Variant report

Variant	nsv1000519
Chromosome Location	chr3:139159300-139206245
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:290)
CpG islands
(count:367)
Chromatin interactive
region (count:14)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:139191977-139192234	K562	blood:	n/a	n/a
2	BACH1	chr3:139194609-139194677	K562	blood:	n/a	n/a
3	BHLHE40	chr3:139192087-139192091	K562	blood:	n/a	n/a
4	BRCA1	chr3:139198154-139198165	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:139177200-139177563	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:139191957-139192273	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr3:139177153-139177627	A549	lung:	n/a	n/a
8	CEBPB	chr3:139192003-139192183	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:139177198-139177560	K562	blood:	n/a	n/a
10	CEBPB	chr3:139177237-139177559	A549	lung:	n/a	n/a
11	CEBPB	chr3:139177245-139177545	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr3:139191910-139192402	HCT-116	colon:	n/a	n/a
13	CEBPB	chr3:139177205-139177555	IMR90	lung:	n/a	n/a
14	CTCF	chr3:139174780-139174930	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr3:139174760-139174910	GM12873	blood:	n/a	n/a
16	CTCF	chr3:139174780-139174930	GM12873	blood:	n/a	n/a
17	CTCF	chr3:139174740-139175010	HVMF	connective:	n/a	n/a
18	CTCF	chr3:139174809-139174900	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr3:139174690-139174985	K562	blood:	n/a	chr3:139174695-139174703
20	CTCF	chr3:139174706-139174950	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr3:139174740-139174890	HFF	foreskin:	n/a	n/a
22	CTCF	chr3:139174720-139174870	RPTEC	kidney:	n/a	n/a
23	CTCF	chr3:139174880-139175030	GM12870	blood:	n/a	n/a
24	CTCF	chr3:139174720-139174870	HPF	lung:	n/a	n/a
25	CTCF	chr3:139174740-139174890	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr3:139185320-139185470	Caco-2	colon:	n/a	n/a
27	CTCF	chr3:139174824-139174948	LNCaP	prostate:	n/a	n/a
28	CTCF	chr3:139174740-139174890	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr3:139174840-139174990	GM12874	blood:	n/a	n/a
30	CTCF	chr3:139161676-139161687	HepG2	liver:	n/a	n/a
31	CTCF	chr3:139185435-139185488	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr3:139174780-139174930	GM12864	blood:	n/a	n/a
33	CTCF	chr3:139174620-139174770	GM12870	blood:	n/a	chr3:139174695-139174703
34	CTCF	chr3:139174720-139174870	GM12865	blood:	n/a	n/a
35	CTCF	chr3:139174799-139174924	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr3:139185433-139185455	A549	lung:	n/a	n/a
37	CTCF	chr3:139185454-139185498	K562	blood:	n/a	n/a
38	CTCF	chr3:139185444-139185456	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:139174760-139174910	HMF	breast:	n/a	n/a
40	CTCF	chr3:139174780-139174930	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr3:139174766-139174934	GM12878	blood:	n/a	n/a
42	CTCF	chr3:139174719-139174942	HepG2	liver:	n/a	n/a
43	CTCF	chr3:139174780-139174930	GM12871	blood:	n/a	n/a
44	CTCF	chr3:139180597-139180659	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:139174660-139174810	GM12868	blood:	n/a	chr3:139174695-139174703
46	CTCF	chr3:139174740-139174890	HPF	lung:	n/a	n/a
47	CTCF	chr3:139174800-139174950	GM12875	blood:	n/a	n/a
48	CTCF	chr3:139185360-139185510	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:139174720-139174870	GM12874	blood:	n/a	n/a
50	CTCF	chr3:139185340-139185490	Hela-S3	cervix:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:139196813-139196863	AG04450	lung:	fetal
2	chr3:139196813-139196863	AG04450	lung:	fetal
3	chr3:139199845-139199895	AG10803	skin:	n/a
4	chr3:139199845-139199895	GM06990	blood:	n/a
5	chr3:139196779-139196829	U87	brain:	n/a
6	chr3:139196779-139196829	HRPEpiC	eye:	n/a
7	chr3:139199845-139199895	PFSK-1	brain:	n/a
8	chr3:139196779-139196829	GM06990	blood:	n/a
9	chr3:139196779-139196829	NH-A	brain:	n/a
10	chr3:139199845-139199895	HNPCEpiC	eye:	n/a
11	chr3:139196779-139196829	T-47D	breast:	n/a
12	chr3:139196779-139196829	H1-hESC	embryonic stem cell:	embryo
13	chr3:139195319-139195369	NB4	blood:	n/a
14	chr3:139195319-139195369	HCPEpiC	choroid plexus:	n/a
15	chr3:139196491-139196541	AG09309	skin:	n/a
16	chr3:139195319-139195369	Jurkat	blood:	n/a
17	chr3:139196491-139196541	K562	blood:	n/a
18	chr3:139196813-139196863	AG09319	gingival:	n/a
19	chr3:139173779-139173829	HCPEpiC	choroid plexus:	n/a
20	chr3:139196491-139196541	GM12892	blood:	n/a
21	chr3:139196779-139196829	HCPEpiC	choroid plexus:	n/a
22	chr3:139196813-139196863	Hela-S3	cervix:	n/a
23	chr3:139196779-139196829	LNCaP	prostate:	n/a
24	chr3:139196491-139196541	Caco-2	colon:	n/a
25	chr3:139173779-139173829	HCF	heart:	n/a
26	chr3:139196813-139196863	SAEC	small airway:	n/a
27	chr3:139173779-139173829	Jurkat	blood:	n/a
28	chr3:139195319-139195369	PANC-1	pancreas:	n/a
29	chr3:139196491-139196541	HMEC	breast:	n/a
30	chr3:139199845-139199895	Hepatocyte	liver:	n/a
31	chr3:139196779-139196829	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:139199845-139199895	HCT-116	colon:	n/a
33	chr3:139196813-139196863	HCPEpiC	choroid plexus:	n/a
34	chr3:139195319-139195369	AG04449	skin:	fetal
35	chr3:139173779-139173829	PANC-1	pancreas:	n/a
36	chr3:139199845-139199895	SAEC	small airway:	n/a
37	chr3:139199845-139199895	IMR90	lung:	fetal
