Variant report

Variant	nsv535841
Chromosome Location	chr2:100072790-100112121
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:100106704-100107165	K562	blood:	n/a	n/a
2	ARID3A	chr2:100087939-100088495	K562	blood:	n/a	n/a
3	ARID3A	chr2:100087382-100087696	K562	blood:	n/a	n/a
4	ARID3A	chr2:100106642-100107333	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:100101926-100102141	K562	blood:	n/a	n/a
6	ATF1	chr2:100094906-100095064	K562	blood:	n/a	n/a
7	ATF2	chr2:100098389-100098667	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:100098321-100098731	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:100106467-100107234	GM12878	blood:	n/a	n/a
10	ATF3	chr2:100106566-100106988	A549	lung:	n/a	n/a
11	ATF3	chr2:100106600-100106832	GM12878	blood:	n/a	n/a
12	ATF3	chr2:100101921-100102207	K562	blood:	n/a	n/a
13	ATF3	chr2:100106345-100106896	K562	blood:	n/a	chr2:100106504-100106513
14	ATF3	chr2:100106585-100106829	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr2:100106451-100106995	GM12878	blood:	n/a	chr2:100106504-100106513
16	ATF3	chr2:100105956-100106296	K562	blood:	n/a	chr2:100106063-100106071
17	ATF3	chr2:100106477-100106874	H1-hESC	embryonic stem cell:	n/a	chr2:100106504-100106513
18	ATF3	chr2:100106507-100106988	HepG2	liver:	n/a	n/a
19	ATF3	chr2:100106558-100107268	HepG2	liver:	n/a	n/a
20	BACH1	chr2:100105699-100107316	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr2:100103095-100103239	K562	blood:	n/a	n/a
22	BACH1	chr2:100112041-100112226	K562	blood:	n/a	n/a
23	BACH1	chr2:100108838-100108869	K562	blood:	n/a	n/a
24	BACH1	chr2:100106288-100107323	K562	blood:	n/a	n/a
25	BCL11A	chr2:100106507-100106931	GM12878	blood:	n/a	chr2:100106509-100106522 chr2:100106587-100106600 chr2:100106779-100106792 chr2:100106752-100106765 chr2:100106688-100106701
26	BCL11A	chr2:100098408-100098588	H1-hESC	embryonic stem cell:	n/a	n/a
27	BCL3	chr2:100106288-100106834	GM12878	blood:	n/a	chr2:100106509-100106522 chr2:100106587-100106600 chr2:100106408-100106421 chr2:100106340-100106353 chr2:100106779-100106792 chr2:100106752-100106765 chr2:100106346-100106355 chr2:100106688-100106701
28	BCLAF1	chr2:100106267-100107231	GM12878	blood:	n/a	chr2:100106509-100106522 chr2:100106587-100106600 chr2:100106408-100106421 chr2:100106340-100106353 chr2:100106779-100106792 chr2:100106752-100106765 chr2:100106346-100106355 chr2:100107150-100107163 chr2:100106688-100106701
29	BCLAF1	chr2:100106213-100106927	K562	blood:	n/a	chr2:100106509-100106522 chr2:100106587-100106600 chr2:100106408-100106421 chr2:100106340-100106353 chr2:100106779-100106792 chr2:100106752-100106765 chr2:100106346-100106355 chr2:100106688-100106701
30	BCLAF1	chr2:100106546-100107257	GM12878	blood:	n/a	chr2:100106587-100106600 chr2:100106779-100106792 chr2:100106752-100106765 chr2:100107150-100107163 chr2:100106688-100106701
31	BHLHE40	chr2:100105969-100107373	K562	blood:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106181-100106197 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106346-100106362 chr2:100106720-100106729 chr2:100106189-100106205
32	BHLHE40	chr2:100106446-100106948	HepG2	liver:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106720-100106729
33	BHLHE40	chr2:100106520-100106893	HepG2	liver:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106720-100106729
34	BHLHE40	chr2:100098590-100098937	K562	blood:	n/a	n/a
35	BHLHE40	chr2:100105996-100107238	GM12878	blood:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106181-100106197 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106346-100106362 chr2:100106720-100106729 chr2:100106189-100106205
36	BHLHE40	chr2:100102274-100102475	K562	blood:	n/a	n/a
37	BHLHE40	chr2:100106535-100107099	A549	lung:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106720-100106729
38	BHLHE40	chr2:100105004-100105678	K562	blood:	n/a	n/a
39	BHLHE40	chr2:100105532-100107280	HepG2	liver:	n/a	chr2:100106719-100106728 chr2:100106720-100106729 chr2:100106714-100106735 chr2:100106181-100106197 chr2:100106718-100106731 chr2:100106721-100106730 chr2:100106346-100106362 chr2:100106720-100106729 chr2:100106189-100106205
