Variant report

Variant	nsv2692
Chromosome Location	chr2:39065768-39111871
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:854)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:39102837-39103146	HepG2	liver:	n/a	n/a
2	ATF2	chr2:39077094-39077589	GM12878	blood:	n/a	n/a
3	ATF3	chr2:39102761-39103189	K562	blood:	n/a	n/a
4	ATF3	chr2:39102558-39103167	A549	lung:	n/a	n/a
5	BACH1	chr2:39102811-39102997	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:39077263-39077563	GM12878	blood:	n/a	n/a
7	BATF	chr2:39077183-39077475	GM12878	blood:	n/a	n/a
8	BCL3	chr2:39102714-39103492	A549	lung:	n/a	chr2:39103181-39103194
9	BCLAF1	chr2:39077190-39077655	GM12878	blood:	n/a	chr2:39077369-39077378
10	BHLHE40	chr2:39102732-39103196	K562	blood:	n/a	n/a
11	BHLHE40	chr2:39102770-39103325	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:39102670-39103437	HepG2	liver:	n/a	n/a
13	BHLHE40	chr2:39077229-39077477	GM12878	blood:	n/a	n/a
14	BRCA1	chr2:39102762-39103510	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr2:39102781-39103189	HepG2	liver:	n/a	n/a
16	BRCA1	chr2:39102777-39103098	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr2:39097075-39097449	K562	blood:	n/a	n/a
18	CBX3	chr2:39102473-39103408	K562	blood:	n/a	n/a
19	CCNT2	chr2:39096636-39096783	K562	blood:	n/a	n/a
20	CCNT2	chr2:39102672-39103209	K562	blood:	n/a	n/a
21	CEBPB	chr2:39083391-39083654	A549	lung:	n/a	n/a
22	CEBPB	chr2:39083328-39083705	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:39094251-39094536	HepG2	liver:	n/a	chr2:39094406-39094417
24	CEBPB	chr2:39086298-39086578	A549	lung:	n/a	n/a
25	CEBPB	chr2:39083311-39083634	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr2:39083170-39083830	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:39083323-39083692	K562	blood:	n/a	n/a
28	CEBPB	chr2:39069122-39069270	HepG2	liver:	n/a	chr2:39069122-39069133
29	CEBPB	chr2:39097477-39097699	HepG2	liver:	n/a	chr2:39097556-39097567
30	CEBPB	chr2:39083331-39083696	IMR90	lung:	n/a	n/a
31	CEBPB	chr2:39083273-39083730	A549	lung:	n/a	n/a
32	CEBPB	chr2:39083334-39083704	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:39083291-39083681	K562	blood:	n/a	n/a
34	CEBPB	chr2:39083331-39083693	A549	lung:	n/a	n/a
35	CEBPB	chr2:39097525-39097649	A549	lung:	n/a	chr2:39097556-39097567
36	CEBPB	chr2:39103009-39103179	HepG2	liver:	n/a	chr2:39103075-39103083
37	CEBPB	chr2:39086317-39086496	HepG2	liver:	n/a	n/a
38	CEBPB	chr2:39094285-39094523	MCF-7	breast:	n/a	chr2:39094406-39094417
39	CEBPB	chr2:39083317-39083619	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr2:39102560-39103205	Hela-S3	cervix:	n/a	chr2:39103075-39103083
41	CEBPB	chr2:39094168-39094506	MCF-7	breast:	n/a	chr2:39094406-39094417
42	CEBPB	chr2:39086489-39086543	K562	blood:	n/a	n/a
43	CEBPB	chr2:39083348-39083680	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:39083366-39083651	MCF-7	breast:	n/a	n/a
45	CEBPD	chr2:39102512-39103258	HepG2	liver:	n/a	n/a
46	CHD1	chr2:39102468-39102478	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr2:39077018-39077113	GM12878	blood:	n/a	n/a
48	CHD1	chr2:39102787-39103066	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr2:39102661-39103151	GM12878	blood:	n/a	n/a
50	CHD2	chr2:39102293-39102341	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:39103037-39103087	ProgFib	skin:	n/a
2	chr2:39103372-39103422	Caco-2	colon:	n/a
3	chr2:39103372-39103422	LNCaP	prostate:	n/a
4	chr2:39102874-39102924	GM12878	blood:	n/a
5	chr2:39104195-39104245	CMK	blood:	n/a
6	chr2:39102955-39103005	PrEC	prostate:	n/a
7	chr2:39102883-39102933	NHBE	bronchial:	n/a
8	chr2:39099230-39099280	ovcar-3	ovarian:	n/a
9	chr2:39103037-39103087	HPAEpiC	pulmonary alveolar:	n/a
10	chr2:39102714-39102764	ECC-1	luminal epithelium:	n/a
11	chr2:39104195-39104245	K562	blood:	n/a
12	chr2:39109167-39109217	BJ	skin:	n/a
13	chr2:39102874-39102924	H1-hESC	embryonic stem cell:	embryo
14	chr2:39103310-39103360	Caco-2	colon:	n/a
15	chr2:39106211-39106261	AG10803	skin:	n/a
16	chr2:39102955-39103005	SKMC	muscle:	n/a
17	chr2:39102883-39102933	HRPEpiC	eye:	n/a
18	chr2:39103277-39103327	HCPEpiC	choroid plexus:	n/a
19	chr2:39106211-39106261	NT2-D1	testis:	n/a
20	chr2:39103068-39103118	HMEC	breast:	n/a
21	chr2:39106211-39106261	NH-A	brain:	n/a
22	chr2:39103037-39103087	HCM	heart:	n/a
23	chr2:39102874-39102924	AG10803	skin:	n/a
24	chr2:39103037-39103087	SK-N-SH_RA	brain:	n/a