38	chr3:139196491-139196541	LNCaP	prostate:	n/a
39	chr3:139196779-139196829	PFSK-1	brain:	n/a
40	chr3:139199845-139199895	NT2-D1	testis:	n/a
41	chr3:139196779-139196829	AG09309	skin:	n/a
42	chr3:139173779-139173829	ovcar-3	ovarian:	n/a
43	chr3:139195319-139195369	LNCaP	prostate:	n/a
44	chr3:139196491-139196541	Jurkat	blood:	n/a
45	chr3:139195319-139195369	NHDF-neo	bronchial:	n/a
46	chr3:139196779-139196829	AG09319	gingival:	n/a
47	chr3:139196491-139196541	SK-N-SH	brain:	n/a
48	chr3:139196813-139196863	HMEC	breast:	n/a
49	chr3:139195319-139195369	U87	brain:	n/a
50	chr3:139199845-139199895	NHBE	bronchial:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:139164444..139166894-chr3:139178847..139180451,2	K562	blood:
2	chr21:46926680..46927202-chr3:139164975..139165475,2	HCT-116	colon:
3	chr3:139187703..139190427-chr3:139192772..139195214,2	K562	blood:
4	chr3:139168645..139171256-chr3:139173067..139176313,3	K562	blood:
5	chr3:139178292..139180286-chr3:139183692..139185516,2	K562	blood:
6	chr3:139165019..139166769-chr3:139169234..139171368,2	MCF-7	breast:
7	chr3:139186237..139189203-chr3:139191374..139194272,2	K562	blood:
8	chr3:139174418..139175114-chr3:139280608..139281156,2	MCF-7	breast:
9	chr3:139156554..139158574-chr3:139162722..139165410,2	MCF-7	breast:
10	chr3:139187703..139190427-chr3:139192772..139195214,2	K562	blood:
11	chr3:139168645..139171256-chr3:139173067..139176313,3	K562	blood:
12	chr3:139164444..139166894-chr3:139178847..139180451,2	K562	blood:
13	chr3:139165019..139166769-chr3:139169234..139171368,2	MCF-7	breast:
14	chr3:139186237..139189203-chr3:139191374..139194272,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS22-1	chr3:139169122-139169255	ENSG00000248932.1
2	lnc-MRPS22-1	chr3:139163021-139165157	NONHSAT092369
3	lnc-MRPS22-1	chr3:139169474-139169503	NONHSAT092358
4	lnc-MRPS22-1	chr3:139170843-139171082	ENSG00000248932.1
5	lnc-MRPS22-1	chr3:139163136-139163452	NONHSAT092368
6	lnc-MRPS22-2	chr3:139185272-139185321	ENSG00000248790.1
7	lnc-MRPS22-1	chr3:139163136-139163167	ENSG00000248932.1
8	lnc-MRPS22-1	chr3:139163136-139163205	ENSG00000248932.1
9	lnc-MRPS22-1	chr3:139163136-139163429	NONHSAT092359
10	lnc-MRPS22-2	chr3:139185415-139185637	ENSG00000248790.1
11	lnc-MRPS22-1	chr3:139163136-139163352	NONHSAT092358

No data

Variant related genes	Relation type
ENSG00000248790	TF binding region
RBP2	TF binding region
ENSG00000248790	CpG island
RBP2	CpG island
ENSG00000248790	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577220322	chr3:139159362-139159363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147187115	chr3:139159365-139159366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552937457	chr3:139159369-139159370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138773573	chr3:139159417-139159418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541697531	chr3:139159430-139159431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555411153	chr3:139159480-139159481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142747211	chr3:139159501-139159502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150719429	chr3:139159504-139159505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181299584	chr3:139159630-139159631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532848412	chr3:139159730-139159731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114106028	chr3:139159737-139159738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11706097	chr3:139159773-139159774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560187407	chr3:139159806-139159807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142800311	chr3:139159829-139159830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528925014	chr3:139159844-139159845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139005405	chr3:139159886-139159887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554061193	chr3:139160006-139160007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531238284	chr3:139160016-139160017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs186829914	chr3:139160022-139160023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375246978	chr3:139160025-139160026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76439201	chr3:139160028-139160029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149855892	chr3:139160031-139160032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191667133	chr3:139160062-139160063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574030047	chr3:139160110-139160111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566515394	chr3:139160122-139160123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs12492812	chr3:139160124-139160125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536425941	chr3:139160186-139160187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs78230813	chr3:139160187-139160188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555757346	chr3:139160188-139160189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181674839	chr3:139160201-139160202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544505212	chr3:139160257-139160258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557659689	