Variant report

Variant	esv1802127
Chromosome Location	chr8:67995266-68076723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:267)
CpG islands
(count:122)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:267 , 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	chr8:68022007-68022483	K562	blood:	n/a	n/a
2	ARID3A	chr8:68032334-68032484	K562	blood:	n/a	n/a
3	ARID3A	chr8:68009478-68009999	K562	blood:	n/a	n/a
4	ARID3A	chr8:68026510-68027171	K562	blood:	n/a	n/a
5	ARID3A	chr8:68065780-68065880	K562	blood:	n/a	n/a
6	ATF1	chr8:68022028-68022347	K562	blood:	n/a	n/a
7	BACH1	chr8:67998010-67998079	K562	blood:	n/a	n/a
8	BACH1	chr8:68013863-68013960	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:68071443-68071797	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:68021797-68022409	K562	blood:	n/a	n/a
11	CBX3	chr8:68021765-68022411	K562	blood:	n/a	n/a
12	CBX3	chr8:68021929-68022308	K562	blood:	n/a	n/a
13	CCNT2	chr8:68026748-68027196	K562	blood:	n/a	n/a
14	CCNT2	chr8:68021959-68022495	K562	blood:	n/a	n/a
15	CEBPB	chr8:68057085-68057376	H1-hESC	embryonic stem cell:	n/a	chr8:68057257-68057268
16	CEBPB	chr8:68044398-68044717	MCF-7	breast:	n/a	chr8:68044543-68044554
17	CEBPB	chr8:68007624-68007824	A549	lung:	n/a	chr8:68007705-68007716
18	CEBPB	chr8:68049232-68049274	K562	blood:	n/a	n/a
19	CEBPB	chr8:68044457-68044696	K562	blood:	n/a	chr8:68044543-68044554
20	CEBPB	chr8:68057162-68057407	MCF-7	breast:	n/a	chr8:68057257-68057268
21	CEBPB	chr8:68057096-68057354	A549	lung:	n/a	chr8:68057257-68057268
22	CEBPB	chr8:68044387-68044724	HepG2	liver:	n/a	chr8:68044543-68044554
23	CEBPB	chr8:68007657-68007868	HepG2	liver:	n/a	chr8:68007705-68007716
24	CEBPB	chr8:68044368-68044721	A549	lung:	n/a	chr8:68044543-68044554
25	CEBPB	chr8:68053740-68053941	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:68044365-68044733	HepG2	liver:	n/a	chr8:68044543-68044554
27	CEBPB	chr8:68053792-68053906	K562	blood:	n/a	n/a
28	CEBPB	chr8:68057093-68057349	IMR90	lung:	n/a	chr8:68057257-68057268
29	CEBPB	chr8:68021686-68022377	K562	blood:	n/a	n/a
30	CEBPB	chr8:67996446-67996798	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:68021700-68022376	K562	blood:	n/a	n/a
32	CEBPB	chr8:68057094-68057354	Hela-S3	cervix:	n/a	chr8:68057257-68057268
33	CEBPB	chr8:68065864-68065964	K562	blood:	n/a	chr8:68065878-68065891
34	CEBPB	chr8:68022022-68022340	K562	blood:	n/a	n/a
35	CEBPB	chr8:68053800-68053928	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:68076544-68076895	HepG2	liver:	n/a	chr8:68076724-68076735
37	CEBPB	chr8:68057084-68057433	K562	blood:	n/a	chr8:68057257-68057268
38	CEBPB	chr8:68040311-68040611	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:68057090-68057352	HepG2	liver:	n/a	chr8:68057257-68057268
40	CEBPB	chr8:68044396-68044716	IMR90	lung:	n/a	chr8:68044543-68044554
41	CEBPB	chr8:68044385-68044681	Hela-S3	cervix:	n/a	chr8:68044543-68044554
42	CEBPB	chr8:68076544-68076875	A549	lung:	n/a	chr8:68076724-68076735
43	CEBPB	chr8:68003361-68003523	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:68007700-68007715	K562	blood:	n/a	n/a
45	CEBPB	chr8:68044426-68044629	HepG2	liver:	n/a	chr8:68044543-68044554
46	CEBPB	chr8:68021723-68021959	K562	blood:	n/a	n/a
47	CEBPD	chr8:68021821-68022549	K562	blood:	n/a	n/a
48	CEBPD	chr8:68021932-68022528	K562	blood:	n/a	n/a
49	CEBPD	chr8:68026644-68027103	K562	blood:	n/a	n/a
50	CEBPD	chr8:68026684-68027035	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67996256-67996306	GM12878	blood:	n/a
2	chr8:68022262-68022312	NHDF-neo	bronchial:	n/a
3	chr8:67996256-67996306	HNPCEpiC	eye:	n/a
4	chr8:67996256-67996306	SK-N-SH	brain:	n/a
5	chr8:67996256-67996306	PrEC	prostate:	n/a
6	chr8:67996256-67996306	SK-N-SH_RA	brain:	n/a
7	chr8:68022262-68022312	CMK	blood:	n/a
8	chr8:67996256-67996306	BE2_C	brain:	n/a
9	chr8:67996256-67996306	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:67996256-67996306	H1-hESC	embryonic stem cell:	embryo
11	chr8:68022262-68022312	AG09309	skin:	n/a
12	chr8:68022262-68022312	H1-hESC	embryonic stem cell:	embryo
13	chr8:68022262-68022312	NHBE	bronchial:	n/a
14	chr8:67996256-67996306	NHDF-neo	bronchial:	n/a
15	chr8:67996256-67996306	HCM	heart:	n/a
16	chr8:68022262-68022312	HRPEpiC	eye:	n/a
17	chr8:67996256-67996306	HRPEpiC	eye:	n/a
18	chr8:68022262-68022312	SAEC	small airway:	n/a
19	chr8:68022262-68022312	AoSMC	blood vessel:	n/a
20	chr8:68022262-68022312	ovcar-3	ovarian:	n/a
