Variant report

Variant	nsv1038535
Chromosome Location	chr16:12620736-12636982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:400)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:12633181-12633355	K562	blood:	n/a	n/a
2	ATF1	chr16:12635640-12635845	K562	blood:	n/a	n/a
3	ATF1	chr16:12633157-12633742	K562	blood:	n/a	n/a
4	ATF2	chr16:12632602-12633937	GM12878	blood:	n/a	n/a
5	ATF2	chr16:12632809-12633811	GM12878	blood:	n/a	n/a
6	ATF2	chr16:12629438-12630541	GM12878	blood:	n/a	n/a
7	ATF2	chr16:12629393-12630582	GM12878	blood:	n/a	n/a
8	ATF3	chr16:12635622-12635902	K562	blood:	n/a	n/a
9	BACH1	chr16:12633143-12633457	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr16:12632913-12633782	GM12878	blood:	n/a	n/a
11	BATF	chr16:12629274-12630385	GM12878	blood:	n/a	n/a
12	BATF	chr16:12632981-12633517	GM12878	blood:	n/a	n/a
13	BATF	chr16:12629811-12630325	GM12878	blood:	n/a	n/a
14	BCL11A	chr16:12633061-12633394	GM12878	blood:	n/a	n/a
15	BCL11A	chr16:12629549-12630405	GM12878	blood:	n/a	chr16:12629725-12629734
16	BCL11A	chr16:12632989-12633622	GM12878	blood:	n/a	n/a
17	BCL11A	chr16:12629995-12630330	GM12878	blood:	n/a	n/a
18	BCL3	chr16:12629874-12630293	GM12878	blood:	n/a	n/a
19	BCL3	chr16:12632947-12633510	GM12878	blood:	n/a	n/a
20	BCL3	chr16:12625852-12626126	GM12878	blood:	n/a	n/a
21	BCL3	chr16:12625872-12626086	GM12878	blood:	n/a	n/a
22	BCL3	chr16:12633003-12633718	GM12878	blood:	n/a	n/a
23	BCL3	chr16:12629387-12630458	GM12878	blood:	n/a	chr16:12629725-12629734
24	BCLAF1	chr16:12632953-12633687	GM12878	blood:	n/a	n/a
25	BCLAF1	chr16:12632789-12633730	GM12878	blood:	n/a	n/a
26	BCLAF1	chr16:12629181-12630446	GM12878	blood:	n/a	chr16:12629725-12629734
27	BCLAF1	chr16:12629271-12630517	GM12878	blood:	n/a	chr16:12629725-12629734
28	BHLHE40	chr16:12632599-12632757	K562	blood:	n/a	n/a
29	BHLHE40	chr16:12635567-12635885	K562	blood:	n/a	n/a
30	BHLHE40	chr16:12632579-12633590	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:12629326-12630373	GM12878	blood:	n/a	n/a
32	CEBPB	chr16:12623436-12623713	K562	blood:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
33	CEBPB	chr16:12635585-12635860	A549	lung:	n/a	chr16:12635747-12635758
34	CEBPB	chr16:12635656-12635804	K562	blood:	n/a	chr16:12635747-12635758
35	CEBPB	chr16:12625755-12626043	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:12633519-12633716	A549	lung:	n/a	n/a
37	CEBPB	chr16:12629933-12630195	GM12878	blood:	n/a	n/a
38	CEBPB	chr16:12623419-12623746	HepG2	liver:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
39	CEBPB	chr16:12623407-12623822	Hela-S3	cervix:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
40	CEBPB	chr16:12635566-12635904	IMR90	lung:	n/a	chr16:12635747-12635758
41	CEBPB	chr16:12635593-12635907	K562	blood:	n/a	chr16:12635747-12635758
42	CEBPB	chr16:12623483-12623827	MCF-7	breast:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
43	CEBPB	chr16:12624483-12624502	K562	blood:	n/a	n/a
44	CEBPB	chr16:12623475-12623675	A549	lung:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
45	CEBPB	chr16:12629765-12630542	GM12878	blood:	n/a	n/a
46	CEBPB	chr16:12636781-12638818	GM12878	blood:	n/a	n/a
47	CEBPB	chr16:12624417-12624559	HepG2	liver:	n/a	chr16:12624468-12624479
48	CEBPB	chr16:12623336-12623837	MCF-7	breast:	n/a	chr16:12623565-12623578 chr16:12623566-12623577
49	CEBPB	chr16:12635568-12635927	HepG2	liver:	n/a	chr16:12635747-12635758 chr16:12635897-12635908
50	CHD1	chr16:12632487-12632686	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12632861-12632911	SK-N-SH_RA	brain:	n/a
2	chr16:12625807-12625857	HCT-116	colon:	n/a
3	chr16:12632861-12632911	GM06990	blood:	n/a
4	chr16:12632861-12632911	HNPCEpiC	eye:	n/a
5	chr16:12625807-12625857	NT2-D1	testis:	n/a
6	chr16:12625807-12625857	AG04449	skin:	fetal
7	chr16:12625807-12625857	AG04450	lung:	fetal
8	chr16:12632861-12632911	HCF	heart:	n/a
9	chr16:12632861-12632911	HCM	heart:	n/a
10	chr16:12632861-12632911	Hepatocyte	liver:	n/a
11	chr16:12625807-12625857	GM12892	blood:	n/a
12	chr16:12632861-12632911	Caco-2	colon:	n/a
13	chr16:12632861-12632911	HRPEpiC	eye:	n/a
14	chr16:12625807-12625857	SK-N-SH_RA	brain:	n/a
15	chr16:12632861-12632911	ProgFib	skin:	n/a
16	chr16:12625807-12625857	NHDF-neo	bronchial:	n/a
17	chr16:12625807-12625857	ProgFib	skin:	n/a
18	chr16:12625807-12625857	ovcar-3	ovarian:	n/a
19	chr16:12625807-12625857	T-47D	breast:	n/a
20	chr16:12632861-12632911	RPTEC	kidney:	n/a
21	chr16:12632861-12632911	AoSMC	blood vessel:	n/a
22	chr16:12625807-12625857	AG10803	skin:	n/a
23	chr16:12632861-12632911	Hela-S3	cervix:	n/a
24	chr16:12632861-12632911	MCF10A-Er-Src	breast:	n/a
25	chr16:12625807-12625857	PANC-1	pancreas:	n/a
26	chr16:12632861-12632911	T-47D	breast:	n/a
27	chr16:12625807-12625857	GM12891	blood:	n/a
28	chr16:12625807-12625857	Hepatocyte	liver:	n/a
29	chr16:12632861-12632911	NB4	blood:	n/a
30	chr16:12625807-12625857	MCF10A-Er-Src	breast:	n/a
