Variant report

Variant	esv3419040
Chromosome Location	chr8:126271495-126339914
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1514)
CpG islands
(count:367)
Chromatin interactive
region (count:101)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1514 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:126291293-126291701	K562	blood:	n/a	n/a
2	ARID3A	chr8:126313175-126313375	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:126283705-126284039	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:126298220-126298510	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:126272253-126272580	K562	blood:	n/a	n/a
6	ARID3A	chr8:126319415-126319746	K562	blood:	n/a	n/a
7	ARID3A	chr8:126290330-126290801	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:126303611-126303860	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:126322014-126322467	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:126286155-126286419	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:126323708-126323731	K562	blood:	n/a	n/a
12	ARID3A	chr8:126286300-126286324	K562	blood:	n/a	n/a
13	ARID3A	chr8:126324850-126325282	K562	blood:	n/a	n/a
14	ARID3A	chr8:126283552-126284086	K562	blood:	n/a	n/a
15	ARID3A	chr8:126285418-126285896	HepG2	liver:	n/a	n/a
16	ATF1	chr8:126286127-126286439	K562	blood:	n/a	n/a
17	ATF1	chr8:126306987-126307275	K562	blood:	n/a	n/a
18	ATF1	chr8:126324894-126325190	K562	blood:	n/a	n/a
19	ATF1	chr8:126283618-126283979	K562	blood:	n/a	n/a
20	ATF2	chr8:126285166-126285723	GM12878	blood:	n/a	n/a
21	ATF2	chr8:126306801-126307606	GM12878	blood:	n/a	n/a
22	ATF2	chr8:126296962-126297414	GM12878	blood:	n/a	n/a
23	ATF2	chr8:126302380-126303082	GM12878	blood:	n/a	n/a
24	ATF2	chr8:126286000-126286442	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr8:126296656-126297570	GM12878	blood:	n/a	n/a
26	ATF2	chr8:126303979-126304584	GM12878	blood:	n/a	n/a
27	ATF2	chr8:126306931-126307567	GM12878	blood:	n/a	n/a
28	ATF2	chr8:126314785-126315735	GM12878	blood:	n/a	n/a
29	ATF2	chr8:126285971-126286560	GM12878	blood:	n/a	n/a
30	ATF2	chr8:126314977-126315701	GM12878	blood:	n/a	n/a
31	ATF2	chr8:126285958-126286462	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr8:126310734-126311162	GM12878	blood:	n/a	n/a
33	ATF3	chr8:126283556-126284115	A549	lung:	n/a	n/a
34	ATF3	chr8:126285332-126286634	HCT-116	colon:	n/a	chr8:126286295-126286308 chr8:126286294-126286309
35	ATF3	chr8:126283441-126284270	HCT-116	colon:	n/a	n/a
36	ATF3	chr8:126283525-126284030	K562	blood:	n/a	n/a
37	ATF3	chr8:126286045-126286544	A549	lung:	n/a	chr8:126286295-126286308 chr8:126286294-126286309
38	ATF3	chr8:126286084-126286490	K562	blood:	n/a	chr8:126286295-126286308 chr8:126286294-126286309
39	ATF3	chr8:126285944-126286611	HCT-116	colon:	n/a	chr8:126286295-126286308 chr8:126286294-126286309
40	BACH1	chr8:126302649-126302876	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr8:126322152-126322160	K562	blood:	n/a	n/a
42	BACH1	chr8:126272395-126272439	K562	blood:	n/a	n/a
43	BACH1	chr8:126302566-126302828	K562	blood:	n/a	n/a
44	BACH1	chr8:126283678-126283893	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:126283627-126284059	K562	blood:	n/a	n/a
46	BATF	chr8:126307002-126307441	GM12878	blood:	n/a	n/a
47	BATF	chr8:126315233-126315667	GM12878	blood:	n/a	n/a
48	BATF	chr8:126315020-126315643	GM12878	blood:	n/a	n/a
49	BATF	chr8:126310822-126311170	GM12878	blood:	n/a	chr8:126310982-126310993
50	BATF	chr8:126304144-126304515	GM12878	blood:	n/a	chr8:126304320-126304331

