Variant report

Variant	nsv917270
Chromosome Location	chr16:46500615-46605059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:549)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 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	BACH1	chr16:46530690-46530890	K562	blood:	n/a	n/a
2	BACH1	chr16:46530728-46530816	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr16:46588341-46588614	GM12878	blood:	n/a	n/a
4	BHLHE40	chr16:46603093-46603220	K562	blood:	n/a	n/a
5	CEBPB	chr16:46553020-46553329	HepG2	liver:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
6	CEBPB	chr16:46553053-46553266	Hela-S3	cervix:	n/a	chr16:46553164-46553181 chr16:46553167-46553180
7	CEBPB	chr16:46534572-46534639	HepG2	liver:	n/a	n/a
8	CTCF	chr16:46588380-46588530	HMEC	breast:	n/a	n/a
9	CTCF	chr16:46588420-46588570	AG09309	skin:	n/a	n/a
10	CTCF	chr16:46588340-46588490	GM06990	blood:	n/a	n/a
11	CTCF	chr16:46508540-46508690	A549	lung:	n/a	n/a
12	CTCF	chr16:46588322-46588569	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr16:46588360-46588510	GM12801	blood:	n/a	n/a
14	CTCF	chr16:46588311-46588605	GM19240	blood:	n/a	n/a
15	CTCF	chr16:46588400-46588550	HVMF	connective:	n/a	n/a
16	CTCF	chr16:46516920-46517070	Caco-2	colon:	n/a	n/a
17	CTCF	chr16:46516880-46517030	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr16:46508420-46508570	HEK293	kidney:	n/a	n/a
19	CTCF	chr16:46588380-46588530	Caco-2	colon:	n/a	n/a
20	CTCF	chr16:46588324-46588611	GM19239	blood:	n/a	n/a
21	CTCF	chr16:46588316-46588592	NHEK	skin:	n/a	n/a
22	CTCF	chr16:46588329-46588598	MCF-7	breast:	n/a	n/a
23	CTCF	chr16:46588360-46588510	AG09319	gingival:	n/a	n/a
24	CTCF	chr16:46588188-46588686	HepG2	liver:	n/a	n/a
25	CTCF	chr16:46588380-46588530	GM12867	blood:	n/a	n/a
26	CTCF	chr16:46516900-46517050	Caco-2	colon:	n/a	n/a
27	CTCF	chr16:46516880-46517030	K562	blood:	n/a	n/a
28	CTCF	chr16:46588360-46588510	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr16:46587940-46588090	AG04450	lung:	n/a	n/a
30	CTCF	chr16:46516902-46517098	K562	blood:	n/a	n/a
31	CTCF	chr16:46588340-46588490	WI-38	lung:	n/a	n/a
32	CTCF	chr16:46588360-46588510	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr16:46588360-46588510	Caco-2	colon:	n/a	n/a
34	CTCF	chr16:46588320-46588470	GM12878	blood:	n/a	n/a
35	CTCF	chr16:46588340-46588490	NB4	blood:	n/a	n/a
36	CTCF	chr16:46516940-46517090	A549	lung:	n/a	n/a
37	CTCF	chr16:46588289-46588556	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr16:46588308-46588600	GM19238	blood:	n/a	n/a
39	CTCF	chr16:46588380-46588530	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr16:46516975-46517025	GM12878	blood:	n/a	n/a
41	CTCF	chr16:46516875-46517117	MCF-7	breast:	n/a	n/a
42	CTCF	chr16:46588380-46588530	GM12868	blood:	n/a	n/a
43	CTCF	chr16:46588360-46588510	BJ	skin:	n/a	n/a
44	CTCF	chr16:46588360-46588510	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr16:46588360-46588510	AG10803	skin:	n/a	n/a
46	CTCF	chr16:46588400-46588550	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr16:46588345-46588560	GM13976	blood:	n/a	n/a
48	CTCF	chr16:46588360-46588510	HPF	lung:	n/a	n/a
49	CTCF	chr16:46588700-46588850	GM12875	blood:	n/a	n/a
50	CTCF	chr16:46588180-46588701	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46603191-46603241	T-47D	breast:	n/a
