Variant report

Variant	nsv1013149
Chromosome Location	chr1:224605943-224646382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1695)
CpG islands
(count:1161)
Chromatin interactive
region (count:89)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1695 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:224645254-224645558	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:224645169-224645579	K562	blood:	n/a	n/a
3	ARID3A	chr1:224622583-224622912	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:224618223-224618880	K562	blood:	n/a	n/a
5	ARID3A	chr1:224620759-224620996	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:224619341-224619938	K562	blood:	n/a	n/a
7	ARID3A	chr1:224620424-224621189	K562	blood:	n/a	n/a
8	ARID3A	chr1:224618196-224618854	HepG2	liver:	n/a	n/a
9	ATF1	chr1:224643837-224643924	K562	blood:	n/a	n/a
10	ATF1	chr1:224622366-224622719	K562	blood:	n/a	chr1:224622509-224622523
11	ATF2	chr1:224622365-224622818	GM12878	blood:	n/a	chr1:224622509-224622523
12	ATF2	chr1:224622416-224622736	GM12878	blood:	n/a	chr1:224622509-224622523
13	ATF2	chr1:224618211-224618596	GM12878	blood:	n/a	n/a
14	ATF3	chr1:224622360-224622709	K562	blood:	n/a	n/a
15	BACH1	chr1:224616627-224616646	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:224616585-224616694	K562	blood:	n/a	n/a
17	BATF	chr1:224618241-224618506	GM12878	blood:	n/a	n/a
18	BCL3	chr1:224622320-224623145	A549	lung:	n/a	chr1:224623074-224623082
19	BCL3	chr1:224622354-224622895	GM12878	blood:	n/a	n/a
20	BCL3	chr1:224622392-224623095	A549	lung:	n/a	chr1:224623074-224623082
21	BCLAF1	chr1:224618169-224618669	GM12878	blood:	n/a	n/a
22	BCLAF1	chr1:224622335-224623088	GM12878	blood:	n/a	chr1:224623074-224623082
23	BHLHE40	chr1:224620832-224620992	K562	blood:	n/a	n/a
24	BHLHE40	chr1:224622416-224622865	A549	lung:	n/a	n/a
25	BHLHE40	chr1:224622399-224623256	HepG2	liver:	n/a	n/a
26	BHLHE40	chr1:224622385-224623559	K562	blood:	n/a	n/a
27	BHLHE40	chr1:224622453-224622706	HepG2	liver:	n/a	n/a
28	BHLHE40	chr1:224622348-224623339	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:224644939-224645377	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:224644666-224645064	K562	blood:	n/a	n/a
31	BHLHE40	chr1:224645288-224645457	K562	blood:	n/a	n/a
32	BRCA1	chr1:224645230-224645603	Hela-S3	cervix:	n/a	chr1:224645575-224645582
33	BRCA1	chr1:224620897-224621113	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr1:224622425-224622722	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr1:224621935-224621958	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr1:224622995-224623460	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr1:224622533-224622818	GM12878	blood:	n/a	n/a
38	CBX3	chr1:224618244-224618862	K562	blood:	n/a	n/a
39	CBX3	chr1:224622348-224623594	K562	blood:	n/a	n/a
40	CBX3	chr1:224620285-224621183	K562	blood:	n/a	n/a
41	CBX3	chr1:224622412-224622884	K562	blood:	n/a	n/a
42	CCNT2	chr1:224622321-224623532	K562	blood:	n/a	n/a
43	CCNT2	chr1:224621435-224622066	K562	blood:	n/a	chr1:224622028-224622037
44	CCNT2	chr1:224620087-224621007	K562	blood:	n/a	chr1:224620927-224620936
45	CEBPB	chr1:224643795-224643801	HepG2	liver:	n/a	n/a
46	CEBPB	chr1:224622758-224623267	ECC-1	luminal epithelium:	n/a	chr1:224622987-224622998
47	CEBPB	chr1:224622826-224623367	A549	lung:	n/a	chr1:224622987-224622998
48	CEBPB	chr1:224616406-224616672	K562	blood:	n/a	n/a
49	CEBPB	chr1:224622422-224623556	K562	blood:	n/a	chr1:224622987-224622998
50	CEBPB	chr1:224622488-224623350	H1-hESC	embryonic stem cell:	n/a	chr1:224622987-224622998

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:224621452-224621502	AG09319	gingival:	n/a
2	chr1:224622813-224622863	AG04450	lung:	fetal
3	chr1:224621452-224621502	AG09319	gingival:	n/a
4	chr1:224622813-224622863	AG04450	lung:	fetal
5	chr1:224620034-224620084	BE2_C	brain:	n/a
6	chr1:224620779-224620829	U87	brain:	n/a
7	chr1:224620806-224620856	HMEC	breast:	n/a
8	chr1:224622417-224622467	K562	blood:	n/a
9	chr1:224622516-224622566	GM19239	blood:	n/a
10	chr1:224622430-224622480	T-47D	breast:	n/a
11	chr1:224622417-224622467	SAEC	small airway:	n/a
12	chr1:224622516-224622566	NT2-D1	testis:	n/a
13	chr1:224622510-224622560	SAEC	small airway:	n/a
14	chr1:224622855-224622905	IMR90	lung:	fetal
15	chr1:224622417-224622467	Hepatocyte	liver:	n/a
16	chr1:224622516-224622566	GM12892	blood:	n/a
17	chr1:224622430-224622480	HCF	heart:	n/a
18	chr1:224622813-224622863	HEK293	kidney:	embryo
19	chr1:224621452-224621502	GM19239	blood:	n/a
20	chr1:224621880-224621930	PrEC	prostate:	n/a
21	chr1:224620806-224620856	HAEpiC	amniotic membrane:	n/a
22	chr1:224621880-224621930	AG10803	skin:	n/a
23	chr1:224622510-224622560	ProgFib	skin:	n/a
24	chr1:224622605-224622655	U87	brain:	n/a
25	chr1:224622430-224622480	NH-A	brain:	n/a
26	chr1:224621880-224621930	AoSMC	blood vessel:	n/a
27	chr1:224620034-224620084	NHDF-neo	bronchial:	n/a
28	chr1:224622516-224622566	HCF	heart:	n/a
