Variant report

Variant	nsv1029449
Chromosome Location	chr9:18414752-18829127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2568)
CpG islands
(count:977)
Chromatin interactive
region (count:41)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:3)

(count:2568 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:18705112-18705234	K562	blood:	n/a	n/a
2	ARID3A	chr9:18456661-18457094	HepG2	liver:	n/a	chr9:18456664-18456680
3	ARID3A	chr9:18452384-18452493	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:18669020-18669356	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:18622195-18622391	HepG2	liver:	n/a	n/a
6	ATF2	chr9:18768932-18769740	GM12878	blood:	n/a	n/a
7	ATF2	chr9:18768817-18769760	GM12878	blood:	n/a	n/a
8	BACH1	chr9:18708496-18708726	H1-hESC	embryonic stem cell:	n/a	chr9:18708633-18708647
9	BACH1	chr9:18821759-18822288	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:18606813-18606827	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:18768943-18769625	GM12878	blood:	n/a	n/a
12	BATF	chr9:18768878-18769670	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:18768959-18769211	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:18768921-18769607	GM12878	blood:	n/a	n/a
15	BCL3	chr9:18768916-18769623	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:18768912-18769756	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:18791280-18791295	K562	blood:	n/a	n/a
18	BRCA1	chr9:18443194-18443410	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr9:18437528-18438248	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr9:18821746-18822028	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr9:18574188-18574199	GM12878	blood:	n/a	n/a
22	BRCA1	chr9:18459902-18460682	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr9:18658837-18659489	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr9:18707230-18707376	A549	lung:	n/a	chr9:18707297-18707314
25	CEBPB	chr9:18578396-18578419	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:18707184-18707437	IMR90	lung:	n/a	chr9:18707297-18707314
27	CEBPB	chr9:18456884-18457194	Hela-S3	cervix:	n/a	chr9:18457081-18457094
28	CEBPB	chr9:18822502-18822702	IMR90	lung:	n/a	chr9:18822560-18822568
29	CEBPB	chr9:18607360-18607559	HepG2	liver:	n/a	chr9:18607503-18607516 chr9:18607502-18607519 chr9:18607503-18607516 chr9:18607504-18607515 chr9:18607503-18607516 chr9:18607503-18607514
30	CEBPB	chr9:18442516-18442940	Hela-S3	cervix:	n/a	chr9:18442652-18442663 chr9:18442654-18442665
31	CEBPB	chr9:18822495-18822766	Hela-S3	cervix:	n/a	chr9:18822560-18822568
32	CEBPB	chr9:18668980-18669271	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:18631227-18631419	K562	blood:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
34	CEBPB	chr9:18806127-18806422	HepG2	liver:	n/a	chr9:18806258-18806267 chr9:18806256-18806267
35	CEBPB	chr9:18658575-18659425	IMR90	lung:	n/a	chr9:18659245-18659262
36	CEBPB	chr9:18472721-18473214	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:18585070-18585095	A549	lung:	n/a	n/a
38	CEBPB	chr9:18424133-18424479	Hela-S3	cervix:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
39	CEBPB	chr9:18756385-18756534	HepG2	liver:	n/a	chr9:18756457-18756468
40	CEBPB	chr9:18631153-18631463	HepG2	liver:	n/a	chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631302-18631311 chr9:18631301-18631312 chr9:18631302-18631311
41	CEBPB	chr9:18474770-18475113	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:18544465-18544730	Hela-S3	cervix:	n/a	chr9:18544557-18544570
43	CEBPB	chr9:18526773-18527003	A549	lung:	n/a	n/a
44	CEBPB	chr9:18756363-18756643	Hela-S3	cervix:	n/a	chr9:18756457-18756468
45	CEBPB	chr9:18424163-18424437	A549	lung:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
46	CEBPB	chr9:18429101-18429513	IMR90	lung:	n/a	chr9:18429301-18429312
47	CEBPB	chr9:18756278-18756653	HepG2	liver:	n/a	chr9:18756457-18756468
48	CEBPB	chr9:18429093-18429510	Hela-S3	cervix:	n/a	chr9:18429301-18429312
49	CEBPB	chr9:18424146-18424500	HepG2	liver:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
50	CEBPB	chr9:18429159-18429386	HepG2	liver:	n/a	chr9:18429301-18429312

