Variant report

Variant	nsv533068
Chromosome Location	chr16:47354593-47559639
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2094)
CpG islands
(count:1163)
Chromatin interactive
region (count:144)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2094 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47507313-47507485	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:47426038-47426363	K562	blood:	n/a	n/a
3	ARID3A	chr16:47507738-47508382	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:47428252-47428453	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47526816-47527197	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:47538556-47538932	K562	blood:	n/a	n/a
7	ARID3A	chr16:47519386-47519410	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:47498536-47498645	K562	blood:	n/a	n/a
9	ARID3A	chr16:47554148-47554743	K562	blood:	n/a	n/a
10	ARID3A	chr16:47499795-47500033	K562	blood:	n/a	n/a
11	ARID3A	chr16:47357253-47357463	HepG2	liver:	n/a	n/a
12	ARID3A	chr16:47524403-47524722	K562	blood:	n/a	n/a
13	ARID3A	chr16:47556945-47557537	HepG2	liver:	n/a	n/a
14	ARID3A	chr16:47421094-47421294	HepG2	liver:	n/a	n/a
15	ARID3A	chr16:47482890-47483076	K562	blood:	n/a	n/a
16	ARID3A	chr16:47509336-47510111	HepG2	liver:	n/a	n/a
17	ARID3A	chr16:47495283-47496261	K562	blood:	n/a	n/a
18	ARID3A	chr16:47484519-47484647	HepG2	liver:	n/a	n/a
19	ARID3A	chr16:47431618-47431623	HepG2	liver:	n/a	n/a
20	ARID3A	chr16:47494825-47496228	HepG2	liver:	n/a	n/a
21	ARID3A	chr16:47533067-47533932	HepG2	liver:	n/a	n/a
22	ARID3A	chr16:47526802-47527555	K562	blood:	n/a	n/a
23	ARID3A	chr16:47500293-47502483	K562	blood:	n/a	n/a
24	ATF1	chr16:47426003-47426482	K562	blood:	n/a	n/a
25	ATF1	chr16:47422668-47422993	K562	blood:	n/a	n/a
26	ATF1	chr16:47501985-47502361	K562	blood:	n/a	n/a
27	ATF1	chr16:47495611-47496214	K562	blood:	n/a	n/a
28	ATF1	chr16:47554214-47554593	K562	blood:	n/a	n/a
29	ATF1	chr16:47427309-47427338	K562	blood:	n/a	n/a
30	ATF1	chr16:47526819-47527180	K562	blood:	n/a	n/a
31	ATF2	chr16:47557169-47557724	GM12878	blood:	n/a	n/a
32	ATF2	chr16:47526273-47527368	GM12878	blood:	n/a	n/a
33	ATF3	chr16:47494883-47495224	GM12878	blood:	n/a	n/a
34	ATF3	chr16:47494617-47495423	HepG2	liver:	n/a	n/a
35	ATF3	chr16:47494770-47495381	GM12878	blood:	n/a	n/a
36	ATF3	chr16:47501997-47502334	K562	blood:	n/a	n/a
37	ATF3	chr16:47494755-47495369	HepG2	liver:	n/a	n/a
38	ATF3	chr16:47494797-47495311	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF3	chr16:47494735-47495286	K562	blood:	n/a	n/a
40	ATF3	chr16:47494783-47495259	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF3	chr16:47494801-47495349	K562	blood:	n/a	n/a
42	BACH1	chr16:47495724-47496205	K562	blood:	n/a	n/a
43	BACH1	chr16:47538552-47539389	K562	blood:	n/a	n/a
44	BACH1	chr16:47495881-47496208	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr16:47495280-47495285	K562	blood:	n/a	n/a
46	BACH1	chr16:47502056-47502356	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr16:47502025-47502424	K562	blood:	n/a	n/a
48	BATF	chr16:47526905-47527207	GM12878	blood:	n/a	n/a
49	BATF	chr16:47364453-47364807	GM12878	blood:	n/a	n/a
50	BATF	chr16:47526497-47527241	GM12878	blood:	n/a	n/a

(count:1163 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47494735-47494785	SKMC	muscle:	n/a
2	chr16:47409367-47409417	HEEpiC	esophagus:	n/a
3	chr16:47492286-47492336	BE2_C	brain:	n/a
4	chr16:47420506-47420556	NHBE	bronchial:	n/a
5	chr16:47494735-47494785	SKMC	muscle:	n/a
6	chr16:47409367-47409417	HEEpiC	esophagus:	n/a
7	chr16:47492286-47492336	BE2_C	brain:	n/a
8	chr16:47420506-47420556	NHBE	bronchial:	n/a
9	chr16:47492286-47492336	BJ	skin:	n/a
10	chr16:47420506-47420556	SK-N-SH_RA	brain:	n/a
11	chr16:47539203-47539253	HCF	heart:	n/a
12	chr16:47494258-47494308	ProgFib	skin:	n/a
13	chr16:47495746-47495796	IMR90	lung:	fetal
14	chr16:47420506-47420556	ovcar-3	ovarian:	n/a
15	chr16:47495746-47495796	HUVEC	blood vessel:	n/a
16	chr16:47495768-47495818	AG04449	skin:	fetal
17	chr16:47409367-47409417	HEK293	kidney:	embryo
18	chr16:47539137-47539187	PFSK-1	brain:	n/a
19	chr16:47494824-47494874	SK-N-SH_RA	brain:	n/a
20	chr16:47494258-47494308	NHDF-neo	bronchial:	n/a
21	chr16:47527034-47527084	HRE	kidney:	n/a
22	chr16:47495746-47495796	PFSK-1	brain:	n/a
23	chr16:47527034-47527084	LNCaP	prostate:	n/a
24	chr16:47409367-47409417	HRPEpiC	eye:	n/a
25	chr16:47494258-47494308	CMK	blood:	n/a
26	chr16:47527034-47527084	HL-60	blood:	n/a
27	chr16:47495110-47495160	HL-60	blood:	n/a
