Variant report

Variant	nsv571465
Chromosome Location	chr16:12625395-12639800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:589)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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	ARID3A	chr16:12637659-12638979	HepG2	liver:	n/a	n/a
3	ATF1	chr16:12635640-12635845	K562	blood:	n/a	n/a
4	ATF1	chr16:12633157-12633742	K562	blood:	n/a	n/a
5	ATF2	chr16:12639568-12640202	GM12878	blood:	n/a	n/a
6	ATF2	chr16:12637898-12638419	GM12878	blood:	n/a	n/a
7	ATF2	chr16:12632809-12633811	GM12878	blood:	n/a	n/a
8	ATF2	chr16:12639659-12640191	GM12878	blood:	n/a	n/a
9	ATF2	chr16:12632602-12633937	GM12878	blood:	n/a	n/a
10	ATF2	chr16:12637132-12637535	GM12878	blood:	n/a	n/a
11	ATF2	chr16:12629393-12630582	GM12878	blood:	n/a	n/a
12	ATF2	chr16:12629438-12630541	GM12878	blood:	n/a	n/a
13	ATF2	chr16:12637025-12638683	GM12878	blood:	n/a	n/a
14	ATF3	chr16:12635622-12635902	K562	blood:	n/a	n/a
15	BACH1	chr16:12633143-12633457	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr16:12632913-12633782	GM12878	blood:	n/a	n/a
17	BATF	chr16:12637100-12637603	GM12878	blood:	n/a	n/a
18	BATF	chr16:12632981-12633517	GM12878	blood:	n/a	n/a
19	BATF	chr16:12629811-12630325	GM12878	blood:	n/a	n/a
20	BATF	chr16:12629274-12630385	GM12878	blood:	n/a	n/a
21	BATF	chr16:12637164-12637545	GM12878	blood:	n/a	n/a
22	BATF	chr16:12637743-12638321	GM12878	blood:	n/a	chr16:12637886-12637896
23	BCL11A	chr16:12629549-12630405	GM12878	blood:	n/a	chr16:12629725-12629734
24	BCL11A	chr16:12632989-12633622	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:12637150-12637604	GM12878	blood:	n/a	n/a
26	BCL11A	chr16:12637890-12638396	GM12878	blood:	n/a	n/a
27	BCL11A	chr16:12633061-12633394	GM12878	blood:	n/a	n/a
28	BCL11A	chr16:12629995-12630330	GM12878	blood:	n/a	n/a
29	BCL11A	chr16:12637166-12637556	GM12878	blood:	n/a	n/a
30	BCL3	chr16:12637811-12638327	GM12878	blood:	n/a	n/a
31	BCL3	chr16:12637165-12637549	GM12878	blood:	n/a	n/a
32	BCL3	chr16:12632947-12633510	GM12878	blood:	n/a	n/a
33	BCL3	chr16:12629387-12630458	GM12878	blood:	n/a	chr16:12629725-12629734
34	BCL3	chr16:12625872-12626086	GM12878	blood:	n/a	n/a
35	BCL3	chr16:12633003-12633718	GM12878	blood:	n/a	n/a
36	BCL3	chr16:12629874-12630293	GM12878	blood:	n/a	n/a
37	BCL3	chr16:12625852-12626126	GM12878	blood:	n/a	n/a
38	BCLAF1	chr16:12629181-12630446	GM12878	blood:	n/a	chr16:12629725-12629734
39	BCLAF1	chr16:12632953-12633687	GM12878	blood:	n/a	n/a
40	BCLAF1	chr16:12637669-12638335	GM12878	blood:	n/a	n/a
41	BCLAF1	chr16:12637158-12638446	GM12878	blood:	n/a	n/a
42	BCLAF1	chr16:12632789-12633730	GM12878	blood:	n/a	n/a
43	BCLAF1	chr16:12629271-12630517	GM12878	blood:	n/a	chr16:12629725-12629734
44	BCLAF1	chr16:12637031-12637643	GM12878	blood:	n/a	n/a
45	BHLHE40	chr16:12639724-12639965	GM12878	blood:	n/a	n/a
46	BHLHE40	chr16:12635567-12635885	K562	blood:	n/a	n/a
