Variant report

Variant	nsv1014638
Chromosome Location	chr1:150647987-150679033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:429)
Chromatin interactive
region (count:39)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:150669521-150670181	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:150668934-150669109	K562	blood:	n/a	n/a
3	ARID3A	chr1:150668117-150668410	K562	blood:	n/a	n/a
4	ARID3A	chr1:150669458-150670246	K562	blood:	n/a	n/a
5	ATF1	chr1:150669547-150670029	K562	blood:	n/a	n/a
6	BACH1	chr1:150668928-150668939	K562	blood:	n/a	n/a
7	BACH1	chr1:150678795-150678810	K562	blood:	n/a	n/a
8	BCL3	chr1:150669301-150670144	A549	lung:	n/a	n/a
9	BHLHE40	chr1:150669725-150669999	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:150669568-150669930	K562	blood:	n/a	n/a
11	BRCA1	chr1:150669458-150670063	Hela-S3	cervix:	n/a	chr1:150669751-150669758
12	CBX3	chr1:150669327-150670139	K562	blood:	n/a	n/a
13	CEBPB	chr1:150648309-150648390	A549	lung:	n/a	n/a
14	CEBPB	chr1:150669483-150670066	Hela-S3	cervix:	n/a	chr1:150669882-150669890
15	CEBPB	chr1:150669362-150670126	MCF-7	breast:	n/a	chr1:150669882-150669890 chr1:150669436-150669449
16	CEBPB	chr1:150669494-150669869	K562	blood:	n/a	n/a
17	CEBPB	chr1:150648337-150648345	K562	blood:	n/a	n/a
18	CEBPB	chr1:150669496-150669938	A549	lung:	n/a	chr1:150669882-150669890
19	CEBPB	chr1:150669565-150669922	HepG2	liver:	n/a	chr1:150669882-150669890
20	CEBPB	chr1:150668232-150668324	K562	blood:	n/a	n/a
21	CEBPB	chr1:150669545-150669987	IMR90	lung:	n/a	chr1:150669882-150669890
22	CEBPZ	chr1:150669516-150670046	HepG2	liver:	n/a	n/a
23	CHD1	chr1:150669371-150669585	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr1:150669443-150669653	GM12878	blood:	n/a	n/a
25	CHD2	chr1:150669396-150670144	GM12878	blood:	n/a	n/a
26	CHD2	chr1:150669499-150670016	HepG2	liver:	n/a	n/a
27	CHD2	chr1:150669410-150670300	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr1:150669083-150670112	Hela-S3	cervix:	n/a	chr1:150669266-150669276
29	CHD2	chr1:150669452-150670078	K562	blood:	n/a	n/a
30	CREB1	chr1:150669321-150670121	HepG2	liver:	n/a	n/a
31	CREB1	chr1:150669355-150670153	HepG2	liver:	n/a	n/a
32	CREB1	chr1:150669444-150669989	A549	lung:	n/a	n/a
33	CREB1	chr1:150669353-150670238	GM12878	blood:	n/a	n/a
34	CREB1	chr1:150669435-150669965	A549	lung:	n/a	n/a
35	CREB1	chr1:150669420-150670149	GM12878	blood:	n/a	n/a
36	CREB1	chr1:150669423-150670041	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr1:150669424-150670110	ECC-1	luminal epithelium:	n/a	n/a
38	CTCF	chr1:150669722-150669871	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr1:150669700-150669850	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr1:150669660-150669810	HCM	heart:	n/a	n/a
41	CTCF	chr1:150669740-150669890	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr1:150669660-150669810	NHLF	lung:	n/a	n/a
