Variant report

Variant	esv3430322
Chromosome Location	chr1:160851829-160920480
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:633)
CpG islands
(count:610)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:633 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:160881283-160881568	K562	blood:	n/a	n/a
2	ATF1	chr1:160919039-160919360	K562	blood:	n/a	n/a
3	ATF1	chr1:160914830-160915136	K562	blood:	n/a	n/a
4	ATF1	chr1:160895577-160895594	K562	blood:	n/a	n/a
5	ATF3	chr1:160895514-160896112	A549	lung:	n/a	n/a
6	ATF3	chr1:160895597-160895919	K562	blood:	n/a	n/a
7	ATF3	chr1:160895552-160896096	A549	lung:	n/a	n/a
8	BHLHE40	chr1:160881275-160881700	K562	blood:	n/a	n/a
9	BHLHE40	chr1:160919047-160919530	K562	blood:	n/a	n/a
10	BHLHE40	chr1:160914798-160915167	K562	blood:	n/a	n/a
11	CBX3	chr1:160918879-160919589	K562	blood:	n/a	n/a
12	CCNT2	chr1:160919222-160919506	K562	blood:	n/a	n/a
13	CCNT2	chr1:160914816-160915424	K562	blood:	n/a	n/a
14	CEBPB	chr1:160912841-160912962	K562	blood:	n/a	n/a
15	CEBPB	chr1:160852973-160853157	HepG2	liver:	n/a	chr1:160853027-160853038
16	CEBPB	chr1:160881426-160881530	K562	blood:	n/a	n/a
17	CEBPB	chr1:160884360-160884367	K562	blood:	n/a	n/a
18	CEBPB	chr1:160884312-160884522	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:160858781-160859054	A549	lung:	n/a	n/a
20	CEBPB	chr1:160912713-160913092	MCF-7	breast:	n/a	n/a
21	CEBPB	chr1:160854148-160854196	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:160912728-160913066	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr1:160918940-160919514	K562	blood:	n/a	n/a
24	CEBPB	chr1:160912752-160912989	A549	lung:	n/a	n/a
25	CEBPB	chr1:160858820-160859043	Hela-S3	cervix:	n/a	n/a
26	CEBPD	chr1:160881154-160881741	K562	blood:	n/a	n/a
27	CEBPD	chr1:160914834-160915230	K562	blood:	n/a	n/a
28	CEBPD	chr1:160914756-160915200	K562	blood:	n/a	n/a
29	CEBPD	chr1:160918804-160919515	K562	blood:	n/a	n/a
30	CREB1	chr1:160904048-160904272	A549	lung:	n/a	n/a
31	CTCF	chr1:160854600-160854750	HCFaa	heart:	n/a	n/a
32	CTCF	chr1:160912776-160912953	GM12891	blood:	n/a	n/a
33	CTCF	chr1:160854456-160854746	HepG2	liver:	n/a	n/a
34	CTCF	chr1:160912800-160912950	GM12874	blood:	n/a	n/a
35	CTCF	chr1:160854540-160854690	GM12867	blood:	n/a	n/a
36	CTCF	chr1:160854540-160854690	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr1:160854626-160854678	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr1:160854587-160854669	GM13977	blood:	n/a	n/a
39	CTCF	chr1:160854409-160854798	HepG2	liver:	n/a	n/a
40	CTCF	chr1:160854529-160854671	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:160912800-160912950	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:160912776-160912925	GM10266	blood:	n/a	n/a
43	CTCF	chr1:160912780-160912930	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:160912756-160912970	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:160912386-160912426	LNCaP	prostate:	n/a	n/a
46	CTCF	chr1:160854529-160854686	GM12892	blood:	n/a	n/a
47	CTCF	chr1:160854540-160854690	HepG2	liver:	n/a	n/a
48	CTCF	chr1:160912800-160912950	AG04450	lung:	n/a	n/a
49	CTCF	chr1:160854463-160854740	GM12878	blood:	n/a	n/a
50	CTCF	chr1:160912780-160912942	ProgFib	skin:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:160856347-160856397	AG04450	lung:	fetal
2	chr1:160856352-160856402	PANC-1	pancreas:	n/a
3	chr1:160855148-160855198	HCM	heart:	n/a
4	chr1:160855077-160855127	HUVEC	blood vessel:	n/a
5	chr1:160856352-160856402	NHBE	bronchial:	n/a
6	chr1:160856347-160856397	ECC-1	luminal epithelium:	n/a
7	chr1:160865097-160865147	GM12891	blood:	n/a
8	chr1:160855148-160855198	PFSK-1	brain:	n/a
9	chr1:160914870-160914920	ProgFib	skin:	n/a
10	chr1:160865146-160865196	SKMC	muscle:	n/a
11	chr1:160914870-160914920	HCF	heart:	n/a
12	chr1:160856352-160856402	AG09309	skin:	n/a
13	chr1:160865097-160865147	HEEpiC	esophagus:	n/a
14	chr1:160856352-160856402	RPTEC	kidney:	n/a
15	chr1:160856352-160856402	K562	blood:	n/a
16	chr1:160865097-160865147	Jurkat	blood:	n/a
17	chr1:160856347-160856397	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:160855077-160855127	HMEC	breast:	n/a
19	chr1:160864761-160864811	NHDF-neo	bronchial:	n/a
20	chr1:160865146-160865196	U87	brain:	n/a
21	chr1:160865146-160865196	PrEC	prostate:	n/a
22	chr1:160865146-160865196	NHDF-neo	bronchial:	n/a
23	chr1:160864761-160864811	PrEC	prostate:	n/a
24	chr1:160856352-160856402	HCPEpiC	choroid plexus:	n/a
25	chr1:160864761-160864811	U87	brain:	n/a
26	chr1:160903135-160903185	T-47D	breast:	n/a
27	chr1:160903135-160903185	NHBE	bronchial:	n/a
28	chr1:160855077-160855127	A549	lung:	n/a
29	chr1:160855148-160855198	HRCEpiC	kidney:	n/a
30	chr1:160856352-160856402	HIPEpiC	eye:	n/a
31	chr1:160856347-160856397	BE2_C	brain:	n/a
32	chr1:160865146-160865196	PFSK-1	brain:	n/a
33	chr1:160865146-160865196	HCF	heart:	n/a
34	chr1:160855148-160855198	AG09309	skin:	n/a
35	chr1:160865146-160865196	SK-N-SH_RA	brain:	n/a
36	chr1:160855148-160855198	ovcar-3	ovarian:	n/a
37	chr1:160855077-160855127	SK-N-SH	brain:	n/a
38	chr1:160865097-160865147	PFSK-1	brain:	n/a
39	chr1:160914870-160914920	AG09319	gingival:	n/a
40	chr1:160855077-160855127	T-47D	breast:	n/a
