Variant report

Variant	nsv591290
Chromosome Location	chr3:111427455-111462570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1145)
CpG islands
(count:490)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:111451923-111452414	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:111445806-111446131	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:111458101-111458451	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:111454105-111454985	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:111436407-111436750	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:111451113-111451510	HepG2	liver:	n/a	n/a
7	ATF2	chr3:111436357-111436771	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:111436325-111436746	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr3:111453975-111454814	HCT-116	colon:	n/a	n/a
10	ATF3	chr3:111454001-111454719	A549	lung:	n/a	n/a
11	ATF3	chr3:111454010-111454671	A549	lung:	n/a	n/a
12	ATF3	chr3:111453955-111454752	HCT-116	colon:	n/a	n/a
13	BACH1	chr3:111436408-111436751	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:111442417-111442770	GM12878	blood:	n/a	chr3:111442616-111442627
15	BATF	chr3:111442425-111442751	GM12878	blood:	n/a	chr3:111442616-111442627
16	BCL3	chr3:111453981-111454688	A549	lung:	n/a	n/a
17	BCL3	chr3:111453969-111454764	A549	lung:	n/a	n/a
18	BHLHE40	chr3:111458164-111458661	HepG2	liver:	n/a	n/a
19	BRCA1	chr3:111456289-111456894	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr3:111434869-111434931	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr3:111458007-111458680	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr3:111453832-111454698	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr3:111436398-111436758	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr3:111453963-111454790	HCT-116	colon:	n/a	n/a
25	CBX3	chr3:111453799-111454737	HCT-116	colon:	n/a	n/a
26	CEBPB	chr3:111453940-111454823	HCT-116	colon:	n/a	chr3:111454441-111454452
27	CEBPB	chr3:111454268-111454498	H1-hESC	embryonic stem cell:	n/a	chr3:111454441-111454452
28	CEBPB	chr3:111458127-111458469	A549	lung:	n/a	n/a
29	CEBPB	chr3:111442478-111442656	A549	lung:	n/a	n/a
30	CEBPB	chr3:111454060-111454713	A549	lung:	n/a	chr3:111454441-111454452
31	CEBPB	chr3:111454083-111455034	A549	lung:	n/a	chr3:111454441-111454452
32	CEBPB	chr3:111456485-111456930	IMR90	lung:	n/a	n/a
33	CEBPB	chr3:111458071-111458680	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:111454219-111454708	MCF-7	breast:	n/a	chr3:111454441-111454452
35	CEBPB	chr3:111456500-111456892	A549	lung:	n/a	n/a
36	CEBPB	chr3:111456379-111456966	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:111442357-111442708	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:111442388-111442725	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:111456479-111456927	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:111454323-111454542	HepG2	liver:	n/a	chr3:111454441-111454452
41	CEBPB	chr3:111458158-111458488	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:111454066-111454640	HepG2	liver:	n/a	chr3:111454441-111454452
43	CEBPB	chr3:111454097-111454660	IMR90	lung:	n/a	chr3:111454441-111454452
44	CEBPB	chr3:111454255-111454640	HepG2	liver:	n/a	chr3:111454441-111454452
45	CEBPB	chr3:111454089-111454687	ECC-1	luminal epithelium:	n/a	chr3:111454441-111454452
46	CEBPB	chr3:111436380-111436774	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:111457919-111459111	HCT-116	colon:	n/a	n/a
48	CEBPB	chr3:111439683-111439733	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:111454245-111454575	HepG2	liver:	n/a	chr3:111454441-111454452
50	CEBPB	chr3:111458054-111458480	IMR90	lung:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:111450718-111450768	ProgFib	skin:	n/a
2	chr3:111456900-111456950	HRPEpiC	eye:	n/a
3	chr3:111450718-111450768	ProgFib	skin:	n/a
4	chr3:111456900-111456950	HRPEpiC	eye:	n/a
5	chr3:111450718-111450768	CMK	blood:	n/a
6	chr3:111456900-111456950	PFSK-1	brain:	n/a
7	chr3:111448206-111448256	GM06990	blood:	n/a
8	chr3:111451090-111451140	GM06990	blood:	n/a
9	chr3:111456900-111456950	HCT-116	colon:	n/a
10	chr3:111456900-111456950	IMR90	lung:	fetal
11	chr3:111442336-111442386	AoSMC	blood vessel:	n/a
12	chr3:111451470-111451520	NHBE	bronchial:	n/a
13	chr3:111451273-111451323	NH-A	brain:	n/a
