Variant report

Variant	nsv899056
Chromosome Location	chr12:47940764-48012390
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:62)
Chromatin interactive
region (count:31)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:48009566-48009824	K562	blood:	n/a	n/a
2	BACH1	chr12:47945511-47945602	K562	blood:	n/a	chr12:47945571-47945585
3	BATF	chr12:47968098-47968398	GM12878	blood:	n/a	n/a
4	BCL3	chr12:47990271-47990556	GM12878	blood:	n/a	n/a
5	CBX3	chr12:48006744-48007063	K562	blood:	n/a	n/a
6	CBX3	chr12:48001220-48001519	K562	blood:	n/a	n/a
7	CBX3	chr12:47999499-47999693	K562	blood:	n/a	n/a
8	CBX3	chr12:47947045-47947272	K562	blood:	n/a	n/a
9	CBX3	chr12:48006668-48007131	HCT-116	colon:	n/a	n/a
10	CBX3	chr12:48006654-48007105	K562	blood:	n/a	n/a
11	CCNT2	chr12:48009615-48009815	K562	blood:	n/a	n/a
12	CEBPB	chr12:48010267-48010601	Hela-S3	cervix:	n/a	chr12:48010454-48010465
13	CEBPB	chr12:48010311-48010625	K562	blood:	n/a	chr12:48010454-48010465
14	CEBPB	chr12:47961516-47961727	IMR90	lung:	n/a	chr12:47961609-47961626
15	CEBPB	chr12:48010270-48010620	IMR90	lung:	n/a	chr12:48010454-48010465
16	CEBPB	chr12:47990257-47990581	HepG2	liver:	n/a	chr12:47990388-47990399
17	CEBPB	chr12:48010262-48010605	A549	lung:	n/a	chr12:48010454-48010465
18	CEBPB	chr12:47990252-47990588	IMR90	lung:	n/a	chr12:47990388-47990399
19	CEBPB	chr12:48010294-48010614	HepG2	liver:	n/a	chr12:48010454-48010465
20	CEBPB	chr12:47990304-47990504	K562	blood:	n/a	chr12:47990388-47990399
21	CEBPB	chr12:47990261-47990663	A549	lung:	n/a	chr12:47990388-47990399
22	CEBPB	chr12:47990321-47990731	Hela-S3	cervix:	n/a	chr12:47990388-47990399
23	CEBPD	chr12:48009505-48009968	K562	blood:	n/a	n/a
24	CTCF	chr12:47940921-47941216	A549	lung:	n/a	n/a
25	CTCF	chr12:47940980-47941130	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr12:47941021-47941106	A549	lung:	n/a	n/a
27	CTCF	chr12:47941023-47941110	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:47940777-47941286	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:47996851-47997024	MCF-7	breast:	n/a	chr12:47996875-47996893 chr12:47996955-47996968
30	CTCF	chr12:47941000-47941150	Caco-2	colon:	n/a	n/a
31	CTCF	chr12:47996800-47996950	Hela-S3	cervix:	n/a	chr12:47996875-47996893
32	CTCF	chr12:47996740-47997037	H1-hESC	embryonic stem cell:	n/a	chr12:47996875-47996893 chr12:47996955-47996968
33	CTCF	chr12:47996907-47996945	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:47940940-47941090	NB4	blood:	n/a	n/a
35	CTCF	chr12:47940920-47941070	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr12:47996800-47996950	MCF-7	breast:	n/a	chr12:47996875-47996893
37	CTCF	chr12:47996733-47997125	K562	blood:	n/a	chr12:47996875-47996893 chr12:47996955-47996968
38	CTCF	chr12:47940960-47941110	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr12:47940980-47941130	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr12:47974986-47975037	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr12:47996900-47997050	BE2_C	brain:	n/a	chr12:47996955-47996968
42	CTCF	chr12:47996916-47996933	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr12:47940980-47941130	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:47940928-47941210	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr12:47940960-47941087	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr12:47941000-47941150	HMEC	breast:	n/a	n/a
47	CTCF	chr12:47940906-47941201	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr12:47941000-47941150	GM12874	blood:	n/a	n/a
49	CTCF	chr12:47996820-47996970	K562	blood:	n/a	chr12:47996875-47996893 chr12:47996955-47996968
50	CTCF	chr12:47940941-47941168	Hela-S3	cervix:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:47985234-47985284	AG10803	skin:	n/a
2	chr12:47985234-47985284	AG10803	skin:	n/a
3	chr12:47985234-47985284	K562	blood:	n/a
4	chr12:47985234-47985284	RPTEC	kidney:	n/a
5	chr12:47985234-47985284	HAEpiC	amniotic membrane:	n/a
6	chr12:47985234-47985284	AG09319	gingival:	n/a
7	chr12:47985234-47985284	HMEC	breast:	n/a
8	chr12:47985234-47985284	HepG2	liver:	n/a
9	chr12:47985234-47985284	SK-N-MC	brain:	n/a
10	chr12:47985234-47985284	GM12892	blood:	n/a
11	chr12:47985234-47985284	Jurkat	blood:	n/a
12	chr12:47985234-47985284	Caco-2	colon:	n/a
13	chr12:47985234-47985284	ovcar-3	ovarian:	n/a
14	chr12:47985234-47985284	IMR90	lung:	fetal
15	chr12:47985234-47985284	Hepatocyte	liver:	n/a
16	chr12:47985234-47985284	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:47985234-47985284	HCPEpiC	choroid plexus:	n/a
18	chr12:47985234-47985284	MCF10A-Er-Src	breast:	n/a
19	chr12:47985234-47985284	PrEC	prostate:	n/a
20	chr12:47985234-47985284	LNCaP	prostate:	n/a
21	chr12:47985234-47985284	HEEpiC	esophagus:	n/a
22	chr12:47985234-47985284	GM12891	blood:	n/a
23	chr12:47985234-47985284	SK-N-SH_RA	brain:	n/a
24	chr12:47985234-47985284	BJ	skin:	n/a
25	chr12:47985234-47985284	ECC-1	luminal epithelium:	n/a
26	chr12:47985234-47985284	T-47D	breast:	n/a
27	chr12:47985234-47985284	PANC-1	pancreas:	n/a
28	chr12:47985234-47985284	Hela-S3	cervix:	n/a
29	chr12:47985234-47985284	AG09309	skin:	n/a
30	chr12:47985234-47985284	CMK	blood:	n/a
31	chr12:47985234-47985284	GM19239	blood:	n/a
32	chr12:47985234-47985284	NH-A	brain:	n/a
33	chr12:47985234-47985284	AG04450	lung:	fetal
34	chr12:47985234-47985284	HCF	heart:	n/a
35	chr12:47985234-47985284	SKMC	muscle:	n/a
36	chr12:47985234-47985284	U87	brain:	n/a
37	chr12:47985234-47985284	HL-60	blood:	n/a
38	chr12:47985234-47985284	HCT-116	colon:	n/a