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:126285443-126285493	ECC-1	luminal epithelium:	n/a
2	chr8:126285443-126285493	ECC-1	luminal epithelium:	n/a
3	chr8:126302396-126302446	K562	blood:	n/a
4	chr8:126302396-126302446	AG04450	lung:	fetal
5	chr8:126302396-126302446	MCF-7	breast:	n/a
6	chr8:126272469-126272519	U87	brain:	n/a
7	chr8:126272469-126272519	AG04450	lung:	fetal
8	chr8:126310179-126310229	NHDF-neo	bronchial:	n/a
9	chr8:126302396-126302446	HEK293	kidney:	embryo
10	chr8:126310179-126310229	K562	blood:	n/a
11	chr8:126285443-126285493	MCF-7	breast:	n/a
12	chr8:126272469-126272519	AG09319	gingival:	n/a
13	chr8:126302396-126302446	SKMC	muscle:	n/a
14	chr8:126310179-126310229	RPTEC	kidney:	n/a
15	chr8:126272469-126272519	HUVEC	blood vessel:	n/a
16	chr8:126272469-126272519	HAEpiC	amniotic membrane:	n/a
17	chr8:126272469-126272519	BE2_C	brain:	n/a
18	chr8:126272469-126272519	SKMC	muscle:	n/a
19	chr8:126291702-126291752	AG04449	skin:	fetal
20	chr8:126310179-126310229	ECC-1	luminal epithelium:	n/a
21	chr8:126320143-126320193	AG09319	gingival:	n/a
22	chr8:126285443-126285493	AG04449	skin:	fetal
23	chr8:126302396-126302446	Jurkat	blood:	n/a
24	chr8:126302396-126302446	U87	brain:	n/a
25	chr8:126285443-126285493	AG04450	lung:	fetal
26	chr8:126310179-126310229	IMR90	lung:	fetal
27	chr8:126302396-126302446	HNPCEpiC	eye:	n/a
28	chr8:126285443-126285493	IMR90	lung:	fetal
29	chr8:126272469-126272519	BJ	skin:	n/a
30	chr8:126272469-126272519	NT2-D1	testis:	n/a
31	chr8:126302396-126302446	GM19239	blood:	n/a
32	chr8:126291702-126291752	NB4	blood:	n/a
33	chr8:126310179-126310229	HRPEpiC	eye:	n/a
34	chr8:126320143-126320193	ECC-1	luminal epithelium:	n/a
35	chr8:126320143-126320193	LNCaP	prostate:	n/a
36	chr8:126320143-126320193	GM12891	blood:	n/a
37	chr8:126302396-126302446	H1-hESC	embryonic stem cell:	embryo
38	chr8:126320143-126320193	GM12878	blood:	n/a
39	chr8:126310179-126310229	MCF10A-Er-Src	breast:	n/a
40	chr8:126302396-126302446	LNCaP	prostate:	n/a
41	chr8:126320143-126320193	PFSK-1	brain:	n/a
42	chr8:126302396-126302446	AoSMC	blood vessel:	n/a
43	chr8:126320143-126320193	K562	blood:	n/a
44	chr8:126302396-126302446	NT2-D1	testis:	n/a
45	chr8:126291702-126291752	BJ	skin:	n/a
46	chr8:126310179-126310229	AG09309	skin:	n/a
47	chr8:126291702-126291752	HRE	kidney:	n/a
48	chr8:126272469-126272519	HCF	heart:	n/a
49	chr8:126291702-126291752	A549	lung:	n/a
50	chr8:126320143-126320193	BE2_C	brain:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:126280606..126282810-chr8:126295937..126297699,2	MCF-7	breast:
2	chr8:126287701..126290542-chr8:126297201..126298945,2	MCF-7	breast:
3	chr8:126290403..126294435-chr8:126303618..126306610,4	K562	blood:
4	chr8:126326305..126327912-chr8:126330901..126332474,2	MCF-7	breast:
5	chr8:126294613..126297401-chr8:126298251..126300790,2	K562	blood:
6	chr8:126287704..126290628-chr8:126303543..126305382,2	MCF-7	breast:
7	chr8:126277652..126280153-chr8:126441312..126443511,2	K562	blood:
8	chr8:126298317..126304061-chr8:126440512..126444095,5	MCF-7	breast:
