Variant report

Variant	nsv546308
Chromosome Location	chr1:58714427-58743499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:366)
CpG islands
(count:978)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:58715990-58716418	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr1:58716043-58716449	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:58715404-58716410	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr1:58714319-58714549	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:58727254-58727400	HepG2	liver:	n/a	chr1:58727327-58727340 chr1:58727329-58727340 chr1:58727329-58727340 chr1:58727327-58727340 chr1:58727327-58727338
6	CEBPB	chr1:58716087-58716404	K562	blood:	n/a	n/a
7	CEBPB	chr1:58716094-58716372	K562	blood:	n/a	n/a
8	CEBPB	chr1:58716163-58716330	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:58726585-58726811	A549	lung:	n/a	chr1:58726655-58726666
10	CEBPB	chr1:58726621-58726706	HepG2	liver:	n/a	chr1:58726655-58726666
11	CEBPB	chr1:58726057-58726249	HepG2	liver:	n/a	chr1:58726184-58726195 chr1:58726186-58726197
12	CEBPB	chr1:58715984-58716420	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:58716094-58716313	HepG2	liver:	n/a	n/a
14	CHD2	chr1:58715956-58716418	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTBP2	chr1:58715231-58716476	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:58717400-58717550	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:58717338-58717678	GM12878	blood:	n/a	n/a
18	CTCF	chr1:58715558-58715669	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr1:58715880-58716030	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr1:58717416-58717614	GM12878	blood:	n/a	n/a
21	CTCF	chr1:58717466-58717586	NHEK	skin:	n/a	n/a
22	CTCF	chr1:58717376-58717598	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr1:58715920-58716070	HFF	foreskin:	n/a	n/a
24	CTCF	chr1:58717440-58717590	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr1:58717284-58717630	K562	blood:	n/a	n/a
26	CTCF	chr1:58717400-58717550	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr1:58717394-58717592	HepG2	liver:	n/a	n/a
28	CTCF	chr1:58717378-58717380	K562	blood:	n/a	n/a
29	CTCF	chr1:58717400-58717550	GM12874	blood:	n/a	n/a
30	CTCF	chr1:58715840-58715990	HAc	cerebellar:	n/a	n/a
31	CTCF	chr1:58717460-58717610	BE2_C	brain:	n/a	n/a
32	CTCF	chr1:58717420-58717570	HEK293	kidney:	n/a	n/a
33	CTCF	chr1:58715940-58716090	AG04449	skin:	n/a	n/a
34	CTCF	chr1:58717466-58717598	A549	lung:	n/a	n/a
35	CTCF	chr1:58715925-58716015	GM12892	blood:	n/a	n/a
36	CTCF	chr1:58717460-58717610	AG04450	lung:	n/a	n/a
37	CTCF	chr1:58717440-58717590	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:58717440-58717590	GM12867	blood:	n/a	n/a
39	CTCF	chr1:58716120-58716270	AG09309	skin:	n/a	n/a
40	CTCF	chr1:58717340-58717490	RPTEC	kidney:	n/a	n/a
41	CTCF	chr1:58717420-58717570	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr1:58717440-58717590	NHLF	lung:	n/a	n/a
43	CTCF	chr1:58717279-58717759	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:58716120-58716270	RPTEC	kidney:	n/a	n/a
45	CTCF	chr1:58717381-58717623	K562	blood:	n/a	n/a
46	CTCF	chr1:58716224-58716294	Gliobla	brain:	n/a	n/a
47	CTCF	chr1:58717420-58717570	GM12872	blood:	n/a	n/a
48	CTCF	chr1:58717420-58717570	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr1:58717440-58717590	HCFaa	heart:	n/a	n/a
50	CTCF	chr1:58717460-58717610	MCF-7	breast:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:58716257-58716307	PrEC	prostate:	n/a
2	chr1:58714452-58714502	AG09309	skin:	n/a
3	chr1:58716257-58716307	PrEC	prostate:	n/a
4	chr1:58714452-58714502	AG09309	skin:	n/a
5	chr1:58716018-58716068	SAEC	small airway:	n/a
6	chr1:58716018-58716068	HepG2	liver:	n/a
7	chr1:58716306-58716356	HUVEC	blood vessel:	n/a
8	chr1:58715747-58715797	MCF-7	breast:	n/a
9	chr1:58717632-58717682	A549	lung:	n/a
10	chr1:58716662-58716712	HCPEpiC	choroid plexus:	n/a
11	chr1:58716257-58716307	MCF10A-Er-Src	breast:	n/a
12	chr1:58740398-58740448	HMEC	breast:	n/a
13	chr1:58716306-58716356	AG09319	gingival:	n/a
14	chr1:58718544-58718594	SK-N-SH_RA	brain:	n/a
15	chr1:58717632-58717682	HCPEpiC	choroid plexus:	n/a
16	chr1:58715499-58715549	HEK293	kidney:	embryo
17	chr1:58740398-58740448	AG10803	skin:	n/a
18	chr1:58715539-58715589	IMR90	lung:	fetal
19	chr1:58716306-58716356	U87	brain:	n/a
20	chr1:58715499-58715549	AG10803	skin:	n/a
21	chr1:58718544-58718594	SKMC	muscle:	n/a
22	chr1:58716306-58716356	RPTEC	kidney:	n/a
23	chr1:58716662-58716712	HL-60	blood:	n/a
24	chr1:58718544-58718594	NH-A	brain:	n/a
25	chr1:58715539-58715589	HEK293	kidney:	embryo
26	chr1:58714452-58714502	Caco-2	colon:	n/a
27	chr1:58716257-58716307	HMEC	breast:	n/a
28	chr1:58717632-58717682	GM12891	blood:	n/a
29	chr1:58716257-58716307	PFSK-1	brain:	n/a
30	chr1:58716306-58716356	SK-N-MC	brain:	n/a
31	chr1:58718544-58718594	HL-60	blood:	n/a
