Variant report

Variant	nsv519645
Chromosome Location	chr8:110602317-110613000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:110605197-110606300	HepG2	liver:	n/a	n/a
2	ATF2	chr8:110604419-110605051	GM12878	blood:	n/a	n/a
3	ATF2	chr8:110606443-110607348	GM12878	blood:	n/a	n/a
4	ATF2	chr8:110604470-110605159	GM12878	blood:	n/a	n/a
5	ATF2	chr8:110608002-110608513	GM12878	blood:	n/a	n/a
6	ATF2	chr8:110607810-110608520	GM12878	blood:	n/a	n/a
7	ATF3	chr8:110605681-110606214	A549	lung:	n/a	n/a
8	BCL11A	chr8:110604550-110604974	GM12878	blood:	n/a	chr8:110604931-110604940
9	BCLAF1	chr8:110604470-110605155	GM12878	blood:	n/a	chr8:110604931-110604940
10	BCLAF1	chr8:110604502-110605022	GM12878	blood:	n/a	chr8:110604931-110604940
11	BHLHE40	chr8:110605586-110606212	HepG2	liver:	n/a	n/a
12	BHLHE40	chr8:110604564-110605005	GM12878	blood:	n/a	n/a
13	CBX3	chr8:110605596-110607241	HCT-116	colon:	n/a	n/a
14	CEBPB	chr8:110605637-110606161	A549	lung:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
15	CEBPB	chr8:110605443-110606208	HepG2	liver:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
16	CEBPB	chr8:110605650-110606058	HepG2	liver:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
17	CEBPB	chr8:110607865-110608093	IMR90	lung:	n/a	chr8:110608006-110608017
18	CEBPB	chr8:110605555-110606846	HCT-116	colon:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
19	CEBPB	chr8:110605650-110606028	HepG2	liver:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
20	CEBPB	chr8:110605391-110606939	HCT-116	colon:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
21	CEBPB	chr8:110605701-110606079	A549	lung:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
22	CEBPB	chr8:110605376-110606212	HepG2	liver:	n/a	chr8:110605887-110605898 chr8:110605887-110605900 chr8:110605889-110605900
23	CEBPB	chr8:110607860-110608155	H1-hESC	embryonic stem cell:	n/a	chr8:110608006-110608017
24	CEBPB	chr8:110607880-110608076	HepG2	liver:	n/a	chr8:110608006-110608017
25	CEBPD	chr8:110605693-110606056	HepG2	liver:	n/a	n/a
26	CEBPZ	chr8:110605662-110605865	HepG2	liver:	n/a	n/a
27	CHD1	chr8:110604415-110604674	GM12878	blood:	n/a	n/a
28	CHD1	chr8:110607566-110608710	GM12878	blood:	n/a	n/a
29	CHD1	chr8:110604940-110605197	GM12878	blood:	n/a	n/a
30	CHD2	chr8:110604632-110604887	GM12878	blood:	n/a	n/a
31	CHD2	chr8:110607744-110608459	GM12878	blood:	n/a	n/a
32	CHD2	chr8:110605695-110606240	HepG2	liver:	n/a	n/a
33	CREB1	chr8:110605480-110606044	A549	lung:	n/a	n/a
34	CREB1	chr8:110608047-110608520	GM12878	blood:	n/a	n/a
35	CREB1	chr8:110605799-110606176	A549	lung:	n/a	n/a
36	CTCF	chr8:110611600-110611750	GM12878	blood:	n/a	n/a
37	CTCF	chr8:110606520-110606670	GM12864	blood:	n/a	n/a
38	CTCF	chr8:110605840-110605990	RPTEC	kidney:	n/a	n/a
39	CUX1	chr8:110604430-110605136	GM12878	blood:	n/a	n/a
40	CUX1	chr8:110607143-110607338	GM12878	blood:	n/a	n/a
41	EBF1	chr8:110604476-110604966	GM12878	blood:	n/a	chr8:110604661-110604670 chr8:110604661-110604671 chr8:110604660-110604671 chr8:110604659-110604672
42	EBF1	chr8:110605954-110606052	GM12878	blood:	n/a	n/a
43	EBF1	chr8:110604428-110605028	GM12878	blood:	n/a	chr8:110604661-110604670 chr8:110604661-110604671 chr8:110604660-110604671 chr8:110604659-110604672
44	EBF1	chr8:110604276-110605151	GM12878	blood:	n/a	chr8:110604661-110604670 chr8:110604661-110604671 chr8:110604660-110604671 chr8:110604659-110604672
45	EBF1	chr8:110608113-110608442	GM12878	blood:	n/a	n/a
46	EBF1	chr8:110608157-110608426	GM12878	blood:	n/a	n/a
47	EBF1	chr8:110606964-110607162	GM12878	blood:	n/a	n/a
48	EBF1	chr8:110608006-110608456	GM12878	blood:	n/a	n/a
49	EP300	chr8:110605351-110606226	HepG2	liver:	n/a	chr8:110605551-110605565
50	EP300	chr8:110605435-110606186	A549	lung:	n/a	chr8:110605551-110605565

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:110608037-110608087	HAEpiC	amniotic membrane:	n/a
2	chr8:110608037-110608087	RPTEC	kidney:	n/a
3	chr8:110608037-110608087	SAEC	small airway:	n/a
4	chr8:110608037-110608087	LNCaP	prostate:	n/a
5	chr8:110608037-110608087	SK-N-SH_RA	brain:	n/a
6	chr8:110608037-110608087	U87	brain:	n/a
7	chr8:110608037-110608087	GM12878	blood:	n/a
8	chr8:110608037-110608087	ECC-1	luminal epithelium:	n/a
9	chr8:110608037-110608087	H1-hESC	embryonic stem cell:	embryo
