Variant report

Variant	nsv1033546
Chromosome Location	chr9:5875201-5900427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:908)
CpG islands
(count:244)
Chromatin interactive
region (count:40)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:908 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:5879451-5879942	K562	blood:	n/a	n/a
2	ARID3A	chr9:5900155-5900946	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:5893874-5894269	HepG2	liver:	n/a	n/a
4	ATF1	chr9:5879431-5879885	K562	blood:	n/a	n/a
5	ATF3	chr9:5879470-5879913	K562	blood:	n/a	n/a
6	ATF3	chr9:5879550-5879783	K562	blood:	n/a	n/a
7	BACH1	chr9:5886147-5886527	H1-hESC	embryonic stem cell:	n/a	chr9:5886178-5886192
8	BACH1	chr9:5876765-5877093	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr9:5879526-5879969	A549	lung:	n/a	n/a
10	BCL3	chr9:5885970-5886631	A549	lung:	n/a	n/a
11	BCLAF1	chr9:5886023-5886513	GM12878	blood:	n/a	n/a
12	BHLHE40	chr9:5897852-5898208	K562	blood:	n/a	n/a
13	BHLHE40	chr9:5895783-5896200	K562	blood:	n/a	n/a
14	BHLHE40	chr9:5886160-5886585	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:5879415-5879885	K562	blood:	n/a	chr9:5879442-5879458
16	BHLHE40	chr9:5886190-5886592	K562	blood:	n/a	n/a
17	BHLHE40	chr9:5886143-5886560	GM12878	blood:	n/a	n/a
18	BRCA1	chr9:5886053-5886313	GM12878	blood:	n/a	n/a
19	BRCA1	chr9:5886138-5886458	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr9:5893757-5894406	HepG2	liver:	n/a	n/a
21	BRCA1	chr9:5879552-5879919	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr9:5879405-5879856	K562	blood:	n/a	n/a
23	CBX3	chr9:5876596-5877260	K562	blood:	n/a	n/a
24	CCNT2	chr9:5879487-5879883	K562	blood:	n/a	n/a
25	CEBPB	chr9:5886158-5886449	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr9:5893927-5894181	HepG2	liver:	n/a	chr9:5894092-5894103
27	CEBPB	chr9:5893726-5894284	HepG2	liver:	n/a	chr9:5894092-5894103
28	CEBPB	chr9:5899522-5899647	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:5886102-5886439	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr9:5898852-5899136	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:5893701-5894286	HepG2	liver:	n/a	chr9:5894092-5894103
32	CEBPB	chr9:5879545-5880038	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:5893779-5894203	HepG2	liver:	n/a	chr9:5894092-5894103
34	CEBPB	chr9:5893964-5894218	A549	lung:	n/a	chr9:5894092-5894103
35	CEBPB	chr9:5879456-5879847	K562	blood:	n/a	n/a
36	CEBPD	chr9:5879468-5879994	K562	blood:	n/a	n/a
37	CEBPD	chr9:5879425-5880002	K562	blood:	n/a	n/a
38	CEBPD	chr9:5893865-5894261	HepG2	liver:	n/a	n/a
39	CHD1	chr9:5885994-5886617	IMR90	lung:	n/a	n/a
40	CHD1	chr9:5886201-5886418	GM12878	blood:	n/a	n/a
41	CHD2	chr9:5886168-5886462	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr9:5879499-5879819	K562	blood:	n/a	n/a
43	CHD2	chr9:5886144-5886720	GM12878	blood:	n/a	n/a
44	CHD2	chr9:5886143-5886439	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr9:5893935-5894288	HepG2	liver:	n/a	n/a
46	CHD2	chr9:5879491-5879915	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr9:5887321-5887371	HepG2	liver:	n/a	n/a
48	CREB1	chr9:5886075-5886552	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr9:5875900-5876050	GM12865	blood:	n/a	n/a
50	CTCF	chr9:5899640-5899790	HUVEC	blood vessel:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:5890900-5890950	ovcar-3	ovarian:	n/a
2	chr9:5891258-5891308	RPTEC	kidney:	n/a
3	chr9:5890866-5890916	NHDF-neo	bronchial:	n/a
4	chr9:5890866-5890916	ECC-1	luminal epithelium:	n/a
5	chr9:5891258-5891308	HPAEpiC	pulmonary alveolar:	n/a
6	chr9:5890866-5890916	K562	blood:	n/a
7	chr9:5890866-5890916	U87	brain:	n/a
8	chr9:5890866-5890916	GM06990	blood:	n/a
9	chr9:5890900-5890950	SK-N-SH_RA	brain:	n/a
10	chr9:5891258-5891308	H1-hESC	embryonic stem cell:	embryo
11	chr9:5890866-5890916	CMK	blood:	n/a
12	chr9:5890900-5890950	BE2_C	brain:	n/a
13	chr9:5890900-5890950	SK-N-SH	brain:	n/a
14	chr9:5890866-5890916	HL-60	blood:	n/a
15	chr9:5893907-5893957	GM12892	blood:	n/a
16	chr9:5893907-5893957	A549	lung:	n/a
17	chr9:5890900-5890950	HNPCEpiC	eye:	n/a
