Variant report

Variant	esv3329643
Chromosome Location	chr8:125494521-125496369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:36)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:36 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:125495455-125495665	K562	blood:	n/a	chr8:125495590-125495601 chr8:125495589-125495600 chr8:125495589-125495602
2	CEBPB	chr8:125495435-125495672	A549	lung:	n/a	chr8:125495590-125495601 chr8:125495589-125495600 chr8:125495589-125495602
3	CEBPB	chr8:125495448-125495743	HepG2	liver:	n/a	chr8:125495590-125495601 chr8:125495589-125495600 chr8:125495589-125495602
4	CEBPB	chr8:125495442-125495738	Hela-S3	cervix:	n/a	chr8:125495590-125495601 chr8:125495589-125495600 chr8:125495589-125495602
5	CEBPB	chr8:125495461-125495748	IMR90	lung:	n/a	chr8:125495590-125495601 chr8:125495589-125495600 chr8:125495589-125495602
6	CTCF	chr8:125494780-125494930	GM12869	blood:	n/a	n/a
7	E2F4	chr8:125496142-125496342	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr8:125495479-125495634	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr8:125495408-125495601	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr8:125495473-125495646	MCF10A-Er-Src	breast:	n/a	n/a
11	FOS	chr8:125495377-125495672	MCF10A-Er-Src	breast:	n/a	n/a
12	FOXA1	chr8:125496200-125496603	T-47D	breast:	n/a	n/a
13	FOXA1	chr8:125496246-125496599	HepG2	liver:	n/a	n/a
14	FOXA1	chr8:125496199-125496507	HepG2	liver:	n/a	n/a
15	FOXA1	chr8:125496238-125496537	HepG2	liver:	n/a	n/a
16	FOXA1	chr8:125496154-125496527	HepG2	liver:	n/a	n/a
17	FOXA1	chr8:125496234-125496611	T-47D	breast:	n/a	n/a
18	FOXA2	chr8:125496315-125496561	HepG2	liver:	n/a	n/a
19	GATA3	chr8:125496222-125496703	T-47D	breast:	n/a	n/a
20	GATA3	chr8:125496254-125496693	T-47D	breast:	n/a	n/a
21	MYC	chr8:125495760-125495769	MCF-7	breast:	n/a	n/a
22	POLR2A	chr8:125495729-125495738	MCF-7	breast:	n/a	n/a
23	POLR2A	chr8:125496361-125496376	MCF-7	breast:	n/a	n/a
24	POLR2A	chr8:125496039-125496201	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr8:125495532-125495549	MCF-7	breast:	n/a	n/a
26	POLR2A	chr8:125495551-125495554	MCF-7	breast:	n/a	n/a
27	POLR2A	chr8:125496350-125496356	MCF-7	breast:	n/a	n/a
28	POLR2A	chr8:125495566-125495614	MCF-7	breast:	n/a	n/a
29	POLR2A	chr8:125495732-125495741	ProgFib	skin:	n/a	n/a
30	POLR2A	chr8:125495750-125495962	MCF-7	breast:	n/a	n/a
31	POLR2A	chr8:125495733-125495835	MCF-7	breast:	n/a	n/a
32	POLR2A	chr8:125496033-125496500	K562	blood:	n/a	n/a
33	POLR2A	chr8:125495701-125495834	MCF-7	breast:	n/a	n/a
34	POLR2A	chr8:125495496-125495508	MCF-7	breast:	n/a	n/a
35	SPI1	chr8:125494212-125494549	HL-60	blood:	n/a	chr8:125494416-125494429
36	STAT3	chr8:125495485-125495685	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125495822-125495872	SAEC	small airway:	n/a
2	chr8:125495822-125495872	HPAEpiC	pulmonary alveolar:	n/a
3	chr8:125495822-125495872	SK-N-SH_RA	brain:	n/a
4	chr8:125495822-125495872	AG04450	lung:	fetal
5	chr8:125495822-125495872	HIPEpiC	eye:	n/a
6	chr8:125495822-125495872	SK-N-MC	brain:	n/a
7	chr8:125495822-125495872	T-47D	breast:	n/a
8	chr8:125495822-125495872	HUVEC	blood vessel:	n/a
9	chr8:125495822-125495872	NH-A	brain:	n/a
10	chr8:125495822-125495872	HAEpiC	amniotic membrane:	n/a
11	chr8:125495822-125495872	Caco-2	colon:	n/a
12	chr8:125495822-125495872	Jurkat	blood:	n/a
13	chr8:125495822-125495872	PFSK-1	brain:	n/a
14	chr8:125495822-125495872	NB4	blood:	n/a
15	chr8:125495822-125495872	HNPCEpiC	eye:	n/a
16	chr8:125495822-125495872	NHBE	bronchial:	n/a
17	chr8:125495822-125495872	HMEC	breast:	n/a
18	chr8:125495822-125495872	HepG2	liver:	n/a
19	chr8:125495822-125495872	MCF10A-Er-Src	breast:	n/a
20	chr8:125495822-125495872	MCF-7	breast:	n/a
21	chr8:125495822-125495872	HCM	heart:	n/a
22	chr8:125495822-125495872	ECC-1	luminal epithelium:	n/a
23	chr8:125495822-125495872	HEEpiC	esophagus:	n/a
24	chr8:125495822-125495872	GM19239	blood:	n/a
25	chr8:125495822-125495872	GM12892	blood:	n/a
26	chr8:125495822-125495872	CMK	blood:	n/a
27	chr8:125495822-125495872	PrEC	prostate:	n/a
28	chr8:125495822-125495872	SK-N-SH	brain:	n/a
29	chr8:125495822-125495872	HCF	heart:	n/a
30	chr8:125495822-125495872	BJ	skin:	n/a
31	chr8:125495822-125495872	GM12878	blood:	n/a
32	chr8:125495822-125495872	HCT-116	colon:	n/a
33	chr8:125495822-125495872	Hepatocyte	liver:	n/a
34	chr8:125495822-125495872	NT2-D1	testis:	n/a
35	chr8:125495822-125495872	GM12891	blood:	n/a
36	chr8:125495822-125495872	IMR90	lung:	fetal
37	chr8:125495822-125495872	PANC-1	pancreas:	n/a
38	chr8:125495822-125495872	GM06990	blood:	n/a
39	chr8:125495822-125495872	SKMC	muscle:	n/a
40	chr8:125495822-125495872	U87	brain:	n/a
