Variant report

Variant	nsv984078
Chromosome Location	chr15:59673640-59683792
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	BHLHE40	chr15:59678603-59678707	A549	lung:	n/a	n/a
2	CEBPB	chr15:59680837-59681165	HepG2	liver:	n/a	chr15:59680978-59680989
3	CEBPB	chr15:59680762-59681241	Hela-S3	cervix:	n/a	chr15:59680978-59680989
4	CEBPB	chr15:59680824-59681107	K562	blood:	n/a	chr15:59680978-59680989
5	CEBPB	chr15:59680808-59681191	A549	lung:	n/a	chr15:59680978-59680989
6	CEBPB	chr15:59680806-59681198	IMR90	lung:	n/a	chr15:59680978-59680989
7	CEBPB	chr15:59680830-59681176	K562	blood:	n/a	chr15:59680978-59680989
8	CEBPB	chr15:59680755-59681245	HCT-116	colon:	n/a	chr15:59680978-59680989
9	CEBPB	chr15:59680609-59681403	A549	lung:	n/a	chr15:59680978-59680989
10	CEBPB	chr15:59680832-59681083	MCF-7	breast:	n/a	chr15:59680978-59680989
11	CEBPB	chr15:59680694-59681297	HCT-116	colon:	n/a	chr15:59680978-59680989
12	CEBPB	chr15:59680732-59681305	A549	lung:	n/a	chr15:59680978-59680989
13	CEBPB	chr15:59681009-59681034	H1-hESC	embryonic stem cell:	n/a	n/a
14	EP300	chr15:59680822-59681212	Hela-S3	cervix:	n/a	chr15:59681014-59681023 chr15:59681015-59681024
15	EP300	chr15:59676752-59676945	GM12878	blood:	n/a	n/a
16	EP300	chr15:59676831-59676973	GM12878	blood:	n/a	n/a
17	FAM48A	chr15:59680918-59680924	GM12878	blood:	n/a	n/a
18	FOS	chr15:59680822-59681241	MCF10A-Er-Src	breast:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
19	FOS	chr15:59680833-59681123	HUVEC	blood vessel:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
20	FOS	chr15:59680822-59681208	MCF10A-Er-Src	breast:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
21	FOS	chr15:59680805-59681216	MCF10A-Er-Src	breast:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
22	FOS	chr15:59680825-59681221	Hela-S3	cervix:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
23	FOS	chr15:59680824-59681225	MCF10A-Er-Src	breast:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681013-59681024 chr15:59681014-59681024
24	FOSL1	chr15:59680757-59681369	HCT-116	colon:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
25	FOSL2	chr15:59680783-59681263	SK-N-SH	brain:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
26	FOSL2	chr15:59680700-59681401	A549	lung:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
27	FOSL2	chr15:59680903-59681192	HepG2	liver:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
28	FOSL2	chr15:59680802-59681207	A549	lung:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
29	JUN	chr15:59680812-59681227	Hela-S3	cervix:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
30	JUN	chr15:59680856-59681133	HepG2	liver:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681015-59681023 chr15:59681014-59681024
31	JUND	chr15:59680750-59681268	SK-N-SH	brain:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681013-59681024 chr15:59681015-59681023 chr15:59681014-59681024
32	JUND	chr15:59673127-59673792	Hela-S3	cervix:	n/a	chr15:59673670-59673679
33	JUND	chr15:59680755-59681264	Hela-S3	cervix:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681013-59681024 chr15:59681015-59681023 chr15:59681014-59681024
34	JUND	chr15:59680833-59681193	HepG2	liver:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681013-59681024 chr15:59681015-59681023 chr15:59681014-59681024
35	JUND	chr15:59673645-59673729	HepG2	liver:	n/a	chr15:59673670-59673679
36	JUND	chr15:59680847-59681244	A549	lung:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681013-59681024 chr15:59681015-59681023 chr15:59681014-59681024
37	JUND	chr15:59680615-59681361	SK-N-SH	brain:	n/a	chr15:59681015-59681022 chr15:59681015-59681024 chr15:59681014-59681023 chr15:59681013-59681024 chr15:59681015-59681023 chr15:59681014-59681024
38	MAFF	chr15:59674352-59674380	K562	blood:	n/a	n/a
39	MYC	chr15:59680827-59681148	MCF10A-Er-Src	breast:	n/a	chr15:59681014-59681023 chr15:59681015-59681024
40	MYC	chr15:59680872-59681194	MCF10A-Er-Src	breast:	n/a	chr15:59681014-59681023 chr15:59681015-59681024
41	POLR2A	chr15:59677967-59677969	Gliobla	brain:	n/a	n/a
42	POLR2A	chr15:59680890-59680974	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr15:59677898-59677952	Gliobla	brain:	n/a	n/a
44	POLR2A	chr15:59678848-59678859	Gliobla	brain:	n/a	n/a
45	RUNX3	chr15:59676667-59677067	GM12878	blood:	n/a	n/a
46	RUNX3	chr15:59676762-59677159	GM12878	blood:	n/a	n/a
47	SPI1	chr15:59683764-59684058	GM12891	blood:	n/a	chr15:59683927-59683940
48	STAT3	chr15:59678674-59678697	MCF10A-Er-Src	breast:	n/a	n/a
49	STAT3	chr15:59676812-59676918	GM12878	blood:	n/a	n/a
50	STAT3	chr15:59675292-59675401	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:59224236..59226115-chr15:59675868..59678075,2	K562	blood:
2	chr15:59663703..59665247-chr15:59672295..59676019,3	MCF-7	breast:
3	chr15:59663626..59666492-chr15:59674182..59676574,2	MCF-7	breast:
4	chr15:59680945..59682711-chr15:59948219..59950781,2	MCF-7	breast:
5	chr15:59673490..59676094-chr16:25768225..25770379,2	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