10	chr8:110608037-110608087	AG10803	skin:	n/a
11	chr8:110608037-110608087	AG04449	skin:	fetal
12	chr8:110608037-110608087	GM06990	blood:	n/a
13	chr8:110608037-110608087	AG04450	lung:	fetal
14	chr8:110608037-110608087	HepG2	liver:	n/a
15	chr8:110608037-110608087	GM19239	blood:	n/a
16	chr8:110608037-110608087	AG09319	gingival:	n/a
17	chr8:110608037-110608087	NH-A	brain:	n/a
18	chr8:110608037-110608087	SK-N-SH	brain:	n/a
19	chr8:110608037-110608087	NB4	blood:	n/a
20	chr8:110608037-110608087	PrEC	prostate:	n/a
21	chr8:110608037-110608087	CMK	blood:	n/a
22	chr8:110608037-110608087	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:110608037-110608087	K562	blood:	n/a
24	chr8:110608037-110608087	NT2-D1	testis:	n/a
25	chr8:110608037-110608087	HUVEC	blood vessel:	n/a
26	chr8:110608037-110608087	HRE	kidney:	n/a
27	chr8:110608037-110608087	GM12891	blood:	n/a
28	chr8:110608037-110608087	HL-60	blood:	n/a
29	chr8:110608037-110608087	AG09309	skin:	n/a
30	chr8:110608037-110608087	Caco-2	colon:	n/a
31	chr8:110608037-110608087	MCF-7	breast:	n/a
32	chr8:110608037-110608087	HNPCEpiC	eye:	n/a
33	chr8:110608037-110608087	NHDF-neo	bronchial:	n/a
34	chr8:110608037-110608087	IMR90	lung:	fetal
35	chr8:110608037-110608087	HEEpiC	esophagus:	n/a
36	chr8:110608037-110608087	HMEC	breast:	n/a
37	chr8:110608037-110608087	T-47D	breast:	n/a
38	chr8:110608037-110608087	SK-N-MC	brain:	n/a
39	chr8:110608037-110608087	AoSMC	blood vessel:	n/a
40	chr8:110608037-110608087	PFSK-1	brain:	n/a
41	chr8:110608037-110608087	GM12892	blood:	n/a
42	chr8:110608037-110608087	HCM	heart:	n/a
43	chr8:110608037-110608087	HCT-116	colon:	n/a
44	chr8:110608037-110608087	SKMC	muscle:	n/a
45	chr8:110608037-110608087	NHBE	bronchial:	n/a
46	chr8:110608037-110608087	HCF	heart:	n/a
47	chr8:110608037-110608087	Hela-S3	cervix:	n/a
48	chr8:110608037-110608087	HRPEpiC	eye:	n/a
49	chr8:110608037-110608087	MCF10A-Er-Src	breast:	n/a
50	chr8:110608037-110608087	ovcar-3	ovarian:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:110601515..110604234-chr8:110611916..110615052,3	MCF-7	breast:
2	chr8:110612107..110614990-chr8:110621772..110623731,2	MCF-7	breast:
3	chr8:110552868..110555274-chr8:110604412..110606695,2	MCF-7	breast:
4	chr8:110587354..110588138-chr8:110605418..110606127,2	MCF-7	breast:
5	chr8:110606587..110608159-chr8:110619850..110621635,2	MCF-7	breast:
6	chr8:110604317..110607760-chr8:110608079..110611073,4	MCF-7	breast:
7	chr8:110588326..110591138-chr8:110601427..110604344,2	MCF-7	breast:
8	chr8:110600715..110602433-chr8:110604852..110607355,2	MCF-7	breast:
9	chr8:110608664..110610842-chr8:110615252..110617482,2	K562	blood:
10	chr8:110605797..110607546-chr8:110612982..110614483,2	MCF-7	breast:
11	chr8:110605754..110608104-chr8:110608990..110611309,2	MCF-7	breast:
12	chr8:110597460..110599576-chr8:110604521..110607030,2	MCF-7	breast:
13	chr8:110605797..110607546-chr8:110612982..110614483,2	MCF-7	breast:
14	chr8:110604868..110607165-chr8:110611365..110613319,2	MCF-7	breast:
15	chr8:110603709..110605508-chr8:110614593..110616929,2	MCF-7	breast:
16	chr8:110599717..110603274-chr8:110604163..110606425,3	MCF-7	breast:
17	chr8:110601011..110602738-chr8:110605572..110607359,2	K562	blood:
18	chr8:110599166..110601638-chr8:110601697..110603770,2	MCF-7	breast:
19	chr20:49345474..49348260-chr8:110608590..110610403,2	MCF-7	breast:
20	chr8:110600715..110602433-chr8:110604852..110607355,2	MCF-7	breast:
21	chr8:110604868..110607165-chr8:110611365..110613319,2	MCF-7	breast:
22	chr8:110599959..110602833-chr8:110655392..110657661,3	MCF-7	breast:
23	chr8:110605754..110608104-chr8:110608990..110611309,2	MCF-7	breast:
24	chr8:110601515..110604234-chr8:110611916..110615052,3	MCF-7	breast:
25	chr8:110603377..110605733-chr8:110607297..110608856,2	K562	blood:
26	chr8:110603080..110605940-chr8:110624770..110626882,2	MCF-7	breast:
27	chr8:110609564..110612150-chr8:110618699..110620279,2	K562	blood:
28	chr8:110344436..110346948-chr8:110603611..110606145,2	MCF-7	breast:
29	chr8:110601011..110602738-chr8:110605572..110607359,2	K562	blood:
30	chr8:110599717..110603274-chr8:110604163..110606425,3	MCF-7	breast:

No data

Variant related genes	Relation type
SYBU	TF binding region
ENSG00000252559	TF binding region
SYBU	CpG island
ENSG00000252559	CpG island
