Variant report

Variant	nsv1032326
Chromosome Location	chr8:86848208-86871596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:0)
Chromatin interactive
region (count:52)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
2	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
3	ARID3A	chr8:86848202-86848466	K562	blood:	n/a	n/a
4	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
5	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
6	ARID3A	chr8:86868281-86868466	K562	blood:	n/a	n/a
7	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
8	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
9	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
10	ATF1	chr8:86851680-86851940	K562	blood:	n/a	n/a
11	ATF3	chr8:86848176-86848532	K562	blood:	n/a	n/a
12	ATF3	chr8:86853960-86854338	K562	blood:	n/a	n/a
13	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
14	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
16	BHLHE40	chr8:86864850-86864971	K562	blood:	n/a	n/a
17	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
18	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
19	BHLHE40	chr8:86848213-86848489	K562	blood:	n/a	n/a
20	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
21	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
22	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
23	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
24	CEBPB	chr8:86855387-86855903	K562	blood:	n/a	n/a
25	CEBPB	chr8:86847657-86848641	MCF-7	breast:	n/a	chr8:86848372-86848383
26	CEBPB	chr8:86847845-86848785	K562	blood:	n/a	chr8:86848372-86848383
27	CEBPB	chr8:86854020-86854265	K562	blood:	n/a	n/a
28	CEBPB	chr8:86855406-86856007	MCF-7	breast:	n/a	n/a
29	CEBPB	chr8:86847995-86848565	HCT-116	colon:	n/a	chr8:86848372-86848383
30	CEBPB	chr8:86848151-86848550	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
31	CEBPB	chr8:86855485-86855973	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:86848095-86848658	HCT-116	colon:	n/a	chr8:86848372-86848383
33	CEBPB	chr8:86848166-86848569	HepG2	liver:	n/a	chr8:86848372-86848383
34	CEBPB	chr8:86848109-86848565	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
35	CEBPB	chr8:86852999-86853917	MCF-7	breast:	n/a	chr8:86853134-86853151
36	CEBPB	chr8:86847793-86848810	A549	lung:	n/a	chr8:86848372-86848383
37	CEBPB	chr8:86847697-86849448	Hela-S3	cervix:	n/a	chr8:86848372-86848383
38	CEBPB	chr8:86858744-86859178	K562	blood:	n/a	chr8:86858989-86859000
39	CEBPB	chr8:86847998-86848696	A549	lung:	n/a	chr8:86848372-86848383
40	CEBPB	chr8:86853219-86853518	K562	blood:	n/a	n/a
41	CEBPB	chr8:86848107-86848605	A549	lung:	n/a	chr8:86848372-86848383
42	CEBPB	chr8:86858898-86859037	HepG2	liver:	n/a	chr8:86858989-86859000
43	CEBPB	chr8:86852955-86853850	MCF-7	breast:	n/a	chr8:86853134-86853151
44	CEBPB	chr8:86848135-86848562	IMR90	lung:	n/a	chr8:86848372-86848383
45	CEBPB	chr8:86848192-86848660	H1-hESC	embryonic stem cell:	n/a	chr8:86848372-86848383
46	CEBPB	chr8:86848079-86848668	MCF-7	breast:	n/a	chr8:86848372-86848383
47	CEBPB	chr8:86848126-86848529	K562	blood:	n/a	chr8:86848372-86848383
48	CEBPB	chr8:86847869-86848819	K562	blood:	n/a	chr8:86848372-86848383
49	CEBPD	chr8:86848072-86848638	K562	blood:	n/a	chr8:86848307-86848318
50	CEBPD	chr8:86848089-86848561	K562	blood:	n/a	chr8:86848307-86848318

No data

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:86864951..86867156-chr8:86950288..86952196,2	K562	blood:
2	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
3	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
4	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
5	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
6	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
7	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
8	chr8:86853963..86856698-chr8:86950908..86953530,2	K562	blood:
9	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
10	chr8:86464673..86465447-chr8:86852772..86853973,3	MCF-7	breast:
11	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
12	chr8:86364996..86367147-chr8:86853567..86855147,2	MCF-7	breast:
13	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
14	chr8:86853239..86855144-chr8:86935082..86937255,2	MCF-7	breast:
15	chr8:86852733..86854770-chr8:86972857..86974930,2	K562	blood:
16	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
17	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
18	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
19	chr8:86852107..86854370-chr8:86972859..86974722,2	MCF-7	breast:
20	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
21	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
22	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:
23	chr8:86868209..86870416-chr8:86917445..86919044,2	K562	blood:
24	chr8:86850726..86853148-chr8:86853230..86857704,4	K562	blood:
25	chr8:86848347..86850172-chr8:86983643..86985301,2	MCF-7	breast:
26	chr8:86852235..86854715-chr8:86982807..86985769,2	MCF-7	breast:
27	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:
28	chr8:86843222..86846042-chr8:86847745..86849520,2	K562	blood:
29	chr8:86852142..86856180-chr8:86917083..86921619,8	MCF-7	breast:
30	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
31	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
32	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
33	chr8:86849344..86852342-chr8:86863151..86865379,2	K562	blood:
34	chr8:86849039..86851736-chr8:87015052..87016845,2	MCF-7	breast:
35	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
36	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
37	chr8:86847849..86857260-chr8:86866079..86880479,25	MCF-7	breast:
38	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
39	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
40	chr8:86849937..86852745-chr8:86855936..86857800,2	K562	blood:
41	chr8:86853963..86856746-chr8:86949985..86952408,2	K562	blood:
42	chr8:86854256..86855844-chr8:86962935..86965322,2	K562	blood:
43	chr8:86867877..86870175-chr8:86957602..86960658,3	K562	blood:
44	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
45	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
46	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
47	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
48	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
49	chr3:61613244..61613971-chr8:86852933..86853873,2	MCF-7	breast:
50	chr8:86865679..86869782-chr8:86870364..86872343,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L2P-2	chr8:86866739-86866829	XLOC_007141
2	lnc-REXO1L2P-2	chr8:86864119-86865001	XLOC_007141
3	lnc-ATP6V0D2-2	chr8:86851934-86852014	NONHSAT127540
4	lnc-ATP6V0D2-2	chr8:86851934-86852014	ENSG00000253154

