Variant report

Variant	nsv874700
Chromosome Location	chr2:100062163-100099989
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:122)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:100087382-100087696	K562	blood:	n/a	n/a
2	ARID3A	chr2:100087939-100088495	K562	blood:	n/a	n/a
3	ATF1	chr2:100094906-100095064	K562	blood:	n/a	n/a
4	ATF2	chr2:100098389-100098667	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:100098321-100098731	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr2:100098408-100098588	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:100098590-100098937	K562	blood:	n/a	n/a
8	BRCA1	chr2:100077545-100077588	GM12878	blood:	n/a	n/a
9	CBX3	chr2:100078566-100078907	K562	blood:	n/a	n/a
10	CBX3	chr2:100087130-100087721	K562	blood:	n/a	n/a
11	CBX3	chr2:100078443-100078932	K562	blood:	n/a	n/a
12	CEBPB	chr2:100092384-100092690	K562	blood:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
13	CEBPB	chr2:100088813-100089065	A549	lung:	n/a	chr2:100088920-100088931
14	CEBPB	chr2:100097912-100098107	K562	blood:	n/a	chr2:100097984-100097995 chr2:100098022-100098031 chr2:100098021-100098032
15	CEBPB	chr2:100097876-100098178	HepG2	liver:	n/a	chr2:100097984-100097995 chr2:100098022-100098031 chr2:100098021-100098032
16	CEBPB	chr2:100088785-100089079	HepG2	liver:	n/a	chr2:100088920-100088931
17	CEBPB	chr2:100092434-100092643	A549	lung:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
18	CEBPB	chr2:100088856-100089028	H1-hESC	embryonic stem cell:	n/a	chr2:100088920-100088931
19	CEBPB	chr2:100092391-100092685	IMR90	lung:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
20	CEBPB	chr2:100092398-100092707	HepG2	liver:	n/a	chr2:100092526-100092539 chr2:100092527-100092538 chr2:100092581-100092593
21	CEBPB	chr2:100088782-100088996	IMR90	lung:	n/a	chr2:100088920-100088931
22	CEBPB	chr2:100088781-100089062	K562	blood:	n/a	chr2:100088920-100088931
23	CEBPB	chr2:100097961-100098049	A549	lung:	n/a	chr2:100097984-100097995 chr2:100098022-100098031 chr2:100098021-100098032
24	CEBPB	chr2:100071610-100071886	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:100076824-100076893	HepG2	liver:	n/a	chr2:100076845-100076856
26	CEBPB	chr2:100074293-100074519	K562	blood:	n/a	n/a
27	CEBPD	chr2:100087372-100087867	K562	blood:	n/a	n/a
28	CEBPZ	chr2:100095232-100095275	HepG2	liver:	n/a	n/a
29	CHD2	chr2:100098360-100098675	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr2:100087131-100087185	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr2:100067976-100068467	GM12878	blood:	n/a	n/a
32	CTCF	chr2:100090720-100090870	AG09319	gingival:	n/a	n/a
33	CTCF	chr2:100090676-100090833	K562	blood:	n/a	n/a
34	CTCF	chr2:100087049-100087096	GM20000	blood:	n/a	n/a
35	CTCF	chr2:100064388-100064442	GM10248	blood:	n/a	n/a
36	CTCF	chr2:100090663-100090887	IMR90	lung:	n/a	n/a
37	CTCF	chr2:100085981-100086001	ProgFib	skin:	n/a	n/a
38	CTCF	chr2:100064223-100064297	Lung_OC	lung:	n/a	n/a
39	CTCF	chr2:100072880-100073030	Caco-2	colon:	n/a	n/a
40	CTCF	chr2:100077120-100077270	HRE	kidney:	n/a	n/a
41	CTCF	chr2:100063360-100063510	AG09309	skin:	n/a	n/a
42	CTCF	chr2:100090783-100090829	HUVEC	blood vessel:	n/a	n/a
43	CUX1	chr2:100087513-100088175	K562	blood:	n/a	n/a
44	E2F4	chr2:100064834-100065440	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr2:100067516-100067716	MCF10A-Er-Src	breast:	n/a	chr2:100067625-100067642 chr2:100067625-100067642
46	EBF1	chr2:100098421-100098764	GM12878	blood:	n/a	chr2:100098579-100098590
47	EGR1	chr2:100096921-100097127	K562	blood:	n/a	chr2:100097042-100097053
48	EGR1	chr2:100096890-100097124	K562	blood:	n/a	chr2:100097042-100097053
49	EP300	chr2:100099758-100099811	K562	blood:	n/a	n/a
50	EP300	chr2:100089312-100089386	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100078174-100078224	NHDF-neo	bronchial:	n/a
2	chr2:100078174-100078224	SAEC	small airway:	n/a
3	chr2:100078174-100078224	HL-60	blood:	n/a
4	chr2:100078174-100078224	SK-N-MC	brain:	n/a
5	chr2:100089996-100090046	K562	blood:	n/a
6	chr2:100089996-100090046	HEK293	kidney:	embryo
7	chr2:100078174-100078224	SK-N-SH_RA	brain:	n/a
8	chr2:100089996-100090046	MCF10A-Er-Src	breast:	n/a
9	chr2:100078174-100078224	Caco-2	colon:	n/a
10	chr2:100089996-100090046	Caco-2	colon:	n/a
11	chr2:100078174-100078224	Hepatocyte	liver:	n/a
12	chr2:100078174-100078224	HAEpiC	amniotic membrane:	n/a
13	chr2:100078174-100078224	HCF	heart:	n/a
14	chr2:100089996-100090046	HL-60	blood:	n/a
15	chr2:100078174-100078224	HRCEpiC	kidney:	n/a
