Variant report

Variant	esv3350498
Chromosome Location	chr1:161374323-161380643
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:75)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:75 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:161377600-161377723	K562	blood:	n/a	n/a
2	ATF2	chr1:161379562-161380002	GM12878	blood:	n/a	n/a
3	BATF	chr1:161379655-161380102	GM12878	blood:	n/a	n/a
4	BATF	chr1:161379614-161379994	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:161379842-161379970	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:161380344-161380544	K562	blood:	n/a	n/a
7	CBX3	chr1:161380161-161380430	K562	blood:	n/a	n/a
8	CBX3	chr1:161379997-161380740	K562	blood:	n/a	n/a
9	CEBPD	chr1:161380318-161380713	K562	blood:	n/a	n/a
10	CTCF	chr1:161376782-161376821	LNCaP	prostate:	n/a	n/a
11	CTCF	chr1:161376618-161376690	GM13976	blood:	n/a	n/a
12	EBF1	chr1:161379681-161380025	GM12878	blood:	n/a	n/a
13	ELF1	chr1:161379911-161380403	GM12878	blood:	n/a	chr1:161380228-161380241
14	ELF1	chr1:161379978-161380437	K562	blood:	n/a	chr1:161380228-161380241
15	EP300	chr1:161380362-161380750	K562	blood:	n/a	n/a
16	EP300	chr1:161377651-161377712	K562	blood:	n/a	n/a
17	GATA1	chr1:161380355-161380776	PBDE	blood:	n/a	n/a
18	GATA2	chr1:161380338-161380784	K562	blood:	n/a	n/a
19	GATA2	chr1:161374082-161374405	K562	blood:	n/a	n/a
20	HEY1	chr1:161376502-161376863	K562	blood:	n/a	n/a
21	IRF1	chr1:161379706-161379865	K562	blood:	n/a	n/a
22	IRF4	chr1:161379550-161380067	GM12878	blood:	n/a	n/a
23	IRF4	chr1:161379615-161380214	GM12878	blood:	n/a	n/a
24	KAP1	chr1:161380120-161380649	K562	blood:	n/a	n/a
25	MAX	chr1:161377259-161377544	K562	blood:	n/a	n/a
26	MAZ	chr1:161377474-161377669	K562	blood:	n/a	n/a
27	MXI1	chr1:161379703-161379894	GM12878	blood:	n/a	n/a
28	MYC	chr1:161376559-161376564	MCF-7	breast:	n/a	n/a
29	NR2F2	chr1:161380044-161380953	K562	blood:	n/a	n/a
30	NR2F2	chr1:161380367-161380722	K562	blood:	n/a	n/a
31	PAX5	chr1:161379600-161379975	GM12878	blood:	n/a	n/a
32	PAX5	chr1:161379604-161380196	GM12878	blood:	n/a	n/a
33	PAX5	chr1:161379602-161379916	GM12878	blood:	n/a	n/a
34	PBX3	chr1:161379644-161379843	GM12878	blood:	n/a	n/a
35	PML	chr1:161380391-161380751	K562	blood:	n/a	n/a
36	POLR2A	chr1:161376315-161376718	GM12891	blood:	n/a	n/a
37	POLR2A	chr1:161379791-161380008	GM12878	blood:	n/a	n/a
38	POLR2A	chr1:161376465-161376719	GM12878	blood:	n/a	n/a
39	POLR2A	chr1:161379860-161380000	GM12878	blood:	n/a	n/a
40	POLR2A	chr1:161379741-161379835	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr1:161376511-161376520	MCF-7	breast:	n/a	n/a
42	POLR2A	chr1:161376041-161376922	GM12878	blood:	n/a	n/a
43	POLR2A	chr1:161376521-161376679	MCF-7	breast:	n/a	n/a
44	POLR2A	chr1:161376522-161376694	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr1:161376441-161376856	GM12891	blood:	n/a	n/a
46	POLR2A	chr1:161376447-161376814	H1-hESC	embryonic stem cell:	n/a	n/a
47	POU2F2	chr1:161378621-161379067	GM12891	blood:	n/a	n/a
48	POU2F2	chr1:161378675-161379146	GM12878	blood:	n/a	n/a
49	POU2F2	chr1:161379541-161379959	GM12878	blood:	n/a	n/a
50	RCOR1	chr1:161375504-161375543	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161375390-161375440	U87	brain:	n/a
2	chr1:161375390-161375440	GM06990	blood:	n/a
3	chr1:161375390-161375440	MCF10A-Er-Src	breast:	n/a
4	chr1:161375390-161375440	HMEC	breast:	n/a
5	chr1:161375390-161375440	GM19239	blood:	n/a
6	chr1:161375390-161375440	GM12892	blood:	n/a
7	chr1:161375390-161375440	LNCaP	prostate:	n/a
8	chr1:161375390-161375440	HRE	kidney:	n/a
9	chr1:161375390-161375440	ECC-1	luminal epithelium:	n/a
10	chr1:161375390-161375440	A549	lung:	n/a
11	chr1:161375390-161375440	SK-N-MC	brain:	n/a
12	chr1:161375390-161375440	HRPEpiC	eye:	n/a
13	chr1:161375390-161375440	NB4	blood:	n/a
14	chr1:161375390-161375440	PFSK-1	brain:	n/a
15	chr1:161375390-161375440	MCF-7	breast:	n/a
16	chr1:161375390-161375440	HCT-116	colon:	n/a
17	chr1:161375390-161375440	CMK	blood:	n/a
18	chr1:161375390-161375440	BE2_C	brain:	n/a
19	chr1:161375390-161375440	T-47D	breast:	n/a
20	chr1:161375390-161375440	HEEpiC	esophagus:	n/a
21	chr1:161375390-161375440	HUVEC	blood vessel:	n/a
22	chr1:161375390-161375440	SK-N-SH_RA	brain:	n/a
23	chr1:161375390-161375440	RPTEC	kidney:	n/a
24	chr1:161375390-161375440	NT2-D1	testis:	n/a
25	chr1:161375390-161375440	NH-A	brain:	n/a
26	chr1:161375390-161375440	AG09309	skin:	n/a
27	chr1:161375390-161375440	HCPEpiC	choroid plexus:	n/a
28	chr1:161375390-161375440	HepG2	liver:	n/a
29	chr1:161375390-161375440	HCM	heart:	n/a
30	chr1:161375390-161375440	NHDF-neo	bronchial:	n/a
31	chr1:161375390-161375440	HL-60	blood:	n/a
32	chr1:161375390-161375440	Jurkat	blood:	n/a
33	chr1:161375390-161375440	HAEpiC	amniotic membrane:	n/a
34	chr1:161375390-161375440	PANC-1	pancreas:	n/a
