Variant report

Variant	nsv566070
Chromosome Location	chr14:105236355-105251720
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	BRCA1	chr14:105242152-105242170	GM12878	blood:	n/a	n/a
2	CBX3	chr14:105237255-105237642	K562	blood:	n/a	n/a
3	CBX3	chr14:105237235-105237617	K562	blood:	n/a	n/a
4	CHD2	chr14:105237398-105237462	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr14:105237331-105237497	HepG2	liver:	n/a	n/a
6	CHD2	chr14:105242131-105242291	K562	blood:	n/a	n/a
7	CTCF	chr14:105237420-105237570	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr14:105237380-105237530	BJ	skin:	n/a	n/a
9	CTCF	chr14:105239880-105240170	A549	lung:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
10	CTCF	chr14:105237360-105237510	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr14:105237364-105237492	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr14:105237380-105237530	K562	blood:	n/a	n/a
13	CTCF	chr14:105237317-105237499	GM19239	blood:	n/a	n/a
14	CTCF	chr14:105237360-105237510	HCT-116	colon:	n/a	n/a
15	CTCF	chr14:105237020-105237170	AoAF	blood vessel:	n/a	n/a
16	CTCF	chr14:105243940-105244090	Hela-S3	cervix:	n/a	chr14:105244038-105244051
17	CTCF	chr14:105237304-105237532	GM12892	blood:	n/a	n/a
18	CTCF	chr14:105237340-105237490	AG09319	gingival:	n/a	n/a
19	CTCF	chr14:105237253-105237607	IMR90	lung:	n/a	n/a
20	CTCF	chr14:105237362-105237510	HepG2	liver:	n/a	n/a
21	CTCF	chr14:105237400-105237550	AG09319	gingival:	n/a	n/a
22	CTCF	chr14:105239980-105240130	Caco-2	colon:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
23	CTCF	chr14:105243881-105244262	H1-hESC	embryonic stem cell:	n/a	chr14:105244152-105244165 chr14:105244038-105244051
24	CTCF	chr14:105239840-105239990	A549	lung:	n/a	n/a
25	CTCF	chr14:105239960-105240110	SAEC	small airway:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
26	CTCF	chr14:105237280-105237430	GM06990	blood:	n/a	n/a
27	CTCF	chr14:105243940-105244090	HPF	lung:	n/a	chr14:105244038-105244051
28	CTCF	chr14:105237360-105237510	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr14:105239930-105240157	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240130-105240148 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
30	CTCF	chr14:105245140-105245290	HEK293	kidney:	n/a	chr14:105245207-105245216
31	CTCF	chr14:105237360-105237510	GM12874	blood:	n/a	n/a
32	CTCF	chr14:105237380-105237530	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr14:105237400-105237550	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr14:105237045-105237675	SK-N-SH	brain:	n/a	n/a
35	CTCF	chr14:105239998-105240096	HepG2	liver:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
36	CTCF	chr14:105237300-105237450	NHLF	lung:	n/a	n/a
37	CTCF	chr14:105244000-105244150	AG04449	skin:	n/a	chr14:105244038-105244051
38	CTCF	chr14:105243960-105244110	SAEC	small airway:	n/a	chr14:105244038-105244051
39	CTCF	chr14:105239960-105240110	HCPEpiC	choroid plexus:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
40	CTCF	chr14:105237360-105237510	GM12868	blood:	n/a	n/a
41	CTCF	chr14:105244020-105244170	SK-N-SH_RA	brain:	n/a	chr14:105244152-105244165 chr14:105244038-105244051
42	CTCF	chr14:105239980-105240130	HMF	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
43	CTCF	chr14:105237360-105237510	AG04449	skin:	n/a	n/a
44	CTCF	chr14:105237360-105237510	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr14:105237360-105237510	GM12865	blood:	n/a	n/a
46	CTCF	chr14:105239900-105240050	GM12878	blood:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
47	CTCF	chr14:105237360-105237510	HCFaa	heart:	n/a	n/a
48	CTCF	chr14:105239969-105240117	MCF-7	breast:	n/a	chr14:105240031-105240041 chr14:105240029-105240042 chr14:105240028-105240049 chr14:105240027-105240043 chr14:105240026-105240044 chr14:105240029-105240038
49	CTCF	chr14:105244020-105244170	HCPEpiC	choroid plexus:	n/a	chr14:105244152-105244165 chr14:105244038-105244051
50	CTCF	chr14:105237347-105237505	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105238924-105238974	HUVEC	blood vessel:	n/a
2	chr14:105238924-105238974	HUVEC	blood vessel:	n/a
3	chr14:105236589-105236639	T-47D	breast:	n/a
4	chr14:105239354-105239404	AG04449	skin:	fetal
5	chr14:105251402-105251452	GM12891	blood:	n/a
