Variant report

Variant	nsv972228
Chromosome Location	chr8:8752697-8759027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:8753115-8753116	K562	blood:	n/a	n/a
2	CEBPB	chr8:8758429-8758585	IMR90	lung:	n/a	chr8:8758494-8758505
3	CTCF	chr8:8759020-8759170	HPF	lung:	n/a	n/a
4	CTCF	chr8:8759000-8759150	HCPEpiC	choroid plexus:	n/a	n/a
5	CTCF	chr8:8759020-8759170	SAEC	small airway:	n/a	n/a
6	CTCF	chr8:8759020-8759170	HMF	breast:	n/a	n/a
7	CTCF	chr8:8759000-8759150	HepG2	liver:	n/a	n/a
8	CTCF	chr8:8759020-8759170	BJ	skin:	n/a	n/a
9	CTCF	chr8:8759000-8759150	HMF	breast:	n/a	n/a
10	CTCF	chr8:8758980-8759130	HCM	heart:	n/a	n/a
11	CTCF	chr8:8756040-8756190	HepG2	liver:	n/a	n/a
12	CTCF	chr8:8759000-8759150	HCM	heart:	n/a	n/a
13	CTCF	chr8:8759000-8759150	HA-sp	spinal cord:	n/a	n/a
14	EP300	chr8:8756928-8757001	K562	blood:	n/a	n/a
15	MAFK	chr8:8752764-8752774	K562	blood:	n/a	n/a
16	MAZ	chr8:8752623-8752757	K562	blood:	n/a	n/a
17	MXI1	chr8:8756942-8756991	K562	blood:	n/a	n/a
18	MYC	chr8:8752622-8752725	K562	blood:	n/a	n/a
19	POLR2A	chr8:8752796-8752813	K562	blood:	n/a	n/a
20	POLR2A	chr8:8752995-8753137	GM12878	blood:	n/a	n/a
21	RAD21	chr8:8758933-8759258	H1-hESC	embryonic stem cell:	n/a	n/a
22	RAD21	chr8:8759009-8759224	H1-hESC	embryonic stem cell:	n/a	n/a
23	RAD21	chr8:8759026-8759226	HepG2	liver:	n/a	n/a
24	RAD21	chr8:8758961-8759253	H1-hESC	embryonic stem cell:	n/a	n/a
25	RAD21	chr8:8758912-8759328	HepG2	liver:	n/a	n/a
26	RCOR1	chr8:8757418-8757515	K562	blood:	n/a	n/a
27	RCOR1	chr8:8752605-8752882	K562	blood:	n/a	n/a
28	RCOR1	chr8:8752742-8752744	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8755272-8755322	HRCEpiC	kidney:	n/a
2	chr8:8755272-8755322	GM19239	blood:	n/a
3	chr8:8755272-8755322	A549	lung:	n/a
4	chr8:8755272-8755322	GM12891	blood:	n/a
5	chr8:8755272-8755322	HUVEC	blood vessel:	n/a
6	chr8:8755272-8755322	GM12892	blood:	n/a
7	chr8:8755272-8755322	HMEC	breast:	n/a
8	chr8:8755272-8755322	LNCaP	prostate:	n/a
9	chr8:8755272-8755322	Jurkat	blood:	n/a
10	chr8:8755272-8755322	HCPEpiC	choroid plexus:	n/a
11	chr8:8755272-8755322	PANC-1	pancreas:	n/a
12	chr8:8755272-8755322	HCT-116	colon:	n/a
13	chr8:8755272-8755322	U87	brain:	n/a
14	chr8:8755272-8755322	AG09319	gingival:	n/a
15	chr8:8755272-8755322	GM12878	blood:	n/a
16	chr8:8755272-8755322	Hepatocyte	liver:	n/a
17	chr8:8755272-8755322	Caco-2	colon:	n/a
18	chr8:8755272-8755322	AG09309	skin:	n/a
19	chr8:8755272-8755322	CMK	blood:	n/a
20	chr8:8755272-8755322	NHBE	bronchial:	n/a
21	chr8:8755272-8755322	HCF	heart:	n/a
22	chr8:8755272-8755322	PrEC	prostate:	n/a
23	chr8:8755272-8755322	T-47D	breast:	n/a
24	chr8:8755272-8755322	HRE	kidney:	n/a
25	chr8:8755272-8755322	NHDF-neo	bronchial:	n/a
26	chr8:8755272-8755322	SAEC	small airway:	n/a
27	chr8:8755272-8755322	SK-N-SH	brain:	n/a
28	chr8:8755272-8755322	AG10803	skin:	n/a
29	chr8:8755272-8755322	ECC-1	luminal epithelium:	n/a
30	chr8:8755272-8755322	ovcar-3	ovarian:	n/a
31	chr8:8755272-8755322	NB4	blood:	n/a
32	chr8:8755272-8755322	HRPEpiC	eye:	n/a
33	chr8:8755272-8755322	AG04450	lung:	fetal
34	chr8:8755272-8755322	AoSMC	blood vessel:	n/a
35	chr8:8755272-8755322	HL-60	blood:	n/a
36	chr8:8755272-8755322	H1-hESC	embryonic stem cell:	embryo
37	chr8:8755272-8755322	HEEpiC	esophagus:	n/a
38	chr8:8755272-8755322	HEK293	kidney:	embryo
39	chr8:8755272-8755322	IMR90	lung:	fetal
40	chr8:8755272-8755322	BE2_C	brain:	n/a
41	chr8:8755272-8755322	GM06990	blood:	n/a
42	chr8:8755272-8755322	SK-N-MC	brain:	n/a
43	chr8:8755272-8755322	NH-A	brain:	n/a
44	chr8:8755272-8755322	ProgFib	skin:	n/a
45	chr8:8755272-8755322	PFSK-1	brain:	n/a
46	chr8:8755272-8755322	MCF-7	breast:	n/a
47	chr8:8755272-8755322	HNPCEpiC	eye:	n/a
48	chr8:8755272-8755322	HCM	heart:	n/a
49	chr8:8755272-8755322	NT2-D1	testis:	n/a
50	chr8:8755272-8755322	SKMC	muscle:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8751885..8754509-chr8:8756832..8758462,2	MCF-7	breast:
2	chr8:8749232..8754669-chr8:8756372..8762618,9	MCF-7	breast:
3	chr8:8750920..8752897-chr8:8753485..8755610,2	MCF-7	breast:
4	chr8:8707079..8709143-chr8:8751442..8753018,2	MCF-7	breast:
5	chr8:8748349..8752697-chr8:8864961..8869329,4	K562	blood:
6	chr8:8756284..8757870-chr8:8861137..8863458,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-682P	TF binding region
