Variant report

Variant	nsv593727
Chromosome Location	chr4:10397327-10694991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3403)
CpG islands
(count:3115)
Chromatin interactive
region (count:176)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3403 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10539570-10539891	K562	blood:	n/a	n/a
2	ARID3A	chr4:10556264-10556699	K562	blood:	n/a	n/a
3	ARID3A	chr4:10539745-10539913	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:10416844-10416961	K562	blood:	n/a	n/a
5	ARID3A	chr4:10405152-10405708	K562	blood:	n/a	n/a
6	ARID3A	chr4:10459741-10459919	K562	blood:	n/a	n/a
7	ARID3A	chr4:10460913-10461399	K562	blood:	n/a	n/a
8	ATF2	chr4:10601067-10601560	GM12878	blood:	n/a	n/a
9	ATF2	chr4:10624419-10624813	GM12878	blood:	n/a	n/a
10	ATF2	chr4:10601095-10601552	GM12878	blood:	n/a	n/a
11	ATF2	chr4:10675370-10675813	GM12878	blood:	n/a	n/a
12	ATF2	chr4:10657639-10658005	GM12878	blood:	n/a	n/a
13	ATF2	chr4:10645150-10645575	GM12878	blood:	n/a	n/a
14	ATF2	chr4:10672922-10673438	GM12878	blood:	n/a	n/a
15	ATF2	chr4:10585640-10586007	GM12878	blood:	n/a	n/a
16	ATF2	chr4:10631025-10631466	GM12878	blood:	n/a	n/a
17	ATF2	chr4:10691734-10692245	GM12878	blood:	n/a	n/a
18	ATF2	chr4:10686127-10686722	GM12878	blood:	n/a	n/a
19	ATF2	chr4:10689657-10690132	GM12878	blood:	n/a	n/a
20	ATF2	chr4:10675331-10675861	GM12878	blood:	n/a	n/a
21	ATF2	chr4:10689554-10690195	GM12878	blood:	n/a	n/a
22	ATF2	chr4:10679636-10680096	GM12878	blood:	n/a	n/a
23	ATF2	chr4:10657553-10658033	GM12878	blood:	n/a	n/a
24	ATF2	chr4:10691679-10692211	GM12878	blood:	n/a	n/a
25	ATF2	chr4:10630985-10631402	GM12878	blood:	n/a	n/a
26	ATF2	chr4:10686178-10686735	GM12878	blood:	n/a	n/a
27	ATF3	chr4:10613160-10613848	HCT-116	colon:	n/a	n/a
28	ATF3	chr4:10497303-10497547	K562	blood:	n/a	n/a
29	ATF3	chr4:10613182-10613769	HCT-116	colon:	n/a	n/a
30	ATF3	chr4:10462880-10463147	K562	blood:	n/a	n/a
31	ATF3	chr4:10551304-10551560	GM12878	blood:	n/a	n/a
32	BACH1	chr4:10462736-10463370	K562	blood:	n/a	n/a
33	BACH1	chr4:10461300-10461416	K562	blood:	n/a	n/a
34	BACH1	chr4:10462826-10463788	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr4:10444197-10445521	K562	blood:	n/a	n/a
36	BACH1	chr4:10645991-10646045	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr4:10446374-10446389	K562	blood:	n/a	n/a
38	BACH1	chr4:10640804-10641050	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr4:10458630-10459108	H1-hESC	embryonic stem cell:	n/a	n/a
40	BATF	chr4:10657633-10657977	GM12878	blood:	n/a	chr4:10657813-10657824 chr4:10657789-10657800
41	BATF	chr4:10624422-10624712	GM12878	blood:	n/a	n/a
42	BATF	chr4:10650167-10650446	GM12878	blood:	n/a	chr4:10650339-10650350
43	BATF	chr4:10642172-10642373	GM12878	blood:	n/a	n/a
44	BATF	chr4:10631064-10631387	GM12878	blood:	n/a	n/a
45	BATF	chr4:10537480-10537757	GM12878	blood:	n/a	n/a
46	BATF	chr4:10461948-10462177	GM12878	blood:	n/a	n/a
47	BATF	chr4:10657617-10658011	GM12878	blood:	n/a	chr4:10657813-10657824 chr4:10657789-10657800
48	BATF	chr4:10675427-10675759	GM12878	blood:	n/a	n/a
49	BATF	chr4:10689708-10690056	GM12878	blood:	n/a	chr4:10689900-10689911
50	BATF	chr4:10649468-10649743	GM12878	blood:	n/a	chr4:10649612-10649623 chr4:10649613-10649623

(count:3115 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10463620-10463670	HRE	kidney:	n/a
2	chr4:10459836-10459886	CMK	blood:	n/a
3	chr4:10459929-10459979	NT2-D1	testis:	n/a
4	chr4:10459141-10459191	SK-N-SH_RA	brain:	n/a
5	chr4:10463620-10463670	HRE	kidney:	n/a
6	chr4:10459836-10459886	CMK	blood:	n/a
7	chr4:10459929-10459979	NT2-D1	testis:	n/a
8	chr4:10459141-10459191	SK-N-SH_RA	brain:	n/a
9	chr4:10458531-10458581	BJ	skin:	n/a
10	chr4:10458165-10458215	LNCaP	prostate:	n/a
