Variant report

Variant	nsv1008381
Chromosome Location	chr1:150721254-150745558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:263)
CpG islands
(count:245)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150737188-150737580	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:150735027-150735152	K562	blood:	n/a	n/a
3	ARID3A	chr1:150721470-150721983	K562	blood:	n/a	n/a
4	ATF1	chr1:150735140-150735301	K562	blood:	n/a	n/a
5	ATF2	chr1:150737922-150738587	GM12878	blood:	n/a	n/a
6	ATF3	chr1:150740092-150740419	K562	blood:	n/a	n/a
7	BATF	chr1:150738059-150738510	GM12878	blood:	n/a	chr1:150738368-150738377
8	BATF	chr1:150737069-150737330	GM12878	blood:	n/a	n/a
9	BATF	chr1:150738024-150738477	GM12878	blood:	n/a	chr1:150738368-150738377
10	BCL3	chr1:150738007-150738423	GM12878	blood:	n/a	chr1:150738330-150738339
11	BCLAF1	chr1:150737911-150738457	GM12878	blood:	n/a	chr1:150738330-150738339
12	BCLAF1	chr1:150737934-150738532	GM12878	blood:	n/a	chr1:150738330-150738339
13	BHLHE40	chr1:150743609-150743633	GM12878	blood:	n/a	n/a
14	BHLHE40	chr1:150738026-150738513	GM12878	blood:	n/a	n/a
15	CCNT2	chr1:150736368-150736679	K562	blood:	n/a	n/a
16	CEBPB	chr1:150737343-150737582	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:150743583-150743617	K562	blood:	n/a	n/a
18	CEBPB	chr1:150743457-150743728	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:150737194-150737676	A549	lung:	n/a	n/a
20	CEBPB	chr1:150740246-150740286	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:150737110-150737710	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:150736963-150737857	A549	lung:	n/a	n/a
23	CEBPB	chr1:150740218-150740447	HepG2	liver:	n/a	chr1:150740301-150740312
24	CEBPB	chr1:150740199-150740439	K562	blood:	n/a	chr1:150740301-150740312
25	CEBPB	chr1:150740122-150740437	K562	blood:	n/a	chr1:150740301-150740312
26	CEBPB	chr1:150740231-150740427	Hela-S3	cervix:	n/a	chr1:150740301-150740312
27	CEBPB	chr1:150740224-150740394	IMR90	lung:	n/a	chr1:150740301-150740312
28	CEBPB	chr1:150744333-150744481	HepG2	liver:	n/a	chr1:150744422-150744433
29	CEBPB	chr1:150737058-150737704	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:150743472-150743639	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:150737278-150737651	A549	lung:	n/a	n/a
32	CEBPB	chr1:150740199-150740399	A549	lung:	n/a	chr1:150740301-150740312
33	CEBPB	chr1:150740214-150740417	K562	blood:	n/a	chr1:150740301-150740312
34	CHD1	chr1:150737238-150738349	GM12878	blood:	n/a	n/a
35	CHD1	chr1:150736265-150736520	GM12878	blood:	n/a	n/a
36	CHD2	chr1:150722139-150722516	K562	blood:	n/a	n/a
37	CREB1	chr1:150743283-150743688	GM12878	blood:	n/a	n/a
38	CREB1	chr1:150737954-150738573	GM12878	blood:	n/a	n/a
39	CTCF	chr1:150727060-150727210	WI-38	lung:	n/a	n/a
40	CTCF	chr1:150727129-150727164	GM10248	blood:	n/a	n/a
41	CTCF	chr1:150743360-150743510	GM12873	blood:	n/a	n/a
42	CTCF	chr1:150732556-150732761	GM12878	blood:	n/a	n/a
43	CTCF	chr1:150732588-150732678	GM13977	blood:	n/a	n/a
44	CTCF	chr1:150732553-150732703	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr1:150744920-150745070	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr1:150732460-150732610	GM12872	blood:	n/a	n/a
47	CTCF	chr1:150744960-150745110	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:150744940-150745090	AG04450	lung:	n/a	n/a
49	CTCF	chr1:150744860-150745010	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr1:150744840-150744990	Caco-2	colon:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150738173-150738223	K562	blood:	n/a
2	chr1:150738173-150738223	K562	blood:	n/a
3	chr1:150737762-150737812	HL-60	blood:	n/a
