Variant report

Variant	nsv901973
Chromosome Location	chr14:56185908-56252062
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	chr14:56188055-56188395	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr14:56246845-56247541	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr14:56216059-56216612	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
10	CEBPB	chr14:56200151-56200351	HepG2	liver:	n/a	n/a
11	CEBPB	chr14:56206596-56207023	MCF-7	breast:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
12	CEBPB	chr14:56216015-56216706	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
13	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
14	CEBPB	chr14:56206674-56206953	IMR90	lung:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
15	CEBPB	chr14:56216122-56216556	A549	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
16	CEBPB	chr14:56206691-56206967	K562	blood:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
17	CEBPB	chr14:56219535-56220200	A549	lung:	n/a	n/a
18	CEBPB	chr14:56219652-56220153	A549	lung:	n/a	n/a
19	CEBPB	chr14:56197253-56197700	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr14:56247933-56248278	K562	blood:	n/a	n/a
21	CEBPB	chr14:56216067-56216656	Hela-S3	cervix:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
22	CEBPB	chr14:56219651-56220076	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr14:56219573-56220424	MCF-7	breast:	n/a	n/a
24	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
25	CEBPB	chr14:56206642-56207436	Hela-S3	cervix:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
26	CEBPB	chr14:56216122-56216559	IMR90	lung:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
27	CEBPB	chr14:56188084-56188481	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:56219644-56220147	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr14:56246757-56247826	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr14:56216172-56216500	HepG2	liver:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
31	CEBPB	chr14:56206661-56206992	HepG2	liver:	n/a	chr14:56206808-56206819 chr14:56206955-56206972 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
32	CEBPB	chr14:56206687-56206907	H1-hESC	embryonic stem cell:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
33	CEBPB	chr14:56216043-56216564	MCF-7	breast:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
34	CEBPB	chr14:56215995-56216640	MCF-7	breast:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
35	CEBPB	chr14:56219448-56220140	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr14:56206649-56206928	A549	lung:	n/a	chr14:56206808-56206819 chr14:56206810-56206821 chr14:56206808-56206821 chr14:56206810-56206819
37	CEBPB	chr14:56188104-56188471	IMR90	lung:	n/a	n/a
38	CEBPB	chr14:56228642-56228829	HepG2	liver:	n/a	chr14:56228678-56228689
39	CEBPB	chr14:56216081-56216495	H1-hESC	embryonic stem cell:	n/a	chr14:56216300-56216311 chr14:56216406-56216419
40	CHD2	chr14:56246835-56247751	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr14:56234598-56234745	K562	blood:	n/a	n/a
42	CHD2	chr14:56188108-56188518	Hela-S3	cervix:	n/a	n/a
43	CHD2	chr14:56216252-56216617	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr14:56248001-56248018	GM12878	blood:	n/a	n/a
45	CHD2	chr14:56219728-56220131	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr14:56216754-56217006	K562	blood:	n/a	n/a
47	CTCF	chr14:56188200-56188350	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr14:56198740-56198890	SAEC	small airway:	n/a	n/a
49	CTCF	chr14:56232860-56233010	K562	blood:	n/a	n/a
50	CTCF	chr14:56198726-56198901	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:56232985-56233035	MCF-7	breast:	n/a
2	chr14:56232985-56233035	MCF-7	breast:	n/a
3	chr14:56207327-56207377	HL-60	blood:	n/a
4	chr14:56228816-56228866	Jurkat	blood:	n/a
5	chr14:56219430-56219480	HCM	heart:	n/a
6	chr14:56228816-56228866	SAEC	small airway:	n/a
7	chr14:56229661-56229711	ECC-1	luminal epithelium:	n/a
8	chr14:56229661-56229711	HRCEpiC	kidney:	n/a
9	chr14:56207327-56207377	HAEpiC	amniotic membrane:	n/a
10	chr14:56232985-56233035	AG10803	skin:	n/a
11	chr14:56232985-56233035	AG09319	gingival:	n/a
12	chr14:56233068-56233118	HRE	kidney:	n/a
13	chr14:56232813-56232863	Hepatocyte	liver:	n/a
14	chr14:56233163-56233213	GM06990	blood:	n/a
15	chr14:56236843-56236893	HEEpiC	esophagus:	n/a
16	chr14:56247892-56247942	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:56219430-56219480	NHDF-neo	bronchial:	n/a
18	chr14:56233163-56233213	HCF	heart:	n/a
19	chr14:56233163-56233213	T-47D	breast:	n/a
20	chr14:56233676-56233726	HRCEpiC	kidney:	n/a
21	chr14:56247892-56247942	PANC-1	pancreas:	n/a