11	chr4:10459435-10459485	Jurkat	blood:	n/a
12	chr4:10463620-10463670	NHBE	bronchial:	n/a
13	chr4:10458918-10458968	U87	brain:	n/a
14	chr4:10462849-10462899	PFSK-1	brain:	n/a
15	chr4:10666415-10666465	ovcar-3	ovarian:	n/a
16	chr4:10459141-10459191	NT2-D1	testis:	n/a
17	chr4:10609880-10609930	HRPEpiC	eye:	n/a
18	chr4:10658271-10658321	HEK293	kidney:	embryo
19	chr4:10462903-10462953	LNCaP	prostate:	n/a
20	chr4:10458531-10458581	HRE	kidney:	n/a
21	chr4:10459435-10459485	ECC-1	luminal epithelium:	n/a
22	chr4:10459219-10459269	ECC-1	luminal epithelium:	n/a
23	chr4:10460009-10460059	SKMC	muscle:	n/a
24	chr4:10602753-10602803	RPTEC	kidney:	n/a
25	chr4:10459435-10459485	AG09319	gingival:	n/a
26	chr4:10458165-10458215	K562	blood:	n/a
27	chr4:10463350-10463400	AG09309	skin:	n/a
28	chr4:10458531-10458581	CMK	blood:	n/a
29	chr4:10686554-10686604	SKMC	muscle:	n/a
30	chr4:10609880-10609930	K562	blood:	n/a
31	chr4:10686335-10686385	MCF-7	breast:	n/a
32	chr4:10686554-10686604	SK-N-MC	brain:	n/a
33	chr4:10459352-10459402	AG10803	skin:	n/a
34	chr4:10585774-10585824	GM12891	blood:	n/a
35	chr4:10531768-10531818	HCM	heart:	n/a
36	chr4:10458454-10458504	HCF	heart:	n/a
37	chr4:10687769-10687819	RPTEC	kidney:	n/a
38	chr4:10459435-10459485	T-47D	breast:	n/a
39	chr4:10459183-10459233	Caco-2	colon:	n/a
40	chr4:10459219-10459269	HCM	heart:	n/a
41	chr4:10443264-10443314	PANC-1	pancreas:	n/a
42	chr4:10602753-10602803	HCPEpiC	choroid plexus:	n/a
43	chr4:10459352-10459402	GM06990	blood:	n/a
44	chr4:10459183-10459233	SK-N-SH_RA	brain:	n/a
45	chr4:10591571-10591621	T-47D	breast:	n/a
46	chr4:10585774-10585824	PANC-1	pancreas:	n/a
47	chr4:10458165-10458215	HepG2	liver:	n/a
48	chr4:10463590-10463640	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:10463749-10463799	HIPEpiC	eye:	n/a
50	chr4:10459836-10459886	GM12892	blood:	n/a

(count:176 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr4:10104180..10106384-chr4:10453224..10455811,2	K562	blood:
2	chr4:10658968..10660496-chr4:10663948..10666416,2	MCF-7	breast:
3	chr4:10166113..10167122-chr4:10405126..10405888,4	K562	blood:
4	chr4:10173514..10177541-chr4:10443857..10446930,3	K562	blood:
5	chr4:10439495..10442453-chr4:10454853..10458527,4	K562	blood:
6	chr4:10119485..10122055-chr4:10473675..10475984,2	K562	blood:
7	chr4:10483661..10485837-chr4:10489240..10491538,2	K562	blood:
8	chr4:10583546..10584400-chr4:11425558..11426293,2	MCF-7	breast:
9	chr4:10417667..10419734-chr4:10446879..10448716,2	K562	blood:
10	chr4:10116151..10120402-chr4:10440722..10445122,4	K562	blood:
11	chr4:10489847..10492535-chr4:10493316..10497082,4	K562	blood:
12	chr4:10100545..10102882-chr4:10446695..10448873,2	K562	blood:
13	chr4:10462498..10464981-chr4:10471870..10474447,2	K562	blood:
14	chr4:10447047..10450143-chr4:10544780..10547664,3	K562	blood:
15	chr4:10414281..10417254-chr4:10441057..10442576,2	K562	blood:
16	chr4:10673794..10675385-chr4:10676849..10678533,2	K562	blood:
17	chr4:10629100..10630665-chr4:10632298..10634083,2	K562	blood:
18	chr4:10120437..10124442-chr4:10402726..10405362,4	K562	blood:
19	chr4:10606286..10608482-chr4:10610172..10612555,2	K562	blood:
20	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
21	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
22	chr4:10439495..10442453-chr4:10454853..10458527,4	K562	blood:
23	chr4:10534187..10535776-chr4:10538246..10540113,2	K562	blood:
24	chr4:10689022..10690915-chr4:10701948..10704455,2	K562	blood:
25	chr4:10462498..10464981-chr4:10471870..10474447,2	K562	blood:
26	chr4:10413005..10416502-chr4:10417554..10421094,3	K562	blood:
27	chr4:10119129..10122077-chr4:10500850..10502742,2	K562	blood:
28	chr4:10565843..10567619-chr4:10571881..10573661,2	K562	blood:
29	chr4:10111136..10113091-chr4:10453721..10455357,2	K562	blood:
30	chr4:10489847..10492535-chr4:10493316..10495674,3	K562	blood:
31	chr4:10166189..10167113-chr4:10551000..10552086,3	MCF-7	breast:
32	chr4:10673504..10675348-chr4:10684233..10687077,2	K562	blood:
33	chr4:10529511..10531855-chr4:10533474..10535069,2	K562	blood:
34	chr17:34890127..34891028-chr4:10458093..10458597,2	HCT-116	colon:
35	chr4:10172802..10175283-chr4:10404131..10407127,2	K562	blood:
36	chr4:10166196..10167366-chr4:10404929..10406035,4	MCF-7	breast:
37	chr4:10164883..10167477-chr4:10450300..10452643,2	K562	blood:
38	chr4:10489847..10492535-chr4:10493316..10495674,3	K562	blood:
39	chr4:10166411..10167001-chr4:10551169..10551934,2	MCF-7	breast:
40	chr4:10513028..10514802-chr4:10517875..10519589,2	K562	blood:
41	chr4:10182377..10184143-chr4:10453503..10455042,2	K562	blood:
42	chr4:10117259..10119774-chr4:10404203..10405780,2	K562	blood:
43	chr4:10120460..10123281-chr4:10421587..10423639,2	K562	blood:
44	chr4:10180113..10182537-chr4:10415151..10418343,3	K562	blood:
45	chr4:10673794..10675385-chr4:10676849..10678533,2	K562	blood:
46	chr4:10119738..10123155-chr4:10543992..10547634,3	K562	blood:
47	chr4:10404962..10406013-chr4:10527520..10528737,3	MCF-7	breast:
48	chr4:10624055..10624663-chr4:10717565..10718180,2	MCF-7	breast:
49	chr4:10133192..10134746-chr4:10556529..10559334,2	K562	blood:
50	chr4:10419551..10421094-chr4:10421815..10424714,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF518B-1	chr4:10433041-10433567	NONHSAT095498
2	lnc-CLNK-2	chr4:10458941-10459034	NONHSAT095502
3	lnc-CLNK-2	chr4:10452511-10454646	NONHSAT095501
4	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095502
5	lnc-CLNK-2	chr4:10456218-10456612	NONHSAT095501
6	lnc-CLNK-2	chr4:10452511-10456612	NONHSAT095503
7	lnc-DRD5-19	chr4:10437730-10438054	NONHSAT095500
8	lnc-DRD5-20	chr4:10439848-10440173	NONHSAT095499
9	lnc-CLNK-2	chr4:10458941-10459032	NONHSAT095501
10	lnc-DRD5-20	chr4:10436252-10437668	NONHSAT095499
11	lnc-DRD5-5	chr4:10686627-10686685	XLOC_003452
12	lnc-DRD5-18	chr4:10419449-10419642	l_2604_chr4:10348296-10419642_testes
13	lnc-DRD5-4	chr4:10404495-10404649	FPKM1_group_22843_transcript_2
14	lnc-DRD5-5	chr4:10693689-10693730	XLOC_003452
15	lnc-DRD5-4	chr4:10404495-10404649	NONHSAT095495
16	lnc-DRD5-4	chr4:10409553-10410132	NONHSAT095495
17	lnc-DRD5-21	chr4:10486610-10487079	NONHSAT095505
18	lnc-CLNK-2	chr4:10458758-10458800	NONHSAT095503
19	lnc-DRD5-4	chr4:10409553-10409610	FPKM1_group_22843_transcript_2
20	lnc-CLNK-1	chr4:10480148-10480547	NONHSAT095504

No data

Variant related genes	Relation type
ENSG00000250613	TF binding region
ENSG00000248419	TF binding region
ZNF518B	TF binding region
ENSG00000249334	TF binding region
CLNK	TF binding region
ENSG00000250613	CpG island
ENSG00000248419	CpG island
ZNF518B	CpG island
ENSG00000249334	CpG island
CLNK	CpG island
ENSG00000251296	chromatin interactions
ENSG00000178163	chromatin interactions
ENSG00000250613	chromatin interactions
ENSG00000141140	chromatin interactions
ENSG00000184886	chromatin interactions
ENSG00000109684	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000248419	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000250505	chromatin interactions
ENSG00000249334	chromatin interactions
ENSG00000248777	chromatin interactions
AKT3	miRNA target sites

Extended variants
information (count: 12586 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:12586 , 50 per page) page: 1 2 3 4 5 6 7 ... 252

