Variant report

Variant	nsv1613
Chromosome Location	chr15:75542832-75588655
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	ARID3A	chr15:75566765-75567085	HepG2	liver:	n/a	n/a
2	BATF	chr15:75566750-75567078	GM12878	blood:	n/a	n/a
3	BATF	chr15:75571142-75571340	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:75575109-75575293	GM12878	blood:	n/a	n/a
5	BCL11A	chr15:75578133-75578306	GM12878	blood:	n/a	n/a
6	BCL11A	chr15:75560181-75560352	GM12878	blood:	n/a	n/a
7	BCL11A	chr15:75571092-75571384	GM12878	blood:	n/a	chr15:75571302-75571309
8	BCL11A	chr15:75553856-75554029	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:75550815-75550962	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:75584457-75584628	GM12878	blood:	n/a	n/a
11	CTCF	chr15:75566840-75566990	GM12865	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
12	CTCF	chr15:75544780-75544930	HBMEC	blood vessel:	n/a	chr15:75544800-75544816
13	CTCF	chr15:75566920-75567070	AG04449	skin:	n/a	n/a
14	CTCF	chr15:75544722-75544901	HepG2	liver:	n/a	chr15:75544800-75544816
15	CTCF	chr15:75544700-75544850	HMF	breast:	n/a	chr15:75544800-75544816
16	CTCF	chr15:75566580-75566730	GM12864	blood:	n/a	n/a
17	CTCF	chr15:75544680-75544830	HPAF	blood vessel:	n/a	chr15:75544800-75544816
18	CTCF	chr15:75584432-75584737	K562	blood:	n/a	chr15:75584587-75584605 chr15:75584590-75584598
19	CTCF	chr15:75566920-75567210	GM12875	blood:	n/a	n/a
20	CTCF	chr15:75560258-75560366	GM20000	blood:	n/a	n/a
21	CTCF	chr15:75566900-75567050	GM12865	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566903-75566921
22	CTCF	chr15:75544720-75544870	AG04450	lung:	n/a	chr15:75544800-75544816
23	CTCF	chr15:75560116-75560472	K562	blood:	n/a	n/a
24	CTCF	chr15:75566820-75566970	GM12869	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
25	CTCF	chr15:75566820-75566970	A549	lung:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
26	CTCF	chr15:75560168-75560461	K562	blood:	n/a	n/a
27	CTCF	chr15:75544720-75544870	MCF-7	breast:	n/a	chr15:75544800-75544816
28	CTCF	chr15:75588550-75588633	GM20000	blood:	n/a	n/a
29	CTCF	chr15:75566788-75567058	Fibrobl	skin:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
30	CTCF	chr15:75544735-75544830	MCF-7	breast:	n/a	chr15:75544800-75544816
31	CTCF	chr15:75566840-75566990	AG04450	lung:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
32	CTCF	chr15:75584490-75584678	Pancreas_OC	pancreas:	n/a	chr15:75584587-75584605 chr15:75584590-75584598
33	CTCF	chr15:75566920-75567210	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr15:75544769-75544859	K562	blood:	n/a	chr15:75544800-75544816
35	CTCF	chr15:75566702-75567007	HepG2	liver:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
36	CTCF	chr15:75566808-75567077	GM20000	blood:	n/a	chr15:75566904-75566920 chr15:75566909-75566918 chr15:75566898-75566919 chr15:75566903-75566921
37	CTCF	chr15:75559908-75560630	A549	lung:	n/a	n/a
38	CTCF	chr15:75566920-75567070	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr15:75566920-75567210	HPF	lung:	n/a	n/a
40	CTCF	chr15:75566920-75567210	AG09319	gingival:	n/a	n/a
41	CTCF	chr15:75566920-75567070	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr15:75544700-75544850	HEEpiC	esophagus:	n/a	chr15:75544800-75544816
43	CTCF	chr15:75566920-75567070	GM12878	blood:	n/a	n/a
44	CTCF	chr15:75560012-75560625	K562	blood:	n/a	n/a
45	CTCF	chr15:75566920-75567210	HMF	breast:	n/a	n/a
46	CTCF	chr15:75544665-75544848	IMR90	lung:	n/a	chr15:75544800-75544816
47	CTCF	chr15:75566920-75567070	HCFaa	heart:	n/a	n/a
48	CTCF	chr15:75566580-75566730	HepG2	liver:	n/a	n/a
49	CTCF	chr15:75566920-75567210	GM12865	blood:	n/a	n/a
50	CTCF	chr15:75566920-75567210	HVMF	connective:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:75575161-75575211	NH-A	brain:	n/a
2	chr15:75586717-75586767	HIPEpiC	eye:	n/a
3	chr15:75575161-75575211	NH-A	brain:	n/a
4	chr15:75586717-75586767	HIPEpiC	eye:	n/a
5	chr15:75587027-75587077	HRCEpiC	kidney:	n/a
6	chr15:75575161-75575211	GM19239	blood:	n/a
7	chr15:75586717-75586767	AG09319	gingival:	n/a
8	chr15:75587027-75587077	AG09309	skin:	n/a
9	chr15:75587027-75587077	Caco-2	colon:	n/a
10	chr15:75586717-75586767	T-47D	breast:	n/a
11	chr15:75587027-75587077	PrEC	prostate:	n/a
12	chr15:75587027-75587077	HEEpiC	esophagus:	n/a
13	chr15:75587027-75587077	HL-60	blood:	n/a
14	chr15:75575161-75575211	H1-hESC	embryonic stem cell:	embryo
15	chr15:75575161-75575211	HCM	heart:	n/a
16	chr15:75551123-75551173	NHBE	bronchial:	n/a
17	chr15:75575161-75575211	GM12878	blood:	n/a
18	chr15:75551123-75551173	HMEC	breast:	n/a
19	chr15:75551123-75551173	PFSK-1	brain:	n/a
20	chr15:75587027-75587077	NHDF-neo	bronchial:	n/a
21	chr15:75551123-75551173	HIPEpiC	eye:	n/a
22	chr15:75587027-75587077	HIPEpiC	eye:	n/a
23	chr15:75551123-75551173	HUVEC	blood vessel:	n/a
24	chr15:75587027-75587077	ECC-1	luminal epithelium:	n/a
25	chr15:75575161-75575211	AG10803	skin:	n/a
26	chr15:75587027-75587077	CMK	blood:	n/a
27	chr15:75575161-75575211	A549	lung:	n/a
28	chr15:75586717-75586767	HNPCEpiC	eye:	n/a
29	chr15:75551123-75551173	HEEpiC	esophagus:	n/a
