Variant report

Variant	nsv543000
Chromosome Location	chr16:82719694-82821762
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:817)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:817 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr16:82734486-82734890	GM12878	blood:	n/a	n/a
2	ATF2	chr16:82734565-82734903	GM12878	blood:	n/a	n/a
3	BATF	chr16:82734563-82734829	GM12878	blood:	n/a	chr16:82734658-82734669
4	BATF	chr16:82768884-82769120	GM12878	blood:	n/a	n/a
5	BATF	chr16:82762566-82762845	GM12878	blood:	n/a	n/a
6	BATF	chr16:82768835-82769108	GM12878	blood:	n/a	n/a
7	BATF	chr16:82769541-82769852	GM12878	blood:	n/a	n/a
8	BCL3	chr16:82819586-82819857	GM12878	blood:	n/a	n/a
9	BCL3	chr16:82769485-82769826	GM12878	blood:	n/a	n/a
10	BCL3	chr16:82734543-82734817	GM12878	blood:	n/a	n/a
11	BHLHE40	chr16:82769364-82769831	GM12878	blood:	n/a	n/a
12	BRCA1	chr16:82729172-82729255	GM12878	blood:	n/a	n/a
13	BRCA1	chr16:82733235-82733712	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr16:82768253-82768514	K562	blood:	n/a	n/a
15	CEBPB	chr16:82734961-82735222	HepG2	liver:	n/a	chr16:82735106-82735117
16	CEBPB	chr16:82794930-82795257	Hela-S3	cervix:	n/a	chr16:82795159-82795172
17	CEBPB	chr16:82735018-82735210	H1-hESC	embryonic stem cell:	n/a	chr16:82735106-82735117
18	CEBPB	chr16:82768963-82769134	IMR90	lung:	n/a	n/a
19	CEBPB	chr16:82795055-82795275	H1-hESC	embryonic stem cell:	n/a	chr16:82795159-82795172
20	CEBPB	chr16:82810428-82810778	HepG2	liver:	n/a	chr16:82810606-82810617
21	CEBPB	chr16:82733173-82733718	HCT-116	colon:	n/a	n/a
22	CEBPB	chr16:82733193-82733720	IMR90	lung:	n/a	n/a
23	CEBPB	chr16:82810502-82810653	K562	blood:	n/a	chr16:82810606-82810617
24	CEBPB	chr16:82781701-82782011	IMR90	lung:	n/a	n/a
25	CEBPB	chr16:82816457-82816749	H1-hESC	embryonic stem cell:	n/a	chr16:82816601-82816612
26	CEBPB	chr16:82773312-82773624	IMR90	lung:	n/a	chr16:82773444-82773453 chr16:82773443-82773454 chr16:82773442-82773455 chr16:82773442-82773453
27	CEBPB	chr16:82793574-82793858	HepG2	liver:	n/a	chr16:82793699-82793710
28	CEBPB	chr16:82773333-82773604	HepG2	liver:	n/a	chr16:82773444-82773453 chr16:82773443-82773454 chr16:82773442-82773455 chr16:82773442-82773453
29	CEBPB	chr16:82806159-82806390	HepG2	liver:	n/a	chr16:82806277-82806288
30	CEBPB	chr16:82734280-82735302	Hela-S3	cervix:	n/a	chr16:82735106-82735117
31	CEBPB	chr16:82734534-82735298	IMR90	lung:	n/a	chr16:82735106-82735117
32	CEBPB	chr16:82727809-82728158	IMR90	lung:	n/a	n/a
33	CEBPB	chr16:82806146-82806407	IMR90	lung:	n/a	chr16:82806277-82806288
34	CEBPB	chr16:82794786-82795354	IMR90	lung:	n/a	chr16:82795159-82795172
35	CEBPB	chr16:82810451-82810782	IMR90	lung:	n/a	chr16:82810606-82810617
36	CEBPB	chr16:82732813-82733796	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:82729707-82729756	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr16:82793367-82793845	IMR90	lung:	n/a	chr16:82793383-82793394 chr16:82793699-82793710
39	CEBPB	chr16:82810463-82810760	A549	lung:	n/a	chr16:82810606-82810617
40	CEBPB	chr16:82794905-82795256	A549	lung:	n/a	chr16:82795159-82795172
41	CEBPB	chr16:82793698-82793750	K562	blood:	n/a	chr16:82793699-82793710
42	CHD2	chr16:82733207-82733714	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr16:82748415-82748521	GM12878	blood:	n/a	n/a
44	CTCF	chr16:82772440-82772590	GM12872	blood:	n/a	chr16:82772478-82772499 chr16:82772483-82772501 chr16:82772489-82772498
45	CTCF	chr16:82772500-82772650	SAEC	small airway:	n/a	n/a
46	CTCF	chr16:82781820-82781970	HPF	lung:	n/a	chr16:82781890-82781911
47	CTCF	chr16:82723990-82724268	GM12878	blood:	n/a	n/a
48	CTCF	chr16:82781800-82781950	AG09309	skin:	n/a	chr16:82781890-82781911
49	CTCF	chr16:82789320-82789470	HCPEpiC	choroid plexus:	n/a	chr16:82789374-82789381
50	CTCF	chr16:82748440-82748590	GM12874	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:82781365-82781415	A549	lung:	n/a
2	chr16:82735595-82735645	AoSMC	blood vessel:	n/a
3	chr16:82735595-82735645	BJ	skin:	n/a
4	chr16:82741062-82741112	IMR90	lung:	fetal
5	chr16:82816457-82816507	SKMC	muscle:	n/a
6	chr16:82781365-82781415	Hepatocyte	liver:	n/a
