Variant report

Variant	nsv905761
Chromosome Location	chr16:31730525-31812442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:223)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:223 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:31750592-31750916	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr16:31775453-31775765	A549	lung:	n/a	chr16:31775622-31775633
3	CEBPB	chr16:31775453-31775770	IMR90	lung:	n/a	chr16:31775622-31775633
4	CEBPB	chr16:31775444-31775809	HepG2	liver:	n/a	chr16:31775622-31775633
5	CEBPB	chr16:31775541-31775735	H1-hESC	embryonic stem cell:	n/a	chr16:31775622-31775633
6	CEBPB	chr16:31775457-31775729	K562	blood:	n/a	chr16:31775622-31775633
7	CTCF	chr16:31750460-31750610	BE2_C	brain:	n/a	n/a
8	CTCF	chr16:31750700-31750850	BE2_C	brain:	n/a	n/a
9	CTCF	chr16:31750720-31750870	AG04449	skin:	n/a	n/a
10	CTCF	chr16:31750600-31750750	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr16:31750700-31750850	HCFaa	heart:	n/a	n/a
12	CTCF	chr16:31733441-31733506	Fibrobl	skin:	n/a	n/a
13	CTCF	chr16:31750600-31750750	GM12872	blood:	n/a	n/a
14	CTCF	chr16:31777196-31777302	GM13976	blood:	n/a	n/a
15	CTCF	chr16:31750720-31750870	HPF	lung:	n/a	n/a
16	CTCF	chr16:31750740-31750890	RPTEC	kidney:	n/a	n/a
17	CTCF	chr16:31748548-31748552	GM20000	blood:	n/a	n/a
18	CTCF	chr16:31750680-31750830	HMF	breast:	n/a	n/a
19	CTCF	chr16:31794895-31794958	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr16:31800818-31800901	Lung_OC	lung:	n/a	n/a
21	CTCF	chr16:31794860-31795010	HEK293	kidney:	n/a	n/a
22	CTCF	chr16:31772327-31772374	Medullo	brain:	n/a	n/a
23	CTCF	chr16:31750680-31750830	GM12873	blood:	n/a	n/a
24	CTCF	chr16:31750660-31750810	HVMF	connective:	n/a	n/a
25	CTCF	chr16:31750700-31750850	HMEC	breast:	n/a	n/a
26	CTCF	chr16:31750620-31750770	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr16:31750700-31750850	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr16:31750640-31750790	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr16:31750711-31750788	MCF-7	breast:	n/a	n/a
30	CTCF	chr16:31750700-31750850	MCF-7	breast:	n/a	n/a
31	CTCF	chr16:31743028-31743084	LNCaP	prostate:	n/a	n/a
32	CTCF	chr16:31750680-31750830	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr16:31812090-31812141	GM20000	blood:	n/a	n/a
34	CTCF	chr16:31750685-31750777	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr16:31764980-31765130	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr16:31809732-31809755	Lung_OC	lung:	n/a	n/a
37	CTCF	chr16:31794895-31794999	K562	blood:	n/a	n/a
38	CTCF	chr16:31750700-31750850	GM12871	blood:	n/a	n/a
39	CTCF	chr16:31771348-31771378	Lung_OC	lung:	n/a	n/a
40	CTCF	chr16:31794860-31795010	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr16:31750620-31750770	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr16:31750620-31750770	HCT-116	colon:	n/a	n/a
43	CTCF	chr16:31750680-31750830	A549	lung:	n/a	n/a
44	CTCF	chr16:31750700-31750850	GM12873	blood:	n/a	n/a
45	CTCF	chr16:31794880-31795030	HepG2	liver:	n/a	n/a
46	CTCF	chr16:31750720-31750870	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr16:31750700-31750850	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr16:31748562-31748609	GM20000	blood:	n/a	n/a
49	CTCF	chr16:31750640-31750790	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr16:31750708-31750844	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:31728442..31730658-chr20:45988564..45991116,2	MCF-7	breast:
2	chr16:31723262..31725200-chr16:31741189..31743578,2	MCF-7	breast:
3	chr16:31482489..31484818-chr16:31728466..31730917,2	MCF-7	breast:
4	chr16:31731395..31734226-chr16:31884146..31887105,3	MCF-7	breast:
5	chr16:31768318..31770553-chr16:31771376..31773000,2	MCF-7	breast:
6	chr16:31768318..31770553-chr16:31771376..31773000,2	MCF-7	breast:
7	chr16:31730337..31731972-chr16:31892630..31894181,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF267-1	chr16:31799523-31801961	ENSG00000259810.1
2	lnc-ZNF720-3	chr16:31770678-31770874	NONHSAT141962
3	lnc-ZNF720-3	chr16:31765087-31765221	NONHSAT141963
4	lnc-ZNF720-3	chr16:31765776-31766116	NONHSAT141961
5	lnc-ZNF720-3	chr16:31765087-31765221	NONHSAT141961
6	lnc-ZNF720-3	chr16:31803951-31804051	NONHSAT141960
7	lnc-ZNF267-1	chr16:31799523-31802314	ENSG00000259810.2
8	lnc-ZNF267-1	chr16:31799523-31800928	ENSG00000261922.1
9	lnc-ZNF720-3	chr16:31765087-31765221	NONHSAT141960
10	lnc-ZNF720-3	chr16:31770678-31770787	NONHSAT141963
11	lnc-ZNF720-3	chr16:31805023-31806190	NONHSAT141960
12	lnc-ZNF720-3	chr16:31804656-31804732	NONHSAT141960
13	lnc-ZNF720-3	chr16:31805023-31805028	NONHSAT141963
14	lnc-ZNF720-3	chr16:31803951-31804051	NONHSAT141963
15	lnc-ZNF720-3	chr16:31804656-31804732	NONHSAT141963
16	lnc-ZNF720-3	chr16:31765087-31765221	NONHSAT141962

