Variant report

Variant	nsv1009935
Chromosome Location	chr3:143497700-143610852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:776)
CpG islands
(count:552)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:143600039-143600234	K562	blood:	n/a	n/a
2	ATF2	chr3:143550046-143550510	GM12878	blood:	n/a	n/a
3	ATF2	chr3:143551130-143551703	GM12878	blood:	n/a	n/a
4	ATF2	chr3:143569668-143570218	GM12878	blood:	n/a	n/a
5	ATF2	chr3:143533293-143533852	GM12878	blood:	n/a	n/a
6	ATF2	chr3:143549981-143550910	GM12878	blood:	n/a	n/a
7	ATF2	chr3:143550821-143551708	GM12878	blood:	n/a	n/a
8	ATF2	chr3:143568557-143569164	GM12878	blood:	n/a	n/a
9	ATF3	chr3:143530518-143530777	K562	blood:	n/a	n/a
10	BACH1	chr3:143589710-143589716	K562	blood:	n/a	n/a
11	BACH1	chr3:143539767-143540024	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:143566636-143566966	K562	blood:	n/a	n/a
13	BACH1	chr3:143506077-143506116	K562	blood:	n/a	n/a
14	BACH1	chr3:143566587-143567111	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr3:143550824-143551198	GM12878	blood:	n/a	n/a
16	BATF	chr3:143567207-143567607	GM12878	blood:	n/a	chr3:143567421-143567432
17	BATF	chr3:143568675-143569126	GM12878	blood:	n/a	chr3:143569072-143569081 chr3:143568916-143568927
18	BATF	chr3:143551239-143551631	GM12878	blood:	n/a	chr3:143551391-143551401 chr3:143551390-143551401
19	BATF	chr3:143550116-143550546	GM12878	blood:	n/a	chr3:143550275-143550285
20	BATF	chr3:143558066-143558444	GM12878	blood:	n/a	n/a
21	BATF	chr3:143567243-143567585	GM12878	blood:	n/a	chr3:143567421-143567432
22	BATF	chr3:143551244-143551604	GM12878	blood:	n/a	chr3:143551391-143551401 chr3:143551390-143551401
23	BATF	chr3:143569705-143570077	GM12878	blood:	n/a	n/a
24	BATF	chr3:143568766-143569102	GM12878	blood:	n/a	chr3:143569072-143569081 chr3:143568916-143568927
25	BATF	chr3:143550051-143550435	GM12878	blood:	n/a	chr3:143550275-143550285
26	BATF	chr3:143533232-143533665	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:143566681-143567031	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:143551314-143551644	GM12878	blood:	n/a	chr3:143551389-143551398 chr3:143551412-143551421
29	BCL11A	chr3:143569728-143570094	GM12878	blood:	n/a	n/a
30	BCL11A	chr3:143568715-143569009	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:143568692-143569195	GM12878	blood:	n/a	n/a
32	BCLAF1	chr3:143550115-143550573	GM12878	blood:	n/a	chr3:143550274-143550283 chr3:143550273-143550282
33	BCLAF1	chr3:143567040-143567571	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:143550035-143550498	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:143566591-143567627	GM12878	blood:	n/a	n/a
36	CCNT2	chr3:143604804-143605090	K562	blood:	n/a	n/a
37	CEBPB	chr3:143607919-143608236	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:143584169-143584375	H1-hESC	embryonic stem cell:	n/a	chr3:143584323-143584334
39	CEBPB	chr3:143530509-143530842	K562	blood:	n/a	chr3:143530654-143530665
40	CEBPB	chr3:143530538-143530690	HepG2	liver:	n/a	chr3:143530654-143530665
41	CEBPB	chr3:143584149-143584501	HepG2	liver:	n/a	chr3:143584323-143584334
42	CEBPB	chr3:143530529-143530789	MCF-7	breast:	n/a	chr3:143530654-143530665
43	CEBPB	chr3:143584195-143584498	A549	lung:	n/a	chr3:143584323-143584334
44	CEBPB	chr3:143566977-143567563	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:143530511-143530790	A549	lung:	n/a	chr3:143530654-143530665
46	CEBPB	chr3:143568806-143569168	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:143584141-143584506	MCF-7	breast:	n/a	chr3:143584323-143584334
48	CEBPB	chr3:143584180-143584487	IMR90	lung:	n/a	chr3:143584323-143584334
49	CEBPB	chr3:143500417-143500497	A549	lung:	n/a	n/a
50	CEBPB	chr3:143530476-143530851	HepG2	liver:	n/a	chr3:143530654-143530665

