Variant report

Variant	esv988172
Chromosome Location	chr1:161051918-161055508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:161052984-161053558	K562	blood:	n/a	n/a
2	ATF3	chr1:161053027-161053547	K562	blood:	n/a	chr1:161053218-161053233
3	ATF3	chr1:161053176-161053518	K562	blood:	n/a	chr1:161053218-161053233
4	ATF3	chr1:161053097-161053313	HepG2	liver:	n/a	chr1:161053218-161053233
5	BHLHE40	chr1:161053160-161053639	K562	blood:	n/a	n/a
6	BRCA1	chr1:161053096-161053542	Hela-S3	cervix:	n/a	chr1:161053314-161053321
7	CBX3	chr1:161053076-161053651	K562	blood:	n/a	n/a
8	CCNT2	chr1:161053202-161053538	K562	blood:	n/a	n/a
9	CEBPB	chr1:161053079-161053680	HepG2	liver:	n/a	n/a
10	CEBPB	chr1:161053158-161053667	K562	blood:	n/a	n/a
11	CEBPB	chr1:161052932-161053700	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr1:161053156-161053810	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr1:161052323-161054117	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:161052959-161053777	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:161052692-161053980	HCT-116	colon:	n/a	n/a
16	CEBPB	chr1:161053304-161053584	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr1:161053360-161053545	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:161053058-161053738	A549	lung:	n/a	n/a
19	CEBPB	chr1:161053083-161054036	IMR90	lung:	n/a	n/a
20	CEBPB	chr1:161053289-161053567	K562	blood:	n/a	n/a
21	CEBPB	chr1:161053064-161053678	A549	lung:	n/a	n/a
22	CEBPB	chr1:161053034-161053774	MCF-7	breast:	n/a	n/a
23	CEBPB	chr1:161053216-161053731	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr1:161053111-161053670	K562	blood:	n/a	n/a
25	CEBPB	chr1:161052979-161053832	A549	lung:	n/a	n/a
26	CEBPB	chr1:161053161-161053666	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:161053298-161053604	HepG2	liver:	n/a	n/a
28	CEBPD	chr1:161053349-161053547	HepG2	liver:	n/a	n/a
29	CHD2	chr1:161053361-161053432	K562	blood:	n/a	n/a
30	CHD2	chr1:161053076-161053647	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr1:161052978-161053563	HepG2	liver:	n/a	chr1:161053219-161053232
32	CREB1	chr1:161052928-161053647	K562	blood:	n/a	chr1:161053219-161053232
33	CREB1	chr1:161052967-161053498	GM12878	blood:	n/a	chr1:161053219-161053232
34	CREB1	chr1:161052923-161053590	ECC-1	luminal epithelium:	n/a	chr1:161053219-161053232
35	CREB1	chr1:161053002-161053628	ECC-1	luminal epithelium:	n/a	chr1:161053219-161053232
36	CREB1	chr1:161053042-161053480	A549	lung:	n/a	chr1:161053219-161053232
37	CREB1	chr1:161053037-161053525	GM12878	blood:	n/a	chr1:161053219-161053232
38	CREB1	chr1:161053039-161053360	H1-hESC	embryonic stem cell:	n/a	chr1:161053219-161053232
39	CREB1	chr1:161052980-161053591	A549	lung:	n/a	chr1:161053219-161053232
40	CREB1	chr1:161052930-161053596	HepG2	liver:	n/a	chr1:161053219-161053232
41	CTCF	chr1:161052860-161053010	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr1:161053440-161053590	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr1:161052900-161053050	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr1:161055120-161055270	HepG2	liver:	n/a	n/a
45	E2F4	chr1:161053248-161053359	MCF10A-Er-Src	breast:	n/a	n/a
46	EGR1	chr1:161053270-161053551	K562	blood:	n/a	n/a
47	ELF1	chr1:161053060-161053929	MCF-7	breast:	n/a	n/a
48	ELK1	chr1:161053092-161053599	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr1:161053297-161053307	K562	blood:	n/a	n/a
50	EP300	chr1:161053167-161053724	T-47D	breast:	n/a	chr1:161053327-161053337