40	BRCA1	chr2:100077545-100077588	GM12878	blood:	n/a	n/a
41	BRCA1	chr2:100106654-100107013	HepG2	liver:	n/a	n/a
42	BRCA1	chr2:100106642-100106788	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr2:100106642-100107258	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr2:100106558-100107241	K562	blood:	n/a	n/a
45	CBX3	chr2:100106595-100107185	K562	blood:	n/a	n/a
46	CBX3	chr2:100078566-100078907	K562	blood:	n/a	n/a
47	CBX3	chr2:100087130-100087721	K562	blood:	n/a	n/a
48	CBX3	chr2:100078443-100078932	K562	blood:	n/a	n/a
49	CCNT2	chr2:100105647-100107150	K562	blood:	n/a	chr2:100106484-100106493 chr2:100106037-100106046 chr2:100106667-100106676 chr2:100106338-100106347 chr2:100106151-100106160 chr2:100106545-100106554
50	CEBPB	chr2:100097912-100098107	K562	blood:	n/a	chr2:100097984-100097995 chr2:100098022-100098031 chr2:100098021-100098032

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:100078174-100078224	SK-N-SH_RA	brain:	n/a
2	chr2:100107157-100107207	HCF	heart:	n/a
3	chr2:100107157-100107207	GM19239	blood:	n/a
4	chr2:100106981-100107031	HCF	heart:	n/a
5	chr2:100106147-100106197	SK-N-SH_RA	brain:	n/a
6	chr2:100105657-100105707	GM12892	blood:	n/a
7	chr2:100106147-100106197	AG09319	gingival:	n/a
8	chr2:100078174-100078224	AG10803	skin:	n/a
9	chr2:100107195-100107245	H1-hESC	embryonic stem cell:	embryo
10	chr2:100106147-100106197	NH-A	brain:	n/a
11	chr2:100107195-100107245	AG09319	gingival:	n/a
12	chr2:100106285-100106335	H1-hESC	embryonic stem cell:	embryo
13	chr2:100106981-100107031	SK-N-SH	brain:	n/a
14	chr2:100105657-100105707	HUVEC	blood vessel:	n/a
15	chr2:100089996-100090046	BE2_C	brain:	n/a
16	chr2:100106981-100107031	A549	lung:	n/a
17	chr2:100105657-100105707	SK-N-SH_RA	brain:	n/a
18	chr2:100109838-100109888	BE2_C	brain:	n/a
19	chr2:100109838-100109888	T-47D	breast:	n/a
20	chr2:100078174-100078224	HL-60	blood:	n/a
21	chr2:100106981-100107031	AoSMC	blood vessel:	n/a
22	chr2:100106147-100106197	Hepatocyte	liver:	n/a
23	chr2:100105657-100105707	HMEC	breast:	n/a
24	chr2:100078174-100078224	NH-A	brain:	n/a
25	chr2:100106285-100106335	Jurkat	blood:	n/a
26	chr2:100106147-100106197	HNPCEpiC	eye:	n/a
27	chr2:100107157-100107207	GM06990	blood:	n/a
28	chr2:100107157-100107207	Caco-2	colon:	n/a
29	chr2:100105657-100105707	HIPEpiC	eye:	n/a
30	chr2:100106981-100107031	ECC-1	luminal epithelium:	n/a
31	chr2:100107195-100107245	AoSMC	blood vessel:	n/a
32	chr2:100107157-100107207	AoSMC	blood vessel:	n/a
33	chr2:100089996-100090046	T-47D	breast:	n/a
34	chr2:100109838-100109888	AG09309	skin:	n/a
35	chr2:100106981-100107031	NB4	blood:	n/a
36	chr2:100109838-100109888	ECC-1	luminal epithelium:	n/a
37	chr2:100107195-100107245	SAEC	small airway:	n/a
38	chr2:100107157-100107207	HRE	kidney:	n/a
39	chr2:100106981-100107031	MCF-7	breast:	n/a
40	chr2:100106285-100106335	HAEpiC	amniotic membrane:	n/a
41	chr2:100078174-100078224	GM12891	blood:	n/a
42	chr2:100106285-100106335	A549	lung:	n/a
43	chr2:100107157-100107207	HRCEpiC	kidney:	n/a
44	chr2:100106147-100106197	NHDF-neo	bronchial:	n/a
45	chr2:100106981-100107031	NT2-D1	testis:	n/a
46	chr2:100107195-100107245	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:100106285-100106335	SK-N-SH	brain:	n/a
48	chr2:100106981-100107031	HRE	kidney:	n/a
49	chr2:100107195-100107245	MCF-7	breast:	n/a
50	chr2:100107157-100107207	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:100106074..100106604-chr6:43021248..43021884,2	Hela-S3	cervix:
2	chr2:100082191..100084657-chr2:100091943..100094929,2	K562	blood:
3	chr2:100100281..100102788-chr2:100105250..100107935,2	MCF-7	breast:
4	chr2:100066768..100070769-chr2:100085883..100089135,3	K562	blood:
5	chr2:100083617..100085558-chr2:100105474..100107901,2	K562	blood:
6	chr2:99952384..99954745-chr2:100101155..100103970,2	K562	blood:
7	chr2:100105579..100107417-chr2:100107751..100110835,3	MCF-7	breast:
8	chr2:99485026..99487433-chr2:100105196..100107704,3	MCF-7	breast:
9	chr2:100079142..100082364-chr2:100082502..100085624,3	K562	blood:
10	chr2:100091037..100094858-chr2:100099869..100102767,4	K562	blood:
11	chr2:100019781..100021613-chr2:100105810..100107711,2	MCF-7	breast:
12	chr2:99796371..99799059-chr2:100100777..100103682,2	MCF-7	breast:
13	chr2:100077312..100079751-chr2:100099970..100102811,3	K562	blood:
14	chr2:99951055..99957153-chr2:100104418..100108530,14	K562	blood:
15	chr2:100091970..100094649-chr2:100104238..100106048,2	MCF-7	breast:
16	chr2:100105801..100108163-chr2:100108777..100110702,3	K562	blood:
17	chr2:100088510..100094256-chr2:100103985..100108648,6	K562	blood:
18	chr2:100104879..100106389-chr2:100120710..100122893,2	MCF-7	breast:
19	chr2:100108007..100111568-chr2:100119889..100123182,3	K562	blood:
20	chr2:99951256..99955616-chr2:100104663..100107649,9	K562	blood:
21	chr2:100103127..100105220-chr2:100105235..100107072,2	MCF-7	breast:
22	chr2:100082529..100085149-chr2:100097513..100099480,2	K562	blood:
23	chr2:100080735..100084657-chr2:100090928..100093443,3	K562	blood:
24	chr2:99952415..99954577-chr2:100101593..100103318,2	MCF-7	breast:
25	chr2:100068951..100071646-chr2:100081782..100083860,2	K562	blood:
26	chr2:100011720..100013891-chr2:100102274..100104165,2	K562	blood:
27	chr2:100075556..100080404-chr2:100103648..100108163,7	K562	blood:
28	chr2:100019850..100022413-chr2:100104870..100107869,3	MCF-7	breast:
29	chr2:100079371..100082089-chr2:100106220..100108086,2	MCF-7	breast:
30	chr2:100083971..100085589-chr2:100104836..100106610,2	MCF-7	breast:
31	chr2:100077312..100079121-chr2:100100989..100102811,2	K562	blood:
32	chr2:100086031..100088660-chr2:100104187..100107882,3	MCF-7	breast:
33	chr2:100064922..100067755-chr2:100103657..100105818,3	MCF-7	breast:
34	chr2:100104533..100107300-chr2:100936927..100940750,3	MCF-7	breast:
35	chr11:63580406..63581266-chr2:100105797..100106443,2	MCF-7	breast:
36	chr2:100081842..100083413-chr2:100104447..100107377,2	MCF-7	breast:
37	chr2:100087595..100089096-chr2:100090818..100093356,2	K562	blood:
38	chr2:100099713..100102517-chr2:100102817..100104971,3	MCF-7	breast:
39	chr15:76603305..76604106-chr2:100105951..100106601,2	Hela-S3	cervix:
40	chr2:99796217..99799127-chr2:100105224..100108883,4	K562	blood:
41	chr2:100088451..100090156-chr2:100093150..100094831,2	MCF-7	breast:
42	chr2:100105839..100108268-chr2:100110978..100113456,2	K562	blood:
43	chr2:100072254..100074226-chr2:100106055..100108821,2	MCF-7	breast:
44	chr2:100080735..100084657-chr2:100090928..100093443,3	K562	blood:
45	chr2:99796217..99798600-chr2:100104908..100107681,3	K562	blood:
46	chr2:27881530..27883047-chr2:100099438..100101050,2	MCF-7	breast:
47	chr2:100084922..100089797-chr2:100104456..100108052,9	MCF-7	breast:
48	chr2:100092416..100102947-chr2:100103557..100108181,19	MCF-7	breast:
49	chr2:100082529..100085149-chr2:100097513..100099480,2	K562	blood:
50	chr2:100088451..100090156-chr2:100093150..100094831,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF5B-1	chr2:100107781-100108142	XLOC_001588

Variant related genes	Relation type
REV1	TF binding region
REV1	CpG island
ENSG00000044090	chromatin interactions
ENSG00000196872	chromatin interactions
ENSG00000158417	chromatin interactions
ENSG00000241962	chromatin interactions
ENSG00000185414	chromatin interactions
ENSG00000115514	chromatin interactions
ENSG00000168005	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000273306	chromatin interactions
ENSG00000158411	chromatin interactions
ENSG00000170500	chromatin interactions
ENSG00000135945	chromatin interactions

Extended variants
