Variant report

Variant	nsv560053
Chromosome Location	chr12:105583877-105651356
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1425)
CpG islands
(count:978)
Chromatin interactive
region (count:86)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1425 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:105629662-105630339	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:105591473-105591516	HepG2	liver:	n/a	n/a
3	ATF1	chr12:105633244-105633314	K562	blood:	n/a	n/a
4	ATF1	chr12:105649824-105650015	K562	blood:	n/a	n/a
5	ATF2	chr12:105630022-105630380	GM12878	blood:	n/a	n/a
6	ATF3	chr12:105629753-105630307	A549	lung:	n/a	n/a
7	BACH1	chr12:105629499-105630249	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr12:105629823-105630623	A549	lung:	n/a	chr12:105630016-105630025 chr12:105629987-105629996
9	BCLAF1	chr12:105629741-105630263	GM12878	blood:	n/a	chr12:105630016-105630025 chr12:105629987-105629996
10	BCLAF1	chr12:105629832-105630264	GM12878	blood:	n/a	chr12:105630016-105630025 chr12:105629987-105629996
11	BHLHE40	chr12:105626000-105626004	A549	lung:	n/a	n/a
12	BHLHE40	chr12:105629385-105630169	K562	blood:	n/a	n/a
13	BHLHE40	chr12:105622370-105622505	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:105620147-105620258	K562	blood:	n/a	n/a
15	BHLHE40	chr12:105629860-105630292	GM12878	blood:	n/a	n/a
16	BRCA1	chr12:105629591-105629777	HepG2	liver:	n/a	n/a
17	BRCA1	chr12:105647641-105647747	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr12:105629877-105630206	K562	blood:	n/a	n/a
19	CCNT2	chr12:105629508-105630253	K562	blood:	n/a	n/a
20	CEBPB	chr12:105633296-105633608	K562	blood:	n/a	n/a
21	CEBPB	chr12:105588806-105589113	HepG2	liver:	n/a	chr12:105588959-105588970
22	CEBPB	chr12:105603377-105603563	IMR90	lung:	n/a	n/a
23	CEBPB	chr12:105620108-105620546	IMR90	lung:	n/a	chr12:105620255-105620266
24	CEBPB	chr12:105630333-105630679	IMR90	lung:	n/a	n/a
25	CEBPB	chr12:105608448-105608590	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:105608393-105608672	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:105604806-105605112	HepG2	liver:	n/a	chr12:105604960-105604969 chr12:105604955-105604972 chr12:105604947-105604958 chr12:105604945-105604962 chr12:105604960-105604971
28	CEBPB	chr12:105608321-105608592	A549	lung:	n/a	n/a
29	CEBPB	chr12:105625237-105625345	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:105608350-105608671	HepG2	liver:	n/a	n/a
31	CEBPB	chr12:105607829-105608873	MCF-7	breast:	n/a	chr12:105608280-105608293
32	CEBPB	chr12:105604782-105605140	A549	lung:	n/a	chr12:105604960-105604969 chr12:105604955-105604972 chr12:105604947-105604958 chr12:105604945-105604962 chr12:105604960-105604971
33	CEBPB	chr12:105608165-105608846	Hela-S3	cervix:	n/a	chr12:105608280-105608293
34	CEBPB	chr12:105651189-105651593	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:105648307-105648603	IMR90	lung:	n/a	n/a
36	CEBPD	chr12:105629979-105630280	HepG2	liver:	n/a	n/a
37	CEBPD	chr12:105629528-105630216	HepG2	liver:	n/a	n/a
38	CHD1	chr12:105629658-105630448	GM12878	blood:	n/a	chr12:105629705-105629715
39	CHD2	chr12:105625287-105625294	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr12:105629663-105630274	Hela-S3	cervix:	n/a	chr12:105629705-105629715
41	CHD2	chr12:105629943-105630193	K562	blood:	n/a	n/a
42	CHD2	chr12:105629581-105629781	HepG2	liver:	n/a	chr12:105629705-105629715
43	CHD2	chr12:105629997-105630094	HepG2	liver:	n/a	n/a
44	CHD2	chr12:105647519-105647879	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr12:105629776-105630221	GM12878	blood:	n/a	n/a
46	CHD2	chr12:105608403-105609093	Hela-S3	cervix:	n/a	n/a
47	CREB1	chr12:105629352-105630342	HepG2	liver:	n/a	n/a
48	CREB1	chr12:105629889-105630303	GM12878	blood:	n/a	n/a
49	CREB1	chr12:105629414-105630296	A549	lung:	n/a	n/a
50	CTCF	chr12:105620100-105620250	HPAF	blood vessel:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:105630036-105630086	BE2_C	brain:	n/a
2	chr12:105629755-105629805	H1-hESC	embryonic stem cell:	embryo
3	chr12:105630036-105630086	BE2_C	brain:	n/a
4	chr12:105629755-105629805	H1-hESC	embryonic stem cell:	embryo
5	chr12:105629518-105629568	Hepatocyte	liver:	n/a
6	chr12:105630720-105630770	HNPCEpiC	eye:	n/a
7	chr12:105622107-105622157	AG10803	skin:	n/a
8	chr12:105622107-105622157	CMK	blood:	n/a
9	chr12:105630771-105630821	Hepatocyte	liver:	n/a
10	chr12:105613925-105613975	AG04449	skin:	fetal
11	chr12:105633626-105633676	PrEC	prostate:	n/a
12	chr12:105630771-105630821	HPAEpiC	pulmonary alveolar:	n/a
13	chr12:105631413-105631463	NT2-D1	testis:	n/a
14	chr12:105626788-105626838	HUVEC	blood vessel:	n/a
15	chr12:105633626-105633676	ECC-1	luminal epithelium:	n/a
16	chr12:105631413-105631463	Hepatocyte	liver:	n/a
17	chr12:105629755-105629805	PrEC	prostate:	n/a
18	chr12:105626788-105626838	HPAEpiC	pulmonary alveolar:	n/a