7	chr16:82816457-82816507	HPAEpiC	pulmonary alveolar:	n/a
8	chr16:82741062-82741112	AG09309	skin:	n/a
9	chr16:82781365-82781415	H1-hESC	embryonic stem cell:	embryo
10	chr16:82735595-82735645	SK-N-SH_RA	brain:	n/a
11	chr16:82735595-82735645	Hela-S3	cervix:	n/a
12	chr16:82781365-82781415	HCF	heart:	n/a
13	chr16:82741062-82741112	HMEC	breast:	n/a
14	chr16:82781365-82781415	GM06990	blood:	n/a
15	chr16:82781365-82781415	AG04449	skin:	fetal
16	chr16:82735595-82735645	SK-N-MC	brain:	n/a
17	chr16:82816457-82816507	HL-60	blood:	n/a
18	chr16:82741062-82741112	SK-N-SH	brain:	n/a
19	chr16:82816457-82816507	ProgFib	skin:	n/a
20	chr16:82816457-82816507	BJ	skin:	n/a
21	chr16:82816457-82816507	NT2-D1	testis:	n/a
22	chr16:82816457-82816507	Hepatocyte	liver:	n/a
23	chr16:82735595-82735645	Jurkat	blood:	n/a
24	chr16:82741062-82741112	PFSK-1	brain:	n/a
25	chr16:82816457-82816507	HAEpiC	amniotic membrane:	n/a
26	chr16:82781365-82781415	K562	blood:	n/a
27	chr16:82741062-82741112	NB4	blood:	n/a
28	chr16:82816457-82816507	NHBE	bronchial:	n/a
29	chr16:82741062-82741112	HEK293	kidney:	embryo
30	chr16:82781365-82781415	AoSMC	blood vessel:	n/a
31	chr16:82741062-82741112	Hela-S3	cervix:	n/a
32	chr16:82781365-82781415	HepG2	liver:	n/a
33	chr16:82741062-82741112	HPAEpiC	pulmonary alveolar:	n/a
34	chr16:82816457-82816507	AG04450	lung:	fetal
35	chr16:82741062-82741112	AG04450	lung:	fetal
36	chr16:82781365-82781415	Caco-2	colon:	n/a
37	chr16:82781365-82781415	SK-N-SH_RA	brain:	n/a
38	chr16:82735595-82735645	IMR90	lung:	fetal
39	chr16:82816457-82816507	HepG2	liver:	n/a
40	chr16:82735595-82735645	NHDF-neo	bronchial:	n/a
41	chr16:82735595-82735645	PrEC	prostate:	n/a
42	chr16:82781365-82781415	HEEpiC	esophagus:	n/a
43	chr16:82735595-82735645	MCF-7	breast:	n/a
44	chr16:82735595-82735645	ProgFib	skin:	n/a
45	chr16:82741062-82741112	H1-hESC	embryonic stem cell:	embryo
46	chr16:82735595-82735645	ovcar-3	ovarian:	n/a
47	chr16:82781365-82781415	CMK	blood:	n/a
48	chr16:82735595-82735645	Caco-2	colon:	n/a
49	chr16:82816457-82816507	SK-N-MC	brain:	n/a
50	chr16:82781365-82781415	ECC-1	luminal epithelium:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:82784687..82786214-chr16:82787764..82790062,2	K562	blood:
2	chr16:82713256..82715722-chr16:82717588..82720342,2	MCF-7	breast:
3	chr16:82771591..82773606-chr16:82773856..82775987,2	MCF-7	breast:
4	chr16:82719977..82722521-chr16:82731834..82734582,2	MCF-7	breast:
5	chr16:82784687..82786214-chr16:82787764..82790062,2	K562	blood:
6	chr16:82810032..82812890-chr16:82813373..82816205,2	K562	blood:
7	chr16:82722552..82724277-chr16:82729529..82732176,2	K562	blood:
8	chr16:82810032..82812890-chr16:82813373..82816205,2	K562	blood:
9	chr16:82719231..82721190-chr16:82722242..82724688,2	K562	blood:
10	chr16:82717088..82721313-chr16:82721815..82725146,5	K562	blood:
11	chr16:82800736..82802731-chr16:82823544..82826539,2	K562	blood:
12	chr16:82758028..82760301-chr16:82761456..82763834,2	K562	blood:
13	chr16:82719231..82721190-chr16:82722242..82724688,2	K562	blood:
14	chr16:82722552..82724277-chr16:82729529..82732176,2	K562	blood:
15	chr16:82771591..82773606-chr16:82773856..82775987,2	MCF-7	breast:
16	chr16:82717088..82721313-chr16:82721815..82725146,5	K562	blood:
17	chr16:82747264..82747918-chr8:126111551..126112155,2	MCF-7	breast:
18	chr16:82762397..82764526-chr16:82767820..82769912,2	MCF-7	breast:
19	chr16:82762397..82764526-chr16:82767820..82769912,2	MCF-7	breast:
20	chr16:82758028..82760301-chr16:82761456..82763834,2	K562	blood:
21	chr16:82719977..82722521-chr16:82731834..82734582,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSD17B2-5	chr16:82756626-82756710	NONHSAT143992
2	lnc-HSD17B2-2	chr16:82806924-82807094	ENSG00000260862.1
3	lnc-HSD17B2-6	chr16:82761080-82761299	NONHSAT143993

miRNA name	Chromosome Location	mirBase accession
hsa-miR-8058	chr16:82722593-82722614	MIMAT0030985

No data

Variant related genes	Relation type
ENSG00000260862	TF binding region
ENSG00000260862	CpG island

Extended variants
