Variant report

Variant	nsv4643
Chromosome Location	chr1:220397642-220442231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:276)
CpG islands
(count:430)
Chromatin interactive
region (count:30)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:276 , 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	chr1:220417486-220417685	K562	blood:	n/a	n/a
2	ARID3A	chr1:220408686-220409116	HepG2	liver:	n/a	n/a
3	BACH1	chr1:220441013-220441325	K562	blood:	n/a	n/a
4	BACH1	chr1:220441007-220441338	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:220397420-220397771	GM12878	blood:	n/a	n/a
6	BATF	chr1:220428578-220428814	GM12878	blood:	n/a	n/a
7	CBX3	chr1:220422956-220423236	HCT-116	colon:	n/a	n/a
8	CBX3	chr1:220422809-220423398	K562	blood:	n/a	n/a
9	CBX3	chr1:220421923-220423589	K562	blood:	n/a	n/a
10	CBX3	chr1:220422096-220422467	K562	blood:	n/a	n/a
11	CEBPB	chr1:220438607-220438720	HepG2	liver:	n/a	chr1:220438642-220438653 chr1:220438618-220438631
12	CEBPB	chr1:220398133-220398286	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:220407761-220407971	K562	blood:	n/a	chr1:220407876-220407889 chr1:220407878-220407889 chr1:220407876-220407889 chr1:220407878-220407887 chr1:220407878-220407887 chr1:220407876-220407889 chr1:220407878-220407887 chr1:220407878-220407887 chr1:220407878-220407889
14	CEBPB	chr1:220398054-220398336	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD1	chr1:220399521-220399538	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr1:220409736-220409821	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:220427512-220427537	GM13976	blood:	n/a	n/a
18	CTCF	chr1:220427495-220427500	GM13976	blood:	n/a	n/a
19	CTCF	chr1:220423480-220423610	K562	blood:	n/a	n/a
20	CTCF	chr1:220399812-220399879	Medullo	brain:	n/a	n/a
21	CTCF	chr1:220409740-220409890	MCF-7	breast:	n/a	n/a
22	CTCF	chr1:220423420-220423570	K562	blood:	n/a	n/a
23	CTCF	chr1:220409760-220409910	HEK293	kidney:	n/a	n/a
24	CTCF	chr1:220426799-220426851	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:220427197-220427257	GM20000	blood:	n/a	n/a
26	CTCF	chr1:220423440-220423590	GM12872	blood:	n/a	n/a
27	CTCF	chr1:220409700-220409850	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr1:220424149-220424201	GM13976	blood:	n/a	n/a
29	CUX1	chr1:220398284-220398299	GM12878	blood:	n/a	n/a
30	CUX1	chr1:220397424-220397851	GM12878	blood:	n/a	n/a
31	CUX1	chr1:220417436-220417627	K562	blood:	n/a	n/a
32	E2F4	chr1:220409386-220409388	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr1:220420864-220421044	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr1:220433932-220433933	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr1:220397485-220397790	GM12878	blood:	n/a	n/a
36	EBF1	chr1:220426669-220426916	GM12878	blood:	n/a	n/a
37	EBF1	chr1:220397501-220397742	GM12878	blood:	n/a	n/a
38	EBF1	chr1:220397468-220397776	GM12878	blood:	n/a	n/a
39	EP300	chr1:220414496-220414657	GM12878	blood:	n/a	n/a
40	EP300	chr1:220417489-220417645	K562	blood:	n/a	n/a
41	EP300	chr1:220432231-220432292	K562	blood:	n/a	n/a
42	EP300	chr1:220397475-220397752	GM12878	blood:	n/a	n/a
43	EP300	chr1:220414846-220414908	K562	blood:	n/a	n/a
44	FAM48A	chr1:220434534-220434733	GM12878	blood:	n/a	n/a
45	FOS	chr1:220408951-220409241	MCF10A-Er-Src	breast:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088
46	FOS	chr1:220408994-220409235	MCF10A-Er-Src	breast:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088
47	FOS	chr1:220408915-220409261	MCF10A-Er-Src	breast:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088
48	FOS	chr1:220408951-220409255	MCF10A-Er-Src	breast:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088
49	FOSL2	chr1:220408881-220409180	MCF-7	breast:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088
50	FOSL2	chr1:220408686-220409370	A549	lung:	n/a	chr1:220409079-220409086 chr1:220409079-220409087 chr1:220409078-220409087 chr1:220409079-220409088

(count:430 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220441596-220441646	BJ	skin:	n/a
2	chr1:220441256-220441306	AG04450	lung:	fetal
3	chr1:220441097-220441147	HRCEpiC	kidney:	n/a
4	chr1:220441596-220441646	BJ	skin:	n/a
5	chr1:220441256-220441306	AG04450	lung:	fetal
6	chr1:220441097-220441147	HRCEpiC	kidney:	n/a
7	chr1:220439792-220439842	CMK	blood:	n/a
