Variant report

Variant	nsv2298
Chromosome Location	chr1:9826286-9857487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:657)
CpG islands
(count:184)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:9844615-9844942	K562	blood:	n/a	n/a
2	ARID3A	chr1:9834781-9835180	K562	blood:	n/a	n/a
3	ARID3A	chr1:9844635-9844937	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:9833259-9833278	K562	blood:	n/a	n/a
5	ATF1	chr1:9834870-9835116	K562	blood:	n/a	n/a
6	ATF2	chr1:9847681-9848137	GM12878	blood:	n/a	n/a
7	ATF2	chr1:9847667-9848191	GM12878	blood:	n/a	n/a
8	BACH1	chr1:9844741-9844941	K562	blood:	n/a	n/a
9	BATF	chr1:9847800-9848204	GM12878	blood:	n/a	n/a
10	BATF	chr1:9843026-9843313	GM12878	blood:	n/a	n/a
11	BATF	chr1:9842988-9843293	GM12878	blood:	n/a	n/a
12	BATF	chr1:9847823-9848098	GM12878	blood:	n/a	n/a
13	BATF	chr1:9849864-9850054	GM12878	blood:	n/a	chr1:9849979-9849990
14	BCL11A	chr1:9847834-9848124	GM12878	blood:	n/a	n/a
15	BCL11A	chr1:9847810-9848149	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:9843078-9843236	GM12878	blood:	n/a	n/a
17	BCL3	chr1:9842936-9843275	GM12878	blood:	n/a	n/a
18	BCLAF1	chr1:9847605-9848283	GM12878	blood:	n/a	n/a
19	BCLAF1	chr1:9844533-9845016	GM12878	blood:	n/a	n/a
20	BHLHE40	chr1:9844644-9844920	K562	blood:	n/a	n/a
21	BHLHE40	chr1:9853476-9853623	K562	blood:	n/a	n/a
22	BHLHE40	chr1:9847773-9848088	GM12878	blood:	n/a	n/a
23	BRCA1	chr1:9844659-9844957	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr1:9840668-9840853	IMR90	lung:	n/a	chr1:9840685-9840698
25	CEBPB	chr1:9836317-9836727	ECC-1	luminal epithelium:	n/a	chr1:9836494-9836505
26	CEBPB	chr1:9836357-9836621	A549	lung:	n/a	chr1:9836494-9836505
27	CEBPB	chr1:9836193-9836726	ECC-1	luminal epithelium:	n/a	chr1:9836494-9836505
28	CEBPB	chr1:9826766-9827252	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:9828112-9828534	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr1:9836436-9836642	H1-hESC	embryonic stem cell:	n/a	chr1:9836494-9836505
31	CEBPB	chr1:9828135-9828460	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr1:9827952-9828438	K562	blood:	n/a	n/a
33	CEBPB	chr1:9836324-9836686	K562	blood:	n/a	chr1:9836494-9836505
34	CEBPB	chr1:9827943-9828502	K562	blood:	n/a	n/a
35	CEBPB	chr1:9836428-9836607	A549	lung:	n/a	chr1:9836494-9836505
36	CEBPB	chr1:9828046-9828395	A549	lung:	n/a	n/a
37	CEBPB	chr1:9836367-9836606	Hela-S3	cervix:	n/a	chr1:9836494-9836505
38	CEBPB	chr1:9836317-9836686	IMR90	lung:	n/a	chr1:9836494-9836505
39	CEBPB	chr1:9840583-9840863	A549	lung:	n/a	chr1:9840685-9840698
40	CEBPB	chr1:9826857-9827070	A549	lung:	n/a	n/a
41	CEBPB	chr1:9847866-9848082	GM12878	blood:	n/a	n/a
42	CEBPB	chr1:9836338-9836671	HepG2	liver:	n/a	chr1:9836494-9836505
43	CEBPB	chr1:9840715-9840882	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:9827967-9828464	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:9836357-9836682	A549	lung:	n/a	chr1:9836494-9836505
46	CEBPB	chr1:9836320-9836639	K562	blood:	n/a	chr1:9836494-9836505
47	CEBPD	chr1:9836676-9837161	K562	blood:	n/a	n/a
48	CEBPD	chr1:9836675-9837238	K562	blood:	n/a	n/a
49	CHD1	chr1:9847761-9848054	GM12878	blood:	n/a	n/a
50	CHD2	chr1:9847801-9848142	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:9844683-9844733	RPTEC	kidney:	n/a
2	chr1:9844683-9844733	RPTEC	kidney:	n/a
3	chr1:9844683-9844733	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:9844683-9844733	ovcar-3	ovarian:	n/a
5	chr1:9852785-9852835	HepG2	liver:	n/a
6	chr1:9852785-9852835	HIPEpiC	eye:	n/a
7	chr1:9847879-9847929	H1-hESC	embryonic stem cell:	embryo
8	chr1:9852785-9852835	GM06990	blood:	n/a
9	chr1:9844683-9844733	HIPEpiC	eye:	n/a
10	chr1:9844683-9844733	AG04450	lung:	fetal
11	chr1:9844683-9844733	AG09319	gingival:	n/a
12	chr1:9847879-9847929	AG04450	lung:	fetal
13	chr1:9852785-9852835	HRCEpiC	kidney:	n/a
14	chr1:9852785-9852835	HRPEpiC	eye:	n/a
