Variant report

Variant	nsv1059363
Chromosome Location	chr16:34935402-35283214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2203)
CpG islands
(count:794)
Chromatin interactive
region (count:1)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2203 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:35249303-35249340	K562	blood:	n/a	n/a
2	ARID3A	chr16:35215806-35216177	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:35281029-35281560	HepG2	liver:	n/a	n/a
4	ATF1	chr16:35277983-35278202	K562	blood:	n/a	n/a
5	ATF1	chr16:35259671-35260040	K562	blood:	n/a	n/a
6	ATF1	chr16:35279340-35279710	K562	blood:	n/a	n/a
7	ATF1	chr16:35280891-35281557	K562	blood:	n/a	n/a
8	ATF1	chr16:35268916-35268944	K562	blood:	n/a	n/a
9	ATF1	chr16:35213351-35213381	K562	blood:	n/a	n/a
10	ATF1	chr16:35267539-35267911	K562	blood:	n/a	n/a
11	ATF1	chr16:35239677-35239877	K562	blood:	n/a	n/a
12	ATF1	chr16:35261366-35261566	K562	blood:	n/a	n/a
13	ATF1	chr16:35264269-35264515	K562	blood:	n/a	n/a
14	ATF1	chr16:35215804-35216177	K562	blood:	n/a	n/a
15	ATF3	chr16:35215892-35216057	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr16:35256899-35257275	K562	blood:	n/a	n/a
17	BACH1	chr16:35266044-35266101	K562	blood:	n/a	n/a
18	BACH1	chr16:35219381-35219757	K562	blood:	n/a	n/a
19	BACH1	chr16:35238579-35238779	K562	blood:	n/a	n/a
20	BATF	chr16:35239497-35239873	GM12878	blood:	n/a	n/a
21	BATF	chr16:35254746-35254977	GM12878	blood:	n/a	n/a
22	BATF	chr16:35215892-35216137	GM12878	blood:	n/a	n/a
23	BATF	chr16:35254458-35254653	GM12878	blood:	n/a	n/a
24	BATF	chr16:35279599-35279898	GM12878	blood:	n/a	n/a
25	BATF	chr16:35253541-35253745	GM12878	blood:	n/a	n/a
26	BATF	chr16:35246110-35246376	GM12878	blood:	n/a	n/a
27	BATF	chr16:35237013-35237332	GM12878	blood:	n/a	n/a
28	BATF	chr16:35245358-35245563	GM12878	blood:	n/a	n/a
29	BATF	chr16:35258431-35258794	GM12878	blood:	n/a	n/a
30	BATF	chr16:35245768-35245957	GM12878	blood:	n/a	n/a
31	BATF	chr16:35247305-35247505	GM12878	blood:	n/a	n/a
32	BATF	chr16:35255675-35256007	GM12878	blood:	n/a	n/a
33	BATF	chr16:35250156-35250514	GM12878	blood:	n/a	n/a
34	BATF	chr16:35221097-35221282	GM12878	blood:	n/a	n/a
35	BATF	chr16:35250134-35250425	GM12878	blood:	n/a	n/a
36	BATF	chr16:35281265-35281451	GM12878	blood:	n/a	n/a
37	BATF	chr16:35252081-35252281	GM12878	blood:	n/a	n/a
38	BATF	chr16:35246081-35246465	GM12878	blood:	n/a	n/a
39	BATF	chr16:35280345-35280653	GM12878	blood:	n/a	n/a
40	BATF	chr16:35227031-35227310	GM12878	blood:	n/a	n/a
41	BATF	chr16:35250603-35250848	GM12878	blood:	n/a	n/a
42	BATF	chr16:35244568-35244723	GM12878	blood:	n/a	n/a
43	BATF	chr16:35231834-35232116	GM12878	blood:	n/a	n/a
44	BATF	chr16:35215869-35216143	GM12878	blood:	n/a	n/a
45	BATF	chr16:35243651-35243855	GM12878	blood:	n/a	n/a
46	BATF	chr16:35261256-35261444	GM12878	blood:	n/a	n/a
47	BATF	chr16:35279610-35279869	GM12878	blood:	n/a	n/a
48	BATF	chr16:35244531-35244748	GM12878	blood:	n/a	n/a
49	BATF	chr16:35274637-35275010	GM12878	blood:	n/a	n/a
50	BATF	chr16:35255667-35255988	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:35029890-35029940	GM12878	blood:	n/a
2	chr16:35029890-35029940	GM12878	blood:	n/a
3	chr16:34984121-34984171	AG09309	skin:	n/a
4	chr16:35029997-35030047	AG09319	gingival:	n/a
5	chr16:35037569-35037619	Jurkat	blood:	n/a
6	chr16:35037569-35037619	PrEC	prostate:	n/a
7	chr16:35029890-35029940	K562	blood:	n/a
8	chr16:35027418-35027468	GM12891	blood:	n/a
9	chr16:35029890-35029940	HCPEpiC	choroid plexus:	n/a
10	chr16:34983912-34983962	GM06990	blood:	n/a
11	chr16:34983615-34983665	ProgFib	skin:	n/a
12	chr16:34983384-34983434	AG10803	skin:	n/a
13	chr16:35029997-35030047	GM19239	blood:	n/a
14	chr16:34979671-34979721	AG09309	skin:	n/a
15	chr16:34983912-34983962	HPAEpiC	pulmonary alveolar:	n/a
16	chr16:34983615-34983665	IMR90	lung:	fetal
17	chr16:34983912-34983962	NT2-D1	testis:	n/a
18	chr16:35029997-35030047	MCF-7	breast:	n/a
19	chr16:35027026-35027076	HL-60	blood:	n/a
20	chr16:35026985-35027035	Jurkat	blood:	n/a
21	chr16:35027418-35027468	AG09319	gingival:	n/a
22	chr16:35037569-35037619	MCF10A-Er-Src	breast:	n/a
23	chr16:34979575-34979625	HCF	heart:	n/a
24	chr16:35027418-35027468	GM06990	blood:	n/a
25	chr16:35027418-35027468	LNCaP	prostate:	n/a
26	chr16:35027418-35027468	HL-60	blood:	n/a
27	chr16:34979575-34979625	AoSMC	blood vessel:	n/a
28	chr16:34979575-34979625	HRPEpiC	eye:	n/a
29	chr16:34979575-34979625	AG10803	skin:	n/a
30	chr16:35030232-35030282	T-47D	breast:	n/a
31	chr16:35026985-35027035	SKMC	muscle:	n/a
32	chr16:34984121-34984171	MCF-7	breast:	n/a
33	chr16:35027026-35027076	U87	brain:	n/a
34	chr16:35029997-35030047	Jurkat	blood:	n/a
35	chr16:34983912-34983962	HRCEpiC	kidney:	n/a
36	chr16:35029890-35029940	HepG2	liver:	n/a
37	chr16:34983384-34983434	AoSMC	blood vessel:	n/a
38	chr16:35037569-35037619	RPTEC	kidney:	n/a
39	chr16:34979671-34979721	AG04449	skin:	fetal
40	chr16:35029997-35030047	HRPEpiC	eye:	n/a
41	chr16:35026985-35027035	GM12892	blood:	n/a
42	chr16:34983912-34983962	BE2_C	brain:	n/a
43	chr16:35029997-35030047	SK-N-MC	brain:	n/a
44	chr16:34983615-34983665	K562	blood:	n/a
45	chr16:35030232-35030282	HCM	heart:	n/a
46	chr16:35037569-35037619	GM12892	blood:	n/a
47	chr16:35029997-35030047	NH-A	brain:	n/a
48	chr16:35029997-35030047	SK-N-SH_RA	brain:	n/a
49	chr16:34984121-34984171	HRPEpiC	eye:	n/a
50	chr16:35029997-35030047	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:35133889..35136586-chr16:35136893..35138863,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2144E22.5.1-35	chr16:35071257-35072103	NONHSAT142246
2	lnc-LINC00273-31	chr16:35036459-35037041	NONHSAT142244
3	lnc-LINC00273-33	chr16:35113407-35113869	NONHSAT142247
4	lnc-LINC00273-9	chr16:35019940-35021258	ENSG00000260611.1
5	lnc-CTD-2144E22.5.1-36	chr16:35146491-35146887	NONHSAT142249
6	lnc-LINC00273-30	chr16:34956639-34956900	NONHSAT142221

