Variant report

Variant	esv1832795
Chromosome Location	chr12:31209204-31261698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1298)
CpG islands
(count:1283)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31227278-31227505	K562	blood:	n/a	n/a
2	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
4	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
5	ATF1	chr12:31230204-31230267	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	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
9	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
10	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
11	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
12	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
13	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
14	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
15	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
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	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
20	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
21	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
24	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
27	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
28	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
31	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	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	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
36	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:31219220-31219425	K562	blood:	n/a	n/a
38	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
39	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
40	CEBPD	chr12:31226951-31227517	K562	blood:	n/a	n/a
41	CEBPD	chr12:31226472-31226934	K562	blood:	n/a	n/a
42	CEBPD	chr12:31219231-31219589	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	chr12:31226517-31227455	Hela-S3	cervix:	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:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31226714-31226764	HepG2	liver:	n/a
2	chr12:31226825-31226875	K562	blood:	n/a
3	chr12:31226714-31226764	HepG2	liver:	n/a
4	chr12:31226825-31226875	K562	blood:	n/a
5	chr12:31226536-31226586	ECC-1	luminal epithelium:	n/a
6	chr12:31241496-31241546	ovcar-3	ovarian:	n/a
7	chr12:31226536-31226586	MCF10A-Er-Src	breast:	n/a
8	chr12:31254036-31254086	AG09309	skin:	n/a
9	chr12:31241496-31241546	HEK293	kidney:	embryo
10	chr12:31254007-31254057	BJ	skin:	n/a
11	chr12:31257362-31257412	HRE	kidney:	n/a
12	chr12:31233201-31233251	HRPEpiC	eye:	n/a
13	chr12:31226801-31226851	RPTEC	kidney:	n/a
14	chr12:31226622-31226672	RPTEC	kidney:	n/a
15	chr12:31241496-31241546	NB4	blood:	n/a
16	chr12:31241496-31241546	HepG2	liver:	n/a
17	chr12:31226606-31226656	HCT-116	colon:	n/a
18	chr12:31226825-31226875	A549	lung:	n/a
19	chr12:31224413-31224463	HCM	heart:	n/a
20	chr12:31254036-31254086	BE2_C	brain:	n/a
21	chr12:31226441-31226491	GM19239	blood:	n/a
22	chr12:31227271-31227321	IMR90	lung:	fetal
23	chr12:31254007-31254057	Hela-S3	cervix:	n/a
24	chr12:31257362-31257412	AG09319	gingival:	n/a
25	chr12:31226718-31226768	NB4	blood:	n/a
26	chr12:31226952-31227002	HPAEpiC	pulmonary alveolar:	n/a
27	chr12:31255279-31255329	HIPEpiC	eye:	n/a
28	chr12:31226441-31226491	BJ	skin:	n/a
29	chr12:31226952-31227002	H1-hESC	embryonic stem cell:	embryo
30	chr12:31233201-31233251	Jurkat	blood:	n/a
31	chr12:31226632-31226682	MCF10A-Er-Src	breast:	n/a
32	chr12:31257362-31257412	GM12878	blood:	n/a
33	chr12:31226714-31226764	HMEC	breast:	n/a
34	chr12:31233201-31233251	HEEpiC	esophagus:	n/a
35	chr12:31256838-31256888	HMEC	breast:	n/a
36	chr12:31226952-31227002	AG09319	gingival:	n/a
37	chr12:31257362-31257412	PrEC	prostate:	n/a
38	chr12:31255279-31255329	GM06990	blood:	n/a
39	chr12:31226952-31227002	A549	lung:	n/a
40	chr12:31226714-31226764	HEEpiC	esophagus:	n/a
41	chr12:31255279-31255329	MCF-7	breast:	n/a
42	chr12:31226632-31226682	RPTEC	kidney:	n/a
43	chr12:31226441-31226491	U87	brain:	n/a
44	chr12:31226441-31226491	NHBE	bronchial:	n/a
45	chr12:31257362-31257412	SK-N-MC	brain:	n/a
46	chr12:31255279-31255329	BJ	skin:	n/a
47	chr12:31230936-31230986	HAEpiC	amniotic membrane:	n/a
48	chr12:31226622-31226672	IMR90	lung:	fetal
49	chr12:31226441-31226491	NHDF-neo	bronchial:	n/a
50	chr12:31226952-31227002	HCT-116	colon:	n/a

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

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

(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
ENSG00000245614	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000209042	chromatin interactions
TBC1D9	miRNA target sites

