Variant report

Variant	nsv558035
Chromosome Location	chr12:31210114-31410821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3004)
CpG islands
(count:2382)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3004 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

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	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:31227121-31227652	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:31391820-31391981	K562	blood:	n/a	n/a
5	ARID3A	chr12:31226612-31226780	HepG2	liver:	n/a	n/a
6	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
7	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
8	ATF1	chr12:31219201-31219422	K562	blood:	n/a	n/a
9	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
10	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
13	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
14	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr12:31226662-31226898	K562	blood:	n/a	n/a
16	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr12:31226535-31226812	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr12:31228050-31228506	GM12878	blood:	n/a	chr12:31228339-31228347
20	BATF	chr12:31226544-31227607	GM12878	blood:	n/a	n/a
21	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
22	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
23	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
24	BATF	chr12:31227825-31228526	GM12878	blood:	n/a	chr12:31228339-31228347
25	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
26	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:31227467-31227641	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
28	BCL11A	chr12:31228004-31228492	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:31226719-31227117	GM12878	blood:	n/a	chr12:31226785-31226794 chr12:31227056-31227065
30	BCL11A	chr12:31227413-31227974	GM12878	blood:	n/a	chr12:31227476-31227485 chr12:31227507-31227514
31	BCL11A	chr12:31228135-31228506	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:31226764-31227047	GM12878	blood:	n/a	chr12:31226785-31226794
33	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
34	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
35	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
36	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
37	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
39	BHLHE40	chr12:31227101-31227187	GM12878	blood:	n/a	n/a
40	BHLHE40	chr12:31227096-31227339	K562	blood:	n/a	chr12:31227176-31227192
41	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
43	BHLHE40	chr12:31219222-31219531	K562	blood:	n/a	n/a
44	BHLHE40	chr12:31226533-31226888	K562	blood:	n/a	n/a
45	BHLHE40	chr12:31226599-31226889	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
48	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
49	BRCA1	chr12:31226630-31226830	GM12878	blood:	n/a	n/a
50	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a

(count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31233201-31233251	AG09309	skin:	n/a
2	chr12:31405369-31405419	HIPEpiC	eye:	n/a
3	chr12:31405359-31405409	HIPEpiC	eye:	n/a
4	chr12:31233201-31233251	AG09309	skin:	n/a
5	chr12:31405369-31405419	HIPEpiC	eye:	n/a
6	chr12:31405359-31405409	HIPEpiC	eye:	n/a
7	chr12:31257362-31257412	HIPEpiC	eye:	n/a
8	chr12:31226606-31226656	GM19239	blood:	n/a
9	chr12:31227271-31227321	Caco-2	colon:	n/a
10	chr12:31254036-31254086	SK-N-SH_RA	brain:	n/a
11	chr12:31254036-31254086	HRPEpiC	eye:	n/a
12	chr12:31360362-31360412	AoSMC	blood vessel:	n/a
13	chr12:31316348-31316398	LNCaP	prostate:	n/a
14	chr12:31241496-31241546	BJ	skin:	n/a
15	chr12:31233201-31233251	RPTEC	kidney:	n/a
16	chr12:31272865-31272915	CMK	blood:	n/a
17	chr12:31276852-31276902	BJ	skin:	n/a
18	chr12:31316348-31316398	AoSMC	blood vessel:	n/a
19	chr12:31230936-31230986	SKMC	muscle:	n/a
20	chr12:31226536-31226586	MCF-7	breast:	n/a
21	chr12:31233201-31233251	GM12892	blood:	n/a
22	chr12:31226536-31226586	HEK293	kidney:	embryo
23	chr12:31316348-31316398	SK-N-SH	brain:	n/a
24	chr12:31405369-31405419	HAEpiC	amniotic membrane:	n/a
25	chr12:31254007-31254057	GM19239	blood:	n/a
26	chr12:31370930-31370980	HRE	kidney:	n/a
27	chr12:31272119-31272169	HRPEpiC	eye:	n/a
28	chr12:31255279-31255329	BE2_C	brain:	n/a
29	chr12:31402470-31402520	AG04449	skin:	fetal
30	chr12:31223310-31223360	AG04450	lung:	fetal
31	chr12:31272119-31272169	Hela-S3	cervix:	n/a
32	chr12:31226801-31226851	HEK293	kidney:	embryo
33	chr12:31276852-31276902	SAEC	small airway:	n/a
34	chr12:31406441-31406491	PFSK-1	brain:	n/a
35	chr12:31360362-31360412	NT2-D1	testis:	n/a
36	chr12:31226718-31226768	AG10803	skin:	n/a
37	chr12:31271429-31271479	AG09319	gingival:	n/a
38	chr12:31226622-31226672	NT2-D1	testis:	n/a
39	chr12:31226622-31226672	BE2_C	brain:	n/a
40	chr12:31256838-31256888	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:31226718-31226768	Caco-2	colon:	n/a
42	chr12:31226952-31227002	NH-A	brain:	n/a
43	chr12:31271783-31271833	HCPEpiC	choroid plexus:	n/a
44	chr12:31272114-31272164	GM12892	blood:	n/a
45	chr12:31233201-31233251	GM06990	blood:	n/a
46	chr12:31272119-31272169	NT2-D1	testis:	n/a
47	chr12:31255279-31255329	SKMC	muscle:	n/a
48	chr12:31226825-31226875	NHDF-neo	bronchial:	n/a
49	chr12:31226632-31226682	PFSK-1	brain:	n/a
50	chr12:31241496-31241546	HCF	heart:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31354080..31355986-chr12:31357943..31360954,3	K562	blood:
2	chr12:31226738..31227630-chr20:47894738..47895520,2	Hela-S3	cervix:
3	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
4	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
5	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
6	chr12:31358059..31360304-chr12:31368898..31371452,2	MCF-7	breast:
7	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
8	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
9	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
10	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
11	chr12:9435913..9436700-chr12:31226425..31227148,3	HCT-116	colon:
12	chr12:31391273..31391961-chr12:31404788..31405659,2	K562	blood:
13	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
14	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
15	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:
16	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
17	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
18	chr12:30999874..31000492-chr12:31398859..31399728,2	K562	blood:
19	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
20	chr12:9436173..9436735-chr12:31226434..31227168,3	Hela-S3	cervix:
21	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
22	chr12:31269781..31270824-chr12:31398705..31400061,4	MCF-7	breast:
23	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
24	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
25	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:
26	chr12:31388279..31391169-chr12:31396495..31398764,2	K562	blood:
27	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
28	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
29	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
30	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
31	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
32	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
2	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
3	lnc-FAM60A-1	chr12:31213594-31213684	ENSG00000245614
4	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
5	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541
6	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
7	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
8	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
9	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-