9	chr8:126318394..126322454-chr8:126322882..126325184,6	K562	blood:
10	chr8:126270583..126272682-chr8:126278710..126280304,2	MCF-7	breast:
11	chr8:126271453..126274338-chr8:126284581..126287313,3	MCF-7	breast:
12	chr8:126298759..126300267-chr8:126304142..126306532,2	MCF-7	breast:
13	chr8:126286342..126289243-chr8:126441006..126444375,7	MCF-7	breast:
14	chr8:126290473..126292876-chr8:126294905..126297324,3	K562	blood:
15	chr8:126272432..126274189-chr8:126283876..126286401,2	MCF-7	breast:
16	chr8:126272432..126274189-chr8:126283876..126286401,2	MCF-7	breast:
17	chr8:126288880..126291551-chr8:126340107..126343091,2	K562	blood:
18	chr8:126270583..126272682-chr8:126278710..126280304,2	MCF-7	breast:
19	chr8:126326305..126327912-chr8:126330901..126332474,2	MCF-7	breast:
20	chr8:126289014..126291245-chr8:126440114..126442015,2	MCF-7	breast:
21	chr8:126290287..126294135-chr8:126298870..126301775,4	K562	blood:
22	chr8:126283879..126287098-chr8:126289140..126291457,3	K562	blood:
23	chr8:126291720..126294435-chr8:126303942..126305549,2	K562	blood:
24	chr2:56773723..56776584-chr8:126325913..126327457,2	MCF-7	breast:
25	chr8:126305198..126307115-chr8:126309185..126311282,2	MCF-7	breast:
26	chr8:126300520..126302327-chr8:126305625..126307763,2	K562	blood:
27	chr8:126319216..126321150-chr8:126442622..126444295,2	MCF-7	breast:
28	chr8:126305198..126307115-chr8:126309185..126311282,2	MCF-7	breast:
29	chr8:126131877..126132657-chr8:126292156..126292668,2	K562	blood:
30	chr8:126320818..126322361-chr8:126441952..126443721,2	K562	blood:
31	chr8:126233282..126235149-chr8:126318935..126321777,2	MCF-7	breast:
32	chr8:126285610..126287271-chr8:126288882..126290405,2	MCF-7	breast:
33	chr8:126283879..126287098-chr8:126289140..126291457,3	K562	blood:
34	chr8:126322775..126325077-chr8:126329486..126331781,2	K562	blood:
35	chr8:126329552..126332451-chr8:126346573..126348088,2	MCF-7	breast:
36	chr8:126287704..126290628-chr8:126303543..126305382,2	MCF-7	breast:
37	chr8:126314491..126316142-chr8:126318788..126320646,2	K562	blood:
38	chr8:126309031..126311192-chr8:126314077..126316163,2	K562	blood:
39	chr8:126291827..126293740-chr8:126301224..126303367,2	MCF-7	breast:
40	chr8:126315465..126318192-chr8:126341334..126342938,2	K562	blood:
41	chr8:126282161..126284585-chr8:126291694..126295212,3	MCF-7	breast:
42	chr8:126268163..126270276-chr8:126271842..126273931,2	MCF-7	breast:
43	chr8:126310853..126313276-chr8:126316044..126318835,2	MCF-7	breast:
44	chr8:126283799..126286168-chr8:126444764..126446499,2	MCF-7	breast:
45	chr8:126302028..126304645-chr8:126442784..126445222,2	K562	blood:
46	chr8:126290887..126293286-chr8:126610271..126611815,2	K562	blood:
47	chr8:126322775..126325077-chr8:126329486..126331781,2	K562	blood:
48	chr8:126303707..126305559-chr8:126307667..126310106,2	K562	blood:
49	chr8:126270332..126273344-chr8:126442265..126444903,5	MCF-7	breast:
50	chr8:126337105..126338773-chr8:126354692..126356214,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIB1-11	chr8:126282846-126283142	NONHSAT128962

