Variant report

Variant	nsv1043995
Chromosome Location	chr15:53907679-53968209
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:273)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:53947832-53947856	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53958161-53958371	HepG2	liver:	n/a	n/a
3	BACH1	chr15:53919759-53919802	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr15:53917634-53917829	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr15:53917502-53917851	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr15:53918831-53919100	A549	lung:	n/a	n/a
7	CEBPB	chr15:53919446-53919796	A549	lung:	n/a	chr15:53919623-53919634
8	CEBPB	chr15:53917269-53917826	A549	lung:	n/a	chr15:53917532-53917543
9	CEBPB	chr15:53917359-53917726	Hela-S3	cervix:	n/a	chr15:53917532-53917543
10	CEBPB	chr15:53928274-53928529	A549	lung:	n/a	chr15:53928415-53928426
11	CEBPB	chr15:53928301-53928577	HepG2	liver:	n/a	chr15:53928415-53928426
12	CEBPB	chr15:53919483-53919789	IMR90	lung:	n/a	chr15:53919623-53919634
13	CEBPB	chr15:53917355-53917715	HepG2	liver:	n/a	chr15:53917532-53917543
14	CEBPB	chr15:53917365-53917680	K562	blood:	n/a	chr15:53917532-53917543
15	CEBPB	chr15:53919464-53919793	HepG2	liver:	n/a	chr15:53919623-53919634
16	CEBPB	chr15:53917355-53917722	IMR90	lung:	n/a	chr15:53917532-53917543
17	CEBPB	chr15:53917422-53917711	MCF-7	breast:	n/a	chr15:53917532-53917543
18	CEBPB	chr15:53917356-53917723	A549	lung:	n/a	chr15:53917532-53917543
19	CEBPB	chr15:53917351-53917766	H1-hESC	embryonic stem cell:	n/a	chr15:53917532-53917543
20	CHD1	chr15:53947735-53947742	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr15:53917498-53918167	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr15:53947740-53947890	Caco-2	colon:	n/a	n/a
23	CTCF	chr15:53958220-53958370	GM12878	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
24	CTCF	chr15:53958360-53958510	A549	lung:	n/a	n/a
25	CTCF	chr15:53958240-53958390	HRE	kidney:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
26	CTCF	chr15:53958340-53958490	GM12864	blood:	n/a	n/a
27	CTCF	chr15:53947716-53947912	HepG2	liver:	n/a	n/a
28	CTCF	chr15:53958160-53958310	HCT-116	colon:	n/a	n/a
29	CTCF	chr15:53958310-53958352	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr15:53958060-53958210	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr15:53947840-53947990	GM12864	blood:	n/a	n/a
32	CTCF	chr15:53958240-53958390	GM12871	blood:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
33	CTCF	chr15:53958260-53958410	WERI-Rb-1	eye:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
34	CTCF	chr15:53947800-53947950	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr15:53947822-53947841	Gliobla	brain:	n/a	n/a
36	CTCF	chr15:53958200-53958350	HepG2	liver:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
37	CTCF	chr15:53958160-53958310	SAEC	small airway:	n/a	n/a
38	CTCF	chr15:53958200-53958350	Caco-2	colon:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
39	CTCF	chr15:53947700-53947850	Caco-2	colon:	n/a	n/a
40	CTCF	chr15:53958180-53958330	HAc	cerebellar:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
41	CTCF	chr15:53947681-53947912	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:53929660-53929810	GM12869	blood:	n/a	n/a
43	CTCF	chr15:53958080-53958230	GM06990	blood:	n/a	n/a
44	CTCF	chr15:53958200-53958350	SK-N-SH_RA	brain:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
45	CTCF	chr15:53947772-53947897	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr15:53961377-53961447	MCF-7	breast:	n/a	n/a
47	CTCF	chr15:53947769-53947942	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:53947780-53947930	HAc	cerebellar:	n/a	n/a
49	CTCF	chr15:53958220-53958370	A549	lung:	n/a	chr15:53958293-53958314 chr15:53958298-53958316
50	CTCF	chr15:53947780-53947930	RPTEC	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53910786-53910836	GM06990	blood:	n/a
2	chr15:53943590-53943640	BE2_C	brain:	n/a
3	chr15:53943590-53943640	NHBE	bronchial:	n/a
4	chr15:53910786-53910836	HRE	kidney:	n/a
5	chr15:53943590-53943640	HIPEpiC	eye:	n/a
6	chr15:53943590-53943640	Hela-S3	cervix:	n/a
7	chr15:53910786-53910836	NB4	blood:	n/a
8	chr15:53943590-53943640	NHDF-neo	bronchial:	n/a
9	chr15:53910786-53910836	HMEC	breast:	n/a
10	chr15:53943590-53943640	HNPCEpiC	eye:	n/a
11	chr15:53943590-53943640	SKMC	muscle:	n/a
12	chr15:53910786-53910836	HepG2	liver:	n/a
13	chr15:53910786-53910836	HRCEpiC	kidney:	n/a
14	chr15:53910786-53910836	ECC-1	luminal epithelium:	n/a
15	chr15:53910786-53910836	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:53910786-53910836	PrEC	prostate:	n/a
17	chr15:53910786-53910836	NT2-D1	testis:	n/a
18	chr15:53943590-53943640	AG10803	skin:	n/a
19	chr15:53943590-53943640	HRCEpiC	kidney:	n/a
20	chr15:53943590-53943640	Jurkat	blood:	n/a
21	chr15:53943590-53943640	HCT-116	colon:	n/a
22	chr15:53943590-53943640	HRPEpiC	eye:	n/a
23	chr15:53910786-53910836	U87	brain:	n/a
24	chr15:53910786-53910836	HCPEpiC	choroid plexus:	n/a
25	chr15:53943590-53943640	NB4	blood:	n/a
26	chr15:53910786-53910836	Hepatocyte	liver:	n/a
27	chr15:53910786-53910836	IMR90	lung:	fetal
28	chr15:53910786-53910836	HEK293	kidney:	embryo
