Variant report

Variant	nsv976565
Chromosome Location	chr12:8315420-8354753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr12:8329523-8329997	GM12878	blood:	n/a	n/a
2	BATF	chr12:8324877-8325190	GM12878	blood:	n/a	n/a
3	BATF	chr12:8329660-8329938	GM12878	blood:	n/a	n/a
4	BATF	chr12:8332681-8332889	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:8324784-8325136	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:8315121-8315536	K562	blood:	n/a	n/a
7	CEBPB	chr12:8350554-8350655	A549	lung:	n/a	n/a
8	CEBPB	chr12:8350414-8350907	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:8350455-8350821	HCT-116	colon:	n/a	n/a
10	CEBPB	chr12:8350339-8350909	IMR90	lung:	n/a	n/a
11	CEBPB	chr12:8350546-8350745	K562	blood:	n/a	n/a
12	CEBPB	chr12:8350634-8350826	K562	blood:	n/a	n/a
13	CTCF	chr12:8332666-8332904	GM12891	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
14	CTCF	chr12:8322768-8322918	K562	blood:	n/a	n/a
15	CTCF	chr12:8340852-8340899	GM13976	blood:	n/a	chr12:8340879-8340895
16	CTCF	chr12:8332660-8332894	Fibrobl	skin:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
17	CTCF	chr12:8332745-8333074	HCT-116	colon:	n/a	n/a
18	CTCF	chr12:8332621-8332912	SK-N-SH_RA	brain:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
19	CTCF	chr12:8332644-8332898	GM19240	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
20	CTCF	chr12:8340661-8341003	A549	lung:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
21	CTCF	chr12:8348240-8348390	HRE	kidney:	n/a	n/a
22	CTCF	chr12:8332720-8332870	HUVEC	blood vessel:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
23	CTCF	chr12:8340780-8340982	MCF-7	breast:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
24	CTCF	chr12:8332640-8332790	HCFaa	heart:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
25	CTCF	chr12:8340860-8341010	HAc	cerebellar:	n/a	chr12:8340880-8340901 chr12:8340879-8340895
26	CTCF	chr12:8350860-8351010	HMEC	breast:	n/a	n/a
27	CTCF	chr12:8332402-8333142	A549	lung:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
28	CTCF	chr12:8332720-8332870	HEK293	kidney:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
29	CTCF	chr12:8332720-8332870	GM12871	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
30	CTCF	chr12:8332682-8332869	K562	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
31	CTCF	chr12:8332720-8332870	GM12866	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
32	CTCF	chr12:8332660-8332810	BE2_C	brain:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
33	CTCF	chr12:8332720-8332870	NHEK	skin:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
34	CTCF	chr12:8332660-8332810	HCT-116	colon:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
35	CTCF	chr12:8332580-8332730	AG04450	lung:	n/a	n/a
36	CTCF	chr12:8340820-8340970	HRPEpiC	eye:	n/a	chr12:8340880-8340901 chr12:8340828-8340849 chr12:8340879-8340895
37	CTCF	chr12:8332692-8332814	MCF-7	breast:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
38	CTCF	chr12:8340860-8341010	BE2_C	brain:	n/a	chr12:8340880-8340901 chr12:8340879-8340895
39	CTCF	chr12:8332640-8332790	HL-60	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
40	CTCF	chr12:8332640-8332790	HPAF	blood vessel:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
41	CTCF	chr12:8332700-8332850	AG09319	gingival:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
42	CTCF	chr12:8332900-8333050	GM12874	blood:	n/a	n/a
43	CTCF	chr12:8332600-8332750	HAc	cerebellar:	n/a	n/a
44	CTCF	chr12:8332720-8332870	GM12873	blood:	n/a	chr12:8332744-8332762 chr12:8332739-8332760
45	CTCF	chr12:8348340-8348490	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr12:8332800-8332950	WI-38	lung:	n/a	n/a
47	CTCF	chr12:8332580-8332730	HCM	heart:	n/a	n/a
48	CTCF	chr12:8347493-8347518	GM10248	blood:	n/a	n/a
49	CTCF	chr12:8348280-8348430	HMF	breast:	n/a	n/a
50	CTCF	chr12:8332618-8332980	A549	lung:	n/a	chr12:8332744-8332762 chr12:8332739-8332760