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18776340-18776390	PrEC	prostate:	n/a
2	chr9:18776340-18776390	PrEC	prostate:	n/a
3	chr9:18605667-18605717	AoSMC	blood vessel:	n/a
4	chr9:18776340-18776390	HIPEpiC	eye:	n/a
5	chr9:18727406-18727456	AG04449	skin:	fetal
6	chr9:18514052-18514102	ovcar-3	ovarian:	n/a
7	chr9:18473902-18473952	NH-A	brain:	n/a
8	chr9:18473902-18473952	GM06990	blood:	n/a
9	chr9:18793879-18793929	HNPCEpiC	eye:	n/a
10	chr9:18473902-18473952	SK-N-MC	brain:	n/a
11	chr9:18474243-18474293	HRE	kidney:	n/a
12	chr9:18777683-18777733	GM12891	blood:	n/a
13	chr9:18474243-18474293	SK-N-MC	brain:	n/a
14	chr9:18473902-18473952	H1-hESC	embryonic stem cell:	embryo
15	chr9:18825658-18825708	IMR90	lung:	fetal
16	chr9:18777683-18777733	IMR90	lung:	fetal
17	chr9:18437917-18437967	HRPEpiC	eye:	n/a
18	chr9:18514052-18514102	HMEC	breast:	n/a
19	chr9:18514052-18514102	CMK	blood:	n/a
20	chr9:18473902-18473952	HRCEpiC	kidney:	n/a
21	chr9:18770966-18771016	Caco-2	colon:	n/a
22	chr9:18490009-18490059	BE2_C	brain:	n/a
23	chr9:18706865-18706915	SAEC	small airway:	n/a
24	chr9:18474243-18474293	HRCEpiC	kidney:	n/a
25	chr9:18727406-18727456	NT2-D1	testis:	n/a
26	chr9:18776340-18776390	SK-N-MC	brain:	n/a
27	chr9:18490009-18490059	BJ	skin:	n/a
28	chr9:18490009-18490059	GM19239	blood:	n/a
29	chr9:18473902-18473952	HEEpiC	esophagus:	n/a
30	chr9:18727406-18727456	ovcar-3	ovarian:	n/a
31	chr9:18622331-18622381	HCT-116	colon:	n/a
32	chr9:18437917-18437967	SK-N-MC	brain:	n/a
33	chr9:18514052-18514102	NT2-D1	testis:	n/a
34	chr9:18605667-18605717	AG04449	skin:	fetal
35	chr9:18777555-18777605	AG04450	lung:	fetal
36	chr9:18473902-18473952	HAEpiC	amniotic membrane:	n/a
37	chr9:18776340-18776390	HEEpiC	esophagus:	n/a
38	chr9:18777683-18777733	HMEC	breast:	n/a
39	chr9:18490009-18490059	AG10803	skin:	n/a
40	chr9:18706865-18706915	RPTEC	kidney:	n/a
41	chr9:18777683-18777733	SK-N-SH	brain:	n/a
42	chr9:18437917-18437967	H1-hESC	embryonic stem cell:	embryo
43	chr9:18770966-18771016	MCF10A-Er-Src	breast:	n/a
44	chr9:18706865-18706915	AG09309	skin:	n/a
45	chr9:18706865-18706915	HRCEpiC	kidney:	n/a
46	chr9:18473902-18473952	Hepatocyte	liver:	n/a
47	chr9:18727406-18727456	Hepatocyte	liver:	n/a
48	chr9:18474243-18474293	AG10803	skin:	n/a
49	chr9:18776940-18776990	BJ	skin:	n/a
50	chr9:18793879-18793929	AG04449	skin:	fetal

