Variant report

Variant	nsv2812
Chromosome Location	chr2:85899944-85929267
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:580)
CpG islands
(count:671)
Chromatin interactive
region (count:29)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:580 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:85929237-85929770	HCT-116	colon:	n/a	n/a
2	ATF3	chr2:85906184-85906724	A549	lung:	n/a	n/a
3	BACH1	chr2:85906329-85906531	K562	blood:	n/a	n/a
4	BCL3	chr2:85906052-85906724	A549	lung:	n/a	n/a
5	BHLHE40	chr2:85914457-85914661	K562	blood:	n/a	chr2:85914497-85914506 chr2:85914496-85914505 chr2:85914491-85914512
6	BHLHE40	chr2:85914370-85914640	A549	lung:	n/a	chr2:85914497-85914506 chr2:85914496-85914505 chr2:85914491-85914512
7	BHLHE40	chr2:85906376-85906649	K562	blood:	n/a	n/a
8	BHLHE40	chr2:85906353-85906635	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:85906354-85906610	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr2:85906578-85906588	GM12878	blood:	n/a	n/a
11	BRCA1	chr2:85906368-85906529	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr2:85906328-85906666	K562	blood:	n/a	n/a
13	CCNT2	chr2:85928847-85928894	K562	blood:	n/a	n/a
14	CEBPB	chr2:85899743-85899973	K562	blood:	n/a	chr2:85899865-85899876
15	CEBPB	chr2:85902158-85902365	A549	lung:	n/a	n/a
16	CEBPB	chr2:85914405-85914644	H1-hESC	embryonic stem cell:	n/a	chr2:85914519-85914532
17	CEBPB	chr2:85914380-85914628	A549	lung:	n/a	chr2:85914519-85914532
18	CEBPB	chr2:85928474-85928724	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:85914334-85914712	Hela-S3	cervix:	n/a	chr2:85914519-85914532
20	CEBPB	chr2:85928481-85928885	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:85929207-85929796	HCT-116	colon:	n/a	n/a
22	CEBPB	chr2:85908115-85908831	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr2:85927841-85928142	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr2:85927812-85928141	IMR90	lung:	n/a	n/a
25	CEBPB	chr2:85927803-85928151	A549	lung:	n/a	n/a
26	CEBPB	chr2:85901630-85901869	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:85901599-85901843	A549	lung:	n/a	n/a
28	CEBPB	chr2:85927720-85928201	A549	lung:	n/a	n/a
29	CEBPB	chr2:85899875-85899986	HepG2	liver:	n/a	n/a
30	CEBPB	chr2:85929177-85929751	A549	lung:	n/a	n/a
31	CEBPB	chr2:85901574-85902386	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr2:85914400-85914661	A549	lung:	n/a	chr2:85914519-85914532
33	CEBPB	chr2:85929159-85929725	HCT-116	colon:	n/a	n/a
34	CEBPB	chr2:85906460-85906569	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:85914409-85914673	IMR90	lung:	n/a	chr2:85914519-85914532
36	CEBPB	chr2:85914289-85914832	A549	lung:	n/a	chr2:85914519-85914532
37	CEBPB	chr2:85928462-85928843	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr2:85906323-85906665	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr2:85929256-85929711	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:85928478-85928799	A549	lung:	n/a	n/a
41	CEBPB	chr2:85927889-85928096	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:85906375-85906658	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:85927910-85928111	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:85902109-85902287	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:85902056-85902392	MCF-7	breast:	n/a	n/a
46	CEBPD	chr2:85923452-85923706	K562	blood:	n/a	n/a
47	CHD2	chr2:85908540-85908801	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr2:85926501-85926815	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr2:85906356-85906633	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr2:85906377-85906520	HepG2	liver:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:85921036-85921086	NHDF-neo	bronchial:	n/a
2	chr2:85914525-85914575	PFSK-1	brain:	n/a
3	chr2:85925749-85925799	HRCEpiC	kidney:	n/a
4	chr2:85921963-85922013	HPAEpiC	pulmonary alveolar:	n/a
5	chr2:85924685-85924735	NB4	blood:	n/a
6	chr2:85921438-85921488	Hela-S3	cervix:	n/a
7	chr2:85921283-85921333	NHBE	bronchial:	n/a
8	chr2:85925749-85925799	HCPEpiC	choroid plexus:	n/a
9	chr2:85925749-85925799	T-47D	breast:	n/a
10	chr2:85920000-85920050	MCF-7	breast:	n/a
11	chr2:85924685-85924735	NH-A	brain:	n/a
12	chr2:85906657-85906707	SKMC	muscle:	n/a
13	chr2:85906657-85906707	HepG2	liver:	n/a
14	chr2:85925749-85925799	GM06990	blood:	n/a
15	chr2:85920000-85920050	Hela-S3	cervix:	n/a
16	chr2:85914525-85914575	LNCaP	prostate:	n/a
17	chr2:85921252-85921302	HCM	heart:	n/a
18	chr2:85921252-85921302	ovcar-3	ovarian:	n/a
19	chr2:85921963-85922013	GM19239	blood:	n/a