31	chr16:12625807-12625857	SAEC	small airway:	n/a
32	chr16:12632861-12632911	AG09309	skin:	n/a
33	chr16:12632861-12632911	BE2_C	brain:	n/a
34	chr16:12632861-12632911	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:12625807-12625857	HNPCEpiC	eye:	n/a
36	chr16:12625807-12625857	HCM	heart:	n/a
37	chr16:12625807-12625857	HEK293	kidney:	embryo
38	chr16:12625807-12625857	Caco-2	colon:	n/a
39	chr16:12625807-12625857	ECC-1	luminal epithelium:	n/a
40	chr16:12632861-12632911	NT2-D1	testis:	n/a
41	chr16:12625807-12625857	HPAEpiC	pulmonary alveolar:	n/a
42	chr16:12632861-12632911	HRCEpiC	kidney:	n/a
43	chr16:12632861-12632911	U87	brain:	n/a
44	chr16:12625807-12625857	HL-60	blood:	n/a
45	chr16:12625807-12625857	U87	brain:	n/a
46	chr16:12625807-12625857	CMK	blood:	n/a
47	chr16:12632861-12632911	BJ	skin:	n/a
48	chr16:12625807-12625857	HEEpiC	esophagus:	n/a
49	chr16:12632861-12632911	NHDF-neo	bronchial:	n/a
50	chr16:12632861-12632911	A549	lung:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:12615906..12618586-chr16:12621155..12622694,2	K562	blood:
2	chr16:12611118..12612757-chr16:12625721..12628602,2	MCF-7	breast:
3	chr16:12606559..12609069-chr16:12621569..12623714,2	MCF-7	breast:
4	chr16:12633130..12635327-chr16:12640812..12643626,2	K562	blood:
5	chr16:12563684..12565962-chr16:12618879..12621631,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000260601	TF binding region
ENSG00000260601	CpG island

Extended variants
information (count: 1933 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1933 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2269445	chr16:12620736-12620737	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs149835948	chr16:12620737-12620738	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146871702	chr16:12620744-12620745	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552222696	chr16:12620758-12620759	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569335169	chr16:12620781-12620782	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190200835	chr16:12620825-12620826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190013	chr16:12620829-12620830	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs72773328	chr16:12620830-12620831	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182833392	chr16:12620844-12620845	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575308716	chr16:12620856-12620857	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs80322340	chr16:12620861-12620862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577489545	chr16:12620885-12620886	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571579587	chr16:12620891-12620892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537600747	chr16:12620901-12620902	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534168647	chr16:12620912-12620913	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs547989215	chr16:12620931-12620932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115696945	chr16:12620932-12620933	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576078542	chr16:12620947-12620948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112638874	chr16:12620957-12620958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185702726	chr16:12620991-12620992	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561701799	chr16:12621006-12621007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527321489	chr16:12621024-12621025	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112702029	chr16:12621026-12621027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs6498315	chr16:12621038-12621039	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs6498316	chr16:12621052-12621053	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs61740759	chr16:12621054-12621055	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549573073	chr16:12621072-12621073	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61744575	chr16:12621073-12621074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114174994	chr16:12621095-12621096	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538331886	chr16:12621096-12621097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567410698	chr16:12621104-12621105	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568410792	chr16:12621105-12621106	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs201338197	chr16:12621123-12621124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189678267	chr16:12621130-12621131	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554462832	chr16:12621138-12621139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577621673	chr16:12621140-12621141	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370059830	chr16:12621154-12621155	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs762792	chr16:12621157-12621158	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs553306809	