47	BHLHE40	chr16:12632599-12632757	K562	blood:	n/a	n/a
48	BHLHE40	chr16:12629326-12630373	GM12878	blood:	n/a	n/a
49	BHLHE40	chr16:12637173-12637633	GM12878	blood:	n/a	n/a
50	BHLHE40	chr16:12637849-12638304	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:12637499-12637549	GM12891	blood:	n/a
2	chr16:12625807-12625857	HRCEpiC	kidney:	n/a
3	chr16:12632861-12632911	U87	brain:	n/a
4	chr16:12637499-12637549	HCPEpiC	choroid plexus:	n/a
5	chr16:12632861-12632911	HEK293	kidney:	embryo
6	chr16:12637499-12637549	HepG2	liver:	n/a
7	chr16:12632861-12632911	HCM	heart:	n/a
8	chr16:12632861-12632911	SK-N-SH_RA	brain:	n/a
9	chr16:12632861-12632911	NT2-D1	testis:	n/a
10	chr16:12637499-12637549	RPTEC	kidney:	n/a
11	chr16:12632861-12632911	HIPEpiC	eye:	n/a
12	chr16:12625807-12625857	HRE	kidney:	n/a
13	chr16:12637499-12637549	HRE	kidney:	n/a
14	chr16:12625807-12625857	GM19239	blood:	n/a
15	chr16:12625807-12625857	HL-60	blood:	n/a
16	chr16:12632861-12632911	PrEC	prostate:	n/a
17	chr16:12632861-12632911	HPAEpiC	pulmonary alveolar:	n/a
18	chr16:12625807-12625857	HPAEpiC	pulmonary alveolar:	n/a
19	chr16:12632861-12632911	SKMC	muscle:	n/a
20	chr16:12632861-12632911	GM19239	blood:	n/a
21	chr16:12632861-12632911	NHDF-neo	bronchial:	n/a
22	chr16:12625807-12625857	AG10803	skin:	n/a
23	chr16:12625807-12625857	MCF-7	breast:	n/a
24	chr16:12632861-12632911	SK-N-SH	brain:	n/a
25	chr16:12632861-12632911	HCT-116	colon:	n/a
26	chr16:12625807-12625857	HCPEpiC	choroid plexus:	n/a
27	chr16:12637499-12637549	HIPEpiC	eye:	n/a
28	chr16:12625807-12625857	HNPCEpiC	eye:	n/a
29	chr16:12625807-12625857	HepG2	liver:	n/a
30	chr16:12625807-12625857	SAEC	small airway:	n/a
31	chr16:12637499-12637549	HMEC	breast:	n/a
32	chr16:12632861-12632911	HCF	heart:	n/a
33	chr16:12637499-12637549	HAEpiC	amniotic membrane:	n/a
34	chr16:12637499-12637549	AoSMC	blood vessel:	n/a
35	chr16:12632861-12632911	HRPEpiC	eye:	n/a
36	chr16:12625807-12625857	K562	blood:	n/a
37	chr16:12632861-12632911	NH-A	brain:	n/a
38	chr16:12637499-12637549	HCT-116	colon:	n/a
39	chr16:12637499-12637549	AG10803	skin:	n/a
40	chr16:12625807-12625857	HAEpiC	amniotic membrane:	n/a
41	chr16:12637499-12637549	Hela-S3	cervix:	n/a
42	chr16:12625807-12625857	ProgFib	skin:	n/a
43	chr16:12632861-12632911	HRE	kidney:	n/a
44	chr16:12637499-12637549	HRCEpiC	kidney:	n/a
45	chr16:12637499-12637549	HPAEpiC	pulmonary alveolar:	n/a
46	chr16:12625807-12625857	SK-N-MC	brain:	n/a
47	chr16:12632861-12632911	AG10803	skin:	n/a
48	chr16:12632861-12632911	Jurkat	blood:	n/a
49	chr16:12625807-12625857	HIPEpiC	eye:	n/a
50	chr16:12637499-12637549	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:12611118..12612757-chr16:12625721..12628602,2	MCF-7	breast:
2	chr16:12633130..12635327-chr16:12640812..12643626,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHISA9-4	chr16:12639339-12639458	ENSG00000260601.1