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
2	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
3	chr9:18705469..18707872-chr9:18709248..18712015,2	MCF-7	breast:
4	chr9:18791200..18791746-chr9:19457106..19458088,3	K562	blood:
5	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
6	chr9:18725510..18728390-chr9:18733590..18735848,2	MCF-7	breast:
7	chr1:149223814..149224438-chr9:18512987..18513487,3	MCF-7	breast:
8	chr9:18824289..18824965-chr9:19028543..19029149,2	MCF-7	breast:
9	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
10	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
11	chr9:18826203..18828034-chr9:18832223..18834749,2	MCF-7	breast:
12	chr9:18769799..18772875-chr9:18776003..18779587,3	K562	blood:
13	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
14	chr9:18254775..18255482-chr9:18823832..18824683,3	MCF-7	breast:
15	chr9:18436804..18438586-chr9:18439890..18441991,2	MCF-7	breast:
16	chr9:18777312..18778984-chr9:18781193..18784128,2	K562	blood:
17	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:
18	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:
19	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
20	chr21:39358274..39359037-chr9:18704805..18705621,2	MCF-7	breast:
21	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
22	chr2:126575127..126575844-chr9:18665491..18666183,2	MCF-7	breast:
23	chr1:149223496..149224418-chr9:18512967..18513967,3	MCF-7	breast:
24	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
25	chr1:149222514..149224923-chr9:18513487..18514987,2	K562	blood:
26	chr9:18745157..18747160-chr9:18747921..18750231,2	MCF-7	breast:
27	chr9:18762802..18765724-chr9:18766149..18769161,3	K562	blood:
28	chr9:18255104..18255666-chr9:18823787..18824360,2	MCF-7	breast:
29	chr9:18733967..18736858-chr9:18739933..18741976,3	MCF-7	breast:
30	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
31	chr1:149223595..149224343-chr9:18512967..18513487,3	Hela-S3	cervix:
32	chr9:18436804..18438586-chr9:18439890..18441991,2	MCF-7	breast:
33	chr9:18722180..18723810-chr9:18726997..18728852,2	K562	blood:
34	chr8:61562599..61565494-chr9:18702295..18704681,2	MCF-7	breast:
35	chr9:18662167..18665769-chr9:18669383..18672936,3	MCF-7	breast:
36	chr9:18734493..18736072-chr9:18736528..18738186,2	MCF-7	breast:
37	chr6:29596747..29597490-chr9:18419651..18420547,2	MCF-7	breast:
38	chr9:18770497..18772251-chr9:18783540..18785289,2	K562	blood:
39	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
40	chr9:18254805..18255425-chr9:18442379..18443060,2	MCF-7	breast:
41	chr9:18552353..18554750-chr9:18819699..18822182,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RRAGA-3	chr9:18651145-18651448	NONHSAT130312
2	lnc-FAM154A-3	chr9:18717972-18718524	NONHSAT130313

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3152-5p	chr9:18573314-18573335	MIMAT0019207
hsa-miR-3152-3p	chr9:18573348-18573369	MIMAT0015025

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADAMTSL1	hsa-miR-25-3p	chr9:18681248-18681269
2	ADAMTSL1	hsa-miR-25-3p	chr9:18681336-18681357
3	ADAMTSL1	hsa-miR-132-3p	chr9:18684803-18684824

Variant related genes	Relation type
RN7SKP258	TF binding region
ADAMTSL1	TF binding region
ENSG00000236857	TF binding region
MIR3152	TF binding region
RN7SKP258	CpG island
ADAMTSL1	CpG island
ENSG00000236857	CpG island
MIR3152	CpG island
ENSG00000206737	chromatin interactions
ENSG00000178031	chromatin interactions

Extended variants
information (count: 18682 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:18682 , 50 per page) page: 1 2 3 4 5 6 7 ... 374