35	chr1:161375390-161375440	HPAEpiC	pulmonary alveolar:	n/a
36	chr1:161375390-161375440	HEK293	kidney:	embryo
37	chr1:161375390-161375440	NHBE	bronchial:	n/a
38	chr1:161375390-161375440	SKMC	muscle:	n/a
39	chr1:161375390-161375440	IMR90	lung:	fetal
40	chr1:161375390-161375440	GM12891	blood:	n/a
41	chr1:161375390-161375440	Hela-S3	cervix:	n/a
42	chr1:161375390-161375440	SAEC	small airway:	n/a
43	chr1:161375390-161375440	Hepatocyte	liver:	n/a
44	chr1:161375390-161375440	HIPEpiC	eye:	n/a
45	chr1:161375390-161375440	ProgFib	skin:	n/a
46	chr1:161375390-161375440	K562	blood:	n/a
47	chr1:161375390-161375440	AG04449	skin:	fetal
48	chr1:161375390-161375440	ovcar-3	ovarian:	n/a
49	chr1:161375390-161375440	BJ	skin:	n/a
50	chr1:161375390-161375440	AG04450	lung:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161122375..161125085-chr1:161376067..161378858,2	K562	blood:
2	chr1:161371806..161374700-chr1:161382431..161384803,2	MCF-7	breast:
3	chr1:161379123..161382070-chr1:161387001..161390523,3	K562	blood:
4	chr1:161372330..161375943-chr1:161377177..161380756,5	K562	blood:
5	chr1:161170434..161172328-chr1:161378596..161380361,2	K562	blood:
6	chr1:161373435..161375369-chr1:161381940..161384249,4	K562	blood:
7	chr1:161367523..161369303-chr1:161373719..161375547,2	MCF-7	breast:
8	chr1:161377159..161380003-chr1:161395367..161397564,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000215840	TF binding region
ENSG00000215840	CpG island
ENSG00000215840	chromatin interactions
ENSG00000143222	chromatin interactions
ENSG00000158864	chromatin interactions

Extended variants
information (count: 231 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:231 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181171083	chr1:161374328-161374329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs35898380	chr1:161374360-161374361	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs569038900	chr1:161374410-161374411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538073645	chr1:161374411-161374412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548682947	chr1:161374412-161374413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12135728	chr1:161374413-161374414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368958130	chr1:161374462-161374463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185357783	chr1:161374515-161374516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553842660	chr1:161374572-161374573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577188581	chr1:161374594-161374595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141693105	chr1:161374603-161374604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs72714996	chr1:161374604-161374605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs576425146	chr1:161374619-161374620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7413615	chr1:161374663-161374664	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs573691982	chr1:161374686-161374687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562494622	chr1:161374698-161374699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560640548	chr1:161374718-161374719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548716424	chr1:161374725-161374726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574153741	chr1:161374850-161374851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189925740	chr1:161374864-161374865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138847374	chr1:161374867-161374868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540326070	chr1:161374984-161374985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34051793	chr1:161375055-161375056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559866883	chr1:161375096-161375097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77703498	chr1:161375114-161375115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76898076	chr1:161375121-161375122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532150705	chr1:161375172-161375173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10157990	chr1:161375174-161375175	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs182501316	chr1:161375182-161375183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548448507	chr1:161375183-161375184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568272067	chr1:161375185-161375186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527740219	chr1:161375197-161375198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547882618	chr1:161375205-161375206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574602069	chr1:161375210-161375211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568033121	chr1:161375211-161375212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10157991	chr1:161375213-161375214	