Variant report

Variant	nsv517557
Chromosome Location	chr6:27356527-27356925
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	chr6:27356437-27356828	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:27356543-27356879	K562	blood:	n/a	n/a
3	ATF2	chr6:27356515-27356961	GM12878	blood:	n/a	n/a
4	ATF2	chr6:27356479-27356915	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:27356395-27356962	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:27356346-27356930	GM12878	blood:	n/a	n/a
7	ATF3	chr6:27356499-27356852	A549	lung:	n/a	n/a
8	ATF3	chr6:27356390-27356930	A549	lung:	n/a	n/a
9	ATF3	chr6:27356439-27356968	K562	blood:	n/a	n/a
10	BACH1	chr6:27356396-27357077	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:27356502-27356863	GM12878	blood:	n/a	n/a
12	BCL3	chr6:27356441-27356912	A549	lung:	n/a	n/a
13	BCLAF1	chr6:27356411-27357053	K562	blood:	n/a	n/a
14	BCLAF1	chr6:27356365-27356967	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:27356253-27357006	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:27356389-27357011	K562	blood:	n/a	n/a
17	BHLHE40	chr6:27356226-27357046	K562	blood:	n/a	n/a
18	BHLHE40	chr6:27356282-27356857	HepG2	liver:	n/a	n/a
19	BRCA1	chr6:27356606-27356910	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr6:27356528-27356880	HepG2	liver:	n/a	n/a
21	CBX3	chr6:27356350-27356928	K562	blood:	n/a	n/a
22	CBX3	chr6:27356238-27357706	K562	blood:	n/a	n/a
23	CCNT2	chr6:27356216-27357079	K562	blood:	n/a	chr6:27356422-27356431
24	CEBPB	chr6:27355900-27356769	HepG2	liver:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
25	CEBPB	chr6:27355860-27356747	IMR90	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
26	CEBPB	chr6:27355827-27356877	H1-hESC	embryonic stem cell:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
27	CEBPB	chr6:27355943-27356733	K562	blood:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
28	CEBPB	chr6:27355966-27356808	Hela-S3	cervix:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
29	CEBPB	chr6:27356370-27356785	HepG2	liver:	n/a	chr6:27356433-27356444
30	CEBPB	chr6:27356207-27357014	GM12878	blood:	n/a	chr6:27356433-27356444
31	CEBPB	chr6:27355805-27356909	ECC-1	luminal epithelium:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
32	CEBPB	chr6:27355921-27357031	A549	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
33	CEBPB	chr6:27356328-27356883	MCF-7	breast:	n/a	chr6:27356433-27356444
34	CEBPB	chr6:27355968-27356744	A549	lung:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
35	CEBPB	chr6:27355927-27356905	K562	blood:	n/a	chr6:27356124-27356135 chr6:27356433-27356444 chr6:27355981-27355990 chr6:27356126-27356135
36	CEBPD	chr6:27356444-27356847	HepG2	liver:	n/a	n/a
37	CEBPD	chr6:27356331-27356922	HepG2	liver:	n/a	n/a
38	CHD2	chr6:27356325-27356815	HepG2	liver:	n/a	n/a
39	CHD2	chr6:27356418-27356847	K562	blood:	n/a	n/a
40	CHD2	chr6:27356460-27356919	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr6:27356376-27356888	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr6:27356506-27356937	GM12878	blood:	n/a	n/a
43	CREB1	chr6:27356313-27356935	H1-hESC	embryonic stem cell:	n/a	n/a
44	CREB1	chr6:27356413-27356898	A549	lung:	n/a	n/a
45	CREB1	chr6:27356195-27357021	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:27356640-27356790	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr6:27356401-27356864	K562	blood:	n/a	n/a
