Variant report

Variant	esv3385958
Chromosome Location	chr1:226117875-226149657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:672)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:262 , 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	chr1:226131440-226131631	K562	blood:	n/a	n/a
2	ARID3A	chr1:226119091-226119687	K562	blood:	n/a	n/a
3	ATF1	chr1:226131403-226131435	K562	blood:	n/a	n/a
4	ATF1	chr1:226119026-226119614	K562	blood:	n/a	n/a
5	ATF3	chr1:226129380-226129628	K562	blood:	n/a	chr1:226129557-226129577 chr1:226129557-226129566 chr1:226129546-226129566
6	BHLHE40	chr1:226118987-226119780	K562	blood:	n/a	n/a
7	BHLHE40	chr1:226123937-226124137	HepG2	liver:	n/a	n/a
8	BHLHE40	chr1:226130286-226130602	GM12878	blood:	n/a	n/a
9	BHLHE40	chr1:226129384-226129726	HepG2	liver:	n/a	chr1:226129551-226129572 chr1:226129556-226129565 chr1:226129557-226129566 chr1:226129557-226129566 chr1:226129555-226129568 chr1:226129558-226129567
10	BHLHE40	chr1:226129542-226129645	GM12878	blood:	n/a	chr1:226129551-226129572 chr1:226129556-226129565 chr1:226129557-226129566 chr1:226129557-226129566 chr1:226129555-226129568 chr1:226129558-226129567
11	BHLHE40	chr1:226138867-226139012	K562	blood:	n/a	n/a
12	BHLHE40	chr1:226129350-226129876	K562	blood:	n/a	chr1:226129551-226129572 chr1:226129556-226129565 chr1:226129557-226129566 chr1:226129557-226129566 chr1:226129555-226129568 chr1:226129558-226129567
13	CBX3	chr1:226131233-226131676	K562	blood:	n/a	n/a
14	CBX3	chr1:226131336-226131617	K562	blood:	n/a	n/a
15	CBX3	chr1:226118728-226119700	K562	blood:	n/a	n/a
16	CCNT2	chr1:226118974-226119424	K562	blood:	n/a	n/a
17	CEBPB	chr1:226133369-226133641	H1-hESC	embryonic stem cell:	n/a	chr1:226133487-226133498 chr1:226133487-226133498
18	CEBPB	chr1:226133480-226133566	K562	blood:	n/a	chr1:226133487-226133498 chr1:226133487-226133498
19	CEBPB	chr1:226145299-226145486	K562	blood:	n/a	n/a
20	CEBPB	chr1:226143821-226143992	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:226122772-226122880	HepG2	liver:	n/a	chr1:226122816-226122829 chr1:226122813-226122830
22	CEBPB	chr1:226122674-226122959	K562	blood:	n/a	chr1:226122816-226122829 chr1:226122813-226122830
23	CEBPB	chr1:226122599-226122957	K562	blood:	n/a	chr1:226122816-226122829 chr1:226122813-226122830
24	CEBPB	chr1:226120820-226121130	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:226144492-226144628	K562	blood:	n/a	n/a
26	CEBPD	chr1:226118890-226119499	K562	blood:	n/a	n/a
27	CHD2	chr1:226119020-226119470	K562	blood:	n/a	n/a
28	CHD2	chr1:226130436-226130532	GM12878	blood:	n/a	n/a
29	CTBP2	chr1:226138444-226139107	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:226143000-226143022	GM10266	blood:	n/a	n/a
31	CTCF	chr1:226138820-226138970	BE2_C	brain:	n/a	chr1:226138926-226138935
32	CTCF	chr1:226118962-226119059	GM20000	blood:	n/a	n/a
33	CTCF	chr1:226138947-226138993	K562	blood:	n/a	n/a
34	CTCF	chr1:226143320-226143470	GM12864	blood:	n/a	n/a
35	CTCF	chr1:226138860-226139010	HepG2	liver:	n/a	chr1:226138926-226138935
36	CTCF	chr1:226143280-226143430	GM12864	blood:	n/a	n/a
37	CTCF	chr1:226132920-226133070	GM12874	blood:	n/a	n/a
38	CTCF	chr1:226127115-226127156	GM12891	blood:	n/a	n/a
39	CTCF	chr1:226127822-226127850	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:226143246-226143462	K562	blood:	n/a	n/a
41	CTCF	chr1:226138840-226138990	K562	blood:	n/a	chr1:226138926-226138935
42	CTCF	chr1:226138840-226138990	HepG2	liver:	n/a	chr1:226138926-226138935
43	CTCF	chr1:226143240-226143390	HepG2	liver:	n/a	n/a
44	CTCF	chr1:226143280-226143430	GM12873	blood:	n/a	n/a
45	CTCF	chr1:226143285-226143425	K562	blood:	n/a	n/a
46	CTCF	chr1:226143220-226143370	GM12873	blood:	n/a	n/a
47	CTCF	chr1:226143300-226143450	GM12869	blood:	n/a	n/a
48	CTCF	chr1:226143340-226143490	GM12864	blood:	n/a	n/a
49	CTCF	chr1:226127697-226127797	GM13976	blood:	n/a	n/a
50	CTCF	chr1:226127026-226127358	H1-hESC	embryonic stem cell:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:226129481-226129531	SK-N-SH	brain:	n/a
2	chr1:226129481-226129531	SK-N-SH	brain:	n/a
3	chr1:226128626-226128676	HCF	heart:	n/a
4	chr1:226129481-226129531	RPTEC	kidney:	n/a
5	chr1:226127694-226127744	HCM	heart:	n/a
6	chr1:226127290-226127340	HL-60	blood:	n/a
7	chr1:226127290-226127340	GM12878	blood:	n/a
8	chr1:226126862-226126912	T-47D	breast:	n/a
9	chr1:226129561-226129611	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:226127694-226127744	AG10803	skin:	n/a
11	chr1:226130366-226130416	ECC-1	luminal epithelium:	n/a
