Variant report

Variant	nsv1010007
Chromosome Location	chr1:169895282-169946436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:169898074-169898510	K562	blood:	n/a	n/a
2	ARID3A	chr1:169898085-169898379	HepG2	liver:	n/a	n/a
3	BCLAF1	chr1:169897998-169898407	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:169895312-169895694	GM12878	blood:	n/a	n/a
5	CBX3	chr1:169897990-169898402	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
7	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
8	CEBPB	chr1:169897984-169898391	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
10	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
11	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
12	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
13	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
14	CEBPB	chr1:169895158-169895662	MCF-7	breast:	n/a	n/a
15	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
16	CHD1	chr1:169898365-169898449	GM12878	blood:	n/a	n/a
17	CTCF	chr1:169898088-169898380	K562	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
18	CTCF	chr1:169898140-169898290	GM12865	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
19	CTCF	chr1:169898180-169898330	HEK293	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
20	CTCF	chr1:169898160-169898310	AG10803	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
21	CTCF	chr1:169898120-169898270	HVMF	connective:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
22	CTCF	chr1:169898113-169898333	GM13976	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
23	CTCF	chr1:169898140-169898290	BJ	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
24	CTCF	chr1:169898160-169898310	NHDF-neo	bronchial:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
25	CTCF	chr1:169898160-169898310	HEK293	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
26	CTCF	chr1:169898120-169898270	GM12873	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
27	CTCF	chr1:169898121-169898335	GM13977	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
28	CTCF	chr1:169898031-169898470	A549	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
29	CTCF	chr1:169898140-169898290	AoAF	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
30	CTCF	chr1:169898060-169898421	A549	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
31	CTCF	chr1:169898031-169898455	IMR90	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
32	CTCF	chr1:169898160-169898310	Caco-2	colon:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
33	CTCF	chr1:169898160-169898310	K562	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
34	CTCF	chr1:169898140-169898290	NHDF-neo	bronchial:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
35	CTCF	chr1:169898200-169898350	HCM	heart:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
36	CTCF	chr1:169898080-169898230	HFF-Myc	foreskin:	n/a	n/a
37	CTCF	chr1:169898140-169898290	SAEC	small airway:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
38	CTCF	chr1:169898099-169898372	Spleen_OC	spleen:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
39	CTCF	chr1:169898088-169898386	HUVEC	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
40	CTCF	chr1:169898180-169898330	GM12878	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
41	CTCF	chr1:169898180-169898330	HRPEpiC	eye:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
42	CTCF	chr1:169898140-169898290	GM12875	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
43	CTCF	chr1:169898160-169898310	NHEK	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
44	CTCF	chr1:169898160-169898310	GM12874	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
45	CTCF	chr1:169898180-169898330	GM12869	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
46	CTCF	chr1:169897868-169898622	A549	lung:	n/a	chr1:169898236-169898244 chr1:169898233-169898254 chr1:169898231-169898249
47	CTCF	chr1:169897840-169897990	NHLF	lung:	n/a	n/a
48	CTCF	chr1:169898140-169898290	Hela-S3	cervix:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
49	CTCF	chr1:169898120-169898270	GM12874	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
50	CTCF	chr1:169897987-169898452	MCF-7	breast:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249

No.	Distal block	Cell Line	Cell type
1	chr1:169896264..169898992-chr1:170499654..170502527,2	MCF-7	breast:
2	chr1:169904469..169905208-chr1:169979740..169980542,2	MCF-7	breast:
3	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
4	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
5	chr1:169909334..169912008-chr1:170041825..170044429,2	MCF-7	breast:
6	chr1:169858457..169860973-chr1:169907396..169909921,2	MCF-7	breast:
7	chr1:169862245..169864105-chr1:169894595..169896381,2	MCF-7	breast:
8	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
9	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
10	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
11	chr1:169883530..169886106-chr1:169901752..169904376,3	K562	blood:
12	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
13	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
14	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
15	chr1:169942236..169943172-chrX:26753938..26754794,2	MCF-7	breast:
16	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
17	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
18	chr1:169897805..169898496-chr1:170898617..170899529,4	MCF-7	breast:
19	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
20	chr1:169819515..169822344-chr1:169896401..169898488,2	MCF-7	breast:
21	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
22	chr1:169891530..169894353-chr1:169899147..169901987,3	K562	blood:
23	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
24	chr1:169909516..169911412-chr20:55839152..55841163,2	MCF-7	breast:
25	chr1:169861655..169864221-chr1:169940931..169943553,2	MCF-7	breast:
26	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
27	chr1:169897753..169898707-chr1:170850760..170851657,6	MCF-7	breast:
28	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
29	chr1:169860365..169863802-chr1:169902105..169905662,4	MCF-7	breast:
30	chr1:169885836..169887922-chr1:169893783..169895856,2	MCF-7	breast:
31	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
32	chr1:169897755..169898590-chr1:170734743..170735498,2	MCF-7	breast:
33	chr1:169897891..169898773-chr1:170898615..170899541,2	MCF-7	breast:
34	chr1:169861783..169864814-chr1:169892837..169895451,3	MCF-7	breast:
35	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCYL3-1	chr1:169927085-169927387	NONHSAT007483

