Variant report

Variant	nsv829672
Chromosome Location	chr3:110206693-110361632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:991)
CpG islands
(count:367)
Chromatin interactive
region (count:47)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:991 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:110339011-110339287	K562	blood:	n/a	n/a
2	ARID3A	chr3:110247380-110248084	K562	blood:	n/a	n/a
3	ARID3A	chr3:110229389-110229704	K562	blood:	n/a	n/a
4	ARID3A	chr3:110222947-110224194	K562	blood:	n/a	n/a
5	ARID3A	chr3:110239851-110240334	K562	blood:	n/a	n/a
6	ARID3A	chr3:110269356-110270029	K562	blood:	n/a	n/a
7	ARID3A	chr3:110344280-110344634	K562	blood:	n/a	n/a
8	ARID3A	chr3:110235328-110235528	K562	blood:	n/a	n/a
9	ATF1	chr3:110223647-110224062	K562	blood:	n/a	n/a
10	ATF1	chr3:110239924-110240245	K562	blood:	n/a	n/a
11	ATF2	chr3:110295750-110296207	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:110239853-110240234	K562	blood:	n/a	n/a
13	ATF3	chr3:110295700-110296333	A549	lung:	n/a	n/a
14	ATF3	chr3:110302100-110302850	A549	lung:	n/a	n/a
15	ATF3	chr3:110302207-110302904	A549	lung:	n/a	n/a
16	ATF3	chr3:110245606-110245939	K562	blood:	n/a	n/a
17	ATF3	chr3:110245673-110245815	K562	blood:	n/a	n/a
18	ATF3	chr3:110344405-110344569	K562	blood:	n/a	n/a
19	ATF3	chr3:110223684-110224032	K562	blood:	n/a	n/a
20	BACH1	chr3:110295457-110296326	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:110239948-110240284	K562	blood:	n/a	n/a
22	BACH1	chr3:110310093-110310161	K562	blood:	n/a	n/a
23	BATF	chr3:110345477-110345909	GM12878	blood:	n/a	chr3:110345613-110345623
24	BATF	chr3:110287191-110287395	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:110317738-110318028	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr3:110302104-110302404	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL11A	chr3:110295758-110296109	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr3:110295827-110296106	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr3:110302187-110302409	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL3	chr3:110295569-110296350	A549	lung:	n/a	n/a
31	BCL3	chr3:110295630-110296266	A549	lung:	n/a	n/a
32	BCL3	chr3:110301985-110302982	A549	lung:	n/a	n/a
33	BHLHE40	chr3:110223596-110224181	K562	blood:	n/a	n/a
34	BHLHE40	chr3:110242580-110242784	K562	blood:	n/a	n/a
35	BHLHE40	chr3:110344340-110344672	K562	blood:	n/a	n/a
36	BHLHE40	chr3:110239814-110240283	K562	blood:	n/a	n/a
37	BRCA1	chr3:110245710-110246410	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr3:110302130-110302724	HCT-116	colon:	n/a	n/a
39	CBX3	chr3:110206753-110206968	K562	blood:	n/a	n/a
40	CBX3	chr3:110286966-110287682	HCT-116	colon:	n/a	n/a
41	CBX3	chr3:110223612-110224055	K562	blood:	n/a	n/a
42	CBX3	chr3:110206695-110207049	K562	blood:	n/a	n/a
43	CBX3	chr3:110295731-110296387	HCT-116	colon:	n/a	n/a
44	CBX3	chr3:110294480-110295010	HCT-116	colon:	n/a	n/a
45	CBX3	chr3:110286951-110287606	HCT-116	colon:	n/a	n/a
46	CBX3	chr3:110239876-110240224	K562	blood:	n/a	n/a
47	CBX3	chr3:110279516-110279782	K562	blood:	n/a	n/a
48	CBX3	chr3:110239735-110240377	HCT-116	colon:	n/a	n/a
49	CBX3	chr3:110247511-110248144	K562	blood:	n/a	n/a
50	CBX3	chr3:110244394-110244807	K562	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:110344165-110344215	AG04449	skin:	fetal
2	chr3:110344165-110344215	AG04449	skin:	fetal
3	chr3:110303472-110303522	GM12891	blood:	n/a
4	chr3:110246985-110247035	SK-N-MC	brain:	n/a
5	chr3:110248442-110248492	ovcar-3	ovarian:	n/a
6	chr3:110246985-110247035	HL-60	blood:	n/a
7	chr3:110250679-110250729	GM12892	blood:	n/a
8	chr3:110303472-110303522	HCT-116	colon:	n/a
9	chr3:110250679-110250729	Hela-S3	cervix:	n/a
10	chr3:110303472-110303522	HEK293	kidney:	embryo
11	chr3:110248442-110248492	HMEC	breast:	n/a
12	chr3:110303472-110303522	Caco-2	colon:	n/a
13	chr3:110344165-110344215	T-47D	breast:	n/a
14	chr3:110246985-110247035	A549	lung:	n/a
15	chr3:110248442-110248492	NH-A	brain:	n/a
16	chr3:110246985-110247035	U87	brain:	n/a
17	chr3:110240891-110240941	Jurkat	blood:	n/a
18	chr3:110344165-110344215	U87	brain:	n/a
19	chr3:110248442-110248492	AG10803	skin:	n/a
20	chr3:110240891-110240941	HIPEpiC	eye:	n/a
21	chr3:110246985-110247035	AG09309	skin:	n/a
