Variant report

Variant	nsv1003588
Chromosome Location	chr1:169895984-169946436
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	chr1:169898085-169898379	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169898074-169898510	K562	blood:	n/a	n/a
3	BCLAF1	chr1:169897998-169898407	GM12878	blood:	n/a	n/a
4	CBX3	chr1:169897990-169898402	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
6	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
7	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
8	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
9	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
10	CEBPB	chr1:169897984-169898391	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
12	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
13	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
14	CHD1	chr1:169898365-169898449	GM12878	blood:	n/a	n/a
15	CTCF	chr1:169898180-169898330	GM12878	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
16	CTCF	chr1:169898079-169898332	SK-N-SH_RA	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
17	CTCF	chr1:169898160-169898310	AG04450	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
18	CTCF	chr1:169898140-169898290	HUVEC	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
19	CTCF	chr1:169898160-169898310	GM12867	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
20	CTCF	chr1:169898120-169898270	HVMF	connective:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
21	CTCF	chr1:169898180-169898330	HA-sp	spinal cord:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
22	CTCF	chr1:169898092-169898361	GM12878	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
23	CTCF	chr1:169914599-169914659	Fibrobl	skin:	n/a	n/a
24	CTCF	chr1:169898260-169898410	WI-38	lung:	n/a	n/a
25	CTCF	chr1:169898160-169898310	GM12878	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
26	CTCF	chr1:169898180-169898330	AG09309	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
27	CTCF	chr1:169898120-169898270	GM12873	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
28	CTCF	chr1:169898160-169898310	HEK293	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
29	CTCF	chr1:169898100-169898358	Hela-S3	cervix:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
30	CTCF	chr1:169898140-169898290	Caco-2	colon:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
31	CTCF	chr1:169897750-169897793	Lung_OC	lung:	n/a	n/a
32	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:169898120-169898270	HepG2	liver:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
34	CTCF	chr1:169898180-169898330	NHEK	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
35	CTCF	chr1:169898160-169898310	NHEK	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
36	CTCF	chr1:169898080-169898230	HCM	heart:	n/a	n/a
37	CTCF	chr1:169898140-169898290	RPTEC	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
38	CTCF	chr1:169898300-169898450	A549	lung:	n/a	n/a
39	CTCF	chr1:169898200-169898350	HPF	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
40	CTCF	chr1:169898160-169898310	SK-N-SH_RA	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
41	CTCF	chr1:169897917-169898404	Medullo	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
42	CTCF	chr1:169898160-169898310	HCPEpiC	choroid plexus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
43	CTCF	chr1:169898088-169898380	K562	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
44	CTCF	chr1:169898180-169898330	HEK293	kidney:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
45	CTCF	chr1:169898160-169898310	AG04449	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
46	CTCF	chr1:169898180-169898330	GM12870	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
47	CTCF	chr1:169898143-169898326	GM10266	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
48	CTCF	chr1:169898031-169898470	A549	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
49	CTCF	chr1:169898140-169898290	GM12865	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
50	CTCF	chr1:169898180-169898330	GM12864	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249

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

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

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

Extended variants
information (count: 1671 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1671 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371612058	chr1:169896001-169896002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs556553914	chr1:169896011-169896012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs12385721	chr1:169896014-169896015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566965298	chr1:169896125-169896126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534238530	chr1:169896258-169896259	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs16862760	chr1:169896351-169896352	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs564179110	chr1:169896353-169896354	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs376648130	chr1:169896387-169896388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs495092	chr1:169896419-169896420	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs546318378	chr1:169896483-169896484	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575417783	chr1:169896514-169896515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35400092	chr1:169896587-169896588	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs151254558	chr1:169896665-169896666	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs527896411	chr1:169896681-169896682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564089656	chr1:169896727-169896728	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs184559931	chr1:169896728-169896729	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539938595	chr1:169896785-169896786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201561807	chr1:169896820-169896821	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373459979	chr1:169896831-169896832	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189475005	chr1:169896895-169896896	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs16862764	chr1:169896934-169896935	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs61806078	chr1:169896963-169896964	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs550890358	chr1:169896973-169896974	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs564192429	chr1:169897021-169897022	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs35115912	chr1:169897058-169897059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs147566794	chr1:169897072-169897073	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528247389	chr1:169897157-169897158	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569555954	chr1:169897159-169897160	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs59851919	chr1:169897193-169897194	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551953150	chr1:169897234-169897235	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs59128071	chr1:169897244-169897245	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs397789861	chr1:169897254-169897255	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs566947458	chr1:169897315-169897316	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs534328676	chr1:169897326-169897327	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2474704	chr1:169897365-169897366	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs567689659	chr1:169897404-169897405	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2474705	chr1:169897417-169897418	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs529172868	chr1:169897479-169897480	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs2474707	chr1:169897486-169897487	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
40	rs545735170	chr1:169897491-169897492	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs80228718	chr1:169897577-169897578	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs12141609	chr1:169897671-169897672	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs117635723	chr1:169897760-169897761	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539974292	chr1:169897792-169897793	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs490000	chr1:169897832-169897833	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
46	rs371125724	chr1:169897840-169897841	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs59281230	chr1:169897858-169897859	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs10690029	chr1:169897862-169897863	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs528927898	chr1:169897880-169897881	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs544211820	chr1:169897881-169897882	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:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

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	chr1:169894200-169903400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:169895000-169896000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr1:169895000-169896400	Enhancers	Dnd41	blood
26	chr1:169895200-169896400	Enhancers	Primary T cells from cord blood	blood
27	chr1:169895600-169898000	Weak transcription	GM12878-XiMat	blood
28	chr1:169895600-169900600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:169895600-169901000	Weak transcription	Fetal Heart	heart
30	chr1:169896000-169896800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr1:169896400-169898000	Weak transcription	Dnd41	blood
32	chr1:169898000-169898200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr1:169898000-169898200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr1:169898000-169898200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr1:169898000-169898200	Enhancers	Dnd41	blood
36	chr1:169898000-169898200	Enhancers	GM12878-XiMat	blood
37	chr1:169898000-169898400	Enhancers	Fetal Kidney	kidney
38	chr1:169898200-169899000	Weak transcription	GM12878-XiMat	blood
39	chr1:169898200-169899200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:169898400-169900800	Weak transcription	Fetal Kidney	kidney
41	chr1:169899200-169900600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr1:169899200-169911400	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:169900600-169900800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:169900600-169901000	Enhancers	Stomach Mucosa	stomach
45	chr1:169900600-169901400	Enhancers	Fetal Lung	lung
46	chr1:169900600-169901400	Enhancers	Fetal Stomach	stomach
47	chr1:169900600-169901600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:169900600-169901600	Enhancers	NHLF	lung
49	chr1:169900600-169901600	Enhancers	Osteobl	bone
50	chr1:169900600-169901800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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