39	chr12:47985234-47985284	AoSMC	blood vessel:	n/a
40	chr12:47985234-47985284	HRPEpiC	eye:	n/a
41	chr12:47985234-47985284	SAEC	small airway:	n/a
42	chr12:47985234-47985284	HNPCEpiC	eye:	n/a
43	chr12:47985234-47985284	HIPEpiC	eye:	n/a
44	chr12:47985234-47985284	NHBE	bronchial:	n/a
45	chr12:47985234-47985284	BE2_C	brain:	n/a
46	chr12:47985234-47985284	HUVEC	blood vessel:	n/a
47	chr12:47985234-47985284	HCM	heart:	n/a
48	chr12:47985234-47985284	GM06990	blood:	n/a
49	chr12:47985234-47985284	ProgFib	skin:	n/a
50	chr12:47985234-47985284	HRE	kidney:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:47978595..47981359-chr12:47984602..47986611,2	K562	blood:
2	chr12:47949400..47951691-chr12:47954293..47957038,2	MCF-7	breast:
3	chr12:47955362..47958310-chr12:48025284..48027406,2	MCF-7	breast:
4	chr12:47951165..47953932-chr12:47955672..47957240,2	MCF-7	breast:
5	chr12:47947520..47950380-chr12:47954557..47956247,2	MCF-7	breast:
6	chr12:47969970..47972142-chr12:47972144..47974115,2	K562	blood:
7	chr12:47988486..47990191-chr12:47994085..47995626,2	MCF-7	breast:
8	chr12:47978595..47981359-chr12:47984602..47986611,2	K562	blood:
9	chr12:47949400..47951691-chr12:47954293..47957038,2	MCF-7	breast:
10	chr12:47995378..47998174-chr12:48001804..48005197,3	K562	blood:
11	chr12:47935247..47938563-chr12:47939699..47941395,3	K562	blood:
12	chr12:47954626..47957338-chr12:47968383..47970833,2	K562	blood:
13	chr12:47969081..47971247-chr12:47974364..47977314,2	MCF-7	breast:
14	chr12:47975336..47978227-chr12:47979914..47982995,4	K562	blood:
15	chr12:47940612..47941519-chr12:48080237..48081015,3	K562	blood:
16	chr12:47969081..47971247-chr12:47974364..47977314,2	MCF-7	breast:
17	chr12:47960869..47963224-chr12:47965190..47966994,3	K562	blood:
18	chr12:47960869..47963224-chr12:47965190..47966994,3	K562	blood:
19	chr12:47969970..47972142-chr12:47972144..47974115,2	K562	blood:
20	chr12:47954626..47957338-chr12:47968383..47970833,2	K562	blood:
21	chr12:47995378..47998174-chr12:48001804..48005197,3	K562	blood:
22	chr12:47951165..47953932-chr12:47955672..47957240,2	MCF-7	breast:
23	chr12:48010127..48013715-chr12:48014407..48017154,4	K562	blood:
24	chr12:47959788..47962194-chr12:47969072..47971219,2	K562	blood:
25	chr12:47974012..47976836-chr12:47979914..47981559,2	K562	blood:
26	chr12:47940639..47941454-chr12:48051090..48052018,3	MCF-7	breast:
27	chr12:47975336..47978227-chr12:47979914..47982995,4	K562	blood:
28	chr12:47959788..47962194-chr12:47969072..47971219,2	K562	blood:
29	chr12:47947520..47950380-chr12:47954557..47956247,2	MCF-7	breast:
30	chr12:47974012..47976836-chr12:47979914..47981559,2	K562	blood:
31	chr12:47988486..47990191-chr12:47994085..47995626,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC48A1-6	chr12:47947058-47947319	expReg_chr12_3796_+
2	lnc-SLC48A1-4	chr12:48001617-48001971	NONHSAT027928

No data

Variant related genes	Relation type
ENSG00000257905	TF binding region
ENSG00000257905	CpG island

Extended variants
information (count: 2628 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7958908	chr12:47940764-47940765	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7959019	chr12:47940829-47940830	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs147216133	chr12:47940840-47940841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12299011	chr12:47940858-47940859	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs77022490	chr12:47940863-47940864	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554196831	chr12:47940912-47940913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73109421	chr12:47940946-47940947	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs370040775	chr12:47940949-47940950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530903951	chr12:47941036-47941037	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551016281	chr12:47941047-47941048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192749034	chr12:47941057-47941058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369809516	chr12:47941122-47941123	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530273029	chr12:47941137-47941138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11168152	chr12:47941152-47941153	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs56095677	chr12:47941167-47941168	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs537793379	chr12:47941177-47941178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368814133	chr12:47941178-47941179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551028937	chr12:47941185-47941186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76860302	chr12:47941206-47941207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537029464	chr12:47941207-47941208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557009076	chr12:47941213-47941214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573875103	chr12:47941219-47941220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536108662	chr12:47941220-47941221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4768830	chr12:47941232-47941233	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs375868749	chr12:47941257-47941258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11168153	chr12:47941279-47941280	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs545538007	chr12:47941323-47941324	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565354784	chr12:47941331-47941332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575582210	chr12:47941356-47941357	