Variant report

Variant	nsv571464
Chromosome Location	chr16:12423557-12449778
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:506)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12435377-12435548	HepG2	liver:	n/a	n/a
2	BHLHE40	chr16:12443836-12444154	K562	blood:	n/a	n/a
3	BHLHE40	chr16:12435349-12435740	HepG2	liver:	n/a	n/a
4	BHLHE40	chr16:12442556-12442849	GM12878	blood:	n/a	n/a
5	BHLHE40	chr16:12434295-12434610	HepG2	liver:	n/a	n/a
6	CBX3	chr16:12435118-12436344	HCT-116	colon:	n/a	n/a
7	CEBPB	chr16:12435361-12435579	HepG2	liver:	n/a	n/a
8	CEBPB	chr16:12434288-12434632	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr16:12435268-12435616	IMR90	lung:	n/a	n/a
10	CEBPB	chr16:12447466-12447520	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr16:12447513-12447591	IMR90	lung:	n/a	chr16:12447541-12447552
12	CEBPB	chr16:12447381-12447657	HepG2	liver:	n/a	chr16:12447541-12447552
13	CEBPB	chr16:12433687-12434238	IMR90	lung:	n/a	n/a
14	CHD2	chr16:12435490-12435652	Hela-S3	cervix:	n/a	n/a
15	CHD2	chr16:12434342-12434600	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr16:12424000-12424150	GM12873	blood:	n/a	n/a
17	CTCF	chr16:12444920-12445070	HRE	kidney:	n/a	n/a
18	CTCF	chr16:12434380-12434530	A549	lung:	n/a	n/a
19	CTCF	chr16:12434400-12434550	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr16:12434400-12434550	GM12870	blood:	n/a	n/a
21	CTCF	chr16:12435440-12435590	HFF	foreskin:	n/a	n/a
22	CTCF	chr16:12434036-12434794	A549	lung:	n/a	n/a
23	CTCF	chr16:12434320-12434470	GM12870	blood:	n/a	n/a
24	CTCF	chr16:12434400-12434550	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr16:12434366-12434538	GM10248	blood:	n/a	n/a
26	CTCF	chr16:12435380-12435530	HRE	kidney:	n/a	n/a
27	CTCF	chr16:12444860-12445010	RPTEC	kidney:	n/a	n/a
28	CTCF	chr16:12435420-12435585	ProgFib	skin:	n/a	n/a
29	CTCF	chr16:12435460-12435610	HMEC	breast:	n/a	n/a
30	CTCF	chr16:12435379-12435618	A549	lung:	n/a	n/a
31	CTCF	chr16:12434320-12434470	NHEK	skin:	n/a	n/a
32	CTCF	chr16:12435459-12435543	GM19238	blood:	n/a	n/a
33	CTCF	chr16:12444900-12445050	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr16:12434340-12434568	A549	lung:	n/a	n/a
35	CTCF	chr16:12444980-12445130	HCT-116	colon:	n/a	n/a
36	CTCF	chr16:12444560-12444710	HEK293	kidney:	n/a	n/a
37	CTCF	chr16:12444740-12444890	GM12875	blood:	n/a	n/a
38	CTCF	chr16:12434360-12434510	HCFaa	heart:	n/a	n/a
39	CTCF	chr16:12424080-12424230	RPTEC	kidney:	n/a	n/a
40	CTCF	chr16:12434373-12434578	GM12891	blood:	n/a	n/a
41	CTCF	chr16:12434289-12434612	HepG2	liver:	n/a	n/a
42	CTCF	chr16:12435320-12435470	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr16:12444920-12445070	GM12868	blood:	n/a	n/a
44	CTCF	chr16:12434380-12434530	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr16:12434400-12434550	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr16:12434400-12434550	K562	blood:	n/a	n/a
47	CTCF	chr16:12434340-12434490	HCM	heart:	n/a	n/a
48	CTCF	chr16:12434352-12434583	MCF-7	breast:	n/a	n/a
49	CTCF	chr16:12435380-12435530	NHLF	lung:	n/a	n/a
50	CTCF	chr16:12434380-12434530	NHLF	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12434580-12434630	AG10803	skin:	n/a
