Variant report

Variant	nsv1052892
Chromosome Location	chr16:12824219-12881078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 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	chr16:12846181-12846420	K562	blood:	n/a	n/a
2	ARID3A	chr16:12851993-12852407	K562	blood:	n/a	n/a
3	ARID3A	chr16:12847867-12848576	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:12858878-12859287	K562	blood:	n/a	n/a
5	ARID3A	chr16:12867870-12867974	K562	blood:	n/a	n/a
6	ATF1	chr16:12867153-12867333	K562	blood:	n/a	n/a
7	ATF1	chr16:12861856-12862131	K562	blood:	n/a	n/a
8	ATF1	chr16:12851970-12852717	K562	blood:	n/a	n/a
9	ATF2	chr16:12843864-12844608	GM12878	blood:	n/a	n/a
10	ATF2	chr16:12843872-12844591	GM12878	blood:	n/a	n/a
11	BACH1	chr16:12834514-12834553	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr16:12843851-12844460	GM12878	blood:	n/a	n/a
13	BATF	chr16:12843817-12844559	GM12878	blood:	n/a	n/a
14	BCL11A	chr16:12843893-12844490	GM12878	blood:	n/a	n/a
15	BCL11A	chr16:12843987-12844351	GM12878	blood:	n/a	n/a
16	BCL3	chr16:12843944-12844423	GM12878	blood:	n/a	n/a
17	BCLAF1	chr16:12843960-12844477	GM12878	blood:	n/a	n/a
18	BCLAF1	chr16:12843852-12844508	GM12878	blood:	n/a	n/a
19	BHLHE40	chr16:12843924-12844488	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:12845974-12846043	GM12878	blood:	n/a	n/a
21	BHLHE40	chr16:12847949-12848189	HepG2	liver:	n/a	n/a
22	BHLHE40	chr16:12851969-12852752	K562	blood:	n/a	n/a
23	CBX3	chr16:12831467-12831701	K562	blood:	n/a	n/a
24	CBX3	chr16:12877971-12878249	K562	blood:	n/a	n/a
25	CCNT2	chr16:12869578-12869952	K562	blood:	n/a	n/a
26	CCNT2	chr16:12851937-12852582	K562	blood:	n/a	n/a
27	CCNT2	chr16:12846163-12846367	K562	blood:	n/a	n/a
28	CEBPB	chr16:12848922-12849070	K562	blood:	n/a	chr16:12849039-12849050 chr16:12849041-12849052
29	CEBPB	chr16:12847779-12847929	A549	lung:	n/a	n/a
30	CEBPB	chr16:12848892-12849153	A549	lung:	n/a	chr16:12849039-12849050 chr16:12849041-12849052
31	CEBPB	chr16:12847730-12847936	HepG2	liver:	n/a	n/a
32	CEBPB	chr16:12848912-12849135	IMR90	lung:	n/a	chr16:12849039-12849050 chr16:12849041-12849052
33	CEBPB	chr16:12848878-12849206	HepG2	liver:	n/a	chr16:12849039-12849050 chr16:12849041-12849052
34	CEBPB	chr16:12848928-12849180	Hela-S3	cervix:	n/a	chr16:12849039-12849050 chr16:12849041-12849052
35	CEBPB	chr16:12847652-12848332	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:12847965-12848292	HepG2	liver:	n/a	n/a
37	CEBPB	chr16:12853163-12853377	HepG2	liver:	n/a	n/a
38	CEBPB	chr16:12865556-12865706	HepG2	liver:	n/a	chr16:12865647-12865658
39	CEBPB	chr16:12827742-12827913	HepG2	liver:	n/a	chr16:12827838-12827847 chr16:12827838-12827849
40	CEBPB	chr16:12836496-12836646	K562	blood:	n/a	chr16:12836546-12836557
41	CEBPB	chr16:12851633-12851658	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:12847744-12847937	K562	blood:	n/a	n/a
43	CEBPB	chr16:12843735-12844684	GM12878	blood:	n/a	n/a
44	CEBPB	chr16:12852122-12852556	K562	blood:	n/a	n/a
45	CEBPB	chr16:12836380-12836670	HepG2	liver:	n/a	chr16:12836546-12836557
46	CEBPB	chr16:12844026-12844367	GM12878	blood:	n/a	n/a
47	CEBPB	chr16:12847589-12848419	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:12847663-12848401	HepG2	liver:	n/a	n/a
49	CEBPD	chr16:12851964-12852382	K562	blood:	n/a	n/a
50	CEBPD	chr16:12847741-12848327	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12853189-12853239	AG10803	skin:	n/a
2	chr16:12875117-12875167	Caco-2	colon:	n/a
3	chr16:12853189-12853239	GM12891	blood:	n/a
4	chr16:12853189-12853239	NHBE	bronchial:	n/a
5	chr16:12853189-12853239	AG04450	lung:	fetal
6	chr16:12875117-12875167	AoSMC	blood vessel:	n/a
7	chr16:12853189-12853239	AoSMC	blood vessel:	n/a
8	chr16:12853189-12853239	AG09319	gingival:	n/a
9	chr16:12875117-12875167	HEEpiC	esophagus:	n/a
10	chr16:12853189-12853239	SK-N-MC	brain:	n/a
11	chr16:12853189-12853239	HRCEpiC	kidney:	n/a
12	chr16:12853189-12853239	PANC-1	pancreas:	n/a
13	chr16:12875117-12875167	HCF	heart:	n/a
14	chr16:12853189-12853239	GM19239	blood:	n/a
15	chr16:12853189-12853239	HEEpiC	esophagus:	n/a
16	chr16:12853189-12853239	HUVEC	blood vessel:	n/a
