Variant report

Variant	nsv1005196
Chromosome Location	chr1:158015996-158065522
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:436)
CpG islands
(count:490)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:158057160-158057363	HepG2	liver:	n/a	n/a
2	ATF2	chr1:158065467-158065885	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr1:158057119-158057540	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr1:158056952-158057428	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:158045818-158046145	IMR90	lung:	n/a	chr1:158045997-158046008
6	CEBPB	chr1:158046021-158046056	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:158029875-158030169	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:158045831-158046158	HepG2	liver:	n/a	chr1:158045997-158046008
9	CEBPB	chr1:158057101-158057513	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr1:158045980-158046107	H1-hESC	embryonic stem cell:	n/a	chr1:158045997-158046008
11	CHD2	chr1:158030128-158030234	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr1:158023361-158023362	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr1:158057456-158057598	HepG2	liver:	n/a	n/a
14	CHD2	chr1:158057165-158057478	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr1:158057240-158057390	WI-38	lung:	n/a	chr1:158057278-158057296
16	CTCF	chr1:158054318-158054371	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:158057200-158057350	HMEC	breast:	n/a	chr1:158057278-158057296
18	CTCF	chr1:158057220-158057370	SK-N-SH_RA	brain:	n/a	chr1:158057278-158057296
19	CTCF	chr1:158057800-158057950	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr1:158057155-158057473	MCF-7	breast:	n/a	chr1:158057278-158057296
21	CTCF	chr1:158057137-158057508	Gliobla	brain:	n/a	chr1:158057278-158057296
22	CTCF	chr1:158057280-158057430	HCT-116	colon:	n/a	n/a
23	CTCF	chr1:158057145-158057507	MCF-7	breast:	n/a	chr1:158057278-158057296
24	CTCF	chr1:158057260-158057410	HPF	lung:	n/a	chr1:158057278-158057296
25	CTCF	chr1:158057240-158057390	NB4	blood:	n/a	chr1:158057278-158057296
26	CTCF	chr1:158065522-158065928	GM12878	blood:	n/a	n/a
27	CTCF	chr1:158065315-158066082	SK-N-SH	brain:	n/a	n/a
28	CTCF	chr1:158057900-158058050	GM12873	blood:	n/a	n/a
29	CTCF	chr1:158057260-158057410	Hela-S3	cervix:	n/a	chr1:158057278-158057296
30	CTCF	chr1:158057260-158057410	AG09309	skin:	n/a	chr1:158057278-158057296
31	CTCF	chr1:158057098-158057597	H1-hESC	embryonic stem cell:	n/a	chr1:158057278-158057296
32	CTCF	chr1:158057240-158057390	GM12865	blood:	n/a	chr1:158057278-158057296
33	CTCF	chr1:158057159-158057459	LNCaP	prostate:	n/a	chr1:158057278-158057296
34	CTCF	chr1:158057260-158057410	HUVEC	blood vessel:	n/a	chr1:158057278-158057296
35	CTCF	chr1:158057525-158057671	GM12892	blood:	n/a	n/a
36	CTCF	chr1:158057240-158057390	HPAF	blood vessel:	n/a	chr1:158057278-158057296
37	CTCF	chr1:158057561-158057611	A549	lung:	n/a	n/a
38	CTCF	chr1:158065488-158065974	K562	blood:	n/a	n/a
39	CTCF	chr1:158057280-158057430	A549	lung:	n/a	n/a
40	CTCF	chr1:158065200-158065350	GM12871	blood:	n/a	n/a
41	CTCF	chr1:158057163-158057480	Fibrobl	skin:	n/a	chr1:158057278-158057296
42	CTCF	chr1:158057220-158057370	GM12874	blood:	n/a	chr1:158057278-158057296
43	CTCF	chr1:158057220-158057370	SAEC	small airway:	n/a	chr1:158057278-158057296
44	CTCF	chr1:158057147-158057461	GM19240	blood:	n/a	chr1:158057278-158057296
45	CTCF	chr1:158057595-158057628	GM12878	blood:	n/a	n/a
46	CTCF	chr1:158057260-158057410	HBMEC	blood vessel:	n/a	chr1:158057278-158057296
47	CTCF	chr1:158057163-158057429	GM10248	blood:	n/a	chr1:158057278-158057296
48	CTCF	chr1:158057220-158057370	HMF	breast:	n/a	chr1:158057278-158057296
49	CTCF	chr1:158057260-158057410	HPAF	blood vessel:	n/a	chr1:158057278-158057296
50	CTCF	chr1:158053340-158053490	HAc	cerebellar:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:158037893-158037943	H1-hESC	embryonic stem cell:	embryo
2	chr1:158028936-158028986	HRPEpiC	eye:	n/a
3	chr1:158037893-158037943	H1-hESC	embryonic stem cell:	embryo
4	chr1:158028936-158028986	HRPEpiC	eye:	n/a
5	chr1:158041312-158041362	HepG2	liver:	n/a
6	chr1:158027914-158027964	Hepatocyte	liver:	n/a
7	chr1:158035207-158035257	T-47D	breast:	n/a
8	chr1:158041312-158041362	MCF10A-Er-Src	breast:	n/a
