Variant report

Variant	nsv4233
Chromosome Location	chr4:10382443-10409916
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:10405152-10405708	K562	blood:	n/a	n/a
2	BHLHE40	chr4:10387822-10388106	K562	blood:	n/a	n/a
3	BHLHE40	chr4:10405415-10405586	K562	blood:	n/a	n/a
4	CCNT2	chr4:10405344-10405663	K562	blood:	n/a	n/a
5	CCNT2	chr4:10387632-10388049	K562	blood:	n/a	n/a
6	CEBPB	chr4:10408033-10408219	K562	blood:	n/a	chr4:10408128-10408141
7	CEBPB	chr4:10405274-10405653	K562	blood:	n/a	n/a
8	CEBPB	chr4:10387651-10387915	K562	blood:	n/a	n/a
9	CTCF	chr4:10405460-10405610	GM12872	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
10	CTCF	chr4:10386763-10386869	NHEK	skin:	n/a	n/a
11	CTCF	chr4:10405468-10405674	HepG2	liver:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
12	CTCF	chr4:10405480-10405630	GM12870	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
13	CTCF	chr4:10405520-10405670	HCT-116	colon:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
14	CTCF	chr4:10405207-10405881	HCT-116	colon:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
15	CTCF	chr4:10405440-10405590	GM12873	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
16	CTCF	chr4:10405358-10405760	H1-hESC	embryonic stem cell:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
17	CTCF	chr4:10405480-10405630	GM06990	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
18	CTCF	chr4:10405343-10405678	MCF-7	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
19	CTCF	chr4:10405462-10405683	MCF-7	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
20	CTCF	chr4:10405858-10405861	LNCaP	prostate:	n/a	n/a
21	CTCF	chr4:10405440-10405590	HCM	heart:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
22	CTCF	chr4:10405480-10405630	HL-60	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
23	CTCF	chr4:10405428-10405698	K562	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
24	CTCF	chr4:10405464-10405691	GM12878	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
25	CTCF	chr4:10405500-10405650	HEK293	kidney:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
26	CTCF	chr4:10405500-10405650	AG10803	skin:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
27	CTCF	chr4:10405500-10405650	NHDF-neo	bronchial:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
28	CTCF	chr4:10405480-10405630	HFF	foreskin:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
29	CTCF	chr4:10405386-10405659	A549	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
30	CTCF	chr4:10405540-10405690	HUVEC	blood vessel:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
31	CTCF	chr4:10405500-10405650	SAEC	small airway:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
32	CTCF	chr4:10405240-10405390	HMEC	breast:	n/a	n/a
33	CTCF	chr4:10405560-10405710	NHEK	skin:	n/a	chr4:10405561-10405579 chr4:10405563-10405576
34	CTCF	chr4:10405453-10405709	Pancreas_OC	pancreas:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
35	CTCF	chr4:10405485-10405650	Hela-S3	cervix:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
36	CTCF	chr4:10405871-10405902	LNCaP	prostate:	n/a	n/a
37	CTCF	chr4:10405457-10405701	LNCaP	prostate:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
38	CTCF	chr4:10405560-10405710	SAEC	small airway:	n/a	chr4:10405561-10405579 chr4:10405563-10405576
39	CTCF	chr4:10405379-10405741	IMR90	lung:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
40	CTCF	chr4:10405480-10405630	GM12801	blood:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
41	CTCF	chr4:10405520-10405670	HRPEpiC	eye:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
42	CTCF	chr4:10405480-10405630	HEEpiC	esophagus:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
43	CTCF	chr4:10405580-10405730	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr4:10405162-10405818	SK-N-SH	brain:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
45	CTCF	chr4:10405480-10405630	HMEC	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
46	CTCF	chr4:10405480-10405630	HBMEC	blood vessel:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
47	CTCF	chr4:10405520-10405670	HepG2	liver:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
48	CTCF	chr4:10405514-10405581	Fibrobl	skin:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
49	CTCF	chr4:10405520-10405670	HMF	breast:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576
50	CTCF	chr4:10405500-10405650	Caco-2	colon:	n/a	chr4:10405556-10405577 chr4:10405561-10405579 chr4:10405563-10405576

