Variant report

Variant	nsv524569
Chromosome Location	chr15:59666992-59712427
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	chr15:59704849-59704998	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:59671156-59671407	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:59671728-59672041	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:59688530-59688760	HepG2	liver:	n/a	n/a
5	ATF2	chr15:59698512-59699056	GM12878	blood:	n/a	n/a
6	ATF2	chr15:59691510-59692436	GM12878	blood:	n/a	n/a
7	ATF2	chr15:59704778-59705802	GM12878	blood:	n/a	n/a
8	ATF2	chr15:59704695-59706120	GM12878	blood:	n/a	n/a
9	ATF2	chr15:59691523-59692242	GM12878	blood:	n/a	n/a
10	ATF3	chr15:59704809-59705486	GM12878	blood:	n/a	n/a
11	BATF	chr15:59705153-59705544	GM12878	blood:	n/a	n/a
12	BATF	chr15:59691664-59692017	GM12878	blood:	n/a	n/a
13	BATF	chr15:59704812-59705675	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:59704757-59705715	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:59691641-59692091	GM12878	blood:	n/a	chr15:59691854-59691863
16	BCL11A	chr15:59691658-59691982	GM12878	blood:	n/a	chr15:59691854-59691863
17	BCL11A	chr15:59704854-59705696	GM12878	blood:	n/a	n/a
18	BCL3	chr15:59691689-59692033	GM12878	blood:	n/a	chr15:59691854-59691863
19	BCL3	chr15:59704861-59705696	GM12878	blood:	n/a	n/a
20	BCL3	chr15:59705078-59705557	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:59704564-59706125	GM12878	blood:	n/a	chr15:59705996-59706005
22	BCLAF1	chr15:59691506-59692889	GM12878	blood:	n/a	chr15:59691854-59691863
23	BCLAF1	chr15:59698552-59699103	GM12878	blood:	n/a	n/a
24	BCLAF1	chr15:59704780-59705833	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:59691424-59692254	GM12878	blood:	n/a	chr15:59691854-59691863
26	BHLHE40	chr15:59704828-59705454	HepG2	liver:	n/a	n/a
27	BHLHE40	chr15:59678603-59678707	A549	lung:	n/a	n/a
28	BHLHE40	chr15:59704817-59705818	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:59691552-59692053	GM12878	blood:	n/a	n/a
30	BRCA1	chr15:59705082-59705429	GM12878	blood:	n/a	n/a
31	BRCA1	chr15:59669029-59669301	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:59680755-59681245	HCT-116	colon:	n/a	chr15:59680978-59680989
33	CEBPB	chr15:59698693-59698860	A549	lung:	n/a	chr15:59698773-59698784
34	CEBPB	chr15:59680830-59681176	K562	blood:	n/a	chr15:59680978-59680989
35	CEBPB	chr15:59670143-59670525	K562	blood:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
36	CEBPB	chr15:59670058-59670528	A549	lung:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
37	CEBPB	chr15:59680732-59681305	A549	lung:	n/a	chr15:59680978-59680989
38	CEBPB	chr15:59688395-59688715	MCF-7	breast:	n/a	chr15:59688597-59688610 chr15:59688597-59688608 chr15:59688598-59688609
39	CEBPB	chr15:59702606-59702861	A549	lung:	n/a	n/a
40	CEBPB	chr15:59670112-59670545	MCF-7	breast:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
41	CEBPB	chr15:59680832-59681083	MCF-7	breast:	n/a	chr15:59680978-59680989
42	CEBPB	chr15:59688538-59688726	HepG2	liver:	n/a	chr15:59688597-59688610 chr15:59688597-59688608 chr15:59688598-59688609
43	CEBPB	chr15:59671740-59672071	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:59670156-59670514	H1-hESC	embryonic stem cell:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
45	CEBPB	chr15:59670028-59670579	Hela-S3	cervix:	n/a	chr15:59670333-59670342 chr15:59670333-59670342 chr15:59670331-59670344 chr15:59670333-59670342 chr15:59670419-59670431 chr15:59670331-59670344 chr15:59670331-59670342
46	CEBPB	chr15:59688523-59688654	Hela-S3	cervix:	n/a	chr15:59688597-59688610 chr15:59688597-59688608 chr15:59688598-59688609
47	CEBPB	chr15:59698648-59698871	K562	blood:	n/a	chr15:59698773-59698784
48	CEBPB	chr15:59671790-59672000	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:59681009-59681034	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr15:59689052-59689065	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:59694115-59694165	HRPEpiC	eye:	n/a
2	chr15:59694115-59694165	HRPEpiC	eye:	n/a
