Variant report

Variant	nsv1040578
Chromosome Location	chr15:49841444-49890789
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:111)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:111 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:49882671-49882822	K562	blood:	n/a	n/a
2	CBX3	chr15:49852297-49852511	K562	blood:	n/a	n/a
3	CEBPB	chr15:49852185-49852249	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr15:49851203-49851523	Hela-S3	cervix:	n/a	chr15:49851344-49851355
5	CEBPB	chr15:49851209-49851512	IMR90	lung:	n/a	chr15:49851344-49851355
6	CEBPB	chr15:49852157-49852250	IMR90	lung:	n/a	n/a
7	CEBPB	chr15:49851268-49851496	HepG2	liver:	n/a	chr15:49851344-49851355
8	CEBPB	chr15:49881371-49881626	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr15:49852119-49852335	K562	blood:	n/a	n/a
10	CEBPB	chr15:49852084-49852279	A549	lung:	n/a	n/a
11	CTCF	chr15:49878644-49878747	LNCaP	prostate:	n/a	n/a
12	CTCF	chr15:49865812-49865877	MCF-7	breast:	n/a	n/a
13	CTCF	chr15:49845880-49846030	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:49841678-49841760	GM13976	blood:	n/a	n/a
15	CTCF	chr15:49865777-49865784	MCF-7	breast:	n/a	n/a
16	CTCF	chr15:49865679-49865766	MCF-7	breast:	n/a	n/a
17	CTCF	chr15:49841702-49841723	Lung_OC	lung:	n/a	n/a
18	CTCF	chr15:49865785-49865786	MCF-7	breast:	n/a	n/a
19	CTCF	chr15:49888795-49888847	Lung_OC	lung:	n/a	n/a
20	CTCF	chr15:49858910-49858964	Medullo	brain:	n/a	n/a
21	CUX1	chr15:49841408-49841645	K562	blood:	n/a	n/a
22	E2F4	chr15:49851300-49851388	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr15:49867799-49867965	MCF10A-Er-Src	breast:	n/a	n/a
24	ELF1	chr15:49885280-49885457	HepG2	liver:	n/a	n/a
25	ELF1	chr15:49885155-49885507	HepG2	liver:	n/a	n/a
26	FOS	chr15:49851188-49851448	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr15:49847779-49848024	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr15:49851248-49851420	MCF10A-Er-Src	breast:	n/a	n/a
29	FOXA1	chr15:49884907-49885210	HepG2	liver:	n/a	n/a
30	FOXA1	chr15:49841528-49841810	HepG2	liver:	n/a	n/a
31	FOXA1	chr15:49884870-49885205	HepG2	liver:	n/a	n/a
32	FOXA1	chr15:49886816-49887102	HepG2	liver:	n/a	n/a
33	FOXA1	chr15:49884882-49885356	HepG2	liver:	n/a	n/a
34	FOXA1	chr15:49884939-49885210	HepG2	liver:	n/a	n/a
35	FOXA2	chr15:49886770-49887012	HepG2	liver:	n/a	n/a
36	FOXA2	chr15:49884914-49885223	A549	lung:	n/a	n/a
37	FOXA2	chr15:49884918-49885225	HepG2	liver:	n/a	n/a
38	GATA1	chr15:49865545-49866171	PBDE	blood:	n/a	n/a
39	GATA2	chr15:49841527-49841823	K562	blood:	n/a	n/a
40	GATA3	chr15:49867956-49868131	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr15:49858514-49858595	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr15:49869701-49870087	MCF-7	breast:	n/a	n/a
43	GATA3	chr15:49862208-49862413	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr15:49887607-49888406	MCF-7	breast:	n/a	n/a
45	HEY1	chr15:49885128-49885393	HepG2	liver:	n/a	n/a
46	HEY1	chr15:49885018-49885369	HepG2	liver:	n/a	n/a
47	IRF1	chr15:49881359-49881597	K562	blood:	n/a	chr15:49881438-49881452 chr15:49881430-49881450 chr15:49881437-49881451 chr15:49881432-49881449 chr15:49881432-49881446 chr15:49881436-49881456 chr15:49881434-49881448 chr15:49881437-49881450 chr15:49881437-49881450 chr15:49881436-49881447 chr15:49881437-49881450 chr15:49881437-49881448 chr15:49881437-49881450 chr15:49881438-49881448
48	IRF1	chr15:49881243-49881595	K562	blood:	n/a	chr15:49881438-49881452 chr15:49881430-49881450 chr15:49881437-49881451 chr15:49881432-49881449 chr15:49881432-49881446 chr15:49881436-49881456 chr15:49881434-49881448 chr15:49881437-49881450 chr15:49881437-49881450 chr15:49881436-49881447 chr15:49881437-49881450 chr15:49881437-49881448 chr15:49881437-49881450 chr15:49881438-49881448
49	JUN	chr15:49847756-49847938	HepG2	liver:	n/a	n/a
50	JUN	chr15:49852400-49852581	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:49843305-49843355	T-47D	breast:	n/a
2	chr15:49843305-49843355	SAEC	small airway:	n/a
