Variant report

Variant	nsv984333
Chromosome Location	chr16:46612389-46633995
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:46616234-46616382	K562	blood:	n/a	n/a
2	ATF1	chr16:46617078-46617217	K562	blood:	n/a	n/a
3	BACH1	chr16:46625336-46625378	K562	blood:	n/a	n/a
4	CBX3	chr16:46620089-46620441	K562	blood:	n/a	n/a
5	CBX3	chr16:46620112-46620343	K562	blood:	n/a	n/a
6	CEBPB	chr16:46614646-46614761	IMR90	lung:	n/a	n/a
7	CEBPB	chr16:46614642-46614766	K562	blood:	n/a	n/a
8	CEBPB	chr16:46616290-46616539	K562	blood:	n/a	n/a
9	CEBPB	chr16:46615792-46615910	HepG2	liver:	n/a	chr16:46615817-46615828
10	CEBPB	chr16:46614675-46614765	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr16:46615804-46615858	K562	blood:	n/a	chr16:46615817-46615828
12	CEBPD	chr16:46616999-46617344	K562	blood:	n/a	n/a
13	CTCF	chr16:46624257-46624347	GM13977	blood:	n/a	n/a
14	CTCF	chr16:46629500-46629650	GM06990	blood:	n/a	n/a
15	CTCF	chr16:46632740-46632890	AG09319	gingival:	n/a	n/a
16	CTCF	chr16:46614643-46614668	Lung_OC	lung:	n/a	n/a
17	EGR1	chr16:46616941-46617237	K562	blood:	n/a	n/a
18	EP300	chr16:46616263-46616460	K562	blood:	n/a	n/a
19	EP300	chr16:46617119-46617273	K562	blood:	n/a	n/a
20	FOS	chr16:46630876-46631171	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr16:46630881-46631153	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr16:46630977-46631146	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr16:46630871-46631184	MCF10A-Er-Src	breast:	n/a	n/a
24	GATA1	chr16:46617824-46618502	PBDE	blood:	n/a	chr16:46618002-46618011
25	GATA1	chr16:46616989-46617412	PBDE	blood:	n/a	chr16:46617174-46617190
26	IRF1	chr16:46616347-46616378	K562	blood:	n/a	n/a
27	JUN	chr16:46628721-46628823	K562	blood:	n/a	n/a
28	JUND	chr16:46617873-46618046	K562	blood:	n/a	chr16:46618004-46618013
29	KAP1	chr16:46620177-46620451	K562	blood:	n/a	n/a
30	MAFF	chr16:46619978-46620262	HepG2	liver:	n/a	n/a
31	MAFF	chr16:46625194-46625547	HepG2	liver:	n/a	chr16:46625351-46625369
32	MAFF	chr16:46625187-46625549	K562	blood:	n/a	chr16:46625351-46625369
33	MAFF	chr16:46620084-46620133	K562	blood:	n/a	n/a
34	MAFF	chr16:46613004-46613095	HepG2	liver:	n/a	chr16:46613026-46613044
35	MAFK	chr16:46619985-46620238	IMR90	lung:	n/a	n/a
36	MAFK	chr16:46625181-46625550	HepG2	liver:	n/a	chr16:46625353-46625368
37	MAFK	chr16:46625182-46625545	IMR90	lung:	n/a	chr16:46625353-46625368
38	MAFK	chr16:46625194-46625536	K562	blood:	n/a	chr16:46625353-46625368
39	MAFK	chr16:46629934-46630134	HepG2	liver:	n/a	chr16:46630093-46630107 chr16:46630092-46630108 chr16:46630090-46630110
40	MAFK	chr16:46625214-46625626	GM12878	blood:	n/a	chr16:46625353-46625368
41	MAFK	chr16:46625245-46625515	Hela-S3	cervix:	n/a	chr16:46625353-46625368
42	MAFK	chr16:46625187-46625541	HepG2	liver:	n/a	chr16:46625353-46625368
43	MAFK	chr16:46619965-46620272	HepG2	liver:	n/a	n/a
44	MAFK	chr16:46625276-46625515	H1-hESC	embryonic stem cell:	n/a	chr16:46625353-46625368
45	MAFK	chr16:46619994-46620239	HepG2	liver:	n/a	n/a
46	MAFK	chr16:46613080-46613083	HepG2	liver:	n/a	n/a
47	MAFK	chr16:46612973-46613143	HepG2	liver:	n/a	chr16:46613030-46613044 chr16:46613027-46613043 chr16:46613032-46613043
48	MAFK	chr16:46620077-46620174	K562	blood:	n/a	n/a
49	MAZ	chr16:46616355-46616502	K562	blood:	n/a	n/a
50	MYC	chr16:46617006-46617165	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46615086-46615136	NHDF-neo	bronchial:	n/a
2	chr16:46615086-46615136	HEK293	kidney:	embryo
3	chr16:46615086-46615136	HNPCEpiC	eye:	n/a
4	chr16:46615086-46615136	T-47D	breast:	n/a
5	chr16:46615086-46615136	RPTEC	kidney:	n/a
6	chr16:46615086-46615136	NH-A	brain:	n/a
7	chr16:46615086-46615136	NHBE	bronchial:	n/a
8	chr16:46615086-46615136	ProgFib	skin:	n/a
9	chr16:46615086-46615136	AoSMC	blood vessel:	n/a
10	chr16:46615086-46615136	SAEC	small airway:	n/a
11	chr16:46615086-46615136	GM19239	blood:	n/a
12	chr16:46615086-46615136	HEEpiC	esophagus:	n/a
13	chr16:46615086-46615136	BE2_C	brain:	n/a
14	chr16:46615086-46615136	ECC-1	luminal epithelium:	n/a
15	chr16:46615086-46615136	GM12892	blood:	n/a
16	chr16:46615086-46615136	SK-N-SH	brain:	n/a
17	chr16:46615086-46615136	LNCaP	prostate:	n/a
18	chr16:46615086-46615136	GM06990	blood:	n/a
19	chr16:46615086-46615136	HUVEC	blood vessel:	n/a
20	chr16:46615086-46615136	HRPEpiC	eye:	n/a
21	chr16:46615086-46615136	AG10803	skin:	n/a
22	chr16:46615086-46615136	HRCEpiC	kidney:	n/a
23	chr16:46615086-46615136	HepG2	liver:	n/a
24	chr16:46615086-46615136	K562	blood:	n/a
25	chr16:46615086-46615136	HCPEpiC	choroid plexus:	n/a
26	chr16:46615086-46615136	HCT-116	colon:	n/a
27	chr16:46615086-46615136	SKMC	muscle:	n/a
28	chr16:46615086-46615136	AG04449	skin:	fetal
29	chr16:46615086-46615136	AG09319	gingival:	n/a
30	chr16:46615086-46615136	AG04450	lung:	fetal
31	chr16:46615086-46615136	H1-hESC	embryonic stem cell:	embryo
32	chr16:46615086-46615136	BJ	skin:	n/a
33	chr16:46615086-46615136	HIPEpiC	eye:	n/a
34	chr16:46615086-46615136	SK-N-MC	brain:	n/a
35	chr16:46615086-46615136	AG09309	skin:	n/a
36	chr16:46615086-46615136	U87	brain:	n/a
