Variant report

Variant	nsv877544
Chromosome Location	chr3:139642572-139688415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:588)
CpG islands
(count:1038)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:139659570-139660082	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:139656575-139656908	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:139656632-139656879	K562	blood:	n/a	n/a
4	BACH1	chr3:139654108-139654260	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:139654516-139654523	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:139659387-139659851	HepG2	liver:	n/a	n/a
7	CCNT2	chr3:139654009-139654199	K562	blood:	n/a	n/a
8	CEBPB	chr3:139656584-139656905	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr3:139683434-139683653	K562	blood:	n/a	chr3:139683575-139683584 chr3:139683574-139683585
10	CEBPB	chr3:139683540-139683654	HepG2	liver:	n/a	chr3:139683575-139683584 chr3:139683574-139683585
11	CEBPB	chr3:139653423-139653643	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr3:139656513-139656962	IMR90	lung:	n/a	n/a
13	CHD2	chr3:139653445-139653754	H1-hESC	embryonic stem cell:	n/a	n/a
14	CHD2	chr3:139654918-139654933	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr3:139653808-139654178	A549	lung:	n/a	chr3:139653971-139653984
16	CREB1	chr3:139653000-139654183	H1-hESC	embryonic stem cell:	n/a	chr3:139653971-139653984
17	CREB1	chr3:139653164-139654436	H1-hESC	embryonic stem cell:	n/a	chr3:139653971-139653984
18	CTBP2	chr3:139653274-139655142	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr3:139653312-139653837	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:139653480-139653630	HEK293	kidney:	n/a	n/a
21	CTCF	chr3:139656620-139656770	HMEC	breast:	n/a	chr3:139656707-139656725
22	CTCF	chr3:139652811-139652910	MCF-7	breast:	n/a	n/a
23	CTCF	chr3:139653460-139653610	Caco-2	colon:	n/a	n/a
24	CTCF	chr3:139642596-139642609	MCF-7	breast:	n/a	n/a
25	CTCF	chr3:139653420-139653570	GM12871	blood:	n/a	n/a
26	CTCF	chr3:139656640-139656790	AG09319	gingival:	n/a	chr3:139656707-139656725
27	CTCF	chr3:139654260-139654410	Caco-2	colon:	n/a	n/a
28	CTCF	chr3:139653600-139653750	GM12870	blood:	n/a	n/a
29	CTCF	chr3:139656640-139656790	AG10803	skin:	n/a	chr3:139656707-139656725
30	CTCF	chr3:139653440-139653590	HEK293	kidney:	n/a	n/a
31	CTCF	chr3:139656600-139656750	RPTEC	kidney:	n/a	chr3:139656707-139656725
32	CTCF	chr3:139653460-139653610	NHEK	skin:	n/a	n/a
33	CTCF	chr3:139656620-139656770	BJ	skin:	n/a	chr3:139656707-139656725
34	CTCF	chr3:139653917-139654434	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:139656600-139656750	GM12867	blood:	n/a	chr3:139656707-139656725
36	CTCF	chr3:139656602-139656805	NHEK	skin:	n/a	chr3:139656707-139656725
37	CTCF	chr3:139656660-139656810	HMF	breast:	n/a	chr3:139656707-139656725
38	CTCF	chr3:139656600-139656750	HL-60	blood:	n/a	chr3:139656707-139656725
39	CTCF	chr3:139653453-139653649	GM19238	blood:	n/a	n/a
40	CTCF	chr3:139656620-139656770	GM12867	blood:	n/a	chr3:139656707-139656725
41	CTCF	chr3:139653420-139653570	AG09309	skin:	n/a	n/a
42	CTCF	chr3:139656602-139656805	GM19238	blood:	n/a	chr3:139656707-139656725
43	CTCF	chr3:139653160-139653310	GM12867	blood:	n/a	n/a
44	CTCF	chr3:139656637-139656802	GM20000	blood:	n/a	chr3:139656707-139656725
45	CTCF	chr3:139653316-139653757	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr3:139653362-139653782	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr3:139656660-139656810	WI-38	lung:	n/a	chr3:139656707-139656725
48	CTCF	chr3:139654180-139654330	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr3:139656601-139656810	Hela-S3	cervix:	n/a	chr3:139656707-139656725
50	CTCF	chr3:139654120-139654270	HMEC	breast:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:139654264-139654314	GM12878	blood:	n/a
2	chr3:139654264-139654314	GM12878	blood:	n/a
3	chr3:139654264-139654314	IMR90	lung:	fetal
4	chr3:139653573-139653623	SAEC	small airway:	n/a
5	chr3:139653328-139653378	U87	brain:	n/a
6	chr3:139678075-139678125	HEK293	kidney:	embryo
7	chr3:139653545-139653595	PANC-1	pancreas:	n/a
8	chr3:139678075-139678125	NB4	blood:	n/a
9	chr3:139658735-139658785	Caco-2	colon:	n/a
10	chr3:139653328-139653378	HCT-116	colon:	n/a
11	chr3:139653872-139653922	SAEC	small airway:	n/a
12	chr3:139653915-139653965	HAEpiC	amniotic membrane:	n/a
13	chr3:139678075-139678125	ovcar-3	ovarian:	n/a
14	chr3:139658735-139658785	RPTEC	kidney:	n/a
15	chr3:139655077-139655127	HIPEpiC	eye:	n/a
16	chr3:139654264-139654314	HEK293	kidney:	embryo
17	chr3:139653545-139653595	LNCaP	prostate:	n/a
18	chr3:139653328-139653378	NHDF-neo	bronchial:	n/a
19	chr3:139653431-139653481	HCT-116	colon:	n/a
20	chr3:139653431-139653481	CMK	blood:	n/a
21	chr3:139655283-139655333	AG09309	skin:	n/a
22	chr3:139678075-139678125	Caco-2	colon:	n/a
23	chr3:139653328-139653378	NHBE	bronchial:	n/a
24	chr3:139653928-139653978	GM19239	blood:	n/a
25	chr3:139655283-139655333	GM12892	blood:	n/a
26	chr3:139655283-139655333	HIPEpiC	eye:	n/a
27	chr3:139653545-139653595	PFSK-1	brain:	n/a
28	chr3:139655283-139655333	NHDF-neo	bronchial:	n/a
29	chr3:139658735-139658785	IMR90	lung:	fetal
30	chr3:139655800-139655850	AG09319	gingival:	n/a
31	chr3:139653872-139653922	GM12878	blood:	n/a
32	chr3:139653928-139653978	MCF10A-Er-Src	breast:	n/a
33	chr3:139653872-139653922	A549	lung:	n/a
34	chr3:139678075-139678125	HCF	heart:	n/a
35	chr3:139653573-139653623	PrEC	prostate:	n/a
