Variant report

Variant	nsv1018922
Chromosome Location	chr8:5474179-5603378
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	BCL11A	chr8:5532714-5533009	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:5572602-5572802	HepG2	liver:	n/a	chr8:5572684-5572695 chr8:5572683-5572694 chr8:5572683-5572696
3	CEBPB	chr8:5480182-5480464	HepG2	liver:	n/a	chr8:5480309-5480320
4	CEBPB	chr8:5513789-5514104	HepG2	liver:	n/a	chr8:5513934-5513945
5	CEBPB	chr8:5584989-5585024	HepG2	liver:	n/a	chr8:5584999-5585010
6	CEBPB	chr8:5532168-5532358	HepG2	liver:	n/a	chr8:5532275-5532288 chr8:5532276-5532287 chr8:5532275-5532286
7	CEBPB	chr8:5532924-5533107	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr8:5527476-5527834	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:5522119-5522167	GM20000	blood:	n/a	n/a
10	CTCF	chr8:5543580-5543730	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
11	CTCF	chr8:5590310-5590375	Fibrobl	skin:	n/a	n/a
12	CTCF	chr8:5543566-5543758	H1-hESC	embryonic stem cell:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
13	CTCF	chr8:5543643-5543834	GM12878	blood:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
14	CTCF	chr8:5543520-5543670	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr8:5543363-5543413	Gliobla	brain:	n/a	n/a
16	CTCF	chr8:5543600-5543750	HEEpiC	esophagus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
17	CTCF	chr8:5543644-5543703	HUVEC	blood vessel:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
18	CTCF	chr8:5543619-5543764	Gliobla	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
19	CTCF	chr8:5543720-5543870	HFF	foreskin:	n/a	n/a
20	CTCF	chr8:5543560-5543710	SK-N-SH_RA	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
21	CTCF	chr8:5543634-5543746	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
22	CTCF	chr8:5543600-5543750	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
23	CTCF	chr8:5543620-5543770	BJ	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
24	CTCF	chr8:5543540-5543690	HAc	cerebellar:	n/a	n/a
25	CTCF	chr8:5543620-5543770	HCPEpiC	choroid plexus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
26	CTCF	chr8:5543639-5543719	HepG2	liver:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
27	CTCF	chr8:5543700-5543850	NB4	blood:	n/a	n/a
28	CTCF	chr8:5543584-5543778	Medullo	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
29	CTCF	chr8:5476080-5476108	GM19239	blood:	n/a	n/a
30	CTCF	chr8:5543560-5543710	NHEK	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
31	CTCF	chr8:5543300-5543450	BJ	skin:	n/a	n/a
32	CTCF	chr8:5543580-5543830	HFF-Myc	foreskin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
33	CTCF	chr8:5543600-5543750	BJ	skin:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
34	CTCF	chr8:5543600-5543750	HRE	kidney:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
35	CTCF	chr8:5543582-5543794	LNCaP	prostate:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
36	CTCF	chr8:5543260-5543410	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr8:5543340-5543490	NHEK	skin:	n/a	n/a
38	CTCF	chr8:5543600-5543750	HMF	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
39	CTCF	chr8:5543560-5543710	HEK293	kidney:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
40	CTCF	chr8:5543660-5543810	WERI-Rb-1	eye:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
41	CTCF	chr8:5520100-5520168	Lung_OC	lung:	n/a	n/a
42	CTCF	chr8:5560300-5560450	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr8:5543540-5543690	BE2_C	brain:	n/a	n/a
44	CTCF	chr8:5543560-5543710	HMEC	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
45	CTCF	chr8:5513960-5514110	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr8:5543652-5543717	MCF-7	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
47	CTCF	chr8:5543660-5543810	HL-60	blood:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
48	CTCF	chr8:5543580-5543730	HCPEpiC	choroid plexus:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
49	CTCF	chr8:5543620-5543770	BE2_C	brain:	n/a	chr8:5543674-5543692 chr8:5543676-5543697
50	CTCF	chr8:5543600-5543750	HMEC	breast:	n/a	chr8:5543674-5543692 chr8:5543676-5543697

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5526092-5526142	U87	brain:	n/a
2	chr8:5526092-5526142	RPTEC	kidney:	n/a
3	chr8:5526092-5526142	HRPEpiC	eye:	n/a
4	chr8:5526092-5526142	NB4	blood:	n/a
5	chr8:5526092-5526142	HIPEpiC	eye:	n/a
6	chr8:5526092-5526142	AG10803	skin:	n/a
7	chr8:5526092-5526142	IMR90	lung:	fetal
8	chr8:5526092-5526142	NH-A	brain:	n/a
9	chr8:5526092-5526142	T-47D	breast:	n/a
10	chr8:5526092-5526142	AG04450	lung:	fetal
11	chr8:5526092-5526142	H1-hESC	embryonic stem cell:	embryo
12	chr8:5526092-5526142	HPAEpiC	pulmonary alveolar:	n/a
13	chr8:5526092-5526142	AoSMC	blood vessel:	n/a
14	chr8:5526092-5526142	PrEC	prostate:	n/a
15	chr8:5526092-5526142	NHDF-neo	bronchial:	n/a
16	chr8:5526092-5526142	AG09319	gingival:	n/a
17	chr8:5526092-5526142	HCT-116	colon:	n/a
18	chr8:5526092-5526142	Caco-2	colon:	n/a
19	chr8:5526092-5526142	LNCaP	prostate:	n/a
20	chr8:5526092-5526142	HNPCEpiC	eye:	n/a
21	chr8:5526092-5526142	SK-N-SH_RA	brain:	n/a
22	chr8:5526092-5526142	PANC-1	pancreas:	n/a
23	chr8:5526092-5526142	CMK	blood:	n/a
