Variant report

Variant	nsv877548
Chromosome Location	chr3:140514022-140590632
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	chr3:140547536-140547736	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:140582604-140582919	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	chr3:140541362-140541793	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr3:140582646-140582715	K562	blood:	n/a	n/a
8	BACH1	chr3:140569657-140569675	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	chr3:140582520-140582700	K562	blood:	n/a	n/a
13	BHLHE40	chr3:140562193-140562481	GM12878	blood:	n/a	n/a
14	CEBPB	chr3:140584271-140584303	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr3:140553951-140554229	MCF-7	breast:	n/a	chr3:140554021-140554032
16	CEBPB	chr3:140553895-140554122	HepG2	liver:	n/a	chr3:140554021-140554032
17	CEBPB	chr3:140578527-140578835	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:140578527-140578802	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr3:140590627-140590784	HepG2	liver:	n/a	chr3:140590723-140590734
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	chr3:140557280-140557476	K562	blood:	n/a	n/a
23	CEBPB	chr3:140539834-140540131	IMR90	lung:	n/a	chr3:140539941-140539952
24	CEBPB	chr3:140539914-140540003	Hela-S3	cervix:	n/a	chr3:140539941-140539952
25	CEBPB	chr3:140578468-140578888	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr3:140578609-140578838	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:140539825-140540092	A549	lung:	n/a	chr3:140539941-140539952
28	CEBPB	chr3:140541106-140541297	K562	blood:	n/a	chr3:140541267-140541280 chr3:140541269-140541280
29	CEBPB	chr3:140539795-140540113	HepG2	liver:	n/a	chr3:140539941-140539952
30	CEBPB	chr3:140539883-140540010	K562	blood:	n/a	chr3:140539941-140539952
31	CHD2	chr3:140561955-140562475	GM12878	blood:	n/a	n/a
32	CTCF	chr3:140582642-140582924	HCT-116	colon:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
33	CTCF	chr3:140582660-140582810	HRPEpiC	eye:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
34	CTCF	chr3:140567560-140567710	GM12864	blood:	n/a	n/a
35	CTCF	chr3:140582720-140582870	NHDF-neo	bronchial:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
36	CTCF	chr3:140582640-140582790	AG09309	skin:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
37	CTCF	chr3:140582620-140582770	NB4	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
38	CTCF	chr3:140582616-140582881	Medullo	brain:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
39	CTCF	chr3:140582640-140582790	AG04449	skin:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
40	CTCF	chr3:140582672-140582829	GM10248	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
41	CTCF	chr3:140567620-140567770	GM12873	blood:	n/a	n/a
42	CTCF	chr3:140582300-140582450	AG04449	skin:	n/a	n/a
43	CTCF	chr3:140582620-140582770	GM12867	blood:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
44	CTCF	chr3:140582649-140582847	Pancreas_OC	pancreas:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
45	CTCF	chr3:140582600-140582750	GM12870	blood:	n/a	n/a
46	CTCF	chr3:140582640-140582790	A549	lung:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
47	CTCF	chr3:140582637-140582864	LNCaP	prostate:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
48	CTCF	chr3:140582640-140582790	HCFaa	heart:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
49	CTCF	chr3:140582660-140582810	AG04450	lung:	n/a	chr3:140582738-140582759 chr3:140582750-140582758 chr3:140582743-140582761 chr3:140582744-140582760
50	CTCF	chr3:140542110-140542179	MCF-7	breast:	n/a	chr3:140542157-140542175 chr3:140542159-140542172 chr3:140542162-140542171

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:140578726-140578776	HL-60	blood:	n/a
2	chr3:140578726-140578776	HL-60	blood:	n/a
3	chr3:140541355-140541405	K562	blood:	n/a
4	chr3:140587268-140587318	AG04449	skin:	fetal
5	chr3:140541355-140541405	RPTEC	kidney:	n/a
6	chr3:140541355-140541405	NH-A	brain:	n/a
7	chr3:140578726-140578776	AG04450	lung:	fetal
8	chr3:140541355-140541405	AG04449	skin:	fetal
9	chr3:140541355-140541405	Caco-2	colon:	n/a
10	chr3:140587268-140587318	BE2_C	brain:	n/a
11	chr3:140541355-140541405	HAEpiC	amniotic membrane:	n/a
12	chr3:140578726-140578776	ovcar-3	ovarian:	n/a
13	chr3:140578726-140578776	U87	brain:	n/a
14	chr3:140541355-140541405	Jurkat	blood:	n/a
15	chr3:140587268-140587318	RPTEC	kidney:	n/a
16	chr3:140541355-140541405	HEEpiC	esophagus:	n/a
17	chr3:140587268-140587318	Hepatocyte	liver:	n/a
18	chr3:140541355-140541405	U87	brain:	n/a
19	chr3:140541355-140541405	NB4	blood:	n/a
20	chr3:140541355-140541405	SK-N-MC	brain:	n/a
21	chr3:140541355-140541405	HEK293	kidney:	embryo
22	chr3:140541355-140541405	SKMC	muscle:	n/a
23	chr3:140587268-140587318	HAEpiC	amniotic membrane:	n/a
24	chr3:140578726-140578776	PFSK-1	brain:	n/a
25	chr3:140541355-140541405	H1-hESC	embryonic stem cell:	embryo
26	chr3:140541355-140541405	Hela-S3	cervix:	n/a
27	chr3:140541355-140541405	LNCaP	prostate:	n/a
28	chr3:140541355-140541405	HNPCEpiC	eye:	n/a