36	chr3:139678075-139678125	HPAEpiC	pulmonary alveolar:	n/a
37	chr3:139654264-139654314	PANC-1	pancreas:	n/a
38	chr3:139655800-139655850	MCF10A-Er-Src	breast:	n/a
39	chr3:139653872-139653922	AG09309	skin:	n/a
40	chr3:139655283-139655333	HCT-116	colon:	n/a
41	chr3:139654740-139654790	HNPCEpiC	eye:	n/a
42	chr3:139654245-139654295	Caco-2	colon:	n/a
43	chr3:139654740-139654790	GM06990	blood:	n/a
44	chr3:139654264-139654314	ovcar-3	ovarian:	n/a
45	chr3:139655283-139655333	GM19239	blood:	n/a
46	chr3:139653928-139653978	H1-hESC	embryonic stem cell:	embryo
47	chr3:139653573-139653623	MCF10A-Er-Src	breast:	n/a
48	chr3:139653573-139653623	NHDF-neo	bronchial:	n/a
49	chr3:139653573-139653623	GM12891	blood:	n/a
50	chr3:139653872-139653922	HCF	heart:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:139438799..139439673-chr3:139652877..139653733,2	MCF-7	breast:
2	chr3:139656013..139657182-chr3:139769630..139770896,8	MCF-7	breast:
3	chr3:139646808..139649286-chr3:139653164..139655013,2	MCF-7	breast:
4	chr3:139656623..139657234-chr3:140218062..140218601,2	MCF-7	breast:
5	chr3:139682760..139685173-chr3:139765720..139767567,2	K562	blood:
6	chr3:139653263..139655437-chr3:139655759..139658179,2	K562	blood:
7	chr3:139683774..139685457-chr3:139686813..139689553,2	K562	blood:
8	chr3:139656565..139657391-chr3:140271192..140271914,2	MCF-7	breast:
9	chr3:139642398..139644174-chr3:139644715..139646232,2	MCF-7	breast:
10	chr3:139662077..139663784-chr3:139663792..139665424,2	MCF-7	breast:
11	chr3:139656272..139658962-chr3:139660762..139664978,3	MCF-7	breast:
12	chr3:139656272..139658962-chr3:139660762..139664978,3	MCF-7	breast:
13	chr3:139662077..139663784-chr3:139663792..139665424,2	MCF-7	breast:
14	chr3:139645968..139647481-chr3:139648116..139649820,2	MCF-7	breast:
15	chr3:139282929..139283874-chr3:139652757..139653752,4	MCF-7	breast:
16	chr3:139683774..139685457-chr3:139686813..139689553,2	K562	blood:
17	chr3:139270922..139271855-chr3:139653137..139653973,3	MCF-7	breast:
18	chr3:139642398..139644174-chr3:139644715..139646232,2	MCF-7	breast:
19	chr3:139654619..139655608-chr3:140217733..140218478,2	MCF-7	breast:
20	chr3:139687470..139689558-chr3:139697247..139698836,2	MCF-7	breast:
21	chr3:139656303..139657655-chr3:139769773..139770917,9	MCF-7	breast:
22	chr3:139641405..139642937-chr3:139647406..139649250,2	K562	blood:
23	chr3:139307203..139308238-chr3:139653078..139653999,6	MCF-7	breast:
24	chr3:139657365..139658949-chr3:139769085..139770688,5	MCF-7	breast:
25	chr3:139645968..139647481-chr3:139648116..139649820,2	MCF-7	breast:
26	chr3:139641405..139642937-chr3:139647406..139649250,2	K562	blood:
27	chr3:139347937..139348556-chr3:139653424..139653964,2	MCF-7	breast:
28	chr3:139673841..139676667-chr3:139679363..139682238,2	K562	blood:
29	chr3:139437070..139437910-chr3:139653098..139654016,8	MCF-7	breast:
30	chr3:139673841..139676667-chr3:139679363..139682238,2	K562	blood:

No data

Variant related genes	Relation type
CLSTN2	TF binding region
CLSTN2	CpG island
ENSG00000158258	chromatin interactions

Extended variants
information (count: 1660 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2349988	chr3:139642572-139642573	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147855519	chr3:139642596-139642597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528997058	chr3:139642618-139642619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549050810	chr3:139642674-139642675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374324104	chr3:139642682-139642683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530630231	chr3:139642691-139642692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557273094	chr3:139642699-139642700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550217120	chr3:139642715-139642716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141401337	chr3:139642717-139642718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146985388	chr3:139642744-139642745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553165985	chr3:139642758-139642759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532773467	chr3:139642764-139642765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573369077	chr3:139642791-139642792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546602148	chr3:139642888-139642889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546012169	chr3:139642889-139642890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs555824739	chr3:139642906-139642907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551925512	chr3:139642912-139642913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs575588063	chr3:139642948-139642949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs544624333	chr3:139643022-139643023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535300467	chr3:139643031-139643032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186706241	chr3:139643090-139643091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533289264	chr3:139643153-139643154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148021131	chr3:139643156-139643157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560126749	chr3:139643211-139643212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529065988	chr3:139643266-139643267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140799834	chr3:139643368-139643369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150110966	chr3:139643372-139643373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191563080	