Variant report

Variant	nsv541341
Chromosome Location	chr12:993822-1034603
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:590)
CpG islands
(count:733)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:590 , 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	ARID3A	chr12:1021263-1021421	K562	blood:	n/a	n/a
2	ARID3A	chr12:1020634-1020950	K562	blood:	n/a	n/a
3	BACH1	chr12:1015861-1016080	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:1013279-1013396	K562	blood:	n/a	n/a
5	BCL3	chr12:1011273-1011475	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:1020590-1020913	K562	blood:	n/a	n/a
7	BRCA1	chr12:1022707-1022779	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr12:1013187-1013658	K562	blood:	n/a	n/a
9	CEBPB	chr12:1027052-1027374	K562	blood:	n/a	n/a
10	CEBPB	chr12:1027022-1027402	A549	lung:	n/a	n/a
11	CEBPB	chr12:1007492-1007702	IMR90	lung:	n/a	n/a
12	CEBPB	chr12:1027047-1027351	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:1027012-1027353	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:1027049-1027428	A549	lung:	n/a	n/a
15	CEBPB	chr12:1027084-1027585	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:1005773-1006185	IMR90	lung:	n/a	n/a
17	CEBPB	chr12:1027014-1027374	HepG2	liver:	n/a	n/a
18	CEBPD	chr12:1020537-1021045	K562	blood:	n/a	n/a
19	CEBPD	chr12:1013147-1013841	K562	blood:	n/a	n/a
20	CEBPD	chr12:1020573-1021073	K562	blood:	n/a	n/a
21	CEBPD	chr12:1013160-1013735	K562	blood:	n/a	n/a
22	CTCF	chr12:994334-994358	GM19238	blood:	n/a	n/a
23	CTCF	chr12:1006620-1006770	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr12:994020-994170	HepG2	liver:	n/a	n/a
25	CTCF	chr12:1023686-1023782	NHEK	skin:	n/a	n/a
26	CTCF	chr12:1032266-1032363	LNCaP	prostate:	n/a	n/a
27	CTCF	chr12:1023560-1023710	RPTEC	kidney:	n/a	n/a
28	CTCF	chr12:1027642-1027715	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:1006660-1006810	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr12:994280-994430	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr12:1027680-1027830	GM12865	blood:	n/a	n/a
32	CTCF	chr12:994300-994450	HEK293	kidney:	n/a	n/a
33	CTCF	chr12:1018720-1018870	A549	lung:	n/a	n/a
34	CTCF	chr12:1027640-1027790	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr12:1027632-1027715	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:1006660-1006810	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr12:1027868-1027923	GM13976	blood:	n/a	n/a
38	CTCF	chr12:994180-994330	AG04449	skin:	n/a	n/a
39	CTCF	chr12:994258-994438	K562	blood:	n/a	n/a
40	CTCF	chr12:1014880-1015030	NHEK	skin:	n/a	n/a
41	CTCF	chr12:1017160-1017310	A549	lung:	n/a	n/a
42	CTCF	chr12:1027640-1027722	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:1006635-1006786	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr12:1006700-1006850	BE2_C	brain:	n/a	n/a
45	CTCF	chr12:994301-994376	HepG2	liver:	n/a	n/a
46	CTCF	chr12:1014920-1015070	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr12:1006700-1006850	BJ	skin:	n/a	n/a
48	CTCF	chr12:1023640-1023790	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr12:1027663-1027693	GM12891	blood:	n/a	n/a
50	CTCF	chr12:1024987-1025063	Lung_OC	lung:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1025529-1025579	HRPEpiC	eye:	n/a
2	chr12:1025529-1025579	HRPEpiC	eye:	n/a
3	chr12:1018307-1018357	Hela-S3	cervix:	n/a
4	chr12:1025663-1025713	HRCEpiC	kidney:	n/a
5	chr12:1017144-1017194	GM06990	blood:	n/a
6	chr12:1026288-1026338	HRE	kidney:	n/a
7	chr12:1026392-1026442	SK-N-SH_RA	brain:	n/a
8	chr12:1026102-1026152	A549	lung:	n/a
9	chr12:1022477-1022527	GM12891	blood:	n/a
10	chr12:1026288-1026338	HCM	heart:	n/a
11	chr12:1026288-1026338	IMR90	lung:	fetal