17	chr16:12875117-12875167	Hepatocyte	liver:	n/a
18	chr16:12853189-12853239	H1-hESC	embryonic stem cell:	embryo
19	chr16:12853189-12853239	AG09309	skin:	n/a
20	chr16:12853189-12853239	SKMC	muscle:	n/a
21	chr16:12875117-12875167	HMEC	breast:	n/a
22	chr16:12875117-12875167	GM12891	blood:	n/a
23	chr16:12875117-12875167	ovcar-3	ovarian:	n/a
24	chr16:12853189-12853239	HCF	heart:	n/a
25	chr16:12875117-12875167	A549	lung:	n/a
26	chr16:12875117-12875167	ECC-1	luminal epithelium:	n/a
27	chr16:12875117-12875167	HPAEpiC	pulmonary alveolar:	n/a
28	chr16:12875117-12875167	HRCEpiC	kidney:	n/a
29	chr16:12875117-12875167	HRPEpiC	eye:	n/a
30	chr16:12875117-12875167	GM19239	blood:	n/a
31	chr16:12875117-12875167	HCM	heart:	n/a
32	chr16:12875117-12875167	SK-N-MC	brain:	n/a
33	chr16:12875117-12875167	HRE	kidney:	n/a
34	chr16:12875117-12875167	SAEC	small airway:	n/a
35	chr16:12875117-12875167	H1-hESC	embryonic stem cell:	embryo
36	chr16:12853189-12853239	PFSK-1	brain:	n/a
37	chr16:12853189-12853239	SAEC	small airway:	n/a
38	chr16:12853189-12853239	MCF10A-Er-Src	breast:	n/a
39	chr16:12853189-12853239	NHDF-neo	bronchial:	n/a
40	chr16:12853189-12853239	Hela-S3	cervix:	n/a
41	chr16:12875117-12875167	CMK	blood:	n/a
42	chr16:12853189-12853239	CMK	blood:	n/a
43	chr16:12853189-12853239	NH-A	brain:	n/a
44	chr16:12875117-12875167	LNCaP	prostate:	n/a
45	chr16:12853189-12853239	PrEC	prostate:	n/a
46	chr16:12853189-12853239	HCPEpiC	choroid plexus:	n/a
47	chr16:12875117-12875167	NHDF-neo	bronchial:	n/a
48	chr16:12875117-12875167	NHBE	bronchial:	n/a
49	chr16:12875117-12875167	SK-N-SH	brain:	n/a
50	chr16:12875117-12875167	K562	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12878457..12880364-chr16:12880659..12882359,2	MCF-7	breast:
2	chr16:12852212..12854597-chr16:12854867..12857733,2	K562	blood:
3	chr16:12816095..12818356-chr16:12821426..12824308,2	MCF-7	breast:
4	chr16:12834774..12836275-chr16:12843130..12845586,2	K562	blood:
5	chr16:12839491..12842213-chr16:12843875..12846809,3	K562	blood:
6	chr16:12837397..12840292-chr16:12850360..12852909,2	K562	blood:
7	chr16:12878873..12880580-chr16:12882969..12884661,2	K562	blood:
8	chr16:12834137..12836275-chr16:12843130..12846539,3	K562	blood:
9	chr16:12823466..12825378-chr16:12892551..12895015,2	K562	blood:
10	chr16:12840444..12842213-chr16:12843875..12846809,2	K562	blood:
11	chr16:12825533..12827033-chr8:2762155..2763733,2	K562	blood:
12	chr16:12878457..12880364-chr16:12880659..12882359,2	MCF-7	breast:
13	chr16:12840444..12842213-chr16:12843875..12846809,2	K562	blood:
14	chr16:12878291..12880312-chr16:12895608..12897646,2	K562	blood:
15	chr16:12880295..12881857-chr16:12883216..12885729,2	MCF-7	breast:
16	chr16:12834137..12836275-chr16:12843130..12846539,3	K562	blood:
17	chr16:12878199..12880560-chr16:12895056..12899012,3	MCF-7	breast:
18	chr16:12834774..12836275-chr16:12843130..12845586,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHISA9-1	chr16:12846877-12846923	NONHSAT140630
2	lnc-SHISA9-2	chr16:12851346-12851692	ENSG00000260378.1
3	lnc-SHISA9-1	chr16:12847678-12847772	NONHSAT140631
4	lnc-SHISA9-1	chr16:12847078-12847244	NONHSAT140630
5	lnc-SHISA9-2	chr16:12847683-12847772	ENSG00000260378.1
6	lnc-SHISA9-2	chr16:12847078-12847244	ENSG00000260378.1
7	lnc-SHISA9-1	chr16:12851346-12853272	NONHSAT140631
8	lnc-SHISA9-1	chr16:12854227-12854937	NONHSAT140630
9	lnc-SHISA9-1	chr16:12851346-12853272	NONHSAT140630
10	lnc-SHISA9-2	chr16:12846848-12846923	ENSG00000260378.1
11	lnc-SHISA9-1	chr16:12854227-12855019	ENSG00000261158.1
12	lnc-SHISA9-1	chr16:12847683-12847772	NONHSAT140630
13	lnc-SHISA9-1	chr16:12853139-12853272	ENSG00000261158.1
14	lnc-SHISA9-2	chr16:12839730-12839835	ENSG00000260378.1
15	lnc-SHISA9-1	chr16:12854227-12854937	NONHSAT140631
16	lnc-SHISA9-1	chr16:12846877-12846923	NONHSAT140631
17	lnc-SHISA9-1	chr16:12847078-12847244	NONHSAT140631

No data

Variant related genes	Relation type
ENSG00000260378	TF binding region
ENSG00000261158	TF binding region
ENSG00000260378	CpG island
ENSG00000261158	CpG island
ENSG00000103381	chromatin interactions
ENSG00000261158	chromatin interactions
ENSG00000260378	chromatin interactions

