Variant report

Variant	nsv946358
Chromosome Location	chr1:156339735-156342442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:156341385-156342160	HepG2	liver:	n/a	n/a
2	BHLHE40	chr1:156341494-156342165	HepG2	liver:	n/a	n/a
3	CEBPB	chr1:156341303-156341719	K562	blood:	n/a	n/a
4	CEBPB	chr1:156341342-156341722	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr1:156341237-156342103	HepG2	liver:	n/a	n/a
6	CEBPB	chr1:156341412-156341766	A549	lung:	n/a	n/a
7	CEBPB	chr1:156341399-156341691	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr1:156341360-156341632	HepG2	liver:	n/a	n/a
9	CEBPB	chr1:156341219-156341828	A549	lung:	n/a	n/a
10	CEBPB	chr1:156341372-156341711	A549	lung:	n/a	n/a
11	CEBPB	chr1:156341328-156341720	K562	blood:	n/a	n/a
12	CEBPB	chr1:156341406-156341668	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr1:156341285-156341779	MCF-7	breast:	n/a	n/a
14	CEBPB	chr1:156341440-156341654	K562	blood:	n/a	n/a
15	CEBPB	chr1:156341236-156342035	HepG2	liver:	n/a	n/a
16	CEBPB	chr1:156341324-156342094	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:156341357-156341705	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:156341666-156341985	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:156341341-156341661	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr1:156341390-156341828	MCF-7	breast:	n/a	n/a
21	CEBPD	chr1:156341244-156342102	HepG2	liver:	n/a	n/a
22	CEBPD	chr1:156341318-156341791	HepG2	liver:	n/a	n/a
23	CHD2	chr1:156341632-156342069	HepG2	liver:	n/a	chr1:156341774-156341784
24	CTCF	chr1:156342362-156342389	HepG2	liver:	n/a	n/a
25	CTCF	chr1:156342140-156342290	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr1:156342410-156342413	HepG2	liver:	n/a	n/a
27	CTCF	chr1:156342320-156342470	HepG2	liver:	n/a	chr1:156342410-156342428 chr1:156342405-156342426
28	CTCF	chr1:156342392-156342409	HepG2	liver:	n/a	n/a
29	CTCF	chr1:156342351-156342358	HepG2	liver:	n/a	n/a
30	EBF1	chr1:156340622-156340703	GM12878	blood:	n/a	n/a
31	EBF1	chr1:156340579-156340837	GM12878	blood:	n/a	chr1:156340693-156340704 chr1:156340693-156340706
32	EGR1	chr1:156341876-156342120	K562	blood:	n/a	n/a
33	EP300	chr1:156341355-156342166	HepG2	liver:	n/a	n/a
34	EP300	chr1:156341110-156342264	HepG2	liver:	n/a	n/a
35	EP300	chr1:156341242-156342192	HepG2	liver:	n/a	n/a
36	FOS	chr1:156341963-156342182	MCF10A-Er-Src	breast:	n/a	chr1:156342162-156342171
37	FOS	chr1:156341882-156342177	MCF10A-Er-Src	breast:	n/a	chr1:156342162-156342171
38	FOS	chr1:156341998-156342075	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL2	chr1:156341310-156342204	HepG2	liver:	n/a	chr1:156341770-156341779 chr1:156342162-156342171
40	FOSL2	chr1:156341586-156342229	HepG2	liver:	n/a	chr1:156341770-156341779 chr1:156342162-156342171
41	FOXA1	chr1:156341264-156342169	HepG2	liver:	n/a	n/a
42	FOXA1	chr1:156341400-156342198	HepG2	liver:	n/a	n/a
43	FOXA1	chr1:156341491-156342249	HepG2	liver:	n/a	n/a
44	FOXA1	chr1:156341383-156342132	HepG2	liver:	n/a	n/a
45	FOXA2	chr1:156341644-156342193	HepG2	liver:	n/a	n/a
