Variant report

Variant	nsv8899
Chromosome Location	chr12:8310078-8380840
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:667)
CpG islands
(count:2443)
Chromatin interactive
region (count:2)
LncRNA
region (count:29)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:667 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:8379562-8379932	GM12878	blood:	n/a	n/a
2	BACH1	chr12:8371647-8371788	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:8332681-8332889	GM12878	blood:	n/a	n/a
4	BATF	chr12:8329660-8329938	GM12878	blood:	n/a	n/a
5	BATF	chr12:8324877-8325190	GM12878	blood:	n/a	n/a
6	BATF	chr12:8329523-8329997	GM12878	blood:	n/a	n/a
7	BATF	chr12:8379573-8380007	GM12878	blood:	n/a	chr12:8379783-8379794
8	BATF	chr12:8379628-8379911	GM12878	blood:	n/a	chr12:8379783-8379794
9	BCL11A	chr12:8379597-8380023	GM12878	blood:	n/a	chr12:8379787-8379796 chr12:8379933-8379946
10	BCL11A	chr12:8379625-8379922	GM12878	blood:	n/a	chr12:8379787-8379796
11	BCL11A	chr12:8324784-8325136	GM12878	blood:	n/a	n/a
12	BCL11A	chr12:8380564-8380764	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:8315121-8315536	K562	blood:	n/a	n/a
14	BHLHE40	chr12:8379952-8380140	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:8350455-8350821	HCT-116	colon:	n/a	n/a
16	CEBPB	chr12:8350554-8350655	A549	lung:	n/a	n/a
17	CEBPB	chr12:8350414-8350907	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:8350634-8350826	K562	blood:	n/a	n/a
19	CEBPB	chr12:8350546-8350745	K562	blood:	n/a	n/a
20	CEBPB	chr12:8350339-8350909	IMR90	lung:	n/a	n/a
21	CTCF	chr12:8340661-8341003	A549	lung:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
22	CTCF	chr12:8332640-8332790	AoAF	blood vessel:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
23	CTCF	chr12:8340815-8340927	Lung_OC	lung:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
24	CTCF	chr12:8332760-8332910	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr12:8340701-8340979	K562	blood:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
26	CTCF	chr12:8340820-8340970	GM12864	blood:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
27	CTCF	chr12:8332753-8332808	HepG2	liver:	n/a	n/a
28	CTCF	chr12:8348320-8348470	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr12:8332640-8332790	HL-60	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
30	CTCF	chr12:8379980-8380130	GM12873	blood:	n/a	n/a
31	CTCF	chr12:8332900-8333050	GM12874	blood:	n/a	n/a
32	CTCF	chr12:8332624-8332907	GM13976	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
33	CTCF	chr12:8340760-8340809	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr12:8352582-8352817	A549	lung:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
35	CTCF	chr12:8348240-8348390	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr12:8364873-8364974	GM10248	blood:	n/a	n/a
37	CTCF	chr12:8332640-8332790	HRPEpiC	eye:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
38	CTCF	chr12:8340616-8340980	K562	blood:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
39	CTCF	chr12:8332700-8332850	HA-sp	spinal cord:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
40	CTCF	chr12:8332640-8332790	NHEK	skin:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
41	CTCF	chr12:8348340-8348490	A549	lung:	n/a	n/a
42	CTCF	chr12:8332720-8332870	NHEK	skin:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
43	CTCF	chr12:8332720-8332870	HepG2	liver:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
44	CTCF	chr12:8332598-8332923	K562	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
45	CTCF	chr12:8332640-8332790	HMEC	breast:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
46	CTCF	chr12:8332745-8333074	HCT-116	colon:	n/a	n/a
47	CTCF	chr12:8332740-8332890	GM12869	blood:	n/a	chr12:8332744-8332762
48	CTCF	chr12:8332651-8332879	ProgFib	skin:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
49	CTCF	chr12:8352700-8352850	HEK293	kidney:	n/a	chr12:8352744-8352762 chr12:8352739-8352760
50	CTCF	chr12:8340860-8341010	A549	lung:	n/a	chr12:8340880-8340901 chr12:8340879-8340895

