Variant report

Variant	esv1804506
Chromosome Location	chr12:8333011-8561680
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3021)
CpG islands
(count:3850)
Chromatin interactive
region (count:4)
LncRNA
region (count:74)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3021 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:8477801-8477893	K562	blood:	n/a	n/a
2	ATF1	chr12:8384340-8384533	K562	blood:	n/a	n/a
3	ATF1	chr12:8477835-8478036	K562	blood:	n/a	n/a
4	ATF2	chr12:8379562-8379932	GM12878	blood:	n/a	n/a
5	ATF3	chr12:8447388-8447568	HepG2	liver:	n/a	n/a
6	BACH1	chr12:8549275-8549403	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:8371647-8371788	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:8472837-8473049	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:8468528-8469314	GM12878	blood:	n/a	n/a
10	BATF	chr12:8384263-8384659	GM12878	blood:	n/a	n/a
11	BATF	chr12:8395305-8395538	GM12878	blood:	n/a	n/a
12	BATF	chr12:8473299-8473507	GM12878	blood:	n/a	n/a
13	BATF	chr12:8486977-8487298	GM12878	blood:	n/a	n/a
14	BATF	chr12:8449447-8449770	GM12878	blood:	n/a	n/a
15	BATF	chr12:8379628-8379911	GM12878	blood:	n/a	chr12:8379783-8379794
16	BATF	chr12:8472172-8472739	GM12878	blood:	n/a	n/a
17	BATF	chr12:8379573-8380007	GM12878	blood:	n/a	chr12:8379783-8379794
18	BATF	chr12:8495427-8495677	GM12878	blood:	n/a	n/a
19	BATF	chr12:8529405-8529600	GM12878	blood:	n/a	n/a
20	BATF	chr12:8394394-8394675	GM12878	blood:	n/a	n/a
21	BATF	chr12:8468641-8469136	GM12878	blood:	n/a	n/a
22	BATF	chr12:8394308-8395112	GM12878	blood:	n/a	chr12:8394791-8394801
23	BATF	chr12:8465483-8465876	GM12878	blood:	n/a	chr12:8465611-8465619
24	BATF	chr12:8465287-8465850	GM12878	blood:	n/a	chr12:8465611-8465619
25	BATF	chr12:8516441-8516876	GM12878	blood:	n/a	n/a
26	BATF	chr12:8384308-8384603	GM12878	blood:	n/a	n/a
27	BATF	chr12:8390044-8390343	GM12878	blood:	n/a	n/a
28	BATF	chr12:8495383-8495701	GM12878	blood:	n/a	n/a
29	BATF	chr12:8472176-8472570	GM12878	blood:	n/a	n/a
30	BATF	chr12:8437659-8437860	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:8394379-8395103	GM12878	blood:	n/a	chr12:8394789-8394798 chr12:8394941-8394950
32	BCL11A	chr12:8384336-8384678	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:8473294-8473468	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:8384233-8384623	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:8495462-8495734	GM12878	blood:	n/a	chr12:8495622-8495631
36	BCL11A	chr12:8394692-8395151	GM12878	blood:	n/a	chr12:8394789-8394798 chr12:8394941-8394950
37	BCL11A	chr12:8449416-8449699	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:8394320-8394628	GM12878	blood:	n/a	n/a
39	BCL11A	chr12:8465466-8465929	GM12878	blood:	n/a	chr12:8465696-8465705
40	BCL11A	chr12:8395308-8395479	GM12878	blood:	n/a	n/a
41	BCL11A	chr12:8465300-8465536	GM12878	blood:	n/a	n/a
42	BCL11A	chr12:8449593-8449779	GM12878	blood:	n/a	n/a
43	BCL11A	chr12:8379625-8379922	GM12878	blood:	n/a	chr12:8379787-8379796
44	BCL11A	chr12:8471330-8471501	GM12878	blood:	n/a	n/a
45	BCL11A	chr12:8474618-8474785	GM12878	blood:	n/a	n/a
46	BCL11A	chr12:8395245-8395510	GM12878	blood:	n/a	n/a
47	BCL11A	chr12:8393785-8393991	GM12878	blood:	n/a	n/a
48	BCL11A	chr12:8464258-8464453	GM12878	blood:	n/a	n/a
49	BCL11A	chr12:8472450-8472705	GM12878	blood:	n/a	n/a
50	BCL11A	chr12:8380564-8380764	GM12878	blood:	n/a	n/a