No data

Variant related genes	Relation type
VN1R70P	TF binding region
RNA5SP417	TF binding region
ENSG00000260611	TF binding region
ENSG00000261122	TF binding region
ENSG00000221580	TF binding region
RNA5SP409	TF binding region
RNA5SP419	TF binding region
RNA5SP407	TF binding region
RNA5SP421	TF binding region
RNA5SP406	TF binding region
RNA5SP408	TF binding region
RNA5SP416	TF binding region
RNA5SP410	TF binding region
RNA5SP413	TF binding region
ENSG00000261782	TF binding region
ENSG00000260522	TF binding region
RNA5SP420	TF binding region
RNA5SP423	TF binding region
RNA5SP415	TF binding region
RNA5SP418	TF binding region
RNA5SP422	TF binding region
HMGN2P41	TF binding region
PPP1R1AP2	TF binding region
VN1R70P	CpG island
RNA5SP417	CpG island
ENSG00000260611	CpG island
ENSG00000261122	CpG island
ENSG00000221580	CpG island
RNA5SP409	CpG island
RNA5SP419	CpG island
RNA5SP407	CpG island
RNA5SP421	CpG island
RNA5SP406	CpG island
RNA5SP408	CpG island
RNA5SP416	CpG island
RNA5SP410	CpG island
RNA5SP413	CpG island
ENSG00000261782	CpG island
ENSG00000260522	CpG island
RNA5SP420	CpG island
RNA5SP423	CpG island
RNA5SP415	CpG island
RNA5SP418	CpG island
RNA5SP422	CpG island
HMGN2P41	CpG island
PPP1R1AP2	CpG island
ENSG00000221580	chromatin interactions

