Variant report

Variant	nsv569132
Chromosome Location	chr15:34877509-34915012
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1031)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1031 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
2	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
3	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
4	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
5	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
6	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
8	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
9	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
10	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
11	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
12	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
13	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
15	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
16	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a
17	BHLHE40	chr15:34880261-34880517	GM12878	blood:	n/a	n/a
18	BHLHE40	chr15:34880263-34880926	K562	blood:	n/a	n/a
19	BHLHE40	chr15:34905607-34905881	K562	blood:	n/a	n/a
20	BHLHE40	chr15:34895468-34895778	HepG2	liver:	n/a	n/a
21	BRCA1	chr15:34880215-34880898	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr15:34880497-34880922	HepG2	liver:	n/a	n/a
23	BRCA1	chr15:34880527-34880886	GM12878	blood:	n/a	n/a
24	BRCA1	chr15:34880268-34880919	H1-hESC	embryonic stem cell:	n/a	n/a
25	CBX3	chr15:34880177-34880935	K562	blood:	n/a	n/a
26	CEBPB	chr15:34900149-34900294	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:34900248-34900270	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:34880150-34880541	K562	blood:	n/a	n/a
29	CEBPB	chr15:34904728-34904797	K562	blood:	n/a	n/a
30	CEBPB	chr15:34892326-34892551	A549	lung:	n/a	chr15:34892539-34892548
31	CEBPB	chr15:34905705-34906062	K562	blood:	n/a	chr15:34905960-34905977
32	CEBPB	chr15:34878509-34878718	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:34911113-34911308	K562	blood:	n/a	n/a
34	CEBPB	chr15:34898327-34898512	Hela-S3	cervix:	n/a	chr15:34898444-34898453 chr15:34898442-34898453 chr15:34898444-34898453 chr15:34898444-34898453 chr15:34898442-34898455 chr15:34898444-34898453
35	CEBPB	chr15:34880180-34880884	K562	blood:	n/a	n/a
36	CEBPB	chr15:34880213-34880530	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr15:34898334-34898590	K562	blood:	n/a	chr15:34898444-34898453 chr15:34898442-34898453 chr15:34898444-34898453 chr15:34898444-34898453 chr15:34898442-34898455 chr15:34898444-34898453
38	CEBPB	chr15:34895509-34895694	HepG2	liver:	n/a	chr15:34895557-34895569
39	CEBPB	chr15:34880261-34880509	MCF-7	breast:	n/a	n/a
40	CEBPB	chr15:34892336-34892561	HepG2	liver:	n/a	chr15:34892539-34892548
41	CEBPB	chr15:34900193-34900303	A549	lung:	n/a	n/a
42	CEBPB	chr15:34897061-34897243	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:34878519-34878707	K562	blood:	n/a	n/a
44	CEBPB	chr15:34903487-34903694	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr15:34892320-34892617	Hela-S3	cervix:	n/a	chr15:34892539-34892548
46	CHD2	chr15:34880229-34880960	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr15:34880247-34880902	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr15:34880173-34880969	K562	blood:	n/a	n/a
49	CHD2	chr15:34880285-34880928	HepG2	liver:	n/a	n/a
50	CTCF	chr15:34913980-34914130	SK-N-SH_RA	brain:	n/a	chr15:34914072-34914093