41	chr8:125495822-125495872	LNCaP	prostate:	n/a
42	chr8:125495822-125495872	HRPEpiC	eye:	n/a
43	chr8:125495822-125495872	K562	blood:	n/a
44	chr8:125495822-125495872	BE2_C	brain:	n/a
45	chr8:125495822-125495872	AG10803	skin:	n/a
46	chr8:125495822-125495872	HRCEpiC	kidney:	n/a
47	chr8:125495822-125495872	H1-hESC	embryonic stem cell:	embryo
48	chr8:125495822-125495872	NHDF-neo	bronchial:	n/a
49	chr8:125495822-125495872	A549	lung:	n/a
50	chr8:125495822-125495872	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:141226994..141229568-chr8:125493170..125494852,2	MCF-7	breast:
2	chr8:125491802..125498170-chr8:125548148..125552034,10	MCF-7	breast:
3	chr8:125494945..125497543-chr8:125548660..125551608,2	K562	blood:
4	chr8:125495517..125498370-chr8:125499214..125502183,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253106	TF binding region
RNF139	TF binding region
ENSG00000253106	CpG island
RNF139	CpG island
ENSG00000253106	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000147684	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564096285	chr8:125494544-125494545	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs533167516	chr8:125494618-125494619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs77481784	chr8:125494644-125494645	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs185798263	chr8:125494729-125494730	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189820548	chr8:125494797-125494798	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs149943774	chr8:125494813-125494814	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569487885	chr8:125494840-125494841	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs118058547	chr8:125494861-125494862	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs552105469	chr8:125494868-125494869	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs571221425	chr8:125494885-125494886	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs114448248	chr8:125494894-125494895	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs4871493	chr8:125494922-125494923	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567235902	chr8:125494933-125494934	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs144121844	chr8:125494934-125494935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543624745	chr8:125494946-125494947	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs180709391	chr8:125495003-125495004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs575837511	chr8:125495031-125495032	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs186105707	chr8:125495058-125495059	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs374246022	chr8:125495076-125495077	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572053475	chr8:125495079-125495080	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376018281	chr8:125495123-125495124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs370373199	chr8:125495133-125495134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs112629245	chr8:125495150-125495151	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143131727	chr8:125495176-125495177	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543128453	chr8:125495177-125495178	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs28635338	chr8:125495182-125495183	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs28549965	chr8:125495184-125495185	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs191875439	chr8:125495186-125495187	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs376318216	chr8:125495199-125495200	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550779916	chr8:125495200-125495201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs28704640	chr8:125495201-125495202	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs371115028	chr8:125495213-125495214	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374074192	chr8:125495217-125495218	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377661619	chr8:125495218-125495219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562715202	chr8:125495219-125495220	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs530210844	chr8:125495220-125495221	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369825859	chr8:125495229-125495230	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs565556490	chr8:125495231-125495232	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs528023124	chr8:125495233-125495234	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs78456204	chr8:125495234-125495235	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs72492813	chr8:125495248-125495249	