No data

Variant related genes	Relation type
ENSG00000253154	TF binding region
ENSG00000253154	chromatin interactions
ENSG00000050820	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000253549	chromatin interactions

Extended variants
information (count: 797 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:797 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17596760	chr8:86848208-86848209	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533606666	chr8:86848220-86848221	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs145539612	chr8:86848223-86848224	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs576714625	chr8:86848260-86848261	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs371264583	chr8:86848266-86848267	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs568807991	chr8:86848347-86848348	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs555926996	chr8:86848378-86848379	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs151291651	chr8:86848389-86848390	Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138101656	chr8:86848404-86848405	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs4960805	chr8:86848406-86848407	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs375699128	chr8:86848495-86848496	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs7840687	chr8:86848522-86848523	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs7388448	chr8:86848528-86848529	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs575102509	chr8:86848540-86848541	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs13281775	chr8:86848607-86848608	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs551638267	chr8:86848621-86848622	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs13260188	chr8:86848622-86848623	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs13260189	chr8:86848624-86848625	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs13260240	chr8:86848670-86848671	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs13260255	chr8:86848687-86848688	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs13260257	chr8:86848690-86848691	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs142678171	chr8:86848723-86848724	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs13282293	chr8:86848724-86848725	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs60186207	chr8:86848752-86848753	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs370440079	chr8:86848780-86848781	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs532366150	chr8:86848871-86848872	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs201631648	chr8:86848891-86848892	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs552536421	chr8:86848894-86848895	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553090453	chr8:86848903-86848904	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35901477	chr8:86848904-86848905	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs59220179	chr8:86848907-86848908	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs562790061	chr8:86848949-86848950	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531615341	chr8:86848994-86848995	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs13254841	chr8:86848999-86849000	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs181184413	chr8:86849052-86849053	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs184513699	chr8:86849150-86849151	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs2930553	chr8:86849171-86849172	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs570517188	chr8:86849213-86849214	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs539203639	chr8:86849231-86849232	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs556101799	chr8:86849248-86849249	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148665455	chr8:86849276-86849277	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs7016829	chr8:86849334-86849335	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs546615947	chr8:86849376-86849377	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs555324704	chr8:86849398-86849399	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs369769579	chr8:86849400-86849401	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs4272430	chr8:86849446-86849447	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs575040600	chr8:86849523-86849524	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs117985643	chr8:86849526-86849527	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575556777	chr8:86849627-86849628	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs560564889	chr8:86849706-86849707	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:575 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86843000-86848600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:86843000-86848800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:86843200-86848400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr8:86843600-86849000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:86844200-86849200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:86844600-86849000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:86845000-86848800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:86845800-86848400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:86845800-86848600	Enhancers	Fetal Lung	lung
10	chr8:86845800-86849000	Weak transcription	HSMM	muscle
11	chr8:86845800-86849400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:86846200-86848600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr8:86846200-86848600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:86846200-86848600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:86846600-86849400	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr8:86846800-86848400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr8:86846800-86850400	Enhancers	Placenta Amnion	Placenta Amnion
18	chr8:86846800-86851600	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:86847000-86848400	Enhancers	NHDF-Ad	bronchial
20	chr8:86847000-86848800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:86847000-86848800	Enhancers	NHEK	skin
22	chr8:86847000-86850400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:86847200-86848400	Enhancers	Brain Hippocampus Middle	brain
24	chr8:86847400-86848400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr8:86847400-86848400	Enhancers	Adipose Nuclei	Adipose
26	chr8:86847400-86848600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:86847400-86851200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:86847600-86848400	Enhancers	Brain Anterior Caudate	brain
29	chr8:86847800-86848400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr8:86847800-86848400	Flanking Active TSS	Hela-S3	cervix
31	chr8:86847800-86848400	Enhancers	NH-A	brain
32	chr8:86847800-86848600	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:86847800-86848600	Enhancers	Liver	Liver
34	chr8:86847800-86848600	Enhancers	Placenta	Placenta
35	chr8:86847800-86848600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr8:86847800-86848800	Weak transcription	NHLF	lung
37	chr8:86848000-86848400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr8:86848000-86848400	Enhancers	Stomach Mucosa	stomach
39	chr8:86848000-86848400	Flanking Active TSS	A549	lung
40	chr8:86848000-86848600	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr8:86848000-86848600	Enhancers	Brain Substantia Nigra	brain
42	chr8:86848000-86849000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:86848200-86848400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr8:86848200-86848400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr8:86848200-86848400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr8:86848200-86848400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr8:86848200-86848400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
48	chr8:86848200-86848600	Flanking Active TSS	K562	blood
49	chr8:86848200-86848800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
50	chr8:86848200-86848800	Enhancers	HMEC	breast

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