41	chr1:160856347-160856397	RPTEC	kidney:	n/a
42	chr1:160865097-160865147	HUVEC	blood vessel:	n/a
43	chr1:160865097-160865147	PANC-1	pancreas:	n/a
44	chr1:160854954-160855004	HCPEpiC	choroid plexus:	n/a
45	chr1:160865097-160865147	MCF-7	breast:	n/a
46	chr1:160856352-160856402	SAEC	small airway:	n/a
47	chr1:160914870-160914920	SK-N-SH	brain:	n/a
48	chr1:160854954-160855004	HAEpiC	amniotic membrane:	n/a
49	chr1:160856347-160856397	HRE	kidney:	n/a
50	chr1:160865097-160865147	HCT-116	colon:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:160850691..160852389-chr1:160852476..160855044,2	MCF-7	breast:
2	chr1:160779866..160781807-chr1:160913798..160915545,2	MCF-7	breast:
3	chr1:160850486..160853249-chr1:160886390..160887944,2	K562	blood:
4	chr1:160872347..160875327-chr1:160877154..160879416,3	K562	blood:
5	chr1:160912472..160913285-chr1:160959725..160960368,3	MCF-7	breast:
6	chr1:160869759..160871916-chr1:160873094..160874895,2	K562	blood:
7	chr1:160912390..160913258-chr1:160920991..160921799,3	MCF-7	breast:
8	chr1:160850691..160852389-chr1:160852476..160855044,2	MCF-7	breast:
9	chr1:160916194..160918562-chr1:160922783..160924481,2	K562	blood:
10	chr1:160915728..160918562-chr1:160922253..160924481,2	K562	blood:
11	chr1:160912415..160913322-chr1:160920810..160921780,7	MCF-7	breast:
12	chr1:160874204..160876595-chr1:160877694..160880011,2	MCF-7	breast:
13	chr1:160872347..160875327-chr1:160877154..160879416,3	K562	blood:
14	chr1:160874204..160876595-chr1:160877694..160880011,2	MCF-7	breast:
15	chr1:160912791..160913358-chr1:160924111..160924969,2	MCF-7	breast:
16	chr1:160869759..160871916-chr1:160873094..160874895,2	K562	blood:
17	chr1:160696688..160697282-chr1:160919145..160920040,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITLN2-1	chr1:160901529-160901967	XLOC_001064
2	lnc-ITLN2-1	chr1:160904035-160904170	XLOC_001064

No data

Variant related genes	Relation type
ENSG00000198358	TF binding region
ENSG00000233691	TF binding region
ENSG00000232188	TF binding region
ENSG00000213080	TF binding region
ITLN1	TF binding region
ENSG00000198358	CpG island
ENSG00000233691	CpG island
ENSG00000232188	CpG island
ENSG00000213080	CpG island
ITLN1	CpG island
ENSG00000158764	chromatin interactions
ENSG00000179914	chromatin interactions

Extended variants
information (count: 2237 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:2237 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138862670	chr1:160851848-160851849	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs370375904	chr1:160851857-160851858	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs375323097	chr1:160851860-160851861	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200697844	chr1:160851867-160851868	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551693271	chr1:160851872-160851873	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs144472647	chr1:160851877-160851878	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138384406	chr1:160851881-160851882	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374425877	chr1:160851882-160851883	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150684937	chr1:160851885-160851886	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs2274908	chr1:160851894-160851895	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs147176765	chr1:160851899-160851900	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147826544	chr1:160851900-160851901	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs142720493	chr1:160851921-160851922	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs151006223	chr1:160851925-160851926	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200007610	chr1:160851930-160851931	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376898715	chr1:160851934-160851935	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs144985706	chr1:160851949-160851950	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs368081658	chr1:160851954-160851955	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs199591422	chr1:160851964-160851965	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs200234260	chr1:160851967-160851968	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117373725	chr1:160851976-160851977	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs201081504	chr1:160851977-160851978	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs200414269	chr1:160852019-160852020	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs2274909	chr1:160852022-160852023	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs575174397	chr1:160852025-160852026	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs2274910	chr1:160852046-160852047	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
