Variant report

Variant	esv1823600
Chromosome Location	chr15:78200594-78219757
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:78219190-78219467	K562	blood:	n/a	n/a
2	BATF	chr15:78200510-78200771	GM12878	blood:	n/a	n/a
3	BATF	chr15:78202770-78203254	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:78202965-78203220	GM12878	blood:	n/a	chr15:78202981-78202994
5	BHLHE40	chr15:78202964-78203186	K562	blood:	n/a	n/a
6	BHLHE40	chr15:78203005-78203198	GM12878	blood:	n/a	n/a
7	BRCA1	chr15:78200667-78200670	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr15:78203014-78203173	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr15:78202751-78203345	K562	blood:	n/a	n/a
10	CBX3	chr15:78200531-78200865	K562	blood:	n/a	n/a
11	CEBPB	chr15:78203019-78203219	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr15:78206647-78206717	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:78206570-78206770	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:78200688-78200932	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr15:78203006-78203201	GM12878	blood:	n/a	n/a
16	CHD2	chr15:78202950-78203024	Hela-S3	cervix:	n/a	n/a
17	CHD2	chr15:78200618-78200951	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr15:78200880-78201030	GM12867	blood:	n/a	n/a
19	CTCF	chr15:78202780-78202930	BE2_C	brain:	n/a	chr15:78202900-78202916 chr15:78202901-78202922 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915
20	CTCF	chr15:78200569-78200823	LNCaP	prostate:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
21	CTCF	chr15:78202540-78202690	GM12878	blood:	n/a	n/a
22	CTCF	chr15:78200640-78200790	NHDF-neo	bronchial:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
23	CTCF	chr15:78207985-78208122	MCF-7	breast:	n/a	n/a
24	CTCF	chr15:78200542-78200842	Hela-S3	cervix:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
25	CTCF	chr15:78202840-78202990	HCPEpiC	choroid plexus:	n/a	chr15:78202900-78202916 chr15:78202901-78202922 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915
26	CTCF	chr15:78200568-78200833	ProgFib	skin:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
27	CTCF	chr15:78202520-78202670	AoAF	blood vessel:	n/a	n/a
28	CTCF	chr15:78202778-78203285	HepG2	liver:	n/a	chr15:78202900-78202916 chr15:78203164-78203180 chr15:78202901-78202922 chr15:78203166-78203175 chr15:78203165-78203186 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915 chr15:78203163-78203181
29	CTCF	chr15:78207991-78208120	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:78200638-78200779	Pancreas_OC	pancreas:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
31	CTCF	chr15:78200660-78200810	GM12878	blood:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
32	CTCF	chr15:78202547-78202649	GM13977	blood:	n/a	n/a
33	CTCF	chr15:78203060-78203210	SK-N-SH_RA	brain:	n/a	chr15:78203164-78203180 chr15:78203166-78203175 chr15:78203165-78203186 chr15:78203163-78203181
34	CTCF	chr15:78202920-78203070	HRE	kidney:	n/a	n/a
35	CTCF	chr15:78200660-78200810	Caco-2	colon:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
36	CTCF	chr15:78202780-78202930	HFF	foreskin:	n/a	chr15:78202900-78202916 chr15:78202901-78202922 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915
37	CTCF	chr15:78200880-78201030	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr15:78200660-78200810	AG04449	skin:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
39	CTCF	chr15:78203000-78203150	WI-38	lung:	n/a	n/a
40	CTCF	chr15:78202900-78203050	GM12873	blood:	n/a	chr15:78202900-78202916 chr15:78202901-78202922 chr15:78202902-78202911 chr15:78202902-78202915
41	CTCF	chr15:78209720-78209870	GM06990	blood:	n/a	chr15:78209735-78209753 chr15:78209742-78209750
42	CTCF	chr15:78200660-78200810	HEEpiC	esophagus:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
43	CTCF	chr15:78202667-78203361	HepG2	liver:	n/a	chr15:78202900-78202916 chr15:78202734-78202752 chr15:78203164-78203180 chr15:78202901-78202922 chr15:78203166-78203175 chr15:78203165-78203186 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915 chr15:78203163-78203181
44	CTCF	chr15:78200660-78200810	K562	blood:	n/a	chr15:78200701-78200714 chr15:78200699-78200715
45	CTCF	chr15:78209720-78209870	WERI-Rb-1	eye:	n/a	chr15:78209735-78209753 chr15:78209742-78209750
46	CTCF	chr15:78202840-78202990	HepG2	liver:	n/a	chr15:78202900-78202916 chr15:78202901-78202922 chr15:78202899-78202917 chr15:78202902-78202911 chr15:78202902-78202915
47	CTCF	chr15:78202980-78203239	ECC-1	luminal epithelium:	n/a	chr15:78203164-78203180 chr15:78203166-78203175 chr15:78203165-78203186 chr15:78203163-78203181
48	CTCF	chr15:78209600-78209750	SAEC	small airway:	n/a	chr15:78209742-78209750
49	CTCF	chr15:78209720-78209870	GM12873	blood:	n/a	chr15:78209735-78209753 chr15:78209742-78209750
50	CTCF	chr15:78200880-78201030	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78219423-78219473	NHDF-neo	bronchial:	n/a
2	chr15:78208251-78208301	AG04449	skin:	fetal
3	chr15:78219423-78219473	NHDF-neo	bronchial:	n/a
4	chr15:78208251-78208301	AG04449	skin:	fetal
5	chr15:78219423-78219473	U87	brain:	n/a
6	chr15:78219748-78219798	PFSK-1	brain:	n/a
7	chr15:78219273-78219323	Jurkat	blood:	n/a
8	chr15:78219748-78219798	ProgFib	skin:	n/a
