Variant report

Variant	nsv542060
Chromosome Location	chr14:42994962-43271733
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	BACH1	chr14:43088748-43088782	K562	blood:	n/a	n/a
2	BRCA1	chr14:43152884-43153470	Hela-S3	cervix:	n/a	n/a
3	BRCA1	chr14:43010506-43011087	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr14:43220007-43220460	MCF-7	breast:	n/a	chr14:43220319-43220332 chr14:43220319-43220330
5	CEBPB	chr14:43200940-43201437	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:43220078-43220475	MCF-7	breast:	n/a	chr14:43220319-43220332 chr14:43220319-43220330
7	CEBPB	chr14:43152867-43153237	HepG2	liver:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
8	CEBPB	chr14:43094448-43094984	HepG2	liver:	n/a	chr14:43094870-43094883 chr14:43094573-43094586 chr14:43094870-43094881
9	CEBPB	chr14:43045458-43045742	HepG2	liver:	n/a	chr14:43045602-43045613
10	CEBPB	chr14:43058937-43059272	HepG2	liver:	n/a	chr14:43059110-43059121
11	CEBPB	chr14:43104496-43104820	HepG2	liver:	n/a	chr14:43104691-43104702 chr14:43104647-43104658
12	CEBPB	chr14:43155323-43155662	HepG2	liver:	n/a	chr14:43155494-43155505
13	CEBPB	chr14:43088861-43089038	A549	lung:	n/a	n/a
14	CEBPB	chr14:43152849-43153141	MCF-7	breast:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
15	CEBPB	chr14:43057650-43057809	HepG2	liver:	n/a	chr14:43057739-43057750
16	CEBPB	chr14:43163290-43163407	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:43058980-43059253	A549	lung:	n/a	chr14:43059110-43059121
18	CEBPB	chr14:43112063-43112289	H1-hESC	embryonic stem cell:	n/a	chr14:43112172-43112183
19	CEBPB	chr14:43006799-43007063	IMR90	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
20	CEBPB	chr14:43269970-43270262	HepG2	liver:	n/a	chr14:43270105-43270116
21	CEBPB	chr14:43257346-43257491	HepG2	liver:	n/a	n/a
22	CEBPB	chr14:43245056-43245279	HepG2	liver:	n/a	chr14:43245175-43245186
23	CEBPB	chr14:43112050-43112355	A549	lung:	n/a	chr14:43112172-43112183
24	CEBPB	chr14:43006817-43007048	A549	lung:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
25	CEBPB	chr14:43152905-43153236	A549	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
26	CEBPB	chr14:43112013-43112367	HepG2	liver:	n/a	chr14:43112172-43112183
27	CEBPB	chr14:43152858-43153242	IMR90	lung:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
28	CEBPB	chr14:43183739-43184211	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:43020465-43020677	HepG2	liver:	n/a	chr14:43020529-43020540
30	CEBPB	chr14:43112055-43112323	Hela-S3	cervix:	n/a	chr14:43112172-43112183
31	CEBPB	chr14:43112026-43112359	IMR90	lung:	n/a	chr14:43112172-43112183
32	CEBPB	chr14:43088915-43089065	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:43155357-43155678	IMR90	lung:	n/a	chr14:43155494-43155505
34	CEBPB	chr14:43098476-43098668	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:43183727-43184112	A549	lung:	n/a	n/a
36	CEBPB	chr14:43152636-43153526	Hela-S3	cervix:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
37	CEBPB	chr14:43071917-43072221	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:43183728-43184158	HepG2	liver:	n/a	n/a
39	CEBPB	chr14:43081131-43081221	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr14:43112099-43112243	K562	blood:	n/a	chr14:43112172-43112183
41	CEBPB	chr14:43010664-43011294	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr14:43203747-43204000	HepG2	liver:	n/a	chr14:43203901-43203912 chr14:43203897-43203910 chr14:43203864-43203875 chr14:43203898-43203909
43	CEBPB	chr14:43220099-43220482	Hela-S3	cervix:	n/a	chr14:43220319-43220332 chr14:43220319-43220330
44	CEBPB	chr14:43152873-43153174	H1-hESC	embryonic stem cell:	n/a	chr14:43153045-43153058 chr14:43153045-43153056 chr14:43153047-43153056 chr14:43153045-43153058 chr14:43153058-43153071 chr14:43153046-43153057
45	CEBPB	chr14:43112092-43112319	MCF-7	breast:	n/a	chr14:43112172-43112183
46	CEBPB	chr14:43186035-43186373	HepG2	liver:	n/a	chr14:43186198-43186209
47	CEBPB	chr14:43009532-43009798	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:43006767-43007104	HepG2	liver:	n/a	chr14:43006914-43006925 chr14:43006916-43006925
49	CEBPB	chr14:42995827-42996065	HepG2	liver:	n/a	chr14:42995926-42995937 chr14:42995924-42995935