43	CTCF	chr1:150652180-150652218	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:150669640-150669790	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr1:150669600-150669750	A549	lung:	n/a	n/a
46	CTCF	chr1:150669720-150669870	AG09309	skin:	n/a	n/a
47	CTCF	chr1:150669680-150669830	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr1:150669900-150670050	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr1:150669620-150669770	GM12868	blood:	n/a	n/a
50	CTCF	chr1:150669700-150669850	K562	blood:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150669977-150670027	HIPEpiC	eye:	n/a
2	chr1:150669681-150669731	SK-N-SH	brain:	n/a
3	chr1:150669977-150670027	HIPEpiC	eye:	n/a
4	chr1:150669681-150669731	SK-N-SH	brain:	n/a
5	chr1:150669796-150669846	SK-N-SH_RA	brain:	n/a
6	chr1:150669681-150669731	AG04450	lung:	fetal
7	chr1:150672619-150672669	SKMC	muscle:	n/a
8	chr1:150672619-150672669	AG04450	lung:	fetal
9	chr1:150670422-150670472	PrEC	prostate:	n/a
10	chr1:150670196-150670246	HRE	kidney:	n/a
11	chr1:150669759-150669809	IMR90	lung:	fetal
12	chr1:150670422-150670472	AoSMC	blood vessel:	n/a
13	chr1:150669681-150669731	HUVEC	blood vessel:	n/a
14	chr1:150670422-150670472	PFSK-1	brain:	n/a
15	chr1:150669977-150670027	ECC-1	luminal epithelium:	n/a
16	chr1:150669759-150669809	AG10803	skin:	n/a
17	chr1:150669796-150669846	GM12878	blood:	n/a
18	chr1:150672619-150672669	HCF	heart:	n/a
19	chr1:150670196-150670246	Caco-2	colon:	n/a
20	chr1:150669977-150670027	HCT-116	colon:	n/a
21	chr1:150670422-150670472	HepG2	liver:	n/a
22	chr1:150670422-150670472	LNCaP	prostate:	n/a
23	chr1:150669977-150670027	NB4	blood:	n/a
24	chr1:150670196-150670246	A549	lung:	n/a
25	chr1:150669796-150669846	HRE	kidney:	n/a
26	chr1:150669796-150669846	MCF-7	breast:	n/a
27	chr1:150669796-150669846	GM06990	blood:	n/a
28	chr1:150672619-150672669	Caco-2	colon:	n/a
29	chr1:150672619-150672669	AG10803	skin:	n/a
30	chr1:150669796-150669846	NH-A	brain:	n/a
31	chr1:150670422-150670472	NHBE	bronchial:	n/a
32	chr1:150669796-150669846	HNPCEpiC	eye:	n/a
33	chr1:150669681-150669731	HRCEpiC	kidney:	n/a
34	chr1:150669681-150669731	HCM	heart:	n/a
35	chr1:150669977-150670027	HL-60	blood:	n/a
36	chr1:150669796-150669846	NHBE	bronchial:	n/a
37	chr1:150669796-150669846	HepG2	liver:	n/a
38	chr1:150670196-150670246	IMR90	lung:	fetal
39	chr1:150670196-150670246	PFSK-1	brain:	n/a
40	chr1:150669759-150669809	GM19239	blood:	n/a
41	chr1:150669977-150670027	RPTEC	kidney:	n/a
42	chr1:150670422-150670472	SK-N-MC	brain:	n/a
43	chr1:150669796-150669846	SK-N-MC	brain:	n/a
44	chr1:150670422-150670472	PANC-1	pancreas:	n/a
45	chr1:150670196-150670246	NB4	blood:	n/a
46	chr1:150669796-150669846	HCPEpiC	choroid plexus:	n/a
47	chr1:150669681-150669731	Jurkat	blood:	n/a
48	chr1:150669681-150669731	AoSMC	blood vessel:	n/a
49	chr1:150669681-150669731	HCPEpiC	choroid plexus:	n/a
50	chr1:150669681-150669731	HEK293	kidney:	embryo

