Variant report

Variant	nsv1016634
Chromosome Location	chr8:5761145-5825529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:154)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:154 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:5765727-5765858	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr8:5766581-5766595	A549	lung:	n/a	n/a
3	CTCF	chr8:5790250-5790429	LNCaP	prostate:	n/a	n/a
4	CTCF	chr8:5790263-5790411	K562	blood:	n/a	n/a
5	CTCF	chr8:5790280-5790430	HL-60	blood:	n/a	n/a
6	CTCF	chr8:5790240-5790390	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr8:5790240-5790390	HEK293	kidney:	n/a	n/a
8	CTCF	chr8:5798380-5798530	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr8:5798480-5798630	A549	lung:	n/a	n/a
10	CTCF	chr8:5790220-5790370	MCF-7	breast:	n/a	n/a
11	CTCF	chr8:5798340-5798490	MCF-7	breast:	n/a	n/a
12	CTCF	chr8:5790273-5790369	HUVEC	blood vessel:	n/a	n/a
13	CTCF	chr8:5790240-5790390	HFF	foreskin:	n/a	n/a
14	CTCF	chr8:5790180-5790330	RPTEC	kidney:	n/a	n/a
15	CTCF	chr8:5790254-5790377	MCF-7	breast:	n/a	n/a
16	CTCF	chr8:5790300-5790450	GM12873	blood:	n/a	n/a
17	CTCF	chr8:5798353-5798573	MCF-7	breast:	n/a	n/a
18	CTCF	chr8:5798365-5798548	HepG2	liver:	n/a	n/a
19	CTCF	chr8:5790200-5790350	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr8:5798372-5798556	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:5790300-5790450	RPTEC	kidney:	n/a	n/a
22	CTCF	chr8:5798360-5798510	HEK293	kidney:	n/a	n/a
23	CTCF	chr8:5790180-5790330	HMF	breast:	n/a	n/a
24	CTCF	chr8:5798264-5798632	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr8:5765000-5765150	GM12866	blood:	n/a	n/a
26	CTCF	chr8:5790260-5790410	NHEK	skin:	n/a	n/a
27	CTCF	chr8:5798364-5798560	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:5798293-5798586	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:5798268-5798623	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:5796519-5796555	LNCaP	prostate:	n/a	n/a
31	CTCF	chr8:5790240-5790390	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr8:5798374-5798543	MCF-7	breast:	n/a	n/a
33	CTCF	chr8:5798357-5798574	MCF-7	breast:	n/a	n/a
34	CTCF	chr8:5798342-5798542	HepG2	liver:	n/a	n/a
35	CTCF	chr8:5790240-5790390	A549	lung:	n/a	n/a
36	CTCF	chr8:5798203-5798596	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr8:5790220-5790370	NHEK	skin:	n/a	n/a
38	CTCF	chr8:5790220-5790370	HMEC	breast:	n/a	n/a
39	CTCF	chr8:5798441-5798516	Gliobla	brain:	n/a	n/a
40	CTCF	chr8:5790251-5790406	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr8:5798340-5798490	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr8:5790200-5790350	BJ	skin:	n/a	n/a
43	CTCF	chr8:5790200-5790350	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr8:5798420-5798570	Caco-2	colon:	n/a	n/a
45	CTCF	chr8:5790240-5790390	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:5790260-5790410	BE2_C	brain:	n/a	n/a
47	CTCF	chr8:5798326-5798597	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr8:5790240-5790390	BJ	skin:	n/a	n/a
49	CTCF	chr8:5790220-5790370	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:5798360-5798510	BE2_C	brain:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:5762990-5763040	MCF10A-Er-Src	breast:	n/a
2	chr8:5762990-5763040	H1-hESC	embryonic stem cell:	embryo
3	chr8:5762990-5763040	CMK	blood:	n/a
4	chr8:5762944-5762994	LNCaP	prostate:	n/a
5	chr8:5762990-5763040	SKMC	muscle:	n/a
6	chr8:5762990-5763040	HL-60	blood:	n/a
7	chr8:5762990-5763040	AG09319	gingival:	n/a
8	chr8:5762944-5762994	AG04449	skin:	fetal
9	chr8:5762944-5762994	HRPEpiC	eye:	n/a
10	chr8:5762944-5762994	IMR90	lung:	fetal
11	chr8:5762990-5763040	ovcar-3	ovarian:	n/a
12	chr8:5762944-5762994	HCT-116	colon:	n/a
13	chr8:5762944-5762994	U87	brain:	n/a
14	chr8:5762944-5762994	H1-hESC	embryonic stem cell:	embryo
15	chr8:5762944-5762994	Hepatocyte	liver:	n/a
16	chr8:5762944-5762994	RPTEC	kidney:	n/a
17	chr8:5762990-5763040	AG04450	lung:	fetal
18	chr8:5762944-5762994	AG09309	skin:	n/a
19	chr8:5762944-5762994	MCF10A-Er-Src	breast:	n/a
20	chr8:5762990-5763040	NHBE	bronchial:	n/a
21	chr8:5762944-5762994	A549	lung:	n/a
22	chr8:5762944-5762994	SK-N-SH_RA	brain:	n/a
23	chr8:5762944-5762994	NHDF-neo	bronchial:	n/a
24	chr8:5762990-5763040	SK-N-SH	brain:	n/a
25	chr8:5762990-5763040	PFSK-1	brain:	n/a
26	chr8:5762944-5762994	GM12891	blood:	n/a
27	chr8:5762944-5762994	HRCEpiC	kidney:	n/a
28	chr8:5762990-5763040	PrEC	prostate:	n/a
29	chr8:5762944-5762994	HEEpiC	esophagus:	n/a
30	chr8:5762990-5763040	GM12878	blood:	n/a
31	chr8:5762944-5762994	NT2-D1	testis:	n/a