32	chr1:58716033-58716083	HRCEpiC	kidney:	n/a
33	chr1:58715747-58715797	AG04450	lung:	fetal
34	chr1:58716257-58716307	MCF-7	breast:	n/a
35	chr1:58715747-58715797	HAEpiC	amniotic membrane:	n/a
36	chr1:58715744-58715794	CMK	blood:	n/a
37	chr1:58716377-58716427	SKMC	muscle:	n/a
38	chr1:58715532-58715582	HUVEC	blood vessel:	n/a
39	chr1:58716377-58716427	IMR90	lung:	fetal
40	chr1:58718544-58718594	K562	blood:	n/a
41	chr1:58716662-58716712	NB4	blood:	n/a
42	chr1:58716018-58716068	Hela-S3	cervix:	n/a
43	chr1:58716033-58716083	HEK293	kidney:	embryo
44	chr1:58716018-58716068	HPAEpiC	pulmonary alveolar:	n/a
45	chr1:58715539-58715589	HRCEpiC	kidney:	n/a
46	chr1:58718544-58718594	HEEpiC	esophagus:	n/a
47	chr1:58716662-58716712	BJ	skin:	n/a
48	chr1:58715747-58715797	HMEC	breast:	n/a
49	chr1:58716257-58716307	Hela-S3	cervix:	n/a
50	chr1:58715747-58715797	HL-60	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:
2	chr1:58711426..58714604-chr1:58717021..58720890,3	K562	blood:
3	chr1:58722416..58724317-chr1:58724409..58727199,2	K562	blood:
4	chr1:58717073..58717741-chr1:59012205..59012834,2	K562	blood:
5	chr1:58740800..58743267-chr1:58744921..58746475,2	K562	blood:
6	chr1:58722434..58724317-chr1:58724409..58727876,3	K562	blood:
7	chr1:58722434..58724317-chr1:58724409..58727876,3	K562	blood:
8	chr1:58711426..58714604-chr1:58717021..58720890,3	K562	blood:

No data

Variant related genes	Relation type
DAB1	TF binding region
DAB1	CpG island
ENSG00000162600	chromatin interactions
ENSG00000173406	chromatin interactions

Extended variants
information (count: 971 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs614373	chr1:58714427-58714428	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567354145	chr1:58714445-58714446	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs536424893	chr1:58714456-58714457	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs144948436	chr1:58714463-58714464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs573210084	chr1:58714485-58714486	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs538913399	chr1:58714487-58714488	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs192432891	chr1:58714504-58714505	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs575167315	chr1:58714574-58714575	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs543980531	chr1:58714588-58714589	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs554601585	chr1:58714598-58714599	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs573916820	chr1:58714651-58714652	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs542776521	chr1:58714673-58714674	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559502636	chr1:58714772-58714773	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528784838	chr1:58714781-58714782	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545677605	chr1:58714804-58714805	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76934468	chr1:58714811-58714812	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375149615	chr1:58714815-58714816	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139349579	chr1:58714855-58714856	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545825118	chr1:58714857-58714858	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531219109	chr1:58714908-58714909	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184883560	chr1:58714911-58714912	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550819962	chr1:58714966-58714967	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567716610	chr1:58714968-58714969	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188148748	chr1:58714981-58714982	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546846109	chr1:58714985-58714986	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566670236	chr1:58714999-58715000	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538976111	chr1:58715008-58715009	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs549437057	chr1:58715073-58715074	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111474486	chr1:58715161-58715162	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs568763342	chr1:58715244-58715245	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537819108	chr1:58715253-58715254	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143771591	chr1:58715300-58715301	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151064229	chr1:58715314-58715315	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184364429	chr1:58715318-58715319	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539916997	chr1:58715351-58715352	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553194693	chr1:58715416-58715417	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573089156	chr1:58715418-58715419	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145480416	