28	chr16:47495541-47495591	PrEC	prostate:	n/a
29	chr16:47539203-47539253	HIPEpiC	eye:	n/a
30	chr16:47362879-47362929	NT2-D1	testis:	n/a
31	chr16:47494711-47494761	HAEpiC	amniotic membrane:	n/a
32	chr16:47539203-47539253	SK-N-MC	brain:	n/a
33	chr16:47539166-47539216	HRE	kidney:	n/a
34	chr16:47495541-47495591	Hela-S3	cervix:	n/a
35	chr16:47494735-47494785	SK-N-SH_RA	brain:	n/a
36	chr16:47362879-47362929	HCF	heart:	n/a
37	chr16:47495113-47495163	NHBE	bronchial:	n/a
38	chr16:47495541-47495591	HIPEpiC	eye:	n/a
39	chr16:47362879-47362929	K562	blood:	n/a
40	chr16:47494824-47494874	AG09319	gingival:	n/a
41	chr16:47494258-47494308	HUVEC	blood vessel:	n/a
42	chr16:47539203-47539253	NT2-D1	testis:	n/a
43	chr16:47539166-47539216	HNPCEpiC	eye:	n/a
44	chr16:47492286-47492336	SK-N-SH_RA	brain:	n/a
45	chr16:47495768-47495818	AG09319	gingival:	n/a
46	chr16:47539137-47539187	SK-N-MC	brain:	n/a
47	chr16:47494735-47494785	MCF-7	breast:	n/a
48	chr16:47362879-47362929	GM12891	blood:	n/a
49	chr16:47362879-47362929	HL-60	blood:	n/a
50	chr16:47497822-47497872	HRPEpiC	eye:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:47480415..47483126-chr16:47520058..47521883,2	K562	blood:
2	chr16:47479859..47483126-chr16:47518741..47522601,4	K562	blood:
3	chr16:47480415..47483126-chr16:47520058..47521883,2	K562	blood:
4	chr16:47538608..47539204-chr19:24184110..24185018,4	MCF-7	breast:
5	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
6	chr16:47177540..47179447-chr16:47502607..47504597,2	K562	blood:
7	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
8	chr16:47506877..47508389-chr16:47511649..47513909,2	K562	blood:
9	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
10	chr16:47404244..47406062-chr16:47411179..47413433,2	K562	blood:
11	chr16:47386165..47387733-chr16:47392448..47394557,2	K562	blood:
12	chr16:47547375..47549482-chr16:47556202..47558891,2	K562	blood:
13	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
14	chr16:47512020..47514843-chr16:47517675..47520024,2	K562	blood:
15	chr16:47386165..47387733-chr16:47392448..47394557,2	K562	blood:
16	chr16:47432128..47434331-chr16:47440523..47442173,2	K562	blood:
17	chr16:47414999..47416779-chr16:47426275..47428924,2	MCF-7	breast:
18	chr16:47416227..47418087-chr16:47500282..47502102,2	K562	blood:
19	chr16:47527728..47529779-chr16:47631706..47633843,2	K562	blood:
20	chr16:47493905..47495976-chr16:47496733..47498612,2	MCF-7	breast:
21	chr16:47502099..47504584-chr16:47526951..47528627,3	K562	blood:
22	chr16:47503547..47505420-chr16:47506732..47508518,2	K562	blood:
23	chr16:47482556..47484709-chr16:47493898..47495616,2	MCF-7	breast:
24	chr16:47493905..47495976-chr16:47496733..47498612,2	MCF-7	breast:
25	chr16:47514982..47517180-chr16:47517561..47520425,2	MCF-7	breast:
26	chr16:47464879..47466397-chr16:47504717..47506667,2	K562	blood:
27	chr16:47500040..47503767-chr16:47514818..47518136,4	K562	blood:
28	chr16:47530496..47533304-chr16:47537314..47539255,2	K562	blood:
29	chr16:47424343..47428876-chr16:47431366..47438255,7	K562	blood:
30	chr16:47530496..47533304-chr16:47537314..47539416,3	K562	blood:
31	chr16:47486141..47491798-chr16:47493044..47496709,8	MCF-7	breast:
32	chr16:47493569..47497883-chr16:47557067..47559084,4	K562	blood:
33	chr16:47533842..47536233-chr16:47541991..47544849,2	K562	blood:
34	chr16:47485624..47489187-chr16:47492609..47496944,6	K562	blood:
35	chr16:47538608..47539232-chr19:24184323..24185236,2	MCF-7	breast:
36	chr16:47500342..47506721-chr16:47514207..47520673,8	K562	blood:
37	chr16:47432128..47434331-chr16:47440523..47442173,2	K562	blood:
38	chr16:47502629..47504464-chr16:47550187..47553009,2	K562	blood:
39	chr16:47489451..47492163-chr16:47492304..47496167,3	K562	blood:
40	chr16:47538608..47539209-chr19:24184105..24184774,2	MCF-7	breast:
41	chr16:47449583..47451141-chr16:47452818..47455615,2	K562	blood:
42	chr16:47352976..47355256-chr16:47362064..47365437,3	K562	blood:
43	chr16:47502808..47504633-chr16:47527127..47529319,2	K562	blood:
44	chr16:47407846..47410097-chr16:47493720..47495618,2	MCF-7	breast:
45	chr16:47493923..47496746-chr16:47529006..47531243,3	K562	blood:
46	chr16:47491892..47494084-chr16:47494205..47496711,2	MCF-7	breast:
47	chr16:47517170..47520211-chr16:47526974..47528925,3	K562	blood:
48	chr16:47503725..47506287-chr16:47510577..47512512,2	K562	blood:
49	chr16:47541164..47545156-chr16:47546024..47549793,5	K562	blood:
50	chr16:47404244..47406062-chr16:47411179..47413433,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-12	chr16:47495240-47495337	NONHSAT142295
2	lnc-GPT2-12	chr16:47497009-47497433	NONHSAT142295

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47484216-47484236

Variant related genes	Relation type
ENSG00000262038	TF binding region
RNA5SP424	TF binding region
PHKB	TF binding region
ITFG1	TF binding region
RNA5SP425	TF binding region
ENSG00000262038	CpG island
RNA5SP424	CpG island
PHKB	CpG island
ITFG1	CpG island
RNA5SP425	CpG island
ENSG00000259918	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000177628	chromatin interactions
ENSG00000212290	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000104613	chromatin interactions
ENSG00000133703	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000162664	chromatin interactions
ENSG00000222268	chromatin interactions

Extended variants
information (count: 6773 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:6773 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184639905	chr16:47354634-47354635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs8057973	chr16:47354669-47354670	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568367858	chr16:47354682-47354683	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs188695185	chr16:47354710-47354711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539269320	chr16:47354721-47354722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557492101	chr16:47354725-47354726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576061381	chr16:47354739-47354740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150764070	chr16:47354863-47354864	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs9635633	chr16:47354883-47354884	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs555112833	chr16:47354919-47354920	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs139215039	chr16:47354973-47354974	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144020536	chr16:47354979-47354980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs191265063	chr16:47354984-47354985	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs34225589	chr16:47354997-47354998	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs572742499	chr16:47354998-47354999	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs75508323	chr16:47355006-47355007	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs183750915	chr16:47355129-47355130	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs569100767	chr16:47355153-47355154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs188476596	chr16:47355200-47355201	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs550236263	chr16:47355335-47355336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35115563	chr16:47355351-47355352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561970853	chr16:47355362-47355363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs529225911	chr16:47355392-47355393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547356571	chr16:47355401-47355402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74765795	chr16:47355411-47355412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs57434681	chr16:47355430-47355431	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140850102	chr16:47355437-47355438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149664486	chr16:47355460-47355461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182019770	chr16:47355470-47355471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555418360	chr16:47355508-47355509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79472053	chr16:47355772-47355773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187624437	chr16:47355780-47355781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189862090	chr16:47355829-47355830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145884782	chr16:47355865-47355866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182056875	chr16:47355867-47355868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546515732	chr16:47355877-47355878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59547333	chr16:47355932-47355933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576560921	chr16:47355970-47355971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543578165	chr16:47355971-47355972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562231342	chr16:47355985-47355986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200880860	