Variant report

Variant	nsv1000254
Chromosome Location	chr1:169203554-169271792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:352)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169235297-169235803	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169240319-169240724	K562	blood:	n/a	n/a
3	ARID3A	chr1:169209995-169210076	K562	blood:	n/a	n/a
4	ARID3A	chr1:169256764-169256929	K562	blood:	n/a	n/a
5	ARID3A	chr1:169219638-169220576	HepG2	liver:	n/a	n/a
6	ATF1	chr1:169210187-169210271	K562	blood:	n/a	n/a
7	ATF1	chr1:169271654-169271659	K562	blood:	n/a	n/a
8	ATF1	chr1:169240334-169240757	K562	blood:	n/a	n/a
9	BHLHE40	chr1:169240319-169240648	K562	blood:	n/a	n/a
10	CBX3	chr1:169250809-169251199	K562	blood:	n/a	n/a
11	CEBPB	chr1:169229862-169230008	K562	blood:	n/a	chr1:169229886-169229899 chr1:169229888-169229897 chr1:169229888-169229897 chr1:169229886-169229897 chr1:169229888-169229897 chr1:169229887-169229898 chr1:169229888-169229897
12	CEBPB	chr1:169209637-169210183	HCT-116	colon:	n/a	n/a
13	CEBPB	chr1:169229825-169229981	HepG2	liver:	n/a	chr1:169229886-169229899 chr1:169229888-169229897 chr1:169229888-169229897 chr1:169229886-169229897 chr1:169229888-169229897 chr1:169229887-169229898 chr1:169229888-169229897
14	CEBPB	chr1:169240163-169240324	K562	blood:	n/a	chr1:169240208-169240219 chr1:169240208-169240219 chr1:169240206-169240219 chr1:169240206-169240219
15	CEBPB	chr1:169268271-169268445	IMR90	lung:	n/a	chr1:169268372-169268385
16	CEBPB	chr1:169217062-169217242	IMR90	lung:	n/a	chr1:169217167-169217178
17	CEBPB	chr1:169219114-169219471	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr1:169256612-169256812	K562	blood:	n/a	n/a
19	CEBPB	chr1:169217146-169217217	HepG2	liver:	n/a	chr1:169217167-169217178
20	CHD2	chr1:169257357-169257565	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:169257368-169257438	Gliobla	brain:	n/a	chr1:169257378-169257396 chr1:169257379-169257395
22	CTCF	chr1:169257400-169257550	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr1:169240580-169240730	HPF	lung:	n/a	n/a
24	CTCF	chr1:169240440-169240590	HCM	heart:	n/a	n/a
25	CTCF	chr1:169240480-169240630	RPTEC	kidney:	n/a	n/a
26	CTCF	chr1:169240600-169240750	HRE	kidney:	n/a	n/a
27	CTCF	chr1:169240565-169240710	LNCaP	prostate:	n/a	n/a
28	CTCF	chr1:169240552-169240712	HepG2	liver:	n/a	n/a
29	CTCF	chr1:169240540-169240690	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr1:169240540-169240690	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:169240540-169240690	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr1:169215445-169215504	Fibrobl	skin:	n/a	n/a
33	CTCF	chr1:169240560-169240710	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr1:169240620-169240770	RPTEC	kidney:	n/a	n/a
35	CTCF	chr1:169240537-169240716	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr1:169240550-169240706	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr1:169240520-169240670	HCFaa	heart:	n/a	n/a
38	CTCF	chr1:169240581-169240651	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:169240420-169240570	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:169240400-169240550	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr1:169240402-169240751	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:169240543-169240697	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:169240560-169240710	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr1:169240520-169240670	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr1:169259970-169260058	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr1:169257260-169257410	SAEC	small airway:	n/a	chr1:169257378-169257396 chr1:169257379-169257395
47	CTCF	chr1:169257300-169257450	AG09309	skin:	n/a	chr1:169257378-169257396 chr1:169257379-169257395
48	CTCF	chr1:169240580-169240730	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr1:169257340-169257490	AG10803	skin:	n/a	chr1:169257378-169257396 chr1:169257379-169257395
50	CTCF	chr1:169257280-169257430	MCF-7	breast:	n/a	chr1:169257378-169257396 chr1:169257379-169257395

