Variant report

Variant	nsv556897
Chromosome Location	chr12:773262-803488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr12:782975-784195	GM12878	blood:	n/a	n/a
5	ATF2	chr12:788224-788729	GM12878	blood:	n/a	n/a
6	ATF2	chr12:794524-795256	GM12878	blood:	n/a	n/a
7	ATF2	chr12:778131-778650	GM12878	blood:	n/a	n/a
8	ATF2	chr12:778081-778740	GM12878	blood:	n/a	n/a
9	ATF2	chr12:775813-776434	GM12878	blood:	n/a	n/a
10	ATF2	chr12:788057-788653	GM12878	blood:	n/a	n/a
11	ATF2	chr12:791586-792067	GM12878	blood:	n/a	n/a
12	ATF2	chr12:782384-782749	GM12878	blood:	n/a	n/a
13	ATF2	chr12:782928-784303	GM12878	blood:	n/a	n/a
14	ATF2	chr12:794559-795159	GM12878	blood:	n/a	n/a
15	ATF2	chr12:775716-776452	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	chr12:786399-786770	GM12878	blood:	n/a	n/a
19	BATF	chr12:786469-786782	GM12878	blood:	n/a	n/a
20	BATF	chr12:775784-776279	GM12878	blood:	n/a	n/a
21	BATF	chr12:790969-791173	GM12878	blood:	n/a	n/a
22	BATF	chr12:801600-801857	GM12878	blood:	n/a	n/a
23	BATF	chr12:783382-783970	GM12878	blood:	n/a	n/a
24	BATF	chr12:778199-778658	GM12878	blood:	n/a	n/a
25	BATF	chr12:794527-794937	GM12878	blood:	n/a	n/a
26	BATF	chr12:783475-783993	GM12878	blood:	n/a	n/a
27	BATF	chr12:775767-776368	GM12878	blood:	n/a	n/a
28	BATF	chr12:788112-788433	GM12878	blood:	n/a	n/a
29	BATF	chr12:778314-778630	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:783502-783933	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:778115-778718	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:783130-783958	GM12878	blood:	n/a	chr12:783189-783198
33	BCL11A	chr12:782391-782737	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:778215-778647	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:775801-776534	GM12878	blood:	n/a	n/a
36	BCL3	chr12:783233-784137	GM12878	blood:	n/a	n/a
37	BCL3	chr12:781840-782241	GM12878	blood:	n/a	n/a
38	BCL3	chr12:778239-778508	GM12878	blood:	n/a	n/a
39	BCL3	chr12:778151-778638	GM12878	blood:	n/a	n/a
40	BCL3	chr12:783332-783983	GM12878	blood:	n/a	n/a
41	BCL3	chr12:781834-782285	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:782970-784046	GM12878	blood:	n/a	chr12:783189-783198
43	BCLAF1	chr12:778063-778594	GM12878	blood:	n/a	n/a
44	BCLAF1	chr12:778166-778659	GM12878	blood:	n/a	n/a
45	BCLAF1	chr12:791584-792121	GM12878	blood:	n/a	n/a
46	BCLAF1	chr12:775857-776470	GM12878	blood:	n/a	n/a
47	BCLAF1	chr12:775761-776529	GM12878	blood:	n/a	n/a
48	BCLAF1	chr12:782298-782809	GM12878	blood:	n/a	n/a
49	BCLAF1	chr12:782875-784143	GM12878	blood:	n/a	chr12:783189-783198
50	BHLHE40	chr12:775741-776749	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:773616-773666	AG04449	skin:	fetal
2	chr12:776351-776401	AG09319	gingival:	n/a
3	chr12:776351-776401	HL-60	blood:	n/a
4	chr12:776351-776401	HRE	kidney:	n/a
5	chr12:773616-773666	RPTEC	kidney:	n/a
6	chr12:776351-776401	H1-hESC	embryonic stem cell:	embryo
7	chr12:776351-776401	SK-N-SH	brain:	n/a
8	chr12:776351-776401	GM19239	blood:	n/a
9	chr12:776351-776401	HepG2	liver:	n/a
10	chr12:776351-776401	AG04449	skin:	fetal
11	chr12:776351-776401	U87	brain:	n/a
12	chr12:773616-773666	NT2-D1	testis:	n/a
13	chr12:773616-773666	HRCEpiC	kidney:	n/a
14	chr12:773616-773666	HNPCEpiC	eye:	n/a
15	chr12:773616-773666	ECC-1	luminal epithelium:	n/a
16	chr12:776351-776401	SK-N-SH_RA	brain:	n/a
17	chr12:776351-776401	AoSMC	blood vessel:	n/a
18	chr12:773616-773666	T-47D	breast:	n/a
19	chr12:773616-773666	BE2_C	brain:	n/a
20	chr12:773616-773666	SAEC	small airway:	n/a
21	chr12:776351-776401	HRCEpiC	kidney:	n/a
22	chr12:773616-773666	K562	blood:	n/a
23	chr12:773616-773666	GM12891	blood:	n/a
24	chr12:773616-773666	HRE	kidney:	n/a
25	chr12:773616-773666	PANC-1	pancreas:	n/a
26	chr12:776351-776401	NHDF-neo	bronchial:	n/a
27	chr12:773616-773666	NHBE	bronchial:	n/a
28	chr12:773616-773666	U87	brain:	n/a
29	chr12:773616-773666	HMEC	breast:	n/a
30	chr12:776351-776401	BE2_C	brain:	n/a
31	chr12:773616-773666	Caco-2	colon:	n/a
32	chr12:776351-776401	SAEC	small airway:	n/a
33	chr12:773616-773666	AG09309	skin:	n/a
34	chr12:773616-773666	HCPEpiC	choroid plexus:	n/a
35	chr12:773616-773666	AoSMC	blood vessel:	n/a
36	chr12:776351-776401	Hepatocyte	liver:	n/a
37	chr12:776351-776401	K562	blood:	n/a
38	chr12:776351-776401	RPTEC	kidney:	n/a
39	chr12:773616-773666	AG04450	lung:	fetal
40	chr12:776351-776401	HCF	heart:	n/a
41	chr12:773616-773666	IMR90	lung:	fetal
42	chr12:773616-773666	HRPEpiC	eye:	n/a
43	chr12:776351-776401	HAEpiC	amniotic membrane:	n/a
44	chr12:776351-776401	PrEC	prostate:	n/a
45	chr12:776351-776401	GM12891	blood:	n/a
46	chr12:773616-773666	NB4	blood:	n/a
47	chr12:773616-773666	BJ	skin:	n/a
48	chr12:776351-776401	PFSK-1	brain:	n/a
49	chr12:776351-776401	HEEpiC	esophagus:	n/a
50	chr12:773616-773666	GM06990	blood:	n/a