9	chr15:78208251-78208301	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:78209119-78209169	HNPCEpiC	eye:	n/a
11	chr15:78209119-78209169	ProgFib	skin:	n/a
12	chr15:78208251-78208301	HL-60	blood:	n/a
13	chr15:78209119-78209169	HEK293	kidney:	embryo
14	chr15:78208251-78208301	GM12891	blood:	n/a
15	chr15:78208251-78208301	PFSK-1	brain:	n/a
16	chr15:78209119-78209169	Jurkat	blood:	n/a
17	chr15:78219748-78219798	HPAEpiC	pulmonary alveolar:	n/a
18	chr15:78219748-78219798	ECC-1	luminal epithelium:	n/a
19	chr15:78208251-78208301	NHBE	bronchial:	n/a
20	chr15:78219273-78219323	SAEC	small airway:	n/a
21	chr15:78209119-78209169	MCF10A-Er-Src	breast:	n/a
22	chr15:78219748-78219798	AG10803	skin:	n/a
23	chr15:78209119-78209169	HepG2	liver:	n/a
24	chr15:78219423-78219473	HAEpiC	amniotic membrane:	n/a
25	chr15:78209119-78209169	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:78219273-78219323	PFSK-1	brain:	n/a
27	chr15:78219273-78219323	ProgFib	skin:	n/a
28	chr15:78219273-78219323	HIPEpiC	eye:	n/a
29	chr15:78219748-78219798	PrEC	prostate:	n/a
30	chr15:78219423-78219473	T-47D	breast:	n/a
31	chr15:78219423-78219473	IMR90	lung:	fetal
32	chr15:78219423-78219473	HCT-116	colon:	n/a
33	chr15:78219273-78219323	GM19239	blood:	n/a
34	chr15:78219423-78219473	PFSK-1	brain:	n/a
35	chr15:78209119-78209169	GM06990	blood:	n/a
36	chr15:78219748-78219798	IMR90	lung:	fetal
37	chr15:78219273-78219323	NB4	blood:	n/a
38	chr15:78208251-78208301	ovcar-3	ovarian:	n/a
39	chr15:78219273-78219323	AoSMC	blood vessel:	n/a
40	chr15:78219273-78219323	BJ	skin:	n/a
41	chr15:78219748-78219798	HepG2	liver:	n/a
42	chr15:78219748-78219798	HRCEpiC	kidney:	n/a
43	chr15:78219273-78219323	A549	lung:	n/a
44	chr15:78208251-78208301	HCPEpiC	choroid plexus:	n/a
45	chr15:78219273-78219323	GM12892	blood:	n/a
46	chr15:78209119-78209169	LNCaP	prostate:	n/a
47	chr15:78208251-78208301	NHDF-neo	bronchial:	n/a
48	chr15:78219423-78219473	BJ	skin:	n/a
49	chr15:78219423-78219473	HCF	heart:	n/a
50	chr15:78219748-78219798	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:78200418..78201162-chr15:78910453..78911204,2	K562	blood:
2	chr15:78200661..78201180-chr15:79032859..79033389,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2D7-4	chr15:78208864-78208974	ENSG00000261244.1
2	lnc-SH2D7-4	chr15:78214120-78214361	ENSG00000261244.1
3	lnc-TBC1D2B-5	chr15:78209065-78209324	NONHSAT047472

Variant related genes	Relation type
ENSG00000260776	TF binding region
ENSG00000261244	TF binding region
RN7SL214P	TF binding region
ENSG00000260776	CpG island
ENSG00000261244	CpG island
RN7SL214P	CpG island

Extended variants
information (count: 1088 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1088 , 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	rs4325522	chr15:78200594-78200595	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544205875	chr15:78200620-78200621	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs146750594	chr15:78200637-78200638	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs535397112	chr15:78200659-78200660	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs141255782	chr15:78200667-78200668	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs4402533	chr15:78200674-78200675	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs539069776	chr15:78200677-78200678	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs111427294	chr15:78200683-78200684	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs559504679	chr15:78200688-78200689	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs12909639	chr15:78200697-78200698	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs12910067	chr15:78200707-78200708	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs575064608	chr15:78200712-78200713	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs542381960	chr15:78200747-78200748	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs563844373	chr15:78200748-78200749	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112555531	chr15:78200750-78200751	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs545882499	chr15:78200789-78200790	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs150459779	chr15:78200790-78200791	Enhancers Weak transcription Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs372942796	chr15:78200805-78200806	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs570728716	chr15:78200851-78200852	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs372753613	chr15:78200866-78200867	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs138255504	chr15:78200870-78200871	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs529067052	chr15:78200911-78200912	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs550708642	chr15:78200969-78200970	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs569058722	chr15:78201004-78201005	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs557765176	chr15:78201013-78201014	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs539719722	chr15:78201043-78201044	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs111437952	chr15:78201095-78201096	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs539716423	chr15:78201177-78201178	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551130603	chr15:78201205-78201206	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs566458993	