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:169258066-169258116	H1-hESC	embryonic stem cell:	embryo
2	chr1:169258066-169258116	AoSMC	blood vessel:	n/a
3	chr1:169258066-169258116	CMK	blood:	n/a
4	chr1:169258066-169258116	AG09309	skin:	n/a
5	chr1:169258066-169258116	HUVEC	blood vessel:	n/a
6	chr1:169258066-169258116	AG04449	skin:	fetal
7	chr1:169258066-169258116	Caco-2	colon:	n/a
8	chr1:169258066-169258116	HIPEpiC	eye:	n/a
9	chr1:169258066-169258116	GM12891	blood:	n/a
10	chr1:169258066-169258116	HCF	heart:	n/a
11	chr1:169258066-169258116	LNCaP	prostate:	n/a
12	chr1:169258066-169258116	NB4	blood:	n/a
13	chr1:169258066-169258116	HCPEpiC	choroid plexus:	n/a
14	chr1:169258066-169258116	HEEpiC	esophagus:	n/a
15	chr1:169258066-169258116	MCF10A-Er-Src	breast:	n/a
16	chr1:169258066-169258116	PrEC	prostate:	n/a
17	chr1:169258066-169258116	HCM	heart:	n/a
18	chr1:169258066-169258116	PANC-1	pancreas:	n/a
19	chr1:169258066-169258116	HEK293	kidney:	embryo
20	chr1:169258066-169258116	SK-N-SH_RA	brain:	n/a
21	chr1:169258066-169258116	GM06990	blood:	n/a
22	chr1:169258066-169258116	Hela-S3	cervix:	n/a
23	chr1:169258066-169258116	HMEC	breast:	n/a
24	chr1:169258066-169258116	HAEpiC	amniotic membrane:	n/a
25	chr1:169258066-169258116	IMR90	lung:	fetal
26	chr1:169258066-169258116	HNPCEpiC	eye:	n/a
27	chr1:169258066-169258116	SK-N-MC	brain:	n/a
28	chr1:169258066-169258116	AG10803	skin:	n/a
29	chr1:169258066-169258116	HCT-116	colon:	n/a
30	chr1:169258066-169258116	MCF-7	breast:	n/a
31	chr1:169258066-169258116	ovcar-3	ovarian:	n/a
32	chr1:169258066-169258116	T-47D	breast:	n/a
33	chr1:169258066-169258116	HepG2	liver:	n/a
34	chr1:169258066-169258116	HL-60	blood:	n/a
35	chr1:169258066-169258116	Hepatocyte	liver:	n/a
36	chr1:169258066-169258116	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:169258066-169258116	NHDF-neo	bronchial:	n/a
38	chr1:169258066-169258116	SAEC	small airway:	n/a
39	chr1:169258066-169258116	AG09319	gingival:	n/a
40	chr1:169258066-169258116	NT2-D1	testis:	n/a
41	chr1:169258066-169258116	AG04450	lung:	fetal
42	chr1:169258066-169258116	Jurkat	blood:	n/a
43	chr1:169258066-169258116	PFSK-1	brain:	n/a
44	chr1:169258066-169258116	GM12892	blood:	n/a
45	chr1:169258066-169258116	NHBE	bronchial:	n/a
46	chr1:169258066-169258116	HRPEpiC	eye:	n/a
47	chr1:169258066-169258116	SKMC	muscle:	n/a
48	chr1:169258066-169258116	BJ	skin:	n/a
49	chr1:169258066-169258116	BE2_C	brain:	n/a
50	chr1:169258066-169258116	GM12878	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
2	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
3	chr1:169208518..169210284-chr1:169213594..169216583,2	K562	blood:
4	chr1:169192162..169194718-chr1:169212473..169215131,2	K562	blood:
5	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
6	chr1:169210215..169210976-chr2:173891921..173892590,2	MCF-7	breast:
7	chr1:169266400..169268623-chr1:169277324..169279302,2	K562	blood:
8	chr1:169267146..169270567-chr1:169272063..169277859,6	K562	blood:
9	chr1:169201903..169204438-chr1:169206741..169208381,2	MCF-7	breast:
10	chr1:169210444..169212042-chr1:169215118..169217438,2	K562	blood:
11	chr1:169249538..169251657-chr1:169297595..169299857,2	MCF-7	breast:
12	chr1:169265989..169270734-chr1:169271559..169276402,6	K562	blood:

No data

Variant related genes	Relation type
NME7	TF binding region
NME7	CpG island
ENSG00000143156	chromatin interactions