chr16:12621171-12621172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2269446	chr16:12621176-12621177	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs138235380	chr16:12621178-12621179	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561643309	chr16:12621181-12621182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs201464597	chr16:12621194-12621195	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367872730	chr16:12621217-12621218	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182640871	chr16:12621237-12621238	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558961153	chr16:12621244-12621245	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540624269	chr16:12621263-12621264	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563784591	chr16:12621274-12621275	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376757529	chr16:12621276-12621277	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs542418285	chr16:12621296-12621297	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Prostate cancer	18632612	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	21858162	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	23813976	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12598800-12622000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr16:12601400-12625400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr16:12602200-12622600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr16:12603200-12626400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr16:12605600-12625000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr16:12605800-12632200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr16:12606000-12623600	Weak transcription	Gastric	stomach
8	chr16:12606000-12632000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr16:12606200-12632400	Weak transcription	Right Atrium	heart
10	chr16:12607000-12623600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr16:12607000-12625600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr16:12607800-12626200	Weak transcription	Brain Germinal Matrix	brain
13	chr16:12608000-12632400	Weak transcription	Rectal Smooth Muscle	rectum
14	chr16:12608200-12624000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr16:12608400-12623800	Weak transcription	Brain Angular Gyrus	brain
16	chr16:12608400-12623800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr16:12608400-12623800	Weak transcription	Brain Substantia Nigra	brain
18	chr16:12608800-12623600	Weak transcription	Brain Hippocampus Middle	brain
19	chr16:12609000-12623600	Weak transcription	Brain Anterior Caudate	brain
20	chr16:12609600-12623600	Weak transcription	Duodenum Mucosa	Duodenum
21	chr16:12609600-12623800	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr16:12610000-12625000	Weak transcription	Fetal Stomach	stomach
23	chr16:12610000-12632400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr16:12610800-12632200	Weak transcription	Psoas Muscle	Psoas
25	chr16:12611600-12632400	Weak transcription	Left Ventricle	heart
26	chr16:12612000-12625400	Weak transcription	Ovary	ovary
27	chr16:12612200-12623800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr16:12612400-12626600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr16:12612400-12626600	Weak transcription	Right Ventricle	heart
30	chr16:12612400-12632000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr16:12612600-12623000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr16:12612600-12626400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr16:12613000-12625400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
35	chr16:12614400-12622400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr16:12614400-12623400	Weak transcription	Placenta	Placenta
37	chr16:12616000-12626600	Weak transcription	Thymus	Thymus
38	chr16:12616200-12623600	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr16:12616200-12623800	Weak transcription	Aorta	Aorta
40	chr16:12617000-12621400	Strong transcription	Primary B cells from peripheral blood	blood
41	chr16:12617000-12626600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr16:12617400-12627000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr16:12618000-12623800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr16:12618200-12621000	Strong transcription	Primary T cells from cord blood	blood
45	chr16:12618400-12620800	Strong transcription	Lung	lung
46	chr16:12618400-12621000	Strong transcription	Adipose Nuclei	Adipose
47	chr16:12618600-12626200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr16:12619000-12622400	Weak transcription	Primary B cells from cord blood	blood
49	chr16:12619000-12626000	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr16:12619000-12632200	Weak transcription	Skeletal Muscle Male	skeletal muscle

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