48	CTCF	chr6:27356636-27356741	Fibrobl	skin:	n/a	n/a
49	CTCF	chr6:27356789-27356896	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr6:27356380-27356530	GM12874	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:27356624-27356674	HCPEpiC	choroid plexus:	n/a
2	chr6:27356624-27356674	HCPEpiC	choroid plexus:	n/a
3	chr6:27356499-27356549	ECC-1	luminal epithelium:	n/a
4	chr6:27356513-27356563	AG09309	skin:	n/a
5	chr6:27356690-27356740	NHBE	bronchial:	n/a
6	chr6:27356509-27356559	HUVEC	blood vessel:	n/a
7	chr6:27356509-27356559	NT2-D1	testis:	n/a
8	chr6:27356690-27356740	SKMC	muscle:	n/a
9	chr6:27356624-27356674	AG10803	skin:	n/a
10	chr6:27356690-27356740	CMK	blood:	n/a
11	chr6:27356690-27356740	T-47D	breast:	n/a
12	chr6:27356509-27356559	AG04449	skin:	fetal
13	chr6:27356509-27356559	HNPCEpiC	eye:	n/a
14	chr6:27356690-27356740	ECC-1	luminal epithelium:	n/a
15	chr6:27356509-27356559	GM12891	blood:	n/a
16	chr6:27356499-27356549	NT2-D1	testis:	n/a
17	chr6:27356499-27356549	AG04449	skin:	fetal
18	chr6:27356513-27356563	HepG2	liver:	n/a
19	chr6:27356690-27356740	HCT-116	colon:	n/a
20	chr6:27356509-27356559	SKMC	muscle:	n/a
21	chr6:27356624-27356674	Caco-2	colon:	n/a
22	chr6:27356513-27356563	Jurkat	blood:	n/a
23	chr6:27356499-27356549	Hela-S3	cervix:	n/a
24	chr6:27356509-27356559	GM12878	blood:	n/a
25	chr6:27356624-27356674	Jurkat	blood:	n/a
26	chr6:27356509-27356559	K562	blood:	n/a
27	chr6:27356624-27356674	U87	brain:	n/a
28	chr6:27356513-27356563	HEEpiC	esophagus:	n/a
29	chr6:27356499-27356549	SKMC	muscle:	n/a
30	chr6:27356499-27356549	SK-N-MC	brain:	n/a
31	chr6:27356690-27356740	IMR90	lung:	fetal
32	chr6:27356499-27356549	ProgFib	skin:	n/a
33	chr6:27356513-27356563	HRCEpiC	kidney:	n/a
34	chr6:27356624-27356674	HNPCEpiC	eye:	n/a
35	chr6:27356690-27356740	HRCEpiC	kidney:	n/a
36	chr6:27356509-27356559	CMK	blood:	n/a
37	chr6:27356690-27356740	PFSK-1	brain:	n/a
38	chr6:27356690-27356740	HAEpiC	amniotic membrane:	n/a
39	chr6:27356499-27356549	PANC-1	pancreas:	n/a
40	chr6:27356499-27356549	RPTEC	kidney:	n/a
41	chr6:27356690-27356740	HEK293	kidney:	embryo
42	chr6:27356624-27356674	NHBE	bronchial:	n/a
43	chr6:27356509-27356559	PrEC	prostate:	n/a
44	chr6:27356513-27356563	NHBE	bronchial:	n/a
45	chr6:27356513-27356563	PFSK-1	brain:	n/a
46	chr6:27356690-27356740	GM19239	blood:	n/a
47	chr6:27356513-27356563	AG09319	gingival:	n/a
48	chr6:27356624-27356674	SAEC	small airway:	n/a
49	chr6:27356509-27356559	Hela-S3	cervix:	n/a
50	chr6:27356624-27356674	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:27291445..27294642-chr6:27355178..27358043,3	MCF-7	breast:
2	chr6:27354651..27357206-chr6:27439212..27442131,3	K562	blood:
3	chr6:27113785..27116304-chr6:27356399..27358052,2	K562	blood:
4	chr6:27341304..27343058-chr6:27356076..27357820,2	MCF-7	breast:
5	chr6:27356907..27359078-chr6:27397692..27399728,2	K562	blood:
6	chr6:27342371..27343890-chr6:27355850..27358027,2	K562	blood:
7	chr6:27356277..27359093-chr6:27439899..27443040,4	MCF-7	breast:
8	chr6:27356362..27358956-chr6:27773296..27775539,3	K562	blood:
9	chr21:27542816..27543374-chr6:27355736..27356540,2	HCT-116	colon:
10	chr6:27114804..27117756-chr6:27356552..27360776,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF184-3	chr6:27356046-27357004	NONHSAT108378
2	lnc-PRSS16-3	chr6:27356683-27356854	NONHSAT108379

