Variant report

Variant	esv3380034
Chromosome Location	chr2:74439354-74533666
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1665)
CpG islands
(count:122)
Chromatin interactive
region (count:133)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1665 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:74477316-74477495	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:74494210-74494595	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:74519889-74520214	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:74469927-74470119	K562	blood:	n/a	n/a
5	ARID3A	chr2:74494181-74494641	K562	blood:	n/a	n/a
6	ARID3A	chr2:74463891-74464189	HepG2	liver:	n/a	n/a
7	ATF1	chr2:74494233-74494557	K562	blood:	n/a	n/a
8	ATF2	chr2:74448623-74449820	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:74443826-74444181	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:74517530-74518015	GM12878	blood:	n/a	n/a
11	ATF2	chr2:74524419-74524995	GM12878	blood:	n/a	n/a
12	BACH1	chr2:74520963-74521163	K562	blood:	n/a	n/a
13	BACH1	chr2:74466609-74466749	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr2:74517571-74517874	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:74524531-74524833	GM12878	blood:	n/a	n/a
16	BCL3	chr2:74446851-74447266	K562	blood:	n/a	n/a
17	BCL3	chr2:74448874-74449557	K562	blood:	n/a	n/a
18	BCL3	chr2:74451570-74452330	A549	lung:	n/a	n/a
19	BCLAF1	chr2:74517475-74518286	GM12878	blood:	n/a	chr2:74518270-74518279
20	BCLAF1	chr2:74517547-74517938	GM12878	blood:	n/a	n/a
21	BCLAF1	chr2:74448855-74449519	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:74521029-74521229	K562	blood:	n/a	n/a
23	BHLHE40	chr2:74519903-74520202	HepG2	liver:	n/a	n/a
24	BHLHE40	chr2:74449355-74449362	HepG2	liver:	n/a	n/a
25	BHLHE40	chr2:74517654-74517928	GM12878	blood:	n/a	n/a
26	BHLHE40	chr2:74513912-74514154	HepG2	liver:	n/a	n/a
27	BHLHE40	chr2:74513834-74514176	K562	blood:	n/a	n/a
28	BHLHE40	chr2:74513984-74514049	A549	lung:	n/a	n/a
29	BHLHE40	chr2:74513919-74514077	GM12878	blood:	n/a	n/a
30	BHLHE40	chr2:74531438-74531752	K562	blood:	n/a	n/a
31	BRCA1	chr2:74459653-74459660	GM12878	blood:	n/a	n/a
32	BRCA1	chr2:74449044-74449056	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr2:74477375-74477493	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr2:74469462-74469867	K562	blood:	n/a	n/a
35	CBX3	chr2:74469476-74469742	K562	blood:	n/a	n/a
36	CBX3	chr2:74466010-74466506	HCT-116	colon:	n/a	n/a
37	CBX3	chr2:74525142-74525547	HCT-116	colon:	n/a	n/a
38	CBX3	chr2:74525161-74525555	HCT-116	colon:	n/a	n/a
39	CBX3	chr2:74466059-74466436	K562	blood:	n/a	n/a
40	CCNT2	chr2:74531556-74531777	K562	blood:	n/a	n/a
41	CCNT2	chr2:74448901-74449742	K562	blood:	n/a	n/a
42	CCNT2	chr2:74444049-74444120	K562	blood:	n/a	n/a
43	CCNT2	chr2:74445822-74446122	K562	blood:	n/a	n/a
44	CEBPB	chr2:74480501-74480710	HepG2	liver:	n/a	chr2:74480594-74480605 chr2:74480594-74480607
45	CEBPB	chr2:74492624-74492704	HepG2	liver:	n/a	chr2:74492671-74492682
46	CEBPB	chr2:74494166-74494520	K562	blood:	n/a	n/a
47	CEBPB	chr2:74494228-74494552	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:74477401-74477423	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:74464044-74464244	K562	blood:	n/a	chr2:74464159-74464170
50	CEBPB	chr2:74451150-74451400	IMR90	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:74477456-74477506	CMK	blood:	n/a
2	chr2:74477456-74477506	U87	brain:	n/a
3	chr2:74448564-74448614	AG04450	lung:	fetal
4	chr2:74477456-74477506	SK-N-SH	brain:	n/a
5	chr2:74448564-74448614	U87	brain:	n/a
6	chr2:74477456-74477506	AoSMC	blood vessel:	n/a
7	chr2:74477456-74477506	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:74448564-74448614	SK-N-SH	brain:	n/a
9	chr2:74477456-74477506	HCF	heart:	n/a
10	chr2:74448564-74448614	T-47D	breast:	n/a
11	chr2:74477456-74477506	PrEC	prostate:	n/a
12	chr2:74448564-74448614	Jurkat	blood:	n/a
13	chr2:74448564-74448614	HAEpiC	amniotic membrane:	n/a
14	chr2:74477456-74477506	HEK293	kidney:	embryo
15	chr2:74477456-74477506	AG09319	gingival:	n/a
16	chr2:74477456-74477506	NHDF-neo	bronchial:	n/a
17	chr2:74448564-74448614	CMK	blood:	n/a
18	chr2:74477456-74477506	Hepatocyte	liver:	n/a
19	chr2:74448564-74448614	A549	lung:	n/a
20	chr2:74477456-74477506	SKMC	muscle:	n/a
21	chr2:74448564-74448614	BJ	skin:	n/a
22	chr2:74477456-74477506	T-47D	breast:	n/a
23	chr2:74448564-74448614	HRE	kidney:	n/a
24	chr2:74448564-74448614	HRPEpiC	eye:	n/a
25	chr2:74477456-74477506	LNCaP	prostate:	n/a
26	chr2:74448564-74448614	HCF	heart:	n/a
