Variant report

Variant	nsv983860
Chromosome Location	chr14:105294291-105307863
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	chr14:105293388-105294331	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr14:105297149-105297499	HepG2	liver:	n/a	n/a
3	BHLHE40	chr14:105297136-105297489	K562	blood:	n/a	n/a
4	CEBPB	chr14:105301155-105301359	K562	blood:	n/a	n/a
5	CEBPD	chr14:105293967-105294310	HepG2	liver:	n/a	n/a
6	CTCF	chr14:105293925-105294331	K562	blood:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
7	CTCF	chr14:105293903-105294307	GM12891	blood:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
8	CTCF	chr14:105294340-105294413	GM12891	blood:	n/a	n/a
9	CTCF	chr14:105293938-105294310	IMR90	lung:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
10	CTCF	chr14:105294160-105294310	HAc	cerebellar:	n/a	n/a
11	CTCF	chr14:105294400-105294550	A549	lung:	n/a	n/a
12	CTCF	chr14:105294260-105294410	GM12864	blood:	n/a	n/a
13	CTCF	chr14:105294420-105294570	HCM	heart:	n/a	n/a
14	CTCF	chr14:105294340-105294490	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr14:105294380-105294530	WI-38	lung:	n/a	n/a
16	CTCF	chr14:105298264-105298324	Kidney_OC	kidney:	n/a	n/a
17	CTCF	chr14:105293869-105294307	A549	lung:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
18	CTCF	chr14:105296910-105296945	GM20000	blood:	n/a	n/a
19	CTCF	chr14:105293849-105294340	MCF-7	breast:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
20	CTCF	chr14:105293665-105294581	HCT-116	colon:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
21	CTCF	chr14:105293947-105294300	T-47D	breast:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
22	CTCF	chr14:105294420-105294570	AG09319	gingival:	n/a	n/a
23	CTCF	chr14:105293843-105294312	H1-hESC	embryonic stem cell:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
24	CTCF	chr14:105293640-105294600	SK-N-SH	brain:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
25	CTCF	chr14:105293945-105294314	K562	blood:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
26	CTCF	chr14:105293877-105294378	H1-hESC	embryonic stem cell:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
27	CTCF	chr14:105293402-105294463	MCF-7	breast:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
28	CTCF	chr14:105294480-105294630	GM12875	blood:	n/a	n/a
29	CTCF	chr14:105293884-105294438	K562	blood:	n/a	chr14:105294124-105294137 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105294152-105294161
30	CTCF	chr14:105293347-105294538	A549	lung:	n/a	chr14:105293855-105293868 chr14:105294124-105294137 chr14:105293381-105293394 chr14:105294123-105294144 chr14:105294121-105294139 chr14:105293852-105293870 chr14:105294152-105294161
31	GABPA	chr14:105293830-105294321	H1-hESC	embryonic stem cell:	n/a	n/a
32	HDAC2	chr14:105292431-105294476	MCF-7	breast:	n/a	n/a
33	HEY1	chr14:105302587-105302834	K562	blood:	n/a	n/a
34	HEY1	chr14:105303006-105303177	K562	blood:	n/a	n/a
35	IRF1	chr14:105295488-105295664	K562	blood:	n/a	n/a
36	JUND	chr14:105295783-105295969	K562	blood:	n/a	n/a
37	MAFK	chr14:105295794-105295956	K562	blood:	n/a	n/a
38	MAX	chr14:105297107-105297483	K562	blood:	n/a	n/a
39	MAX	chr14:105293343-105294356	A549	lung:	n/a	n/a
40	MAX	chr14:105293266-105294348	MCF-7	breast:	n/a	chr14:105293285-105293295
41	MAX	chr14:105297290-105297455	K562	blood:	n/a	n/a
42	MAZ	chr14:105293754-105294339	K562	blood:	n/a	n/a
43	MAZ	chr14:105293875-105294321	HepG2	liver:	n/a	n/a
44	MAZ	chr14:105292365-105294484	IMR90	lung:	n/a	chr14:105293285-105293295
45	MYC	chr14:105293894-105294292	H1-hESC	embryonic stem cell:	n/a	n/a
46	MYC	chr14:105297357-105297390	GM12878	blood:	n/a	n/a
47	POLR2A	chr14:105302777-105302883	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr14:105302634-105302762	A549	lung:	n/a	n/a
49	POLR2A	chr14:105302473-105302948	GM12878	blood:	n/a	n/a
50	POLR2A	chr14:105302976-105303249	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105302637-105302687	Hela-S3	cervix:	n/a
2	chr14:105302637-105302687	ProgFib	skin:	n/a
3	chr14:105306646-105306696	CMK	blood:	n/a
4	chr14:105303134-105303184	LNCaP	prostate:	n/a
5	chr14:105306646-105306696	U87	brain:	n/a
6	chr14:105303134-105303184	MCF-7	breast:	n/a
7	chr14:105306646-105306696	HCM	heart:	n/a
8	chr14:105302637-105302687	HUVEC	blood vessel:	n/a
9	chr14:105303134-105303184	ECC-1	luminal epithelium:	n/a
10	chr14:105302637-105302687	AG04450	lung:	fetal
11	chr14:105302637-105302687	HCM	heart:	n/a
12	chr14:105297364-105297414	NH-A	brain:	n/a
13	chr14:105302637-105302687	HRCEpiC	kidney:	n/a
14	chr14:105297364-105297414	K562	blood:	n/a
15	chr14:105303134-105303184	GM19239	blood:	n/a
16	chr14:105306646-105306696	GM12892	blood:	n/a
17	chr14:105306646-105306696	HIPEpiC	eye:	n/a
18	chr14:105303134-105303184	HEEpiC	esophagus:	n/a
19	chr14:105306646-105306696	ProgFib	skin:	n/a
20	chr14:105302637-105302687	AG09319	gingival:	n/a
21	chr14:105306646-105306696	NB4	blood:	n/a
22	chr14:105297364-105297414	GM12891	blood:	n/a
23	chr14:105297364-105297414	A549	lung:	n/a
24	chr14:105295832-105295882	IMR90	lung:	fetal
25	chr14:105306646-105306696	HAEpiC	amniotic membrane:	n/a
26	chr14:105295832-105295882	CMK	blood:	n/a
27	chr14:105303134-105303184	Caco-2	colon:	n/a
28	chr14:105302637-105302687	HEEpiC	esophagus:	n/a
29	chr14:105303134-105303184	HPAEpiC	pulmonary alveolar:	n/a
30	chr14:105303134-105303184	GM12892	blood:	n/a
31	chr14:105295832-105295882	BJ	skin:	n/a
32	chr14:105297364-105297414	NHDF-neo	bronchial:	n/a