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6835730	chr4:10397327-10397328	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs185129134	chr4:10397370-10397371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546736916	chr4:10397396-10397397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546864113	chr4:10397414-10397415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376027426	chr4:10397491-10397492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568181364	chr4:10397560-10397561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535293292	chr4:10397616-10397617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568432308	chr4:10397626-10397627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112805002	chr4:10397665-10397666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146836643	chr4:10397682-10397683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs539046095	chr4:10397685-10397686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73809406	chr4:10397756-10397757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs572857591	chr4:10397758-10397759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112262683	chr4:10397785-10397786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553504773	chr4:10397815-10397816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575064749	chr4:10397884-10397885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542477205	chr4:10397895-10397896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563966372	chr4:10397917-10397918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576010075	chr4:10397937-10397938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546178210	chr4:10397943-10397944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191219754	chr4:10397991-10397992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528555154	chr4:10397999-10398000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546753194	chr4:10398012-10398013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562242591	chr4:10398014-10398015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550956813	chr4:10398049-10398050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569240782	chr4:10398052-10398053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139370212	chr4:10398091-10398092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567113685	chr4:10398098-10398099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568767849	chr4:10398101-10398102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150043398	chr4:10398137-10398138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551323341	chr4:10398162-10398163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566368109	chr4:10398225-10398226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183341985	chr4:10398259-10398260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539954324	chr4:10398266-10398267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555155870	chr4:10398280-10398281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573826675	chr4:10398302-10398303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536009098	chr4:10398309-10398310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115374903	chr4:10398329-10398330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575975974	chr4:10398332-10398333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs187638630	chr4:10398370-10398371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564826794	chr4:10398371-10398372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573137198	chr4:10398402-10398403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs4389568	chr4:10398427-10398428	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs373123473	chr4:10398444-10398445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561845748	chr4:10398461-10398462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191502423	