Variant report

Variant	esv3494304
Chromosome Location	chr12:31206205-31263015
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1446)
CpG islands
(count:1284)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1446 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
3	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
4	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
5	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
6	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
7	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
9	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
10	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
11	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
12	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
13	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
14	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
15	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
17	BCL11A	chr12:31227467-31227641	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	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
20	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
21	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
26	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
27	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
29	BHLHE40	chr12:31226599-31226889	GM12878	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	chr12:31226185-31227769	K562	blood:	n/a	n/a
33	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
34	CBX3	chr12:31219097-31219592	K562	blood:	n/a	n/a
35	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
37	CEBPB	chr12:31219220-31219425	K562	blood:	n/a	n/a
38	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
39	CEBPB	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
40	CEBPD	chr12:31226472-31226934	K562	blood:	n/a	n/a
41	CEBPD	chr12:31219231-31219589	K562	blood:	n/a	n/a
42	CEBPD	chr12:31226951-31227517	K562	blood:	n/a	n/a
43	CHD1	chr12:31227630-31227808	GM12878	blood:	n/a	n/a
44	CHD1	chr12:31226926-31227309	GM12878	blood:	n/a	n/a
45	CHD1	chr12:31226593-31226634	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr12:31226547-31226796	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr12:31226529-31227290	GM12878	blood:	n/a	n/a
48	CHD2	chr12:31226553-31227372	K562	blood:	n/a	n/a
49	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
50	CHD2	chr12:31227458-31227537	HepG2	liver:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31226606-31226656	CMK	blood:	n/a
2	chr12:31226952-31227002	HRE	kidney:	n/a
3	chr12:31226622-31226672	HRPEpiC	eye:	n/a
4	chr12:31226606-31226656	CMK	blood:	n/a
5	chr12:31226952-31227002	HRE	kidney:	n/a
6	chr12:31226622-31226672	HRPEpiC	eye:	n/a
7	chr12:31226632-31226682	GM06990	blood:	n/a
8	chr12:31241496-31241546	MCF10A-Er-Src	breast:	n/a
9	chr12:31254036-31254086	GM06990	blood:	n/a
10	chr12:31256838-31256888	MCF-7	breast:	n/a
11	chr12:31255279-31255329	NT2-D1	testis:	n/a
12	chr12:31226441-31226491	HNPCEpiC	eye:	n/a
13	chr12:31256838-31256888	GM12892	blood:	n/a
14	chr12:31230936-31230986	RPTEC	kidney:	n/a
15	chr12:31256838-31256888	PFSK-1	brain:	n/a
16	chr12:31255279-31255329	Jurkat	blood:	n/a
17	chr12:31226714-31226764	AG10803	skin:	n/a
18	chr12:31255279-31255329	HEEpiC	esophagus:	n/a
19	chr12:31226825-31226875	HMEC	breast:	n/a
20	chr12:31257362-31257412	K562	blood:	n/a
21	chr12:31226801-31226851	MCF-7	breast:	n/a
22	chr12:31255279-31255329	AoSMC	blood vessel:	n/a
23	chr12:31257362-31257412	GM12891	blood:	n/a
24	chr12:31226606-31226656	HEEpiC	esophagus:	n/a
25	chr12:31226718-31226768	HCM	heart:	n/a
26	chr12:31230936-31230986	HAEpiC	amniotic membrane:	n/a
27	chr12:31226622-31226672	HEK293	kidney:	embryo
28	chr12:31224413-31224463	NT2-D1	testis:	n/a
29	chr12:31226801-31226851	T-47D	breast:	n/a
30	chr12:31223310-31223360	PFSK-1	brain:	n/a
31	chr12:31226801-31226851	NB4	blood:	n/a
32	chr12:31226952-31227002	IMR90	lung:	fetal
33	chr12:31254007-31254057	GM12891	blood:	n/a
34	chr12:31254036-31254086	SK-N-MC	brain:	n/a
35	chr12:31226718-31226768	PrEC	prostate:	n/a
36	chr12:31230936-31230986	BJ	skin:	n/a
37	chr12:31226632-31226682	LNCaP	prostate:	n/a
38	chr12:31226952-31227002	K562	blood:	n/a
39	chr12:31226606-31226656	IMR90	lung:	fetal
40	chr12:31226536-31226586	SAEC	small airway:	n/a
41	chr12:31226718-31226768	HCF	heart:	n/a
42	chr12:31226801-31226851	NT2-D1	testis:	n/a
43	chr12:31230936-31230986	HNPCEpiC	eye:	n/a
44	chr12:31255279-31255329	MCF10A-Er-Src	breast:	n/a
45	chr12:31227271-31227321	HCT-116	colon:	n/a
46	chr12:31226536-31226586	HEK293	kidney:	embryo
47	chr12:31257362-31257412	HCF	heart:	n/a
48	chr12:31255279-31255329	PrEC	prostate:	n/a
49	chr12:31226952-31227002	GM19239	blood:	n/a
50	chr12:31256838-31256888	MCF10A-Er-Src	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
2	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
3	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
4	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
5	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
6	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:

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

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

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
DDX11	CpG island
ENSG00000177410	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000013573	chromatin interactions
TBC1D9	miRNA target sites

Extended variants
information (count: 2673 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2673 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191270747	chr12:31206213-31206214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565578018	chr12:31206241-31206242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183131591	chr12:31206261-31206262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201348601	chr12:31206267-31206268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75928383	chr12:31206292-31206293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563797883	chr12:31206294-31206295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371644850	chr12:31206316-31206317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149350129	chr12:31206344-31206345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185402147	chr12:31206370-31206371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs530946765	chr12:31206377-31206378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189819300	chr12:31206486-31206487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182179455	chr12:31206549-31206550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570104381	chr12:31206569-31206570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs71444373	chr12:31206586-31206587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368117273	chr12:31206587-31206588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539293988	chr12:31206588-31206589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201068386	chr12:31206603-31206604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201285513	chr12:31206611-31206612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537449438	chr12:31206676-31206677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs552242546	chr12:31206747-31206748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371660888	chr12:31206748-31206749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35020	chr12:31206764-31206765	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs200069279	chr12:31206796-31206797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372085631	chr12:31206797-31206798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534578232	chr12:31206812-31206813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187798226	chr12:31206813-31206814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552769304	chr12:31206815-31206816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574279447	chr12:31206859-31206860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs149112616	chr12:31206887-31206888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140417780	chr12:31206901-31206902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575203481	chr12:31206935-31206936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140874858	chr12:31207000-31207001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs369594145	chr12:31207034-31207035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183528874	chr12:31207123-31207124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs373497672	chr12:31207124-31207125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35019	chr12:31207178-31207179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs147445862	chr12:31207206-31207207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs371846034	chr12:31207222-31207223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111667299	chr12:31207260-31207261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560021988	chr12:31207272-31207273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530305590	chr12:31207273-31207274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542387021	chr12:31207287-31207288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370592400	chr12:31207288-31207289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373554301	chr12:31207289-31207290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563772434	chr12:31207290-31207291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530868313	chr12:31207327-31207328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552557304	chr12:31207353-31207354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149187130	chr12:31207358-31207359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188536908	chr12:31207364-31207365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61919881	chr12:31207498-31207499	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:1378 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31189800-31225400	Weak transcription	Fetal Stomach	stomach
2	chr12:31202200-31219400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:31203200-31207600	Enhancers	Fetal Thymus	thymus
4	chr12:31204200-31206800	Enhancers	Thymus	Thymus
5	chr12:31205000-31206400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:31205000-31210400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr12:31205400-31207000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:31205400-31207000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:31206000-31206600	Enhancers	NH-A	brain
10	chr12:31206000-31206800	Enhancers	HepG2	liver
11	chr12:31206000-31207000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:31206200-31206400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr12:31206200-31206400	Enhancers	Left Ventricle	heart
14	chr12:31206200-31206600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr12:31206200-31206600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:31206200-31206600	Enhancers	Fetal Intestine Large	intestine
17	chr12:31206200-31206800	Enhancers	HSMMtube	muscle
18	chr12:31206200-31207000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr12:31206200-31207000	Enhancers	HSMM	muscle
20	chr12:31206400-31206600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr12:31206400-31207800	Enhancers	Fetal Heart	heart
22	chr12:31206600-31206800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr12:31206600-31210400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:31206600-31210800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:31206600-31211200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr12:31206800-31211600	Weak transcription	Thymus	Thymus
27	chr12:31207600-31213800	Weak transcription	Fetal Thymus	thymus
28	chr12:31208400-31210000	Weak transcription	Fetal Muscle Trunk	muscle
29	chr12:31210000-31210800	Strong transcription	Fetal Muscle Trunk	muscle
30	chr12:31210400-31210800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr12:31210400-31210800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:31210400-31210800	Enhancers	NHEK	skin
33	chr12:31210800-31212800	Weak transcription	Fetal Muscle Trunk	muscle
34	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr12:31211800-31212000	Enhancers	K562	blood
36	chr12:31213800-31214000	Enhancers	Fetal Thymus	thymus
37	chr12:31215200-31215600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr12:31216200-31217400	Weak transcription	K562	blood
39	chr12:31217400-31217600	Enhancers	K562	blood
40	chr12:31217600-31219200	Weak transcription	K562	blood
41	chr12:31219200-31219600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:31219200-31220000	Enhancers	K562	blood
43	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:31220400-31221000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:31220400-31221200	Enhancers	HMEC	breast
46	chr12:31220400-31221200	Enhancers	NHEK	skin
47	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:31221200-31225400	Weak transcription	HMEC	breast

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