20	chr2:85914525-85914575	NT2-D1	testis:	n/a
21	chr2:85921252-85921302	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:85906657-85906707	CMK	blood:	n/a
23	chr2:85920000-85920050	ProgFib	skin:	n/a
24	chr2:85921438-85921488	ECC-1	luminal epithelium:	n/a
25	chr2:85925749-85925799	GM19239	blood:	n/a
26	chr2:85920000-85920050	AoSMC	blood vessel:	n/a
27	chr2:85924685-85924735	BE2_C	brain:	n/a
28	chr2:85921252-85921302	HCF	heart:	n/a
29	chr2:85921283-85921333	T-47D	breast:	n/a
30	chr2:85920000-85920050	HepG2	liver:	n/a
31	chr2:85921529-85921579	GM12891	blood:	n/a
32	chr2:85906657-85906707	SK-N-MC	brain:	n/a
33	chr2:85925749-85925799	AG09319	gingival:	n/a
34	chr2:85914525-85914575	NH-A	brain:	n/a
35	chr2:85921529-85921579	ProgFib	skin:	n/a
36	chr2:85921438-85921488	CMK	blood:	n/a
37	chr2:85921036-85921086	Hela-S3	cervix:	n/a
38	chr2:85921283-85921333	PANC-1	pancreas:	n/a
39	chr2:85920000-85920050	AG09319	gingival:	n/a
40	chr2:85921963-85922013	HRE	kidney:	n/a
41	chr2:85921438-85921488	BE2_C	brain:	n/a
42	chr2:85921036-85921086	HCT-116	colon:	n/a
43	chr2:85914525-85914575	NB4	blood:	n/a
44	chr2:85925749-85925799	NHDF-neo	bronchial:	n/a
45	chr2:85921252-85921302	HMEC	breast:	n/a
46	chr2:85924685-85924735	AG09309	skin:	n/a
47	chr2:85906657-85906707	HRE	kidney:	n/a
48	chr2:85921283-85921333	NH-A	brain:	n/a
49	chr2:85921529-85921579	NHBE	bronchial:	n/a
50	chr2:85921252-85921302	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:85924610..85926408-chr2:85954711..85957464,2	K562	blood:
2	chr2:85921436..85923058-chr2:85925193..85926829,2	K562	blood:
3	chr2:85901871..85904801-chr2:85904981..85906586,2	MCF-7	breast:
4	chr2:85895587..85899828-chr2:85904456..85908043,4	K562	blood:
5	chr2:85896506..85899590-chr2:85901147..85903484,4	K562	blood:
6	chr2:85919636..85921243-chr2:85926613..85928346,2	MCF-7	breast:
7	chr2:85901871..85904801-chr2:85904981..85906586,2	MCF-7	breast:
8	chr2:85900096..85901739-chr2:85904881..85906884,2	K562	blood:
9	chr2:85905086..85909626-chr2:85912458..85918293,6	K562	blood:
10	chr2:85905984..85906919-chr2:85955820..85956730,3	MCF-7	breast:
11	chr2:85906061..85906876-chr2:85945247..85945851,2	MCF-7	breast:
12	chr2:85914382..85917156-chr2:85991881..85994505,2	MCF-7	breast:
13	chr2:85906761..85907337-chr2:86041197..86041830,2	K562	blood:
14	chr2:85895416..85898828-chr2:85901766..85904071,3	K562	blood:
15	chr2:85917153..85919926-chr2:85924436..85926788,2	K562	blood:
16	chr2:85900096..85901739-chr2:85904881..85906884,2	K562	blood:
17	chr2:85905086..85906749-chr2:85913552..85916158,2	K562	blood:
18	chr2:85915170..85916745-chr2:85920753..85922786,2	K562	blood:
19	chr2:85906030..85906925-chr2:86041040..86041639,4	MCF-7	breast:
20	chr2:85912358..85914098-chr2:85920772..85923092,2	K562	blood:
21	chr2:85919636..85921243-chr2:85926613..85928346,2	MCF-7	breast:
22	chr2:85839135..85840661-chr2:85928083..85930394,2	MCF-7	breast:
23	chr2:85904933..85907760-chr2:85933076..85936019,2	MCF-7	breast:
24	chr2:85917153..85919926-chr2:85924436..85926788,2	K562	blood:
25	chr2:85886384..85888298-chr2:85898868..85900454,2	MCF-7	breast:
26	chr2:85906071..85907432-chr2:85933759..85935058,9	MCF-7	breast:
27	chr2:85892613..85895581-chr2:85898917..85901318,2	K562	blood:
28	chr2:85928909..85931848-chr2:86021884..86024213,2	K562	blood:
29	chr2:85899004..85901888-chr2:85989811..85991933,2	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNLY-2	chr2:85923081-85923179	NONHSAT072044
2	lnc-GNLY-3	chr2:85904630-85905146	l_1876_chr2:85898899-85905283_thyroid
3	lnc-GNLY-3	chr2:85904630-85906025	NONHSAT072038
4	lnc-GNLY-2	chr2:85925687-85925870	NONHSAT072043
5	lnc-GNLY-2	chr2:85912298-85912344	NONHSAT072039
6	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072039
7	lnc-GNLY-2	chr2:85924111-85924224	NONHSAT072044
8	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072041
9	lnc-GNLY-2	chr2:85921451-85921593	NONHSAT072041
10	lnc-GNLY-2	chr2:85921465-85922546	NONHSAT072043
11	lnc-GNLY-2	chr2:85922027-85922309	NONHSAT072045
12	lnc-SFTPB-2	chr2:85913176-85914170	NONHSAT072040
13	lnc-GNLY-2	chr2:85921876-85922046	NONHSAT072041
14	lnc-GNLY-2	chr2:85921876-85922546	NONHSAT072042
15	lnc-GNLY-2	chr2:85921455-85921593	NONHSAT072042
16	lnc-GNLY-2	chr2:85921876-85922046	NONHSAT072044
17	lnc-GNLY-2	chr2:85923081-85923179	NONHSAT072043
18	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072044
19	lnc-GNLY-2	chr2:85921549-85921593	NONHSAT072044
20	lnc-GNLY-3	chr2:85905160-85905283	l_1876_chr2:85898899-85905283_thyroid