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535243947	chr9:18420819-18420820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146293865	chr9:18420823-18420824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35254758	chr9:18420826-18420827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536689363	chr9:18420839-18420840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554623170	chr9:18420840-18420841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs139546126	chr9:18420861-18420862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184735657	chr9:18420863-18420864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548281479	chr9:18420960-18420961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs1340049	chr9:18420972-18420973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs954527	chr9:18420986-18420987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537060814	chr9:18420989-18420990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34902749	chr9:18421001-18421002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35729329	chr9:18421004-18421005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552184113	chr9:18421014-18421015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142651181	chr9:18421017-18421018	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535054616	chr9:18421026-18421027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7032022	chr9:18421037-18421038	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574943251	chr9:18421087-18421088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536020217	chr9:18421112-18421113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190004254	chr9:18421131-18421132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7046726	chr9:18421132-18421133	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545893230	chr9:18421139-18421140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564119587	chr9:18421180-18421181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146043210	chr9:18421181-18421182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540169145	chr9:18421209-18421210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561973192	chr9:18421239-18421240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577542955	chr9:18421244-18421245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533129457	chr9:18421249-18421250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550325354	chr9:18421256-18421257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562324252	chr9:18421257-18421258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115317131	chr9:18421269-18421270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552249388	chr9:18421379-18421380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376153874	chr9:18421399-18421400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs181232034	chr9:18421426-18421427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs76361169	chr9:18421437-18421438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572984677	chr9:18421447-18421448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371249477	chr9:18421450-18421451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568704062	chr9:18421452-18421453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374369199	chr9:18421571-18421572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34138828	chr9:18421578-18421579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386733288	chr9:18421586-18421587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75079900	chr9:18421590-18421591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185677500	chr9:18421612-18421613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189019956	chr9:18421626-18421627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575906973	chr9:18421723-18421724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541642442	chr9:18421734-18421735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149707547	chr9:18421748-18421749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572755298	chr9:18421815-18421816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540199689	chr9:18421817-18421818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575145820	chr9:18421851-18421852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20841430	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:4335 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18420800-18424400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:18421000-18421200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:18421000-18422800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr9:18421400-18421800	Enhancers	Left Ventricle	heart
5	chr9:18421400-18422400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:18421400-18423200	Enhancers	Fetal Heart	heart
7	chr9:18421800-18422200	Weak transcription	Left Ventricle	heart
8	chr9:18421800-18422800	Enhancers	Osteobl	bone
9	chr9:18422000-18422400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:18422000-18423000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:18422200-18422800	Enhancers	HMEC	breast
12	chr9:18422200-18423000	Enhancers	Left Ventricle	heart
13	chr9:18422200-18423000	Enhancers	HSMM	muscle
14	chr9:18422400-18422800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr9:18422400-18422800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:18422400-18422800	Enhancers	Muscle Satellite Cultured Cells	--
17	chr9:18422400-18422800	Enhancers	HSMMtube	muscle
18	chr9:18422400-18423600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr9:18422800-18424000	Weak transcription	Osteobl	bone
20	chr9:18423000-18428800	Weak transcription	HSMM	muscle
21	chr9:18423200-18428800	Weak transcription	Fetal Heart	heart
22	chr9:18423600-18424600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr9:18423600-18424600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:18424000-18424400	Enhancers	Osteobl	bone
25	chr9:18424400-18427600	Weak transcription	Osteobl	bone
26	chr9:18424600-18427000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:18424600-18427600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:18426600-18426800	Enhancers	Aorta	Aorta
29	chr9:18426800-18427800	Weak transcription	Aorta	Aorta
30	chr9:18427000-18427200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr9:18427200-18427800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:18427400-18431400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:18427600-18428000	Enhancers	Stomach Smooth Muscle	stomach
34	chr9:18427600-18428800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr9:18427600-18428800	Enhancers	HUVEC	blood vessel
36	chr9:18427600-18429400	Enhancers	Adipose Nuclei	Adipose
37	chr9:18427600-18429800	Enhancers	NHDF-Ad	bronchial
38	chr9:18427600-18432800	Enhancers	Osteobl	bone
39	chr9:18427800-18428400	Enhancers	Colon Smooth Muscle	Colon
40	chr9:18427800-18428600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr9:18427800-18428600	Enhancers	Aorta	Aorta
42	chr9:18427800-18431000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:18428000-18429200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr9:18428400-18428800	Weak transcription	Colon Smooth Muscle	Colon
45	chr9:18428400-18429000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr9:18428600-18429600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:18428600-18430800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:18428800-18429200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr9:18428800-18429400	Enhancers	Colon Smooth Muscle	Colon
50	chr9:18428800-18429600	Enhancers	Fetal Heart	heart

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