8	chr1:220441097-220441147	AG04450	lung:	fetal
9	chr1:220441596-220441646	HCT-116	colon:	n/a
10	chr1:220441596-220441646	AG04450	lung:	fetal
11	chr1:220408360-220408410	HCM	heart:	n/a
12	chr1:220441256-220441306	Jurkat	blood:	n/a
13	chr1:220439792-220439842	NB4	blood:	n/a
14	chr1:220439792-220439842	MCF-7	breast:	n/a
15	chr1:220408360-220408410	HEK293	kidney:	embryo
16	chr1:220439792-220439842	Jurkat	blood:	n/a
17	chr1:220408360-220408410	U87	brain:	n/a
18	chr1:220408360-220408410	SAEC	small airway:	n/a
19	chr1:220441097-220441147	NT2-D1	testis:	n/a
20	chr1:220440947-220440997	H1-hESC	embryonic stem cell:	embryo
21	chr1:220441256-220441306	NT2-D1	testis:	n/a
22	chr1:220415655-220415705	HRE	kidney:	n/a
23	chr1:220408360-220408410	SKMC	muscle:	n/a
24	chr1:220415655-220415705	LNCaP	prostate:	n/a
25	chr1:220440947-220440997	SAEC	small airway:	n/a
26	chr1:220415655-220415705	HCPEpiC	choroid plexus:	n/a
27	chr1:220440947-220440997	HCF	heart:	n/a
28	chr1:220441097-220441147	PFSK-1	brain:	n/a
29	chr1:220441256-220441306	IMR90	lung:	fetal
30	chr1:220440947-220440997	HEEpiC	esophagus:	n/a
31	chr1:220415655-220415705	Hepatocyte	liver:	n/a
32	chr1:220440947-220440997	AG09319	gingival:	n/a
33	chr1:220441256-220441306	NH-A	brain:	n/a
34	chr1:220408360-220408410	AG04449	skin:	fetal
35	chr1:220415655-220415705	HL-60	blood:	n/a
36	chr1:220408360-220408410	HCPEpiC	choroid plexus:	n/a
37	chr1:220441256-220441306	NHDF-neo	bronchial:	n/a
38	chr1:220439792-220439842	HEK293	kidney:	embryo
39	chr1:220439792-220439842	ProgFib	skin:	n/a
40	chr1:220439792-220439842	SK-N-SH	brain:	n/a
41	chr1:220441256-220441306	HMEC	breast:	n/a
42	chr1:220439792-220439842	NH-A	brain:	n/a
43	chr1:220441097-220441147	SK-N-SH_RA	brain:	n/a
44	chr1:220440947-220440997	HRPEpiC	eye:	n/a
45	chr1:220439792-220439842	HRPEpiC	eye:	n/a
46	chr1:220415655-220415705	CMK	blood:	n/a
47	chr1:220415655-220415705	AoSMC	blood vessel:	n/a
48	chr1:220441097-220441147	AG10803	skin:	n/a
49	chr1:220441256-220441306	GM12892	blood:	n/a
50	chr1:220415655-220415705	AG09309	skin:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:220440528..220443413-chr1:220443546..220445862,4	MCF-7	breast:
2	chr1:220405526..220409117-chr1:220409485..220413749,4	K562	blood:
3	chr1:220415502..220418514-chr1:220424873..220426907,3	K562	blood:
4	chr1:220395865..220398692-chr1:220400712..220402951,3	K562	blood:
5	chr1:220218323..220221198-chr1:220420169..220422135,2	K562	blood:
6	chr1:220398979..220400909-chr1:220405433..220407745,2	K562	blood:
7	chr1:220403586..220405327-chr1:220408780..220410379,2	K562	blood:
8	chr1:220401657..220404587-chr1:220444540..220446507,3	K562	blood:
9	chr1:220390706..220392701-chr1:220399648..220402266,2	K562	blood:
10	chr1:220396718..220399259-chr1:220445966..220447617,2	MCF-7	breast:
11	chr1:220420506..220423214-chr1:220434683..220436632,3	K562	blood:
12	chr1:220415502..220418514-chr1:220424873..220426907,3	K562	blood:
13	chr1:220409924..220412280-chr1:220442735..220445695,2	K562	blood:
14	chr1:220420506..220423214-chr1:220434683..220436632,3	K562	blood:
15	chr1:220378470..220380460-chr1:220408418..220411307,2	K562	blood:
16	chr1:220403586..220405327-chr1:220408780..220410379,2	K562	blood:
17	chr1:220398979..220400909-chr1:220405433..220407745,2	K562	blood:
18	chr1:220415384..220417325-chr1:220437558..220439400,2	K562	blood:
19	chr1:220401875..220404587-chr1:220444180..220446507,2	K562	blood:
20	chr1:220401289..220404210-chr1:220406154..220407744,2	MCF-7	breast:
21	chr1:220386418..220388172-chr1:220398105..220400996,2	K562	blood:
22	chr1:220415384..220417325-chr1:220437558..220439400,2	K562	blood:
23	chr1:220401289..220404210-chr1:220406154..220407744,2	MCF-7	breast:
24	chr1:220396351..220398828-chr1:220410943..220412922,2	K562	blood:
25	chr1:220396351..220398828-chr1:220410943..220412922,2	K562	blood:
26	chr1:220403099..220406087-chr1:220921390..220923561,2	MCF-7	breast:
27	chr1:220438275..220439851-chr1:220451270..220453670,2	K562	blood:
28	chr1:220395865..220398692-chr1:220400712..220402951,3	K562	blood:
29	chr1:220437133..220439238-chr1:220458442..220459950,2	K562	blood:
30	chr1:220405526..220409117-chr1:220409485..220413749,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BPNT1-2	chr1:220439327-220441093	NONHSAT009593
