Variant report

Variant	nsv875019
Chromosome Location	chr2:128340855-128408170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1344)
CpG islands
(count:2198)
Chromatin interactive
region (count:97)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:128349048-128349416	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:128402852-128402944	HepG2	liver:	n/a	n/a
3	ATF1	chr2:128395319-128395639	K562	blood:	n/a	n/a
4	ATF1	chr2:128358801-128358803	K562	blood:	n/a	n/a
5	ATF2	chr2:128395260-128395633	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:128395213-128395669	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:128390643-128391096	GM12878	blood:	n/a	n/a
8	ATF2	chr2:128407243-128407554	GM12878	blood:	n/a	n/a
9	ATF2	chr2:128348914-128349416	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr2:128401745-128401880	K562	blood:	n/a	n/a
11	BACH1	chr2:128343035-128343230	K562	blood:	n/a	n/a
12	BACH1	chr2:128349033-128349329	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr2:128395358-128395563	GM12878	blood:	n/a	n/a
14	BATF	chr2:128377445-128377648	GM12878	blood:	n/a	chr2:128377561-128377570
15	BCL11A	chr2:128390676-128391052	GM12878	blood:	n/a	n/a
16	BCLAF1	chr2:128349073-128349341	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:128396128-128396261	K562	blood:	n/a	n/a
18	BHLHE40	chr2:128407395-128407643	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:128407298-128407596	K562	blood:	n/a	n/a
20	BHLHE40	chr2:128385528-128385592	K562	blood:	n/a	n/a
21	BHLHE40	chr2:128349045-128349370	K562	blood:	n/a	n/a
22	BHLHE40	chr2:128395747-128395861	K562	blood:	n/a	n/a
23	BRCA1	chr2:128407346-128407624	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:128348982-128349342	K562	blood:	n/a	n/a
25	CCNT2	chr2:128395299-128395499	K562	blood:	n/a	n/a
26	CCNT2	chr2:128404581-128404775	K562	blood:	n/a	chr2:128404664-128404684
27	CEBPB	chr2:128395866-128396205	HepG2	liver:	n/a	chr2:128396018-128396029
28	CEBPB	chr2:128349000-128349373	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr2:128387560-128388007	MCF-7	breast:	n/a	chr2:128387774-128387785
30	CEBPB	chr2:128395924-128396209	H1-hESC	embryonic stem cell:	n/a	chr2:128396018-128396029
31	CEBPB	chr2:128349084-128349423	HepG2	liver:	n/a	n/a
32	CEBPB	chr2:128395924-128396104	HepG2	liver:	n/a	chr2:128396018-128396029
33	CEBPB	chr2:128395844-128396166	K562	blood:	n/a	chr2:128396018-128396029
34	CEBPB	chr2:128395864-128396191	HepG2	liver:	n/a	chr2:128396018-128396029
35	CEBPB	chr2:128395872-128396195	IMR90	lung:	n/a	chr2:128396018-128396029
36	CEBPB	chr2:128387706-128387873	HepG2	liver:	n/a	chr2:128387774-128387785
37	CEBPB	chr2:128402725-128402856	HepG2	liver:	n/a	chr2:128402781-128402792
38	CEBPB	chr2:128395370-128395570	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:128349142-128349337	HepG2	liver:	n/a	n/a
40	CEBPB	chr2:128395817-128396208	K562	blood:	n/a	chr2:128396018-128396029
41	CEBPB	chr2:128349086-128349381	K562	blood:	n/a	n/a
42	CEBPB	chr2:128395791-128396221	MCF-7	breast:	n/a	chr2:128396018-128396029
43	CEBPB	chr2:128387780-128387794	A549	lung:	n/a	n/a
44	CEBPD	chr2:128349131-128349314	HepG2	liver:	n/a	n/a
45	CHD2	chr2:128349251-128349257	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr2:128398116-128398212	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr2:128349131-128349289	HepG2	liver:	n/a	n/a
48	CHD2	chr2:128407348-128407622	HepG2	liver:	n/a	n/a
49	CHD2	chr2:128349065-128349344	K562	blood:	n/a	n/a
50	CHD2	chr2:128348982-128349275	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2198 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:128403133-128403183	HL-60	blood:	n/a
2	chr2:128389103-128389153	H1-hESC	embryonic stem cell:	embryo
3	chr2:128403133-128403183	HL-60	blood:	n/a
4	chr2:128389103-128389153	H1-hESC	embryonic stem cell:	embryo
5	chr2:128350748-128350798	SK-N-SH_RA	brain:	n/a
6	chr2:128350572-128350622	NHBE	bronchial:	n/a
7	chr2:128366594-128366644	NB4	blood:	n/a
8	chr2:128395196-128395246	GM19239	blood:	n/a
9	chr2:128366514-128366564	NT2-D1	testis:	n/a
10	chr2:128389207-128389257	HEEpiC	esophagus:	n/a
11	chr2:128381835-128381885	SAEC	small airway:	n/a
12	chr2:128407154-128407204	HEK293	kidney:	embryo
13	chr2:128351542-128351592	U87	brain:	n/a
14	chr2:128380062-128380112	ECC-1	luminal epithelium:	n/a
15	chr2:128396059-128396109	HRPEpiC	eye:	n/a
16	chr2:128348899-128348949	PFSK-1	brain:	n/a
17	chr2:128403286-128403336	SAEC	small airway:	n/a
18	chr2:128403084-128403134	HRE	kidney:	n/a
19	chr2:128350306-128350356	RPTEC	kidney:	n/a
20	chr2:128378434-128378484	PFSK-1	brain:	n/a
21	chr2:128402415-128402465	HNPCEpiC	eye:	n/a
22	chr2:128389112-128389162	SK-N-MC	brain:	n/a
23	chr2:128348899-128348949	HRE	kidney:	n/a
24	chr2:128347901-128347951	K562	blood:	n/a
