Variant report

Variant	nsv569234
Chromosome Location	chr15:41815649-41822302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr15:41822080-41823482	SK-N-SH	brain:	n/a	n/a
2	POLR2A	chr15:41815053-41816353	HepG2	liver:	n/a	n/a
3	POLR2A	chr15:41815971-41816235	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr15:41816085-41816497	K562	blood:	n/a	n/a
5	POLR2A	chr15:41814961-41815817	K562	blood:	n/a	n/a
6	POLR2A	chr15:41817165-41817186	GM12878	blood:	n/a	n/a
7	POLR2A	chr15:41815978-41816225	ECC-1	luminal epithelium:	n/a	n/a
8	POLR2A	chr15:41818730-41818818	HepG2	liver:	n/a	n/a
9	POLR2A	chr15:41820564-41820749	K562	blood:	n/a	n/a
10	POLR2A	chr15:41818851-41818885	HepG2	liver:	n/a	n/a
11	POLR2A	chr15:41816512-41816525	HepG2	liver:	n/a	n/a
12	POLR2A	chr15:41816556-41816581	HepG2	liver:	n/a	n/a
13	POLR2A	chr15:41816714-41817267	HepG2	liver:	n/a	n/a
14	POLR2A	chr15:41815729-41815794	K562	blood:	n/a	n/a
15	POLR2A	chr15:41821733-41821872	GM12878	blood:	n/a	n/a
16	POLR2A	chr15:41817140-41817369	K562	blood:	n/a	n/a
17	POLR2A	chr15:41815436-41816037	K562	blood:	n/a	n/a
18	POLR2A	chr15:41816260-41816655	K562	blood:	n/a	n/a
19	POLR2A	chr15:41815975-41816173	K562	blood:	n/a	n/a
20	POLR2A	chr15:41817401-41817499	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr15:41816835-41817482	K562	blood:	n/a	n/a
22	POLR2A	chr15:41819512-41819727	K562	blood:	n/a	n/a
23	POLR2A	chr15:41816044-41816374	GM12892	blood:	n/a	n/a
24	POLR2A	chr15:41816876-41817276	K562	blood:	n/a	n/a
25	POLR2A	chr15:41815628-41815702	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr15:41816200-41816583	K562	blood:	n/a	n/a
27	POLR2A	chr15:41816264-41816410	H1-hESC	embryonic stem cell:	n/a	n/a
28	POLR2A	chr15:41816608-41816693	HepG2	liver:	n/a	n/a
29	POLR2A	chr15:41821939-41822063	K562	blood:	n/a	n/a
30	POLR2A	chr15:41818641-41818701	HepG2	liver:	n/a	n/a
31	POLR2A	chr15:41818556-41818617	HepG2	liver:	n/a	n/a
32	POLR2A	chr15:41816380-41816477	HepG2	liver:	n/a	n/a
33	POLR2A	chr15:41817923-41817952	HepG2	liver:	n/a	n/a
34	POLR2A	chr15:41815808-41816030	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr15:41817039-41817171	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr15:41822250-41822655	K562	blood:	n/a	n/a
37	POLR2A	chr15:41815114-41815707	K562	blood:	n/a	n/a
38	POLR2A	chr15:41817143-41817340	K562	blood:	n/a	n/a
39	POLR2A	chr15:41816108-41816351	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr15:41817611-41817812	HepG2	liver:	n/a	n/a
41	POLR2A	chr15:41820620-41820651	HepG2	liver:	n/a	n/a
42	POLR2A	chr15:41816174-41816428	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr15:41815569-41815735	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr15:41816360-41816361	HepG2	liver:	n/a	n/a
45	TCF7L2	chr15:41817129-41817225	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41820721-41820771	BJ	skin:	n/a
2	chr15:41820721-41820771	HEK293	kidney:	embryo
