Variant report

Variant	esv3490861
Chromosome Location	chr3:49196144-49198530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr3:49196216-49196670	GM12878	blood:	n/a	n/a
2	ESR1	chr3:49196254-49196538	ECC-1	luminal epithelium:	n/a	n/a
3	ESR1	chr3:49196080-49196633	ECC-1	luminal epithelium:	n/a	n/a
4	ESR1	chr3:49196254-49196584	ECC-1	luminal epithelium:	n/a	n/a
5	ESR1	chr3:49196177-49196674	ECC-1	luminal epithelium:	n/a	n/a
6	ESR1	chr3:49196135-49196627	ECC-1	luminal epithelium:	n/a	n/a
7	ESRRA	chr3:49195135-49196546	GM12878	blood:	n/a	chr3:49196315-49196327 chr3:49195752-49195762 chr3:49195747-49195759
8	MTA3	chr3:49196235-49196583	GM12878	blood:	n/a	n/a
9	MTA3	chr3:49194918-49196655	GM12878	blood:	n/a	n/a
10	NFATC1	chr3:49196036-49196783	GM12878	blood:	n/a	n/a
11	NFATC1	chr3:49194899-49196736	GM12878	blood:	n/a	n/a
12	NFIC	chr3:49196150-49196734	ECC-1	luminal epithelium:	n/a	n/a
13	NR2C2	chr3:49195532-49196187	GM12878	blood:	n/a	chr3:49195743-49195758 chr3:49195747-49195756 chr3:49195745-49195758
14	NR2F2	chr3:49196135-49196686	MCF-7	breast:	n/a	n/a
15	POLR2A	chr3:49198371-49198430	GM12878	blood:	n/a	n/a
16	POLR2A	chr3:49194658-49196735	MCF10A-Er-Src	breast:	n/a	n/a
17	POLR2A	chr3:49195848-49196750	GM12878	blood:	n/a	n/a
18	POLR2A	chr3:49198510-49204140	GM12892	blood:	n/a	n/a
19	POLR2A	chr3:49195957-49196683	K562	blood:	n/a	n/a
20	POLR2A	chr3:49197414-49197768	GM12891	blood:	n/a	n/a
21	POLR2A	chr3:49197538-49197701	HepG2	liver:	n/a	n/a
22	POLR2A	chr3:49195237-49196660	HCT-116	colon:	n/a	n/a
23	POLR2A	chr3:49198029-49198473	HCT-116	colon:	n/a	n/a
24	POLR2A	chr3:49197536-49197865	GM12878	blood:	n/a	n/a
25	POLR2A	chr3:49196138-49196663	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr3:49197529-49197734	MCF-7	breast:	n/a	n/a
27	POLR2A	chr3:49195103-49196558	PBDE	blood:	n/a	n/a
28	POLR2A	chr3:49198116-49198377	GM12878	blood:	n/a	n/a
29	POLR2A	chr3:49195921-49196749	GM12892	blood:	n/a	n/a
30	POLR2A	chr3:49194982-49196593	GM12878	blood:	n/a	n/a
31	POLR2A	chr3:49194754-49196672	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr3:49197967-49198493	U87	brain:	n/a	n/a
33	POLR2A	chr3:49197475-49197793	GM12891	blood:	n/a	n/a
34	POLR2A	chr3:49195763-49196678	GM12892	blood:	n/a	n/a
35	POLR2A	chr3:49197534-49197716	HCT-116	colon:	n/a	n/a
36	POLR2A	chr3:49195998-49197769	HepG2	liver:	n/a	n/a
37	POLR2A	chr3:49197991-49198468	GM12892	blood:	n/a	n/a
38	POLR2A	chr3:49197525-49197712	A549	lung:	n/a	n/a
39	POLR2A	chr3:49198196-49198375	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr3:49197486-49197768	U87	brain:	n/a	n/a
41	POLR2A	chr3:49197990-49198468	GM12891	blood:	n/a	n/a
42	POLR2A	chr3:49197973-49198354	U87	brain:	n/a	n/a
43	POLR2A	chr3:49198039-49198411	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:49197504-49197737	HCT-116	colon:	n/a	n/a
45	POLR2A	chr3:49197498-49197732	A549	lung:	n/a	n/a
46	POLR2A	chr3:49196322-49196578	GM12878	blood:	n/a	n/a
47	POLR2A	chr3:49196187-49196433	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr3:49197489-49197727	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr3:49196433-49196721	GM12891	blood:	n/a	n/a
50	POLR2A	chr3:49197496-49197798	GM12891	blood:	n/a	n/a

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:49043216..49045196-chr3:49196235..49197868,2	K562	blood:
2	chr3:49197673..49199686-chr3:49449232..49451070,2	K562	blood:
3	chr3:49189882..49192619-chr3:49194424..49197107,3	MCF-7	breast:
4	chr3:49168509..49171088-chr3:49198215..49200498,3	K562	blood:
5	chr3:49057940..49060006-chr3:49197956..49200673,2	MCF-7	breast:
6	chr3:49141127..49143388-chr3:49194740..49196446,2	MCF-7	breast:
7	chr3:49062671..49068005-chr3:49193889..49197259,7	MCF-7	breast:
8	chr3:49198168..49200645-chr3:49211215..49212732,2	K562	blood:
9	chr3:49193599..49196325-chr3:49216577..49219891,3	MCF-7	breast:
10	chr3:49070051..49071657-chr3:49195116..49197322,2	MCF-7	breast:
11	chr3:49173300..49174828-chr3:49194938..49196550,2	K562	blood:
12	chr3:49166454..49167956-chr3:49197730..49200400,2	K562	blood:
13	chr3:49188624..49190754-chr3:49194222..49196176,2	K562	blood:
14	chr3:49063218..49064787-chr3:49194853..49197640,2	K562	blood:
15	chr3:49058901..49061123-chr3:49194988..49197137,2	MCF-7	breast:
16	chr3:49195402..49201533-chr3:49207296..49212401,9	MCF-7	breast:
17	chr3:49195403..49197616-chr3:49208526..49210728,2	K562	blood:
18	chr3:49042896..49045458-chr3:49193854..49196447,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000270441	TF binding region
ENSG00000172053	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000178252	chromatin interactions
ENSG00000207605	chromatin interactions
ENSG00000185909	chromatin interactions
ENSG00000067560	chromatin interactions
ENSG00000198218	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000145022	chromatin interactions
ENSG00000178035	chromatin interactions
ENSG00000172037	chromatin interactions
ENSG00000272434	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546522572	chr3:49196149-49196150	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs112410524	chr3:49196176-49196177	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs564635441	chr3:49196188-49196189	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs528738137	chr3:49196197-49196198	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs567663538	chr3:49196321-49196322	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs60587322	chr3:49196418-49196419	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs534876047	chr3:49196446-49196447	Weak transcription Enhancers Strong transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs565375756	chr3:49196451-49196452	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs572481939	chr3:49196459-49196460	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs528992083	chr3:49196460-49196461	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs550241846	chr3:49196499-49196500	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs568761814	chr3:49196538-49196539	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs191299512	chr3:49196569-49196570	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs551511333	chr3:49196572-49196573	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs566655419	chr3:49196590-49196591	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs534064826	chr3:49196605-49196606	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs553417985	chr3:49196626-49196627	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs568448202	chr3:49196645-49196646	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs528362127	