chr3:139643388-139643389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112132040	chr3:139643404-139643405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550965985	chr3:139643407-139643408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570874041	chr3:139643419-139643420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370813490	chr3:139643437-139643438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1834503	chr3:139643459-139643460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs2010357	chr3:139643464-139643465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs980337	chr3:139643561-139643562	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs2010367	chr3:139643592-139643593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs115757960	chr3:139643754-139643755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183861902	chr3:139643773-139643774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9985239	chr3:139643881-139643882	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs35399326	chr3:139643907-139643908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138399699	chr3:139643915-139643916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs540564337	chr3:139643977-139643978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs560393528	chr3:139644082-139644083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141554838	chr3:139644087-139644088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542817848	chr3:139644134-139644135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553304632	chr3:139644154-139644155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192717460	chr3:139644159-139644160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185127931	chr3:139644193-139644194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541681641	chr3:139644226-139644227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148811208	chr3:139644285-139644286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139642400-139642800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:139642800-139651600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:139645400-139646000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:139646000-139647600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:139647400-139647600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:139647400-139647800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:139647400-139647800	Enhancers	HMEC	breast
8	chr3:139647600-139647800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr3:139647600-139649200	Enhancers	Ovary	ovary
10	chr3:139647800-139648800	Weak transcription	HMEC	breast
11	chr3:139648000-139649600	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:139648800-139649600	Enhancers	HMEC	breast
13	chr3:139649600-139653400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr3:139651400-139651800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr3:139651600-139651800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr3:139651600-139651800	Enhancers	Spleen	Spleen
17	chr3:139651800-139653200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr3:139651800-139653200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:139652400-139652600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
20	chr3:139652400-139652600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
21	chr3:139652600-139652800	Enhancers	Brain Hippocampus Middle	brain
22	chr3:139653200-139653400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
25	chr3:139653200-139653400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr3:139653200-139653400	Bivalent Enhancer	Adipose Nuclei	Adipose
27	chr3:139653200-139653400	Enhancers	Brain Angular Gyrus	brain
28	chr3:139653200-139653400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
29	chr3:139653200-139653400	Enhancers	Ovary	ovary
30	chr3:139653200-139653400	Enhancers	Pancreas	Pancrea
31	chr3:139653200-139653400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr3:139653200-139653400	Flanking Bivalent TSS/Enh	HSMMtube	muscle
33	chr3:139653200-139653600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:139653200-139653600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:139653200-139653600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:139653200-139653600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:139653200-139653600	Bivalent Enhancer	Fetal Intestine Small	intestine
38	chr3:139653200-139653600	Bivalent Enhancer	Placenta	Placenta
39	chr3:139653200-139654000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:139653200-139654200	Enhancers	Fetal Brain Male	brain
41	chr3:139653200-139654800	Active TSS	Brain Anterior Caudate	brain
42	chr3:139653200-139655000	Active TSS	Brain Cingulate Gyrus	brain
43	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
44	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
45	chr3:139653200-139655200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
46	chr3:139653200-139655400	Active TSS	Pancreatic Islets	Pancreatic Islet
47	chr3:139653200-139655600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr3:139653200-139655600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr3:139653200-139656000	Active TSS	Brain Inferior Temporal Lobe	brain
50	chr3:139653400-139653600	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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