3	chr15:41820721-41820771	Hepatocyte	liver:	n/a
4	chr15:41820721-41820771	SK-N-SH_RA	brain:	n/a
5	chr15:41820721-41820771	IMR90	lung:	fetal
6	chr15:41820721-41820771	T-47D	breast:	n/a
7	chr15:41820721-41820771	CMK	blood:	n/a
8	chr15:41820721-41820771	HRE	kidney:	n/a
9	chr15:41820721-41820771	A549	lung:	n/a
10	chr15:41820721-41820771	AG09319	gingival:	n/a
11	chr15:41820721-41820771	HCT-116	colon:	n/a
12	chr15:41820721-41820771	HMEC	breast:	n/a
13	chr15:41820721-41820771	PFSK-1	brain:	n/a
14	chr15:41820721-41820771	ovcar-3	ovarian:	n/a
15	chr15:41820721-41820771	HRCEpiC	kidney:	n/a
16	chr15:41820721-41820771	ECC-1	luminal epithelium:	n/a
17	chr15:41820721-41820771	U87	brain:	n/a
18	chr15:41820721-41820771	PANC-1	pancreas:	n/a
19	chr15:41820721-41820771	GM12878	blood:	n/a
20	chr15:41820721-41820771	RPTEC	kidney:	n/a
21	chr15:41820721-41820771	Hela-S3	cervix:	n/a
22	chr15:41820721-41820771	HUVEC	blood vessel:	n/a
23	chr15:41820721-41820771	Caco-2	colon:	n/a
24	chr15:41820721-41820771	AG04450	lung:	fetal
25	chr15:41820721-41820771	AoSMC	blood vessel:	n/a
26	chr15:41820721-41820771	HAEpiC	amniotic membrane:	n/a
27	chr15:41820721-41820771	SKMC	muscle:	n/a
28	chr15:41820721-41820771	AG10803	skin:	n/a
29	chr15:41820721-41820771	NH-A	brain:	n/a
30	chr15:41820721-41820771	HRPEpiC	eye:	n/a
31	chr15:41820721-41820771	LNCaP	prostate:	n/a
32	chr15:41820721-41820771	BE2_C	brain:	n/a
33	chr15:41820721-41820771	MCF-7	breast:	n/a
34	chr15:41820721-41820771	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:41820721-41820771	AG09309	skin:	n/a
36	chr15:41820721-41820771	SAEC	small airway:	n/a
37	chr15:41820721-41820771	HEEpiC	esophagus:	n/a
38	chr15:41820721-41820771	NT2-D1	testis:	n/a
39	chr15:41820721-41820771	HL-60	blood:	n/a
40	chr15:41820721-41820771	GM19239	blood:	n/a
41	chr15:41820721-41820771	PrEC	prostate:	n/a
42	chr15:41820721-41820771	HNPCEpiC	eye:	n/a
43	chr15:41820721-41820771	MCF10A-Er-Src	breast:	n/a
44	chr15:41820721-41820771	HCF	heart:	n/a
45	chr15:41820721-41820771	SK-N-MC	brain:	n/a
46	chr15:41820721-41820771	ProgFib	skin:	n/a
47	chr15:41820721-41820771	SK-N-SH	brain:	n/a
48	chr15:41820721-41820771	K562	blood:	n/a
49	chr15:41820721-41820771	HCM	heart:	n/a
50	chr15:41820721-41820771	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:41811420..41814118-chr15:41817482..41820204,2	K562	blood:
2	chr15:41821217..41823173-chr15:41825451..41828342,2	K562	blood:
3	chr15:41813214..41815755-chr15:41821195..41823682,2	K562	blood:
4	chr15:41813214..41815867-chr15:41821195..41823790,3	K562	blood:
5	chr15:41784591..41787497-chr15:41813598..41816388,3	K562	blood:
6	chr15:41819746..41824231-chr15:41825451..41829235,5	K562	blood:
7	chr15:41812182..41819156-chr15:41830894..41838104,9	K562	blood:
8	chr15:41814934..41817190-chr15:41828140..41829699,2	MCF-7	breast:
9	chr15:41791755..41794361-chr15:41822033..41824334,2	K562	blood:

No data

Variant related genes	Relation type
RPAP1	TF binding region
RPAP1	CpG island
ENSG00000137825	chromatin interactions
ENSG00000103932	chromatin interactions

Extended variants
information (count: 313 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2297377	chr15:41815649-41815650	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557770566	chr15:41815731-41815732	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs577838582	chr15:41815749-41815750	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs149477926	chr15:41815754-41815755	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs563277218	chr15:41815756-41815757	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs529024328	chr15:41815781-41815782	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs542737131	chr15:41815791-41815792	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs143933505	chr15:41815798-41815799	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs528702081	chr15:41815799-41815800	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs551924332	chr15:41815805-41815806	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs565454874	chr15:41815806-41815807	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs531221356	chr15:41815895-41815896	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs117391509	chr15:41815914-41815915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201033681	chr15:41815932-41815933	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs200468439	chr15:41815934-41815935	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs376121881	chr15:41815952-41815953	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs200318959	chr15:41815968-41815969	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs35841360	chr15:41815996-41815997	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs546698821	chr15:41815997-41815998	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs375474364	chr15:41816020-41816021	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs34601962	chr15:41816029-41816030	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369954246	chr15:41816072-41816073	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs199643044	chr15:41816130-41816131	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs372213286	chr15:41816146-41816147	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376586068	chr15:41816153-41816154	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs557896983	chr15:41816186-41816187	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs2297378	chr15:41816190-41816191	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs201561284	chr15:41816196-41816197	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs373352914	chr15:41816217-41816218	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs376409007	chr15:41816218-41816219	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs117189559	chr15:41816259-41816260	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs373394008	chr15:41816270-41816271	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs377361732	chr15:41816275-41816276	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs200806598	chr15:41816282-41816283	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs542600446	chr15:41816293-41816294	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs202122322	chr15:41816311-41816312	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs371439385	chr15:41816319-41816320	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs146202371	chr15:41816320-41816321	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs182734566	chr15:41816323-41816324	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs148404660	chr15:41816354-41816355	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374561656	chr15:41816366-41816367	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148641695	chr15:41816391-41816392	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545307017	chr15:41816409-41816410	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565456152	chr15:41816428-41816429	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs142484175	chr15:41816429-41816430	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377353071	chr15:41816446-41816447	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200383908	chr15:41816481-41816482	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370667528	chr15:41816490-41816491	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367928671	chr15:41816497-41816498	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs201521511	chr15:41816500-41816501	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41801800-41819000	Weak transcription	Hela-S3	cervix
2	chr15:41806200-41820400	Weak transcription	HSMM	muscle
3	chr15:41806200-41822600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:41806400-41818600	Weak transcription	Primary B cells from cord blood	blood
5	chr15:41806400-41835200	Weak transcription	Right Atrium	heart
6	chr15:41806600-41817000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr15:41806600-41818800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr15:41806600-41818800	Weak transcription	GM12878-XiMat	blood
9	chr15:41806600-41819000	Weak transcription	HUVEC	blood vessel
10	chr15:41806600-41819200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr15:41806600-41824600	Weak transcription	Fetal Kidney	kidney
12	chr15:41806600-41835200	Weak transcription	Fetal Heart	heart
13	chr15:41806800-41818200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr15:41806800-41818400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr15:41806800-41818600	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr15:41806800-41818800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr15:41806800-41818800	Weak transcription	Stomach Mucosa	stomach
18	chr15:41806800-41822400	Weak transcription	NH-A	brain
19	chr15:41807000-41816400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr15:41807200-41819400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr15:41807200-41835600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr15:41808000-41829600	Strong transcription	Fetal Stomach	stomach
23	chr15:41808200-41818200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr15:41808200-41820600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr15:41808600-41823000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr15:41808600-41829200	Strong transcription	Skeletal Muscle Female	skeletal muscle
27	chr15:41808600-41829600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:41808600-41835400	Weak transcription	Fetal Brain Male	brain
29	chr15:41808800-41829600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr15:41809000-41829400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:41809000-41829400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr15:41809600-41829200	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr15:41809600-41829400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:41809800-41818600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:41810000-41815800	Weak transcription	Colon Smooth Muscle	Colon
36	chr15:41810000-41820400	Weak transcription	Small Intestine	intestine
37	chr15:41810200-41818400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr15:41810200-41819000	Weak transcription	HSMMtube	muscle
39	chr15:41810400-41817000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr15:41810400-41818600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:41810400-41819400	Weak transcription	Psoas Muscle	Psoas
42	chr15:41810600-41818600	Weak transcription	HMEC	breast
43	chr15:41810600-41818800	Weak transcription	K562	blood
44	chr15:41811400-41818600	Weak transcription	HepG2	liver
45	chr15:41811400-41819200	Weak transcription	A549	lung
46	chr15:41811600-41829600	Strong transcription	Fetal Intestine Large	intestine
47	chr15:41811600-41829800	Strong transcription	Fetal Muscle Leg	muscle
48	chr15:41811800-41817400	Strong transcription	NHEK	skin
49	chr15:41811800-41829400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:41811800-41829400	Strong transcription	Brain Hippocampus Middle	brain

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