29	chr1:224622813-224622863	T-47D	breast:	n/a
30	chr1:224622131-224622181	Caco-2	colon:	n/a
31	chr1:224622510-224622560	BJ	skin:	n/a
32	chr1:224620034-224620084	HCPEpiC	choroid plexus:	n/a
33	chr1:224621834-224621884	Hela-S3	cervix:	n/a
34	chr1:224622126-224622176	HAEpiC	amniotic membrane:	n/a
35	chr1:224621861-224621911	MCF-7	breast:	n/a
36	chr1:224621880-224621930	MCF10A-Er-Src	breast:	n/a
37	chr1:224622430-224622480	GM06990	blood:	n/a
38	chr1:224620779-224620829	SK-N-SH	brain:	n/a
39	chr1:224622598-224622648	HMEC	breast:	n/a
40	chr1:224621861-224621911	GM12878	blood:	n/a
41	chr1:224621834-224621884	MCF-7	breast:	n/a
42	chr1:224621452-224621502	GM12891	blood:	n/a
43	chr1:224622510-224622560	Caco-2	colon:	n/a
44	chr1:224621880-224621930	IMR90	lung:	fetal
45	chr1:224622813-224622863	GM12891	blood:	n/a
46	chr1:224644750-224644800	HepG2	liver:	n/a
47	chr1:224620806-224620856	HUVEC	blood vessel:	n/a
48	chr1:224620034-224620084	CMK	blood:	n/a
49	chr1:224621861-224621911	IMR90	lung:	fetal
50	chr1:224620806-224620856	GM19239	blood:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:224370348..224372775-chr1:224619496..224622200,4	K562	blood:
2	chr1:224627143..224628933-chr1:224633589..224638837,4	MCF-7	breast:
3	chr1:224607859..224609701-chr1:224614855..224617759,2	MCF-7	breast:
4	chr1:224636445..224639746-chr1:224642433..224645284,3	K562	blood:
5	chr1:224633115..224636329-chr1:224637747..224639820,3	K562	blood:
6	chr1:224637202..224641034-chr1:224641889..224644811,3	K562	blood:
7	chr1:224604661..224609524-chr1:224620120..224624801,9	MCF-7	breast:
8	chr1:224615678..224629188-chr1:224635437..224647951,56	MCF-7	breast:
9	chr1:224621190..224622071-chr1:224645300..224645919,2	MCF-7	breast:
10	chr1:224633115..224636329-chr1:224637747..224639820,3	K562	blood:
11	chr1:224610939..224613102-chr1:224621309..224623672,2	MCF-7	breast:
12	chr1:224629495..224631561-chr1:224643787..224646406,3	K562	blood:
13	chr1:224613670..224615210-chr1:224641405..224643090,2	MCF-7	breast:
14	chr1:224629495..224631561-chr1:224643787..224646406,3	K562	blood:
15	chr1:224621280..224621884-chr1:224644931..224645508,2	K562	blood:
16	chr1:224629011..224632657-chr1:224632773..224636127,4	K562	blood:
17	chr1:224624808..224626574-chr1:224690723..224692820,2	K562	blood:
18	chr1:223885488..223886561-chr1:224644979..224645876,5	K562	blood:
19	chr1:224617091..224617963-chr19:47729258..47729978,2	NB4	blood:
20	chr1:224623991..224626334-chr1:224637841..224639342,2	K562	blood:
21	chr1:224607158..224609951-chr1:224643885..224645714,2	K562	blood:
22	chr1:224369742..224372382-chr1:224618245..224620019,2	MCF-7	breast:
23	chr1:224622290..224622794-chr10:98591846..98592614,2	Hela-S3	cervix:
24	chr1:224620032..224622500-chr1:224629192..224631427,3	MCF-7	breast:
25	chr1:224627143..224628933-chr1:224633589..224638837,4	MCF-7	breast:
26	chr1:224641326..224643104-chr1:224643904..224646218,2	MCF-7	breast:
27	chr1:224633064..224636103-chr1:224643208..224646617,3	K562	blood:
28	chr1:224620202..224624138-chr1:224637608..224640207,3	MCF-7	breast:
29	chr1:224606906..224609708-chr1:224624793..224626933,3	MCF-7	breast:
30	chr1:224644724..224648422-chr1:224649777..224653927,3	K562	blood:
31	chr1:224595603..224601847-chr1:224621020..224623770,7	MCF-7	breast:
32	chr1:224640045..224642435-chr1:224680202..224683058,2	MCF-7	breast:
33	chr1:224629011..224632657-chr1:224632773..224636127,4	K562	blood:
34	chr1:224604963..224607322-chr1:224610128..224612873,2	MCF-7	breast:
35	chr1:224634502..224636379-chr1:224636698..224640995,4	K562	blood:
36	chr1:224370348..224372410-chr1:224620146..224621939,2	K562	blood:
37	chr1:224303666..224304411-chr1:224645043..224645567,2	K562	blood:
38	chr1:224607859..224609701-chr1:224614855..224617759,2	MCF-7	breast:
39	chr1:224602276..224606277-chr1:224608631..224611582,5	MCF-7	breast:
40	chr1:224238230..224238917-chr1:224645015..224645671,2	K562	blood:
41	chr1:224621761..224622518-chr1:224642077..224642647,2	MCF-7	breast:
42	chr1:224642182..224643861-chr1:225117106..225119317,2	MCF-7	breast:
43	chr1:224602276..224606277-chr1:224608631..224611582,5	MCF-7	breast:
44	chr1:224606906..224609708-chr1:224624793..224626933,3	MCF-7	breast:
45	chr1:224640725..224643210-chr1:224646698..224648571,2	K562	blood:
46	chr1:224637202..224641034-chr1:224641889..224644811,3	K562	blood:
47	chr1:224575555..224578052-chr1:224610141..224612570,2	MCF-7	breast:
48	chr1:224544325..224548164-chr1:224620481..224623704,4	K562	blood:
49	chr1:224634502..224636379-chr1:224636698..224640995,4	K562	blood:
50	chr1:224586518..224588836-chr1:224621196..224623489,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNIH3-2	chr1:224627334-224627476	NONHSAT009806
2	lnc-NVL-2	chr1:224624523-224624723	XLOC_001227
3	lnc-CNIH3-2	chr1:224624195-224624607	NONHSAT009806
4	lnc-CNIH3-2	chr1:224645272-224646480	NONHSAT009806
5	lnc-CNIH3-2	chr1:224644440-224644974	NONHSAT009806
6	lnc-CNIH3-2	chr1:224644385-224644623	NONHSAT009807