3	chr15:59700360-59700410	GM19239	blood:	n/a
4	chr15:59701812-59701862	AG09309	skin:	n/a
5	chr15:59701812-59701862	HMEC	breast:	n/a
6	chr15:59701812-59701862	HRPEpiC	eye:	n/a
7	chr15:59700360-59700410	SAEC	small airway:	n/a
8	chr15:59701812-59701862	HEEpiC	esophagus:	n/a
9	chr15:59694115-59694165	SK-N-SH	brain:	n/a
10	chr15:59667752-59667802	SK-N-SH	brain:	n/a
11	chr15:59700360-59700410	SK-N-SH	brain:	n/a
12	chr15:59694115-59694165	NT2-D1	testis:	n/a
13	chr15:59694115-59694165	AoSMC	blood vessel:	n/a
14	chr15:59701812-59701862	HEK293	kidney:	embryo
15	chr15:59667752-59667802	Hela-S3	cervix:	n/a
16	chr15:59700360-59700410	HCT-116	colon:	n/a
17	chr15:59700360-59700410	K562	blood:	n/a
18	chr15:59701812-59701862	LNCaP	prostate:	n/a
19	chr15:59667752-59667802	AG04449	skin:	fetal
20	chr15:59694115-59694165	PANC-1	pancreas:	n/a
21	chr15:59667752-59667802	A549	lung:	n/a
22	chr15:59694115-59694165	BE2_C	brain:	n/a
23	chr15:59701812-59701862	NHBE	bronchial:	n/a
24	chr15:59667752-59667802	NH-A	brain:	n/a
25	chr15:59700360-59700410	Hela-S3	cervix:	n/a
26	chr15:59701812-59701862	HRE	kidney:	n/a
27	chr15:59700360-59700410	HL-60	blood:	n/a
28	chr15:59667752-59667802	U87	brain:	n/a
29	chr15:59701812-59701862	SAEC	small airway:	n/a
30	chr15:59700360-59700410	Caco-2	colon:	n/a
31	chr15:59694115-59694165	NB4	blood:	n/a
32	chr15:59701812-59701862	H1-hESC	embryonic stem cell:	embryo
33	chr15:59667752-59667802	MCF-7	breast:	n/a
34	chr15:59667752-59667802	HEK293	kidney:	embryo
35	chr15:59667752-59667802	HCM	heart:	n/a
36	chr15:59701812-59701862	GM12892	blood:	n/a
37	chr15:59700360-59700410	ovcar-3	ovarian:	n/a
38	chr15:59701812-59701862	IMR90	lung:	fetal
39	chr15:59694115-59694165	NH-A	brain:	n/a
40	chr15:59700360-59700410	HRPEpiC	eye:	n/a
41	chr15:59667752-59667802	GM06990	blood:	n/a
42	chr15:59667752-59667802	AG09319	gingival:	n/a
43	chr15:59701812-59701862	HRCEpiC	kidney:	n/a
44	chr15:59701812-59701862	GM19239	blood:	n/a
45	chr15:59701812-59701862	BJ	skin:	n/a
46	chr15:59700360-59700410	GM06990	blood:	n/a
47	chr15:59700360-59700410	HCF	heart:	n/a
48	chr15:59701812-59701862	K562	blood:	n/a
49	chr15:59667752-59667802	SAEC	small airway:	n/a
50	chr15:59701812-59701862	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:146556062..146556589-chr15:59704212..59704713,2	Hela-S3	cervix:
2	chr15:59663703..59665247-chr15:59672295..59676019,3	MCF-7	breast:
3	chr15:59466869..59467465-chr15:59704534..59705044,2	MCF-7	breast:
4	chr15:59684140..59687063-chr15:59689972..59692965,2	K562	blood:
5	chr15:59702973..59705551-chr15:59735416..59737691,2	K562	blood:
6	chr15:59663626..59666492-chr15:59674182..59676574,2	MCF-7	breast:
7	chr15:59539475..59539997-chr15:59704300..59705075,2	MCF-7	breast:
8	chr15:59224236..59226115-chr15:59675868..59678075,2	K562	blood:
9	chr15:59669107..59671939-chr15:59729142..59731544,2	MCF-7	breast:
10	chr15:59673490..59676094-chr16:25768225..25770379,2	MCF-7	breast:
11	chr15:59665017..59667143-chr15:59670371..59671925,2	MCF-7	breast:
12	chr15:59663587..59666015-chr15:59667547..59669051,2	MCF-7	breast:
13	chr15:59664112..59666783-chr15:59703908..59705716,2	MCF-7	breast:
14	chr15:59684140..59687063-chr15:59689972..59692965,2	K562	blood:
15	chr15:59680945..59682711-chr15:59948219..59950781,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LDHAL6B-3	chr15:59678953-59679083	NONHSAT044165
2	lnc-LDHAL6B-2	chr15:59678005-59678092	ucscGeneNc_uc002agy_1
3	lnc-LDHAL6B-2	chr15:59683896-59684732	ucscGeneNc_uc002agy_1
4	lnc-LDHAL6B-3	chr15:59694475-59694557	NONHSAT044165

Variant related genes	Relation type
ENSG00000259750	TF binding region
ENSG00000259674	TF binding region
MYO1E	TF binding region
ENSG00000200252	TF binding region
ENSG00000238767	TF binding region
ENSG00000259750	CpG island
ENSG00000259674	CpG island
MYO1E	CpG island
ENSG00000200252	CpG island
ENSG00000238767	CpG island
ENSG00000137776	chromatin interactions
ENSG00000157470	chromatin interactions
ENSG00000157483	chromatin interactions
ENSG00000140307	chromatin interactions

Extended variants