30	chr15:75587027-75587077	NH-A	brain:	n/a
31	chr15:75551123-75551173	H1-hESC	embryonic stem cell:	embryo
32	chr15:75587027-75587077	RPTEC	kidney:	n/a
33	chr15:75586717-75586767	HEK293	kidney:	embryo
34	chr15:75587027-75587077	HRPEpiC	eye:	n/a
35	chr15:75551123-75551173	Jurkat	blood:	n/a
36	chr15:75587027-75587077	LNCaP	prostate:	n/a
37	chr15:75587027-75587077	SKMC	muscle:	n/a
38	chr15:75551123-75551173	HCPEpiC	choroid plexus:	n/a
39	chr15:75575161-75575211	GM12891	blood:	n/a
40	chr15:75587027-75587077	SK-N-MC	brain:	n/a
41	chr15:75575161-75575211	NHDF-neo	bronchial:	n/a
42	chr15:75586717-75586767	MCF-7	breast:	n/a
43	chr15:75551123-75551173	MCF-7	breast:	n/a
44	chr15:75586717-75586767	HEEpiC	esophagus:	n/a
45	chr15:75575161-75575211	AG09319	gingival:	n/a
46	chr15:75575161-75575211	IMR90	lung:	fetal
47	chr15:75586717-75586767	AG10803	skin:	n/a
48	chr15:75587027-75587077	PFSK-1	brain:	n/a
49	chr15:75551123-75551173	GM06990	blood:	n/a
50	chr15:75551123-75551173	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:75321592..75322142-chr15:75566565..75567153,2	MCF-7	breast:
2	chr15:74600289..74600861-chr15:75566666..75567634,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAN2C1-9	chr15:75564454-75564996	ncRnaDb_ncrna_FR096405_1
2	lnc-GOLGA6D-3	chr15:75560749-75561024	NONHSAT047302
3	lnc-GOLGA6C-1	chr15:75585025-75585300	NONHSAT047303

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA6A	hsa-miR-192-5p	chr15:75562833-75562852

Variant related genes	Relation type
GOLGA6D	TF binding region
NIFKP4	TF binding region
RN7SL489P	TF binding region
RN7SL327P	TF binding region
ENSG00000260104	TF binding region
GOLGA6C	TF binding region
GOLGA6D	CpG island
NIFKP4	CpG island
RN7SL489P	CpG island
RN7SL327P	CpG island
ENSG00000260104	CpG island
GOLGA6C	CpG island

Extended variants
information (count: 389 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142592259	chr15:75542838-75542839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532566883	chr15:75542840-75542841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552751338	chr15:75542847-75542848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144936869	chr15:75542897-75542898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371456625	chr15:75542923-75542924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573652492	chr15:75542934-75542935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112070588	chr15:75542936-75542937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113966788	chr15:75542947-75542948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372096104	chr15:75543130-75543131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552990059	chr15:75543136-75543137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567965684	chr15:75543173-75543174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35217305	chr15:75543283-75543284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs367596606	chr15:75543296-75543297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535427793	chr15:75543309-75543310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557726413	chr15:75543339-75543340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575993436	chr15:75543348-75543349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546448052	chr15:75543397-75543398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60485089	chr15:75543442-75543443	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143461567	chr15:75543468-75543469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559779873	chr15:75543570-75543571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148004443	chr15:75543600-75543601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529318859	chr15:75543639-75543640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563280104	chr15:75543684-75543685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530733051	chr15:75543685-75543686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192852774	chr15:75543739-75543740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570319956	chr15:75543740-75543741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140799974	chr15:75543779-75543780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546423821	chr15:75543780-75543781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369527942	chr15:75543791-75543792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150127678	chr15:75543792-75543793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138591739	chr15:75543830-75543831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556974898	chr15:75543861-75543862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141813026	chr15:75543866-75543867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540152660	chr15:75543891-75543892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558452759	chr15:75543895-75543896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548599307	chr15:75543917-75543918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573361504	chr15:75543934-75543935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540820765	