2	chr16:12442738-12442788	Caco-2	colon:	n/a
3	chr16:12442738-12442788	LNCaP	prostate:	n/a
4	chr16:12434580-12434630	HUVEC	blood vessel:	n/a
5	chr16:12434580-12434630	RPTEC	kidney:	n/a
6	chr16:12442738-12442788	HNPCEpiC	eye:	n/a
7	chr16:12434580-12434630	HEEpiC	esophagus:	n/a
8	chr16:12434580-12434630	HL-60	blood:	n/a
9	chr16:12442738-12442788	GM19239	blood:	n/a
10	chr16:12442738-12442788	U87	brain:	n/a
11	chr16:12434580-12434630	ProgFib	skin:	n/a
12	chr16:12442738-12442788	NHDF-neo	bronchial:	n/a
13	chr16:12442738-12442788	NHBE	bronchial:	n/a
14	chr16:12434580-12434630	NB4	blood:	n/a
15	chr16:12442738-12442788	SKMC	muscle:	n/a
16	chr16:12434580-12434630	K562	blood:	n/a
17	chr16:12442738-12442788	HRE	kidney:	n/a
18	chr16:12442738-12442788	A549	lung:	n/a
19	chr16:12442738-12442788	ovcar-3	ovarian:	n/a
20	chr16:12442738-12442788	NH-A	brain:	n/a
21	chr16:12434580-12434630	GM12891	blood:	n/a
22	chr16:12442738-12442788	HAEpiC	amniotic membrane:	n/a
23	chr16:12434580-12434630	BE2_C	brain:	n/a
24	chr16:12434580-12434630	NHDF-neo	bronchial:	n/a
25	chr16:12434580-12434630	NHBE	bronchial:	n/a
26	chr16:12434580-12434630	HRE	kidney:	n/a
27	chr16:12442738-12442788	SK-N-SH_RA	brain:	n/a
28	chr16:12442738-12442788	Hela-S3	cervix:	n/a
29	chr16:12442738-12442788	HRCEpiC	kidney:	n/a
30	chr16:12434580-12434630	HRCEpiC	kidney:	n/a
31	chr16:12434580-12434630	U87	brain:	n/a
32	chr16:12434580-12434630	H1-hESC	embryonic stem cell:	embryo
33	chr16:12442738-12442788	AG04449	skin:	fetal
34	chr16:12442738-12442788	Hepatocyte	liver:	n/a
35	chr16:12434580-12434630	HCF	heart:	n/a
36	chr16:12434580-12434630	HCM	heart:	n/a
37	chr16:12442738-12442788	AoSMC	blood vessel:	n/a
38	chr16:12442738-12442788	HUVEC	blood vessel:	n/a
39	chr16:12442738-12442788	NB4	blood:	n/a
40	chr16:12434580-12434630	HCT-116	colon:	n/a
41	chr16:12442738-12442788	HMEC	breast:	n/a
42	chr16:12434580-12434630	HepG2	liver:	n/a
43	chr16:12442738-12442788	PANC-1	pancreas:	n/a
44	chr16:12442738-12442788	SK-N-SH	brain:	n/a
45	chr16:12442738-12442788	BJ	skin:	n/a
46	chr16:12442738-12442788	AG10803	skin:	n/a
47	chr16:12442738-12442788	AG09309	skin:	n/a
48	chr16:12434580-12434630	ovcar-3	ovarian:	n/a
49	chr16:12434580-12434630	ECC-1	luminal epithelium:	n/a
50	chr16:12434580-12434630	GM12892	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12434031..12434617-chr16:12912936..12913439,2	K562	blood:
2	chr16:12434163..12434889-chr16:12562200..12562981,2	MCF-7	breast:
3	chr16:12434404..12435162-chr16:12548365..12549293,2	MCF-7	breast:
4	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:
5	chr16:12434411..12435246-chr16:12667446..12668002,2	MCF-7	breast:
6	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
7	chr16:12433483..12435044-chr16:12435490..12437605,2	K562	blood:
8	chr16:12434035..12434594-chr16:12912889..12913804,2	MCF-7	breast:
9	chr16:12426103..12428836-chr16:12432217..12434096,4	K562	blood:
10	chr16:12415388..12417131-chr16:12421455..12424382,2	MCF-7	breast:
11	chr16:12426103..12428836-chr16:12432217..12434096,4	K562	blood:
12	chr16:12426504..12430184-chr16:12432340..12435917,5	K562	blood:

No data

Variant related genes	Relation type
SNX29	TF binding region
SNX29	CpG island

Extended variants
information (count: 1328 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1328 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs209836	chr16:12423557-12423558	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551819996	chr16:12423565-12423566	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558996475	chr16:12423566-12423567	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571897016	chr16:12423568-12423569	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536691171	chr16:12423591-12423592	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556949198	chr16:12423603-12423604	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72786356	chr16:12423617-12423618	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536317436	chr16:12423626-12423627	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182070035	chr16:12423704-12423705	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs158476	chr16:12423706-12423707	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs545180522	chr16:12423713-12423714	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs558625885	chr16:12423740-12423741	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141298428	chr16:12423751-12423752	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs117880683	chr16:12423752-12423753	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs145079182	chr16:12423757-12423758	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115193548	chr16:12423782-12423783	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559404219	chr16:12423799-12423800	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186662287	chr16:12423833-12423834	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76100837	chr16:12423848-12423849	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565442388	chr16:12423883-12423884	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34534162	chr16:12423894-12423895	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150391762	chr16:12423906-12423907	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74542017	chr16:12423909-12423910	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192378037	chr16:12423992-12423993	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368367003	chr16:12423993-12423994	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138662464	chr16:12423995-12423996	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555579402	chr16:12424068-12424069	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184764347	chr16:12424081-12424082	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567241265	chr16:12424089-12424090	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149307519	chr16:12424105-12424106	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546760012	chr16:12424129-12424130	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566560391	chr16:12424151-12424152	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538458664	chr16:12424170-12424171	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558680555	chr16:12424217-12424218	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575466912	chr16:12424219-12424220	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs158475	chr16:12424239-12424240	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554423245	chr16:12424248-12424249	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs158474	chr16:12424286-12424287	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542600649	chr16:12424303-12424304	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs17817646	chr16:12424313-12424314	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190182280	chr16:12424331-12424332	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs144590600	chr16:12424341-12424342	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs370509139	chr16:12424353-12424354	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565442004	chr16:12424362-12424363	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563289331	chr16:12424371-12424372	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13331380	chr16:12424372-12424373	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs192959612	chr16:12424386-12424387	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80165102	chr16:12424390-12424391	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529762515	chr16:12424408-12424409	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs376201088	chr16:12424468-12424469	Enhancers Weak transcription Genic 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
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:506 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12371400-12456800	Weak transcription	Aorta	Aorta
2	chr16:12404200-12427400	Weak transcription	Primary T cells from cord blood	blood
3	chr16:12405600-12426400	Weak transcription	Lung	lung
4	chr16:12405600-12442400	Weak transcription	Spleen	Spleen
5	chr16:12410000-12456600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr16:12410200-12424400	Weak transcription	Right Atrium	heart
7	chr16:12410200-12464800	Weak transcription	Gastric	stomach
8	chr16:12414400-12431400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:12414800-12432000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr16:12415000-12424600	Weak transcription	Esophagus	oesophagus
11	chr16:12415000-12431600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr16:12415400-12435400	Weak transcription	Pancreas	Pancrea
13	chr16:12415600-12425200	Weak transcription	Primary B cells from cord blood	blood
14	chr16:12416000-12423800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr16:12416200-12427600	Weak transcription	Thymus	Thymus
16	chr16:12416800-12438600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr16:12417800-12424200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr16:12418400-12426400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr16:12418400-12433400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr16:12418400-12433400	Weak transcription	Brain Substantia Nigra	brain
21	chr16:12418400-12438400	Weak transcription	Brain Anterior Caudate	brain
22	chr16:12418600-12424600	Weak transcription	Psoas Muscle	Psoas
23	chr16:12421600-12428400	Enhancers	Stomach Smooth Muscle	stomach
24	chr16:12421800-12423800	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr16:12421800-12425400	Enhancers	Colon Smooth Muscle	Colon
26	chr16:12422000-12424000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr16:12422000-12432200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr16:12422400-12424400	Weak transcription	Rectal Smooth Muscle	rectum
29	chr16:12422400-12424400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr16:12422600-12423600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr16:12422600-12425400	Enhancers	GM12878-XiMat	blood
32	chr16:12422800-12424600	Weak transcription	Adipose Nuclei	Adipose
33	chr16:12422800-12424800	Weak transcription	Liver	Liver
34	chr16:12423000-12423600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr16:12423000-12424400	Weak transcription	Fetal Stomach	stomach
36	chr16:12423000-12425000	Enhancers	Left Ventricle	heart
37	chr16:12423000-12425000	Enhancers	Right Ventricle	heart
38	chr16:12423000-12425600	Enhancers	Fetal Heart	heart
39	chr16:12423000-12426800	Enhancers	Fetal Muscle Leg	muscle
40	chr16:12423200-12424600	Weak transcription	Ovary	ovary
41	chr16:12423200-12425400	Genic enhancers	Primary B cells from peripheral blood	blood
42	chr16:12423400-12423800	Enhancers	Fetal Brain Female	brain
43	chr16:12423400-12423800	Enhancers	HSMMtube	muscle
44	chr16:12423600-12425400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr16:12423600-12425400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr16:12423800-12424400	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr16:12423800-12425000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr16:12423800-12426000	Weak transcription	Fetal Brain Female	brain
49	chr16:12423800-12433600	Weak transcription	HSMMtube	muscle
50	chr16:12424000-12424400	Enhancers	Primary neutrophils fromperipheralblood	blood

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