7	lnc-CNIH3-2	chr1:224645508-224646893	NONHSAT009808
8	lnc-CNIH3-2	chr1:224625685-224626248	NONHSAT009806
9	lnc-CNIH3-2	chr1:224623283-224623314	NONHSAT009806
10	lnc-CNIH3-2	chr1:224622627-224622889	NONHSAT009804
11	lnc-CNIH3-2	chr1:224622614-224622889	NONHSAT009803
12	lnc-CNIH3-2	chr1:224622362-224622564	NONHSAT009801
13	lnc-CNIH3-2	chr1:224629729-224630159	NONHSAT009806
14	lnc-CNIH3-2	chr1:224626494-224626907	NONHSAT009806
15	lnc-NVL-2	chr1:224623157-224623593	XLOC_001227
16	lnc-CNIH3-2	chr1:224622442-224622564	NONHSAT009802
17	lnc-CNIH3-2	chr1:224630165-224630269	NONHSAT009806
18	lnc-CNIH3-2	chr1:224626267-224626350	NONHSAT009806

No data

Variant related genes	Relation type
CNIH3	TF binding region
WDR26	TF binding region
CNIH3	CpG island
WDR26	CpG island
ENSG00000202538	chromatin interactions
ENSG00000143786	chromatin interactions
ENSG00000143753	chromatin interactions
ENSG00000162923	chromatin interactions
ENSG00000143514	chromatin interactions
ENSG00000266618	chromatin interactions
ENSG00000143756	chromatin interactions
ENSG00000143771	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000196233	chromatin interactions
ARHGAP12	miRNA target sites
SPOPL	miRNA target sites

Extended variants
information (count: 1352 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1352 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373462234	chr1:224605950-224605951	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs140689711	chr1:224605976-224605977	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs148170824	chr1:224606027-224606028	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs542538921	chr1:224606030-224606031	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200825616	chr1:224606040-224606041	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs77704730	chr1:224606052-224606053	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs77585756	chr1:224606055-224606056	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543649206	chr1:224606060-224606061	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs565415424	chr1:224606064-224606065	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374705168	chr1:224606065-224606066	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532451573	chr1:224606196-224606197	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547460318	chr1:224606221-224606222	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs10495219	chr1:224606249-224606250	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs529998020	chr1:224606346-224606347	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs549264181	chr1:224606349-224606350	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567446134	chr1:224606353-224606354	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538085404	chr1:224606385-224606386	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183058679	chr1:224606419-224606420	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571394390	chr1:224606423-224606424	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs148389992	chr1:224606440-224606441	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114764476	chr1:224606450-224606451	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572078434	chr1:224606568-224606569	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576025362	chr1:224606621-224606622	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs374805055	chr1:224606629-224606630	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542596203	chr1:224606645-224606646	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs185947853	chr1:224606692-224606693	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs576652422	chr1:224606701-224606702	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544025528	chr1:224606714-224606715	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565363554	chr1:224606750-224606751	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs143992815	chr1:224606751-224606752	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146506096	chr1:224606809-224606810	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs115722240	chr1:224606816-224606817	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369062324	chr1:224606837-224606838	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs141132876	chr1:224606843-224606844	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs191112672	chr1:224606858-224606859	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs561271885	chr1:224606905-224606906	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs114508491	chr1:224606959-224606960	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs71644784	chr1:224606997-224606998	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550021396	chr1:224607014-224607015	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571481458	chr1:224607053-224607054	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115056568	