Variant report

Variant	nsv818876
Chromosome Location	chr12:772458-796131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:427)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:775968-776208	K562	blood:	n/a	n/a
2	ARID3A	chr12:781997-782473	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:783640-783703	K562	blood:	n/a	n/a
4	ATF2	chr12:788224-788729	GM12878	blood:	n/a	n/a
5	ATF2	chr12:788057-788653	GM12878	blood:	n/a	n/a
6	ATF2	chr12:791586-792067	GM12878	blood:	n/a	n/a
7	ATF2	chr12:794524-795256	GM12878	blood:	n/a	n/a
8	ATF2	chr12:778131-778650	GM12878	blood:	n/a	n/a
9	ATF2	chr12:794559-795159	GM12878	blood:	n/a	n/a
10	ATF2	chr12:775716-776452	GM12878	blood:	n/a	n/a
11	ATF2	chr12:775813-776434	GM12878	blood:	n/a	n/a
12	ATF2	chr12:782975-784195	GM12878	blood:	n/a	n/a
13	ATF2	chr12:782928-784303	GM12878	blood:	n/a	n/a
14	ATF2	chr12:782384-782749	GM12878	blood:	n/a	n/a
15	ATF2	chr12:778081-778740	GM12878	blood:	n/a	n/a
16	BACH1	chr12:776410-776946	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:776346-776887	K562	blood:	n/a	n/a
18	BATF	chr12:775767-776368	GM12878	blood:	n/a	n/a
19	BATF	chr12:788112-788433	GM12878	blood:	n/a	n/a
20	BATF	chr12:786399-786770	GM12878	blood:	n/a	n/a
21	BATF	chr12:775784-776279	GM12878	blood:	n/a	n/a
22	BATF	chr12:778199-778658	GM12878	blood:	n/a	n/a
23	BATF	chr12:790969-791173	GM12878	blood:	n/a	n/a
24	BATF	chr12:783382-783970	GM12878	blood:	n/a	n/a
25	BATF	chr12:772752-773049	GM12878	blood:	n/a	n/a
26	BATF	chr12:783475-783993	GM12878	blood:	n/a	n/a
27	BATF	chr12:794527-794937	GM12878	blood:	n/a	n/a
28	BATF	chr12:778314-778630	GM12878	blood:	n/a	n/a
29	BATF	chr12:786469-786782	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:778115-778718	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:783130-783958	GM12878	blood:	n/a	chr12:783189-783198
32	BCL11A	chr12:775801-776534	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:782391-782737	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:778215-778647	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:783502-783933	GM12878	blood:	n/a	n/a
36	BCL3	chr12:781834-782285	GM12878	blood:	n/a	n/a
37	BCL3	chr12:783332-783983	GM12878	blood:	n/a	n/a
38	BCL3	chr12:783233-784137	GM12878	blood:	n/a	n/a
39	BCL3	chr12:781840-782241	GM12878	blood:	n/a	n/a
40	BCL3	chr12:778239-778508	GM12878	blood:	n/a	n/a
41	BCL3	chr12:778151-778638	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:791584-792121	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:775761-776529	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:782298-782809	GM12878	blood:	n/a	n/a
45	BCLAF1	chr12:782970-784046	GM12878	blood:	n/a	chr12:783189-783198
46	BCLAF1	chr12:778166-778659	GM12878	blood:	n/a	n/a
47	BCLAF1	chr12:782875-784143	GM12878	blood:	n/a	chr12:783189-783198
48	BCLAF1	chr12:778063-778594	GM12878	blood:	n/a	n/a
49	BCLAF1	chr12:775857-776470	GM12878	blood:	n/a	n/a
50	BHLHE40	chr12:791720-792133	GM12878	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:772861-772911	MCF10A-Er-Src	breast:	n/a
2	chr12:773616-773666	SK-N-MC	brain:	n/a
3	chr12:773616-773666	NHBE	bronchial:	n/a
4	chr12:772982-773032	HEEpiC	esophagus:	n/a
5	chr12:772966-773016	HRE	kidney:	n/a
