Variant report

Variant	nsv971152
Chromosome Location	chr7:6485642-6509340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1182)
CpG islands
(count:915)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6488139-6488172	K562	blood:	n/a	n/a
2	ARID3A	chr7:6488936-6489138	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6486701-6486946	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6490873-6491305	K562	blood:	n/a	n/a
5	ARID3A	chr7:6488062-6488548	HepG2	liver:	n/a	n/a
6	ATF1	chr7:6490921-6491255	K562	blood:	n/a	n/a
7	ATF1	chr7:6493526-6493770	K562	blood:	n/a	n/a
8	ATF2	chr7:6487336-6487955	GM12878	blood:	n/a	n/a
9	ATF2	chr7:6486523-6487023	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:6486610-6487004	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:6487386-6487931	A549	lung:	n/a	n/a
12	ATF3	chr7:6488075-6488312	K562	blood:	n/a	n/a
13	ATF3	chr7:6487977-6488395	K562	blood:	n/a	n/a
14	ATF3	chr7:6487381-6487905	A549	lung:	n/a	n/a
15	ATF3	chr7:6487978-6488464	A549	lung:	n/a	n/a
16	ATF3	chr7:6488046-6488342	HepG2	liver:	n/a	n/a
17	ATF3	chr7:6487909-6488473	A549	lung:	n/a	n/a
18	ATF3	chr7:6487409-6487848	K562	blood:	n/a	n/a
19	ATF3	chr7:6487423-6487720	K562	blood:	n/a	n/a
20	BACH1	chr7:6486734-6487392	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr7:6488084-6488303	GM12878	blood:	n/a	n/a
22	BCL3	chr7:6487927-6488489	A549	lung:	n/a	n/a
23	BCL3	chr7:6487027-6487786	A549	lung:	n/a	n/a
24	BCL3	chr7:6507378-6507738	A549	lung:	n/a	n/a
25	BCL3	chr7:6493126-6493626	A549	lung:	n/a	n/a
26	BCL3	chr7:6487925-6488405	A549	lung:	n/a	n/a
27	BCLAF1	chr7:6487250-6487905	GM12878	blood:	n/a	n/a
28	BDP1	chr7:6487975-6488322	Hela-S3	cervix:	n/a	n/a
29	BHLHE40	chr7:6489539-6489776	HepG2	liver:	n/a	n/a
30	BHLHE40	chr7:6488081-6488448	A549	lung:	n/a	n/a
31	BHLHE40	chr7:6486647-6486947	HepG2	liver:	n/a	n/a
32	BHLHE40	chr7:6488134-6488146	GM12878	blood:	n/a	n/a
33	BHLHE40	chr7:6488086-6488434	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:6488045-6488452	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:6490897-6491300	K562	blood:	n/a	n/a
36	BHLHE40	chr7:6487350-6488448	K562	blood:	n/a	chr7:6487666-6487682
37	BHLHE40	chr7:6487250-6489027	HepG2	liver:	n/a	chr7:6487666-6487682 chr7:6488890-6488906
38	BHLHE40	chr7:6486581-6487037	K562	blood:	n/a	n/a
39	BRCA1	chr7:6487419-6487619	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr7:6487407-6488336	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr7:6486488-6488335	K562	blood:	n/a	n/a
42	CBX3	chr7:6488029-6488311	K562	blood:	n/a	n/a
43	CCNT2	chr7:6488085-6488244	K562	blood:	n/a	n/a
44	CCNT2	chr7:6486637-6487804	K562	blood:	n/a	n/a
45	CCNT2	chr7:6490886-6491272	K562	blood:	n/a	n/a
46	CEBPB	chr7:6489595-6489867	A549	lung:	n/a	chr7:6489689-6489700
47	CEBPB	chr7:6486649-6486935	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:6489591-6489761	HepG2	liver:	n/a	chr7:6489689-6489700
49	CEBPB	chr7:6488056-6488446	ECC-1	luminal epithelium:	n/a	chr7:6488194-6488205
50	CEBPB	chr7:6490245-6490568	HepG2	liver:	n/a	chr7:6490404-6490415

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6487775-6487825	HMEC	breast:	n/a
2	chr7:6485717-6485767	GM19239	blood:	n/a
3	chr7:6490427-6490477	ProgFib	skin:	n/a
4	chr7:6485717-6485767	Caco-2	colon:	n/a
5	chr7:6487749-6487799	MCF-7	breast:	n/a
6	chr7:6485717-6485767	HCPEpiC	choroid plexus:	n/a
7	chr7:6487342-6487392	HNPCEpiC	eye:	n/a
8	chr7:6487775-6487825	GM12892	blood:	n/a
9	chr7:6487775-6487825	T-47D	breast:	n/a
10	chr7:6493555-6493605	ECC-1	luminal epithelium:	n/a
11	chr7:6488916-6488966	NHDF-neo	bronchial:	n/a
12	chr7:6487989-6488039	HEEpiC	esophagus:	n/a
13	chr7:6493555-6493605	GM12891	blood:	n/a
14	chr7:6487510-6487560	CMK	blood:	n/a
15	chr7:6501749-6501799	T-47D	breast:	n/a
16	chr7:6487989-6488039	AG09309	skin:	n/a
17	chr7:6488668-6488718	ECC-1	luminal epithelium:	n/a
18	chr7:6487775-6487825	NB4	blood:	n/a
19	chr7:6487512-6487562	ovcar-3	ovarian:	n/a
