Variant report

Variant	esv3356749
Chromosome Location	chr6:27155446-27163661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:27154842..27156986-chr6:27301919..27304257,2	K562	blood:
2	chr6:27130956..27132580-chr6:27154818..27157126,2	K562	blood:
3	chr6:27148219..27154668-chr6:27154722..27158254,9	K562	blood:
4	chr6:27155275..27158320-chr6:27568064..27571527,3	K562	blood:
5	chr6:27143412..27146140-chr6:27152536..27156532,5	K562	blood:
6	chr6:27156417..27159630-chr6:27160529..27165919,7	K562	blood:
7	chr6:27114939..27117742-chr6:27153749..27157823,5	K562	blood:
8	chr6:27154773..27157322-chr6:27634142..27636330,2	MCF-7	breast:
9	chr6:27155262..27157566-chr6:27266020..27269001,2	K562	blood:
10	chr6:27154198..27156038-chr6:27159087..27161685,2	MCF-7	breast:
11	chr6:27154554..27158026-chr6:27757603..27761465,4	K562	blood:
12	chr6:27155655..27157705-chr6:27862759..27864468,2	K562	blood:
13	chr6:27156279..27157260-chr6:27759304..27760417,5	K562	blood:
14	chr6:27154198..27156038-chr6:27159087..27161685,2	MCF-7	breast:
15	chr6:27160523..27163263-chr6:27832952..27835255,2	K562	blood:
16	chr6:27155324..27157508-chr6:27634451..27636223,2	K562	blood:
17	chr6:27145758..27149060-chr6:27154386..27156904,3	MCF-7	breast:
18	chr6:27114727..27117926-chr6:27154560..27156609,3	K562	blood:
19	chr6:27154865..27156812-chr6:27464410..27466083,2	K562	blood:
20	chr6:27124780..27127221-chr6:27160550..27163070,2	K562	blood:
21	chr6:27150672..27153341-chr6:27153761..27155795,3	MCF-7	breast:
22	chr6:27154833..27157823-chr6:27782934..27785900,2	K562	blood:
23	chr6:27154220..27156812-chr6:27776425..27779440,4	K562	blood:
24	chr6:27155406..27158362-chr6:27858378..27860998,5	K562	blood:
25	chr6:27153641..27158263-chr6:27858563..27861801,5	K562	blood:
26	chr6:27154260..27155926-chr6:27167713..27170180,2	K562	blood:
27	chr6:27130515..27132785-chr6:27154818..27157852,3	K562	blood:
28	chr6:27156028..27157789-chr6:27774192..27775722,2	K562	blood:
29	chr6:27162610..27164330-chr6:27172522..27175063,2	K562	blood:
30	chr6:27156508..27159438-chr6:27571250..27573740,2	K562	blood:
31	chr6:27155042..27157581-chr6:27762343..27765282,2	K562	blood:
32	chr6:27161961..27163515-chr6:27727995..27729647,2	K562	blood:
33	chr6:27156417..27159630-chr6:27160529..27165919,7	K562	blood:
34	chr6:27133928..27135511-chr6:27156341..27158260,2	K562	blood:
35	chr6:27155528..27159493-chr6:27776465..27779576,3	K562	blood:
36	chr6:27145218..27148337-chr6:27151646..27158450,9	MCF-7	breast:
37	chr6:27150639..27152459-chr6:27154596..27157395,2	MCF-7	breast:
38	chr6:27154579..27158488-chr6:27757538..27761648,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000184825	chromatin interactions
ENSG00000198374	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000203813	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000185130	chromatin interactions
ENSG00000265565	chromatin interactions

