Variant report

Variant	nsv510665
Chromosome Location	chr15:72374862-72407548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:183)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72402687-72403203	HepG2	liver:	n/a	n/a
2	BCL3	chr15:72402707-72403203	A549	lung:	n/a	n/a
3	CEBPB	chr15:72402810-72403001	A549	lung:	n/a	n/a
4	CEBPB	chr15:72395407-72395583	A549	lung:	n/a	n/a
5	CEBPB	chr15:72395417-72395537	K562	blood:	n/a	n/a
6	CEBPB	chr15:72395429-72395522	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr15:72395404-72395606	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr15:72402826-72403026	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:72395338-72395630	IMR90	lung:	n/a	n/a
10	CEBPB	chr15:72402709-72403232	A549	lung:	n/a	n/a
11	CEBPB	chr15:72395416-72395749	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr15:72390648-72390890	HepG2	liver:	n/a	chr15:72390741-72390752
13	CEBPB	chr15:72395315-72395674	MCF-7	breast:	n/a	n/a
14	CEBPB	chr15:72390575-72390900	K562	blood:	n/a	chr15:72390741-72390752
15	CHD2	chr15:72406654-72406661	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr15:72378260-72378410	RPTEC	kidney:	n/a	n/a
17	CTCF	chr15:72378345-72378449	NHEK	skin:	n/a	n/a
18	CTCF	chr15:72378342-72378466	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr15:72378531-72378580	MCF-7	breast:	n/a	n/a
20	CTCF	chr15:72378331-72378479	HepG2	liver:	n/a	n/a
21	CTCF	chr15:72383432-72383510	LNCaP	prostate:	n/a	n/a
22	CTCF	chr15:72378326-72378486	MCF-7	breast:	n/a	n/a
23	CTCF	chr15:72378320-72378470	SAEC	small airway:	n/a	n/a
24	CTCF	chr15:72378303-72378513	MCF-7	breast:	n/a	n/a
25	CTCF	chr15:72378382-72378455	GM19238	blood:	n/a	n/a
26	CTCF	chr15:72378867-72378949	MCF-7	breast:	n/a	n/a
27	CTCF	chr15:72378315-72378539	MCF-7	breast:	n/a	n/a
28	CTCF	chr15:72378308-72378522	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:72378316-72378655	MCF-7	breast:	n/a	n/a
30	CTCF	chr15:72378306-72378525	MCF-7	breast:	n/a	n/a
31	CTCF	chr15:72378280-72378430	MCF-7	breast:	n/a	n/a
32	CTCF	chr15:72378829-72378967	MCF-7	breast:	n/a	n/a
33	CTCF	chr15:72378593-72378600	MCF-7	breast:	n/a	n/a
34	CUX1	chr15:72385300-72385313	GM12878	blood:	n/a	n/a
35	CUX1	chr15:72400450-72400732	K562	blood:	n/a	n/a
36	EP300	chr15:72405900-72406171	T-47D	breast:	n/a	n/a
37	EP300	chr15:72402557-72403271	A549	lung:	n/a	chr15:72402842-72402852
38	EP300	chr15:72405799-72406303	T-47D	breast:	n/a	n/a
39	EP300	chr15:72402551-72403286	A549	lung:	n/a	chr15:72402842-72402852
40	FOS	chr15:72399440-72399785	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr15:72399499-72399762	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr15:72399439-72399773	MCF10A-Er-Src	breast:	n/a	n/a
43	FOSL2	chr15:72402702-72403262	A549	lung:	n/a	n/a
44	FOSL2	chr15:72402706-72403138	A549	lung:	n/a	n/a
45	FOXA1	chr15:72405938-72406347	HepG2	liver:	n/a	chr15:72406121-72406136
46	FOXA1	chr15:72402680-72403099	HepG2	liver:	n/a	n/a
47	FOXA1	chr15:72405937-72406319	T-47D	breast:	n/a	chr15:72406121-72406136
48	FOXA1	chr15:72406001-72406326	HepG2	liver:	n/a	chr15:72406121-72406136
49	FOXA1	chr15:72402675-72403101	HepG2	liver:	n/a	n/a
50	FOXA1	chr15:72402711-72403022	T-47D	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72406824-72406874	BJ	skin:	n/a
2	chr15:72406824-72406874	AG10803	skin:	n/a
3	chr15:72405733-72405783	HPAEpiC	pulmonary alveolar:	n/a
4	chr15:72405733-72405783	CMK	blood:	n/a