18	chr9:5893907-5893957	HRCEpiC	kidney:	n/a
19	chr9:5891258-5891308	U87	brain:	n/a
20	chr9:5890866-5890916	HRCEpiC	kidney:	n/a
21	chr9:5890900-5890950	ProgFib	skin:	n/a
22	chr9:5890900-5890950	SK-N-MC	brain:	n/a
23	chr9:5893907-5893957	HMEC	breast:	n/a
24	chr9:5890900-5890950	AG09319	gingival:	n/a
25	chr9:5890866-5890916	GM12892	blood:	n/a
26	chr9:5891258-5891308	IMR90	lung:	fetal
27	chr9:5890900-5890950	HIPEpiC	eye:	n/a
28	chr9:5890866-5890916	SK-N-MC	brain:	n/a
29	chr9:5893907-5893957	ovcar-3	ovarian:	n/a
30	chr9:5890866-5890916	HUVEC	blood vessel:	n/a
31	chr9:5890866-5890916	T-47D	breast:	n/a
32	chr9:5891258-5891308	AoSMC	blood vessel:	n/a
33	chr9:5891258-5891308	SK-N-SH_RA	brain:	n/a
34	chr9:5890900-5890950	GM12892	blood:	n/a
35	chr9:5893907-5893957	T-47D	breast:	n/a
36	chr9:5890866-5890916	NH-A	brain:	n/a
37	chr9:5893907-5893957	AG10803	skin:	n/a
38	chr9:5893907-5893957	CMK	blood:	n/a
39	chr9:5890900-5890950	SKMC	muscle:	n/a
40	chr9:5890900-5890950	HMEC	breast:	n/a
41	chr9:5890866-5890916	Hepatocyte	liver:	n/a
42	chr9:5890900-5890950	NH-A	brain:	n/a
43	chr9:5890900-5890950	BJ	skin:	n/a
44	chr9:5893907-5893957	AoSMC	blood vessel:	n/a
45	chr9:5893907-5893957	GM12891	blood:	n/a
46	chr9:5893907-5893957	GM12878	blood:	n/a
47	chr9:5890866-5890916	HEEpiC	esophagus:	n/a
48	chr9:5891258-5891308	HIPEpiC	eye:	n/a
49	chr9:5893907-5893957	NHDF-neo	bronchial:	n/a
50	chr9:5890900-5890950	GM19239	blood:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:5892941..5894729-chr9:6007050..6009397,2	MCF-7	breast:
2	chr9:5878375..5880151-chr9:6078401..6080050,2	K562	blood:
3	chr9:5894386..5896231-chr9:5898006..5899746,2	MCF-7	breast:
4	chr9:5799071..5800155-chr9:5899057..5900015,4	MCF-7	breast:
5	chr9:5885755..5886725-chr9:6049470..6050448,5	K562	blood:
6	chr9:5887261..5887765-chr9:6007127..6007900,2	NB4	blood:
7	chr9:5886155..5886775-chr9:5898962..5899536,2	K562	blood:
8	chr9:5885723..5886777-chr9:5899071..5900066,3	MCF-7	breast:
9	chr9:5886155..5886775-chr9:5898962..5899536,2	K562	blood:
10	chr9:5839459..5843654-chr9:5878363..5884455,6	MCF-7	breast:
11	chr9:5880522..5882906-chr9:5883810..5886379,2	K562	blood:
12	chr9:5798897..5800040-chr9:5885951..5886842,5	MCF-7	breast:
13	chr9:5885881..5887710-chr9:5891218..5893485,2	K562	blood:
14	chr9:5868662..5871145-chr9:5874957..5877904,2	MCF-7	breast:
15	chr9:5828344..5834722-chr9:5880387..5886482,7	MCF-7	breast:
16	chr9:5885108..5886777-chr9:6014239..6017219,2	MCF-7	breast:
17	chr9:5880522..5882906-chr9:5883810..5886379,2	K562	blood:
18	chr9:5829712..5832967-chr9:5877183..5879900,5	MCF-7	breast:
19	chr9:5871955..5874825-chr9:5876474..5878566,2	MCF-7	breast:
20	chr9:5869406..5870321-chr9:5886024..5886748,3	K562	blood:
21	chr9:5894261..5896922-chr9:5907318..5910115,2	MCF-7	breast:
22	chr9:5886469..5887983-chr9:6006752..6008775,2	MCF-7	breast:
23	chr9:5885830..5887288-chr9:6054244..6055346,7	MCF-7	breast:
24	chr9:5885869..5886582-chr9:6049601..6050363,3	MCF-7	breast:
25	chr9:5885059..5887812-chr9:6005618..6008458,2	K562	blood:
26	chr9:5864598..5866719-chr9:5878064..5881327,3	MCF-7	breast:
27	chr9:5894386..5896231-chr9:5898006..5899746,2	MCF-7	breast:
28	chr9:5886316..5888360-chr9:6049322..6051751,2	MCF-7	breast:
29	chr3:95018524..95019390-chr9:5887461..5888104,2	MCF-7	breast:
30	chr9:5832530..5834263-chr9:5898379..5901171,2	MCF-7	breast:
31	chr9:5798939..5799987-chr9:5899066..5899993,6	MCF-7	breast:
32	chr9:5869892..5870408-chr9:5899019..5899560,2	K562	blood:
33	chr9:5875561..5878927-chr9:6007054..6010083,3	K562	blood:
34	chr9:5870831..5873725-chr9:5878360..5881340,2	K562	blood:
35	chr9:5869625..5872282-chr9:5874318..5876632,2	K562	blood:
36	chr9:5886117..5886694-chr9:6054993..6055882,2	MCF-7	breast:
37	chr9:5885723..5886777-chr9:5899071..5900066,3	MCF-7	breast:
38	chr9:5870416..5872339-chr9:5877036..5879791,2	K562	blood:
39	chr9:5885173..5887992-chr9:5891542..5893097,2	MCF-7	breast:
40	chr9:5869343..5870326-chr9:5886000..5886537,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1432-2	chr9:5897557-5897653	NONHSAT130117
2	lnc-ERMP1-4	chr9:5898937-5899255	NONHSAT130119
