Variant report

Variant	nsv899009
Chromosome Location	chr12:39284077-39441096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1972)
CpG islands
(count:978)
Chromatin interactive
region (count:40)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1972 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:39300558-39300682	K562	blood:	n/a	n/a
2	ARID3A	chr12:39285777-39286637	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:39300494-39300860	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:39397543-39397858	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:39377087-39377287	HepG2	liver:	n/a	n/a
6	ATF1	chr12:39284008-39284252	K562	blood:	n/a	n/a
7	ATF1	chr12:39436838-39437126	K562	blood:	n/a	n/a
8	ATF2	chr12:39300305-39300945	GM12878	blood:	n/a	n/a
9	ATF2	chr12:39298537-39299243	GM12878	blood:	n/a	n/a
10	ATF2	chr12:39300121-39301011	GM12878	blood:	n/a	n/a
11	ATF2	chr12:39298529-39299822	GM12878	blood:	n/a	n/a
12	ATF3	chr12:39300365-39300843	A549	lung:	n/a	n/a
13	ATF3	chr12:39298460-39299097	A549	lung:	n/a	chr12:39299077-39299086
14	ATF3	chr12:39299347-39299915	A549	lung:	n/a	n/a
15	ATF3	chr12:39285710-39286359	A549	lung:	n/a	n/a
16	ATF3	chr12:39300228-39300807	A549	lung:	n/a	chr12:39300324-39300337
17	ATF3	chr12:39285802-39286224	A549	lung:	n/a	n/a
18	BACH1	chr12:39298839-39300096	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:39406696-39407064	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:39300395-39300863	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr12:39286146-39286543	GM12878	blood:	n/a	n/a
22	BATF	chr12:39300359-39300867	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:39300494-39300852	GM12878	blood:	n/a	chr12:39300564-39300577
24	BCL3	chr12:39300378-39300735	GM12878	blood:	n/a	chr12:39300564-39300577
25	BCL3	chr12:39285771-39286377	A549	lung:	n/a	chr12:39286325-39286332
26	BCL3	chr12:39298956-39299761	A549	lung:	n/a	chr12:39298957-39298970
27	BCL3	chr12:39298658-39299050	GM12878	blood:	n/a	chr12:39298957-39298970
28	BCL3	chr12:39285844-39286500	A549	lung:	n/a	chr12:39286325-39286332
29	BCLAF1	chr12:39298496-39299659	GM12878	blood:	n/a	chr12:39298957-39298970
30	BCLAF1	chr12:39300289-39300959	GM12878	blood:	n/a	chr12:39300564-39300577
31	BCLAF1	chr12:39298576-39299858	GM12878	blood:	n/a	chr12:39298957-39298970
32	BCLAF1	chr12:39300278-39300864	GM12878	blood:	n/a	chr12:39300564-39300577
33	BHLHE40	chr12:39298621-39299502	K562	blood:	n/a	n/a
34	BHLHE40	chr12:39300370-39301239	GM12878	blood:	n/a	n/a
35	BHLHE40	chr12:39300420-39300708	K562	blood:	n/a	n/a
36	BHLHE40	chr12:39285799-39286240	A549	lung:	n/a	n/a
37	BHLHE40	chr12:39292224-39292367	GM12878	blood:	n/a	n/a
38	BHLHE40	chr12:39298710-39299023	A549	lung:	n/a	n/a
39	BHLHE40	chr12:39313132-39313245	K562	blood:	n/a	n/a
40	BHLHE40	chr12:39298606-39300030	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:39296363-39296497	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:39300332-39300812	HepG2	liver:	n/a	n/a
43	BHLHE40	chr12:39285981-39286182	K562	blood:	n/a	n/a
44	BHLHE40	chr12:39285801-39286415	HepG2	liver:	n/a	n/a
45	BHLHE40	chr12:39284315-39284633	GM12878	blood:	n/a	chr12:39284487-39284496 chr12:39284487-39284496
46	BHLHE40	chr12:39298120-39298226	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:39288323-39288627	GM12878	blood:	n/a	chr12:39288427-39288448 chr12:39288431-39288444
48	BRCA1	chr12:39298568-39299415	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr12:39300482-39300623	HepG2	liver:	n/a	n/a
50	BRCA1	chr12:39436806-39437549	Hela-S3	cervix:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:39299716-39299766	HMEC	breast:	n/a
2	chr12:39300744-39300794	HNPCEpiC	eye:	n/a
3	chr12:39299716-39299766	HMEC	breast:	n/a
4	chr12:39300744-39300794	HNPCEpiC	eye:	n/a
5	chr12:39299726-39299776	PFSK-1	brain:	n/a
6	chr12:39299364-39299414	H1-hESC	embryonic stem cell:	embryo
7	chr12:39296476-39296526	A549	lung:	n/a
8	chr12:39299726-39299776	MCF-7	breast:	n/a
9	chr12:39299844-39299894	AoSMC	blood vessel:	n/a
10	chr12:39298639-39298689	SK-N-SH_RA	brain:	n/a
11	chr12:39300744-39300794	HCM	heart:	n/a
12	chr12:39299726-39299776	MCF10A-Er-Src	breast:	n/a
13	chr12:39298824-39298874	HCPEpiC	choroid plexus:	n/a
14	chr12:39299726-39299776	AG04449	skin:	fetal
15	chr12:39300744-39300794	RPTEC	kidney:	n/a
16	chr12:39299716-39299766	ProgFib	skin:	n/a
17	chr12:39299501-39299551	NT2-D1	testis:	n/a
18	chr12:39302027-39302077	HUVEC	blood vessel:	n/a
