Variant report

Variant	nsv876836
Chromosome Location	chr3:59500394-59664687
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1062)
CpG islands
(count:549)
Chromatin interactive
region (count:24)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1062 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:59593395-59593580	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:59561182-59561539	K562	blood:	n/a	n/a
3	ATF2	chr3:59526458-59526871	GM12878	blood:	n/a	n/a
4	ATF2	chr3:59552084-59552714	GM12878	blood:	n/a	n/a
5	ATF2	chr3:59526362-59526892	GM12878	blood:	n/a	n/a
6	ATF2	chr3:59552167-59552639	GM12878	blood:	n/a	n/a
7	ATF3	chr3:59545554-59545797	K562	blood:	n/a	n/a
8	ATF3	chr3:59650067-59650586	A549	lung:	n/a	n/a
9	BACH1	chr3:59561316-59561497	K562	blood:	n/a	n/a
10	BATF	chr3:59552130-59552654	GM12878	blood:	n/a	n/a
11	BATF	chr3:59566745-59567115	GM12878	blood:	n/a	chr3:59566993-59567001 chr3:59566948-59566959
12	BATF	chr3:59552139-59552671	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:59552163-59552630	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:59552149-59552712	GM12878	blood:	n/a	n/a
15	BCL3	chr3:59650007-59650553	A549	lung:	n/a	n/a
16	BCL3	chr3:59649988-59650620	A549	lung:	n/a	n/a
17	BCL3	chr3:59552099-59552595	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:59526434-59526792	GM12878	blood:	n/a	chr3:59526549-59526558
19	BCLAF1	chr3:59552242-59552645	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:59561146-59561474	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:59561180-59561474	K562	blood:	n/a	n/a
22	BHLHE40	chr3:59526353-59526844	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:59561069-59561492	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:59552179-59552771	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:59561225-59561514	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr3:59541320-59541709	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:59552092-59552763	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:59544954-59545907	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:59567068-59567390	HepG2	liver:	n/a	chr3:59567199-59567210
30	CEBPB	chr3:59649776-59650736	MCF-7	breast:	n/a	chr3:59650631-59650643 chr3:59650374-59650385 chr3:59650375-59650386
31	CEBPB	chr3:59653709-59653972	IMR90	lung:	n/a	chr3:59653858-59653869
32	CEBPB	chr3:59545365-59546017	HCT-116	colon:	n/a	n/a
33	CEBPB	chr3:59649665-59650712	MCF-7	breast:	n/a	chr3:59650631-59650643 chr3:59650374-59650385 chr3:59650375-59650386
34	CEBPB	chr3:59650189-59650561	HepG2	liver:	n/a	chr3:59650374-59650385 chr3:59650375-59650386
35	CEBPB	chr3:59545459-59545896	A549	lung:	n/a	n/a
36	CEBPB	chr3:59545484-59545826	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:59646516-59647195	A549	lung:	n/a	chr3:59646894-59646903 chr3:59646892-59646905
38	CEBPB	chr3:59646653-59647137	ECC-1	luminal epithelium:	n/a	chr3:59646894-59646903 chr3:59646892-59646905
39	CEBPB	chr3:59618695-59618973	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:59659002-59659220	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:59649754-59650589	IMR90	lung:	n/a	chr3:59650374-59650385 chr3:59650375-59650386
42	CEBPB	chr3:59521729-59522020	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:59545351-59545970	HCT-116	colon:	n/a	n/a
44	CEBPB	chr3:59559767-59560006	A549	lung:	n/a	n/a
45	CEBPB	chr3:59646788-59647107	ECC-1	luminal epithelium:	n/a	chr3:59646894-59646903 chr3:59646892-59646905
46	CEBPB	chr3:59545368-59545976	A549	lung:	n/a	n/a
47	CEBPB	chr3:59545462-59545842	A549	lung:	n/a	n/a
48	CEBPB	chr3:59649790-59650569	HepG2	liver:	n/a	chr3:59650374-59650385 chr3:59650375-59650386
49	CEBPB	chr3:59627318-59627649	HepG2	liver:	n/a	chr3:59627501-59627510 chr3:59627501-59627510 chr3:59627499-59627512 chr3:59627499-59627512 chr3:59627501-59627510 chr3:59627499-59627512 chr3:59627499-59627510 chr3:59627500-59627511 chr3:59627501-59627510 chr3:59627499-59627510
50	CEBPB	chr3:59545488-59545824	MCF-7	breast:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:59526404-59526454	HMEC	breast:	n/a
2	chr3:59644285-59644335	Hepatocyte	liver:	n/a
3	chr3:59526404-59526454	A549	lung:	n/a