20	chr7:6487749-6487799	HEK293	kidney:	embryo
21	chr7:6487510-6487560	HRPEpiC	eye:	n/a
22	chr7:6487775-6487825	PFSK-1	brain:	n/a
23	chr7:6487739-6487789	HPAEpiC	pulmonary alveolar:	n/a
24	chr7:6501749-6501799	IMR90	lung:	fetal
25	chr7:6488916-6488966	PFSK-1	brain:	n/a
26	chr7:6487342-6487392	NHDF-neo	bronchial:	n/a
27	chr7:6485717-6485767	Jurkat	blood:	n/a
28	chr7:6493555-6493605	SK-N-MC	brain:	n/a
29	chr7:6488916-6488966	AG04450	lung:	fetal
30	chr7:6485717-6485767	PrEC	prostate:	n/a
31	chr7:6487749-6487799	ProgFib	skin:	n/a
32	chr7:6487512-6487562	GM12878	blood:	n/a
33	chr7:6487512-6487562	HMEC	breast:	n/a
34	chr7:6487739-6487789	U87	brain:	n/a
35	chr7:6488668-6488718	NHDF-neo	bronchial:	n/a
36	chr7:6487999-6488049	HEEpiC	esophagus:	n/a
37	chr7:6487512-6487562	MCF10A-Er-Src	breast:	n/a
38	chr7:6485717-6485767	HRE	kidney:	n/a
39	chr7:6487775-6487825	AG04450	lung:	fetal
40	chr7:6487999-6488049	HMEC	breast:	n/a
41	chr7:6487749-6487799	SK-N-SH	brain:	n/a
42	chr7:6493555-6493605	A549	lung:	n/a
43	chr7:6493555-6493605	HIPEpiC	eye:	n/a
44	chr7:6487739-6487789	LNCaP	prostate:	n/a
45	chr7:6487775-6487825	HRPEpiC	eye:	n/a
46	chr7:6487512-6487562	HL-60	blood:	n/a
47	chr7:6487989-6488039	HCPEpiC	choroid plexus:	n/a
48	chr7:6488916-6488966	GM12892	blood:	n/a
49	chr7:6485717-6485767	Hepatocyte	liver:	n/a
50	chr7:6488916-6488966	SK-N-SH_RA	brain:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6499717..6507603-chr7:6511410..6517764,12	K562	blood:
2	chr5:68485539..68486202-chr7:6487649..6488157,2	Hela-S3	cervix:
3	chr7:6500350..6502598-chr7:6505904..6507972,2	MCF-7	breast:
4	chr7:6495113..6497493-chr7:6497529..6500079,3	MCF-7	breast:
5	chr7:6445380..6448087-chr7:6488948..6490884,2	K562	blood:
6	chr7:6504061..6507520-chr7:6522286..6524549,3	K562	blood:
7	chr7:6488240..6490209-chr7:6490613..6492203,2	MCF-7	breast:
8	chr7:6503445..6506169-chr7:6511956..6514111,2	K562	blood:
9	chr7:6484395..6490398-chr7:6492212..6496662,5	MCF-7	breast:
10	chr7:6497678..6499764-chr7:6515399..6517836,2	K562	blood:
11	chr7:6486266..6487977-chr7:6489365..6491007,2	MCF-7	breast:
12	chr7:6500350..6502598-chr7:6505904..6507972,2	MCF-7	breast:
13	chr7:6486201..6489628-chr7:6522463..6525039,4	MCF-7	breast:
14	chr7:6495113..6497493-chr7:6497529..6500079,3	MCF-7	breast:
15	chr7:6143603..6145893-chr7:6507665..6509813,2	MCF-7	breast:
16	chr7:6505053..6507706-chr7:6514500..6517460,3	K562	blood:
17	chr7:6474092..6477009-chr7:6483600..6487126,3	K562	blood:
18	chr7:6487071..6489296-chr7:6498689..6501637,2	MCF-7	breast:
19	chr7:6488240..6490209-chr7:6490613..6492203,2	MCF-7	breast:
20	chr7:6500191..6503008-chr7:6519492..6521377,2	K562	blood:
21	chr7:6487534..6489634-chr7:6491176..6495271,6	MCF-7	breast:
22	chr7:6492564..6494087-chr7:6514495..6516683,2	K562	blood:
23	chr7:6501893..6503760-chr7:6541357..6543829,2	MCF-7	breast:
24	chr7:6485398..6489202-chr7:6520855..6525273,5	MCF-7	breast:
25	chr7:6486167..6489212-chr7:6498721..6504081,5	MCF-7	breast:
26	chr7:6412857..6414877-chr7:6485942..6488132,2	MCF-7	breast:
27	chr12:64797367..64798283-chr7:6487421..6487959,2	Hela-S3	cervix:
28	chr7:6499949..6501557-chr7:6518916..6521343,2	MCF-7	breast:
29	chr7:6486176..6487864-chr7:6615659..6618201,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRID2IP-4	chr7:6486625-6486971	expReg_chr7_744_-

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KDELR2	hsa-miR-124-3p	chr7:6502583-6502596
2	KDELR2	hsa-miR-124-3p	chr7:6502583-6502602
3	KDELR2	hsa-miR-124-3p	chr7:6502588-6502582

Variant related genes	Relation type
DAGLB	TF binding region
DAGLB	CpG island
ENSG00000164535	chromatin interactions
ENSG00000153044	chromatin interactions
ENSG00000136238	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000184575	chromatin interactions
ENSG00000106346	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000136240	chromatin interactions

Extended variants