22	chr14:56232985-56233035	HCM	heart:	n/a
23	chr14:56231604-56231654	HRPEpiC	eye:	n/a
24	chr14:56233178-56233228	PANC-1	pancreas:	n/a
25	chr14:56232985-56233035	NB4	blood:	n/a
26	chr14:56216951-56217001	Caco-2	colon:	n/a
27	chr14:56232650-56232700	NHDF-neo	bronchial:	n/a
28	chr14:56216951-56217001	HIPEpiC	eye:	n/a
29	chr14:56236843-56236893	AG04450	lung:	fetal
30	chr14:56236843-56236893	HEK293	kidney:	embryo
31	chr14:56232921-56232971	T-47D	breast:	n/a
32	chr14:56232985-56233035	HNPCEpiC	eye:	n/a
33	chr14:56228816-56228866	GM12892	blood:	n/a
34	chr14:56233163-56233213	ProgFib	skin:	n/a
35	chr14:56233178-56233228	PFSK-1	brain:	n/a
36	chr14:56232921-56232971	HepG2	liver:	n/a
37	chr14:56216951-56217001	HRCEpiC	kidney:	n/a
38	chr14:56228816-56228866	SK-N-SH_RA	brain:	n/a
39	chr14:56233163-56233213	HNPCEpiC	eye:	n/a
40	chr14:56233068-56233118	SKMC	muscle:	n/a
41	chr14:56232650-56232700	Caco-2	colon:	n/a
42	chr14:56229661-56229711	GM19239	blood:	n/a
43	chr14:56232985-56233035	HEK293	kidney:	embryo
44	chr14:56236843-56236893	NB4	blood:	n/a
45	chr14:56233163-56233213	BE2_C	brain:	n/a
46	chr14:56236843-56236893	HCPEpiC	choroid plexus:	n/a
47	chr14:56228816-56228866	HUVEC	blood vessel:	n/a
48	chr14:56231604-56231654	RPTEC	kidney:	n/a
49	chr14:56233676-56233726	ECC-1	luminal epithelium:	n/a
50	chr14:56233178-56233228	HCM	heart:	n/a

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

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

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: 2562 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2562 , 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	rs8010380	chr14:56185908-56185909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563559874	chr14:56185925-56185926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140262027	chr14:56185935-56185936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149804381	chr14:56185976-56185977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs182614894	chr14:56186005-56186006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528545628	chr14:56186014-56186015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373566836	chr14:56186015-56186016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1953354	chr14:56186034-56186035	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs565881286	chr14:56186085-56186086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536579827	chr14:56186172-56186173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs145737337	chr14:56186301-56186302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs564174945	chr14:56186330-56186331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115973779	chr14:56186356-56186357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577539652	chr14:56186357-56186358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188133887	chr14:56186375-56186376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540240375	chr14:56186405-56186406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369169251	chr14:56186477-56186478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs12436057	chr14:56186617-56186618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs149781145	chr14:56186623-56186624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377555849	chr14:56186627-56186628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184272124	chr14:56186657-56186658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs148931777	chr14:56186663-56186664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77330353	chr14:56186674-56186675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76877562	chr14:56186697-56186698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542192238	chr14:56186742-56186743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73289549	chr14:56186755-56186756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs73289551	chr14:56186793-56186794	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs369642437	chr14:56186804-56186805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138210953	chr14:56186824-56186825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543033311	chr14:56186825-56186826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35332726	chr14:56186826-56186827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564429960	chr14:56186862-56186863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs8015113	chr14:56186878-56186879	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs8015120	chr14:56186890-56186891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559623530	