Variant report

Variant	nsv569491
Chromosome Location	chr15:54260920-54397493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:563)
CpG islands
(count:551)
Chromatin interactive
region (count:23)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr15:54270443-54270603	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr15:54269100-54269383	GM12878	blood:	n/a	chr15:54269243-54269254
3	BCL3	chr15:54375816-54376051	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:54270556-54270727	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:54358727-54358963	GM12878	blood:	n/a	n/a
6	BHLHE40	chr15:54269170-54269333	HepG2	liver:	n/a	n/a
7	BHLHE40	chr15:54375171-54375297	GM12878	blood:	n/a	n/a
8	BHLHE40	chr15:54267062-54267260	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:54269065-54269371	GM12878	blood:	n/a	n/a
10	BRCA1	chr15:54376140-54376218	GM12878	blood:	n/a	n/a
11	BRCA1	chr15:54375208-54375398	GM12878	blood:	n/a	n/a
12	CEBPB	chr15:54327869-54328210	HepG2	liver:	n/a	chr15:54328041-54328052
13	CEBPB	chr15:54327914-54328190	A549	lung:	n/a	chr15:54328041-54328052
14	CEBPB	chr15:54334058-54334298	IMR90	lung:	n/a	n/a
15	CEBPB	chr15:54317233-54317453	IMR90	lung:	n/a	n/a
16	CEBPB	chr15:54272984-54273248	HepG2	liver:	n/a	chr15:54273084-54273095
17	CEBPB	chr15:54338360-54338559	A549	lung:	n/a	n/a
18	CEBPB	chr15:54264954-54265172	HepG2	liver:	n/a	chr15:54265094-54265107 chr15:54265094-54265105 chr15:54265096-54265107
19	CEBPB	chr15:54327868-54328211	Hela-S3	cervix:	n/a	chr15:54328041-54328052
20	CEBPB	chr15:54335334-54335567	HepG2	liver:	n/a	chr15:54335407-54335420 chr15:54335407-54335420
21	CHD1	chr15:54271429-54271624	GM12878	blood:	n/a	n/a
22	CHD1	chr15:54275962-54276044	GM12878	blood:	n/a	n/a
23	CHD1	chr15:54375292-54375397	GM12878	blood:	n/a	n/a
24	CHD1	chr15:54270369-54270604	GM12878	blood:	n/a	n/a
25	CHD2	chr15:54395054-54395191	GM12878	blood:	n/a	n/a
26	CHD2	chr15:54383047-54383312	GM12878	blood:	n/a	chr15:54383265-54383275
27	CHD2	chr15:54269281-54269328	HepG2	liver:	n/a	n/a
28	CHD2	chr15:54380837-54380897	GM12878	blood:	n/a	n/a
29	CHD2	chr15:54270395-54270817	GM12878	blood:	n/a	n/a
30	CHD2	chr15:54375592-54375770	GM12878	blood:	n/a	n/a
31	CHD2	chr15:54375231-54375384	GM12878	blood:	n/a	n/a
32	CTCF	chr15:54375160-54375310	WI-38	lung:	n/a	n/a
33	CTCF	chr15:54269116-54269346	MCF-7	breast:	n/a	n/a
34	CTCF	chr15:54375117-54375400	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr15:54375160-54375310	MCF-7	breast:	n/a	n/a
36	CTCF	chr15:54269140-54269290	SAEC	small airway:	n/a	n/a
37	CTCF	chr15:54375061-54375391	K562	blood:	n/a	n/a
38	CTCF	chr15:54375160-54375310	HepG2	liver:	n/a	n/a
39	CTCF	chr15:54269072-54269438	MCF-7	breast:	n/a	n/a
40	CTCF	chr15:54269146-54269262	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr15:54375463-54375535	GM10248	blood:	n/a	n/a
42	CTCF	chr15:54375180-54375330	GM12868	blood:	n/a	n/a
43	CTCF	chr15:54375131-54375344	HepG2	liver:	n/a	n/a
44	CTCF	chr15:54358550-54358924	GM12878	blood:	n/a	n/a
45	CTCF	chr15:54375160-54375310	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr15:54374967-54375523	MCF-7	breast:	n/a	n/a
47	CTCF	chr15:54269120-54269270	HCFaa	heart:	n/a	n/a
48	CTCF	chr15:54375129-54375386	NHEK	skin:	n/a	n/a
49	CTCF	chr15:54375093-54375457	Gliobla	brain:	n/a	n/a
50	CTCF	chr15:54375160-54375310	GM12873	blood:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54271167-54271217	MCF-7	breast:	n/a
2	chr15:54305206-54305256	PFSK-1	brain:	n/a
3	chr15:54271167-54271217	MCF-7	breast:	n/a
4	chr15:54305206-54305256	PFSK-1	brain:	n/a
5	chr15:54303927-54303977	GM12892	blood:	n/a
6	chr15:54270557-54270607	HPAEpiC	pulmonary alveolar:	n/a
7	chr15:54304950-54305000	RPTEC	kidney:	n/a
8	chr15:54304950-54305000	AG09309	skin:	n/a
9	chr15:54270947-54270997	Jurkat	blood:	n/a
10	chr15:54270947-54270997	HRPEpiC	eye:	n/a
11	chr15:54305206-54305256	HAEpiC	amniotic membrane:	n/a
12	chr15:54303927-54303977	SAEC	small airway:	n/a
13	chr15:54303927-54303977	Jurkat	blood:	n/a
