Variant report

Variant	nsv820251
Chromosome Location	chr8:38848740-38853026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:85)
CpG islands
(count:62)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:85 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:38852772-38853117	HepG2	liver:	n/a	n/a
2	CHD1	chr8:38852795-38859264	IMR90	lung:	n/a	chr8:38854280-38854290 chr8:38854954-38854964
3	CTCF	chr8:38852980-38853130	GM12873	blood:	n/a	chr8:38853084-38853092
4	CTCF	chr8:38852820-38852970	GM12874	blood:	n/a	n/a
5	CTCF	chr8:38852740-38852890	HEEpiC	esophagus:	n/a	n/a
6	CTCF	chr8:38852866-38852955	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr8:38852820-38852970	NHEK	skin:	n/a	n/a
8	CTCF	chr8:38852820-38852970	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr8:38852800-38852950	HVMF	connective:	n/a	n/a
10	CTCF	chr8:38852740-38852890	A549	lung:	n/a	n/a
11	CTCF	chr8:38852820-38852970	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr8:38852720-38852870	HCPEpiC	choroid plexus:	n/a	n/a
13	CTCF	chr8:38852820-38852970	BJ	skin:	n/a	n/a
14	CTCF	chr8:38852800-38852950	BE2_C	brain:	n/a	n/a
15	CTCF	chr8:38852740-38852890	HBMEC	blood vessel:	n/a	n/a
16	CTCF	chr8:38852820-38852970	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr8:38852960-38853110	A549	lung:	n/a	chr8:38853084-38853092
18	CTCF	chr8:38852760-38852910	HMF	breast:	n/a	n/a
19	CTCF	chr8:38852760-38852910	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr8:38852900-38853050	SAEC	small airway:	n/a	n/a
21	CTCF	chr8:38852740-38852890	HPF	lung:	n/a	n/a
22	CTCF	chr8:38852620-38852770	AG09319	gingival:	n/a	n/a
23	CTCF	chr8:38852800-38852950	HEK293	kidney:	n/a	n/a
24	CTCF	chr8:38852780-38852930	HMEC	breast:	n/a	n/a
25	CTCF	chr8:38852780-38852930	BE2_C	brain:	n/a	n/a
26	CTCF	chr8:38852800-38852950	GM12873	blood:	n/a	n/a
27	CTCF	chr8:38852600-38852750	HCT-116	colon:	n/a	n/a
28	CTCF	chr8:38852800-38852950	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr8:38852800-38852950	GM12864	blood:	n/a	n/a
30	CTCF	chr8:38852800-38852950	HPF	lung:	n/a	n/a
31	CTCF	chr8:38852820-38852970	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:38852900-38853050	NHLF	lung:	n/a	n/a
33	CTCF	chr8:38852860-38853110	GM12872	blood:	n/a	chr8:38853084-38853092
34	CTCF	chr8:38852760-38852910	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr8:38852840-38852990	RPTEC	kidney:	n/a	n/a
36	CTCF	chr8:38852660-38852810	HCM	heart:	n/a	n/a
37	CTCF	chr8:38852860-38853010	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr8:38852820-38852970	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr8:38852800-38852950	AG04449	skin:	n/a	n/a
40	CTCF	chr8:38852720-38852870	GM12873	blood:	n/a	n/a
41	CTCF	chr8:38852800-38852950	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr8:38852820-38852970	HepG2	liver:	n/a	n/a
43	CTCF	chr8:38852800-38852950	AG04450	lung:	n/a	n/a
44	CTCF	chr8:38852760-38852910	AG10803	skin:	n/a	n/a
45	CTCF	chr8:38852740-38852890	HAc	cerebellar:	n/a	n/a
46	CTCF	chr8:38852780-38852930	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:38852840-38852990	GM12867	blood:	n/a	n/a
48	CTCF	chr8:38852800-38852950	GM12872	blood:	n/a	n/a
49	CTCF	chr8:38852760-38852910	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr8:38852840-38852990	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:38851155-38851205	Hepatocyte	liver:	n/a
2	chr8:38851155-38851205	Hepatocyte	liver:	n/a
3	chr8:38851155-38851205	HRE	kidney:	n/a
4	chr8:38851155-38851205	SKMC	muscle:	n/a
5	chr8:38851155-38851205	HIPEpiC	eye:	n/a
6	chr8:38851155-38851205	HUVEC	blood vessel:	n/a
7	chr8:38851155-38851205	T-47D	breast:	n/a
8	chr8:38851155-38851205	HEK293	kidney:	embryo
9	chr8:38851155-38851205	HepG2	liver:	n/a
10	chr8:38851155-38851205	HMEC	breast:	n/a
11	chr8:38851155-38851205	AG09319	gingival:	n/a
12	chr8:38851155-38851205	U87	brain:	n/a
13	chr8:38851155-38851205	NH-A	brain:	n/a
14	chr8:38851155-38851205	A549	lung:	n/a
15	chr8:38851155-38851205	NHBE	bronchial:	n/a
16	chr8:38851155-38851205	NB4	blood:	n/a
17	chr8:38851155-38851205	HCF	heart:	n/a
18	chr8:38851155-38851205	NT2-D1	testis:	n/a
19	chr8:38851155-38851205	H1-hESC	embryonic stem cell:	embryo
20	chr8:38851155-38851205	BJ	skin:	n/a
21	chr8:38851155-38851205	SAEC	small airway:	n/a
22	chr8:38851155-38851205	PANC-1	pancreas:	n/a
23	chr8:38851155-38851205	HEEpiC	esophagus:	n/a
24	chr8:38851155-38851205	ovcar-3	ovarian:	n/a
25	chr8:38851155-38851205	HCM	heart:	n/a
26	chr8:38851155-38851205	PFSK-1	brain:	n/a
27	chr8:38851155-38851205	HAEpiC	amniotic membrane:	n/a
28	chr8:38851155-38851205	AoSMC	blood vessel:	n/a
29	chr8:38851155-38851205	CMK	blood:	n/a
30	chr8:38851155-38851205	AG10803	skin:	n/a
31	chr8:38851155-38851205	AG04450	lung:	fetal
32	chr8:38851155-38851205	HCPEpiC	choroid plexus:	n/a
33	chr8:38851155-38851205	SK-N-SH_RA	brain:	n/a
34	chr8:38851155-38851205	SK-N-MC	brain:	n/a
35	chr8:38851155-38851205	LNCaP	prostate:	n/a
36	chr8:38851155-38851205	AG09309	skin:	n/a
37	chr8:38851155-38851205	SK-N-SH	brain:	n/a
38	chr8:38851155-38851205	Hela-S3	cervix:	n/a