chr3:49196668-49196669	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs11429215	chr3:49196669-49196670	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs397777944	chr3:49196678-49196679	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs372695608	chr3:49196718-49196719	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs557487633	chr3:49196721-49196722	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs575652948	chr3:49196724-49196725	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs546085091	chr3:49196759-49196760	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs558304514	chr3:49196763-49196764	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs115297924	chr3:49196824-49196825	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs540511618	chr3:49196836-49196837	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs561376065	chr3:49196861-49196862	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs183492661	chr3:49196870-49196871	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs578010827	chr3:49196877-49196878	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs188842080	chr3:49196916-49196917	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs541214481	chr3:49196917-49196918	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs9681947	chr3:49196925-49196926	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs551306592	chr3:49196931-49196932	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs193227205	chr3:49196937-49196938	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs560257419	chr3:49196975-49196976	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs560937499	chr3:49196976-49196977	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs527621965	chr3:49196980-49196981	Weak transcription Enhancers Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs557287025	chr3:49197027-49197028	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs568513420	chr3:49197052-49197053	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs535840184	chr3:49197063-49197064	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs144786725	chr3:49197108-49197109	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs370198784	chr3:49197126-49197127	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs147799508	chr3:49197133-49197134	Weak transcription Strong transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs185471518	chr3:49197162-49197163	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs374129008	chr3:49197185-49197186	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs573366762	chr3:49197200-49197201	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs534270825	chr3:49197211-49197212	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs529997720	chr3:49197215-49197216	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medullary thyroid carcinoma	18765511	CNVD
abnormal development	18461090	CNVD
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:49172200-49200400	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:49186200-49198800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr3:49186800-49198800	Weak transcription	Pancreas	Pancrea
4	chr3:49191000-49198800	Weak transcription	Ovary	ovary
5	chr3:49191000-49199800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:49191400-49198800	Weak transcription	Gastric	stomach
7	chr3:49191400-49199000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:49191600-49200200	Weak transcription	Esophagus	oesophagus
9	chr3:49192000-49198000	Weak transcription	Thymus	Thymus
10	chr3:49192200-49198600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr3:49194400-49198200	Weak transcription	Brain Germinal Matrix	brain
12	chr3:49194400-49199000	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr3:49194600-49198200	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr3:49194600-49198800	Weak transcription	Stomach Smooth Muscle	stomach
15	chr3:49194800-49198200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr3:49195000-49196400	Enhancers	HepG2	liver
17	chr3:49195000-49198200	Weak transcription	Fetal Brain Female	brain
18	chr3:49195000-49198200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr3:49195000-49199600	Weak transcription	Rectal Smooth Muscle	rectum
20	chr3:49195200-49197000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:49195200-49199400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr3:49195200-49200400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr3:49195200-49202400	Weak transcription	Fetal Kidney	kidney
24	chr3:49195400-49196400	Weak transcription	Hela-S3	cervix
25	chr3:49195400-49198800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr3:49195400-49200400	Weak transcription	Brain Angular Gyrus	brain
27	chr3:49195600-49196600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:49195600-49196600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:49195600-49196800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr3:49195600-49198200	Weak transcription	Primary B cells from peripheral blood	blood
31	chr3:49195600-49198200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr3:49195600-49198600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:49195600-49198600	Weak transcription	Fetal Muscle Leg	muscle
34	chr3:49195600-49198800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:49195600-49198800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr3:49195600-49198800	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr3:49195600-49199000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:49195600-49199400	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr3:49195600-49199400	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr3:49195600-49200200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr3:49195600-49200200	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr3:49195600-49200400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:49195600-49200400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr3:49195600-49200400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:49195600-49200400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr3:49195600-49202200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:49195800-49198000	Weak transcription	Fetal Intestine Small	intestine
48	chr3:49195800-49198200	Weak transcription	Brain Substantia Nigra	brain
49	chr3:49195800-49198800	Weak transcription	Fetal Intestine Large	intestine
50	chr3:49195800-49199600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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