information (count: 1408 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1408 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142375612	chr2:100072797-100072798	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576051662	chr2:100072851-100072852	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541558020	chr2:100072879-100072880	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78886329	chr2:100072898-100072899	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs28369955	chr2:100072915-100072916	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558876747	chr2:100072924-100072925	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs187225243	chr2:100072951-100072952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577380648	chr2:100072986-100072987	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190058110	chr2:100073060-100073061	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs28369954	chr2:100073082-100073083	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs7580448	chr2:100073130-100073131	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs569192958	chr2:100073177-100073178	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181705544	chr2:100073328-100073329	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs548747688	chr2:100073338-100073339	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10183488	chr2:100073402-100073403	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568662711	chr2:100073425-100073426	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574851157	chr2:100073501-100073502	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534351597	chr2:100073504-100073505	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs9308821	chr2:100073512-100073513	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186020800	chr2:100073544-100073545	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs539756636	chr2:100073647-100073648	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs556106002	chr2:100073699-100073700	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575974553	chr2:100073757-100073758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541519049	chr2:100073767-100073768	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561486078	chr2:100073770-100073771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571817158	chr2:100073790-100073791	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540780803	chr2:100073822-100073823	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564142756	chr2:100073884-100073885	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190369687	chr2:100073887-100073888	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146901325	chr2:100073910-100073911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs202176815	chr2:100073941-100073942	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145842145	chr2:100073965-100073966	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs12465846	chr2:100073971-100073972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs568523497	chr2:100073990-100073991	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs527811493	chr2:100074062-100074063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs36007747	chr2:100074071-100074072	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547973827	chr2:100074074-100074075	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570988831	chr2:100074103-100074104	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs143745505	chr2:100074138-100074139	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs62155805	chr2:100074147-100074148	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371360329	chr2:100074149-100074150	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556628782	chr2:100074162-100074163	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569622790	chr2:100074184-100074185	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs182631425	chr2:100074266-100074267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185489522	chr2:100074282-100074283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190840916	chr2:100074302-100074303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148149570	chr2:100074321-100074322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549630340	chr2:100074328-100074329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557913710	chr2:100074360-100074361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577808971	chr2:100074364-100074365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	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
