Variant report

Variant	nsv831260
Chromosome Location	chr8:20907266-21097125
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	ATF2	chr8:21039702-21040202	GM12878	blood:	n/a	n/a
2	ATF2	chr8:21032011-21032389	GM12878	blood:	n/a	n/a
3	ATF2	chr8:21039736-21040167	GM12878	blood:	n/a	n/a
4	BACH1	chr8:21035178-21035180	K562	blood:	n/a	n/a
5	BATF	chr8:20961550-20961882	GM12878	blood:	n/a	chr8:20961720-20961731
6	BATF	chr8:21039791-21040093	GM12878	blood:	n/a	n/a
7	BATF	chr8:21039838-21040187	GM12878	blood:	n/a	n/a
8	BATF	chr8:20961526-20961830	GM12878	blood:	n/a	chr8:20961720-20961731
9	BCL11A	chr8:21039822-21040106	GM12878	blood:	n/a	n/a
10	BCL11A	chr8:21032090-21032306	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:21039777-21040139	GM12878	blood:	n/a	n/a
12	BCL3	chr8:21000353-21000601	GM12878	blood:	n/a	chr8:21000463-21000472 chr8:21000464-21000473
13	BCL3	chr8:21017363-21018430	GM12878	blood:	n/a	n/a
14	BCL3	chr8:21017339-21018243	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:21039870-21040070	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:21032073-21032327	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:21096295-21096298	K562	blood:	n/a	n/a
18	CEBPB	chr8:20913877-20914202	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:20913886-20914184	A549	lung:	n/a	n/a
20	CEBPB	chr8:20916902-20917149	K562	blood:	n/a	chr8:20917030-20917041
21	CEBPB	chr8:20913882-20914203	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:20913845-20914246	MCF-7	breast:	n/a	n/a
23	CEBPB	chr8:20925030-20925226	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:20913887-20914170	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:20916875-20917150	IMR90	lung:	n/a	chr8:20917030-20917041
26	CEBPB	chr8:20913900-20914163	K562	blood:	n/a	n/a
27	CEBPB	chr8:21066713-21066847	A549	lung:	n/a	n/a
28	CEBPB	chr8:20916934-20917174	H1-hESC	embryonic stem cell:	n/a	chr8:20917030-20917041
29	CEBPB	chr8:21005690-21005742	HepG2	liver:	n/a	chr8:21005710-21005721
30	CEBPB	chr8:21096322-21096357	K562	blood:	n/a	n/a
31	CEBPB	chr8:21071954-21072206	HepG2	liver:	n/a	chr8:21072084-21072095
32	CEBPB	chr8:21073119-21073178	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:20929353-20929765	HepG2	liver:	n/a	chr8:20929621-20929634 chr8:20929621-20929632
34	CEBPB	chr8:20969875-20969923	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:21084807-21085012	MCF-7	breast:	n/a	n/a
36	CEBPB	chr8:20951952-20952054	K562	blood:	n/a	n/a
37	CEBPB	chr8:20949761-20949783	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:20916891-20917209	HepG2	liver:	n/a	chr8:20917030-20917041
39	CEBPB	chr8:21071950-21072152	IMR90	lung:	n/a	chr8:21072084-21072095
40	CHD1	chr8:21032115-21032389	GM12878	blood:	n/a	n/a
41	CREB1	chr8:21039817-21040281	GM12878	blood:	n/a	n/a
42	CREB1	chr8:21039816-21040284	GM12878	blood:	n/a	n/a
43	CTCF	chr8:20913894-20914221	K562	blood:	n/a	n/a
44	CTCF	chr8:20974380-20974530	WERI-Rb-1	eye:	n/a	n/a
45	CTCF	chr8:20986832-20987011	LNCaP	prostate:	n/a	chr8:20986931-20986949 chr8:20986934-20986943 chr8:20986933-20986954 chr8:20986934-20986947
46	CTCF	chr8:20986840-20986990	HRE	kidney:	n/a	chr8:20986931-20986949 chr8:20986934-20986943 chr8:20986933-20986954 chr8:20986934-20986947
47	CTCF	chr8:20986762-20986964	A549	lung:	n/a	chr8:20986931-20986949 chr8:20986934-20986943 chr8:20986933-20986954 chr8:20986934-20986947
48	CTCF	chr8:20974462-20974472	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr8:20986827-20987047	MCF-7	breast:	n/a	chr8:20986931-20986949 chr8:20986934-20986943 chr8:20986933-20986954 chr8:20986934-20986947
50	CTCF	chr8:20913980-20914130	HRPEpiC	eye:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:20919649..20922445-chr8:20924691..20927492,3	K562	blood:
2	chr8:21015073..21016879-chr8:21019625..21021848,2	K562	blood:
3	chr8:20983096..20985679-chr8:20989458..20991827,2	K562	blood:
4	chr8:20984570..20986928-chr8:20991210..20994043,2	K562	blood:
5	chr8:21000566..21002926-chr8:21006520..21008330,2	K562	blood:
6	chr8:21039519..21041986-chr8:21043567..21045082,2	K562	blood:
7	chr8:21015073..21016879-chr8:21019625..21021848,2	K562	blood:
8	chr8:21085653..21087927-chr8:21091745..21093754,2	K562	blood:
9	chr8:20983096..20985679-chr8:20989458..20991827,2	K562	blood:
10	chr8:21046396..21048432-chr8:21052883..21055018,2	K562	blood:
11	chr8:21000646..21002417-chr8:21003581..21006297,2	K562	blood:
12	chr8:20920073..20922021-chr8:20924691..20926689,2	K562	blood:
13	chr8:20940533..20944455-chr8:21040696..21044387,3	K562	blood:
14	chr8:20986575..20987388-chr8:21641622..21642126,2	MCF-7	breast:
15	chr8:20920073..20922021-chr8:20924691..20926689,2	K562	blood:
16	chr8:21000566..21002926-chr8:21006520..21008330,2	K562	blood:
17	chr8:20919649..20922445-chr8:20924691..20927492,3	K562	blood:
18	chr8:20950968..20952803-chr8:20959075..20960715,2	K562	blood:
19	chr8:20940533..20944455-chr8:21040696..21044387,3	K562	blood:
20	chr8:21039519..21041986-chr8:21043567..21045082,2	K562	blood:
21	chr8:20950968..20952803-chr8:20959075..20960715,2	K562	blood:
22	chr8:21085653..21087927-chr8:21091745..21093754,2	K562	blood:
23	chr8:21000646..21002417-chr8:21003581..21006297,2	K562	blood:
24	chr8:20984570..20986928-chr8:20991210..20994043,2	K562	blood:
25	chr8:21046396..21048432-chr8:21052883..21055018,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GFRA2-6	chr8:21030675-21030922	l_3557_chr8:20853997-20856467_brain
2	lnc-GFRA2-6	chr8:20961661-20961726	l_3557_chr8:20853997-20856467_brain
3	lnc-GFRA2-2	chr8:20986395-20986642	XLOC_007019
4	lnc-GFRA2-2	chr8:20917383-20917446	XLOC_007019

Variant related genes	Relation type
ENSG00000215945	TF binding region

Extended variants
information (count: 7070 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:7070 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189340507	chr8:20907316-20907317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192595386	chr8:20907381-20907382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541024995	chr8:20907426-20907427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553308451	chr8:20907427-20907428	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116704108	chr8:20907428-20907429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544893710	chr8:20907462-20907463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183715839	chr8:20907463-20907464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530601174	chr8:20907464-20907465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs58110635	chr8:20907465-20907466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560173076	chr8:20907487-20907488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561042166	chr8:20907504-20907505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148549187	chr8:20907538-20907539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs546547795	chr8:20907547-20907548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34527344	chr8:20907550-20907551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112321062	chr8:20907552-20907553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532811527	chr8:20907559-20907560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113181150	chr8:20907567-20907568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114215003	chr8:20907595-20907596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146568449	chr8:20907613-20907614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74830061	chr8:20907650-20907651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555549013	chr8:20907666-20907667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567324292	chr8:20907680-20907681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534612880	chr8:20907751-20907752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552972750	chr8:20907766-20907767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141304601	chr8:20907784-20907785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557517072	chr8:20907804-20907805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556963894	chr8:20907811-20907812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542086320	chr8:20907827-20907828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1546710	chr8:20907847-20907848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs572780462	chr8:20907852-20907853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542409164	chr8:20907964-20907965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527912953	chr8:20907979-20907980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528530198	chr8:20908034-20908035	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540252847	chr8:20908055-20908056	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564966466	chr8:20908074-20908075	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532388136	chr8:20908101-20908102	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35517020	chr8:20908109-20908110	