15	chr1:9852785-9852835	AG09319	gingival:	n/a
16	chr1:9847879-9847929	RPTEC	kidney:	n/a
17	chr1:9852785-9852835	MCF-7	breast:	n/a
18	chr1:9852785-9852835	SKMC	muscle:	n/a
19	chr1:9847879-9847929	HCM	heart:	n/a
20	chr1:9852785-9852835	HCPEpiC	choroid plexus:	n/a
21	chr1:9852785-9852835	SK-N-SH	brain:	n/a
22	chr1:9844683-9844733	NT2-D1	testis:	n/a
23	chr1:9844683-9844733	GM12891	blood:	n/a
24	chr1:9844683-9844733	H1-hESC	embryonic stem cell:	embryo
25	chr1:9847879-9847929	HL-60	blood:	n/a
26	chr1:9847879-9847929	NHDF-neo	bronchial:	n/a
27	chr1:9844683-9844733	HUVEC	blood vessel:	n/a
28	chr1:9847879-9847929	HEK293	kidney:	embryo
29	chr1:9844683-9844733	AG04449	skin:	fetal
30	chr1:9852785-9852835	H1-hESC	embryonic stem cell:	embryo
31	chr1:9847879-9847929	ovcar-3	ovarian:	n/a
32	chr1:9844683-9844733	BJ	skin:	n/a
33	chr1:9852785-9852835	LNCaP	prostate:	n/a
34	chr1:9844683-9844733	SK-N-SH	brain:	n/a
35	chr1:9847879-9847929	HNPCEpiC	eye:	n/a
36	chr1:9844683-9844733	BE2_C	brain:	n/a
37	chr1:9847879-9847929	HRPEpiC	eye:	n/a
38	chr1:9844683-9844733	Jurkat	blood:	n/a
39	chr1:9852785-9852835	SK-N-SH_RA	brain:	n/a
40	chr1:9847879-9847929	MCF-7	breast:	n/a
41	chr1:9844683-9844733	HRPEpiC	eye:	n/a
42	chr1:9852785-9852835	AG04449	skin:	fetal
43	chr1:9847879-9847929	Caco-2	colon:	n/a
44	chr1:9847879-9847929	Jurkat	blood:	n/a
45	chr1:9852785-9852835	HMEC	breast:	n/a
46	chr1:9847879-9847929	AoSMC	blood vessel:	n/a
47	chr1:9852785-9852835	GM12892	blood:	n/a
48	chr1:9847879-9847929	ECC-1	luminal epithelium:	n/a
49	chr1:9844683-9844733	ECC-1	luminal epithelium:	n/a
50	chr1:9852785-9852835	Hepatocyte	liver:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:9686719..9688039-chr1:9844321..9845208,3	K562	blood:
2	chr1:9828487..9830236-chr1:9832238..9835058,2	MCF-7	breast:
3	chr1:9834329..9836774-chr1:9865219..9869770,4	K562	blood:
4	chr1:9828487..9830236-chr1:9832238..9835058,2	MCF-7	breast:
5	chr1:9833791..9835454-chr1:9838985..9841128,2	K562	blood:
6	chr1:9832750..9834507-chr1:9841729..9844026,2	K562	blood:
7	chr1:9828174..9830133-chr1:10270143..10271916,2	K562	blood:
8	chr1:9851605..9853089-chr1:9927228..9928149,4	MCF-7	breast:
9	chr1:9827688..9830515-chr1:9884401..9886148,2	MCF-7	breast:
10	chr1:9836345..9837855-chr1:9905780..9908681,2	K562	blood:
11	chr1:9847449..9849226-chr1:9882664..9884165,2	MCF-7	breast:
12	chr1:9849986..9852429-chr1:9882664..9886615,3	MCF-7	breast:
13	chr1:9852437..9854426-chr1:9882312..9884327,2	MCF-7	breast:
14	chr1:9844361..9845392-chr1:9927251..9928213,4	MCF-7	breast:
15	chr1:9851033..9853778-chr1:9882451..9884467,4	MCF-7	breast:
16	chr1:9855972..9858555-chr1:9861978..9863923,2	MCF-7	breast:
17	chr1:9832750..9834507-chr1:9841729..9844026,2	K562	blood:
18	chr1:9852615..9854985-chr1:9884936..9886688,2	MCF-7	breast:
19	chr1:9844090..9846323-chr1:9883653..9885317,2	MCF-7	breast:
20	chr1:9687069..9687927-chr1:9844746..9845711,2	MCF-7	breast:
21	chr1:9844311..9845253-chr1:9926813..9928252,17	K562	blood:
22	chr1:9821662..9824159-chr1:9828181..9830598,2	K562	blood:
23	chr1:9749103..9751299-chr1:9843003..9845112,2	K562	blood:
24	chr1:9850230..9850981-chr1:220848009..220848904,2	MCF-7	breast:
25	chr1:9838012..9841968-chr1:9843309..9844971,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIK3CD-2	chr1:9840880-9840958	NONHSAT000820
2	lnc-PIK3CD-1	chr1:9830964-9832799	predAs_engstrom06_BG189868_1
3	lnc-PIK3CD-2	chr1:9841132-9841298	NONHSAT000820

No data

Variant related genes	Relation type
ENSG00000271264	TF binding region
ENSG00000271264	CpG island
ENSG00000223989	chromatin interactions
ENSG00000171603	chromatin interactions
ENSG00000271264	chromatin interactions
ENSG00000054523	chromatin interactions

Extended variants
