Variant report

Variant	esv2830098
Chromosome Location	chr1:227295716-227422234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:753)
CpG islands
(count:61)
Chromatin interactive
region (count:79)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:753 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:227358074-227358482	K562	blood:	n/a	n/a
2	ARID3A	chr1:227372087-227372239	K562	blood:	n/a	n/a
3	ARID3A	chr1:227361299-227361515	K562	blood:	n/a	n/a
4	ARID3A	chr1:227319080-227319280	K562	blood:	n/a	n/a
5	ATF1	chr1:227357826-227358453	K562	blood:	n/a	n/a
6	ATF1	chr1:227413464-227413737	K562	blood:	n/a	n/a
7	BACH1	chr1:227363300-227363678	K562	blood:	n/a	n/a
8	BACH1	chr1:227404157-227404185	K562	blood:	n/a	n/a
9	BACH1	chr1:227418237-227418332	K562	blood:	n/a	n/a
10	BACH1	chr1:227379815-227380280	K562	blood:	n/a	n/a
11	BACH1	chr1:227379784-227380406	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr1:227379385-227379648	GM12878	blood:	n/a	n/a
13	BATF	chr1:227379413-227379619	GM12878	blood:	n/a	n/a
14	BATF	chr1:227315567-227315918	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:227357092-227357408	K562	blood:	n/a	n/a
16	BHLHE40	chr1:227410896-227410905	K562	blood:	n/a	n/a
17	BRCA1	chr1:227319002-227319254	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr1:227413255-227413986	HCT-116	colon:	n/a	n/a
19	CCNT2	chr1:227401058-227401258	K562	blood:	n/a	n/a
20	CCNT2	chr1:227358183-227358571	K562	blood:	n/a	n/a
21	CCNT2	chr1:227334421-227334611	K562	blood:	n/a	n/a
22	CEBPB	chr1:227338717-227338920	HepG2	liver:	n/a	chr1:227338774-227338785
23	CEBPB	chr1:227346510-227346825	K562	blood:	n/a	n/a
24	CEBPB	chr1:227413356-227413930	HCT-116	colon:	n/a	n/a
25	CEBPB	chr1:227380998-227381251	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:227336277-227336518	K562	blood:	n/a	n/a
27	CEBPB	chr1:227346511-227346813	A549	lung:	n/a	n/a
28	CEBPB	chr1:227403870-227404070	K562	blood:	n/a	n/a
29	CEBPB	chr1:227338614-227338940	K562	blood:	n/a	chr1:227338774-227338785
30	CEBPB	chr1:227322718-227323063	K562	blood:	n/a	n/a
31	CEBPB	chr1:227319032-227319072	K562	blood:	n/a	n/a
32	CEBPB	chr1:227346500-227346801	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:227336332-227336521	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:227413291-227413878	IMR90	lung:	n/a	n/a
35	CEBPB	chr1:227398410-227398629	HepG2	liver:	n/a	n/a
36	CEBPB	chr1:227346535-227346798	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:227413379-227413890	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr1:227378050-227378326	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:227399543-227399575	HepG2	liver:	n/a	chr1:227399552-227399563
40	CEBPB	chr1:227361781-227362125	IMR90	lung:	n/a	n/a
41	CEBPB	chr1:227381046-227381285	A549	lung:	n/a	n/a
42	CEBPB	chr1:227413496-227413884	K562	blood:	n/a	n/a
43	CEBPB	chr1:227381130-227381159	K562	blood:	n/a	n/a
44	CEBPB	chr1:227413524-227413816	K562	blood:	n/a	n/a
45	CEBPB	chr1:227413355-227413962	HCT-116	colon:	n/a	n/a
46	CEBPB	chr1:227375229-227375258	A549	lung:	n/a	n/a
47	CEBPB	chr1:227318964-227319214	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:227382927-227383043	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:227375213-227375374	HepG2	liver:	n/a	chr1:227375280-227375291
50	CEBPB	chr1:227346577-227346829	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:227327429-227327479	HL-60	blood:	n/a
2	chr1:227327429-227327479	SKMC	muscle:	n/a
3	chr1:227327429-227327479	H1-hESC	embryonic stem cell:	embryo
4	chr1:227327429-227327479	NHBE	bronchial:	n/a
5	chr1:227327429-227327479	U87	brain:	n/a
6	chr1:227327429-227327479	HIPEpiC	eye:	n/a
7	chr1:227327429-227327479	PrEC	prostate:	n/a
8	chr1:227327429-227327479	PANC-1	pancreas:	n/a
9	chr1:227327429-227327479	NB4	blood:	n/a
10	chr1:227327429-227327479	HUVEC	blood vessel:	n/a
11	chr1:227327429-227327479	HEEpiC	esophagus:	n/a
12	chr1:227327429-227327479	A549	lung:	n/a
13	chr1:227327429-227327479	ovcar-3	ovarian:	n/a
14	chr1:227327429-227327479	NT2-D1	testis:	n/a
15	chr1:227327429-227327479	IMR90	lung:	fetal
16	chr1:227327429-227327479	CMK	blood:	n/a
17	chr1:227327429-227327479	HRPEpiC	eye:	n/a
18	chr1:227327429-227327479	AG10803	skin:	n/a
19	chr1:227327429-227327479	AG09319	gingival:	n/a
20	chr1:227327429-227327479	ECC-1	luminal epithelium:	n/a
21	chr1:227327429-227327479	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:227327429-227327479	HNPCEpiC	eye:	n/a
23	chr1:227327429-227327479	GM12878	blood:	n/a
24	chr1:227327429-227327479	SK-N-MC	brain:	n/a
25	chr1:227327429-227327479	Hela-S3	cervix:	n/a
26	chr1:227327429-227327479	AG04449	skin:	fetal
27	chr1:227327429-227327479	NHDF-neo	bronchial:	n/a
