Variant report

Variant	nsv899500
Chromosome Location	chr12:105742674-105803028
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:870)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:870 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:105777106-105777465	HepG2	liver:	n/a	n/a
2	ATF2	chr12:105745785-105746226	GM12878	blood:	n/a	n/a
3	ATF2	chr12:105745773-105746233	GM12878	blood:	n/a	n/a
4	ATF2	chr12:105750815-105751589	GM12878	blood:	n/a	n/a
5	BACH1	chr12:105748359-105748431	K562	blood:	n/a	n/a
6	BACH1	chr12:105746778-105747104	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr12:105750923-105751527	GM12878	blood:	n/a	chr12:105751380-105751390
8	BATF	chr12:105745917-105746230	GM12878	blood:	n/a	n/a
9	BATF	chr12:105745789-105746206	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:105745760-105746255	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:105745868-105746174	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:105750764-105751375	GM12878	blood:	n/a	chr12:105751033-105751042
13	BCLAF1	chr12:105750862-105751424	GM12878	blood:	n/a	chr12:105751033-105751042
14	BCLAF1	chr12:105745775-105746292	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:105748545-105748836	IMR90	lung:	n/a	chr12:105748703-105748714
16	CEBPB	chr12:105777190-105777468	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:105758171-105758235	A549	lung:	n/a	n/a
18	CEBPB	chr12:105762889-105763177	IMR90	lung:	n/a	n/a
19	CEBPB	chr12:105751033-105751519	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:105756566-105756832	HepG2	liver:	n/a	n/a
21	CEBPB	chr12:105749696-105749932	A549	lung:	n/a	chr12:105749913-105749922
22	CEBPB	chr12:105793280-105793501	K562	blood:	n/a	chr12:105793361-105793372
23	CEBPB	chr12:105748538-105748872	HepG2	liver:	n/a	chr12:105748703-105748714
24	CEBPB	chr12:105748672-105748779	K562	blood:	n/a	chr12:105748703-105748714
25	CEBPB	chr12:105793233-105793519	A549	lung:	n/a	chr12:105793361-105793372
26	CEBPB	chr12:105793262-105793516	IMR90	lung:	n/a	chr12:105793361-105793372
27	CEBPB	chr12:105750918-105751786	GM12878	blood:	n/a	n/a
28	CEBPB	chr12:105779021-105779204	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:105748537-105748848	A549	lung:	n/a	chr12:105748703-105748714
30	CEBPB	chr12:105793202-105793492	Hela-S3	cervix:	n/a	chr12:105793361-105793372
31	CEBPB	chr12:105793210-105793558	HepG2	liver:	n/a	chr12:105793361-105793372
32	CEBPB	chr12:105749608-105749944	IMR90	lung:	n/a	chr12:105749913-105749922
33	CEBPB	chr12:105756621-105756835	A549	lung:	n/a	n/a
34	CHD2	chr12:105777087-105777465	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr12:105746710-105746934	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr12:105762980-105763130	AG09309	skin:	n/a	n/a
37	CTCF	chr12:105777240-105777390	GM12871	blood:	n/a	chr12:105777301-105777319 chr12:105777307-105777316 chr12:105777296-105777317
38	CTCF	chr12:105772800-105772950	GM12869	blood:	n/a	n/a
39	CTCF	chr12:105777118-105777432	ECC-1	luminal epithelium:	n/a	chr12:105777301-105777319 chr12:105777307-105777316 chr12:105777296-105777317
40	CTCF	chr12:105777220-105777370	HBMEC	blood vessel:	n/a	chr12:105777301-105777319 chr12:105777307-105777316 chr12:105777296-105777317
41	CTCF	chr12:105777240-105777390	MCF-7	breast:	n/a	chr12:105777301-105777319 chr12:105777307-105777316 chr12:105777296-105777317
42	CTCF	chr12:105777220-105777370	NB4	blood:	n/a	chr12:105777301-105777319 chr12:105777307-105777316 chr12:105777296-105777317
43	CTCF	chr12:105772740-105772890	GM12873	blood:	n/a	n/a
44	CTCF	chr12:105772938-105773117	HepG2	liver:	n/a	n/a
45	CTCF	chr12:105772700-105772850	BJ	skin:	n/a	n/a
46	CTCF	chr12:105762980-105763130	HMF	breast:	n/a	n/a
47	CTCF	chr12:105785089-105785140	GM10266	blood:	n/a	n/a
48	CTCF	chr12:105772662-105773060	MCF-7	breast:	n/a	n/a
49	CTCF	chr12:105762957-105763052	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:105772680-105772930	HMEC	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:105759219-105759269	HepG2	liver:	n/a
2	chr12:105759219-105759269	HRE	kidney:	n/a
3	chr12:105759219-105759269	MCF-7	breast:	n/a
4	chr12:105747184-105747234	Hepatocyte	liver:	n/a
5	chr12:105744023-105744073	HEEpiC	esophagus:	n/a
6	chr12:105759219-105759269	Jurkat	blood:	n/a
7	chr12:105744023-105744073	HEK293	kidney:	embryo
8	chr12:105761853-105761903	SKMC	muscle:	n/a
