Variant report

Variant	nsv894134
Chromosome Location	chr9:136839840-136892523
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2433)
CpG islands
(count:1955)
Chromatin interactive
region (count:110)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2433 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:136889805-136890105	K562	blood:	n/a	n/a
2	ARID3A	chr9:136890416-136890552	K562	blood:	n/a	n/a
3	ARID3A	chr9:136876031-136876182	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:136856048-136856079	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:136859562-136859782	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:136890361-136890664	HepG2	liver:	n/a	n/a
7	ATF2	chr9:136890271-136890720	GM12878	blood:	n/a	n/a
8	ATF2	chr9:136890042-136890385	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:136890308-136890719	A549	lung:	n/a	chr9:136890464-136890473
10	ATF3	chr9:136890380-136890723	A549	lung:	n/a	chr9:136890464-136890473
11	ATF3	chr9:136890447-136890733	K562	blood:	n/a	chr9:136890464-136890473
12	ATF3	chr9:136885323-136885812	HCT-116	colon:	n/a	n/a
13	BACH1	chr9:136858165-136858241	K562	blood:	n/a	n/a
14	BACH1	chr9:136857281-136858367	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:136856855-136856872	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:136856324-136856351	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr9:136879263-136879437	GM12878	blood:	n/a	n/a
18	BCL11A	chr9:136879082-136879526	GM12878	blood:	n/a	n/a
19	BCL3	chr9:136885430-136885587	GM12878	blood:	n/a	n/a
20	BCL3	chr9:136857104-136857688	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857667-136857680 chr9:136857587-136857600
21	BCL3	chr9:136857966-136858629	A549	lung:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
22	BCLAF1	chr9:136890309-136890720	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:136857182-136857925	GM12878	blood:	n/a	chr9:136857527-136857540 chr9:136857722-136857735 chr9:136857667-136857680 chr9:136857587-136857600 chr9:136857703-136857716
24	BCLAF1	chr9:136857949-136858391	GM12878	blood:	n/a	chr9:136858041-136858050 chr9:136858023-136858032 chr9:136858029-136858038
25	BHLHE40	chr9:136859506-136859800	K562	blood:	n/a	n/a
26	BHLHE40	chr9:136869721-136869754	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:136890128-136890704	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:136856410-136856656	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:136857175-136857795	GM12878	blood:	n/a	chr9:136857723-136857739
30	BHLHE40	chr9:136869497-136870038	HepG2	liver:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
31	BHLHE40	chr9:136858022-136858718	GM12878	blood:	n/a	chr9:136858292-136858308
32	BHLHE40	chr9:136843682-136844132	HepG2	liver:	n/a	chr9:136843822-136843838
33	BHLHE40	chr9:136857536-136857643	K562	blood:	n/a	n/a
34	BHLHE40	chr9:136869547-136869987	K562	blood:	n/a	chr9:136869715-136869728 chr9:136869957-136869973 chr9:136869906-136869915 chr9:136869716-136869725
35	BHLHE40	chr9:136857238-136857657	HepG2	liver:	n/a	n/a
36	BHLHE40	chr9:136890947-136891211	GM12878	blood:	n/a	n/a
37	BHLHE40	chr9:136859537-136859868	GM12878	blood:	n/a	n/a
38	BHLHE40	chr9:136890357-136891137	K562	blood:	n/a	n/a
39	BHLHE40	chr9:136858375-136858412	K562	blood:	n/a	n/a
40	BRCA1	chr9:136857229-136857386	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:136859495-136859859	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr9:136859697-136859701	GM12878	blood:	n/a	n/a
43	BRCA1	chr9:136843712-136843912	HepG2	liver:	n/a	n/a
44	BRCA1	chr9:136889902-136890644	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr9:136856472-136856482	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr9:136859571-136859661	HepG2	liver:	n/a	n/a
47	BRCA1	chr9:136858624-136858795	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr9:136879187-136879552	K562	blood:	n/a	n/a
49	CBX3	chr9:136890207-136890673	K562	blood:	n/a	n/a
50	CBX3	chr9:136879192-136879515	K562	blood:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:136861819-136861869	NT2-D1	testis:	n/a
2	chr9:136889061-136889111	AG10803	skin:	n/a
3	chr9:136856435-136856485	AoSMC	blood vessel:	n/a
4	chr9:136861819-136861869	NT2-D1	testis:	n/a
5	chr9:136889061-136889111	AG10803	skin:	n/a
6	chr9:136856435-136856485	AoSMC	blood vessel:	n/a
7	chr9:136858308-136858358	Caco-2	colon:	n/a
8	chr9:136845816-136845866	Hela-S3	cervix:	n/a
9	chr9:136857190-136857240	HRPEpiC	eye:	n/a
10	chr9:136844768-136844818	SAEC	small airway:	n/a
11	chr9:136857190-136857240	HCT-116	colon:	n/a
12	chr9:136855902-136855952	HRCEpiC	kidney:	n/a
13	chr9:136890014-136890064	SKMC	muscle:	n/a
14	chr9:136876905-136876955	HCPEpiC	choroid plexus:	n/a
15	chr9:136882828-136882878	A549	lung:	n/a
16	chr9:136858308-136858358	BE2_C	brain:	n/a
17	chr9:136856352-136856402	RPTEC	kidney:	n/a
18	chr9:136882828-136882878	AG09309	skin:	n/a
19	chr9:136879298-136879348	GM12892	blood:	n/a
