Variant report

Variant	nsv877143
Chromosome Location	chr3:87630433-87860130
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1188)
CpG islands
(count:611)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:87846361-87847423	K562	blood:	n/a	n/a
2	ARID3A	chr3:87852889-87853083	K562	blood:	n/a	n/a
3	ARID3A	chr3:87847637-87848059	K562	blood:	n/a	n/a
4	ARID3A	chr3:87856389-87856892	K562	blood:	n/a	n/a
5	ARID3A	chr3:87854872-87855404	K562	blood:	n/a	n/a
6	ARID3A	chr3:87853726-87854283	K562	blood:	n/a	n/a
7	ARID3A	chr3:87820565-87820676	K562	blood:	n/a	n/a
8	ARID3A	chr3:87837578-87837623	K562	blood:	n/a	n/a
9	ARID3A	chr3:87850727-87851027	K562	blood:	n/a	n/a
10	ARID3A	chr3:87845165-87845971	K562	blood:	n/a	n/a
11	ATF1	chr3:87661797-87661994	K562	blood:	n/a	n/a
12	ATF1	chr3:87845222-87845685	K562	blood:	n/a	n/a
13	ATF1	chr3:87839831-87840243	K562	blood:	n/a	n/a
14	ATF1	chr3:87847026-87847435	K562	blood:	n/a	n/a
15	ATF1	chr3:87676571-87676792	K562	blood:	n/a	n/a
16	ATF2	chr3:87723828-87724353	GM12878	blood:	n/a	n/a
17	ATF2	chr3:87723887-87724325	GM12878	blood:	n/a	n/a
18	ATF3	chr3:87845316-87845788	K562	blood:	n/a	n/a
19	BACH1	chr3:87841454-87842181	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr3:87820557-87820578	K562	blood:	n/a	n/a
21	BACH1	chr3:87841407-87841692	K562	blood:	n/a	n/a
22	BCL11A	chr3:87670905-87671200	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:87723571-87723850	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:87723898-87724281	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:87723845-87724273	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:87777026-87777188	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr3:87776930-87777274	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCLAF1	chr3:87845143-87845687	K562	blood:	n/a	n/a
29	BHLHE40	chr3:87820480-87820751	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:87854760-87855262	GM12878	blood:	n/a	n/a
31	BHLHE40	chr3:87849772-87849912	K562	blood:	n/a	n/a
32	BHLHE40	chr3:87723553-87724426	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:87845112-87845719	K562	blood:	n/a	n/a
34	BHLHE40	chr3:87842682-87842708	K562	blood:	n/a	n/a
35	BHLHE40	chr3:87846439-87847356	K562	blood:	n/a	n/a
36	BHLHE40	chr3:87841624-87842476	K562	blood:	n/a	chr3:87841931-87841947 chr3:87841808-87841824 chr3:87841972-87841988 chr3:87842037-87842053
37	BHLHE40	chr3:87854742-87855265	K562	blood:	n/a	n/a
38	BHLHE40	chr3:87844618-87844835	K562	blood:	n/a	n/a
39	CBX3	chr3:87790020-87790221	K562	blood:	n/a	n/a
40	CBX3	chr3:87664686-87664965	K562	blood:	n/a	n/a
41	CBX3	chr3:87656185-87656439	K562	blood:	n/a	n/a
42	CBX3	chr3:87664665-87664997	K562	blood:	n/a	n/a
43	CBX3	chr3:87805024-87805380	K562	blood:	n/a	n/a
44	CBX3	chr3:87845223-87845642	K562	blood:	n/a	n/a
45	CBX3	chr3:87656209-87656523	K562	blood:	n/a	n/a
46	CBX3	chr3:87789999-87790224	K562	blood:	n/a	n/a
47	CCNT2	chr3:87845078-87845730	K562	blood:	n/a	n/a
48	CCNT2	chr3:87841691-87842470	K562	blood:	n/a	chr3:87841941-87841950
49	CCNT2	chr3:87846951-87847362	K562	blood:	n/a	chr3:87847349-87847358
50	CEBPB	chr3:87665485-87665674	A549	lung:	n/a	chr3:87665588-87665599

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:87811194-87811244	T-47D	breast:	n/a
2	chr3:87811194-87811244	T-47D	breast:	n/a
3	chr3:87842246-87842296	AG10803	skin:	n/a
4	chr3:87811194-87811244	SK-N-MC	brain:	n/a
5	chr3:87728433-87728483	Jurkat	blood:	n/a
6	chr3:87843755-87843805	AG04450	lung:	fetal
7	chr3:87728433-87728483	GM12891	blood:	n/a
8	chr3:87842246-87842296	HNPCEpiC	eye:	n/a
9	chr3:87811194-87811244	IMR90	lung:	fetal
10	chr3:87842246-87842296	GM12878	blood:	n/a
11	chr3:87839841-87839891	ovcar-3	ovarian:	n/a
12	chr3:87810762-87810812	ECC-1	luminal epithelium:	n/a
13	chr3:87839841-87839891	GM19239	blood:	n/a
14	chr3:87728433-87728483	RPTEC	kidney:	n/a
15	chr3:87729320-87729370	ECC-1	luminal epithelium:	n/a
16	chr3:87842019-87842069	HCM	heart:	n/a
17	chr3:87846180-87846230	NHBE	bronchial:	n/a
18	chr3:87729320-87729370	GM12891	blood:	n/a
19	chr3:87842246-87842296	GM12892	blood:	n/a
20	chr3:87811194-87811244	K562	blood:	n/a
21	chr3:87842246-87842296	SK-N-SH	brain:	n/a