12	chr12:1022780-1022830	LNCaP	prostate:	n/a
13	chr12:1005734-1005784	HRPEpiC	eye:	n/a
14	chr12:1025529-1025579	NB4	blood:	n/a
15	chr12:1026102-1026152	SK-N-MC	brain:	n/a
16	chr12:1026392-1026442	T-47D	breast:	n/a
17	chr12:1022780-1022830	PrEC	prostate:	n/a
18	chr12:1025663-1025713	AG04449	skin:	fetal
19	chr12:1022780-1022830	NH-A	brain:	n/a
20	chr12:1022780-1022830	PFSK-1	brain:	n/a
21	chr12:1018307-1018357	AG04449	skin:	fetal
22	chr12:1017144-1017194	U87	brain:	n/a
23	chr12:1022477-1022527	PrEC	prostate:	n/a
24	chr12:1026288-1026338	RPTEC	kidney:	n/a
25	chr12:1025529-1025579	SKMC	muscle:	n/a
26	chr12:1017144-1017194	ECC-1	luminal epithelium:	n/a
27	chr12:1025663-1025713	GM06990	blood:	n/a
28	chr12:1022477-1022527	NHBE	bronchial:	n/a
29	chr12:1025663-1025713	HepG2	liver:	n/a
30	chr12:1026369-1026419	A549	lung:	n/a
31	chr12:1025663-1025713	NB4	blood:	n/a
32	chr12:1022780-1022830	PANC-1	pancreas:	n/a
33	chr12:1025663-1025713	LNCaP	prostate:	n/a
34	chr12:1017144-1017194	MCF-7	breast:	n/a
35	chr12:1017144-1017194	LNCaP	prostate:	n/a
36	chr12:1025529-1025579	PANC-1	pancreas:	n/a
37	chr12:1025663-1025713	A549	lung:	n/a
38	chr12:1025529-1025579	SK-N-SH_RA	brain:	n/a
39	chr12:1026369-1026419	AG04449	skin:	fetal
40	chr12:1018307-1018357	GM12878	blood:	n/a
41	chr12:1026102-1026152	AG04450	lung:	fetal
42	chr12:1018307-1018357	PANC-1	pancreas:	n/a
43	chr12:1026369-1026419	AG09319	gingival:	n/a
44	chr12:1026288-1026338	CMK	blood:	n/a
45	chr12:1026288-1026338	ProgFib	skin:	n/a
46	chr12:1026369-1026419	HEK293	kidney:	embryo
47	chr12:1026392-1026442	Hepatocyte	liver:	n/a
48	chr12:1022780-1022830	HIPEpiC	eye:	n/a
49	chr12:1022477-1022527	ovcar-3	ovarian:	n/a
50	chr12:1022477-1022527	Caco-2	colon:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1000108..1002926-chr12:1003679..1005359,2	K562	blood:
2	chr12:1004472..1007497-chr12:1008864..1013280,3	K562	blood:
3	chr12:1007023..1009524-chr12:1012315..1014770,2	MCF-7	breast:
4	chr12:1014162..1017622-chr12:1021413..1026114,4	K562	blood:
5	chr12:993243..995222-chr12:1008926..1011772,2	K562	blood:
6	chr12:1011965..1016701-chr12:1017001..1021007,7	K562	blood:
7	chr12:1018385..1020466-chr12:1036158..1038882,2	MCF-7	breast:
8	chr12:978470..980054-chr12:995425..998345,2	K562	blood:
9	chr12:1014162..1017622-chr12:1021413..1026114,4	K562	blood:
10	chr12:1007023..1009524-chr12:1012315..1014770,2	MCF-7	breast:
11	chr12:1008526..1010244-chr12:1013943..1016449,2	K562	blood:
12	chr12:1009803..1012282-chr12:1013308..1015371,2	MCF-7	breast:
13	chr12:1011675..1016122-chr12:1018154..1021007,6	K562	blood:
14	chr12:1005997..1008361-chr12:1009600..1011843,2	K562	blood:
15	chr12:1011675..1016122-chr12:1018154..1021007,6	K562	blood:
16	chr12:1011965..1016701-chr12:1017001..1021007,7	K562	blood:
17	chr12:990717..994064-chr12:994788..999202,4	K562	blood:
18	chr12:1026662..1028225-chr12:1041093..1043045,2	K562	blood:
19	chr12:985828..988420-chr12:992932..994549,2	K562	blood:
20	chr12:1022033..1023631-chr12:1025919..1029696,3	K562	blood:
21	chr12:1005428..1007462-chr12:1013958..1015805,2	K562	blood:
22	chr12:1004472..1007497-chr12:1008864..1013280,3	K562	blood:
23	chr12:1000108..1002926-chr12:1003679..1005359,2	K562	blood:
24	chr12:1014378..1016436-chr12:1021383..1023969,3	MCF-7	breast:
25	chr12:1009803..1012282-chr12:1013308..1015371,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ2-4	chr12:1023577-1023698	NONHSAT025375
2	lnc-ERC1-3	chr12:1011722-1016190	NONHSAT025371
3	lnc-NINJ2-4	chr12:1025510-1025748	NONHSAT025375
4	lnc-NINJ2-4	chr12:1022400-1022618	NONHSAT025375
5	lnc-NINJ2-4	chr12:1022525-1022618	NONHSAT025376
6	lnc-NINJ2-4	chr12:1023060-1023364	NONHSAT025376
7	lnc-NINJ2-4	chr12:1023060-1023287	NONHSAT025375

