Variant report

Variant	nsv1024397
Chromosome Location	chr8:35296922-35424277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:705)
CpG islands
(count:549)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:705 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:35359837-35359860	K562	blood:	n/a	n/a
2	ATF2	chr8:35402728-35403206	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:35345895-35346297	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:35402765-35403153	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:35402916-35403184	H1-hESC	embryonic stem cell:	n/a	chr8:35402948-35402962
6	BACH1	chr8:35424139-35424252	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr8:35307562-35307906	GM12878	blood:	n/a	n/a
8	CEBPB	chr8:35321610-35322016	H1-hESC	embryonic stem cell:	n/a	chr8:35321795-35321806
9	CEBPB	chr8:35321610-35321982	HepG2	liver:	n/a	chr8:35321795-35321806
10	CEBPB	chr8:35363377-35363478	A549	lung:	n/a	n/a
11	CEBPB	chr8:35345918-35346225	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:35363368-35363566	HepG2	liver:	n/a	n/a
13	CEBPB	chr8:35321655-35321970	ECC-1	luminal epithelium:	n/a	chr8:35321795-35321806
14	CEBPB	chr8:35303084-35303393	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:35321615-35321951	K562	blood:	n/a	chr8:35321795-35321806
16	CEBPB	chr8:35367904-35368119	A549	lung:	n/a	n/a
17	CEBPB	chr8:35367625-35367771	K562	blood:	n/a	n/a
18	CEBPB	chr8:35321618-35321977	IMR90	lung:	n/a	chr8:35321795-35321806
19	CEBPB	chr8:35317694-35318060	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:35321631-35321976	A549	lung:	n/a	chr8:35321795-35321806
21	CEBPB	chr8:35344529-35344911	IMR90	lung:	n/a	n/a
22	CHD1	chr8:35401521-35401688	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr8:35352773-35352813	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:35345682-35345722	HepG2	liver:	n/a	n/a
25	CHD2	chr8:35371858-35371940	HepG2	liver:	n/a	n/a
26	CHD2	chr8:35402907-35403123	H1-hESC	embryonic stem cell:	n/a	n/a
27	CREB1	chr8:35402825-35403248	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr8:35346002-35346191	A549	lung:	n/a	n/a
29	CTCF	chr8:35346000-35346150	AG10803	skin:	n/a	n/a
30	CTCF	chr8:35345972-35346203	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:35346030-35346171	GM19238	blood:	n/a	n/a
32	CTCF	chr8:35345940-35346090	GM12874	blood:	n/a	n/a
33	CTCF	chr8:35346040-35346190	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr8:35324000-35324150	AG09319	gingival:	n/a	chr8:35324073-35324091 chr8:35324075-35324096
35	CTCF	chr8:35340840-35340990	HMEC	breast:	n/a	n/a
36	CTCF	chr8:35382618-35382697	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:35323880-35324030	HMEC	breast:	n/a	n/a
38	CTCF	chr8:35296920-35297070	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:35371734-35371816	Fibrobl	skin:	n/a	n/a
40	CTCF	chr8:35296780-35296930	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:35296820-35296970	RPTEC	kidney:	n/a	n/a
42	CTCF	chr8:35402940-35403090	SK-N-SH_RA	brain:	n/a	chr8:35403034-35403052 chr8:35403036-35403049
43	CTCF	chr8:35326940-35327090	GM12865	blood:	n/a	n/a
44	CTCF	chr8:35323980-35324130	AG10803	skin:	n/a	chr8:35324073-35324091 chr8:35324075-35324096