information (count: 6024 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6024 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138678262	chr16:82719697-82719698	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs112340250	chr16:82719699-82719700	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370150765	chr16:82719729-82719730	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144960303	chr16:82719730-82719731	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552074000	chr16:82719783-82719784	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192233959	chr16:82719823-82719824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs8060937	chr16:82719836-82719837	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs546341335	chr16:82719837-82719838	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs567860709	chr16:82719842-82719843	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs149114795	chr16:82719885-82719886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550338743	chr16:82719902-82719903	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568858761	chr16:82719912-82719913	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143208131	chr16:82719929-82719930	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559302340	chr16:82719930-82719931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs571111003	chr16:82719970-82719971	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77492656	chr16:82719982-82719983	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148272798	chr16:82719988-82719989	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184762862	chr16:82720013-82720014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574871976	chr16:82720028-82720029	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534041105	chr16:82720089-82720090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557145300	chr16:82720106-82720107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575609537	chr16:82720111-82720112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557337262	chr16:82720113-82720114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545748109	chr16:82720156-82720157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3891658	chr16:82720168-82720169	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs116525038	chr16:82720182-82720183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376394538	chr16:82720197-82720198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs189486790	chr16:82720203-82720204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540077014	chr16:82720205-82720206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561903464	chr16:82720206-82720207	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3845200	chr16:82720208-82720209	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs80355210	chr16:82720213-82720214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532962206	chr16:82720218-82720219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191422217	chr16:82720235-82720236	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs202201635	chr16:82720243-82720244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3852739	chr16:82720245-82720246	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs184517752	chr16:82720258-82720259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs117074004	chr16:82720266-82720267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146238390	chr16:82720274-82720275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535636910	chr16:82720311-82720312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs16958271	chr16:82720313-82720314	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575600622	chr16:82720328-82720329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551042886	chr16:82720342-82720343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189787522	chr16:82720343-82720344	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557720502	chr16:82720353-82720354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572836382	chr16:82720364-82720365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540113843	chr16:82720391-82720392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549097583	chr16:82720420-82720421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117405863	chr16:82720452-82720453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115619764	chr16:82720459-82720460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Non-small cell lung cancer	21829676	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16461572	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Alveolar capillary dysplasia	19500772	CNVD