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs187174923	chr1:161375214-161375215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs535754458	chr1:161375260-161375261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555491908	chr1:161375416-161375417	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs114882903	chr1:161375433-161375434	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs373086235	chr1:161375499-161375500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547110907	chr1:161375500-161375501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553866357	chr1:161375620-161375621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112705999	chr1:161375625-161375626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
45	rs545832828	chr1:161375666-161375667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73024097	chr1:161375674-161375675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs556235142	chr1:161375684-161375685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74124950	chr1:161375694-161375695	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs542150511	chr1:161375739-161375740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576676262	chr1:161375788-161375789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161370400-161375400	Weak transcription	Ovary	ovary
2	chr1:161370400-161379200	Weak transcription	Stomach Mucosa	stomach
3	chr1:161370400-161380000	Weak transcription	Gastric	stomach
4	chr1:161370600-161375200	Weak transcription	Hela-S3	cervix
5	chr1:161370600-161378600	Weak transcription	Fetal Heart	heart
6	chr1:161370600-161381800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr1:161370800-161374400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr1:161370800-161374800	Weak transcription	Fetal Brain Male	brain
9	chr1:161370800-161379200	Weak transcription	Colonic Mucosa	Colon
10	chr1:161371000-161374400	Weak transcription	Fetal Lung	lung
11	chr1:161371000-161378800	Weak transcription	Duodenum Mucosa	Duodenum
12	chr1:161371000-161378800	Weak transcription	Fetal Intestine Small	intestine
13	chr1:161371000-161379000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr1:161371000-161379000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr1:161371000-161379000	Weak transcription	Right Atrium	heart
16	chr1:161371000-161379400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr1:161371000-161381400	Weak transcription	Esophagus	oesophagus
18	chr1:161371000-161387800	Weak transcription	Spleen	Spleen
19	chr1:161371200-161378800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr1:161371200-161379000	Weak transcription	Psoas Muscle	Psoas
21	chr1:161371400-161378400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr1:161371400-161379000	Weak transcription	Primary B cells from peripheral blood	blood
23	chr1:161371600-161379000	Weak transcription	Right Ventricle	heart
24	chr1:161372200-161379800	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr1:161372400-161375400	Weak transcription	Pancreas	Pancrea
26	chr1:161372600-161374400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:161372800-161377400	Weak transcription	Fetal Intestine Large	intestine
28	chr1:161373400-161374600	Enhancers	HepG2	liver
29	chr1:161373800-161374400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr1:161374000-161374800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:161374000-161377600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr1:161374000-161379000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr1:161374200-161374600	Enhancers	K562	blood
34	chr1:161374200-161378800	Weak transcription	Left Ventricle	heart
35	chr1:161374200-161380000	Weak transcription	Small Intestine	intestine
36	chr1:161374400-161374800	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr1:161374400-161374800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr1:161374400-161374800	Enhancers	Fetal Lung	lung
39	chr1:161374400-161375400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:161374600-161377200	Weak transcription	K562	blood
41	chr1:161374600-161378600	Weak transcription	HepG2	liver
42	chr1:161374800-161375000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr1:161374800-161375000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr1:161374800-161379800	Weak transcription	Fetal Lung	lung
45	chr1:161374800-161380000	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr1:161375000-161377400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr1:161375400-161375600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:161375400-161375600	Enhancers	Ovary	ovary
49	chr1:161375400-161376800	Enhancers	Pancreas	Pancrea
50	chr1:161376200-161377600	Weak transcription	H9 Cell Line	embryonic stem cell

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