28	chr1:227327429-227327479	HEK293	kidney:	embryo
29	chr1:227327429-227327479	HCF	heart:	n/a
30	chr1:227327429-227327479	LNCaP	prostate:	n/a
31	chr1:227327429-227327479	HepG2	liver:	n/a
32	chr1:227327429-227327479	Caco-2	colon:	n/a
33	chr1:227327429-227327479	GM12892	blood:	n/a
34	chr1:227327429-227327479	HMEC	breast:	n/a
35	chr1:227327429-227327479	SK-N-SH_RA	brain:	n/a
36	chr1:227327429-227327479	SK-N-SH	brain:	n/a
37	chr1:227327429-227327479	ProgFib	skin:	n/a
38	chr1:227327429-227327479	GM06990	blood:	n/a
39	chr1:227327429-227327479	K562	blood:	n/a
40	chr1:227327429-227327479	HCPEpiC	choroid plexus:	n/a
41	chr1:227327429-227327479	HAEpiC	amniotic membrane:	n/a
42	chr1:227327429-227327479	AG09309	skin:	n/a
43	chr1:227327429-227327479	HRE	kidney:	n/a
44	chr1:227327429-227327479	AG04450	lung:	fetal
45	chr1:227327429-227327479	GM19239	blood:	n/a
46	chr1:227327429-227327479	GM12891	blood:	n/a
47	chr1:227327429-227327479	NH-A	brain:	n/a
48	chr1:227327429-227327479	AoSMC	blood vessel:	n/a
49	chr1:227327429-227327479	HRCEpiC	kidney:	n/a
50	chr1:227327429-227327479	RPTEC	kidney:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:227318905..227319442-chr1:227625175..227625871,2	MCF-7	breast:
2	chr1:227314587..227318154-chr1:227324311..227326852,3	MCF-7	breast:
3	chr1:227314492..227316043-chr1:227318628..227320566,2	K562	blood:
4	chr1:227127149..227129305-chr1:227309091..227310783,2	MCF-7	breast:
5	chr1:227402647..227405396-chr1:227406531..227409406,3	K562	blood:
6	chr1:227312511..227315121-chr1:227315946..227317817,2	K562	blood:
7	chr1:227396969..227399919-chr1:227412592..227414970,2	MCF-7	breast:
8	chr1:227361245..227362795-chr1:227368024..227369819,2	K562	blood:
9	chr1:227314492..227316043-chr1:227318628..227320566,2	K562	blood:
10	chr1:227361245..227362795-chr1:227368024..227369819,2	K562	blood:
11	chr1:227319022..227319798-chr1:227635073..227635816,2	MCF-7	breast:
12	chr1:227373675..227376391-chr1:227377073..227380557,3	K562	blood:
13	chr1:227365251..227367190-chr1:227371984..227375259,3	K562	blood:
14	chr1:227405924..227407789-chr1:227409135..227411231,2	K562	blood:
15	chr1:227422234..227422915-chr1:227623464..227624323,2	MCF-7	breast:
16	chr1:227316215..227319084-chr1:227324943..227327660,2	K562	blood:
17	chr1:227411051..227412753-chr1:227415183..227417286,2	MCF-7	breast:
18	chr1:227316215..227319084-chr1:227324943..227327660,2	K562	blood:
19	chr1:227357663..227359363-chr1:227504376..227506174,2	K562	blood:
20	chr1:227100489..227101122-chr1:227314586..227315189,2	MCF-7	breast:
21	chr1:227421745..227423708-chr1:227616261..227618228,2	MCF-7	breast:
22	chr1:227379953..227381548-chr1:227386329..227389074,2	K562	blood:
23	chr1:227373675..227376391-chr1:227377073..227380557,3	K562	blood:
24	chr1:227379953..227381548-chr1:227386329..227389074,2	K562	blood:
25	chr1:227315023..227317648-chr1:227321044..227323168,2	K562	blood:
26	chr1:227356009..227359900-chr1:227368469..227370220,4	K562	blood:
27	chr1:227361494..227363417-chr1:227400194..227402831,2	K562	blood:
28	chr1:227356009..227359900-chr1:227368469..227370220,4	K562	blood:
29	chr1:227319066..227320904-chr1:227331310..227334061,2	K562	blood:
30	chr1:227365298..227367002-chr1:227505047..227506997,2	K562	blood:
31	chr1:227414219..227417070-chr1:227421056..227422767,2	K562	blood:
32	chr1:227125600..227128392-chr1:227333735..227336576,2	MCF-7	breast:
33	chr1:227361494..227363417-chr1:227400194..227402831,2	K562	blood:
34	chr1:227360407..227362745-chr1:227368024..227370354,2	K562	blood:
35	chr1:227288769..227292259-chr1:227294331..227298471,4	K562	blood:
36	chr1:227100305..227100846-chr1:227318760..227319399,2	MCF-7	breast:
37	chr1:227383751..227387113-chr1:227389765..227393443,4	K562	blood:
38	chr1:227383842..227386781-chr1:227388623..227390741,2	K562	blood:
39	chr1:227315023..227317648-chr1:227321044..227323168,2	K562	blood:
40	chr1:227319086..227319624-chr1:227625143..227626016,2	K562	blood:
41	chr1:227411051..227412753-chr1:227415183..227417286,2	MCF-7	breast:
42	chr1:227327635..227329514-chr1:227357311..227359633,2	K562	blood:
43	chr1:227405924..227407789-chr1:227409135..227411231,2	K562	blood:
44	chr1:227344361..227346262-chr1:227357856..227360838,2	K562	blood:
45	chr1:227402647..227405396-chr1:227406531..227409406,3	K562	blood:
46	chr1:227400709..227402426-chr1:227403946..227405462,2	K562	blood:
47	chr1:227319076..227321131-chr1:227322486..227324185,2	K562	blood:
48	chr1:227360994..227362712-chr1:227365141..227367307,2	K562	blood:
49	chr1:227314587..227318154-chr1:227324311..227326852,3	MCF-7	breast:
50	chr1:227383842..227386781-chr1:227388623..227390741,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADCK3-6	chr1:227421970-227422486	NONHSAT009917
