Variant report

Variant	nsv430537
Chromosome Location	chr12:121487632-121579955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2424)
CpG islands
(count:1100)
Chromatin interactive
region (count:99)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2424 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:121497991-121498204	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:121523699-121523880	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:121566791-121567654	K562	blood:	n/a	n/a
4	ARID3A	chr12:121548072-121548453	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:121566854-121567036	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:121562061-121562665	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:121554555-121555038	HepG2	liver:	n/a	n/a
8	ATF1	chr12:121562281-121562579	K562	blood:	n/a	n/a
9	ATF1	chr12:121551788-121552180	K562	blood:	n/a	n/a
10	ATF1	chr12:121558234-121558481	K562	blood:	n/a	n/a
11	ATF1	chr12:121569831-121570036	K562	blood:	n/a	n/a
12	ATF1	chr12:121548142-121548488	K562	blood:	n/a	n/a
13	ATF1	chr12:121529137-121529138	K562	blood:	n/a	n/a
14	ATF1	chr12:121554252-121554339	K562	blood:	n/a	n/a
15	ATF1	chr12:121570380-121570704	K562	blood:	n/a	n/a
16	ATF1	chr12:121566717-121567709	K562	blood:	n/a	n/a
17	ATF2	chr12:121533611-121534068	GM12878	blood:	n/a	n/a
18	ATF2	chr12:121566714-121567459	GM12878	blood:	n/a	n/a
19	ATF2	chr12:121547862-121548404	GM12878	blood:	n/a	n/a
20	ATF2	chr12:121566798-121567437	GM12878	blood:	n/a	n/a
21	ATF2	chr12:121548101-121548552	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr12:121576172-121576432	K562	blood:	n/a	n/a
23	ATF3	chr12:121562132-121562469	A549	lung:	n/a	n/a
24	ATF3	chr12:121548098-121548416	K562	blood:	n/a	n/a
25	ATF3	chr12:121562110-121562601	HCT-116	colon:	n/a	n/a
26	ATF3	chr12:121523628-121523846	HepG2	liver:	n/a	n/a
27	ATF3	chr12:121488586-121488835	GM12878	blood:	n/a	n/a
28	ATF3	chr12:121562226-121562539	K562	blood:	n/a	n/a
29	BACH1	chr12:121533616-121534030	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr12:121533719-121533919	K562	blood:	n/a	n/a
31	BATF	chr12:121533751-121534150	GM12878	blood:	n/a	n/a
32	BATF	chr12:121547894-121548437	GM12878	blood:	n/a	n/a
33	BATF	chr12:121537496-121537848	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:121537441-121537694	GM12878	blood:	n/a	n/a
35	BCL11A	chr12:121533546-121533936	GM12878	blood:	n/a	n/a
36	BCL11A	chr12:121537435-121537840	GM12878	blood:	n/a	n/a
37	BCL11A	chr12:121547886-121548416	GM12878	blood:	n/a	n/a
38	BCL11A	chr12:121547884-121548479	GM12878	blood:	n/a	n/a
39	BCL3	chr12:121533635-121534282	A549	lung:	n/a	chr12:121534235-121534244 chr12:121534236-121534245
40	BCL3	chr12:121562161-121562550	A549	lung:	n/a	chr12:121562488-121562497
41	BCLAF1	chr12:121547881-121548461	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:121498339-121498687	GM12878	blood:	n/a	n/a
43	BCLAF1	chr12:121566680-121567405	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:121558260-121558488	K562	blood:	n/a	n/a
45	BHLHE40	chr12:121576146-121576345	K562	blood:	n/a	n/a
46	BHLHE40	chr12:121566812-121567545	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:121570483-121571033	K562	blood:	n/a	n/a
48	BHLHE40	chr12:121533271-121534064	K562	blood:	n/a	chr12:121533663-121533679 chr12:121533363-121533372 chr12:121533362-121533371 chr12:121533362-121533371 chr12:121533361-121533370 chr12:121533356-121533377
49	BHLHE40	chr12:121551869-121552119	K562	blood:	n/a	n/a
50	BHLHE40	chr12:121566732-121567393	K562	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121570081-121570131	HRPEpiC	eye:	n/a
2	chr12:121534028-121534078	MCF-7	breast:	n/a
3	chr12:121570081-121570131	HRPEpiC	eye:	n/a
4	chr12:121534028-121534078	MCF-7	breast:	n/a
5	chr12:121533801-121533851	GM06990	blood:	n/a
6	chr12:121533801-121533851	HRPEpiC	eye:	n/a
7	chr12:121570752-121570802	HRCEpiC	kidney:	n/a
8	chr12:121513978-121514028	AoSMC	blood vessel:	n/a
9	chr12:121570677-121570727	HCT-116	colon:	n/a
10	chr12:121571068-121571118	GM19239	blood:	n/a
11	chr12:121569924-121569974	PrEC	prostate:	n/a
12	chr12:121570875-121570925	Hepatocyte	liver:	n/a
13	chr12:121571068-121571118	ECC-1	luminal epithelium:	n/a
14	chr12:121498343-121498393	SKMC	muscle:	n/a
15	chr12:121570616-121570666	HNPCEpiC	eye:	n/a
16	chr12:121570677-121570727	HIPEpiC	eye:	n/a
17	chr12:121533475-121533525	SK-N-MC	brain:	n/a
18	chr12:121570571-121570621	Hela-S3	cervix:	n/a
19	chr12:121533801-121533851	GM12891	blood:	n/a
20	chr12:121534028-121534078	HCT-116	colon:	n/a
21	chr12:121569969-121570019	HCM	heart:	n/a
22	chr12:121571068-121571118	H1-hESC	embryonic stem cell:	embryo