(count:3850 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8557855-8557905	AoSMC	blood vessel:	n/a
2	chr12:8375674-8375724	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:8376090-8376140	IMR90	lung:	fetal
4	chr12:8546330-8546380	HEEpiC	esophagus:	n/a
5	chr12:8539716-8539766	SKMC	muscle:	n/a
6	chr12:8398718-8398768	IMR90	lung:	fetal
7	chr12:8337217-8337267	HEK293	kidney:	embryo
8	chr12:8557855-8557905	AoSMC	blood vessel:	n/a
9	chr12:8375674-8375724	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:8376090-8376140	IMR90	lung:	fetal
11	chr12:8546330-8546380	HEEpiC	esophagus:	n/a
12	chr12:8539716-8539766	SKMC	muscle:	n/a
13	chr12:8398718-8398768	IMR90	lung:	fetal
14	chr12:8337217-8337267	HEK293	kidney:	embryo
15	chr12:8433230-8433280	RPTEC	kidney:	n/a
16	chr12:8543333-8543383	BE2_C	brain:	n/a
17	chr12:8542524-8542574	SK-N-SH_RA	brain:	n/a
18	chr12:8371626-8371676	GM12891	blood:	n/a
19	chr12:8380360-8380410	PFSK-1	brain:	n/a
20	chr12:8375674-8375724	HUVEC	blood vessel:	n/a
21	chr12:8371924-8371974	SK-N-SH_RA	brain:	n/a
22	chr12:8395493-8395543	K562	blood:	n/a
23	chr12:8474132-8474182	HAEpiC	amniotic membrane:	n/a
24	chr12:8395821-8395871	PFSK-1	brain:	n/a
25	chr12:8396581-8396631	HL-60	blood:	n/a
26	chr12:8380785-8380835	K562	blood:	n/a
27	chr12:8372182-8372232	AG04449	skin:	fetal
28	chr12:8395821-8395871	HMEC	breast:	n/a
29	chr12:8396581-8396631	ovcar-3	ovarian:	n/a
30	chr12:8396767-8396817	GM19239	blood:	n/a
31	chr12:8551501-8551551	PANC-1	pancreas:	n/a
32	chr12:8549243-8549293	SK-N-SH	brain:	n/a
33	chr12:8336589-8336639	GM12892	blood:	n/a
34	chr12:8380785-8380835	GM12878	blood:	n/a
35	chr12:8374133-8374183	SK-N-MC	brain:	n/a
36	chr12:8392560-8392610	PANC-1	pancreas:	n/a
37	chr12:8380785-8380835	HEK293	kidney:	embryo
38	chr12:8380785-8380835	GM06990	blood:	n/a
39	chr12:8376090-8376140	BE2_C	brain:	n/a
40	chr12:8542839-8542889	HEEpiC	esophagus:	n/a
41	chr12:8392560-8392610	SK-N-MC	brain:	n/a
42	chr12:8374206-8374256	HEK293	kidney:	embryo
43	chr12:8380891-8380941	SK-N-SH_RA	brain:	n/a
44	chr12:8396581-8396631	HepG2	liver:	n/a
45	chr12:8396767-8396817	H1-hESC	embryonic stem cell:	embryo
46	chr12:8376943-8376993	AG09309	skin:	n/a
47	chr12:8337217-8337267	SK-N-MC	brain:	n/a
48	chr12:8380472-8380522	HCF	heart:	n/a
49	chr12:8395875-8395925	NB4	blood:	n/a
50	chr12:8372478-8372528	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:8377558..8379489-chr12:8392400..8395227,2	K562	blood:
2	chr12:8377558..8379489-chr12:8392400..8395227,2	K562	blood:
3	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:
4	chr12:8261371..8262028-chr12:8384017..8384906,5	MCF-7	breast:

(count:74 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC6A-1	chr12:8475457-8475704	ENSG00000256101
2	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
3	lnc-CLEC6A-2	chr12:8521588-8521956	NONHSAT026334
4	lnc-ZNF705A-1	chr12:8347873-8348008	ENSG00000226711.2
5	lnc-ZNF705A-1	chr12:8356654-8356771	ENSG00000226711.2
6	lnc-ZNF705A-3	chr12:8448589-8448704	ENSG00000250937
7	lnc-ZNF705A-1	chr12:8341163-8341241	NONHSAT026297
8	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
9	lnc-FAM90A1-1	chr12:8393238-8394790	NONHSAT026319
10	lnc-CLEC4E-2	chr12:8542866-8543107	ENSG00000226091.2
11	lnc-CLEC6A-2	chr12:8472977-8473022	ENSG00000256552.1
12	lnc-ZNF705A-1	chr12:8346799-8347077	NONHSAT026297
13	lnc-CLEC4E-2	chr12:8522809-8523025	NONHSAT026332
14	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
15	lnc-CLEC4E-2	chr12:8549019-8549212	NONHSAT026335
16	lnc-ZNF705A-2	chr12:8391333-8394905	NONHSAT026320
17	lnc-ZNF705A-3	chr12:8449260-8450140	ENSG00000250937
18	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
19	lnc-ZNF705A-1	chr12:8347026-8347077	ENSG00000226711.2
20	lnc-CLEC4E-2	chr12:8522931-8523025	NONHSAT026335
21	lnc-ZNF705A-2	chr12:8388478-8388595	ENSG00000215241
22	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
23	lnc-CLEC6A-2	chr12:8521578-8522151	ENSG00000256552.1
24	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
25	lnc-ZNF705A-1	chr12:8341081-8341131	ENSG00000226711.2
26	lnc-ZNF705A-1	chr12:8347873-8348248	ENSG00000226711.2
27	lnc-CLEC4E-2	chr12:8509559-8509737	ENSG00000226091.2
28	lnc-ZNF705A-1	chr12:8341068-8341133	ENSG00000256703.1
29	lnc-CLEC4E-2	chr12:8542866-8543348	NR_024420
30	lnc-CLEC4E-2	chr12:8542866-8543348	ENSG00000226091.2
31	lnc-FAM90A1-1	chr12:8389318-8391345	NONHSAT026319
32	lnc-CLEC4E-2	chr12:8527013-8527109	ENSG00000226091.2
33	lnc-ZNF705A-3	chr12:8430651-8430757	ENSG00000250937
34	lnc-ZNF705A-1	chr12:8368402-8368631	ENSG00000226711.2
35	lnc-CLEC4E-2	chr12:8522809-8523025	ENSG00000226091.2
36	lnc-ZNF705A-1	chr12:8378474-8378624	NONHSAT026297
37	lnc-CLEC4E-2	chr12:8536701-8537017	ENSG00000226091.2
38	lnc-ZNF705A-1	chr12:8347529-8347872	ENSG00000226711.2
39	lnc-ZNF705A-2	chr12:8391333-8391510	ENSG00000215241
40	lnc-ZNF705A-2	chr12:8388526-8388595	ENSG00000215241
41	lnc-FAM90A1-2	chr12:8352195-8352416	NONHSAT026302
42	lnc-CLEC4E-2	chr12:8538284-8538442	ENSG00000226091.2
43	lnc-ZNF705A-3	chr12:8444364-8444483	ENSG00000250937
44	lnc-CLEC4E-2	chr12:8539359-8540500	ENSG00000226091.2
45	lnc-ZNF705A-3	chr12:8447315-8447576	ENSG00000250937
46	lnc-ZNF705A-1	chr12:8356654-8356724	ENSG00000226711.2
47	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
48	lnc-CLEC4E-2	chr12:8523906-8524036	ENSG00000226091.2
49	lnc-CLEC4E-2	chr12:8537740-8537895	ENSG00000226091.2
50	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2

No data

Variant related genes	Relation type
FAM90A1	TF binding region
ENPP7P5	TF binding region
ENSG00000244050	TF binding region
ENSG00000256101	TF binding region
LINC00937	TF binding region
FAM86FP	TF binding region
FAM66C	TF binding region
ENSG00000256552	TF binding region
ENSG00000221104	TF binding region
ALG1L10P	TF binding region
ENSG00000221307	TF binding region
ENSG00000256136	TF binding region
ENSG00000266026	TF binding region
RPS3AP43	TF binding region
ENSG00000215241	TF binding region
FAM90A1	CpG island
ENPP7P5	CpG island
ENSG00000244050	CpG island
ENSG00000256101	CpG island
LINC00937	CpG island
FAM86FP	CpG island
FAM66C	CpG island
ENSG00000256552	CpG island
ENSG00000221104	CpG island
ALG1L10P	CpG island
ENSG00000221307	CpG island
ENSG00000256136	CpG island
ENSG00000266026	CpG island
RPS3AP43	CpG island
ENSG00000215241	CpG island
ENSG00000215374	chromatin interactions

