Variant report

Variant	nsv659
Chromosome Location	chr12:31203746-31249055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1181)
CpG islands
(count:977)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
4	ARID3A	chr12:31205625-31205628	HepG2	liver:	n/a	n/a
5	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
6	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
7	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
8	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
10	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
11	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
12	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
13	BATF	chr12:31204619-31204884	GM12878	blood:	n/a	n/a
14	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
15	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
16	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
18	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
19	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
21	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
22	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31203581-31203781	K562	blood:	n/a	n/a
24	BHLHE40	chr12:31204659-31204964	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
26	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
27	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
30	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
32	CBX3	chr12:31219097-31219592	K562	blood:	n/a	n/a
33	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
34	CBX3	chr12:31226185-31227769	K562	blood:	n/a	n/a
35	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr12:31205640-31205849	IMR90	lung:	n/a	n/a
37	CEBPB	chr12:31219220-31219425	K562	blood:	n/a	n/a
38	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
40	CEBPB	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
41	CEBPD	chr12:31219231-31219589	K562	blood:	n/a	n/a
42	CEBPD	chr12:31226472-31226934	K562	blood:	n/a	n/a
43	CEBPD	chr12:31226951-31227517	K562	blood:	n/a	n/a
44	CHD1	chr12:31227630-31227808	GM12878	blood:	n/a	n/a
45	CHD1	chr12:31226593-31226634	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr12:31226926-31227309	GM12878	blood:	n/a	n/a
47	CHD2	chr12:31226528-31227169	HepG2	liver:	n/a	n/a
48	CHD2	chr12:31226517-31227455	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr12:31226547-31226796	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:31226529-31227290	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31226801-31226851	NHDF-neo	bronchial:	n/a
2	chr12:31226801-31226851	NHDF-neo	bronchial:	n/a
3	chr12:31226622-31226672	HIPEpiC	eye:	n/a
4	chr12:31226622-31226672	PFSK-1	brain:	n/a
5	chr12:31223310-31223360	Hepatocyte	liver:	n/a
6	chr12:31223310-31223360	SK-N-SH	brain:	n/a
7	chr12:31226622-31226672	MCF10A-Er-Src	breast:	n/a
8	chr12:31226718-31226768	NH-A	brain:	n/a
9	chr12:31226801-31226851	AG09319	gingival:	n/a
10	chr12:31233201-31233251	HEK293	kidney:	embryo
11	chr12:31226441-31226491	HPAEpiC	pulmonary alveolar:	n/a
12	chr12:31226441-31226491	U87	brain:	n/a
13	chr12:31224413-31224463	ProgFib	skin:	n/a
14	chr12:31223310-31223360	HIPEpiC	eye:	n/a
15	chr12:31226952-31227002	NHDF-neo	bronchial:	n/a
16	chr12:31226632-31226682	HRCEpiC	kidney:	n/a
17	chr12:31226441-31226491	HEK293	kidney:	embryo
18	chr12:31226606-31226656	LNCaP	prostate:	n/a
19	chr12:31233201-31233251	HAEpiC	amniotic membrane:	n/a
20	chr12:31226952-31227002	AG04449	skin:	fetal
21	chr12:31223310-31223360	HCF	heart:	n/a
22	chr12:31227271-31227321	HUVEC	blood vessel:	n/a
23	chr12:31226825-31226875	NT2-D1	testis:	n/a
24	chr12:31226801-31226851	SK-N-SH_RA	brain:	n/a
25	chr12:31226718-31226768	HepG2	liver:	n/a
26	chr12:31226632-31226682	HRPEpiC	eye:	n/a
27	chr12:31224413-31224463	GM06990	blood:	n/a
28	chr12:31227271-31227321	PFSK-1	brain:	n/a
29	chr12:31226536-31226586	SK-N-SH	brain:	n/a
30	chr12:31226441-31226491	MCF-7	breast:	n/a
31	chr12:31226801-31226851	HCM	heart:	n/a
32	chr12:31233201-31233251	ovcar-3	ovarian:	n/a
33	chr12:31224413-31224463	RPTEC	kidney:	n/a
34	chr12:31241496-31241546	NHDF-neo	bronchial:	n/a
35	chr12:31226622-31226672	ECC-1	luminal epithelium:	n/a
36	chr12:31241496-31241546	HEK293	kidney:	embryo
37	chr12:31226952-31227002	PFSK-1	brain:	n/a
38	chr12:31233201-31233251	SKMC	muscle:	n/a
39	chr12:31226622-31226672	ProgFib	skin:	n/a
40	chr12:31226718-31226768	AG09319	gingival:	n/a
41	chr12:31226825-31226875	U87	brain:	n/a
42	chr12:31226718-31226768	HCT-116	colon:	n/a
43	chr12:31226632-31226682	SK-N-SH	brain:	n/a
44	chr12:31226536-31226586	GM19239	blood:	n/a
45	chr12:31226714-31226764	NB4	blood:	n/a
46	chr12:31224413-31224463	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:31226606-31226656	ECC-1	luminal epithelium:	n/a
48	chr12:31226825-31226875	GM12891	blood:	n/a
49	chr12:31230936-31230986	HIPEpiC	eye:	n/a
50	chr12:31241496-31241546	CMK	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
2	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
3	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
4	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
5	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-1	chr12:31213594-31213684	ENSG00000245614
2	lnc-FAM60A-1	chr12:31203850-31204329	ENSG00000245614