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	WNK1	hsa-miR-215-5p	chr12:1018500-1018520
2	WNK1	hsa-miR-320a	chr12:1018546-1018552
3	WNK1	hsa-miR-215-5p	chr12:1018513-1018519
4	RAD52	hsa-miR-373-3p	chr12:1022377-1022402
5	WNK1	hsa-miR-192-5p	chr12:1018513-1018519
6	WNK1	hsa-miR-193b-3p	chr12:1019197-1019218
7	WNK1	hsa-miR-192-5p	chr12:1018500-1018520
8	WNK1	hsa-miR-320a	chr12:1018534-1018553
9	WNK1	hsa-miR-320a	chr12:1018156-1018177

Variant related genes	Relation type
WNK1	TF binding region
RAD52	TF binding region
WNK1	CpG island
RAD52	CpG island
ENSG00000060237	chromatin interactions
ENSG00000002016	chromatin interactions

Extended variants
information (count: 1767 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1767 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149186881	chr12:993829-993830	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs570079182	chr12:993849-993850	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143361850	chr12:993869-993870	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375565845	chr12:993905-993906	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112190167	chr12:993906-993907	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs7300444	chr12:993930-993931	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs369511479	chr12:993957-993958	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs200513331	chr12:993961-993962	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541776516	chr12:993973-993974	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140473724	chr12:994001-994002	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145701154	chr12:994008-994009	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs10849577	chr12:994014-994015	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs201608137	chr12:994017-994018	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534565611	chr12:994068-994069	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142787842	chr12:994074-994075	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574069625	chr12:994100-994101	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs375915349	chr12:994101-994102	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs56088924	chr12:994137-994138	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs146024504	chr12:994139-994140	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138777852	chr12:994195-994196	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149295230	chr12:994203-994204	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs370543517	chr12:994249-994250	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144574489	chr12:994268-994269	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs72650730	chr12:994290-994291	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs72650731	chr12:994291-994292	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372955308	chr12:994298-994299	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535135770	chr12:994303-994304	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376176091	chr12:994306-994307	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142543401	chr12:994324-994325	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200205583	chr12:994350-994351	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368621387	chr12:994354-994355	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370909801	chr12:994361-994362	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367898105	chr12:994418-994419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201525324	chr12:994434-994435	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs56107487	chr12:994473-994474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575881382	chr12:994483-994484	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7955371	chr12:994487-994488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs200827492	chr12:994495-994496	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543991926	chr12:994502-994503	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs186880440	chr12:994530-994531	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146861951	chr12:994534-994535	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577520430	chr12:994545-994546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541711074	chr12:994548-994549	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375717084	chr12:994550-994551	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530093512	chr12:994552-994553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567183841	chr12:994573-994574	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs72650732	chr12:994575-994576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs56351358	chr12:994607-994608	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs367712687	chr12:994630-994631	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs563801917	chr12:994663-994664	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	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
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Schizophrenia	23813976	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Autism	22495311	CNVD
Pancreatic cancer	17952125	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1191 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:928200-994400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:962200-1002600	Strong transcription	Dnd41	blood
3	chr12:962200-1012400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr12:964200-1007600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr12:964400-1042200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:964600-1027200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr12:965800-1014000	Strong transcription	Primary neutrophils fromperipheralblood	blood
8	chr12:965800-1028400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr12:966000-1002200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:966000-1012200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:966000-1014800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:967200-1005800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr12:968600-1006400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr12:980000-1013200	Strong transcription	Primary T helper cells fromperipheralblood	blood
15	chr12:982200-1027000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr12:986000-996800	Strong transcription	Fetal Thymus	thymus
17	chr12:986200-1002400	Strong transcription	Left Ventricle	heart
18	chr12:986200-1042200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr12:986400-999800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr12:986400-1014800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:986600-999800	Strong transcription	HepG2	liver
22	chr12:986600-1012000	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr12:986600-1012000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:986600-1012200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:986800-996200	Strong transcription	K562	blood
26	chr12:986800-1002000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:986800-1014600	Strong transcription	Primary B cells from peripheral blood	blood
28	chr12:986800-1028400	Strong transcription	Placenta	Placenta
29	chr12:987000-998800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr12:987000-999800	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:987000-999800	Strong transcription	Brain Anterior Caudate	brain
32	chr12:987000-1000000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr12:987000-1000200	Strong transcription	Thymus	Thymus
34	chr12:987000-1000400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr12:987000-1000400	Strong transcription	HMEC	breast
36	chr12:987000-1001200	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr12:987000-1001400	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr12:987000-1001800	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr12:987000-1002000	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr12:987000-1002000	Strong transcription	Duodenum Mucosa	Duodenum
41	chr12:987000-1002000	Strong transcription	A549	lung
42	chr12:987000-1002400	Strong transcription	Primary hematopoietic stem cells	blood
43	chr12:987000-1002600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:987000-1007000	Strong transcription	HUVEC	blood vessel
45	chr12:987000-1007200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
46	chr12:987000-1011200	Strong transcription	Liver	Liver
47	chr12:987000-1012600	Strong transcription	Primary T cells from cord blood	blood
48	chr12:987000-1014800	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr12:987000-1017600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:987000-1020800	Strong transcription	Adipose Nuclei	Adipose

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