2	lnc-BPNT1-2	chr1:220439521-220441057	NONHSAT009594
3	lnc-BPNT1-2	chr1:220440048-220441259	NONHSAT009595

No data

Variant related genes	Relation type
AURKAPS1	TF binding region
MORF4L1P1	TF binding region
AURKAPS1	CpG island
MORF4L1P1	CpG island
ENSG00000118873	chromatin interactions
ENSG00000136628	chromatin interactions
ENSG00000117791	chromatin interactions

Extended variants
information (count: 1521 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569423683	chr1:220397698-220397699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563071201	chr1:220397715-220397716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370518392	chr1:220397746-220397747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150936547	chr1:220397801-220397802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140764415	chr1:220397845-220397846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530982666	chr1:220397907-220397908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs575024264	chr1:220397912-220397913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532235118	chr1:220397925-220397926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150125402	chr1:220397987-220397988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577119307	chr1:220398011-220398012	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545645229	chr1:220398039-220398040	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376458586	chr1:220398040-220398041	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562822129	chr1:220398055-220398056	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115530073	chr1:220398058-220398059	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541851653	chr1:220398080-220398081	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561345174	chr1:220398081-220398082	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575053768	chr1:220398182-220398183	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs527248848	chr1:220398209-220398210	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368183374	chr1:220398236-220398237	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147823750	chr1:220398274-220398275	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76707019	chr1:220398357-220398358	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547281173	chr1:220398393-220398394	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4274069	chr1:220398404-220398405	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183359849	chr1:220398412-220398413	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569566048	chr1:220398415-220398416	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187869784	chr1:220398419-220398420	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4274070	chr1:220398520-220398521	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548608966	chr1:220398529-220398530	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568466740	chr1:220398570-220398571	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534141899	chr1:220398583-220398584	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554323835	chr1:220398596-220398597	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577384275	chr1:220398597-220398598	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570746499	chr1:220398643-220398644	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191229366	chr1:220398645-220398646	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs372326490	chr1:220398689-220398690	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141287582	chr1:220398737-220398738	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs145130031	chr1:220398767-220398768	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576334699	chr1:220398775-220398776	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146986754	chr1:220398812-220398813	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147616890	chr1:220399021-220399022	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554331725	chr1:220399121-220399122	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs138174615	chr1:220399127-220399128	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566302669	chr1:220399180-220399181	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571725301	