29	chr3:140587268-140587318	IMR90	lung:	fetal
30	chr3:140587268-140587318	SK-N-MC	brain:	n/a
31	chr3:140578726-140578776	HCT-116	colon:	n/a
32	chr3:140578726-140578776	Jurkat	blood:	n/a
33	chr3:140541355-140541405	T-47D	breast:	n/a
34	chr3:140578726-140578776	Caco-2	colon:	n/a
35	chr3:140578726-140578776	NT2-D1	testis:	n/a
36	chr3:140541355-140541405	SK-N-SH	brain:	n/a
37	chr3:140541355-140541405	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:140578726-140578776	SKMC	muscle:	n/a
39	chr3:140578726-140578776	NHBE	bronchial:	n/a
40	chr3:140578726-140578776	A549	lung:	n/a
41	chr3:140578726-140578776	GM12878	blood:	n/a
42	chr3:140578726-140578776	IMR90	lung:	fetal
43	chr3:140541355-140541405	GM12891	blood:	n/a
44	chr3:140587268-140587318	GM12892	blood:	n/a
45	chr3:140541355-140541405	Hepatocyte	liver:	n/a
46	chr3:140587268-140587318	HIPEpiC	eye:	n/a
47	chr3:140587268-140587318	AoSMC	blood vessel:	n/a
48	chr3:140587268-140587318	NHBE	bronchial:	n/a
49	chr3:140578726-140578776	BE2_C	brain:	n/a
50	chr3:140541355-140541405	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:140271820..140272427-chr3:140582348..140582959,2	K562	blood:
2	chr3:140560323..140562507-chr3:140565228..140567400,2	MCF-7	breast:
3	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
4	chr3:139847498..139848064-chr3:140582279..140583196,3	MCF-7	breast:
5	chr3:140554185..140556969-chr3:140557455..140559405,2	MCF-7	breast:
6	chr3:140567340..140568277-chrX:19340677..19341645,2	MCF-7	breast:
7	chr3:140586905..140589436-chr3:140659176..140661455,2	K562	blood:
8	chr3:140582774..140583595-chr3:140910775..140911453,2	K562	blood:
9	chr3:140455659..140456657-chr3:140582285..140583107,3	MCF-7	breast:
10	chr3:140590326..140591145-chr5:7456282..7457279,2	MCF-7	breast:
11	chr3:140560323..140562507-chr3:140565228..140567400,2	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: 1961 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1961 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6779600	chr3:140514022-140514023	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545929763	chr3:140514026-140514027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs77401039	chr3:140514066-140514067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371177760	chr3:140514067-140514068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80068642	chr3:140514068-140514069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564029424	chr3:140514076-140514077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373097376	chr3:140514100-140514101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6767120	chr3:140514171-140514172	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs201639750	chr3:140514228-140514229	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189981924	chr3:140514329-140514330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6779910	chr3:140514357-140514358	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs76892564	chr3:140514358-140514359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547250337	chr3:140514363-140514364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138828201	chr3:140527814-140527815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114713081	chr3:140527869-140527870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375954163	chr3:140527872-140527873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528061239	chr3:140527902-140527903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546606210	chr3:140527957-140527958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs78015242	chr3:140528013-140528014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182720585	chr3:140528016-140528017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2102875	chr3:140528025-140528026	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569074055	chr3:140528037-140528038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs80269770	chr3:140528118-140528119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115806913	chr3:140528147-140528148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74364894	chr3:140528189-140528190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75736875	chr3:140528190-140528191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138137203	chr3:140528205-140528206	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs78775635	chr3:140528277-140528278	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs11711297	chr3:140528321-140528322	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562894377	chr3:140528330-140528331	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs78119486	chr3:140528341-140528342	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs9835982	chr3:140528353-140528354	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs560630311	chr3:140528382-140528383	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs551880169	chr3:140528403-140528404	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs546242242	chr3:140528421-140528422	