(count:2443 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8376943-8376993	LNCaP	prostate:	n/a
2	chr12:8376090-8376140	HL-60	blood:	n/a
3	chr12:8374206-8374256	Caco-2	colon:	n/a
4	chr12:8376943-8376993	LNCaP	prostate:	n/a
5	chr12:8376090-8376140	HL-60	blood:	n/a
6	chr12:8374206-8374256	Caco-2	colon:	n/a
7	chr12:8374133-8374183	ECC-1	luminal epithelium:	n/a
8	chr12:8324628-8324678	HNPCEpiC	eye:	n/a
9	chr12:8376943-8376993	IMR90	lung:	fetal
10	chr12:8372478-8372528	HRE	kidney:	n/a
11	chr12:8324998-8325048	HEK293	kidney:	embryo
12	chr12:8329330-8329380	HCF	heart:	n/a
13	chr12:8324628-8324678	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:8378308-8378358	HCF	heart:	n/a
15	chr12:8332808-8332858	HRPEpiC	eye:	n/a
16	chr12:8380360-8380410	PANC-1	pancreas:	n/a
17	chr12:8378308-8378358	AG10803	skin:	n/a
18	chr12:8332156-8332206	IMR90	lung:	fetal
19	chr12:8333192-8333242	SK-N-SH	brain:	n/a
20	chr12:8329330-8329380	GM06990	blood:	n/a
21	chr12:8372478-8372528	NH-A	brain:	n/a
22	chr12:8324998-8325048	HAEpiC	amniotic membrane:	n/a
23	chr12:8333010-8333060	HCT-116	colon:	n/a
24	chr12:8380127-8380177	AG09309	skin:	n/a
25	chr12:8332156-8332206	BE2_C	brain:	n/a
26	chr12:8325216-8325266	PrEC	prostate:	n/a
27	chr12:8332808-8332858	SKMC	muscle:	n/a
28	chr12:8373953-8374003	HCT-116	colon:	n/a
29	chr12:8380472-8380522	HMEC	breast:	n/a
30	chr12:8376943-8376993	H1-hESC	embryonic stem cell:	embryo
31	chr12:8325216-8325266	HCPEpiC	choroid plexus:	n/a
32	chr12:8337217-8337267	Caco-2	colon:	n/a
33	chr12:8371812-8371862	IMR90	lung:	fetal
34	chr12:8331979-8332029	LNCaP	prostate:	n/a
35	chr12:8371626-8371676	HCM	heart:	n/a
36	chr12:8374206-8374256	HNPCEpiC	eye:	n/a
37	chr12:8378308-8378358	HCM	heart:	n/a
38	chr12:8377808-8377858	HCF	heart:	n/a
39	chr12:8371812-8371862	GM12891	blood:	n/a
40	chr12:8372182-8372232	SAEC	small airway:	n/a
41	chr12:8376943-8376993	Caco-2	colon:	n/a
42	chr12:8331979-8332029	HRCEpiC	kidney:	n/a
43	chr12:8380286-8380336	RPTEC	kidney:	n/a
44	chr12:8375674-8375724	LNCaP	prostate:	n/a
45	chr12:8378308-8378358	GM12891	blood:	n/a
46	chr12:8332640-8332690	HRE	kidney:	n/a
47	chr12:8332156-8332206	AG09319	gingival:	n/a
48	chr12:8324628-8324678	HRCEpiC	kidney:	n/a
49	chr12:8329330-8329380	PrEC	prostate:	n/a
50	chr12:8324998-8325048	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:8377558..8379489-chr12:8392400..8395227,2	K562	blood:
2	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:

(count:29 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF705A-1	chr12:8346127-8346251	ENSG00000226711.2
2	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
3	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
4	lnc-ZNF705A-1	chr12:8346800-8347077	ENSG00000226711.2
5	lnc-ZNF705A-1	chr12:8341163-8341241	NONHSAT026297
6	lnc-ZNF705A-1	chr12:8348853-8349114	ENSG00000226711.2
7	lnc-ZNF705A-1	chr12:8356654-8356771	ENSG00000226711.2
8	lnc-ZNF705A-1	chr12:8346799-8347077	NONHSAT026297
9	lnc-ZNF705A-1	chr12:8347873-8348008	ENSG00000226711.2
10	lnc-FAM90A1-2	chr12:8352195-8352416	NONHSAT026302
11	lnc-ZNF705A-1	chr12:8347026-8347077	ENSG00000226711.2
12	lnc-ZNF705A-1	chr12:8347016-8347077	ENSG00000226711.2
13	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
14	lnc-ZNF705A-1	chr12:8328453-8328538	ENSG00000256703.1
15	lnc-ZNF705A-1	chr12:8346799-8347077	ENSG00000226711.2
16	lnc-ZNF705A-1	chr12:8341081-8341131	ENSG00000226711.2
17	lnc-ZNF705A-1	chr12:8378474-8378624	NONHSAT026297
18	lnc-ZNF705A-1	chr12:8368402-8368631	ENSG00000226711.2
19	lnc-ZNF705A-1	chr12:8341068-8341133	ENSG00000256703.1
20	lnc-ZNF705A-1	chr12:8347529-8347872	ENSG00000226711.2
21	lnc-ZNF705A-1	chr12:8347873-8348248	ENSG00000226711.2
22	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
23	lnc-ZNF705A-1	chr12:8356654-8356724	ENSG00000226711.2
24	lnc-ZNF705A-1	chr12:8329595-8329781	ENSG00000256703.1
25	lnc-ZNF705A-1	chr12:8378905-8379047	NONHSAT026297
26	lnc-ZNF705A-1	chr12:8347325-8347392	ENSG00000226711.2
27	lnc-ZNF705A-1	chr12:8346895-8346923	ENSG00000226711.2
28	lnc-ZNF705A-1	chr12:8347016-8347077	ENSG00000226711.2
29	lnc-FAM90A1-2	chr12:8359252-8359306	NONHSAT026302