chr1:220399202-220399203	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113329276	chr1:220399314-220399315	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540599492	chr1:220399316-220399317	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563868688	chr1:220399324-220399325	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149542290	chr1:220399327-220399328	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535434438	chr1:220399384-220399385	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555343680	chr1:220399391-220399392	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1364 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220325000-220398400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:220374600-220407600	Weak transcription	Fetal Brain Male	brain
3	chr1:220378800-220398200	Weak transcription	Psoas Muscle	Psoas
4	chr1:220378800-220398200	Weak transcription	Small Intestine	intestine
5	chr1:220379000-220418200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:220379200-220400400	Weak transcription	Right Ventricle	heart
7	chr1:220379200-220409600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:220379200-220410800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr1:220379200-220422600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr1:220380400-220398200	Weak transcription	Brain Anterior Caudate	brain
11	chr1:220380400-220400800	Weak transcription	Spleen	Spleen
12	chr1:220381200-220422000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:220384000-220399400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:220384200-220398200	Weak transcription	Aorta	Aorta
15	chr1:220384200-220398200	Weak transcription	Stomach Smooth Muscle	stomach
16	chr1:220384200-220398600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr1:220384200-220398800	Weak transcription	Fetal Intestine Small	intestine
18	chr1:220384200-220400000	Weak transcription	Pancreas	Pancrea
19	chr1:220384200-220400200	Weak transcription	Fetal Muscle Leg	muscle
20	chr1:220384200-220400400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr1:220384200-220402800	Weak transcription	NHLF	lung
22	chr1:220384200-220404400	Weak transcription	Ovary	ovary
23	chr1:220384200-220408800	Weak transcription	A549	lung
24	chr1:220384200-220420600	Weak transcription	Fetal Kidney	kidney
25	chr1:220384200-220423000	Weak transcription	Esophagus	oesophagus
26	chr1:220384200-220425800	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr1:220384400-220398200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr1:220384400-220400200	Weak transcription	Fetal Muscle Trunk	muscle
29	chr1:220384400-220413400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr1:220384800-220398000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr1:220384800-220398200	Weak transcription	Rectal Smooth Muscle	rectum
32	chr1:220384800-220398800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:220384800-220398800	Weak transcription	Fetal Intestine Large	intestine
34	chr1:220384800-220399000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr1:220384800-220399000	Weak transcription	Colonic Mucosa	Colon
36	chr1:220384800-220400000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:220384800-220400000	Weak transcription	Left Ventricle	heart
38	chr1:220384800-220400800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr1:220384800-220401000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:220384800-220401800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr1:220384800-220404400	Weak transcription	HSMMtube	muscle
42	chr1:220384800-220408000	Weak transcription	Hela-S3	cervix
43	chr1:220384800-220417000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr1:220385000-220403400	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr1:220385000-220403800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr1:220385000-220405000	Weak transcription	Placenta	Placenta
47	chr1:220385200-220397800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr1:220385400-220398200	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr1:220385400-220409000	Weak transcription	NH-A	brain
50	chr1:220385400-220419400	Weak transcription	HUVEC	blood vessel

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