Variant report

Variant	nsv870239
Chromosome Location	chr12:31207051-31339312
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1902)
CpG islands
(count:1894)
Chromatin interactive
region (count:7)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1902 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

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	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
5	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
6	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
7	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
9	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
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	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
14	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
15	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
16	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
18	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
20	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
21	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
22	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
23	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
24	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
27	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
28	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
29	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
30	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
31	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
32	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
33	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
34	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
36	BRCA1	chr12:31226555-31227323	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
38	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
39	CBX3	chr12:31219097-31219592	K562	blood:	n/a	n/a
40	CBX3	chr12:31226185-31227769	K562	blood:	n/a	n/a
41	CBX3	chr12:31224793-31225171	K562	blood:	n/a	n/a
42	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
43	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
45	CEBPB	chr12:31226508-31227197	GM12878	blood:	n/a	chr12:31227015-31227027
46	CEBPB	chr12:31219220-31219425	K562	blood:	n/a	n/a
47	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
48	CEBPB	chr12:31226603-31227301	Hela-S3	cervix:	n/a	chr12:31227015-31227027
49	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
50	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a

(count:1894 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31226714-31226764	AoSMC	blood vessel:	n/a
2	chr12:31272112-31272162	HRE	kidney:	n/a
3	chr12:31270326-31270376	GM12892	blood:	n/a
4	chr12:31226714-31226764	AoSMC	blood vessel:	n/a
5	chr12:31272112-31272162	HRE	kidney:	n/a
6	chr12:31270326-31270376	GM12892	blood:	n/a
7	chr12:31254036-31254086	HCPEpiC	choroid plexus:	n/a
8	chr12:31274424-31274474	HNPCEpiC	eye:	n/a
9	chr12:31254036-31254086	AG10803	skin:	n/a
10	chr12:31276852-31276902	HUVEC	blood vessel:	n/a
11	chr12:31230936-31230986	HCPEpiC	choroid plexus:	n/a
12	chr12:31226801-31226851	PANC-1	pancreas:	n/a
13	chr12:31254036-31254086	H1-hESC	embryonic stem cell:	embryo
14	chr12:31270326-31270376	ECC-1	luminal epithelium:	n/a
15	chr12:31254007-31254057	U87	brain:	n/a
16	chr12:31226622-31226672	Hela-S3	cervix:	n/a
17	chr12:31272112-31272162	HMEC	breast:	n/a
18	chr12:31276852-31276902	T-47D	breast:	n/a
19	chr12:31230936-31230986	AG04450	lung:	fetal
20	chr12:31226622-31226672	BE2_C	brain:	n/a
21	chr12:31274424-31274474	GM12891	blood:	n/a
22	chr12:31226825-31226875	AG04450	lung:	fetal
23	chr12:31271783-31271833	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:31241496-31241546	BJ	skin:	n/a
25	chr12:31272119-31272169	ECC-1	luminal epithelium:	n/a
26	chr12:31254007-31254057	IMR90	lung:	fetal
27	chr12:31274424-31274474	HMEC	breast:	n/a
28	chr12:31254007-31254057	NB4	blood:	n/a
29	chr12:31255279-31255329	SK-N-SH_RA	brain:	n/a
30	chr12:31230936-31230986	HEEpiC	esophagus:	n/a
31	chr12:31226714-31226764	NH-A	brain:	n/a
32	chr12:31226441-31226491	SK-N-SH	brain:	n/a
33	chr12:31226825-31226875	K562	blood:	n/a
34	chr12:31272119-31272169	HRCEpiC	kidney:	n/a
35	chr12:31233201-31233251	MCF10A-Er-Src	breast:	n/a
36	chr12:31226718-31226768	IMR90	lung:	fetal
37	chr12:31257362-31257412	HCM	heart:	n/a
38	chr12:31254007-31254057	SKMC	muscle:	n/a
39	chr12:31226606-31226656	HAEpiC	amniotic membrane:	n/a
40	chr12:31226441-31226491	SK-N-SH_RA	brain:	n/a
41	chr12:31226622-31226672	SKMC	muscle:	n/a
42	chr12:31223310-31223360	U87	brain:	n/a
43	chr12:31272865-31272915	AG04450	lung:	fetal
44	chr12:31257362-31257412	PrEC	prostate:	n/a
45	chr12:31226622-31226672	ProgFib	skin:	n/a
46	chr12:31226718-31226768	MCF-7	breast:	n/a
47	chr12:31255279-31255329	PrEC	prostate:	n/a
48	chr12:31227271-31227321	BJ	skin:	n/a
49	chr12:31241496-31241546	HRCEpiC	kidney:	n/a
50	chr12:31316348-31316398	ovcar-3	ovarian:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9620209..9621328-chr12:31206996..31207808,4	MCF-7	breast:
2	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
3	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
4	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
5	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
6	chr12:9620489..9621323-chr12:31206721..31207493,2	MCF-7	breast:
7	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
2	lnc-FAM60A-1	chr12:31213594-31213684	ENSG00000245614
3	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
4	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
5	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
6	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
ENSG00000177359	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
ENSG00000177359	CpG island
DDX11	CpG island
ENSG00000177410	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000124201	chromatin interactions
TBC1D9	miRNA target sites

