Variant report

Variant	nsv904207
Chromosome Location	chr15:50290295-50352945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:850)
CpG islands
(count:307)
Chromatin interactive
region (count:62)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:50295957-50296257	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:50347722-50347835	K562	blood:	n/a	n/a
3	ARID3A	chr15:50343998-50344331	HepG2	liver:	n/a	n/a
4	ATF1	chr15:50350381-50350590	K562	blood:	n/a	n/a
5	ATF1	chr15:50300325-50300362	K562	blood:	n/a	n/a
6	ATF2	chr15:50295912-50296587	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:50296014-50296624	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr15:50295806-50296215	A549	lung:	n/a	n/a
9	ATF3	chr15:50343969-50344296	K562	blood:	n/a	n/a
10	ATF3	chr15:50295945-50296303	GM12878	blood:	n/a	n/a
11	ATF3	chr15:50295965-50296248	K562	blood:	n/a	n/a
12	ATF3	chr15:50343869-50344464	A549	lung:	n/a	n/a
13	BCL3	chr15:50343838-50344498	A549	lung:	n/a	n/a
14	BHLHE40	chr15:50295925-50296300	HepG2	liver:	n/a	n/a
15	BHLHE40	chr15:50301988-50302148	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:50295915-50296281	K562	blood:	n/a	n/a
17	BHLHE40	chr15:50295908-50296250	GM12878	blood:	n/a	n/a
18	BRCA1	chr15:50295529-50296306	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr15:50295970-50296552	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr15:50295894-50296315	K562	blood:	n/a	n/a
21	CEBPB	chr15:50344010-50344350	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr15:50343972-50344371	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:50343986-50344448	HCT-116	colon:	n/a	n/a
24	CEBPB	chr15:50341916-50342564	A549	lung:	n/a	n/a
25	CEBPB	chr15:50295439-50295817	A549	lung:	n/a	n/a
26	CEBPB	chr15:50309916-50309981	A549	lung:	n/a	n/a
27	CEBPB	chr15:50343871-50344450	MCF-7	breast:	n/a	n/a
28	CEBPB	chr15:50343993-50344314	K562	blood:	n/a	n/a
29	CEBPB	chr15:50343729-50344508	A549	lung:	n/a	n/a
30	CEBPB	chr15:50343938-50344364	A549	lung:	n/a	n/a
31	CEBPB	chr15:50309855-50310029	K562	blood:	n/a	n/a
32	CEBPB	chr15:50295478-50295695	A549	lung:	n/a	n/a
33	CEBPB	chr15:50309786-50310024	IMR90	lung:	n/a	n/a
34	CEBPB	chr15:50295447-50296251	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr15:50343884-50344423	A549	lung:	n/a	n/a
36	CEBPB	chr15:50295464-50296420	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr15:50343938-50344348	HepG2	liver:	n/a	n/a
38	CEBPB	chr15:50347182-50347920	IMR90	lung:	n/a	n/a
39	CEBPB	chr15:50343844-50344476	MCF-7	breast:	n/a	n/a
40	CEBPB	chr15:50343992-50344290	K562	blood:	n/a	n/a
41	CEBPB	chr15:50295354-50296246	A549	lung:	n/a	n/a
42	CEBPB	chr15:50343964-50344366	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:50295500-50295692	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:50339134-50339302	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:50341895-50342459	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:50295589-50295658	K562	blood:	n/a	n/a
47	CHD2	chr15:50295895-50296286	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr15:50295944-50296616	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr15:50301661-50302193	GM12878	blood:	n/a	n/a
50	CHD2	chr15:50295938-50296228	GM12878	blood:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:50296100-50296150	HRPEpiC	eye:	n/a
2	chr15:50344782-50344832	SK-N-MC	brain:	n/a
3	chr15:50296100-50296150	HRPEpiC	eye:	n/a
4	chr15:50344782-50344832	SK-N-MC	brain:	n/a
5	chr15:50350432-50350482	PFSK-1	brain:	n/a
6	chr15:50350432-50350482	ProgFib	skin:	n/a
7	chr15:50344782-50344832	T-47D	breast:	n/a
8	chr15:50352288-50352338	HCPEpiC	choroid plexus:	n/a
9	chr15:50344782-50344832	NB4	blood:	n/a
10	chr15:50352288-50352338	SK-N-MC	brain:	n/a
11	chr15:50344782-50344832	AG09309	skin:	n/a
12	chr15:50344782-50344832	SAEC	small airway:	n/a
13	chr15:50316779-50316829	HCM	heart:	n/a
14	chr15:50344782-50344832	HCT-116	colon:	n/a
15	chr15:50296100-50296150	PFSK-1	brain:	n/a
16	chr15:50296100-50296150	ProgFib	skin:	n/a
17	chr15:50344782-50344832	HepG2	liver:	n/a
18	chr15:50350432-50350482	SK-N-MC	brain:	n/a
19	chr15:50296100-50296150	HCF	heart:	n/a
20	chr15:50296100-50296150	NHBE	bronchial:	n/a
21	chr15:50352288-50352338	ovcar-3	ovarian:	n/a
22	chr15:50316779-50316829	SKMC	muscle:	n/a
23	chr15:50350432-50350482	GM06990	blood:	n/a
24	chr15:50344782-50344832	ProgFib	skin:	n/a
25	chr15:50296100-50296150	SKMC	muscle:	n/a