33	chr14:105295832-105295882	AG04450	lung:	fetal
34	chr14:105306646-105306696	AG10803	skin:	n/a
35	chr14:105302637-105302687	GM06990	blood:	n/a
36	chr14:105302637-105302687	NB4	blood:	n/a
37	chr14:105302637-105302687	SK-N-MC	brain:	n/a
38	chr14:105297364-105297414	HCF	heart:	n/a
39	chr14:105295832-105295882	SK-N-SH_RA	brain:	n/a
40	chr14:105303134-105303184	HL-60	blood:	n/a
41	chr14:105295832-105295882	Caco-2	colon:	n/a
42	chr14:105302637-105302687	PANC-1	pancreas:	n/a
43	chr14:105302637-105302687	NHBE	bronchial:	n/a
44	chr14:105303134-105303184	HCT-116	colon:	n/a
45	chr14:105295832-105295882	SK-N-MC	brain:	n/a
46	chr14:105297364-105297414	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:105306646-105306696	HRE	kidney:	n/a
48	chr14:105297364-105297414	ProgFib	skin:	n/a
49	chr14:105303134-105303184	HRPEpiC	eye:	n/a
50	chr14:105302637-105302687	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105226070..105227570-chr14:105291620..105294600,2	MCF-7	breast:
2	chr14:105294072..105294589-chr14:105362751..105363336,2	MCF-7	breast:
3	chr14:105218306..105221418-chr14:105291704..105295058,3	MCF-7	breast:
4	chr14:105264645..105268219-chr14:105292165..105294813,6	K562	blood:
5	chr14:105268427..105271161-chr14:105291567..105294333,2	K562	blood:
6	chr14:105289983..105292400-chr14:105295807..105297431,2	MCF-7	breast:
7	chr14:105235443..105237438-chr14:105291289..105294293,4	K562	blood:
8	chr14:105293628..105294624-chr14:105337330..105337838,2	MCF-7	breast:
9	chr14:105291374..105295422-chr14:105328190..105336195,18	MCF-7	breast:
10	chr14:105280966..105282808-chr14:105292129..105294295,2	K562	blood:
11	chr14:105298884..105302177-chr14:105308001..105311152,3	MCF-7	breast:
12	chr14:105292450..105295087-chr14:105329500..105333525,7	MCF-7	breast:
13	chr14:105233810..105238299-chr14:105291361..105295745,6	K562	blood:
14	chr14:105287225..105290811-chr14:105291462..105294551,5	K562	blood:
15	chr14:105292878..105295272-chr14:105309126..105311348,2	MCF-7	breast:
16	chr14:105293691..105294557-chr14:105406827..105407640,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKT1-3	chr14:105297175-105297508	NONHSAT040287

Variant related genes	Relation type
ENSG00000258811	TF binding region
RPS26P49	TF binding region
RPS2P4	TF binding region
ENSG00000258811	CpG island
RPS26P49	CpG island
RPS2P4	CpG island
ENSG00000258811	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000184990	chromatin interactions
ENSG00000258701	chromatin interactions

Extended variants
information (count: 421 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550940573	chr14:105294318-105294319	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs75925957	chr14:105294325-105294326	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563875766	chr14:105294346-105294347	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs193043397	chr14:105294363-105294364	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs547138349	chr14:105294385-105294386	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs566850900	chr14:105294387-105294388	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs569397779	chr14:105294434-105294435	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs529476015	chr14:105294496-105294497	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs538692967	chr14:105294525-105294526	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs374293170	chr14:105294690-105294691	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs557618958	chr14:105294753-105294754	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs553417342	chr14:105294754-105294755	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs12883252	chr14:105294786-105294787	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs12882529	chr14:105294833-105294834	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs370003048	chr14:105294843-105294844	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs373644409	chr14:105294870-105294871	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs531444201	chr14:105294907-105294908	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs12882165	chr14:105294917-105294918	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs549595505	chr14:105294955-105294956	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs373758720	chr14:105294956-105294957	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs574305496	chr14:105294965-105294966	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs12882729	chr14:105294997-105294998	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs12882465	chr14:105294998-105294999	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs565781100	chr14:105295007-105295008	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs534740414	chr14:105295030-105295031	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs12882590	chr14:105295037-105295038	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs12882849	chr14:105295041-105295042	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539910900	chr14:105295059-105295060	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12882619	chr14:105295102-105295103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs553476840	chr14:105295116-105295117	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs370479867	chr14:105295137-105295138	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576414412	chr14:105295151-105295152	