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143532568-143532618	PrEC	prostate:	n/a
2	chr3:143559620-143559670	NHBE	bronchial:	n/a
3	chr3:143567031-143567081	HMEC	breast:	n/a
4	chr3:143532568-143532618	PrEC	prostate:	n/a
5	chr3:143559620-143559670	NHBE	bronchial:	n/a
6	chr3:143567031-143567081	HMEC	breast:	n/a
7	chr3:143559620-143559670	A549	lung:	n/a
8	chr3:143526770-143526820	AG04449	skin:	fetal
9	chr3:143501281-143501331	HRPEpiC	eye:	n/a
10	chr3:143567031-143567081	GM12891	blood:	n/a
11	chr3:143501281-143501331	HRCEpiC	kidney:	n/a
12	chr3:143532568-143532618	Hepatocyte	liver:	n/a
13	chr3:143607961-143608011	IMR90	lung:	fetal
14	chr3:143567492-143567542	AG04449	skin:	fetal
15	chr3:143559620-143559670	T-47D	breast:	n/a
16	chr3:143532568-143532618	GM12878	blood:	n/a
17	chr3:143505340-143505390	HIPEpiC	eye:	n/a
18	chr3:143501281-143501331	GM12878	blood:	n/a
19	chr3:143526770-143526820	HepG2	liver:	n/a
20	chr3:143501281-143501331	GM12891	blood:	n/a
21	chr3:143559620-143559670	NB4	blood:	n/a
22	chr3:143526770-143526820	NHDF-neo	bronchial:	n/a
23	chr3:143501281-143501331	SKMC	muscle:	n/a
24	chr3:143567492-143567542	HIPEpiC	eye:	n/a
25	chr3:143501281-143501331	ECC-1	luminal epithelium:	n/a
26	chr3:143532568-143532618	AG04450	lung:	fetal
27	chr3:143501281-143501331	HL-60	blood:	n/a
28	chr3:143501281-143501331	NHDF-neo	bronchial:	n/a
29	chr3:143526770-143526820	SAEC	small airway:	n/a
30	chr3:143505340-143505390	HNPCEpiC	eye:	n/a
31	chr3:143526770-143526820	U87	brain:	n/a
32	chr3:143501281-143501331	HUVEC	blood vessel:	n/a
33	chr3:143566850-143566900	NHDF-neo	bronchial:	n/a
34	chr3:143567031-143567081	Caco-2	colon:	n/a
35	chr3:143607961-143608011	SK-N-SH	brain:	n/a
36	chr3:143526770-143526820	GM19239	blood:	n/a
37	chr3:143532568-143532618	LNCaP	prostate:	n/a
38	chr3:143566850-143566900	Hepatocyte	liver:	n/a
39	chr3:143566850-143566900	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:143559620-143559670	HCT-116	colon:	n/a
41	chr3:143505340-143505390	HRE	kidney:	n/a
42	chr3:143559620-143559670	H1-hESC	embryonic stem cell:	embryo
43	chr3:143607961-143608011	HIPEpiC	eye:	n/a
44	chr3:143505340-143505390	HMEC	breast:	n/a
45	chr3:143501281-143501331	AoSMC	blood vessel:	n/a
46	chr3:143532568-143532618	HRE	kidney:	n/a
47	chr3:143567031-143567081	HRPEpiC	eye:	n/a
48	chr3:143566850-143566900	PANC-1	pancreas:	n/a
49	chr3:143505340-143505390	Jurkat	blood:	n/a
50	chr3:143526770-143526820	HCT-116	colon:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:143548374..143549959-chr3:143555685..143558599,3	MCF-7	breast:
2	chr3:143607627..143609347-chr3:143688609..143690879,2	MCF-7	breast:
3	chr3:143556738..143559123-chr3:143561803..143563430,2	MCF-7	breast:
4	chr3:143604103..143606429-chr3:143613609..143616531,3	K562	blood:
5	chr1:225997868..225998526-chr3:143572696..143573196,2	K562	blood:
6	chr3:143534241..143536547-chr3:143539436..143542162,2	K562	blood:
7	chr10:29692522..29694043-chr3:143572695..143574216,2	MCF-7	breast:
8	chr3:143552824..143555742-chr3:143557678..143559714,2	K562	blood:
9	chr3:143572196..143573196-chr8:43094222..43095523,3	HCT-116	colon:
10	chr3:143531756..143533614-chr3:143541669..143543725,2	MCF-7	breast:
11	chr3:143566553..143569042-chr3:143690803..143692633,2	MCF-7	breast:
12	chr3:143607486..143610242-chr3:143690819..143692656,2	K562	blood:
13	chr3:143552824..143555742-chr3:143557678..143559714,2	K562	blood:
14	chr3:143604929..143607401-chr3:143613434..143616389,2	K562	blood:
15	chr3:143607160..143610158-chr3:143611331..143613238,2	K562	blood:
16	chr3:143531756..143533614-chr3:143541669..143543725,2	MCF-7	breast:
17	chr3:143556738..143559123-chr3:143561803..143563430,2	MCF-7	breast:
18	chr3:143604403..143605317-chr3:143669942..143670478,2	K562	blood:
19	chr3:143604467..143605336-chr3:143669926..143671031,5	MCF-7	breast:
20	chr3:143548374..143549959-chr3:143555685..143558599,3	MCF-7	breast:
21	chr3:143610538..143615148-chr3:143689957..143693126,6	MCF-7	breast:
22	chr3:143572695..143573196-chr8:43096744..43097413,2	MCF-7	breast:
23	chr3:143534241..143536547-chr3:143539436..143542162,2	K562	blood:
24	chr3:143572714..143574427-chr3:143574833..143577632,2	K562	blood:
25	chr3:143560889..143563208-chr3:143565981..143568974,3	MCF-7	breast:
26	chr3:143514332..143514918-chr3:143670242..143670855,2	MCF-7	breast:
27	chr3:143540836..143543345-chr3:143547418..143549416,3	MCF-7	breast:
28	chr3:143540836..143543345-chr3:143547418..143549416,3	MCF-7	breast:
29	chr3:143601941..143604638-chr3:143689903..143691740,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAQR9-7	chr3:143566436-143566825	NONHSAT092530
2	lnc-PAQR9-7	chr3:143566990-143567311	NONHSAT092530

