Variant report

Variant	nsv536689
Chromosome Location	chr3:110209344-110559021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1701)
CpG islands
(count:855)
Chromatin interactive
region (count:64)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:110269356-110270029	K562	blood:	n/a	n/a
2	ARID3A	chr3:110247380-110248084	K562	blood:	n/a	n/a
3	ARID3A	chr3:110239851-110240334	K562	blood:	n/a	n/a
4	ARID3A	chr3:110491707-110493063	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:110222947-110224194	K562	blood:	n/a	n/a
6	ARID3A	chr3:110229389-110229704	K562	blood:	n/a	n/a
7	ARID3A	chr3:110462094-110462434	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:110339011-110339287	K562	blood:	n/a	n/a
9	ARID3A	chr3:110235328-110235528	K562	blood:	n/a	n/a
10	ARID3A	chr3:110344280-110344634	K562	blood:	n/a	n/a
11	ATF1	chr3:110223647-110224062	K562	blood:	n/a	n/a
12	ATF1	chr3:110239924-110240245	K562	blood:	n/a	n/a
13	ATF2	chr3:110295750-110296207	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:110532964-110533649	GM12878	blood:	n/a	n/a
15	ATF2	chr3:110430649-110431131	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr3:110430615-110431161	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr3:110302100-110302850	A549	lung:	n/a	n/a
18	ATF3	chr3:110344405-110344569	K562	blood:	n/a	n/a
19	ATF3	chr3:110295700-110296333	A549	lung:	n/a	n/a
20	ATF3	chr3:110245673-110245815	K562	blood:	n/a	n/a
21	ATF3	chr3:110223684-110224032	K562	blood:	n/a	n/a
22	ATF3	chr3:110245606-110245939	K562	blood:	n/a	n/a
23	ATF3	chr3:110302207-110302904	A549	lung:	n/a	n/a
24	ATF3	chr3:110239853-110240234	K562	blood:	n/a	n/a
25	BACH1	chr3:110310093-110310161	K562	blood:	n/a	n/a
26	BACH1	chr3:110239948-110240284	K562	blood:	n/a	n/a
27	BACH1	chr3:110373934-110373954	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr3:110295457-110296326	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr3:110486727-110486959	GM12878	blood:	n/a	chr3:110486867-110486878
30	BATF	chr3:110533351-110533666	GM12878	blood:	n/a	n/a
31	BATF	chr3:110532917-110533342	GM12878	blood:	n/a	chr3:110533127-110533137 chr3:110533126-110533137 chr3:110533123-110533133
32	BATF	chr3:110532924-110533300	GM12878	blood:	n/a	chr3:110533127-110533137 chr3:110533126-110533137 chr3:110533123-110533133
33	BATF	chr3:110455224-110455485	GM12878	blood:	n/a	n/a
34	BATF	chr3:110287191-110287395	GM12878	blood:	n/a	n/a
35	BATF	chr3:110345477-110345909	GM12878	blood:	n/a	chr3:110345613-110345623
36	BCL11A	chr3:110302104-110302404	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr3:110430733-110430982	H1-hESC	embryonic stem cell:	n/a	n/a
38	BCL11A	chr3:110532958-110533252	GM12878	blood:	n/a	chr3:110533125-110533134 chr3:110533126-110533135
39	BCL11A	chr3:110430736-110430988	H1-hESC	embryonic stem cell:	n/a	n/a
40	BCL11A	chr3:110295758-110296109	H1-hESC	embryonic stem cell:	n/a	n/a
41	BCL11A	chr3:110317738-110318028	H1-hESC	embryonic stem cell:	n/a	n/a
42	BCL11A	chr3:110295827-110296106	H1-hESC	embryonic stem cell:	n/a	n/a
43	BCL11A	chr3:110302187-110302409	H1-hESC	embryonic stem cell:	n/a	n/a
44	BCL3	chr3:110301985-110302982	A549	lung:	n/a	n/a
45	BCL3	chr3:110295630-110296266	A549	lung:	n/a	n/a
46	BCL3	chr3:110295569-110296350	A549	lung:	n/a	n/a
47	BHLHE40	chr3:110223596-110224181	K562	blood:	n/a	n/a
48	BHLHE40	chr3:110492187-110492694	HepG2	liver:	n/a	n/a
49	BHLHE40	chr3:110344340-110344672	K562	blood:	n/a	n/a
50	BHLHE40	chr3:110239814-110240283	K562	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:110533292-110533342	AG09319	gingival:	n/a
2	chr3:110533292-110533342	AG09319	gingival:	n/a
3	chr3:110344165-110344215	GM12891	blood:	n/a
4	chr3:110376551-110376601	SKMC	muscle:	n/a
5	chr3:110446221-110446271	GM06990	blood:	n/a
6	chr3:110240891-110240941	Jurkat	blood:	n/a
7	chr3:110510470-110510520	GM12891	blood:	n/a
8	chr3:110246985-110247035	GM12892	blood:	n/a
9	chr3:110250679-110250729	AG10803	skin:	n/a
10	chr3:110446221-110446271	AG09309	skin:	n/a
11	chr3:110246985-110247035	MCF10A-Er-Src	breast:	n/a
12	chr3:110303472-110303522	GM12891	blood:	n/a
13	chr3:110246985-110247035	NHBE	bronchial:	n/a
14	chr3:110533292-110533342	HNPCEpiC	eye:	n/a
15	chr3:110376551-110376601	GM12878	blood:	n/a
16	chr3:110363281-110363331	HEEpiC	esophagus:	n/a
17	chr3:110303472-110303522	PFSK-1	brain:	n/a
18	chr3:110363228-110363278	PANC-1	pancreas:	n/a
19	chr3:110248442-110248492	SKMC	muscle:	n/a
20	chr3:110533292-110533342	SAEC	small airway:	n/a
21	chr3:110240891-110240941	BE2_C	brain:	n/a
22	chr3:110510470-110510520	HRE	kidney:	n/a