5	chr15:72406367-72406417	BE2_C	brain:	n/a
6	chr15:72406367-72406417	U87	brain:	n/a
7	chr15:72405733-72405783	AoSMC	blood vessel:	n/a
8	chr15:72405733-72405783	Hepatocyte	liver:	n/a
9	chr15:72405733-72405783	HRE	kidney:	n/a
10	chr15:72405733-72405783	HCT-116	colon:	n/a
11	chr15:72406367-72406417	T-47D	breast:	n/a
12	chr15:72406824-72406874	HRPEpiC	eye:	n/a
13	chr15:72406824-72406874	HRE	kidney:	n/a
14	chr15:72406824-72406874	HAEpiC	amniotic membrane:	n/a
15	chr15:72406367-72406417	GM06990	blood:	n/a
16	chr15:72405733-72405783	Caco-2	colon:	n/a
17	chr15:72406824-72406874	PANC-1	pancreas:	n/a
18	chr15:72406824-72406874	NB4	blood:	n/a
19	chr15:72406367-72406417	PANC-1	pancreas:	n/a
20	chr15:72406824-72406874	HUVEC	blood vessel:	n/a
21	chr15:72405733-72405783	NH-A	brain:	n/a
22	chr15:72405733-72405783	SK-N-SH_RA	brain:	n/a
23	chr15:72405733-72405783	U87	brain:	n/a
24	chr15:72406824-72406874	Hela-S3	cervix:	n/a
25	chr15:72405733-72405783	HNPCEpiC	eye:	n/a
26	chr15:72406367-72406417	SK-N-SH_RA	brain:	n/a
27	chr15:72405733-72405783	IMR90	lung:	fetal
28	chr15:72405733-72405783	SK-N-MC	brain:	n/a
29	chr15:72405733-72405783	PANC-1	pancreas:	n/a
30	chr15:72406824-72406874	ProgFib	skin:	n/a
31	chr15:72406824-72406874	Hepatocyte	liver:	n/a
32	chr15:72405733-72405783	RPTEC	kidney:	n/a
33	chr15:72406367-72406417	NT2-D1	testis:	n/a
34	chr15:72406367-72406417	AG09319	gingival:	n/a
35	chr15:72405733-72405783	AG09319	gingival:	n/a
36	chr15:72405733-72405783	ovcar-3	ovarian:	n/a
37	chr15:72405733-72405783	HEK293	kidney:	embryo
38	chr15:72406367-72406417	HIPEpiC	eye:	n/a
39	chr15:72406824-72406874	A549	lung:	n/a
40	chr15:72405733-72405783	HCM	heart:	n/a
41	chr15:72406367-72406417	HNPCEpiC	eye:	n/a
42	chr15:72405733-72405783	AG04450	lung:	fetal
43	chr15:72406367-72406417	NB4	blood:	n/a
44	chr15:72406367-72406417	HEEpiC	esophagus:	n/a
45	chr15:72406367-72406417	Hela-S3	cervix:	n/a
46	chr15:72406367-72406417	ovcar-3	ovarian:	n/a
47	chr15:72406824-72406874	GM12892	blood:	n/a
48	chr15:72406824-72406874	HCPEpiC	choroid plexus:	n/a
49	chr15:72406824-72406874	HMEC	breast:	n/a
50	chr15:72405733-72405783	NHDF-neo	bronchial:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:72405635..72407377-chr15:72409076..72410696,2	K562	blood:
2	chr15:72401062..72403312-chr15:72406877..72409075,2	K562	blood:
3	chr15:72398478..72400917-chr15:72408968..72411115,2	MCF-7	breast:
4	chr15:72378259..72378845-chr15:72448189..72448926,2	MCF-7	breast:
5	chr15:72383759..72385848-chr15:72409093..72411983,2	MCF-7	breast:
6	chr15:72399406..72401734-chr15:72404487..72406226,2	K562	blood:
7	chr15:72394985..72397263-chr15:72398518..72401032,2	MCF-7	breast:
8	chr15:72399406..72401734-chr15:72404487..72406226,2	K562	blood:
9	chr15:72394985..72397263-chr15:72398518..72401032,2	MCF-7	breast:
10	chr15:72394930..72397507-chr15:72409085..72411660,2	MCF-7	breast:
11	chr15:72401062..72403312-chr15:72406877..72409075,2	K562	blood:
12	chr15:72393359..72395081-chr15:72408256..72411185,2	K562	blood:
13	chr15:72380042..72381883-chr15:72383169..72385505,2	MCF-7	breast:
14	chr15:72399130..72400833-chr15:72405712..72408016,2	MCF-7	breast:
15	chr15:72398905..72401840-chr15:72409196..72411848,3	K562	blood:
16	chr15:72380042..72381883-chr15:72383169..72385505,2	MCF-7	breast:
17	chr15:72398211..72399947-chr15:72411763..72414182,2	MCF-7	breast:
18	chr15:72398664..72401840-chr15:72410348..72413852,3	K562	blood:

No data

Variant related genes	Relation type
SENP8	TF binding region
SENP8	CpG island
ENSG00000066933	chromatin interactions
ENSG00000166192	chromatin interactions

Extended variants
information (count: 1217 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180811034	chr15:72374886-72374887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138651902	chr15:72374889-72374890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12771836	chr15:72374901-72374902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367547590	chr15:72374952-72374953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141689316	chr15:72374979-72374980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs186529674	chr15:72375006-72375007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376747927	chr15:72375038-72375039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552874738	chr15:72375049-72375050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28796596	chr15:72375055-72375056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564770938	chr15:72375062-72375063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs11744720	chr15:72375064-72375065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs28824293	chr15:72375073-72375074	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs547114976	chr15:72375076-72375077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs551126814	chr15:72375077-72375078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191391096	chr15:72375110-72375111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183467806	chr15:72375134-72375135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569477071	chr15:72375135-72375136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs80321052	chr15:72375145-72375146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79476659	chr15:72375146-72375147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79874203	chr15:72375152-72375153	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185906535	chr15:72375157-72375158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77614217	chr15:72375160-72375161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78833108	chr15:72375161-72375162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs74781528	chr15:72375163-72375164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78959007	chr15:72375164-72375165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs78325489	chr15:72375177-72375178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75287210	chr15:72375178-72375179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78752727	chr15:72375182-72375183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75790824	chr15:72375201-72375202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532891781	chr15:72375206-72375207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs76534275	chr15:72375247-72375248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76106923	chr15:72375255-72375256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75802159	chr15:72375270-72375271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558384213	chr15:72375274-72375275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79247819	chr15:72375275-72375276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78883687	chr15:72375276-72375277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75674389	chr15:72375293-72375294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79710518	chr15:72375296-72375297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533623135	chr15:72375321-72375322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34705283	chr15:72375337-72375338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs28879707	chr15:72375338-72375339	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs191117886	chr15:72375344-72375345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35094660	chr15:72375387-72375388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574856636	chr15:72375407-72375408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542378956	chr15:72375447-72375448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs555148850	chr15:72375461-72375462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551210692	chr15:72375462-72375463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183257559	chr15:72375487-72375488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546427435	chr15:72375497-72375498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564789747	chr15:72375506-72375507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	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
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72351200-72395800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:72353600-72379600	Weak transcription	Primary T cells from cord blood	blood
3	chr15:72354000-72378400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:72355800-72376200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:72361600-72377400	Weak transcription	Fetal Intestine Small	intestine
6	chr15:72361600-72390600	Weak transcription	Aorta	Aorta
7	chr15:72361600-72391400	Weak transcription	Ovary	ovary
8	chr15:72367200-72407600	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:72367800-72377400	Weak transcription	Fetal Stomach	stomach
10	chr15:72370000-72378400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr15:72370800-72378600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr15:72371200-72377400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr15:72371400-72376800	Weak transcription	Fetal Brain Female	brain
14	chr15:72371400-72379600	Weak transcription	Brain Anterior Caudate	brain
15	chr15:72372200-72378000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr15:72372200-72399400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr15:72373600-72378400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:72373600-72394400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:72374000-72375400	Enhancers	HSMMtube	muscle
20	chr15:72374400-72375400	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr15:72374600-72375200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr15:72374800-72375000	Enhancers	Right Ventricle	heart
23	chr15:72374800-72375400	Enhancers	Psoas Muscle	Psoas
24	chr15:72375000-72379400	Weak transcription	Right Ventricle	heart
25	chr15:72375000-72408200	Weak transcription	Primary B cells from cord blood	blood
26	chr15:72375200-72376600	Weak transcription	Fetal Lung	lung
27	chr15:72375200-72378800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:72375400-72376800	Weak transcription	HSMMtube	muscle
29	chr15:72375400-72377800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr15:72375400-72378400	Weak transcription	Psoas Muscle	Psoas
31	chr15:72375800-72395600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:72376200-72377000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:72376400-72378400	Weak transcription	Esophagus	oesophagus
34	chr15:72376400-72381400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:72376600-72377000	Strong transcription	Fetal Lung	lung
36	chr15:72376800-72377000	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
37	chr15:72376800-72377200	ZNF genes & repeats	Fetal Brain Female	brain
38	chr15:72376800-72379000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:72376800-72379200	Enhancers	HSMMtube	muscle
40	chr15:72377000-72378000	Weak transcription	Fetal Lung	lung
41	chr15:72377000-72378800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr15:72377000-72379800	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr15:72377200-72388200	Weak transcription	Fetal Brain Female	brain
44	chr15:72377400-72377600	ZNF genes & repeats	Fetal Stomach	stomach
45	chr15:72377400-72378600	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr15:72377400-72379400	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr15:72377600-72378200	Weak transcription	Fetal Stomach	stomach
48	chr15:72377600-72381800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr15:72377800-72378000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr15:72377800-72378200	Enhancers	Skeletal Muscle Male	skeletal muscle

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