2	liver:	n/a	n/a
31	BHLHE40	chr7:149470761-149470937	K562	blood:	n/a	n/a
32	BHLHE40	chr7:149469561-149469696	K562	blood:	n/a	n/a
33	BHLHE40	chr7:149468449-149469169	K562	blood:	n/a	n/a
34	BHLHE40	chr7:149470191-149470441	K562	blood:	n/a	chr7:149470279-149470295
35	BHLHE40	chr7:149524649-149524883	K562	blood:	n/a	n/a
36	BHLHE40	chr7:149519647-149519856	K562	blood:	n/a	n/a
37	BHLHE40	chr7:149504258-149504411	K562	blood:	n/a	n/a
38	BHLHE40	chr7:149480644-149480682	K562	blood:	n/a	n/a
39	BHLHE40	chr7:149474321-149474331	K562	blood:	n/a	n/a
40	BHLHE40	chr7:149489080-149489398	K562	blood:	n/a	n/a
41	BHLHE40	chr7:149486849-149486853	K562	blood:	n/a	n/a
42	BHLHE40	chr7:149473430-149473809	K562	blood:	n/a	n/a
43	BHLHE40	chr7:149484475-149485102	K562	blood:	n/a	n/a
44	BHLHE40	chr7:149468628-149469161	GM12878	blood:	n/a	n/a
45	BHLHE40	chr7:149532297-149532624	K562	blood:	n/a	n/a
46	BHLHE40	chr7:149534828-149536545	K562	blood:	n/a	chr7:149535444-149535460 chr7:149535441-149535457 chr7:149535627-149535643
47	BHLHE40	chr7:149487231-149487628	K562	blood:	n/a	n/a
48	BHLHE40	chr7:149509091-149509224	K562	blood:	n/a	n/a
49	BHLHE40	chr7:149523724-149523906	K562	blood:	n/a	n/a
50	BHLHE40	chr7:149508490-149508616	K562	blood:	n/a	n/a

(count:3239 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149473097-149473147	NHDF-neo	bronchial:	n/a
2	chr7:149487338-149487388	AG10803	skin:	n/a
3	chr7:149489783-149489833	PrEC	prostate:	n/a
4	chr7:149473178-149473228	PANC-1	pancreas:	n/a
5	chr7:149535361-149535411	HRPEpiC	eye:	n/a
6	chr7:149532221-149532271	BJ	skin:	n/a
7	chr7:149473097-149473147	NHDF-neo	bronchial:	n/a
8	chr7:149487338-149487388	AG10803	skin:	n/a
9	chr7:149489783-149489833	PrEC	prostate:	n/a
10	chr7:149473178-149473228	PANC-1	pancreas:	n/a
11	chr7:149535361-149535411	HRPEpiC	eye:	n/a
12	chr7:149532221-149532271	BJ	skin:	n/a
13	chr7:149535383-149535433	SK-N-SH	brain:	n/a
14	chr7:149470343-149470393	BE2_C	brain:	n/a
15	chr7:149476924-149476974	Hela-S3	cervix:	n/a
16	chr7:149535717-149535767	HMEC	breast:	n/a
17	chr7:149535383-149535433	RPTEC	kidney:	n/a
18	chr7:149519042-149519092	HCT-116	colon:	n/a
19	chr7:149517519-149517569	SK-N-SH_RA	brain:	n/a
20	chr7:149488213-149488263	U87	brain:	n/a
21	chr7:149535071-149535121	BJ	skin:	n/a
22	chr7:149473097-149473147	HUVEC	blood vessel:	n/a
23	chr7:149470343-149470393	Caco-2	colon:	n/a
24	chr7:149517519-149517569	AG09309	skin:	n/a
25	chr7:149517605-149517655	NHBE	bronchial:	n/a
26	chr7:149469722-149469772	NHBE	bronchial:	n/a
27	chr7:149489783-149489833	HCPEpiC	choroid plexus:	n/a
28	chr7:149535378-149535428	AG09319	gingival:	n/a
29	chr7:149535383-149535433	H1-hESC	embryonic stem cell:	embryo
30	chr7:149470343-149470393	NHDF-neo	bronchial:	n/a
31	chr7:149473097-149473147	AG10803	skin:	n/a
32	chr7:149519042-149519092	PFSK-1	brain:	n/a
33	chr7:149535246-149535296	NT2-D1	testis:	n/a
34	chr7:149471044-149471094	AoSMC	blood vessel:	n/a
35	chr7:149470820-149470870	AG04450	lung:	fetal
36	chr7:149519042-149519092	MCF-7	breast:	n/a
37	chr7:149536854-149536904	NB4	blood:	n/a
38	chr7:149535071-149535121	HCT-116	colon:	n/a
39	chr7:149480305-149480355	T-47D	breast:	n/a
40	chr7:149488213-149488263	Caco-2	colon:	n/a
41	chr7:149470694-149470744	SAEC	small airway:	n/a
42	chr7:149517605-149517655	HMEC	breast:	n/a
43	chr7:149535402-149535452	PFSK-1	brain:	n/a
44	chr7:149519165-149519215	K562	blood:	n/a
45	chr7:149487338-149487388	GM12892	blood:	n/a
46	chr7:149485712-149485762	HUVEC	blood vessel:	n/a
47	chr7:149535378-149535428	PrEC	prostate:	n/a
48	chr7:149487749-149487799	HCF	heart:	n/a
49	chr7:149535717-149535767	RPTEC	kidney:	n/a
50	chr7:149487338-149487388	HEK293	kidney:	embryo

(count:145 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:149471231..149473426-chr7:149502540..149505740,3	MCF-7	breast:
2	chr7:149359338..149360344-chr7:149496249..149497433,4	K562	blood:
3	chr7:149504416..149504923-chr7:149545982..149546934,2	K562	blood:
4	chr7:149520043..149524365-chr7:149535249..149538309,4	MCF-7	breast:
5	chr10:8096209..8098721-chr7:149471620..149473923,2	MCF-7	breast:
6	chr7:149478286..149483291-chr7:149484543..149488292,6	K562	blood:
7	chr7:149534869..149537140-chr7:149569608..149571872,2	MCF-7	breast:
8	chr7:149503828..149507340-chr7:149518386..149521542,3	K562	blood:
9	chr7:149518113..149520685-chr7:149524328..149527196,4	MCF-7	breast:
10	chr7:149534468..149539239-chr7:149549126..149555518,7	MCF-7	breast:
11	chr7:149473801..149475401-chr7:149492673..149494757,2	MCF-7	breast:
12	chr7:149491656..149493796-chr7:149550496..149553442,2	MCF-7	breast:
13	chr7:149535432..149538355-chr7:150102358..150106003,3	MCF-7	breast:
14	chr7:149359595..149361550-chr7:149476876..149478987,2	K562	blood:
15	chr7:149450723..149451333-chr7:149487310..149488062,2	K562	blood:
16	chr7:149471379..149473903-chr7:149490121..149491823,3	MCF-7	breast:
17	chr7:149466134..149470595-chr7:149532425..149537706,5	MCF-7	breast:
18	chr7:149468811..149471165-chr7:149492241..149495834,3	K562	blood:
19	chr7:149487412..149490099-chr7:149499430..149501914,2	K562	blood:
20	chr7:149538606..149540564-chr7:149551907..149553835,2	MCF-7	breast:
21	chr7:149538288..149539809-chr7:149546755..149548278,2	MCF-7	breast:
22	chr7:149520369..149522519-chr7:149531265..149532920,2	K562	blood:
23	chr7:149158020..149159528-chr7:149468647..149470369,2	K562	blood:
24	chr1:144533785..144534480-chr7:149535088..149535984,2	Hela-S3	cervix:
25	chr7:149470006..149471576-chr7:149569800..149572611,2	MCF-7	breast:
26	chr7:149482558..149484845-chr7:149519799..149522299,2	K562	blood:
27	chr7:149320616..149324173-chr7:149466840..149469728,4	K562	blood:
28	chr7:149487842..149489605-chr7:149493457..149495726,2	MCF-7	breast:
29	chr7:149492814..149494456-chr7:149502531..149504471,2	K562	blood:
30	chr7:149486170..149487742-chr7:149495791..149498541,2	K562	blood:
31	chr7:149459369..149463521-chr7:149463788..149469028,7	MCF-7	breast:
32	chr7:149475777..149478196-chr7:149495163..149497885,2	K562	blood:
33	chr7:149479781..149482192-chr7:149551108..149553438,2	MCF-7	breast:
34	chr7:149536256..149537911-chr7:149545323..149547402,2	K562	blood:
35	chr7:149473801..149475401-chr7:149492673..149494757,2	MCF-7	breast:
36	chr7:149492594..149494537-chr7:149501792..149504524,2	MCF-7	breast:
37	chr7:149359887..149360749-chr7:149496598..149497119,2	MCF-7	breast:
38	chr7:149501055..149503338-chr7:149561332..149564151,2	MCF-7	breast:
39	chr7:149484023..149486893-chr7:149499166..149501510,2	K562	blood:
40	chr7:149470907..149472534-chr7:149538103..149539944,2	MCF-7	breast:
41	chr7:149517716..149520406-chr7:149521366..149523449,3	K562	blood:
42	chr7:149467627..149470524-chr7:149529860..149532491,2	K562	blood:
43	chr7:149469487..149472454-chr7:149520687..149524368,4	MCF-7	breast:
44	chr7:149473373..149475721-chr7:149519077..149521805,2	MCF-7	breast:
45	chr7:149520043..149524365-chr7:149535249..149538309,4	MCF-7	breast:
46	chr7:149479515..149482094-chr7:149544911..149547463,2	MCF-7	breast:
47	chr7:149508450..149510500-chr7:149518652..149520983,2	K562	blood:
48	chr7:149517716..149520406-chr7:149521366..149523449,3	K562	blood:
49	chr7:149516696..149519376-chr7:149534960..149537116,2	MCF-7	breast:
50	chr7:149409957..149411791-chr7:149503300..149505720,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF862-1	chr7:149521826-149522213	NONHSAT124065
2	lnc-ZNF862-1	chr7:149522364-149522480	ENSG00000197558.7
3	lnc-ZNF862-1	chr7:149493695-149493834	NONHSAT124049
4	lnc-ZNF862-1	chr7:149480195-149480379	ENSG00000197558.7
5	lnc-ZNF862-1	chr7:149494360-149494432	NONHSAT124049
6	lnc-ZNF862-1	chr7:149524858-149524980	ENSG00000197558.7
7	lnc-ZNF862-1	chr7:149473524-149473617	ENSG00000197558.7
8	lnc-ZNF862-1	chr7:149475870-149476028	ENSG00000197558.7
9	lnc-ZNF862-1	chr7:149520813-149520937	ENSG00000197558.7
10	lnc-ZNF862-1	chr7:149519233-149519286	ENSG00000197558.7
11	lnc-KRBA1-2	chr7:149470297-149473130	NONHSAT124042
12	lnc-ZNF862-1	chr7:149524858-149525016	NONHSAT124065
13	lnc-ZNF862-1	chr7:149496922-149497125	NONHSAT124049
14	lnc-ZNF862-1	chr7:149528224-149528823	NONHSAT124068
15	lnc-ZNF862-1	chr7:149525922-149526085	NONHSAT124068
16	lnc-ZNF862-1	chr7:149479270-149479387	ENSG00000197558.7
17	lnc-ATP6V0E2-6	chr7:149535464-149535550	NONHSAT124069
18	lnc-ZNF862-1	chr7:149522364-149522480	NONHSAT124065

No data

Variant related genes	Relation type
ZNF862	TF binding region
SSPO	TF binding region
ZNF467	TF binding region
ZNF862	CpG island
SSPO	CpG island
ZNF467	CpG island
ENSG00000201699	chromatin interactions
ENSG00000196453	chromatin interactions
ENSG00000107485	chromatin interactions
ENSG00000133624	chromatin interactions
