Variant report

Variant	nsv1039820
Chromosome Location	chr14:45298012-45361409
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	BATF	chr14:45358994-45359377	GM12878	blood:	n/a	n/a
2	BATF	chr14:45361242-45361482	GM12878	blood:	n/a	n/a
3	BATF	chr14:45361234-45361562	GM12878	blood:	n/a	n/a
4	BCL11A	chr14:45358948-45359357	GM12878	blood:	n/a	n/a
5	BCL11A	chr14:45359009-45359260	GM12878	blood:	n/a	n/a
6	CBX3	chr14:45302559-45303057	HCT-116	colon:	n/a	n/a
7	CEBPB	chr14:45304361-45304445	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr14:45302511-45302996	HCT-116	colon:	n/a	n/a
9	CEBPB	chr14:45308593-45308878	HepG2	liver:	n/a	chr14:45308721-45308732 chr14:45308719-45308730
10	CEBPB	chr14:45308596-45308858	A549	lung:	n/a	chr14:45308721-45308732 chr14:45308719-45308730
11	CEBPB	chr14:45319836-45320101	IMR90	lung:	n/a	n/a
12	CTCF	chr14:45315540-45315690	NHEK	skin:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
13	CTCF	chr14:45315560-45315710	AG10803	skin:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
14	CTCF	chr14:45315489-45315748	Hela-S3	cervix:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
15	CTCF	chr14:45316800-45316950	AG10803	skin:	n/a	n/a
16	CTCF	chr14:45315480-45315630	HFF	foreskin:	n/a	chr14:45315609-45315630
17	CTCF	chr14:45323460-45323610	GM12874	blood:	n/a	n/a
18	CTCF	chr14:45323474-45323580	GM12878	blood:	n/a	n/a
19	CTCF	chr14:45315497-45315747	Pancreas_OC	pancreas:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
20	CTCF	chr14:45315485-45315755	MCF-7	breast:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
21	CTCF	chr14:45315277-45315914	SK-N-SH	brain:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
22	CTCF	chr14:45315600-45315750	WI-38	lung:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
23	CTCF	chr14:45315419-45315832	IMR90	lung:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
24	CTCF	chr14:45315540-45315690	NHDF-neo	bronchial:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
25	CTCF	chr14:45315890-45316001	GM10266	blood:	n/a	n/a
26	CTCF	chr14:45315520-45315670	GM12873	blood:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
27	CTCF	chr14:45356550-45356771	K562	blood:	n/a	chr14:45356671-45356687
28	CTCF	chr14:45323420-45323570	GM12865	blood:	n/a	n/a
29	CTCF	chr14:45315580-45315730	GM12874	blood:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
30	CTCF	chr14:45315580-45315730	HCT-116	colon:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
31	CTCF	chr14:45315560-45315710	GM12875	blood:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
32	CTCF	chr14:45329700-45329850	GM12873	blood:	n/a	n/a
33	CTCF	chr14:45315540-45315690	HCM	heart:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
34	CTCF	chr14:45315540-45315690	HCPEpiC	choroid plexus:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
35	CTCF	chr14:45315540-45315690	WERI-Rb-1	eye:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
36	CTCF	chr14:45323400-45323550	GM12878	blood:	n/a	n/a
37	CTCF	chr14:45315501-45315765	SK-N-SH_RA	brain:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
38	CTCF	chr14:45315560-45315710	HEEpiC	esophagus:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
39	CTCF	chr14:45315540-45315690	GM12866	blood:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
40	CTCF	chr14:45323493-45323549	GM10266	blood:	n/a	n/a
41	CTCF	chr14:45315560-45315710	HRPEpiC	eye:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
42	CTCF	chr14:45332101-45332123	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:45315540-45315690	HRE	kidney:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
44	CTCF	chr14:45315468-45315773	HUVEC	blood vessel:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
45	CTCF	chr14:45323420-45323570	HMF	breast:	n/a	n/a
46	CTCF	chr14:45315560-45315710	HCM	heart:	n/a	chr14:45315609-45315630 chr14:45315614-45315632
47	CTCF	chr14:45314840-45314990	BJ	skin:	n/a	n/a
48	CTCF	chr14:45307923-45307956	Lung_OC	lung:	n/a	n/a
49	CTCF	chr14:45323452-45323607	K562	blood:	n/a	n/a
50	CTCF	chr14:45323459-45323577	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:45356797-45356847	ProgFib	skin:	n/a
2	chr14:45356797-45356847	ProgFib	skin:	n/a
3	chr14:45356233-45356283	IMR90	lung:	fetal
4	chr14:45356233-45356283	GM12891	blood:	n/a
5	chr14:45356185-45356235	NHDF-neo	bronchial:	n/a
6	chr14:45353678-45353728	PrEC	prostate:	n/a
7	chr14:45356673-45356723	HEK293	kidney:	embryo
8	chr14:45356607-45356657	HEEpiC	esophagus:	n/a
9	chr14:45360220-45360270	AG04450	lung:	fetal
10	chr14:45357076-45357126	SKMC	muscle:	n/a
11	chr14:45356892-45356942	GM12878	blood:	n/a
12	chr14:45356233-45356283	HCM	heart:	n/a
13	chr14:45356673-45356723	SK-N-SH_RA	brain:	n/a
14	chr14:45356673-45356723	HepG2	liver:	n/a
15	chr14:45357076-45357126	Hepatocyte	liver:	n/a
16	chr14:45356607-45356657	NHDF-neo	bronchial:	n/a
17	chr14:45356797-45356847	SAEC	small airway:	n/a
18	chr14:45360220-45360270	GM12891	blood:	n/a
19	chr14:45353678-45353728	HRCEpiC	kidney:	n/a
20	chr14:45360220-45360270	GM12878	blood:	n/a
21	chr14:45356233-45356283	NHBE	bronchial:	n/a
22	chr14:45356892-45356942	SAEC	small airway:	n/a
23	chr14:45356233-45356283	HCPEpiC	choroid plexus:	n/a