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs368206010	chr8:125495251-125495252	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372596259	chr8:125495264-125495265	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs370370558	chr8:125495268-125495269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs373715299	chr8:125495270-125495271	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs375520286	chr8:125495285-125495286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369445348	chr8:125495287-125495288	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373873894	chr8:125495288-125495289	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs80027151	chr8:125495294-125495295	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372288388	chr8:125495296-125495297	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:141)

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
Multiple myeloma	17550852	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
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125488000-125503400	Weak transcription	Spleen	Spleen
2	chr8:125488200-125498200	Weak transcription	Esophagus	oesophagus
3	chr8:125488200-125515800	Weak transcription	Lung	lung
4	chr8:125488200-125550400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:125489000-125496200	Weak transcription	Colonic Mucosa	Colon
6	chr8:125489000-125497200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:125489000-125498200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr8:125489000-125498200	Weak transcription	Placenta	Placenta
9	chr8:125489000-125501800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:125489000-125503400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr8:125489000-125505800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr8:125489000-125519800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:125489000-125531200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:125489000-125541200	Weak transcription	Gastric	stomach
15	chr8:125489000-125543400	Weak transcription	Small Intestine	intestine
16	chr8:125489200-125495800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:125489200-125496200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr8:125489200-125496200	Weak transcription	Fetal Stomach	stomach
19	chr8:125489200-125496400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr8:125489200-125496400	Weak transcription	NH-A	brain
21	chr8:125489200-125497200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr8:125489200-125498000	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:125489200-125498000	Weak transcription	Fetal Muscle Leg	muscle
24	chr8:125489200-125498200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:125489200-125498200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr8:125489200-125498200	Weak transcription	Aorta	Aorta
27	chr8:125489200-125498200	Weak transcription	Right Ventricle	heart
28	chr8:125489200-125498200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr8:125489200-125498200	Weak transcription	Thymus	Thymus
30	chr8:125489200-125498400	Weak transcription	Fetal Brain Male	brain
31	chr8:125489200-125498600	Weak transcription	A549	lung
32	chr8:125489200-125498600	Weak transcription	HSMMtube	muscle
33	chr8:125489400-125497800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:125489400-125498000	Weak transcription	Fetal Kidney	kidney
35	chr8:125489400-125498000	Weak transcription	Stomach Smooth Muscle	stomach
36	chr8:125489400-125498200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr8:125489400-125498200	Weak transcription	HSMM	muscle
38	chr8:125489400-125498400	Weak transcription	NHEK	skin
39	chr8:125489400-125501800	Weak transcription	Fetal Intestine Small	intestine
40	chr8:125489600-125494800	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr8:125489600-125497800	Weak transcription	Primary hematopoietic stem cells	blood
42	chr8:125489600-125498000	Weak transcription	Fetal Intestine Large	intestine
43	chr8:125489600-125498200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr8:125489600-125498200	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr8:125489600-125498200	Weak transcription	HMEC	breast
46	chr8:125489600-125498600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr8:125489800-125496400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:125489800-125498000	Weak transcription	Duodenum Mucosa	Duodenum
49	chr8:125490000-125496000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr8:125490000-125496200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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