Extended variants
information (count: 2547 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2547 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13374140	chr1:169203619-169203620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560494236	chr1:169203633-169203634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200636505	chr1:169203637-169203638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575422702	chr1:169203676-169203677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530528505	chr1:169203679-169203680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192417204	chr1:169203684-169203685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2300159	chr1:169203693-169203694	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs558030081	chr1:169203697-169203698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs569416719	chr1:169203738-169203739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144080110	chr1:169203750-169203751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377510970	chr1:169203752-169203753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573414765	chr1:169203766-169203767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540635676	chr1:169203796-169203797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114714687	chr1:169203800-169203801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142229997	chr1:169203844-169203845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184969139	chr1:169203846-169203847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563517306	chr1:169203847-169203848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530724083	chr1:169203854-169203855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59283002	chr1:169203943-169203944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545974839	chr1:169203979-169203980	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs151185507	chr1:169204007-169204008	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs115285296	chr1:169204094-169204095	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546598179	chr1:169204143-169204144	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529734282	chr1:169204162-169204163	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs10919102	chr1:169204219-169204220	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112602896	chr1:169204268-169204269	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs140301383	chr1:169204336-169204337	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs550257798	chr1:169204354-169204355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568565446	chr1:169204364-169204365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144390206	chr1:169204378-169204379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557894565	chr1:169204384-169204385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34165486	chr1:169204409-169204410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs36013941	chr1:169204410-169204411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567172318	chr1:169204424-169204425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202081199	chr1:169204429-169204430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374917505	chr1:169204436-169204437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369230839	chr1:169204462-169204463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566797678	chr1:169204492-169204493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188217703	chr1:169204554-169204555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544766138	chr1:169204594-169204595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556699867	chr1:169204629-169204630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs12741540	chr1:169204640-169204641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs181018110	chr1:169204644-169204645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372959772	chr1:169204733-169204734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146996423	chr1:169204834-169204835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531371494	chr1:169204836-169204837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184756362	chr1:169204848-169204849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533861612	chr1:169204850-169204851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561769493	chr1:169204863-169204864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528860543	chr1:169204865-169204866	Weak transcription 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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169172400-169207600	Weak transcription	Esophagus	oesophagus
2	chr1:169172600-169227000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:169176600-169206200	Weak transcription	Aorta	Aorta
4	chr1:169177400-169207400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr1:169180000-169210000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:169180600-169206200	Weak transcription	Left Ventricle	heart
7	chr1:169182800-169205400	Weak transcription	Adipose Nuclei	Adipose
8	chr1:169184400-169206200	Weak transcription	Lung	lung
9	chr1:169184800-169207400	Weak transcription	Ovary	ovary
10	chr1:169187600-169207800	Weak transcription	Primary T cells from cord blood	blood
11	chr1:169187800-169211800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr1:169192200-169209600	Weak transcription	NHEK	skin
13	chr1:169192400-169210000	Weak transcription	Brain Hippocampus Middle	brain
14	chr1:169194000-169210000	Weak transcription	NHDF-Ad	bronchial
15	chr1:169194800-169207400	Weak transcription	Primary B cells from cord blood	blood
16	chr1:169194800-169214000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:169195200-169207600	Weak transcription	Fetal Lung	lung
18	chr1:169195400-169207600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr1:169197000-169204600	Weak transcription	HUVEC	blood vessel
20	chr1:169197200-169206200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:169197200-169207600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:169197200-169210200	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr1:169197600-169210200	Weak transcription	Brain Substantia Nigra	brain
24	chr1:169198000-169209800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:169198600-169205200	Weak transcription	Fetal Kidney	kidney
26	chr1:169199200-169205000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr1:169199200-169210200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr1:169199200-169211600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:169199600-169209800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr1:169200800-169204000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr1:169201000-169207800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:169201000-169212800	Weak transcription	Psoas Muscle	Psoas
33	chr1:169201200-169204600	Weak transcription	Rectal Smooth Muscle	rectum
34	chr1:169201200-169205000	Weak transcription	Colon Smooth Muscle	Colon
35	chr1:169202400-169208800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr1:169202800-169205400	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr1:169203200-169205400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:169203600-169206800	Enhancers	Liver	Liver
39	chr1:169204000-169204200	Enhancers	HepG2	liver
40	chr1:169204600-169205000	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr1:169204600-169205200	Enhancers	HUVEC	blood vessel
42	chr1:169204600-169206200	Enhancers	Rectal Smooth Muscle	rectum
43	chr1:169205000-169205400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:169205000-169206400	Enhancers	Colon Smooth Muscle	Colon
45	chr1:169205200-169209800	Weak transcription	HUVEC	blood vessel
46	chr1:169205400-169205600	Enhancers	Adipose Nuclei	Adipose
47	chr1:169205400-169205600	Enhancers	Fetal Heart	heart
48	chr1:169205400-169205600	Enhancers	Right Ventricle	heart
49	chr1:169205400-169205600	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr1:169205400-169206400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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