24	chr8:5526092-5526142	PFSK-1	brain:	n/a
25	chr8:5526092-5526142	GM19239	blood:	n/a
26	chr8:5526092-5526142	GM06990	blood:	n/a
27	chr8:5526092-5526142	AG04449	skin:	fetal
28	chr8:5526092-5526142	HUVEC	blood vessel:	n/a
29	chr8:5526092-5526142	SK-N-MC	brain:	n/a
30	chr8:5526092-5526142	HAEpiC	amniotic membrane:	n/a
31	chr8:5526092-5526142	HCPEpiC	choroid plexus:	n/a
32	chr8:5526092-5526142	NT2-D1	testis:	n/a
33	chr8:5526092-5526142	K562	blood:	n/a
34	chr8:5526092-5526142	BE2_C	brain:	n/a
35	chr8:5526092-5526142	Jurkat	blood:	n/a
36	chr8:5526092-5526142	Hepatocyte	liver:	n/a
37	chr8:5526092-5526142	HMEC	breast:	n/a
38	chr8:5526092-5526142	MCF10A-Er-Src	breast:	n/a
39	chr8:5526092-5526142	NHBE	bronchial:	n/a
40	chr8:5526092-5526142	HEK293	kidney:	embryo
41	chr8:5526092-5526142	GM12891	blood:	n/a
42	chr8:5526092-5526142	HCM	heart:	n/a
43	chr8:5526092-5526142	GM12892	blood:	n/a
44	chr8:5526092-5526142	SK-N-SH	brain:	n/a
45	chr8:5526092-5526142	MCF-7	breast:	n/a
46	chr8:5526092-5526142	HepG2	liver:	n/a
47	chr8:5526092-5526142	ProgFib	skin:	n/a
48	chr8:5526092-5526142	HEEpiC	esophagus:	n/a
49	chr8:5526092-5526142	A549	lung:	n/a
50	chr8:5526092-5526142	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:47028381..47029208-chr8:5581216..5581723,2	MCF-7	breast:
2	chr8:5543604..5544126-chr8:5997197..5997756,2	MCF-7	breast:
3	chr1:14651092..14651694-chr8:5507747..5508432,2	MCF-7	breast:
4	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:
5	chr8:5539160..5541154-chr8:5572222..5575011,2	K562	blood:
6	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
7	chr8:5535511..5537996-chr8:5538816..5540687,2	K562	blood:
8	chr8:5524220..5526546-chr8:5527520..5529311,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD1-6	chr8:5522226-5522711	ENSG00000254007
2	lnc-CSMD1-6	chr8:5517201-5517508	ENSG00000254007
3	lnc-CSMD1-6	chr8:5522226-5522285	XLOC_006981
4	lnc-CSMD1-6	chr8:5517279-5517508	XLOC_006981
5	lnc-CSMD1-6	chr8:5527471-5527599	ENSG00000254007

Variant related genes	Relation type
ENSG00000254007	TF binding region
ENSG00000254007	CpG island
ENSG00000254007	chromatin interactions
STRBP	miRNA target sites
STRADB	miRNA target sites

Extended variants
information (count: 3400 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:3400 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557761190	chr8:5474183-5474184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs116513653	chr8:5474189-5474190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537162845	chr8:5474190-5474191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555143679	chr8:5474198-5474199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574980976	chr8:5474199-5474200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541981851	chr8:5474221-5474222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554087829	chr8:5474238-5474239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149792524	chr8:5474246-5474247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545821981	chr8:5474249-5474250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554903287	chr8:5474265-5474266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564491911	chr8:5474274-5474275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531573522	chr8:5474275-5474276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77005282	chr8:5474284-5474285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148882569	chr8:5474304-5474305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs377532240	chr8:5474347-5474348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1076275	chr8:5474369-5474370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185247815	chr8:5474370-5474371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559709154	chr8:5474396-5474397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142592473	chr8:5474407-5474408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147644078	chr8:5474411-5474412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs569653534	chr8:5474428-5474429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536598985	chr8:5474463-5474464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549073920	chr8:5474465-5474466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114847451	chr8:5474471-5474472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115306408	chr8:5474483-5474484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116025884	chr8:5474511-5474512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572441008	chr8:5474539-5474540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539761043	chr8:5474571-5474572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190004881	chr8:5474583-5474584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182790667	chr8:5474596-5474597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543443630	chr8:5474603-5474604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186601246	chr8:5474619-5474620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574158301	chr8:5474620-5474621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113382669	chr8:5474634-5474635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191445560	chr8:5474636-5474637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs578135751	