45	CTCF	chr8:35346020-35346170	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr8:35346040-35346163	GM12892	blood:	n/a	n/a
47	CTCF	chr8:35346032-35346206	GM12878	blood:	n/a	n/a
48	CTCF	chr8:35346040-35346190	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr8:35296690-35297219	SK-N-SH	brain:	n/a	n/a
50	CTCF	chr8:35346040-35346190	SAEC	small airway:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35392042-35392092	NB4	blood:	n/a
2	chr8:35401670-35401720	U87	brain:	n/a
3	chr8:35403156-35403206	SK-N-SH_RA	brain:	n/a
4	chr8:35391321-35391371	AG04450	lung:	fetal
5	chr8:35401742-35401792	GM12892	blood:	n/a
6	chr8:35401742-35401792	H1-hESC	embryonic stem cell:	embryo
7	chr8:35401670-35401720	NT2-D1	testis:	n/a
8	chr8:35391321-35391371	Caco-2	colon:	n/a
9	chr8:35392042-35392092	SK-N-SH	brain:	n/a
10	chr8:35391321-35391371	NHBE	bronchial:	n/a
11	chr8:35401742-35401792	HRPEpiC	eye:	n/a
12	chr8:35403156-35403206	BE2_C	brain:	n/a
13	chr8:35401670-35401720	MCF-7	breast:	n/a
14	chr8:35401313-35401363	SK-N-SH_RA	brain:	n/a
15	chr8:35401670-35401720	HRCEpiC	kidney:	n/a
16	chr8:35401742-35401792	SK-N-MC	brain:	n/a
17	chr8:35401908-35401958	NHBE	bronchial:	n/a
18	chr8:35417823-35417873	K562	blood:	n/a
19	chr8:35391321-35391371	AoSMC	blood vessel:	n/a
20	chr8:35392042-35392092	HRCEpiC	kidney:	n/a
21	chr8:35392042-35392092	HEK293	kidney:	embryo
22	chr8:35391321-35391371	PFSK-1	brain:	n/a
23	chr8:35391321-35391371	SK-N-SH	brain:	n/a
24	chr8:35417823-35417873	HEEpiC	esophagus:	n/a
25	chr8:35403156-35403206	ovcar-3	ovarian:	n/a
26	chr8:35391321-35391371	LNCaP	prostate:	n/a
27	chr8:35417823-35417873	HRCEpiC	kidney:	n/a
28	chr8:35401313-35401363	RPTEC	kidney:	n/a
29	chr8:35392042-35392092	AG04450	lung:	fetal
30	chr8:35401670-35401720	HepG2	liver:	n/a
31	chr8:35392042-35392092	Hela-S3	cervix:	n/a
32	chr8:35391321-35391371	HNPCEpiC	eye:	n/a
33	chr8:35392042-35392092	BE2_C	brain:	n/a
34	chr8:35401908-35401958	Hela-S3	cervix:	n/a
35	chr8:35401908-35401958	HIPEpiC	eye:	n/a
36	chr8:35401670-35401720	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:35403156-35403206	CMK	blood:	n/a
38	chr8:35401670-35401720	PFSK-1	brain:	n/a
39	chr8:35401313-35401363	ECC-1	luminal epithelium:	n/a
40	chr8:35401908-35401958	AG04449	skin:	fetal
41	chr8:35401742-35401792	HCF	heart:	n/a
42	chr8:35297622-35297672	AG10803	skin:	n/a
43	chr8:35401670-35401720	HCF	heart:	n/a
44	chr8:35401908-35401958	Jurkat	blood:	n/a
45	chr8:35401670-35401720	HIPEpiC	eye:	n/a
46	chr8:35403156-35403206	GM06990	blood:	n/a
47	chr8:35417823-35417873	H1-hESC	embryonic stem cell:	embryo
48	chr8:35401742-35401792	AG09319	gingival:	n/a
49	chr8:35401313-35401363	AG04450	lung:	fetal
50	chr8:35403156-35403206	HUVEC	blood vessel:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:35309662..35311958-chr8:35313825..35315981,2	K562	blood:
2	chr8:35323883..35324476-chr8:36630898..36631416,2	MCF-7	breast:
3	chr8:35296451..35297364-chr8:35998554..35999313,2	MCF-7	breast:
4	chr8:35296849..35299028-chr8:35299266..35301130,2	MCF-7	breast:
5	chr4:159096504..159097300-chr8:35345684..35346534,2	MCF-7	breast:
6	chr8:35309662..35311958-chr8:35313825..35315981,2	K562	blood:
7	chr8:35296849..35299028-chr8:35299266..35301130,2	MCF-7	breast:

No data

Variant related genes	Relation type
UNC5D	TF binding region
LSM12P1	TF binding region
UNC5D	CpG island
LSM12P1	CpG island

Extended variants
information (count: 4519 )
Associated
traits (count: 119 )

Variant overlapped rSNPs/rCNVs (count:4519 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369563942	chr8:35296965-35296966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143888252	chr8:35296986-35296987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs564616700	chr8:35296988-35296989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184267208	chr8:35296989-35296990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs187490369	chr8:35297106-35297107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559058967	chr8:35297110-35297111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373828250	chr8:35297124-35297125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146403186	chr8:35297144-35297145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372302836	chr8:35297147-35297148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191645276	chr8:35297155-35297156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148501164	chr8:35297158-35297159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375550353	chr8:35297192-35297193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142815405	chr8:35297224-35297225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570940718	chr8:35297231-35297232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560243490	chr8:35297253-35297254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551573027	chr8:35297293-35297294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535208228	chr8:35297297-35297298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs151052950	chr8:35297315-35297316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs568315990	chr8:35297325-35297326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140992954	chr8:35297327-35297328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs75010618	chr8:35297364-35297365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569543386	chr8:35297376-35297377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142598212	chr8:35297402-35297403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs367631579	chr8:35297424-35297425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536834640	chr8:35297453-35297454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558297361	chr8:35297531-35297532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114422089	chr8:35297597-35297598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149810984	chr8:35297619-35297620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184153028	chr8:35297644-35297645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56198320	chr8:35297664-35297665	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs552432636	chr8:35297686-35297687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540873979	chr8:35297702-35297703	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189857402	chr8:35297718-35297719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180716863	chr8:35297723-35297724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531161483	chr8:35297726-35297727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184534547	chr8:35297733-35297734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79766763	chr8:35297769-35297770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75855303	chr8:35297800-35297801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190269632	chr8:35297824-35297825	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147821796	chr8:35297845-35297846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529267435	chr8:35297889-35297890	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182491270	chr8:35297903-35297904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186026526	chr8:35297919-35297920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536920413	chr8:35297938-35297939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141370321	chr8:35298095-35298096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544636506	chr8:35298134-35298135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147004652	chr8:35298144-35298145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs16883929	chr8:35298232-35298233	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190789001	chr8:35298240-35298241	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574405094	chr8:35298251-35298252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:119)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	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
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
Seminomas	18059402	CNVD
Lung cancer	18438408	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
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35295400-35317000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr8:35296800-35298000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:35297000-35297800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:35297000-35298600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:35297400-35297800	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:35297600-35297800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:35297600-35298000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr8:35297800-35302600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr8:35297800-35303000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr8:35298000-35299200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:35302600-35303200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr8:35303000-35303200	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr8:35303000-35303200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr8:35303000-35303400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr8:35303200-35307000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:35303200-35311800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr8:35305000-35313800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr8:35305800-35310200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:35308400-35311800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr8:35310200-35311800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr8:35310800-35311400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:35311400-35311600	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:35311400-35312000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
24	chr8:35311800-35312000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:35311800-35312600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
26	chr8:35311800-35315600	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr8:35312600-35316600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr8:35313000-35314200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:35313600-35314400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr8:35313800-35314400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:35314000-35314200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr8:35314000-35314200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:35314200-35316600	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr8:35314400-35315800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr8:35314400-35316600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr8:35314600-35315600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:35315600-35317000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr8:35315600-35318000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:35315600-35318200	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr8:35315600-35319400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr8:35315800-35316000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr8:35316000-35316400	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr8:35316000-35319200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr8:35316400-35319200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:35316600-35317400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr8:35316600-35318400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:35316600-35319000	Enhancers	H1 Cell Line	embryonic stem cell
48	chr8:35316600-35319200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:35316800-35317800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:35316800-35318000	Enhancers	Fetal Brain Male	brain

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