Extended variants
information (count: 3973 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3973 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183528874	chr12:31207123-31207124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373497672	chr12:31207124-31207125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35019	chr12:31207178-31207179	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs147445862	chr12:31207206-31207207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371846034	chr12:31207222-31207223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111667299	chr12:31207260-31207261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560021988	chr12:31207272-31207273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530305590	chr12:31207273-31207274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542387021	chr12:31207287-31207288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370592400	chr12:31207288-31207289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373554301	chr12:31207289-31207290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563772434	chr12:31207290-31207291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530868313	chr12:31207327-31207328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552557304	chr12:31207353-31207354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149187130	chr12:31207358-31207359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188536908	chr12:31207364-31207365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61919881	chr12:31207498-31207499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528413315	chr12:31207532-31207533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373874019	chr12:31207644-31207645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546482167	chr12:31207658-31207659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567962126	chr12:31207688-31207689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs535273367	chr12:31207701-31207702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556698447	chr12:31207702-31207703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35018	chr12:31207707-31207708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539134650	chr12:31207724-31207725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557764338	chr12:31207732-31207733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372206647	chr12:31207744-31207745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369785778	chr12:31207755-31207756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192877730	chr12:31207814-31207815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140518926	chr12:31207821-31207822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12305860	chr12:31207844-31207845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553697215	chr12:31207855-31207856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142175845	chr12:31208071-31208072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184281746	chr12:31208072-31208073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542448466	chr12:31208082-31208083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs146412813	chr12:31208093-31208094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531056057	chr12:31208108-31208109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545958110	chr12:31208110-31208111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71223840	chr12:31208119-31208120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs71223839	chr12:31208156-31208157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377175402	chr12:31208188-31208189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71223838	chr12:31208203-31208204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564546320	chr12:31208208-31208209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568520135	chr12:31208209-31208210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529493989	chr12:31208231-31208232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71223837	chr12:31208237-31208238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546543592	chr12:31208261-31208262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200504031	chr12:31208358-31208359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550940629	chr12:31208450-31208451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188670274	chr12:31208464-31208465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

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	chr12:31205000-31210400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:31206400-31207800	Enhancers	Fetal Heart	heart
6	chr12:31206600-31210400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:31206600-31210800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr12:31206600-31211200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr12:31206800-31211600	Weak transcription	Thymus	Thymus
10	chr12:31207600-31213800	Weak transcription	Fetal Thymus	thymus
11	chr12:31208400-31210000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr12:31210000-31210800	Strong transcription	Fetal Muscle Trunk	muscle
13	chr12:31210400-31210800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr12:31210400-31210800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:31210400-31210800	Enhancers	NHEK	skin
16	chr12:31210800-31212800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:31211800-31212000	Enhancers	K562	blood
19	chr12:31213800-31214000	Enhancers	Fetal Thymus	thymus
20	chr12:31215200-31215600	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr12:31216200-31217400	Weak transcription	K562	blood
22	chr12:31217400-31217600	Enhancers	K562	blood
23	chr12:31217600-31219200	Weak transcription	K562	blood
24	chr12:31219200-31219600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:31219200-31220000	Enhancers	K562	blood
26	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:31220400-31221000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr12:31220400-31221200	Enhancers	HMEC	breast
29	chr12:31220400-31221200	Enhancers	NHEK	skin
30	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:31221200-31225400	Weak transcription	HMEC	breast
34	chr12:31221200-31225600	Weak transcription	NHEK	skin
35	chr12:31221400-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr12:31221600-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr12:31225000-31225200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr12:31225000-31225200	Enhancers	Dnd41	blood
39	chr12:31225200-31225400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr12:31225200-31225400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:31225200-31225400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr12:31225200-31225400	Active TSS	Fetal Thymus	thymus
43	chr12:31225200-31225400	Active TSS	Hela-S3	cervix
44	chr12:31225200-31225600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr12:31225200-31225600	Enhancers	HepG2	liver
46	chr12:31225200-31225600	Enhancers	K562	blood
47	chr12:31225200-31225800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr12:31225200-31226200	Flanking Active TSS	Dnd41	blood
49	chr12:31225200-31228000	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr12:31225200-31228400	Active TSS	HUES6 Cell Line	embryonic stem cell

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