Variant report

Variant	esv1941080
Chromosome Location	chr14:72490613-72491036
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	CEBPB	chr14:72489676-72491241	GM12878	blood:	n/a	chr14:72490500-72490512
2	CEBPB	chr14:72490726-72490946	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr14:72490860-72491010	HCT-116	colon:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
4	CTCF	chr14:72490840-72490990	HCM	heart:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
5	CTCF	chr14:72490860-72491010	HRE	kidney:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
6	CTCF	chr14:72490523-72491217	A549	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
7	CTCF	chr14:72490760-72491010	ProgFib	skin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
8	CTCF	chr14:72490800-72490950	AG04450	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
9	CTCF	chr14:72490860-72491010	GM12873	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
10	CTCF	chr14:72490900-72491050	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr14:72490840-72490990	GM12864	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
12	CTCF	chr14:72490880-72491030	HCPEpiC	choroid plexus:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
13	CTCF	chr14:72490600-72490750	HCM	heart:	n/a	n/a
14	CTCF	chr14:72490840-72490990	A549	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
15	CTCF	chr14:72490840-72490990	HFF-Myc	foreskin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
16	CTCF	chr14:72490860-72491010	HA-sp	spinal cord:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
17	CTCF	chr14:72490860-72491010	SAEC	small airway:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
18	CTCF	chr14:72490616-72491124	GM12878	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
19	CTCF	chr14:72490744-72491004	HUVEC	blood vessel:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
20	CTCF	chr14:72490743-72491029	A549	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
21	CTCF	chr14:72490721-72491064	IMR90	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
22	CTCF	chr14:72490773-72491027	LNCaP	prostate:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
23	CTCF	chr14:72490840-72490990	Hela-S3	cervix:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
24	CTCF	chr14:72490840-72490990	HA-sp	spinal cord:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
25	CTCF	chr14:72490840-72490990	AG04449	skin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
26	CTCF	chr14:72490840-72490990	NHLF	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
27	CTCF	chr14:72490600-72490750	K562	blood:	n/a	n/a
28	CTCF	chr14:72490560-72490710	AG10803	skin:	n/a	n/a
29	CTCF	chr14:72490820-72490970	GM12865	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
30	CTCF	chr14:72490780-72490930	HCFaa	heart:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
31	CTCF	chr14:72490800-72490950	GM12866	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
32	CTCF	chr14:72490815-72491008	GM20000	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
33	CTCF	chr14:72490776-72491034	GM10248	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
34	CTCF	chr14:72490840-72490990	GM12868	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
35	CTCF	chr14:72490820-72490970	MCF-7	breast:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
36	CTCF	chr14:72490563-72490613	GM10266	blood:	n/a	n/a
37	CTCF	chr14:72490840-72490990	GM12867	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
38	CTCF	chr14:72490760-72490995	GM13977	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
39	CTCF	chr14:72490847-72491041	NHEK	skin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
40	CTCF	chr14:72490714-72491081	K562	blood:	n/a	chr14:72490893-72490902 chr14:72490892-72490913 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490891-72490907
41	CTCF	chr14:72490780-72490930	GM12869	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
42	CTCF	chr14:72490709-72491023	Spleen_OC	spleen:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
43	CTCF	chr14:72490860-72491010	WI-38	lung:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
44	CTCF	chr14:72490767-72491033	GM10266	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
45	CTCF	chr14:72490780-72490930	GM12872	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
46	CTCF	chr14:72490819-72491045	GM19240	blood:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
47	CTCF	chr14:72490620-72490770	GM12870	blood:	n/a	n/a
48	CTCF	chr14:72490830-72491008	Fibrobl	skin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913
49	CTCF	chr14:72490760-72490910	BJ	skin:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906
50	CTCF	chr14:72490829-72490994	HepG2	liver:	n/a	chr14:72490891-72490907 chr14:72490893-72490902 chr14:72490890-72490908 chr14:72490893-72490906 chr14:72490892-72490913