14	chr3:111436574-111436624	HRE	kidney:	n/a
15	chr3:111451470-111451520	GM12891	blood:	n/a
16	chr3:111456900-111456950	AG09319	gingival:	n/a
17	chr3:111448206-111448256	AG10803	skin:	n/a
18	chr3:111456900-111456950	HEK293	kidney:	embryo
19	chr3:111442336-111442386	HCF	heart:	n/a
20	chr3:111456900-111456950	NH-A	brain:	n/a
21	chr3:111436574-111436624	HMEC	breast:	n/a
22	chr3:111450718-111450768	NB4	blood:	n/a
23	chr3:111436574-111436624	HRPEpiC	eye:	n/a
24	chr3:111442336-111442386	SAEC	small airway:	n/a
25	chr3:111436574-111436624	NH-A	brain:	n/a
26	chr3:111451273-111451323	HCT-116	colon:	n/a
27	chr3:111436574-111436624	ovcar-3	ovarian:	n/a
28	chr3:111450718-111450768	Caco-2	colon:	n/a
29	chr3:111442336-111442386	HCPEpiC	choroid plexus:	n/a
30	chr3:111436574-111436624	MCF10A-Er-Src	breast:	n/a
31	chr3:111442336-111442386	NHBE	bronchial:	n/a
32	chr3:111451273-111451323	AG09309	skin:	n/a
33	chr3:111442336-111442386	PrEC	prostate:	n/a
34	chr3:111451470-111451520	HL-60	blood:	n/a
35	chr3:111436574-111436624	HPAEpiC	pulmonary alveolar:	n/a
36	chr3:111450718-111450768	AG04450	lung:	fetal
37	chr3:111436574-111436624	A549	lung:	n/a
38	chr3:111436574-111436624	HL-60	blood:	n/a
39	chr3:111451470-111451520	PANC-1	pancreas:	n/a
40	chr3:111450718-111450768	HEK293	kidney:	embryo
41	chr3:111451273-111451323	HUVEC	blood vessel:	n/a
42	chr3:111448206-111448256	HL-60	blood:	n/a
43	chr3:111436574-111436624	NHDF-neo	bronchial:	n/a
44	chr3:111436574-111436624	HEK293	kidney:	embryo
45	chr3:111451273-111451323	NT2-D1	testis:	n/a
46	chr3:111456900-111456950	Hepatocyte	liver:	n/a
47	chr3:111451470-111451520	AG09319	gingival:	n/a
48	chr3:111448206-111448256	K562	blood:	n/a
49	chr3:111456900-111456950	AoSMC	blood vessel:	n/a
50	chr3:111448206-111448256	HCPEpiC	choroid plexus:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:111433009..111433546-chr3:111686227..111687119,2	MCF-7	breast:
2	chr3:111456141..111458585-chr3:111526075..111527610,2	MCF-7	breast:
3	chr3:111435949..111437121-chr3:111578992..111579967,7	MCF-7	breast:
4	chr3:111452923..111457246-chr3:111577346..111581538,6	MCF-7	breast:
5	chr3:111436015..111437110-chr3:111686600..111687236,4	MCF-7	breast:
6	chr3:111410859..111413288-chr3:111426130..111428349,2	MCF-7	breast:
7	chr3:111448469..111451104-chr3:111452736..111455582,2	MCF-7	breast:
8	chr3:111435344..111436034-chr3:111659001..111659706,2	K562	blood:
9	chr3:111436461..111439454-chr3:111578478..111580162,2	MCF-7	breast:
10	chr3:111434533..111435893-chr3:111686244..111687114,4	MCF-7	breast:
11	chr3:111436245..111438347-chr3:111577161..111580902,4	MCF-7	breast:
12	chr3:111459238..111460946-chr3:111462346..111465281,2	MCF-7	breast:
13	chr3:111296456..111297303-chr3:111434475..111435453,4	MCF-7	breast:
14	chr3:111436107..111437022-chr3:111686211..111687194,8	K562	blood:
15	chr3:111436056..111437320-chr3:111577599..111579917,18	MCF-7	breast:
16	chr3:111448052..111452466-chr3:111452775..111456031,4	MCF-7	breast:
17	chr3:111453729..111455773-chr3:111578184..111580273,2	MCF-7	breast:
18	chr3:111413561..111415397-chr3:111433422..111435003,2	MCF-7	breast:
19	chr3:111457259..111459990-chr3:111577947..111581239,4	MCF-7	breast:
20	chr3:111425995..111428417-chr3:111430718..111432943,2	MCF-7	breast:
21	chr3:111452077..111454237-chr3:111460686..111462940,2	K562	blood:
22	chr3:111448469..111451104-chr3:111452736..111455582,2	MCF-7	breast:
23	chr1:234297659..234298530-chr3:111435438..111436357,2	MCF-7	breast:
24	chr3:111387271..111388418-chr3:111434523..111435377,4	MCF-7	breast:
25	chr3:111452077..111454237-chr3:111460686..111462940,2	K562	blood:
26	chr3:111435213..111435852-chr3:111686469..111687089,2	MCF-7	breast:
27	chr3:111387866..111388370-chr3:111434530..111435197,2	MCF-7	breast:
28	chr3:111387525..111388405-chr3:111434480..111435434,2	K562	blood:
29	chr3:111436073..111437457-chr3:111686120..111687700,18	MCF-7	breast:
30	chr3:111448045..111449995-chr3:111576976..111579247,2	MCF-7	breast:
31	chr3:111459238..111460946-chr3:111462346..111465281,2	MCF-7	breast:
32	chr3:111436392..111436951-chr3:111732026..111733001,2	MCF-7	breast:
33	chr3:111436085..111436804-chr3:111732107..111732656,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHLDB2-1	chr3:111451308-111451550	NONHSAT091150

