Variant report

Variant	nsv877549
Chromosome Location	chr3:140521178-140590632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:140582604-140582919	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140547536-140547736	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:140582617-140582913	K562	blood:	n/a	n/a
4	ATF2	chr3:140562011-140562511	GM12878	blood:	n/a	n/a
5	ATF2	chr3:140564672-140565199	GM12878	blood:	n/a	n/a
6	BACH1	chr3:140569657-140569675	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:140582646-140582715	K562	blood:	n/a	n/a
8	BACH1	chr3:140541362-140541793	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr3:140562108-140562470	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:140562021-140562506	GM12878	blood:	n/a	chr3:140562252-140562261
11	BCL11A	chr3:140562101-140562449	GM12878	blood:	n/a	chr3:140562252-140562261
12	BHLHE40	chr3:140562193-140562481	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:140582520-140582700	K562	blood:	n/a	n/a
14	CEBPB	chr3:140541106-140541297	K562	blood:	n/a	chr3:140541267-140541280 chr3:140541269-140541280
15	CEBPB	chr3:140553951-140554229	MCF-7	breast:	n/a	chr3:140554021-140554032
16	CEBPB	chr3:140539883-140540010	K562	blood:	n/a	chr3:140539941-140539952
17	CEBPB	chr3:140578527-140578802	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr3:140578527-140578835	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr3:140578468-140578888	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr3:140545802-140545921	K562	blood:	n/a	chr3:140545861-140545874 chr3:140545861-140545874 chr3:140545901-140545912 chr3:140545863-140545874 chr3:140545863-140545874
21	CEBPB	chr3:140578494-140578848	MCF-7	breast:	n/a	n/a
22	CEBPB	chr3:140539825-140540092	A549	lung:	n/a	chr3:140539941-140539952
23	CEBPB	chr3:140539914-140540003	Hela-S3	cervix:	n/a	chr3:140539941-140539952
24	CEBPB	chr3:140584271-140584303	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:140553895-140554122	HepG2	liver:	n/a	chr3:140554021-140554032
26	CEBPB	chr3:140578609-140578838	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:140557280-140557476	K562	blood:	n/a	n/a
28	CEBPB	chr3:140539834-140540131	IMR90	lung:	n/a	chr3:140539941-140539952
29	CEBPB	chr3:140539795-140540113	HepG2	liver:	n/a	chr3:140539941-140539952
30	CEBPB	chr3:140590627-140590784	HepG2	liver:	n/a	chr3:140590723-140590734
31	CHD2	chr3:140561955-140562475	GM12878	blood:	n/a	n/a
32	CTCF	chr3:140583032-140583124	K562	blood:	n/a	n/a
33	CTCF	chr3:140582980-140583130	SAEC	small airway:	n/a	n/a
34	CTCF	chr3:140527820-140527970	GM12873	blood:	n/a	n/a
35	CTCF	chr3:140567630-140567813	GM19240	blood:	n/a	n/a
36	CTCF	chr3:140567734-140567743	GM20000	blood:	n/a	n/a
37	CTCF	chr3:140582561-140582920	H1-hESC	embryonic stem cell:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
38	CTCF	chr3:140567640-140567790	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:140567700-140567850	GM06990	blood:	n/a	n/a
40	CTCF	chr3:140562195-140562368	GM12878	blood:	n/a	n/a
41	CTCF	chr3:140582600-140582925	K562	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
42	CTCF	chr3:140583000-140583150	GM12873	blood:	n/a	n/a
43	CTCF	chr3:140582680-140582830	Caco-2	colon:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
44	CTCF	chr3:140583352-140583420	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr3:140582659-140582759	H1-hESC	embryonic stem cell:	n/a	chr3:140582738-140582759 chr3:140582750-140582758
46	CTCF	chr3:140582586-140582938	HepG2	liver:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
47	CTCF	chr3:140582640-140582790	GM12875	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
48	CTCF	chr3:140542080-140542230	GM12872	blood:	n/a	chr3:140542157-140542175 chr3:140542159-140542172 chr3:140542162-140542171
49	CTCF	chr3:140583025-140583043	GM13977	blood:	n/a	n/a
50	CTCF	chr3:140567660-140567810	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140587268-140587318	HAEpiC	amniotic membrane:	n/a
2	chr3:140578726-140578776	HCPEpiC	choroid plexus:	n/a
3	chr3:140541355-140541405	Jurkat	blood:	n/a
4	chr3:140587268-140587318	GM12878	blood:	n/a
5	chr3:140587268-140587318	GM19239	blood:	n/a
6	chr3:140578726-140578776	LNCaP	prostate:	n/a
7	chr3:140578726-140578776	HUVEC	blood vessel:	n/a
8	chr3:140541355-140541405	MCF-7	breast:	n/a
9	chr3:140578726-140578776	BE2_C	brain:	n/a
10	chr3:140587268-140587318	HCPEpiC	choroid plexus:	n/a
11	chr3:140541355-140541405	HRE	kidney:	n/a
12	chr3:140587268-140587318	HCM	heart:	n/a
13	chr3:140541355-140541405	PrEC	prostate:	n/a
14	chr3:140578726-140578776	PFSK-1	brain:	n/a
15	chr3:140587268-140587318	NHBE	bronchial:	n/a
16	chr3:140578726-140578776	ProgFib	skin:	n/a
17	chr3:140587268-140587318	SK-N-SH_RA	brain:	n/a
18	chr3:140541355-140541405	NHBE	bronchial:	n/a
19	chr3:140587268-140587318	Hepatocyte	liver:	n/a
20	chr3:140578726-140578776	HNPCEpiC	eye:	n/a
21	chr3:140541355-140541405	SKMC	muscle:	n/a
22	chr3:140541355-140541405	NB4	blood:	n/a
23	chr3:140587268-140587318	BE2_C	brain:	n/a
24	chr3:140541355-140541405	HCM	heart:	n/a
25	chr3:140541355-140541405	SK-N-SH	brain:	n/a
26	chr3:140578726-140578776	K562	blood:	n/a