50	CEBPB	chr14:43098443-43098643	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:43123081-43123131	NT2-D1	testis:	n/a
2	chr14:43123081-43123131	SK-N-SH_RA	brain:	n/a
3	chr14:43123081-43123131	Hela-S3	cervix:	n/a
4	chr14:43123081-43123131	HUVEC	blood vessel:	n/a
5	chr14:43123081-43123131	PANC-1	pancreas:	n/a
6	chr14:43123081-43123131	HCT-116	colon:	n/a
7	chr14:43123081-43123131	AG04450	lung:	fetal
8	chr14:43123081-43123131	H1-hESC	embryonic stem cell:	embryo
9	chr14:43123081-43123131	MCF-7	breast:	n/a
10	chr14:43123081-43123131	HRPEpiC	eye:	n/a
11	chr14:43123081-43123131	HRCEpiC	kidney:	n/a
12	chr14:43123081-43123131	AG04449	skin:	fetal
13	chr14:43123081-43123131	GM06990	blood:	n/a
14	chr14:43123081-43123131	MCF10A-Er-Src	breast:	n/a
15	chr14:43123081-43123131	AG09309	skin:	n/a
16	chr14:43123081-43123131	HEEpiC	esophagus:	n/a
17	chr14:43123081-43123131	LNCaP	prostate:	n/a
18	chr14:43123081-43123131	HNPCEpiC	eye:	n/a
19	chr14:43123081-43123131	SAEC	small airway:	n/a
20	chr14:43123081-43123131	SK-N-SH	brain:	n/a
21	chr14:43123081-43123131	HMEC	breast:	n/a
22	chr14:43123081-43123131	HIPEpiC	eye:	n/a
23	chr14:43123081-43123131	GM19239	blood:	n/a
24	chr14:43123081-43123131	NB4	blood:	n/a
25	chr14:43123081-43123131	BJ	skin:	n/a
26	chr14:43123081-43123131	U87	brain:	n/a
27	chr14:43123081-43123131	PrEC	prostate:	n/a
28	chr14:43123081-43123131	GM12891	blood:	n/a
29	chr14:43123081-43123131	HRE	kidney:	n/a
30	chr14:43123081-43123131	HCF	heart:	n/a
31	chr14:43123081-43123131	K562	blood:	n/a
32	chr14:43123081-43123131	SKMC	muscle:	n/a
33	chr14:43123081-43123131	Caco-2	colon:	n/a
34	chr14:43123081-43123131	ovcar-3	ovarian:	n/a
35	chr14:43123081-43123131	RPTEC	kidney:	n/a
36	chr14:43123081-43123131	AoSMC	blood vessel:	n/a
37	chr14:43123081-43123131	GM12892	blood:	n/a
38	chr14:43123081-43123131	HAEpiC	amniotic membrane:	n/a
39	chr14:43123081-43123131	ECC-1	luminal epithelium:	n/a
40	chr14:43123081-43123131	A549	lung:	n/a
41	chr14:43123081-43123131	HCM	heart:	n/a
42	chr14:43123081-43123131	NHBE	bronchial:	n/a
43	chr14:43123081-43123131	CMK	blood:	n/a
44	chr14:43123081-43123131	T-47D	breast:	n/a
45	chr14:43123081-43123131	ProgFib	skin:	n/a
46	chr14:43123081-43123131	BE2_C	brain:	n/a
47	chr14:43123081-43123131	HCPEpiC	choroid plexus:	n/a
48	chr14:43123081-43123131	IMR90	lung:	fetal
49	chr14:43123081-43123131	AG09319	gingival:	n/a
50	chr14:43123081-43123131	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr14:43227995..43229990-chr14:43231177..43232780,2	MCF-7	breast:
2	chr14:43214694..43216920-chr14:43221221..43223715,2	MCF-7	breast:
3	chr14:43134052..43134776-chr3:181029654..181030646,2	MCF-7	breast:
4	chr14:43227995..43229990-chr14:43231177..43232780,2	MCF-7	breast:
5	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
6	chr14:43030553..43031053-chr17:8338863..8339416,2	Hela-S3	cervix:
7	chr14:43169956..43172607-chr14:43173470..43175872,2	MCF-7	breast:
8	chr14:42579463..42579970-chr14:43055430..43056355,2	MCF-7	breast:
9	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
10	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
11	chr14:43199863..43201590-chr14:43205073..43207655,2	MCF-7	breast:
12	chr14:43169956..43172607-chr14:43173470..43175872,2	MCF-7	breast:
13	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
14	chr14:43140328..43142020-chr14:43153445..43155405,2	MCF-7	breast:
15	chr14:43180662..43182425-chr14:43185874..43188790,2	MCF-7	breast:
16	chr14:43214694..43216920-chr14:43221221..43223715,2	MCF-7	breast:
17	chr14:43078769..43080628-chr14:43081211..43084199,2	MCF-7	breast:
18	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:
19	chr14:43180662..43182425-chr14:43185874..43188790,2	MCF-7	breast:
20	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
21	chr14:43258257..43260320-chr6:32934540..32936791,2	MCF-7	breast:
22	chr14:43199863..43201590-chr14:43205073..43207655,2	MCF-7	breast:
23	chr14:43090850..43092635-chr14:43095537..43098102,2	K562	blood:
24	chr14:43055616..43058571-chr14:43062767..43065185,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-2	chr14:42997872-42998091	ENSG00000258850.1
2	lnc-RP11-214N1.1.1-1	chr14:43172308-43172404	ENSG00000258394.1
3	lnc-RP11-214N1.1.1-2	chr14:42997872-42998001	NONHSAT036588
4	lnc-RP11-214N1.1.1-3	chr14:43078071-43078780	NONHSAT036591
