Variant report

Variant	nsv818139
Chromosome Location	chr3:50144951-50174572
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1162)
CpG islands
(count:184)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:50158921-50159391	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr3:50158911-50159394	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr3:50158840-50159409	GM12878	blood:	n/a	n/a
4	BACH1	chr3:50159135-50159316	K562	blood:	n/a	n/a
5	BACH1	chr3:50163136-50163153	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr3:50170240-50170366	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr3:50158817-50159345	A549	lung:	n/a	n/a
8	BCL3	chr3:50158162-50158458	GM12878	blood:	n/a	n/a
9	BCL3	chr3:50157818-50159337	A549	lung:	n/a	n/a
10	BCLAF1	chr3:50158568-50159471	GM12878	blood:	n/a	chr3:50159417-50159425
11	BCLAF1	chr3:50160591-50161105	GM12878	blood:	n/a	n/a
12	BCLAF1	chr3:50158710-50159430	GM12878	blood:	n/a	chr3:50159417-50159425
13	BHLHE40	chr3:50159114-50159308	K562	blood:	n/a	n/a
14	BHLHE40	chr3:50159107-50159200	GM12878	blood:	n/a	n/a
15	BRCA1	chr3:50158773-50159282	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr3:50159080-50159306	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:50159687-50159805	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:50149929-50150097	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:50165121-50165437	A549	lung:	n/a	chr3:50165136-50165147
20	CEBPB	chr3:50173260-50173281	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:50149891-50150137	HepG2	liver:	n/a	n/a
22	CEBPB	chr3:50173208-50173309	HepG2	liver:	n/a	n/a
23	CEBPB	chr3:50165314-50165440	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:50165103-50165442	IMR90	lung:	n/a	chr3:50165136-50165147
25	CEBPB	chr3:50165127-50165332	HepG2	liver:	n/a	chr3:50165136-50165147
26	CEBPB	chr3:50147575-50147633	HepG2	liver:	n/a	chr3:50147594-50147605
27	CEBPB	chr3:50149859-50150148	IMR90	lung:	n/a	n/a
28	CHD2	chr3:50158578-50158724	HepG2	liver:	n/a	n/a
29	CHD2	chr3:50159071-50159189	GM12878	blood:	n/a	n/a
30	CHD2	chr3:50158916-50159341	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr3:50158500-50158526	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr3:50158585-50159495	K562	blood:	n/a	n/a
33	CHD2	chr3:50163056-50163245	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:50160818-50160987	HepG2	liver:	n/a	n/a
35	CHD2	chr3:50159112-50159400	HepG2	liver:	n/a	n/a
36	CHD2	chr3:50160386-50160551	HepG2	liver:	n/a	n/a
37	CHD2	chr3:50163909-50164038	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr3:50162079-50162080	HepG2	liver:	n/a	n/a
39	CTCF	chr3:50159120-50159270	GM06990	blood:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172
40	CTCF	chr3:50159024-50159249	GM20000	blood:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172
41	CTCF	chr3:50151660-50151810	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr3:50158803-50158927	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr3:50158979-50159320	NHEK	skin:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172
44	CTCF	chr3:50159100-50159250	SK-N-SH_RA	brain:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172
45	CTCF	chr3:50158902-50159308	Kidney_OC	kidney:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172
46	CTCF	chr3:50159615-50159767	GM12891	blood:	n/a	chr3:50159697-50159715 chr3:50159700-50159713
47	CTCF	chr3:50158428-50159936	SK-N-SH	brain:	n/a	chr3:50159156-50159177 chr3:50158486-50158499 chr3:50159157-50159166 chr3:50159697-50159715 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159700-50159713 chr3:50159159-50159169 chr3:50159154-50159172
48	CTCF	chr3:50160040-50160190	HCFaa	heart:	n/a	chr3:50160124-50160145 chr3:50160122-50160140
49	CTCF	chr3:50159820-50159970	HAc	cerebellar:	n/a	n/a
50	CTCF	chr3:50159080-50159230	BJ	skin:	n/a	chr3:50159156-50159177 chr3:50159157-50159166 chr3:50159157-50159170 chr3:50159155-50159171 chr3:50159159-50159169 chr3:50159154-50159172

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:50155956-50156006	SK-N-MC	brain:	n/a
2	chr3:50155956-50156006	SK-N-MC	brain:	n/a
3	chr3:50162322-50162372	ProgFib	skin:	n/a
4	chr3:50163269-50163319	HRPEpiC	eye:	n/a
5	chr3:50155956-50156006	HCPEpiC	choroid plexus:	n/a
6	chr3:50162322-50162372	Hela-S3	cervix:	n/a
7	chr3:50162322-50162372	HRPEpiC	eye:	n/a
8	chr3:50163269-50163319	NB4	blood:	n/a
9	chr3:50162322-50162372	HRE	kidney:	n/a
10	chr3:50162322-50162372	HNPCEpiC	eye:	n/a
11	chr3:50155956-50156006	HRE	kidney:	n/a
12	chr3:50163269-50163319	HepG2	liver:	n/a
13	chr3:50155956-50156006	HMEC	breast:	n/a
