Variant report

Variant	nsv890977
Chromosome Location	chr8:69173049-69236718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:177)
CpG islands
(count:62)
Chromatin interactive
region (count:4)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:177 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:69227774-69227939	K562	blood:	n/a	n/a
2	BACH1	chr8:69207698-69207805	K562	blood:	n/a	n/a
3	BACH1	chr8:69218330-69218530	K562	blood:	n/a	n/a
4	BCL3	chr8:69208381-69208746	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:69218442-69218815	K562	blood:	n/a	n/a
6	BHLHE40	chr8:69183640-69183747	GM12878	blood:	n/a	n/a
7	CEBPB	chr8:69181605-69181846	HepG2	liver:	n/a	chr8:69181693-69181704 chr8:69181692-69181705
8	CEBPB	chr8:69181615-69181856	H1-hESC	embryonic stem cell:	n/a	chr8:69181693-69181704 chr8:69181692-69181705
9	CEBPB	chr8:69208457-69208763	MCF-7	breast:	n/a	n/a
10	CHD1	chr8:69179058-69179073	GM12878	blood:	n/a	n/a
11	CHD1	chr8:69218317-69218685	GM12878	blood:	n/a	n/a
12	CHD1	chr8:69211429-69211450	GM12878	blood:	n/a	n/a
13	CHD2	chr8:69218449-69218649	K562	blood:	n/a	n/a
14	CTCF	chr8:69196020-69196170	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr8:69196040-69196190	HCPEpiC	choroid plexus:	n/a	n/a
16	CTCF	chr8:69196020-69196170	AoAF	blood vessel:	n/a	n/a
17	CTCF	chr8:69196100-69196250	NHDF-neo	bronchial:	n/a	n/a
18	CTCF	chr8:69196060-69196210	AG09319	gingival:	n/a	n/a
19	CTCF	chr8:69195980-69196130	NHEK	skin:	n/a	n/a
20	CTCF	chr8:69196040-69196190	HVMF	connective:	n/a	n/a
21	CTCF	chr8:69196040-69196190	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr8:69198020-69198170	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr8:69219748-69219767	ProgFib	skin:	n/a	n/a
24	CTCF	chr8:69196120-69196270	GM12872	blood:	n/a	n/a
25	CTCF	chr8:69174300-69174450	BJ	skin:	n/a	n/a
26	CTCF	chr8:69196000-69196150	AG04450	lung:	n/a	n/a
27	CTCF	chr8:69196040-69196190	BJ	skin:	n/a	n/a
28	CTCF	chr8:69196140-69196290	RPTEC	kidney:	n/a	n/a
29	CTCF	chr8:69195980-69196130	HMEC	breast:	n/a	n/a
30	CTCF	chr8:69196060-69196210	AG10803	skin:	n/a	n/a
31	CTCF	chr8:69196000-69196150	AG09309	skin:	n/a	n/a
32	CTCF	chr8:69196060-69196210	GM12873	blood:	n/a	n/a
33	CTCF	chr8:69197980-69198130	GM12873	blood:	n/a	n/a
34	CTCF	chr8:69196060-69196210	HMEC	breast:	n/a	n/a
35	CTCF	chr8:69196020-69196170	HEK293	kidney:	n/a	n/a
36	CTCF	chr8:69195940-69196090	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr8:69195980-69196130	AG04449	skin:	n/a	n/a
38	CTCF	chr8:69196040-69196190	HMF	breast:	n/a	n/a
39	CTCF	chr8:69195880-69196030	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:69195960-69196110	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:69195940-69196090	AG04450	lung:	n/a	n/a
42	CTCF	chr8:69196100-69196250	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr8:69196080-69196230	HCFaa	heart:	n/a	n/a
44	CTCF	chr8:69196080-69196230	GM12864	blood:	n/a	n/a
45	CTCF	chr8:69196020-69196170	HRE	kidney:	n/a	n/a
46	CTCF	chr8:69225926-69225981	GM10248	blood:	n/a	n/a
47	CTCF	chr8:69196062-69196197	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr8:69229745-69229787	GM10248	blood:	n/a	n/a