25	chr2:128407068-128407118	AoSMC	blood vessel:	n/a
26	chr2:128348899-128348949	NHDF-neo	bronchial:	n/a
27	chr2:128350306-128350356	ECC-1	luminal epithelium:	n/a
28	chr2:128347901-128347951	SK-N-SH	brain:	n/a
29	chr2:128403286-128403336	GM12878	blood:	n/a
30	chr2:128382383-128382433	AoSMC	blood vessel:	n/a
31	chr2:128382383-128382433	AG09309	skin:	n/a
32	chr2:128366324-128366374	SKMC	muscle:	n/a
33	chr2:128402415-128402465	K562	blood:	n/a
34	chr2:128388876-128388926	Hela-S3	cervix:	n/a
35	chr2:128350306-128350356	PANC-1	pancreas:	n/a
36	chr2:128381653-128381703	ECC-1	luminal epithelium:	n/a
37	chr2:128381689-128381739	ovcar-3	ovarian:	n/a
38	chr2:128366594-128366644	CMK	blood:	n/a
39	chr2:128382383-128382433	HRPEpiC	eye:	n/a
40	chr2:128378434-128378484	GM12878	blood:	n/a
41	chr2:128405844-128405894	HNPCEpiC	eye:	n/a
42	chr2:128381653-128381703	U87	brain:	n/a
43	chr2:128402415-128402465	HRPEpiC	eye:	n/a
44	chr2:128350442-128350492	SAEC	small airway:	n/a
45	chr2:128354089-128354139	PANC-1	pancreas:	n/a
46	chr2:128350748-128350798	NHBE	bronchial:	n/a
47	chr2:128381745-128381795	NHDF-neo	bronchial:	n/a
48	chr2:128402294-128402344	H1-hESC	embryonic stem cell:	embryo
49	chr2:128366324-128366374	HEK293	kidney:	embryo
50	chr2:128366514-128366564	NHBE	bronchial:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:128350066..128351938-chr2:128352163..128353978,2	MCF-7	breast:
2	chr2:128334136..128336410-chr2:128339156..128341197,2	MCF-7	breast:
3	chr2:128367073..128368593-chr2:128390549..128393243,2	K562	blood:
4	chr2:128385318..128388983-chr2:128393086..128394739,3	MCF-7	breast:
5	chr2:128391814..128393751-chr2:128458053..128460441,2	MCF-7	breast:
6	chr2:128364338..128366836-chr2:212139739..212142572,2	MCF-7	breast:
7	chr2:128266465..128268562-chr2:128395784..128397620,2	MCF-7	breast:
8	chr2:128341026..128343432-chr2:128406208..128408267,2	MCF-7	breast:
9	chr2:128376581..128378906-chr2:128380891..128383389,2	K562	blood:
10	chr2:128375941..128378223-chr2:128378920..128381001,2	K562	blood:
11	chr2:128396062..128398700-chr2:128403094..128404905,3	K562	blood:
12	chr2:128340070..128342294-chr2:128344591..128347137,2	K562	blood:
13	chr2:128402343..128404793-chr2:128407484..128409770,2	MCF-7	breast:
14	chr2:128380533..128382202-chr2:128389367..128391180,2	K562	blood:
15	chr2:128386978..128389867-chr2:128392766..128396164,5	MCF-7	breast:
16	chr2:128349348..128351904-chr2:128462965..128465382,2	MCF-7	breast:
17	chr2:128283338..128286732-chr2:128405209..128408607,3	MCF-7	breast:
18	chr2:128372780..128375078-chr2:128457805..128460523,2	MCF-7	breast:
19	chr2:128349507..128351016-chr2:128354758..128356667,2	K562	blood:
20	chr2:128349507..128351016-chr2:128354758..128356667,2	K562	blood:
21	chr2:128370249..128372116-chr2:128372361..128374948,2	MCF-7	breast:
22	chr2:128282210..128283932-chr2:128379234..128381110,2	MCF-7	breast:
23	chr2:128345319..128347126-chr2:128457834..128460214,2	K562	blood:
24	chr2:128348754..128349757-chr2:128407019..128407967,16	MCF-7	breast:
25	chr2:128404401..128407109-chr2:128457505..128460604,3	K562	blood:
26	chr2:128356185..128358427-chr2:128361989..128364155,2	MCF-7	breast:
27	chr2:128372104..128373861-chr2:128379908..128381447,2	K562	blood:
28	chr17:41464681..41467245-chr2:128400919..128402419,3	K562	blood:
29	chr2:128389876..128393259-chr2:128457359..128460267,4	K562	blood:
30	chr2:128281499..128284149-chr2:128402816..128405194,3	K562	blood:
31	chr2:128378927..128382378-chr2:128457870..128460162,3	MCF-7	breast:
32	chr2:128368208..128370995-chr2:128394997..128397698,2	K562	blood:
33	chr2:128379152..128382886-chr2:128385919..128388760,4	K562	blood:
34	chr2:128371727..128374321-chr2:128457294..128459838,2	K562	blood:
35	chr2:128348736..128349703-chr2:128407022..128407964,6	K562	blood:
36	chr2:128393595..128398988-chr2:128401355..128406842,9	K562	blood:
37	chr2:128399188..128401329-chr2:128456948..128459490,2	MCF-7	breast:
38	chr2:128349017..128351644-chr2:128387621..128389792,2	MCF-7	breast:
39	chr2:128399168..128401965-chr2:128403212..128405574,3	MCF-7	breast:
40	chr2:128367073..128368593-chr2:128390549..128393243,2	K562	blood:
41	chr2:128370249..128372116-chr2:128372361..128374948,2	MCF-7	breast:
42	chr2:128388188..128389976-chr2:128397282..128399225,3	MCF-7	breast:
43	chr2:128396263..128398888-chr2:128399161..128401002,2	MCF-7	breast:
44	chr2:128372104..128373861-chr2:128379908..128381447,2	K562	blood:
45	chr2:128385318..128388983-chr2:128393086..128394739,3	MCF-7	breast:
46	chr2:128348828..128349586-chr2:128398143..128398870,2	MCF-7	breast:
47	chr2:128356185..128358427-chr2:128361989..128364155,2	MCF-7	breast:
48	chr2:128386610..128389542-chr2:128567624..128570008,2	MCF-7	breast:
49	chr2:128396263..128398888-chr2:128399161..128401002,2	MCF-7	breast:
50	chr2:128348763..128349664-chr2:128408092..128409288,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR17-2	chr2:128360094-128360482	expReg_chr2_9268_+
2	lnc-GPR17-1	chr2:128366260-128366776	l_1945_chr2:128361165-128366776_ovary
3	lnc-LIMS2-2	chr2:128383572-128384423	ENSG00000272789.1
4	lnc-LIMS2-1	chr2:128394380-128394796	NONHSAT074176
5	lnc-GPR17-1	chr2:128361166-128363412	l_1945_chr2:128361165-128366776_ovary
6	lnc-LIMS2-1	chr2:128391285-128394251	NONHSAT074176
7	lnc-LIMS2-3	chr2:128345637-128345930	expReg_chr2_9243_-

No data

Variant related genes	Relation type
GPR17	TF binding region
LIMS2	TF binding region
ENSG00000272789	TF binding region
MYO7B	TF binding region
GPR17	CpG island
LIMS2	CpG island
ENSG00000272789	CpG island
MYO7B	CpG island
ENSG00000144230	chromatin interactions
ENSG00000169994	chromatin interactions
ENSG00000272789	chromatin interactions
ENSG00000072163	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000136709	chromatin interactions
ENSG00000163166	chromatin interactions
ENSG00000264462	chromatin interactions
ENSG00000173349	chromatin interactions

Extended variants
information (count: 3287 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3287 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11693296	chr2:128340855-128340856	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190753363	chr2:128340861-128340862	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181956362	chr2:128340876-128340877	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13025351	chr2:128340901-128340902	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs11693303	chr2:128340902-128340903	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145833879	chr2:128340922-128340923	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563158681	chr2:128340929-128340930	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184226200	chr2:128340940-128340941	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528333145	chr2:128340942-128340943	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551288000	chr2:128340950-128340951	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs565048234	chr2:128340990-128340991	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188984805	chr2:128341011-128341012	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181045539	chr2:128341096-128341097	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186716513	chr2:128341116-128341117	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532008596	chr2:128341122-128341123	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs12616515	chr2:128341142-128341143	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535449807	chr2:128341154-128341155	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549314381	chr2:128341178-128341179	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs566246957	chr2:128341197-128341198	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535285126	chr2:128341216-128341217	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs568393758	chr2:128341262-128341263	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190708121	chr2:128341297-128341298	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs578102648	chr2:128341334-128341335	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs532081691	chr2:128341410-128341411	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs537171247	chr2:128341484-128341485	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs80141995	chr2:128341485-128341486	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs4283359	chr2:128341495-128341496	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573719420	chr2:128341509-128341510	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs35131095	chr2:128341532-128341533	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs76870472	chr2:128341533-128341534	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542639149	chr2:128341550-128341551	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs4436901	chr2:128341566-128341567	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs77795299	chr2:128341568-128341569	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573061443	chr2:128341580-128341581	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs148969909	chr2:128341587-128341588	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs545262599	chr2:128341598-128341599	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs10928772	chr2:128341603-128341604	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs530718322	chr2:128341644-128341645	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs143819345	chr2:128341662-128341663	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs563440617	chr2:128341697-128341698	