6	chr12:773616-773666	PFSK-1	brain:	n/a
7	chr12:772982-773032	A549	lung:	n/a
8	chr12:772688-772738	Hela-S3	cervix:	n/a
9	chr12:772529-772579	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:773616-773666	AG04450	lung:	fetal
11	chr12:772982-773032	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:776351-776401	SK-N-MC	brain:	n/a
13	chr12:773616-773666	RPTEC	kidney:	n/a
14	chr12:772688-772738	NH-A	brain:	n/a
15	chr12:772966-773016	U87	brain:	n/a
16	chr12:776351-776401	ECC-1	luminal epithelium:	n/a
17	chr12:772966-773016	SK-N-MC	brain:	n/a
18	chr12:772529-772579	GM12891	blood:	n/a
19	chr12:772966-773016	HPAEpiC	pulmonary alveolar:	n/a
20	chr12:776351-776401	GM12878	blood:	n/a
21	chr12:772966-773016	MCF-7	breast:	n/a
22	chr12:772688-772738	AG09309	skin:	n/a
23	chr12:772861-772911	NT2-D1	testis:	n/a
24	chr12:772688-772738	HNPCEpiC	eye:	n/a
25	chr12:772861-772911	A549	lung:	n/a
26	chr12:773616-773666	H1-hESC	embryonic stem cell:	embryo
27	chr12:772688-772738	HRE	kidney:	n/a
28	chr12:772529-772579	K562	blood:	n/a
29	chr12:772966-773016	AG09309	skin:	n/a
30	chr12:772688-772738	HEEpiC	esophagus:	n/a
31	chr12:772861-772911	SK-N-SH_RA	brain:	n/a
32	chr12:772982-773032	H1-hESC	embryonic stem cell:	embryo
33	chr12:772861-772911	HUVEC	blood vessel:	n/a
34	chr12:773616-773666	HCPEpiC	choroid plexus:	n/a
35	chr12:776351-776401	HUVEC	blood vessel:	n/a
36	chr12:772688-772738	T-47D	breast:	n/a
37	chr12:773616-773666	GM06990	blood:	n/a
38	chr12:772688-772738	MCF10A-Er-Src	breast:	n/a
39	chr12:772966-773016	GM19239	blood:	n/a
40	chr12:772966-773016	AG04450	lung:	fetal
41	chr12:776351-776401	HRE	kidney:	n/a
42	chr12:772861-772911	PrEC	prostate:	n/a
43	chr12:773616-773666	A549	lung:	n/a
44	chr12:772982-773032	NHBE	bronchial:	n/a
45	chr12:776351-776401	HepG2	liver:	n/a
46	chr12:776351-776401	AG10803	skin:	n/a
47	chr12:772688-772738	GM12891	blood:	n/a
48	chr12:773616-773666	NT2-D1	testis:	n/a
49	chr12:772688-772738	HL-60	blood:	n/a
50	chr12:772982-773032	PFSK-1	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:751811..754307-chr12:785925..788890,4	MCF-7	breast:
2	chr12:784539..786532-chr12:803214..805167,2	K562	blood:
3	chr12:752374..754889-chr12:785771..788046,2	K562	blood:
4	chr12:764195..765871-chr12:773990..776397,2	K562	blood:
5	chr12:756195..759652-chr12:773829..776440,3	MCF-7	breast:
6	chr12:774861..777730-chr12:780859..783120,2	K562	blood:
7	chr12:754920..757056-chr12:790543..792765,2	K562	blood:
8	chr12:774861..777730-chr12:780859..783120,2	K562	blood:
9	chr12:750256..753677-chr12:768929..774136,4	MCF-7	breast:
10	chr12:752037..753643-chr12:774666..777308,2	K562	blood:
11	chr12:775656..779828-chr12:858965..863317,6	K562	blood:
12	chr12:751083..753301-chr12:777175..779752,2	MCF-7	breast:
13	chr12:751801..754339-chr12:772154..775493,3	MCF-7	breast:
14	chr12:769742..773483-chr12:773969..776715,3	K562	blood:
15	chr12:795680..800126-chr12:801859..804463,4	K562	blood:
16	chr12:775430..777687-chr12:860597..863456,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALNT3-2	chr12:772483-772872	ENSG00000177406.4
2	lnc-NINJ2-1	chr12:783967-784185	ENSG00000256672
3	lnc-NINJ2-1	chr12:793161-793293	ENSG00000256672
4	lnc-NINJ2-1	chr12:790918-791061	ENSG00000256672

