Variant report

Variant	nsv535838
Chromosome Location	chr2:99335416-99358356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:622)
CpG islands
(count:732)
Chromatin interactive
region (count:26)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99347710-99347908	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:99351261-99351842	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:99352884-99353266	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:99348284-99349093	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:99351304-99351833	K562	blood:	n/a	n/a
6	ARID3A	chr2:99344181-99344479	HepG2	liver:	n/a	n/a
7	ATF1	chr2:99351376-99351732	K562	blood:	n/a	n/a
8	BACH1	chr2:99347838-99348187	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:99346840-99346973	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr2:99346571-99347012	HepG2	liver:	n/a	chr2:99346971-99346987
11	BHLHE40	chr2:99347751-99348118	GM12878	blood:	n/a	chr2:99348042-99348058
12	BRCA1	chr2:99343443-99343614	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr2:99347882-99347930	GM12878	blood:	n/a	n/a
14	BRCA1	chr2:99347750-99347916	HepG2	liver:	n/a	n/a
15	CBX3	chr2:99351253-99351632	K562	blood:	n/a	n/a
16	CCNT2	chr2:99351308-99351749	K562	blood:	n/a	chr2:99351739-99351748
17	CCNT2	chr2:99347175-99347456	K562	blood:	n/a	n/a
18	CEBPB	chr2:99351443-99351657	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:99352867-99353318	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:99352837-99353271	A549	lung:	n/a	n/a
21	CEBPB	chr2:99343237-99343538	Hela-S3	cervix:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
22	CEBPB	chr2:99346243-99346870	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:99352906-99353320	MCF-7	breast:	n/a	n/a
24	CEBPB	chr2:99348446-99348773	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:99343215-99343547	IMR90	lung:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
26	CEBPB	chr2:99343221-99343577	K562	blood:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
27	CEBPB	chr2:99352912-99353177	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr2:99343232-99343529	A549	lung:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
29	CEBPB	chr2:99348514-99348710	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:99348249-99348809	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:99343257-99343478	H1-hESC	embryonic stem cell:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
32	CEBPB	chr2:99343208-99343574	HepG2	liver:	n/a	chr2:99343393-99343404 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343393-99343402 chr2:99343391-99343402
33	CEBPD	chr2:99346652-99347301	HepG2	liver:	n/a	n/a
34	CEBPD	chr2:99351255-99351835	K562	blood:	n/a	n/a
35	CEBPD	chr2:99347647-99347927	HepG2	liver:	n/a	n/a
36	CEBPD	chr2:99347639-99347979	HepG2	liver:	n/a	n/a
37	CEBPD	chr2:99351301-99351703	K562	blood:	n/a	n/a
38	CHD1	chr2:99348067-99348246	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr2:99347958-99347989	GM12878	blood:	n/a	n/a
40	CHD2	chr2:99347101-99347164	HepG2	liver:	n/a	n/a
41	CHD2	chr2:99347694-99348352	GM12878	blood:	n/a	n/a
42	CHD2	chr2:99347720-99348370	HepG2	liver:	n/a	n/a
43	CREB1	chr2:99346553-99348804	HepG2	liver:	n/a	n/a
44	CREB1	chr2:99347648-99348058	A549	lung:	n/a	n/a
45	CREB1	chr2:99351272-99351910	HepG2	liver:	n/a	n/a
46	CTCF	chr2:99347447-99347452	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr2:99347300-99347450	GM06990	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
48	CTCF	chr2:99347300-99347450	MCF-7	breast:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
49	CTCF	chr2:99347300-99347450	GM12869	blood:	n/a	chr2:99347374-99347382 chr2:99347371-99347389
50	CTCF	chr2:99347330-99347336	NHEK	skin:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99342685-99342735	AG04450	lung:	fetal
2	chr2:99347979-99348029	IMR90	lung:	fetal
3	chr2:99342986-99343036	GM12891	blood:	n/a
4	chr2:99347987-99348037	IMR90	lung:	fetal