12	chr1:226124569-226124619	AG04449	skin:	fetal
13	chr1:226129481-226129531	PFSK-1	brain:	n/a
14	chr1:226127113-226127163	ProgFib	skin:	n/a
15	chr1:226129481-226129531	HRE	kidney:	n/a
16	chr1:226126862-226126912	GM12891	blood:	n/a
17	chr1:226130366-226130416	RPTEC	kidney:	n/a
18	chr1:226128626-226128676	CMK	blood:	n/a
19	chr1:226127113-226127163	NB4	blood:	n/a
20	chr1:226126862-226126912	HPAEpiC	pulmonary alveolar:	n/a
21	chr1:226128626-226128676	ECC-1	luminal epithelium:	n/a
22	chr1:226127113-226127163	PFSK-1	brain:	n/a
23	chr1:226127290-226127340	HRCEpiC	kidney:	n/a
24	chr1:226129561-226129611	GM06990	blood:	n/a
25	chr1:226127290-226127340	AG09319	gingival:	n/a
26	chr1:226129481-226129531	AoSMC	blood vessel:	n/a
27	chr1:226124569-226124619	HEEpiC	esophagus:	n/a
28	chr1:226128626-226128676	AoSMC	blood vessel:	n/a
29	chr1:226129561-226129611	HepG2	liver:	n/a
30	chr1:226130366-226130416	HIPEpiC	eye:	n/a
31	chr1:226128626-226128676	ProgFib	skin:	n/a
32	chr1:226130366-226130416	NT2-D1	testis:	n/a
33	chr1:226128626-226128676	AG04449	skin:	fetal
34	chr1:226130366-226130416	Hela-S3	cervix:	n/a
35	chr1:226130366-226130416	GM12891	blood:	n/a
36	chr1:226129824-226129874	HEK293	kidney:	embryo
37	chr1:226127113-226127163	Caco-2	colon:	n/a
38	chr1:226127113-226127163	HAEpiC	amniotic membrane:	n/a
39	chr1:226130366-226130416	HUVEC	blood vessel:	n/a
40	chr1:226124569-226124619	NT2-D1	testis:	n/a
41	chr1:226127290-226127340	AG09309	skin:	n/a
42	chr1:226124569-226124619	HCM	heart:	n/a
43	chr1:226129824-226129874	AG09309	skin:	n/a
44	chr1:226126862-226126912	IMR90	lung:	fetal
45	chr1:226127113-226127163	ECC-1	luminal epithelium:	n/a
46	chr1:226127290-226127340	AoSMC	blood vessel:	n/a
47	chr1:226129824-226129874	BJ	skin:	n/a
48	chr1:226129561-226129611	AG04450	lung:	fetal
49	chr1:226126862-226126912	U87	brain:	n/a
50	chr1:226126862-226126912	HEEpiC	esophagus:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:226141982..226145434-chr1:226148441..226150785,5	K562	blood:
2	chr1:226108026..226109867-chr1:226122182..226124487,2	K562	blood:
3	chr1:226131302..226133654-chr1:226147607..226150224,2	K562	blood:
4	chr1:226141982..226145141-chr1:226147810..226150785,4	K562	blood:
5	chr1:226096836..226099303-chr1:226126858..226129548,2	K562	blood:
6	chr1:226080382..226082754-chr1:226132657..226134532,2	K562	blood:
7	chr1:226055732..226058409-chr1:226119393..226121117,2	K562	blood:
8	chr1:226131302..226133654-chr1:226147607..226150224,2	K562	blood:
9	chr1:226103278..226105384-chr1:226143217..226145668,2	K562	blood:
10	chr1:226109718..226113155-chr1:226118910..226121755,3	K562	blood:
11	chr1:226141982..226145434-chr1:226148441..226150785,5	K562	blood:
12	chr1:226131582..226134772-chr1:226137252..226139972,3	K562	blood:
13	chr1:226115016..226118116-chr1:226129058..226132265,3	K562	blood:
14	chr1:226132398..226133993-chr1:226259835..226261737,2	K562	blood:
15	chr1:226141982..226145141-chr1:226147810..226150785,4	K562	blood:
16	chr1:225974348..225976521-chr1:226121252..226124139,2	K562	blood:
17	chr1:226131824..226133632-chr1:226138472..226140922,2	K562	blood:
18	chr1:226109266..226111565-chr1:226131902..226133596,2	K562	blood:
19	chr1:226145697..226148596-chr1:226148752..226151369,2	K562	blood:
20	chr1:226147096..226148688-chr1:226148752..226150265,2	K562	blood:
21	chr1:226119249..226122725-chr1:226127061..226129247,3	K562	blood:
22	chr1:226147096..226148688-chr1:226148752..226150265,2	K562	blood:
23	chr1:226110303..226113969-chr1:226129213..226132274,3	MCF-7	breast:
24	chr1:226145697..226148596-chr1:226148752..226151369,2	K562	blood:
25	chr1:226106739..226108269-chr1:226135055..226137378,2	K562	blood:
26	chr1:226133155..226134935-chr1:226134938..226137202,2	K562	blood:
27	chr1:225668021..225670369-chr1:226148124..226150238,2	MCF-7	breast:
28	chr1:226141035..226142644-chr1:226145004..226147535,2	K562	blood:
29	chr1:226070080..226072229-chr1:226145455..226147029,2	K562	blood:
30	chr1:226131582..226134772-chr1:226137252..226139972,3	K562	blood:
31	chr1:226141035..226142644-chr1:226145004..226147535,2	K562	blood:
32	chr1:226110665..226113538-chr1:226134928..226137142,2	K562	blood:
33	chr1:225824935..225826508-chr1:226133985..226136055,2	K562	blood:
34	chr1:226127800..226129740-chr1:226134309..226137044,3	K562	blood:
35	chr1:226070563..226073306-chr1:226118336..226120549,2	K562	blood:
36	chr1:226133155..226134935-chr1:226134938..226137202,2	K562	blood:
37	chr1:226069198..226071720-chr1:226149361..226151916,2	MCF-7	breast:
38	chr1:226147735..226150048-chr1:226187163..226189644,2	K562	blood:
39	chr1:226119019..226120944-chr1:226187286..226188826,2	K562	blood:
40	chr1:226128883..226131588-chr1:226148529..226150758,3	K562	blood:
41	chr1:226107771..226111419-chr1:226132837..226135522,3	MCF-7	breast:
42	chr1:226148548..226150301-chr1:226188144..226190996,2	K562	blood:
43	chr1:226131824..226133632-chr1:226138472..226140922,2	K562	blood:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	LEFTY2	hsa-miR-302a-3p	chr1:226124963-226124988
2	LEFTY2	hsa-miR-302d-3p	chr1:226124963-226124986
3	LEFTY2	hsa-miR-302a-3p	chr1:226124969-226124962
4	LEFTY2	hsa-miR-302d-3p	chr1:226124969-226124962

Variant related genes	Relation type
ENSG00000248322	TF binding region
NDUFA3P3	TF binding region
LEFTY2	TF binding region
ENSG00000248322	CpG island
NDUFA3P3	CpG island
LEFTY2	CpG island
ENSG00000143768	chromatin interactions
ENSG00000196187	chromatin interactions
ENSG00000143811	chromatin interactions
ENSG00000243709	chromatin interactions

Extended variants
information (count: 1189 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74189679	chr1:226117921-226117922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs200754358	chr1:226117928-226117929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs578073350	chr1:226117931-226117932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs367782265	chr1:226117942-226117943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs554256436	chr1:226117945-226117946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572476236	chr1:226117960-226117961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs543302507	chr1:226117962-226117963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs571463294	chr1:226117969-226117970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61835187	chr1:226117976-226117977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372381764	chr1:226117992-226117993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs61835188	chr1:226118013-226118014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189325005	chr1:226118035-226118036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs373515985	chr1:226118056-226118057	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs376370049	chr1:226118061-226118062	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375580999	chr1:226118063-226118064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs370983096	chr1:226118067-226118068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs76927821	chr1:226118072-226118073	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575656162	chr1:226118091-226118092	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564815351	chr1:226118095-226118096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532276468	chr1:226118159-226118160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549008030	chr1:226118202-226118203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139087562	chr1:226118203-226118204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181981175	chr1:226118204-226118205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs529654848	chr1:226118207-226118208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548052111	chr1:226118213-226118214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544880613	chr1:226118214-226118215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563074255	chr1:226118333-226118334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75753793	chr1:226118336-226118337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542968839	chr1:226118356-226118357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200305035	chr1:226118357-226118358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs199992866	chr1:226118364-226118365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141547822	chr1:226118383-226118384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542081418	chr1:226118387-226118388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147103743	chr1:226118406-226118407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10915901	chr1:226118468-226118469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs368773938	chr1:226118553-226118554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77353856	chr1:226118772-226118773	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs34338801	chr1:226118798-226118799	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs375533778	chr1:226118891-226118892	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs187315825	