Variant report

Variant	nsv1042146
Chromosome Location	chr16:12208242-12256699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:295)
CpG islands
(count:732)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12243354-12243549	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:12236580-12236915	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:12245167-12245225	HepG2	liver:	n/a	n/a
4	ATF2	chr16:12254465-12255152	GM12878	blood:	n/a	n/a
5	ATF2	chr16:12254616-12255135	GM12878	blood:	n/a	n/a
6	BACH1	chr16:12238319-12238479	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr16:12215466-12215475	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr16:12248132-12248148	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr16:12254703-12255013	GM12878	blood:	n/a	chr16:12254928-12254941
10	BATF	chr16:12254603-12255131	GM12878	blood:	n/a	chr16:12254928-12254941
11	BCL11A	chr16:12211022-12211352	GM12878	blood:	n/a	n/a
12	BCL3	chr16:12227549-12227967	GM12878	blood:	n/a	n/a
13	BCL3	chr16:12226116-12226508	GM12878	blood:	n/a	n/a
14	BCL3	chr16:12254620-12255048	GM12878	blood:	n/a	chr16:12254941-12254950 chr16:12254772-12254781
15	BHLHE40	chr16:12236528-12236852	HepG2	liver:	n/a	n/a
16	BHLHE40	chr16:12254677-12255163	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:12249200-12249317	K562	blood:	n/a	chr16:12249228-12249241 chr16:12249229-12249238
18	BHLHE40	chr16:12239983-12240047	K562	blood:	n/a	n/a
19	BHLHE40	chr16:12244466-12244701	K562	blood:	n/a	n/a
20	BHLHE40	chr16:12256051-12256137	K562	blood:	n/a	n/a
21	CEBPB	chr16:12213537-12213862	IMR90	lung:	n/a	n/a
22	CEBPB	chr16:12214130-12214784	IMR90	lung:	n/a	n/a
23	CEBPB	chr16:12226214-12226490	K562	blood:	n/a	chr16:12226341-12226352
24	CEBPB	chr16:12245018-12245300	IMR90	lung:	n/a	chr16:12245164-12245175
25	CEBPB	chr16:12252077-12252733	IMR90	lung:	n/a	n/a
26	CEBPB	chr16:12211438-12211685	IMR90	lung:	n/a	chr16:12211487-12211498 chr16:12211555-12211566
27	CEBPB	chr16:12211429-12211646	Hela-S3	cervix:	n/a	chr16:12211487-12211498 chr16:12211555-12211566
28	CEBPB	chr16:12226297-12226442	HepG2	liver:	n/a	chr16:12226341-12226352
29	CEBPB	chr16:12244979-12245344	HepG2	liver:	n/a	chr16:12245164-12245175
30	CEBPB	chr16:12211430-12211687	K562	blood:	n/a	chr16:12211487-12211498 chr16:12211555-12211566
31	CEBPB	chr16:12218428-12218483	IMR90	lung:	n/a	n/a
32	CEBPB	chr16:12226166-12226528	IMR90	lung:	n/a	chr16:12226341-12226352
33	CEBPB	chr16:12211401-12211679	HepG2	liver:	n/a	chr16:12211487-12211498 chr16:12211555-12211566
34	CEBPB	chr16:12211405-12211640	A549	lung:	n/a	chr16:12211487-12211498 chr16:12211555-12211566
35	CEBPB	chr16:12236659-12236895	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:12213485-12213861	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:12245051-12245251	A549	lung:	n/a	chr16:12245164-12245175
38	CEBPB	chr16:12235256-12235260	HepG2	liver:	n/a	n/a
39	CEBPD	chr16:12239772-12240135	K562	blood:	n/a	n/a
40	CHD2	chr16:12217653-12217709	K562	blood:	n/a	n/a
41	CREB1	chr16:12238219-12238592	K562	blood:	n/a	n/a
42	CTCF	chr16:12249040-12249190	HAc	cerebellar:	n/a	n/a
43	CTCF	chr16:12252880-12253030	GM12864	blood:	n/a	n/a
44	CTCF	chr16:12211129-12211205	GM10266	blood:	n/a	n/a
45	CTCF	chr16:12243820-12243970	HepG2	liver:	n/a	n/a
46	CTCF	chr16:12231150-12231353	HepG2	liver:	n/a	chr16:12231254-12231270
47	CTCF	chr16:12231140-12231290	HepG2	liver:	n/a	chr16:12231254-12231270
48	CTCF	chr16:12252980-12253130	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr16:12229160-12229310	GM06990	blood:	n/a	n/a
50	CTCF	chr16:12231181-12231305	K562	blood:	n/a	chr16:12231254-12231270

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12211098-12211148	ovcar-3	ovarian:	n/a
2	chr16:12210834-12210884	HRE	kidney:	n/a
3	chr16:12226852-12226902	Jurkat	blood:	n/a
4	chr16:12214807-12214857	HepG2	liver:	n/a
5	chr16:12212548-12212598	Caco-2	colon:	n/a
6	chr16:12210910-12210960	HEK293	kidney:	embryo
7	chr16:12211322-12211372	HCPEpiC	choroid plexus:	n/a
8	chr16:12210656-12210706	SAEC	small airway:	n/a
9	chr16:12212548-12212598	A549	lung:	n/a
10	chr16:12211322-12211372	AG04450	lung:	fetal
11	chr16:12211098-12211148	RPTEC	kidney:	n/a
12	chr16:12209538-12209588	HEEpiC	esophagus:	n/a
13	chr16:12212548-12212598	Jurkat	blood:	n/a
14	chr16:12211322-12211372	SKMC	muscle:	n/a
15	chr16:12209538-12209588	AG09309	skin:	n/a
16	chr16:12226852-12226902	HCF	heart:	n/a
17	chr16:12214807-12214857	ovcar-3	ovarian:	n/a
18	chr16:12241554-12241604	GM12878	blood:	n/a
19	chr16:12250718-12250768	NHBE	bronchial:	n/a
20	chr16:12241554-12241604	ovcar-3	ovarian:	n/a
21	chr16:12210834-12210884	GM12878	blood:	n/a
22	chr16:12211186-12211236	HCT-116	colon:	n/a
23	chr16:12211322-12211372	HL-60	blood:	n/a
24	chr16:12226852-12226902	HNPCEpiC	eye:	n/a
25	chr16:12226852-12226902	HAEpiC	amniotic membrane:	n/a
26	chr16:12210910-12210960	HMEC	breast:	n/a
27	chr16:12210910-12210960	HRE	kidney:	n/a
28	chr16:12226852-12226902	GM19239	blood:	n/a
29	chr16:12211186-12211236	A549	lung:	n/a
30	chr16:12212548-12212598	GM06990	blood:	n/a
31	chr16:12210834-12210884	HCF	heart:	n/a
32	chr16:12250718-12250768	HCM	heart:	n/a
33	chr16:12226852-12226902	HepG2	liver:	n/a
34	chr16:12241554-12241604	PrEC	prostate:	n/a
35	chr16:12214807-12214857	AG04450	lung:	fetal
36	chr16:12214807-12214857	MCF-7	breast:	n/a
37	chr16:12250718-12250768	HCPEpiC	choroid plexus:	n/a
38	chr16:12210834-12210884	AG09319	gingival:	n/a
39	chr16:12210656-12210706	BJ	skin:	n/a