Extended variants
information (count: 2484 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:2484 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144257682	chr12:31209222-31209223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575849271	chr12:31209249-31209250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148322237	chr12:31209253-31209254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11051223	chr12:31209254-31209255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs2543202	chr12:31209287-31209288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534573422	chr12:31209296-31209297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573025635	chr12:31209301-31209302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540310357	chr12:31209357-31209358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71440924	chr12:31209412-31209413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374048856	chr12:31209580-31209581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs544539942	chr12:31209586-31209587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562641929	chr12:31209607-31209608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs61919885	chr12:31209633-31209634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574687825	chr12:31209639-31209640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367651118	chr12:31209694-31209695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371937159	chr12:31209739-31209740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs244498	chr12:31209744-31209745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143338420	chr12:31209777-31209778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146024525	chr12:31209792-31209793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368720171	chr12:31209863-31209864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551300282	chr12:31209869-31209870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560360237	chr12:31209871-31209872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372308736	chr12:31209958-31209959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377042225	chr12:31209972-31209973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201365137	chr12:31210035-31210036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549082772	chr12:31210037-31210038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs151290606	chr12:31210071-31210072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73089779	chr12:31210080-31210081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549711603	chr12:31210087-31210088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs244496	chr12:31210114-31210115	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs141732020	chr12:31210122-31210123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558099786	chr12:31210140-31210141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186814350	chr12:31210171-31210172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs147744030	chr12:31210278-31210279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142664192	chr12:31210314-31210315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528503771	chr12:31210318-31210319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573749193	chr12:31210338-31210339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369634214	chr12:31210410-31210411	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540881752	chr12:31210517-31210518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113636946	chr12:31210518-31210519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115604859	chr12:31210547-31210548	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556484539	chr12:31210605-31210606	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577878670	chr12:31210642-31210643	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113457381	chr12:31210666-31210667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79963429	chr12:31210669-31210670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560423263	chr12:31210676-31210677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7973425	chr12:31210677-31210678	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
48	rs190372647	chr12:31210760-31210761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368788057	chr12:31210805-31210806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551138729	chr12:31210809-31210810	Weak transcription	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:1352 , 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	chr12:31205000-31210400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr12:31206600-31210400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:31206600-31210800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:31206600-31211200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:31206800-31211600	Weak transcription	Thymus	Thymus
8	chr12:31207600-31213800	Weak transcription	Fetal Thymus	thymus
9	chr12:31208400-31210000	Weak transcription	Fetal Muscle Trunk	muscle
10	chr12:31210000-31210800	Strong transcription	Fetal Muscle Trunk	muscle
11	chr12:31210400-31210800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:31210400-31210800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:31210400-31210800	Enhancers	NHEK	skin
14	chr12:31210800-31212800	Weak transcription	Fetal Muscle Trunk	muscle
15	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr12:31211800-31212000	Enhancers	K562	blood
17	chr12:31213800-31214000	Enhancers	Fetal Thymus	thymus
18	chr12:31215200-31215600	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr12:31216200-31217400	Weak transcription	K562	blood
20	chr12:31217400-31217600	Enhancers	K562	blood
21	chr12:31217600-31219200	Weak transcription	K562	blood
22	chr12:31219200-31219600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:31219200-31220000	Enhancers	K562	blood
24	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:31220400-31221000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:31220400-31221200	Enhancers	HMEC	breast
27	chr12:31220400-31221200	Enhancers	NHEK	skin
28	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr12:31221200-31225400	Weak transcription	HMEC	breast
32	chr12:31221200-31225600	Weak transcription	NHEK	skin
33	chr12:31221400-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:31221600-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:31225000-31225200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr12:31225000-31225200	Enhancers	Dnd41	blood
37	chr12:31225200-31225400	Enhancers	H1 Cell Line	embryonic stem cell
38	chr12:31225200-31225400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:31225200-31225400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:31225200-31225400	Active TSS	Fetal Thymus	thymus
41	chr12:31225200-31225400	Active TSS	Hela-S3	cervix
42	chr12:31225200-31225600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr12:31225200-31225600	Enhancers	HepG2	liver
44	chr12:31225200-31225600	Enhancers	K562	blood
45	chr12:31225200-31225800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:31225200-31226200	Flanking Active TSS	Dnd41	blood
47	chr12:31225200-31228000	Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr12:31225200-31228400	Active TSS	HUES6 Cell Line	embryonic stem cell
49	chr12:31225200-31228600	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr12:31225400-31225600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links