25	chr2:39099230-39099280	HEK293	kidney:	embryo
26	chr2:39103302-39103352	GM12892	blood:	n/a
27	chr2:39103068-39103118	AG09319	gingival:	n/a
28	chr2:39104195-39104245	HRPEpiC	eye:	n/a
29	chr2:39109167-39109217	GM06990	blood:	n/a
30	chr2:39102955-39103005	SK-N-MC	brain:	n/a
31	chr2:39109167-39109217	AG10803	skin:	n/a
32	chr2:39102714-39102764	AG04449	skin:	fetal
33	chr2:39103302-39103352	HIPEpiC	eye:	n/a
34	chr2:39102883-39102933	AG09319	gingival:	n/a
35	chr2:39099230-39099280	HepG2	liver:	n/a
36	chr2:39103037-39103087	HAEpiC	amniotic membrane:	n/a
37	chr2:39103277-39103327	BE2_C	brain:	n/a
38	chr2:39106211-39106261	BJ	skin:	n/a
39	chr2:39102955-39103005	K562	blood:	n/a
40	chr2:39102883-39102933	K562	blood:	n/a
41	chr2:39103037-39103087	HMEC	breast:	n/a
42	chr2:39103310-39103360	HRCEpiC	kidney:	n/a
43	chr2:39103277-39103327	ovcar-3	ovarian:	n/a
44	chr2:39103310-39103360	U87	brain:	n/a
45	chr2:39103310-39103360	SK-N-SH	brain:	n/a
46	chr2:39104195-39104245	A549	lung:	n/a
47	chr2:39103310-39103360	HMEC	breast:	n/a
48	chr2:39104195-39104245	AG04450	lung:	fetal
49	chr2:39102874-39102924	MCF-7	breast:	n/a
50	chr2:39102714-39102764	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:39064983..39068575-chr2:39101517..39104346,3	MCF-7	breast:
2	chr2:39075448..39080892-chr2:39081993..39084972,5	K562	blood:
3	chr2:39102312..39104681-chr2:39105607..39108211,2	K562	blood:
4	chr2:39086851..39091387-chr2:39094171..39096771,4	K562	blood:
5	chr2:39060938..39063167-chr2:39068142..39070499,2	K562	blood:
6	chr2:39086851..39091387-chr2:39094171..39096771,4	K562	blood:
7	chr2:39067403..39069873-chr2:39082049..39084866,2	K562	blood:
8	chr2:38973701..38976718-chr2:39077217..39081288,3	K562	blood:
9	chr2:38973415..38975366-chr2:39100938..39103537,2	K562	blood:
10	chr2:38971477..38974181-chr2:39070212..39071979,2	K562	blood:
11	chr2:39089505..39093700-chr2:39094409..39098372,5	K562	blood:
12	chr2:39075448..39080892-chr2:39081993..39084972,5	K562	blood:
13	chr2:38977106..38980095-chr2:39079432..39082390,2	K562	blood:
14	chr2:39089505..39093700-chr2:39094409..39098372,5	K562	blood:
15	chr2:39082200..39083996-chr2:39090256..39092735,2	MCF-7	breast:
16	chr2:38975762..38977938-chr2:39078854..39080619,2	K562	blood:
17	chr2:38976936..38979845-chr2:39101241..39105632,7	K562	blood:
18	chr2:38977039..38980057-chr2:39069909..39072529,4	K562	blood:
19	chr2:39068375..39070499-chr2:39072460..39074648,2	K562	blood:
20	chr2:39092323..39097069-chr2:39100019..39103136,5	MCF-7	breast:
21	chr2:38976661..38978798-chr2:39083252..39086476,5	MCF-7	breast:
22	chr2:39106402..39108515-chr2:39149048..39151113,2	MCF-7	breast:
23	chr2:38977620..38979260-chr2:39085026..39086818,2	K562	blood:
24	chr2:39079613..39082361-chr2:39103056..39104740,2	MCF-7	breast:
25	chr2:39076189..39078927-chr4:92754563..92756152,2	MCF-7	breast:
26	chr2:38977140..38978650-chr2:39068514..39070309,2	K562	blood:
27	chr2:39102843..39105265-chr2:39108661..39111288,2	MCF-7	breast:
28	chr2:39106547..39110069-chr2:39150032..39154401,3	K562	blood:
29	chr2:39082200..39083996-chr2:39090256..39092735,2	MCF-7	breast:
30	chr2:39065545..39067577-chr2:39069948..39073607,4	K562	blood:
31	chr2:39068375..39070499-chr2:39072460..39074648,2	K562	blood:
32	chr2:38977475..38979317-chr2:39084775..39086818,3	K562	blood:
33	chr2:39052271..39054519-chr2:39105359..39107014,2	K562	blood:
34	chr2:39094395..39096056-chr2:39119130..39121663,2	K562	blood:
35	chr2:38977095..38978891-chr2:39077165..39078784,2	MCF-7	breast:
36	chr2:39088675..39091170-chr2:39093044..39095216,2	MCF-7	breast:
37	chr2:38969744..38972668-chr2:39079063..39081917,2	K562	blood:
38	chr2:39060039..39062647-chr2:39091366..39093415,2	K562	blood:
39	chr2:39092323..39097069-chr2:39100019..39103136,5	MCF-7	breast:
40	chr2:38977123..38979933-chr2:39076809..39078622,2	K562	blood:
41	chr2:38976877..38979785-chr2:39100480..39105632,13	K562	blood:
42	chr2:38977095..38979491-chr2:39071029..39074824,4	K562	blood:
43	chr2:39065545..39067577-chr2:39069948..39073607,4	K562	blood:
44	chr2:39097841..39100728-chr2:39103293..39104847,2	MCF-7	breast:
45	chr2:39097841..39100728-chr2:39103293..39104847,2	MCF-7	breast:
46	chr2:39065831..39067433-chr2:39089862..39092131,2	K562	blood:
47	chr2:39088675..39091170-chr2:39093044..39095216,2	MCF-7	breast:
48	chr2:39094336..39097317-chr2:39099432..39100935,2	K562	blood:
49	chr2:39095857..39098722-chr2:39101020..39103452,2	MCF-7	breast:
50	chr2:39065831..39067433-chr2:39089862..39092131,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MORN2-1	chr2:39088862-39088895	ENSG00000225284.1
2	lnc-SRSF7-3	chr2:39073209-39073418	expReg_chr2_2809_-
3	lnc-MORN2-1	chr2:39089760-39090275	ENSG00000225284.1

No data

Variant related genes	Relation type
MORN2	TF binding region
RNU6-851P	TF binding region
ENSG00000225284	TF binding region
DHX57	TF binding region
MORN2	CpG island
RNU6-851P	CpG island
ENSG00000225284	CpG island
DHX57	CpG island
ENSG00000115875	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000225284	chromatin interactions
ENSG00000188010	chromatin interactions
ENSG00000163214	chromatin interactions

Extended variants
information (count: 2026 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2026 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567318627	chr2:39065808-39065809	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs528076432	chr2:39065908-39065909	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs116701216	chr2:39065910-39065911	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs61442219	chr2:39065957-39065958	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs560913433	chr2:39065989-39065990	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571340911	chr2:39066002-39066003	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186371611	chr2:39066015-39066016	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs557125550	chr2:39066026-39066027	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs140894638	chr2:39066051-39066052	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374932868	chr2:39066076-39066077	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs192083253	chr2:39066082-39066083	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs573734663	chr2:39066127-39066128	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs533867634	chr2:39066142-39066143	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534715263	chr2:39066149-39066150	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183405521	chr2:39066197-39066198	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs546370118	chr2:39066214-39066215	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373363175	chr2:39066221-39066222	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377547537	chr2:39066296-39066297	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs545132992	chr2:39066297-39066298	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs563947459	chr2:39066304-39066305	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564657138	chr2:39066363-39066364	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575747612	chr2:39066367-39066368	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs112462334	chr2:39066381-39066382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561581524	chr2:39066423-39066424	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs113366132	chr2:39066438-39066439	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs369327667	chr2:39066467-39066468	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs528767298	chr2:39066477-39066478	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546621610	chr2:39066532-39066533	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564683409	chr2:39066558-39066559	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532272144	chr2:39066582-39066583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573363644	chr2:39066593-39066594	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs7598052	chr2:39066608-39066609	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs10708087	chr2:39066700-39066701	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567073053	chr2:39066713-39066714	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs62142679	chr2:39066715-39066716	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs7598403	chr2:39066756-39066757	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs569060074	chr2:39066818-39066819	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144710821	chr2:39066840-39066841	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs547948849	chr2:39066847-39066848	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566453855	chr2:39066857-39066858	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376793761	chr2:39066930-39066931	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs142981533	