14	chr3:50163269-50163319	A549	lung:	n/a
15	chr3:50162322-50162372	NH-A	brain:	n/a
16	chr3:50162322-50162372	Jurkat	blood:	n/a
17	chr3:50155956-50156006	Caco-2	colon:	n/a
18	chr3:50162322-50162372	HepG2	liver:	n/a
19	chr3:50155956-50156006	HUVEC	blood vessel:	n/a
20	chr3:50155956-50156006	NB4	blood:	n/a
21	chr3:50155956-50156006	HL-60	blood:	n/a
22	chr3:50155956-50156006	PANC-1	pancreas:	n/a
23	chr3:50155956-50156006	ProgFib	skin:	n/a
24	chr3:50155956-50156006	AoSMC	blood vessel:	n/a
25	chr3:50155956-50156006	HIPEpiC	eye:	n/a
26	chr3:50162322-50162372	GM06990	blood:	n/a
27	chr3:50162322-50162372	GM12892	blood:	n/a
28	chr3:50155956-50156006	LNCaP	prostate:	n/a
29	chr3:50155956-50156006	SK-N-SH	brain:	n/a
30	chr3:50162322-50162372	HIPEpiC	eye:	n/a
31	chr3:50155956-50156006	PrEC	prostate:	n/a
32	chr3:50162322-50162372	RPTEC	kidney:	n/a
33	chr3:50163269-50163319	AG09319	gingival:	n/a
34	chr3:50155956-50156006	Hepatocyte	liver:	n/a
35	chr3:50163269-50163319	AG09309	skin:	n/a
36	chr3:50163269-50163319	HCPEpiC	choroid plexus:	n/a
37	chr3:50163269-50163319	GM12878	blood:	n/a
38	chr3:50155956-50156006	K562	blood:	n/a
39	chr3:50163269-50163319	T-47D	breast:	n/a
40	chr3:50163269-50163319	SAEC	small airway:	n/a
41	chr3:50162322-50162372	BJ	skin:	n/a
42	chr3:50162322-50162372	HEEpiC	esophagus:	n/a
43	chr3:50162322-50162372	MCF-7	breast:	n/a
44	chr3:50155956-50156006	SKMC	muscle:	n/a
45	chr3:50155956-50156006	SAEC	small airway:	n/a
46	chr3:50155956-50156006	U87	brain:	n/a
47	chr3:50163269-50163319	AG10803	skin:	n/a
48	chr3:50162322-50162372	NHDF-neo	bronchial:	n/a
49	chr3:50163269-50163319	HIPEpiC	eye:	n/a
50	chr3:50162322-50162372	ECC-1	luminal epithelium:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:50159119..50159942-chr3:50191580..50192142,2	MCF-7	breast:
2	chr3:50170263..50171999-chr3:50174884..50177139,2	MCF-7	breast:
3	chr3:50156913..50158492-chr3:50221059..50222752,2	K562	blood:
4	chr3:50157879..50160528-chr3:50162974..50166130,4	K562	blood:
5	chr3:50171631..50173640-chr3:50177307..50179987,2	K562	blood:
6	chr3:50159102..50161217-chr3:50161241..50163893,2	MCF-7	breast:
7	chr3:50159102..50161217-chr3:50161241..50163893,2	MCF-7	breast:
8	chr3:50157801..50161419-chr3:50224013..50228566,6	MCF-7	breast:
9	chr3:50126403..50128325-chr3:50160017..50162244,2	K562	blood:
10	chr3:50159863..50162699-chr3:50227102..50229015,2	MCF-7	breast:
11	chr3:50164397..50164965-chr3:50226441..50226966,2	K562	blood:
12	chr3:50150753..50152851-chr3:50154115..50156768,2	K562	blood:
13	chr3:50157579..50160318-chr3:50233509..50235124,2	MCF-7	breast:
14	chr3:50161300..50163134-chr3:50195216..50197721,2	MCF-7	breast:
15	chr3:50164743..50166299-chr3:50183403..50185616,2	MCF-7	breast:
16	chr3:50150154..50152874-chr3:50153182..50156279,3	K562	blood:
17	chr3:50164487..50165036-chr3:50302247..50302879,2	MCF-7	breast:
18	chr3:50160797..50162684-chr3:50168795..50170458,2	K562	blood:
19	chr3:50160721..50162724-chr3:50168795..50173383,5	K562	blood:
20	chr3:50150154..50152874-chr3:50153182..50156279,3	K562	blood:
21	chr3:50171634..50174420-chr3:50273113..50275042,2	MCF-7	breast:
22	chr3:50172563..50177055-chr3:50182695..50185570,4	MCF-7	breast:
23	chr3:50159011..50159688-chr3:50191786..50192464,2	MCF-7	breast:
24	chr3:50160600..50163125-chr3:50165110..50166972,2	K562	blood:
25	chr3:50157123..50160509-chr3:50182287..50185771,3	MCF-7	breast:
26	chr3:50158102..50159885-chr3:50296008..50298288,2	MCF-7	breast:
27	chr3:50158625..50159212-chr3:50263622..50264247,2	K562	blood:
28	chr3:50144744..50147316-chr3:50219770..50222620,2	K562	blood:
29	chr3:50149445..50151714-chr3:50193369..50195764,2	MCF-7	breast:
30	chr3:50159660..50164036-chr3:50192840..50194687,5	MCF-7	breast:
31	chr3:50161158..50162921-chr3:50305977..50308672,2	MCF-7	breast:
32	chr3:50160236..50162661-chr3:50199284..50201968,2	MCF-7	breast:
33	chr3:50161160..50162683-chr3:50271555..50274143,2	MCF-7	breast:
34	chr3:50164220..50165841-chr3:50169417..50171104,2	MCF-7	breast:
35	chr3:50166461..50169382-chr3:50192185..50193904,2	MCF-7	breast:
36	chr3:50157403..50159553-chr3:50273403..50275024,2	K562	blood:
37	chr3:50171126..50173864-chr3:50190598..50194091,3	MCF-7	breast:
38	chr3:50164983..50167115-chr3:50208238..50210374,2	MCF-7	breast:
39	chr3:50157890..50164898-chr3:50186493..50191745,15	MCF-7	breast:
40	chr3:50149717..50151316-chr3:50273425..50276151,2	MCF-7	breast:
41	chr3:50159116..50159819-chr3:50183361..50183915,2	MCF-7	breast:
42	chr3:50171431..50173846-chr3:50174182..50176296,2	K562	blood:
43	chr3:50157983..50159948-chr3:50231806..50233770,3	K562	blood:
44	chr3:50159053..50159645-chr3:50263405..50264051,2	MCF-7	breast:
45	chr3:50160721..50162724-chr3:50168795..50173383,5	K562	blood:
46	chr3:50154064..50156374-chr3:50184030..50185702,2	MCF-7	breast:
47	chr3:50162229..50165038-chr3:50305683..50307880,2	MCF-7	breast:
48	chr3:50159501..50162170-chr3:50213209..50216428,3	K562	blood:
49	chr3:50131320..50133089-chr3:50157321..50159844,2	K562	blood:
50	chr3:50160600..50163125-chr3:50165110..50166972,2	K562	blood:

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RBM5	hsa-miR-30a-5p	chr3:50156150-50156171

Variant related genes	Relation type
RBM5	TF binding region
RBM5	CpG island
ENSG00000264706	chromatin interactions
ENSG00000230454	chromatin interactions
ENSG00000001617	chromatin interactions
ENSG00000164076	chromatin interactions
ENSG00000114353	chromatin interactions
ENSG00000003756	chromatin interactions
ENSG00000207922	chromatin interactions
ENSG00000235016	chromatin interactions
ENSG00000012171	chromatin interactions
ENSG00000114349	chromatin interactions

Extended variants
information (count: 1032 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1061474	chr3:50144951-50144952	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs368640807	chr3:50144969-50144970	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs371984080	chr3:50144972-50144973	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs371337648	chr3:50144989-50144990	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374315579	chr3:50145010-50145011	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs535200928	chr3:50145028-50145029	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368199438	chr3:50145042-50145043	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375767951	chr3:50145079-50145080	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs563893929	chr3:50145082-50145083	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186139207	chr3:50145083-50145084	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs551857748	chr3:50145095-50145096	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374531852	chr3:50145100-50145101	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371569911	chr3:50145105-50145106	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs71080575	chr3:50145128-50145129	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs570169675	chr3:50145140-50145141	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs190606791	chr3:50145143-50145144	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145241894	chr3:50145155-50145156	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs546926879	chr3:50145156-50145157	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571400095	chr3:50145190-50145191	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149150469	chr3:50145201-50145202	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs367942409	chr3:50145222-50145223	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368918565	chr3:50145263-50145264	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs144989528	chr3:50145293-50145294	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538704873	chr3:50145314-50145315	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs534906792	chr3:50145321-50145322	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558227117	chr3:50145323-50145324	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs557036070	chr3:50145333-50145334	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs146773930	chr3:50145360-50145361	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs559103655	chr3:50145366-50145367	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs577407574	chr3:50145367-50145368	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140724462	chr3:50145370-50145371	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs553312795	chr3:50145371-50145372	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536263741	chr3:50145379-50145380	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575067541	chr3:50145398-50145399	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542527287	chr3:50145407-50145408	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs145867347	chr3:50145410-50145411	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148691467	chr3:50145541-50145542	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs200288461	chr3:50145551-50145552	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201247964	chr3:50145596-50145597	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17050921	chr3:50145623-50145624	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs371342266	chr3:50145662-50145663	