19	chr12:39298824-39298874	MCF10A-Er-Src	breast:	n/a
20	chr12:39298824-39298874	GM19239	blood:	n/a
21	chr12:39299716-39299766	AG10803	skin:	n/a
22	chr12:39298639-39298689	AG10803	skin:	n/a
23	chr12:39299326-39299376	H1-hESC	embryonic stem cell:	embryo
24	chr12:39299726-39299776	LNCaP	prostate:	n/a
25	chr12:39298824-39298874	PrEC	prostate:	n/a
26	chr12:39299364-39299414	ProgFib	skin:	n/a
27	chr12:39296476-39296526	SAEC	small airway:	n/a
28	chr12:39299364-39299414	NT2-D1	testis:	n/a
29	chr12:39296476-39296526	SK-N-SH	brain:	n/a
30	chr12:39299364-39299414	ECC-1	luminal epithelium:	n/a
31	chr12:39300142-39300192	SK-N-SH	brain:	n/a
32	chr12:39299546-39299596	SK-N-SH_RA	brain:	n/a
33	chr12:39299844-39299894	LNCaP	prostate:	n/a
34	chr12:39299844-39299894	AG04449	skin:	fetal
35	chr12:39299326-39299376	NH-A	brain:	n/a
36	chr12:39299132-39299182	HCF	heart:	n/a
37	chr12:39300744-39300794	T-47D	breast:	n/a
38	chr12:39302027-39302077	HCT-116	colon:	n/a
39	chr12:39300744-39300794	HCPEpiC	choroid plexus:	n/a
40	chr12:39299546-39299596	HNPCEpiC	eye:	n/a
41	chr12:39298639-39298689	Hela-S3	cervix:	n/a
42	chr12:39296476-39296526	HCM	heart:	n/a
43	chr12:39302027-39302077	K562	blood:	n/a
44	chr12:39299726-39299776	HCF	heart:	n/a
45	chr12:39300142-39300192	AoSMC	blood vessel:	n/a
46	chr12:39299726-39299776	BJ	skin:	n/a
47	chr12:39299716-39299766	Caco-2	colon:	n/a
48	chr12:39302027-39302077	HPAEpiC	pulmonary alveolar:	n/a
49	chr12:39299132-39299182	NB4	blood:	n/a
50	chr12:39302027-39302077	PANC-1	pancreas:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:39298720..39299544-chr8:95565528..95566062,2	Hela-S3	cervix:
2	chr12:39294074..39295589-chr12:39295957..39298877,2	K562	blood:
3	chr12:39290114..39292966-chr12:39295688..39297919,2	K562	blood:
4	chr12:39396332..39398967-chr12:39400620..39403550,2	K562	blood:
5	chr12:39320556..39323665-chr12:39326717..39328717,3	K562	blood:
6	chr12:39406167..39408502-chr12:39412272..39414594,2	K562	blood:
7	chr12:39378140..39380661-chr12:39381373..39384205,2	MCF-7	breast:
8	chr12:39299427..39300247-chr6:17706649..17707521,2	Hela-S3	cervix:
9	chr12:39298727..39299416-chr20:30328091..30329027,2	Hela-S3	cervix:
10	chr12:39298324..39299381-chr7:141251113..141251796,3	Hela-S3	cervix:
11	chr12:39300010..39300760-chr3:119814285..119814942,2	Hela-S3	cervix:
12	chr12:38721798..38722714-chr12:39305427..39306254,2	MCF-7	breast:
13	chr12:39314380..39315501-chr12:39497292..39498019,4	MCF-7	breast:
14	chr12:39314606..39315315-chr12:39497081..39498041,2	K562	blood:
15	chr12:39429919..39432388-chr12:39432739..39435549,2	K562	blood:
16	chr12:39290114..39292966-chr12:39295688..39297919,2	K562	blood:
17	chr12:39343718..39345753-chr12:39348375..39350244,2	K562	blood:
18	chr12:39299074..39299955-chr9:26892301..26892993,2	Hela-S3	cervix:
19	chr12:39299154..39299960-chr4:40632090..40632777,2	Hela-S3	cervix:
20	chr12:39295565..39299427-chr12:39307532..39310185,3	K562	blood:
21	chr1:45196572..45197199-chr12:39300046..39300549,2	Hela-S3	cervix:
22	chr12:39433107..39434027-chr17:57914832..57915487,2	MCF-7	breast:
23	chr12:39268478..39271402-chr12:39288578..39290820,2	K562	blood:
24	chr12:39406167..39408502-chr12:39412272..39414594,2	K562	blood:
25	chr12:39314389..39315587-chr12:39497082..39498251,11	MCF-7	breast:
26	chr12:39298360..39299282-chr5:99870676..99871194,2	Hela-S3	cervix:
27	chr12:39315885..39316656-chr16:75018113..75018792,2	MCF-7	breast:
28	chr12:39320556..39323665-chr12:39326717..39328717,3	K562	blood:
29	chr12:39343718..39345753-chr12:39348375..39350244,2	K562	blood:
30	chr12:39342874..39345523-chr12:39354497..39356508,3	K562	blood:
31	chr12:39429919..39432388-chr12:39432739..39435549,2	K562	blood:
32	chr12:39295565..39299427-chr12:39307532..39310185,3	K562	blood:
33	chr12:39285246..39287445-chr12:39289748..39291988,2	K562	blood:
34	chr12:39294074..39295589-chr12:39295957..39298877,2	K562	blood:
35	chr12:39342874..39345523-chr12:39354497..39356508,3	K562	blood:
36	chr12:39285246..39287445-chr12:39289748..39291988,2	K562	blood:
37	chr12:39378140..39380661-chr12:39381373..39384205,2	MCF-7	breast:
38	chr12:39319182..39321686-chr4:39639319..39641692,2	MCF-7	breast:
39	chr12:39300444..39301044-chr12:39497356..39498030,2	K562	blood:
40	chr12:39396332..39398967-chr12:39400620..39403550,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-3	chr12:39388605-39388738	NONHSAT027694
2	lnc-ALG10B-1	chr12:39303112-39303322	NONHSAT027691
