Variant report

Variant	nsv611357
Chromosome Location	chr8:53445500-53505755
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	ARID3A	chr8:53490305-53490673	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:53490268-53490616	K562	blood:	n/a	n/a
3	ATF2	chr8:53502312-53502692	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:53476807-53478567	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:53502214-53502830	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:53474425-53474625	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr8:53502345-53502607	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr8:53490163-53490169	K562	blood:	n/a	n/a
9	CBX3	chr8:53459232-53459585	K562	blood:	n/a	n/a
10	CEBPB	chr8:53504545-53504779	K562	blood:	n/a	chr8:53504612-53504623
11	CEBPB	chr8:53484150-53484340	HepG2	liver:	n/a	chr8:53484205-53484216
12	CEBPB	chr8:53473626-53474007	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:53504483-53504758	IMR90	lung:	n/a	chr8:53504612-53504623
14	CEBPB	chr8:53475202-53475451	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:53500301-53500400	K562	blood:	n/a	n/a
16	CEBPB	chr8:53473588-53474038	A549	lung:	n/a	n/a
17	CEBPB	chr8:53482192-53482440	A549	lung:	n/a	chr8:53482355-53482366
18	CEBPB	chr8:53473661-53473959	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:53500260-53500488	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:53475278-53475403	HepG2	liver:	n/a	n/a
21	CEBPB	chr8:53504508-53504688	HepG2	liver:	n/a	chr8:53504612-53504623
22	CEBPB	chr8:53473666-53473994	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:53500247-53500519	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:53482232-53482516	HepG2	liver:	n/a	chr8:53482355-53482366
25	CEBPB	chr8:53473675-53474000	A549	lung:	n/a	n/a
26	CEBPB	chr8:53473671-53473965	K562	blood:	n/a	n/a
27	CEBPB	chr8:53473645-53474169	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr8:53478215-53478807	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr8:53474867-53474966	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD1	chr8:53490413-53490437	GM12878	blood:	n/a	n/a
31	CTBP2	chr8:53476833-53478582	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr8:53490140-53490290	HCT-116	colon:	n/a	n/a
33	CTCF	chr8:53490315-53490604	Spleen_OC	spleen:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
34	CTCF	chr8:53490420-53490570	AG09319	gingival:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
35	CTCF	chr8:53490268-53490553	K562	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
36	CTCF	chr8:53490120-53490270	GM12873	blood:	n/a	n/a
37	CTCF	chr8:53490400-53490550	HepG2	liver:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
38	CTCF	chr8:53474606-53474756	H1-hESC	embryonic stem cell:	n/a	chr8:53474668-53474681
39	CTCF	chr8:53490400-53490550	NHDF-neo	bronchial:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
40	CTCF	chr8:53490400-53490550	AG04450	lung:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
41	CTCF	chr8:53476385-53476498	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:53500348-53500445	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:53490340-53490490	NHEK	skin:	n/a	chr8:53490468-53490486 chr8:53490469-53490485
44	CTCF	chr8:53490728-53490771	Gliobla	brain:	n/a	n/a
45	CTCF	chr8:53474604-53474742	Medullo	brain:	n/a	chr8:53474668-53474681
46	CTCF	chr8:53490380-53490530	GM12865	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
47	CTCF	chr8:53490160-53490310	GM12868	blood:	n/a	n/a
48	CTCF	chr8:53490360-53490510	GM12878	blood:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491
49	CTCF	chr8:53474480-53474630	A549	lung:	n/a	n/a
50	CTCF	chr8:53490380-53490530	AoAF	blood vessel:	n/a	chr8:53490468-53490486 chr8:53490469-53490485 chr8:53490470-53490491

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:53450729-53450779	GM12878	blood:	n/a
2	chr8:53450729-53450779	GM12878	blood:	n/a
3	chr8:53450729-53450779	SAEC	small airway:	n/a
4	chr8:53499582-53499632	PFSK-1	brain:	n/a
5	chr8:53476865-53476915	GM19239	blood:	n/a
6	chr8:53490251-53490301	HUVEC	blood vessel:	n/a
7	chr8:53478706-53478756	PANC-1	pancreas:	n/a
8	chr8:53478074-53478124	GM12891	blood:	n/a
9	chr8:53474030-53474080	HUVEC	blood vessel:	n/a
10	chr8:53477881-53477931	HRE	kidney:	n/a
11	chr8:53477545-53477595	T-47D	breast:	n/a
12	chr8:53456003-53456053	AG04449	skin:	fetal
13	chr8:53478102-53478152	MCF10A-Er-Src	breast:	n/a
14	chr8:53478454-53478504	ovcar-3	ovarian:	n/a
15	chr8:53485670-53485720	GM19239	blood:	n/a
16	chr8:53478624-53478674	RPTEC	kidney:	n/a
17	chr8:53474887-53474937	GM19239	blood:	n/a
18	chr8:53456003-53456053	HEK293	kidney:	embryo
19	chr8:53499582-53499632	HCM	heart:	n/a
20	chr8:53478624-53478674	HUVEC	blood vessel:	n/a
21	chr8:53471884-53471934	HCM	heart:	n/a
22	chr8:53474030-53474080	GM12891	blood:	n/a
23	chr8:53471884-53471934	HRE	kidney:	n/a
24	chr8:53499558-53499608	HL-60	blood:	n/a
25	chr8:53476943-53476993	CMK	blood:	n/a
26	chr8:53478454-53478504	HCT-116	colon:	n/a
27	chr8:53478102-53478152	HEEpiC	esophagus:	n/a
28	chr8:53478624-53478674	HepG2	liver:	n/a
29	chr8:53499582-53499632	HEK293	kidney:	embryo
30	chr8:53450729-53450779	Jurkat	blood:	n/a
31	chr8:53490251-53490301	HPAEpiC	pulmonary alveolar:	n/a
32	chr8:53485670-53485720	BJ	skin:	n/a
33	chr8:53490251-53490301	SKMC	muscle:	n/a
34	chr8:53477545-53477595	SK-N-SH	brain:	n/a
35	chr8:53476943-53476993	Caco-2	colon:	n/a
36	chr8:53477264-53477314	HL-60	blood:	n/a
37	chr8:53474030-53474080	AoSMC	blood vessel:	n/a
38	chr8:53478454-53478504	SK-N-SH_RA	brain:	n/a
39	chr8:53478053-53478103	CMK	blood:	n/a
40	chr8:53456003-53456053	A549	lung:	n/a
41	chr8:53478074-53478124	PrEC	prostate:	n/a
42	chr8:53499558-53499608	CMK	blood:	n/a
43	chr8:53476943-53476993	T-47D	breast:	n/a
44	chr8:53476865-53476915	IMR90	lung:	fetal
45	chr8:53478053-53478103	PrEC	prostate:	n/a
46	chr8:53477881-53477931	H1-hESC	embryonic stem cell:	embryo
47	chr8:53450729-53450779	SK-N-MC	brain:	n/a
48	chr8:53478074-53478124	NHBE	bronchial:	n/a
49	chr8:53474030-53474080	PANC-1	pancreas:	n/a
50	chr8:53485670-53485720	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:53490029..53490926-chr8:53861444..53862393,2	MCF-7	breast:
2	chr8:53490108..53490739-chr8:53649694..53650429,2	MCF-7	breast:

Variant related genes	Relation type
FAM150A	TF binding region
FAM150A	CpG island

Extended variants
information (count: 1804 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1804 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13278871	chr8:53445500-53445501	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148770132	chr8:53445544-53445545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541307765	chr8:53445546-53445547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577695943	chr8:53445548-53445549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572592932	chr8:53445565-53445566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77603971	chr8:53445576-53445577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564757798	chr8:53445607-53445608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535240952	chr8:53445655-53445656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544686305	chr8:53445682-53445683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs55868469	chr8:53445696-53445697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532054556	chr8:53445745-53445746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558237591	chr8:53445747-53445748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543934150	chr8:53445754-53445755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142427210	chr8:53445759-53445760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529687833	chr8:53445787-53445788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548171472	chr8:53445832-53445833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182952455	chr8:53445862-53445863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76879765	chr8:53445877-53445878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75651715	chr8:53445882-53445883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79767041	chr8:53445883-53445884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200557203	chr8:53445884-53445885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs201618616	chr8:53445885-53445886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141930498	chr8:53446122-53446123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546859139	chr8:53446190-53446191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571904257	chr8:53446207-53446208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539125617	chr8:53446258-53446259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187467933	chr8:53446310-53446311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs531398083	chr8:53446326-53446327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569379328	chr8:53446334-53446335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375169397	chr8:53446349-53446350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536215115	chr8:53446457-53446458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192022377	chr8:53446474-53446475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577805820	chr8:53446527-53446528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573024519	chr8:53446557-53446558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184204809	chr8:53446579-53446580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543233147	chr8:53446607-53446608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540546947	chr8:53446611-53446612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35937020	chr8:53446634-53446635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558312022	chr8:53446650-53446651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148648836	chr8:53446690-53446691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370023713	chr8:53446694-53446695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563568309	chr8:53446711-53446712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115005342	chr8:53446735-53446736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188761070	chr8:53446845-53446846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562197006	chr8:53446861-53446862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529804728	chr8:53446992-53446993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576263263	chr8:53447135-53447136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541425794	chr8:53447141-53447142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560124198	chr8:53447213-53447214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs192718762	chr8:53447216-53447217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:53444800-53446000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:53445400-53446400	Enhancers	Fetal Lung	lung
3	chr8:53446000-53446400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:53446000-53446600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:53446400-53453200	Weak transcription	Fetal Lung	lung
6	chr8:53446600-53448400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:53448400-53448800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:53448800-53453000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:53453000-53454000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:53453200-53453400	Enhancers	Fetal Lung	lung
11	chr8:53454000-53455200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr8:53455200-53456200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:53455800-53456800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:53455800-53457200	Bivalent Enhancer	Dnd41	blood
15	chr8:53456200-53456400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:53456400-53457200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:53457200-53458600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:53458600-53460800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:53460800-53467800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:53467600-53475000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr8:53467800-53468600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr8:53467800-53468600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr8:53468200-53468400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr8:53468200-53468400	Enhancers	Esophagus	oesophagus
25	chr8:53468400-53471600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr8:53468600-53469600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr8:53469600-53470000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:53470000-53471000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr8:53470800-53471400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
30	chr8:53471000-53471400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr8:53471000-53471400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:53471000-53472000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:53471000-53472400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr8:53471000-53472400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:53471200-53471600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr8:53471200-53471600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr8:53471200-53471800	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr8:53471200-53471800	Active TSS	iPS-18 Cell Line	embryonic stem cell
39	chr8:53471200-53472000	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr8:53471400-53471600	Flanking Active TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr8:53471400-53471600	Flanking Active TSS	H1 Cell Line	embryonic stem cell
42	chr8:53471400-53472000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr8:53471600-53471800	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:53471600-53471800	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr8:53471600-53472000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr8:53471600-53472000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr8:53471600-53472000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr8:53471800-53472000	Flanking Active TSS	H1 Cell Line	embryonic stem cell
49	chr8:53471800-53472000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr8:53471800-53472000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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