Variant report

Variant	esv3448312
Chromosome Location	chr15:73995047-73996564
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:73996208-73996365	GM13976	blood:	n/a	n/a
2	CTCF	chr15:73996260-73996410	SK-N-SH_RA	brain:	n/a	n/a
3	CTCF	chr15:73994920-73995070	HepG2	liver:	n/a	n/a
4	CTCF	chr15:73995191-73995200	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr15:73996220-73996370	WERI-Rb-1	eye:	n/a	n/a
6	CTCF	chr15:73996260-73996410	HEK293	kidney:	n/a	n/a
7	CTCF	chr15:73995251-73995324	MCF-7	breast:	n/a	n/a
8	CTCF	chr15:73996250-73996371	Gliobla	brain:	n/a	n/a
9	CTCF	chr15:73996306-73996347	Kidney_OC	kidney:	n/a	n/a
10	CTCF	chr15:73996230-73996308	ProgFib	skin:	n/a	n/a
11	CTCF	chr15:73994920-73995070	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr15:73996240-73996390	HepG2	liver:	n/a	n/a
13	CTCF	chr15:73996229-73996406	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:73996220-73996370	HCFaa	heart:	n/a	n/a
15	CTCF	chr15:73994920-73995070	HEK293	kidney:	n/a	n/a
16	CTCF	chr15:73994940-73995090	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr15:73994756-73995139	K562	blood:	n/a	n/a
18	CTCF	chr15:73996171-73996496	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr15:73996237-73996409	A549	lung:	n/a	n/a
20	CTCF	chr15:73996220-73996370	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr15:73996100-73996250	HRE	kidney:	n/a	n/a
22	CTCF	chr15:73996137-73996528	K562	blood:	n/a	n/a
23	CTCF	chr15:73996280-73996430	GM12871	blood:	n/a	n/a
24	CTCF	chr15:73996218-73996404	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:73996280-73996430	HCT-116	colon:	n/a	n/a
26	CTCF	chr15:73996229-73996401	MCF-7	breast:	n/a	n/a
27	CTCF	chr15:73996205-73996412	NHEK	skin:	n/a	n/a
28	CTCF	chr15:73994920-73995070	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr15:73994920-73995070	SAEC	small airway:	n/a	n/a
30	CTCF	chr15:73995232-73995248	GM12891	blood:	n/a	n/a
31	CTCF	chr15:73996320-73996470	HMEC	breast:	n/a	n/a
32	CTCF	chr15:73996260-73996410	GM12872	blood:	n/a	n/a
33	CTCF	chr15:73996300-73996450	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr15:73996320-73996470	GM12873	blood:	n/a	n/a
35	CTCF	chr15:73996060-73996210	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr15:73996240-73996390	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr15:73994752-73995062	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr15:73996256-73996358	GM19239	blood:	n/a	n/a
39	CTCF	chr15:73996283-73996402	K562	blood:	n/a	n/a
40	CTCF	chr15:73996320-73996470	Caco-2	colon:	n/a	n/a
41	CTCF	chr15:73994900-73995050	HCT-116	colon:	n/a	n/a
42	CTCF	chr15:73994920-73995070	Caco-2	colon:	n/a	n/a
43	CTCF	chr15:73996040-73996190	HEK293	kidney:	n/a	n/a
44	CTCF	chr15:73996320-73996470	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr15:73996260-73996410	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr15:73996340-73996490	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr15:73996300-73996450	NB4	blood:	n/a	n/a
48	CTCF	chr15:73995227-73995317	MCF-7	breast:	n/a	n/a
49	CTCF	chr15:73995240-73995403	GM19239	blood:	n/a	n/a
50	CTCF	chr15:73994900-73995050	HCFaa	heart:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:73996358-73996408	T-47D	breast:	n/a
2	chr15:73996268-73996318	HRE	kidney:	n/a
3	chr15:73996268-73996318	PFSK-1	brain:	n/a
4	chr15:73996194-73996244	GM12878	blood:	n/a
5	chr15:73996358-73996408	HCM	heart:	n/a
6	chr15:73996358-73996408	HCPEpiC	choroid plexus:	n/a
7	chr15:73996268-73996318	HNPCEpiC	eye:	n/a
8	chr15:73996268-73996318	BJ	skin:	n/a
9	chr15:73996358-73996408	Caco-2	colon:	n/a
10	chr15:73996194-73996244	Jurkat	blood:	n/a
11	chr15:73996194-73996244	SK-N-SH	brain:	n/a
12	chr15:73996358-73996408	GM12878	blood:	n/a
13	chr15:73996358-73996408	Hepatocyte	liver:	n/a
14	chr15:73996268-73996318	PANC-1	pancreas:	n/a
15	chr15:73996194-73996244	HL-60	blood:	n/a
16	chr15:73996194-73996244	NHBE	bronchial:	n/a
17	chr15:73996194-73996244	PFSK-1	brain:	n/a
18	chr15:73996268-73996318	K562	blood:	n/a
19	chr15:73996358-73996408	GM12891	blood:	n/a
20	chr15:73996358-73996408	HNPCEpiC	eye:	n/a
21	chr15:73996194-73996244	MCF-7	breast:	n/a
22	chr15:73996194-73996244	AG04449	skin:	fetal
23	chr15:73996194-73996244	ProgFib	skin:	n/a
24	chr15:73996358-73996408	Hela-S3	cervix:	n/a
25	chr15:73996358-73996408	NH-A	brain:	n/a
26	chr15:73996194-73996244	SAEC	small airway:	n/a
27	chr15:73996358-73996408	ovcar-3	ovarian:	n/a
28	chr15:73996194-73996244	AoSMC	blood vessel:	n/a
29	chr15:73996194-73996244	SK-N-MC	brain:	n/a
30	chr15:73996194-73996244	HCM	heart:	n/a
31	chr15:73996358-73996408	U87	brain:	n/a
32	chr15:73996358-73996408	SK-N-MC	brain:	n/a
33	chr15:73996358-73996408	MCF10A-Er-Src	breast:	n/a
34	chr15:73996358-73996408	BJ	skin:	n/a
35	chr15:73996268-73996318	SK-N-MC	brain:	n/a
36	chr15:73996194-73996244	HEEpiC	esophagus:	n/a