3	lnc-ALG10B-1	chr12:39300141-39300495	NONHSAT027691
4	lnc-ALG10B-2	chr12:39317620-39317740	XLOC_009709
5	lnc-ALG10B-2	chr12:39313439-39313539	XLOC_009709
6	lnc-CPNE8-3	chr12:39390514-39390684	NONHSAT027694
7	lnc-ALG10B-1	chr12:39300253-39300495	ENSG00000257718.1
8	lnc-ALG10B-1	chr12:39303112-39303394	ENSG00000257718.1

No data

Variant related genes	Relation type
ENSG00000257718	TF binding region
CPNE8	TF binding region
ENSG00000252801	TF binding region
ENSG00000257586	TF binding region
ENSG00000257718	CpG island
CPNE8	CpG island
ENSG00000252801	CpG island
ENSG00000257586	CpG island
ENSG00000164944	chromatin interactions
ENSG00000255458	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000103091	chromatin interactions
ENSG00000174132	chromatin interactions
ENSG00000163683	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000124789	chromatin interactions
ENSG00000163694	chromatin interactions
ENSG00000006530	chromatin interactions
ENSG00000247877	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000253704	chromatin interactions
ENSG00000120159	chromatin interactions

Extended variants
information (count: 2357 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2357 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11169908	chr12:39284077-39284078	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190259391	chr12:39284123-39284124	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs60605001	chr12:39284156-39284157	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs541492512	chr12:39284169-39284170	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs377428550	chr12:39284184-39284185	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150555144	chr12:39284186-39284187	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs561371553	chr12:39284281-39284282	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs369878635	chr12:39284301-39284302	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs530379566	chr12:39284340-39284341	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs76139934	chr12:39284344-39284345	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs538615816	chr12:39284370-39284371	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs181597153	chr12:39284371-39284372	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs78756189	chr12:39284380-39284381	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs78491400	chr12:39284449-39284450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs114842286	chr12:39284586-39284587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs144721711	chr12:39284589-39284590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555071364	chr12:39284599-39284600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186571622	chr12:39284623-39284624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537409342	chr12:39284637-39284638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557067562	chr12:39284667-39284668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145759736	chr12:39284678-39284679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577866179	chr12:39284703-39284704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs58697274	chr12:39284738-39284739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545765879	chr12:39284797-39284798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377303956	chr12:39284838-39284839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190982316	chr12:39284875-39284876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572677007	chr12:39284880-39284881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541531562	chr12:39284916-39284917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7307683	chr12:39284923-39284924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs530512920	chr12:39284924-39284925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544243123	chr12:39284940-39284941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7308580	chr12:39284958-39284959	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs61937842	chr12:39284970-39284971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369624282	chr12:39284978-39284979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1516557	chr12:39284985-39284986	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs142776860	chr12:39285008-39285009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529748363	chr12:39285024-39285025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566297484	