27	chr3:140578726-140578776	Jurkat	blood:	n/a
28	chr3:140578726-140578776	NH-A	brain:	n/a
29	chr3:140578726-140578776	MCF10A-Er-Src	breast:	n/a
30	chr3:140541355-140541405	K562	blood:	n/a
31	chr3:140541355-140541405	AG04449	skin:	fetal
32	chr3:140587268-140587318	SKMC	muscle:	n/a
33	chr3:140587268-140587318	AG10803	skin:	n/a
34	chr3:140541355-140541405	HUVEC	blood vessel:	n/a
35	chr3:140578726-140578776	HRE	kidney:	n/a
36	chr3:140541355-140541405	HRPEpiC	eye:	n/a
37	chr3:140578726-140578776	GM19239	blood:	n/a
38	chr3:140541355-140541405	ProgFib	skin:	n/a
39	chr3:140578726-140578776	HCM	heart:	n/a
40	chr3:140578726-140578776	SK-N-MC	brain:	n/a
41	chr3:140541355-140541405	ECC-1	luminal epithelium:	n/a
42	chr3:140541355-140541405	LNCaP	prostate:	n/a
43	chr3:140541355-140541405	AG04450	lung:	fetal
44	chr3:140578726-140578776	HEK293	kidney:	embryo
45	chr3:140578726-140578776	MCF-7	breast:	n/a
46	chr3:140587268-140587318	SK-N-MC	brain:	n/a
47	chr3:140587268-140587318	PANC-1	pancreas:	n/a
48	chr3:140541355-140541405	HMEC	breast:	n/a
49	chr3:140541355-140541405	HepG2	liver:	n/a
50	chr3:140587268-140587318	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140271820..140272427-chr3:140582348..140582959,2	K562	blood:
2	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
3	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
4	chr3:140560323..140562507-chr3:140565228..140567400,2	MCF-7	breast:
5	chr3:140586905..140589436-chr3:140659176..140661455,2	K562	blood:
6	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:
7	chr3:140582774..140583595-chr3:140910775..140911453,2	K562	blood:
8	chr3:139847498..139848064-chr3:140582279..140583196,3	MCF-7	breast:
9	chr3:140560323..140562507-chr3:140565228..140567400,2	MCF-7	breast:
10	chr3:140567340..140568277-chrX:19340677..19341645,2	MCF-7	breast:
11	chr3:140590326..140591145-chr5:7456282..7457279,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-4	chr3:140583917-140586625	ENSG00000261826.1

Variant related genes	Relation type
ENSG00000261826	TF binding region
ENSG00000261826	CpG island
ENSG00000114120	chromatin interactions

Extended variants
information (count: 1948 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138828201	chr3:140527814-140527815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114713081	chr3:140527869-140527870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375954163	chr3:140527872-140527873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528061239	chr3:140527902-140527903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546606210	chr3:140527957-140527958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78015242	chr3:140528013-140528014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182720585	chr3:140528016-140528017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2102875	chr3:140528025-140528026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs569074055	chr3:140528037-140528038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs80269770	chr3:140528118-140528119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115806913	chr3:140528147-140528148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74364894	chr3:140528189-140528190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs75736875	chr3:140528190-140528191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138137203	chr3:140528205-140528206	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs78775635	chr3:140528277-140528278	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs11711297	chr3:140528321-140528322	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs562894377	chr3:140528330-140528331	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs78119486	chr3:140528341-140528342	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs9835982	chr3:140528353-140528354	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560630311	chr3:140528382-140528383	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs551880169	chr3:140528403-140528404	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs546242242	chr3:140528421-140528422	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs142619205	chr3:140528458-140528459	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs565419944	chr3:140528495-140528496	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs116474909	chr3:140528507-140528508	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs77980144	chr3:140528559-140528560	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs569214598	chr3:140528588-140528589	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs536434440	chr3:140528607-140528608	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188239194	chr3:140528609-140528610	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs534330848	chr3:140528650-140528651	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs75521451	chr3:140528657-140528658	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs534312073	chr3:140528688-140528689	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs536755909	chr3:140528712-140528713	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs547738320	chr3:140528719-140528720	