46	FOXA2	chr1:156341328-156341641	HepG2	liver:	n/a	n/a
47	HDAC2	chr1:156341316-156342211	HepG2	liver:	n/a	n/a
48	HDAC2	chr1:156341208-156342164	HepG2	liver:	n/a	n/a
49	HEY1	chr1:156341184-156343184	HepG2	liver:	n/a	n/a
50	HEY1	chr1:156341169-156342527	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:156341523-156341573	SK-N-MC	brain:	n/a
2	chr1:156341523-156341573	U87	brain:	n/a
3	chr1:156341523-156341573	AG09319	gingival:	n/a
4	chr1:156341523-156341573	PANC-1	pancreas:	n/a
5	chr1:156341523-156341573	K562	blood:	n/a
6	chr1:156341523-156341573	RPTEC	kidney:	n/a
7	chr1:156341523-156341573	HCT-116	colon:	n/a
8	chr1:156341523-156341573	H1-hESC	embryonic stem cell:	embryo
9	chr1:156341523-156341573	ProgFib	skin:	n/a
10	chr1:156341523-156341573	PrEC	prostate:	n/a
11	chr1:156341523-156341573	ovcar-3	ovarian:	n/a
12	chr1:156341523-156341573	MCF-7	breast:	n/a
13	chr1:156341523-156341573	A549	lung:	n/a
14	chr1:156341523-156341573	MCF10A-Er-Src	breast:	n/a
15	chr1:156341523-156341573	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:156341523-156341573	NH-A	brain:	n/a
17	chr1:156341523-156341573	Jurkat	blood:	n/a
18	chr1:156341523-156341573	AG10803	skin:	n/a
19	chr1:156341523-156341573	HUVEC	blood vessel:	n/a
20	chr1:156341523-156341573	HL-60	blood:	n/a
21	chr1:156341523-156341573	SKMC	muscle:	n/a
22	chr1:156341523-156341573	CMK	blood:	n/a
23	chr1:156341523-156341573	HNPCEpiC	eye:	n/a
24	chr1:156341523-156341573	BE2_C	brain:	n/a
25	chr1:156341523-156341573	NB4	blood:	n/a
26	chr1:156341523-156341573	AoSMC	blood vessel:	n/a
27	chr1:156341523-156341573	NT2-D1	testis:	n/a
28	chr1:156341523-156341573	HMEC	breast:	n/a
29	chr1:156341523-156341573	HEK293	kidney:	embryo
30	chr1:156341523-156341573	AG04450	lung:	fetal
31	chr1:156341523-156341573	LNCaP	prostate:	n/a
32	chr1:156341523-156341573	SK-N-SH_RA	brain:	n/a
33	chr1:156341523-156341573	HRCEpiC	kidney:	n/a
34	chr1:156341523-156341573	SK-N-SH	brain:	n/a
35	chr1:156341523-156341573	GM12891	blood:	n/a
36	chr1:156341523-156341573	GM12878	blood:	n/a
37	chr1:156341523-156341573	IMR90	lung:	fetal
38	chr1:156341523-156341573	HEEpiC	esophagus:	n/a
39	chr1:156341523-156341573	HCM	heart:	n/a
40	chr1:156341523-156341573	HCPEpiC	choroid plexus:	n/a
41	chr1:156341523-156341573	HCF	heart:	n/a
42	chr1:156341523-156341573	NHDF-neo	bronchial:	n/a
43	chr1:156341523-156341573	HepG2	liver:	n/a
44	chr1:156341523-156341573	GM06990	blood:	n/a
45	chr1:156341523-156341573	HIPEpiC	eye:	n/a
46	chr1:156341523-156341573	PFSK-1	brain:	n/a
47	chr1:156341523-156341573	GM12892	blood:	n/a
48	chr1:156341523-156341573	BJ	skin:	n/a
49	chr1:156341523-156341573	Hepatocyte	liver:	n/a
50	chr1:156341523-156341573	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:156305358..156309501-chr1:156336177..156340436,7	MCF-7	breast:
2	chr1:156341941..156343974-chr1:156352114..156354913,2	K562	blood:
3	chr1:156326557..156327290-chr1:156342036..156342992,2	MCF-7	breast:
4	chr1:156335306..156343282-chr1:156347773..156352892,8	MCF-7	breast:

No data

Variant related genes	Relation type
CCT3	TF binding region
CCT3	CpG island
ENSG00000132677	chromatin interactions
ENSG00000163468	chromatin interactions
ENSG00000163467	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533693520	chr1:156339736-156339737	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs545613438	chr1:156339752-156339753	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs74229290	chr1:156339756-156339757	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs77115412	chr1:156339776-156339777	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs146050212	chr1:156339845-156339846	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs567523642	chr1:156339874-156339875	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs528501139	chr1:156339878-156339879	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs12048396	chr1:156339935-156339936	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs367876027	chr1:156339966-156339967	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs538375407	chr1:156339967-156339968	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs546714016	chr1:156339968-156339969	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs139786238	chr1:156340022-156340023	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs189274869	chr1:156340038-156340039	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs149364770	chr1:156340045-156340046	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs181850252	chr1:156340055-156340056	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs569526816	chr1:156340067-156340068	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs536703340	chr1:156340068-156340069	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs58162377	chr1:156340108-156340109	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs555462570	chr1:156340136-156340137	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs573525212	chr1:156340144-156340145	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs12048454	chr1:156340156-156340157	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs144731218	chr1:156340161-156340162	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs186918788	chr1:156340206-156340207	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs4661039	chr1:156340213-156340214	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs145536681	chr1:156340226-156340227	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs10668520	chr1:156340242-156340243	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs189816950	chr1:156340264-156340265	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs181374591	chr1:156340276-156340277	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs542720123	chr1:156340321-156340322	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs368579369	chr1:156340345-156340346	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs11264478	chr1:156340352-156340353	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs59248542	chr1:156340406-156340407	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs75307368	chr1:156340424-156340425	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs60879830	chr1:156340426-156340427	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs12129175	chr1:156340428-156340429	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs374645933	chr1:156340432-156340433	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs12036869	chr1:156340483-156340484	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs199797795	chr1:156340549-156340550	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs189906493	chr1:156340550-156340551	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571347699	chr1:156340586-156340587	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140993086	chr1:156340595-156340596	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs2985714	chr1:156340618-156340619	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs144215990	chr1:156340724-156340725	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372234779	chr1:156340774-156340775	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs537268531	chr1:156340782-156340783	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs548943142	chr1:156340801-156340802	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182234282	chr1:156340970-156340971	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs76319808	chr1:156340971-156340972	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs74611157	chr1:156340972-156340973	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs534458476	chr1:156340985-156340986	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Breast cancer	17393978	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
Esophageal squamous carcinoma	18350619	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
Cancer	17060936	CNVD
Multiple myeloma	16616336	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD

Chromatin state (count:101 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:156338200-156341400	Weak transcription	Hela-S3	cervix
2	chr1:156338600-156339800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
3	chr1:156338600-156339800	Flanking Active TSS	Liver	Liver
4	chr1:156338800-156339800	Flanking Active TSS	Spleen	Spleen
5	chr1:156338800-156339800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
6	chr1:156339000-156339800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
7	chr1:156339000-156339800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr1:156339000-156339800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr1:156339000-156339800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
10	chr1:156339200-156339800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
11	chr1:156339400-156339800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
12	chr1:156339400-156339800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:156339400-156339800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
14	chr1:156339400-156339800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
15	chr1:156339400-156339800	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
16	chr1:156339400-156339800	Bivalent Enhancer	Fetal Lung	lung
17	chr1:156339400-156339800	Enhancers	Pancreas	Pancrea
18	chr1:156339400-156339800	Enhancers	Right Ventricle	heart
19	chr1:156339400-156341400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:156339400-156341800	Weak transcription	Brain Anterior Caudate	brain
21	chr1:156339600-156339800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
22	chr1:156339600-156339800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr1:156339600-156339800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
24	chr1:156339600-156339800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:156339600-156339800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr1:156339600-156339800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
27	chr1:156339600-156339800	Enhancers	Esophagus	oesophagus
28	chr1:156339600-156339800	Bivalent/Poised TSS	Fetal Kidney	kidney
29	chr1:156339600-156339800	Active TSS	Ovary	ovary
30	chr1:156339600-156339800	Flanking Bivalent TSS/Enh	HepG2	liver
31	chr1:156339600-156340000	Flanking Active TSS	Fetal Intestine Large	intestine
32	chr1:156339600-156341200	Weak transcription	Adipose Nuclei	Adipose
33	chr1:156339600-156341400	Weak transcription	A549	lung
34	chr1:156339600-156341800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:156339600-156358000	Weak transcription	Right Atrium	heart
36	chr1:156339800-156340000	Enhancers	Liver	Liver
37	chr1:156339800-156340000	Active TSS	Fetal Intestine Small	intestine
38	chr1:156339800-156340200	Weak transcription	Ovary	ovary
39	chr1:156339800-156340400	Active TSS	HepG2	liver
40	chr1:156339800-156341000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr1:156339800-156342600	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr1:156339800-156342800	Weak transcription	Pancreas	Pancrea
43	chr1:156339800-156343800	Weak transcription	Right Ventricle	heart
44	chr1:156340000-156340600	Weak transcription	Liver	Liver
45	chr1:156340000-156341000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr1:156340000-156341600	Enhancers	Fetal Intestine Large	intestine
47	chr1:156340000-156343000	Enhancers	Fetal Intestine Small	intestine
48	chr1:156340200-156341400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr1:156340200-156344400	Enhancers	Ovary	ovary
50	chr1:156340400-156343000	Flanking Active TSS	HepG2	liver

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