Variant report

Variant	nsv469739
Chromosome Location	chr12:33738564-33922234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:966)
CpG islands
(count:122)
Chromatin interactive
region (count:106)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:33740984-33742025	K562	blood:	n/a	n/a
2	ARID3A	chr12:33831095-33831857	K562	blood:	n/a	n/a
3	ARID3A	chr12:33806348-33806595	K562	blood:	n/a	n/a
4	ARID3A	chr12:33905885-33906235	K562	blood:	n/a	n/a
5	ARID3A	chr12:33807257-33807627	K562	blood:	n/a	n/a
6	ATF1	chr12:33807257-33807582	K562	blood:	n/a	n/a
7	ATF1	chr12:33740996-33741606	K562	blood:	n/a	n/a
8	ATF1	chr12:33749134-33749614	K562	blood:	n/a	n/a
9	ATF1	chr12:33837952-33838076	K562	blood:	n/a	n/a
10	ATF1	chr12:33918231-33918238	K562	blood:	n/a	n/a
11	ATF1	chr12:33905799-33906217	K562	blood:	n/a	n/a
12	ATF2	chr12:33740950-33741433	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr12:33741735-33742256	GM12878	blood:	n/a	n/a
14	ATF2	chr12:33740922-33741468	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr12:33806344-33806588	K562	blood:	n/a	n/a
16	ATF3	chr12:33740980-33741602	K562	blood:	n/a	n/a
17	BACH1	chr12:33854735-33854758	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:33847319-33847363	K562	blood:	n/a	n/a
19	BACH1	chr12:33812366-33812495	K562	blood:	n/a	n/a
20	BACH1	chr12:33751125-33751167	K562	blood:	n/a	n/a
21	BACH1	chr12:33905912-33906117	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:33807354-33807505	K562	blood:	n/a	n/a
23	BACH1	chr12:33740516-33741383	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr12:33741913-33742237	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:33802958-33803315	H1-hESC	embryonic stem cell:	n/a	chr12:33803028-33803037
26	BCL11A	chr12:33741023-33741182	H1-hESC	embryonic stem cell:	n/a	n/a
27	BHLHE40	chr12:33759702-33760074	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:33867451-33867477	K562	blood:	n/a	n/a
29	BHLHE40	chr12:33741303-33741660	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:33759769-33760039	K562	blood:	n/a	n/a
31	BHLHE40	chr12:33806387-33806560	K562	blood:	n/a	n/a
32	BHLHE40	chr12:33741030-33741823	K562	blood:	n/a	n/a
33	BHLHE40	chr12:33905773-33906139	K562	blood:	n/a	n/a
34	BRCA1	chr12:33740352-33740651	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr12:33770729-33771117	K562	blood:	n/a	n/a
36	CBX3	chr12:33803718-33804191	K562	blood:	n/a	n/a
37	CBX3	chr12:33772340-33772799	K562	blood:	n/a	n/a
38	CBX3	chr12:33770775-33771015	K562	blood:	n/a	n/a
39	CBX3	chr12:33740710-33741670	K562	blood:	n/a	n/a
40	CBX3	chr12:33905727-33906205	K562	blood:	n/a	n/a
41	CBX3	chr12:33803725-33804117	K562	blood:	n/a	n/a
42	CBX3	chr12:33770149-33770498	K562	blood:	n/a	n/a
43	CCNT2	chr12:33741067-33741621	K562	blood:	n/a	n/a
44	CEBPB	chr12:33839411-33839655	K562	blood:	n/a	n/a
45	CEBPB	chr12:33830997-33831470	K562	blood:	n/a	n/a
46	CEBPB	chr12:33821466-33821658	A549	lung:	n/a	chr12:33821568-33821579
47	CEBPB	chr12:33884502-33884721	HepG2	liver:	n/a	chr12:33884579-33884590
48	CEBPB	chr12:33740231-33740646	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr12:33843240-33843532	A549	lung:	n/a	chr12:33843373-33843384
50	CEBPB	chr12:33843303-33843542	HepG2	liver:	n/a	chr12:33843373-33843384

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:33750494-33750544	GM12891	blood:	n/a
2	chr12:33750494-33750544	NHDF-neo	bronchial:	n/a
3	chr12:33787337-33787387	Caco-2	colon:	n/a
4	chr12:33787337-33787387	HepG2	liver:	n/a
5	chr12:33787337-33787387	HEK293	kidney:	embryo
6	chr12:33750494-33750544	SK-N-SH	brain:	n/a
7	chr12:33787337-33787387	SK-N-SH_RA	brain:	n/a
8	chr12:33750494-33750544	SK-N-MC	brain:	n/a
9	chr12:33787337-33787387	HEEpiC	esophagus:	n/a
10	chr12:33787337-33787387	HUVEC	blood vessel:	n/a
11	chr12:33787337-33787387	GM06990	blood:	n/a
12	chr12:33787337-33787387	MCF10A-Er-Src	breast:	n/a
13	chr12:33787337-33787387	GM12891	blood:	n/a
14	chr12:33787337-33787387	A549	lung:	n/a
15	chr12:33787337-33787387	SKMC	muscle:	n/a
16	chr12:33750494-33750544	BE2_C	brain:	n/a
17	chr12:33787337-33787387	BJ	skin:	n/a
18	chr12:33750494-33750544	PrEC	prostate:	n/a
19	chr12:33750494-33750544	MCF10A-Er-Src	breast:	n/a
20	chr12:33787337-33787387	HL-60	blood:	n/a
21	chr12:33750494-33750544	HAEpiC	amniotic membrane:	n/a
22	chr12:33787337-33787387	HCM	heart:	n/a
23	chr12:33787337-33787387	ovcar-3	ovarian:	n/a
24	chr12:33750494-33750544	HRPEpiC	eye:	n/a
25	chr12:33750494-33750544	ProgFib	skin:	n/a
26	chr12:33787337-33787387	GM19239	blood:	n/a