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8333192-8333242	MCF-7	breast:	n/a
2	chr12:8333192-8333242	MCF-7	breast:	n/a
3	chr12:8331979-8332029	AG09319	gingival:	n/a
4	chr12:8332810-8332860	LNCaP	prostate:	n/a
5	chr12:8324998-8325048	HAEpiC	amniotic membrane:	n/a
6	chr12:8332881-8332931	HEK293	kidney:	embryo
7	chr12:8332156-8332206	PANC-1	pancreas:	n/a
8	chr12:8337217-8337267	HRCEpiC	kidney:	n/a
9	chr12:8332881-8332931	ProgFib	skin:	n/a
10	chr12:8333192-8333242	SKMC	muscle:	n/a
11	chr12:8332881-8332931	IMR90	lung:	fetal
12	chr12:8332810-8332860	PrEC	prostate:	n/a
13	chr12:8324628-8324678	GM12892	blood:	n/a
14	chr12:8333192-8333242	HUVEC	blood vessel:	n/a
15	chr12:8337217-8337267	HL-60	blood:	n/a
16	chr12:8332152-8332202	HRCEpiC	kidney:	n/a
17	chr12:8333192-8333242	Caco-2	colon:	n/a
18	chr12:8329330-8329380	HEK293	kidney:	embryo
19	chr12:8336589-8336639	HIPEpiC	eye:	n/a
20	chr12:8336589-8336639	PFSK-1	brain:	n/a
21	chr12:8331979-8332029	SK-N-SH_RA	brain:	n/a
22	chr12:8331979-8332029	AoSMC	blood vessel:	n/a
23	chr12:8324628-8324678	LNCaP	prostate:	n/a
24	chr12:8332808-8332858	HRCEpiC	kidney:	n/a
25	chr12:8337217-8337267	HEEpiC	esophagus:	n/a
26	chr12:8333010-8333060	RPTEC	kidney:	n/a
27	chr12:8332808-8332858	IMR90	lung:	fetal
28	chr12:8329330-8329380	HEEpiC	esophagus:	n/a
29	chr12:8324153-8324203	HUVEC	blood vessel:	n/a
30	chr12:8332737-8332787	HEK293	kidney:	embryo
31	chr12:8332881-8332931	U87	brain:	n/a
32	chr12:8332152-8332202	T-47D	breast:	n/a
33	chr12:8324153-8324203	Hepatocyte	liver:	n/a
34	chr12:8324153-8324203	NH-A	brain:	n/a
35	chr12:8332808-8332858	AG09309	skin:	n/a
36	chr12:8333010-8333060	MCF-7	breast:	n/a
37	chr12:8324628-8324678	HCM	heart:	n/a
38	chr12:8329330-8329380	T-47D	breast:	n/a
39	chr12:8332881-8332931	AG04450	lung:	fetal
40	chr12:8324153-8324203	K562	blood:	n/a
41	chr12:8331979-8332029	AG09309	skin:	n/a
42	chr12:8332640-8332690	GM06990	blood:	n/a
43	chr12:8336589-8336639	AG04449	skin:	fetal
44	chr12:8324628-8324678	GM19239	blood:	n/a
45	chr12:8324998-8325048	HL-60	blood:	n/a
46	chr12:8332152-8332202	NB4	blood:	n/a
47	chr12:8329330-8329380	SKMC	muscle:	n/a
48	chr12:8324153-8324203	A549	lung:	n/a
49	chr12:8336589-8336639	T-47D	breast:	n/a
50	chr12:8332737-8332787	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:8332362..8333276-chr8:7212481..7212992,2	MCF-7	breast:

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

Variant related genes	Relation type
FAM66C	TF binding region
ZNF705A	TF binding region
FAM66C	CpG island
ZNF705A	CpG island
ENSG00000215374	chromatin interactions