4	chr3:59646860-59646910	HAEpiC	amniotic membrane:	n/a
5	chr3:59521337-59521387	SK-N-MC	brain:	n/a
6	chr3:59640236-59640286	MCF-7	breast:	n/a
7	chr3:59560961-59561011	GM06990	blood:	n/a
8	chr3:59521337-59521387	AG10803	skin:	n/a
9	chr3:59560961-59561011	U87	brain:	n/a
10	chr3:59627287-59627337	K562	blood:	n/a
11	chr3:59501481-59501531	A549	lung:	n/a
12	chr3:59560961-59561011	HEK293	kidney:	embryo
13	chr3:59644285-59644335	MCF10A-Er-Src	breast:	n/a
14	chr3:59640236-59640286	LNCaP	prostate:	n/a
15	chr3:59526404-59526454	H1-hESC	embryonic stem cell:	embryo
16	chr3:59521337-59521387	AG04450	lung:	fetal
17	chr3:59646860-59646910	Hela-S3	cervix:	n/a
18	chr3:59644285-59644335	PFSK-1	brain:	n/a
19	chr3:59645614-59645664	H1-hESC	embryonic stem cell:	embryo
20	chr3:59526404-59526454	HUVEC	blood vessel:	n/a
21	chr3:59627287-59627337	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:59526404-59526454	LNCaP	prostate:	n/a
23	chr3:59646860-59646910	PANC-1	pancreas:	n/a
24	chr3:59644285-59644335	RPTEC	kidney:	n/a
25	chr3:59646860-59646910	BJ	skin:	n/a
26	chr3:59501481-59501531	Jurkat	blood:	n/a
27	chr3:59521337-59521387	HIPEpiC	eye:	n/a
28	chr3:59645614-59645664	NT2-D1	testis:	n/a
29	chr3:59644285-59644335	Hela-S3	cervix:	n/a
30	chr3:59627287-59627337	HCM	heart:	n/a
31	chr3:59640236-59640286	GM12891	blood:	n/a
32	chr3:59560961-59561011	ECC-1	luminal epithelium:	n/a
33	chr3:59640236-59640286	MCF10A-Er-Src	breast:	n/a
34	chr3:59646860-59646910	NB4	blood:	n/a
35	chr3:59560961-59561011	AG04450	lung:	fetal
36	chr3:59640236-59640286	GM19239	blood:	n/a
37	chr3:59501481-59501531	AG09319	gingival:	n/a
38	chr3:59645614-59645664	Caco-2	colon:	n/a
39	chr3:59646860-59646910	HUVEC	blood vessel:	n/a
40	chr3:59646860-59646910	HCF	heart:	n/a
41	chr3:59640236-59640286	AG10803	skin:	n/a
42	chr3:59627287-59627337	HAEpiC	amniotic membrane:	n/a
43	chr3:59501481-59501531	PrEC	prostate:	n/a
44	chr3:59640236-59640286	HPAEpiC	pulmonary alveolar:	n/a
45	chr3:59645614-59645664	NB4	blood:	n/a
46	chr3:59640236-59640286	BJ	skin:	n/a
47	chr3:59645614-59645664	NHBE	bronchial:	n/a
48	chr3:59501481-59501531	HRE	kidney:	n/a
49	chr3:59640236-59640286	HMEC	breast:	n/a
50	chr3:59645614-59645664	ovcar-3	ovarian:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:59593238..59594045-chr3:59842694..59843779,3	MCF-7	breast:
2	chr3:58980166..58981001-chr3:59560879..59561772,2	MCF-7	breast:
3	chr3:59560813..59561442-chr3:59843559..59844061,2	MCF-7	breast:
4	chr3:59586558..59588987-chr3:59590319..59592657,2	K562	blood:
5	chr3:59561232..59561846-chr3:59795242..59795895,3	MCF-7	breast:
6	chr3:59524667..59527497-chr3:59528444..59530855,2	K562	blood:
7	chr3:59524667..59527497-chr3:59528444..59530855,2	K562	blood:
8	chr3:59560756..59561799-chr3:61367133..61368119,4	K562	blood:
9	chr20:1798049..1800079-chr3:59632520..59635313,2	MCF-7	breast:
10	chr3:59649290..59650251-chr3:59988158..59988824,3	MCF-7	breast:
11	chr3:59586558..59588987-chr3:59590319..59592657,2	K562	blood:
12	chr3:59510111..59512291-chr3:59513698..59516687,2	K562	blood:
13	chr3:59560988..59561827-chr3:59795202..59795948,3	MCF-7	breast:
14	chr3:59560849..59562291-chr3:59843175..59844082,5	MCF-7	breast:
15	chr3:59549975..59552166-chr3:59555008..59557289,2	K562	blood:
16	chr3:59610769..59613089-chr3:59615642..59618440,2	K562	blood:
17	chr3:59400041..59401605-chr3:59564601..59566183,2	MCF-7	breast:
18	chr3:59593056..59594000-chr3:59795106..59795983,2	MCF-7	breast:
19	chr3:59549975..59552166-chr3:59555008..59557289,2	K562	blood:
20	chr3:59629969..59632394-chr3:59636625..59638438,2	K562	blood:
21	chr3:59629969..59632394-chr3:59636625..59638438,2	K562	blood:
22	chr3:59649290..59649811-chr3:59988158..59988814,2	MCF-7	breast:
23	chr3:59510111..59512291-chr3:59513698..59516687,2	K562	blood:
24	chr3:59610769..59613089-chr3:59615642..59618440,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FHIT-1	chr3:59643972-59644000	XLOC_003142
2	lnc-KCTD6-7	chr3:59521589-59522141	NONHSAT090151
3	lnc-FHIT-1	chr3:59643971-59643973	FPKM1_group_21266_transcript_1
4	lnc-FHIT-1	chr3:59627440-59627638	FPKM1_group_21266_transcript_1
5	lnc-FHIT-1	chr3:59643971-59644000	NONHSAT090152
6	lnc-FHIT-1	chr3:59627440-59627638	NONHSAT090152