ENSG00000164896	chromatin interactions
ENSG00000197558	chromatin interactions
ENSG00000171130	chromatin interactions
ENSG00000106479	chromatin interactions
ENSG00000196456	chromatin interactions
ENSG00000133619	chromatin interactions
ENSG00000204934	chromatin interactions
ENSG00000181444	chromatin interactions
TMEM109	miRNA target sites

Extended variants
information (count: 4101 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4101 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs855675	chr7:149465674-149465675	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542259903	chr7:149465686-149465687	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148937527	chr7:149465690-149465691	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143703420	chr7:149465765-149465766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371911551	chr7:149465870-149465871	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553530835	chr7:149465871-149465872	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113680332	chr7:149466051-149466052	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550029484	chr7:149466060-149466061	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192558755	chr7:149466080-149466081	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77195367	chr7:149466083-149466084	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555254562	chr7:149466126-149466127	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199666652	chr7:149466129-149466130	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201453089	chr7:149466148-149466149	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567452310	chr7:149466149-149466150	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376640503	chr7:149466159-149466160	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535804166	chr7:149466188-149466189	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs200671338	chr7:149466200-149466201	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146526438	chr7:149466205-149466206	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs151076217	chr7:149466219-149466220	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs563045809	chr7:149466221-149466222	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369922355	chr7:149466243-149466244	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs34873220	chr7:149466251-149466252	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200125804	chr7:149466270-149466271	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs140993808	chr7:149466271-149466272	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376158234	chr7:149466274-149466275	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558365906	chr7:149466284-149466285	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140317564	chr7:149466333-149466334	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537735902	chr7:149466429-149466430	Bivalent Enhancer Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576527465	chr7:149466511-149466512	Bivalent Enhancer Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs183522463	chr7:149466513-149466514	Bivalent Enhancer Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574260064	chr7:149466616-149466617	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542574074	chr7:149466683-149466684	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544056674	chr7:149466725-149466726	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552716726	chr7:149466728-149466729	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572588724	chr7:149466767-149466768	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544745765	chr7:149466768-149466769	Bivalent Enhancer Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564735375	chr7:149466805-149466806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs530572471	chr7:149466810-149466811	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs544013931	chr7:149466840-149466841	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561203387	chr7:149466856-149466857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529968898	chr7:149466884-149466885	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs145466028	chr7:149466897-149466898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565972661	chr7:149466920-149466921	