MFHAS1	TF binding region
RNU6-682P	CpG island
MFHAS1	CpG island
ENSG00000104626	chromatin interactions
ENSG00000147324	chromatin interactions
ENSG00000200713	chromatin interactions

Extended variants
information (count: 297 )
Associated
traits (count: 140 )

Variant overlapped rSNPs/rCNVs (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548537768	chr8:8752707-8752708	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs372639726	chr8:8752716-8752717	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs565679252	chr8:8752721-8752722	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs560473402	chr8:8752727-8752728	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs190264842	chr8:8752784-8752785	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs551501286	chr8:8752801-8752802	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs35820021	chr8:8752804-8752805	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs537279344	chr8:8752811-8752812	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs115894931	chr8:8752843-8752844	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs182150466	chr8:8752851-8752852	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs536557747	chr8:8752880-8752881	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs186753840	chr8:8752881-8752882	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs116295905	chr8:8752885-8752886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs36025219	chr8:8752890-8752891	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs558265865	chr8:8752919-8752920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs113156397	chr8:8752923-8752924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3834747	chr8:8752930-8752931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397961561	chr8:8752931-8752932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372257869	chr8:8752934-8752935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs66997485	chr8:8752935-8752936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372925465	chr8:8752954-8752955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117514834	chr8:8752998-8752999	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs192388577	chr8:8753015-8753016	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs183950955	chr8:8753023-8753024	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs116779374	chr8:8753051-8753052	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs551503108	chr8:8753104-8753105	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs188507356	chr8:8753178-8753179	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs559083628	chr8:8753186-8753187	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs138664110	chr8:8753203-8753204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs36061325	chr8:8753216-8753217	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs551856269	chr8:8753224-8753225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76118851	chr8:8753230-8753231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144583134	chr8:8753239-8753240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75465272	chr8:8753282-8753283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566846000	chr8:8753305-8753306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567470058	chr8:8753346-8753347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536545428	chr8:8753442-8753443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112954786	chr8:8753458-8753459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546911922	chr8:8753472-8753473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192913480	chr8:8753488-8753489	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs535045653	chr8:8753524-8753525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs28711612	chr8:8753538-8753539	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs577680009	chr8:8753540-8753541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113407228	chr8:8753544-8753545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557087151	chr8:8753569-8753570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs59044850	chr8:8753572-8753573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112332876	chr8:8753620-8753621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368895544	chr8:8753658-8753659	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554658958	chr8:8753659-8753660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148037148	chr8:8753668-8753669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:140)