27	chr12:33787337-33787387	PFSK-1	brain:	n/a
28	chr12:33787337-33787387	GM12892	blood:	n/a
29	chr12:33750494-33750544	IMR90	lung:	fetal
30	chr12:33787337-33787387	AG04449	skin:	fetal
31	chr12:33787337-33787387	NB4	blood:	n/a
32	chr12:33750494-33750544	A549	lung:	n/a
33	chr12:33750494-33750544	HNPCEpiC	eye:	n/a
34	chr12:33750494-33750544	PANC-1	pancreas:	n/a
35	chr12:33787337-33787387	Jurkat	blood:	n/a
36	chr12:33787337-33787387	HAEpiC	amniotic membrane:	n/a
37	chr12:33787337-33787387	T-47D	breast:	n/a
38	chr12:33750494-33750544	Jurkat	blood:	n/a
39	chr12:33750494-33750544	LNCaP	prostate:	n/a
40	chr12:33787337-33787387	SAEC	small airway:	n/a
41	chr12:33750494-33750544	HMEC	breast:	n/a
42	chr12:33750494-33750544	HRCEpiC	kidney:	n/a
43	chr12:33787337-33787387	H1-hESC	embryonic stem cell:	embryo
44	chr12:33787337-33787387	RPTEC	kidney:	n/a
45	chr12:33750494-33750544	K562	blood:	n/a
46	chr12:33750494-33750544	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:33787337-33787387	PrEC	prostate:	n/a
48	chr12:33750494-33750544	Hela-S3	cervix:	n/a
49	chr12:33787337-33787387	AG04450	lung:	fetal
50	chr12:33787337-33787387	NT2-D1	testis:	n/a

(count:106 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:33795771..33798343-chr12:33800787..33802349,2	K562	blood:
2	chr12:33903835..33905859-chr12:33907919..33910698,2	MCF-7	breast:
3	chr12:33825675..33828123-chr8:42750828..42752625,2	MCF-7	breast:
4	chr12:33901002..33902516-chr12:33905016..33907291,2	MCF-7	breast:
5	chr12:33828756..33830899-chr12:33837528..33839909,2	MCF-7	breast:
6	chr12:33590911..33594784-chr12:33761182..33765828,4	MCF-7	breast:
7	chr12:33741049..33744622-chr12:33756451..33760061,5	MCF-7	breast:
8	chr12:32908104..32910738-chr12:33762406..33764699,2	MCF-7	breast:
9	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
10	chr12:33737757..33739747-chr12:33741389..33743027,2	MCF-7	breast:
11	chr12:33593109..33594784-chr12:33753664..33755603,2	MCF-7	breast:
12	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
13	chr12:33589726..33596989-chr12:33737254..33743557,12	MCF-7	breast:
14	chr12:33073552..33076364-chr12:33762087..33763941,2	MCF-7	breast:
15	chr12:33748144..33750127-chr12:33751970..33754633,2	K562	blood:
16	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
17	chr12:33749299..33751532-chr12:33760036..33763741,3	MCF-7	breast:
18	chr12:33591707..33594309-chr12:33773793..33775557,2	MCF-7	breast:
19	chr12:33737682..33739227-chr12:33743519..33746177,2	K562	blood:
20	chr12:33753748..33755380-chr12:33758835..33761146,2	K562	blood:
21	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
22	chr12:33807598..33810256-chr12:33811118..33813511,2	K562	blood:
23	chr12:33799617..33801183-chr8:42749699..42752602,2	MCF-7	breast:
24	chr12:33831200..33833987-chr12:33837460..33839264,2	K562	blood:
25	chr12:33579807..33580648-chr12:33758471..33759360,2	MCF-7	breast:
26	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
27	chr12:32906746..32910896-chr12:33738987..33744699,5	MCF-7	breast:
28	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
29	chr12:33762584..33764416-chr12:33765590..33768500,2	MCF-7	breast:
30	chr12:33796695..33799615-chr12:33802612..33805057,2	K562	blood:
31	chr12:33735767..33737470-chr12:33737741..33739409,2	K562	blood:
32	chr12:33851368..33853439-chr12:33854297..33856163,2	K562	blood:
33	chr12:33590728..33593622-chr12:33761421..33764471,4	MCF-7	breast:
34	chr12:33740590..33741231-chr12:33762284..33763123,2	MCF-7	breast:
35	chr12:33809313..33810966-chr12:33832220..33835115,2	K562	blood:
36	chr12:31834709..31836887-chr12:33736084..33739059,2	K562	blood:
37	chr12:33585788..33587542-chr12:33741964..33743676,2	MCF-7	breast:
38	chr12:33815236..33817568-chr12:33820316..33823181,2	K562	blood:
39	chr12:33590801..33593904-chr12:33746085..33748903,3	MCF-7	breast:
40	chr12:33752192..33755696-chr12:33757650..33764170,6	MCF-7	breast:
41	chr12:33817225..33819690-chr12:33823230..33824769,2	MCF-7	breast:
42	chr12:33762272..33764150-chr8:42748547..42750407,2	MCF-7	breast:
43	chr12:33734204..33736505-chr12:33740513..33742206,2	K562	blood:
44	chr12:33757088..33759339-chr12:33761312..33763614,2	K562	blood:
45	chr12:33749840..33752814-chr12:33754848..33757190,2	K562	blood:
46	chr12:33758071..33760342-chr12:33762792..33765785,2	MCF-7	breast:
47	chr12:33758791..33761325-chr12:33805781..33808679,2	K562	blood:
48	chr12:33829191..33832015-chr12:33832800..33835417,2	K562	blood:
49	chr12:33041897..33044565-chr12:33740312..33741870,2	K562	blood:
50	chr12:33730883..33732707-chr12:33745155..33746710,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ALG10-6	chr12:33870788-33871152	NONHSAT027645

No data

Variant related genes	Relation type
ENSG00000270807	TF binding region
ENSG00000270807	CpG island
ENSG00000131931	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000110975	chromatin interactions
ENSG00000139131	chromatin interactions
ENSG00000120925	chromatin interactions
ENSG00000168172	chromatin interactions
ENSG00000171148	chromatin interactions
ENSG00000184697	chromatin interactions
ENSG00000266044	chromatin interactions

Extended variants
information (count: 2922 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2922 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539705034	chr12:33738587-33738588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs181400769	chr12:33738599-33738600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186751020	chr12:33738610-33738611	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191999598	chr12:33738724-33738725	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs141987320	chr12:33738729-33738730	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs183808003	chr12:33738755-33738756	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544705522	chr12:33738805-33738806	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs815027	chr12:33738814-33738815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs577970794	chr12:33738831-33738832	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540314913	chr12:33738847-33738848	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559676051	chr12:33738881-33738882	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs528430583	chr12:33738952-33738953	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs542023687	chr12:33739010-33739011	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs146299833	chr12:33739019-33739020	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs558388174	chr12:33739021-33739022	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs530488563	chr12:33739030-33739031	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs575888290	chr12:33739033-33739034	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs550662089	chr12:33739038-33739039	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs570306806	chr12:33739057-33739058	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs532940412	chr12:33739063-33739064	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs546232660	chr12:33739092-33739093	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs138245365	chr12:33739093-33739094	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs535776755	chr12:33739153-33739154	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs549128468	chr12:33739154-33739155	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542879778	chr12:33739171-33739172	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs569114523	chr12:33739206-33739207	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs149576378	chr12:33739208-33739209	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558227036	chr12:33739246-33739247	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs2633744	chr12:33739297-33739298	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs200601679	chr12:33739302-33739303	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs368670573	chr12:33739375-33739376	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs144048558	chr12:33739427-33739428	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs708147	chr12:33739541-33739542	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187466620	chr12:33739551-33739552	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs542160947	chr12:33739563-33739564	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs561825037	chr12:33739597-33739598	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs575399951	chr12:33739619-33739620	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs553462092	chr12:33739627-33739628	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs114463090	chr12:33739655-33739656	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574824886	chr12:33739660-33739661	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs564201208	chr12:33739727-33739728	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs532920936	chr12:33739728-33739729	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs148655602	