chr2:39066988-39066989	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs577948350	chr2:39067023-39067024	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539171783	chr2:39067058-39067059	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs191208577	chr2:39067113-39067114	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575772947	chr2:39067115-39067116	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561884951	chr2:39067126-39067127	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs562263827	chr2:39067165-39067166	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543263630	chr2:39067231-39067232	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182405193	chr2:39067261-39067262	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	16272173	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

Chromatin state (count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39006400-39085600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr2:39022000-39066800	Weak transcription	Stomach Mucosa	stomach
3	chr2:39026600-39079800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr2:39030600-39088200	Weak transcription	Fetal Heart	heart
5	chr2:39032800-39072800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr2:39038800-39095600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:39038800-39102200	Weak transcription	Gastric	stomach
8	chr2:39039000-39085400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:39039000-39090000	Weak transcription	Esophagus	oesophagus
10	chr2:39039000-39101200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:39039000-39102000	Weak transcription	Colonic Mucosa	Colon
12	chr2:39040000-39069000	Strong transcription	Fetal Muscle Leg	muscle
13	chr2:39042800-39080600	Weak transcription	Small Intestine	intestine
14	chr2:39043600-39079800	Weak transcription	Right Ventricle	heart
15	chr2:39046000-39073200	Weak transcription	Pancreas	Pancrea
16	chr2:39046200-39070200	Weak transcription	NHLF	lung
17	chr2:39050400-39072800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:39050400-39079800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr2:39050400-39079800	Weak transcription	Spleen	Spleen
20	chr2:39050400-39088000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr2:39051000-39068600	Weak transcription	HMEC	breast
22	chr2:39052200-39068600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr2:39053200-39068600	Weak transcription	Brain Substantia Nigra	brain
24	chr2:39053200-39069600	Weak transcription	HUVEC	blood vessel
25	chr2:39053800-39068200	Weak transcription	HSMM	muscle
26	chr2:39053800-39068400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:39053800-39068600	Weak transcription	Aorta	Aorta
28	chr2:39053800-39068800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr2:39053800-39080200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr2:39053800-39080600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr2:39054200-39076400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:39055000-39080000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr2:39055200-39068800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr2:39055200-39085600	Weak transcription	Psoas Muscle	Psoas
35	chr2:39055600-39071600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:39055600-39073200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr2:39055600-39080000	Weak transcription	NH-A	brain
38	chr2:39055600-39080600	Weak transcription	Hela-S3	cervix
39	chr2:39055600-39080600	Weak transcription	K562	blood
40	chr2:39055800-39071200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:39056600-39066000	Strong transcription	Primary T cells from cord blood	blood
42	chr2:39056600-39066000	Strong transcription	A549	lung
43	chr2:39057000-39086200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:39057200-39066600	Strong transcription	Stomach Smooth Muscle	stomach
45	chr2:39057200-39067000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr2:39057200-39071400	Strong transcription	Fetal Muscle Trunk	muscle
47	chr2:39058000-39068400	Weak transcription	Brain Angular Gyrus	brain
48	chr2:39058000-39087800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr2:39059000-39066400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr2:39060000-39080000	Weak transcription	Lung	lung

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