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12163538	chr3:50145694-50145695	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545975791	chr3:50145696-50145697	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563882793	chr3:50145700-50145701	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs376849156	chr3:50145727-50145728	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs369922395	chr3:50145729-50145730	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528152155	chr3:50145730-50145731	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs546222776	chr3:50145754-50145755	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568062016	chr3:50145843-50145844	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs9852055	chr3:50145869-50145870	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Adrenocortical carcinoma	18281524	CNVD
Cancer	20164919	CNVD
Autism	20531469	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50127400-50150000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:50127800-50157800	Strong transcription	H9 Cell Line	embryonic stem cell
3	chr3:50128000-50152600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:50128000-50157800	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:50128000-50158000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:50128000-50158000	Strong transcription	Fetal Muscle Trunk	muscle
7	chr3:50128200-50152800	Strong transcription	H1 Cell Line	embryonic stem cell
8	chr3:50128200-50158800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:50128400-50148800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr3:50128400-50157800	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr3:50128400-50158200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr3:50128400-50158400	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr3:50128400-50159000	Strong transcription	Lung	lung
14	chr3:50128600-50148800	Strong transcription	Fetal Muscle Leg	muscle
15	chr3:50128600-50156200	Strong transcription	Ovary	ovary
16	chr3:50128600-50158000	Strong transcription	NH-A	brain
17	chr3:50128600-50158400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:50128600-50158400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
19	chr3:50128600-50158600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr3:50128600-50158600	Strong transcription	Colonic Mucosa	Colon
21	chr3:50128600-50158800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr3:50128600-50158800	Strong transcription	Brain Germinal Matrix	brain
23	chr3:50128600-50158800	Strong transcription	Placenta Amnion	Placenta Amnion
24	chr3:50128600-50159000	Strong transcription	Brain Angular Gyrus	brain
25	chr3:50128600-50159000	Strong transcription	Placenta	Placenta
26	chr3:50128600-50159000	Strong transcription	Sigmoid Colon	Sigmoid Colon
27	chr3:50128600-50159200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:50128600-50159200	Strong transcription	Liver	Liver
29	chr3:50128600-50159200	Strong transcription	NHEK	skin
30	chr3:50128600-50160400	Strong transcription	Fetal Thymus	thymus
31	chr3:50128800-50149000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr3:50128800-50156600	Strong transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:50128800-50156600	Strong transcription	Brain Substantia Nigra	brain
34	chr3:50128800-50158600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr3:50128800-50158600	Strong transcription	HMEC	breast
36	chr3:50128800-50159000	Strong transcription	Brain Anterior Caudate	brain
37	chr3:50129000-50158600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:50129000-50158600	Strong transcription	Duodenum Mucosa	Duodenum
39	chr3:50129000-50158800	Strong transcription	Fetal Intestine Large	intestine
40	chr3:50129000-50159000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr3:50129000-50159200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:50129000-50159200	Strong transcription	Primary B cells from peripheral blood	blood
43	chr3:50129000-50159400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr3:50129000-50159400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr3:50129000-50160000	Strong transcription	Fetal Stomach	stomach
46	chr3:50129000-50160000	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr3:50129000-50160800	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr3:50129200-50147600	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr3:50129200-50147800	Strong transcription	Skeletal Muscle Male	skeletal muscle
50	chr3:50129200-50148400	Strong transcription	Hela-S3	cervix

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