21	lnc-GNLY-2	chr2:85923081-85923229	NONHSAT072042
22	lnc-GNLY-2	chr2:85923081-85923853	NONHSAT072039
23	lnc-GNLY-2	chr2:85923081-85923617	NONHSAT072041
24	lnc-GNLY-2	chr2:85922443-85922546	NONHSAT072045
25	lnc-GNLY-2	chr2:85924111-85924800	NONHSAT072043
26	lnc-GNLY-2	chr2:85923081-85923655	NONHSAT072045

No data

Variant related genes	Relation type
GNLY	TF binding region
SFTPB	TF binding region
ENSG00000203363	TF binding region
GNLY	CpG island
SFTPB	CpG island
ENSG00000203363	CpG island
ENSG00000168878	chromatin interactions
ENSG00000168887	chromatin interactions
ENSG00000168883	chromatin interactions
ENSG00000115523	chromatin interactions
ENSG00000203363	chromatin interactions
ENSG00000199687	chromatin interactions

Extended variants
information (count: 1170 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1170 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567939556	chr2:85900021-85900022	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373639444	chr2:85900033-85900034	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191550288	chr2:85900089-85900090	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs367620493	chr2:85900106-85900107	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs571942304	chr2:85900140-85900141	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs545734893	chr2:85900154-85900155	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs72923102	chr2:85900183-85900184	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs149947909	chr2:85900322-85900323	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543570767	chr2:85900380-85900381	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs562252063	chr2:85900427-85900428	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184175764	chr2:85900457-85900458	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533716979	chr2:85900484-85900485	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187194096	chr2:85900492-85900493	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559951345	chr2:85900572-85900573	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs375317057	chr2:85900597-85900598	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs551715565	chr2:85900639-85900640	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs112936493	chr2:85900663-85900664	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs72925004	chr2:85900710-85900711	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs76174197	chr2:85900746-85900747	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs140957566	chr2:85900780-85900781	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567904896	chr2:85900786-85900787	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535312178	chr2:85900795-85900796	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192002130	chr2:85900799-85900800	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565924307	chr2:85900821-85900822	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144826810	chr2:85900852-85900853	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113649271	chr2:85900858-85900859	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs369454745	chr2:85900861-85900862	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575988065	chr2:85900879-85900880	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77412032	chr2:85900900-85900901	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs13414643	chr2:85900905-85900906	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138582783	chr2:85900930-85900931	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559711337	chr2:85900932-85900933	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140307031	chr2:85900999-85901000	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs545402191	chr2:85901000-85901001	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs563681744	chr2:85901008-85901009	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376302848	chr2:85901020-85901021	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530853372	chr2:85901037-85901038	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs185353717	chr2:85901055-85901056	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs560999274	chr2:85901081-85901082	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs544264224	chr2:85901192-85901193	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs528572743	chr2:85901203-85901204	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547542096	chr2:85901204-85901205	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs143434010	