Variant report

Variant	nsv901974
Chromosome Location	chr14:56192577-56252062
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	ATF1	chr14:56247898-56248141	K562	blood:	n/a	n/a
2	BCL3	chr14:56219661-56220203	A549	lung:	n/a	n/a
3	BCL3	chr14:56219701-56220211	A549	lung:	n/a	n/a
4	BHLHE40	chr14:56229831-56229884	A549	lung:	n/a	n/a
5	BHLHE40	chr14:56229447-56229780	GM12878	blood:	n/a	n/a
6	BRCA1	chr14:56246068-56246093	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr14:56246845-56247541	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:56216067-56216656	Hela-S3	cervix:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
9	CEBPB	chr14:56216059-56216612	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
10	CEBPB	chr14:56206649-56206928	A549	lung:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
11	CEBPB	chr14:56219573-56220424	MCF-7	breast:	n/a	n/a
12	CEBPB	chr14:56216122-56216556	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
13	CEBPB	chr14:56247933-56248278	K562	blood:	n/a	n/a
14	CEBPB	chr14:56219652-56220153	A549	lung:	n/a	n/a
15	CEBPB	chr14:56216122-56216559	IMR90	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
16	CEBPB	chr14:56216043-56216564	MCF-7	breast:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
17	CEBPB	chr14:56216015-56216706	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
18	CEBPB	chr14:56206674-56206953	IMR90	lung:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
19	CEBPB	chr14:56219651-56220076	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr14:56206606-56206988	ECC-1	luminal epithelium:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
21	CEBPB	chr14:56216172-56216500	HepG2	liver:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
22	CEBPB	chr14:56219448-56220140	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr14:56200151-56200351	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:56206642-56207436	Hela-S3	cervix:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
25	CEBPB	chr14:56206661-56206992	HepG2	liver:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
26	CEBPB	chr14:56206691-56206967	K562	blood:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
27	CEBPB	chr14:56197253-56197700	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:56228642-56228829	HepG2	liver:	n/a	chr14:56228678-56228689
29	CEBPB	chr14:56246757-56247826	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:56215995-56216640	MCF-7	breast:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
31	CEBPB	chr14:56219644-56220147	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr14:56206596-56207023	MCF-7	breast:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
33	CEBPB	chr14:56206687-56206907	H1-hESC	embryonic stem cell:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
34	CEBPB	chr14:56216081-56216495	H1-hESC	embryonic stem cell:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
35	CEBPB	chr14:56219535-56220200	A549	lung:	n/a	n/a
36	CEBPB	chr14:56206659-56207049	ECC-1	luminal epithelium:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
37	CHD2	chr14:56234598-56234745	K562	blood:	n/a	n/a
38	CHD2	chr14:56219728-56220131	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr14:56216252-56216617	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr14:56248001-56248018	GM12878	blood:	n/a	n/a
41	CHD2	chr14:56246835-56247751	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr14:56198700-56198850	Caco-2	colon:	n/a	n/a
43	CTCF	chr14:56206500-56206650	HepG2	liver:	n/a	n/a
44	CTCF	chr14:56203840-56203990	GM12875	blood:	n/a	n/a
45	CTCF	chr14:56198340-56198490	BJ	skin:	n/a	n/a
46	CTCF	chr14:56198470-56198536	GM19239	blood:	n/a	n/a
47	CTCF	chr14:56232860-56233010	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr14:56220719-56220876	Hela-S3	cervix:	n/a	chr14:56220780-56220793
49	CTCF	chr14:56198695-56198973	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr14:56198700-56198850	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56232985-56233035	GM12878	blood:	n/a
2	chr14:56233676-56233726	HMEC	breast:	n/a
3	chr14:56216951-56217001	Jurkat	blood:	n/a
4	chr14:56247892-56247942	GM12892	blood:	n/a