chr15:78201219-78201220	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs192037099	chr15:78201227-78201228	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs555524162	chr15:78201269-78201270	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs573745425	chr15:78201321-78201322	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs386785574	chr15:78201340-78201341	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs12910712	chr15:78201342-78201343	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs535643482	chr15:78201349-78201350	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs12912242	chr15:78201444-78201445	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs12911012	chr15:78201454-78201455	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs557767581	chr15:78201455-78201456	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs12911015	chr15:78201460-78201461	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs12911022	chr15:78201468-78201469	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs12911476	chr15:78201515-78201516	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs12911037	chr15:78201521-78201522	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs552220360	chr15:78201531-78201532	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs544123922	chr15:78201536-78201537	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs142723742	chr15:78201537-78201538	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs386785575	chr15:78201538-78201539	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs375104038	chr15:78201539-78201540	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs184193580	chr15:78201542-78201543	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs12911348	chr15:78201589-78201590	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78180000-78215600	Weak transcription	Right Atrium	heart
2	chr15:78192000-78202800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr15:78197000-78201000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:78198600-78200600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr15:78199400-78201600	Weak transcription	Right Ventricle	heart
6	chr15:78200200-78201000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:78200200-78201400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:78200200-78201600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr15:78200200-78203000	Enhancers	Colonic Mucosa	Colon
10	chr15:78200400-78200600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr15:78200400-78200600	Flanking Active TSS	Hela-S3	cervix
12	chr15:78200400-78200800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr15:78200400-78201200	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr15:78200400-78201200	Enhancers	HSMMtube	muscle
15	chr15:78200400-78201400	Enhancers	HSMM	muscle
16	chr15:78200400-78202400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:78200400-78202800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:78200400-78202800	Enhancers	Fetal Intestine Small	intestine
19	chr15:78200400-78203200	Enhancers	Esophagus	oesophagus
20	chr15:78200400-78203200	Enhancers	Stomach Mucosa	stomach
21	chr15:78200400-78203800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:78200600-78200800	Active TSS	Hela-S3	cervix
23	chr15:78200600-78201000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:78200600-78201200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr15:78200600-78201400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr15:78200600-78201800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:78200600-78202000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr15:78200600-78202800	Enhancers	Fetal Muscle Trunk	muscle
29	chr15:78200800-78201000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr15:78200800-78201000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr15:78200800-78201000	Bivalent Enhancer	Fetal Stomach	stomach
32	chr15:78200800-78201000	Flanking Active TSS	HepG2	liver
33	chr15:78200800-78201000	Enhancers	K562	blood
34	chr15:78200800-78201200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr15:78200800-78201200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr15:78200800-78201200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
37	chr15:78200800-78201200	Enhancers	NH-A	brain
38	chr15:78200800-78201400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr15:78200800-78201400	Enhancers	Fetal Muscle Leg	muscle
40	chr15:78200800-78201400	Flanking Active TSS	Hela-S3	cervix
41	chr15:78200800-78201800	Bivalent Enhancer	Placenta	Placenta
42	chr15:78200800-78202800	Enhancers	Fetal Intestine Large	intestine
43	chr15:78200800-78202800	Enhancers	A549	lung
44	chr15:78201000-78201400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr15:78201000-78201400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:78201000-78201400	Enhancers	HepG2	liver
47	chr15:78201000-78202800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr15:78201000-78202800	Weak transcription	Fetal Thymus	thymus
49	chr15:78201200-78202600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr15:78201200-78202600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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