chr2:85901240-85901241	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147973785	chr2:85901243-85901244	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539704408	chr2:85901246-85901247	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs72925006	chr2:85901292-85901293	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs373495300	chr2:85901310-85901311	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537001660	chr2:85901318-85901319	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs115104676	chr2:85901319-85901320	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs573745796	chr2:85901346-85901347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
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
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	18438408	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16272173	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:597 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:85883600-85900000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr2:85886400-85901000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:85887000-85905800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:85891000-85905800	Weak transcription	Right Atrium	heart
5	chr2:85893000-85903000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr2:85894000-85905000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr2:85895600-85900800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:85896200-85901200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:85896400-85900600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:85896600-85900600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:85896600-85901200	Weak transcription	Lung	lung
12	chr2:85897200-85900000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr2:85897200-85905600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr2:85898800-85900000	Enhancers	Primary B cells from cord blood	blood
15	chr2:85899200-85902000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr2:85899400-85900600	Enhancers	Placenta	Placenta
17	chr2:85899600-85900000	Enhancers	GM12878-XiMat	blood
18	chr2:85899600-85902400	Enhancers	Adipose Nuclei	Adipose
19	chr2:85899800-85900200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr2:85899800-85900200	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr2:85899800-85902200	Enhancers	NHDF-Ad	bronchial
22	chr2:85900000-85900400	Enhancers	Brain Hippocampus Middle	brain
23	chr2:85900000-85900600	Enhancers	Primary B cells from peripheral blood	blood
24	chr2:85900000-85900800	Weak transcription	Primary B cells from cord blood	blood
25	chr2:85900000-85901000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr2:85900200-85901000	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr2:85900200-85901400	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr2:85900200-85902000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:85900200-85902200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:85900400-85901200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr2:85900400-85905600	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:85900600-85901000	Weak transcription	Placenta	Placenta
33	chr2:85900600-85901400	Enhancers	Primary hematopoietic stem cells	blood
34	chr2:85900600-85902200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr2:85900600-85902800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:85900600-85906200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr2:85900800-85901000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr2:85900800-85901200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr2:85900800-85902600	Enhancers	Primary B cells from cord blood	blood
40	chr2:85901000-85901400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr2:85901000-85901400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
42	chr2:85901000-85901800	Enhancers	H9 Cell Line	embryonic stem cell
43	chr2:85901000-85902200	Enhancers	Placenta	Placenta
44	chr2:85901200-85902200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr2:85901200-85902800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr2:85901200-85902800	Enhancers	Lung	lung
47	chr2:85901200-85902800	Enhancers	Psoas Muscle	Psoas
48	chr2:85901200-85903400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr2:85901200-85906000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr2:85901400-85901600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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