9	chr12:105759219-105759269	HMEC	breast:	n/a
10	chr12:105744023-105744073	ovcar-3	ovarian:	n/a
11	chr12:105759219-105759269	HEEpiC	esophagus:	n/a
12	chr12:105747184-105747234	HRE	kidney:	n/a
13	chr12:105744023-105744073	T-47D	breast:	n/a
14	chr12:105747184-105747234	NB4	blood:	n/a
15	chr12:105744023-105744073	K562	blood:	n/a
16	chr12:105761853-105761903	GM12891	blood:	n/a
17	chr12:105747184-105747234	K562	blood:	n/a
18	chr12:105759219-105759269	NHDF-neo	bronchial:	n/a
19	chr12:105747184-105747234	SK-N-SH	brain:	n/a
20	chr12:105744023-105744073	HNPCEpiC	eye:	n/a
21	chr12:105747184-105747234	AG10803	skin:	n/a
22	chr12:105744023-105744073	Hela-S3	cervix:	n/a
23	chr12:105747184-105747234	GM12878	blood:	n/a
24	chr12:105744023-105744073	AG04449	skin:	fetal
25	chr12:105747184-105747234	PANC-1	pancreas:	n/a
26	chr12:105747184-105747234	GM06990	blood:	n/a
27	chr12:105744023-105744073	ProgFib	skin:	n/a
28	chr12:105747184-105747234	SK-N-MC	brain:	n/a
29	chr12:105761853-105761903	NHDF-neo	bronchial:	n/a
30	chr12:105759219-105759269	GM19239	blood:	n/a
31	chr12:105761853-105761903	GM12892	blood:	n/a
32	chr12:105744023-105744073	AG10803	skin:	n/a
33	chr12:105759219-105759269	SK-N-SH_RA	brain:	n/a
34	chr12:105761853-105761903	NH-A	brain:	n/a
35	chr12:105747184-105747234	PFSK-1	brain:	n/a
36	chr12:105744023-105744073	HPAEpiC	pulmonary alveolar:	n/a
37	chr12:105759219-105759269	BE2_C	brain:	n/a
38	chr12:105761853-105761903	HMEC	breast:	n/a
39	chr12:105761853-105761903	HepG2	liver:	n/a
40	chr12:105744023-105744073	SAEC	small airway:	n/a
41	chr12:105747184-105747234	GM19239	blood:	n/a
42	chr12:105744023-105744073	ECC-1	luminal epithelium:	n/a
43	chr12:105744023-105744073	A549	lung:	n/a
44	chr12:105747184-105747234	AG09319	gingival:	n/a
45	chr12:105761853-105761903	HNPCEpiC	eye:	n/a
46	chr12:105747184-105747234	PrEC	prostate:	n/a
47	chr12:105761853-105761903	SK-N-SH	brain:	n/a
48	chr12:105761853-105761903	K562	blood:	n/a
49	chr12:105761853-105761903	AG10803	skin:	n/a
50	chr12:105759219-105759269	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:105598458..105599984-chr12:105777215..105778784,2	MCF-7	breast:
2	chr12:105734973..105737533-chr12:105761292..105763629,2	MCF-7	breast:
3	chr12:105746552..105749035-chr12:105752419..105755099,2	K562	blood:
4	chr12:105794772..105797299-chr12:105799465..105802543,3	K562	blood:
5	chr12:105752392..105754695-chr12:105757650..105760428,2	MCF-7	breast:
6	chr12:105714730..105715298-chr12:105772516..105773065,3	MCF-7	breast:
7	chr12:105765326..105767170-chr12:105773876..105775781,2	MCF-7	breast:
8	chr12:105713189..105714168-chr12:105776809..105777553,3	MCF-7	breast:
9	chr12:105724394..105725093-chr12:105772133..105773100,3	MCF-7	breast:
10	chr12:105741772..105743921-chr12:105752449..105754219,2	MCF-7	breast:
11	chr12:105673064..105673821-chr12:105772193..105773537,4	MCF-7	breast:
12	chr12:105753779..105755590-chr12:105767042..105768690,2	MCF-7	breast:
13	chr12:105627950..105630649-chr12:105770738..105772692,2	MCF-7	breast:
14	chr12:105744909..105747333-chr12:105755240..105757076,3	K562	blood:
15	chr12:105740078..105742393-chr12:105756994..105759086,2	MCF-7	breast:
16	chr12:105765326..105767170-chr12:105773876..105775781,2	MCF-7	breast:
17	chr12:105782673..105785080-chr12:105794485..105797067,2	MCF-7	breast:
18	chr12:105499961..105503110-chr12:105776663..105778620,3	MCF-7	breast:
19	chr12:105672864..105673858-chr12:105772686..105773396,2	MCF-7	breast:
20	chr12:105782673..105785080-chr12:105794485..105797067,2	MCF-7	breast:
21	chr12:105742172..105744127-chr12:105746507..105748716,2	K562	blood:
22	chr12:105682504..105683036-chr12:105776820..105777391,2	MCF-7	breast:
23	chr12:105746012..105748494-chr12:105749131..105751106,2	MCF-7	breast:
24	chr12:105752392..105754695-chr12:105757650..105760428,2	MCF-7	breast:
25	chr12:105753779..105755590-chr12:105767042..105768690,2	MCF-7	breast:
26	chr12:105741772..105743921-chr12:105752449..105754219,2	MCF-7	breast:
27	chr12:105794772..105797299-chr12:105799465..105802543,3	K562	blood:
28	chr12:104595039..104595617-chr12:105776853..105777524,2	K562	blood:
29	chr12:105672889..105673823-chr12:105777116..105777625,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APPL2-3	chr12:105766175-105766461	NONHSAT030451
2	lnc-C12orf75-3	chr12:105759585-105760242	NONHSAT030449
3	lnc-C12orf75-1	chr12:105789468-105789491	XLOC_009868