chr1:226119005-226119006	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369829160	chr1:226119021-226119022	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143609186	chr1:226119046-226119047	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548013326	chr1:226119047-226119048	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs559667189	chr1:226119051-226119052	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs59087995	chr1:226119057-226119058	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs555283537	chr1:226119074-226119075	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs58429683	chr1:226119110-226119111	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543647235	chr1:226119124-226119125	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565427829	chr1:226119127-226119128	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs10915902	chr1:226119236-226119237	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:90)

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
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:226112600-226125200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:226112600-226126800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr1:226112600-226126800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr1:226112800-226120800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:226112800-226126800	Weak transcription	Right Atrium	heart
6	chr1:226113000-226124000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:226113000-226124400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr1:226113800-226118200	Enhancers	Primary T cells fromperipheralblood	blood
9	chr1:226114600-226120600	Weak transcription	Osteobl	bone
10	chr1:226114800-226118800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr1:226114800-226127000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr1:226116200-226118600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:226116400-226124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr1:226116600-226126800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr1:226117200-226118400	Weak transcription	Fetal Thymus	thymus
16	chr1:226117400-226118800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr1:226117600-226118000	Weak transcription	K562	blood
18	chr1:226117600-226118200	Weak transcription	Primary T cells from cord blood	blood
19	chr1:226118000-226118600	Enhancers	K562	blood
20	chr1:226118400-226118600	Enhancers	Fetal Thymus	thymus
21	chr1:226118400-226119000	Enhancers	Brain Germinal Matrix	brain
22	chr1:226118600-226119000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:226118600-226119600	Flanking Active TSS	K562	blood
24	chr1:226118800-226119000	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr1:226118800-226119000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr1:226118800-226119600	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:226118800-226119800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:226119200-226119400	Enhancers	Primary T cells from cord blood	blood
29	chr1:226119600-226121000	Enhancers	K562	blood
30	chr1:226120600-226121000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr1:226120600-226121000	Enhancers	NHEK	skin
32	chr1:226120600-226121400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr1:226120600-226121400	Enhancers	HMEC	breast
34	chr1:226120600-226121400	Enhancers	Osteobl	bone
35	chr1:226120800-226121000	Enhancers	NHDF-Ad	bronchial
36	chr1:226120800-226121200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr1:226120800-226121400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:226121000-226122400	Weak transcription	K562	blood
39	chr1:226121000-226123800	Weak transcription	NHEK	skin
40	chr1:226121000-226124400	Weak transcription	NHDF-Ad	bronchial
41	chr1:226121400-226124000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr1:226121400-226124000	Weak transcription	HMEC	breast
43	chr1:226121400-226124400	Weak transcription	Osteobl	bone
44	chr1:226122400-226122600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:226122400-226123000	Enhancers	K562	blood
46	chr1:226122600-226124000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr1:226123000-226124400	Weak transcription	K562	blood
48	chr1:226124000-226124200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:226124000-226124200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:226124000-226124200	Enhancers	NHEK	skin

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