chr3:139160319-139160320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577960655	chr3:139160408-139160409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76728176	chr3:139160416-139160417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560253893	chr3:139160427-139160428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529018340	chr3:139160444-139160445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545485462	chr3:139160476-139160477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144857962	chr3:139160498-139160499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562513339	chr3:139160523-139160524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531099993	chr3:139160570-139160571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186327476	chr3:139160594-139160595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570933565	chr3:139160595-139160596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114859909	chr3:139160610-139160611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546808576	chr3:139160650-139160651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs566599908	chr3:139160672-139160673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10935328	chr3:139160675-139160676	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs555437494	chr3:139160706-139160707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372709868	chr3:139160765-139160766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191074757	chr3:139160843-139160844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1371340	chr3:139160906-139160907	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:55)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139136400-139166200	Weak transcription	Fetal Brain Female	brain
2	chr3:139138600-139166200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr3:139138600-139170400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr3:139139600-139160000	Weak transcription	Fetal Brain Male	brain
5	chr3:139141200-139160000	Weak transcription	Lung	lung
6	chr3:139141400-139167000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:139142200-139172200	Weak transcription	Fetal Heart	heart
8	chr3:139142800-139162600	Weak transcription	Psoas Muscle	Psoas
9	chr3:139142800-139169000	Weak transcription	Aorta	Aorta
10	chr3:139142800-139176800	Weak transcription	Fetal Stomach	stomach
11	chr3:139144800-139173200	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr3:139145200-139164400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:139145200-139170400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:139147400-139160200	Weak transcription	Brain Angular Gyrus	brain
15	chr3:139148000-139160000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr3:139149800-139170600	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr3:139152200-139159800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:139154000-139167000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr3:139154200-139165600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr3:139154200-139168200	Weak transcription	Fetal Intestine Small	intestine
21	chr3:139154200-139171200	Weak transcription	Right Atrium	heart
22	chr3:139154200-139173600	Weak transcription	Ovary	ovary
23	chr3:139154200-139178600	Weak transcription	Left Ventricle	heart
24	chr3:139154400-139159600	Weak transcription	HSMM	muscle
25	chr3:139154400-139166200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:139154400-139167000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:139154800-139165200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:139158000-139160800	Enhancers	Brain Substantia Nigra	brain
29	chr3:139158200-139160000	Enhancers	Brain Anterior Caudate	brain
30	chr3:139158200-139160400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:139158200-139161400	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr3:139158600-139166200	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:139158600-139172600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr3:139158600-139174800	Weak transcription	Adipose Nuclei	Adipose
35	chr3:139158800-139166000	Weak transcription	HSMMtube	muscle
36	chr3:139159000-139159400	Weak transcription	Brain Hippocampus Middle	brain
37	chr3:139159200-139159400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr3:139159400-139159800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:139159400-139161000	Enhancers	Brain Hippocampus Middle	brain
40	chr3:139159400-139162200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:139159600-139159800	Enhancers	HSMM	muscle
42	chr3:139159600-139161400	Enhancers	Brain Germinal Matrix	brain
43	chr3:139159800-139160200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:139159800-139160600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:139160000-139160600	Enhancers	Fetal Brain Male	brain
46	chr3:139160000-139160600	Enhancers	Lung	lung
47	chr3:139160000-139161000	Enhancers	Brain Cingulate Gyrus	brain
48	chr3:139160000-139162800	Weak transcription	Brain Anterior Caudate	brain
49	chr3:139160200-139160800	Enhancers	Brain Angular Gyrus	brain
50	chr3:139160200-139174800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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