Variant report

Variant	nsv605885
Chromosome Location	chr7:3337081-3340551
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:306)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:3340510-3340769	HepG2	liver:	n/a	n/a
2	BACH1	chr7:3339959-3340991	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr7:3340395-3340873	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537 chr7:3340744-3340757
4	BCLAF1	chr7:3340441-3340719	GM12878	blood:	n/a	chr7:3340634-3340647 chr7:3340524-3340537
5	BHLHE40	chr7:3340387-3340937	GM12878	blood:	n/a	chr7:3340519-3340535 chr7:3340527-3340543
6	BHLHE40	chr7:3340409-3341002	HepG2	liver:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
7	BHLHE40	chr7:3340404-3341008	K562	blood:	n/a	chr7:3340932-3340948 chr7:3340519-3340535 chr7:3340527-3340543
8	CBX3	chr7:3340484-3340710	K562	blood:	n/a	n/a
9	CBX3	chr7:3340439-3340719	K562	blood:	n/a	n/a
10	CBX3	chr7:3340323-3340885	HCT-116	colon:	n/a	n/a
11	CCNT2	chr7:3340411-3341005	K562	blood:	n/a	n/a
12	CHD1	chr7:3340292-3340917	IMR90	lung:	n/a	n/a
13	CHD2	chr7:3340519-3340719	GM12878	blood:	n/a	n/a
14	CHD2	chr7:3340511-3340673	HepG2	liver:	n/a	n/a
15	CHD2	chr7:3339627-3339800	HepG2	liver:	n/a	n/a
16	CHD2	chr7:3340488-3340695	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr7:3340365-3341037	HepG2	liver:	n/a	n/a
18	CREB1	chr7:3340132-3341053	A549	lung:	n/a	n/a
19	CTBP2	chr7:3340345-3341019	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:3340499-3340752	A549	lung:	n/a	n/a
21	CTCF	chr7:3340410-3340708	HepG2	liver:	n/a	chr7:3340483-3340496
22	CTCF	chr7:3340300-3340450	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr7:3340396-3340852	GM12878	blood:	n/a	chr7:3340483-3340496
24	CTCF	chr7:3340520-3340670	GM12870	blood:	n/a	n/a
25	CTCF	chr7:3340456-3340765	Gliobla	brain:	n/a	chr7:3340483-3340496
26	CTCF	chr7:3340460-3340610	GM12868	blood:	n/a	chr7:3340483-3340496
27	CTCF	chr7:3340540-3340690	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr7:3340462-3340772	NHEK	skin:	n/a	chr7:3340483-3340496
29	CTCF	chr7:3340540-3340690	GM12874	blood:	n/a	n/a
30	CTCF	chr7:3340540-3340690	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr7:3340540-3340690	SAEC	small airway:	n/a	n/a
32	CTCF	chr7:3340179-3341039	A549	lung:	n/a	chr7:3340483-3340496
33	CTCF	chr7:3340502-3340744	GM13976	blood:	n/a	n/a
34	CTCF	chr7:3340280-3340430	AG04450	lung:	n/a	n/a
35	CTCF	chr7:3340470-3340763	MCF-7	breast:	n/a	chr7:3340483-3340496
36	CTCF	chr7:3340520-3340670	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr7:3340540-3340690	GM12867	blood:	n/a	n/a
38	CTCF	chr7:3340520-3340670	AG10803	skin:	n/a	n/a
39	CTCF	chr7:3340520-3340670	GM12866	blood:	n/a	n/a
40	CTCF	chr7:3340540-3340690	HAc	cerebellar:	n/a	n/a
41	CTCF	chr7:3340328-3340344	GM12878	blood:	n/a	n/a
42	CTCF	chr7:3340393-3340825	H1-hESC	embryonic stem cell:	n/a	chr7:3340483-3340496
43	CTCF	chr7:3340385-3340749	H1-hESC	embryonic stem cell:	n/a	chr7:3340483-3340496