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PLCXD2	hsa-miR-16-5p	chr3:111445122-111445146

Variant related genes	Relation type
PLCXD2	TF binding region
PHLDB2	TF binding region
PLCXD2	CpG island
PHLDB2	CpG island
ENSG00000240891	chromatin interactions
ENSG00000144824	chromatin interactions

Extended variants
information (count: 1245 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1245 , 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	rs1877575	chr3:111427455-111427456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112022969	chr3:111427460-111427461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs139814643	chr3:111427527-111427528	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs34873993	chr3:111427536-111427537	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547812707	chr3:111427547-111427548	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567936532	chr3:111427637-111427638	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145016073	chr3:111427647-111427648	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189551222	chr3:111427672-111427673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182213132	chr3:111427713-111427714	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367869512	chr3:111427720-111427721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73852864	chr3:111427723-111427724	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114743996	chr3:111427835-111427836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs138307886	chr3:111427841-111427842	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371262663	chr3:111427852-111427853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73852865	chr3:111427867-111427868	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541199265	chr3:111427883-111427884	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs372466061	chr3:111427938-111427939	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376526607	chr3:111427939-111427940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs77158477	chr3:111427957-111427958	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373289554	chr3:111427973-111427974	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554590357	chr3:111428019-111428020	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193138960	chr3:111428073-111428074	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575949088	chr3:111428106-111428107	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377408588	chr3:111428137-111428138	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185211250	chr3:111428146-111428147	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531981391	chr3:111428227-111428228	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546077033	chr3:111428257-111428258	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76157107	chr3:111428309-111428310	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs545622821	chr3:111428312-111428313	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79588369	chr3:111428314-111428315	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs372111744	chr3:111428315-111428316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559385516	chr3:111428324-111428325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs57059255	chr3:111428330-111428331	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73852867	chr3:111428331-111428332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs564828793	chr3:111428332-111428333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201841913	chr3:111428333-111428334	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs73852868	chr3:111428335-111428336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552569468	chr3:111428341-111428342	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547940929	chr3:111428372-111428373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs188479151	chr3:111428378-111428379	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs530374410	chr3:111428433-111428434	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9879325	chr3:111428467-111428468	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs184038763	chr3:111428500-111428501	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs4381908	chr3:111428527-111428528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs558817253	