16	chr2:100089996-100090046	ECC-1	luminal epithelium:	n/a
17	chr2:100089996-100090046	AG09309	skin:	n/a
18	chr2:100089996-100090046	HAEpiC	amniotic membrane:	n/a
19	chr2:100078174-100078224	SKMC	muscle:	n/a
20	chr2:100089996-100090046	AG04449	skin:	fetal
21	chr2:100078174-100078224	H1-hESC	embryonic stem cell:	embryo
22	chr2:100089996-100090046	AG10803	skin:	n/a
23	chr2:100089996-100090046	HCF	heart:	n/a
24	chr2:100089996-100090046	HCM	heart:	n/a
25	chr2:100078174-100078224	AoSMC	blood vessel:	n/a
26	chr2:100089996-100090046	HRPEpiC	eye:	n/a
27	chr2:100078174-100078224	NH-A	brain:	n/a
28	chr2:100078174-100078224	AG09319	gingival:	n/a
29	chr2:100078174-100078224	HMEC	breast:	n/a
30	chr2:100089996-100090046	HEEpiC	esophagus:	n/a
31	chr2:100089996-100090046	IMR90	lung:	fetal
32	chr2:100089996-100090046	NHBE	bronchial:	n/a
33	chr2:100089996-100090046	A549	lung:	n/a
34	chr2:100089996-100090046	T-47D	breast:	n/a
35	chr2:100089996-100090046	CMK	blood:	n/a
36	chr2:100078174-100078224	IMR90	lung:	fetal
37	chr2:100089996-100090046	ProgFib	skin:	n/a
38	chr2:100078174-100078224	AG10803	skin:	n/a
39	chr2:100089996-100090046	SK-N-SH_RA	brain:	n/a
40	chr2:100078174-100078224	ovcar-3	ovarian:	n/a
41	chr2:100078174-100078224	HepG2	liver:	n/a
42	chr2:100089996-100090046	PFSK-1	brain:	n/a
43	chr2:100078174-100078224	HNPCEpiC	eye:	n/a
44	chr2:100089996-100090046	AG04450	lung:	fetal
45	chr2:100089996-100090046	AoSMC	blood vessel:	n/a
46	chr2:100078174-100078224	PrEC	prostate:	n/a
47	chr2:100078174-100078224	BJ	skin:	n/a
48	chr2:100078174-100078224	HEEpiC	esophagus:	n/a
49	chr2:100078174-100078224	GM12892	blood:	n/a
50	chr2:100089996-100090046	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:100077312..100079121-chr2:100100989..100102811,2	K562	blood:
2	chr2:100086031..100088660-chr2:100104187..100107882,3	MCF-7	breast:
3	chr2:100059250..100062216-chr2:100105245..100107789,2	MCF-7	breast:
4	chr2:100081842..100083413-chr2:100104447..100107377,2	MCF-7	breast:
5	chr2:100065120..100066698-chr2:100069712..100072523,2	MCF-7	breast:
6	chr2:100065327..100067396-chr2:100072129..100074926,2	K562	blood:
7	chr2:100066815..100068950-chr2:100081584..100083548,2	K562	blood:
8	chr2:100064922..100067755-chr2:100103657..100105818,3	MCF-7	breast:
9	chr2:100053808..100056700-chr2:100061249..100063281,2	K562	blood:
10	chr2:100066768..100070769-chr2:100085883..100089135,3	K562	blood:
11	chr2:100092416..100102947-chr2:100103557..100108181,19	MCF-7	breast:
12	chr2:100082529..100085149-chr2:100097513..100099480,2	K562	blood:
13	chr2:100065327..100067396-chr2:100072129..100074926,2	K562	blood:
14	chr2:100068825..100071556-chr2:100104542..100107022,2	MCF-7	breast:
15	chr2:100078933..100081024-chr2:100087446..100090857,3	K562	blood:
16	chr2:100061358..100063213-chr2:100063988..100066181,2	MCF-7	breast:
17	chr2:100091441..100093893-chr2:100095526..100097800,4	K562	blood:
18	chr2:100087595..100089096-chr2:100090818..100093356,2	K562	blood:
19	chr2:100084922..100089797-chr2:100104456..100108052,9	MCF-7	breast:
20	chr2:100099713..100102517-chr2:100102817..100104971,3	MCF-7	breast:
21	chr2:100061358..100063213-chr2:100063988..100066181,2	MCF-7	breast:
22	chr2:100077312..100079751-chr2:100099970..100102811,3	K562	blood:
23	chr2:100083617..100085558-chr2:100105474..100107901,2	K562	blood:
24	chr2:100072001..100074970-chr2:100080545..100083472,2	MCF-7	breast:
25	chr2:100091970..100094649-chr2:100104238..100106048,2	MCF-7	breast:
26	chr2:100045628..100047326-chr2:100061347..100063062,2	K562	blood:
27	chr2:100068951..100071646-chr2:100081782..100083860,2	K562	blood:
28	chr2:100082529..100085149-chr2:100097513..100099480,2	K562	blood:
29	chr2:100082191..100084657-chr2:100091943..100094929,2	K562	blood:
30	chr2:100061386..100063394-chr2:100105518..100107666,2	K562	blood:
31	chr2:100088451..100090156-chr2:100093150..100094831,2	MCF-7	breast:
32	chr2:100091441..100093893-chr2:100095526..100097800,4	K562	blood:
33	chr2:100072001..100074970-chr2:100080545..100083472,2	MCF-7	breast:
34	chr2:100068951..100071646-chr2:100081782..100083860,2	K562	blood:
35	chr2:100088510..100094256-chr2:100103985..100108648,6	K562	blood:
36	chr2:100072254..100074226-chr2:100106055..100108821,2	MCF-7	breast:
37	chr2:100091037..100094858-chr2:100099869..100102767,4	K562	blood:
38	chr2:100079371..100082089-chr2:100106220..100108086,2	MCF-7	breast:
39	chr2:100083971..100085589-chr2:100104836..100106610,2	MCF-7	breast:
40	chr2:100088451..100090156-chr2:100093150..100094831,2	MCF-7	breast:
41	chr2:100091037..100094858-chr2:100099869..100102767,4	K562	blood:
42	chr2:100080735..100084657-chr2:100090928..100093443,3	K562	blood:
43	chr2:100079142..100082364-chr2:100082502..100085624,3	K562	blood:
44	chr2:100075556..100080404-chr2:100103648..100108163,7	K562	blood:
45	chr2:27881530..27883047-chr2:100099438..100101050,2	MCF-7	breast:
46	chr2:100082191..100084657-chr2:100091943..100094929,2	K562	blood:
47	chr2:100087595..100089096-chr2:100090818..100093356,2	K562	blood:
48	chr2:100071675..100073794-chr2:100105117..100106832,2	K562	blood:
49	chr2:100065120..100066698-chr2:100069712..100072523,2	MCF-7	breast:
50	chr2:100080735..100084657-chr2:100090928..100093443,3	K562	blood:

No data

Variant related genes	Relation type
REV1	TF binding region
REV1	CpG island
ENSG00000135945	chromatin interactions

Extended variants
information (count: 1349 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1349 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3792135	chr2:100062163-100062164	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs558752701	chr2:100062244-100062245	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2053916	chr2:100062248-100062249	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138510455	chr2:100062363-100062364	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144117763	chr2:100062378-100062379	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554617036	chr2:100062414-100062415	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372545854	chr2:100062431-100062432	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147289749	chr2:100062450-100062451	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554242422	chr2:100062466-100062467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs369069898	chr2:100062467-100062468	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12986447	chr2:100062474-100062475	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559702238	chr2:100062591-100062592	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs377083132	chr2:100062622-100062623	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200429376	chr2:100062757-100062758	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs528534652	chr2:100062899-100062900	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138909598	chr2:100062919-100062920	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565119764	chr2:100062987-100062988	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs189120867	chr2:100063039-100063040	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181501234	chr2:100063061-100063062	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184961587	chr2:100063064-100063065	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149477923	chr2:100063111-100063112	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546230055	chr2:100063137-100063138	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566492271	chr2:100063250-100063251	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs116316872	chr2:100063289-100063290	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs368768627	chr2:100063290-100063291	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374589982	chr2:100063325-100063326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552329719	chr2:100063339-100063340	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs569070077	chr2:100063342-100063343	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567938715	chr2:100063355-100063356	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs562265427	chr2:100063463-100063464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537689283	chr2:100063486-100063487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554760902	chr2:100063496-100063497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189686201	chr2:100063560-100063561	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530976428	chr2:100063680-100063681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7563455	chr2:100063681-100063682	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs572932848	chr2:100063707-100063708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7563462	chr2:100063708-100063709	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs565083359	chr2:100063727-100063728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201585307	chr2:100063761-100063762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373172649	chr2:100063784-100063785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544437405	