5	lnc-RP11-214N1.1.1-2	chr14:42998014-42998060	NONHSAT036588
6	lnc-RP11-214N1.1.1-1	chr14:43172607-43172858	ENSG00000258394.1

Variant related genes	Relation type
ENSG00000258622	TF binding region
ENSG00000258505	TF binding region
ENSG00000258622	CpG island
ENSG00000258505	CpG island
ENSG00000204256	chromatin interactions
ENSG00000166579	chromatin interactions
ENSG00000204257	chromatin interactions

Extended variants
information (count: 2580 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2580 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547717821	chr14:42994963-42994964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565713389	chr14:42995041-42995042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533201197	chr14:42995102-42995103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11412462	chr14:42995137-42995138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551450886	chr14:42995155-42995156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112031563	chr14:42995157-42995158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12147919	chr14:42995182-42995183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs368466842	chr14:42995186-42995187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs74049214	chr14:42995189-42995190	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs113922113	chr14:42995290-42995291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556055731	chr14:42995415-42995416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139185009	chr14:42995464-42995465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371412106	chr14:42995476-42995477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12436904	chr14:42995533-42995534	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144434139	chr14:42995539-42995540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572063653	chr14:42995549-42995550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536265121	chr14:42995561-42995562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74049223	chr14:42995641-42995642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182142951	chr14:42995644-42995645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs367825058	chr14:42995727-42995728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145365057	chr14:42995753-42995754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186860739	chr14:42995756-42995757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148761765	chr14:42995778-42995779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541321167	chr14:42995800-42995801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559660805	chr14:42995838-42995839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533455135	chr14:42995851-42995852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74049225	chr14:42995921-42995922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563720333	chr14:42995922-42995923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs530874045	chr14:42995949-42995950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549488857	chr14:42995977-42995978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200429006	chr14:42995992-42995993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199647963	chr14:42996054-42996055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556462851	chr14:42996064-42996065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544991021	chr14:42996069-42996070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568160589	chr14:42996124-42996125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8004487	chr14:42996125-42996126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs142457777	chr14:42996134-42996135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558502209	chr14:42996213-42996214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17113136	chr14:42996220-42996221	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs539766224	chr14:42996305-42996306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577789426	chr14:42996315-42996316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115156398	chr14:42996321-42996322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114430937	chr14:42996358-42996359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs17697838	