Variant report

Variant	nsv520421
Chromosome Location	chr8:35155517-35479468
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	ATF1	chr8:35359837-35359860	K562	blood:	n/a	n/a
2	ATF2	chr8:35234476-35235286	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:35402765-35403153	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:35402728-35403206	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:35449456-35450056	GM12878	blood:	n/a	n/a
6	ATF2	chr8:35234691-35235234	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:35449571-35450010	GM12878	blood:	n/a	n/a
8	ATF2	chr8:35345895-35346297	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:35424139-35424252	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:35180822-35181005	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr8:35181513-35182272	H1-hESC	embryonic stem cell:	n/a	chr8:35181773-35181787 chr8:35181784-35181798
12	BACH1	chr8:35234711-35235215	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:35402916-35403184	H1-hESC	embryonic stem cell:	n/a	chr8:35402948-35402962
14	BACH1	chr8:35253656-35253963	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:35181721-35181921	K562	blood:	n/a	chr8:35181773-35181787 chr8:35181784-35181798
16	BACH1	chr8:35189339-35189377	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr8:35234788-35235130	H1-hESC	embryonic stem cell:	n/a	chr8:35234889-35234897
18	BCL11A	chr8:35234816-35235153	H1-hESC	embryonic stem cell:	n/a	chr8:35234889-35234897
19	BCL3	chr8:35307562-35307906	GM12878	blood:	n/a	n/a
20	BRCA1	chr8:35184325-35184525	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr8:35317694-35318060	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:35321610-35322016	H1-hESC	embryonic stem cell:	n/a	chr8:35321795-35321806
23	CEBPB	chr8:35184658-35185589	ECC-1	luminal epithelium:	n/a	chr8:35184680-35184697
24	CEBPB	chr8:35214780-35214969	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:35219453-35219855	A549	lung:	n/a	chr8:35219500-35219513 chr8:35219502-35219511 chr8:35219502-35219511 chr8:35219715-35219724 chr8:35219715-35219724 chr8:35219715-35219724 chr8:35219502-35219511
26	CEBPB	chr8:35219552-35219752	HepG2	liver:	n/a	chr8:35219715-35219724 chr8:35219715-35219724 chr8:35219715-35219724
27	CEBPB	chr8:35185121-35185532	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr8:35363377-35363478	A549	lung:	n/a	n/a
29	CEBPB	chr8:35345918-35346225	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr8:35156126-35156359	A549	lung:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218
31	CEBPB	chr8:35344529-35344911	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:35287390-35287620	IMR90	lung:	n/a	chr8:35287480-35287491
33	CEBPB	chr8:35266416-35266558	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr8:35219599-35219640	K562	blood:	n/a	n/a
35	CEBPB	chr8:35219449-35219861	IMR90	lung:	n/a	chr8:35219500-35219513 chr8:35219502-35219511 chr8:35219502-35219511 chr8:35219715-35219724 chr8:35219715-35219724 chr8:35219715-35219724 chr8:35219502-35219511
36	CEBPB	chr8:35156041-35156392	HepG2	liver:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218
37	CEBPB	chr8:35287408-35287608	K562	blood:	n/a	chr8:35287480-35287491
38	CEBPB	chr8:35213182-35213362	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:35287338-35287618	HepG2	liver:	n/a	chr8:35287480-35287491
40	CEBPB	chr8:35367625-35367771	K562	blood:	n/a	n/a
41	CEBPB	chr8:35321610-35321982	HepG2	liver:	n/a	chr8:35321795-35321806
42	CEBPB	chr8:35250632-35250640	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:35321615-35321951	K562	blood:	n/a	chr8:35321795-35321806
44	CEBPB	chr8:35321618-35321977	IMR90	lung:	n/a	chr8:35321795-35321806
45	CEBPB	chr8:35363368-35363566	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:35184745-35185054	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr8:35321631-35321976	A549	lung:	n/a	chr8:35321795-35321806
48	CEBPB	chr8:35287374-35287642	A549	lung:	n/a	chr8:35287480-35287491
49	CEBPB	chr8:35321655-35321970	ECC-1	luminal epithelium:	n/a	chr8:35321795-35321806
50	CEBPB	chr8:35156083-35156363	IMR90	lung:	n/a	chr8:35156207-35156218 chr8:35156209-35156220 chr8:35156209-35156218

