Variant report

Variant	nsv605327
Chromosome Location	chr6:167185674-167360389
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2312)
CpG islands
(count:3787)
Chromatin interactive
region (count:87)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167200218-167200546	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167264235-167264605	K562	blood:	n/a	n/a
3	ARID3A	chr6:167356202-167356749	K562	blood:	n/a	n/a
4	ARID3A	chr6:167353960-167354308	K562	blood:	n/a	n/a
5	ARID3A	chr6:167188768-167188974	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167324658-167325218	K562	blood:	n/a	n/a
7	ATF1	chr6:167328715-167329352	K562	blood:	n/a	n/a
8	ATF1	chr6:167356210-167356679	K562	blood:	n/a	n/a
9	ATF1	chr6:167260351-167260433	K562	blood:	n/a	n/a
10	ATF1	chr6:167324192-167325358	K562	blood:	n/a	n/a
11	ATF1	chr6:167320881-167321225	K562	blood:	n/a	n/a
12	ATF1	chr6:167190190-167190394	K562	blood:	n/a	n/a
13	ATF1	chr6:167238143-167238339	K562	blood:	n/a	n/a
14	ATF1	chr6:167264121-167264564	K562	blood:	n/a	n/a
15	ATF1	chr6:167213787-167214099	K562	blood:	n/a	n/a
16	ATF1	chr6:167287376-167287880	K562	blood:	n/a	n/a
17	ATF1	chr6:167240077-167240150	K562	blood:	n/a	n/a
18	ATF1	chr6:167255068-167255231	K562	blood:	n/a	n/a
19	ATF1	chr6:167345566-167345627	K562	blood:	n/a	n/a
20	ATF2	chr6:167243498-167244485	GM12878	blood:	n/a	n/a
21	ATF2	chr6:167320633-167321310	GM12878	blood:	n/a	n/a
22	ATF2	chr6:167243583-167244420	GM12878	blood:	n/a	n/a
23	ATF2	chr6:167200233-167200574	GM12878	blood:	n/a	n/a
24	ATF2	chr6:167247521-167247974	GM12878	blood:	n/a	n/a
25	ATF2	chr6:167247492-167247983	GM12878	blood:	n/a	n/a
26	ATF2	chr6:167263194-167263607	GM12878	blood:	n/a	n/a
27	ATF3	chr6:167356221-167356691	K562	blood:	n/a	n/a
28	BACH1	chr6:167196277-167196415	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:167198886-167198899	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167276270-167276880	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167354196-167354394	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167216081-167216348	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167290924-167291004	K562	blood:	n/a	n/a
34	BACH1	chr6:167354162-167354365	K562	blood:	n/a	n/a
35	BACH1	chr6:167317880-167318113	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr6:167197282-167197733	GM12878	blood:	n/a	n/a
37	BATF	chr6:167247528-167247858	GM12878	blood:	n/a	n/a
38	BATF	chr6:167243652-167243968	GM12878	blood:	n/a	n/a
39	BATF	chr6:167263166-167263351	GM12878	blood:	n/a	n/a
40	BATF	chr6:167243631-167244353	GM12878	blood:	n/a	n/a
41	BATF	chr6:167197269-167197664	GM12878	blood:	n/a	n/a
42	BATF	chr6:167320864-167321175	GM12878	blood:	n/a	n/a
43	BATF	chr6:167263100-167263391	GM12878	blood:	n/a	n/a
44	BATF	chr6:167247594-167247848	GM12878	blood:	n/a	n/a
45	BCL11A	chr6:167243593-167243973	GM12878	blood:	n/a	n/a
46	BCL11A	chr6:167244040-167244445	GM12878	blood:	n/a	n/a
47	BCL11A	chr6:167197263-167197805	GM12878	blood:	n/a	n/a
48	BCL11A	chr6:167243668-167243958	GM12878	blood:	n/a	n/a
49	BCL11A	chr6:167244064-167244380	GM12878	blood:	n/a	n/a
50	BCL11A	chr6:167197224-167197721	GM12878	blood:	n/a	n/a