Ovarian cancer	21781307	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
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2018 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100006000-100081200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr2:100021200-100077800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:100032600-100078000	Weak transcription	Psoas Muscle	Psoas
4	chr2:100034200-100088800	Weak transcription	Small Intestine	intestine
5	chr2:100036800-100074800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:100038200-100073800	Weak transcription	Esophagus	oesophagus
7	chr2:100041400-100077800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:100041600-100083400	Weak transcription	Brain Substantia Nigra	brain
9	chr2:100048200-100090600	Weak transcription	Stomach Mucosa	stomach
10	chr2:100053800-100075800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:100055400-100083200	Weak transcription	Right Ventricle	heart
12	chr2:100055600-100078200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr2:100055600-100079800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:100055800-100072800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr2:100055800-100076200	Weak transcription	Aorta	Aorta
16	chr2:100055800-100076400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr2:100055800-100089000	Weak transcription	Pancreas	Pancrea
18	chr2:100055800-100092600	Weak transcription	Gastric	stomach
19	chr2:100056600-100091000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr2:100057200-100073000	Weak transcription	NHLF	lung
21	chr2:100057200-100076000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:100057400-100077800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:100057400-100078000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr2:100058200-100077800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr2:100060400-100079200	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr2:100061800-100079200	Strong transcription	Primary T cells fromperipheralblood	blood
27	chr2:100061800-100079400	Strong transcription	Liver	Liver
28	chr2:100062200-100074400	Strong transcription	Fetal Thymus	thymus
29	chr2:100062200-100079000	Strong transcription	Primary B cells from peripheral blood	blood
30	chr2:100062200-100080600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:100062200-100080600	Strong transcription	HepG2	liver
32	chr2:100062400-100079200	Strong transcription	Primary T helper cells fromperipheralblood	blood
33	chr2:100062600-100079200	Strong transcription	Duodenum Mucosa	Duodenum
34	chr2:100063400-100074200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:100063400-100074600	Strong transcription	Rectal Mucosa Donor 29	rectum
36	chr2:100063400-100078400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:100063400-100078800	Strong transcription	Adipose Nuclei	Adipose
38	chr2:100063400-100079200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr2:100063800-100078400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr2:100063800-100078400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr2:100064000-100074800	Strong transcription	Placenta	Placenta
42	chr2:100064000-100078800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:100065400-100072800	Weak transcription	Fetal Brain Male	brain
44	chr2:100065400-100076000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr2:100065400-100078600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr2:100065400-100087400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr2:100065600-100075800	Weak transcription	Colonic Mucosa	Colon
48	chr2:100065600-100077200	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr2:100065600-100077600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr2:100065800-100075600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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