37	chr16:46615086-46615136	ovcar-3	ovarian:	n/a
38	chr16:46615086-46615136	HL-60	blood:	n/a
39	chr16:46615086-46615136	HPAEpiC	pulmonary alveolar:	n/a
40	chr16:46615086-46615136	HMEC	breast:	n/a
41	chr16:46615086-46615136	IMR90	lung:	fetal
42	chr16:46615086-46615136	HCF	heart:	n/a
43	chr16:46615086-46615136	PFSK-1	brain:	n/a
44	chr16:46615086-46615136	HAEpiC	amniotic membrane:	n/a
45	chr16:46615086-46615136	GM12878	blood:	n/a
46	chr16:46615086-46615136	Hela-S3	cervix:	n/a
47	chr16:46615086-46615136	MCF10A-Er-Src	breast:	n/a
48	chr16:46615086-46615136	Caco-2	colon:	n/a
49	chr16:46615086-46615136	NT2-D1	testis:	n/a
50	chr16:46615086-46615136	A549	lung:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46627736..46629535-chr16:46636596..46638732,2	K562	blood:
2	chr16:46607322..46610381-chr16:46616231..46620606,3	K562	blood:
3	chr16:46632468..46635763-chr16:46636250..46638765,3	K562	blood:
4	chr16:46624881..46627555-chr16:46632548..46635416,2	K562	blood:
5	chr16:46632677..46635528-chr16:46640441..46642160,2	K562	blood:
6	chr16:46598432..46601412-chr16:46613348..46615647,2	K562	blood:
7	chr16:46628966..46631349-chr16:46648629..46650816,2	K562	blood:
8	chr16:46624881..46627555-chr16:46632548..46635416,2	K562	blood:

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SHCBP1	hsa-miR-33a-5p	chr16:46615444-46615464
2	SHCBP1	hsa-miR-340-5p	chr16:46614530-46614551
3	SHCBP1	hsa-miR-19b-3p	chr16:46615488-46615482
4	SHCBP1	hsa-miR-425-5p	chr16:46615267-46615289
5	SHCBP1	hsa-miR-19b-3p	chr16:46615193-46615218
6	SHCBP1	hsa-miR-19b-3p	chr16:46615604-46615597
7	SHCBP1	hsa-miR-340-5p	chr16:46615462-46615482
8	SHCBP1	hsa-miR-19b-3p	chr16:46615598-46615621

Variant related genes	Relation type
SHCBP1	TF binding region
SHCBP1	CpG island
ENSG00000171241	chromatin interactions
ENSG00000260251	chromatin interactions

Extended variants
information (count: 650 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:650 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190070659	chr16:46612425-46612426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542960110	chr16:46612562-46612563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371717553	chr16:46612590-46612591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375969224	chr16:46612774-46612775	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6598661	chr16:46612780-46612781	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536590627	chr16:46612796-46612797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139937585	chr16:46612812-46612813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368568048	chr16:46612825-46612826	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573133180	chr16:46612883-46612884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371926728	chr16:46612913-46612914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533391379	chr16:46612950-46612951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534008341	chr16:46613049-46613050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558649293	chr16:46613052-46613053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577129193	chr16:46613083-46613084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374919534	chr16:46613108-46613109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76057578	chr16:46613135-46613136	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77415906	chr16:46613136-46613137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561037727	chr16:46613158-46613159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs368992701	chr16:46613238-46613239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574676068	chr16:46613272-46613273	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577442531	chr16:46613291-46613292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531565440	chr16:46613293-46613294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542187296	chr16:46613423-46613424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs60938441	chr16:46613451-46613452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527501804	chr16:46613504-46613505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143924159	chr16:46613533-46613534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147239153	chr16:46613541-46613542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531158989	chr16:46613576-46613577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568004568	chr16:46613713-46613714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536531550	chr16:46613777-46613778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576425960	chr16:46613821-46613822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183058565	chr16:46613898-46613899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566697473	chr16:46613906-46613907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534141539	chr16:46613930-46613931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs148725754	chr16:46613973-46613974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565032116	