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149486606	chr14:105295199-105295200	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551381656	chr14:105295219-105295220	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565569524	chr14:105295245-105295246	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531063560	chr14:105295253-105295254	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs571278756	chr14:105295291-105295292	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs544905771	chr14:105295357-105295358	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs115528857	chr14:105295382-105295383	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189305178	chr14:105295393-105295394	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs547101468	chr14:105295437-105295438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs567013711	chr14:105295452-105295453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs73350387	chr14:105295475-105295476	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs556980103	chr14:105295488-105295489	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573738233	chr14:105295580-105295581	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs112837176	chr14:105295593-105295594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569247078	chr14:105295596-105295597	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537712524	chr14:105295607-105295608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs180988498	chr14:105295622-105295623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567890645	chr14:105295639-105295640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	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
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105291800-105294400	Enhancers	Spleen	Spleen
2	chr14:105292000-105294400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr14:105292000-105294400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
4	chr14:105292200-105294400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr14:105292800-105294400	Enhancers	Gastric	stomach
6	chr14:105292800-105294400	Enhancers	Stomach Mucosa	stomach
7	chr14:105292800-105294600	Bivalent Enhancer	Fetal Thymus	thymus
8	chr14:105293000-105294400	Bivalent Enhancer	Primary B cells from cord blood	blood
9	chr14:105293000-105294400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
10	chr14:105293400-105294400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr14:105293400-105294400	Flanking Active TSS	Adipose Nuclei	Adipose
12	chr14:105293400-105294400	Flanking Active TSS	Colonic Mucosa	Colon
13	chr14:105293400-105294400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
14	chr14:105293400-105294400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
15	chr14:105293400-105294600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr14:105293400-105294600	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr14:105293600-105294400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr14:105293600-105294400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
19	chr14:105293600-105294400	Enhancers	Fetal Heart	heart
20	chr14:105293600-105294400	Flanking Active TSS	Fetal Lung	lung
21	chr14:105293600-105294600	Flanking Active TSS	Fetal Intestine Small	intestine
22	chr14:105293800-105294400	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr14:105293800-105294400	Enhancers	Placenta	Placenta
24	chr14:105293800-105294400	Enhancers	Left Ventricle	heart
25	chr14:105293800-105294400	Enhancers	Ovary	ovary
26	chr14:105294000-105294400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr14:105294000-105294400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:105294000-105294400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr14:105294000-105294400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
30	chr14:105294000-105294400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr14:105294000-105294400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr14:105294000-105294400	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr14:105294000-105294400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr14:105294000-105294400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
35	chr14:105294000-105294400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr14:105294000-105294400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
37	chr14:105294000-105294400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr14:105294000-105294400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr14:105294000-105294400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:105294000-105294400	Enhancers	Liver	Liver
41	chr14:105294000-105294400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
42	chr14:105294000-105294400	Enhancers	Brain Hippocampus Middle	brain
43	chr14:105294000-105294400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr14:105294000-105294400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr14:105294000-105294400	Enhancers	Pancreas	Pancrea
46	chr14:105294000-105294400	Active TSS	Rectal Smooth Muscle	rectum
47	chr14:105294000-105294400	Enhancers	Osteobl	bone
48	chr14:105294000-105294600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr14:105294000-105294600	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr14:105294000-105294600	Enhancers	Primary B cells from peripheral blood	blood

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