Variant report

Variant	esv1817077
Chromosome Location	chr12:31229417-31354483
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1043)
CpG islands
(count:1100)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1043 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
2	ATF1	chr12:31230204-31230267	K562	blood:	n/a	n/a
3	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
6	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
7	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
8	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
9	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
10	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
14	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
16	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
17	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
18	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
19	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
21	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
22	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
23	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
24	CEBPB	chr12:31231821-31232014	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:31232555-31232661	HepG2	liver:	n/a	n/a
26	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
27	CHD2	chr12:31271974-31272145	GM12878	blood:	n/a	n/a
28	CHD2	chr12:31270114-31270314	GM12878	blood:	n/a	n/a
29	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a
31	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
32	CHD2	chr12:31270194-31270459	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTBP2	chr12:31271446-31272443	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr12:31270123-31270826	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr12:31270451-31270519	Spleen_OC	spleen:	n/a	n/a
36	CTCF	chr12:31251032-31251134	GM12892	blood:	n/a	n/a
37	CTCF	chr12:31340460-31340480	GM13976	blood:	n/a	n/a
38	CTCF	chr12:31269968-31270406	HepG2	liver:	n/a	n/a
39	CTCF	chr12:31304409-31304525	A549	lung:	n/a	n/a
40	CTCF	chr12:31330652-31330768	GM19239	blood:	n/a	chr12:31330654-31330675
41	CTCF	chr12:31304437-31304526	GM19238	blood:	n/a	n/a
42	CTCF	chr12:31278702-31278731	LNCaP	prostate:	n/a	n/a
43	CTCF	chr12:31330576-31330804	A549	lung:	n/a	chr12:31330654-31330675
44	CTCF	chr12:31270019-31270364	MCF-7	breast:	n/a	n/a
45	CTCF	chr12:31304382-31304560	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:31270079-31270311	GM10266	blood:	n/a	n/a
47	CTCF	chr12:31270160-31270310	WI-38	lung:	n/a	n/a
48	CTCF	chr12:31330420-31330570	HPF	lung:	n/a	n/a
49	CTCF	chr12:31270113-31270275	HepG2	liver:	n/a	n/a
50	CTCF	chr12:31270500-31270650	HCPEpiC	choroid plexus:	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	chr12:31254007-31254057	HEK293	kidney:	embryo
2	chr12:31272865-31272915	GM12892	blood:	n/a
3	chr12:31254007-31254057	HEK293	kidney:	embryo
4	chr12:31272865-31272915	GM12892	blood:	n/a
5	chr12:31272112-31272162	AG09319	gingival:	n/a
6	chr12:31255279-31255329	HepG2	liver:	n/a
7	chr12:31272112-31272162	GM12891	blood:	n/a
8	chr12:31257362-31257412	GM12878	blood:	n/a
9	chr12:31233201-31233251	ovcar-3	ovarian:	n/a
10	chr12:31272114-31272164	GM12891	blood:	n/a
11	chr12:31274424-31274474	Caco-2	colon:	n/a
12	chr12:31233201-31233251	HCF	heart:	n/a
13	chr12:31271783-31271833	HCM	heart:	n/a
14	chr12:31257362-31257412	HRPEpiC	eye:	n/a
15	chr12:31256838-31256888	HL-60	blood:	n/a
16	chr12:31274424-31274474	AG04450	lung:	fetal
17	chr12:31271429-31271479	NHDF-neo	bronchial:	n/a
18	chr12:31316348-31316398	PANC-1	pancreas:	n/a
19	chr12:31272114-31272164	HRE	kidney:	n/a
20	chr12:31256838-31256888	HCF	heart:	n/a
21	chr12:31272865-31272915	HCPEpiC	choroid plexus:	n/a
22	chr12:31274424-31274474	BE2_C	brain:	n/a
23	chr12:31255279-31255329	HPAEpiC	pulmonary alveolar:	n/a
24	chr12:31272865-31272915	PFSK-1	brain:	n/a
25	chr12:31272865-31272915	GM06990	blood:	n/a
26	chr12:31256838-31256888	GM19239	blood:	n/a
27	chr12:31272119-31272169	ECC-1	luminal epithelium:	n/a
28	chr12:31255279-31255329	SK-N-SH_RA	brain:	n/a
29	chr12:31276852-31276902	SK-N-MC	brain:	n/a
30	chr12:31276852-31276902	ovcar-3	ovarian:	n/a
31	chr12:31254036-31254086	HRE	kidney:	n/a
32	chr12:31271429-31271479	HPAEpiC	pulmonary alveolar:	n/a
33	chr12:31316348-31316398	ovcar-3	ovarian:	n/a
34	chr12:31316348-31316398	HRPEpiC	eye:	n/a
35	chr12:31271783-31271833	HIPEpiC	eye:	n/a
36	chr12:31271783-31271833	A549	lung:	n/a
37	chr12:31316348-31316398	NT2-D1	testis:	n/a
38	chr12:31316348-31316398	MCF10A-Er-Src	breast:	n/a
39	chr12:31256838-31256888	HRCEpiC	kidney:	n/a
40	chr12:31316348-31316398	HRE	kidney:	n/a
41	chr12:31233201-31233251	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:31255279-31255329	MCF-7	breast:	n/a
43	chr12:31272119-31272169	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:31270326-31270376	AG09309	skin:	n/a
45	chr12:31271783-31271833	PANC-1	pancreas:	n/a
46	chr12:31316348-31316398	HMEC	breast:	n/a
47	chr12:31255279-31255329	AG09309	skin:	n/a
48	chr12:31272114-31272164	HAEpiC	amniotic membrane:	n/a
49	chr12:31274424-31274474	AG10803	skin:	n/a
50	chr12:31256838-31256888	H1-hESC	embryonic stem cell:	embryo