24	chr14:45356673-45356723	NHDF-neo	bronchial:	n/a
25	chr14:45356233-45356283	HRPEpiC	eye:	n/a
26	chr14:45357076-45357126	GM06990	blood:	n/a
27	chr14:45357076-45357126	CMK	blood:	n/a
28	chr14:45357076-45357126	HCM	heart:	n/a
29	chr14:45356892-45356942	SK-N-MC	brain:	n/a
30	chr14:45357076-45357126	HCT-116	colon:	n/a
31	chr14:45356185-45356235	LNCaP	prostate:	n/a
32	chr14:45356892-45356942	ProgFib	skin:	n/a
33	chr14:45356233-45356283	HCF	heart:	n/a
34	chr14:45356233-45356283	Jurkat	blood:	n/a
35	chr14:45353678-45353728	H1-hESC	embryonic stem cell:	embryo
36	chr14:45356185-45356235	AG10803	skin:	n/a
37	chr14:45356233-45356283	BE2_C	brain:	n/a
38	chr14:45356797-45356847	PrEC	prostate:	n/a
39	chr14:45356892-45356942	ECC-1	luminal epithelium:	n/a
40	chr14:45360220-45360270	A549	lung:	n/a
41	chr14:45356892-45356942	SK-N-SH	brain:	n/a
42	chr14:45353678-45353728	MCF-7	breast:	n/a
43	chr14:45356797-45356847	RPTEC	kidney:	n/a
44	chr14:45356607-45356657	HMEC	breast:	n/a
45	chr14:45360220-45360270	HL-60	blood:	n/a
46	chr14:45356233-45356283	Hepatocyte	liver:	n/a
47	chr14:45353678-45353728	ECC-1	luminal epithelium:	n/a
48	chr14:45356185-45356235	PFSK-1	brain:	n/a
49	chr14:45356185-45356235	HAEpiC	amniotic membrane:	n/a
50	chr14:45356797-45356847	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:45126668..45127459-chr14:45315563..45316088,2	MCF-7	breast:
2	chr14:45355758..45358329-chr14:45365529..45367662,3	MCF-7	breast:
3	chr14:45331974..45334102-chr14:45335344..45337812,2	MCF-7	breast:
4	chr14:45360749..45362918-chr14:45364710..45368351,3	MCF-7	breast:
5	chr14:45354185..45356391-chr14:45360074..45361840,2	MCF-7	breast:
6	chr14:45355784..45358308-chr14:45369191..45370698,2	MCF-7	breast:
7	chr14:45354185..45356391-chr14:45360074..45361840,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf28-2	chr14:45311363-45311409	l_978_chr14:45283074-45311409_kidney
2	lnc-C14orf28-2	chr14:45311089-45311174	l_978_chr14:45283074-45311409_kidney
3	lnc-KLHL28-2	chr14:45346077-45346703	ENSG00000258633.1

Variant related genes	Relation type
ENSG00000259000	TF binding region
ENSG00000259046	TF binding region
ENSG00000258509	TF binding region
ENSG00000259000	CpG island
ENSG00000259046	CpG island
ENSG00000258509	CpG island
ENSG00000179476	chromatin interactions
ENSG00000259000	chromatin interactions
ENSG00000258633	chromatin interactions

Extended variants
information (count: 1161 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1958262	chr14:45298012-45298013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs536352704	chr14:45298093-45298094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554909545	chr14:45298113-45298114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141265607	chr14:45298126-45298127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367838966	chr14:45298158-45298159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs75742746	chr14:45298245-45298246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184471778	chr14:45298393-45298394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190510528	chr14:45298395-45298396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375280110	chr14:45298447-45298448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369372313	chr14:45298476-45298477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150733602	chr14:45298555-45298556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139093575	chr14:45298571-45298572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79694771	chr14:45298607-45298608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111272844	chr14:45298614-45298615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570666795	chr14:45298621-45298622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527341592	chr14:45298639-45298640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552433776	chr14:45298678-45298679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570382098	chr14:45298728-45298729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558844830	chr14:45298814-45298815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115461660	chr14:45298843-45298844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549521975	chr14:45298868-45298869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182332498	chr14:45298869-45298870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185941419	chr14:45298993-45298994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554812688	chr14:45299006-45299007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566837137	chr14:45299048-45299049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140709401	chr14:45299057-45299058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373189622	chr14:45299089-45299090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558924625	chr14:45299099-45299100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143899355	chr14:45299113-45299114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188743254	chr14:45299175-45299176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181227408	chr14:45299180-45299181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575123459	chr14:45299185-45299186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs141005020	