information (count: 2009 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2009 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6494105	chr15:59666992-59666993	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538055373	chr15:59667095-59667096	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201035163	chr15:59667222-59667223	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs141307971	chr15:59667232-59667233	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs574553248	chr15:59667300-59667301	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs145254692	chr15:59667320-59667321	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs61371124	chr15:59667336-59667337	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11071433	chr15:59667389-59667390	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545747855	chr15:59667420-59667421	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564252204	chr15:59667458-59667459	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs10687299	chr15:59667489-59667490	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs142810908	chr15:59667490-59667491	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542024902	chr15:59667514-59667515	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs536716080	chr15:59667516-59667517	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs200759096	chr15:59667518-59667519	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs188933679	chr15:59667519-59667520	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs543875092	chr15:59667535-59667536	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs181681739	chr15:59667624-59667625	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529479489	chr15:59667661-59667662	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10851653	chr15:59667687-59667688	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs559948962	chr15:59667690-59667691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs567986620	chr15:59667753-59667754	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs527291793	chr15:59667800-59667801	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs552168819	chr15:59667803-59667804	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs570585535	chr15:59667849-59667850	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs371603960	chr15:59667855-59667856	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs537967933	chr15:59667864-59667865	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs373625525	chr15:59667871-59667872	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs530627924	chr15:59667876-59667877	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs184640311	chr15:59667884-59667885	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs189427692	chr15:59667887-59667888	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs147683951	chr15:59667894-59667895	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs553787462	chr15:59667929-59667930	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs571971816	chr15:59667949-59667950	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs539466989	chr15:59667972-59667973	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs182462665	chr15:59667986-59667987	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs550792380	chr15:59668009-59668010	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs375081316	chr15:59668051-59668052	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs576010323	chr15:59668060-59668061	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs142440997	chr15:59668062-59668063	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562208610	chr15:59668079-59668080	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570550376	chr15:59668094-59668095	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs574155003	chr15:59668101-59668102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs374528468	chr15:59668193-59668194	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs56021112	chr15:59668207-59668208	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs34378607	chr15:59668208-59668209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185805835	chr15:59668251-59668252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs377085891	chr15:59668260-59668261	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs560103547	chr15:59668290-59668291	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs533640017	chr15:59668298-59668299	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Mental retardation	17124404	CNVD