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34880284-34880334	Hela-S3	cervix:	n/a
2	chr15:34880284-34880334	ovcar-3	ovarian:	n/a
3	chr15:34880284-34880334	HCF	heart:	n/a
4	chr15:34880284-34880334	SK-N-SH	brain:	n/a
5	chr15:34880284-34880334	BJ	skin:	n/a
6	chr15:34880284-34880334	LNCaP	prostate:	n/a
7	chr15:34880284-34880334	T-47D	breast:	n/a
8	chr15:34880284-34880334	NB4	blood:	n/a
9	chr15:34880284-34880334	Caco-2	colon:	n/a
10	chr15:34880284-34880334	MCF-7	breast:	n/a
11	chr15:34880284-34880334	AG04450	lung:	fetal
12	chr15:34880284-34880334	AG04449	skin:	fetal
13	chr15:34880284-34880334	NT2-D1	testis:	n/a
14	chr15:34880284-34880334	HEEpiC	esophagus:	n/a
15	chr15:34880284-34880334	AoSMC	blood vessel:	n/a
16	chr15:34880284-34880334	SAEC	small airway:	n/a
17	chr15:34880284-34880334	HAEpiC	amniotic membrane:	n/a
18	chr15:34880284-34880334	NHBE	bronchial:	n/a
19	chr15:34880284-34880334	BE2_C	brain:	n/a
20	chr15:34880284-34880334	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:34880284-34880334	PANC-1	pancreas:	n/a
22	chr15:34880284-34880334	HepG2	liver:	n/a
23	chr15:34880284-34880334	U87	brain:	n/a
24	chr15:34880284-34880334	HMEC	breast:	n/a
25	chr15:34880284-34880334	GM06990	blood:	n/a
26	chr15:34880284-34880334	HRE	kidney:	n/a
27	chr15:34880284-34880334	H1-hESC	embryonic stem cell:	embryo
28	chr15:34880284-34880334	NH-A	brain:	n/a
29	chr15:34880284-34880334	AG10803	skin:	n/a
30	chr15:34880284-34880334	Hepatocyte	liver:	n/a
31	chr15:34880284-34880334	HCM	heart:	n/a
32	chr15:34880284-34880334	GM12891	blood:	n/a
33	chr15:34880284-34880334	SK-N-SH_RA	brain:	n/a
34	chr15:34880284-34880334	AG09309	skin:	n/a
35	chr15:34880284-34880334	HIPEpiC	eye:	n/a
36	chr15:34880284-34880334	Jurkat	blood:	n/a
37	chr15:34880284-34880334	HUVEC	blood vessel:	n/a
38	chr15:34880284-34880334	PrEC	prostate:	n/a
39	chr15:34880284-34880334	HRPEpiC	eye:	n/a
40	chr15:34880284-34880334	GM19239	blood:	n/a
41	chr15:34880284-34880334	ECC-1	luminal epithelium:	n/a
42	chr15:34880284-34880334	HEK293	kidney:	embryo
43	chr15:34880284-34880334	HNPCEpiC	eye:	n/a
44	chr15:34880284-34880334	K562	blood:	n/a
45	chr15:34880284-34880334	MCF10A-Er-Src	breast:	n/a
46	chr15:34880284-34880334	HRCEpiC	kidney:	n/a
47	chr15:34880284-34880334	AG09319	gingival:	n/a
48	chr15:34880284-34880334	HCT-116	colon:	n/a
49	chr15:34880284-34880334	GM12892	blood:	n/a
50	chr15:34880284-34880334	A549	lung:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
2	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
3	chr13:92448522..92450690-chr15:34895323..34897374,2	K562	blood:
4	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
5	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
6	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
7	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
8	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
9	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
10	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
11	chr15:34892499..34894333-chr15:34896967..34899231,2	K562	blood:
12	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
13	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
14	chr15:34330686..34332519-chr15:34889794..34891923,2	MCF-7	breast:
15	chr15:34659441..34662117-chr15:34875107..34877933,3	K562	blood:
16	chr15:34879223..34881623-chr15:34893177..34895546,2	K562	blood:
17	chr15:34892499..34894333-chr15:34896967..34899231,2	K562	blood:
18	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
19	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
20	chr15:34664329..34667047-chr15:34894143..34895743,2	MCF-7	breast:
21	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
22	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
23	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
24	chr15:34908586..34909269-chr15:35212549..35213068,2	MCF-7	breast:
25	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
26	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
27	chr15:34876102..34877627-chr15:34879229..34881136,2	MCF-7	breast:
28	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
29	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
30	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
31	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
32	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
33	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:

No data

Variant related genes	Relation type
GOLGA8A	TF binding region
ENSG00000252425	TF binding region
GOLGA8B	TF binding region
GOLGA8A	CpG island
ENSG00000252425	CpG island
GOLGA8B	CpG island
ENSG00000182117	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000259904	chromatin interactions
ENSG00000128463	chromatin interactions