No data

Variant related genes	Relation type
ENSG00000235110	TF binding region
SLC9A9	TF binding region
ENSG00000235110	CpG island
SLC9A9	CpG island
ENSG00000235110	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000181804	chromatin interactions

Extended variants
information (count: 4199 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:4199 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543993950	chr3:143497731-143497732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562095809	chr3:143497764-143497765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529455898	chr3:143497807-143497808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145497752	chr3:143497898-143497899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374768165	chr3:143497903-143497904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs74750922	chr3:143497918-143497919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147269902	chr3:143497964-143497965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569720476	chr3:143497980-143497981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532500776	chr3:143498016-143498017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112237102	chr3:143498054-143498055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536790163	chr3:143498207-143498208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113848661	chr3:143498211-143498212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188354583	chr3:143498254-143498255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567306936	chr3:143498256-143498257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534826082	chr3:143498294-143498295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193193200	chr3:143498335-143498336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578019680	chr3:143498359-143498360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140950134	chr3:143498369-143498370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144795266	chr3:143498376-143498377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116086745	chr3:143498380-143498381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536781477	chr3:143498405-143498406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562228996	chr3:143498465-143498466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573869447	chr3:143498555-143498556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6805483	chr3:143498566-143498567	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs559604991	chr3:143498621-143498622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151330528	chr3:143498630-143498631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs567096397	chr3:143498640-143498641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs13059339	chr3:143498642-143498643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs558781114	chr3:143498677-143498678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563088869	chr3:143498730-143498731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182911813	chr3:143498750-143498751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114066654	chr3:143498755-143498756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140583398	chr3:143498775-143498776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534787250	chr3:143498872-143498873	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546850327	chr3:143498896-143498897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571563116	chr3:143498942-143498943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538889324	chr3:143498974-143498975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557231776	chr3:143499073-143499074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576325500	chr3:143499145-143499146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537476075	chr3:143499152-143499153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577131816	chr3:143499153-143499154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555560005	chr3:143499179-143499180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544573475	chr3:143499183-143499184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368579405	chr3:143499202-143499203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111291405	chr3:143499215-143499216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541219520	chr3:143499282-143499283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116779390	chr3:143499326-143499327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs577817554	chr3:143499327-143499328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545334168	chr3:143499346-143499347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371162445	chr3:143499347-143499348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
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
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
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143476600-143500400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:143492400-143513000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:143494600-143505200	Weak transcription	NHLF	lung
4	chr3:143494800-143498800	Weak transcription	Primary T cells from cord blood	blood
5	chr3:143494800-143500600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:143494800-143500600	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr3:143494800-143505200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr3:143494800-143505200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr3:143494800-143505200	Weak transcription	Fetal Lung	lung
10	chr3:143494800-143505400	Weak transcription	Brain Angular Gyrus	brain
11	chr3:143494800-143505400	Weak transcription	Right Atrium	heart
12	chr3:143494800-143515600	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr3:143494800-143515800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr3:143495000-143505400	Weak transcription	Colon Smooth Muscle	Colon
15	chr3:143496200-143500800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr3:143496200-143505200	Weak transcription	Brain Substantia Nigra	brain
17	chr3:143498800-143499600	Strong transcription	Primary T cells from cord blood	blood
18	chr3:143499000-143505200	Weak transcription	Aorta	Aorta
19	chr3:143499600-143512800	Weak transcription	Primary T cells from cord blood	blood
20	chr3:143500400-143503000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:143500600-143502000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr3:143500600-143502200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:143500600-143502200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:143500600-143502800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr3:143500600-143503200	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:143500800-143501200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:143500800-143501800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:143500800-143502400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:143500800-143503000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr3:143501200-143501600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr3:143501600-143502200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr3:143501600-143502200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr3:143501600-143503000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:143501800-143502800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr3:143502000-143502200	Enhancers	Spleen	Spleen
36	chr3:143502000-143505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr3:143502200-143503200	Enhancers	Fetal Heart	heart
38	chr3:143502200-143503400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr3:143502400-143502800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr3:143502600-143503400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr3:143502800-143503000	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:143502800-143503000	Enhancers	Osteobl	bone
43	chr3:143502800-143503200	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:143503000-143503200	Enhancers	HSMMtube	muscle
45	chr3:143503000-143505200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr3:143503000-143505200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr3:143503000-143505400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr3:143503000-143505400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr3:143503200-143503800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:143503200-143505200	Weak transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links