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150668347..150671201-chr1:150671621..150673676,2	MCF-7	breast:
2	chr1:150600957..150603301-chr1:150669104..150670860,3	MCF-7	breast:
3	chr1:150550587..150552161-chr1:150659135..150662073,2	MCF-7	breast:
4	chr1:150657524..150659198-chr1:150659977..150662845,2	MCF-7	breast:
5	chr1:150661949..150665249-chr1:150666928..150670811,7	K562	blood:
6	chr1:150600872..150603791-chr1:150659144..150663270,3	MCF-7	breast:
7	chr1:150551078..150552936-chr1:150667990..150671349,4	K562	blood:
8	chr1:150668066..150670376-chr1:150778150..150781017,2	K562	blood:
9	chr1:150549499..150551723-chr1:150674236..150676416,2	K562	blood:
10	chr1:150656265..150658079-chr1:150660051..150662794,2	K562	blood:
11	chr1:150668066..150670256-chr1:150778150..150780706,2	K562	blood:
12	chr1:150611643..150613854-chr1:150667499..150669234,2	K562	blood:
13	chr1:150601610..150603438-chr1:150651701..150654487,2	K562	blood:
14	chr1:150672673..150675324-chr1:150676637..150678852,2	K562	blood:
15	chr1:150334566..150337465-chr1:150678330..150680323,3	K562	blood:
16	chr1:150648019..150649950-chr1:150651188..150654049,2	MCF-7	breast:
17	chr1:150652709..150655600-chr1:150657493..150660351,2	MCF-7	breast:
18	chr1:150600620..150604710-chr1:150667156..150670884,6	K562	blood:
19	chr1:150656265..150658079-chr1:150660051..150662794,2	K562	blood:
20	chr1:150670046..150672281-chr1:150847927..150849937,2	MCF-7	breast:
21	chr1:150667811..150671175-chr1:150944483..150949055,4	MCF-7	breast:
22	chr1:150600782..150602798-chr1:150645652..150648306,2	MCF-7	breast:
23	chr1:150594892..150596447-chr1:150663377..150666210,2	K562	blood:
24	chr1:150588429..150591209-chr1:150660064..150661641,2	K562	blood:
25	chr1:150533613..150535919-chr1:150668275..150670992,2	MCF-7	breast:
26	chr1:150661949..150664649-chr1:150666977..150670248,3	K562	blood:
27	chr1:150538247..150539989-chr1:150652708..150654425,2	K562	blood:
28	chr1:150551507..150553628-chr1:150668472..150670953,2	K562	blood:
29	chr1:150657524..150659198-chr1:150659977..150662845,2	MCF-7	breast:
30	chr1:150540683..150542229-chr1:150664945..150667122,2	K562	blood:
31	chr1:150651534..150653959-chr1:150654025..150657023,2	MCF-7	breast:
32	chr1:150600649..150603708-chr1:150666872..150671304,5	K562	blood:
33	chr1:150651534..150653959-chr1:150654025..150657023,2	MCF-7	breast:
34	chr1:150669609..150671897-chr1:150782631..150785278,2	K562	blood:
35	chr1:150648019..150649950-chr1:150651188..150654049,2	MCF-7	breast:
36	chr1:150662766..150666731-chr1:150669381..150672304,3	MCF-7	breast:
37	chr1:150652709..150655600-chr1:150657493..150660351,2	MCF-7	breast:
38	chr1:150672673..150675324-chr1:150676637..150678852,2	K562	blood:
39	chr1:150668010..150669720-chr1:150777076..150779971,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLPH3L-2	chr1:150671330-150671441	NONHSAT006324
2	lnc-GOLPH3L-2	chr1:150670867-150671210	NONHSAT006324
3	lnc-GOLPH3L-2	chr1:150676753-150676783	NONHSAT006324
4	lnc-GOLPH3L-2	chr1:150672588-150672659	NONHSAT006324
5	lnc-GOLPH3L-2	chr1:150675786-150675869	NONHSAT006324
6	lnc-GOLPH3L-2	chr1:150676594-150676670	NONHSAT006324

