Variant report

Variant	nsv615214
Chromosome Location	chr9:116125789-116149967
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:856)
CpG islands
(count:366)
Chromatin interactive
region (count:78)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116131138-116131767	K562	blood:	n/a	n/a
2	ARID3A	chr9:116139127-116139456	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:116145354-116145483	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:116127307-116127593	K562	blood:	n/a	n/a
5	ARID3A	chr9:116144360-116144724	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:116141440-116141630	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:116126185-116126530	K562	blood:	n/a	n/a
8	ARID3A	chr9:116149786-116150559	HepG2	liver:	n/a	n/a
9	ATF1	chr9:116126194-116126233	K562	blood:	n/a	n/a
10	ATF1	chr9:116131294-116131700	K562	blood:	n/a	n/a
11	ATF2	chr9:116143051-116143619	GM12878	blood:	n/a	n/a
12	ATF2	chr9:116138986-116139353	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr9:116139055-116139313	K562	blood:	n/a	n/a
14	ATF3	chr9:116126158-116126331	K562	blood:	n/a	n/a
15	ATF3	chr9:116126089-116126414	K562	blood:	n/a	n/a
16	BACH1	chr9:116139114-116139222	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr9:116130706-116130708	K562	blood:	n/a	n/a
18	BATF	chr9:116143108-116143589	GM12878	blood:	n/a	n/a
19	BATF	chr9:116143136-116143558	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:116143244-116143474	GM12878	blood:	n/a	n/a
21	BCL11A	chr9:116143154-116143562	GM12878	blood:	n/a	n/a
22	BCL3	chr9:116143133-116143500	GM12878	blood:	n/a	n/a
23	BCLAF1	chr9:116143172-116143521	GM12878	blood:	n/a	n/a
24	BCLAF1	chr9:116138877-116139188	GM12878	blood:	n/a	n/a
25	BCLAF1	chr9:116143129-116143573	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:116132005-116132020	K562	blood:	n/a	n/a
27	BHLHE40	chr9:116139475-116139701	K562	blood:	n/a	n/a
28	BHLHE40	chr9:116138930-116139215	GM12878	blood:	n/a	n/a
29	BHLHE40	chr9:116143071-116143530	GM12878	blood:	n/a	n/a
30	BHLHE40	chr9:116131110-116131598	K562	blood:	n/a	n/a
31	CBX3	chr9:116138878-116139282	K562	blood:	n/a	n/a
32	CCNT2	chr9:116131132-116132132	K562	blood:	n/a	chr9:116131405-116131425 chr9:116131461-116131481
33	CCNT2	chr9:116138987-116139670	K562	blood:	n/a	chr9:116139645-116139654
34	CEBPB	chr9:116141306-116141356	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:116127974-116128268	K562	blood:	n/a	n/a
36	CEBPB	chr9:116128066-116128170	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:116126158-116126817	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr9:116144314-116144678	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:116141307-116141312	K562	blood:	n/a	n/a
40	CEBPB	chr9:116144344-116144600	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:116149923-116150291	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:116131063-116131683	K562	blood:	n/a	n/a
43	CEBPB	chr9:116126184-116126709	K562	blood:	n/a	n/a
44	CEBPB	chr9:116145310-116145644	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:116126079-116126663	K562	blood:	n/a	n/a
46	CEBPB	chr9:116144366-116144768	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:116144339-116144636	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:116127860-116128361	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:116126365-116126702	MCF-7	breast:	n/a	n/a
50	CEBPB	chr9:116144358-116144768	MCF-7	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116139085-116139135	GM12878	blood:	n/a
2	chr9:116135281-116135331	HAEpiC	amniotic membrane:	n/a
3	chr9:116139085-116139135	SKMC	muscle:	n/a
4	chr9:116138128-116138178	HCPEpiC	choroid plexus:	n/a
5	chr9:116138128-116138178	HEEpiC	esophagus:	n/a
6	chr9:116137097-116137147	HCPEpiC	choroid plexus:	n/a
7	chr9:116133216-116133266	PFSK-1	brain:	n/a
8	chr9:116138128-116138178	LNCaP	prostate:	n/a
9	chr9:116135281-116135331	Jurkat	blood:	n/a
10	chr9:116135281-116135331	HUVEC	blood vessel:	n/a
11	chr9:116133216-116133266	HAEpiC	amniotic membrane:	n/a
12	chr9:116138128-116138178	ProgFib	skin:	n/a
13	chr9:116143143-116143193	MCF10A-Er-Src	breast:	n/a
14	chr9:116137097-116137147	PANC-1	pancreas:	n/a
15	chr9:116133216-116133266	MCF-7	breast:	n/a
16	chr9:116139085-116139135	HNPCEpiC	eye:	n/a
17	chr9:116135281-116135331	NB4	blood:	n/a
18	chr9:116138128-116138178	BE2_C	brain:	n/a
19	chr9:116139085-116139135	HCF	heart:	n/a
20	chr9:116137097-116137147	ovcar-3	ovarian:	n/a
21	chr9:116139085-116139135	SK-N-SH	brain:	n/a
22	chr9:116138128-116138178	HNPCEpiC	eye:	n/a
23	chr9:116133216-116133266	HEEpiC	esophagus:	n/a
24	chr9:116143143-116143193	HCPEpiC	choroid plexus:	n/a