4	lnc-C12orf75-1	chr12:105793147-105793278	NONHSAT030453

No data

Variant related genes	Relation type
C12orf75	TF binding region
C12orf75	CpG island
ENSG00000235162	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000136044	chromatin interactions
ZNF280C	miRNA target sites

Extended variants
information (count: 2210 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2210 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2888846	chr12:105742674-105742675	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35329316	chr12:105742680-105742681	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs5800663	chr12:105742687-105742688	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs571230822	chr12:105742693-105742694	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537193432	chr12:105742737-105742738	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs190023352	chr12:105742747-105742748	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573257837	chr12:105742759-105742760	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs535847201	chr12:105742810-105742811	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs183292639	chr12:105742841-105742842	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572816281	chr12:105742849-105742850	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs137860284	chr12:105742859-105742860	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368709490	chr12:105742866-105742867	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs11112488	chr12:105742939-105742940	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs377283139	chr12:105742954-105742955	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs76583350	chr12:105742995-105742996	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186536272	chr12:105743016-105743017	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191686570	chr12:105743045-105743046	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560056768	chr12:105743048-105743049	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs528820458	chr12:105743049-105743050	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183522960	chr12:105743082-105743083	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571849711	chr12:105743186-105743187	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188072221	chr12:105743226-105743227	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527482100	chr12:105743289-105743290	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs550603393	chr12:105743300-105743301	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34346262	chr12:105743347-105743348	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs535811501	chr12:105743386-105743387	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552583205	chr12:105743399-105743400	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs143549908	chr12:105743408-105743409	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs192728337	chr12:105743409-105743410	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558465112	chr12:105743424-105743425	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575356798	chr12:105743442-105743443	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548683701	chr12:105743469-105743470	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs544081617	chr12:105743490-105743491	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10861403	chr12:105743603-105743604	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs574199620	chr12:105743616-105743617	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs73401756	chr12:105743657-105743658	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs559829702	chr12:105743691-105743692	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142822147	chr12:105743694-105743695	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs182676878	chr12:105743703-105743704	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535868133	chr12:105743717-105743718	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs531105181	chr12:105743750-105743751	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575251466	chr12:105743755-105743756	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs4964360	chr12:105743869-105743870	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs560977810	chr12:105743949-105743950	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs186580981	chr12:105743989-105743990	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs529767255	chr12:105744023-105744024	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs546185109	chr12:105744104-105744105	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566171620	chr12:105744105-105744106	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs538266019	chr12:105744142-105744143	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs35281951	chr12:105744234-105744235	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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