26	chr15:50352288-50352338	AoSMC	blood vessel:	n/a
27	chr15:50296100-50296150	BJ	skin:	n/a
28	chr15:50350432-50350482	HEEpiC	esophagus:	n/a
29	chr15:50296100-50296150	Jurkat	blood:	n/a
30	chr15:50344782-50344832	RPTEC	kidney:	n/a
31	chr15:50344782-50344832	BE2_C	brain:	n/a
32	chr15:50344782-50344832	PANC-1	pancreas:	n/a
33	chr15:50352288-50352338	HEK293	kidney:	embryo
34	chr15:50316779-50316829	AG04449	skin:	fetal
35	chr15:50350432-50350482	HepG2	liver:	n/a
36	chr15:50316779-50316829	ovcar-3	ovarian:	n/a
37	chr15:50296100-50296150	MCF10A-Er-Src	breast:	n/a
38	chr15:50316779-50316829	A549	lung:	n/a
39	chr15:50296100-50296150	PANC-1	pancreas:	n/a
40	chr15:50352288-50352338	HL-60	blood:	n/a
41	chr15:50296100-50296150	HAEpiC	amniotic membrane:	n/a
42	chr15:50344782-50344832	HMEC	breast:	n/a
43	chr15:50296100-50296150	U87	brain:	n/a
44	chr15:50350432-50350482	MCF10A-Er-Src	breast:	n/a
45	chr15:50316779-50316829	Jurkat	blood:	n/a
46	chr15:50350432-50350482	CMK	blood:	n/a
47	chr15:50352288-50352338	AG09309	skin:	n/a
48	chr15:50344782-50344832	HL-60	blood:	n/a
49	chr15:50344782-50344832	HCF	heart:	n/a
50	chr15:50350432-50350482	HAEpiC	amniotic membrane:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:50300655..50303212-chr15:50310956..50313515,2	MCF-7	breast:
2	chr15:50193943..50194801-chr15:50295649..50296194,2	MCF-7	breast:
3	chr15:49813884..49814632-chr15:50343852..50344661,2	MCF-7	breast:
4	chr15:50296030..50296784-chr15:50438463..50439304,2	MCF-7	breast:
5	chr15:49911881..49914598-chr15:50296077..50298742,3	MCF-7	breast:
6	chr15:49763327..49764266-chr15:50295694..50296534,2	K562	blood:
7	chr15:50332088..50333712-chr15:50350541..50352729,2	MCF-7	breast:
8	chr15:50168577..50169691-chr15:50343449..50344653,12	MCF-7	breast:
9	chr15:50168671..50170291-chr15:50295598..50297002,27	MCF-7	breast:
10	chr15:50331487..50333450-chr15:50352450..50354634,2	K562	blood:
11	chr15:50346066..50347875-chr15:50350812..50353705,2	MCF-7	breast:
12	chr15:50297914..50300377-chr15:50303552..50305087,2	K562	blood:
13	chr15:50295364..50296554-chr15:50343746..50344327,4	MCF-7	breast:
14	chr15:50313089..50314715-chr15:50316842..50319496,2	K562	blood:
15	chr15:50295364..50296554-chr15:50343746..50344327,4	MCF-7	breast:
16	chr15:50291875..50294417-chr15:50301462..50303817,2	MCF-7	breast:
17	chr15:50295676..50296612-chr15:50343747..50344632,9	MCF-7	breast:
18	chr15:49813709..49814641-chr15:50343905..50344674,5	MCF-7	breast:
19	chr15:50291875..50294417-chr15:50301462..50303817,2	MCF-7	breast:
20	chr15:50167838..50170752-chr15:50297771..50300862,3	MCF-7	breast:
21	chr15:50300799..50302850-chr15:50303826..50306378,3	K562	blood:
22	chr15:50168665..50170078-chr15:50295569..50296665,10	MCF-7	breast:
23	chr15:50277715..50280459-chr15:50288291..50290867,2	MCF-7	breast:
24	chr15:50299476..50301572-chr15:50306400..50308140,2	MCF-7	breast:
25	chr15:50330960..50333313-chr15:50430196..50432185,2	MCF-7	breast:
26	chr15:49527514..49528112-chr15:50295833..50296585,3	K562	blood:
27	chr15:50342963..50345133-chr15:50348674..50350890,2	MCF-7	breast:
28	chr15:50321086..50325244-chr15:50330201..50333799,4	MCF-7	breast:
29	chr15:50343838..50344709-chr15:50437300..50438173,3	MCF-7	breast:
30	chr15:50342963..50345133-chr15:50348674..50350890,2	MCF-7	breast:
31	chr15:50295676..50296612-chr15:50343747..50344632,9	MCF-7	breast:
32	chr15:50293833..50297239-chr15:50342287..50344568,3	MCF-7	breast:
33	chr15:50346066..50347875-chr15:50350812..50353705,2	MCF-7	breast:
34	chr15:50331487..50333450-chr15:50352450..50354634,2	K562	blood:
35	chr15:50166426..50168186-chr15:50342851..50345400,2	MCF-7	breast:
36	chr15:50295757..50297489-chr15:50308752..50310287,2	MCF-7	breast:
37	chr15:50299476..50301572-chr15:50306400..50308140,2	MCF-7	breast:
38	chr15:49813707..49814631-chr15:50295905..50296603,3	MCF-7	breast:
39	chr15:50332088..50333712-chr15:50350541..50352729,2	MCF-7	breast:
40	chr15:50293833..50297239-chr15:50342287..50344568,3	MCF-7	breast:
41	chr15:50287759..50289399-chr15:50326998..50328987,2	MCF-7	breast:
42	chr15:50300655..50303212-chr15:50310956..50313515,2	MCF-7	breast:
43	chr15:50297914..50300377-chr15:50303552..50305087,2	K562	blood:
44	chr15:50349881..50352868-chr15:50355491..50358841,3	MCF-7	breast:
45	chr15:50168669..50169329-chr15:50343948..50344644,2	MCF-7	breast:
46	chr15:49898446..49899204-chr15:50344444..50344972,2	MCF-7	breast:
47	chr15:49898616..49899303-chr15:50295594..50296454,4	MCF-7	breast:
48	chr15:49930312..49931293-chr15:50295864..50296533,3	MCF-7	breast:
49	chr15:50343799..50344658-chr15:50430684..50431213,3	MCF-7	breast:
50	chr15:49763251..49764501-chr15:50295657..50296544,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf33-1	chr15:50303042-50303114	NONHSAT042399

No data

Variant related genes	Relation type
ATP8B4	TF binding region
ATP8B4	CpG island
ENSG00000104043	chromatin interactions
ENSG00000244879	chromatin interactions
ENSG00000104047	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000166262	chromatin interactions

Extended variants
information (count: 2259 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2413998	chr15:50290295-50290296	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34025439	chr15:50290306-50290307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9302151	chr15:50290361-50290362	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs560175193	chr15:50290376-50290377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367870444	chr15:50290380-50290381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74825048	chr15:50290382-50290383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549072514	chr15:50290393-50290394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567484237	chr15:50290473-50290474	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs182854297	chr15:50290506-50290507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186126140	chr15:50290514-50290515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571497236	chr15:50290517-50290518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538911897	chr15:50290526-50290527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371423895	chr15:50290564-50290565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551393349	chr15:50290578-50290579	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190992381	chr15:50290633-50290634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374520217	chr15:50290637-50290638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555403258	chr15:50290638-50290639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368763071	chr15:50290644-50290645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183556159	chr15:50290645-50290646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561021847	chr15:50290662-50290663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577737862	chr15:50290709-50290710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556711301	chr15:50290741-50290742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs578212683	chr15:50290752-50290753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545249451	chr15:50290807-50290808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545661339	chr15:50290821-50290822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560213901	chr15:50290844-50290845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs201519575	chr15:50290881-50290882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572037087	chr15:50290888-50290889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542753304	chr15:50290891-50290892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560917836	chr15:50290904-50290905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs531431787	chr15:50290977-50290978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62021041	chr15:50290982-50290983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549750040	chr15:50291001-50291002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs28833309	chr15:50291156-50291157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7182705	chr15:50291232-50291233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs75262180	chr15:50291233-50291234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547259465	chr15:50291239-50291240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547964276	chr15:50291259-50291260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75334793	chr15:50291282-50291283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56061303	chr15:50291302-50291303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566541051	chr15:50291309-50291310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187777730	chr15:50291364-50291365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs57881230	chr15:50291511-50291512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567697439	chr15:50291541-50291542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538321748	chr15:50291605-50291606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556508505	chr15:50291734-50291735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4550392	chr15:50291750-50291751	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs538979825	chr15:50291766-50291767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192460332	chr15:50291799-50291800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572071693	chr15:50291819-50291820	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	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