25	chr9:116138128-116138178	GM06990	blood:	n/a
26	chr9:116137097-116137147	T-47D	breast:	n/a
27	chr9:116133216-116133266	SK-N-SH	brain:	n/a
28	chr9:116135281-116135331	HCPEpiC	choroid plexus:	n/a
29	chr9:116143143-116143193	GM12892	blood:	n/a
30	chr9:116137097-116137147	BJ	skin:	n/a
31	chr9:116133216-116133266	NHBE	bronchial:	n/a
32	chr9:116135281-116135331	AG10803	skin:	n/a
33	chr9:116139085-116139135	NHDF-neo	bronchial:	n/a
34	chr9:116137097-116137147	HCM	heart:	n/a
35	chr9:116138128-116138178	HCT-116	colon:	n/a
36	chr9:116135281-116135331	K562	blood:	n/a
37	chr9:116135281-116135331	GM12892	blood:	n/a
38	chr9:116139085-116139135	HCT-116	colon:	n/a
39	chr9:116138128-116138178	AoSMC	blood vessel:	n/a
40	chr9:116143143-116143193	BE2_C	brain:	n/a
41	chr9:116137097-116137147	GM12878	blood:	n/a
42	chr9:116133216-116133266	PrEC	prostate:	n/a
43	chr9:116138128-116138178	NHBE	bronchial:	n/a
44	chr9:116133216-116133266	HEK293	kidney:	embryo
45	chr9:116133216-116133266	SAEC	small airway:	n/a
46	chr9:116137097-116137147	ECC-1	luminal epithelium:	n/a
47	chr9:116135281-116135331	LNCaP	prostate:	n/a
48	chr9:116139085-116139135	MCF10A-Er-Src	breast:	n/a
49	chr9:116139085-116139135	RPTEC	kidney:	n/a
50	chr9:116139085-116139135	Hepatocyte	liver:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:116127286..116129224-chr9:116135348..116138252,2	K562	blood:
2	chr9:116116765..116119707-chr9:116134717..116136429,2	K562	blood:
3	chr9:116118659..116121326-chr9:116124549..116126674,2	MCF-7	breast:
4	chr9:116125138..116127996-chr9:116129478..116132469,3	K562	blood:
5	chr15:80215740..80216631-chr9:116137961..116138854,2	Hela-S3	cervix:
6	chr9:116139132..116139813-chr9:116162815..116163745,2	MCF-7	breast:
7	chr9:116101733..116104316-chr9:116133698..116137362,3	K562	blood:
8	chr9:116124595..116126724-chr9:116133634..116135834,3	K562	blood:
9	chr9:116124299..116128919-chr9:116129296..116133206,5	K562	blood:
10	chr9:116117613..116119725-chr9:116129685..116131579,2	MCF-7	breast:
11	chr9:116129075..116133029-chr9:116162215..116166672,4	K562	blood:
12	chr9:116110642..116113360-chr9:116143045..116146049,5	MCF-7	breast:
13	chr9:116142555..116147503-chr9:116159083..116164157,6	MCF-7	breast:
14	chr9:116116183..116118289-chr9:116124994..116127482,2	K562	blood:
15	chr9:116132959..116135893-chr9:116149192..116150775,2	MCF-7	breast:
16	chr9:116137731..116139998-chr9:116170716..116173211,2	K562	blood:
17	chr9:116110267..116113559-chr9:116127795..116130030,3	MCF-7	breast:
18	chr9:116142961..116144680-chr9:116145190..116147516,2	MCF-7	breast:
19	chr9:116079936..116083155-chr9:116131441..116134734,3	MCF-7	breast:
20	chr15:79351623..79352456-chr9:116148392..116149161,2	MCF-7	breast:
21	chr9:116149427..116152233-chr9:116182929..116184530,2	K562	blood:
22	chr9:116119995..116122506-chr9:116129873..116132566,2	MCF-7	breast:
23	chr9:116127846..116129499-chr9:116156115..116158388,2	K562	blood:
24	chr9:116148030..116156107-chr9:116161914..116166950,9	MCF-7	breast:
25	chr9:116037280..116038788-chr9:116133892..116135424,2	MCF-7	breast:
26	chr9:116103291..116106183-chr9:116133139..116134993,2	K562	blood:
27	chr9:116068239..116070626-chr9:116128043..116129865,2	MCF-7	breast:
28	chr9:116071329..116074445-chr9:116134233..116136581,3	MCF-7	breast:
29	chr9:116133150..116137640-chr9:116162561..116165581,6	MCF-7	breast:
30	chr9:116124595..116126724-chr9:116133634..116135834,3	K562	blood:
31	chr9:116137751..116140184-chr9:116144665..116146448,2	K562	blood:
32	chr9:116108846..116117047-chr9:116126327..116140994,30	MCF-7	breast:
33	chr9:116133477..116135690-chr9:116141217..116143043,2	K562	blood:
34	chr9:116061990..116065430-chr9:116133757..116136498,3	MCF-7	breast:
35	chr9:116129625..116132113-chr9:116158128..116160524,2	MCF-7	breast:
36	chr9:116122597..116124839-chr9:116128759..116130936,3	MCF-7	breast:
37	chr9:116138257..116141960-chr9:116162197..116164966,3	K562	blood:
38	chr9:116149664..116152667-chr9:116172993..116176331,3	K562	blood:
39	chr9:116142961..116144680-chr9:116145190..116147516,2	MCF-7	breast:
40	chr9:116100614..116105784-chr9:116143158..116149337,5	MCF-7	breast:
41	chr9:116125138..116127996-chr9:116129478..116132469,3	K562	blood:
42	chr9:116137664..116140470-chr9:116160302..116166802,9	MCF-7	breast:
43	chr9:116149635..116151577-chr9:116153234..116155559,2	MCF-7	breast:
44	chr9:116135295..116143276-chr9:116169551..116176415,12	MCF-7	breast:
45	chr9:116127286..116129224-chr9:116135348..116138252,2	K562	blood:
46	chr9:116147693..116150594-chr9:116171749..116173878,2	MCF-7	breast:
47	chr9:116135343..116137901-chr9:116159656..116162633,2	K562	blood:
48	chr9:116131952..116133539-chr9:116342073..116343791,2	MCF-7	breast:
49	chr9:116070123..116071918-chr9:116134499..116138293,3	MCF-7	breast:
50	chr9:116136647..116140990-chr9:116144919..116148634,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALAD-1	chr9:116146660-116147175	expReg_chr9_5901_-

No data

Variant related genes	Relation type
HDHD3	TF binding region
HDHD3	CpG island
ENSG00000105193	chromatin interactions
ENSG00000119411	chromatin interactions
ENSG00000180953	chromatin interactions
ENSG00000119431	chromatin interactions
ENSG00000259332	chromatin interactions
ENSG00000148225	chromatin interactions
ENSG00000176386	chromatin interactions
ENSG00000138835	chromatin interactions
ENSG00000196235	chromatin interactions
ENSG00000148218	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000165188	chromatin interactions
ENSG00000136875	chromatin interactions

Extended variants
information (count: 1080 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1080 , 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	rs10981769	chr9:116125789-116125790	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10981770	chr9:116125802-116125803	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs10981771	chr9:116125811-116125812	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs141556166	chr9:116125849-116125850	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs566975016	chr9:116125853-116125854	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs118066331	chr9:116125888-116125889	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs538495849	chr9:116125898-116125899	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs7045901	chr9:116125926-116125927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs188079133	chr9:116125927-116125928	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs373083116	chr9:116125940-116125941	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs375174917	chr9:116125952-116125953	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs7045908	chr9:116125980-116125981	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs554818453	chr9:116125993-116125994	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs574351590	chr9:116126005-116126006	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs540192843	chr9:116126025-116126026	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs386737781	chr9:116126026-116126027	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs59285217	chr9:116126030-116126031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs543800901	chr9:116126047-116126048	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs546447855	chr9:116126048-116126049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs10981772	chr9:116126072-116126073	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs181038937	chr9:116126088-116126089	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs11788954	chr9:116126117-116126118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs10981773	chr9:116126135-116126136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs187158918	chr9:116126146-116126147	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs71491088	chr9:116126152-116126153	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs71367721	chr9:116126154-116126155	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs558369308	chr9:116126175-116126176	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs57026104	chr9:116126181-116126182	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs534791554	chr9:116126185-116126186	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs531186983	chr9:116126187-116126188	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs553309219	chr9:116126192-116126193	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs192511528	chr9:116126206-116126207	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs183252331	chr9:116126230-116126231	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs547384959	chr9:116126248-116126249	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs570643141	chr9:116126256-116126257	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs369167827	chr9:116126278-116126279	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs115731496	chr9:116126280-116126281	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs11793368	chr9:116126311-116126312	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