No data

Variant related genes	Relation type
FAM90A1	TF binding region
ENSG00000244050	TF binding region
FAM66C	TF binding region
ALG1L10P	TF binding region
ENSG00000266026	TF binding region
ZNF705A	TF binding region
FAM90A1	CpG island
ENSG00000244050	CpG island
FAM66C	CpG island
ALG1L10P	CpG island
ENSG00000266026	CpG island
ZNF705A	CpG island
ENSG00000215374	chromatin interactions

Extended variants
information (count: 2081 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568796677	chr12:8310096-8310097	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs372319575	chr12:8310108-8310109	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs114842103	chr12:8310134-8310135	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs527505515	chr12:8310169-8310170	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs116592898	chr12:8310255-8310256	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs147749393	chr12:8310261-8310262	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs541506186	chr12:8310396-8310397	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs375496818	chr12:8310421-8310422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs74060105	chr12:8310460-8310461	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs117153680	chr12:8310484-8310485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs57915390	chr12:8310538-8310539	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs4294628	chr12:8310539-8310540	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs58877610	chr12:8310552-8310553	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs4284474	chr12:8310591-8310592	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs376342466	chr12:8310651-8310652	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs529549070	chr12:8310810-8310811	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs4348974	chr12:8310823-8310824	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs149832372	chr12:8310835-8310836	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs74060106	chr12:8310837-8310838	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs536108192	chr12:8310842-8310843	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs534903871	chr12:8310859-8310860	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs373112466	chr12:8310860-8310861	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs144944409	chr12:8310919-8310920	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61330021	chr12:8310949-8310950	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs186740851	chr12:8310950-8310951	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115945660	chr12:8311042-8311043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149069690	chr12:8311067-8311068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10770254	chr12:8311188-8311189	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576407102	chr12:8311262-8311263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143083020	chr12:8311268-8311269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs191593748	chr12:8311283-8311284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138503738	chr12:8311342-8311343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184912953	chr12:8311343-8311344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6486850	chr12:8311376-8311377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs6486851	chr12:8311423-8311424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs190411876	chr12:8311460-8311461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374009704	chr12:8311522-8311523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140247586	chr12:8311528-8311529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76962630	chr12:8311563-8311564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs181623709	chr12:8311583-8311584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145527184	chr12:8311596-8311597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374526874	chr12:8311637-8311638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112598060	chr12:8311643-8311644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs561425562	chr12:8311649-8311650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185224031	chr12:8311651-8311652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111472458	chr12:8311681-8311682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141724965	chr12:8311711-8311712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189725336	chr12:8311787-8311788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181103864	chr12:8311802-8311803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150575168	chr12:8311839-8311840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
early-passage human iPS cells	21368824	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8306400-8311000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:8306600-8311000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr12:8308600-8310800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr12:8308600-8310800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr12:8308800-8310600	Enhancers	HMEC	breast
6	chr12:8309000-8310400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr12:8309000-8310600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:8309200-8310200	Enhancers	K562	blood
9	chr12:8309200-8310200	Enhancers	Osteobl	bone
10	chr12:8309200-8310600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:8309200-8310600	Enhancers	NH-A	brain
12	chr12:8309200-8311000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr12:8309400-8310200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr12:8309400-8310200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr12:8309400-8310400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:8309400-8310400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr12:8309400-8310600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:8309400-8310600	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:8309600-8310600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:8309600-8311000	Flanking Active TSS	A549	lung
21	chr12:8309600-8314600	Weak transcription	Primary T cells from cord blood	blood
22	chr12:8309800-8310600	Enhancers	Primary hematopoietic stem cells	blood
23	chr12:8310000-8310600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:8310000-8310800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr12:8310000-8310800	Enhancers	HUVEC	blood vessel
26	chr12:8310200-8310400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr12:8310200-8314800	Weak transcription	K562	blood
28	chr12:8310800-8311200	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr12:8311000-8311200	Enhancers	A549	lung
30	chr12:8311000-8314600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr12:8314600-8315200	Enhancers	Primary T cells from cord blood	blood
32	chr12:8314600-8315400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr12:8314800-8315400	Enhancers	K562	blood
34	chr12:8324800-8325000	Enhancers	Brain Hippocampus Middle	brain
35	chr12:8325000-8325400	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr12:8325000-8325400	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr12:8325000-8325400	Enhancers	GM12878-XiMat	blood
38	chr12:8325400-8332600	Weak transcription	Brain Hippocampus Middle	brain
39	chr12:8332000-8334600	Active TSS	Brain Anterior Caudate	brain
40	chr12:8332400-8332800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr12:8332400-8332800	Flanking Active TSS	Dnd41	blood
42	chr12:8332400-8334200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:8332600-8333000	Active TSS	Primary B cells from cord blood	blood
44	chr12:8332600-8333000	Active TSS	Primary T cells from cord blood	blood
45	chr12:8332600-8333000	Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr12:8332600-8333000	Active TSS	Fetal Kidney	kidney
47	chr12:8332600-8333000	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr12:8332600-8333200	Active TSS	Primary B cells from peripheral blood	blood
49	chr12:8332600-8333200	Active TSS	Primary hematopoietic stem cells	blood
50	chr12:8332600-8333200	Active TSS	Primary T helper naive cells from peripheral blood	blood

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