ENSG00000248050	chromatin interactions
ENSG00000147642	chromatin interactions
ENSG00000120526	chromatin interactions
ENSG00000120533	chromatin interactions
ENSG00000124171	chromatin interactions
ENSG00000252559	chromatin interactions

Extended variants
information (count: 369 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6990312	chr8:110602317-110602318	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565521454	chr8:110602401-110602402	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs527564503	chr8:110602479-110602480	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547104659	chr8:110602527-110602528	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs570424091	chr8:110602548-110602549	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184672253	chr8:110602563-110602564	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189386728	chr8:110602570-110602571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76757611	chr8:110602639-110602640	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs11315086	chr8:110602640-110602641	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs398009330	chr8:110602650-110602651	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs182592528	chr8:110602755-110602756	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs570268114	chr8:110602772-110602773	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548155620	chr8:110602779-110602780	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs568365157	chr8:110602794-110602795	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536031232	chr8:110602802-110602803	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs556112677	chr8:110602804-110602805	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs372675561	chr8:110602812-110602813	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs184314912	chr8:110602826-110602827	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs189293746	chr8:110602834-110602835	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs557185753	chr8:110602858-110602859	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557915440	chr8:110602876-110602877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs556289895	chr8:110602888-110602889	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs148644299	chr8:110602917-110602918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371691270	chr8:110602918-110602919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575950907	chr8:110602947-110602948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562612240	chr8:110602994-110602995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577925988	chr8:110602996-110602997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138825004	chr8:110602997-110602998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577157808	chr8:110602999-110603000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs11412488	chr8:110603003-110603004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10691264	chr8:110603009-110603010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs180870030	chr8:110603030-110603031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186394823	chr8:110603158-110603159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17450520	chr8:110603219-110603220	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs116497906	chr8:110603232-110603233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74785237	chr8:110603255-110603256	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527634941	chr8:110603261-110603262	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs138693918	chr8:110603360-110603361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563935903	chr8:110603367-110603368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73702899	chr8:110603392-110603393	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7826188	chr8:110603398-110603399	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs572315970	chr8:110603409-110603410	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149358488	chr8:110603414-110603415	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs528983239	chr8:110603440-110603441	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2703382	chr8:110603479-110603480	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs144128198	chr8:110603566-110603567	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535050743	chr8:110603581-110603582	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs552001884	chr8:110603639-110603640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs571571306	chr8:110603691-110603692	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs71564046	chr8:110603722-110603723	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	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