Extended variants
information (count: 352 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:352 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73740444	chr6:27155473-27155474	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs858974	chr6:27155474-27155475	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs116005859	chr6:27155485-27155486	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs564094809	chr6:27155524-27155525	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs182596879	chr6:27155525-27155526	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs550506661	chr6:27155540-27155541	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs145030337	chr6:27155545-27155546	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs113014817	chr6:27155588-27155589	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs858975	chr6:27155623-27155624	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566106133	chr6:27155673-27155674	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs111638235	chr6:27155678-27155679	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs149348640	chr6:27155684-27155685	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs144643810	chr6:27155705-27155706	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs148054724	chr6:27155737-27155738	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs187307211	chr6:27155751-27155752	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs556931474	chr6:27155829-27155830	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs535054679	chr6:27155836-27155837	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs191395975	chr6:27155838-27155839	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs143704110	chr6:27155843-27155844	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs858976	chr6:27155844-27155845	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs201367448	chr6:27155851-27155852	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs147197000	chr6:27155964-27155965	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs572121662	chr6:27155967-27155968	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs541132974	chr6:27155970-27155971	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs564131515	chr6:27156006-27156007	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs577804481	chr6:27156015-27156016	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs35605769	chr6:27156032-27156033	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs398084849	chr6:27156033-27156034	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs536153341	chr6:27156045-27156046	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs200816881	chr6:27156047-27156048	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs12196889	chr6:27156095-27156096	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs563121164	chr6:27156178-27156179	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs529605160	chr6:27156184-27156185	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs1102560	chr6:27156273-27156274	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs183959965	chr6:27156317-27156318	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs369649299	chr6:27156505-27156506	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs551547995	chr6:27156541-27156542	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs372058850	chr6:27156556-27156557	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs567773952	chr6:27156562-27156563	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs60266855	chr6:27156573-27156574	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs537122914	chr6:27156584-27156585	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs34176287	chr6:27156620-27156621	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs368090790	chr6:27156721-27156722	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs188863511	chr6:27156725-27156726	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs116191177	chr6:27156767-27156768	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs528375802	chr6:27156810-27156811	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs140456965	chr6:27156821-27156822	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs144354458	chr6:27156827-27156828	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs555329006	chr6:27156829-27156830	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs1102561	chr6:27156836-27156837	Flanking Active TSS Weak transcription Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD

Chromatin state (count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27146600-27155800	Weak transcription	Spleen	Spleen
2	chr6:27147000-27155600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:27155000-27155600	Enhancers	Stomach Mucosa	stomach
4	chr6:27155000-27157000	Active TSS	Right Atrium	heart
5	chr6:27155200-27155600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:27155200-27155600	Enhancers	Fetal Thymus	thymus
7	chr6:27155200-27155600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:27155200-27155600	Enhancers	Dnd41	blood
9	chr6:27155200-27156400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr6:27155200-27156600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:27155200-27156800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:27155200-27156800	Active TSS	Osteobl	bone
13	chr6:27155200-27157000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:27155400-27155600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:27155400-27155600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
16	chr6:27155400-27155600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:27155400-27155600	Active TSS	Primary B cells from cord blood	blood
18	chr6:27155400-27155600	Enhancers	Primary B cells from peripheral blood	blood
19	chr6:27155400-27155600	Active TSS	Primary T cells from cord blood	blood
20	chr6:27155400-27155600	Enhancers	Primary hematopoietic stem cells	blood
21	chr6:27155400-27155600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:27155400-27155600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr6:27155400-27155600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr6:27155400-27155600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr6:27155400-27155600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr6:27155400-27155600	Enhancers	Liver	Liver
27	chr6:27155400-27155600	Enhancers	Brain Angular Gyrus	brain
28	chr6:27155400-27155600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr6:27155400-27155600	Enhancers	Brain Substantia Nigra	brain
30	chr6:27155400-27155600	Enhancers	Fetal Heart	heart
31	chr6:27155400-27155600	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr6:27155400-27155600	Enhancers	Placenta	Placenta
33	chr6:27155400-27155600	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr6:27155400-27155600	Flanking Active TSS	GM12878-XiMat	blood
35	chr6:27155400-27155600	Enhancers	Hela-S3	cervix
36	chr6:27155400-27155600	Bivalent/Poised TSS	HepG2	liver
37	chr6:27155400-27155600	Enhancers	NHEK	skin
38	chr6:27155400-27155800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
39	chr6:27155400-27155800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:27155400-27155800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
41	chr6:27155400-27155800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:27155400-27155800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr6:27155400-27155800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr6:27155400-27155800	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr6:27155400-27155800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr6:27155400-27155800	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr6:27155400-27155800	Active TSS	Rectal Smooth Muscle	rectum
48	chr6:27155400-27155800	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr6:27155400-27156000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
50	chr6:27155400-27156000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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