32	chr8:5762990-5763040	LNCaP	prostate:	n/a
33	chr8:5762990-5763040	AG09309	skin:	n/a
34	chr8:5762944-5762994	PrEC	prostate:	n/a
35	chr8:5762990-5763040	Hela-S3	cervix:	n/a
36	chr8:5762944-5762994	HL-60	blood:	n/a
37	chr8:5762990-5763040	AG04449	skin:	fetal
38	chr8:5762990-5763040	HUVEC	blood vessel:	n/a
39	chr8:5762944-5762994	BJ	skin:	n/a
40	chr8:5762990-5763040	HCF	heart:	n/a
41	chr8:5762944-5762994	HAEpiC	amniotic membrane:	n/a
42	chr8:5762990-5763040	HMEC	breast:	n/a
43	chr8:5762944-5762994	HMEC	breast:	n/a
44	chr8:5762944-5762994	K562	blood:	n/a
45	chr8:5762990-5763040	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:5762990-5763040	HAEpiC	amniotic membrane:	n/a
47	chr8:5762944-5762994	GM12892	blood:	n/a
48	chr8:5762944-5762994	GM19239	blood:	n/a
49	chr8:5762944-5762994	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:5762944-5762994	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:5775799..5778570-chr8:6262790..6264825,2	K562	blood:
2	chr8:5797855..5798416-chr8:5934095..5934883,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-12	chr8:5768467-5768758	NONHSAT124763

No data

Variant related genes	Relation type
RN7SKP159	TF binding region
RN7SKP159	CpG island
ENSG00000147316	chromatin interactions
ENSG00000246089	chromatin interactions

Extended variants
information (count: 2125 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:2125 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17075051	chr8:5761145-5761146	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548494818	chr8:5761170-5761171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549421682	chr8:5761204-5761205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376766843	chr8:5761233-5761234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs527739001	chr8:5761240-5761241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145958864	chr8:5761253-5761254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570486707	chr8:5761308-5761309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139717055	chr8:5761319-5761320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556457948	chr8:5761323-5761324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568240774	chr8:5761332-5761333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553423308	chr8:5761342-5761343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535685690	chr8:5761343-5761344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs116755402	chr8:5761344-5761345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114767942	chr8:5761360-5761361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545866621	chr8:5761377-5761378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187776606	chr8:5761384-5761385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144379060	chr8:5761389-5761390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192520637	chr8:5761398-5761399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563244055	chr8:5761407-5761408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs61590929	chr8:5761416-5761417	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs2703244	chr8:5761421-5761422	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs151127411	chr8:5761429-5761430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539489634	chr8:5761431-5761432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527805618	chr8:5761446-5761447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552220807	chr8:5761483-5761484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74300032	chr8:5761494-5761495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531621509	chr8:5761495-5761496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549903189	chr8:5761513-5761514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568381974	chr8:5761517-5761518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183631823	chr8:5761525-5761526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553934825	chr8:5761539-5761540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs79570452	chr8:5761556-5761557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373946587	chr8:5761557-5761558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201075935	chr8:5761567-5761568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565850370	chr8:5761587-5761588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138628931	chr8:5761616-5761617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200685896	chr8:5761623-5761624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201912129	