No data

Variant related genes	Relation type
GOLPH3L	TF binding region
HORMAD1	TF binding region
RNU6-1042P	TF binding region
GOLPH3L	CpG island
HORMAD1	CpG island
RNU6-1042P	CpG island
ENSG00000231073	chromatin interactions
ENSG00000264584	chromatin interactions
ENSG00000200175	chromatin interactions
ENSG00000143437	chromatin interactions
ENSG00000163125	chromatin interactions
ENSG00000143420	chromatin interactions
ENSG00000206931	chromatin interactions
ENSG00000143457	chromatin interactions
ENSG00000143418	chromatin interactions
ENSG00000264508	chromatin interactions
ENSG00000143452	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000143387	chromatin interactions
ENSG00000203804	chromatin interactions

Extended variants
information (count: 866 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:866 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11204693	chr1:150647987-150647988	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587709721	chr1:150648056-150648057	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369709115	chr1:150648070-150648071	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs59381208	chr1:150648096-150648097	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587609162	chr1:150648147-150648148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139785695	chr1:150648207-150648208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587745418	chr1:150648208-150648209	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587619147	chr1:150648231-150648232	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs58158655	chr1:150648256-150648257	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs397981523	chr1:150648283-150648284	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs79733056	chr1:150648284-150648285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587692946	chr1:150648300-150648301	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200242510	chr1:150648431-150648432	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs587750327	chr1:150648442-150648443	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201186737	chr1:150648453-150648454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587648100	chr1:150648462-150648463	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372094254	chr1:150648463-150648464	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77316446	chr1:150648464-150648465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144497175	chr1:150648467-150648468	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs587613863	chr1:150648490-150648491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74593888	chr1:150648512-150648513	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79583600	chr1:150648515-150648516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76227187	chr1:150648517-150648518	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587689187	chr1:150648542-150648543	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376883215	chr1:150648587-150648588	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587644912	chr1:150648606-150648607	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs57502737	chr1:150648613-150648614	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs587702278	chr1:150648672-150648673	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs587761781	chr1:150648788-150648789	Weak transcription Genic enhancers Enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs587659042	chr1:150648827-150648828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34267816	chr1:150648841-150648842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587708818	chr1:150648912-150648913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587719338	chr1:150648947-150648948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587604183	chr1:150648948-150648949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369872160	chr1:150648991-150648992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201058883	chr1:150649034-150649035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12064548	chr1:150649180-150649181	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs377647231	chr1:150649205-150649206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587596993	chr1:150649211-150649212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12095002	chr1:150649249-150649250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs373851358	chr1:150649273-150649274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587752244	chr1:150649284-150649285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113561392	chr1:150649362-150649363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143722760	chr1:150649401-150649402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187206992	chr1:150649403-150649404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587739318	chr1:150649440-150649441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189271927	chr1:150649510-150649511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12064701	chr1:150649514-150649515	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs587748839	chr1:150649607-150649608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587622605	chr1:150649623-150649624	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD

Chromatin state (count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:150603200-150661200	Weak transcription	Brain Substantia Nigra	brain
2	chr1:150603400-150668200	Weak transcription	Brain Germinal Matrix	brain
3	chr1:150608600-150668600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:150618800-150660400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr1:150621000-150660800	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:150621200-150660400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr1:150621200-150664800	Weak transcription	Fetal Brain Female	brain
8	chr1:150621200-150665000	Weak transcription	Fetal Kidney	kidney
9	chr1:150621200-150669400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:150621400-150660400	Weak transcription	HSMM	muscle
11	chr1:150621800-150661200	Weak transcription	NHDF-Ad	bronchial
12	chr1:150621800-150668600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr1:150622000-150661400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:150622000-150668600	Weak transcription	HSMMtube	muscle
15	chr1:150622000-150669400	Weak transcription	Esophagus	oesophagus
16	chr1:150622200-150660600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr1:150623200-150648400	Weak transcription	Lung	lung
18	chr1:150623200-150668600	Weak transcription	Brain Angular Gyrus	brain
19	chr1:150623400-150663000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:150630000-150664800	Weak transcription	Thymus	Thymus
21	chr1:150630800-150656200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr1:150631800-150665400	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr1:150632400-150669000	Weak transcription	Aorta	Aorta
24	chr1:150632600-150654200	Weak transcription	Ovary	ovary
25	chr1:150632600-150658400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:150632600-150665000	Weak transcription	Colonic Mucosa	Colon
27	chr1:150632600-150668200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr1:150633000-150668600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr1:150633200-150656400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr1:150633200-150656400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:150633200-150669200	Weak transcription	Left Ventricle	heart
32	chr1:150633400-150656400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr1:150633400-150660600	Weak transcription	Fetal Lung	lung
34	chr1:150633400-150665000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr1:150634200-150653600	Weak transcription	Osteobl	bone
36	chr1:150634200-150654400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr1:150634400-150648200	Weak transcription	NHLF	lung
38	chr1:150634400-150653000	Weak transcription	Fetal Muscle Trunk	muscle
39	chr1:150634400-150654000	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:150634400-150656400	Weak transcription	Primary B cells from cord blood	blood
41	chr1:150634600-150651600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr1:150634600-150656200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr1:150634600-150656400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr1:150634600-150656400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr1:150634600-150658800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:150634600-150660400	Weak transcription	K562	blood
47	chr1:150634600-150660800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr1:150634600-150661200	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr1:150634600-150664800	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr1:150634800-150658600	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

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