chr16:46613977-46613978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577272366	chr16:46613986-46613987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538003884	chr16:46613988-46613989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558338612	chr16:46614056-46614057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537561610	chr16:46614067-46614068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199591996	chr16:46614116-46614117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556515195	chr16:46614117-46614118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574777135	chr16:46614232-46614233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375868096	chr16:46614302-46614303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542125888	chr16:46614355-46614356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187394389	chr16:46614402-46614403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114722965	chr16:46614478-46614479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12928618	chr16:46614595-46614596	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568268549	chr16:46614643-46614644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534219469	chr16:46614694-46614695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Autism	19955444	CNVD
Schizophrenia	19955444	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
Non-syndromic sensorineural hearing loss	18451855	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	chr16:46607000-46616000	Weak transcription	Brain Germinal Matrix	brain
2	chr16:46607200-46614800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr16:46607600-46614800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr16:46607600-46615000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr16:46607600-46615000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr16:46607800-46612800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr16:46607800-46614600	Weak transcription	HUVEC	blood vessel
8	chr16:46607800-46614800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr16:46607800-46614800	Weak transcription	GM12878-XiMat	blood
10	chr16:46607800-46628800	Weak transcription	NHEK	skin
11	chr16:46608000-46614600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr16:46608000-46614600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr16:46608000-46614800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr16:46608000-46615000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr16:46608000-46615000	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr16:46608000-46615000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:46608000-46615000	Weak transcription	HSMM	muscle
18	chr16:46608000-46615000	Weak transcription	K562	blood
19	chr16:46608000-46615200	Weak transcription	HMEC	breast
20	chr16:46608000-46615200	Weak transcription	NH-A	brain
21	chr16:46608000-46615200	Weak transcription	NHDF-Ad	bronchial
22	chr16:46608000-46615400	Weak transcription	Osteobl	bone
23	chr16:46608000-46615600	Weak transcription	HepG2	liver
24	chr16:46608000-46615800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr16:46608000-46615800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr16:46608000-46616200	Weak transcription	A549	lung
27	chr16:46608000-46616400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr16:46608000-46617000	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr16:46608000-46619000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr16:46608000-46619800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr16:46608000-46629000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr16:46608000-46631000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr16:46608000-46633400	Weak transcription	Hela-S3	cervix
34	chr16:46608000-46637400	Weak transcription	NHLF	lung
35	chr16:46608000-46654200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr16:46608200-46614600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr16:46608200-46614600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr16:46608200-46615600	Weak transcription	Fetal Stomach	stomach
39	chr16:46609000-46614800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr16:46609200-46615000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr16:46609400-46615600	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr16:46609400-46646400	Weak transcription	Fetal Heart	heart
43	chr16:46610200-46614600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr16:46610200-46615000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:46610400-46619600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr16:46610600-46613400	Strong transcription	Dnd41	blood
47	chr16:46610600-46615000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr16:46611200-46616400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr16:46611800-46614600	Weak transcription	Primary hematopoietic stem cells	blood
50	chr16:46611800-46615000	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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