14	chr15:54270661-54270711	SKMC	muscle:	n/a
15	chr15:54305206-54305256	HRE	kidney:	n/a
16	chr15:54271167-54271217	AG10803	skin:	n/a
17	chr15:54270693-54270743	HEK293	kidney:	embryo
18	chr15:54271167-54271217	HL-60	blood:	n/a
19	chr15:54305206-54305256	GM12891	blood:	n/a
20	chr15:54304778-54304828	AG09319	gingival:	n/a
21	chr15:54271167-54271217	NB4	blood:	n/a
22	chr15:54271167-54271217	CMK	blood:	n/a
23	chr15:54270557-54270607	HEK293	kidney:	embryo
24	chr15:54304778-54304828	HUVEC	blood vessel:	n/a
25	chr15:54304950-54305000	HCM	heart:	n/a
26	chr15:54270693-54270743	AG09319	gingival:	n/a
27	chr15:54270557-54270607	GM12892	blood:	n/a
28	chr15:54304950-54305000	AG04450	lung:	fetal
29	chr15:54270947-54270997	HRE	kidney:	n/a
30	chr15:54270947-54270997	PANC-1	pancreas:	n/a
31	chr15:54270557-54270607	PFSK-1	brain:	n/a
32	chr15:54270693-54270743	PrEC	prostate:	n/a
33	chr15:54304950-54305000	GM06990	blood:	n/a
34	chr15:54270947-54270997	IMR90	lung:	fetal
35	chr15:54270661-54270711	HRCEpiC	kidney:	n/a
36	chr15:54304778-54304828	HAEpiC	amniotic membrane:	n/a
37	chr15:54271167-54271217	HEEpiC	esophagus:	n/a
38	chr15:54270661-54270711	PFSK-1	brain:	n/a
39	chr15:54303927-54303977	HRE	kidney:	n/a
40	chr15:54271167-54271217	PrEC	prostate:	n/a
41	chr15:54303927-54303977	Caco-2	colon:	n/a
42	chr15:54304950-54305000	AG10803	skin:	n/a
43	chr15:54304778-54304828	MCF10A-Er-Src	breast:	n/a
44	chr15:54270693-54270743	PFSK-1	brain:	n/a
45	chr15:54304950-54305000	GM12891	blood:	n/a
46	chr15:54304950-54305000	H1-hESC	embryonic stem cell:	embryo
47	chr15:54304778-54304828	SK-N-MC	brain:	n/a
48	chr15:54304950-54305000	HCF	heart:	n/a
49	chr15:54271167-54271217	HCM	heart:	n/a
50	chr15:54270557-54270607	NH-A	brain:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
2	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
3	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
4	chr15:54266407..54270072-chr15:55486535..55491034,4	MCF-7	breast:
5	chr15:54367693..54370404-chr15:54374986..54376971,2	MCF-7	breast:
6	chr15:54268767..54269686-chr15:54375127..54375711,4	MCF-7	breast:
7	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
8	chr15:54374784..54375687-chr15:55460665..55461171,2	MCF-7	breast:
9	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
10	chr15:54272577..54275424-chr15:54278207..54281083,2	MCF-7	breast:
11	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
12	chr15:54298660..54299394-chr15:54317743..54318508,2	MCF-7	breast:
13	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
14	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
15	chr15:54254977..54255831-chr15:54374717..54376166,5	MCF-7	breast:
16	chr15:54375029..54375976-chr15:55400805..55401778,3	MCF-7	breast:
17	chr15:54323697..54325296-chr15:54326702..54328336,2	MCF-7	breast:
18	chr15:54254685..54255342-chr15:54375170..54375703,2	MCF-7	breast:
19	chr15:54307497..54309750-chr15:54313366..54316109,2	K562	blood:
20	chr15:54322544..54324113-chr15:54326394..54329349,2	K562	blood:
21	chr15:54355045..54357590-chr15:54360185..54362187,2	K562	blood:
22	chr15:54316286..54318779-chr15:54320377..54322655,2	MCF-7	breast:
23	chr15:54374868..54376175-chr15:55400827..55401744,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-1	chr15:54267015-54267165	ENSG00000259669.1
2	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
3	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
4	lnc-WDR72-1	chr15:54268965-54269105	ENSG00000259669.1
5	lnc-WDR72-1	chr15:54267015-54267206	NONHSAT140240
6	lnc-WDR72-1	chr15:54264867-54264981	ENSG00000259669.1
7	lnc-WDR72-1	chr15:54267015-54267147	ENSG00000259669.1
8	lnc-WDR72-1	chr15:54264872-54264981	NONHSAT140240
9	lnc-WDR72-1	chr15:54267015-54267136	ENSG00000259669.1

No data

Variant related genes	Relation type
ENSG00000259669	TF binding region
UNC13C	TF binding region
ENSG00000259619	TF binding region
ENSG00000259669	CpG island
UNC13C	CpG island
ENSG00000259619	CpG island
ENSG00000137876	chromatin interactions