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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50268600-50290400	Strong transcription	Primary hematopoietic stem cells	blood
2	chr15:50278000-50301600	Weak transcription	Liver	Liver
3	chr15:50282000-50295600	Weak transcription	Adipose Nuclei	Adipose
4	chr15:50282200-50290400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr15:50283000-50290800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr15:50283400-50290400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr15:50287400-50294400	Weak transcription	Fetal Stomach	stomach
8	chr15:50287600-50296000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:50288400-50294000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr15:50288600-50293600	Weak transcription	Colon Smooth Muscle	Colon
11	chr15:50289600-50291800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr15:50290000-50291800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr15:50290200-50291600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:50290200-50291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:50290400-50291800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr15:50290400-50291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:50290400-50292000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr15:50290800-50291600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr15:50291600-50294600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr15:50291600-50294600	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr15:50291800-50292800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr15:50291800-50293600	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr15:50291800-50293800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr15:50291800-50294800	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr15:50291800-50296200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr15:50292000-50292600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr15:50292000-50292600	Strong transcription	Primary hematopoietic stem cells	blood
28	chr15:50292600-50294200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr15:50292600-50295600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:50292800-50294400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr15:50293600-50293800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr15:50293600-50293800	Enhancers	Ovary	ovary
33	chr15:50293600-50296200	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr15:50293600-50296400	Enhancers	Colon Smooth Muscle	Colon
35	chr15:50293600-50297200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:50293800-50294400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr15:50293800-50295800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:50293800-50296000	Weak transcription	Ovary	ovary
39	chr15:50294000-50294800	Enhancers	Rectal Smooth Muscle	rectum
40	chr15:50294200-50295600	Strong transcription	Primary hematopoietic stem cells	blood
41	chr15:50294400-50294600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr15:50294400-50294600	Enhancers	Fetal Intestine Small	intestine
43	chr15:50294400-50294600	Enhancers	Fetal Stomach	stomach
44	chr15:50294400-50295000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr15:50294400-50295400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:50294600-50294800	Enhancers	Brain Substantia Nigra	brain
47	chr15:50294600-50295600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr15:50294600-50295600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr15:50294600-50295600	Weak transcription	Fetal Intestine Small	intestine
50	chr15:50294600-50295600	Weak transcription	Fetal Stomach	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links