chr4:10398481-10398482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573043557	chr4:10398511-10398512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145399721	chr4:10398589-10398590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533666733	chr4:10398599-10398600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4698048	chr4:10398635-10398636	Weak transcription Enhancers Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3094 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10387000-10403600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:10396800-10399600	Enhancers	HMEC	breast
3	chr4:10397000-10399000	Enhancers	NHEK	skin
4	chr4:10397000-10400000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:10397200-10399200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:10397400-10398400	Enhancers	K562	blood
7	chr4:10397600-10399000	Enhancers	Fetal Thymus	thymus
8	chr4:10397800-10398400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr4:10398400-10403400	Weak transcription	K562	blood
10	chr4:10398600-10398800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
11	chr4:10399000-10405600	Weak transcription	NHEK	skin
12	chr4:10399200-10402800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:10399600-10400000	Weak transcription	HMEC	breast
14	chr4:10400000-10400400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:10400000-10400600	Enhancers	HMEC	breast
16	chr4:10400400-10400600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:10400600-10405200	Weak transcription	HMEC	breast
18	chr4:10400600-10405400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:10402800-10403000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:10403400-10406000	Enhancers	K562	blood
21	chr4:10405200-10405800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:10405200-10406000	Enhancers	HMEC	breast
23	chr4:10405400-10406000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:10405600-10406000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:10405600-10406000	Enhancers	NHEK	skin
26	chr4:10405600-10406400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr4:10406000-10408800	Weak transcription	K562	blood
28	chr4:10407400-10407600	Enhancers	Fetal Heart	heart
29	chr4:10407600-10408600	Weak transcription	Fetal Heart	heart
30	chr4:10408200-10408600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:10408600-10410600	Enhancers	Fetal Heart	heart
32	chr4:10408600-10421000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:10408800-10409200	Enhancers	Gastric	stomach
34	chr4:10408800-10410200	Enhancers	K562	blood
35	chr4:10409400-10410800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:10409400-10410800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:10410200-10416600	Weak transcription	K562	blood
38	chr4:10410600-10417800	Weak transcription	Fetal Heart	heart
39	chr4:10412200-10412800	Active TSS	Placenta	Placenta
40	chr4:10413200-10414000	Enhancers	Ovary	ovary
41	chr4:10413600-10415600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr4:10413800-10416000	Enhancers	Primary B cells from cord blood	blood
43	chr4:10413800-10416000	Enhancers	Primary B cells from peripheral blood	blood
44	chr4:10414600-10415200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr4:10414600-10415400	Enhancers	GM12878-XiMat	blood
46	chr4:10414800-10415800	Enhancers	Primary T cells from cord blood	blood
47	chr4:10415200-10417000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr4:10415600-10415800	Enhancers	Thymus	Thymus
49	chr4:10415600-10416600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr4:10415800-10417600	Weak transcription	Primary T cells from cord blood	blood

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