No data

Variant related genes	Relation type
DDX11-AS1	TF binding region
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
ENSG00000270766	TF binding region
ENSG00000270395	TF binding region
DDX11	TF binding region
DDX11-AS1	CpG island
ENSG00000243517	CpG island
ENSG00000177359	CpG island
ENSG00000270926	CpG island
ENSG00000212533	CpG island
ENSG00000270766	CpG island
ENSG00000270395	CpG island
DDX11	CpG island
ENSG00000013573	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000270766	chromatin interactions
ENSG00000111788	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000209042	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000177410	chromatin interactions
ENSG00000270395	chromatin interactions
TBC1D9	miRNA target sites

Extended variants
information (count: 6257 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6257 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs244496	chr12:31210114-31210115	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs141732020	chr12:31210122-31210123	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558099786	chr12:31210140-31210141	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186814350	chr12:31210171-31210172	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147744030	chr12:31210278-31210279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142664192	chr12:31210314-31210315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528503771	chr12:31210318-31210319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573749193	chr12:31210338-31210339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369634214	chr12:31210410-31210411	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540881752	chr12:31210517-31210518	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113636946	chr12:31210518-31210519	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115604859	chr12:31210547-31210548	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556484539	chr12:31210605-31210606	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577878670	chr12:31210642-31210643	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113457381	chr12:31210666-31210667	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs79963429	chr12:31210669-31210670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560423263	chr12:31210676-31210677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7973425	chr12:31210677-31210678	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
19	rs190372647	chr12:31210760-31210761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368788057	chr12:31210805-31210806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551138729	chr12:31210809-31210810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2543203	chr12:31210840-31210841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531402935	chr12:31210882-31210883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139049821	chr12:31210890-31210891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2543204	chr12:31210931-31210932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144934691	chr12:31210949-31210950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61919887	chr12:31210995-31210996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533493141	chr12:31211016-31211017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs74087903	chr12:31211121-31211122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566772650	chr12:31211131-31211132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534127409	chr12:31211152-31211153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145542717	chr12:31211155-31211156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555497935	chr12:31211166-31211167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567666901	chr12:31211170-31211171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538307160	chr12:31211184-31211185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556311150	chr12:31211187-31211188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577954670	chr12:31211189-31211190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545013833	chr12:31211214-31211215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375354933	chr12:31211220-31211221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554103508	chr12:31211251-31211252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572329380	chr12:31211350-31211351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181644111	chr12:31211377-31211378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561035712	chr12:31211380-31211381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531335556	chr12:31211420-31211421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185652481	chr12:31211468-31211469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564772278	chr12:31211475-31211476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373076547	chr12:31211498-31211499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532132296	chr12:31211499-31211500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550171898	chr12:31211512-31211513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546943809	chr12:31211530-31211531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2605 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

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	chr12:31210000-31210800	Strong transcription	Fetal Muscle Trunk	muscle
10	chr12:31210400-31210800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr12:31210400-31210800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:31210400-31210800	Enhancers	NHEK	skin
13	chr12:31210800-31212800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr12:31210800-31225200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:31211800-31212000	Enhancers	K562	blood
16	chr12:31213800-31214000	Enhancers	Fetal Thymus	thymus
17	chr12:31215200-31215600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr12:31216200-31217400	Weak transcription	K562	blood
19	chr12:31217400-31217600	Enhancers	K562	blood
20	chr12:31217600-31219200	Weak transcription	K562	blood
21	chr12:31219200-31219600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr12:31219200-31220000	Enhancers	K562	blood
23	chr12:31219600-31225600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr12:31220400-31221000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:31220400-31221200	Enhancers	HMEC	breast
26	chr12:31220400-31221200	Enhancers	NHEK	skin
27	chr12:31220800-31221400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:31220800-31221600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:31221000-31225600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:31221200-31225400	Weak transcription	HMEC	breast
31	chr12:31221200-31225600	Weak transcription	NHEK	skin
32	chr12:31221400-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:31221600-31225600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:31225000-31225200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr12:31225000-31225200	Enhancers	Dnd41	blood
36	chr12:31225200-31225400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr12:31225200-31225400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:31225200-31225400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:31225200-31225400	Active TSS	Fetal Thymus	thymus
40	chr12:31225200-31225400	Active TSS	Hela-S3	cervix
41	chr12:31225200-31225600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr12:31225200-31225600	Enhancers	HepG2	liver
43	chr12:31225200-31225600	Enhancers	K562	blood
44	chr12:31225200-31225800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr12:31225200-31226200	Flanking Active TSS	Dnd41	blood
46	chr12:31225200-31228000	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr12:31225200-31228400	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr12:31225200-31228600	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr12:31225400-31225600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:31225400-31225600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived

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