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:72490712-72490762	AG09319	gingival:	n/a
2	chr14:72490712-72490762	SK-N-SH	brain:	n/a
3	chr14:72490712-72490762	IMR90	lung:	fetal
4	chr14:72490712-72490762	HCF	heart:	n/a
5	chr14:72490712-72490762	LNCaP	prostate:	n/a
6	chr14:72490712-72490762	ovcar-3	ovarian:	n/a
7	chr14:72490712-72490762	AG10803	skin:	n/a
8	chr14:72490712-72490762	HUVEC	blood vessel:	n/a
9	chr14:72490712-72490762	SKMC	muscle:	n/a
10	chr14:72490712-72490762	RPTEC	kidney:	n/a
11	chr14:72490712-72490762	NT2-D1	testis:	n/a
12	chr14:72490712-72490762	CMK	blood:	n/a
13	chr14:72490712-72490762	A549	lung:	n/a
14	chr14:72490712-72490762	MCF10A-Er-Src	breast:	n/a
15	chr14:72490712-72490762	GM12891	blood:	n/a
16	chr14:72490712-72490762	ProgFib	skin:	n/a
17	chr14:72490712-72490762	MCF-7	breast:	n/a
18	chr14:72490712-72490762	NHBE	bronchial:	n/a
19	chr14:72490712-72490762	H1-hESC	embryonic stem cell:	embryo
20	chr14:72490712-72490762	HAEpiC	amniotic membrane:	n/a
21	chr14:72490712-72490762	HCPEpiC	choroid plexus:	n/a
22	chr14:72490712-72490762	Hepatocyte	liver:	n/a
23	chr14:72490712-72490762	AG04450	lung:	fetal
24	chr14:72490712-72490762	SK-N-SH_RA	brain:	n/a
25	chr14:72490712-72490762	AG09309	skin:	n/a
26	chr14:72490712-72490762	HNPCEpiC	eye:	n/a
27	chr14:72490712-72490762	HL-60	blood:	n/a
28	chr14:72490712-72490762	T-47D	breast:	n/a
29	chr14:72490712-72490762	GM12878	blood:	n/a
30	chr14:72490712-72490762	HRCEpiC	kidney:	n/a
31	chr14:72490712-72490762	U87	brain:	n/a
32	chr14:72490712-72490762	HRE	kidney:	n/a
33	chr14:72490712-72490762	NB4	blood:	n/a
34	chr14:72490712-72490762	Caco-2	colon:	n/a
35	chr14:72490712-72490762	PANC-1	pancreas:	n/a
36	chr14:72490712-72490762	HepG2	liver:	n/a
37	chr14:72490712-72490762	BE2_C	brain:	n/a
38	chr14:72490712-72490762	BJ	skin:	n/a
39	chr14:72490712-72490762	GM06990	blood:	n/a
40	chr14:72490712-72490762	Jurkat	blood:	n/a
41	chr14:72490712-72490762	SK-N-MC	brain:	n/a
42	chr14:72490712-72490762	HCM	heart:	n/a
43	chr14:72490712-72490762	GM19239	blood:	n/a
44	chr14:72490712-72490762	HMEC	breast:	n/a
45	chr14:72490712-72490762	AoSMC	blood vessel:	n/a
46	chr14:72490712-72490762	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:72490712-72490762	HIPEpiC	eye:	n/a
48	chr14:72490712-72490762	HEK293	kidney:	embryo
49	chr14:72490712-72490762	SAEC	small airway:	n/a
50	chr14:72490712-72490762	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:72398692..72399639-chr14:72490586..72491393,3	MCF-7	breast:
2	chr14:72482931..72485550-chr14:72489530..72491362,2	MCF-7	breast:
3	chr14:72490629..72491408-chr14:72758856..72759783,5	MCF-7	breast:
4	chr14:72490402..72491111-chr14:72887191..72887990,2	MCF-7	breast:
5	chr14:72489255..72491408-chr14:72757396..72759777,2	MCF-7	breast:
6	chr14:72490617..72491401-chr14:72887032..72887742,2	K562	blood:

Variant related genes	Relation type
ENSG00000200298	TF binding region
ENSG00000200298	CpG island
ENSG00000182732	chromatin interactions

Extended variants
information (count: 32 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146511994	chr14:72490616-72490617	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs555964771	chr14:72490634-72490635	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567982603	chr14:72490651-72490652	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs11846932	chr14:72490662-72490663	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs181974269	chr14:72490663-72490664	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs386778686	chr14:72490678-72490679	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs11846989	chr14:72490679-72490680	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557543878	chr14:72490680-72490681	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576106956	chr14:72490694-72490695	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs544782466	chr14:72490711-72490712	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371356820	chr14:72490712-72490713	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs10137125	chr14:72490717-72490718	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs542536451	chr14:72490725-72490726	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186200807	chr14:72490753-72490754	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs527671416	chr14:72490757-72490758	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs552569725	chr14:72490762-72490763	Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs76096283	chr14:72490793-72490794	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs57712462	chr14:72490794-72490795	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs202142370	chr14:72490798-72490799	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531710183	chr14:72490821-72490822	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549528165	chr14:72490823-72490824	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs386778687	chr14:72490840-72490841	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs386508599	chr14:72490843-72490844	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs567919712	chr14:72490851-72490852	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535304536	chr14:72490856-72490857	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs548092372	chr14:72490872-72490873	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs142283270	chr14:72490913-72490914	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565990525	chr14:72490923-72490924	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539032885	chr14:72490937-72490938	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs8021632	chr14:72490980-72490981	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs576013578	chr14:72491014-72491015	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6574039	chr14:72491015-72491016	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:68)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72489200-72491000	Enhancers	HMEC	breast
2	chr14:72489600-72491200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr14:72489600-72491200	Enhancers	Adipose Nuclei	Adipose
4	chr14:72489600-72491200	Enhancers	GM12878-XiMat	blood
5	chr14:72489800-72491600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr14:72490000-72494800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:72490200-72490800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr14:72490200-72490800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr14:72490200-72490800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:72490200-72490800	Enhancers	Fetal Muscle Leg	muscle
11	chr14:72490200-72490800	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr14:72490200-72490800	Flanking Active TSS	NHEK	skin
13	chr14:72490200-72491200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr14:72490200-72491200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr14:72490200-72491600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:72490400-72490800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr14:72490400-72490800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:72490400-72491200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr14:72490400-72491200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:72490400-72491200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr14:72490400-72491200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr14:72490400-72491200	Enhancers	Left Ventricle	heart
23	chr14:72490600-72491200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr14:72490800-72491200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr14:72490800-72491200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:72490800-72491400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr14:72490800-72491600	Enhancers	NHEK	skin
28	chr14:72491000-72491400	Enhancers	Right Atrium	heart
29	chr14:72491000-72491800	Enhancers	Fetal Heart	heart

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