(count:3787 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167276275-167276325	SK-N-MC	brain:	n/a
2	chr6:167314433-167314483	HEEpiC	esophagus:	n/a
3	chr6:167279026-167279076	MCF-7	breast:	n/a
4	chr6:167188753-167188803	HRPEpiC	eye:	n/a
5	chr6:167276359-167276409	SK-N-SH_RA	brain:	n/a
6	chr6:167276275-167276325	SK-N-MC	brain:	n/a
7	chr6:167314433-167314483	HEEpiC	esophagus:	n/a
8	chr6:167279026-167279076	MCF-7	breast:	n/a
9	chr6:167188753-167188803	HRPEpiC	eye:	n/a
10	chr6:167276359-167276409	SK-N-SH_RA	brain:	n/a
11	chr6:167276650-167276700	HRE	kidney:	n/a
12	chr6:167312423-167312473	GM12891	blood:	n/a
13	chr6:167276650-167276700	NHBE	bronchial:	n/a
14	chr6:167192573-167192623	GM06990	blood:	n/a
15	chr6:167263025-167263075	ProgFib	skin:	n/a
16	chr6:167314233-167314283	ProgFib	skin:	n/a
17	chr6:167284353-167284403	PrEC	prostate:	n/a
18	chr6:167250429-167250479	IMR90	lung:	fetal
19	chr6:167275684-167275734	AG09319	gingival:	n/a
20	chr6:167314962-167315012	GM19239	blood:	n/a
21	chr6:167276359-167276409	HEK293	kidney:	embryo
22	chr6:167313144-167313194	HRE	kidney:	n/a
23	chr6:167190149-167190199	HNPCEpiC	eye:	n/a
24	chr6:167250429-167250479	CMK	blood:	n/a
25	chr6:167317799-167317849	A549	lung:	n/a
26	chr6:167263193-167263243	SK-N-SH	brain:	n/a
27	chr6:167192488-167192538	GM12891	blood:	n/a
28	chr6:167313267-167313317	AG04450	lung:	fetal
29	chr6:167313144-167313194	GM12892	blood:	n/a
30	chr6:167275781-167275831	HNPCEpiC	eye:	n/a
31	chr6:167287812-167287862	SAEC	small airway:	n/a
32	chr6:167287812-167287862	AG10803	skin:	n/a
33	chr6:167284353-167284403	HRPEpiC	eye:	n/a
34	chr6:167275755-167275805	Caco-2	colon:	n/a
35	chr6:167202522-167202572	Hela-S3	cervix:	n/a
36	chr6:167190226-167190276	HEEpiC	esophagus:	n/a
37	chr6:167314433-167314483	Caco-2	colon:	n/a
38	chr6:167275755-167275805	HRE	kidney:	n/a
39	chr6:167276359-167276409	HepG2	liver:	n/a
40	chr6:167283835-167283885	NH-A	brain:	n/a
41	chr6:167318108-167318158	GM12878	blood:	n/a
42	chr6:167263454-167263504	Jurkat	blood:	n/a
43	chr6:167280873-167280923	SAEC	small airway:	n/a
44	chr6:167284353-167284403	RPTEC	kidney:	n/a
45	chr6:167263193-167263243	Hepatocyte	liver:	n/a
46	chr6:167250513-167250563	SK-N-MC	brain:	n/a
47	chr6:167275832-167275882	GM06990	blood:	n/a
48	chr6:167314233-167314283	BE2_C	brain:	n/a
49	chr6:167250541-167250591	AG10803	skin:	n/a
50	chr6:167280873-167280923	GM12878	blood:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:167185035..167187575-chr6:167358179..167360344,2	K562	blood:
2	chr6:167188128..167189127-chr6:167402681..167403785,5	MCF-7	breast:
3	chr6:167188403..167189352-chr6:167555280..167555897,4	K562	blood:
4	chr6:167187491..167191588-chr6:167191761..167196442,4	K562	blood:
5	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
6	chr6:167316933..167319053-chr6:167320800..167322909,2	K562	blood:
7	chr6:167327598..167330047-chr6:167367070..167369538,2	K562	blood:
8	chr6:167353995..167356024-chr6:167413983..167416895,2	K562	blood:
9	chr6:167200059..167200966-chr6:167402403..167403438,4	K562	blood:
10	chr6:167200327..167200836-chr6:167459295..167459843,2	K562	blood:
11	chr6:167356381..167359345-chr6:167359373..167361500,2	K562	blood:
12	chr6:167320098..167322424-chr6:167348297..167350309,2	K562	blood:
13	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
14	chr6:167339433..167341286-chr6:167346948..167348863,2	K562	blood:
15	chr6:167232177..167234702-chr6:167235338..167237852,2	K562	blood:
16	chr6:167274608..167276505-chr6:167368344..167370567,2	MCF-7	breast:
17	chr6:167244883..167247077-chr6:167250402..167252258,2	K562	blood:
18	chr6:167327579..167329886-chr6:167332499..167334100,2	K562	blood:
19	chr6:167187421..167189873-chr6:167410909..167412648,3	MCF-7	breast:
20	chr6:167285809..167288027-chr6:167289441..167291420,2	K562	blood:
21	chr6:167344148..167347081-chr6:167347085..167349759,2	K562	blood:
22	chr6:167324257..167326145-chr6:167328411..167330868,2	K562	blood:
23	chr6:167179347..167182239-chr6:167183994..167186208,2	K562	blood:
24	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
25	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:
26	chr6:167198453..167200233-chr6:167409946..167412844,2	K562	blood:
27	chr6:167339433..167341286-chr6:167346948..167348863,2	K562	blood:
28	chr6:167172089..167173654-chr6:167192090..167194256,2	K562	blood:
29	chr6:167186547..167188661-chr6:167553295..167555799,2	K562	blood:
30	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
31	chr6:167307243..167309166-chr6:167369086..167371594,2	MCF-7	breast:
32	chr6:167263153..167265718-chr6:167272365..167274771,2	K562	blood:
33	chr6:167287783..167290388-chr6:167293843..167295742,3	K562	blood:
34	chr6:167187969..167188996-chr6:167555512..167556325,4	MCF-7	breast:
35	chr6:167287783..167289646-chr6:167293843..167295409,2	K562	blood:
36	chr6:167187491..167189760-chr6:167193508..167196442,3	K562	blood:
37	chr6:167320098..167322424-chr6:167348297..167350309,2	K562	blood:
38	chr6:167212524..167215294-chr6:167216154..167217898,2	K562	blood:
39	chr6:167221917..167225316-chr6:167226153..167228902,3	K562	blood:
40	chr6:167244459..167246952-chr6:167353805..167356355,2	K562	blood:
41	chr6:167356381..167359345-chr6:167359373..167361500,2	K562	blood:
42	chr6:167120732..167121236-chr6:167185691..167186290,2	MCF-7	breast:
43	chr6:167324476..167326634-chr6:167338829..167341348,2	K562	blood:
44	chr6:167234510..167236019-chr6:167237889..167239702,2	MCF-7	breast:
45	chr6:167280811..167283547-chr6:167284862..167287593,2	K562	blood:
46	chr6:167212524..167215294-chr6:167216154..167217898,2	K562	blood:
47	chr6:167187491..167191588-chr6:167191761..167196442,4	K562	blood:
48	chr6:167188755..167189454-chr6:167555413..167556221,2	MCF-7	breast:
49	chr6:166870182..166872414-chr6:167234943..167236564,2	K562	blood:
50	chr6:167218838..167220495-chr6:167220755..167222846,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASET2-3	chr6:167315613-167316152	NONHSAT116059
2	lnc-RPS6KA2-2	chr6:167357853-167360151	NONHSAT116065
3	lnc-FGFR1OP-1	chr6:167319514-167321259	l_3322_chr6:167314133-167321259_testes
4	lnc-RNASET2-3	chr6:167317848-167318299	NONHSAT116059
5	lnc-FGFR1OP-11	chr6:167237176-167237266	NONHSAT116055
6	lnc-FGFR1OP-11	chr6:167237778-167238313	NONHSAT116055
7	lnc-FGFR1OP-1	chr6:167317788-167318557	NR_046644
8	lnc-FGFR1OP-1	chr6:167321422-167321647	l_3322_chr6:167314133-167321259_testes
9	lnc-FGFR1OP-1	chr6:167317788-167318323	XLOC_005539
10	lnc-FGFR1OP-10	chr6:167242352-167242576	l_3320_chr6:167242351-167255400_testes
11	lnc-FGFR1OP-1	chr6:167317186-167317276	XLOC_005539
12	lnc-FGFR1OP-10	chr6:167254947-167255400	l_3320_chr6:167242351-167255400_testes
13	lnc-FGFR1OP-1	chr6:167314134-167317318	l_3322_chr6:167314133-167321259_testes
14	lnc-FGFR1OP-1	chr6:167317186-167317276	NR_046644
15	lnc-RNASET2-2	chr6:167346863-167347624	NONHSAT116063