7	lnc-FHIT-1	chr3:59627441-59627638	XLOC_003142

No data

Variant related genes	Relation type
ENSG00000241804	TF binding region
ENSG00000242545	TF binding region
ENSG00000241804	CpG island
ENSG00000242545	CpG island
ENSG00000230839	chromatin interactions
PCGF3	miRNA target sites
GNAI2	miRNA target sites

Extended variants
information (count: 6186 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:6186 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7340603	chr3:59500394-59500395	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs145884194	chr3:59500400-59500401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs199623445	chr3:59500474-59500475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573921068	chr3:59500478-59500479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9826715	chr3:59500479-59500480	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73082832	chr3:59500496-59500497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577014527	chr3:59500522-59500523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115880835	chr3:59500547-59500548	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs9844389	chr3:59500557-59500558	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143804669	chr3:59500589-59500590	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549949366	chr3:59500607-59500608	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs189172220	chr3:59500623-59500624	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192872800	chr3:59500654-59500655	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs547634335	chr3:59500720-59500721	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565832175	chr3:59500747-59500748	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs34126751	chr3:59500779-59500780	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs28488791	chr3:59500784-59500785	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs386661390	chr3:59500839-59500840	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs113476403	chr3:59500840-59500841	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73837326	chr3:59500841-59500842	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs79506037	chr3:59500850-59500851	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs185455792	chr3:59500857-59500858	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138489009	chr3:59500921-59500922	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28606076	chr3:59500930-59500931	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs553155936	chr3:59500954-59500955	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs578082402	chr3:59500977-59500978	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs375769688	chr3:59500984-59500985	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs545726658	chr3:59501012-59501013	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs558279945	chr3:59501024-59501025	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs563825874	chr3:59501033-59501034	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs143946859	chr3:59501108-59501109	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543428449	chr3:59501113-59501114	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs146555492	chr3:59501132-59501133	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529000090	chr3:59501136-59501137	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547473601	chr3:59501157-59501158	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs139135767	chr3:59501196-59501197	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577024092	chr3:59501197-59501198	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs532979069	chr3:59501227-59501228	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs74509558	chr3:59501257-59501258	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs113996820	chr3:59501332-59501333	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs12629410	chr3:59501351-59501352	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs536911233	chr3:59501355-59501356	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs34448606	chr3:59501444-59501445	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs60616246	