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161053558-161053608	Hela-S3	cervix:	n/a
2	chr1:161053558-161053608	ovcar-3	ovarian:	n/a
3	chr1:161053558-161053608	HCM	heart:	n/a
4	chr1:161053558-161053608	HCT-116	colon:	n/a
5	chr1:161053558-161053608	HUVEC	blood vessel:	n/a
6	chr1:161053558-161053608	PFSK-1	brain:	n/a
7	chr1:161053558-161053608	A549	lung:	n/a
8	chr1:161053558-161053608	U87	brain:	n/a
9	chr1:161053558-161053608	HAEpiC	amniotic membrane:	n/a
10	chr1:161053558-161053608	SK-N-SH_RA	brain:	n/a
11	chr1:161053558-161053608	HEK293	kidney:	embryo
12	chr1:161053558-161053608	SAEC	small airway:	n/a
13	chr1:161053558-161053608	SK-N-MC	brain:	n/a
14	chr1:161053558-161053608	IMR90	lung:	fetal
15	chr1:161053558-161053608	PANC-1	pancreas:	n/a
16	chr1:161053558-161053608	NB4	blood:	n/a
17	chr1:161053558-161053608	RPTEC	kidney:	n/a
18	chr1:161053558-161053608	GM12878	blood:	n/a
19	chr1:161053558-161053608	HL-60	blood:	n/a
20	chr1:161053558-161053608	HMEC	breast:	n/a
21	chr1:161053558-161053608	AG04450	lung:	fetal
22	chr1:161053558-161053608	HRE	kidney:	n/a
23	chr1:161053558-161053608	Hepatocyte	liver:	n/a
24	chr1:161053558-161053608	Jurkat	blood:	n/a
25	chr1:161053558-161053608	HepG2	liver:	n/a
26	chr1:161053558-161053608	NHDF-neo	bronchial:	n/a
27	chr1:161053558-161053608	AG09319	gingival:	n/a
28	chr1:161053558-161053608	HRCEpiC	kidney:	n/a
29	chr1:161053558-161053608	HCPEpiC	choroid plexus:	n/a
30	chr1:161053558-161053608	NHBE	bronchial:	n/a
31	chr1:161053558-161053608	NH-A	brain:	n/a
32	chr1:161053558-161053608	BJ	skin:	n/a
33	chr1:161053558-161053608	BE2_C	brain:	n/a
34	chr1:161053558-161053608	H1-hESC	embryonic stem cell:	embryo
35	chr1:161053558-161053608	HEEpiC	esophagus:	n/a
36	chr1:161053558-161053608	MCF10A-Er-Src	breast:	n/a
37	chr1:161053558-161053608	Caco-2	colon:	n/a
38	chr1:161053558-161053608	K562	blood:	n/a
39	chr1:161053558-161053608	T-47D	breast:	n/a
40	chr1:161053558-161053608	LNCaP	prostate:	n/a
41	chr1:161053558-161053608	PrEC	prostate:	n/a
42	chr1:161053558-161053608	ProgFib	skin:	n/a
43	chr1:161053558-161053608	CMK	blood:	n/a
44	chr1:161053558-161053608	HRPEpiC	eye:	n/a
45	chr1:161053558-161053608	MCF-7	breast:	n/a
46	chr1:161053558-161053608	SKMC	muscle:	n/a
47	chr1:161053558-161053608	NT2-D1	testis:	n/a
48	chr1:161053558-161053608	AoSMC	blood vessel:	n/a
49	chr1:161053558-161053608	AG04449	skin:	fetal
50	chr1:161053558-161053608	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160989645..160990508-chr1:161052915..161053846,2	MCF-7	breast:
2	chr1:161014972..161017157-chr1:161051557..161054618,4	MCF-7	breast:
3	chr1:161012288..161019472-chr1:161047717..161055328,13	MCF-7	breast:
4	chr1:161051876..161054238-chr1:161125249..161127981,2	K562	blood:
5	chr1:161052998..161054950-chr1:161128036..161130636,2	MCF-7	breast:
6	chr1:161052309..161054886-chr1:161086826..161089196,2	MCF-7	breast:
7	chr1:161051125..161053415-chr1:161074658..161077254,2	MCF-7	breast:
8	chr1:161015304..161016112-chr1:161053054..161053924,2	MCF-7	breast:
9	chr1:161051697..161056385-chr1:161085679..161090534,7	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHDC9-1	chr1:161054727-161054818	NONHSAT007099
2	lnc-KLHDC9-1	chr1:161054727-161054818	ENSG00000228917.1
3	lnc-KLHDC9-1	chr1:161053627-161054602	NONHSAT007099
4	lnc-KLHDC9-1	chr1:161054255-161054602	ENSG00000228917.1