3	chr15:49843305-49843355	GM12892	blood:	n/a
4	chr15:49843305-49843355	HUVEC	blood vessel:	n/a
5	chr15:49843305-49843355	GM19239	blood:	n/a
6	chr15:49843305-49843355	HRE	kidney:	n/a
7	chr15:49843305-49843355	HCM	heart:	n/a
8	chr15:49843305-49843355	IMR90	lung:	fetal
9	chr15:49843305-49843355	HIPEpiC	eye:	n/a
10	chr15:49843305-49843355	BJ	skin:	n/a
11	chr15:49843305-49843355	HCF	heart:	n/a
12	chr15:49843305-49843355	Hela-S3	cervix:	n/a
13	chr15:49843305-49843355	U87	brain:	n/a
14	chr15:49843305-49843355	AG09319	gingival:	n/a
15	chr15:49843305-49843355	HPAEpiC	pulmonary alveolar:	n/a
16	chr15:49843305-49843355	K562	blood:	n/a
17	chr15:49843305-49843355	AG04449	skin:	fetal
18	chr15:49843305-49843355	HNPCEpiC	eye:	n/a
19	chr15:49843305-49843355	AG04450	lung:	fetal
20	chr15:49843305-49843355	H1-hESC	embryonic stem cell:	embryo
21	chr15:49843305-49843355	NB4	blood:	n/a
22	chr15:49843305-49843355	Hepatocyte	liver:	n/a
23	chr15:49843305-49843355	ovcar-3	ovarian:	n/a
24	chr15:49843305-49843355	HEK293	kidney:	embryo
25	chr15:49843305-49843355	Caco-2	colon:	n/a
26	chr15:49843305-49843355	A549	lung:	n/a
27	chr15:49843305-49843355	HCT-116	colon:	n/a
28	chr15:49843305-49843355	HRCEpiC	kidney:	n/a
29	chr15:49843305-49843355	HRPEpiC	eye:	n/a
30	chr15:49843305-49843355	Jurkat	blood:	n/a
31	chr15:49843305-49843355	PrEC	prostate:	n/a
32	chr15:49843305-49843355	LNCaP	prostate:	n/a
33	chr15:49843305-49843355	AoSMC	blood vessel:	n/a
34	chr15:49843305-49843355	SK-N-SH	brain:	n/a
35	chr15:49843305-49843355	CMK	blood:	n/a
36	chr15:49843305-49843355	HepG2	liver:	n/a
37	chr15:49843305-49843355	SK-N-MC	brain:	n/a
38	chr15:49843305-49843355	MCF10A-Er-Src	breast:	n/a
39	chr15:49843305-49843355	ProgFib	skin:	n/a
40	chr15:49843305-49843355	HMEC	breast:	n/a
41	chr15:49843305-49843355	BE2_C	brain:	n/a
42	chr15:49843305-49843355	NT2-D1	testis:	n/a
43	chr15:49843305-49843355	NH-A	brain:	n/a
44	chr15:49843305-49843355	HL-60	blood:	n/a
45	chr15:49843305-49843355	SKMC	muscle:	n/a
46	chr15:49843305-49843355	AG10803	skin:	n/a
47	chr15:49843305-49843355	HEEpiC	esophagus:	n/a
48	chr15:49843305-49843355	GM12891	blood:	n/a
49	chr15:49843305-49843355	HAEpiC	amniotic membrane:	n/a
50	chr15:49843305-49843355	NHBE	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:49848023..49849744-chr15:49849965..49852877,2	MCF-7	breast:
2	chr15:49850414..49853063-chr15:49861863..49863640,2	MCF-7	breast:
3	chr15:49849928..49852326-chr15:49917906..49919869,2	MCF-7	breast:
4	chr15:49850123..49851824-chr15:49869687..49871274,2	MCF-7	breast:
5	chr15:49850123..49851824-chr15:49869687..49871274,2	MCF-7	breast:
6	chr15:49857009..49858910-chr15:49862176..49864573,2	K562	blood:
7	chr15:49857690..49860916-chr15:49911493..49914714,3	MCF-7	breast:
8	chr15:49848023..49849744-chr15:49849965..49852877,2	MCF-7	breast:
9	chr15:49857009..49858910-chr15:49862176..49864573,2	K562	blood:
10	chr15:49845853..49848692-chr15:49911908..49914705,2	MCF-7	breast:
11	chr15:49850414..49853063-chr15:49861863..49863640,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP8B4-1	chr15:49866935-49867306	NONHSAT042381
2	lnc-ATP8B4-1	chr15:49881973-49882204	NONHSAT042381
3	lnc-ATP8B4-1	chr15:49868938-49869042	NONHSAT042381
4	lnc-ATP8B4-1	chr15:49880213-49880280	NONHSAT042382
5	lnc-ATP8B4-1	chr15:49869826-49869861	NONHSAT042381
6	lnc-ATP8B4-1	chr15:49880213-49880280	NONHSAT042381
7	lnc-ATP8B4-1	chr15:49881971-49882204	NONHSAT042383
8	lnc-ATP8B4-1	chr15:49867058-49867306	NONHSAT042382
9	lnc-ATP8B4-1	chr15:49881973-49882204	NONHSAT042382

No data

Variant related genes	Relation type
FAM227B	TF binding region
FAM227B	CpG island
ENSG00000104047	chromatin interactions
ENSG00000166262	chromatin interactions

Extended variants