chr3:111428563-111428564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73852870	chr3:111428580-111428581	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531423966	chr3:111428591-111428592	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534535344	chr3:111428612-111428613	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188725098	chr3:111428638-111428639	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574395538	chr3:111428647-111428648	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111410200-111428400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr3:111410200-111433200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:111410600-111443400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:111412800-111430800	Weak transcription	Duodenum Mucosa	Duodenum
5	chr3:111415200-111454200	Weak transcription	Small Intestine	intestine
6	chr3:111415600-111430800	Weak transcription	Osteobl	bone
7	chr3:111415600-111431000	Weak transcription	HMEC	breast
8	chr3:111415600-111436000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:111415600-111436400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:111416200-111431200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr3:111418200-111442000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:111419000-111436000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr3:111419000-111436200	Weak transcription	Stomach Mucosa	stomach
14	chr3:111419600-111428600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:111419600-111431000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:111419600-111431000	Weak transcription	GM12878-XiMat	blood
17	chr3:111420400-111450600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr3:111420600-111445600	Weak transcription	HepG2	liver
19	chr3:111421400-111434600	Weak transcription	A549	lung
20	chr3:111422000-111433400	Weak transcription	HSMMtube	muscle
21	chr3:111422200-111431000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:111422600-111430800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:111423200-111430400	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr3:111423200-111434600	Weak transcription	HUVEC	blood vessel
25	chr3:111424600-111428400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr3:111424600-111441800	Weak transcription	Thymus	Thymus
27	chr3:111425000-111431400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr3:111425800-111441200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr3:111425800-111443800	Weak transcription	Dnd41	blood
30	chr3:111426200-111431200	Weak transcription	Esophagus	oesophagus
31	chr3:111426400-111430200	Weak transcription	Brain Germinal Matrix	brain
32	chr3:111426600-111428400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr3:111426600-111430000	Strong transcription	Primary B cells from peripheral blood	blood
34	chr3:111426800-111427600	Strong transcription	Fetal Intestine Small	intestine
35	chr3:111426800-111427600	Strong transcription	Sigmoid Colon	Sigmoid Colon
36	chr3:111426800-111428000	Strong transcription	Fetal Thymus	thymus
37	chr3:111426800-111428800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr3:111426800-111429400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr3:111426800-111429800	Strong transcription	Primary T cells from cord blood	blood
40	chr3:111426800-111429800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr3:111426800-111430600	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr3:111426800-111430800	Strong transcription	Primary T cells fromperipheralblood	blood
43	chr3:111426800-111431000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr3:111426800-111436400	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr3:111427000-111428600	Strong transcription	Placenta	Placenta
46	chr3:111427000-111428800	Strong transcription	Primary B cells from cord blood	blood
47	chr3:111427000-111428800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
48	chr3:111427000-111429000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:111427000-111429000	Strong transcription	Primary hematopoietic stem cells	blood
50	chr3:111427000-111431200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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