40	chr16:12210656-12210706	MCF10A-Er-Src	breast:	n/a
41	chr16:12210834-12210884	HCPEpiC	choroid plexus:	n/a
42	chr16:12226852-12226902	NHBE	bronchial:	n/a
43	chr16:12212548-12212598	HNPCEpiC	eye:	n/a
44	chr16:12211098-12211148	HCF	heart:	n/a
45	chr16:12210834-12210884	HIPEpiC	eye:	n/a
46	chr16:12210834-12210884	SK-N-SH_RA	brain:	n/a
47	chr16:12250718-12250768	PFSK-1	brain:	n/a
48	chr16:12211322-12211372	BE2_C	brain:	n/a
49	chr16:12210834-12210884	HMEC	breast:	n/a
50	chr16:12226852-12226902	Hepatocyte	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12251094..12253122-chr16:12351083..12352799,2	MCF-7	breast:
2	chr16:12235977..12239654-chr16:12243100..12246222,3	K562	blood:
3	chr16:12235799..12238230-chr16:12240005..12241977,2	MCF-7	breast:
4	chr16:12225063..12228356-chr16:12228504..12231414,3	K562	blood:
5	chr16:12225063..12228356-chr16:12228504..12231414,3	K562	blood:
6	chr16:12213304..12215275-chr16:12226853..12228529,2	MCF-7	breast:
7	chr16:12231008..12232542-chr16:12255971..12258594,2	K562	blood:
8	chr16:12241354..12243525-chr16:12245349..12247031,2	K562	blood:
9	chr16:12207504..12209871-chr16:12211621..12214983,3	K562	blood:
10	chr16:12240782..12243525-chr16:12245349..12247044,3	K562	blood:
11	chr16:12215027..12215616-chr8:139698499..139699323,2	MCF-7	breast:
12	chr16:12192648..12195630-chr16:12219371..12221424,2	MCF-7	breast:
13	chr16:12241354..12243525-chr16:12245349..12247031,2	K562	blood:
14	chr16:12212007..12215167-chr16:12222860..12225449,4	MCF-7	breast:
15	chr16:12240782..12243525-chr16:12245349..12247044,3	K562	blood:
16	chr16:12231008..12232542-chr16:12255971..12258594,2	K562	blood:
17	chr16:12235977..12239654-chr16:12243100..12246222,3	K562	blood:
18	chr16:12236133..12238164-chr16:12283683..12286173,2	MCF-7	breast:
19	chr16:12213304..12215275-chr16:12226853..12228529,2	MCF-7	breast:
20	chr16:12207504..12209871-chr16:12211621..12214983,3	K562	blood:
21	chr16:12253223..12255934-chr16:12258590..12260441,2	K562	blood:
22	chr16:12235799..12238230-chr16:12240005..12241977,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island
ENSG00000048471	chromatin interactions

Extended variants
information (count: 2549 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8051768	chr16:12208242-12208243	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183863291	chr16:12208247-12208248	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs551869688	chr16:12208256-12208257	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs80188659	chr16:12208268-12208269	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs537646723	chr16:12208277-12208278	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs188640042	chr16:12208321-12208322	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs4781183	chr16:12208326-12208327	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs536629641	chr16:12208375-12208376	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs553438679	chr16:12208395-12208396	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542498042	chr16:12208399-12208400	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs559251332	chr16:12208408-12208409	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566889710	chr16:12208427-12208428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374949142	chr16:12208440-12208441	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559099541	chr16:12208502-12208503	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575756734	chr16:12208534-12208535	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537185319	chr16:12208560-12208561	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550984124	chr16:12208566-12208567	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554731684	chr16:12208594-12208595	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs555238422	chr16:12208645-12208646	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76978124	chr16:12208697-12208698	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111998428	chr16:12208730-12208731	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180700941	chr16:12208766-12208767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138282663	chr16:12208767-12208768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551294510	chr16:12208781-12208782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532001218	chr16:12208793-12208794	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186102444	chr16:12208820-12208821	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190614887	chr16:12208825-12208826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368310428	chr16:12208836-12208837	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142783814	chr16:12208844-12208845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115629068	chr16:12208874-12208875	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs182222121	chr16:12208920-12208921	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374536743	chr16:12208930-12208931	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374965016	chr16:12208948-12208949	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547737772	chr16:12208957-12208958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566828314	chr16:12208967-12208968	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538854444	chr16:12209008-12209009	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs116130354	chr16:12209018-12209019	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539047509	