Variant report

Variant	nsv564693
Chromosome Location	chr14:44840554-44927624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:264)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:264 , 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	chr14:44918300-44918537	K562	blood:	n/a	n/a
2	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
4	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
5	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
6	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
8	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
9	CEBPB	chr14:44845840-44846035	A549	lung:	n/a	n/a
10	CEBPB	chr14:44865546-44865783	Hela-S3	cervix:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
11	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
12	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
13	CEBPB	chr14:44859620-44859752	H1-hESC	embryonic stem cell:	n/a	chr14:44859701-44859712
14	CEBPB	chr14:44862132-44862411	HepG2	liver:	n/a	chr14:44862299-44862316 chr14:44862302-44862315
15	CEBPB	chr14:44865478-44865918	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
16	CEBPB	chr14:44865476-44865832	A549	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
17	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
18	CEBPB	chr14:44865449-44865776	MCF-7	breast:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
19	CEBPB	chr14:44860656-44860866	HepG2	liver:	n/a	chr14:44860752-44860763
20	CEBPB	chr14:44892241-44892441	IMR90	lung:	n/a	chr14:44892371-44892382
21	CEBPB	chr14:44859595-44859755	HepG2	liver:	n/a	chr14:44859701-44859712
22	CEBPB	chr14:44892321-44892509	HepG2	liver:	n/a	chr14:44892371-44892382
23	CEBPD	chr14:44918203-44918635	K562	blood:	n/a	n/a
24	CEBPD	chr14:44918285-44918591	K562	blood:	n/a	n/a
25	CTCF	chr14:44922545-44923128	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:44884447-44884520	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr14:44922681-44922975	T-47D	breast:	n/a	n/a
28	CTCF	chr14:44922804-44922869	NHEK	skin:	n/a	n/a
29	CTCF	chr14:44922760-44922910	MCF-7	breast:	n/a	n/a
30	CTCF	chr14:44922811-44922942	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr14:44922769-44922938	LNCaP	prostate:	n/a	n/a
32	CTCF	chr14:44922763-44922910	LNCaP	prostate:	n/a	n/a
33	CTCF	chr14:44922840-44922990	MCF-7	breast:	n/a	n/a
34	CTCF	chr14:44922829-44922893	K562	blood:	n/a	n/a
35	CTCF	chr14:44922568-44923005	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:44922768-44922939	MCF-7	breast:	n/a	n/a
37	CTCF	chr14:44922602-44923043	T-47D	breast:	n/a	n/a
38	CTCF	chr14:44867820-44867970	HepG2	liver:	n/a	n/a
39	CTCF	chr14:44922780-44922930	NHEK	skin:	n/a	n/a
40	CTCF	chr14:44882613-44882697	Lung_OC	lung:	n/a	n/a
41	CTCF	chr14:44857548-44857591	GM13977	blood:	n/a	n/a
42	CTCF	chr14:44846025-44846080	GM13976	blood:	n/a	n/a
43	CTCF	chr14:44894642-44894669	GM13976	blood:	n/a	n/a
44	CTCF	chr14:44890993-44890999	GM13976	blood:	n/a	n/a
45	CTCF	chr14:44926160-44926203	GM10266	blood:	n/a	n/a
46	CTCF	chr14:44922746-44922968	GM12878	blood:	n/a	n/a
47	CTCF	chr14:44922840-44922990	NHEK	skin:	n/a	n/a
48	CTCF	chr14:44922798-44922912	Gliobla	brain:	n/a	n/a
49	CTCF	chr14:44890953-44890989	GM13976	blood:	n/a	n/a
50	CTCF	chr14:44922737-44922969	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44853952-44854002	HCPEpiC	choroid plexus:	n/a
2	chr14:44853952-44854002	GM12892	blood:	n/a
3	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
4	chr14:44853952-44854002	SK-N-SH	brain:	n/a
5	chr14:44853952-44854002	GM12891	blood:	n/a
6	chr14:44853952-44854002	PFSK-1	brain:	n/a
7	chr14:44853952-44854002	ECC-1	luminal epithelium:	n/a
8	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
9	chr14:44853952-44854002	HepG2	liver:	n/a
10	chr14:44853952-44854002	MCF-7	breast:	n/a
11	chr14:44853952-44854002	MCF10A-Er-Src	breast:	n/a
12	chr14:44853952-44854002	K562	blood:	n/a
13	chr14:44853952-44854002	HL-60	blood:	n/a
14	chr14:44853952-44854002	Hepatocyte	liver:	n/a
15	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
16	chr14:44853952-44854002	HRCEpiC	kidney:	n/a
17	chr14:44853952-44854002	AG04450	lung:	fetal
18	chr14:44853952-44854002	A549	lung:	n/a
19	chr14:44853952-44854002	ProgFib	skin:	n/a
20	chr14:44853952-44854002	BE2_C	brain:	n/a
21	chr14:44853952-44854002	GM06990	blood:	n/a
22	chr14:44853952-44854002	HNPCEpiC	eye:	n/a
23	chr14:44853952-44854002	NH-A	brain:	n/a
24	chr14:44853952-44854002	NT2-D1	testis:	n/a
25	chr14:44853952-44854002	PrEC	prostate:	n/a
26	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
27	chr14:44853952-44854002	HIPEpiC	eye:	n/a
28	chr14:44853952-44854002	U87	brain:	n/a
29	chr14:44853952-44854002	Caco-2	colon:	n/a
30	chr14:44853952-44854002	CMK	blood:	n/a
31	chr14:44853952-44854002	HMEC	breast:	n/a
32	chr14:44853952-44854002	NHDF-neo	bronchial:	n/a
33	chr14:44853952-44854002	GM19239	blood:	n/a
34	chr14:44853952-44854002	SAEC	small airway:	n/a
35	chr14:44853952-44854002	HRPEpiC	eye:	n/a