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10405694-10405744	HCM	heart:	n/a
2	chr4:10405694-10405744	AG04450	lung:	fetal
3	chr4:10405694-10405744	Hepatocyte	liver:	n/a
4	chr4:10405694-10405744	U87	brain:	n/a
5	chr4:10405694-10405744	SK-N-MC	brain:	n/a
6	chr4:10405694-10405744	SK-N-SH	brain:	n/a
7	chr4:10405694-10405744	HCPEpiC	choroid plexus:	n/a
8	chr4:10405694-10405744	NB4	blood:	n/a
9	chr4:10405694-10405744	AG04449	skin:	fetal
10	chr4:10405694-10405744	SKMC	muscle:	n/a
11	chr4:10405694-10405744	HRE	kidney:	n/a
12	chr4:10405694-10405744	ovcar-3	ovarian:	n/a
13	chr4:10405694-10405744	SAEC	small airway:	n/a
14	chr4:10405694-10405744	GM19239	blood:	n/a
15	chr4:10405694-10405744	MCF-7	breast:	n/a
16	chr4:10405694-10405744	HRPEpiC	eye:	n/a
17	chr4:10405694-10405744	PFSK-1	brain:	n/a
18	chr4:10405694-10405744	Caco-2	colon:	n/a
19	chr4:10405694-10405744	HRCEpiC	kidney:	n/a
20	chr4:10405694-10405744	HepG2	liver:	n/a
21	chr4:10405694-10405744	HEK293	kidney:	embryo
22	chr4:10405694-10405744	GM12892	blood:	n/a
23	chr4:10405694-10405744	HAEpiC	amniotic membrane:	n/a
24	chr4:10405694-10405744	IMR90	lung:	fetal
25	chr4:10405694-10405744	LNCaP	prostate:	n/a
26	chr4:10405694-10405744	NH-A	brain:	n/a
27	chr4:10405694-10405744	GM06990	blood:	n/a
28	chr4:10405694-10405744	HIPEpiC	eye:	n/a
29	chr4:10405694-10405744	BJ	skin:	n/a
30	chr4:10405694-10405744	T-47D	breast:	n/a
31	chr4:10405694-10405744	HEEpiC	esophagus:	n/a
32	chr4:10405694-10405744	A549	lung:	n/a
33	chr4:10405694-10405744	HCT-116	colon:	n/a
34	chr4:10405694-10405744	SK-N-SH_RA	brain:	n/a
35	chr4:10405694-10405744	PrEC	prostate:	n/a
36	chr4:10405694-10405744	MCF10A-Er-Src	breast:	n/a
37	chr4:10405694-10405744	NT2-D1	testis:	n/a
38	chr4:10405694-10405744	AG09319	gingival:	n/a
39	chr4:10405694-10405744	GM12878	blood:	n/a
40	chr4:10405694-10405744	H1-hESC	embryonic stem cell:	embryo
41	chr4:10405694-10405744	HMEC	breast:	n/a
42	chr4:10405694-10405744	ProgFib	skin:	n/a
43	chr4:10405694-10405744	K562	blood:	n/a
44	chr4:10405694-10405744	RPTEC	kidney:	n/a
45	chr4:10405694-10405744	ECC-1	luminal epithelium:	n/a
46	chr4:10405694-10405744	AG10803	skin:	n/a
47	chr4:10405694-10405744	GM12891	blood:	n/a
48	chr4:10405694-10405744	AoSMC	blood vessel:	n/a
49	chr4:10405694-10405744	HNPCEpiC	eye:	n/a
50	chr4:10405694-10405744	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10180539..10184306-chr4:10401076..10403855,3	K562	blood:
2	chr4:10380945..10383777-chr4:10383962..10385513,2	K562	blood:
3	chr4:10406734..10408445-chr4:10443381..10446084,2	K562	blood:
4	chr4:10182452..10185153-chr4:10405566..10407454,2	K562	blood:
5	chr4:10377322..10379936-chr4:10386087..10389023,2	K562	blood:
6	chr4:10031896..10034212-chr4:10409451..10411616,2	K562	blood:
7	chr4:10404962..10406013-chr4:10527520..10528737,3	MCF-7	breast:
8	chr4:10370932..10373880-chr4:10390683..10392321,2	K562	blood:
9	chr4:10405058..10406722-chr4:10414024..10415781,2	K562	blood:
10	chr4:10391155..10393700-chr4:10401011..10403355,4	MCF-7	breast:
11	chr17:59945131..59945952-chr4:10405006..10405538,2	MCF-7	breast:
12	chr4:10194015..10194637-chr4:10405680..10406337,2	MCF-7	breast:
13	chr4:10166113..10167122-chr4:10405126..10405888,4	K562	blood:
14	chr4:10181802..10184742-chr4:10401642..10403855,2	K562	blood:
15	chr4:10118696..10122262-chr4:10407294..10411909,5	K562	blood:
16	chr4:10117259..10123841-chr4:10401893..10417202,19	K562	blood:
17	chr4:10166648..10168321-chr4:10402902..10405737,2	K562	blood:
18	chr4:10187984..10188890-chr4:10405320..10406071,3	MCF-7	breast:
19	chr4:10186739..10189194-chr4:10403510..10406450,4	K562	blood:
20	chr4:10385942..10388810-chr4:10389542..10391176,2	K562	blood:
21	chr4:10116794..10121385-chr4:10387531..10390337,4	K562	blood:
22	chr4:10166236..10167092-chr4:10405236..10406016,3	MCF-7	breast:
23	chr4:10172802..10175283-chr4:10404131..10407127,2	K562	blood:
24	chr4:10117806..10121732-chr4:10389330..10392612,4	K562	blood:
25	chr4:10117259..10119774-chr4:10404203..10405780,2	K562	blood:
26	chr4:10390019..10393146-chr4:10400722..10404569,4	K562	blood:
27	chr4:10161526..10162602-chr4:10405096..10406350,5	K562	blood:
28	chr4:10380945..10383777-chr4:10383962..10385513,2	K562	blood:
29	chr4:10374180..10377123-chr4:10380489..10383795,3	K562	blood:
30	chr4:10120437..10124442-chr4:10402726..10405362,4	K562	blood:
31	chr4:10158544..10160312-chr4:10404691..10406060,12	K562	blood:
32	chr4:10185450..10187184-chr4:10401056..10402949,2	K562	blood:
33	chr4:10391155..10393700-chr4:10401011..10403355,4	MCF-7	breast:
34	chr4:10390019..10393146-chr4:10400722..10404569,4	K562	blood:
35	chr4:10179301..10181367-chr4:10408418..10410454,2	K562	blood:
36	chr4:10179643..10181436-chr4:10389855..10391388,2	K562	blood:
37	chr4:10187220..10189194-chr4:10403510..10406450,3	K562	blood:
38	chr4:10166196..10167366-chr4:10404929..10406035,4	MCF-7	breast:
39	chr4:10184632..10187184-chr4:10400763..10402949,2	K562	blood:
40	chr4:10159016..10159805-chr4:10405257..10406163,3	MCF-7	breast:
41	chr4:10385942..10388810-chr4:10389542..10391176,2	K562	blood:
42	chr4:10201021..10203569-chr4:10408297..10410976,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DRD5-4	chr4:10409553-10409610	FPKM1_group_22843_transcript_2
2	lnc-DRD5-4	chr4:10404495-10404649	FPKM1_group_22843_transcript_2
3	lnc-DRD5-4	chr4:10409553-10410132	NONHSAT095495
4	lnc-DRD5-4	chr4:10404495-10404649	NONHSAT095495

Variant related genes	Relation type
ENSG00000250613	TF binding region
ENSG00000250613	CpG island
ENSG00000223086	chromatin interactions
ENSG00000071127	chromatin interactions
ENSG00000248777	chromatin interactions

Extended variants
information (count: 1272 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116716044	chr4:10382500-10382501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs533088605	chr4:10382520-10382521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552492897	chr4:10382529-10382530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571455610	chr4:10382578-10382579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538536255	chr4:10382604-10382605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113232757	chr4:10382613-10382614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs56413923	chr4:10382629-10382630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12509659	chr4:10382649-10382650	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191211951	chr4:10382670-10382671	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183333079	chr4:10382699-10382700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12501750	chr4:10382709-10382710	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs115501633	chr4:10382742-10382743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs575879497	chr4:10382743-10382744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148461710	chr4:10382749-10382750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535799049	chr4:10382774-10382775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554721544	chr4:10382823-10382824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78311580	chr4:10382832-10382833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187628962	chr4:10382840-10382841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573003553	chr4:10382850-10382851	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191746326	chr4:10382864-10382865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs80152809	chr4:10382865-10382866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142632159	chr4:10382878-10382879	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs115816663	chr4:10382888-10382889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116713180	chr4:10382910-10382911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs577618755	chr4:10382963-10382964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544112119	chr4:10382967-10382968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545099227	chr4:10382968-10382969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140905753	chr4:10382974-10382975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554190296	chr4:10382985-10382986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145765287	chr4:10382998-10382999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183319380	chr4:10383000-10383001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7677806	chr4:10383005-10383006	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs147772368	chr4:10383013-10383014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375448559	chr4:10383056-10383057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569237573	chr4:10383064-10383065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs369554362	chr4:10383067-10383068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539507361	chr4:10383086-10383087	