Variant related genes	Relation type
ZNF391	TF binding region
ZNF391	CpG island
ENSG00000220758	chromatin interactions
ENSG00000197903	chromatin interactions
ENSG00000273492	chromatin interactions
ENSG00000184825	chromatin interactions
ENSG00000217862	chromatin interactions
ENSG00000096654	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000142192	chromatin interactions
ENSG00000124613	chromatin interactions

Extended variants
information (count: 19 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13220817	chr6:27356527-27356528	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540280297	chr6:27356540-27356541	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
3	rs555938981	chr6:27356541-27356542	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
4	rs528423366	chr6:27356597-27356598	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
5	rs533634800	chr6:27356605-27356606	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
6	rs551404610	chr6:27356625-27356626	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
7	rs190651366	chr6:27356630-27356631	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
8	rs374834053	chr6:27356633-27356634	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
9	rs62622793	chr6:27356647-27356648	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs550756047	chr6:27356710-27356711	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
11	rs567410150	chr6:27356740-27356741	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
12	rs182509236	chr6:27356767-27356768	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
13	rs188001937	chr6:27356783-27356784	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
14	rs566458918	chr6:27356817-27356818	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
15	rs538592631	chr6:27356844-27356845	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
16	rs4713091	chr6:27356867-27356868	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs386698288	chr6:27356900-27356901	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
18	rs10807020	chr6:27356902-27356903	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs10807021	chr6:27356925-27356926	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:100)

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
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD

Chromatin state (count:150 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27355000-27357400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:27355600-27357600	Active TSS	iPS-18 Cell Line	embryonic stem cell
3	chr6:27355600-27358400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:27355800-27356600	Active TSS	Fetal Muscle Trunk	muscle
5	chr6:27355800-27356800	Active TSS	Colonic Mucosa	Colon
6	chr6:27355800-27357000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:27355800-27357000	Active TSS	Brain Angular Gyrus	brain
8	chr6:27355800-27357000	Active TSS	HMEC	breast
9	chr6:27355800-27357200	Active TSS	Muscle Satellite Cultured Cells	--
10	chr6:27355800-27357200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:27355800-27357200	Active TSS	Aorta	Aorta
12	chr6:27355800-27357200	Active TSS	Brain Hippocampus Middle	brain
13	chr6:27355800-27357200	Active TSS	Fetal Brain Male	brain
14	chr6:27355800-27357200	Active TSS	Right Ventricle	heart
15	chr6:27355800-27357200	Active TSS	A549	lung
16	chr6:27355800-27357200	Flanking Active TSS	HUVEC	blood vessel
17	chr6:27355800-27357200	Active TSS	K562	blood
18	chr6:27355800-27357200	Active TSS	NHDF-Ad	bronchial
19	chr6:27355800-27357400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr6:27355800-27357400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:27355800-27357400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:27355800-27357400	Active TSS	Brain Cingulate Gyrus	brain
23	chr6:27355800-27357400	Active TSS	Fetal Brain Female	brain
24	chr6:27355800-27357400	Active TSS	Fetal Intestine Small	intestine
25	chr6:27355800-27357400	Active TSS	Rectal Smooth Muscle	rectum
26	chr6:27355800-27357400	Active TSS	NHLF	lung
27	chr6:27355800-27357600	Active TSS	H9 Cell Line	embryonic stem cell
28	chr6:27355800-27357600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr6:27355800-27357600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr6:27355800-27357600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:27355800-27357600	Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr6:27355800-27357600	Active TSS	Stomach Smooth Muscle	stomach
33	chr6:27355800-27357600	Active TSS	NHEK	skin
34	chr6:27355800-27357800	Active TSS	ES-I3 Cell Line	embryonic stem cell
35	chr6:27355800-27357800	Active TSS	H1 Cell Line	embryonic stem cell
36	chr6:27355800-27357800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr6:27355800-27357800	Active TSS	GM12878-XiMat	blood
38	chr6:27355800-27358000	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr6:27355800-27358000	Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr6:27356000-27356600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr6:27356000-27356600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr6:27356000-27356800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:27356000-27356800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr6:27356000-27356800	Active TSS	Thymus	Thymus
45	chr6:27356000-27356800	Bivalent/Poised TSS	HepG2	liver
46	chr6:27356000-27357000	Active TSS	Fetal Lung	lung
47	chr6:27356000-27357000	Active TSS	Left Ventricle	heart
48	chr6:27356000-27357000	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr6:27356000-27357000	Active TSS	HSMMtube	muscle
50	chr6:27356000-27357200	Active TSS	Primary T killer memory cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links