5	chr14:56207327-56207377	MCF10A-Er-Src	breast:	n/a
6	chr14:56232650-56232700	Caco-2	colon:	n/a
7	chr14:56233178-56233228	HCF	heart:	n/a
8	chr14:56233163-56233213	NH-A	brain:	n/a
9	chr14:56232650-56232700	PFSK-1	brain:	n/a
10	chr14:56233676-56233726	T-47D	breast:	n/a
11	chr14:56232650-56232700	Hepatocyte	liver:	n/a
12	chr14:56216951-56217001	AG10803	skin:	n/a
13	chr14:56228816-56228866	LNCaP	prostate:	n/a
14	chr14:56233178-56233228	HMEC	breast:	n/a
15	chr14:56233068-56233118	ovcar-3	ovarian:	n/a
16	chr14:56229661-56229711	SKMC	muscle:	n/a
17	chr14:56219430-56219480	GM06990	blood:	n/a
18	chr14:56229661-56229711	NB4	blood:	n/a
19	chr14:56247892-56247942	AG09309	skin:	n/a
20	chr14:56233178-56233228	GM19239	blood:	n/a
21	chr14:56229661-56229711	SK-N-MC	brain:	n/a
22	chr14:56232921-56232971	LNCaP	prostate:	n/a
23	chr14:56232813-56232863	HCF	heart:	n/a
24	chr14:56231604-56231654	T-47D	breast:	n/a
25	chr14:56231604-56231654	U87	brain:	n/a
26	chr14:56219430-56219480	HRCEpiC	kidney:	n/a
27	chr14:56225464-56225514	AG09319	gingival:	n/a
28	chr14:56225464-56225514	HEEpiC	esophagus:	n/a
29	chr14:56225464-56225514	Hepatocyte	liver:	n/a
30	chr14:56207327-56207377	U87	brain:	n/a
31	chr14:56232650-56232700	ovcar-3	ovarian:	n/a
32	chr14:56228816-56228866	T-47D	breast:	n/a
33	chr14:56233676-56233726	BE2_C	brain:	n/a
34	chr14:56225464-56225514	GM12892	blood:	n/a
35	chr14:56216951-56217001	GM19239	blood:	n/a
36	chr14:56233068-56233118	PFSK-1	brain:	n/a
37	chr14:56207327-56207377	NHBE	bronchial:	n/a
38	chr14:56225464-56225514	K562	blood:	n/a
39	chr14:56232813-56232863	H1-hESC	embryonic stem cell:	embryo
40	chr14:56232921-56232971	HCF	heart:	n/a
41	chr14:56225464-56225514	HNPCEpiC	eye:	n/a
42	chr14:56229661-56229711	MCF-7	breast:	n/a
43	chr14:56232650-56232700	GM06990	blood:	n/a
44	chr14:56232921-56232971	HRCEpiC	kidney:	n/a
45	chr14:56233178-56233228	CMK	blood:	n/a
46	chr14:56207327-56207377	PANC-1	pancreas:	n/a
47	chr14:56247892-56247942	HepG2	liver:	n/a
48	chr14:56232650-56232700	NHDF-neo	bronchial:	n/a
49	chr14:56233676-56233726	CMK	blood:	n/a
50	chr14:56233068-56233118	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:56198714..56199586-chr14:56889085..56889797,2	MCF-7	breast:
2	chr14:56245870..56248010-chr14:56260063..56261577,2	K562	blood:
3	chr14:56209789..56211421-chr14:56215723..56218469,2	MCF-7	breast:
4	chr14:56207915..56209917-chr14:56216169..56218035,2	MCF-7	breast:
5	chr14:56220561..56223458-chr14:56223829..56226647,2	K562	blood:
6	chr14:56219849..56221518-chr14:56225046..56227362,2	MCF-7	breast:
7	chr14:56226675..56229343-chr14:56231799..56234788,2	K562	blood:
8	chr14:56209789..56211421-chr14:56215723..56218469,2	MCF-7	breast:
9	chr14:56220561..56223458-chr14:56223829..56226647,2	K562	blood:
10	chr14:56209875..56212045-chr14:56256095..56258296,2	MCF-7	breast:
11	chr14:56197898..56198585-chr14:56888977..56889535,2	MCF-7	breast:
12	chr14:56221789..56224702-chr14:56769776..56771612,2	K562	blood:
13	chr14:56207915..56209917-chr14:56216169..56218035,2	MCF-7	breast:
14	chr14:56224023..56226441-chr14:56261049..56262918,2	MCF-7	breast:
15	chr14:56238761..56241278-chr14:56243560..56245184,2	MCF-7	breast:
16	chr14:56215726..56218304-chr14:56218749..56222273,3	K562	blood:
17	chr14:56207089..56208058-chr14:56265155..56265723,2	MCF-7	breast:
18	chr14:56198273..56199200-chr14:56551636..56552463,2	MCF-7	breast:
19	chr14:56198307..56199262-chr14:56551982..56552868,6	MCF-7	breast:
20	chr14:56248252..56249940-chr14:56263162..56264665,2	MCF-7	breast:
21	chr14:56215726..56218304-chr14:56218749..56222273,3	K562	blood:
22	chr14:56238761..56241278-chr14:56243560..56245184,2	MCF-7	breast:
23	chr14:56219849..56221518-chr14:56225046..56227362,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KTN1-AS1-1	chr14:56249127-56249299	ENSG00000258791.2
2	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.3
3	lnc-KTN1-1	chr14:56239474-56239567	ENSG00000258784.1
4	lnc-KTN1-1	chr14:56238349-56238423	ENSG00000258784.1
5	lnc-KTN1-AS1-1	chr14:56247864-56248070	ENSG00000258791.2
6	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037027
7	lnc-KTN1-AS1-1	chr14:56247854-56249698	XLOC_011037