No data

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

Extended variants
information (count: 2002 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2002 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1794304	chr16:12625395-12625396	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531880159	chr16:12625404-12625405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145965786	chr16:12625407-12625408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529539280	chr16:12625410-12625411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542948413	chr16:12625417-12625418	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs559486294	chr16:12625433-12625434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139889346	chr16:12625449-12625450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551143323	chr16:12625454-12625455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62026883	chr16:12625481-12625482	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs192715943	chr16:12625490-12625491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150676571	chr16:12625513-12625514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539161742	chr16:12625515-12625516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77411296	chr16:12625517-12625518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372490083	chr16:12625526-12625527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553316390	chr16:12625532-12625533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566518574	chr16:12625535-12625536	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538827186	chr16:12625542-12625543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557929295	chr16:12625552-12625553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149858067	chr16:12625559-12625560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552371705	chr16:12625566-12625567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548031862	chr16:12625574-12625575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571077294	chr16:12625578-12625579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76385589	chr16:12625579-12625580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115955584	chr16:12625587-12625588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184742617	chr16:12625592-12625593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534779916	chr16:12625619-12625620	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs169774	chr16:12625626-12625627	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs528638922	chr16:12625628-12625629	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545577151	chr16:12625630-12625631	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565388143	chr16:12625642-12625643	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530610357	chr16:12625647-12625648	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373641353	chr16:12625654-12625655	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145682586	chr16:12625658-12625659	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549974486	chr16:12625659-12625660	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184127	chr16:12625662-12625663	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs1794305	chr16:12625689-12625690	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7192166	chr16:12625699-12625700	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189516469	chr16:12625735-12625736	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538595225	chr16:12625741-12625742	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552344495	chr16:12625758-12625759	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs114976000	chr16:12625763-12625764	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537114461	chr16:12625781-12625782	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373067167	chr16:12625789-12625790	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557055090	chr16:12625790-12625791	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573653138	chr16:12625791-12625792	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181519563	chr16:12625807-12625808	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184654083	chr16:12625811-12625812	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189789776	chr16:12625829-12625830	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145387972	chr16:12625832-12625833	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368537710	chr16:12625836-12625837	Enhancers Weak transcription Strong transcription	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
Mental retardation	17847001	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12601400-12625400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr16:12603200-12626400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr16:12605800-12632200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr16:12606000-12632000	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr16:12606200-12632400	Weak transcription	Right Atrium	heart
6	chr16:12607000-12625600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr16:12607800-12626200	Weak transcription	Brain Germinal Matrix	brain
8	chr16:12608000-12632400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr16:12610000-12632400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr16:12610800-12632200	Weak transcription	Psoas Muscle	Psoas
11	chr16:12611600-12632400	Weak transcription	Left Ventricle	heart
12	chr16:12612000-12625400	Weak transcription	Ovary	ovary
13	chr16:12612400-12626600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr16:12612400-12626600	Weak transcription	Right Ventricle	heart
15	chr16:12612400-12632000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr16:12612600-12626400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr16:12613000-12625400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr16:12613000-12670800	Weak transcription	Pancreas	Pancrea
19	chr16:12616000-12626600	Weak transcription	Thymus	Thymus
20	chr16:12617000-12626600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr16:12617400-12627000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr16:12618600-12626200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr16:12619000-12626000	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr16:12619000-12632200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr16:12619800-12632000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr16:12620600-12625400	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr16:12620600-12630200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr16:12620800-12625400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr16:12620800-12625400	Weak transcription	Liver	Liver
30	chr16:12621000-12632400	Weak transcription	Adipose Nuclei	Adipose
31	chr16:12621600-12625800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr16:12621600-12628000	Weak transcription	GM12878-XiMat	blood
33	chr16:12622400-12625800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr16:12623000-12625400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr16:12623000-12625600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr16:12623600-12625600	Enhancers	Duodenum Mucosa	Duodenum
37	chr16:12623600-12627200	Enhancers	Brain Hippocampus Middle	brain
38	chr16:12623800-12625400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr16:12623800-12627000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr16:12623800-12627400	Enhancers	Brain Substantia Nigra	brain
41	chr16:12624000-12625400	Weak transcription	Placenta	Placenta
42	chr16:12624000-12625400	Weak transcription	Gastric	stomach
43	chr16:12624000-12625600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr16:12624000-12631600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr16:12624000-12632000	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr16:12624000-12632400	Weak transcription	Aorta	Aorta
47	chr16:12624000-12632600	Weak transcription	Lung	lung
48	chr16:12624200-12625400	Weak transcription	Brain Angular Gyrus	brain
49	chr16:12624200-12625600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr16:12624200-12625600	Weak transcription	Brain Anterior Caudate	brain

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