chr14:42996368-42996369	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs140465940	chr14:42996393-42996394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147031610	chr14:42996405-42996406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541185901	chr14:42996406-42996407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559521072	chr14:42996415-42996416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7142011	chr14:42996458-42996459	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs147700665	chr14:42996467-42996468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Burkitt''s lymphoma	19759907	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
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	20967226	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42993200-42996600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr14:42996600-42997200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr14:42997200-42997600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr14:43002400-43002800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:43002400-43003000	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr14:43002800-43010800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:43004400-43004800	Active TSS	A549	lung
8	chr14:43004600-43004800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr14:43010600-43011200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:43010600-43011400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr14:43010800-43011400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:43011000-43011400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:43011000-43011600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:43011200-43011600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:43013600-43013800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:43017400-43017800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr14:43017800-43019800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr14:43018800-43020200	Enhancers	Fetal Heart	heart
19	chr14:43019000-43020200	Enhancers	Fetal Brain Male	brain
20	chr14:43019400-43020200	Enhancers	Fetal Brain Female	brain
21	chr14:43020200-43023400	Weak transcription	Fetal Heart	heart
22	chr14:43023400-43023800	Flanking Active TSS	Fetal Heart	heart
23	chr14:43023800-43024800	Enhancers	Fetal Heart	heart
24	chr14:43024800-43025200	Flanking Active TSS	Fetal Heart	heart
25	chr14:43025200-43026600	Enhancers	Fetal Heart	heart
26	chr14:43025800-43026200	Enhancers	Fetal Brain Female	brain
27	chr14:43030000-43031400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr14:43031200-43033200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:43031400-43031800	Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr14:43031400-43033200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:43031800-43032000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr14:43031800-43033000	Enhancers	Primary hematopoietic stem cells	blood
33	chr14:43032000-43032400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:43032000-43032400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr14:43032400-43033200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr14:43034400-43035400	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr14:43035400-43038400	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr14:43038000-43038800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr14:43038200-43038800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:43038400-43038800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr14:43040200-43041200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:43064200-43064400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr14:43071200-43072000	Enhancers	Fetal Lung	lung
44	chr14:43072000-43075400	Weak transcription	Fetal Lung	lung
45	chr14:43075200-43075400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr14:43078200-43078600	Enhancers	Brain Angular Gyrus	brain
47	chr14:43078200-43078600	Enhancers	Brain Hippocampus Middle	brain
48	chr14:43078200-43078600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr14:43084800-43085000	Enhancers	Fetal Heart	heart
50	chr14:43094800-43095000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links