Variant report

Variant	nsv872534
Chromosome Location	chr1:169533266-169561274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:663)
CpG islands
(count:488)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169539100-169539788	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169555576-169556383	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:169541178-169542037	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:169557339-169558326	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:169537700-169538082	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:169545546-169546227	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:169534688-169535455	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:169553882-169554484	HepG2	liver:	n/a	n/a
9	BHLHE40	chr1:169555531-169556131	HepG2	liver:	n/a	chr1:169555776-169555792
10	BHLHE40	chr1:169545709-169546119	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:169555793-169555821	K562	blood:	n/a	n/a
12	BRCA1	chr1:169555543-169556228	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:169534549-169535050	A549	lung:	n/a	chr1:169534774-169534785
14	CEBPB	chr1:169555556-169555899	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:169557411-169557791	HepG2	liver:	n/a	chr1:169557645-169557656
16	CEBPB	chr1:169534588-169534946	A549	lung:	n/a	chr1:169534774-169534785
17	CEBPB	chr1:169539292-169539700	HepG2	liver:	n/a	n/a
18	CEBPB	chr1:169534594-169535003	HepG2	liver:	n/a	chr1:169534774-169534785
19	CEBPB	chr1:169534622-169534947	H1-hESC	embryonic stem cell:	n/a	chr1:169534774-169534785
20	CEBPB	chr1:169534530-169534891	HepG2	liver:	n/a	chr1:169534774-169534785
21	CEBPB	chr1:169557409-169557718	HepG2	liver:	n/a	chr1:169557645-169557656
22	CEBPB	chr1:169534530-169534929	MCF-7	breast:	n/a	chr1:169534774-169534785
23	CEBPB	chr1:169534607-169534960	Hela-S3	cervix:	n/a	chr1:169534774-169534785
24	CEBPB	chr1:169541501-169541833	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:169539310-169539666	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:169534594-169534964	K562	blood:	n/a	chr1:169534774-169534785
27	CEBPB	chr1:169557445-169557832	HepG2	liver:	n/a	chr1:169557645-169557656
28	CEBPB	chr1:169539303-169539617	HepG2	liver:	n/a	n/a
29	CEBPB	chr1:169557480-169557715	HepG2	liver:	n/a	chr1:169557645-169557656
30	CEBPB	chr1:169534587-169534954	IMR90	lung:	n/a	chr1:169534774-169534785
31	CEBPB	chr1:169539347-169539662	HepG2	liver:	n/a	n/a
32	CEBPB	chr1:169534487-169535019	MCF-7	breast:	n/a	chr1:169534774-169534785
33	CEBPD	chr1:169555423-169555855	HepG2	liver:	n/a	n/a
34	CHD2	chr1:169555624-169555920	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:169555560-169556175	HepG2	liver:	n/a	n/a
36	CTCF	chr1:169555581-169555909	IMR90	lung:	n/a	chr1:169555637-169555650
37	CTCF	chr1:169555640-169555790	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr1:169555606-169555835	GM13977	blood:	n/a	chr1:169555637-169555650
39	CTCF	chr1:169555660-169555810	SAEC	small airway:	n/a	n/a
40	CTCF	chr1:169555578-169555871	MCF-7	breast:	n/a	chr1:169555637-169555650
41	CTCF	chr1:169555383-169556090	A549	lung:	n/a	chr1:169555637-169555650 chr1:169555902-169555910
42	CTCF	chr1:169555613-169555860	Spleen_OC	spleen:	n/a	chr1:169555637-169555650
43	CTCF	chr1:169555660-169555810	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr1:169555560-169555858	K562	blood:	n/a	chr1:169555637-169555650
45	CTCF	chr1:169558080-169558230	GM12865	blood:	n/a	n/a
46	CTCF	chr1:169555640-169555790	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr1:169555560-169555866	GM19239	blood:	n/a	chr1:169555637-169555650
48	CTCF	chr1:169555680-169555830	GM12866	blood:	n/a	n/a
49	CTCF	chr1:169555560-169555710	A549	lung:	n/a	chr1:169555637-169555650
50	CTCF	chr1:169555565-169555884	MCF-7	breast:	n/a	chr1:169555637-169555650