27	chr2:74477456-74477506	K562	blood:	n/a
28	chr2:74448564-74448614	PFSK-1	brain:	n/a
29	chr2:74477456-74477506	A549	lung:	n/a
30	chr2:74477456-74477506	HAEpiC	amniotic membrane:	n/a
31	chr2:74477456-74477506	GM12891	blood:	n/a
32	chr2:74477456-74477506	Jurkat	blood:	n/a
33	chr2:74448564-74448614	SAEC	small airway:	n/a
34	chr2:74448564-74448614	HUVEC	blood vessel:	n/a
35	chr2:74448564-74448614	GM12891	blood:	n/a
36	chr2:74448564-74448614	GM12892	blood:	n/a
37	chr2:74477456-74477506	Hela-S3	cervix:	n/a
38	chr2:74477456-74477506	MCF10A-Er-Src	breast:	n/a
39	chr2:74448564-74448614	AoSMC	blood vessel:	n/a
40	chr2:74448564-74448614	SK-N-SH_RA	brain:	n/a
41	chr2:74477456-74477506	HRCEpiC	kidney:	n/a
42	chr2:74477456-74477506	AG10803	skin:	n/a
43	chr2:74477456-74477506	RPTEC	kidney:	n/a
44	chr2:74477456-74477506	IMR90	lung:	fetal
45	chr2:74448564-74448614	SKMC	muscle:	n/a
46	chr2:74477456-74477506	GM06990	blood:	n/a
47	chr2:74448564-74448614	Hela-S3	cervix:	n/a
48	chr2:74477456-74477506	SK-N-MC	brain:	n/a
49	chr2:74448564-74448614	LNCaP	prostate:	n/a
50	chr2:74448564-74448614	IMR90	lung:	fetal

(count:133 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:74475432..74477293-chr2:74687364..74689653,2	MCF-7	breast:
2	chr2:74346199..74346887-chr2:74488452..74489322,3	MCF-7	breast:
3	chr2:74512494..74514343-chr2:74657604..74660593,2	MCF-7	breast:
4	chr2:74495487..74498408-chr2:74499846..74503643,4	K562	blood:
5	chr2:74513138..74514789-chr2:74518325..74520415,2	MCF-7	breast:
6	chr2:74477004..74477578-chr2:74814578..74815241,2	K562	blood:
7	chr2:74434810..74438446-chr2:74445370..74448587,3	MCF-7	breast:
8	chr2:74492389..74495530-chr2:74618766..74620808,3	MCF-7	breast:
9	chr2:74477174..74477874-chr2:74561684..74562548,3	MCF-7	breast:
10	chr2:74500884..74503924-chr2:74506466..74508793,4	K562	blood:
11	chr2:74447215..74450146-chr2:74463449..74466578,3	K562	blood:
12	chr2:74487300..74489151-chr2:74489519..74492583,3	K562	blood:
13	chr2:74516653..74519345-chr2:74527381..74530006,3	K562	blood:
14	chr2:74474393..74476736-chr2:74479092..74481052,2	K562	blood:
15	chr2:74424362..74427305-chr2:74471867..74475240,3	K562	blood:
16	chr2:74469977..74471909-chr2:74474642..74477346,2	K562	blood:
17	chr2:74466425..74468753-chr2:74472765..74474388,2	K562	blood:
18	chr2:74375171..74377057-chr2:74458721..74461004,2	K562	blood:
19	chr2:74435328..74437744-chr2:74484533..74487667,3	MCF-7	breast:
20	chr2:74403803..74406060-chr2:74446250..74448222,2	MCF-7	breast:
21	chr2:74447215..74450146-chr2:74463449..74465120,2	K562	blood:
22	chr2:74374912..74375452-chr2:74488427..74489083,2	MCF-7	breast:
23	chr2:74491562..74493273-chr2:74497523..74500245,2	MCF-7	breast:
24	chr2:74495113..74497380-chr2:74500287..74503029,2	MCF-7	breast:
25	chr2:74435694..74437496-chr2:74451439..74453723,2	MCF-7	breast:
26	chr2:74478235..74480981-chr2:74481514..74484984,3	MCF-7	breast:
27	chr2:74516504..74518624-chr2:74518820..74521491,2	K562	blood:
28	chr2:74446614..74449007-chr2:74477377..74479575,2	K562	blood:
29	chr2:74474110..74476610-chr2:74483390..74486162,3	MCF-7	breast:
30	chr2:74424696..74427673-chr2:74460558..74464630,6	MCF-7	breast:
31	chr2:74474393..74476736-chr2:74479092..74481052,2	K562	blood:
32	chr2:74457826..74461318-chr2:74461527..74466761,7	K562	blood:
33	chr2:74466425..74468633-chr2:74471671..74474388,2	K562	blood:
34	chr2:74469853..74472729-chr2:74479366..74481244,2	MCF-7	breast:
35	chr2:74478235..74480981-chr2:74481514..74484984,3	MCF-7	breast:
36	chr2:74453950..74456295-chr2:74468210..74469726,2	K562	blood:
37	chr2:74519106..74521397-chr2:74523008..74525063,2	K562	blood:
38	chr2:74500884..74502937-chr2:74506466..74508655,3	K562	blood:
39	chr2:74469720..74472104-chr2:74477669..74480121,2	K562	blood:
40	chr2:74485713..74488456-chr2:74492837..74494369,2	K562	blood:
41	chr2:74449058..74450989-chr2:74745319..74747786,2	K562	blood:
42	chr2:74481714..74484157-chr2:74616620..74619291,2	MCF-7	breast:
43	chr2:74449407..74451288-chr2:74565740..74568302,2	K562	blood:
44	chr2:74452405..74454369-chr2:74458052..74460977,2	MCF-7	breast:
45	chr2:74404101..74407081-chr2:74456321..74458789,3	MCF-7	breast:
46	chr2:74500884..74502937-chr2:74506466..74508655,3	K562	blood:
47	chr2:74209451..74212429-chr2:74510433..74512189,2	MCF-7	breast:
48	chr2:74493932..74494789-chr2:74561661..74562579,7	MCF-7	breast:
49	chr2:74446879..74448831-chr2:74595217..74597589,2	K562	blood:
50	chr2:74488137..74490835-chr2:74493877..74495627,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTHFD2-3	chr2:74496082-74497200	ucscGeneNc_uc002sla_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MTHFD2	hsa-miR-421	chr2:74442280-74442305

Variant related genes	Relation type
SLC4A5	TF binding region
SLC4A5	CpG island
ENSG00000115307	chromatin interactions
ENSG00000188687	chromatin interactions
ENSG00000204843	chromatin interactions
ENSG00000225439	chromatin interactions
ENSG00000115275	chromatin interactions
ENSG00000204822	chromatin interactions
ENSG00000114978	chromatin interactions
ENSG00000163170	chromatin interactions
ENSG00000114993	chromatin interactions
ENSG00000235499	chromatin interactions
ENSG00000115317	chromatin interactions
ENSG00000065911	chromatin interactions

Extended variants
information (count: 3626 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3626 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13011529	chr2:74439356-74439357	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs57461008	chr2:74439357-74439358	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574276605	chr2:74439363-74439364	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531670145	chr2:74439380-74439381	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs398042480	chr2:74439391-74439392	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190659598	chr2:74439471-74439472	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10189152	chr2:74439522-74439523	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550290163	chr2:74439585-74439586	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545089156	chr2:74439595-74439596	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560509697	chr2:74439609-74439610	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562264302	chr2:74439662-74439663	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572828418	chr2:74439734-74439735	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201212703	chr2:74439772-74439773	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146865338	chr2:74439796-74439797	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529048548	chr2:74439829-74439830	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs183662805	chr2:74439832-74439833	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374104260	chr2:74439849-74439850	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559711007	chr2:74439885-74439886	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528063910	chr2:74439949-74439950	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs115376565	chr2:74439951-74439952	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs533020984	chr2:74439963-74439964	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs551120613	chr2:74439973-74439974	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs140710681	chr2:74440022-74440023	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528034523	chr2:74440036-74440037	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs397779252	chr2:74440047-74440048	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs529558032	chr2:74440066-74440067	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs367897245	chr2:74440114-74440115	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs549696954	chr2:74440251-74440252	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs10192236	chr2:74440303-74440304	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188004013	chr2:74440318-74440319	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs571932651	chr2:74440319-74440320	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192839061	chr2:74440327-74440328	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561586239	chr2:74440328-74440329	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548099274	chr2:74440360-74440361	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111889001	chr2:74440397-74440398	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs377733991	chr2:74440398-74440399	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10638050	chr2:74440421-74440422	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs7562660	chr2:74440426-74440427	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553782117	chr2:74440440-74440441	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540126681	chr2:74440447-74440448	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs6546894	chr2:74440466-74440467	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs540180264	chr2:74440636-74440637	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs550448998	chr2:74440675-74440676	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555243354	chr2:74440676-74440677	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573835743	chr2:74440719-74440720	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs13398979	chr2:74440744-74440745	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs117739871	chr2:74440746-74440747	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562683973	chr2:74440762-74440763	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570440205	chr2:74440797-74440798	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553547865	chr2:74440811-74440812	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