information (count: 1361 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1361 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185154942	chr1:9826290-9826291	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs4385713	chr1:9826312-9826313	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs77094336	chr1:9826313-9826314	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs571139645	chr1:9826347-9826348	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs534879116	chr1:9826397-9826398	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553511095	chr1:9826409-9826410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189681357	chr1:9826439-9826440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561785337	chr1:9826445-9826446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535537504	chr1:9826454-9826455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150365787	chr1:9826488-9826489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575262197	chr1:9826528-9826529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547589564	chr1:9826556-9826557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58685630	chr1:9826571-9826572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376959655	chr1:9826579-9826580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138124173	chr1:9826610-9826611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557731983	chr1:9826664-9826665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573111540	chr1:9826715-9826716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs58790250	chr1:9826729-9826730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540185479	chr1:9826754-9826755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561903428	chr1:9826770-9826771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529116965	chr1:9826773-9826774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141155110	chr1:9826875-9826876	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192824570	chr1:9826876-9826877	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs567557139	chr1:9826879-9826880	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184394408	chr1:9826897-9826898	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112096336	chr1:9826930-9826931	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144761115	chr1:9826944-9826945	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563340989	chr1:9826994-9826995	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547020814	chr1:9826995-9826996	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568639102	chr1:9826996-9826997	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138700653	chr1:9827034-9827035	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549068112	chr1:9827040-9827041	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568985902	chr1:9827066-9827067	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78223112	chr1:9827085-9827086	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149580607	chr1:9827092-9827093	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374451452	chr1:9827104-9827105	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540510249	chr1:9827119-9827120	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556165262	chr1:9827141-9827142	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11805962	chr1:9827177-9827178	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs573454046	chr1:9827184-9827185	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144293170	chr1:9827201-9827202	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115699691	chr1:9827248-9827249	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148288025	chr1:9827260-9827261	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs367627022	chr1:9827289-9827290	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528287830	chr1:9827301-9827302	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113562751	chr1:9827338-9827339	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546426990	chr1:9827367-9827368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571088646	chr1:9827371-9827372	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371226313	chr1:9827373-9827374	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180774049	chr1:9827434-9827435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	20406844	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:9801200-9837800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr1:9801400-9854200	Weak transcription	Fetal Kidney	kidney