39	chr8:38851155-38851205	K562	blood:	n/a
40	chr8:38851155-38851205	HL-60	blood:	n/a
41	chr8:38851155-38851205	RPTEC	kidney:	n/a
42	chr8:38851155-38851205	GM12878	blood:	n/a
43	chr8:38851155-38851205	BE2_C	brain:	n/a
44	chr8:38851155-38851205	GM06990	blood:	n/a
45	chr8:38851155-38851205	ECC-1	luminal epithelium:	n/a
46	chr8:38851155-38851205	HNPCEpiC	eye:	n/a
47	chr8:38851155-38851205	MCF10A-Er-Src	breast:	n/a
48	chr8:38851155-38851205	ProgFib	skin:	n/a
49	chr8:38851155-38851205	HRPEpiC	eye:	n/a
50	chr8:38851155-38851205	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:38847973..38851292-chr8:38852746..38855360,5	MCF-7	breast:
2	chr8:38642891..38646001-chr8:38852513..38856801,5	K562	blood:
3	chr8:38841597..38844221-chr8:38849102..38850866,2	MCF-7	breast:
4	chr8:38849585..38851368-chr8:38856687..38858833,2	MCF-7	breast:
5	chr8:38842260..38845059-chr8:38847931..38850445,2	MCF-7	breast:
6	chr8:38643651..38646089-chr8:38852696..38855577,2	MCF-7	breast:
7	chr8:38829292..38831588-chr8:38847607..38850439,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf86-7	chr8:38851064-38851555	NONHSAT126138
2	lnc-C8orf86-7	chr8:38849013-38849064	NONHSAT126138

No data

Variant related genes	Relation type
ADAM9	TF binding region
TM2D2	TF binding region
ADAM9	CpG island
TM2D2	CpG island
ENSG00000253645	chromatin interactions
ENSG00000168615	chromatin interactions
ENSG00000147526	chromatin interactions
ENSG00000169490	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:175 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149260396	chr8:38848749-38848750	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs547752295	chr8:38848750-38848751	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs559680482	chr8:38848753-38848754	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs3183442	chr8:38848757-38848758	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs369201513	chr8:38848787-38848788	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs58771784	chr8:38848808-38848809	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548090259	chr8:38848827-38848828	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4733895	chr8:38848850-38848851	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs140076526	chr8:38848917-38848918	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs374696018	chr8:38848923-38848924	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs201350341	chr8:38848950-38848951	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs144339648	chr8:38849005-38849006	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs371560347	chr8:38849016-38849017	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs374889594	chr8:38849042-38849043	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs552227296	chr8:38849045-38849046	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs201500324	chr8:38849058-38849059	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs199615903	chr8:38849069-38849070	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs200354734	chr8:38849076-38849077	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs200606749	chr8:38849104-38849105	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs111722842	chr8:38849139-38849140	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs547104703	chr8:38849201-38849202	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs181773068	chr8:38849209-38849210	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs566037071	chr8:38849251-38849252	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186881646	chr8:38849268-38849269	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs554883918	chr8:38849344-38849345	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs192255994	chr8:38849355-38849356	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs183924896	chr8:38849365-38849366	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs184898342	chr8:38849368-38849369	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs375798507	chr8:38849374-38849375	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs577357279	chr8:38849432-38849433	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs541438505	chr8:38849451-38849452	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs189803160	chr8:38849528-38849529	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530029033	chr8:38849538-38849539	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs542078567	chr8:38849550-38849551	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs369775301	chr8:38849617-38849618	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs149980120	chr8:38849667-38849668	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563365170	chr8:38849735-38849736	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs62504415	chr8:38849792-38849793	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs111646684	chr8:38849823-38849824	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs36088130	chr8:38849849-38849850	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552025884	