Extended variants
information (count: 1075 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4924045	chr15:34877509-34877510	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565792384	chr15:34877516-34877517	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs377619419	chr15:34877673-34877674	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs115942485	chr15:34877694-34877695	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs552013493	chr15:34877790-34877791	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs184944779	chr15:34877858-34877859	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs189458884	chr15:34877862-34877863	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs556130727	chr15:34877906-34877907	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs574216539	chr15:34877936-34877937	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535039255	chr15:34877962-34877963	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs147133735	chr15:34877971-34877972	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs578055219	chr15:34878038-34878039	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545136321	chr15:34878080-34878081	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141056091	chr15:34878086-34878087	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144940701	chr15:34878102-34878103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs180850377	chr15:34878214-34878215	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs373795348	chr15:34878217-34878218	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529149211	chr15:34878218-34878219	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs547375354	chr15:34878235-34878236	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs560950603	chr15:34878344-34878345	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs147949124	chr15:34878351-34878352	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs532949866	chr15:34878358-34878359	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs28834189	chr15:34878365-34878366	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs551548694	chr15:34878426-34878427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184916196	chr15:34878430-34878431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs139359680	chr15:34878452-34878453	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs571181604	chr15:34878476-34878477	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371183408	chr15:34878517-34878518	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs72486689	chr15:34878597-34878598	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs532319082	chr15:34878613-34878614	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs188106002	chr15:34878645-34878646	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs12441873	chr15:34878685-34878686	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370158219	chr15:34878696-34878697	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs182025903	chr15:34878717-34878718	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs571597672	chr15:34878756-34878757	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs113944020	chr15:34878760-34878761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs12441909	chr15:34878809-34878810	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187100286	chr15:34878839-34878840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7179269	chr15:34878900-34878901	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs191950662	chr15:34878903-34878904	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs575303456	chr15:34878927-34878928	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs543238351	chr15:34878943-34878944	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs555225609	chr15:34878944-34878945	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs4923708	chr15:34878993-34878994	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs554680961	chr15:34879075-34879076	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs569814142	chr15:34879091-34879092	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs146567308	chr15:34879092-34879093	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs398118731	chr15:34879102-34879103	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs537102576	chr15:34879104-34879105	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559595165	chr15:34879121-34879122	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34876000-34877800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr15:34876600-34878600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:34876600-34880200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr15:34876600-34880400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr15:34876600-34880400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr15:34876600-34880400	Weak transcription	Brain Substantia Nigra	brain
7	chr15:34876600-34880400	Weak transcription	Right Atrium	heart
8	chr15:34876600-34880400	Weak transcription	Thymus	Thymus
9	chr15:34876800-34877600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:34876800-34877600	Enhancers	Liver	Liver
11	chr15:34876800-34877600	Enhancers	K562	blood
12	chr15:34876800-34877800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr15:34876800-34879200	Weak transcription	A549	lung
14	chr15:34876800-34880000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr15:34876800-34880000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:34876800-34880000	Weak transcription	NHEK	skin
17	chr15:34876800-34880200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:34876800-34880200	Weak transcription	Osteobl	bone
19	chr15:34876800-34880400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr15:34876800-34880400	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr15:34876800-34880400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr15:34876800-34880400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr15:34876800-34880400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr15:34876800-34880400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr15:34876800-34880400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:34876800-34880400	Weak transcription	Adipose Nuclei	Adipose
27	chr15:34876800-34880400	Weak transcription	Ovary	ovary
28	chr15:34876800-34880400	Weak transcription	Hela-S3	cervix
29	chr15:34876800-34880400	Weak transcription	HSMMtube	muscle
30	chr15:34876800-34880600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr15:34876800-34880600	Weak transcription	Esophagus	oesophagus
32	chr15:34877000-34877600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:34877000-34880200	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr15:34877000-34880400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr15:34877200-34877600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
36	chr15:34877200-34877600	Bivalent Enhancer	Fetal Brain Female	brain
37	chr15:34877200-34880400	Weak transcription	HMEC	breast
38	chr15:34877400-34877600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr15:34877400-34877600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
40	chr15:34877400-34880200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr15:34877400-34880400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:34877400-34880400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr15:34877400-34880400	Weak transcription	Fetal Heart	heart
44	chr15:34877400-34880400	Weak transcription	HepG2	liver
45	chr15:34877600-34877800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
46	chr15:34877600-34880200	Weak transcription	Liver	Liver
47	chr15:34877600-34880200	Weak transcription	K562	blood
48	chr15:34877600-34880400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr15:34877800-34880400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr15:34877800-34880400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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