chr12:33739746-33739747	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs144540194	chr12:33739787-33739788	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs529501164	chr12:33739903-33739904	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs189616233	chr12:33739911-33739912	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs569494671	chr12:33739945-33739946	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs113127376	chr12:33739985-33739986	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs538423409	chr12:33740000-33740001	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs115013600	chr12:33740006-33740007	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chordoma	18071362	CNVD
Lung cancer	18438408	CNVD
Cancer	21272361	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Tetralogy of Fallot	22912587	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:33733200-33741400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:33734800-33739600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr12:33735200-33739400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr12:33735400-33739600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:33735600-33739200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:33737000-33740800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr12:33738800-33740400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr12:33738800-33743600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr12:33739200-33743400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr12:33739200-33743800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:33739200-33744400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:33739400-33740600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr12:33739400-33740800	Enhancers	Muscle Satellite Cultured Cells	--
14	chr12:33739600-33740200	Enhancers	K562	blood
15	chr12:33739600-33740400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr12:33739600-33740600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:33739600-33740800	Enhancers	Hela-S3	cervix
18	chr12:33739600-33741000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr12:33739600-33741000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr12:33739600-33741200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr12:33739600-33742000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:33739600-33743600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:33739800-33741000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr12:33739800-33741400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:33739800-33743000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr12:33739800-33743600	Enhancers	HMEC	breast
27	chr12:33740000-33741000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr12:33740000-33742000	Enhancers	HSMM	muscle
29	chr12:33740000-33742200	Enhancers	NH-A	brain
30	chr12:33740000-33743600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr12:33740200-33740400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr12:33740200-33740400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:33740200-33740400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr12:33740200-33741000	Flanking Active TSS	K562	blood
35	chr12:33740200-33741600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:33740200-33742000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr12:33740400-33740800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr12:33740400-33741000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:33740400-33741200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr12:33740400-33741400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr12:33740400-33741400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:33740400-33741400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr12:33740600-33740800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr12:33740600-33741000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr12:33740800-33741000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr12:33740800-33741200	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr12:33740800-33741400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr12:33740800-33741400	Enhancers	Fetal Intestine Large	intestine
49	chr12:33740800-33741400	Enhancers	NHEK	skin
50	chr12:33740800-33741600	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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