chr1:58715437-58715438	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189152186	chr1:58715463-58715464	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546670768	chr1:58715545-58715546	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541718253	chr1:58715732-58715733	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530828428	chr1:58715736-58715737	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114988039	chr1:58715744-58715745	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61779232	chr1:58715755-58715756	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576103	chr1:58715779-58715780	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530264314	chr1:58715787-58715788	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547107571	chr1:58715822-58715823	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs117567026	chr1:58715824-58715825	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs561958667	chr1:58715829-58715830	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs181814740	chr1:58715839-58715840	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Meckel-Gruber syndrome	21572526	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	16616336	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:58713000-58716800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
2	chr1:58713200-58714600	Bivalent/Poised TSS	Fetal Brain Female	brain
3	chr1:58713600-58714600	Bivalent Enhancer	Liver	Liver
4	chr1:58713600-58715200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
5	chr1:58713800-58714600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
6	chr1:58713800-58714600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
7	chr1:58713800-58714600	Enhancers	Left Ventricle	heart
8	chr1:58713800-58715000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:58713800-58715200	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr1:58713800-58715600	Enhancers	Rectal Smooth Muscle	rectum
11	chr1:58713800-58715800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
12	chr1:58713800-58716000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
13	chr1:58714000-58714600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:58714000-58714600	Active TSS	Brain Angular Gyrus	brain
15	chr1:58714000-58714800	Flanking Bivalent TSS/Enh	Brain Anterior Caudate	brain
16	chr1:58714000-58715000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
17	chr1:58714000-58715200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:58714000-58715200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
19	chr1:58714200-58714600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
20	chr1:58714200-58714600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr1:58714200-58714600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
22	chr1:58714200-58714600	Bivalent Enhancer	Fetal Heart	heart
23	chr1:58714200-58714800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
24	chr1:58714200-58714800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr1:58714200-58714800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
26	chr1:58714200-58714800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:58714200-58714800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:58714200-58715000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:58714200-58715000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:58714200-58715200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
31	chr1:58714200-58715400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
32	chr1:58714200-58715800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
33	chr1:58714200-58716200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
34	chr1:58714200-58716200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:58714200-58716200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr1:58714400-58714600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
37	chr1:58714400-58714600	Flanking Bivalent TSS/Enh	Brain Substantia Nigra	brain
38	chr1:58714400-58714600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
39	chr1:58714400-58714600	Flanking Active TSS	Fetal Brain Male	brain
40	chr1:58714400-58714600	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
41	chr1:58714400-58714600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
42	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
43	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
45	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
47	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
48	chr1:58714400-58714800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
49	chr1:58714400-58715000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
50	chr1:58714400-58715200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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