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169555944-169555994	PFSK-1	brain:	n/a
2	chr1:169556657-169556707	GM12878	blood:	n/a
3	chr1:169558925-169558975	PANC-1	pancreas:	n/a
4	chr1:169555674-169555724	K562	blood:	n/a
5	chr1:169556657-169556707	HepG2	liver:	n/a
6	chr1:169555773-169555823	GM12892	blood:	n/a
7	chr1:169555944-169555994	MCF-7	breast:	n/a
8	chr1:169555681-169555731	HCPEpiC	choroid plexus:	n/a
9	chr1:169555944-169555994	SKMC	muscle:	n/a
10	chr1:169556657-169556707	ECC-1	luminal epithelium:	n/a
11	chr1:169555805-169555855	GM12891	blood:	n/a
12	chr1:169555944-169555994	HRE	kidney:	n/a
13	chr1:169558925-169558975	GM12878	blood:	n/a
14	chr1:169555805-169555855	GM12878	blood:	n/a
15	chr1:169555773-169555823	SAEC	small airway:	n/a
16	chr1:169555805-169555855	A549	lung:	n/a
17	chr1:169556022-169556072	NB4	blood:	n/a
18	chr1:169555674-169555724	GM12892	blood:	n/a
19	chr1:169556022-169556072	NT2-D1	testis:	n/a
20	chr1:169555805-169555855	AG04450	lung:	fetal
21	chr1:169555674-169555724	A549	lung:	n/a
22	chr1:169555773-169555823	HCF	heart:	n/a
23	chr1:169556657-169556707	IMR90	lung:	fetal
24	chr1:169555674-169555724	Hela-S3	cervix:	n/a
25	chr1:169555674-169555724	NHBE	bronchial:	n/a
26	chr1:169555944-169555994	LNCaP	prostate:	n/a
27	chr1:169556022-169556072	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:169555674-169555724	SK-N-SH	brain:	n/a
29	chr1:169555681-169555731	LNCaP	prostate:	n/a
30	chr1:169555674-169555724	SAEC	small airway:	n/a
31	chr1:169558925-169558975	IMR90	lung:	fetal
32	chr1:169558925-169558975	AG04449	skin:	fetal
33	chr1:169558925-169558975	NHBE	bronchial:	n/a
34	chr1:169555805-169555855	Hela-S3	cervix:	n/a
35	chr1:169555944-169555994	AG04449	skin:	fetal
36	chr1:169555674-169555724	PrEC	prostate:	n/a
37	chr1:169555944-169555994	NH-A	brain:	n/a
38	chr1:169555944-169555994	HCF	heart:	n/a
39	chr1:169556022-169556072	CMK	blood:	n/a
40	chr1:169555681-169555731	ProgFib	skin:	n/a
41	chr1:169556657-169556707	AG10803	skin:	n/a
42	chr1:169555773-169555823	LNCaP	prostate:	n/a
43	chr1:169558925-169558975	CMK	blood:	n/a
44	chr1:169555773-169555823	HL-60	blood:	n/a
45	chr1:169555805-169555855	HCT-116	colon:	n/a
46	chr1:169556022-169556072	HAEpiC	amniotic membrane:	n/a
47	chr1:169555805-169555855	Hepatocyte	liver:	n/a
48	chr1:169555773-169555823	HRPEpiC	eye:	n/a
49	chr1:169556657-169556707	GM12892	blood:	n/a
50	chr1:169555944-169555994	A549	lung:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169554006..169554804-chrX:81997894..81998531,2	MCF-7	breast:
2	chr1:169539510..169541317-chr1:169543367..169545442,2	K562	blood:
3	chr1:169541824..169543359-chr1:169543755..169546590,2	MCF-7	breast:
4	chr1:169543905..169545512-chr1:169548629..169550660,2	K562	blood:
5	chr1:169454435..169456317-chr1:169545578..169547535,2	MCF-7	breast:
6	chr1:169531774..169534548-chr1:169536079..169538530,2	K562	blood:
7	chr1:169543905..169545512-chr1:169548629..169550660,2	K562	blood:
8	chr1:169529558..169531629-chr1:169534485..169537061,2	K562	blood:
9	chr1:169541824..169543359-chr1:169543755..169546590,2	MCF-7	breast:
10	chr1:169555910..169558714-chr1:169805893..169807663,2	K562	blood:
11	chr1:169453485..169455825-chr1:169552064..169553822,2	K562	blood:
12	chr1:169539510..169541317-chr1:169543367..169545442,2	K562	blood:
13	chr1:169531774..169534548-chr1:169536079..169538530,2	K562	blood:
14	chr1:169553531..169554398-chr1:169563651..169564307,2	MCF-7	breast:

No data

Variant related genes	Relation type
SELP	TF binding region
F5	TF binding region
SELP	CpG island
F5	CpG island
ENSG00000213062	chromatin interactions
ENSG00000117479	chromatin interactions