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs551004670	chr2:128341700-128341701	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs144080203	chr2:128341722-128341723	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs374298824	chr2:128341727-128341728	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs368262229	chr2:128341750-128341751	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372272451	chr2:128341758-128341759	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs376811050	chr2:128341769-128341770	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs181001303	chr2:128341772-128341773	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs200853784	chr2:128341790-128341791	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs146427264	chr2:128341802-128341803	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs61742021	chr2:128341813-128341814	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Mental retardation	17621639	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Medulloblastoma	16968546	CNVD
Neurocytoma	17123091	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1585 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:128321600-128352200	Strong transcription	Fetal Intestine Small	intestine
2	chr2:128328000-128370200	Weak transcription	Small Intestine	intestine
3	chr2:128330000-128350600	Strong transcription	Fetal Intestine Large	intestine
4	chr2:128330200-128346400	Strong transcription	Rectal Mucosa Donor 31	rectum
5	chr2:128330400-128349800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr2:128330800-128346600	Strong transcription	Rectal Mucosa Donor 29	rectum
7	chr2:128334400-128376400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr2:128335600-128348800	Weak transcription	Spleen	Spleen
9	chr2:128335800-128346000	Weak transcription	Pancreas	Pancrea
10	chr2:128337400-128356000	Strong transcription	Sigmoid Colon	Sigmoid Colon
11	chr2:128338200-128342400	Strong transcription	Colonic Mucosa	Colon
12	chr2:128338800-128342200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr2:128340400-128342600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr2:128341200-128341600	Enhancers	Fetal Thymus	thymus
15	chr2:128341600-128344200	Weak transcription	Fetal Thymus	thymus
16	chr2:128342200-128344800	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr2:128342400-128345400	Weak transcription	Colonic Mucosa	Colon
18	chr2:128342600-128343800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr2:128343000-128344000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr2:128343000-128344200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr2:128343200-128343600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr2:128343200-128343600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr2:128343600-128344400	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:128343800-128344000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr2:128343800-128346200	Enhancers	Dnd41	blood
26	chr2:128344000-128344200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:128344200-128344800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr2:128344200-128345000	Enhancers	Fetal Thymus	thymus
29	chr2:128344200-128350400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:128344400-128344600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:128344400-128345000	Enhancers	Primary B cells from peripheral blood	blood
32	chr2:128344400-128346000	Enhancers	Placenta	Placenta
33	chr2:128344800-128346000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:128344800-128347600	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr2:128345000-128348800	Weak transcription	Primary B cells from peripheral blood	blood
36	chr2:128345400-128346400	Strong transcription	Colonic Mucosa	Colon
37	chr2:128346000-128346200	Enhancers	Pancreas	Pancrea
38	chr2:128346000-128347600	Weak transcription	Placenta	Placenta
39	chr2:128346200-128347600	Weak transcription	Dnd41	blood
40	chr2:128346400-128347800	Weak transcription	Colonic Mucosa	Colon
41	chr2:128346400-128347800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:128346600-128347400	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr2:128347400-128351600	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr2:128347600-128348600	Strong transcription	Primary neutrophils fromperipheralblood	blood
45	chr2:128347600-128349800	Enhancers	Placenta	Placenta
46	chr2:128347600-128353400	Weak transcription	Right Atrium	heart
47	chr2:128347600-128354800	Weak transcription	Thymus	Thymus
48	chr2:128347600-128355600	Enhancers	Dnd41	blood
49	chr2:128347800-128352000	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr2:128347800-128352200	Strong transcription	Colonic Mucosa	Colon

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