chr15:75544001-75544002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555623545	chr15:75544005-75544006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574066638	chr15:75544042-75544043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544348722	chr15:75544065-75544066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs568507478	chr15:75544077-75544078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146279307	chr15:75544102-75544103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138151959	chr15:75544104-75544105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545692978	chr15:75544125-75544126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551048240	chr15:75544165-75544166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564035091	chr15:75544203-75544204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150862212	chr15:75544246-75544247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546756897	chr15:75544261-75544262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561658317	chr15:75544265-75544266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
small cell lung cancer	20016488	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
Congenital diaphragmatic hernia	21085971	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Epilepsy	22083797	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Myelofibrosis	22110671	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75538000-75545400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:75540200-75544600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:75542400-75544600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:75542400-75544600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr15:75542400-75545400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr15:75542600-75544600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr15:75544600-75544800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr15:75544600-75544800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr15:75544600-75546200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr15:75544600-75547000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr15:75544800-75545200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:75544800-75545400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr15:75545200-75545600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr15:75545400-75545800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:75545400-75546200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
16	chr15:75545400-75546200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr15:75545400-75546200	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr15:75545600-75546200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr15:75545600-75546200	Enhancers	HepG2	liver
20	chr15:75545600-75546400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr15:75546000-75546400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr15:75566200-75567200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr15:75566400-75568000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr15:75566600-75567200	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr15:75566600-75567200	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr15:75566800-75567200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr15:75566800-75567400	Enhancers	Liver	Liver
28	chr15:75567000-75567200	Enhancers	Spleen	Spleen
29	chr15:75567000-75567200	Bivalent Enhancer	HepG2	liver
30	chr15:75567000-75567400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:75567000-75567400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr15:75567000-75567600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:75567200-75568000	Weak transcription	Spleen	Spleen
34	chr15:75567200-75571000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr15:75567200-75571000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr15:75567600-75568000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr15:75568000-75568200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr15:75568000-75568400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr15:75568000-75568400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:75568000-75568400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:75568000-75568400	Active TSS	Spleen	Spleen
42	chr15:75568200-75568400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:75570800-75571200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:75570800-75571200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr15:75570800-75571200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr15:75570800-75571200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr15:75571000-75571200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr15:75571000-75571200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr15:75571000-75571200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr15:75571000-75571200	Enhancers	iPS-18 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links