No data

Variant related genes	Relation type
RNASET2	TF binding region
RPS6KA2	TF binding region
ENSG00000197146	TF binding region
RPS6KA2-AS1	TF binding region
RNASET2	CpG island
RPS6KA2	CpG island
ENSG00000197146	CpG island
RPS6KA2-AS1	CpG island
ENSG00000231654	chromatin interactions
ENSG00000249141	chromatin interactions
ENSG00000213066	chromatin interactions
ENSG00000272980	chromatin interactions
ENSG00000265828	chromatin interactions
ENSG00000026297	chromatin interactions
ENSG00000197146	chromatin interactions
ENSG00000227598	chromatin interactions

Extended variants
information (count: 7570 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:7570 , 50 per page) page: 1 2 3 4 5 6 7 ... 152

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6456123	chr6:167185674-167185675	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144334798	chr6:167185695-167185696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs34022746	chr6:167185734-167185735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs116715054	chr6:167185751-167185752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540175849	chr6:167185782-167185783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs537572962	chr6:167185806-167185807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556198032	chr6:167185862-167185863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs563562300	chr6:167185899-167185900	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140843017	chr6:167185922-167185923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372668624	chr6:167185949-167185950	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs17590608	chr6:167186024-167186025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs191701443	chr6:167186042-167186043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543161799	chr6:167186049-167186050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543287709	chr6:167186054-167186055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs79280772	chr6:167186065-167186066	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs62438720	chr6:167186112-167186113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs547396265	chr6:167186128-167186129	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs559719187	chr6:167186153-167186154	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117841668	chr6:167186154-167186155	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs11755085	chr6:167186188-167186189	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368345608	chr6:167186214-167186215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183917232	chr6:167186215-167186216	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs551649037	chr6:167186264-167186265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs76168680	chr6:167186271-167186272	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144705475	chr6:167186327-167186328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2072637	chr6:167186353-167186354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
27	rs549255478	chr6:167186355-167186356	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567174696	chr6:167186433-167186434	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200432364	chr6:167186443-167186444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs188244044	chr6:167186462-167186463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147880702	chr6:167186463-167186464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs58374957	chr6:167186482-167186483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368586801	chr6:167186509-167186510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs76829116	chr6:167186521-167186522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572282027	chr6:167186593-167186594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542971716	chr6:167186652-167186653	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs57722156	chr6:167186663-167186664	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs73035537	chr6:167186737-167186738	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78375724	chr6:167186739-167186740	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35517912	chr6:167186748-167186749	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543752153	chr6:167186769-167186770	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs62438721	chr6:167186776-167186777	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532694795	chr6:167186835-167186836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547897175	chr6:167186840-167186841	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs397832487	chr6:167186875-167186876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs193102024	chr6:167186879-167186880	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549024954	chr6:167186920-167186921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560227933	chr6:167186944-167186945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531214520	chr6:167186991-167186992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549785477	chr6:167187010-167187011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Autism	22549408	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	CNVD

Chromatin state (count:1805 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167173400-167189000	Weak transcription	Brain Anterior Caudate	brain
2	chr6:167180200-167186000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr6:167182200-167218600	Weak transcription	Right Atrium	heart
4	chr6:167184200-167189000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:167184400-167189000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167184800-167187800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:167184800-167188800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:167185200-167186800	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr6:167185200-167189000	Weak transcription	Fetal Thymus	thymus
10	chr6:167186600-167186800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:167186600-167186800	Bivalent Enhancer	Placenta	Placenta
12	chr6:167186800-167188800	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr6:167188400-167189200	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr6:167188400-167189600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr6:167188600-167189200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr6:167188800-167189200	Enhancers	Primary B cells from peripheral blood	blood
17	chr6:167188800-167189600	Flanking Bivalent TSS/Enh	HepG2	liver
18	chr6:167188800-167190800	Enhancers	Primary neutrophils fromperipheralblood	blood
19	chr6:167189000-167189200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:167189000-167189200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
21	chr6:167189000-167189400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr6:167189000-167189400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr6:167189000-167189400	Enhancers	Brain Anterior Caudate	brain
24	chr6:167189000-167189400	Enhancers	Fetal Brain Male	brain
25	chr6:167189000-167189400	Bivalent Enhancer	K562	blood
26	chr6:167189000-167189600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr6:167189000-167189600	Enhancers	Fetal Thymus	thymus
28	chr6:167189400-167190600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr6:167189400-167192200	Weak transcription	Fetal Brain Male	brain
30	chr6:167189600-167193200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr6:167190000-167190400	Enhancers	Lung	lung
32	chr6:167190400-167195200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr6:167190800-167191000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr6:167190800-167195200	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr6:167192200-167192400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr6:167192200-167192800	Enhancers	Fetal Brain Male	brain
37	chr6:167192400-167192800	Enhancers	Fetal Brain Female	brain
38	chr6:167192400-167192800	Enhancers	Pancreas	Pancrea
39	chr6:167192400-167195200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr6:167192600-167192800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr6:167193000-167193400	Enhancers	Pancreas	Pancrea
42	chr6:167193200-167193800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:167193800-167194800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:167194800-167195200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr6:167195200-167195400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:167195200-167195400	Enhancers	Brain Inferior Temporal Lobe	brain
47	chr6:167195200-167196200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr6:167195400-167196200	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr6:167196200-167196400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr6:167196400-167198600	Weak transcription	Brain Inferior Temporal Lobe	brain

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