9	chr1:158035207-158035257	RPTEC	kidney:	n/a
10	chr1:158028936-158028986	AoSMC	blood vessel:	n/a
11	chr1:158041312-158041362	GM06990	blood:	n/a
12	chr1:158029978-158030028	IMR90	lung:	fetal
13	chr1:158028936-158028986	AG10803	skin:	n/a
14	chr1:158028936-158028986	T-47D	breast:	n/a
15	chr1:158037893-158037943	PrEC	prostate:	n/a
16	chr1:158047439-158047489	H1-hESC	embryonic stem cell:	embryo
17	chr1:158028936-158028986	AG09319	gingival:	n/a
18	chr1:158027914-158027964	BJ	skin:	n/a
19	chr1:158047439-158047489	SAEC	small airway:	n/a
20	chr1:158027914-158027964	AG04449	skin:	fetal
21	chr1:158047439-158047489	SK-N-MC	brain:	n/a
22	chr1:158029978-158030028	ECC-1	luminal epithelium:	n/a
23	chr1:158019222-158019272	NH-A	brain:	n/a
24	chr1:158041312-158041362	SAEC	small airway:	n/a
25	chr1:158027914-158027964	HEEpiC	esophagus:	n/a
26	chr1:158029978-158030028	K562	blood:	n/a
27	chr1:158019222-158019272	Hepatocyte	liver:	n/a
28	chr1:158035207-158035257	HL-60	blood:	n/a
29	chr1:158037893-158037943	PANC-1	pancreas:	n/a
30	chr1:158041312-158041362	H1-hESC	embryonic stem cell:	embryo
31	chr1:158037893-158037943	NHBE	bronchial:	n/a
32	chr1:158035207-158035257	PFSK-1	brain:	n/a
33	chr1:158019222-158019272	SKMC	muscle:	n/a
34	chr1:158028936-158028986	BJ	skin:	n/a
35	chr1:158029978-158030028	AG10803	skin:	n/a
36	chr1:158027914-158027964	Caco-2	colon:	n/a
37	chr1:158037893-158037943	HAEpiC	amniotic membrane:	n/a
38	chr1:158041312-158041362	SK-N-SH	brain:	n/a
39	chr1:158041312-158041362	HCPEpiC	choroid plexus:	n/a
40	chr1:158041312-158041362	SKMC	muscle:	n/a
41	chr1:158019222-158019272	SK-N-SH_RA	brain:	n/a
42	chr1:158029978-158030028	HCPEpiC	choroid plexus:	n/a
43	chr1:158035207-158035257	GM19239	blood:	n/a
44	chr1:158028936-158028986	MCF10A-Er-Src	breast:	n/a
45	chr1:158027914-158027964	GM12878	blood:	n/a
46	chr1:158047439-158047489	MCF-7	breast:	n/a
47	chr1:158029978-158030028	NT2-D1	testis:	n/a
48	chr1:158029978-158030028	GM12878	blood:	n/a
49	chr1:158028936-158028986	HIPEpiC	eye:	n/a
50	chr1:158037893-158037943	HCF	heart:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:157967091..157967967-chr1:158056917..158057710,2	MCF-7	breast:
2	chr1:158048939..158051558-chr1:158056001..158058414,2	K562	blood:
3	chr1:158052197..158054065-chr1:158057202..158058918,2	K562	blood:
4	chr1:157957635..157958557-chr1:158056642..158057313,2	MCF-7	breast:
5	chr1:158063066..158067831-chr1:158068647..158073940,6	K562	blood:
6	chr1:157933081..157934129-chr1:158056881..158057890,3	MCF-7	breast:
7	chr1:158045418..158047759-chr1:158047962..158051460,3	MCF-7	breast:
8	chr1:158057302..158058215-chr1:158087580..158088116,2	MCF-7	breast:
9	chr1:157938968..157940216-chr1:158056696..158058127,7	MCF-7	breast:
10	chr1:158037503..158040836-chr1:158048548..158051276,3	MCF-7	breast:
11	chr1:158020778..158022913-chr1:158023711..158025340,2	K562	blood:
12	chr1:158048699..158051003-chr1:158054119..158055695,2	K562	blood:
13	chr1:158045418..158047759-chr1:158047962..158051460,3	MCF-7	breast:
14	chr1:157961475..157962440-chr1:158056771..158057768,8	MCF-7	breast:
15	chr1:158050284..158053478-chr1:158072717..158076426,3	K562	blood:
16	chr1:158014548..158016120-chr1:158017209..158018949,2	MCF-7	breast:
17	chr1:157961448..157962029-chr1:158056905..158057718,2	K562	blood:
18	chr1:158056895..158057743-chr1:158091127..158091633,2	MCF-7	breast:
19	chr1:158048699..158051003-chr1:158054119..158055695,2	K562	blood:
20	chr1:158020778..158022913-chr1:158023711..158025340,2	K562	blood:
21	chr1:158020017..158022610-chr1:158028062..158030654,2	K562	blood:
22	chr1:158055734..158058404-chr1:158065518..158067250,2	MCF-7	breast:
23	chr1:158044161..158046672-chr1:158053347..158055156,2	K562	blood:
24	chr1:158037503..158040836-chr1:158048548..158051276,3	MCF-7	breast:
25	chr1:158047303..158050333-chr1:158050962..158053728,3	K562	blood:
26	chr1:158047303..158050333-chr1:158050962..158053728,3	K562	blood:
27	chr1:158014548..158016120-chr1:158017209..158018949,2	MCF-7	breast:
28	chr1:157933123..157934067-chr1:158056815..158057738,4	K562	blood:
29	chr1:157939154..157940337-chr1:158056815..158057875,10	MCF-7	breast:
30	chr1:158044161..158046672-chr1:158053347..158055156,2	K562	blood:
31	chr1:158020017..158022610-chr1:158028062..158030654,2	K562	blood:
32	chr1:158052197..158054065-chr1:158057202..158058918,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KIRREL	hsa-miR-335-5p	chr1:158065436-158065459
2	KIRREL	hsa-miR-335-5p	chr1:158064975-158064998

Variant related genes	Relation type
KIRREL	TF binding region
KIRREL	CpG island
ENSG00000183853	chromatin interactions

Extended variants
information (count: 1899 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1899 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1925033	chr1:158015996-158015997	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544184432	chr1:158016013-158016014	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562481457	chr1:158016053-158016054	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113707221	chr1:158016077-158016078	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529986012	chr1:158016110-158016111	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542123762	chr1:158016118-158016119	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560221597	chr1:158016170-158016171	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs76787699	chr1:158016195-158016196	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527470672	chr1:158016243-158016244	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552132506	chr1:158016257-158016258	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571669074	chr1:158016258-158016259	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532479977	chr1:158016284-158016285	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141721331	chr1:158016292-158016293	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552824433	chr1:158016357-158016358	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80179247	chr1:158016417-158016418	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536277270	chr1:158016447-158016448	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555230268	chr1:158016492-158016493	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567094139	chr1:158016530-158016531	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180839495	chr1:158016531-158016532	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146283534	chr1:158016538-158016539	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs114626782	chr1:158016553-158016554	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537957887	chr1:158016697-158016698	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556318752	chr1:158016778-158016779	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs530195686	chr1:158016784-158016785	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7413362	chr1:158016788-158016789	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529567991	chr1:158016810-158016811	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138143790	chr1:158016816-158016817	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542154744	chr1:158016832-158016833	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142639883	chr1:158016850-158016851	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545943251	chr1:158016851-158016852	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564142984	chr1:158016885-158016886	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563427818	chr1:158016953-158016954	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150825936	chr1:158016984-158016985	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550641010	chr1:158017021-158017022	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4480346	chr1:158017046-158017047	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139233329	chr1:158017118-158017119	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530028829	chr1:158017142-158017143	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549554297	chr1:158017155-158017156	Weak transcription Genic enhancers Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150019778	chr1:158017222-158017223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4971122	chr1:158017250-158017251	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs534239519	chr1:158017377-158017378	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374937787	