39	rs137876970	chr9:116126328-116126329	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs149491974	chr9:116126329-116126330	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs7046353	chr9:116126332-116126333	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs554574076	chr9:116126334-116126335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs577352334	chr9:116126335-116126336	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs568333429	chr9:116126388-116126389	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs533814300	chr9:116126402-116126403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs553780854	chr9:116126475-116126476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs201380812	chr9:116126476-116126477	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs577046628	chr9:116126534-116126535	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs143950364	chr9:116126538-116126539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs111573629	chr9:116126575-116126576	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1199 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116113000-116135600	Weak transcription	Colonic Mucosa	Colon
2	chr9:116113000-116138000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr9:116113400-116135200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:116113800-116137800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr9:116114000-116127400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr9:116114200-116136400	Weak transcription	Primary B cells from cord blood	blood
7	chr9:116115400-116135000	Weak transcription	Esophagus	oesophagus
8	chr9:116115600-116132800	Weak transcription	Fetal Intestine Large	intestine
9	chr9:116115800-116125800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr9:116116400-116137000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr9:116116600-116126400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr9:116120200-116126400	Strong transcription	Fetal Intestine Small	intestine
13	chr9:116120200-116131800	Weak transcription	Lung	lung
14	chr9:116120400-116127200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr9:116121600-116126400	Strong transcription	Primary hematopoietic stem cells	blood
16	chr9:116123000-116132800	Weak transcription	Fetal Stomach	stomach
17	chr9:116123200-116129200	Enhancers	Hela-S3	cervix
18	chr9:116123200-116131800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:116123200-116136400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:116123600-116138200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:116123800-116130400	Weak transcription	Stomach Mucosa	stomach
22	chr9:116124000-116135000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr9:116124000-116135000	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr9:116124000-116135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:116124000-116135600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr9:116124200-116127800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:116124400-116128400	Weak transcription	Rectal Mucosa Donor 29	rectum
28	chr9:116124400-116131600	Weak transcription	Pancreas	Pancrea
29	chr9:116124400-116135600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr9:116124800-116125800	Weak transcription	K562	blood
31	chr9:116124800-116128800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr9:116124800-116134200	Weak transcription	Brain Anterior Caudate	brain
33	chr9:116124800-116134400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr9:116124800-116135000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:116124800-116135200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:116124800-116135400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:116124800-116135800	Weak transcription	Brain Substantia Nigra	brain
38	chr9:116125000-116130600	Weak transcription	Gastric	stomach
39	chr9:116125000-116138000	Weak transcription	Fetal Kidney	kidney
40	chr9:116125200-116133600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:116125200-116135000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr9:116125800-116126800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr9:116125800-116128200	Enhancers	K562	blood
44	chr9:116126200-116134400	Weak transcription	Placenta	Placenta
45	chr9:116126400-116127400	Weak transcription	Primary hematopoietic stem cells	blood
46	chr9:116126400-116128200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr9:116126400-116128600	Weak transcription	Fetal Intestine Small	intestine
48	chr9:116126800-116133200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:116127200-116127800	Enhancers	Fetal Heart	heart
50	chr9:116127200-116128400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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