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35401908-35401958	BE2_C	brain:	n/a
2	chr8:35401908-35401958	BE2_C	brain:	n/a
3	chr8:35186363-35186413	NT2-D1	testis:	n/a
4	chr8:35391321-35391371	PFSK-1	brain:	n/a
5	chr8:35401742-35401792	GM12891	blood:	n/a
6	chr8:35401313-35401363	LNCaP	prostate:	n/a
7	chr8:35452334-35452384	Hela-S3	cervix:	n/a
8	chr8:35391321-35391371	LNCaP	prostate:	n/a
9	chr8:35417823-35417873	Caco-2	colon:	n/a
10	chr8:35417823-35417873	AG04449	skin:	fetal
11	chr8:35401313-35401363	SAEC	small airway:	n/a
12	chr8:35401670-35401720	Hela-S3	cervix:	n/a
13	chr8:35297622-35297672	LNCaP	prostate:	n/a
14	chr8:35401908-35401958	HNPCEpiC	eye:	n/a
15	chr8:35401908-35401958	AG04450	lung:	fetal
16	chr8:35401742-35401792	HCPEpiC	choroid plexus:	n/a
17	chr8:35401908-35401958	HEK293	kidney:	embryo
18	chr8:35186363-35186413	Hepatocyte	liver:	n/a
19	chr8:35186363-35186413	CMK	blood:	n/a
20	chr8:35186363-35186413	NB4	blood:	n/a
21	chr8:35403156-35403206	HUVEC	blood vessel:	n/a
22	chr8:35297622-35297672	NT2-D1	testis:	n/a
23	chr8:35186363-35186413	HRE	kidney:	n/a
24	chr8:35440771-35440821	HMEC	breast:	n/a
25	chr8:35186363-35186413	HEEpiC	esophagus:	n/a
26	chr8:35186363-35186413	A549	lung:	n/a
27	chr8:35440771-35440821	Hela-S3	cervix:	n/a
28	chr8:35452334-35452384	ECC-1	luminal epithelium:	n/a
29	chr8:35235229-35235279	NT2-D1	testis:	n/a
30	chr8:35417823-35417873	BJ	skin:	n/a
31	chr8:35401742-35401792	NB4	blood:	n/a
32	chr8:35297622-35297672	CMK	blood:	n/a
33	chr8:35401742-35401792	AG10803	skin:	n/a
34	chr8:35237424-35237474	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:35452334-35452384	SK-N-SH	brain:	n/a
36	chr8:35401908-35401958	HL-60	blood:	n/a
37	chr8:35440771-35440821	MCF-7	breast:	n/a
38	chr8:35401670-35401720	NB4	blood:	n/a
39	chr8:35403156-35403206	HNPCEpiC	eye:	n/a
40	chr8:35392042-35392092	MCF-7	breast:	n/a
41	chr8:35297622-35297672	NH-A	brain:	n/a
42	chr8:35235229-35235279	HCM	heart:	n/a
43	chr8:35233248-35233298	CMK	blood:	n/a
44	chr8:35403156-35403206	CMK	blood:	n/a
45	chr8:35401313-35401363	HEK293	kidney:	embryo
46	chr8:35403156-35403206	AG04449	skin:	fetal
47	chr8:35186363-35186413	HCPEpiC	choroid plexus:	n/a
48	chr8:35252359-35252409	AG09319	gingival:	n/a
49	chr8:35186363-35186413	U87	brain:	n/a
50	chr8:35417823-35417873	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr8:35431521..35433590-chr8:35435377..35437047,2	K562	blood:
2	chr4:159096504..159097300-chr8:35345684..35346534,2	MCF-7	breast:
3	chr8:35309662..35311958-chr8:35313825..35315981,2	K562	blood:
4	chr8:35431521..35433590-chr8:35435377..35437047,2	K562	blood:
5	chr8:35452680..35453282-chr8:35998615..35999410,2	MCF-7	breast:
6	chr8:35309662..35311958-chr8:35313825..35315981,2	K562	blood:
7	chr8:35323883..35324476-chr8:36630898..36631416,2	MCF-7	breast:
8	chr8:35296849..35299028-chr8:35299266..35301130,2	MCF-7	breast:
9	chr8:35236339..35238040-chr8:35238233..35240737,2	K562	blood:
10	chr8:35236339..35238040-chr8:35238233..35240737,2	K562	blood:
11	chr8:35296451..35297364-chr8:35998554..35999313,2	MCF-7	breast:
12	chr8:35296849..35299028-chr8:35299266..35301130,2	MCF-7	breast:

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

Extended variants
information (count: 11453 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:11453 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7003669	chr8:35155517-35155518	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537514750	chr8:35155518-35155519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566064042	chr8:35155581-35155582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558686841	chr8:35155588-35155589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577142478	chr8:35155597-35155598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538951722	chr8:35155673-35155674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545043508	chr8:35155678-35155679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35946405	chr8:35155725-35155726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539405131	chr8:35155730-35155731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2056768	chr8:35155736-35155737	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs542882070	chr8:35155817-35155818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575271582	chr8:35155821-35155822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539225769	chr8:35155826-35155827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543475659	chr8:35155872-35155873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368384344	chr8:35155915-35155916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576427381	chr8:35155983-35155984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113331472	chr8:35155989-35155990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs540603711	chr8:35156003-35156004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35299004	chr8:35156104-35156105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs386412555	chr8:35156105-35156106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs71278800	chr8:35156125-35156126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201479843	chr8:35156126-35156127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181279307	chr8:35156130-35156131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112168374	chr8:35156139-35156140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185961446	chr8:35156140-35156141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530319891	chr8:35156141-35156142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs548386749	chr8:35156159-35156160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570187257	chr8:35156204-35156205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2980400	chr8:35156214-35156215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149718344	chr8:35156235-35156236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561096210	chr8:35156285-35156286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552608420	chr8:35156292-35156293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146228677	chr8:35156296-35156297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535063905	chr8:35156309-35156310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189919136	chr8:35156314-35156315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565986240	chr8:35156318-35156319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181888907	chr8:35156322-35156323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2980401	chr8:35156356-35156357	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs186529919	chr8:35156361-35156362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543235374	chr8:35156369-35156370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140081673	chr8:35156446-35156447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554444453	chr8:35156481-35156482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540666231	chr8:35156509-35156510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558883086	chr8:35156561-35156562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190627931	chr8:35156604-35156605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542484058	chr8:35156637-35156638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143661020	chr8:35156657-35156658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146794097	chr8:35156664-35156665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs114224226	chr8:35156687-35156688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77636624	chr8:35156784-35156785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35144600-35156800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr8:35144800-35158400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr8:35146600-35160800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:35152000-35155600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr8:35152000-35160800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr8:35152400-35156800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:35154800-35156000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr8:35155000-35155600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:35155200-35155800	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:35155400-35155800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:35155400-35155800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:35155400-35155800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr8:35155400-35155800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:35155400-35156000	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:35155400-35157000	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:35155600-35156000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:35155800-35158200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr8:35155800-35158600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr8:35155800-35159400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr8:35155800-35166800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr8:35156000-35158200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr8:35156800-35157200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:35156800-35157600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:35157600-35158400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr8:35158200-35159000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
26	chr8:35158200-35159000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr8:35158200-35159200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
28	chr8:35158400-35158800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:35158400-35159200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
30	chr8:35158600-35159200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
31	chr8:35158800-35159800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:35159000-35159200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr8:35159000-35159400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr8:35159000-35161000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:35159200-35159800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr8:35159200-35160800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr8:35159200-35162200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr8:35159200-35178200	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr8:35159400-35160000	Enhancers	H9 Cell Line	embryonic stem cell
40	chr8:35159400-35160000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:35159400-35160200	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:35159600-35160200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr8:35159800-35160000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr8:35159800-35161800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:35160000-35160400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr8:35160000-35161000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:35160000-35161200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr8:35160200-35160600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr8:35160200-35160600	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:35160400-35161800	Enhancers	HUES6 Cell Line	embryonic stem cell

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