21	chr8:67996256-67996306	AG04450	lung:	fetal
22	chr8:67996256-67996306	GM12891	blood:	n/a
23	chr8:67996256-67996306	NT2-D1	testis:	n/a
24	chr8:68022262-68022312	AG04449	skin:	fetal
25	chr8:67996256-67996306	HCPEpiC	choroid plexus:	n/a
26	chr8:67996256-67996306	HRCEpiC	kidney:	n/a
27	chr8:67996256-67996306	A549	lung:	n/a
28	chr8:67996256-67996306	HCF	heart:	n/a
29	chr8:68022262-68022312	ECC-1	luminal epithelium:	n/a
30	chr8:67996256-67996306	HL-60	blood:	n/a
31	chr8:67996256-67996306	PFSK-1	brain:	n/a
32	chr8:67996256-67996306	PANC-1	pancreas:	n/a
33	chr8:68022262-68022312	ProgFib	skin:	n/a
34	chr8:67996256-67996306	AG09309	skin:	n/a
35	chr8:68022262-68022312	NH-A	brain:	n/a
36	chr8:67996256-67996306	Caco-2	colon:	n/a
37	chr8:67996256-67996306	CMK	blood:	n/a
38	chr8:68022262-68022312	GM12891	blood:	n/a
39	chr8:67996256-67996306	T-47D	breast:	n/a
40	chr8:68022262-68022312	HUVEC	blood vessel:	n/a
41	chr8:68022262-68022312	HEEpiC	esophagus:	n/a
42	chr8:67996256-67996306	K562	blood:	n/a
43	chr8:68022262-68022312	HCT-116	colon:	n/a
44	chr8:68022262-68022312	HCF	heart:	n/a
45	chr8:68022262-68022312	GM12892	blood:	n/a
46	chr8:68022262-68022312	BJ	skin:	n/a
47	chr8:68022262-68022312	MCF-7	breast:	n/a
48	chr8:68022262-68022312	NT2-D1	testis:	n/a
49	chr8:68022262-68022312	Caco-2	colon:	n/a
50	chr8:68022262-68022312	BE2_C	brain:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
2	chr8:68059036..68061219-chr8:68063581..68066022,2	K562	blood:
3	chr8:67976406..67978604-chr8:68001660..68003649,2	K562	blood:
4	chr8:67990677..67996100-chr8:67997550..68001970,5	K562	blood:
5	chr8:67977500..67979616-chr8:68012864..68015307,2	MCF-7	breast:
6	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
7	chr8:68053402..68056915-chr8:68068462..68071572,3	K562	blood:
8	chr8:68059036..68061219-chr8:68063581..68066022,2	K562	blood:
9	chr8:67831819..67834409-chr8:68034635..68036146,2	K562	blood:
10	chr8:67976148..67978802-chr8:68002770..68006546,3	K562	blood:
11	chr8:67972943..67975596-chr8:68018499..68020394,2	MCF-7	breast:
12	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
13	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
14	chr8:67985384..67988219-chr8:68025028..68027428,3	K562	blood:
15	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
16	chr8:67990308..67993966-chr8:67998315..68001185,4	K562	blood:
17	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
18	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
19	chr8:68030814..68032510-chr8:68038981..68041972,2	K562	blood:
20	chr8:68066129..68069885-chr8:68074156..68076683,4	K562	blood:
21	chr8:67975625..67978171-chr8:68007327..68009716,2	MCF-7	breast:
22	chr8:68034598..68037205-chr8:68038455..68041133,2	MCF-7	breast:
23	chr8:68038512..68041443-chr8:68043392..68045199,2	MCF-7	breast:
24	chr8:68019313..68021388-chr8:68023240..68024925,2	K562	blood:
25	chr8:67973427..67978093-chr8:68011189..68018690,8	K562	blood:
26	chr8:67831601..67833863-chr8:68059505..68062271,2	MCF-7	breast:
27	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
28	chr8:68021467..68023804-chr8:68064580..68067516,2	K562	blood:
29	chr8:68039129..68041953-chr8:68044102..68045625,2	K562	blood:
30	chr8:68074799..68076714-chr8:68078840..68080441,2	K562	blood:
31	chr8:67973913..67977272-chr8:68024656..68026462,3	K562	blood:
32	chr8:68034598..68037205-chr8:68038455..68041133,2	MCF-7	breast:
33	chr8:67978540..67980056-chr8:67997064..67998672,2	K562	blood:
34	chr8:67831270..67834163-chr8:68004872..68007019,2	K562	blood:
35	chr8:67831901..67834274-chr8:68007659..68009308,2	K562	blood:
36	chr8:68006861..68009461-chr8:68010974..68012762,2	K562	blood:
37	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
38	chr8:67977046..67978803-chr8:67992749..67996349,3	K562	blood:
39	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
40	chr2:88315577..88316138-chr8:68058073..68058573,2	MCF-7	breast:
41	chr8:67830248..67833464-chr8:68001607..68004691,3	K562	blood:
42	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
43	chr8:68049843..68052686-chr8:68057977..68059611,2	K562	blood:
44	chr8:68038512..68041443-chr8:68043392..68045199,2	MCF-7	breast:
45	chr8:67996527..67998674-chr8:68001336..68003420,2	K562	blood:
46	chr8:68062959..68065035-chr8:68067846..68069927,2	MCF-7	breast:
47	chr8:68021467..68023804-chr8:68064580..68067516,2	K562	blood:
48	chr8:67969000..67971915-chr8:68028216..68029773,2	K562	blood:
49	chr8:67997747..68001730-chr8:68001894..68004625,4	K562	blood:
50	chr8:67973320..67975625-chr8:67995468..67997290,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COPS5-1	chr8:67997226-67997654	expReg_chr8_3344_-

No data

Variant related genes	Relation type
RNA5SP268	TF binding region
ENSG00000250869	TF binding region
CSPP1	TF binding region
COPS5	TF binding region
RNA5SP268	CpG island
ENSG00000250869	CpG island
CSPP1	CpG island
COPS5	CpG island
ENSG00000252637	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000266491	chromatin interactions

Extended variants
information (count: 2556 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2556 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13278667	chr8:67995266-67995267	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs540422438	chr8:67995301-67995302	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560320698	chr8:67995369-67995370	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs13277391	chr8:67995377-67995378	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs185793763	chr8:67995432-67995433	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569439379	chr8:67995481-67995482	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529353128	chr8:67995495-67995496	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs543122452	chr8:67995545-67995546	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs562711467	chr8:67995581-67995582	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs538037379	chr8:67995591-67995592	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs531599665	chr8:67995594-67995595	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs75671377	chr8:67995724-67995725	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs75931073	chr8:67995783-67995784	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs373485985	chr8:67995785-67995786	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs55758408	chr8:67995808-67995809	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs571600286	chr8:67995822-67995823	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs578170969	chr8:67995921-67995922	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs181338803	chr8:67995951-67995952	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs186343860	chr8:67995955-67995956	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567885718	chr8:67995969-67995970	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs190798881	chr8:67996026-67996027	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs535169936	chr8:67996092-67996093	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs537837237	chr8:67996140-67996141	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs555462751	chr8:67996179-67996180	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs538448660	chr8:67996187-67996188	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs537829087	chr8:67996248-67996249	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs557830673	chr8:67996262-67996263	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545705855	chr8:67996299-67996300	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs182841853	chr8:67996367-67996368	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs553650644	chr8:67996371-67996372	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs573800749	chr8:67996446-67996447	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs186566284	chr8:67996475-67996476	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs140212635	chr8:67996544-67996545	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs531732923	chr8:67996572-67996573	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs190971380	chr8:67996573-67996574	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs145624696	chr8:67996608-67996609	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs117672318	chr8:67996687-67996688	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs147727151	chr8:67996705-67996706	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs149191066	chr8:67996721-67996722	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs142372809	chr8:67996732-67996733	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs530321352	chr8:67996746-67996747	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs373153790	chr8:67996753-67996754	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529041099	chr8:67996815-67996816	