information (count: 1190 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1190 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376919352	chr7:6485654-6485655	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs201095630	chr7:6485668-6485669	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs138752821	chr7:6485700-6485701	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs370262270	chr7:6485738-6485739	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs78373085	chr7:6485740-6485741	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs372982163	chr7:6485741-6485742	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568580768	chr7:6485759-6485760	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs114879948	chr7:6485773-6485774	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs185023987	chr7:6485775-6485776	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs566351136	chr7:6485812-6485813	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs115718913	chr7:6485825-6485826	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs558164148	chr7:6485827-6485828	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12666019	chr7:6485848-6485849	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs149448344	chr7:6485872-6485873	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188180342	chr7:6485892-6485893	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs376793508	chr7:6485941-6485942	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7793715	chr7:6485942-6485943	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs368720822	chr7:6485943-6485944	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs368915094	chr7:6485944-6485945	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs34692184	chr7:6485960-6485961	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs548012209	chr7:6485961-6485962	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs147145685	chr7:6485969-6485970	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs570404859	chr7:6486000-6486001	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs541969922	chr7:6486001-6486002	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140376861	chr7:6486017-6486018	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs60802552	chr7:6486022-6486023	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557237090	chr7:6486028-6486029	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545428033	chr7:6486038-6486039	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs28670897	chr7:6486042-6486043	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs563754541	chr7:6486048-6486049	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs531179704	chr7:6486057-6486058	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs147296881	chr7:6486064-6486065	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs7797644	chr7:6486067-6486068	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs561779461	chr7:6486093-6486094	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs373297535	chr7:6486105-6486106	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs13222147	chr7:6486143-6486144	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs13222155	chr7:6486147-6486148	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs180974893	chr7:6486163-6486164	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs7810332	chr7:6486219-6486220	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs186198340	chr7:6486264-6486265	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs73342968	chr7:6486328-6486329	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541205298	chr7:6486367-6486368	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs540191629	chr7:6486368-6486369	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs374105320	chr7:6486377-6486378	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs71539940	chr7:6486405-6486406	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs71539941	chr7:6486412-6486413	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs570090374	chr7:6486428-6486429	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs537397534	chr7:6486430-6486431	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs114702204	chr7:6486432-6486433	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs567741666	chr7:6486552-6486553	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1153 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6453000-6486800	Weak transcription	Small Intestine	intestine