22	chr3:110303472-110303522	AG09309	skin:	n/a
23	chr3:110240891-110240941	HAEpiC	amniotic membrane:	n/a
24	chr3:110250679-110250729	T-47D	breast:	n/a
25	chr3:110344165-110344215	A549	lung:	n/a
26	chr3:110344165-110344215	GM12891	blood:	n/a
27	chr3:110344165-110344215	HCF	heart:	n/a
28	chr3:110240891-110240941	AG04450	lung:	fetal
29	chr3:110248442-110248492	NB4	blood:	n/a
30	chr3:110344165-110344215	AoSMC	blood vessel:	n/a
31	chr3:110246985-110247035	GM06990	blood:	n/a
32	chr3:110248442-110248492	HRCEpiC	kidney:	n/a
33	chr3:110248442-110248492	HIPEpiC	eye:	n/a
34	chr3:110344165-110344215	AG04450	lung:	fetal
35	chr3:110344165-110344215	CMK	blood:	n/a
36	chr3:110248442-110248492	GM12892	blood:	n/a
37	chr3:110303472-110303522	HRPEpiC	eye:	n/a
38	chr3:110246985-110247035	Hepatocyte	liver:	n/a
39	chr3:110248442-110248492	K562	blood:	n/a
40	chr3:110246985-110247035	HEK293	kidney:	embryo
41	chr3:110303472-110303522	HCM	heart:	n/a
42	chr3:110303472-110303522	CMK	blood:	n/a
43	chr3:110240891-110240941	BE2_C	brain:	n/a
44	chr3:110344165-110344215	HRPEpiC	eye:	n/a
45	chr3:110248442-110248492	NHDF-neo	bronchial:	n/a
46	chr3:110246985-110247035	T-47D	breast:	n/a
47	chr3:110240891-110240941	AG09319	gingival:	n/a
48	chr3:110250679-110250729	GM12878	blood:	n/a
49	chr3:110246985-110247035	HRPEpiC	eye:	n/a
50	chr3:110246985-110247035	AoSMC	blood vessel:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:110223100..110226514-chr3:110228942..110230704,3	K562	blood:
2	chr3:110337784..110340050-chr3:110340181..110342150,2	MCF-7	breast:
3	chr3:110279243..110282023-chr3:110283429..110285882,2	K562	blood:
4	chr3:110282414..110285256-chr3:110286686..110288676,2	K562	blood:
5	chr3:110228265..110231031-chr3:110237827..110239739,2	K562	blood:
6	chr3:110276449..110278320-chr3:110281402..110283554,3	K562	blood:
7	chr3:110224350..110227035-chr3:110267483..110270332,2	K562	blood:
8	chr3:110302646..110303511-chr3:110658446..110659012,2	MCF-7	breast:
9	chr19:49845864..49846607-chr3:110315550..110316370,2	MCF-7	breast:
10	chr3:110256128..110258374-chr3:110259929..110261455,2	K562	blood:
11	chr3:110232519..110235271-chr3:110279973..110282638,2	K562	blood:
12	chr3:110224350..110227035-chr3:110267483..110270332,2	K562	blood:
13	chr3:110240019..110241918-chr3:110243471..110245418,2	K562	blood:
14	chr3:110223795..110225407-chr3:110236340..110238461,2	K562	blood:
15	chr3:110279243..110282023-chr3:110283429..110285882,2	K562	blood:
16	chr3:110222894..110225675-chr3:110240158..110242098,2	K562	blood:
17	chr3:110248230..110250752-chr3:110252528..110254988,2	K562	blood:
18	chr3:110269319..110271663-chr3:110272777..110274394,2	K562	blood:
19	chr3:110226107..110231031-chr3:110235797..110240409,5	K562	blood:
20	chr3:110223081..110225312-chr3:110255969..110257984,2	K562	blood:
21	chr3:110233003..110234859-chr3:110246795..110249588,2	K562	blood:
22	chr3:110195963..110198828-chr3:110223194..110225023,2	K562	blood:
23	chr3:110282414..110285256-chr3:110286686..110288676,2	K562	blood:
24	chr3:110223100..110226514-chr3:110228942..110230704,3	K562	blood:
25	chr3:110223795..110225407-chr3:110236340..110238461,2	K562	blood:
26	chr3:110361104..110363034-chr3:110366368..110368463,2	MCF-7	breast:
27	chr3:110240019..110241918-chr3:110243471..110245418,2	K562	blood:
28	chr3:110245688..110247478-chr3:110251852..110254191,2	K562	blood:
29	chr3:110222894..110225675-chr3:110240158..110242098,2	K562	blood:
30	chr3:110240671..110243637-chr3:110277371..110279265,2	K562	blood:
31	chr3:110228265..110231031-chr3:110237827..110239739,2	K562	blood:
32	chr3:110235029..110237272-chr3:110238334..110239946,2	K562	blood:
33	chr3:110226107..110231031-chr3:110235797..110240409,5	K562	blood:
34	chr3:110202579..110205350-chr3:110208750..110211546,2	K562	blood:
35	chr3:110232263..110233795-chr3:110237768..110239573,2	K562	blood:
36	chr3:110234753..110236641-chr3:110241075..110242689,2	K562	blood:
37	chr3:110240671..110243637-chr3:110277371..110279265,2	K562	blood:
38	chr3:110234753..110236641-chr3:110241075..110242689,2	K562	blood:
39	chr3:110337784..110340050-chr3:110340181..110342150,2	MCF-7	breast:
40	chr3:110232519..110235271-chr3:110279973..110282638,2	K562	blood:
41	chr3:110223081..110225312-chr3:110255969..110257984,2	K562	blood:
42	chr3:110256128..110258374-chr3:110259929..110261455,2	K562	blood:
43	chr3:110235029..110237272-chr3:110238334..110239946,2	K562	blood:
44	chr3:110245688..110247478-chr3:110251852..110254191,2	K562	blood:
45	chr3:110276449..110278320-chr3:110281402..110283554,3	K562	blood:
46	chr3:110200269..110202547-chr3:110206926..110209174,2	K562	blood:
47	chr3:110232263..110233795-chr3:110237768..110239573,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 4707 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4707 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572626386	chr3:110206700-110206701	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs12633463	chr3:110206748-110206749	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs12638763	chr3:110206753-110206754	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555857051	chr3:110206754-110206755	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs569375161	chr3:110206769-110206770	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs9878382	chr3:110206782-110206783	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs558145459	chr3:110206804-110206805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs577984077	chr3:110206844-110206845	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs188606796	chr3:110206847-110206848	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs554212216	chr3:110206856-110206857	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs573857231	chr3:110206867-110206868	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs542819233	chr3:110206873-110206874	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs181425046	chr3:110206891-110206892	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs139401890	chr3:110206941-110206942	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs371130737	chr3:110207104-110207105	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs544812269	chr3:110207114-110207115	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs564876943	chr3:110207149-110207150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs80181483	chr3:110207202-110207203	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs547662017	chr3:110207281-110207282	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs567575802	chr3:110207296-110207297	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs2203187	chr3:110207342-110207343	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs62271588	chr3:110207363-110207364	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs578127786	chr3:110207400-110207401	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs185831383	chr3:110207406-110207407	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538319548	chr3:110207433-110207434	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs557996663	chr3:110207481-110207482	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs113492675	chr3:110207503-110207504	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs539093904	chr3:110207517-110207518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs553990665	chr3:110207531-110207532	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs191041580	chr3:110207548-110207549	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs11713405	chr3:110207556-110207557	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10511286	chr3:110207583-110207584	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs556324108	chr3:110207585-110207586	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs76027108	chr3:110207643-110207644	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs545084244	chr3:110207652-110207653	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs559951318	chr3:110207661-110207662	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs564871585	chr3:110207767-110207768	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs181944165	chr3:110207822-110207823	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs187344451	chr3:110207880-110207881	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs62271589	chr3:110207909-110207910	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs150042987	chr3:110207915-110207916	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs35391921	chr3:110207917-110207918	