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
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	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
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Hepatocellular carcinoma	16750200	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74427400-74441000	Weak transcription	Colon Smooth Muscle	Colon
2	chr2:74427400-74441200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:74427400-74448400	Weak transcription	Brain Anterior Caudate	brain
4	chr2:74427400-74453000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr2:74427400-74453200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr2:74427400-74460200	Weak transcription	Brain Substantia Nigra	brain
7	chr2:74427400-74462000	Weak transcription	Brain Angular Gyrus	brain
8	chr2:74427400-74484400	Weak transcription	Fetal Lung	lung
9	chr2:74427600-74442600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:74427800-74494200	Weak transcription	Brain Germinal Matrix	brain
11	chr2:74428000-74448600	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr2:74428600-74449600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:74429000-74450600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr2:74429000-74453200	Weak transcription	Ovary	ovary
15	chr2:74429200-74452800	Weak transcription	Fetal Heart	heart
16	chr2:74432200-74441600	Strong transcription	Fetal Muscle Trunk	muscle
17	chr2:74432600-74444600	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr2:74432800-74441800	Strong transcription	Fetal Muscle Leg	muscle
19	chr2:74433600-74441800	Strong transcription	Fetal Stomach	stomach
20	chr2:74433600-74443000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:74433600-74444200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
22	chr2:74433600-74447200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr2:74433600-74447400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:74433600-74447600	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr2:74433600-74447600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr2:74433600-74448400	Weak transcription	Brain Hippocampus Middle	brain
27	chr2:74433800-74439400	Weak transcription	Aorta	Aorta
28	chr2:74433800-74439600	Weak transcription	Fetal Intestine Small	intestine
29	chr2:74433800-74447400	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr2:74433800-74447400	Strong transcription	Dnd41	blood
31	chr2:74433800-74447600	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr2:74433800-74447600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:74433800-74448400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:74433800-74449200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr2:74433800-74449200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr2:74433800-74449400	Strong transcription	NHEK	skin
37	chr2:74433800-74449600	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr2:74433800-74449800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr2:74433800-74461800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr2:74434000-74444800	Strong transcription	Hela-S3	cervix
41	chr2:74434000-74453000	Weak transcription	Psoas Muscle	Psoas
42	chr2:74434200-74439400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr2:74434200-74440600	Weak transcription	Spleen	Spleen
44	chr2:74434200-74442000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:74434200-74447600	Strong transcription	HMEC	breast
46	chr2:74434200-74449400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:74434200-74449800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr2:74434400-74447600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:74434600-74447600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr2:74434600-74448800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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