information (count: 1598 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1598 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533625664	chr15:49845856-49845857	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548993779	chr15:49845868-49845869	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs372768971	chr15:49845873-49845874	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs28822970	chr15:49845874-49845875	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs369139935	chr15:49845896-49845897	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571478575	chr15:49845914-49845915	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556896134	chr15:49845941-49845942	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs80023777	chr15:49846058-49846059	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs368762244	chr15:49846087-49846088	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs539236040	chr15:49846089-49846090	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs372674735	chr15:49846092-49846093	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs534773311	chr15:49846102-49846103	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs554043843	chr15:49846117-49846118	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572530280	chr15:49846131-49846132	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs184372485	chr15:49846169-49846170	ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs189149795	chr15:49846273-49846274	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560987117	chr15:49846277-49846278	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576024366	chr15:49846314-49846315	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs543366540	chr15:49846339-49846340	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376062700	chr15:49846350-49846351	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs182031073	chr15:49846375-49846376	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533044744	chr15:49846389-49846390	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532344966	chr15:49846409-49846410	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs551576488	chr15:49846423-49846424	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs74014341	chr15:49846426-49846427	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527418774	chr15:49846472-49846473	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549093066	chr15:49846495-49846496	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145985663	chr15:49846520-49846521	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537847372	chr15:49846530-49846531	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184435328	chr15:49846580-49846581	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs8030761	chr15:49846603-49846604	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs538940856	chr15:49846604-49846605	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs138650492	chr15:49846614-49846615	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149321656	chr15:49846671-49846672	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs536799882	chr15:49846672-49846673	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs115596760	chr15:49846685-49846686	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs576087725	chr15:49846699-49846700	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543428153	chr15:49846799-49846800	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377345026	chr15:49846802-49846803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs114524690	chr15:49846818-49846819	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs577899391	chr15:49846869-49846870	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560762617	chr15:49846925-49846926	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs144467325	chr15:49846949-49846950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs527494154	chr15:49847005-49847006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189282126	chr15:49847017-49847018	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538000710	chr15:49847028-49847029	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs560979245	chr15:49847059-49847060	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs79072480	chr15:49847089-49847090	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs574164998	chr15:49847099-49847100	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs118060816	chr15:49847143-49847144	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49846000-49846200	ZNF genes & repeats	Pancreas	Pancrea