VACTERL syndrome	21315191	CNVD
T-cell lymphomas	19863542	CNVD
Developmental delay	19490664	CNVD
Neuroblastoma	18923191	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Autism	20531469	CNVD

Chromatin state (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82694200-82728400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr16:82695400-82726600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr16:82709600-82724200	Weak transcription	Aorta	Aorta
4	chr16:82709600-82728000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr16:82709800-82727000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr16:82710000-82727200	Weak transcription	NH-A	brain
7	chr16:82713000-82720600	Strong transcription	HSMM	muscle
8	chr16:82716600-82720600	Weak transcription	Psoas Muscle	Psoas
9	chr16:82716600-82721200	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr16:82717000-82721200	Weak transcription	Right Ventricle	heart
11	chr16:82717200-82721400	Weak transcription	Left Ventricle	heart
12	chr16:82717200-82722400	Weak transcription	Fetal Intestine Large	intestine
13	chr16:82717200-82726600	Weak transcription	HMEC	breast
14	chr16:82717600-82721200	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr16:82718000-82726400	Weak transcription	NHEK	skin
16	chr16:82718200-82720400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr16:82718200-82721400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr16:82718400-82720000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr16:82718600-82720400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr16:82719200-82720000	Enhancers	Thymus	Thymus
21	chr16:82719400-82723000	Weak transcription	Fetal Intestine Small	intestine
22	chr16:82719400-82728600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr16:82719600-82727200	Weak transcription	HSMMtube	muscle
24	chr16:82720000-82722600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr16:82720400-82722000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr16:82720400-82722200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:82720600-82721000	Enhancers	Psoas Muscle	Psoas
28	chr16:82720600-82724200	Weak transcription	HSMM	muscle
29	chr16:82721000-82721600	Weak transcription	Psoas Muscle	Psoas
30	chr16:82721200-82721800	Enhancers	Right Ventricle	heart
31	chr16:82721200-82722000	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr16:82721200-82722200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr16:82721400-82722000	Enhancers	Left Ventricle	heart
34	chr16:82721400-82724800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr16:82721600-82722600	Enhancers	Psoas Muscle	Psoas
36	chr16:82721800-82728400	Weak transcription	Right Ventricle	heart
37	chr16:82722000-82726600	Weak transcription	Left Ventricle	heart
38	chr16:82722000-82728200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr16:82722200-82726800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr16:82722400-82723000	Enhancers	Fetal Intestine Large	intestine
41	chr16:82722600-82726000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr16:82722600-82731600	Weak transcription	Psoas Muscle	Psoas
43	chr16:82723000-82726600	Weak transcription	Fetal Intestine Large	intestine
44	chr16:82723200-82723600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr16:82723200-82726600	Weak transcription	Fetal Intestine Small	intestine
46	chr16:82724200-82725000	Strong transcription	Aorta	Aorta
47	chr16:82724200-82726200	Strong transcription	HSMM	muscle
48	chr16:82724800-82726800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr16:82725000-82730600	Weak transcription	Aorta	Aorta
50	chr16:82726000-82729000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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