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs142619205	chr3:140528458-140528459	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs565419944	chr3:140528495-140528496	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs116474909	chr3:140528507-140528508	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs77980144	chr3:140528559-140528560	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs569214598	chr3:140528588-140528589	Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536434440	chr3:140528607-140528608	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs188239194	chr3:140528609-140528610	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs534330848	chr3:140528650-140528651	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs75521451	chr3:140528657-140528658	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs534312073	chr3:140528688-140528689	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs536755909	chr3:140528712-140528713	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs547738320	chr3:140528719-140528720	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs78825396	chr3:140528738-140528739	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs191490622	chr3:140528758-140528759	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs114861980	chr3:140528778-140528779	Enhancers Flanking Active TSS	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:198 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140512800-140514400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr3:140527800-140528200	Enhancers	Adipose Nuclei	Adipose
3	chr3:140527800-140528600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr3:140527800-140528600	Enhancers	Fetal Muscle Leg	muscle
5	chr3:140527800-140528800	Enhancers	Primary B cells from peripheral blood	blood
6	chr3:140528000-140528400	Enhancers	Primary B cells from cord blood	blood
7	chr3:140528000-140528400	Enhancers	HSMMtube	muscle
8	chr3:140528000-140528600	Enhancers	Lung	lung
9	chr3:140528200-140528600	Enhancers	Fetal Muscle Trunk	muscle
10	chr3:140528200-140528800	Enhancers	Placenta	Placenta
11	chr3:140528200-140529000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:140528200-140529000	Flanking Active TSS	Adipose Nuclei	Adipose
13	chr3:140528400-140528600	ZNF genes & repeats	Right Atrium	heart
14	chr3:140528400-140528800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:140533200-140533600	ZNF genes & repeats	Psoas Muscle	Psoas
16	chr3:140533600-140533800	Enhancers	Primary B cells from cord blood	blood
17	chr3:140533800-140535200	Weak transcription	Primary B cells from cord blood	blood
18	chr3:140534800-140536000	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:140535000-140536000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr3:140535000-140536000	Enhancers	GM12878-XiMat	blood
21	chr3:140535200-140536000	Enhancers	Primary B cells from cord blood	blood
22	chr3:140535400-140535800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr3:140535400-140535800	Enhancers	Adipose Nuclei	Adipose
24	chr3:140535600-140535800	Enhancers	Fetal Muscle Leg	muscle
25	chr3:140535600-140536000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:140535800-140540800	Weak transcription	Fetal Muscle Leg	muscle
27	chr3:140536000-140541400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr3:140539000-140539200	Enhancers	HSMMtube	muscle
29	chr3:140539200-140539800	Weak transcription	HSMMtube	muscle
30	chr3:140539800-140542600	Enhancers	HSMMtube	muscle
31	chr3:140540200-140540800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr3:140540200-140540800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr3:140540200-140542600	Enhancers	HepG2	liver
34	chr3:140540600-140541600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:140540800-140541800	Enhancers	Fetal Muscle Leg	muscle
36	chr3:140541000-140541800	Enhancers	Fetal Thymus	thymus
37	chr3:140541000-140542200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:140541000-140542400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:140541000-140542400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:140541200-140542600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr3:140541400-140542000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:140541400-140542200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr3:140541400-140542400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr3:140541400-140542400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr3:140541400-140542600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr3:140541400-140542600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr3:140541600-140542000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:140541800-140542200	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr3:140542000-140542600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:140542000-140551400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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