23	chr12:121498343-121498393	HCT-116	colon:	n/a
24	chr12:121570571-121570621	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:121534028-121534078	NH-A	brain:	n/a
26	chr12:121570677-121570727	ProgFib	skin:	n/a
27	chr12:121571068-121571118	AG09319	gingival:	n/a
28	chr12:121535941-121535991	HRCEpiC	kidney:	n/a
29	chr12:121533833-121533883	K562	blood:	n/a
30	chr12:121570081-121570131	ECC-1	luminal epithelium:	n/a
31	chr12:121569969-121570019	HCPEpiC	choroid plexus:	n/a
32	chr12:121570081-121570131	AG04450	lung:	fetal
33	chr12:121534028-121534078	HEK293	kidney:	embryo
34	chr12:121530737-121530787	BJ	skin:	n/a
35	chr12:121533475-121533525	HCF	heart:	n/a
36	chr12:121535941-121535991	AG04450	lung:	fetal
37	chr12:121535941-121535991	GM06990	blood:	n/a
38	chr12:121513978-121514028	SK-N-SH_RA	brain:	n/a
39	chr12:121533833-121533883	GM06990	blood:	n/a
40	chr12:121534028-121534078	PFSK-1	brain:	n/a
41	chr12:121570616-121570666	HCM	heart:	n/a
42	chr12:121570875-121570925	K562	blood:	n/a
43	chr12:121570571-121570621	ECC-1	luminal epithelium:	n/a
44	chr12:121498343-121498393	MCF-7	breast:	n/a
45	chr12:121534028-121534078	K562	blood:	n/a
46	chr12:121570875-121570925	ovcar-3	ovarian:	n/a
47	chr12:121570571-121570621	CMK	blood:	n/a
48	chr12:121535941-121535991	SAEC	small airway:	n/a
49	chr12:121570677-121570727	SK-N-SH_RA	brain:	n/a
50	chr12:121513978-121514028	HRE	kidney:	n/a

(count:99 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:121498251..121499029-chr12:121533532..121534500,2	MCF-7	breast:
2	chr12:121442844..121443785-chr12:121547734..121548804,3	K562	blood:
3	chr12:121490675..121493658-chr12:121495456..121497011,2	K562	blood:
4	chr12:121498418..121499035-chr12:121547998..121548758,2	K562	blood:
5	chr12:121533067..121535799-chr12:121628437..121630049,2	K562	blood:
6	chr12:121020917..121021868-chr12:121533219..121533885,3	K562	blood:
7	chr12:121442839..121443768-chr12:121497604..121498594,3	MCF-7	breast:
8	chr12:121533631..121534218-chr12:121667773..121668734,2	K562	blood:
9	chr12:121564281..121567226-chr12:121569639..121571152,2	MCF-7	breast:
10	chr12:121521823..121524170-chr12:121665223..121666931,2	MCF-7	breast:
11	chr12:121547752..121548609-chr12:121647435..121648349,3	MCF-7	breast:
12	chr12:121575022..121577625-chr12:121581601..121583531,2	MCF-7	breast:
13	chr12:121552705..121555604-chr12:121668224..121669822,2	MCF-7	breast:
14	chr12:121561171..121566774-chr12:121646455..121649214,5	MCF-7	breast:
15	chr12:121547911..121548611-chr12:121647690..121648251,2	MCF-7	breast:
16	chr12:121523299..121524824-chr12:121646920..121648679,2	MCF-7	breast:
17	chr12:121566845..121568445-chr12:121570737..121572613,2	K562	blood:
18	chr12:121555909..121558170-chr12:121651475..121654023,2	K562	blood:
19	chr12:121495209..121497796-chr12:121499977..121502641,3	K562	blood:
20	chr12:121488415..121490899-chr12:121492548..121494191,2	K562	blood:
21	chr12:121566738..121568870-chr12:121570376..121572315,2	MCF-7	breast:
22	chr12:121488470..121488989-chr3:111085239..111085759,2	MCF-7	breast:
23	chr12:121481372..121483233-chr12:121486748..121488250,2	K562	blood:
24	chr12:121462116..121464172-chr12:121497468..121500006,2	MCF-7	breast:
25	chr12:121552789..121554818-chr12:121661360..121664343,2	MCF-7	breast:
26	chr12:121550087..121552294-chr12:121646919..121649909,2	MCF-7	breast:
27	chr12:121473524..121476101-chr12:121524769..121527497,2	K562	blood:
28	chr12:121442823..121443336-chr12:121547928..121548775,2	MCF-7	breast:
29	chr12:121540942..121542575-chr12:121550109..121552835,2	K562	blood:
30	chr12:121574197..121575819-chr12:121598623..121600574,2	MCF-7	breast:
31	chr12:121501042..121502570-chr12:121660337..121662789,2	MCF-7	breast:
32	chr12:121488415..121490899-chr12:121492548..121494191,2	K562	blood:
33	chr12:121499402..121500015-chr12:121931705..121932231,2	MCF-7	breast:
34	chr12:121498108..121499039-chr12:121533443..121534521,4	MCF-7	breast:
35	chr12:121559081..121561979-chr12:121605012..121606674,2	MCF-7	breast:
36	chr12:121562465..121564050-chr12:121566966..121568974,2	MCF-7	breast:
37	chr12:121569906..121572539-chr12:121647803..121649868,2	MCF-7	breast:
38	chr12:121509410..121511926-chr12:121521670..121523636,2	K562	blood:
39	chr12:121498058..121498974-chr12:121533466..121534380,2	K562	blood:
40	chr12:121563121..121566575-chr12:121568260..121572155,4	K562	blood:
41	chr12:121547509..121549908-chr12:121645627..121647537,2	MCF-7	breast:
42	chr12:121017782..121019527-chr12:121520951..121522619,2	MCF-7	breast:
43	chr12:121569636..121570366-chr12:121640682..121641273,2	MCF-7	breast:
44	chr12:121509410..121511926-chr12:121521670..121523636,2	K562	blood:
45	chr12:121550438..121552806-chr12:121556760..121558947,2	K562	blood:
