Variant report

Variant	esv3328739
Chromosome Location	chr8:126452520-126454568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr8:126452873-126453180	GM12878	blood:	n/a	n/a
2	CBX3	chr8:126451425-126453375	HCT-116	colon:	n/a	n/a
3	CEBPB	chr8:126451435-126453300	HCT-116	colon:	n/a	n/a
4	EBF1	chr8:126452546-126452758	GM12878	blood:	n/a	chr8:126452671-126452682 chr8:126452673-126452682 chr8:126452673-126452682 chr8:126452672-126452682
5	ELF1	chr8:126451427-126453026	HCT-116	colon:	n/a	chr8:126452598-126452609
6	FOS	chr8:126452863-126453176	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr8:126452887-126453162	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr8:126452828-126453177	MCF10A-Er-Src	breast:	n/a	n/a
9	FOSL1	chr8:126451441-126453353	HCT-116	colon:	n/a	n/a
10	JUND	chr8:126451409-126453313	HCT-116	colon:	n/a	n/a
11	MAX	chr8:126451479-126453254	HCT-116	colon:	n/a	chr8:126452445-126452456
12	MAX	chr8:126451413-126453303	HCT-116	colon:	n/a	chr8:126452445-126452456
13	MYC	chr8:126452541-126452713	MCF10A-Er-Src	breast:	n/a	n/a
14	MYC	chr8:126452883-126453177	MCF10A-Er-Src	breast:	n/a	n/a
15	MYC	chr8:126453046-126453079	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr8:126451790-126452526	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr8:126451676-126453099	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr8:126440811-126453303	HCT-116	colon:	n/a	n/a
19	POLR2A	chr8:126453008-126453025	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr8:126451558-126453433	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr8:126451655-126452938	PANC-1	pancreas:	n/a	n/a
22	POLR2A	chr8:126451698-126453343	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr8:126451764-126453189	HepG2	liver:	n/a	n/a
24	POLR2A	chr8:126453874-126454168	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr8:126443504-126453314	A549	lung:	n/a	n/a
26	POLR2A	chr8:126451647-126452910	HCT-116	colon:	n/a	n/a
27	POLR2A	chr8:126443517-126453304	HepG2	liver:	n/a	n/a
28	POLR2A	chr8:126451421-126453714	HL-60	blood:	n/a	n/a
29	POLR2A	chr8:126451742-126452584	U87	brain:	n/a	n/a
30	POLR2A	chr8:126453007-126453224	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr8:126453012-126453115	GM12878	blood:	n/a	n/a
32	POLR2A	chr8:126451705-126452841	SK-N-MC	brain:	n/a	n/a
33	POLR2A	chr8:126451742-126452743	U87	brain:	n/a	n/a
34	POLR2A	chr8:126452800-126453189	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr8:126451681-126452728	HUVEC	blood vessel:	n/a	n/a
36	POLR2A	chr8:126441360-126452957	GM12878	blood:	n/a	n/a
37	POLR2A	chr8:126451643-126453320	GM12892	blood:	n/a	n/a
38	POLR2A	chr8:126449545-126452900	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr8:126440867-126453568	IMR90	lung:	n/a	n/a
40	POLR2A	chr8:126454032-126454538	HepG2	liver:	n/a	n/a
41	POLR2A	chr8:126453924-126454800	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr8:126451437-126453693	HL-60	blood:	n/a	n/a
43	POLR2A	chr8:126453809-126454547	IMR90	lung:	n/a	n/a
44	POLR2A	chr8:126451679-126453299	GM12878	blood:	n/a	n/a
45	POLR2A	chr8:126451360-126452652	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr8:126449286-126453223	MCF10A-Er-Src	breast:	n/a	n/a
47	POLR2A	chr8:126451732-126453121	GM12878	blood:	n/a	n/a
48	POLR2A	chr8:126450089-126452594	Hela-S3	cervix:	n/a	n/a
49	RAD21	chr8:126451421-126453364	HCT-116	colon:	n/a	n/a
50	RAD21	chr8:126451740-126453206	IMR90	lung:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr8:126450829..126453336-chr8:126485586..126487093,2	MCF-7	breast:
2	chr8:126450499..126452520-chr8:126526931..126528561,2	K562	blood:
3	chr8:126103757..126106407-chr8:126451002..126452588,2	MCF-7	breast:
4	chr8:126202921..126205556-chr8:126450247..126452721,2	K562	blood:
5	chr8:126453555..126455063-chr8:126584275..126586099,2	MCF-7	breast:
6	chr8:126452402..126454551-chr8:126832949..126835244,2	K562	blood:

No data

Variant related genes	Relation type
RN7SL590P	TF binding region
ENSG00000164961	chromatin interactions
ENSG00000156831	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543297867	chr8:126452526-126452527	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs563074634	chr8:126452589-126452590	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77593609	chr8:126452628-126452629	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs72647353	chr8:126452721-126452722	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs539926857	chr8:126452739-126452740	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551978727	chr8:126452815-126452816	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs186230224	chr8:126452861-126452862	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs552679387	chr8:126452867-126452868	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143577704	chr8:126452929-126452930	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs578128025	chr8:126452946-126452947	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs189721445	chr8:126452965-126452966	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs547520413	chr8:126453004-126453005	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs371181787	chr8:126453067-126453068	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs562436851	chr8:126453076-126453077	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs550033558	chr8:126453101-126453102	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564927021	chr8:126453110-126453111	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150876018	chr8:126453125-126453126	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs139376637	chr8:126453183-126453184	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs576025201	chr8:126453199-126453200	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs76593452	chr8:126453220-126453221	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533982461	chr8:126453258-126453259	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs201993317	chr8:126453321-126453322	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs367953738	chr8:126453328-126453329	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs75617280	chr8:126453330-126453331	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs200989651	chr8:126453332-126453333	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs146449783	chr8:126453351-126453352	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs374251475	chr8:126453361-126453362	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs60258141	chr8:126453362-126453363	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs10956246	chr8:126453363-126453364	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs74745796	chr8:126453365-126453366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs10956247	chr8:126453366-126453367	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs57460861	chr8:126453368-126453369	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs66953250	chr8:126453381-126453382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs6995783	chr8:126453382-126453383	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs72087760	chr8:126453396-126453397	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs554015524	chr8:126453493-126453494	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs368357512	chr8:126453533-126453534	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs75223307	chr8:126453605-126453606	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs368449058	chr8:126453608-126453609	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs113007674	chr8:126453618-126453619	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs558649736	chr8:126453693-126453694	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs562926124	chr8:126453696-126453697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372427381	chr8:126453725-126453726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183822541	chr8:126453736-126453737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545725891	chr8:126453784-126453785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143538805	chr8:126453835-126453836	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376976715	chr8:126453837-126453838	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs10097356	chr8:126453864-126453865	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs527937497	chr8:126453882-126453883	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs547504410	chr8:126453900-126453901	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
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
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Gastric cancer	21635755	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126447000-126458800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:126448000-126453400	Weak transcription	Stomach Mucosa	stomach
3	chr8:126448600-126457800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:126448600-126458600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr8:126449000-126459000	Weak transcription	HSMM	muscle
6	chr8:126449200-126457200	Weak transcription	Fetal Heart	heart
7	chr8:126449400-126452800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:126449400-126453000	Weak transcription	Gastric	stomach
9	chr8:126449400-126458600	Weak transcription	Esophagus	oesophagus
10	chr8:126450400-126452600	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:126450400-126452600	Weak transcription	GM12878-XiMat	blood
12	chr8:126450600-126453200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr8:126450600-126457600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr8:126450600-126463800	Weak transcription	Hela-S3	cervix
15	chr8:126450800-126452600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr8:126450800-126452600	Weak transcription	Fetal Thymus	thymus
17	chr8:126450800-126452800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr8:126450800-126452800	Weak transcription	Thymus	Thymus
19	chr8:126450800-126453000	Weak transcription	Aorta	Aorta
20	chr8:126450800-126453200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr8:126450800-126454600	Weak transcription	Pancreas	Pancrea
22	chr8:126450800-126457000	Weak transcription	K562	blood
23	chr8:126450800-126457200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:126450800-126457400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:126450800-126457600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:126450800-126457800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr8:126450800-126458000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr8:126450800-126458600	Weak transcription	Stomach Smooth Muscle	stomach
29	chr8:126450800-126458800	Weak transcription	Fetal Stomach	stomach
30	chr8:126451000-126452600	Weak transcription	Fetal Brain Female	brain
31	chr8:126451000-126452800	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr8:126451000-126454400	Weak transcription	Duodenum Mucosa	Duodenum
33	chr8:126451000-126454600	Weak transcription	Primary B cells from cord blood	blood
34	chr8:126451000-126457000	Weak transcription	Fetal Muscle Trunk	muscle
35	chr8:126451000-126457400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr8:126451000-126457600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr8:126451000-126458400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr8:126451000-126462400	Weak transcription	Liver	Liver
39	chr8:126451200-126452600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr8:126451200-126452800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr8:126451200-126452800	Weak transcription	Fetal Intestine Large	intestine
42	chr8:126451200-126452800	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr8:126451200-126452800	Weak transcription	HUVEC	blood vessel
44	chr8:126451200-126454400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:126451200-126458200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr8:126451400-126453000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr8:126451400-126453000	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr8:126451600-126452800	Enhancers	A549	lung
49	chr8:126451600-126453000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:126451600-126453200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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