Variant report

Variant	nsv1037114
Chromosome Location	chr14:82123315-82241676
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	ARID3A	chr14:82129357-82129431	HepG2	liver:	n/a	n/a
2	BACH1	chr14:82199769-82199770	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr14:82222336-82222595	K562	blood:	n/a	n/a
4	CEBPB	chr14:82234938-82235036	A549	lung:	n/a	chr14:82234961-82234970 chr14:82234959-82234970
5	CEBPB	chr14:82223192-82223412	HepG2	liver:	n/a	chr14:82223312-82223323
6	CEBPB	chr14:82240243-82240541	MCF-7	breast:	n/a	n/a
7	CTCF	chr14:82176720-82176870	K562	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
8	CTCF	chr14:82176573-82176942	H1-hESC	embryonic stem cell:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
9	CTCF	chr14:82176720-82176870	GM12867	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
10	CTCF	chr14:82176700-82176850	GM12868	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
11	CTCF	chr14:82176781-82176817	A549	lung:	n/a	n/a
12	CTCF	chr14:82176720-82176870	SK-N-SH_RA	brain:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
13	CTCF	chr14:82176660-82176902	Gliobla	brain:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
14	CTCF	chr14:82176647-82176912	LNCaP	prostate:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
15	CTCF	chr14:82176720-82176870	GM12869	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
16	CTCF	chr14:82176700-82176850	HEK293	kidney:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
17	CTCF	chr14:82176773-82176791	MCF-7	breast:	n/a	chr14:82176773-82176791
18	CTCF	chr14:82140387-82140523	MCF-7	breast:	n/a	n/a
19	CTCF	chr14:82176740-82176890	HCPEpiC	choroid plexus:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
20	CTCF	chr14:82143420-82143570	MCF-7	breast:	n/a	chr14:82143482-82143491
21	CTCF	chr14:82176800-82176950	NHDF-neo	bronchial:	n/a	n/a
22	CTCF	chr14:82176720-82176870	GM06990	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
23	CTCF	chr14:82176667-82176906	MCF-7	breast:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
24	CTCF	chr14:82204380-82204530	Caco-2	colon:	n/a	chr14:82204478-82204499
25	CTCF	chr14:82176639-82176903	HepG2	liver:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
26	CTCF	chr14:82210738-82210798	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr14:82176696-82176883	ProgFib	skin:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
28	CTCF	chr14:82176570-82176575	Medullo	brain:	n/a	n/a
29	CTCF	chr14:82176740-82176890	SK-N-SH_RA	brain:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
30	CTCF	chr14:82176605-82176897	A549	lung:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
31	CTCF	chr14:82176740-82176890	GM12873	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
32	CTCF	chr14:82140393-82140510	MCF-7	breast:	n/a	n/a
33	CTCF	chr14:82135469-82135487	ProgFib	skin:	n/a	n/a
34	CTCF	chr14:82203620-82203770	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr14:82176619-82176953	K562	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
36	CTCF	chr14:82176700-82176850	HCFaa	heart:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
37	CTCF	chr14:82176720-82176870	HMF	breast:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
38	CTCF	chr14:82176700-82176850	HRPEpiC	eye:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
39	CTCF	chr14:82176720-82176870	SAEC	small airway:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
40	CTCF	chr14:82176760-82176910	HFF	foreskin:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
41	CTCF	chr14:82136416-82136418	GM10248	blood:	n/a	n/a
42	CTCF	chr14:82176700-82176850	HCM	heart:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
43	CTCF	chr14:82176686-82176836	GM20000	blood:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