chr8:5474666-5474667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142267078	chr8:5474678-5474679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs183761644	chr8:5474683-5474684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374012284	chr8:5474704-5474705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2725668	chr8:5474720-5474721	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs563397450	chr8:5474735-5474736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73660162	chr8:5474744-5474745	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs567051485	chr8:5474746-5474747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367562337	chr8:5474749-5474750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370437218	chr8:5474751-5474752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187480468	chr8:5474776-5474777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528850994	chr8:5474788-5474789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138638490	chr8:5474828-5474829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192443330	chr8:5474883-5474884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs13259632	chr8:5474893-5474894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:130)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	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
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	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
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Chronic myeloid leukemia	21384125	CNVD
Tetralogy of Fallot	22912587	CNVD
Type 2 diabetes	21526130	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD
Obesity	21131291	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5472600-5476200	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr8:5472800-5476800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:5475000-5476400	Enhancers	Spleen	Spleen
4	chr8:5475200-5475600	Enhancers	Brain Anterior Caudate	brain
5	chr8:5475400-5475600	Enhancers	Brain Substantia Nigra	brain
6	chr8:5475400-5476200	Enhancers	Esophagus	oesophagus
7	chr8:5475400-5476400	Enhancers	Lung	lung
8	chr8:5476000-5476200	Enhancers	Stomach Smooth Muscle	stomach
9	chr8:5476800-5477600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr8:5485400-5486200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr8:5485400-5486200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr8:5499800-5500200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:5503000-5508000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:5511000-5511800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr8:5514000-5514600	Enhancers	Fetal Muscle Leg	muscle
16	chr8:5518400-5518600	Enhancers	H9 Cell Line	embryonic stem cell
17	chr8:5518600-5522200	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr8:5518800-5519000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:5521200-5521400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr8:5522200-5522400	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:5522400-5525800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr8:5522800-5523000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr8:5523400-5525400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr8:5524600-5526000	Enhancers	Fetal Brain Male	brain
25	chr8:5525000-5526600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr8:5525400-5528000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:5525400-5528200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr8:5525400-5528200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr8:5525600-5526400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:5525600-5528200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:5525800-5526000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:5525800-5526000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:5525800-5526000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:5525800-5528000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:5526000-5526200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr8:5526000-5526200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:5526000-5527000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:5526000-5528800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr8:5526200-5526400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
40	chr8:5526200-5527200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr8:5526200-5527400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr8:5526400-5526600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr8:5526400-5527400	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr8:5526600-5527000	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr8:5526600-5527400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:5527000-5527800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr8:5527000-5528000	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr8:5527200-5527400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:5527200-5527800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr8:5527200-5527800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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