Variant report

Variant	esv3444323
Chromosome Location	chr6:4078453-4080526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:27)
CpG islands
(count:612)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:27 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:4079362-4079553	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:4078964-4079020	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:4078638-4078736	HepG2	liver:	n/a	n/a
4	CTCF	chr6:4079100-4079250	HCM	heart:	n/a	n/a
5	CTCF	chr6:4079060-4079210	HUVEC	blood vessel:	n/a	n/a
6	E2F6	chr6:4078558-4079475	H1-hESC	embryonic stem cell:	n/a	n/a
7	E2F6	chr6:4078511-4079484	H1-hESC	embryonic stem cell:	n/a	n/a
8	GABPA	chr6:4079332-4079671	H1-hESC	embryonic stem cell:	n/a	n/a
9	GABPA	chr6:4079038-4079512	H1-hESC	embryonic stem cell:	n/a	n/a
10	GTF2F1	chr6:4079087-4079193	H1-hESC	embryonic stem cell:	n/a	n/a
11	MAX	chr6:4078644-4079326	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr6:4078667-4079409	H1-hESC	embryonic stem cell:	n/a	n/a
13	MYC	chr6:4078974-4079111	H1-hESC	embryonic stem cell:	n/a	n/a
14	NANOG	chr6:4078977-4079228	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr6:4078958-4078970	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr6:4079027-4079106	H1-hESC	embryonic stem cell:	n/a	n/a
17	POLR2A	chr6:4078818-4078950	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr6:4078757-4078812	MCF-7	breast:	n/a	n/a
19	POLR2A	chr6:4080261-4080352	K562	blood:	n/a	n/a
20	POLR2A	chr6:4079815-4079821	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr6:4079174-4079257	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr6:4079509-4079856	K562	blood:	n/a	n/a
23	TBP	chr6:4078762-4079466	H1-hESC	embryonic stem cell:	n/a	n/a
24	USF1	chr6:4078884-4079265	H1-hESC	embryonic stem cell:	n/a	n/a
25	USF1	chr6:4078931-4079186	H1-hESC	embryonic stem cell:	n/a	n/a
26	USF2	chr6:4079046-4079126	H1-hESC	embryonic stem cell:	n/a	n/a
27	ZNF143	chr6:4079477-4079596	H1-hESC	embryonic stem cell:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:4078970-4079020	U87	brain:	n/a
2	chr6:4079704-4079754	U87	brain:	n/a
3	chr6:4078970-4079020	U87	brain:	n/a
4	chr6:4079704-4079754	U87	brain:	n/a
5	chr6:4079649-4079699	HEEpiC	esophagus:	n/a
6	chr6:4078943-4078993	GM19239	blood:	n/a
7	chr6:4079342-4079392	PFSK-1	brain:	n/a
8	chr6:4079350-4079400	SK-N-SH_RA	brain:	n/a
9	chr6:4078959-4079009	H1-hESC	embryonic stem cell:	embryo
10	chr6:4079704-4079754	NT2-D1	testis:	n/a
11	chr6:4079572-4079622	NHDF-neo	bronchial:	n/a
12	chr6:4078970-4079020	T-47D	breast:	n/a
13	chr6:4079350-4079400	AG04449	skin:	fetal
14	chr6:4079350-4079400	U87	brain:	n/a
15	chr6:4079649-4079699	LNCaP	prostate:	n/a
16	chr6:4078959-4079009	PFSK-1	brain:	n/a
17	chr6:4078970-4079020	SK-N-SH	brain:	n/a
18	chr6:4078943-4078993	HEEpiC	esophagus:	n/a
19	chr6:4078970-4079020	HMEC	breast:	n/a
20	chr6:4078959-4079009	BE2_C	brain:	n/a
21	chr6:4078959-4079009	NH-A	brain:	n/a
22	chr6:4079350-4079400	HCM	heart:	n/a
23	chr6:4079704-4079754	Hepatocyte	liver:	n/a
24	chr6:4079704-4079754	HCPEpiC	choroid plexus:	n/a
25	chr6:4079572-4079622	HCM	heart:	n/a
26	chr6:4079649-4079699	IMR90	lung:	fetal
27	chr6:4078943-4078993	SK-N-SH_RA	brain:	n/a
28	chr6:4079534-4079584	LNCaP	prostate:	n/a
29	chr6:4078959-4079009	ECC-1	luminal epithelium:	n/a
30	chr6:4079342-4079392	K562	blood:	n/a
31	chr6:4078959-4079009	HCT-116	colon:	n/a
32	chr6:4079534-4079584	HEK293	kidney:	embryo
33	chr6:4079350-4079400	NH-A	brain:	n/a
34	chr6:4078943-4078993	SAEC	small airway:	n/a
35	chr6:4079534-4079584	GM12878	blood:	n/a
36	chr6:4078959-4079009	SK-N-MC	brain:	n/a
37	chr6:4078943-4078993	NH-A	brain:	n/a
38	chr6:4078943-4078993	T-47D	breast:	n/a
39	chr6:4079649-4079699	NB4	blood:	n/a
40	chr6:4078970-4079020	HCM	heart:	n/a
41	chr6:4079350-4079400	MCF-7	breast:	n/a
42	chr6:4078943-4078993	HEK293	kidney:	embryo
43	chr6:4079528-4079578	HIPEpiC	eye:	n/a
44	chr6:4079704-4079754	ECC-1	luminal epithelium:	n/a
45	chr6:4079649-4079699	HepG2	liver:	n/a
46	chr6:4079534-4079584	AG04450	lung:	fetal
47	chr6:4079649-4079699	PrEC	prostate:	n/a
48	chr6:4079534-4079584	PrEC	prostate:	n/a
49	chr6:4078943-4078993	HepG2	liver:	n/a
50	chr6:4079704-4079754	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:4076386..4078865-chr6:4079874..4083762,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf201-4	chr6:4079440-4079914	NR_104464
2	lnc-ECI2-6	chr6:4079086-4079455	NONHSAT107292
3	lnc-ECI2-5	chr6:4078218-4078499	NONHSAT107295
4	lnc-C6orf201-4	chr6:4076360-4079955	NONHSAT107293