4	chr1:150738173-150738223	BE2_C	brain:	n/a
5	chr1:150737762-150737812	T-47D	breast:	n/a
6	chr1:150722805-150722855	AG09319	gingival:	n/a
7	chr1:150722805-150722855	ProgFib	skin:	n/a
8	chr1:150722805-150722855	BJ	skin:	n/a
9	chr1:150738905-150738955	GM12891	blood:	n/a
10	chr1:150737762-150737812	NHDF-neo	bronchial:	n/a
11	chr1:150738905-150738955	HCT-116	colon:	n/a
12	chr1:150738905-150738955	HCF	heart:	n/a
13	chr1:150738173-150738223	SK-N-SH	brain:	n/a
14	chr1:150737762-150737812	Hela-S3	cervix:	n/a
15	chr1:150722805-150722855	HCPEpiC	choroid plexus:	n/a
16	chr1:150722805-150722855	SK-N-SH	brain:	n/a
17	chr1:150722805-150722855	HIPEpiC	eye:	n/a
18	chr1:150722805-150722855	HUVEC	blood vessel:	n/a
19	chr1:150722805-150722855	HL-60	blood:	n/a
20	chr1:150722805-150722855	H1-hESC	embryonic stem cell:	embryo
21	chr1:150737762-150737812	AG10803	skin:	n/a
22	chr1:150738173-150738223	MCF10A-Er-Src	breast:	n/a
23	chr1:150738173-150738223	HRCEpiC	kidney:	n/a
24	chr1:150722805-150722855	HRE	kidney:	n/a
25	chr1:150738173-150738223	AoSMC	blood vessel:	n/a
26	chr1:150738905-150738955	Caco-2	colon:	n/a
27	chr1:150737762-150737812	BE2_C	brain:	n/a
28	chr1:150722805-150722855	T-47D	breast:	n/a
29	chr1:150738905-150738955	NT2-D1	testis:	n/a
30	chr1:150722805-150722855	HRPEpiC	eye:	n/a
31	chr1:150737762-150737812	HCM	heart:	n/a
32	chr1:150737762-150737812	HCT-116	colon:	n/a
33	chr1:150738173-150738223	HCM	heart:	n/a
34	chr1:150722805-150722855	Hela-S3	cervix:	n/a
35	chr1:150738173-150738223	GM12892	blood:	n/a
36	chr1:150737762-150737812	MCF-7	breast:	n/a
37	chr1:150722805-150722855	Jurkat	blood:	n/a
38	chr1:150738173-150738223	PFSK-1	brain:	n/a
39	chr1:150737762-150737812	PFSK-1	brain:	n/a
40	chr1:150738173-150738223	AG04450	lung:	fetal
41	chr1:150738905-150738955	SKMC	muscle:	n/a
42	chr1:150722805-150722855	HMEC	breast:	n/a
43	chr1:150737762-150737812	HCPEpiC	choroid plexus:	n/a
44	chr1:150738173-150738223	T-47D	breast:	n/a
45	chr1:150738173-150738223	U87	brain:	n/a
46	chr1:150722805-150722855	K562	blood:	n/a
47	chr1:150738905-150738955	HAEpiC	amniotic membrane:	n/a
48	chr1:150737762-150737812	H1-hESC	embryonic stem cell:	embryo
49	chr1:150722805-150722855	HRCEpiC	kidney:	n/a
50	chr1:150737762-150737812	HAEpiC	amniotic membrane:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150550688..150552369-chr1:150735871..150738707,2	MCF-7	breast:
2	chr1:150737960..150741233-chr1:150743077..150746063,3	K562	blood:
3	chr1:150738126..150741415-chr1:150742001..150744824,3	MCF-7	breast:
4	chr1:150725025..150727549-chr1:150728831..150731687,2	K562	blood:
5	chr1:150600704..150602423-chr1:150722921..150725680,2	MCF-7	breast:
6	chr1:150724802..150727328-chr1:150746278..150749231,2	MCF-7	breast:
7	chr1:150733435..150736065-chr1:150737703..150739768,2	K562	blood:
8	chr1:150730585..150733903-chr1:150734445..150737358,3	K562	blood:
9	chr1:150725025..150727549-chr1:150728831..150731687,2	K562	blood:
10	chr1:150718367..150722446-chr1:150727232..150730438,3	K562	blood:
11	chr1:150543916..150546115-chr1:150744599..150746718,2	K562	blood:
12	chr1:150731143..150734388-chr1:150735639..150737851,3	MCF-7	breast:
13	chr1:150718367..150722446-chr1:150727232..150730438,3	K562	blood:
14	chr1:150638939..150641718-chr1:150729032..150731135,2	K562	blood:
15	chr1:150720934..150724836-chr1:150780473..150783915,3	K562	blood:
16	chr1:150741916..150744860-chr1:150749050..150751954,2	K562	blood:
17	chr1:150742855..150744803-chr1:150749653..150752578,2	MCF-7	breast:
18	chr1:150743215..150744968-chr1:150746292..150748650,2	MCF-7	breast:
19	chr1:150720840..150722838-chr1:150897246..150898815,2	K562	blood:

No data

Variant related genes	Relation type
CTSS	TF binding region
CTSS	CpG island
ENSG00000143420	chromatin interactions
ENSG00000143379	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000143387	chromatin interactions
ENSG00000163131	chromatin interactions

Extended variants
information (count: 670 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:670 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587600186	chr1:150721403-150721404	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs368672285	chr1:150721412-150721413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs587707613	chr1:150721435-150721436	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587606092	chr1:150721453-150721454	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs587680558	chr1:150721465-150721466	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190309842	chr1:150721506-150721507	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs587594544	chr1:150721543-150721544	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs181085131	chr1:150721561-150721562	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs184319490	chr1:150721583-150721584	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs587620848	chr1:150721682-150721683	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs587683953	chr1:150721683-150721684	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs189262671	chr1:150721891-150721892	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149953139	chr1:150721900-150721901	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs371666863	chr1:150721914-150721915	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs587687958	chr1:150721916-150721917	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181261562	chr1:150721928-150721929	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs145017122	chr1:150722000-150722001	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs72704615	chr1:150722010-150722011	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376154753	chr1:150722043-150722044	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372453458	chr1:150722073-150722074	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587632563	chr1:150722076-150722077	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111672603	chr1:150722256-150722257	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs377511536	chr1:150722311-150722312	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs185319034	chr1:150722328-150722329	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs34888280	chr1:150722358-150722359	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587649336	chr1:150722430-150722431	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs587704673	chr1:150722442-150722443	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs376261246	chr1:150722462-150722463	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs201032560	chr1:150722464-150722465	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138263900	chr1:150722511-150722512	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs372474770	chr1:150722546-150722547	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1059605	chr1:150722576-150722577	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs147260142	chr1:150722586-150722587	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs375763218	chr1:150722662-150722663	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs112376067	chr1:150722703-150722704	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs587615128	chr1:150722733-150722734	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs181460361	chr1:150722806-150722807	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs587724190	chr1:150722823-150722824	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs11587444	chr1:150722844-150722845	Weak transcription Strong transcription Enhancers Genic enhancers	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs587670084	chr1:150722884-150722885	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113207686	chr1:150722900-150722901	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35102178	chr1:150722909-150722910	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587733194	chr1:150723063-150723064	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs587630503	chr1:150723146-150723147	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587669433	chr1:150723199-150723200	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs587749037	chr1:150723219-150723220	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs80183777	chr1:150723224-150723225	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587622451	chr1:150723289-150723290	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs371743311	chr1:150723323-150723324	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs587746473	chr1:150723357-150723358	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Cancer	23975201	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:629 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150701400-150727400	Weak transcription	Left Ventricle	heart
2	chr1:150704000-150736600	Weak transcription	Fetal Stomach	stomach
3	chr1:150705400-150723800	Weak transcription	Gastric	stomach
4	chr1:150705600-150723800	Weak transcription	Thymus	Thymus
5	chr1:150708400-150733000	Weak transcription	Fetal Intestine Large	intestine
6	chr1:150709000-150723800	Weak transcription	Esophagus	oesophagus
7	chr1:150709000-150727400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr1:150710200-150729200	Weak transcription	Psoas Muscle	Psoas
9	chr1:150711000-150735600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr1:150712000-150737800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:150714600-150723800	Weak transcription	Fetal Intestine Small	intestine
12	chr1:150714800-150732200	Weak transcription	Stomach Mucosa	stomach
13	chr1:150715600-150728000	Weak transcription	Brain Anterior Caudate	brain
14	chr1:150715800-150736200	Weak transcription	Small Intestine	intestine
15	chr1:150716600-150737000	Weak transcription	Pancreas	Pancrea
16	chr1:150717000-150721600	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr1:150717000-150724200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr1:150717000-150724400	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr1:150717000-150730800	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr1:150717000-150731000	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr1:150717000-150731400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:150717000-150732000	Strong transcription	Primary B cells from cord blood	blood
23	chr1:150717000-150732200	Strong transcription	Primary B cells from peripheral blood	blood
24	chr1:150717000-150732200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:150717000-150732400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr1:150717000-150732800	Strong transcription	Duodenum Mucosa	Duodenum
27	chr1:150717000-150733000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr1:150717200-150721400	Strong transcription	Sigmoid Colon	Sigmoid Colon
29	chr1:150717200-150728000	Strong transcription	Primary T helper naive cells from peripheral blood	blood
30	chr1:150717200-150730600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:150717200-150730800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr1:150717200-150731000	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr1:150717200-150733600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:150717400-150722800	Strong transcription	GM12878-XiMat	blood
35	chr1:150717400-150723000	Strong transcription	Primary hematopoietic stem cells	blood
36	chr1:150717400-150730600	Strong transcription	Primary T cells from cord blood	blood
37	chr1:150717400-150731400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr1:150719600-150724000	Weak transcription	Adipose Nuclei	Adipose
39	chr1:150719600-150724200	Weak transcription	Lung	lung
40	chr1:150719800-150726600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:150720000-150723000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:150720000-150727400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr1:150720200-150722200	Strong transcription	Spleen	Spleen
44	chr1:150720200-150722600	Weak transcription	Liver	Liver
45	chr1:150720200-150724200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr1:150720200-150736200	Weak transcription	Colonic Mucosa	Colon
47	chr1:150720400-150723600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr1:150720400-150725600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr1:150720400-150727000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr1:150720600-150737800	Weak transcription	Brain Substantia Nigra	brain

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