Gastrointestinal stromal cancer	20877625	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59662600-59667600	Active TSS	GM12878-XiMat	blood
2	chr15:59665400-59667000	Enhancers	Small Intestine	intestine
3	chr15:59665400-59667400	Weak transcription	Gastric	stomach
4	chr15:59665800-59668800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr15:59665800-59674000	Weak transcription	Fetal Kidney	kidney
6	chr15:59665800-59675800	Weak transcription	Brain Hippocampus Middle	brain
7	chr15:59665800-59678400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr15:59665800-59680200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr15:59665800-59691800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:59666000-59667000	Weak transcription	Aorta	Aorta
11	chr15:59666000-59667000	Enhancers	HepG2	liver
12	chr15:59666000-59667400	Enhancers	Primary B cells from cord blood	blood
13	chr15:59666000-59672600	Weak transcription	Placenta	Placenta
14	chr15:59666000-59674400	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr15:59666000-59674800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr15:59666000-59676400	Weak transcription	Colon Smooth Muscle	Colon
17	chr15:59666000-59677000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr15:59666000-59678400	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:59666000-59678400	Weak transcription	Rectal Smooth Muscle	rectum
20	chr15:59666000-59678800	Weak transcription	Fetal Lung	lung
21	chr15:59666000-59680800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr15:59666200-59667000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:59666200-59667200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:59666200-59667400	Enhancers	Fetal Intestine Large	intestine
25	chr15:59666200-59671200	Weak transcription	Fetal Intestine Small	intestine
26	chr15:59666200-59671800	Weak transcription	Duodenum Mucosa	Duodenum
27	chr15:59666200-59673200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr15:59666200-59674000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr15:59666200-59680400	Weak transcription	Fetal Stomach	stomach
30	chr15:59666200-59680600	Weak transcription	NHEK	skin
31	chr15:59666200-59681800	Weak transcription	Ovary	ovary
32	chr15:59666400-59667200	Flanking Active TSS	A549	lung
33	chr15:59666400-59667200	Enhancers	Hela-S3	cervix
34	chr15:59666400-59667400	Enhancers	Fetal Heart	heart
35	chr15:59666400-59667600	Enhancers	Liver	Liver
36	chr15:59666400-59667600	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr15:59666400-59680600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr15:59666600-59667800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr15:59666800-59667400	Enhancers	Stomach Mucosa	stomach
40	chr15:59666800-59674000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:59667000-59667400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:59667000-59667600	Enhancers	Aorta	Aorta
43	chr15:59667000-59671200	Weak transcription	HepG2	liver
44	chr15:59667200-59667400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr15:59667200-59667800	Enhancers	A549	lung
46	chr15:59667200-59670000	Weak transcription	Hela-S3	cervix
47	chr15:59667400-59669000	Weak transcription	Primary B cells from cord blood	blood
48	chr15:59667400-59671400	Weak transcription	Fetal Intestine Large	intestine
49	chr15:59667400-59672800	Weak transcription	Stomach Mucosa	stomach
50	chr15:59667400-59674800	Weak transcription	Fetal Heart	heart

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