37	chr15:73996358-73996408	NB4	blood:	n/a
38	chr15:73996268-73996318	HPAEpiC	pulmonary alveolar:	n/a
39	chr15:73996194-73996244	HPAEpiC	pulmonary alveolar:	n/a
40	chr15:73996358-73996408	HEEpiC	esophagus:	n/a
41	chr15:73996194-73996244	IMR90	lung:	fetal
42	chr15:73996194-73996244	T-47D	breast:	n/a
43	chr15:73996194-73996244	NHDF-neo	bronchial:	n/a
44	chr15:73996358-73996408	BE2_C	brain:	n/a
45	chr15:73996194-73996244	HUVEC	blood vessel:	n/a
46	chr15:73996358-73996408	GM19239	blood:	n/a
47	chr15:73996268-73996318	HepG2	liver:	n/a
48	chr15:73996194-73996244	K562	blood:	n/a
49	chr15:73996268-73996318	HMEC	breast:	n/a
50	chr15:73996194-73996244	HRCEpiC	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:73992648..73995502-chr15:73997951..74000936,2	MCF-7	breast:
2	chr15:73975584..73976331-chr15:73994335..73995109,2	MCF-7	breast:
3	chr15:73975489..73977527-chr15:73994222..73997098,2	MCF-7	breast:
4	chr15:73993873..73996840-chr15:74002371..74004783,2	MCF-7	breast:
5	chr15:73996066..73998855-chr15:74002172..74005149,2	MCF-7	breast:

No data

Variant related genes	Relation type
CD276	TF binding region
CD276	CpG island
ENSG00000103855	chromatin interactions

Extended variants
information (count: 108 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:108 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535801324	chr15:73995051-73995052	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs545149233	chr15:73995066-73995067	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372595808	chr15:73995093-73995094	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs71399752	chr15:73995124-73995125	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548539544	chr15:73995127-73995128	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs111801073	chr15:73995165-73995166	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs11574479	chr15:73995173-73995174	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs146911233	chr15:73995180-73995181	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs561421890	chr15:73995185-73995186	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs145891493	chr15:73995188-73995189	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs531910633	chr15:73995198-73995199	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs186688946	chr15:73995200-73995201	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571322872	chr15:73995210-73995211	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs532441600	chr15:73995213-73995214	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs202232823	chr15:73995228-73995229	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374564457	chr15:73995233-73995234	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368243594	chr15:73995236-73995237	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs199719127	chr15:73995238-73995239	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs138502254	chr15:73995239-73995240	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs142744437	chr15:73995247-73995248	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs555581349	chr15:73995262-73995263	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372836595	chr15:73995272-73995273	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375773746	chr15:73995284-73995285	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567423683	chr15:73995285-73995286	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs144253368	chr15:73995293-73995294	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs148316620	chr15:73995319-73995320	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs141481664	chr15:73995329-73995330	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556169986	chr15:73995361-73995362	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368756883	chr15:73995369-73995370	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs199765601	chr15:73995370-73995371	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376536679	chr15:73995371-73995372	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577717498	chr15:73995384-73995385	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184115783	chr15:73995386-73995387	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs376623449	chr15:73995399-73995400	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs11574480	chr15:73995431-73995432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555400591	chr15:73995458-73995459	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139330740	chr15:73995462-73995463	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs371713870	chr15:73995476-73995477	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369275458	chr15:73995477-73995478	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77067414	