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556457346	chr4:10383087-10383088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551867284	chr4:10383095-10383096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566520365	chr4:10383106-10383107	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533723787	chr4:10383107-10383108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188328903	chr4:10383108-10383109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578101263	chr4:10383121-10383122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573595428	chr4:10383122-10383123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537753185	chr4:10383129-10383130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545290482	chr4:10383158-10383159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141188150	chr4:10383184-10383185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577584484	chr4:10383193-10383194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544751506	chr4:10383221-10383222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560173810	chr4:10383223-10383224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10374200-10386600	Weak transcription	K562	blood
2	chr4:10382000-10383400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:10382000-10383600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:10382200-10383400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:10382200-10383400	Enhancers	NHEK	skin
6	chr4:10382200-10383600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:10382200-10383600	Enhancers	HMEC	breast
8	chr4:10382400-10384400	Weak transcription	Thymus	Thymus
9	chr4:10383400-10386400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr4:10383400-10386400	Weak transcription	NHEK	skin
11	chr4:10383400-10386600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:10383600-10386200	Weak transcription	HMEC	breast
13	chr4:10383600-10386600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:10384400-10384600	Enhancers	Fetal Thymus	thymus
15	chr4:10384400-10389000	Enhancers	Thymus	Thymus
16	chr4:10384600-10385200	Weak transcription	Fetal Thymus	thymus
17	chr4:10385200-10388200	Enhancers	Fetal Thymus	thymus
18	chr4:10385600-10386400	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr4:10385800-10386600	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr4:10386200-10387800	Enhancers	HMEC	breast
21	chr4:10386400-10387800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:10386400-10388000	Enhancers	NHEK	skin
23	chr4:10386600-10387000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:10386600-10387800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:10386600-10388800	Enhancers	K562	blood
26	chr4:10387000-10403600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:10387800-10391800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:10387800-10397000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:10390000-10391000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:10390000-10391600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:10390000-10392200	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:10390200-10392200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:10390200-10392400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:10390400-10391400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr4:10391000-10391400	Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr4:10391000-10391800	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr4:10391400-10392000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr4:10391800-10392000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:10396800-10399600	Enhancers	HMEC	breast
40	chr4:10397000-10399000	Enhancers	NHEK	skin
41	chr4:10397000-10400000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:10397200-10399200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr4:10397400-10398400	Enhancers	K562	blood
44	chr4:10397600-10399000	Enhancers	Fetal Thymus	thymus
45	chr4:10397800-10398400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr4:10398400-10403400	Weak transcription	K562	blood
47	chr4:10398600-10398800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
48	chr4:10399000-10405600	Weak transcription	NHEK	skin
49	chr4:10399200-10402800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:10399600-10400000	Weak transcription	HMEC	breast

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