6	chr14:105242373-105242423	NT2-D1	testis:	n/a
7	chr14:105239544-105239594	SK-N-SH_RA	brain:	n/a
8	chr14:105248634-105248684	HNPCEpiC	eye:	n/a
9	chr14:105244271-105244321	Jurkat	blood:	n/a
10	chr14:105236538-105236588	SK-N-MC	brain:	n/a
11	chr14:105236654-105236704	PANC-1	pancreas:	n/a
12	chr14:105239544-105239594	HEK293	kidney:	embryo
13	chr14:105239544-105239594	IMR90	lung:	fetal
14	chr14:105238745-105238795	HPAEpiC	pulmonary alveolar:	n/a
15	chr14:105251402-105251452	AG10803	skin:	n/a
16	chr14:105238745-105238795	BE2_C	brain:	n/a
17	chr14:105246532-105246582	NB4	blood:	n/a
18	chr14:105239544-105239594	AG04449	skin:	fetal
19	chr14:105238773-105238823	GM06990	blood:	n/a
20	chr14:105236538-105236588	SKMC	muscle:	n/a
21	chr14:105239354-105239404	NB4	blood:	n/a
22	chr14:105238745-105238795	Hepatocyte	liver:	n/a
23	chr14:105238745-105238795	RPTEC	kidney:	n/a
24	chr14:105244271-105244321	HNPCEpiC	eye:	n/a
25	chr14:105248634-105248684	A549	lung:	n/a
26	chr14:105236538-105236588	HCPEpiC	choroid plexus:	n/a
27	chr14:105246708-105246758	RPTEC	kidney:	n/a
28	chr14:105239857-105239907	CMK	blood:	n/a
29	chr14:105248634-105248684	U87	brain:	n/a
30	chr14:105251610-105251660	HNPCEpiC	eye:	n/a
31	chr14:105248634-105248684	Jurkat	blood:	n/a
32	chr14:105238924-105238974	LNCaP	prostate:	n/a
33	chr14:105240263-105240313	A549	lung:	n/a
34	chr14:105240170-105240220	ovcar-3	ovarian:	n/a
35	chr14:105239457-105239507	HUVEC	blood vessel:	n/a
36	chr14:105236538-105236588	PrEC	prostate:	n/a
37	chr14:105236538-105236588	HCT-116	colon:	n/a
38	chr14:105244271-105244321	HEK293	kidney:	embryo
39	chr14:105251610-105251660	HPAEpiC	pulmonary alveolar:	n/a
40	chr14:105240263-105240313	HRCEpiC	kidney:	n/a
41	chr14:105238745-105238795	HCM	heart:	n/a
42	chr14:105240170-105240220	HRE	kidney:	n/a
43	chr14:105239354-105239404	HRCEpiC	kidney:	n/a
44	chr14:105246708-105246758	NB4	blood:	n/a
45	chr14:105240170-105240220	AG09319	gingival:	n/a
46	chr14:105246708-105246758	GM06990	blood:	n/a
47	chr14:105236538-105236588	GM12891	blood:	n/a
48	chr14:105240263-105240313	SKMC	muscle:	n/a
49	chr14:105240263-105240313	GM19239	blood:	n/a
50	chr14:105238745-105238795	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:105219091..105223015-chr14:105243213..105247150,4	MCF-7	breast:
2	chr14:105234538..105236569-chr14:105286438..105288492,2	K562	blood:
3	chr14:105239791..105242217-chr14:105329726..105333005,4	MCF-7	breast:
4	chr14:105146944..105148675-chr14:105240764..105242693,2	MCF-7	breast:
5	chr14:105188904..105192093-chr14:105240193..105242599,4	MCF-7	breast:
6	chr14:105238572..105242731-chr14:105243797..105248047,10	MCF-7	breast:
7	chr14:105188439..105190556-chr14:105236596..105238485,2	K562	blood:
8	chr14:105198092..105200035-chr14:105235985..105237545,2	K562	blood:
9	chr14:105242733..105245405-chr14:105245728..105247914,2	MCF-7	breast:
10	chr14:105239842..105240752-chr14:105259046..105260243,3	MCF-7	breast:
11	chr14:105238572..105242731-chr14:105243797..105248047,10	MCF-7	breast:
12	chr14:105250763..105252757-chr14:105330393..105333309,2	K562	blood:
13	chr14:105219457..105221671-chr14:105233976..105237421,3	K562	blood:
14	chr14:105246961..105249735-chr14:105330074..105332395,2	MCF-7	breast:
15	chr14:105219054..105221939-chr14:105234928..105236625,2	MCF-7	breast:
16	chr14:105217283..105220523-chr14:105237983..105243269,6	MCF-7	breast:
17	chr14:105236868..105239092-chr14:105267183..105269745,2	K562	blood:
18	chr14:105239243..105243388-chr14:105243994..105248690,7	MCF-7	breast:
19	chr14:105234268..105237912-chr14:105260331..105262677,3	K562	blood:
20	chr14:105206877..105208659-chr14:105234732..105236587,2	MCF-7	breast:
21	chr14:105239243..105243388-chr14:105243994..105248690,7	MCF-7	breast:
22	chr14:105193685..105196531-chr14:105242046..105243557,2	MCF-7	breast:
23	chr14:105234579..105236355-chr14:105286684..105287712,12	MCF-7	breast:
24	chr14:105218074..105222224-chr14:105239346..105242379,3	MCF-7	breast:
25	chr14:105247569..105249557-chr14:105347096..105349716,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHNAK2-9	chr14:105241347-105241468	ucscGeneNc_uc001ysc_2
2	lnc-SIVA1-1	chr14:105235984-105236608	ENSG00000258430.1
3	lnc-AHNAK2-9	chr14:105241749-105241984	ucscGeneNc_uc001ysc_2

Variant related genes	Relation type