chr14:56186893-56186894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs61976652	chr14:56186900-56186901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548053331	chr14:56186909-56186910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs8014725	chr14:56186953-56186954	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs190575201	chr14:56186970-56186971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552190741	chr14:56186977-56186978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571727644	chr14:56187130-56187131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570109507	chr14:56187135-56187136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534439085	chr14:56187149-56187150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552634465	chr14:56187211-56187212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534066048	chr14:56187219-56187220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529384834	chr14:56187303-56187304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574158271	chr14:56187328-56187329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559028376	chr14:56187355-56187356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547747012	chr14:56187394-56187395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557224913	chr14:56187434-56187435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:560 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56154000-56191000	Weak transcription	Aorta	Aorta
2	chr14:56179800-56188800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:56179800-56189000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr14:56183400-56187600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr14:56183400-56187800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:56183400-56188000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:56185600-56189200	Weak transcription	HSMMtube	muscle
8	chr14:56185800-56187600	Weak transcription	Hela-S3	cervix
9	chr14:56187600-56187800	Enhancers	HSMM	muscle
10	chr14:56187600-56188400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr14:56187600-56188600	Enhancers	NHDF-Ad	bronchial
12	chr14:56187600-56188800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:56187600-56188800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr14:56187600-56188800	Enhancers	NHEK	skin
15	chr14:56187600-56189200	Enhancers	Hela-S3	cervix
16	chr14:56187800-56188600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:56187800-56188600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr14:56187800-56188600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr14:56187800-56188600	Enhancers	HUVEC	blood vessel
20	chr14:56187800-56188800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr14:56187800-56188800	Enhancers	NH-A	brain
22	chr14:56187800-56189000	Enhancers	HMEC	breast
23	chr14:56188000-56188400	Enhancers	Stomach Mucosa	stomach
24	chr14:56188000-56188600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr14:56188200-56188400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr14:56188200-56188400	Enhancers	Pancreas	Pancrea
27	chr14:56188200-56189000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr14:56188200-56189000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:56188200-56190200	Enhancers	Brain Germinal Matrix	brain
30	chr14:56188400-56189400	Weak transcription	Pancreas	Pancrea
31	chr14:56188800-56189200	Enhancers	Brain Cingulate Gyrus	brain
32	chr14:56189000-56189200	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr14:56189000-56189800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:56189400-56189800	Enhancers	Pancreas	Pancrea
35	chr14:56189800-56190800	Weak transcription	Pancreas	Pancrea
36	chr14:56191000-56191200	ZNF genes & repeats	Aorta	Aorta
37	chr14:56191000-56191200	Enhancers	Pancreas	Pancrea
38	chr14:56191200-56206600	Weak transcription	Aorta	Aorta
39	chr14:56195600-56195800	Enhancers	Small Intestine	intestine
40	chr14:56196400-56198600	Enhancers	A549	lung
41	chr14:56197000-56199200	Enhancers	Fetal Thymus	thymus
42	chr14:56197000-56201000	Enhancers	Hela-S3	cervix
43	chr14:56197200-56197800	Enhancers	Primary hematopoietic stem cells	blood
44	chr14:56197200-56197800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr14:56197200-56197800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr14:56197200-56197800	Enhancers	Dnd41	blood
47	chr14:56197200-56197800	Enhancers	HepG2	liver
48	chr14:56197200-56197800	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr14:56197200-56198000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr14:56197400-56197600	Enhancers	Small Intestine	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links