chr1:224607119-224607120	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs547516491	chr1:224607120-224607121	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565775301	chr1:224607121-224607122	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs536283484	chr1:224607141-224607142	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs12737765	chr1:224607151-224607152	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs367707141	chr1:224607177-224607178	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs61138605	chr1:224607183-224607184	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370469962	chr1:224607214-224607215	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs139095966	chr1:224607229-224607230	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143097789	chr1:224607242-224607243	Strong transcription Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Congenital diaphragmatic hernia	21085971	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
Autism	20808228	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
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Leukoplakia	24403051	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224547400-224618600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:224572000-224617800	Strong transcription	Fetal Thymus	thymus
3	chr1:224572400-224617600	Strong transcription	Placenta	Placenta
4	chr1:224572600-224617600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:224572600-224617600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:224572600-224618400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:224573200-224618400	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr1:224573200-224618400	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:224573600-224614200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr1:224573600-224618200	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:224573800-224615200	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr1:224574000-224613600	Strong transcription	Adipose Nuclei	Adipose
13	chr1:224574600-224613600	Strong transcription	Duodenum Mucosa	Duodenum
14	chr1:224575000-224607600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr1:224575200-224607600	Strong transcription	Fetal Intestine Large	intestine
16	chr1:224575200-224613800	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr1:224575200-224616600	Strong transcription	Dnd41	blood
18	chr1:224575200-224616800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr1:224576200-224614000	Strong transcription	Fetal Muscle Trunk	muscle
20	chr1:224576400-224614600	Strong transcription	HSMM	muscle
21	chr1:224577000-224617400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:224578800-224614000	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr1:224578800-224617200	Strong transcription	Liver	Liver
24	chr1:224579600-224617400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr1:224579800-224616000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr1:224581800-224615800	Strong transcription	K562	blood
27	chr1:224589000-224611200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:224590400-224612600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr1:224591200-224613000	Strong transcription	Primary T helper cells fromperipheralblood	blood
30	chr1:224591400-224607800	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr1:224593400-224617000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr1:224593800-224613600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:224595400-224613400	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr1:224595400-224618000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr1:224595600-224613200	Strong transcription	HUVEC	blood vessel
36	chr1:224596000-224608800	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr1:224596200-224614400	Strong transcription	NHDF-Ad	bronchial
38	chr1:224596200-224614600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr1:224596200-224615400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr1:224596600-224611600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr1:224596600-224614200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:224596600-224614600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:224596800-224614200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:224597200-224607800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:224597200-224613600	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr1:224597600-224612200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr1:224597600-224616200	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr1:224598200-224617000	Strong transcription	Fetal Muscle Leg	muscle
49	chr1:224598400-224612400	Strong transcription	Brain Substantia Nigra	brain
50	chr1:224598800-224609000	Weak transcription	Esophagus	oesophagus

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