8	lnc-KTN1-1	chr14:56239707-56239921	ENSG00000258784.1
9	lnc-KTN1-AS1-1	chr14:56249144-56249698	ENSG00000258791.2
10	lnc-KTN1-2	chr14:56221453-56222019	NONHSAT037023
11	lnc-KTN1-AS1-1	chr14:56247432-56247714	NONHSAT037025
12	lnc-KTN1-AS1-1	chr14:56248785-56249492	ENSG00000258791.2
13	lnc-KTN1-AS1-1	chr14:56247800-56248072	NONHSAT037025
14	lnc-KTN1-1	chr14:56214926-56215000	ENSG00000258784.1
15	lnc-KTN1-AS1-1	chr14:56247853-56249698	NONHSAT037026

Variant related genes	Relation type
ENSG00000258784	TF binding region
RPL13AP3	TF binding region
ENSG00000258784	CpG island
RPL13AP3	CpG island
ENSG00000258791	chromatin interactions
ENSG00000177350	chromatin interactions

Extended variants
information (count: 2341 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2341 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2152284	chr14:56192577-56192578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76337534	chr14:56192654-56192655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530867951	chr14:56192659-56192660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542240251	chr14:56192721-56192722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550040674	chr14:56192727-56192728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571461133	chr14:56192739-56192740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538961678	chr14:56192744-56192745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140522905	chr14:56192750-56192751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17128756	chr14:56192794-56192795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs536250788	chr14:56192800-56192801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368652628	chr14:56192810-56192811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565101936	chr14:56192927-56192928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554230456	chr14:56192934-56192935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2184558	chr14:56192952-56192953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144270037	chr14:56192957-56192958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187748383	chr14:56193002-56193003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577007093	chr14:56193033-56193034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35098897	chr14:56193096-56193097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs560017221	chr14:56193133-56193134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574986120	chr14:56193142-56193143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs367738363	chr14:56193219-56193220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542215312	chr14:56193226-56193227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10129414	chr14:56193272-56193273	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs57452319	chr14:56193313-56193314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199986581	chr14:56193318-56193319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531073101	chr14:56193348-56193349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550255273	chr14:56193353-56193354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112857224	chr14:56193375-56193376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565107744	chr14:56193383-56193384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532361140	chr14:56193406-56193407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547583695	chr14:56193412-56193413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565976342	chr14:56193434-56193435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536149453	chr14:56193469-56193470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10129360	chr14:56193481-56193482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs192186650	chr14:56193500-56193501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141179593	chr14:56193514-56193515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185094409	chr14:56193515-56193516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576502231	chr14:56193516-56193517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561240980	chr14:56193520-56193521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs145172977	