36	chr14:44853952-44854002	AG10803	skin:	n/a
37	chr14:44853952-44854002	IMR90	lung:	fetal
38	chr14:44853952-44854002	SKMC	muscle:	n/a
39	chr14:44853952-44854002	RPTEC	kidney:	n/a
40	chr14:44853952-44854002	GM12878	blood:	n/a
41	chr14:44853952-44854002	HRE	kidney:	n/a
42	chr14:44853952-44854002	HCM	heart:	n/a
43	chr14:44853952-44854002	Jurkat	blood:	n/a
44	chr14:44853952-44854002	SK-N-SH_RA	brain:	n/a
45	chr14:44853952-44854002	ovcar-3	ovarian:	n/a
46	chr14:44853952-44854002	HCT-116	colon:	n/a
47	chr14:44853952-44854002	SK-N-MC	brain:	n/a
48	chr14:44853952-44854002	Hela-S3	cervix:	n/a
49	chr14:44853952-44854002	NB4	blood:	n/a
50	chr14:44853952-44854002	LNCaP	prostate:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
2	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
3	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
4	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
5	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
6	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
7	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
2	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
3	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
4	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
5	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
6	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126
7	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
8	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
9	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
10	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126
11	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
12	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969

No data

Variant related genes	Relation type
ENSG00000258969	TF binding region
ENSG00000259126	TF binding region
ENSG00000258969	CpG island
ENSG00000259126	CpG island
ENSG00000259126	chromatin interactions
FAM134B	miRNA target sites
B4GALT1	miRNA target sites

Extended variants
information (count: 1861 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1861 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs950265	chr14:44840554-44840555	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533017179	chr14:44840588-44840589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs373478272	chr14:44840607-44840608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145022962	chr14:44840614-44840615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564110759	chr14:44840615-44840616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531585544	chr14:44840616-44840617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs949776	chr14:44840663-44840664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568453232	chr14:44840711-44840712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs189315323	chr14:44840726-44840727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs547966112	chr14:44840740-44840741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566387075	chr14:44840758-44840759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540105953	chr14:44840773-44840774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557810210	chr14:44840814-44840815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193197052	chr14:44840847-44840848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138084248	chr14:44840894-44840895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149536657	chr14:44840900-44840901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555482996	chr14:44840942-44840943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573605937	chr14:44840967-44840968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185112696	chr14:44841051-44841052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552712598	chr14:44841078-44841079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577536471	chr14:44841104-44841105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544928858	chr14:44841113-44841114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189967679	chr14:44841141-44841142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111757877	chr14:44841229-44841230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534728846	chr14:44841281-44841282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554238498	chr14:44841351-44841352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376458655	chr14:44841367-44841368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148250212	chr14:44841389-44841390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568068277	chr14:44841576-44841577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141274690	chr14:44841580-44841581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548190375	chr14:44841653-44841654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75301488	chr14:44841681-44841682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147375058	