22	chr3:87843755-87843805	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:87728433-87728483	ECC-1	luminal epithelium:	n/a
24	chr3:87846180-87846230	HCT-116	colon:	n/a
25	chr3:87839841-87839891	HUVEC	blood vessel:	n/a
26	chr3:87810762-87810812	NHDF-neo	bronchial:	n/a
27	chr3:87842019-87842069	HNPCEpiC	eye:	n/a
28	chr3:87839841-87839891	PANC-1	pancreas:	n/a
29	chr3:87810762-87810812	Caco-2	colon:	n/a
30	chr3:87842398-87842448	H1-hESC	embryonic stem cell:	embryo
31	chr3:87843755-87843805	Jurkat	blood:	n/a
32	chr3:87842019-87842069	HMEC	breast:	n/a
33	chr3:87842398-87842448	AoSMC	blood vessel:	n/a
34	chr3:87811194-87811244	MCF-7	breast:	n/a
35	chr3:87846180-87846230	SKMC	muscle:	n/a
36	chr3:87810762-87810812	HRCEpiC	kidney:	n/a
37	chr3:87842246-87842296	LNCaP	prostate:	n/a
38	chr3:87842019-87842069	LNCaP	prostate:	n/a
39	chr3:87810762-87810812	HIPEpiC	eye:	n/a
40	chr3:87842246-87842296	ProgFib	skin:	n/a
41	chr3:87842019-87842069	HRE	kidney:	n/a
42	chr3:87810762-87810812	LNCaP	prostate:	n/a
43	chr3:87842398-87842448	HCM	heart:	n/a
44	chr3:87843755-87843805	U87	brain:	n/a
45	chr3:87846180-87846230	Jurkat	blood:	n/a
46	chr3:87810762-87810812	HCT-116	colon:	n/a
47	chr3:87842398-87842448	HL-60	blood:	n/a
48	chr3:87846180-87846230	PrEC	prostate:	n/a
49	chr3:87811194-87811244	RPTEC	kidney:	n/a
50	chr3:87842246-87842296	MCF10A-Er-Src	breast:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:87808352..87810255-chr3:87812136..87814576,2	MCF-7	breast:
2	chr3:87789321..87792117-chr3:87796229..87798081,2	MCF-7	breast:
3	chr3:87827898..87830613-chr3:87841535..87843509,2	K562	blood:
4	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
5	chr3:87346989..87347924-chr3:87820302..87821498,3	MCF-7	breast:
6	chr3:87745181..87747327-chr3:87772407..87775801,3	K562	blood:
7	chr3:87835402..87838110-chr3:87839403..87841793,3	K562	blood:
8	chr3:87773985..87776726-chr3:87783571..87785837,2	MCF-7	breast:
9	chr3:87670698..87673462-chr3:87676763..87678506,2	K562	blood:
10	chr3:87849890..87852917-chr3:87853922..87857395,3	K562	blood:
11	chr3:87670698..87673462-chr3:87675838..87678506,3	K562	blood:
12	chr3:87805200..87807448-chr3:87809033..87811045,2	K562	blood:
13	chr3:87787506..87789179-chr3:87800683..87802189,2	MCF-7	breast:
14	chr3:87808352..87810255-chr3:87812136..87814576,2	MCF-7	breast:
15	chr3:87820271..87821383-chr3:88051902..88052924,6	MCF-7	breast:
16	chr3:87774485..87776498-chr3:87777273..87779870,3	MCF-7	breast:
17	chr3:87834701..87839368-chr3:87839393..87843561,7	K562	blood:
18	chr3:87670698..87673462-chr3:87675838..87678506,3	K562	blood:
19	chr3:87752670..87754550-chr3:87776800..87779392,2	MCF-7	breast:
20	chr3:87835402..87838110-chr3:87839403..87841793,3	K562	blood:
21	chr3:87843885..87846211-chr3:87904754..87906414,2	K562	blood:
22	chr3:87774485..87776498-chr3:87777273..87779870,3	MCF-7	breast:
23	chr3:87805200..87807448-chr3:87809033..87811045,2	K562	blood:
24	chr3:87849890..87852917-chr3:87853922..87857395,3	K562	blood:
25	chr3:87805630..87807898-chr3:87809132..87811197,2	MCF-7	breast:
26	chr3:87820697..87821585-chr3:88052369..88052934,2	MCF-7	breast:
27	chr3:87745181..87747327-chr3:87772407..87775801,3	K562	blood:
28	chr3:87347562..87348198-chr3:87820743..87821251,2	MCF-7	breast:
29	chr3:87805630..87807898-chr3:87809132..87811197,2	MCF-7	breast:
30	chr3:87859784..87864231-chr3:87868098..87870648,4	K562	blood:
31	chr3:87773985..87776726-chr3:87783571..87785837,2	MCF-7	breast:
32	chr3:87752670..87754550-chr3:87776800..87779392,2	MCF-7	breast:
33	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
34	chr3:87845525..87848228-chr3:87871993..87873515,2	K562	blood:
35	chr3:87787506..87789179-chr3:87800683..87802189,2	MCF-7	breast:
36	chr3:87670698..87673462-chr3:87676763..87678506,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHMP2B-3	chr3:87643988-87644526	NONHSAT090690
2	lnc-POU1F1-1	chr3:87679451-87680769	NONHSAT090691

No data

Variant related genes	Relation type
ENSG00000239572	TF binding region
RNU6-873P	TF binding region
PSMC1P6	TF binding region
APOOP2	TF binding region
ENSG00000239572	CpG island
RNU6-873P	CpG island
PSMC1P6	CpG island