3	lnc-KIAA1432-2	chr9:5892511-5892551	NONHSAT130117

No data

Variant related genes	Relation type
MLANA	TF binding region
ENSG00000238654	TF binding region
MLANA	CpG island
ENSG00000238654	CpG island
ENSG00000183354	chromatin interactions
ENSG00000137040	chromatin interactions
ENSG00000263575	chromatin interactions
ENSG00000099219	chromatin interactions
ENSG00000120215	chromatin interactions

Extended variants
information (count: 1092 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7848093	chr9:5875201-5875202	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569886883	chr9:5875219-5875220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7862229	chr9:5875256-5875257	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555906177	chr9:5875259-5875260	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574002866	chr9:5875264-5875265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369564555	chr9:5875267-5875268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10739078	chr9:5875294-5875295	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553133855	chr9:5875299-5875300	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577956626	chr9:5875316-5875317	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185192014	chr9:5875369-5875370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563613556	chr9:5875372-5875373	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143747178	chr9:5875381-5875382	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542774624	chr9:5875396-5875397	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561525840	chr9:5875399-5875400	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190886136	chr9:5875415-5875416	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529017331	chr9:5875418-5875419	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs536093660	chr9:5875432-5875433	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547450788	chr9:5875446-5875447	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565566873	chr9:5875517-5875518	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375327891	chr9:5875519-5875520	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532926694	chr9:5875556-5875557	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554894098	chr9:5875562-5875563	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569925314	chr9:5875574-5875575	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552865843	chr9:5875614-5875615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146844582	chr9:5875616-5875617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs182019465	chr9:5875631-5875632	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs572686801	chr9:5875641-5875642	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113514101	chr9:5875656-5875657	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs10975330	chr9:5875669-5875670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs80193588	chr9:5875677-5875678	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567446455	chr9:5875686-5875687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs6477016	chr9:5875690-5875691	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs144456927	chr9:5875746-5875747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369319955	chr9:5875750-5875751	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs532926426	chr9:5875767-5875768	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185716357	chr9:5875779-5875780	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs557244246	chr9:5875792-5875793	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs575488661	chr9:5875811-5875812	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7023910	chr9:5875821-5875822	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542901208	chr9:5875834-5875835	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs368774889	chr9:5875857-5875858	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561354090	chr9:5875867-5875868	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573362656	chr9:5875922-5875923	