46	chr12:121525079..121528154-chr12:121532572..121535295,3	MCF-7	breast:
47	chr12:121532324..121533988-chr12:121647782..121650405,2	MCF-7	breast:
48	chr12:121502918..121505798-chr12:121509128..121510948,2	K562	blood:
49	chr12:121495209..121497796-chr12:121499977..121502641,3	K562	blood:
50	chr12:121550877..121553101-chr12:121566808..121569789,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-P2RX7-2	chr12:121555321-121555362	XLOC_009912
2	lnc-P2RX7-2	chr12:121557252-121558609	XLOC_009912
3	lnc-P2RX7-2	chr12:121557252-121557692	XLOC_009912
4	lnc-P2RX7-2	chr12:121556258-121556287	XLOC_009912
5	lnc-P2RX7-6	chr12:121517645-121517927	NONHSAT031263

No data

Variant related genes	Relation type
ENSG00000201945	TF binding region
P2RX7	TF binding region
ENSG00000223538	TF binding region
ENSG00000256963	TF binding region
ENSG00000201945	CpG island
P2RX7	CpG island
ENSG00000223538	CpG island
ENSG00000256963	CpG island
ENSG00000256963	chromatin interactions
ENSG00000167272	chromatin interactions
ENSG00000257053	chromatin interactions
ENSG00000135124	chromatin interactions
ENSG00000089041	chromatin interactions
HIVEP2	miRNA target sites

Extended variants
information (count: 3559 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:3559 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2708101	chr12:121487632-121487633	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73214187	chr12:121487658-121487659	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs79692207	chr12:121487663-121487664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569704080	chr12:121487697-121487698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2708100	chr12:121487745-121487746	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs572344688	chr12:121487763-121487764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551739545	chr12:121487784-121487785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73419642	chr12:121487800-121487801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534216531	chr12:121487810-121487811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554396953	chr12:121487827-121487828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567771829	chr12:121487891-121487892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551197253	chr12:121487921-121487922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77581164	chr12:121487940-121487941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577210376	chr12:121487943-121487944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556405608	chr12:121487948-121487949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541174285	chr12:121488057-121488058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78249402	chr12:121488115-121488116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539072356	chr12:121488124-121488125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs566137617	chr12:121488137-121488138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546277164	chr12:121488163-121488164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs376368605	chr12:121488219-121488220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113439611	chr12:121488279-121488280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562871444	chr12:121488312-121488313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182747302	chr12:121488338-121488339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78622253	chr12:121488339-121488340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541336689	chr12:121488344-121488345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs2258844	chr12:121488372-121488373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs3850514	chr12:121488423-121488424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs543579617	chr12:121488480-121488481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561967367	chr12:121488515-121488516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3850515	chr12:121488519-121488520	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs551802674	chr12:121488560-121488561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375101392	chr12:121488575-121488576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144256377	chr12:121488576-121488577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78671297	chr12:121488593-121488594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112008215	chr12:121488611-121488612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558954408	chr12:121488637-121488638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567922223	chr12:121488656-121488657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577444512	