49	CTCF	chr8:69196120-69196270	K562	blood:	n/a	n/a
50	CTCF	chr8:69229926-69229993	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69216882-69216932	SKMC	muscle:	n/a
2	chr8:69216882-69216932	SKMC	muscle:	n/a
3	chr8:69216882-69216932	HAEpiC	amniotic membrane:	n/a
4	chr8:69216882-69216932	U87	brain:	n/a
5	chr8:69216882-69216932	HL-60	blood:	n/a
6	chr8:69216882-69216932	H1-hESC	embryonic stem cell:	embryo
7	chr8:69216882-69216932	MCF10A-Er-Src	breast:	n/a
8	chr8:69216882-69216932	NB4	blood:	n/a
9	chr8:69216882-69216932	A549	lung:	n/a
10	chr8:69216882-69216932	SAEC	small airway:	n/a
11	chr8:69216882-69216932	HRPEpiC	eye:	n/a
12	chr8:69216882-69216932	HIPEpiC	eye:	n/a
13	chr8:69216882-69216932	AG10803	skin:	n/a
14	chr8:69216882-69216932	HepG2	liver:	n/a
15	chr8:69216882-69216932	Hepatocyte	liver:	n/a
16	chr8:69216882-69216932	ovcar-3	ovarian:	n/a
17	chr8:69216882-69216932	HEEpiC	esophagus:	n/a
18	chr8:69216882-69216932	NH-A	brain:	n/a
19	chr8:69216882-69216932	HCM	heart:	n/a
20	chr8:69216882-69216932	SK-N-SH_RA	brain:	n/a
21	chr8:69216882-69216932	HRCEpiC	kidney:	n/a
22	chr8:69216882-69216932	LNCaP	prostate:	n/a
23	chr8:69216882-69216932	T-47D	breast:	n/a
24	chr8:69216882-69216932	HCF	heart:	n/a
25	chr8:69216882-69216932	HMEC	breast:	n/a
26	chr8:69216882-69216932	PFSK-1	brain:	n/a
27	chr8:69216882-69216932	Hela-S3	cervix:	n/a
28	chr8:69216882-69216932	HCPEpiC	choroid plexus:	n/a
29	chr8:69216882-69216932	HEK293	kidney:	embryo
30	chr8:69216882-69216932	BJ	skin:	n/a
31	chr8:69216882-69216932	AG09319	gingival:	n/a
32	chr8:69216882-69216932	RPTEC	kidney:	n/a
33	chr8:69216882-69216932	GM12892	blood:	n/a
34	chr8:69216882-69216932	GM12878	blood:	n/a
35	chr8:69216882-69216932	IMR90	lung:	fetal
36	chr8:69216882-69216932	K562	blood:	n/a
37	chr8:69216882-69216932	Jurkat	blood:	n/a
38	chr8:69216882-69216932	SK-N-SH	brain:	n/a
39	chr8:69216882-69216932	HNPCEpiC	eye:	n/a
40	chr8:69216882-69216932	NT2-D1	testis:	n/a
41	chr8:69216882-69216932	AG04449	skin:	fetal
42	chr8:69216882-69216932	MCF-7	breast:	n/a
43	chr8:69216882-69216932	PrEC	prostate:	n/a
44	chr8:69216882-69216932	NHDF-neo	bronchial:	n/a
45	chr8:69216882-69216932	GM12891	blood:	n/a
46	chr8:69216882-69216932	CMK	blood:	n/a
47	chr8:69216882-69216932	HUVEC	blood vessel:	n/a
48	chr8:69216882-69216932	AG09309	skin:	n/a
49	chr8:69216882-69216932	PANC-1	pancreas:	n/a
50	chr8:69216882-69216932	Caco-2	colon:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:69172089..69174443-chr8:69177342..69179034,2	K562	blood:
2	chr8:69172089..69174443-chr8:69177342..69179034,2	K562	blood:
3	chr8:69214227..69216220-chr8:69229088..69230981,2	K562	blood:
4	chr8:69214227..69216220-chr8:69229088..69230981,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-664D7.4.1-4	chr8:69215703-69217036	NR_038877
2	lnc-RP11-664D7.4.1-4	chr8:69224379-69224452	NONHSAT127094
3	lnc-RP11-664D7.4.1-4	chr8:69214472-69216749	NONHSAT127093
4	lnc-RP11-664D7.4.1-4	chr8:69218753-69218833	NR_038877
5	lnc-RP11-664D7.4.1-4	chr8:69218753-69218833	NONHSAT127094
6	lnc-RP11-664D7.4.1-4	chr8:69216867-69217036	NONHSAT127094
7	lnc-RP11-664D7.4.1-5	chr8:69205681-69206053	NONHSAT127092