23	chr3:110246985-110247035	HepG2	liver:	n/a
24	chr3:110376551-110376601	A549	lung:	n/a
25	chr3:110344165-110344215	GM12892	blood:	n/a
26	chr3:110246985-110247035	Hela-S3	cervix:	n/a
27	chr3:110240891-110240941	U87	brain:	n/a
28	chr3:110363281-110363331	HCF	heart:	n/a
29	chr3:110248442-110248492	Hepatocyte	liver:	n/a
30	chr3:110240891-110240941	SKMC	muscle:	n/a
31	chr3:110363222-110363272	HRE	kidney:	n/a
32	chr3:110240891-110240941	K562	blood:	n/a
33	chr3:110246985-110247035	HCPEpiC	choroid plexus:	n/a
34	chr3:110303472-110303522	HCF	heart:	n/a
35	chr3:110248442-110248492	PFSK-1	brain:	n/a
36	chr3:110246985-110247035	Caco-2	colon:	n/a
37	chr3:110510470-110510520	LNCaP	prostate:	n/a
38	chr3:110363281-110363331	NHBE	bronchial:	n/a
39	chr3:110240891-110240941	PANC-1	pancreas:	n/a
40	chr3:110248442-110248492	HAEpiC	amniotic membrane:	n/a
41	chr3:110240891-110240941	GM06990	blood:	n/a
42	chr3:110501630-110501680	GM12878	blood:	n/a
43	chr3:110376551-110376601	NHDF-neo	bronchial:	n/a
44	chr3:110363281-110363331	HAEpiC	amniotic membrane:	n/a
45	chr3:110510470-110510520	PrEC	prostate:	n/a
46	chr3:110363281-110363331	RPTEC	kidney:	n/a
47	chr3:110446221-110446271	HNPCEpiC	eye:	n/a
48	chr3:110376551-110376601	GM19239	blood:	n/a
49	chr3:110344165-110344215	A549	lung:	n/a
50	chr3:110510470-110510520	T-47D	breast:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr19:49845864..49846607-chr3:110315550..110316370,2	MCF-7	breast:
2	chr3:110374889..110375647-chr5:134724423..134725132,2	MCF-7	breast:
3	chr3:110405694..110407709-chr3:110411526..110413966,2	K562	blood:
4	chr3:110282414..110285256-chr3:110286686..110288676,2	K562	blood:
5	chr3:110531400..110533494-chr3:110558447..110560628,2	K562	blood:
6	chr3:110222894..110225675-chr3:110240158..110242098,2	K562	blood:
7	chr10:125136292..125137128-chr3:110437815..110438528,2	MCF-7	breast:
8	chr3:110245688..110247478-chr3:110251852..110254191,2	K562	blood:
9	chr3:110234753..110236641-chr3:110241075..110242689,2	K562	blood:
10	chr3:110443436..110447134-chr3:110454733..110457934,4	K562	blood:
11	chr3:110448604..110450202-chr3:110451942..110453671,2	MCF-7	breast:
12	chr3:110437982..110441695-chr3:110441982..110447721,6	K562	blood:
13	chr3:110228265..110231031-chr3:110237827..110239739,2	K562	blood:
14	chr3:110240019..110241918-chr3:110243471..110245418,2	K562	blood:
15	chr3:110448604..110450202-chr3:110451942..110453671,2	MCF-7	breast:
16	chr3:110361104..110363034-chr3:110366368..110368463,2	MCF-7	breast:
17	chr3:110226107..110231031-chr3:110235797..110240409,5	K562	blood:
18	chr3:110223795..110225407-chr3:110236340..110238461,2	K562	blood:
19	chr3:110223081..110225312-chr3:110255969..110257984,2	K562	blood:
20	chr3:110232519..110235271-chr3:110279973..110282638,2	K562	blood:
21	chr3:110235029..110237272-chr3:110238334..110239946,2	K562	blood:
22	chr3:110226107..110231031-chr3:110235797..110240409,5	K562	blood:
23	chr3:110256128..110258374-chr3:110259929..110261455,2	K562	blood:
24	chr3:110224350..110227035-chr3:110267483..110270332,2	K562	blood:
25	chr3:110361104..110363034-chr3:110366368..110368463,2	MCF-7	breast:
26	chr3:110223795..110225407-chr3:110236340..110238461,2	K562	blood:
27	chr3:110195963..110198828-chr3:110223194..110225023,2	K562	blood:
28	chr3:110232263..110233795-chr3:110237768..110239573,2	K562	blood:
29	chr3:110235029..110237272-chr3:110238334..110239946,2	K562	blood:
30	chr3:110279243..110282023-chr3:110283429..110285882,2	K562	blood:
31	chr3:109749391..109751192-chr3:110500927..110502696,2	K562	blood:
32	chr3:110279243..110282023-chr3:110283429..110285882,2	K562	blood:
33	chr3:110405694..110407709-chr3:110411526..110413966,2	K562	blood:
34	chr3:110232263..110233795-chr3:110237768..110239573,2	K562	blood:
35	chr3:110240019..110241918-chr3:110243471..110245418,2	K562	blood:
36	chr3:110232519..110235271-chr3:110279973..110282638,2	K562	blood:
37	chr3:110223100..110226514-chr3:110228942..110230704,3	K562	blood:
38	chr3:110248230..110250752-chr3:110252528..110254988,2	K562	blood:
39	chr3:110302646..110303511-chr3:110658446..110659012,2	MCF-7	breast:
40	chr3:110276449..110278320-chr3:110281402..110283554,3	K562	blood:
41	chr3:110245688..110247478-chr3:110251852..110254191,2	K562	blood:
42	chr3:110240671..110243637-chr3:110277371..110279265,2	K562	blood:
43	chr3:110223100..110226514-chr3:110228942..110230704,3	K562	blood:
44	chr3:110457222..110459502-chr3:110460960..110463894,2	K562	blood:
45	chr3:110531400..110533494-chr3:110558447..110560628,2	K562	blood:
46	chr3:110223081..110225312-chr3:110255969..110257984,2	K562	blood:
47	chr3:110234753..110236641-chr3:110241075..110242689,2	K562	blood:
48	chr3:110451364..110453338-chr3:110456908..110458980,2	K562	blood:
49	chr3:110202579..110205350-chr3:110208750..110211546,2	K562	blood:
50	chr3:110240671..110243637-chr3:110277371..110279265,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-553A10.1.1-2	chr3:110247848-110248015	XLOC_003212
2	lnc-RP11-553A10.1.1-2	chr3:110247508-110247602	XLOC_003212
3	lnc-RP11-553A10.1.1-2	chr3:110248177-110248429	XLOC_003212
4	lnc-RP11-553A10.1.1-2	chr3:110246329-110246613	XLOC_003212

No data

Variant related genes	Relation type
ENSG00000201426	TF binding region
ENSG00000244722	TF binding region
RNU6ATAC15P	TF binding region
ENSG00000240895	TF binding region
ENSG00000201426	CpG island
ENSG00000244722	CpG island
RNU6ATAC15P	CpG island
ENSG00000240895	CpG island
ENSG00000221206	chromatin interactions
ENSG00000113648	chromatin interactions
ENSG00000240895	chromatin interactions
ENSG00000201426	chromatin interactions

Extended variants
information (count: 10128 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:10128 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576803414	chr3:110209353-110209354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554188754	chr3:110209357-110209358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77350793	chr3:110209375-110209376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187815481	chr3:110209422-110209423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572662731	chr3:110209443-110209444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs13069621	chr3:110209493-110209494	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561017755	chr3:110209518-110209519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141977794	chr3:110209541-110209542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144500690	chr3:110209571-110209572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143642425	chr3:110209573-110209574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543544520	chr3:110209595-110209596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145753215	chr3:110209632-110209633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35156093	chr3:110209637-110209638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs552582627	chr3:110209638-110209639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115575755	chr3:110209699-110209700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs4402956	chr3:110209713-110209714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13070606	chr3:110209814-110209815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs548817697	chr3:110209820-110209821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375054172	chr3:110209865-110209866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192618818	chr3:110209866-110209867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs368071800	chr3:110209886-110209887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148280889	chr3:110210019-110210020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73211497	chr3:110210022-110210023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550700488	chr3:110210078-110210079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189148352	chr3:110210087-110210088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs16856944	chr3:110210108-110210109	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs540717565	chr3:110210113-110210114	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552946090	chr3:110210118-110210119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140393125	chr3:110210148-110210149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62271591	chr3:110210174-110210175	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs555126627	chr3:110210245-110210246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181082859	chr3:110210251-110210252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147553924	chr3:110210262-110210263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs16856946	chr3:110210285-110210286	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs2063567	chr3:110210309-110210310	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs577119805	chr3:110210398-110210399	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114430107	chr3:110210406-110210407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559765731	chr3:110210459-110210460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1398416	