chr14:56193528-56193529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189778781	chr14:56193535-56193536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575118023	chr14:56193572-56193573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542155591	chr14:56193587-56193588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181261249	chr14:56193588-56193589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575690234	chr14:56193669-56193670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148470213	chr14:56193700-56193701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564590726	chr14:56193701-56193702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184477373	chr14:56193710-56193711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148982949	chr14:56193760-56193761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376894204	chr14:56193784-56193785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56191200-56206600	Weak transcription	Aorta	Aorta
2	chr14:56195600-56195800	Enhancers	Small Intestine	intestine
3	chr14:56196400-56198600	Enhancers	A549	lung
4	chr14:56197000-56199200	Enhancers	Fetal Thymus	thymus
5	chr14:56197000-56201000	Enhancers	Hela-S3	cervix
6	chr14:56197200-56197800	Enhancers	Primary hematopoietic stem cells	blood
7	chr14:56197200-56197800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:56197200-56197800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr14:56197200-56197800	Enhancers	Dnd41	blood
10	chr14:56197200-56197800	Enhancers	HepG2	liver
11	chr14:56197200-56197800	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr14:56197200-56198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr14:56197400-56197600	Enhancers	Small Intestine	intestine
14	chr14:56197400-56197800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:56197400-56197800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:56197400-56197800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr14:56197400-56198000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr14:56197400-56198600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr14:56197400-56198600	Enhancers	Brain Angular Gyrus	brain
20	chr14:56197400-56198600	Enhancers	Brain Hippocampus Middle	brain
21	chr14:56197400-56198600	Enhancers	Brain Substantia Nigra	brain
22	chr14:56197400-56198600	Enhancers	Fetal Brain Male	brain
23	chr14:56197400-56198600	Enhancers	Thymus	Thymus
24	chr14:56197400-56199600	Enhancers	Stomach Mucosa	stomach
25	chr14:56197600-56197800	Enhancers	Fetal Intestine Large	intestine
26	chr14:56197600-56198200	Enhancers	Colon Smooth Muscle	Colon
27	chr14:56197600-56198600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr14:56197600-56198600	Enhancers	Brain Cingulate Gyrus	brain
29	chr14:56197600-56198600	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr14:56197800-56198200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr14:56197800-56198600	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr14:56198000-56198600	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr14:56198400-56198600	Enhancers	Fetal Intestine Large	intestine
34	chr14:56198400-56198600	Enhancers	Gastric	stomach
35	chr14:56198600-56198800	Enhancers	Small Intestine	intestine
36	chr14:56198600-56199600	Weak transcription	Fetal Brain Male	brain
37	chr14:56198600-56200200	Weak transcription	Thymus	Thymus
38	chr14:56198600-56219400	Weak transcription	Gastric	stomach
39	chr14:56199200-56200200	Weak transcription	Fetal Thymus	thymus
40	chr14:56199600-56201000	Enhancers	Fetal Brain Male	brain
41	chr14:56200200-56200800	Enhancers	Fetal Thymus	thymus
42	chr14:56200200-56200800	Enhancers	Thymus	Thymus
43	chr14:56200200-56201600	Enhancers	Stomach Mucosa	stomach
44	chr14:56200800-56203800	Weak transcription	Thymus	Thymus
45	chr14:56201200-56201600	Enhancers	HSMMtube	muscle
46	chr14:56203600-56203800	Enhancers	Fetal Thymus	thymus
47	chr14:56203800-56204000	Enhancers	Thymus	Thymus
48	chr14:56204000-56211400	Weak transcription	Thymus	Thymus
49	chr14:56205600-56207800	Enhancers	Fetal Kidney	kidney
50	chr14:56206000-56208000	Enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links