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575620180	chr8:20908115-20908116	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113481789	chr8:20908120-20908121	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546070902	chr8:20908121-20908122	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551298705	chr8:20908140-20908141	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115413148	chr8:20908156-20908157	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530319544	chr8:20908167-20908168	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145071773	chr8:20908210-20908211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151242996	chr8:20908213-20908214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534681350	chr8:20908219-20908220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376685978	chr8:20908221-20908222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571258770	chr8:20908222-20908223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188433345	chr8:20908227-20908228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557223338	chr8:20908244-20908245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20900400-20917600	Weak transcription	Psoas Muscle	Psoas
2	chr8:20907400-20908400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr8:20908000-20908200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:20908000-20908200	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr8:20911200-20913800	Enhancers	Fetal Brain Male	brain
6	chr8:20911600-20912000	Enhancers	Fetal Brain Female	brain
7	chr8:20912000-20912200	Weak transcription	Fetal Brain Female	brain
8	chr8:20912200-20912600	Enhancers	Fetal Brain Female	brain
9	chr8:20912400-20913600	Enhancers	Aorta	Aorta
10	chr8:20912600-20913600	Weak transcription	Fetal Brain Female	brain
11	chr8:20913400-20914800	Enhancers	Liver	Liver
12	chr8:20913400-20915000	Enhancers	Pancreas	Pancrea
13	chr8:20913600-20914000	Weak transcription	Aorta	Aorta
14	chr8:20913800-20914000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:20913800-20914000	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr8:20913800-20917800	Weak transcription	Fetal Brain Male	brain
17	chr8:20914000-20914200	Enhancers	Aorta	Aorta
18	chr8:20914200-20925600	Weak transcription	Aorta	Aorta
19	chr8:20916000-20918400	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr8:20916600-20918000	Weak transcription	Fetal Brain Female	brain
21	chr8:20916800-20918400	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr8:20917600-20917800	Enhancers	Psoas Muscle	Psoas
23	chr8:20917800-20918200	Weak transcription	Psoas Muscle	Psoas
24	chr8:20917800-20919000	Enhancers	Fetal Brain Male	brain
25	chr8:20918000-20918800	Enhancers	Fetal Brain Female	brain
26	chr8:20918200-20919600	Enhancers	Psoas Muscle	Psoas
27	chr8:20918400-20918800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr8:20918400-20918800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr8:20918800-20919000	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr8:20918800-20919200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr8:20920800-20922200	Enhancers	Pancreas	Pancrea
32	chr8:20921400-20922400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr8:20922200-20922600	Weak transcription	Pancreas	Pancrea
34	chr8:20922200-20922600	Enhancers	HepG2	liver
35	chr8:20922600-20926000	Enhancers	Pancreas	Pancrea
36	chr8:20924200-20926200	Enhancers	Placenta	Placenta
37	chr8:20924200-20926600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:20925000-20925400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr8:20925000-20926000	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr8:20925000-20926600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr8:20925200-20925400	Flanking Active TSS	Hela-S3	cervix
42	chr8:20925200-20925600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr8:20925200-20926000	Enhancers	Adipose Nuclei	Adipose
44	chr8:20925200-20926000	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr8:20925200-20926200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr8:20925200-20926200	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr8:20925400-20925600	Enhancers	Hela-S3	cervix
48	chr8:20925400-20925800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr8:20925400-20926000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:20925400-20926000	Enhancers	Left Ventricle	heart

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