19	chr12:105630720-105630770	HCT-116	colon:	n/a
20	chr12:105629798-105629848	GM06990	blood:	n/a
21	chr12:105633626-105633676	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:105593962-105594012	MCF-7	breast:	n/a
23	chr12:105593962-105594012	GM06990	blood:	n/a
24	chr12:105629798-105629848	HRCEpiC	kidney:	n/a
25	chr12:105629798-105629848	Hepatocyte	liver:	n/a
26	chr12:105630059-105630109	ProgFib	skin:	n/a
27	chr12:105629518-105629568	U87	brain:	n/a
28	chr12:105630063-105630113	AG10803	skin:	n/a
29	chr12:105629755-105629805	NHDF-neo	bronchial:	n/a
30	chr12:105630720-105630770	HIPEpiC	eye:	n/a
31	chr12:105630771-105630821	GM12878	blood:	n/a
32	chr12:105630205-105630255	GM12892	blood:	n/a
33	chr12:105630059-105630109	BJ	skin:	n/a
34	chr12:105629755-105629805	HMEC	breast:	n/a
35	chr12:105630059-105630109	HUVEC	blood vessel:	n/a
36	chr12:105630063-105630113	NT2-D1	testis:	n/a
37	chr12:105622107-105622157	ovcar-3	ovarian:	n/a
38	chr12:105631413-105631463	HEK293	kidney:	embryo
39	chr12:105605477-105605527	SK-N-MC	brain:	n/a
40	chr12:105629798-105629848	NHDF-neo	bronchial:	n/a
41	chr12:105629518-105629568	PANC-1	pancreas:	n/a
42	chr12:105629798-105629848	HCT-116	colon:	n/a
43	chr12:105629755-105629805	AG09319	gingival:	n/a
44	chr12:105629798-105629848	SK-N-MC	brain:	n/a
45	chr12:105622107-105622157	Hepatocyte	liver:	n/a
46	chr12:105626788-105626838	HRPEpiC	eye:	n/a
47	chr12:105630036-105630086	MCF10A-Er-Src	breast:	n/a
48	chr12:105626788-105626838	Jurkat	blood:	n/a
49	chr12:105630063-105630113	HepG2	liver:	n/a
50	chr12:105622107-105622157	NHBE	bronchial:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:105629542..105630454-chr19:18392234..18393176,2	Hela-S3	cervix:
2	chr12:105608691..105610894-chr12:105612066..105614500,4	MCF-7	breast:
3	chr12:105606787..105609967-chr12:105617120..105620044,3	MCF-7	breast:
4	chr12:105499144..105502991-chr12:105627617..105631044,5	MCF-7	breast:
5	chr12:105636186..105637706-chr17:16342913..16345886,3	K562	blood:
6	chr12:105500608..105502385-chr12:105631430..105634044,2	K562	blood:
7	chr12:105587133..105589303-chr12:105595164..105597360,2	MCF-7	breast:
8	chr12:105632034..105634612-chr12:105649228..105651077,2	MCF-7	breast:
9	chr12:105586360..105589934-chr12:105601343..105605180,3	MCF-7	breast:
10	chr12:105598232..105600634-chr12:105603530..105606133,2	K562	blood:
11	chr12:105596266..105598085-chr12:105600191..105602690,2	K562	blood:
12	chr12:105629495..105630048-chr20:30696905..30697754,2	Hela-S3	cervix:
13	chr12:105501229..105503953-chr12:105621352..105624637,3	MCF-7	breast:
14	chr12:105586360..105589934-chr12:105601343..105605180,3	MCF-7	breast:
15	chr12:105595599..105598152-chr12:105628448..105630073,2	MCF-7	breast:
16	chr12:105499627..105501658-chr12:105620143..105622423,2	K562	blood:
17	chr12:105628535..105631470-chr12:105631945..105633798,3	K562	blood:
18	chr12:105501422..105503562-chr12:105608423..105610224,2	MCF-7	breast:
19	chr12:105608691..105610894-chr12:105612066..105614500,4	MCF-7	breast:
20	chr12:105628268..105630407-chr12:105646094..105648967,2	MCF-7	breast:
21	chr12:105628535..105631488-chr12:105632035..105634749,3	K562	blood:
22	chr12:105606787..105609967-chr12:105617120..105620044,3	MCF-7	breast:
23	chr12:105592344..105594615-chr12:105595221..105597389,2	MCF-7	breast:
24	chr12:105606486..105608815-chr12:105609324..105611383,2	K562	blood:
25	chr12:105606486..105608815-chr12:105609324..105611383,2	K562	blood:
26	chr12:105500023..105502355-chr12:105628064..105629909,2	K562	blood:
27	chr12:105646719..105649373-chr12:105657582..105659204,2	K562	blood:
28	chr12:105556392..105559099-chr12:105584648..105587108,2	K562	blood:
29	chr12:105599435..105602379-chr12:105626303..105628956,2	K562	blood:
30	chr12:105620755..105625323-chr12:105625745..105629848,5	K562	blood:
31	chr12:105630089..105632839-chr12:105665320..105668612,3	MCF-7	breast:
32	chr12:105604459..105610765-chr12:105612400..105619000,9	MCF-7	breast:
33	chr12:105501251..105503302-chr12:105608033..105610589,2	MCF-7	breast:
34	chr12:105627501..105631320-chr12:105637092..105641109,6	MCF-7	breast:
35	chr12:105628928..105631591-chr12:105632421..105636831,6	MCF-7	breast:
36	chr12:105585594..105587866-chr12:105590129..105592324,2	MCF-7	breast:
37	chr12:105501540..105503183-chr12:105627693..105630661,2	MCF-7	breast:
38	chr12:105615953..105617646-chr12:105655942..105657913,2	MCF-7	breast:
39	chr12:105632034..105634612-chr12:105649228..105651077,2	MCF-7	breast:
40	chr12:105611067..105613851-chr12:105616365..105618135,2	MCF-7	breast:
41	chr12:105599435..105602379-chr12:105626303..105628956,2	K562	blood:
42	chr12:105609229..105612971-chr12:105615964..105620947,4	K562	blood:
43	chr12:105500023..105504653-chr12:105628064..105630551,4	K562	blood:
44	chr12:105607304..105609527-chr12:105723338..105725728,2	MCF-7	breast:
45	chr12:105611185..105613030-chr12:105615764..105617845,2	MCF-7	breast:
46	chr12:105628899..105630525-chr15:65596241..65598833,2	MCF-7	breast:
47	chr12:105598458..105599984-chr12:105777215..105778784,2	MCF-7	breast:
48	chr12:105602998..105604968-chr12:105605214..105607629,2	MCF-7	breast:
49	chr12:105592344..105594615-chr12:105595221..105597389,2	MCF-7	breast:
50	chr12:105589883..105591833-chr12:105596630..105599143,3	K562	blood:

No data

Variant related genes	Relation type
APPL2	TF binding region
C12orf75	TF binding region
APPL2	CpG island
C12orf75	CpG island
ENSG00000198431	chromatin interactions
ENSG00000101337	chromatin interactions
ENSG00000136044	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000117318	chromatin interactions
ENSG00000235162	chromatin interactions
ENSG00000247240	chromatin interactions
ENSG00000138629	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000266651	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000175061	chromatin interactions
ENSG00000059804	chromatin interactions

Extended variants
information (count: 2765 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2765 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2272495	chr12:105583877-105583878	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200542741	chr12:105583880-105583881	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576659482	chr12:105583968-105583969	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs568041214	chr12:105584040-105584041	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148713024	chr12:105584121-105584122	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570052615	chr12:105584146-105584147	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs547228636	chr12:105584175-105584176	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs566845726	chr12:105584178-105584179	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs539122579	chr12:105584186-105584187	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs558641887	chr12:105584216-105584217	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs569253212	chr12:105584229-105584230	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs538513211	chr12:105584254-105584255	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs555281740	chr12:105584327-105584328	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs575245023	chr12:105584407-105584408	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs540822265	chr12:105584422-105584423	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs116959144	chr12:105584470-105584471	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs74802930	chr12:105584489-105584490	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs545898179	chr12:105584537-105584538	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs59618886	chr12:105584558-105584559	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs191001909	chr12:105584701-105584702	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562568777	chr12:105584727-105584728	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs75636247	chr12:105584751-105584752	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs537409461	chr12:105584756-105584757	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561636169	chr12:105584768-105584769	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs78695030	chr12:105584790-105584791	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs60732733	chr12:105584834-105584835	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs151266741	chr12:105584851-105584852	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs182787925	chr12:105584877-105584878	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555490789	chr12:105584920-105584921	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs559962969	chr12:105584972-105584973	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564428646	chr12:105584994-105584995	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs532468447	chr12:105585051-105585052	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs552662953	chr12:105585057-105585058	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569283606	chr12:105585154-105585155	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79385818	chr12:105585239-105585240	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs548644169	chr12:105585246-105585247	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568766659	chr12:105585261-105585262	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs145509832	chr12:105585296-105585297	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs187436925	chr12:105585303-105585304	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs577389115	chr12:105585313-105585314	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs539671713	