Variant related genes	Relation type
RN7SL269P	TF binding region
ENSG00000101144	chromatin interactions
ENSG00000231407	chromatin interactions
ENSG00000120370	chromatin interactions
ENSG00000075945	chromatin interactions
ENSG00000000457	chromatin interactions

Extended variants
information (count: 1704 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1704 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2806390	chr1:169895316-169895317	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs140824895	chr1:169895333-169895334	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144574953	chr1:169895434-169895435	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192877123	chr1:169895468-169895469	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs184422510	chr1:169895470-169895471	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552266586	chr1:169895496-169895497	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573184736	chr1:169895556-169895557	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540646970	chr1:169895557-169895558	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs533986087	chr1:169895567-169895568	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs534891700	chr1:169895579-169895580	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs562021294	chr1:169895586-169895587	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs377129399	chr1:169895619-169895620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563375618	chr1:169895674-169895675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530714222	chr1:169895677-169895678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs552011851	chr1:169895717-169895718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs2750020	chr1:169895723-169895724	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs528143487	chr1:169895737-169895738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs7526925	chr1:169895739-169895740	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377663941	chr1:169895745-169895746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs187270899	chr1:169895778-169895779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138382361	chr1:169895815-169895816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112339572	chr1:169895816-169895817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs201550590	chr1:169895822-169895823	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs1159379	chr1:169895825-169895826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs114533683	chr1:169895827-169895828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201844200	chr1:169895831-169895832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs398053516	chr1:169895843-169895844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs3068642	chr1:169895844-169895845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375567601	chr1:169895845-169895846	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs6684078	chr1:169895868-169895869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs6659747	chr1:169895874-169895875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs192554348	chr1:169895894-169895895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs6672703	chr1:169895970-169895971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371612058	chr1:169896001-169896002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs556553914	chr1:169896011-169896012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs12385721	chr1:169896014-169896015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566965298	chr1:169896125-169896126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs534238530	chr1:169896258-169896259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs16862760	chr1:169896351-169896352	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564179110	chr1:169896353-169896354	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376648130	chr1:169896387-169896388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs495092	chr1:169896419-169896420	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs546318378	chr1:169896483-169896484	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575417783	chr1:169896514-169896515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs35400092	chr1:169896587-169896588	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs151254558	chr1:169896665-169896666	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs527896411	chr1:169896681-169896682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs564089656	chr1:169896727-169896728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184559931	chr1:169896728-169896729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539938595	chr1:169896785-169896786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169876200-169903600	Weak transcription	Aorta	Aorta
2	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr1:169881400-169901000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr1:169884200-169913000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr1:169884600-169900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:169884600-169900600	Weak transcription	NHDF-Ad	bronchial
7	chr1:169885200-169900800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:169885400-169913200	Weak transcription	Ovary	ovary
9	chr1:169885600-169903200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr1:169885800-169896600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:169885800-169898000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr1:169886400-169913000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr1:169887000-169911400	Weak transcription	Left Ventricle	heart
15	chr1:169888800-169900600	Weak transcription	Fetal Stomach	stomach
16	chr1:169889600-169900600	Weak transcription	Fetal Lung	lung
17	chr1:169889800-169898000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr1:169890800-169906200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr1:169891000-169896800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr1:169891000-169898200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr1:169891000-169911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr1:169891000-169913200	Weak transcription	Adipose Nuclei	Adipose
23	chr1:169892800-169895600	Enhancers	Fetal Heart	heart
24	chr1:169894000-169895400	Enhancers	HSMMtube	muscle
25	chr1:169894200-169903400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr1:169894600-169895400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:169894800-169895400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr1:169894800-169895400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:169895000-169895400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr1:169895000-169896000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:169895000-169896400	Enhancers	Dnd41	blood
32	chr1:169895200-169895400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr1:169895200-169895400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:169895200-169895400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr1:169895200-169895400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr1:169895200-169895400	Enhancers	Fetal Intestine Small	intestine
37	chr1:169895200-169895400	Flanking Active TSS	GM12878-XiMat	blood
38	chr1:169895200-169895600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:169895200-169895600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr1:169895200-169896400	Enhancers	Primary T cells from cord blood	blood
41	chr1:169895400-169895600	Active TSS	GM12878-XiMat	blood
42	chr1:169895600-169898000	Weak transcription	GM12878-XiMat	blood
43	chr1:169895600-169900600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr1:169895600-169901000	Weak transcription	Fetal Heart	heart
45	chr1:169896000-169896800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:169896400-169898000	Weak transcription	Dnd41	blood
47	chr1:169898000-169898200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr1:169898000-169898200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
49	chr1:169898000-169898200	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr1:169898000-169898200	Enhancers	Dnd41	blood

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