Extended variants
information (count: 14291 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:14291 , 50 per page) page: 1 2 3 4 5 6 7 ... 286

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550761450	chr16:34935674-34935675	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs182554508	chr16:34935675-34935676	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs536912699	chr16:34935684-34935685	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs531373249	chr16:34935708-34935709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs548605943	chr16:34935715-34935716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs566830977	chr16:34935718-34935719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs371338043	chr16:34935721-34935722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs560123768	chr16:34935848-34935849	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs151211344	chr16:34935864-34935865	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs571318126	chr16:34935930-34935931	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs8055664	chr16:34935934-34935935	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570936613	chr16:34935961-34935962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs375305173	chr16:34935965-34935966	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs75770674	chr16:34935966-34935967	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs542078264	chr16:34935974-34935975	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs553795645	chr16:34935977-34935978	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs138130570	chr16:34935978-34935979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs373059339	chr16:34936017-34936018	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs565922712	chr16:34936046-34936047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs376470115	chr16:34936053-34936054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs531298603	chr16:34936060-34936061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs375054495	chr16:34936085-34936086	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs200886223	chr16:34936087-34936088	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs187178868	chr16:34936095-34936096	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs189968666	chr16:34936146-34936147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs180830875	chr16:34936246-34936247	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs143666301	chr16:34936266-34936267	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs145851643	chr16:34936281-34936282	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs185188676	chr16:34936302-34936303	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs138557737	chr16:34936339-34936340	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs544849025	chr16:34936346-34936347	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs368109992	chr16:34936347-34936348	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs538295318	chr16:34936372-34936373	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs556403231	chr16:34936392-34936393	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs568210168	chr16:34936466-34936467	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs150823588	chr16:34936487-34936488	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs565587545	chr16:34936488-34936489	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs535275946	chr16:34936527-34936528	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs190332491	chr16:34936528-34936529	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs536929823	chr16:34936552-34936553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs370670329	chr16:34936562-34936563	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs536458166	chr16:34936604-34936605	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs182510255	chr16:34936611-34936612	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs554757725	chr16:34936617-34936618	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs8045492	chr16:34936623-34936624	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs34581256	chr16:34936681-34936682	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs113325079	chr16:34936719-34936720	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs376557953	chr16:34936721-34936722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs543087284	chr16:34936743-34936744	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs558727948	chr16:34936754-34936755	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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	17603634	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
Ductal carcinoma	22052326	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
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Disorders of sex development	21048976	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Medulloblastoma	21163964	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:34935600-34937200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr16:34938200-34939400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr16:34943800-34944200	Active TSS	Fetal Heart	heart
4	chr16:34944200-34946000	Weak transcription	Fetal Heart	heart
5	chr16:34945200-34947600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr16:34945400-34946800	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr16:34945600-34946200	Enhancers	Left Ventricle	heart
8	chr16:34945600-34946200	Enhancers	Right Atrium	heart
9	chr16:34946000-34946400	Active TSS	Fetal Heart	heart
10	chr16:34946200-34947600	Weak transcription	Right Atrium	heart
11	chr16:34947600-34947800	Enhancers	Right Atrium	heart
12	chr16:34948400-34948600	Enhancers	Left Ventricle	heart
13	chr16:34948800-34949800	ZNF genes & repeats	Adipose Nuclei	Adipose
14	chr16:34949200-34949800	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
15	chr16:34957200-34958400	ZNF genes & repeats	Dnd41	blood
16	chr16:34959200-34960400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
17	chr16:34959400-34959600	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr16:34959600-34965000	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr16:34960200-34960600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr16:34960600-34961000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr16:34960800-34961200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr16:34961000-34961200	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr16:34961200-34963000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr16:34963000-34964400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr16:34964400-34965400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr16:34965000-34965800	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr16:34965400-34967400	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chr16:34965800-34966800	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr16:34966800-34968000	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr16:34967200-34969200	Enhancers	NHEK	skin
31	chr16:34968000-34970800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr16:34969000-34970200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr16:34970000-34971200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr16:34978800-34980400	Enhancers	NHEK	skin
35	chr16:34979800-34989600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr16:34980400-34989000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr16:34983000-34988400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
38	chr16:34983600-34986400	ZNF genes & repeats	Fetal Stomach	stomach
39	chr16:34984200-34986200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr16:34985600-34986600	Enhancers	NHEK	skin
41	chr16:34987000-34989000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr16:34988800-34989000	ZNF genes & repeats	Brain Germinal Matrix	brain
43	chr16:34999000-35000000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr16:35006800-35009000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
45	chr16:35013200-35014000	ZNF genes & repeats	Dnd41	blood
46	chr16:35015200-35015800	Active TSS	Liver	Liver
47	chr16:35017200-35020600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr16:35018200-35018800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
49	chr16:35021400-35025800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr16:35022000-35023600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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