2	lnc-ADCK3-2	chr1:227370568-227371145	ENSG00000228625.1
3	lnc-ADCK3-2	chr1:227368150-227368283	ENSG00000228625.1
4	lnc-ITPKB-3	chr1:227297151-227297275	NONHSAT009914
5	lnc-ADCK3-2	chr1:227366034-227366135	ENSG00000228625.1

No data

Variant related genes	Relation type
CDC42BPA	TF binding region
ENSG00000228729	TF binding region
ENSG00000228625	TF binding region
CDC42BPA	CpG island
ENSG00000228729	CpG island
ENSG00000228625	CpG island
ENSG00000143776	chromatin interactions
ENSG00000242757	chromatin interactions
ENSG00000228729	chromatin interactions
ENSG00000163050	chromatin interactions
ENSG00000228625	chromatin interactions

Extended variants
information (count: 4905 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4905 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6664803	chr1:227295716-227295717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142688824	chr1:227295741-227295742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541820335	chr1:227295890-227295891	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188487217	chr1:227295899-227295900	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544879774	chr1:227295912-227295913	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375543239	chr1:227295934-227295935	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs559835379	chr1:227295942-227295943	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563681067	chr1:227295982-227295983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72748192	chr1:227296009-227296010	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs549257929	chr1:227296018-227296019	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs566953867	chr1:227296045-227296046	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs477373	chr1:227296082-227296083	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs148035994	chr1:227296110-227296111	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs531094672	chr1:227296119-227296120	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549334677	chr1:227296120-227296121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61836470	chr1:227296123-227296124	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112620261	chr1:227296125-227296126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs141184111	chr1:227296133-227296134	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150740177	chr1:227296153-227296154	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567043775	chr1:227296159-227296160	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35006467	chr1:227296161-227296162	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552767386	chr1:227296188-227296189	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147074189	chr1:227296266-227296267	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534269767	chr1:227296274-227296275	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs583729	chr1:227296300-227296301	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192158906	chr1:227296302-227296303	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544632488	chr1:227296329-227296330	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs183876887	chr1:227296354-227296355	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12404627	chr1:227296369-227296370	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545475591	chr1:227296384-227296385	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564546661	chr1:227296437-227296438	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs188650740	chr1:227296525-227296526	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115337938	chr1:227296531-227296532	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs560866035	chr1:227296548-227296549	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs367911270	chr1:227296555-227296556	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533698138	chr1:227296557-227296558	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139121040	chr1:227296585-227296586	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs482032	chr1:227296587-227296588	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs386639938	chr1:227296624-227296625	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs79424821	chr1:227296626-227296627	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs34413773	chr1:227296681-227296682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566979461	chr1:227296691-227296692	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534387210	chr1:227296698-227296699	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs191250331	chr1:227296715-227296716	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184673977	chr1:227296744-227296745	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189188369	chr1:227296751-227296752	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559830166	chr1:227296810-227296811	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374927073	chr1:227296811-227296812	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs567981418	chr1:227296877-227296878	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs538499605	chr1:227296882-227296883	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