44	CTCF	chr14:82206352-82206390	GM20000	blood:	n/a	n/a
45	CTCF	chr14:82176700-82176850	Caco-2	colon:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
46	CTCF	chr14:82176760-82176910	BE2_C	brain:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
47	CTCF	chr14:82176680-82176830	NHEK	skin:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
48	CTCF	chr14:82138506-82138559	Lung_OC	lung:	n/a	n/a
49	CTCF	chr14:82176700-82176886	Lung_OC	lung:	n/a	chr14:82176775-82176796 chr14:82176773-82176791
50	CTCF	chr14:82140360-82140519	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:82124963-82125013	Caco-2	colon:	n/a
2	chr14:82124963-82125013	BE2_C	brain:	n/a
3	chr14:82148289-82148339	HAEpiC	amniotic membrane:	n/a
4	chr14:82148289-82148339	BE2_C	brain:	n/a
5	chr14:82124963-82125013	HNPCEpiC	eye:	n/a
6	chr14:82135353-82135403	HRPEpiC	eye:	n/a
7	chr14:82124963-82125013	GM12891	blood:	n/a
8	chr14:82135353-82135403	NT2-D1	testis:	n/a
9	chr14:82148289-82148339	RPTEC	kidney:	n/a
10	chr14:82124963-82125013	NHBE	bronchial:	n/a
11	chr14:82124963-82125013	Jurkat	blood:	n/a
12	chr14:82124963-82125013	GM12878	blood:	n/a
13	chr14:82148289-82148339	HRCEpiC	kidney:	n/a
14	chr14:82124963-82125013	HRE	kidney:	n/a
15	chr14:82135353-82135403	PANC-1	pancreas:	n/a
16	chr14:82135353-82135403	Caco-2	colon:	n/a
17	chr14:82148289-82148339	Hela-S3	cervix:	n/a
18	chr14:82124963-82125013	HEEpiC	esophagus:	n/a
19	chr14:82135353-82135403	PrEC	prostate:	n/a
20	chr14:82135353-82135403	A549	lung:	n/a
21	chr14:82124963-82125013	LNCaP	prostate:	n/a
22	chr14:82124963-82125013	HCPEpiC	choroid plexus:	n/a
23	chr14:82124963-82125013	A549	lung:	n/a
24	chr14:82124963-82125013	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:82135353-82135403	AG04450	lung:	fetal
26	chr14:82135353-82135403	HNPCEpiC	eye:	n/a
27	chr14:82135353-82135403	AG09309	skin:	n/a
28	chr14:82124963-82125013	HRPEpiC	eye:	n/a
29	chr14:82124963-82125013	MCF10A-Er-Src	breast:	n/a
30	chr14:82135353-82135403	HIPEpiC	eye:	n/a
31	chr14:82124963-82125013	U87	brain:	n/a
32	chr14:82148289-82148339	ECC-1	luminal epithelium:	n/a
33	chr14:82135353-82135403	MCF10A-Er-Src	breast:	n/a
34	chr14:82124963-82125013	HRCEpiC	kidney:	n/a
35	chr14:82148289-82148339	NB4	blood:	n/a
36	chr14:82124963-82125013	SKMC	muscle:	n/a
37	chr14:82124963-82125013	BJ	skin:	n/a
38	chr14:82135353-82135403	ECC-1	luminal epithelium:	n/a
39	chr14:82135353-82135403	HMEC	breast:	n/a
40	chr14:82135353-82135403	HCF	heart:	n/a
41	chr14:82135353-82135403	NH-A	brain:	n/a
42	chr14:82135353-82135403	BE2_C	brain:	n/a
43	chr14:82135353-82135403	HCT-116	colon:	n/a
44	chr14:82124963-82125013	SAEC	small airway:	n/a
45	chr14:82124963-82125013	GM19239	blood:	n/a
46	chr14:82148289-82148339	NT2-D1	testis:	n/a
47	chr14:82124963-82125013	IMR90	lung:	fetal
48	chr14:82148289-82148339	SK-N-SH_RA	brain:	n/a
49	chr14:82135353-82135403	SAEC	small airway:	n/a
50	chr14:82148289-82148339	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:82167442..82169869-chr14:82176351..82178755,2	MCF-7	breast:
2	chr14:82167442..82169869-chr14:82176351..82178755,2	MCF-7	breast:
3	chr14:82195306..82196922-chr14:82198362..82200231,2	K562	blood:
4	chr14:82176321..82177178-chr14:83538011..83538873,2	MCF-7	breast:
5	chr14:82195306..82196922-chr14:82198362..82200231,2	K562	blood:
6	chr14:82134770..82137572-chr20:47128262..47129981,2	MCF-7	breast:
7	chr14:82211114..82211614-chr20:35089840..35090389,2	Hela-S3	cervix:
8	chr14:82091384..82092373-chr14:82204011..82204637,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-2	chr14:82194124-82194564	ENSG00000258718
2	lnc-SEL1L-2	chr14:82206581-82206616	ENSG00000258718
3	lnc-TSHR-4	chr14:82218461-82218586	ENSG00000259035
4	lnc-TSHR-4	chr14:82207346-82207439	ENSG00000259035