44	CTCF	chr7:3340520-3340670	NHEK	skin:	n/a	n/a
45	CTCF	chr7:3340540-3340690	GM12878	blood:	n/a	n/a
46	CTCF	chr7:3340491-3340803	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr7:3340312-3340320	GM19240	blood:	n/a	n/a
48	CTCF	chr7:3340140-3340290	NHEK	skin:	n/a	n/a
49	CTCF	chr7:3340464-3340791	Lung_OC	lung:	n/a	chr7:3340483-3340496
50	CTCF	chr7:3340520-3340670	A549	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:3338498-3338548	Jurkat	blood:	n/a
2	chr7:3338498-3338548	Jurkat	blood:	n/a
3	chr7:3338723-3338773	HCF	heart:	n/a
4	chr7:3340459-3340509	AG10803	skin:	n/a
5	chr7:3339766-3339816	HIPEpiC	eye:	n/a
6	chr7:3338498-3338548	GM06990	blood:	n/a
7	chr7:3338498-3338548	U87	brain:	n/a
8	chr7:3339766-3339816	PFSK-1	brain:	n/a
9	chr7:3340459-3340509	HUVEC	blood vessel:	n/a
10	chr7:3339766-3339816	NB4	blood:	n/a
11	chr7:3337443-3337493	ovcar-3	ovarian:	n/a
12	chr7:3338723-3338773	HRPEpiC	eye:	n/a
13	chr7:3339766-3339816	SK-N-MC	brain:	n/a
14	chr7:3339766-3339816	SKMC	muscle:	n/a
15	chr7:3339766-3339816	U87	brain:	n/a
16	chr7:3338723-3338773	NH-A	brain:	n/a
17	chr7:3337443-3337493	HCT-116	colon:	n/a
18	chr7:3338498-3338548	IMR90	lung:	fetal
19	chr7:3338723-3338773	SKMC	muscle:	n/a
20	chr7:3338498-3338548	GM19239	blood:	n/a
21	chr7:3340459-3340509	PANC-1	pancreas:	n/a
22	chr7:3338723-3338773	Jurkat	blood:	n/a
23	chr7:3338498-3338548	ProgFib	skin:	n/a
24	chr7:3337443-3337493	BE2_C	brain:	n/a
25	chr7:3339766-3339816	HNPCEpiC	eye:	n/a
26	chr7:3340459-3340509	AG04450	lung:	fetal
27	chr7:3337443-3337493	A549	lung:	n/a
28	chr7:3338723-3338773	H1-hESC	embryonic stem cell:	embryo
29	chr7:3338498-3338548	SK-N-SH_RA	brain:	n/a
30	chr7:3339766-3339816	MCF-7	breast:	n/a
31	chr7:3338723-3338773	Hela-S3	cervix:	n/a
32	chr7:3337443-3337493	MCF10A-Er-Src	breast:	n/a
33	chr7:3337443-3337493	ProgFib	skin:	n/a
34	chr7:3337443-3337493	SKMC	muscle:	n/a
35	chr7:3338498-3338548	PANC-1	pancreas:	n/a
36	chr7:3338498-3338548	BE2_C	brain:	n/a
37	chr7:3339766-3339816	IMR90	lung:	fetal
38	chr7:3339766-3339816	HCPEpiC	choroid plexus:	n/a
39	chr7:3338723-3338773	HUVEC	blood vessel:	n/a
40	chr7:3339766-3339816	HRE	kidney:	n/a
41	chr7:3340459-3340509	NB4	blood:	n/a
42	chr7:3340459-3340509	ovcar-3	ovarian:	n/a
43	chr7:3338723-3338773	HepG2	liver:	n/a
44	chr7:3337443-3337493	SK-N-SH_RA	brain:	n/a
45	chr7:3340459-3340509	GM19239	blood:	n/a
46	chr7:3338498-3338548	NHDF-neo	bronchial:	n/a
47	chr7:3340459-3340509	SK-N-MC	brain:	n/a
48	chr7:3339766-3339816	T-47D	breast:	n/a
49	chr7:3340459-3340509	A549	lung:	n/a
50	chr7:3338723-3338773	HAEpiC	amniotic membrane:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:3250247..3250807-chr7:3340190..3341077,3	MCF-7	breast:
2	chr7:3339718..3341766-chr7:3458306..3459954,2	K562	blood:
3	chr7:3254030..3256348-chr7:3338235..3340171,2	MCF-7	breast:
4	chr7:3194510..3195232-chr7:3340158..3340723,2	MCF-7	breast:
5	chr7:3340063..3340822-chr7:3439252..3440083,5	MCF-7	breast:

No data

Variant related genes	Relation type
SDK1	TF binding region
SDK1	CpG island
ENSG00000211544	chromatin interactions

Extended variants
information (count: 227 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:227 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10266927	chr7:3337081-3337082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565495211	chr7:3337144-3337145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs180982890	chr7:3337163-3337164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201638159	chr7:3337175-3337176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187328574	chr7:3337180-3337181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190544188	chr7:3337203-3337204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370059666	chr7:3337216-3337217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569867550	chr7:3337224-3337225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564048833	chr7:3337231-3337232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs117088427	chr7:3337239-3337240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115012853	chr7:3337263-3337264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35883661	chr7:3337273-3337274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs397814955	chr7:3337275-3337276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4047371	chr7:3337276-3337277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114462790	chr7:3337281-3337282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1464884	chr7:3337284-3337285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386709451	chr7:3337293-3337294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539752082	chr7:3337294-3337295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs376369315	chr7:3337299-3337300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113528208	chr7:3337320-3337321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs73286334	chr7:3337323-3337324	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs202240329	chr7:3337336-3337337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs75203648	chr7:3337344-3337345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs13245913	chr7:3337347-3337348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs71527439	chr7:3337350-3337351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71527440	chr7:3337353-3337354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199770646	chr7:3337354-3337355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs13233687	chr7:3337358-3337359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563731255	chr7:3337370-3337371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533777181	chr7:3337371-3337372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144770370	chr7:3337410-3337411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147898043	chr7:3337435-3337436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564566238	chr7:3337488-3337489	Weak transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs533504098	chr7:3337547-3337548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570924472	chr7:3337559-3337560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566706052	chr7:3337561-3337562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529310106	chr7:3337565-3337566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572315708	chr7:3337573-3337574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139909415	chr7:3337585-3337586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142765961	chr7:3337594-3337595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564637661	chr7:3337624-3337625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs557972379	chr7:3337639-3337640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs571518207	chr7:3337645-3337646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533607239	chr7:3337651-3337652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs369488361	chr7:3337710-3337711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553856126	chr7:3337781-3337782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573519423	chr7:3337783-3337784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542639900	chr7:3337785-3337786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs151117030	chr7:3337830-3337831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528581986	chr7:3337858-3337859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Chordoma	21602918	CNVD
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Nasopharyngeal cancer	20548289	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
Spondylocostal dysostosis	21085971	CNVD
Mental retardation	17901693	CNVD
Heart disease	21282601	CNVD
Glioblastoma multiforme	22286061	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	21645411	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3334800-3338400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:3334800-3339600	Weak transcription	Pancreas	Pancrea
3	chr7:3335000-3340000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:3337000-3337600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:3337000-3338400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:3337600-3339800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:3338200-3339000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:3338200-3339400	Enhancers	Adipose Nuclei	Adipose
9	chr7:3338400-3338600	Enhancers	H9 Cell Line	embryonic stem cell
10	chr7:3338400-3338600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:3338400-3339400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr7:3338600-3338800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:3338600-3339000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:3338600-3339600	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr7:3338600-3340200	Enhancers	NHDF-Ad	bronchial
16	chr7:3339000-3339400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:3339000-3339800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:3339200-3339800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr7:3339200-3339800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:3339200-3340000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr7:3339400-3339600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
22	chr7:3339400-3339600	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr7:3339400-3339600	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr7:3339400-3339600	Bivalent Enhancer	HepG2	liver
25	chr7:3339400-3339800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
26	chr7:3339400-3339800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:3339400-3339800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
28	chr7:3339400-3339800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr7:3339400-3339800	Bivalent Enhancer	Brain Germinal Matrix	brain
30	chr7:3339400-3340000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:3339400-3340000	Bivalent Enhancer	Duodenum Mucosa	Duodenum
32	chr7:3339400-3340200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr7:3339400-3340200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
34	chr7:3339400-3340200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr7:3339400-3340200	Bivalent Enhancer	Fetal Thymus	thymus
36	chr7:3339400-3340600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
37	chr7:3339400-3340600	Bivalent Enhancer	Placenta	Placenta
38	chr7:3339600-3339800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
39	chr7:3339600-3339800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:3339600-3339800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
41	chr7:3339600-3339800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
42	chr7:3339600-3339800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
43	chr7:3339600-3339800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr7:3339600-3339800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr7:3339600-3339800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr7:3339600-3339800	Enhancers	Fetal Heart	heart
47	chr7:3339600-3339800	Enhancers	Pancreas	Pancrea
48	chr7:3339600-3339800	Enhancers	Right Ventricle	heart
49	chr7:3339600-3340000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr7:3339600-3340000	Enhancers	H9 Cell Line	embryonic stem cell

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