APOOP2	CpG island
ENSG00000200703	chromatin interactions
ENSG00000239572	chromatin interactions

Extended variants
information (count: 4306 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:4306 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138265810	chr3:87636034-87636035	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs4859086	chr3:87636057-87636058	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs545741646	chr3:87636068-87636069	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs184557623	chr3:87636081-87636082	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs149643913	chr3:87636117-87636118	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs201918070	chr3:87636124-87636125	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs544570379	chr3:87636152-87636153	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs562709490	chr3:87636178-87636179	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs111375132	chr3:87636195-87636196	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189937216	chr3:87636223-87636224	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs192195610	chr3:87636224-87636225	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs527883929	chr3:87636226-87636227	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs4859087	chr3:87636245-87636246	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs571103984	chr3:87636295-87636296	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs538129246	chr3:87636305-87636306	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs549765814	chr3:87636314-87636315	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs9836770	chr3:87636331-87636332	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs567925060	chr3:87636348-87636349	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs535182068	chr3:87636368-87636369	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs183580395	chr3:87636394-87636395	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs571949237	chr3:87636396-87636397	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs539232508	chr3:87636404-87636405	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs557655368	chr3:87636416-87636417	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576304476	chr3:87636450-87636451	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs200143835	chr3:87636460-87636461	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs543317137	chr3:87636468-87636469	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs562910004	chr3:87636469-87636470	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs532380074	chr3:87636473-87636474	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188267289	chr3:87636508-87636509	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542388940	chr3:87636510-87636511	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs9874465	chr3:87636514-87636515	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs527916815	chr3:87636549-87636550	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs141519988	chr3:87636567-87636568	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs150755814	chr3:87636568-87636569	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532043485	chr3:87636570-87636571	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs12108006	chr3:87636588-87636589	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139207531	chr3:87636592-87636593	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570468605	chr3:87640301-87640302	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs144399870	chr3:87640343-87640344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs4858965	chr3:87640363-87640364	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185733317	chr3:87640364-87640365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs372651743	chr3:87640368-87640369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545887296	chr3:87640381-87640382	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs535146566	chr3:87640385-87640386	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs189662011	chr3:87640402-87640403	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs559155211	chr3:87640422-87640423	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs562580833	chr3:87640423-87640424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539765533	chr3:87640424-87640425	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557756342	chr3:87640445-87640446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371932601	chr3:87640458-87640459	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