No data

Variant related genes	Relation type
NINJ2	TF binding region
ENSG00000256672	TF binding region
NINJ2	CpG island
ENSG00000256672	CpG island
ENSG00000171840	chromatin interactions
ENSG00000060237	chromatin interactions
ENSG00000177406	chromatin interactions

Extended variants
information (count: 1000 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3782851	chr12:772458-772459	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375586297	chr12:772521-772522	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs569602741	chr12:772527-772528	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs530757674	chr12:772534-772535	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs529249945	chr12:772544-772545	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs184687485	chr12:772553-772554	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs570353758	chr12:772564-772565	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs150600623	chr12:772596-772597	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs552805082	chr12:772600-772601	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs148175381	chr12:772619-772620	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs139615750	chr12:772623-772624	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs150678610	chr12:772649-772650	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs34737022	chr12:772656-772657	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs369334042	chr12:772657-772658	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs4980959	chr12:772673-772674	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs553291953	chr12:772678-772679	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs200138347	chr12:772688-772689	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs577184405	chr12:772722-772723	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs541486834	chr12:772740-772741	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs146623012	chr12:772790-772791	Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs115202674	chr12:772819-772820	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs530170954	chr12:772823-772824	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs541618822	chr12:772897-772898	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs3809265	chr12:772928-772929	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs149306006	chr12:772971-772972	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs75104885	chr12:772983-772984	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs552195658	chr12:773003-773004	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs17693182	chr12:773051-773052	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3809264	chr12:773056-773057	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs546600455	chr12:773077-773078	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs542337667	chr12:773097-773098	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs74478678	chr12:773098-773099	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs115369746	chr12:773135-773136	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs562356290	chr12:773166-773167	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs570266081	chr12:773173-773174	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537707289	chr12:773178-773179	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559010156	chr12:773198-773199	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577494820	chr12:773246-773247	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs17754970	chr12:773262-773263	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs181476337	chr12:773278-773279	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs77338221	chr12:773312-773313	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567926086	chr12:773325-773326	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372392686	chr12:773334-773335	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs61916681	chr12:773336-773337	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs185070741	chr12:773339-773340	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs201554184	chr12:773363-773364	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116297710	chr12:773379-773380	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs146235957	chr12:773424-773425	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs189867710	chr12:773437-773438	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs3809263	chr12:773456-773457	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:83)

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
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:753400-776000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:756800-776000	Weak transcription	A549	lung
3	chr12:760600-776600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:770200-773600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
5	chr12:770400-773000	Enhancers	Primary B cells from cord blood	blood
6	chr12:770400-773000	Enhancers	Primary hematopoietic stem cells	blood
7	chr12:770400-773000	Active TSS	Brain Hippocampus Middle	brain
8	chr12:770600-773000	Enhancers	Right Ventricle	heart
9	chr12:770600-773200	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr12:770800-773000	Enhancers	Fetal Heart	heart
11	chr12:771000-773200	Active TSS	Brain Anterior Caudate	brain
12	chr12:771000-773200	Enhancers	Spleen	Spleen
13	chr12:771200-772800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr12:771200-773200	Active TSS	Brain Substantia Nigra	brain
15	chr12:771400-772800	Enhancers	Fetal Stomach	stomach
16	chr12:771400-772800	Active TSS	Rectal Smooth Muscle	rectum
17	chr12:771400-773000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr12:771400-773000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr12:771400-773000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:771400-773000	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr12:771400-773000	Active TSS	Brain Cingulate Gyrus	brain
22	chr12:771400-773200	Active TSS	Brain Angular Gyrus	brain
23	chr12:771400-773600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr12:771400-773600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr12:771400-776200	Weak transcription	Lung	lung
26	chr12:771600-772600	Active TSS	Rectal Mucosa Donor 29	rectum
27	chr12:771600-772800	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr12:771600-772800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr12:771600-772800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr12:771600-773000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:771800-772600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr12:771800-772600	Enhancers	Primary B cells from peripheral blood	blood
33	chr12:771800-772600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr12:771800-772600	Bivalent Enhancer	Fetal Kidney	kidney
35	chr12:771800-772600	Enhancers	Fetal Lung	lung
36	chr12:771800-772600	Flanking Active TSS	Fetal Muscle Leg	muscle
37	chr12:771800-772600	Weak transcription	Psoas Muscle	Psoas
38	chr12:771800-772600	Active TSS	NHDF-Ad	bronchial
39	chr12:771800-772800	Enhancers	Aorta	Aorta
40	chr12:771800-772800	Active TSS	Duodenum Smooth Muscle	Duodenum
41	chr12:771800-772800	Enhancers	Pancreas	Pancrea
42	chr12:771800-772800	Flanking Active TSS	Thymus	Thymus
43	chr12:771800-772800	Bivalent Enhancer	Dnd41	blood
44	chr12:771800-772800	Flanking Active TSS	HMEC	breast
45	chr12:771800-772800	Enhancers	NH-A	brain
46	chr12:771800-773000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:771800-773000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr12:771800-773000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr12:771800-773000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr12:771800-773000	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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