chr16:47356029-47356030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570895170	chr16:47356077-47356078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186158613	chr16:47356086-47356087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115612046	chr16:47356168-47356169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559320294	chr16:47356169-47356170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533101514	chr16:47356226-47356227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551640326	chr16:47356236-47356237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569779422	chr16:47356243-47356244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530754932	chr16:47356245-47356246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149001952	chr16:47356293-47356294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4647 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47311400-47362200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr16:47333400-47371600	Weak transcription	Esophagus	oesophagus
3	chr16:47333600-47354600	Weak transcription	HSMMtube	muscle
4	chr16:47334000-47354600	Weak transcription	HSMM	muscle
5	chr16:47334400-47355200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr16:47334400-47357000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr16:47334400-47357400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr16:47334400-47371200	Weak transcription	Aorta	Aorta
9	chr16:47334400-47371600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr16:47334400-47371600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr16:47334600-47372800	Weak transcription	Primary T cells from cord blood	blood
12	chr16:47342800-47364800	Weak transcription	Primary B cells from cord blood	blood
13	chr16:47344600-47371600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr16:47344800-47354600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr16:47344800-47358800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr16:47344800-47370200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr16:47345200-47357600	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr16:47346200-47371600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr16:47346400-47371400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr16:47346400-47371400	Weak transcription	Dnd41	blood
21	chr16:47346400-47371400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr16:47346800-47371600	Weak transcription	Primary T helper cells PMA-I stimulated	--
23	chr16:47350600-47371000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr16:47351400-47370200	Weak transcription	Ovary	ovary
25	chr16:47351800-47357200	Weak transcription	Right Ventricle	heart
26	chr16:47354200-47355800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr16:47354400-47354800	Enhancers	NHDF-Ad	bronchial
28	chr16:47354400-47354800	Enhancers	NHLF	lung
29	chr16:47354400-47355400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:47354600-47354800	Enhancers	HSMM	muscle
31	chr16:47354600-47355200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr16:47354600-47355200	Enhancers	HSMMtube	muscle
33	chr16:47354800-47355200	Enhancers	Fetal Heart	heart
34	chr16:47354800-47355200	Flanking Active TSS	NHDF-Ad	bronchial
35	chr16:47355200-47355600	Enhancers	NHDF-Ad	bronchial
36	chr16:47355200-47371600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr16:47355800-47357800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr16:47357000-47357200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr16:47357200-47357400	Enhancers	Right Ventricle	heart
40	chr16:47357600-47357800	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr16:47360400-47371600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr16:47361600-47371400	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr16:47362600-47371600	Weak transcription	Left Ventricle	heart
44	chr16:47362800-47363600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr16:47362800-47364000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr16:47363200-47364000	Enhancers	Colon Smooth Muscle	Colon
47	chr16:47364600-47370200	Weak transcription	Pancreas	Pancrea
48	chr16:47364800-47365400	Strong transcription	Primary B cells from cord blood	blood
49	chr16:47365200-47371200	Weak transcription	Lung	lung
50	chr16:47365400-47371000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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