27	rs562918918	chr1:160852056-160852057	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573658807	chr1:160852066-160852067	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542668441	chr1:160852116-160852117	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11265508	chr1:160852125-160852126	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs528286113	chr1:160852142-160852143	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6427552	chr1:160852167-160852168	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs565161800	chr1:160852172-160852173	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73027849	chr1:160852188-160852189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs538700799	chr1:160852223-160852224	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572425579	chr1:160852244-160852245	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181755062	chr1:160852270-160852271	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142992711	chr1:160852298-160852299	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543068207	chr1:160852331-160852332	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs536355163	chr1:160852338-160852339	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs373321005	chr1:160852344-160852345	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185252935	chr1:160852350-160852351	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs376790564	chr1:160852359-160852360	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs151083269	chr1:160852367-160852368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558695224	chr1:160852395-160852396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575556175	chr1:160852454-160852455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538105253	chr1:160852455-160852456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371167225	chr1:160852490-160852491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141068321	chr1:160852493-160852494	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs146787017	chr1:160852499-160852500	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160846800-160854200	Weak transcription	Fetal Intestine Small	intestine
2	chr1:160847200-160852400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr1:160847600-160853800	Weak transcription	Spleen	Spleen
4	chr1:160849000-160852200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:160849200-160855400	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr1:160849400-160854200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:160851000-160855400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr1:160851200-160852800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr1:160852200-160852400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:160852400-160855000	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr1:160852800-160855000	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr1:160853400-160853600	Enhancers	Gastric	stomach
13	chr1:160853600-160854400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:160853600-160854600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr1:160853600-160858800	Weak transcription	Gastric	stomach
16	chr1:160853800-160854600	Enhancers	Spleen	Spleen
17	chr1:160854200-160854600	Active TSS	Fetal Intestine Small	intestine
18	chr1:160854200-160854600	Enhancers	Lung	lung
19	chr1:160854200-160855000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:160854400-160854600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:160854600-160855400	Enhancers	Fetal Heart	heart
22	chr1:160854800-160855000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:160854800-160855200	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:160854800-160855400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:160855400-160857000	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr1:160855400-160857000	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr1:160855400-160860200	Weak transcription	Fetal Heart	heart
28	chr1:160857000-160857800	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr1:160857000-160857800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr1:160857800-160858800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr1:160857800-160858800	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr1:160858800-160859000	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr1:160858800-160859000	Enhancers	Gastric	stomach
34	chr1:160858800-160859000	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr1:160858800-160859200	Enhancers	HUVEC	blood vessel
36	chr1:160859000-160859600	Weak transcription	Gastric	stomach
37	chr1:160859600-160859800	Enhancers	Gastric	stomach
38	chr1:160860200-160861400	Enhancers	Fetal Heart	heart
39	chr1:160870200-160875600	Weak transcription	Spleen	Spleen
40	chr1:160871400-160871600	Enhancers	Right Atrium	heart
41	chr1:160871600-160872000	Enhancers	Ovary	ovary
42	chr1:160871600-160874200	Weak transcription	Right Atrium	heart
43	chr1:160872000-160873600	Weak transcription	Ovary	ovary
44	chr1:160872200-160872800	Enhancers	Gastric	stomach
45	chr1:160872800-160875200	Weak transcription	Gastric	stomach
46	chr1:160873600-160877200	Enhancers	Ovary	ovary
47	chr1:160873800-160875000	Enhancers	Fetal Heart	heart
48	chr1:160874200-160875400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr1:160874200-160875800	Enhancers	Right Atrium	heart
50	chr1:160874400-160875000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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