chr12:105585349-105585350	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs76657638	chr12:105585470-105585471	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs191273552	chr12:105585487-105585488	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371259913	chr12:105585491-105585492	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs147716531	chr12:105585519-105585520	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561347217	chr12:105585529-105585530	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370440032	chr12:105585531-105585532	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs2246510	chr12:105585543-105585544	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs564100106	chr12:105585549-105585550	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs183024577	chr12:105585555-105585556	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2633 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105522600-105586000	Weak transcription	Stomach Mucosa	stomach
2	chr12:105546800-105625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:105558200-105587200	Weak transcription	Psoas Muscle	Psoas
4	chr12:105558800-105615200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr12:105561400-105598400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr12:105568000-105589400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr12:105571400-105617800	Weak transcription	K562	blood
8	chr12:105576000-105593200	Strong transcription	Muscle Satellite Cultured Cells	--
9	chr12:105576000-105595600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:105576400-105585600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:105576400-105606000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr12:105577000-105607200	Strong transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:105577200-105584000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:105577200-105584000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr12:105577200-105587400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr12:105577200-105589400	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:105577200-105592200	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr12:105577400-105592800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:105577400-105593600	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr12:105577400-105616200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr12:105577600-105589200	Strong transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:105577800-105585600	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr12:105577800-105585800	Strong transcription	Brain Anterior Caudate	brain
24	chr12:105577800-105586400	Strong transcription	Brain Substantia Nigra	brain
25	chr12:105577800-105586800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr12:105577800-105589600	Strong transcription	Primary B cells from peripheral blood	blood
27	chr12:105577800-105591200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:105577800-105591400	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr12:105577800-105592200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr12:105577800-105592600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr12:105577800-105593400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr12:105577800-105594200	Strong transcription	Fetal Intestine Large	intestine
33	chr12:105577800-105594400	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr12:105577800-105595200	Strong transcription	Left Ventricle	heart
35	chr12:105577800-105598600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:105577800-105598800	Strong transcription	Rectal Mucosa Donor 29	rectum
37	chr12:105577800-105599400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr12:105577800-105602600	Strong transcription	Fetal Thymus	thymus
39	chr12:105577800-105603600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr12:105577800-105605400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr12:105577800-105605600	Strong transcription	Primary B cells from cord blood	blood
42	chr12:105577800-105607400	Strong transcription	Duodenum Mucosa	Duodenum
43	chr12:105578000-105584000	Strong transcription	NHDF-Ad	bronchial
44	chr12:105578000-105585800	Strong transcription	Brain Hippocampus Middle	brain
45	chr12:105578000-105586200	Strong transcription	HUVEC	blood vessel
46	chr12:105578000-105586400	Strong transcription	Adipose Nuclei	Adipose
47	chr12:105578000-105588600	Strong transcription	Liver	Liver
48	chr12:105578000-105589400	Strong transcription	Primary T cells from cord blood	blood
49	chr12:105578000-105589400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr12:105578000-105590800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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