3	chr1:9804400-9836600	Weak transcription	Small Intestine	intestine
4	chr1:9804600-9836600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:9810000-9832400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:9810200-9829200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:9811600-9832400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr1:9811600-9832400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:9811800-9832400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr1:9811800-9857000	Weak transcription	Aorta	Aorta
11	chr1:9812400-9832200	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr1:9812600-9829000	Weak transcription	Stomach Mucosa	stomach
13	chr1:9812800-9831000	Weak transcription	Colon Smooth Muscle	Colon
14	chr1:9813400-9829000	Weak transcription	Colonic Mucosa	Colon
15	chr1:9813400-9830400	Weak transcription	GM12878-XiMat	blood
16	chr1:9813600-9831800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:9813600-9832400	Weak transcription	Right Ventricle	heart
18	chr1:9813800-9832400	Weak transcription	Adipose Nuclei	Adipose
19	chr1:9813800-9852200	Weak transcription	Right Atrium	heart
20	chr1:9814200-9827000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr1:9815400-9829200	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr1:9815400-9831600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:9815400-9832400	Weak transcription	Fetal Intestine Large	intestine
24	chr1:9815400-9832600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr1:9815600-9829600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr1:9815600-9830800	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr1:9816400-9831800	Weak transcription	Brain Germinal Matrix	brain
28	chr1:9816600-9842400	Weak transcription	HUVEC	blood vessel
29	chr1:9819600-9826800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr1:9820000-9826800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr1:9820000-9826800	Weak transcription	Brain Substantia Nigra	brain
32	chr1:9820200-9832400	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr1:9820400-9831600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr1:9820400-9832400	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr1:9820400-9832600	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr1:9820400-9832600	Weak transcription	Ovary	ovary
37	chr1:9820600-9826800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr1:9820600-9832400	Weak transcription	Left Ventricle	heart
39	chr1:9820600-9832600	Weak transcription	Fetal Lung	lung
40	chr1:9820600-9836200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr1:9821000-9832400	Weak transcription	Esophagus	oesophagus
42	chr1:9821200-9827000	Weak transcription	Brain Anterior Caudate	brain
43	chr1:9821200-9827000	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr1:9821200-9829200	Weak transcription	Pancreas	Pancrea
45	chr1:9821200-9832400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:9821200-9832400	Weak transcription	HepG2	liver
47	chr1:9822000-9832400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr1:9822000-9832400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr1:9822000-9832400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr1:9822200-9829200	Weak transcription	Primary T cells fromperipheralblood	blood

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