No data

Variant related genes	Relation type
C6orf201	TF binding region
FAM217A	TF binding region
C6orf201	CpG island
FAM217A	CpG island
ENSG00000252668	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530676690	chr6:4078482-4078483	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs147624349	chr6:4078489-4078490	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs6930491	chr6:4078518-4078519	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs539830442	chr6:4078609-4078610	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs556724300	chr6:4078633-4078634	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs146263068	chr6:4078690-4078691	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs186925762	chr6:4078691-4078692	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs682063	chr6:4078728-4078729	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs555548413	chr6:4078733-4078734	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs650183	chr6:4078734-4078735	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs369320440	chr6:4078782-4078783	Weak transcription Enhancers Bivalent Enhancer	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs372910451	chr6:4078811-4078812	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs191385909	chr6:4078812-4078813	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs555759526	chr6:4078814-4078815	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs185068115	chr6:4078970-4078971	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs542991171	chr6:4079019-4079020	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs78652484	chr6:4079036-4079037	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs528997458	chr6:4079064-4079065	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs542315228	chr6:4079110-4079111	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs562307567	chr6:4079126-4079127	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs527874806	chr6:4079138-4079139	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs548145268	chr6:4079187-4079188	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs571139970	chr6:4079194-4079195	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs376139305	chr6:4079202-4079203	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs652493	chr6:4079210-4079211	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs550215961	chr6:4079237-4079238	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs570027939	chr6:4079248-4079249	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs13203009	chr6:4079250-4079251	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs377493266	chr6:4079255-4079256	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs34907568	chr6:4079278-4079279	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs555576706	chr6:4079320-4079321	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs7756630	chr6:4079334-4079335	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534502078	chr6:4079372-4079373	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs13202297	chr6:4079378-4079379	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs557657253	chr6:4079385-4079386	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs147974084	chr6:4079415-4079416	Enhancers Weak transcription	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs112823213	chr6:4079511-4079512	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs543276694	chr6:4079529-4079530	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs367750182	chr6:4079567-4079568	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs10080424	chr6:4079581-4079582	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs588158	chr6:4079592-4079593	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576670383	chr6:4079627-4079628	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs559170119	chr6:4079637-4079638	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs572631289	chr6:4079652-4079653	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs13202659	chr6:4079656-4079657	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs80018662	chr6:4079679-4079680	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs664839	chr6:4079688-4079689	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs533677333	chr6:4079696-4079697	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs550450914	chr6:4079721-4079722	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs201784902	chr6:4079730-4079731	Enhancers Weak transcription	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Uveal melanoma	20484589	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
small cell lung cancer	20016488	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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:4063400-4078800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:4066800-4079600	Weak transcription	NHLF	lung
3	chr6:4067000-4082400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:4074400-4083000	Weak transcription	Pancreas	Pancrea
5	chr6:4078200-4084600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:4078600-4078800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:4078600-4079000	Bivalent Enhancer	Fetal Intestine Small	intestine
8	chr6:4078600-4079200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr6:4078800-4079000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:4078800-4079000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:4078800-4079000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
12	chr6:4078800-4079000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:4078800-4079000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:4078800-4079000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:4078800-4079000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr6:4078800-4079200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr6:4078800-4079200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr6:4078800-4079200	Enhancers	Placenta Amnion	Placenta Amnion
19	chr6:4078800-4079400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:4079000-4079200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:4079000-4079200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr6:4079000-4079200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr6:4079000-4079200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:4079000-4079200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr6:4079000-4079200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:4079000-4079200	Bivalent Enhancer	Lung	lung
27	chr6:4079000-4079200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
28	chr6:4079000-4079400	Enhancers	Primary hematopoietic stem cells	blood
29	chr6:4079000-4079400	Enhancers	Right Atrium	heart
30	chr6:4079000-4082400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr6:4079200-4079400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr6:4079200-4079400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr6:4079200-4079800	Enhancers	H1 Cell Line	embryonic stem cell
34	chr6:4079200-4080000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr6:4079400-4092000	Weak transcription	Right Atrium	heart
36	chr6:4079600-4079800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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