chr8:38849856-38849857	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs570210609	chr8:38849860-38849861	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs528128866	chr8:38849864-38849865	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs534239844	chr8:38849889-38849890	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs558782858	chr8:38849890-38849891	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs141513768	chr8:38849902-38849903	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs57298254	chr8:38849905-38849906	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182420523	chr8:38849912-38849913	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570189809	chr8:38849930-38849931	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555854799	chr8:38849983-38849984	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
Melanoma	18172304	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	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
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	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
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Adrenocortical carcinoma	18281524	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Lung cancer	21569311	CNVD
Breast cancer	21364760	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:38824200-38848800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:38832400-38848800	Weak transcription	Pancreas	Pancrea
3	chr8:38832600-38848800	Weak transcription	Gastric	stomach
4	chr8:38832600-38848800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:38832600-38853000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:38835800-38848800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr8:38845200-38851600	Strong transcription	Primary B cells from peripheral blood	blood
8	chr8:38845400-38852000	Strong transcription	Osteobl	bone
9	chr8:38845600-38851600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:38845800-38851400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr8:38845800-38851800	Strong transcription	Fetal Muscle Leg	muscle
12	chr8:38846000-38851200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:38846000-38852400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr8:38846200-38851400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr8:38846200-38851400	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr8:38846200-38851400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr8:38846400-38849800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr8:38846400-38850400	Strong transcription	Dnd41	blood
19	chr8:38846400-38850600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr8:38846400-38851600	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr8:38846400-38852200	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr8:38846400-38852400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr8:38846400-38852400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr8:38846400-38852600	Strong transcription	Fetal Muscle Trunk	muscle
25	chr8:38846600-38850600	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr8:38846600-38851400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:38846600-38851600	Strong transcription	Fetal Intestine Large	intestine
28	chr8:38846600-38851600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr8:38846600-38852200	Weak transcription	Fetal Heart	heart
30	chr8:38846600-38852400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:38846600-38853000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr8:38846800-38850800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:38846800-38851200	Strong transcription	Primary T cells fromperipheralblood	blood
34	chr8:38846800-38851200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr8:38846800-38851200	Strong transcription	Fetal Stomach	stomach
36	chr8:38846800-38851600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr8:38846800-38852200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:38847000-38848800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr8:38847000-38851600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:38847200-38849000	Weak transcription	Fetal Kidney	kidney
41	chr8:38847400-38852000	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr8:38847400-38852000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:38847400-38852200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr8:38847400-38852400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr8:38847400-38852800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:38847600-38849000	Strong transcription	Small Intestine	intestine
47	chr8:38847600-38849400	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr8:38847600-38849600	Strong transcription	Primary neutrophils fromperipheralblood	blood
49	chr8:38847600-38850000	Strong transcription	HUVEC	blood vessel
50	chr8:38847600-38850200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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