Chromatin state (count:1192 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105725600-105747200	Weak transcription	Gastric	stomach
2	chr12:105729800-105749400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:105730600-105755400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:105734800-105744000	Weak transcription	Thymus	Thymus
5	chr12:105734800-105744000	Weak transcription	HSMMtube	muscle
6	chr12:105734800-105750200	Weak transcription	Primary T cells from cord blood	blood
7	chr12:105734800-105750800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr12:105734800-105776600	Weak transcription	Esophagus	oesophagus
9	chr12:105735000-105776600	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr12:105735200-105750800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:105735400-105742800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr12:105735400-105756800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:105735600-105743800	Weak transcription	Aorta	Aorta
14	chr12:105735600-105744000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:105735600-105744000	Weak transcription	NHEK	skin
16	chr12:105735600-105745400	Weak transcription	Fetal Thymus	thymus
17	chr12:105735600-105746200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr12:105735600-105749200	Weak transcription	HMEC	breast
19	chr12:105735600-105750600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr12:105735600-105753800	Weak transcription	Fetal Stomach	stomach
21	chr12:105735600-105766800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:105735600-105776600	Weak transcription	Fetal Intestine Small	intestine
23	chr12:105735800-105743200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:105736200-105745400	Weak transcription	Primary B cells from peripheral blood	blood
25	chr12:105736200-105749200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:105736600-105743800	Weak transcription	GM12878-XiMat	blood
27	chr12:105737400-105743000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:105738000-105742800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:105738000-105746000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr12:105738000-105752000	Weak transcription	Spleen	Spleen
31	chr12:105738200-105744000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr12:105738200-105744000	Weak transcription	HSMM	muscle
33	chr12:105738200-105745400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:105738200-105745400	Weak transcription	Psoas Muscle	Psoas
35	chr12:105738200-105745800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr12:105738200-105746000	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr12:105738200-105746400	Weak transcription	NH-A	brain
38	chr12:105738200-105750600	Weak transcription	Primary B cells from cord blood	blood
39	chr12:105739000-105745600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:105740600-105742800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr12:105740800-105743400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:105740800-105744600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr12:105741000-105744000	Weak transcription	A549	lung
44	chr12:105741200-105742800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:105741400-105742800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr12:105741400-105743200	Enhancers	NHLF	lung
47	chr12:105741400-105746000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:105741600-105743400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:105741800-105742800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr12:105741800-105742800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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