No data

Variant related genes	Relation type
ENSG00000259810	TF binding region
ENSG00000261457	TF binding region
ENSG00000185947	chromatin interactions
ENSG00000140682	chromatin interactions
ENSG00000261731	chromatin interactions
ENSG00000197302	chromatin interactions

Extended variants
information (count: 2717 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2717 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17519579	chr16:31730525-31730526	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548379827	chr16:31730537-31730538	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs566642861	chr16:31730546-31730547	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs552128293	chr16:31730618-31730619	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527585269	chr16:31730621-31730622	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552457218	chr16:31730855-31730856	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs75841415	chr16:31730876-31730877	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1073513	chr16:31730892-31730893	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs193005824	chr16:31731013-31731014	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145013280	chr16:31731089-31731090	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535169968	chr16:31731166-31731167	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs574052614	chr16:31731232-31731233	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9928006	chr16:31731233-31731234	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs74536439	chr16:31731234-31731235	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs546098429	chr16:31731235-31731236	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184728616	chr16:31731259-31731260	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576075509	chr16:31731286-31731287	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543782831	chr16:31731291-31731292	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561898621	chr16:31731327-31731328	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529409485	chr16:31731328-31731329	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143523098	chr16:31731416-31731417	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541119673	chr16:31731432-31731433	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149103455	chr16:31731443-31731444	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs9940126	chr16:31731446-31731447	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs75027371	chr16:31731467-31731468	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs552550750	chr16:31731589-31731590	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187493677	chr16:31731616-31731617	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs546514728	chr16:31731617-31731618	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143191600	chr16:31731636-31731637	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs192011261	chr16:31731643-31731644	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs567939030	chr16:31731674-31731675	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148181667	chr16:31731774-31731775	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547050338	chr16:31731871-31731872	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565975241	chr16:31731895-31731896	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184784743	chr16:31731931-31731932	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374350974	chr16:31731936-31731937	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539643017	chr16:31731946-31731947	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142697779	chr16:31731969-31731970	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs371064232	chr16:31731970-31731971	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576688763	chr16:31731986-31731987	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs537318319	chr16:31731989-31731990	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555734924	chr16:31732004-31732005	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544774413	chr16:31732019-31732020	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs371132282	chr16:31732020-31732021	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117806831	chr16:31732036-31732037	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573908242	chr16:31732048-31732049	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs115189766	chr16:31732051-31732052	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7359491	chr16:31732056-31732057	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs572296898	chr16:31732099-31732100	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546007377	chr16:31732108-31732109	Weak transcription ZNF genes & repeats Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
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	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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Sezary syndrome	18413736	CNVD
Wilms tumour	21544195	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1517 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31725400-31742000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:31725600-31735800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr16:31725800-31753400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:31726000-31742400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr16:31726000-31747400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr16:31726200-31730600	Strong transcription	Fetal Muscle Trunk	muscle
7	chr16:31726200-31734200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr16:31726200-31736600	Weak transcription	Aorta	Aorta
9	chr16:31726200-31736800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr16:31726200-31742600	Weak transcription	Ovary	ovary
11	chr16:31726200-31745600	Weak transcription	Colonic Mucosa	Colon
12	chr16:31726400-31736000	Strong transcription	Cortex derived primary cultured neurospheres	brain
13	chr16:31726400-31736600	Weak transcription	Small Intestine	intestine
14	chr16:31726400-31750000	Weak transcription	HUVEC	blood vessel
15	chr16:31726400-31750800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr16:31726600-31730600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr16:31726600-31731200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr16:31726600-31734400	Weak transcription	Fetal Kidney	kidney
19	chr16:31726600-31734600	Weak transcription	Fetal Brain Male	brain
20	chr16:31726600-31734800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr16:31726600-31734800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr16:31726600-31736000	Weak transcription	Placenta	Placenta
23	chr16:31726600-31736200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr16:31726600-31740000	Weak transcription	NHDF-Ad	bronchial
25	chr16:31726600-31741000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr16:31726600-31743200	Weak transcription	Brain Cingulate Gyrus	brain
27	chr16:31726600-31744000	Weak transcription	K562	blood
28	chr16:31726600-31748600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr16:31726800-31736800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr16:31727000-31732200	ZNF genes & repeats	GM12878-XiMat	blood
31	chr16:31727000-31745000	Weak transcription	HMEC	breast
32	chr16:31727200-31734000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr16:31727200-31736200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr16:31727200-31758800	Weak transcription	Fetal Thymus	thymus
35	chr16:31727200-31760000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr16:31727400-31733600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr16:31727400-31736000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
38	chr16:31727400-31736600	Weak transcription	Brain Hippocampus Middle	brain
39	chr16:31727600-31733800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr16:31727600-31734400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr16:31727600-31736800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr16:31727600-31741000	Weak transcription	Fetal Heart	heart
43	chr16:31727600-31743400	Weak transcription	NHEK	skin
44	chr16:31727600-31758400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:31727800-31731400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr16:31727800-31731400	Weak transcription	NHLF	lung
47	chr16:31727800-31733200	Weak transcription	Stomach Mucosa	stomach
48	chr16:31727800-31733800	Weak transcription	Osteobl	bone
49	chr16:31727800-31734000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr16:31727800-31734600	Weak transcription	HepG2	liver

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