chr1:158017392-158017393	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114250888	chr1:158017436-158017437	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112081799	chr1:158017535-158017536	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144283898	chr1:158017537-158017538	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76222637	chr1:158017566-158017567	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs77480197	chr1:158017592-158017593	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574630336	chr1:158017617-158017618	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535380963	chr1:158017634-158017635	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572834336	chr1:158017688-158017689	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21045282	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:157997600-158047600	Weak transcription	Dnd41	blood
2	chr1:158001200-158047400	Weak transcription	Thymus	Thymus
3	chr1:158002400-158025400	Weak transcription	Fetal Brain Female	brain
4	chr1:158008000-158019600	Weak transcription	Colonic Mucosa	Colon
5	chr1:158008200-158018400	Weak transcription	Spleen	Spleen
6	chr1:158008200-158023000	Weak transcription	A549	lung
7	chr1:158008200-158024600	Weak transcription	Placenta	Placenta
8	chr1:158009400-158024400	Weak transcription	Hela-S3	cervix
9	chr1:158009600-158022600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:158010000-158023000	Weak transcription	HSMM	muscle
11	chr1:158010200-158020600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:158011000-158017200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr1:158012200-158019800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:158012400-158017200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:158012800-158016800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr1:158012800-158017000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr1:158012800-158017200	Enhancers	Lung	lung
18	chr1:158013000-158016200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr1:158013000-158016400	Enhancers	Fetal Muscle Leg	muscle
20	chr1:158013000-158016600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr1:158013000-158016600	Enhancers	Right Atrium	heart
22	chr1:158013000-158017200	Enhancers	Ovary	ovary
23	chr1:158013000-158020600	Enhancers	Fetal Lung	lung
24	chr1:158013200-158017400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr1:158013400-158017800	Enhancers	Adipose Nuclei	Adipose
26	chr1:158013400-158020600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:158013600-158020600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:158013600-158025600	Weak transcription	Brain Germinal Matrix	brain
29	chr1:158013800-158017000	Strong transcription	NHEK	skin
30	chr1:158013800-158027000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:158014000-158016800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:158014200-158018200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:158014200-158018800	Enhancers	Fetal Kidney	kidney
34	chr1:158014600-158016000	Enhancers	Osteobl	bone
35	chr1:158014600-158016200	Enhancers	Colon Smooth Muscle	Colon
36	chr1:158014600-158016200	Enhancers	NH-A	brain
37	chr1:158014600-158016600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr1:158014600-158016600	Enhancers	NHDF-Ad	bronchial
39	chr1:158014600-158016800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:158014600-158017600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:158014800-158016000	Enhancers	Pancreas	Pancrea
42	chr1:158014800-158016000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr1:158014800-158016000	Enhancers	HMEC	breast
44	chr1:158014800-158016200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:158014800-158016200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:158014800-158016200	Enhancers	Rectal Smooth Muscle	rectum
47	chr1:158014800-158016200	Enhancers	NHLF	lung
48	chr1:158014800-158016400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr1:158014800-158016600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr1:158014800-158016600	Enhancers	HUES48 Cell Line	embryonic stem cell

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