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs545035281	chr9:5876002-5876003	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs145420870	chr9:5876024-5876025	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575341285	chr9:5876077-5876078	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs532966296	chr9:5876152-5876153	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs551348965	chr9:5876167-5876168	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563270512	chr9:5876176-5876177	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs530867232	chr9:5876217-5876218	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Renal cell carcinoma	21215367	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:5834400-5886000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr9:5840400-5921600	Weak transcription	Right Ventricle	heart
3	chr9:5840600-5879800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:5847800-5876200	Weak transcription	Brain Angular Gyrus	brain
5	chr9:5852200-5897000	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr9:5852400-5878800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:5853800-5895600	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr9:5854400-5886200	Weak transcription	Brain Anterior Caudate	brain
9	chr9:5855600-5876600	Weak transcription	Fetal Stomach	stomach
10	chr9:5856600-5880000	Weak transcription	Esophagus	oesophagus
11	chr9:5856800-5895600	Weak transcription	Brain Substantia Nigra	brain
12	chr9:5858600-5876600	Weak transcription	Aorta	Aorta
13	chr9:5858600-5885800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr9:5859000-5876800	Weak transcription	Left Ventricle	heart
15	chr9:5859000-5895600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:5859000-5906600	Weak transcription	Ovary	ovary
17	chr9:5859200-5919800	Weak transcription	Fetal Brain Female	brain
18	chr9:5859800-5876600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:5863400-5876800	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr9:5863400-5895600	Weak transcription	Fetal Intestine Small	intestine
21	chr9:5863600-5896600	Weak transcription	Pancreas	Pancrea
22	chr9:5864800-5880800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:5864800-5881400	Weak transcription	Spleen	Spleen
24	chr9:5864800-5895600	Weak transcription	Gastric	stomach
25	chr9:5865200-5881000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr9:5865200-5886000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr9:5870000-5886400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr9:5870200-5876000	Weak transcription	HMEC	breast
29	chr9:5870200-5876600	Weak transcription	Placenta	Placenta
30	chr9:5870400-5876800	Weak transcription	HepG2	liver
31	chr9:5870800-5895600	Weak transcription	Stomach Smooth Muscle	stomach
32	chr9:5871000-5876400	Weak transcription	Lung	lung
33	chr9:5871000-5895600	Weak transcription	Brain Hippocampus Middle	brain
34	chr9:5871000-5920000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr9:5871200-5898400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr9:5872600-5879400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr9:5873200-5876800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr9:5873600-5875600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:5873800-5875600	Enhancers	Primary T cells from cord blood	blood
40	chr9:5873800-5876000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr9:5873800-5876000	Enhancers	Fetal Thymus	thymus
42	chr9:5874200-5875400	Enhancers	Primary hematopoietic stem cells	blood
43	chr9:5874200-5876200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr9:5874200-5876600	Weak transcription	Hela-S3	cervix
45	chr9:5874200-5877200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr9:5874400-5876200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr9:5875000-5875400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr9:5875200-5875600	Enhancers	Thymus	Thymus
49	chr9:5875200-5876400	Enhancers	K562	blood
50	chr9:5875400-5875600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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