chr14:45299248-45299249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560016522	chr14:45299256-45299257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs527398576	chr14:45299340-45299341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185623412	chr14:45299348-45299349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563744502	chr14:45299353-45299354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566367791	chr14:45299403-45299404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531464992	chr14:45299414-45299415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144953154	chr14:45299449-45299450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs191405134	chr14:45299453-45299454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147962571	chr14:45299476-45299477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548649811	chr14:45299483-45299484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs138603413	chr14:45299518-45299519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs386381251	chr14:45299525-45299526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375814835	chr14:45299528-45299529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566816919	chr14:45299574-45299575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534320696	chr14:45299588-45299589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535253134	chr14:45299616-45299617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555607408	chr14:45299668-45299669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
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
Schizophrenia	23813976	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:45297800-45299200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr14:45297800-45302400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr14:45298400-45299400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:45299200-45300400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr14:45299400-45302400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:45299800-45300000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr14:45300400-45301600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:45301600-45301800	Enhancers	NHDF-Ad	bronchial
9	chr14:45301600-45305000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr14:45301800-45302200	Weak transcription	NHDF-Ad	bronchial
11	chr14:45301800-45303600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr14:45302200-45304000	Enhancers	NHDF-Ad	bronchial
13	chr14:45302400-45303600	Enhancers	Fetal Kidney	kidney
14	chr14:45302400-45303800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:45302400-45303800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:45302400-45304000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr14:45302600-45303200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:45303000-45303800	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr14:45303400-45303800	Enhancers	Fetal Lung	lung
20	chr14:45303400-45303800	Enhancers	NHLF	lung
21	chr14:45303400-45304200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:45303800-45304800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr14:45303800-45309000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:45304800-45305000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr14:45305000-45314400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr14:45309000-45309400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr14:45309800-45311000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr14:45311000-45311400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:45314400-45314800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:45314600-45315000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr14:45314800-45315800	Enhancers	Fetal Heart	heart
32	chr14:45314800-45317400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr14:45315200-45315600	Enhancers	Brain Angular Gyrus	brain
34	chr14:45315200-45315600	Active TSS	Brain Hippocampus Middle	brain
35	chr14:45315200-45315600	Enhancers	Brain Substantia Nigra	brain
36	chr14:45315200-45315600	Enhancers	Colon Smooth Muscle	Colon
37	chr14:45315200-45315800	Enhancers	Liver	Liver
38	chr14:45315400-45315600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr14:45315400-45315600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr14:45315400-45315600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr14:45315400-45315800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
42	chr14:45317400-45317600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr14:45329400-45330200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr14:45329600-45330000	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr14:45329600-45330000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr14:45329600-45330200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr14:45329600-45330200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr14:45329600-45330200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:45333000-45333600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:45333400-45334200	Enhancers	Fetal Stomach	stomach

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