chr3:110210464-110210465	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs150361484	chr3:110210465-110210466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1398415	chr3:110210507-110210508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138038553	chr3:110210528-110210529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550365181	chr3:110210550-110210551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142509645	chr3:110210574-110210575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539036811	chr3:110210605-110210606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184920917	chr3:110210622-110210623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79268671	chr3:110210623-110210624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4682588	chr3:110210628-110210629	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555288277	chr3:110210639-110210640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537695448	chr3:110210655-110210656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Burkitt''s lymphoma	20823134	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1338 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110209200-110211400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:110209800-110211000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:110210000-110210600	Enhancers	H1 Cell Line	embryonic stem cell
4	chr3:110210000-110210800	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr3:110210000-110211000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:110210000-110211000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:110210200-110210400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:110210200-110211000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr3:110210200-110211000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr3:110210800-110211600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr3:110211400-110211600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:110211600-110212000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:110211600-110213400	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr3:110211600-110213400	Enhancers	Fetal Lung	lung
15	chr3:110211800-110212200	Enhancers	Duodenum Mucosa	Duodenum
16	chr3:110212000-110212200	Enhancers	Fetal Intestine Small	intestine
17	chr3:110212400-110214000	Enhancers	Fetal Brain Male	brain
18	chr3:110212600-110213000	Enhancers	Fetal Intestine Large	intestine
19	chr3:110212600-110213600	Enhancers	Fetal Brain Female	brain
20	chr3:110213000-110214000	Weak transcription	Fetal Intestine Large	intestine
21	chr3:110213800-110214400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:110214000-110214200	Enhancers	Fetal Intestine Large	intestine
23	chr3:110214000-110214600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:110214000-110214600	Enhancers	Fetal Intestine Small	intestine
25	chr3:110214400-110214600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:110223000-110223200	Enhancers	K562	blood
27	chr3:110223200-110223800	Flanking Active TSS	K562	blood
28	chr3:110223800-110226000	Active TSS	K562	blood
29	chr3:110226000-110230000	Weak transcription	K562	blood
30	chr3:110230000-110232000	Enhancers	K562	blood
31	chr3:110231200-110232000	Enhancers	Fetal Brain Male	brain
32	chr3:110231400-110232400	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr3:110231600-110232000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:110231600-110232200	Enhancers	NHEK	skin
35	chr3:110232000-110234400	Weak transcription	K562	blood
36	chr3:110232000-110245200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:110234400-110234600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
38	chr3:110234400-110235000	Enhancers	K562	blood
39	chr3:110235000-110235400	Weak transcription	K562	blood
40	chr3:110235400-110236200	Enhancers	K562	blood
41	chr3:110236200-110236800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:110236200-110239400	Weak transcription	K562	blood
43	chr3:110237800-110238400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:110238400-110239600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:110239400-110240000	Enhancers	K562	blood
46	chr3:110239400-110240200	Enhancers	NHEK	skin
47	chr3:110239400-110240600	Enhancers	NHDF-Ad	bronchial
48	chr3:110239400-110241000	Enhancers	NHLF	lung
49	chr3:110239400-110241400	Enhancers	HUVEC	blood vessel
50	chr3:110239600-110240400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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