5	chr2:99346635-99346685	K562	blood:	n/a
6	chr2:99347979-99348029	SAEC	small airway:	n/a
7	chr2:99347854-99347904	Hela-S3	cervix:	n/a
8	chr2:99351550-99351600	K562	blood:	n/a
9	chr2:99342685-99342735	HMEC	breast:	n/a
10	chr2:99347987-99348037	AG09319	gingival:	n/a
11	chr2:99346635-99346685	PANC-1	pancreas:	n/a
12	chr2:99342986-99343036	AG09319	gingival:	n/a
13	chr2:99346902-99346952	HRPEpiC	eye:	n/a
14	chr2:99347979-99348029	AG09309	skin:	n/a
15	chr2:99351550-99351600	HEK293	kidney:	embryo
16	chr2:99346902-99346952	HL-60	blood:	n/a
17	chr2:99346818-99346868	Hela-S3	cervix:	n/a
18	chr2:99351550-99351600	HRPEpiC	eye:	n/a
19	chr2:99346818-99346868	NHDF-neo	bronchial:	n/a
20	chr2:99347987-99348037	NHBE	bronchial:	n/a
21	chr2:99347854-99347904	K562	blood:	n/a
22	chr2:99347987-99348037	NT2-D1	testis:	n/a
23	chr2:99346635-99346685	SK-N-SH_RA	brain:	n/a
24	chr2:99347422-99347472	Caco-2	colon:	n/a
25	chr2:99347422-99347472	GM19239	blood:	n/a
26	chr2:99351550-99351600	SK-N-SH	brain:	n/a
27	chr2:99346635-99346685	SK-N-SH	brain:	n/a
28	chr2:99346818-99346868	A549	lung:	n/a
29	chr2:99342685-99342735	HCPEpiC	choroid plexus:	n/a
30	chr2:99342986-99343036	LNCaP	prostate:	n/a
31	chr2:99342685-99342735	A549	lung:	n/a
32	chr2:99346818-99346868	PrEC	prostate:	n/a
33	chr2:99347854-99347904	AG04449	skin:	fetal
34	chr2:99346902-99346952	MCF-7	breast:	n/a
35	chr2:99346635-99346685	SKMC	muscle:	n/a
36	chr2:99351550-99351600	NT2-D1	testis:	n/a
37	chr2:99348232-99348282	BJ	skin:	n/a
38	chr2:99346902-99346952	NHBE	bronchial:	n/a
39	chr2:99342685-99342735	HepG2	liver:	n/a
40	chr2:99348176-99348226	Hepatocyte	liver:	n/a
41	chr2:99348232-99348282	Caco-2	colon:	n/a
42	chr2:99347854-99347904	ovcar-3	ovarian:	n/a
43	chr2:99347979-99348029	AG04450	lung:	fetal
44	chr2:99342986-99343036	PANC-1	pancreas:	n/a
45	chr2:99347854-99347904	HRE	kidney:	n/a
46	chr2:99347979-99348029	GM06990	blood:	n/a
47	chr2:99347854-99347904	ProgFib	skin:	n/a
48	chr2:99351550-99351600	Jurkat	blood:	n/a
49	chr2:99347979-99348029	SK-N-MC	brain:	n/a
50	chr2:99342986-99343036	GM06990	blood:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:99343338..99345259-chr2:99346373..99348700,3	MCF-7	breast:
2	chr2:99342228..99344879-chr2:99346177..99348874,2	K562	blood:
3	chr2:99336480..99339286-chr2:99347871..99349769,2	MCF-7	breast:
4	chr2:99352944..99355702-chr2:99450894..99453779,2	MCF-7	breast:
5	chr2:99342228..99344879-chr2:99346177..99348874,2	K562	blood:
6	chr2:99097067..99098913-chr2:99352317..99355051,2	MCF-7	breast:
7	chr2:99356397..99359071-chr2:99359903..99362484,2	K562	blood:
8	chr2:99336480..99339286-chr2:99347871..99349769,2	MCF-7	breast:
9	chr2:99343338..99345259-chr2:99346373..99348700,3	MCF-7	breast:
10	chr2:99334681..99338238-chr2:99344696..99347399,3	MCF-7	breast:
11	chr2:99316162..99318899-chr2:99339583..99342162,2	MCF-7	breast:
12	chr2:99221557..99223102-chr2:99346482..99348239,2	MCF-7	breast:
13	chr2:99358144..99360845-chr2:99364555..99366061,2	MCF-7	breast:
14	chr2:99345368..99349321-chr2:99385005..99390572,6	MCF-7	breast:
15	chr2:99345360..99347894-chr2:99396622..99399352,2	MCF-7	breast:
16	chr2:99344922..99348721-chr2:99382903..99389092,6	MCF-7	breast:
17	chr2:99342514..99344879-chr2:99346177..99348798,2	K562	blood:
18	chr2:99338843..99341034-chr2:99341737..99344169,2	MCF-7	breast:
19	chr2:99346676..99348606-chr2:99349694..99353065,3	MCF-7	breast:
20	chr2:99334922..99337052-chr2:99339872..99343548,3	MCF-7	breast:
21	chr2:99342514..99344879-chr2:99346177..99348798,2	K562	blood:
22	chr2:99348346..99350092-chr2:99446085..99447956,2	MCF-7	breast:
23	chr2:99344987..99348857-chr2:99353398..99358314,5	MCF-7	breast:
24	chr2:99352512..99355304-chr2:99377484..99380437,2	MCF-7	breast:
25	chr2:99329459..99332003-chr2:99335709..99337859,2	MCF-7	breast:
26	chr2:99341666..99344183-chr2:99455107..99457899,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC50-1	chr2:99348118-99348158	XLOC_001587
2	lnc-UNC50-1	chr2:99347828-99348158	NONHSAT072721