Variant related genes	Relation type
ENSG00000238767	TF binding region
ENSG00000157470	chromatin interactions
ENSG00000140307	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000157483	chromatin interactions

Extended variants
information (count: 456 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:456 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193122076	chr15:59673701-59673702	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs534077016	chr15:59673723-59673724	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549922084	chr15:59673733-59673734	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112625583	chr15:59673739-59673740	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs75489970	chr15:59673767-59673768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535396940	chr15:59673785-59673786	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs111584673	chr15:59673788-59673789	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377172841	chr15:59673794-59673795	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs11383358	chr15:59673795-59673796	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553644755	chr15:59673800-59673801	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs200211937	chr15:59673808-59673809	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs397933520	chr15:59673812-59673813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs79435986	chr15:59673827-59673828	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565786685	chr15:59673828-59673829	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs539405764	chr15:59673834-59673835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs557984192	chr15:59673906-59673907	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs12913287	chr15:59673981-59673982	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543528996	chr15:59673989-59673990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143728773	chr15:59674011-59674012	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs574274511	chr15:59674055-59674056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541792728	chr15:59674081-59674082	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560040759	chr15:59674108-59674109	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs527293583	chr15:59674109-59674110	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs28714594	chr15:59674179-59674180	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs74017765	chr15:59674180-59674181	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs534408187	chr15:59674196-59674197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549596446	chr15:59674197-59674198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567956157	chr15:59674218-59674219	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529052770	chr15:59674256-59674257	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547295407	chr15:59674294-59674295	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs79441379	chr15:59674331-59674332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs539466884	chr15:59674382-59674383	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs558159391	chr15:59674416-59674417	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569933138	chr15:59674455-59674456	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147230208	chr15:59674456-59674457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs555576287	chr15:59674478-59674479	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140493321	chr15:59674506-59674507	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs576484923	chr15:59674518-59674519	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs541597982	chr15:59674562-59674563	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs543608915	chr15:59674575-59674576	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553719323	chr15:59674588-59674589	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs578243246	chr15:59674599-59674600	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201190524	chr15:59674603-59674604	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs377477155	chr15:59674604-59674605	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs201191951	chr15:59674605-59674606	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs79923685	chr15:59674637-59674638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372093506	chr15:59674721-59674722	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535207818	chr15:59674727-59674728	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs531200951	chr15:59674729-59674730	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs188324584	chr15:59674733-59674734	Weak transcription Strong 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:128 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59665800-59674000	Weak transcription	Fetal Kidney	kidney
2	chr15:59665800-59675800	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:59665800-59678400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:59665800-59680200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr15:59665800-59691800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:59666000-59674400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr15:59666000-59674800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:59666000-59676400	Weak transcription	Colon Smooth Muscle	Colon
9	chr15:59666000-59677000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr15:59666000-59678400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr15:59666000-59678400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr15:59666000-59678800	Weak transcription	Fetal Lung	lung
13	chr15:59666000-59680800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:59666200-59674000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr15:59666200-59680400	Weak transcription	Fetal Stomach	stomach
16	chr15:59666200-59680600	Weak transcription	NHEK	skin
17	chr15:59666200-59681800	Weak transcription	Ovary	ovary
18	chr15:59666400-59680600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr15:59666800-59674000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr15:59667400-59674800	Weak transcription	Fetal Heart	heart
21	chr15:59667400-59691800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr15:59667600-59674200	Weak transcription	Liver	Liver
23	chr15:59670400-59675800	Weak transcription	GM12878-XiMat	blood
24	chr15:59670400-59685000	Weak transcription	Primary B cells from cord blood	blood
25	chr15:59670600-59676200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr15:59671600-59674800	Weak transcription	HepG2	liver
27	chr15:59671600-59675200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr15:59672600-59674400	Enhancers	Placenta	Placenta
29	chr15:59672600-59675200	Strong transcription	Aorta	Aorta
30	chr15:59672800-59673800	Enhancers	Hela-S3	cervix
31	chr15:59673200-59674400	Strong transcription	Stomach Smooth Muscle	stomach
32	chr15:59673400-59674800	Weak transcription	Duodenum Mucosa	Duodenum
33	chr15:59673400-59677000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:59673600-59673800	Enhancers	A549	lung
35	chr15:59673600-59674800	Weak transcription	Fetal Intestine Large	intestine
36	chr15:59673600-59675200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:59673600-59675600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr15:59673600-59676000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr15:59673600-59678800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr15:59673600-59685200	Weak transcription	Fetal Intestine Small	intestine
41	chr15:59673800-59680600	Weak transcription	A549	lung
42	chr15:59674000-59674800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr15:59674000-59674800	Strong transcription	Fetal Kidney	kidney
44	chr15:59674000-59675200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr15:59674200-59674600	Strong transcription	Liver	Liver
46	chr15:59674400-59674800	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr15:59674400-59674800	Weak transcription	Placenta	Placenta
48	chr15:59674400-59682200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr15:59674600-59677000	Weak transcription	Liver	Liver
50	chr15:59674800-59675000	Enhancers	Duodenum Mucosa	Duodenum

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