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000212533	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000212533	CpG island
DDX11	CpG island
ENSG00000111788	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000209042	chromatin interactions
ANKRD29	miRNA target sites
TBC1D9	miRNA target sites

Extended variants
information (count: 1986 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1986 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369705670	chr12:31203751-31203752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560455103	chr12:31203870-31203871	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs563503031	chr12:31203905-31203906	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs11051222	chr12:31203920-31203921	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs192560872	chr12:31203956-31203957	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs7309642	chr12:31203966-31203967	Enhancers Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs561103007	chr12:31203984-31203985	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs141317898	chr12:31203998-31203999	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs549949333	chr12:31204012-31204013	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs73082891	chr12:31204033-31204034	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs532193563	chr12:31204049-31204050	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs547094466	chr12:31204074-31204075	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs565640369	chr12:31204076-31204077	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs528005896	chr12:31204102-31204103	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs184816801	chr12:31204166-31204167	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs567560158	chr12:31204172-31204173	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs538043650	chr12:31204195-31204196	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs556668674	chr12:31204204-31204205	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs571658212	chr12:31204216-31204217	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs187658196	chr12:31204290-31204291	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs146991734	chr12:31204314-31204315	Enhancers Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs572392014	chr12:31204344-31204345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192985983	chr12:31204402-31204403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73089771	chr12:31204420-31204421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
25	rs576358842	chr12:31204422-31204423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149123503	chr12:31204448-31204449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565058591	chr12:31204465-31204466	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148193800	chr12:31204492-31204493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541098747	chr12:31204503-31204504	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372814434	chr12:31204504-31204505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559119751	chr12:31204524-31204525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377255991	chr12:31204587-31204588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374273826	chr12:31204606-31204607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185123593	chr12:31204660-31204661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549310262	chr12:31204744-31204745	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565158067	chr12:31204766-31204767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77669025	chr12:31204790-31204791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531842690	chr12:31204792-31204793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78526719	chr12:31204802-31204803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200841619	chr12:31204818-31204819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550120760	chr12:31204826-31204827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147702878	chr12:31204835-31204836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571792894	chr12:31204836-31204837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371177360	chr12:31204846-31204847	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142119864	chr12:31204861-31204862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554233512	chr12:31204920-31204921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139752685	chr12:31204921-31204922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375578522	chr12:31205026-31205027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144219038	chr12:31205083-31205084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576422156	chr12:31205124-31205125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31189800-31225400	Weak transcription	Fetal Stomach	stomach
2	chr12:31195000-31206200	Weak transcription	Left Ventricle	heart
3	chr12:31202200-31219400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr12:31202800-31205000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr12:31203200-31207600	Enhancers	Fetal Thymus	thymus
6	chr12:31203400-31204000	Enhancers	NH-A	brain
7	chr12:31203800-31204000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:31203800-31205600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:31204000-31205400	Weak transcription	NH-A	brain
10	chr12:31204200-31205000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:31204200-31206800	Enhancers	Thymus	Thymus
12	chr12:31204400-31205000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr12:31204400-31205000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr12:31204400-31205000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:31204400-31205400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:31204400-31205400	Enhancers	Primary B cells from peripheral blood	blood
17	chr12:31204400-31205800	Enhancers	Dnd41	blood
18	chr12:31204600-31205000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:31204600-31205000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr12:31204600-31205000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr12:31204600-31205400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr12:31204600-31205400	Enhancers	GM12878-XiMat	blood
23	chr12:31204800-31205600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr12:31205000-31206000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:31205000-31206200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:31205000-31206200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:31205000-31206400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:31205000-31210400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:31205200-31205600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr12:31205400-31205600	Enhancers	NH-A	brain
31	chr12:31205400-31205800	Enhancers	HSMMtube	muscle
32	chr12:31205400-31205800	Enhancers	Osteobl	bone
33	chr12:31205400-31207000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:31205400-31207000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr12:31205600-31206000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:31205600-31206000	Weak transcription	NH-A	brain
37	chr12:31205600-31206200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:31205800-31206200	Weak transcription	HSMMtube	muscle
39	chr12:31206000-31206200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:31206000-31206600	Enhancers	NH-A	brain
41	chr12:31206000-31206800	Enhancers	HepG2	liver
42	chr12:31206000-31207000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:31206200-31206400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr12:31206200-31206400	Enhancers	Left Ventricle	heart
45	chr12:31206200-31206600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:31206200-31206600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr12:31206200-31206600	Enhancers	Fetal Intestine Large	intestine
48	chr12:31206200-31206800	Enhancers	HSMMtube	muscle
49	chr12:31206200-31207000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr12:31206200-31207000	Enhancers	HSMM	muscle

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