chr3:59501445-59501446	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs77863308	chr3:59501446-59501447	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs555360619	chr3:59501448-59501449	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs112702504	chr3:59501449-59501450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs567277427	chr3:59501452-59501453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs534804526	chr3:59501475-59501476	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs143041993	chr3:59501489-59501490	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Cancer	18162546	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1003 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59492400-59501000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:59498000-59500600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr3:59498200-59500600	Weak transcription	Primary T cells from cord blood	blood
4	chr3:59499600-59503200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:59500200-59500400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:59500200-59500600	Enhancers	Dnd41	blood
7	chr3:59500200-59503800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:59500400-59501600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr3:59500600-59501200	Enhancers	Primary T cells from cord blood	blood
10	chr3:59500600-59501400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr3:59500600-59501600	Flanking Active TSS	Dnd41	blood
12	chr3:59500600-59501800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr3:59500600-59501800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:59500600-59502200	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:59500800-59502000	Enhancers	Brain Hippocampus Middle	brain
16	chr3:59501000-59502000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:59501000-59502000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr3:59501000-59502000	Enhancers	Brain Substantia Nigra	brain
19	chr3:59501000-59502000	Enhancers	Fetal Brain Female	brain
20	chr3:59501000-59502200	Enhancers	Brain Cingulate Gyrus	brain
21	chr3:59501200-59501600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr3:59501200-59501800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:59501200-59502000	Enhancers	Brain Germinal Matrix	brain
24	chr3:59501200-59502000	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr3:59501200-59502200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:59501200-59502800	Weak transcription	Primary T cells from cord blood	blood
27	chr3:59501200-59503600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:59501400-59501800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:59501400-59502200	Enhancers	Brain Anterior Caudate	brain
30	chr3:59501400-59502800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr3:59501400-59503800	Enhancers	Fetal Lung	lung
32	chr3:59501600-59502000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:59501600-59502200	Enhancers	Dnd41	blood
34	chr3:59501600-59503000	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr3:59501600-59503800	Enhancers	Fetal Kidney	kidney
36	chr3:59501800-59502200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr3:59502000-59503000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:59502000-59503000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:59502200-59502600	Weak transcription	Dnd41	blood
40	chr3:59502600-59503200	Enhancers	Pancreas	Pancrea
41	chr3:59502600-59503400	Enhancers	Dnd41	blood
42	chr3:59502800-59503200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr3:59502800-59503200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr3:59502800-59503600	Enhancers	Primary T cells from cord blood	blood
45	chr3:59503000-59503400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr3:59503000-59503400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:59503000-59503400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:59503000-59503600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr3:59503000-59505200	Enhancers	Stomach Mucosa	stomach
50	chr3:59503200-59503400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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