chr16:12209021-12209022	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559081178	chr16:12209022-12209023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs569296016	chr16:12209032-12209033	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538411042	chr16:12209036-12209037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74887023	chr16:12209041-12209042	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570876722	chr16:12209044-12209045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34126591	chr16:12209103-12209104	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141572561	chr16:12209119-12209120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186026532	chr16:12209143-12209144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368532007	chr16:12209147-12209148	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs114495733	chr16:12209148-12209149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576387221	chr16:12209169-12209170	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545440331	chr16:12209180-12209181	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	17603634	CNVD
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22102821	CNVD
Autism	22495311	CNVD
idiopathic generalized epilepsy	19843651	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Intellectual disability	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelofibrosis	22110671	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	19786961	CNVD
Mental retardation	19786961	CNVD
Schizophrenia	19786961	CNVD
Mental retardation	19951919	CNVD
Autism	18791038	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Malignant germ cell tumour	17285132	CNVD
Autism	17480035	CNVD
Schizophrenia	19955444	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD

Chromatin state (count:1364 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12184400-12231200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr16:12186800-12213400	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr16:12189800-12209600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr16:12189800-12220400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr16:12190000-12220200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr16:12190000-12220400	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr16:12190200-12210600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:12190800-12210600	Weak transcription	Pancreas	Pancrea
9	chr16:12191200-12223200	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr16:12191400-12213600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr16:12192000-12213800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr16:12192000-12214600	Weak transcription	Right Atrium	heart
13	chr16:12192400-12210400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr16:12192400-12213200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr16:12192400-12213200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr16:12192800-12213600	Weak transcription	Adipose Nuclei	Adipose
17	chr16:12194000-12212600	Weak transcription	Ovary	ovary
18	chr16:12194000-12213000	Weak transcription	Right Ventricle	heart
19	chr16:12194000-12215200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr16:12194200-12210600	Weak transcription	NHEK	skin
21	chr16:12198200-12227800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr16:12200200-12220200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr16:12200400-12209200	Weak transcription	Gastric	stomach
24	chr16:12200400-12210600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr16:12200400-12210600	Weak transcription	Aorta	Aorta
26	chr16:12200600-12210400	Weak transcription	Lung	lung
27	chr16:12200600-12213000	Weak transcription	Fetal Heart	heart
28	chr16:12200600-12215400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr16:12201000-12209200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr16:12201000-12210400	Weak transcription	Thymus	Thymus
31	chr16:12202000-12209400	Weak transcription	GM12878-XiMat	blood
32	chr16:12204600-12208400	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr16:12204800-12208400	Enhancers	Primary hematopoietic stem cells	blood
34	chr16:12204800-12222000	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr16:12205000-12208400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:12205000-12208400	Enhancers	Brain Anterior Caudate	brain
37	chr16:12205400-12210600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr16:12205400-12210600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr16:12205400-12213400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr16:12205800-12213600	Weak transcription	Stomach Smooth Muscle	stomach
41	chr16:12206000-12210000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr16:12206200-12208800	Weak transcription	Primary B cells from peripheral blood	blood
43	chr16:12206400-12210200	Weak transcription	Fetal Stomach	stomach
44	chr16:12206800-12208400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr16:12206800-12208400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr16:12206800-12208400	Enhancers	Fetal Brain Female	brain
47	chr16:12206800-12212600	Weak transcription	HepG2	liver
48	chr16:12207000-12208400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr16:12207000-12208400	Enhancers	Brain Cingulate Gyrus	brain
50	chr16:12207200-12208400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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