chr8:5761626-5761627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149876399	chr8:5761627-5761628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188437182	chr8:5761642-5761643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139984439	chr8:5761648-5761649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112475060	chr8:5761688-5761689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368970203	chr8:5761689-5761690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544388789	chr8:5761694-5761695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192697645	chr8:5761723-5761724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184994969	chr8:5761725-5761726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574948784	chr8:5761735-5761736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78465456	chr8:5761736-5761737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575080580	chr8:5761766-5761767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572605215	chr8:5761781-5761782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Schizophrenia	20967226	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:5760200-5761600	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr8:5760800-5761600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr8:5761000-5761400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:5761000-5761600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr8:5761400-5762000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:5761400-5763400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr8:5761600-5762000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:5761600-5763400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr8:5761600-5763400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr8:5762000-5762200	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:5762000-5762200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:5762000-5762400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:5762200-5764000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr8:5762200-5764600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:5763400-5763600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr8:5763400-5764200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr8:5763400-5764600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:5763400-5765600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr8:5763400-5765800	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr8:5763600-5764200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr8:5763600-5764600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr8:5763800-5764600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr8:5764000-5764200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:5764000-5764600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr8:5764600-5765000	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr8:5764600-5765400	Enhancers	H9 Cell Line	embryonic stem cell
27	chr8:5764600-5765600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:5765000-5765600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr8:5772600-5774600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:5773000-5774800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:5792200-5794800	Enhancers	Dnd41	blood
32	chr8:5796200-5796600	Enhancers	Fetal Heart	heart
33	chr8:5806600-5809600	Weak transcription	Fetal Heart	heart
34	chr8:5809600-5810800	Enhancers	Fetal Heart	heart
35	chr8:5815200-5816000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:5815400-5816000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:5815600-5815800	Weak transcription	Fetal Heart	heart
38	chr8:5815800-5816000	Enhancers	Fetal Heart	heart
39	chr8:5816000-5818600	Weak transcription	Fetal Heart	heart
40	chr8:5816000-5819200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:5816000-5819400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr8:5818600-5820600	Enhancers	Fetal Heart	heart
43	chr8:5819200-5820600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr8:5819400-5820600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:5819600-5820800	Enhancers	Fetal Brain Male	brain
46	chr8:5819800-5820200	Enhancers	Fetal Lung	lung
47	chr8:5819800-5820800	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr8:5820000-5821600	Enhancers	Primary hematopoietic stem cells	blood
49	chr8:5820200-5820600	Enhancers	Brain Germinal Matrix	brain
50	chr8:5820200-5820600	Enhancers	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links