Extended variants
information (count: 776 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192163071	chr12:8322589-8322590	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs367944845	chr12:8322642-8322643	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs538270528	chr12:8322653-8322654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184526288	chr12:8322691-8322692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs111353743	chr12:8322726-8322727	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs35676407	chr12:8322781-8322782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs145174240	chr12:8322788-8322789	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs138852339	chr12:8322790-8322791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144679128	chr12:8322791-8322792	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs141364610	chr12:8322792-8322793	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs74240328	chr12:8322817-8322818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs117841484	chr12:8322829-8322830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs534382352	chr12:8322841-8322842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs181868640	chr12:8322869-8322870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs376901866	chr12:8322874-8322875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs369672333	chr12:8322905-8322906	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377590419	chr12:8322953-8322954	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs529901127	chr12:8324169-8324170	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs566160932	chr12:8324183-8324184	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs11502587	chr12:8324652-8324653	Inactive region	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs11043734	chr12:8324663-8324664	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs11613962	chr12:8324717-8324718	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs111931230	chr12:8324850-8324851	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs138640726	chr12:8324941-8324942	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs12369280	chr12:8325018-8325019	Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs189846990	chr12:8325022-8325023	Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs71042340	chr12:8325091-8325092	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs148922259	chr12:8325092-8325093	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs531602510	chr12:8325216-8325217	Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs74060111	chr12:8325226-8325227	Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568474094	chr12:8325318-8325319	Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs537710994	chr12:8325392-8325393	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146325917	chr12:8325402-8325403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs59495395	chr12:8325443-8325444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs112844519	chr12:8325444-8325445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577416313	chr12:8325445-8325446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34787357	chr12:8325462-8325463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs113804827	chr12:8325558-8325559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4242878	chr12:8325660-8325661	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs540053913	chr12:8325662-8325663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558365805	chr12:8325672-8325673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575339294	chr12:8325738-8325739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375073873	chr12:8325815-8325816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543984264	chr12:8325883-8325884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368063135	chr12:8325904-8325905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572582741	chr12:8325937-8325938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554098346	chr12:8325939-8325940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541447469	chr12:8325995-8325996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4242879	chr12:8326009-8326010	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs183200577	chr12:8326193-8326194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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

Chromatin state (count:243 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8324800-8325000	Enhancers	Brain Hippocampus Middle	brain
2	chr12:8325000-8325400	Flanking Active TSS	Brain Hippocampus Middle	brain
3	chr12:8325000-8325400	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr12:8325000-8325400	Enhancers	GM12878-XiMat	blood
5	chr12:8325400-8332600	Weak transcription	Brain Hippocampus Middle	brain
6	chr12:8332000-8334600	Active TSS	Brain Anterior Caudate	brain
7	chr12:8332400-8332800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr12:8332400-8332800	Flanking Active TSS	Dnd41	blood
9	chr12:8332400-8334200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:8332600-8333000	Active TSS	Primary B cells from cord blood	blood
11	chr12:8332600-8333000	Active TSS	Primary T cells from cord blood	blood
12	chr12:8332600-8333000	Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr12:8332600-8333000	Active TSS	Fetal Kidney	kidney
14	chr12:8332600-8333000	Active TSS	Monocytes-CD14+_RO01746	blood
15	chr12:8332600-8333200	Active TSS	Primary B cells from peripheral blood	blood
16	chr12:8332600-8333200	Active TSS	Primary hematopoietic stem cells	blood
17	chr12:8332600-8333200	Active TSS	Primary T helper naive cells from peripheral blood	blood
18	chr12:8332600-8333200	Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr12:8332600-8333200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr12:8332600-8333200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
21	chr12:8332600-8333400	Active TSS	H1 Cell Line	embryonic stem cell
22	chr12:8332600-8333400	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr12:8332600-8333400	Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr12:8332600-8333400	Active TSS	Primary T cells fromperipheralblood	blood
25	chr12:8332600-8333400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
26	chr12:8332600-8333400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:8332600-8333400	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:8332600-8333400	Active TSS	Adipose Nuclei	Adipose
29	chr12:8332600-8333400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
30	chr12:8332600-8333400	Active TSS	Fetal Intestine Large	intestine
31	chr12:8332600-8333400	Active TSS	Fetal Thymus	thymus
32	chr12:8332600-8333400	Active TSS	HSMM	muscle
33	chr12:8332600-8333400	Active TSS	NHEK	skin
34	chr12:8332600-8333600	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr12:8332600-8333600	Active TSS	Fetal Muscle Trunk	muscle
36	chr12:8332600-8333600	Active TSS	Ovary	ovary
37	chr12:8332600-8333600	Active TSS	HMEC	breast
38	chr12:8332600-8333800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr12:8332600-8333800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:8332600-8333800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr12:8332600-8333800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:8332600-8333800	Active TSS	Brain Cingulate Gyrus	brain
43	chr12:8332600-8333800	Active TSS	Brain Hippocampus Middle	brain
44	chr12:8332600-8333800	Active TSS	A549	lung
45	chr12:8332600-8334000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:8332600-8334000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:8332600-8334000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:8332600-8334000	Active TSS	Stomach Smooth Muscle	stomach
49	chr12:8332600-8334200	Active TSS	Fetal Brain Female	brain
50	chr12:8332600-8334600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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