29	chr15:53943590-53943640	HRE	kidney:	n/a
30	chr15:53943590-53943640	GM06990	blood:	n/a
31	chr15:53943590-53943640	HCF	heart:	n/a
32	chr15:53910786-53910836	SK-N-SH	brain:	n/a
33	chr15:53943590-53943640	SK-N-MC	brain:	n/a
34	chr15:53910786-53910836	GM12892	blood:	n/a
35	chr15:53910786-53910836	PFSK-1	brain:	n/a
36	chr15:53910786-53910836	SK-N-SH_RA	brain:	n/a
37	chr15:53910786-53910836	HCM	heart:	n/a
38	chr15:53943590-53943640	HEK293	kidney:	embryo
39	chr15:53943590-53943640	RPTEC	kidney:	n/a
40	chr15:53943590-53943640	Hepatocyte	liver:	n/a
41	chr15:53943590-53943640	ovcar-3	ovarian:	n/a
42	chr15:53910786-53910836	MCF10A-Er-Src	breast:	n/a
43	chr15:53910786-53910836	GM12878	blood:	n/a
44	chr15:53910786-53910836	AG04450	lung:	fetal
45	chr15:53910786-53910836	HL-60	blood:	n/a
46	chr15:53943590-53943640	AG04450	lung:	fetal
47	chr15:53943590-53943640	AoSMC	blood vessel:	n/a
48	chr15:53910786-53910836	HRPEpiC	eye:	n/a
49	chr15:53943590-53943640	BJ	skin:	n/a
50	chr15:53943590-53943640	HCPEpiC	choroid plexus:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53072550..53073539-chr15:53947412..53948347,3	MCF-7	breast:
2	chr15:53057704..53058252-chr15:53950484..53951446,2	MCF-7	breast:
3	chr15:53057663..53058643-chr15:53947402..53948111,2	MCF-7	breast:
4	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
5	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
6	chr15:53958809..53961070-chr15:53966400..53969207,2	MCF-7	breast:
7	chr15:53676366..53677226-chr15:53947378..53948497,3	MCF-7	breast:
8	chr15:53945998..53946891-chr15:54009249..54010202,2	MCF-7	breast:
9	chr15:53072427..53073417-chr15:53957937..53958702,5	MCF-7	breast:
10	chr15:53949957..53952071-chr15:53952352..53954072,2	MCF-7	breast:
11	chr15:53926573..53928626-chr15:53929111..53931457,2	K562	blood:
12	chr15:53920296..53922661-chr20:30119400..30121230,2	MCF-7	breast:
13	chr15:53676762..53677326-chr15:53957733..53958557,2	MCF-7	breast:
14	chr15:53926573..53928626-chr15:53929111..53931457,2	K562	blood:

No data

Variant related genes	Relation type
RNU2-53P	TF binding region
RNU2-53P	CpG island
ENSG00000169856	chromatin interactions

Extended variants
information (count: 2443 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16966318	chr15:53907679-53907680	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114363728	chr15:53907709-53907710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146417353	chr15:53907716-53907717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557128345	chr15:53907717-53907718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs201086977	chr15:53907729-53907730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187218340	chr15:53907760-53907761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76886815	chr15:53907780-53907781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115484883	chr15:53907805-53907806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540230903	chr15:53907807-53907808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202019287	chr15:53907825-53907826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150164663	chr15:53907900-53907901	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs16966320	chr15:53907906-53907907	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs148877909	chr15:53907946-53907947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs17730281	chr15:53907948-53907949	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
15	rs191971924	chr15:53907952-53907953	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369011394	chr15:53907959-53907960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116496912	chr15:53907991-53907992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143898711	chr15:53908012-53908013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147252875	chr15:53908020-53908021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200326734	chr15:53908027-53908028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs374963913	chr15:53908033-53908034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370789138	chr15:53908043-53908044	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150548151	chr15:53908046-53908047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560525261	chr15:53908054-53908055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs267607178	chr15:53908055-53908056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60404950	chr15:53908062-53908063	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150903344	chr15:53908064-53908065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs202146135	chr15:53908073-53908074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569519028	chr15:53908076-53908077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533610307	chr15:53908102-53908103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138555114	chr15:53908104-53908105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs550592919	chr15:53908135-53908136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375032585	chr15:53908138-53908139	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372174379	