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
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:87636000-87636600	Active TSS	Fetal Heart	heart
2	chr3:87645400-87646200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr3:87646000-87646400	Enhancers	Sigmoid Colon	Sigmoid Colon
4	chr3:87646200-87648000	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:87648000-87648600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr3:87649400-87650200	Enhancers	Hela-S3	cervix
7	chr3:87655600-87656600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:87657000-87657800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
9	chr3:87662000-87664400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:87664200-87664600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
11	chr3:87664400-87664800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:87664400-87665000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr3:87664600-87664800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr3:87664800-87665200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:87664800-87669800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr3:87666800-87667000	Bivalent Enhancer	Esophagus	oesophagus
17	chr3:87675000-87676000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:87675600-87676400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr3:87675600-87677200	Enhancers	K562	blood
20	chr3:87676400-87677000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr3:87676600-87677200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr3:87683000-87683200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:87683000-87683400	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
24	chr3:87683200-87683400	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:87686600-87687600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr3:87686800-87687400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:87686800-87687400	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:87686800-87687600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:87687000-87687400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr3:87687000-87687400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr3:87687000-87687400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:87687600-87694000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr3:87693800-87694200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
34	chr3:87693800-87694200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:87694000-87695400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr3:87694000-87695600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr3:87694000-87695600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr3:87694000-87695600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr3:87694200-87695200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:87694200-87695200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:87695200-87695400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr3:87695200-87695400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:87702600-87702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:87702800-87703000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:87702800-87703600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:87703600-87706000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:87722800-87723200	Bivalent Enhancer	GM12878-XiMat	blood
48	chr3:87723200-87724600	Enhancers	GM12878-XiMat	blood
49	chr3:87723600-87724400	Enhancers	Primary B cells from peripheral blood	blood
50	chr3:87723600-87724600	Bivalent Enhancer	Primary B cells from cord blood	blood

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