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs76857624	chr3:110207986-110207987	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs191067169	chr3:110208031-110208032	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs563448710	chr3:110208059-110208060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs533467340	chr3:110208106-110208107	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs532250866	chr3:110208144-110208145	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs550858710	chr3:110208159-110208160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs115010565	chr3:110208168-110208169	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs78277077	chr3:110208174-110208175	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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

Chromatin state (count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110206200-110208200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:110208200-110208800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:110208800-110209200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:110209200-110211400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:110209800-110211000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:110210000-110210600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr3:110210000-110210800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:110210000-110211000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:110210000-110211000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:110210200-110210400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:110210200-110211000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:110210200-110211000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr3:110210800-110211600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr3:110211400-110211600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:110211600-110212000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:110211600-110213400	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr3:110211600-110213400	Enhancers	Fetal Lung	lung
18	chr3:110211800-110212200	Enhancers	Duodenum Mucosa	Duodenum
19	chr3:110212000-110212200	Enhancers	Fetal Intestine Small	intestine
20	chr3:110212400-110214000	Enhancers	Fetal Brain Male	brain
21	chr3:110212600-110213000	Enhancers	Fetal Intestine Large	intestine
22	chr3:110212600-110213600	Enhancers	Fetal Brain Female	brain
23	chr3:110213000-110214000	Weak transcription	Fetal Intestine Large	intestine
24	chr3:110213800-110214400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:110214000-110214200	Enhancers	Fetal Intestine Large	intestine
26	chr3:110214000-110214600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:110214000-110214600	Enhancers	Fetal Intestine Small	intestine
28	chr3:110214400-110214600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:110223000-110223200	Enhancers	K562	blood
30	chr3:110223200-110223800	Flanking Active TSS	K562	blood
31	chr3:110223800-110226000	Active TSS	K562	blood
32	chr3:110226000-110230000	Weak transcription	K562	blood
33	chr3:110230000-110232000	Enhancers	K562	blood
34	chr3:110231200-110232000	Enhancers	Fetal Brain Male	brain
35	chr3:110231400-110232400	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr3:110231600-110232000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr3:110231600-110232200	Enhancers	NHEK	skin
38	chr3:110232000-110234400	Weak transcription	K562	blood
39	chr3:110232000-110245200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:110234400-110234600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
41	chr3:110234400-110235000	Enhancers	K562	blood
42	chr3:110235000-110235400	Weak transcription	K562	blood
43	chr3:110235400-110236200	Enhancers	K562	blood
44	chr3:110236200-110236800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:110236200-110239400	Weak transcription	K562	blood
46	chr3:110237800-110238400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:110238400-110239600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:110239400-110240000	Enhancers	K562	blood
49	chr3:110239400-110240200	Enhancers	NHEK	skin
50	chr3:110239400-110240600	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links