Extended variants
information (count: 7402 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:7402 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11830824	chr12:8333105-8333106	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs188575728	chr12:8333133-8333134	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs368587453	chr12:8333135-8333136	Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4619218	chr12:8333260-8333261	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs12427270	chr12:8333274-8333275	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs529440349	chr12:8333467-8333468	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7298250	chr12:8333499-8333500	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144106958	chr12:8333565-8333566	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs74060113	chr12:8333566-8333567	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs55851344	chr12:8333567-8333568	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs146350099	chr12:8333623-8333624	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs139700857	chr12:8333728-8333729	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs180715696	chr12:8333876-8333877	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs185154331	chr12:8333880-8333881	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112891986	chr12:8333960-8333961	Active TSS Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs143242142	chr12:8334050-8334051	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549203931	chr12:8334052-8334053	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34118930	chr12:8334077-8334078	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565940543	chr12:8334103-8334104	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376780169	chr12:8334145-8334146	Active TSS Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189273902	chr12:8334230-8334231	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs182332820	chr12:8334321-8334322	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs367588676	chr12:8334330-8334331	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs371819550	chr12:8334353-8334354	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs12426297	chr12:8334366-8334367	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs34215999	chr12:8334421-8334422	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs369388950	chr12:8334478-8334479	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs187393385	chr12:8334533-8334534	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs111810997	chr12:8334609-8334610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191847795	chr12:8334770-8334771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11043787	chr12:8334942-8334943	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs570393379	chr12:8335027-8335028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs11614995	chr12:8335081-8335082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4523762	chr12:8335159-8335160	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs183053875	chr12:8335201-8335202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4414303	chr12:8335227-8335228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs576299533	chr12:8335236-8335237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140905344	chr12:8335317-8335318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373352788	chr12:8335368-8335369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377525254	chr12:8335401-8335402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368883103	chr12:8335434-8335435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111452066	chr12:8335478-8335479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113627194	chr12:8335482-8335483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185549420	chr12:8335589-8335590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373081778	chr12:8335627-8335628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs375962694	chr12:8335674-8335675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112427115	chr12:8335682-8335683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71451945	chr12:8335697-8335698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs371164018	chr12:8335698-8335699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201085497	chr12:8335718-8335719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1506 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8332000-8334600	Active TSS	Brain Anterior Caudate	brain
2	chr12:8332400-8334200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:8332600-8333200	Active TSS	Primary B cells from peripheral blood	blood
4	chr12:8332600-8333200	Active TSS	Primary hematopoietic stem cells	blood
5	chr12:8332600-8333200	Active TSS	Primary T helper naive cells from peripheral blood	blood
6	chr12:8332600-8333200	Active TSS	Primary T helper cells PMA-I stimulated	--
7	chr12:8332600-8333200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
8	chr12:8332600-8333200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
9	chr12:8332600-8333400	Active TSS	H1 Cell Line	embryonic stem cell
10	chr12:8332600-8333400	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr12:8332600-8333400	Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr12:8332600-8333400	Active TSS	Primary T cells fromperipheralblood	blood
13	chr12:8332600-8333400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
14	chr12:8332600-8333400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:8332600-8333400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr12:8332600-8333400	Active TSS	Adipose Nuclei	Adipose
17	chr12:8332600-8333400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
18	chr12:8332600-8333400	Active TSS	Fetal Intestine Large	intestine
19	chr12:8332600-8333400	Active TSS	Fetal Thymus	thymus
20	chr12:8332600-8333400	Active TSS	HSMM	muscle
21	chr12:8332600-8333400	Active TSS	NHEK	skin
22	chr12:8332600-8333600	Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr12:8332600-8333600	Active TSS	Fetal Muscle Trunk	muscle
24	chr12:8332600-8333600	Active TSS	Ovary	ovary
25	chr12:8332600-8333600	Active TSS	HMEC	breast
26	chr12:8332600-8333800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:8332600-8333800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:8332600-8333800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:8332600-8333800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:8332600-8333800	Active TSS	Brain Cingulate Gyrus	brain
31	chr12:8332600-8333800	Active TSS	Brain Hippocampus Middle	brain
32	chr12:8332600-8333800	Active TSS	A549	lung
33	chr12:8332600-8334000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:8332600-8334000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr12:8332600-8334000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr12:8332600-8334000	Active TSS	Stomach Smooth Muscle	stomach
37	chr12:8332600-8334200	Active TSS	Fetal Brain Female	brain
38	chr12:8332600-8334600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:8332800-8333200	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr12:8332800-8333200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr12:8332800-8333200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:8332800-8333200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr12:8332800-8333200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:8332800-8333200	Active TSS	Primary monocytes fromperipheralblood	blood
45	chr12:8332800-8333200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr12:8332800-8333200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr12:8332800-8333200	Active TSS	Aorta	Aorta
48	chr12:8332800-8333200	Active TSS	Duodenum Mucosa	Duodenum
49	chr12:8332800-8333200	Active TSS	Placenta Amnion	Placenta Amnion
50	chr12:8332800-8333200	Active TSS	Rectal Mucosa Donor 31	rectum

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