ENSG00000259669	chromatin interactions

Extended variants
information (count: 4348 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4348 , 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	rs9972357	chr15:54260920-54260921	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150435164	chr15:54260944-54260945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549908921	chr15:54260953-54260954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138361918	chr15:54260999-54261000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538609348	chr15:54261002-54261003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs552563654	chr15:54261016-54261017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576905183	chr15:54261038-54261039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560772711	chr15:54261041-54261042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566208939	chr15:54261049-54261050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74492274	chr15:54261050-54261051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545728587	chr15:54261060-54261061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143846597	chr15:54261117-54261118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201486533	chr15:54261135-54261136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113664627	chr15:54261169-54261170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs189830552	chr15:54264879-54264880	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs4776196	chr15:54264891-54264892	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555214429	chr15:54266459-54266460	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561790827	chr15:54266470-54266471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187168291	chr15:54266479-54266480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536372089	chr15:54266521-54266522	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555880217	chr15:54266535-54266536	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576031339	chr15:54266540-54266541	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs2711595	chr15:54266579-54266580	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs192176230	chr15:54266593-54266594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572031400	chr15:54266627-54266628	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369449633	chr15:54266670-54266671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540795158	chr15:54266701-54266702	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs560783135	chr15:54266715-54266716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs17731753	chr15:54266750-54266751	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs543935179	chr15:54266776-54266777	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs377155891	chr15:54266777-54266778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs563639686	chr15:54266852-54266853	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115697057	chr15:54266865-54266866	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs114243842	chr15:54266867-54266868	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566340225	chr15:54266911-54266912	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528826826	chr15:54266931-54266932	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547294613	chr15:54266935-54266936	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs67773288	chr15:54266936-54266937	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs398027349	chr15:54266947-54266948	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200804038	chr15:54266949-54266950	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs184490356	chr15:54266994-54266995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs139387571	chr15:54267034-54267035	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs56974799	chr15:54267069-54267070	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs535957932	chr15:54267096-54267097	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs150048722	chr15:54267117-54267118	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs569655338	chr15:54267130-54267131	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs528861605	chr15:54267133-54267134	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs190277429	chr15:54267137-54267138	Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs116680128	chr15:54267154-54267155	Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs182447697	chr15:54267169-54267170	Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54259800-54261200	Enhancers	Fetal Lung	lung