chr14:44841697-44841698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113837629	chr14:44841702-44841703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117476592	chr14:44841709-44841710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs533545382	chr14:44841721-44841722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28735647	chr14:44841729-44841730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552140107	chr14:44841788-44841789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572507660	chr14:44841855-44841856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537303305	chr14:44841856-44841857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570246766	chr14:44841898-44841899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78698400	chr14:44841941-44841942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111714841	chr14:44841949-44841950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567368920	chr14:44841968-44841969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534383938	chr14:44841973-44841974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115315265	chr14:44842023-44842024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557335053	chr14:44842082-44842083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551034775	chr14:44842168-44842169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577449179	chr14:44842178-44842179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs544794281	chr14:44842184-44842185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44838400-44842600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr14:44839400-44841200	Weak transcription	Fetal Intestine Large	intestine
3	chr14:44839600-44841400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr14:44839800-44841200	Weak transcription	HMEC	breast
5	chr14:44840200-44841200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr14:44840800-44842400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr14:44841200-44841800	Enhancers	HMEC	breast
8	chr14:44841200-44842400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:44841200-44842600	Enhancers	Fetal Intestine Large	intestine
10	chr14:44841400-44841800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:44841800-44842400	Weak transcription	HMEC	breast
12	chr14:44842400-44842600	Enhancers	HMEC	breast
13	chr14:44843400-44850200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr14:44845200-44846600	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr14:44848000-44849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:44848400-44849200	Enhancers	Adipose Nuclei	Adipose
17	chr14:44849200-44851000	Weak transcription	Adipose Nuclei	Adipose
18	chr14:44849200-44851600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr14:44850200-44851000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr14:44851000-44852800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr14:44851000-44853600	Enhancers	Adipose Nuclei	Adipose
22	chr14:44851600-44853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr14:44852600-44852800	Enhancers	Ovary	ovary
24	chr14:44852800-44853600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:44853000-44853600	Enhancers	Fetal Stomach	stomach
26	chr14:44853400-44853600	Enhancers	Ovary	ovary
27	chr14:44853400-44853800	Enhancers	Fetal Brain Female	brain
28	chr14:44853800-44857400	Weak transcription	Fetal Brain Female	brain
29	chr14:44854200-44854400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:44857400-44857600	Enhancers	Fetal Brain Female	brain
31	chr14:44861800-44862400	Enhancers	Fetal Intestine Large	intestine
32	chr14:44862400-44862800	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr14:44872000-44872600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr14:44872000-44874400	Enhancers	Fetal Brain Male	brain
35	chr14:44872400-44874600	Enhancers	Fetal Brain Female	brain
36	chr14:44872600-44874000	Enhancers	Fetal Heart	heart
37	chr14:44873200-44874600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr14:44873400-44874400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:44873600-44874600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr14:44873600-44874600	Enhancers	Adipose Nuclei	Adipose
41	chr14:44873600-44875200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr14:44873800-44874200	Enhancers	Fetal Kidney	kidney
43	chr14:44874200-44874600	Enhancers	Fetal Lung	lung
44	chr14:44881200-44882400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr14:44881600-44882600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:44881600-44882600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr14:44882000-44882600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr14:44882000-44882600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr14:44882000-44882600	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr14:44882000-44882600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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