Disease	PMID	Source
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
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
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
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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Bipolar disorder	19114987	CNVD
Gastric cancer	17229543	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8751400-8752800	Enhancers	Primary T killer memory cells from peripheral blood	blood
2	chr8:8751600-8753000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:8751600-8753200	Enhancers	Primary T cells fromperipheralblood	blood
4	chr8:8751600-8775000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:8751800-8752800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:8751800-8752800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:8751800-8752800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr8:8751800-8753000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr8:8751800-8753000	Enhancers	K562	blood
10	chr8:8751800-8753200	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr8:8751800-8753200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr8:8751800-8753200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr8:8751800-8753200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr8:8751800-8753200	Enhancers	Fetal Thymus	thymus
15	chr8:8751800-8753200	Enhancers	HepG2	liver
16	chr8:8751800-8753400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr8:8751800-8755200	Weak transcription	Fetal Heart	heart
18	chr8:8751800-8756200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr8:8751800-8756800	Weak transcription	Duodenum Mucosa	Duodenum
20	chr8:8751800-8756800	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr8:8751800-8757800	Weak transcription	Small Intestine	intestine
22	chr8:8751800-8759000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:8752000-8752800	Enhancers	Dnd41	blood
24	chr8:8752000-8753200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr8:8752000-8753400	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr8:8752000-8755400	Weak transcription	Fetal Lung	lung
27	chr8:8752000-8756400	Weak transcription	Thymus	Thymus
28	chr8:8752000-8757000	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr8:8752200-8756800	Weak transcription	Fetal Intestine Small	intestine
30	chr8:8752200-8758200	Weak transcription	Brain Cingulate Gyrus	brain
31	chr8:8752200-8759000	Weak transcription	Stomach Smooth Muscle	stomach
32	chr8:8752400-8752800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr8:8752400-8752800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:8752400-8753000	Enhancers	Placenta	Placenta
35	chr8:8752400-8753200	Enhancers	Primary T cells from cord blood	blood
36	chr8:8752400-8753200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:8752600-8752800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:8752600-8752800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr8:8752600-8752800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr8:8752600-8752800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr8:8752600-8752800	Enhancers	Muscle Satellite Cultured Cells	--
42	chr8:8752600-8753200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:8752800-8753000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:8752800-8753000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:8752800-8753000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:8752800-8753200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr8:8752800-8756400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr8:8752800-8757400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr8:8752800-8775000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr8:8753000-8753200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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