No data

Variant related genes	Relation type
RN7SL329P	TF binding region
RN7SL329P	CpG island
ENSG00000242170	chromatin interactions
ENSG00000173334	chromatin interactions
ENSG00000249242	chromatin interactions

Extended variants
information (count: 2631 )
Associated
traits (count: 147 )

Variant overlapped rSNPs/rCNVs (count:2631 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567131900	chr8:126271564-126271565	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562278226	chr8:126271591-126271592	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529616668	chr8:126271607-126271608	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549745439	chr8:126271678-126271679	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544943403	chr8:126271741-126271742	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144691028	chr8:126271805-126271806	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs143712812	chr8:126271824-126271825	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374204554	chr8:126271888-126271889	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs562835983	chr8:126271893-126271894	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551427595	chr8:126271894-126271895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530124430	chr8:126271927-126271928	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs571269786	chr8:126271947-126271948	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs34313605	chr8:126271948-126271949	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs371592977	chr8:126271955-126271956	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs553354446	chr8:126271995-126271996	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs573346009	chr8:126272061-126272062	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs536129859	chr8:126272131-126272132	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185060310	chr8:126272177-126272178	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146231031	chr8:126272187-126272188	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544898934	chr8:126272193-126272194	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs188699643	chr8:126272204-126272205	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578041011	chr8:126272239-126272240	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144147194	chr8:126272287-126272288	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs375865994	chr8:126272378-126272379	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566847494	chr8:126272419-126272420	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529348596	chr8:126272447-126272448	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549684707	chr8:126272495-126272496	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs563060430	chr8:126272498-126272499	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs193173382	chr8:126272534-126272535	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs374279014	chr8:126272536-126272537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs185025658	chr8:126272555-126272556	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs551689082	chr8:126272596-126272597	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs368996805	chr8:126272645-126272646	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs10283134	chr8:126272646-126272647	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs189872053	chr8:126272681-126272682	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs72720574	chr8:126272685-126272686	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs181033820	chr8:126272689-126272690	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs183973961	chr8:126272692-126272693	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs563231108	chr8:126272719-126272720	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs188310095	chr8:126272751-126272752	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs78129809	chr8:126272757-126272758	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs556849810	chr8:126272775-126272776	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538785770	chr8:126272784-126272785	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs180781489	chr8:126272799-126272800	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs187587302	chr8:126272825-126272826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547974450	chr8:126272826-126272827	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs191847285	chr8:126272829-126272830	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560604823	chr8:126272840-126272841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs10283200	chr8:126272860-126272861	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182012589	chr8:126272878-126272879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:147)

Disease	PMID	Source
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
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Ovarian cancer	21240255	CNVD
Glioma	20126413	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126239600-126274000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr8:126251400-126272000	Weak transcription	Fetal Intestine Small	intestine
3	chr8:126255200-126271600	Weak transcription	Right Atrium	heart
4	chr8:126255400-126287800	Weak transcription	Primary B cells from cord blood	blood
5	chr8:126256200-126271600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:126256400-126271800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:126257400-126273600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr8:126261400-126286000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr8:126261600-126272600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr8:126262200-126288200	Weak transcription	Ovary	ovary
11	chr8:126263400-126279000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:126264400-126272000	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:126264800-126310600	Weak transcription	Aorta	Aorta
14	chr8:126265600-126274800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr8:126265600-126296600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:126265800-126272000	Weak transcription	Adipose Nuclei	Adipose
17	chr8:126266000-126273400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:126266200-126274000	Weak transcription	Fetal Thymus	thymus
19	chr8:126267400-126271600	Weak transcription	Gastric	stomach
20	chr8:126267400-126276400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr8:126267800-126273200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr8:126267800-126274600	Weak transcription	Primary T cells from cord blood	blood
23	chr8:126267800-126276200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr8:126268000-126273400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr8:126268200-126271600	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:126268200-126273200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr8:126268200-126273800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr8:126268600-126280800	Weak transcription	Primary monocytes fromperipheralblood	blood
29	chr8:126270200-126272800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr8:126270400-126271800	Weak transcription	NHEK	skin
31	chr8:126270800-126272200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:126271000-126271600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr8:126271000-126271800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr8:126271400-126271600	Enhancers	Lung	lung
35	chr8:126271400-126271600	Enhancers	Psoas Muscle	Psoas
36	chr8:126271400-126271800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:126271400-126271800	Weak transcription	K562	blood
38	chr8:126271400-126272200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr8:126271400-126272800	Flanking Active TSS	Hela-S3	cervix
40	chr8:126271600-126271800	Enhancers	Right Atrium	heart
41	chr8:126271600-126272400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:126271600-126272600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr8:126271600-126273600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:126271600-126273800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:126271600-126275600	Weak transcription	Psoas Muscle	Psoas
46	chr8:126271800-126272000	Enhancers	A549	lung
47	chr8:126271800-126272200	Weak transcription	Right Atrium	heart
48	chr8:126271800-126272200	Enhancers	NHEK	skin
49	chr8:126271800-126272800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:126271800-126272800	Enhancers	Placenta Amnion	Placenta Amnion

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