Extended variants
information (count: 1059 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6678795	chr1:169533266-169533267	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185145331	chr1:169533310-169533311	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs61805772	chr1:169533346-169533347	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs562737413	chr1:169533350-169533351	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs369422919	chr1:169533356-169533357	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs551429876	chr1:169533379-169533380	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs566448198	chr1:169533400-169533401	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs527254990	chr1:169533401-169533402	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs35852972	chr1:169533402-169533403	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs141129349	chr1:169533407-169533408	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs538173271	chr1:169533416-169533417	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs112641077	chr1:169533436-169533437	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs150716552	chr1:169533452-169533453	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs137938060	chr1:169533525-169533526	Weak transcription Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs724510	chr1:169533710-169533711	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs538881071	chr1:169533730-169533731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570262263	chr1:169533734-169533735	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554190720	chr1:169533741-169533742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs724509	chr1:169533744-169533745	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536637560	chr1:169533756-169533757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555047699	chr1:169533762-169533763	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137956128	chr1:169533775-169533776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572191994	chr1:169533777-169533778	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572814536	chr1:169533784-169533785	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571743711	chr1:169533814-169533815	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562662796	chr1:169533817-169533818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs724508	chr1:169533845-169533846	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs111310239	chr1:169533848-169533849	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115955140	chr1:169533877-169533878	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142224328	chr1:169533898-169533899	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557474603	chr1:169533919-169533920	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548550411	chr1:169533943-169533944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370194204	chr1:169533975-169533976	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188875550	chr1:169533985-169533986	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146404119	chr1:169533997-169533998	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs724507	chr1:169534028-169534029	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs139661191	chr1:169534054-169534055	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539181999	chr1:169534096-169534097	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547714618	chr1:169534123-169534124	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2236871	chr1:169534149-169534150	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs181636176	chr1:169534167-169534168	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563271479	chr1:169534183-169534184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186334065	chr1:169534223-169534224	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576477907	chr1:169534238-169534239	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537447613	chr1:169534239-169534240	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563983809	chr1:169534240-169534241	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577902965	chr1:169534268-169534269	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545186955	chr1:169534280-169534281	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573484095	chr1:169534281-169534282	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571790420	chr1:169534288-169534289	Strong transcription Weak transcription Bivalent Enhancer Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
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
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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169505800-169534800	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr1:169506200-169542800	Weak transcription	Right Ventricle	heart
3	chr1:169524600-169541800	Weak transcription	Placenta	Placenta
4	chr1:169528600-169533400	Weak transcription	Stomach Mucosa	stomach
5	chr1:169530200-169535400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr1:169530200-169539000	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr1:169530400-169534000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr1:169530800-169534800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr1:169531600-169534800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:169532400-169534600	Strong transcription	Liver	Liver
11	chr1:169533000-169533600	ZNF genes & repeats	HepG2	liver
12	chr1:169533200-169551600	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr1:169533400-169544600	Enhancers	Stomach Mucosa	stomach
14	chr1:169533600-169534200	Strong transcription	HepG2	liver
15	chr1:169534000-169541400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr1:169534200-169534400	Bivalent Enhancer	Small Intestine	intestine
17	chr1:169534200-169537000	Genic enhancers	HepG2	liver
18	chr1:169534400-169536000	Enhancers	Duodenum Mucosa	Duodenum
19	chr1:169534600-169534800	Genic enhancers	Liver	Liver
20	chr1:169534600-169535800	Enhancers	HUVEC	blood vessel
21	chr1:169534600-169537400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr1:169534800-169535200	Enhancers	Primary hematopoietic stem cells	blood
23	chr1:169534800-169535400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr1:169534800-169535400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr1:169534800-169535600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
26	chr1:169534800-169535600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr1:169534800-169535600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:169534800-169535600	Enhancers	Dnd41	blood
29	chr1:169534800-169535800	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr1:169534800-169535800	Enhancers	NHEK	skin
31	chr1:169534800-169538800	Enhancers	Liver	Liver
32	chr1:169535000-169535600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr1:169535000-169535600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr1:169535000-169535600	Enhancers	Thymus	Thymus
35	chr1:169535000-169535800	Enhancers	Fetal Kidney	kidney
36	chr1:169535000-169535800	Enhancers	HMEC	breast
37	chr1:169535200-169535600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:169535200-169535600	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr1:169535200-169535800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr1:169535200-169535800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:169535400-169535600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr1:169535400-169540200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr1:169535600-169536000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr1:169535600-169538000	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr1:169535600-169539400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:169535800-169541600	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr1:169536000-169536200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr1:169536000-169539000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr1:169536200-169536400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:169536200-169536400	Enhancers	Left Ventricle	heart

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