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184688714	chr12:47941359-47941360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188787730	chr12:47941363-47941364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11168154	chr12:47941409-47941410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs150506453	chr12:47941423-47941424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546851815	chr12:47941499-47941500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370656668	chr12:47941509-47941510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547186523	chr12:47941528-47941529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540038995	chr12:47941548-47941549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs142152104	chr12:47941561-47941562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529703598	chr12:47941604-47941605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs564694778	chr12:47941605-47941606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192155918	chr12:47941617-47941618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550552527	chr12:47941633-47941634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184699950	chr12:47941634-47941635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112854065	chr12:47941672-47941673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377328315	chr12:47941711-47941712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553275484	chr12:47941756-47941757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189116637	chr12:47941769-47941770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538817516	chr12:47941782-47941783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112320024	chr12:47941820-47941821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559132619	chr12:47941907-47941908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Neurodevelopmental disorder	22521361	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47932200-47944800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr12:47938800-47942000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr12:47939200-47941400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:47939400-47940800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:47940000-47940800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:47940200-47940800	Enhancers	Primary B cells from cord blood	blood
7	chr12:47940800-47944400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr12:47940800-47944800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:47941200-47941400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:47941400-47945200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:47941400-47945200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:47942000-47945200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr12:47943000-47943200	Enhancers	HMEC	breast
14	chr12:47943400-47945200	Weak transcription	HMEC	breast
15	chr12:47943600-47951600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:47944200-47944600	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr12:47944200-47946000	Enhancers	Fetal Stomach	stomach
18	chr12:47944200-47946400	Enhancers	Rectal Smooth Muscle	rectum
19	chr12:47944200-47953000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:47944400-47946400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr12:47944400-47946400	Enhancers	Colon Smooth Muscle	Colon
22	chr12:47944600-47945600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr12:47944800-47945200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:47944800-47945600	Enhancers	Brain Angular Gyrus	brain
25	chr12:47944800-47945600	Enhancers	Stomach Smooth Muscle	stomach
26	chr12:47944800-47945600	Flanking Active TSS	NHDF-Ad	bronchial
27	chr12:47944800-47946600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr12:47945000-47946400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:47945200-47945600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr12:47945200-47945600	Enhancers	HMEC	breast
31	chr12:47945200-47945600	Enhancers	HSMMtube	muscle
32	chr12:47945200-47945600	Bivalent Enhancer	Osteobl	bone
33	chr12:47945200-47945800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr12:47945200-47945800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:47945200-47945800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr12:47945200-47945800	Enhancers	A549	lung
37	chr12:47945200-47946000	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr12:47945400-47945800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr12:47945600-47946000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:47945600-47946000	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr12:47945600-47946000	Enhancers	NHDF-Ad	bronchial
42	chr12:47945800-47946200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr12:47945800-47947200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:47946000-47947000	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr12:47946400-47946800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr12:47946400-47947000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:47946400-47949800	Weak transcription	Colon Smooth Muscle	Colon
48	chr12:47946600-47947200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
49	chr12:47946800-47947400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr12:47947000-47947400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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