AKT1	TF binding region
AKT1	CpG island
ENSG00000184990	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000256050	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000185100	chromatin interactions

Extended variants
information (count: 833 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1130245	chr14:105236355-105236356	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs41307094	chr14:105236377-105236378	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532385857	chr14:105236403-105236404	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs34558581	chr14:105236410-105236411	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs61761249	chr14:105236429-105236430	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs112281303	chr14:105236448-105236449	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs373002859	chr14:105236508-105236509	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs537945247	chr14:105236539-105236540	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs548181379	chr14:105236542-105236543	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs17846826	chr14:105236557-105236558	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17846821	chr14:105236568-105236569	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs553657544	chr14:105236592-105236593	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs11555430	chr14:105236629-105236630	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs573353277	chr14:105236630-105236631	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs368920620	chr14:105236631-105236632	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539258432	chr14:105236641-105236642	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs558891046	chr14:105236643-105236644	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs370987171	chr14:105236654-105236655	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs375585585	chr14:105236655-105236656	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs373329736	chr14:105236661-105236662	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs377339529	chr14:105236662-105236663	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs111793056	chr14:105236670-105236671	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs192237287	chr14:105236671-105236672	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs200508405	chr14:105236672-105236673	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs555187157	chr14:105236684-105236685	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs201291259	chr14:105236685-105236686	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs200213561	chr14:105236690-105236691	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184263655	chr14:105236705-105236706	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs113547523	chr14:105236727-105236728	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144112075	chr14:105236732-105236733	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs11555435	chr14:105236740-105236741	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs139394285	chr14:105236741-105236742	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs113777945	chr14:105236760-105236761	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs151052051	chr14:105236765-105236766	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs548780765	chr14:105236768-105236769	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs201152786	chr14:105236770-105236771	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs140998189	chr14:105236778-105236779	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs562695830	chr14:105236824-105236825	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531400798	chr14:105236844-105236845	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs548338247	chr14:105236859-105236860	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs111489239	chr14:105236862-105236863	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs568038730	chr14:105236911-105236912	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs527327617	chr14:105236915-105236916	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs113635490	chr14:105236948-105236949	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs567110708	