20	chr9:136879298-136879348	LNCaP	prostate:	n/a
21	chr9:136889061-136889111	ProgFib	skin:	n/a
22	chr9:136847709-136847759	H1-hESC	embryonic stem cell:	embryo
23	chr9:136857244-136857294	BE2_C	brain:	n/a
24	chr9:136860187-136860237	Jurkat	blood:	n/a
25	chr9:136882828-136882878	H1-hESC	embryonic stem cell:	embryo
26	chr9:136891620-136891670	SAEC	small airway:	n/a
27	chr9:136858163-136858213	SKMC	muscle:	n/a
28	chr9:136844768-136844818	Hela-S3	cervix:	n/a
29	chr9:136891078-136891128	NH-A	brain:	n/a
30	chr9:136890014-136890064	HIPEpiC	eye:	n/a
31	chr9:136861819-136861869	Caco-2	colon:	n/a
32	chr9:136844768-136844818	AG09319	gingival:	n/a
33	chr9:136857244-136857294	T-47D	breast:	n/a
34	chr9:136876905-136876955	A549	lung:	n/a
35	chr9:136877010-136877060	HCPEpiC	choroid plexus:	n/a
36	chr9:136879746-136879796	NB4	blood:	n/a
37	chr9:136890948-136890998	LNCaP	prostate:	n/a
38	chr9:136856352-136856402	NB4	blood:	n/a
39	chr9:136890014-136890064	HCM	heart:	n/a
40	chr9:136890014-136890064	HCPEpiC	choroid plexus:	n/a
41	chr9:136869371-136869421	GM12878	blood:	n/a
42	chr9:136858680-136858730	NT2-D1	testis:	n/a
43	chr9:136879746-136879796	GM06990	blood:	n/a
44	chr9:136860187-136860237	HepG2	liver:	n/a
45	chr9:136858680-136858730	SKMC	muscle:	n/a
46	chr9:136858308-136858358	A549	lung:	n/a
47	chr9:136847709-136847759	IMR90	lung:	fetal
48	chr9:136891620-136891670	HepG2	liver:	n/a
49	chr9:136860187-136860237	ovcar-3	ovarian:	n/a
50	chr9:136856352-136856402	MCF10A-Er-Src	breast:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:136802379..136804423-chr9:136852709..136855178,2	MCF-7	breast:
2	chr7:26239812..26240720-chr9:136846541..136847167,2	Hela-S3	cervix:
3	chr9:136819196..136821510-chr9:136837894..136840389,2	K562	blood:
4	chr9:136372726..136374611-chr9:136854336..136856756,2	MCF-7	breast:
5	chr9:136839997..136844319-chr9:136851053..136854251,5	MCF-7	breast:
6	chr9:136592345..136593069-chr9:136859637..136860159,2	MCF-7	breast:
7	chr9:136859431..136860674-chr9:136964030..136964900,5	MCF-7	breast:
8	chr9:136867977..136869664-chr9:136870201..136872512,2	MCF-7	breast:
9	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
10	chr9:136683788..136685445-chr9:136846019..136848764,2	MCF-7	breast:
11	chr9:136855434..136861951-chr9:136862866..136866695,10	MCF-7	breast:
12	chr9:136836160..136840287-chr9:136840459..136843890,5	MCF-7	breast:
13	chr9:136746415..136748463-chr9:136851208..136853267,2	MCF-7	breast:
14	chr9:136834147..136836110-chr9:136837222..136840817,3	MCF-7	breast:
15	chr9:136657461..136661655-chr9:136857893..136859866,4	K562	blood:
16	chr9:136849949..136852879-chr9:136857069..136859221,2	K562	blood:
17	chr9:136706030..136708990-chr9:136860281..136862454,2	MCF-7	breast:
18	chr9:136739328..136742123-chr9:136841796..136845434,3	MCF-7	breast:
19	chr9:136890470..136892525-chr9:136914394..136917333,2	K562	blood:
20	chr9:136607827..136608773-chr9:136859602..136860351,4	MCF-7	breast:
21	chr9:136856397..136858189-chr9:136860981..136863697,2	K562	blood:
22	chr9:136647409..136647939-chr9:136859642..136860182,3	K562	blood:
23	chr9:136625089..136627399-chr9:136858004..136860328,2	MCF-7	breast:
24	chr9:136743217..136745167-chr9:136838200..136840998,2	MCF-7	breast:
25	chr9:136824147..136826582-chr9:136846037..136848091,2	MCF-7	breast:
26	chr9:136888985..136892489-chr9:136929943..136933995,5	K562	blood:
27	chr9:136594711..136597550-chr9:136858767..136860355,2	MCF-7	breast:
28	chr22:43010797..43011769-chr9:136856743..136857657,2	Hela-S3	cervix:
29	chr9:136862110..136863707-chr9:136863725..136867446,4	MCF-7	breast:
30	chr9:136868478..136870718-chr9:136870776..136873148,2	K562	blood:
31	chr9:136857193..136859735-chr9:136888278..136891342,4	MCF-7	breast:
32	chr9:136600362..136604558-chr9:136857405..136860234,5	MCF-7	breast:
33	chr9:136840954..136843930-chr9:136846251..136850265,3	K562	blood:
34	chr9:136867977..136869664-chr9:136870201..136872512,2	MCF-7	breast:
35	chr9:136856689..136859629-chr9:136860948..136863697,2	K562	blood:
36	chr9:136827453..136828973-chr9:136850064..136852455,2	MCF-7	breast:
37	chr9:136862110..136863707-chr9:136863725..136867446,4	MCF-7	breast:
38	chr9:136657412..136658751-chr9:136858523..136860164,12	K562	blood:
39	chr9:136592463..136593107-chr9:136859236..136860141,3	MCF-7	breast:
40	chr9:136889377..136892336-chr9:136904315..136908613,4	MCF-7	breast:
41	chr9:136888457..136893834-chr9:136930854..136936517,11	MCF-7	breast:
42	chr17:58677435..58680394-chr9:136857896..136860386,2	MCF-7	breast:
43	chr9:136655962..136656512-chr9:136858875..136859685,2	K562	blood:
44	chr9:136679694..136681677-chr9:136851207..136853977,2	MCF-7	breast:
45	chr9:136859325..136860777-chr9:136964002..136965283,7	MCF-7	breast:
46	chr1:16678857..16679483-chr9:136857773..136858655,2	Hela-S3	cervix:
47	chr9:136751034..136753056-chr9:136851311..136853643,2	MCF-7	breast:
48	chr9:136747429..136748291-chr9:136859497..136860075,2	MCF-7	breast:
49	chr9:136890645..136892420-chr9:136892471..136894163,2	K562	blood:
50	chr9:136667141..136668984-chr9:136855421..136857150,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR5-3	chr9:136892273-136892384	ENSG00000235106
2	lnc-WDR5-3	chr9:136890561-136890658	NONHSAT135349
3	lnc-WDR5-7	chr9:136857728-136861324	NONHSAT135347
4	lnc-WDR5-3	chr9:136890967-136891212	NONHSAT135349
5	lnc-WDR5-3	chr9:136890608-136890658	ENSG00000235106
6	lnc-WDR5-3	chr9:136891330-136891671	ENSG00000235106
7	lnc-WDR5-3	chr9:136890967-136891212	ENSG00000235106
8	lnc-WDR5-3	chr9:136891330-136891671	NONHSAT135349

No data

Variant related genes	Relation type
LINC00094	TF binding region
VAV2	TF binding region
LINC00094	CpG island
VAV2	CpG island
ENSG00000235106	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000169925	chromatin interactions
ENSG00000235138	chromatin interactions
ENSG00000196363	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000123453	chromatin interactions
ENSG00000273249	chromatin interactions
ENSG00000136450	chromatin interactions
ENSG00000270022	chromatin interactions
ENSG00000174282	chromatin interactions
ENSG00000037637	chromatin interactions
ENSG00000170836	chromatin interactions
ENSG00000160293	chromatin interactions
ENSG00000100227	chromatin interactions
ENSG00000055070	chromatin interactions
ENSG00000181222	chromatin interactions
MRPL19	miRNA target sites
PRKAA1	miRNA target sites
CSE1L	miRNA target sites
CCND2	miRNA target sites

Extended variants
information (count: 2486 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2486 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs679106	chr9:136839840-136839841	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535261718	chr9:136839848-136839849	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs553942718	chr9:136839850-136839851	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs571955828	chr9:136839854-136839855	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs535706299	chr9:136839869-136839870	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545682602	chr9:136839875-136839876	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs678744	chr9:136839888-136839889	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11270393	chr9:136839891-136839892	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs535244173	chr9:136839904-136839905	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs58320170	chr9:136839910-136839911	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs576803797	chr9:136839935-136839936	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544613734	chr9:136839962-136839963	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs562804358	chr9:136839986-136839987	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs146578450	chr9:136840058-136840059	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs397772972	chr9:136840062-136840063	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs142838785	chr9:136840066-136840067	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs187777904	chr9:136840072-136840073	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs560668105	chr9:136840127-136840128	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs527931629	chr9:136840130-136840131	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs72619336	chr9:136840152-136840153	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs564799668	chr9:136840154-136840155	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs192772861	chr9:136840175-136840176	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs146250667	chr9:136840176-136840177	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs10115680	chr9:136840192-136840193	Weak transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs543438640	chr9:136840214-136840215	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556948980	chr9:136840226-136840227	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs375213404	chr9:136840251-136840252	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547215737	chr9:136840276-136840277	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs386739219	chr9:136840289-136840290	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2519134	chr9:136840291-136840292	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs7027965	chr9:136840323-136840324	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557601969	chr9:136840331-136840332	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575945897	chr9:136840335-136840336	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537808077	chr9:136840387-136840388	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2519133	chr9:136840389-136840390	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574789639	chr9:136840404-136840405	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542302318	chr9:136840438-136840439	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560604835	