chr12:121488668-121488669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571188203	chr12:121488669-121488670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56345498	chr12:121488683-121488684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187165244	chr12:121488684-121488685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570207003	chr12:121488738-121488739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191670050	chr12:121488776-121488777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370471415	chr12:121488831-121488832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs16950755	chr12:121488876-121488877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs549822407	chr12:121488882-121488883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569681868	chr12:121488890-121488891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554594182	chr12:121488899-121488900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535568447	chr12:121488940-121488941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1667 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121486600-121497400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:121494200-121494400	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr12:121494800-121497400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr12:121495000-121495600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr12:121495000-121496000	Enhancers	HepG2	liver
6	chr12:121495400-121495600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr12:121495400-121495600	Enhancers	Brain Substantia Nigra	brain
8	chr12:121495600-121495800	Enhancers	Ovary	ovary
9	chr12:121495600-121497800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr12:121495600-121498000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr12:121495600-121498000	Weak transcription	Brain Substantia Nigra	brain
12	chr12:121495800-121496000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr12:121495800-121496000	Enhancers	Fetal Thymus	thymus
14	chr12:121495800-121496000	Enhancers	Pancreas	Pancrea
15	chr12:121495800-121497400	Weak transcription	Ovary	ovary
16	chr12:121496000-121496200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:121496200-121497400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:121496200-121497400	Weak transcription	Fetal Thymus	thymus
19	chr12:121496400-121497600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:121497000-121498200	Weak transcription	Pancreas	Pancrea
21	chr12:121497200-121497800	Enhancers	Fetal Muscle Trunk	muscle
22	chr12:121497200-121497800	Enhancers	GM12878-XiMat	blood
23	chr12:121497200-121497800	Enhancers	NHDF-Ad	bronchial
24	chr12:121497200-121498000	Enhancers	Primary T cells fromperipheralblood	blood
25	chr12:121497200-121498000	Enhancers	Fetal Muscle Leg	muscle
26	chr12:121497400-121497600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr12:121497400-121497600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr12:121497400-121497800	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr12:121497400-121497800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:121497400-121497800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr12:121497400-121497800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr12:121497400-121497800	Enhancers	Adipose Nuclei	Adipose
33	chr12:121497400-121497800	Enhancers	Ovary	ovary
34	chr12:121497400-121497800	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr12:121497400-121497800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
36	chr12:121497400-121497800	Enhancers	Hela-S3	cervix
37	chr12:121497400-121497800	Enhancers	HepG2	liver
38	chr12:121497400-121498000	Enhancers	Primary B cells from peripheral blood	blood
39	chr12:121497400-121498000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr12:121497400-121498000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:121497400-121498000	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr12:121497400-121498000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:121497400-121498000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:121497400-121498000	Enhancers	Placenta	Placenta
45	chr12:121497400-121498000	Enhancers	Fetal Thymus	thymus
46	chr12:121497400-121498400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:121497400-121498400	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr12:121497400-121498600	Active TSS	Rectal Smooth Muscle	rectum
49	chr12:121497600-121497800	Enhancers	Liver	Liver
50	chr12:121497600-121498000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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