chr12:39285046-39285047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180959787	chr12:39285089-39285090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548707697	chr12:39285102-39285103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs7307936	chr12:39285106-39285107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs61937843	chr12:39285250-39285251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78326599	chr12:39285252-39285253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs75865525	chr12:39285265-39285266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569808929	chr12:39285271-39285272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186162095	chr12:39285301-39285302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11832454	chr12:39285332-39285333	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs539745251	chr12:39285342-39285343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141134740	chr12:39285399-39285400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12305985	chr12:39285409-39285410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:39204000-39284800	Weak transcription	Lung	lung
2	chr12:39269800-39285800	Weak transcription	Osteobl	bone
3	chr12:39271800-39297200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:39277800-39287200	Weak transcription	Aorta	Aorta
5	chr12:39278200-39284400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:39279800-39285800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr12:39280000-39285600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:39280400-39287200	Weak transcription	Colonic Mucosa	Colon
9	chr12:39280800-39285800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:39281000-39285800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr12:39281000-39286000	Weak transcription	Gastric	stomach
12	chr12:39282000-39284800	Weak transcription	Right Atrium	heart
13	chr12:39282200-39285800	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr12:39282800-39285200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:39282800-39285200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr12:39283000-39284600	Enhancers	Stomach Mucosa	stomach
17	chr12:39283200-39284600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:39283200-39285000	Enhancers	Primary hematopoietic stem cells	blood
19	chr12:39283400-39284400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:39283400-39285800	Enhancers	Liver	Liver
21	chr12:39283600-39284600	Enhancers	Colon Smooth Muscle	Colon
22	chr12:39283600-39285800	Weak transcription	Esophagus	oesophagus
23	chr12:39283800-39284400	Weak transcription	Fetal Intestine Small	intestine
24	chr12:39283800-39284600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr12:39283800-39285000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr12:39283800-39285800	Weak transcription	Left Ventricle	heart
27	chr12:39283800-39285800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr12:39284000-39284200	Enhancers	Adipose Nuclei	Adipose
29	chr12:39284000-39284400	Flanking Active TSS	A549	lung
30	chr12:39284000-39284400	Enhancers	Hela-S3	cervix
31	chr12:39284000-39284600	Enhancers	HMEC	breast
32	chr12:39284000-39284600	Enhancers	HUVEC	blood vessel
33	chr12:39284000-39284600	Enhancers	NHEK	skin
34	chr12:39284000-39285000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:39284200-39289600	Weak transcription	Adipose Nuclei	Adipose
36	chr12:39284400-39284600	Enhancers	Fetal Intestine Small	intestine
37	chr12:39284400-39284600	Enhancers	A549	lung
38	chr12:39284400-39285000	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr12:39284400-39285600	Weak transcription	Hela-S3	cervix
40	chr12:39284400-39285800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:39284600-39285600	Weak transcription	Fetal Intestine Small	intestine
42	chr12:39284600-39285600	Weak transcription	A549	lung
43	chr12:39284600-39285800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:39284600-39285800	Weak transcription	Stomach Mucosa	stomach
45	chr12:39284600-39285800	Weak transcription	HMEC	breast
46	chr12:39284600-39286000	Weak transcription	Colon Smooth Muscle	Colon
47	chr12:39284600-39286000	Weak transcription	NHEK	skin
48	chr12:39284600-39289200	Weak transcription	HUVEC	blood vessel
49	chr12:39284800-39286000	Enhancers	Lung	lung
50	chr12:39284800-39286400	Enhancers	Right Atrium	heart

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