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:
2	chr12:31354080..31355986-chr12:31357943..31360954,3	K562	blood:
3	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
4	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
2	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066
3	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
4	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
5	lnc-FAM60A-7	chr12:31265915-31266017	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
ENSG00000245614	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000243517	chromatin interactions
ENSG00000013573	chromatin interactions

Extended variants
information (count: 3128 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3128 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372745922	chr12:31229417-31229418	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs4931426	chr12:31229428-31229429	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs562455713	chr12:31229434-31229435	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs183631732	chr12:31229437-31229438	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs146392946	chr12:31229459-31229460	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs571019279	chr12:31229469-31229470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535237381	chr12:31229478-31229479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4931427	chr12:31229485-31229486	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs568245856	chr12:31229510-31229511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535539314	chr12:31229566-31229567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs556976735	chr12:31229631-31229632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541124030	chr12:31229649-31229650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559787008	chr12:31229667-31229668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575232944	chr12:31229810-31229811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539404997	chr12:31229812-31229813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs60118847	chr12:31229822-31229823	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs2543258	chr12:31229826-31229827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189554313	chr12:31229850-31229851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201511526	chr12:31229879-31229880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540448789	chr12:31229883-31229884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561847451	chr12:31229907-31229908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530180125	chr12:31229941-31229942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs61917187	chr12:31229946-31229947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181971994	chr12:31230003-31230004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544319270	chr12:31230076-31230077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200128383	chr12:31230085-31230086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563704893	chr12:31230101-31230102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562519545	chr12:31230116-31230117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201015721	chr12:31230122-31230123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531205804	chr12:31230149-31230150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs36123089	chr12:31230182-31230183	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs2241287	chr12:31230223-31230224	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs190102477	chr12:31230245-31230246	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
34	rs528761660	chr12:31230263-31230264	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
35	rs528677208	chr12:31230290-31230291	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
36	rs11051236	chr12:31230300-31230301	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs535602012	chr12:31230339-31230340	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550665203	chr12:31230340-31230341	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149803189	chr12:31230354-31230355	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539841385	chr12:31230390-31230391	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565747836	chr12:31230415-31230416	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs71440932	chr12:31230420-31230421	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs71440933	chr12:31230428-31230429	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566792036	chr12:31230430-31230431	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533834285	chr12:31230477-31230478	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555644955	chr12:31230479-31230480	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373502811	chr12:31230507-31230508	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544379510	chr12:31230534-31230535	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556312195	chr12:31230539-31230540	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554110413	chr12:31230548-31230549	Weak transcription Strong transcription Genic enhancers Enhancers	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
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

Chromatin state (count:1579 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227600-31235600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:31227600-31235800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:31227600-31236800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:31227600-31237000	Weak transcription	Aorta	Aorta
5	chr12:31227800-31232400	Weak transcription	Spleen	Spleen
6	chr12:31227800-31232800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr12:31227800-31233600	Weak transcription	Fetal Intestine Large	intestine
8	chr12:31227800-31234000	Weak transcription	Esophagus	oesophagus
9	chr12:31227800-31235600	Weak transcription	Primary B cells from cord blood	blood
10	chr12:31227800-31235600	Weak transcription	Fetal Intestine Small	intestine
11	chr12:31227800-31235800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr12:31227800-31236000	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr12:31227800-31236800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr12:31227800-31236800	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:31227800-31237000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr12:31227800-31237000	Weak transcription	Gastric	stomach
17	chr12:31227800-31237000	Weak transcription	Lung	lung
18	chr12:31227800-31237000	Weak transcription	Right Ventricle	heart
19	chr12:31227800-31237400	Weak transcription	Ovary	ovary
20	chr12:31227800-31240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr12:31227800-31242000	Weak transcription	Left Ventricle	heart
22	chr12:31227800-31242600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
24	chr12:31228000-31230200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:31228000-31230200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr12:31228000-31230200	Weak transcription	HUVEC	blood vessel
27	chr12:31228000-31230800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr12:31228000-31230800	Weak transcription	Fetal Stomach	stomach
29	chr12:31228000-31230800	Weak transcription	HSMM	muscle
30	chr12:31228000-31230800	Weak transcription	NH-A	brain
31	chr12:31228000-31230800	Weak transcription	Osteobl	bone
32	chr12:31228000-31231000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr12:31228000-31231000	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:31228000-31231200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr12:31228000-31231400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr12:31228000-31232400	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr12:31228000-31232400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:31228000-31232800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr12:31228000-31232800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr12:31228000-31232800	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr12:31228000-31233000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr12:31228000-31233000	Weak transcription	NHEK	skin
43	chr12:31228000-31233600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr12:31228000-31233600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr12:31228000-31233800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr12:31228000-31233800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr12:31228000-31234000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr12:31228000-31234200	Weak transcription	Fetal Muscle Leg	muscle
49	chr12:31228000-31235200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr12:31228000-31235600	Weak transcription	Thymus	Thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links