2	chr15:49846600-49846800	Enhancers	Right Ventricle	heart
3	chr15:49846800-49850800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:49846800-49852800	Weak transcription	Right Ventricle	heart
5	chr15:49850400-49851600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr15:49850800-49851600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:49850800-49851600	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr15:49850800-49851800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
9	chr15:49850800-49851800	Enhancers	Hela-S3	cervix
10	chr15:49851000-49851600	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr15:49851000-49851800	ZNF genes & repeats	Primary monocytes fromperipheralblood	blood
12	chr15:49851400-49851600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr15:49851400-49851600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr15:49851600-49851800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
15	chr15:49851800-49855200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr15:49855200-49856200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
17	chr15:49856200-49897400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr15:49859600-49860200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr15:49861600-49868200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr15:49862600-49863400	Enhancers	Primary T cells from cord blood	blood
21	chr15:49862600-49869600	Weak transcription	Brain Angular Gyrus	brain
22	chr15:49863400-49864600	Weak transcription	Primary T cells from cord blood	blood
23	chr15:49863400-49874800	Weak transcription	Fetal Kidney	kidney
24	chr15:49863800-49865600	Weak transcription	Left Ventricle	heart
25	chr15:49863800-49865600	Weak transcription	Ovary	ovary
26	chr15:49863800-49881400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr15:49864000-49866400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:49864000-49873000	Weak transcription	HSMM	muscle
29	chr15:49864600-49865200	ZNF genes & repeats	Primary T cells from cord blood	blood
30	chr15:49864600-49866400	Weak transcription	Lung	lung
31	chr15:49864600-49866800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:49864600-49867000	Weak transcription	Fetal Stomach	stomach
33	chr15:49864600-49878200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr15:49864800-49865000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr15:49864800-49878600	Weak transcription	Primary B cells from cord blood	blood
36	chr15:49864800-49881600	Weak transcription	Brain Substantia Nigra	brain
37	chr15:49865000-49865200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
38	chr15:49865000-49866800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
39	chr15:49865000-49875400	Weak transcription	HSMMtube	muscle
40	chr15:49865000-49880400	Weak transcription	Fetal Lung	lung
41	chr15:49865200-49866400	Weak transcription	Primary T cells from cord blood	blood
42	chr15:49865200-49866800	Strong transcription	Primary hematopoietic stem cells	blood
43	chr15:49865400-49881400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr15:49865400-49881800	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr15:49865600-49865800	ZNF genes & repeats	Gastric	stomach
46	chr15:49865600-49866400	Weak transcription	Liver	Liver
47	chr15:49865600-49866800	Strong transcription	Left Ventricle	heart
48	chr15:49865600-49866800	Strong transcription	Ovary	ovary
49	chr15:49865800-49868400	Weak transcription	Gastric	stomach
50	chr15:49865800-49870400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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