No data

Variant related genes	Relation type
RPL31P40	TF binding region
ENSG00000248801	TF binding region
RPL31P40	CpG island
ENSG00000248801	CpG island

Extended variants
information (count: 1241 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1241 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7463341	chr8:69173049-69173050	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73683422	chr8:69173080-69173081	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs552202050	chr8:69173129-69173130	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs546765722	chr8:69173213-69173214	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs567072622	chr8:69173229-69173230	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs565644046	chr8:69173238-69173239	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs370091656	chr8:69173261-69173262	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554690372	chr8:69173275-69173276	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs568202688	chr8:69173297-69173298	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs537641581	chr8:69173324-69173325	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs557485189	chr8:69173344-69173345	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs193132571	chr8:69173471-69173472	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs182718475	chr8:69173491-69173492	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs553416566	chr8:69173522-69173523	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs10103223	chr8:69173543-69173544	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs369949040	chr8:69173575-69173576	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs572883711	chr8:69173671-69173672	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544646773	chr8:69173879-69173880	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187043957	chr8:69173896-69173897	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs561840005	chr8:69173900-69173901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs530865787	chr8:69173949-69173950	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs151051987	chr8:69173983-69173984	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs114070840	chr8:69173990-69173991	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs368568567	chr8:69173996-69173997	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs76149106	chr8:69174057-69174058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554385580	chr8:69174068-69174069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191538763	chr8:69174136-69174137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111498702	chr8:69174151-69174152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139768696	chr8:69174170-69174171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs183694482	chr8:69174223-69174224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537105743	chr8:69174290-69174291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188067752	chr8:69174334-69174335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75646616	chr8:69174358-69174359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs117019704	chr8:69174361-69174362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553617609	chr8:69174458-69174459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117402602	chr8:69174459-69174460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs75544924	chr8:69174470-69174471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79667588	chr8:69174506-69174507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575252380	chr8:69174580-69174581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149811273	chr8:69174582-69174583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564453421	chr8:69174584-69174585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs147924550	chr8:69174702-69174703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141788692	chr8:69174703-69174704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559682551	chr8:69174705-69174706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528350172	chr8:69174707-69174708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545919007	chr8:69174744-69174745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373607669	chr8:69174767-69174768	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145628913	chr8:69174806-69174807	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs367664767	chr8:69174845-69174846	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs545169876	chr8:69174855-69174856	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:141 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69167000-69173600	Weak transcription	Esophagus	oesophagus
2	chr8:69170000-69173200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:69170200-69173200	Weak transcription	Aorta	Aorta
4	chr8:69170400-69173600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:69172200-69173200	Enhancers	Fetal Stomach	stomach
6	chr8:69172200-69173800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:69172200-69173800	Flanking Active TSS	NHDF-Ad	bronchial
8	chr8:69172400-69173200	Weak transcription	Left Ventricle	heart
9	chr8:69172400-69173600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:69172600-69173800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:69172800-69173600	Active TSS	NHLF	lung
12	chr8:69172800-69173800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:69172800-69174000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
14	chr8:69173000-69173200	Flanking Active TSS	Rectal Smooth Muscle	rectum
15	chr8:69173000-69173400	Enhancers	Primary hematopoietic stem cells	blood
16	chr8:69173000-69173400	Active TSS	A549	lung
17	chr8:69173000-69173400	Active TSS	HSMMtube	muscle
18	chr8:69173000-69173400	Active TSS	HUVEC	blood vessel
19	chr8:69173000-69173600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr8:69173000-69173600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr8:69173000-69173600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:69173000-69173600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr8:69173000-69173600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:69173000-69173600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:69173000-69173600	Active TSS	Duodenum Mucosa	Duodenum
26	chr8:69173000-69173600	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr8:69173000-69173600	Active TSS	Ovary	ovary
28	chr8:69173000-69173600	Active TSS	Right Atrium	heart
29	chr8:69173000-69173800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr8:69173000-69173800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr8:69173000-69173800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:69173000-69173800	Flanking Active TSS	Adipose Nuclei	Adipose
33	chr8:69173000-69173800	Active TSS	Osteobl	bone
34	chr8:69173200-69173400	Flanking Active TSS	Liver	Liver
35	chr8:69173200-69173600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:69173200-69173600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:69173200-69173600	Enhancers	Aorta	Aorta
38	chr8:69173200-69173600	Active TSS	Brain Hippocampus Middle	brain
39	chr8:69173200-69173600	Enhancers	Fetal Lung	lung
40	chr8:69173200-69173600	Active TSS	Fetal Muscle Leg	muscle
41	chr8:69173200-69173600	Active TSS	Fetal Stomach	stomach
42	chr8:69173200-69173600	Active TSS	Rectal Mucosa Donor 31	rectum
43	chr8:69173200-69173600	Active TSS	Rectal Smooth Muscle	rectum
44	chr8:69173200-69173600	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr8:69173200-69173600	Active TSS	Stomach Smooth Muscle	stomach
46	chr8:69173200-69173800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr8:69173200-69173800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr8:69173200-69173800	Enhancers	Left Ventricle	heart
49	chr8:69173200-69173800	Enhancers	Psoas Muscle	Psoas
50	chr8:69173200-69173800	Active TSS	Rectal Mucosa Donor 29	rectum

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