chr15:73995481-73995482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs531850674	chr15:73995483-73995484	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543728797	chr15:73995533-73995534	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373034101	chr15:73995548-73995549	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10152662	chr15:73995588-73995589	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs10152645	chr15:73995603-73995604	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs547809128	chr15:73995689-73995690	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376518259	chr15:73995707-73995708	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs566036505	chr15:73995723-73995724	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530238341	chr15:73995745-73995746	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548887823	chr15:73995768-73995769	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Lung cancer	18438408	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
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	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
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	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:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73978800-74000800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr15:73979400-73996400	Weak transcription	A549	lung
3	chr15:73984600-73995400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:73988800-73996200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:73989600-73996200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr15:73989600-73996800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr15:73989800-73995400	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr15:73989800-73995800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr15:73989800-73996400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr15:73989800-73996800	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:73989800-73997000	Weak transcription	Hela-S3	cervix
12	chr15:73989800-74000600	Weak transcription	Esophagus	oesophagus
13	chr15:73989800-74001600	Strong transcription	Fetal Intestine Small	intestine
14	chr15:73989800-74008800	Weak transcription	Small Intestine	intestine
15	chr15:73990000-73996200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr15:73990000-73997600	Weak transcription	Fetal Kidney	kidney
17	chr15:73990000-73999800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr15:73990000-74012000	Weak transcription	Fetal Brain Male	brain
19	chr15:73990200-74007200	Weak transcription	Stomach Mucosa	stomach
20	chr15:73990200-74007600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:73990400-74007200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:73990400-74007600	Strong transcription	Fetal Stomach	stomach
23	chr15:73990600-73996800	Weak transcription	Fetal Lung	lung
24	chr15:73990600-73999400	Weak transcription	Left Ventricle	heart
25	chr15:73990600-74006600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr15:73990600-74007400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:73990600-74018800	Weak transcription	Right Atrium	heart
28	chr15:73990800-73996200	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr15:73990800-73996400	Weak transcription	Rectal Smooth Muscle	rectum
30	chr15:73990800-73996400	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr15:73990800-73997400	Weak transcription	Brain Substantia Nigra	brain
32	chr15:73990800-73997600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:73990800-74009200	Weak transcription	Psoas Muscle	Psoas
34	chr15:73991000-74003400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr15:73991200-74001600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr15:73991400-74004800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:73991400-74007200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr15:73991800-73997000	Weak transcription	HSMMtube	muscle
39	chr15:73992000-73997000	Weak transcription	HSMM	muscle
40	chr15:73992200-74007400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:73992400-73995600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:73992600-73995400	Weak transcription	Colon Smooth Muscle	Colon
43	chr15:73992600-73995600	Weak transcription	Right Ventricle	heart
44	chr15:73992600-73996800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr15:73992600-73997000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:73992600-74000600	Weak transcription	Brain Angular Gyrus	brain
47	chr15:73992600-74002400	Weak transcription	Fetal Heart	heart
48	chr15:73992600-74007400	Strong transcription	Fetal Muscle Trunk	muscle
49	chr15:73992800-73995200	Weak transcription	Placenta	Placenta
50	chr15:73992800-73996400	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links