chr9:136840456-136840457	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534556496	chr9:136840528-136840529	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573686973	chr9:136840623-136840624	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189454833	chr9:136840624-136840625	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs546443713	chr9:136840636-136840637	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs564736311	chr9:136840642-136840643	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532041516	chr9:136840686-136840687	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549465366	chr9:136840759-136840760	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561715942	chr9:136840765-136840766	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs809737	chr9:136840824-136840825	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs547067433	chr9:136840841-136840842	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs181556143	chr9:136840853-136840854	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375729706	chr9:136840858-136840859	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Hepatocellular carcinoma	22174799	CNVD
Bladder cancer	21909424	CNVD
Cancer	17160897	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20932292	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:1938 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:136832000-136840800	Enhancers	Primary B cells from cord blood	blood
2	chr9:136832400-136842400	Enhancers	Primary B cells from peripheral blood	blood
3	chr9:136832600-136843800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr9:136832800-136844200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:136833600-136842000	Enhancers	Pancreas	Pancrea
6	chr9:136833800-136840200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:136834000-136840000	Enhancers	Fetal Muscle Trunk	muscle
8	chr9:136834000-136840400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:136834200-136840400	Enhancers	Spleen	Spleen
10	chr9:136835000-136840000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr9:136835200-136848600	Enhancers	Fetal Intestine Large	intestine
12	chr9:136835400-136840000	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr9:136835400-136848800	Genic enhancers	Fetal Intestine Small	intestine
14	chr9:136835600-136840200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr9:136835600-136840600	Enhancers	Stomach Mucosa	stomach
16	chr9:136835800-136854800	Weak transcription	A549	lung
17	chr9:136836000-136840400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr9:136836600-136840000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr9:136836800-136843800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr9:136836800-136844000	Weak transcription	NHDF-Ad	bronchial
21	chr9:136837200-136842400	Weak transcription	NHLF	lung
22	chr9:136837400-136840400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:136837400-136840800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr9:136837400-136842000	Weak transcription	Ovary	ovary
25	chr9:136837400-136851400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr9:136837400-136854800	Weak transcription	HMEC	breast
27	chr9:136837600-136845000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr9:136837600-136845000	Weak transcription	Fetal Kidney	kidney
29	chr9:136837800-136844000	Weak transcription	Colon Smooth Muscle	Colon
30	chr9:136837800-136850600	Weak transcription	NHEK	skin
31	chr9:136838000-136854800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr9:136838400-136840200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr9:136838400-136840200	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr9:136838400-136840600	Enhancers	Lung	lung
35	chr9:136838400-136841600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr9:136838400-136841600	Weak transcription	Fetal Stomach	stomach
37	chr9:136838600-136840200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr9:136838800-136840000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr9:136838800-136840200	Enhancers	Right Atrium	heart
40	chr9:136838800-136840200	Enhancers	Right Ventricle	heart
41	chr9:136838800-136841000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr9:136839000-136842000	Weak transcription	Fetal Lung	lung
43	chr9:136839000-136844000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:136839000-136844000	Weak transcription	Esophagus	oesophagus
45	chr9:136839000-136844400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr9:136839000-136844400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr9:136839200-136840400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr9:136839200-136840600	Enhancers	Placenta	Placenta
49	chr9:136839200-136841400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr9:136839200-136843400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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