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs78825396	chr3:140528738-140528739	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs191490622	chr3:140528758-140528759	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs114861980	chr3:140528778-140528779	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs144062890	chr3:140528797-140528798	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs148655888	chr3:140528808-140528809	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs78743105	chr3:140528814-140528815	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559269909	chr3:140528817-140528818	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs11707358	chr3:140528842-140528843	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs117035429	chr3:140528844-140528845	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs35328449	chr3:140528933-140528934	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs564875480	chr3:140528944-140528945	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs375249715	chr3:140528949-140528950	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs544257866	chr3:140528954-140528955	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs116151028	chr3:140528989-140528990	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs539141581	chr3:140533214-140533215	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs74493348	chr3:140533261-140533262	ZNF genes & repeats	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
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
abnormal development	18461090	CNVD
Schizophrenia	17989066	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140527800-140528200	Enhancers	Adipose Nuclei	Adipose
2	chr3:140527800-140528600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr3:140527800-140528600	Enhancers	Fetal Muscle Leg	muscle
4	chr3:140527800-140528800	Enhancers	Primary B cells from peripheral blood	blood
5	chr3:140528000-140528400	Enhancers	Primary B cells from cord blood	blood
6	chr3:140528000-140528400	Enhancers	HSMMtube	muscle
7	chr3:140528000-140528600	Enhancers	Lung	lung
8	chr3:140528200-140528600	Enhancers	Fetal Muscle Trunk	muscle
9	chr3:140528200-140528800	Enhancers	Placenta	Placenta
10	chr3:140528200-140529000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:140528200-140529000	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr3:140528400-140528600	ZNF genes & repeats	Right Atrium	heart
13	chr3:140528400-140528800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:140533200-140533600	ZNF genes & repeats	Psoas Muscle	Psoas
15	chr3:140533600-140533800	Enhancers	Primary B cells from cord blood	blood
16	chr3:140533800-140535200	Weak transcription	Primary B cells from cord blood	blood
17	chr3:140534800-140536000	Enhancers	Primary B cells from peripheral blood	blood
18	chr3:140535000-140536000	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr3:140535000-140536000	Enhancers	GM12878-XiMat	blood
20	chr3:140535200-140536000	Enhancers	Primary B cells from cord blood	blood
21	chr3:140535400-140535800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
22	chr3:140535400-140535800	Enhancers	Adipose Nuclei	Adipose
23	chr3:140535600-140535800	Enhancers	Fetal Muscle Leg	muscle
24	chr3:140535600-140536000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:140535800-140540800	Weak transcription	Fetal Muscle Leg	muscle
26	chr3:140536000-140541400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr3:140539000-140539200	Enhancers	HSMMtube	muscle
28	chr3:140539200-140539800	Weak transcription	HSMMtube	muscle
29	chr3:140539800-140542600	Enhancers	HSMMtube	muscle
30	chr3:140540200-140540800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:140540200-140540800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:140540200-140542600	Enhancers	HepG2	liver
33	chr3:140540600-140541600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:140540800-140541800	Enhancers	Fetal Muscle Leg	muscle
35	chr3:140541000-140541800	Enhancers	Fetal Thymus	thymus
36	chr3:140541000-140542200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr3:140541000-140542400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:140541000-140542400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr3:140541200-140542600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:140541400-140542000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr3:140541400-140542200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:140541400-140542400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:140541400-140542400	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr3:140541400-140542600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr3:140541400-140542600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:140541600-140542000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:140541800-140542200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:140542000-140542600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:140542000-140551400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:140542200-140542600	Enhancers	Lung	lung

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