No data

Variant related genes	Relation type
MGAT4A	TF binding region
MGAT4A	CpG island
ENSG00000238830	chromatin interactions
ENSG00000226791	chromatin interactions
ENSG00000201070	chromatin interactions
ENSG00000183513	chromatin interactions
ENSG00000071073	chromatin interactions

Extended variants
information (count: 775 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182617336	chr2:99335505-99335506	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs141182113	chr2:99335506-99335507	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs1399512	chr2:99335547-99335548	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs186804867	chr2:99335556-99335557	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs201550371	chr2:99335622-99335623	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs199646612	chr2:99335625-99335626	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10191603	chr2:99335626-99335627	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149887794	chr2:99335628-99335629	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551177988	chr2:99335650-99335651	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs548072301	chr2:99335718-99335719	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567818868	chr2:99335722-99335723	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536830555	chr2:99335807-99335808	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs147213531	chr2:99335892-99335893	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566948550	chr2:99335908-99335909	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs533565361	chr2:99335976-99335977	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191259833	chr2:99335992-99335993	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs184795521	chr2:99336006-99336007	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536899611	chr2:99336011-99336012	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140581648	chr2:99336028-99336029	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs573543215	chr2:99336036-99336037	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs6737760	chr2:99336044-99336045	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs144533728	chr2:99336070-99336071	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187691052	chr2:99336146-99336147	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545005900	chr2:99336179-99336180	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564699774	chr2:99336196-99336197	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147814112	chr2:99336210-99336211	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs574681101	chr2:99336249-99336250	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542005479	chr2:99336278-99336279	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs551030450	chr2:99336330-99336331	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561563105	chr2:99336342-99336343	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530345869	chr2:99336404-99336405	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374494243	chr2:99336470-99336471	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs192146966	chr2:99336480-99336481	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185167575	chr2:99336555-99336556	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs552543214	chr2:99336556-99336557	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569118181	chr2:99336588-99336589	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538231097	chr2:99336589-99336590	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs112631083	chr2:99336593-99336594	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs28783173	chr2:99336608-99336609	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536077077	chr2:99336619-99336620	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189583502	chr2:99336649-99336650	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372102285	chr2:99336672-99336673	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141809289	chr2:99336702-99336703	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535362351	chr2:99336784-99336785	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs544733405	chr2:99336802-99336803	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181119064	chr2:99336804-99336805	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184752418	chr2:99336835-99336836	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs544204365	chr2:99336845-99336846	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs561601823	chr2:99336860-99336861	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540296808	chr2:99336863-99336864	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1188 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99303200-99336400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr2:99316600-99336400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:99319200-99336800	Weak transcription	Spleen	Spleen
4	chr2:99321000-99336200	Weak transcription	Fetal Stomach	stomach
5	chr2:99321600-99336600	Weak transcription	Fetal Kidney	kidney
6	chr2:99322000-99336800	Weak transcription	Colonic Mucosa	Colon
7	chr2:99322200-99336200	Weak transcription	Fetal Intestine Large	intestine
8	chr2:99324200-99336600	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr2:99325600-99336800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr2:99326400-99336000	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr2:99326400-99336800	Weak transcription	Aorta	Aorta
12	chr2:99326400-99342600	Weak transcription	Adipose Nuclei	Adipose
13	chr2:99326400-99343600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr2:99326400-99346400	Weak transcription	Fetal Muscle Leg	muscle
15	chr2:99326600-99336800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr2:99326600-99336800	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr2:99326600-99336800	Weak transcription	Rectal Smooth Muscle	rectum
18	chr2:99326600-99340000	Weak transcription	Brain Angular Gyrus	brain
19	chr2:99326800-99336600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr2:99326800-99336600	Weak transcription	Brain Hippocampus Middle	brain
21	chr2:99326800-99336800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr2:99326800-99337000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:99326800-99342600	Weak transcription	Liver	Liver
24	chr2:99326800-99343800	Weak transcription	Small Intestine	intestine
25	chr2:99327200-99336800	Weak transcription	Brain Anterior Caudate	brain
26	chr2:99327800-99336000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
27	chr2:99328000-99335600	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr2:99328400-99336600	Weak transcription	Primary B cells from cord blood	blood
29	chr2:99328400-99336800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr2:99328600-99336600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:99328600-99336800	Weak transcription	Left Ventricle	heart
32	chr2:99328800-99337000	Weak transcription	Psoas Muscle	Psoas
33	chr2:99329400-99336600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:99329600-99339600	Weak transcription	Right Atrium	heart
35	chr2:99330600-99336600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr2:99330800-99336400	Genic enhancers	Primary T cells fromperipheralblood	blood
37	chr2:99330800-99336400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr2:99331200-99337400	Weak transcription	HUVEC	blood vessel
39	chr2:99332600-99336200	Strong transcription	Fetal Intestine Small	intestine
40	chr2:99332600-99337200	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr2:99333000-99336400	Genic enhancers	Primary T cells from cord blood	blood
42	chr2:99333000-99336400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
43	chr2:99333000-99342800	Strong transcription	Primary monocytes fromperipheralblood	blood
44	chr2:99333200-99336600	Weak transcription	Primary B cells from peripheral blood	blood
45	chr2:99333400-99337400	Strong transcription	Duodenum Mucosa	Duodenum
46	chr2:99333600-99335600	Strong transcription	Sigmoid Colon	Sigmoid Colon
47	chr2:99334000-99339400	Strong transcription	Dnd41	blood
48	chr2:99334200-99335600	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr2:99334200-99343200	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr2:99334400-99339400	Weak transcription	Esophagus	oesophagus

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