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542739668	chr7:149466923-149466924	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs188158237	chr7:149466961-149466962	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs73168054	chr7:149466984-149466985	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs181116721	chr7:149466989-149466990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572763866	chr7:149467005-149467006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs557286370	chr7:149467024-149467025	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567920407	chr7:149467034-149467035	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2042 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149451200-149468400	Weak transcription	Right Atrium	heart
2	chr7:149460600-149468200	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:149460800-149467600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr7:149460800-149467800	Strong transcription	Primary T cells from cord blood	blood
5	chr7:149461000-149467000	Strong transcription	Lung	lung
6	chr7:149461000-149467200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr7:149461000-149467800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr7:149461600-149467600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:149461600-149467800	Weak transcription	Dnd41	blood
10	chr7:149462000-149467800	Weak transcription	Ovary	ovary
11	chr7:149462400-149466200	Strong transcription	Pancreas	Pancrea
12	chr7:149462400-149466600	Strong transcription	Stomach Smooth Muscle	stomach
13	chr7:149462400-149468000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr7:149462600-149466400	Strong transcription	Liver	Liver
15	chr7:149462800-149467600	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr7:149463000-149468200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr7:149463000-149468400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr7:149463200-149466200	Strong transcription	Spleen	Spleen
19	chr7:149463200-149466400	Strong transcription	Adipose Nuclei	Adipose
20	chr7:149463800-149467800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr7:149464000-149468000	Weak transcription	Brain Anterior Caudate	brain
22	chr7:149464200-149467600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr7:149464200-149467600	Weak transcription	Fetal Thymus	thymus
24	chr7:149464200-149467800	Weak transcription	Thymus	Thymus
25	chr7:149464200-149468000	Weak transcription	Colonic Mucosa	Colon
26	chr7:149464200-149468000	Strong transcription	Fetal Lung	lung
27	chr7:149464400-149467600	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr7:149464400-149467800	Strong transcription	Fetal Stomach	stomach
29	chr7:149464600-149468400	Weak transcription	Aorta	Aorta
30	chr7:149464800-149466200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:149464800-149468000	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:149465000-149465800	Strong transcription	K562	blood
33	chr7:149465000-149467000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr7:149465200-149466400	Strong transcription	Left Ventricle	heart
35	chr7:149465400-149465800	Strong transcription	Brain Cingulate Gyrus	brain
36	chr7:149465400-149465800	Strong transcription	Duodenum Mucosa	Duodenum
37	chr7:149465400-149466600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr7:149465400-149466800	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr7:149465400-149467000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr7:149465400-149467000	Strong transcription	Gastric	stomach
41	chr7:149465400-149467600	Strong transcription	Fetal Kidney	kidney
42	chr7:149465400-149467600	Strong transcription	Placenta	Placenta
43	chr7:149465600-149466400	Strong transcription	Colon Smooth Muscle	Colon
44	chr7:149465600-149466600	Strong transcription	Esophagus	oesophagus
45	chr7:149465800-149466600	Weak transcription	K562	blood
46	chr7:149465800-149468200	Weak transcription	Brain Cingulate Gyrus	brain
47	chr7:149465800-149468200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:149466200-149466400	Genic enhancers	Spleen	Spleen
49	chr7:149466200-149467600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:149466200-149467600	Weak transcription	Pancreas	Pancrea

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