chr14:105237010-105237011	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs150070451	chr14:105237027-105237028	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs368913986	chr14:105237029-105237030	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs538965403	chr14:105237052-105237053	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs61761248	chr14:105237070-105237071	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112458264	chr14:105237081-105237082	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Breast cancer	20932292	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105221600-105253800	Weak transcription	Psoas Muscle	Psoas
2	chr14:105221800-105248200	Weak transcription	Fetal Brain Male	brain
3	chr14:105222800-105237400	Weak transcription	Fetal Kidney	kidney
4	chr14:105224200-105237200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr14:105224400-105237200	Weak transcription	Brain Substantia Nigra	brain
6	chr14:105225800-105238800	Weak transcription	Small Intestine	intestine
7	chr14:105226000-105237200	Weak transcription	Brain Angular Gyrus	brain
8	chr14:105226000-105237200	Weak transcription	NHDF-Ad	bronchial
9	chr14:105226000-105237600	Weak transcription	Aorta	Aorta
10	chr14:105226200-105241600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr14:105226400-105237000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr14:105226400-105237000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr14:105226600-105237000	Weak transcription	Colon Smooth Muscle	Colon
14	chr14:105226600-105237000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr14:105226600-105237200	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr14:105227200-105237200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr14:105227400-105237200	Weak transcription	Left Ventricle	heart
18	chr14:105228000-105237200	Weak transcription	NHEK	skin
19	chr14:105228000-105237600	Weak transcription	GM12878-XiMat	blood
20	chr14:105228200-105237600	Weak transcription	HSMMtube	muscle
21	chr14:105228400-105237200	Weak transcription	Brain Hippocampus Middle	brain
22	chr14:105229000-105236800	Weak transcription	Primary T cells from cord blood	blood
23	chr14:105233000-105237200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:105233200-105237200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr14:105233200-105237400	Weak transcription	HSMM	muscle
26	chr14:105233600-105236600	Genic enhancers	Spleen	Spleen
27	chr14:105233600-105236800	Genic enhancers	Fetal Muscle Trunk	muscle
28	chr14:105233600-105237600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr14:105233800-105236800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr14:105234600-105236400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr14:105234800-105236400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr14:105234800-105236400	Genic enhancers	Fetal Muscle Leg	muscle
33	chr14:105234800-105236400	Genic enhancers	Fetal Stomach	stomach
34	chr14:105235000-105237400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:105235200-105236800	Enhancers	K562	blood
36	chr14:105235400-105236400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:105235400-105236400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr14:105235400-105236600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr14:105235400-105236600	Weak transcription	Esophagus	oesophagus
40	chr14:105235400-105236800	Weak transcription	Brain Cingulate Gyrus	brain
41	chr14:105235400-105236800	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr14:105235400-105237000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr14:105235400-105237000	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr14:105235400-105237000	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr14:105235400-105237000	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr14:105235400-105237000	Weak transcription	Brain Anterior Caudate	brain
47	chr14:105235400-105237200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr14:105235400-105237200	Strong transcription	Thymus	Thymus
49	chr14:105235400-105237200	Weak transcription	Hela-S3	cervix
50	chr14:105235400-105237200	Weak transcription	HUVEC	blood vessel

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