2	chr15:54267000-54267200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:54267400-54269600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr15:54269200-54269400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
5	chr15:54269200-54269400	Enhancers	Esophagus	oesophagus
6	chr15:54269200-54269400	Enhancers	Fetal Intestine Small	intestine
7	chr15:54269200-54270000	Enhancers	Fetal Brain Female	brain
8	chr15:54269200-54270000	Enhancers	Fetal Lung	lung
9	chr15:54269200-54277200	Active TSS	Aorta	Aorta
10	chr15:54269400-54270400	Weak transcription	Esophagus	oesophagus
11	chr15:54269600-54269800	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr15:54269800-54270000	Bivalent Enhancer	Brain Hippocampus Middle	brain
13	chr15:54269800-54274800	Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr15:54270000-54270200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr15:54270000-54270200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr15:54270000-54270200	Bivalent Enhancer	Brain Cingulate Gyrus	brain
17	chr15:54270000-54270200	Enhancers	Brain Germinal Matrix	brain
18	chr15:54270000-54270200	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr15:54270000-54270200	Active TSS	Fetal Brain Male	brain
20	chr15:54270000-54270400	Flanking Active TSS	Fetal Brain Female	brain
21	chr15:54270000-54270600	Flanking Active TSS	Fetal Lung	lung
22	chr15:54270000-54270800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
23	chr15:54270000-54271600	Active TSS	Stomach Smooth Muscle	stomach
24	chr15:54270200-54270400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
25	chr15:54270200-54270400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr15:54270200-54270400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
28	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
29	chr15:54270200-54270400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
30	chr15:54270200-54270400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr15:54270200-54270400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:54270200-54270400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr15:54270200-54270400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:54270200-54270400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr15:54270200-54270400	Active TSS	Fetal Intestine Small	intestine
36	chr15:54270200-54270400	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
37	chr15:54270200-54270400	Active TSS	Fetal Muscle Leg	muscle
38	chr15:54270200-54270400	Enhancers	Gastric	stomach
39	chr15:54270200-54270400	Enhancers	Ovary	ovary
40	chr15:54270200-54270400	Enhancers	Pancreas	Pancrea
41	chr15:54270200-54270400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr15:54270200-54270400	Active TSS	Rectal Smooth Muscle	rectum
43	chr15:54270200-54270400	Active TSS	A549	lung
44	chr15:54270200-54270600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:54270200-54270600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:54270200-54270600	Flanking Active TSS	Brain Anterior Caudate	brain
47	chr15:54270200-54270600	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
48	chr15:54270200-54270600	Flanking Active TSS	Brain Germinal Matrix	brain
49	chr15:54270200-54270600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
50	chr15:54270200-54270600	Flanking Active TSS	Fetal Brain Male	brain

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