Variant related genes	Relation type
ENSG00000258718	TF binding region
ENSG00000258841	TF binding region
ENSG00000259035	TF binding region
ENSG00000258718	CpG island
ENSG00000258841	CpG island
ENSG00000259035	CpG island
ENSG00000080845	chromatin interactions

Extended variants
information (count: 2998 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2998 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12436893	chr14:82123315-82123316	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140512596	chr14:82123352-82123353	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs559438332	chr14:82123446-82123447	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529694767	chr14:82123449-82123450	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs542181172	chr14:82123663-82123664	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550239815	chr14:82123672-82123673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs370987341	chr14:82123678-82123679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186283491	chr14:82123687-82123688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373984111	chr14:82123714-82123715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150015240	chr14:82123723-82123724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10150305	chr14:82123743-82123744	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528631509	chr14:82123765-82123766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546665972	chr14:82123773-82123774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568148868	chr14:82123782-82123783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574782089	chr14:82123809-82123810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557254434	chr14:82123881-82123882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569487438	chr14:82123882-82123883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539655402	chr14:82123898-82123899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199810883	chr14:82123919-82123920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34443421	chr14:82123921-82123922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375358834	chr14:82123924-82123925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560786723	chr14:82123948-82123949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558370839	chr14:82123983-82123984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573355131	chr14:82124012-82124013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541157641	chr14:82124028-82124029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76816735	chr14:82124127-82124128	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568583690	chr14:82124148-82124149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140344416	chr14:82124185-82124186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114345602	chr14:82124248-82124249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563581413	chr14:82124260-82124261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572803274	chr14:82124319-82124320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530872763	chr14:82124444-82124445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191894090	chr14:82124451-82124452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564332473	chr14:82124501-82124502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528256555	chr14:82124503-82124504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145400889	chr14:82124522-82124523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10873339	chr14:82124646-82124647	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs529254167	chr14:82124664-82124665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138169863	chr14:82124740-82124741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569148821	chr14:82124761-82124762	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1958206	chr14:82124795-82124796	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1958207	chr14:82124804-82124805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567090283	chr14:82124828-82124829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534358264	chr14:82124838-82124839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141106547	chr14:82124839-82124840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181957438	chr14:82124944-82124945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535530738	chr14:82124962-82124963	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs10133076	chr14:82125033-82125034	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs1958208	chr14:82125040-82125041	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs73348047	chr14:82125053-82125054	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:69)

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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:82121800-82123800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr14:82121800-82124800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr14:82122000-82124000	Enhancers	Brain Cingulate Gyrus	brain
4	chr14:82122200-82124600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr14:82122200-82124800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:82122400-82123400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr14:82122400-82123600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:82122400-82124600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr14:82122600-82123400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr14:82122600-82123400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr14:82122600-82124800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr14:82122800-82123400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr14:82122800-82123400	Active TSS	Brain Anterior Caudate	brain
14	chr14:82122800-82123600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr14:82122800-82123600	Enhancers	Aorta	Aorta
16	chr14:82122800-82123600	Active TSS	Ovary	ovary
17	chr14:82123000-82123400	Active TSS	Adipose Nuclei	Adipose
18	chr14:82123000-82123400	Active TSS	Brain Inferior Temporal Lobe	brain
19	chr14:82123000-82123400	Active TSS	Right Atrium	heart
20	chr14:82123000-82123600	Flanking Active TSS	Brain Hippocampus Middle	brain
21	chr14:82123200-82123800	Enhancers	Brain Substantia Nigra	brain
22	chr14:82123200-82126200	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr14:82123400-82123600	Enhancers	H1 Cell Line	embryonic stem cell
24	chr14:82123400-82123600	Enhancers	Brain Anterior Caudate	brain
25	chr14:82123400-82124000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr14:82123400-82124400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:82123400-82124800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr14:82123600-82124400	Enhancers	Brain Germinal Matrix	brain
29	chr14:82123600-82124400	Enhancers	Brain Hippocampus Middle	brain
30	chr14:82123600-82124400	Weak transcription	Ovary	ovary
31	chr14:82123600-82124800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr14:82123600-82124800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr14:82123600-82126200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:82123600-82128600	Weak transcription	Aorta	Aorta
35	chr14:82123800-82129000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr14:82124200-82124400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr14:82124400-82124600	Enhancers	H1 Cell Line	embryonic stem cell
38	chr14:82124400-82125000	Enhancers	Ovary	ovary
39	chr14:82124400-82126600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:82124600-82125800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr14:82124600-82126000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr14:82124800-82126000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr14:82124800-82126000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr14:82124800-82126200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:82124800-82126200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr14:82124800-82126200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr14:82125000-82125400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr14:82125800-82126600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr14:82126000-82126600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr14:82126000-82126600	Enhancers	HUES64 Cell Line	embryonic stem cell

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