chr15:53908146-53908147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs28470860	chr15:53908224-53908225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570420538	chr15:53908226-53908227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150040344	chr15:53908274-53908275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372698012	chr15:53908280-53908281	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568484297	chr15:53908302-53908303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374643853	chr15:53908323-53908324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553075314	chr15:53908326-53908327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201438175	chr15:53908369-53908370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535620312	chr15:53908370-53908371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs555400617	chr15:53908375-53908376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146114056	chr15:53908433-53908434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377509506	chr15:53908459-53908460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368859127	chr15:53908461-53908462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372511714	chr15:53908481-53908482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35549748	chr15:53908497-53908498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111808423	chr15:53908513-53908514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53900400-53908400	Strong transcription	Liver	Liver
2	chr15:53905200-53910800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr15:53905200-53918200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:53908400-53918400	Weak transcription	Liver	Liver
5	chr15:53910600-53911200	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr15:53910800-53911200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:53910800-53911800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr15:53910800-53911800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr15:53911000-53912000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr15:53911200-53912000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr15:53911200-53916600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:53911600-53912200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr15:53911800-53917400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr15:53911800-53917400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr15:53912000-53912800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr15:53912000-53916200	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr15:53912200-53916600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:53912800-53916400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:53914200-53916600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr15:53916200-53917200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr15:53916400-53916800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr15:53916400-53917400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr15:53916600-53916800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr15:53916600-53916800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr15:53916600-53917400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr15:53916600-53918600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr15:53916600-53918800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:53916800-53917800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr15:53916800-53918400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr15:53917000-53917600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr15:53917000-53918200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr15:53917200-53917600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr15:53917200-53918200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr15:53917400-53917600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
35	chr15:53917400-53918000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr15:53917400-53918200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr15:53917400-53918600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr15:53917400-53919000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr15:53917600-53917800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr15:53917600-53918000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr15:53917600-53918800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr15:53917800-53918000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr15:53917800-53918400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr15:53918000-53918400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr15:53918000-53919200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr15:53918200-53918400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr15:53918200-53918600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:53918200-53918600	ZNF genes & repeats	Pancreas	Pancrea
49	chr15:53918200-53918800	Enhancers	H1 Cell Line	embryonic stem cell
50	chr15:53918200-53918800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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