2	chr7:6456800-6486800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:6465000-6486600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr7:6465800-6486400	Weak transcription	Colonic Mucosa	Colon
5	chr7:6466000-6486400	Weak transcription	Aorta	Aorta
6	chr7:6476200-6486400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:6476400-6486400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr7:6478800-6486000	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:6478800-6486600	Weak transcription	Fetal Heart	heart
10	chr7:6479000-6486000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:6479200-6486400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr7:6479400-6486400	Weak transcription	Right Atrium	heart
13	chr7:6479800-6485800	Strong transcription	Fetal Thymus	thymus
14	chr7:6481000-6485800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr7:6481200-6485800	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:6481200-6486000	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:6481200-6486000	Strong transcription	Fetal Stomach	stomach
18	chr7:6481400-6485800	Strong transcription	H1 Cell Line	embryonic stem cell
19	chr7:6481400-6485800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr7:6481400-6485800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:6481400-6485800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:6481400-6485800	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr7:6481400-6485800	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:6481400-6485800	Strong transcription	Fetal Muscle Trunk	muscle
25	chr7:6481400-6486400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr7:6481600-6485800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:6481600-6485800	Strong transcription	Liver	Liver
28	chr7:6481600-6485800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
29	chr7:6481600-6485800	Strong transcription	Spleen	Spleen
30	chr7:6481800-6485800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
31	chr7:6481800-6485800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr7:6482000-6485800	Strong transcription	Gastric	stomach
33	chr7:6482000-6486400	Weak transcription	GM12878-XiMat	blood
34	chr7:6482200-6485800	Genic enhancers	Hela-S3	cervix
35	chr7:6482200-6486200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:6482200-6486200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr7:6482200-6486400	Weak transcription	Stomach Mucosa	stomach
38	chr7:6482400-6486400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr7:6482400-6486400	Weak transcription	Brain Angular Gyrus	brain
40	chr7:6483000-6486000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:6483800-6485800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr7:6484000-6485800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:6484200-6485800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:6484200-6485800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:6484200-6485800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:6484200-6485800	Strong transcription	HUVEC	blood vessel
47	chr7:6484200-6485800	Strong transcription	K562	blood
48	chr7:6484200-6485800	Strong transcription	NHEK	skin
49	chr7:6484200-6486000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:6484200-6486000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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