No data

Variant related genes	Relation type
ENSG00000228917	TF binding region
ENSG00000228917	CpG island
ENSG00000158773	chromatin interactions
ENSG00000143256	chromatin interactions
ENSG00000143258	chromatin interactions
ENSG00000158793	chromatin interactions
ENSG00000224985	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12138659	chr1:161051928-161051929	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556863796	chr1:161051978-161051979	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs192721639	chr1:161051980-161051981	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs558158378	chr1:161051983-161051984	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs575233994	chr1:161051987-161051988	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs182379349	chr1:161051988-161051989	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs117194117	chr1:161052054-161052055	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs377129872	chr1:161052093-161052094	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs573234457	chr1:161052095-161052096	Weak transcription Enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs76394572	chr1:161052120-161052121	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs558955857	chr1:161052138-161052139	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs373591385	chr1:161052247-161052248	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537909199	chr1:161052248-161052249	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs188417738	chr1:161052267-161052268	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs554387713	chr1:161052340-161052341	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs574927526	chr1:161052367-161052368	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs116102952	chr1:161052419-161052420	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs530250623	chr1:161052469-161052470	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs114313460	chr1:161052499-161052500	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs146859502	chr1:161052506-161052507	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs528221237	chr1:161052523-161052524	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs112466152	chr1:161052557-161052558	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs149892837	chr1:161052629-161052630	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs530683305	chr1:161052672-161052673	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs550874782	chr1:161052800-161052801	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs546699456	chr1:161052835-161052836	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs367772272	chr1:161052852-161052853	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs372121706	chr1:161052887-161052888	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs191762639	chr1:161052896-161052897	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs536460094	chr1:161052900-161052901	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs61801075	chr1:161052935-161052936	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs149024125	chr1:161052937-161052938	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs539162386	chr1:161052943-161052944	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs558662641	chr1:161052947-161052948	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs575609551	chr1:161052964-161052965	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs116520365	chr1:161052973-161052974	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs555244293	chr1:161053054-161053055	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs574837550	chr1:161053093-161053094	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs143046198	chr1:161053123-161053124	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs560345062	chr1:161053160-161053161	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs374497302	chr1:161053181-161053182	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs368748140	chr1:161053190-161053191	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs545105177	chr1:161053212-161053213	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs564699751	chr1:161053218-161053219	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs530531735	chr1:161053277-161053278	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs74932391	chr1:161053300-161053301	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs184640746	chr1:161053303-161053304	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs561156764	chr1:161053371-161053372	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs76291054	chr1:161053409-161053410	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs546794784	chr1:161053410-161053411	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
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	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161039600-161066800	Weak transcription	Right Atrium	heart
2	chr1:161039800-161052600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:161039800-161053000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:161040200-161052600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:161040200-161052800	Weak transcription	Colonic Mucosa	Colon
6	chr1:161043600-161052800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr1:161043800-161052200	Weak transcription	Spleen	Spleen
8	chr1:161045000-161052400	Weak transcription	A549	lung
9	chr1:161045000-161053200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr1:161047400-161053400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr1:161047600-161052200	Weak transcription	Pancreas	Pancrea
12	chr1:161047600-161053000	Weak transcription	HepG2	liver
13	chr1:161049000-161055000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr1:161049200-161055600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:161049400-161052800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr1:161049400-161053600	Enhancers	Placenta Amnion	Placenta Amnion
17	chr1:161049400-161056400	Enhancers	HMEC	breast
18	chr1:161049400-161056600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:161049600-161054600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr1:161049800-161052800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:161049800-161052800	Enhancers	Placenta	Placenta
22	chr1:161049800-161054600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:161050000-161052200	Weak transcription	Gastric	stomach
24	chr1:161050000-161052800	Enhancers	NHEK	skin
25	chr1:161050000-161057800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:161050200-161055800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr1:161050400-161052800	Enhancers	Hela-S3	cervix
28	chr1:161050400-161053600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:161050600-161053600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr1:161050800-161052800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr1:161050800-161052800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr1:161050800-161053000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr1:161051000-161054800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr1:161051000-161055800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr1:161051200-161052400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:161051200-161052400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr1:161051200-161052400	Weak transcription	NHDF-Ad	bronchial
38	chr1:161051200-161052600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr1:161051200-161052600	Weak transcription	Osteobl	bone
40	chr1:161051200-161052800	Weak transcription	NH-A	brain
41	chr1:161051200-161052800	Weak transcription	NHLF	lung
42	chr1:161051200-161053800	Enhancers	Stomach Mucosa	stomach
43	chr1:161051200-161055600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr1:161051400-161052600	Weak transcription	HSMM	muscle
45	chr1:161051400-161052800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr1:161051400-161053000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:161051600-161052400	Active TSS	Esophagus	oesophagus
48	chr1:161051600-161052400	Weak transcription	Lung	lung
49	chr1:161051600-161052600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr1:161051600-161052600	Weak transcription	HSMMtube	muscle

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