chr2:100063816-100063817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7572779	chr2:100063844-100063845	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs373024038	chr2:100063902-100063903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10865031	chr2:100063923-100063924	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs369833498	chr2:100063938-100063939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146189117	chr2:100063954-100063955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560169060	chr2:100063956-100063957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532192037	chr2:100064052-100064053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552294878	chr2:100064071-100064072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11899745	chr2:100064072-100064073	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1535 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100005800-100062600	Strong transcription	Dnd41	blood
2	chr2:100005800-100066000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:100006000-100081200	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr2:100021200-100077800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:100032600-100078000	Weak transcription	Psoas Muscle	Psoas
6	chr2:100034200-100088800	Weak transcription	Small Intestine	intestine
7	chr2:100036800-100074800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr2:100038200-100063200	Weak transcription	Fetal Intestine Small	intestine
9	chr2:100038200-100073800	Weak transcription	Esophagus	oesophagus
10	chr2:100041400-100077800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:100041600-100083400	Weak transcription	Brain Substantia Nigra	brain
12	chr2:100042800-100065000	Weak transcription	Lung	lung
13	chr2:100045000-100064200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr2:100045400-100068200	Weak transcription	Ovary	ovary
15	chr2:100047800-100063200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr2:100048200-100090600	Weak transcription	Stomach Mucosa	stomach
17	chr2:100048400-100067800	Weak transcription	Fetal Heart	heart
18	chr2:100048600-100064000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr2:100048600-100068200	Weak transcription	Spleen	Spleen
20	chr2:100048800-100070400	Weak transcription	Fetal Brain Female	brain
21	chr2:100050000-100065000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:100051800-100064600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr2:100053800-100075800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:100055400-100083200	Weak transcription	Right Ventricle	heart
25	chr2:100055600-100062200	Weak transcription	Brain Hippocampus Middle	brain
26	chr2:100055600-100063800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:100055600-100064000	Weak transcription	Stomach Smooth Muscle	stomach
28	chr2:100055600-100065000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr2:100055600-100065000	Weak transcription	Brain Cingulate Gyrus	brain
30	chr2:100055600-100065000	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:100055600-100065000	Weak transcription	NH-A	brain
32	chr2:100055600-100065400	Weak transcription	Brain Germinal Matrix	brain
33	chr2:100055600-100068600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr2:100055600-100071200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr2:100055600-100078200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:100055600-100079800	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr2:100055800-100062600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:100055800-100063200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr2:100055800-100063800	Weak transcription	Fetal Stomach	stomach
40	chr2:100055800-100064000	Weak transcription	HMEC	breast
41	chr2:100055800-100064200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr2:100055800-100064200	Weak transcription	HSMMtube	muscle
43	chr2:100055800-100064200	Weak transcription	Osteobl	bone
44	chr2:100055800-100064400	Weak transcription	Colonic Mucosa	Colon
45	chr2:100055800-100065000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr2:100055800-100067800	Weak transcription	Fetal Lung	lung
47	chr2:100055800-100072200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr2:100055800-100072800	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr2:100055800-100076200	Weak transcription	Aorta	Aorta
50	chr2:100055800-100076400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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