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs376956242	chr8:67996816-67996817	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs183134638	chr8:67996834-67996835	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs533850283	chr8:67996866-67996867	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs558439399	chr8:67996877-67996878	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs571903166	chr8:67996975-67996976	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs544175572	chr8:67996983-67996984	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs187587967	chr8:67996984-67996985	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	17142309	CNVD
Glioblastoma multiforme	19115005	CNVD
Breast cancer	22522925	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1817 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67977600-67998200	Weak transcription	Gastric	stomach
2	chr8:67977800-68009200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:67977800-68010000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr8:67977800-68013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr8:67977800-68021800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:67977800-68044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr8:67978000-67995400	Weak transcription	Colonic Mucosa	Colon
8	chr8:67978000-67996800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr8:67978000-68012200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:67978200-68006000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr8:67978200-68012600	Weak transcription	HUVEC	blood vessel
12	chr8:67978200-68074400	Weak transcription	Esophagus	oesophagus
13	chr8:67978400-68044800	Weak transcription	Brain Angular Gyrus	brain
14	chr8:67978400-68045600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr8:67978600-67998000	Weak transcription	NHEK	skin
16	chr8:67978600-68007000	Weak transcription	Brain Substantia Nigra	brain
17	chr8:67978600-68008000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:67978600-68031200	Weak transcription	Fetal Heart	heart
19	chr8:67978600-68074200	Weak transcription	Psoas Muscle	Psoas
20	chr8:67978800-68044200	Weak transcription	Colon Smooth Muscle	Colon
21	chr8:67979400-68013200	Weak transcription	Pancreas	Pancrea
22	chr8:67984200-68009200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr8:67986400-68045400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr8:67988000-68004800	Weak transcription	Thymus	Thymus
25	chr8:67988200-68007000	Weak transcription	Fetal Brain Male	brain
26	chr8:67988200-68007000	Weak transcription	Fetal Kidney	kidney
27	chr8:67988200-68014000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr8:67988200-68038800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:67988200-68074800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr8:67988400-68002800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
31	chr8:67988400-68035000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr8:67990400-68074400	Weak transcription	Spleen	Spleen
33	chr8:67990800-67996000	Weak transcription	NH-A	brain
34	chr8:67990800-68009600	Weak transcription	Small Intestine	intestine
35	chr8:67991000-67999000	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:67991000-68021400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:67991200-68011400	Weak transcription	Fetal Intestine Small	intestine
38	chr8:67991200-68035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:67991400-67997800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr8:67991600-68007800	Weak transcription	Right Ventricle	heart
41	chr8:67991800-67996000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr8:67991800-68003000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:67991800-68006200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:67991800-68036800	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr8:67992000-67999400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr8:67992000-67999600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr8:67992200-67995800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr8:67992200-67995800	Weak transcription	NHDF-Ad	bronchial
49	chr8:67992200-68002600	Weak transcription	Primary B cells from peripheral blood	blood
50	chr8:67993000-67998400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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