(count:18 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NINJ2-1	chr12:790918-791061	ENSG00000256672
2	lnc-NINJ2-1	chr12:783967-784185	ENSG00000256672
3	lnc-WNK1-1	chr12:799000-799203	XLOC_009614
4	lnc-NINJ2-1	chr12:793161-793293	ENSG00000256672

No data

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

Extended variants
information (count: 1246 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1246 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	rs181476337	chr12:773278-773279	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs77338221	chr12:773312-773313	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567926086	chr12:773325-773326	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372392686	chr12:773334-773335	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs61916681	chr12:773336-773337	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs185070741	chr12:773339-773340	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201554184	chr12:773363-773364	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs116297710	chr12:773379-773380	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146235957	chr12:773424-773425	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs189867710	chr12:773437-773438	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	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
13	rs181134547	chr12:773474-773475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186254927	chr12:773487-773488	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs3840792	chr12:773543-773544	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs368434530	chr12:773553-773554	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs397849939	chr12:773554-773555	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs376734954	chr12:773555-773556	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139275226	chr12:773617-773618	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs190776193	chr12:773660-773661	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs528949370	chr12:773677-773678	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550711358	chr12:773703-773704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570235046	chr12:773719-773720	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182013501	chr12:773770-773771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs552771853	chr12:773777-773778	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186391128	chr12:773830-773831	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs535378583	chr12:773847-773848	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs371843995	chr12:773852-773853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs533418446	chr12:773882-773883	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574504852	chr12:773916-773917	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs144050150	chr12:773953-773954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146441229	chr12:773972-773973	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs575359934	chr12:774002-774003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551377050	chr12:774044-774045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75456748	chr12:774056-774057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs148612304	chr12:774105-774106	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs190896110	chr12:774107-774108	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376501874	chr12:774160-774161	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs540524390	chr12:774173-774174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369243285	chr12:774197-774198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs561626377	chr12:774200-774201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528918843	chr12:774250-774251	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs537577688	chr12:774259-774260	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs550623869	chr12:774273-774274	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs74964131	chr12:774276-774277	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs12820097	chr12:774295-774296	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs533090330	chr12:774310-774311	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs545129894	chr12:774311-774312	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs372151623	chr12:774369-774370	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs142056351	chr12:774372-774373	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

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:621 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr12:771400-773600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:771400-773600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr12:771400-776200	Weak transcription	Lung	lung
8	chr12:772200-774200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr12:772400-773400	Enhancers	Liver	Liver
10	chr12:772400-773600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:772600-775400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr12:772600-775800	Enhancers	GM12878-XiMat	blood
13	chr12:772600-776200	Weak transcription	HSMM	muscle
14	chr12:772800-773600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr12:772800-773600	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr12:772800-773600	Bivalent Enhancer	HepG2	liver
17	chr12:772800-773600	Enhancers	K562	blood
18	chr12:772800-774000	Enhancers	Primary T cells from cord blood	blood
19	chr12:772800-774000	Weak transcription	Ovary	ovary
20	chr12:772800-774000	Enhancers	Thymus	Thymus
21	chr12:772800-775600	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr12:772800-775800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:772800-775800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr12:772800-776200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr12:772800-776200	Weak transcription	HSMMtube	muscle
26	chr12:772800-776400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:772800-776400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:772800-777000	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr12:772800-786600	Enhancers	Fetal Thymus	thymus
30	chr12:773000-773400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr12:773000-773400	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr12:773000-773400	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr12:773000-773600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:773000-773600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:773000-773600	Enhancers	Adipose Nuclei	Adipose
36	chr12:773000-774200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr12:773000-774200	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr12:773000-774600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr12:773000-774600	Weak transcription	Fetal Heart	heart
40	chr12:773000-775600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr12:773000-775800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr12:773000-776000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:773000-776000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr12:773000-776000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr12:773000-776000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr12:773000-776000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr12:773000-776200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr12:773000-776200	Weak transcription	Right Atrium	heart
49	chr12:773000-776200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr12:773000-776200	Weak transcription	NHDF-Ad	bronchial

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