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
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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Barrett''s adenocarcinoma	18663352	CNVD

Chromatin state (count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110553800-110613000	Weak transcription	NHLF	lung
2	chr8:110587800-110605800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:110590000-110605600	Weak transcription	K562	blood
4	chr8:110590200-110654800	Weak transcription	Lung	lung
5	chr8:110591600-110609400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:110592200-110604600	Weak transcription	Gastric	stomach
7	chr8:110594800-110606000	Weak transcription	Fetal Brain Male	brain
8	chr8:110596800-110608400	Enhancers	Fetal Intestine Large	intestine
9	chr8:110597800-110608400	Enhancers	Fetal Intestine Small	intestine
10	chr8:110598400-110602800	Enhancers	Liver	Liver
11	chr8:110598400-110605800	Weak transcription	Fetal Brain Female	brain
12	chr8:110598400-110607800	Weak transcription	Esophagus	oesophagus
13	chr8:110598600-110603600	Enhancers	Duodenum Mucosa	Duodenum
14	chr8:110598800-110605400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:110598800-110615000	Weak transcription	Ovary	ovary
16	chr8:110599400-110603200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:110599600-110602400	Enhancers	Colon Smooth Muscle	Colon
18	chr8:110599800-110603400	Enhancers	Hela-S3	cervix
19	chr8:110600000-110603200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr8:110600000-110605000	Weak transcription	Colonic Mucosa	Colon
21	chr8:110600200-110604600	Weak transcription	Pancreas	Pancrea
22	chr8:110600600-110602400	Enhancers	HepG2	liver
23	chr8:110600600-110602600	Enhancers	HUVEC	blood vessel
24	chr8:110601000-110602400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr8:110601000-110602800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:110601000-110604400	Weak transcription	Small Intestine	intestine
27	chr8:110601000-110605200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr8:110601200-110602600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:110601200-110602600	Enhancers	Stomach Smooth Muscle	stomach
30	chr8:110601400-110602400	Enhancers	Muscle Satellite Cultured Cells	--
31	chr8:110601400-110602400	Enhancers	Brain Angular Gyrus	brain
32	chr8:110601400-110602400	Enhancers	Brain Cingulate Gyrus	brain
33	chr8:110601400-110602600	Enhancers	Adipose Nuclei	Adipose
34	chr8:110601400-110602600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr8:110601400-110603200	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr8:110601400-110603400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:110601400-110603600	Enhancers	Rectal Mucosa Donor 29	rectum
38	chr8:110601600-110602400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr8:110601600-110602400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr8:110601600-110602400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:110601600-110602400	Enhancers	Psoas Muscle	Psoas
42	chr8:110601600-110602400	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr8:110601600-110602600	Enhancers	Brain Anterior Caudate	brain
44	chr8:110601600-110602600	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr8:110601600-110602600	Enhancers	Rectal Smooth Muscle	rectum
46	chr8:110601600-110602800	Enhancers	Right Atrium	heart
47	chr8:110601800-110602400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:110601800-110602400	Enhancers	Brain Germinal Matrix	brain
49	chr8:110601800-110602400	Weak transcription	Fetal Muscle Leg	muscle
50	chr8:110601800-110604600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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