Extended variants
information (count: 2815 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2815 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571087065	chr16:12824233-12824234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540026339	chr16:12824257-12824258	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111812740	chr16:12824267-12824268	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576043703	chr16:12824271-12824272	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558909504	chr16:12824272-12824273	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575763043	chr16:12824292-12824293	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567953608	chr16:12824323-12824324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112001545	chr16:12824335-12824336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555311601	chr16:12824407-12824408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72779061	chr16:12824415-12824416	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540956777	chr16:12824462-12824463	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111460996	chr16:12824466-12824467	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567207738	chr16:12824469-12824470	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372111386	chr16:12824499-12824500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554603529	chr16:12824506-12824507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190299405	chr16:12824529-12824530	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537160396	chr16:12824530-12824531	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181709257	chr16:12824573-12824574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185955861	chr16:12824623-12824624	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72779063	chr16:12824643-12824644	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs147248030	chr16:12824647-12824648	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559701618	chr16:12824690-12824691	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112194728	chr16:12824717-12824718	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76886694	chr16:12824745-12824746	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188762215	chr16:12824746-12824747	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139453433	chr16:12824760-12824761	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548147114	chr16:12824804-12824805	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113197057	chr16:12824845-12824846	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78281848	chr16:12824856-12824857	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374123287	chr16:12824913-12824914	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532300149	chr16:12824914-12824915	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181084041	chr16:12824929-12824930	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545664213	chr16:12824933-12824934	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112577250	chr16:12824940-12824941	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538816090	chr16:12824963-12824964	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112509468	chr16:12824978-12824979	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11645533	chr16:12824989-12824990	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368421258	chr16:12825001-12825002	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71386717	chr16:12825013-12825014	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560566643	chr16:12825014-12825015	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113434760	chr16:12825021-12825022	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397700514	chr16:12825028-12825029	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112486774	chr16:12825074-12825075	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185989431	chr16:12825079-12825080	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540615860	chr16:12825097-12825098	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191179750	chr16:12825101-12825102	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182554843	chr16:12825124-12825125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531490226	chr16:12825135-12825136	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375377391	chr16:12825142-12825143	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563469720	chr16:12825200-12825201	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	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