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
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
Breast cancer	17603634	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
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Basal cell lymphoma	17053054	CNVD
Autism	14699429	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Fumarase deficiency	21572526	CNVD
Autism	17483303	CNVD
Kartagener syndrome	16639409	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:227209200-227301600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:227214800-227329200	Weak transcription	Right Ventricle	heart
3	chr1:227247400-227299800	Weak transcription	HMEC	breast
4	chr1:227251000-227300000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:227257800-227312200	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:227259400-227349000	Weak transcription	Colonic Mucosa	Colon
7	chr1:227271800-227299600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:227272800-227331000	Weak transcription	Lung	lung
9	chr1:227273000-227312400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr1:227275800-227302600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr1:227277200-227302600	Weak transcription	Brain Substantia Nigra	brain
12	chr1:227279800-227299000	Weak transcription	Placenta	Placenta
13	chr1:227280800-227298800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:227282600-227318000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:227285600-227297600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr1:227285600-227308600	Weak transcription	Pancreas	Pancrea
17	chr1:227285600-227313800	Weak transcription	Gastric	stomach
18	chr1:227286400-227328200	Weak transcription	Brain Germinal Matrix	brain
19	chr1:227287400-227360800	Weak transcription	Psoas Muscle	Psoas
20	chr1:227288000-227326400	Weak transcription	A549	lung
21	chr1:227288200-227296400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr1:227288200-227332400	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr1:227288400-227297600	Weak transcription	NH-A	brain
24	chr1:227288400-227299400	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:227288400-227299400	Weak transcription	Ovary	ovary
26	chr1:227288400-227299600	Weak transcription	Brain Cingulate Gyrus	brain
27	chr1:227288400-227299600	Weak transcription	Osteobl	bone
28	chr1:227288400-227302200	Weak transcription	Fetal Brain Male	brain
29	chr1:227288400-227343000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr1:227288400-227398000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr1:227288600-227296200	Weak transcription	K562	blood
32	chr1:227288600-227298600	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr1:227288600-227298600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr1:227288600-227298800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:227288600-227299200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:227288600-227299200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:227288600-227299200	Weak transcription	Aorta	Aorta
38	chr1:227288600-227299200	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr1:227288600-227299400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr1:227288600-227299600	Weak transcription	Brain Anterior Caudate	brain
41	chr1:227288600-227310800	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr1:227288600-227312200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr1:227288600-227313000	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr1:227288600-227316000	Weak transcription	Fetal Muscle Trunk	muscle
45	chr1:227288600-227328200	Weak transcription	Fetal Stomach	stomach
46	chr1:227288600-227332400	Weak transcription	NHLF	lung
47	chr1:227288600-227333600	Weak transcription	Esophagus	oesophagus
48	chr1:227288800-227299600	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr1:227288800-227317200	Weak transcription	NHEK	skin
50	chr1:227288800-227330000	Weak transcription	NHDF-Ad	bronchial

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