Breast cancer	21858162	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12753400-12836000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr16:12798400-12825800	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr16:12798600-12825800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr16:12798600-12836800	Weak transcription	Placenta	Placenta
5	chr16:12798800-12826600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr16:12813200-12826200	Strong transcription	HepG2	liver
7	chr16:12814000-12826200	Weak transcription	Brain Angular Gyrus	brain
8	chr16:12814200-12825600	Weak transcription	Liver	Liver
9	chr16:12814600-12825600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr16:12817800-12827400	Weak transcription	Esophagus	oesophagus
11	chr16:12818400-12826200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr16:12818400-12834400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr16:12818600-12826200	Weak transcription	Aorta	Aorta
14	chr16:12818600-12826200	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr16:12819800-12825600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr16:12821600-12826200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr16:12822000-12825800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr16:12822400-12824600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr16:12822400-12824600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr16:12822400-12824600	Enhancers	HSMMtube	muscle
21	chr16:12822600-12824400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr16:12822600-12824800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr16:12822600-12824800	Enhancers	Osteobl	bone
24	chr16:12822800-12824800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr16:12822800-12824800	Enhancers	NHDF-Ad	bronchial
26	chr16:12823200-12824400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr16:12823200-12824600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr16:12823200-12824600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr16:12823200-12825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr16:12823200-12826000	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr16:12823800-12824800	Enhancers	HUVEC	blood vessel
32	chr16:12823800-12826400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr16:12824000-12824600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr16:12824000-12826400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:12824200-12824600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr16:12824200-12826200	Weak transcription	HSMM	muscle
37	chr16:12824400-12824600	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr16:12824400-12829000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:12824600-12824800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr16:12824600-12826200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr16:12824600-12826200	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr16:12824600-12826200	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr16:12824600-12828200	Weak transcription	HSMMtube	muscle
44	chr16:12824800-12825400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr16:12824800-12826200	Weak transcription	HUVEC	blood vessel
46	chr16:12824800-12828600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr16:12824800-12847800	Weak transcription	Osteobl	bone
48	chr16:12825000-12825400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr16:12825400-12825600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr16:12825400-12829000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin

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