2	chr16:46603191-46603241	H1-hESC	embryonic stem cell:	embryo
3	chr16:46603321-46603371	GM06990	blood:	n/a
4	chr16:46588509-46588559	LNCaP	prostate:	n/a
5	chr16:46603015-46603065	AG09319	gingival:	n/a
6	chr16:46603021-46603071	GM19239	blood:	n/a
7	chr16:46603059-46603109	GM19239	blood:	n/a
8	chr16:46602737-46602787	NHDF-neo	bronchial:	n/a
9	chr16:46602737-46602787	GM19239	blood:	n/a
10	chr16:46603059-46603109	ECC-1	luminal epithelium:	n/a
11	chr16:46604297-46604347	HCF	heart:	n/a
12	chr16:46603021-46603071	HCPEpiC	choroid plexus:	n/a
13	chr16:46603321-46603371	AG04449	skin:	fetal
14	chr16:46603259-46603309	HRPEpiC	eye:	n/a
15	chr16:46603021-46603071	GM12878	blood:	n/a
16	chr16:46603321-46603371	GM12878	blood:	n/a
17	chr16:46603059-46603109	HUVEC	blood vessel:	n/a
18	chr16:46604297-46604347	GM12892	blood:	n/a
19	chr16:46603059-46603109	AG09319	gingival:	n/a
20	chr16:46603321-46603371	K562	blood:	n/a
21	chr16:46603059-46603109	GM06990	blood:	n/a
22	chr16:46603015-46603065	MCF10A-Er-Src	breast:	n/a
23	chr16:46604297-46604347	NHBE	bronchial:	n/a
24	chr16:46603015-46603065	PFSK-1	brain:	n/a
25	chr16:46603015-46603065	K562	blood:	n/a
26	chr16:46603191-46603241	Caco-2	colon:	n/a
27	chr16:46588509-46588559	NHDF-neo	bronchial:	n/a
28	chr16:46603321-46603371	AG09309	skin:	n/a
29	chr16:46603259-46603309	IMR90	lung:	fetal
30	chr16:46588509-46588559	SK-N-MC	brain:	n/a
31	chr16:46603321-46603371	BE2_C	brain:	n/a
32	chr16:46603015-46603065	GM19239	blood:	n/a
33	chr16:46604297-46604347	AG09319	gingival:	n/a
34	chr16:46603259-46603309	HNPCEpiC	eye:	n/a
35	chr16:46603321-46603371	HRPEpiC	eye:	n/a
36	chr16:46602737-46602787	HCT-116	colon:	n/a
37	chr16:46603259-46603309	SK-N-MC	brain:	n/a
38	chr16:46603021-46603071	HNPCEpiC	eye:	n/a
39	chr16:46603021-46603071	AG04449	skin:	fetal
40	chr16:46603021-46603071	GM06990	blood:	n/a
41	chr16:46603015-46603065	NB4	blood:	n/a
42	chr16:46603015-46603065	HAEpiC	amniotic membrane:	n/a
43	chr16:46603021-46603071	NB4	blood:	n/a
44	chr16:46588509-46588559	HCF	heart:	n/a
45	chr16:46603259-46603309	A549	lung:	n/a
46	chr16:46602737-46602787	HL-60	blood:	n/a
47	chr16:46602737-46602787	AoSMC	blood vessel:	n/a
48	chr16:46603059-46603109	Jurkat	blood:	n/a
49	chr16:46603321-46603371	U87	brain:	n/a
50	chr16:46603021-46603071	NH-A	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:46588077..46588805-chr16:46640597..46641513,2	MCF-7	breast:
2	chr16:46589331..46591714-chr16:46654314..46656100,2	K562	blood:
3	chr16:46588378..46588920-chr16:46662972..46663507,2	K562	blood:
4	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
5	chr16:46530274..46532917-chr16:46535064..46536684,2	K562	blood:
6	chr16:46598432..46601412-chr16:46613348..46615647,2	K562	blood:
7	chr11:125334060..125334821-chr16:46593821..46594420,2	HCT-116	colon:
8	chr16:46601237..46602830-chr16:46605603..46608385,2	K562	blood:
9	chr16:46603053..46604562-chr16:46606887..46609535,2	MCF-7	breast:
10	chr16:46511252..46512930-chr16:46534367..46536672,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SHCBP1-3	chr16:46509678-46509906	NONHSAT142250
2	lnc-SHCBP1-3	chr16:46512241-46512351	NONHSAT142250
3	lnc-SHCBP1-3	chr16:46508034-46508241	NONHSAT142250

No data

Variant related genes	Relation type
ANKRD26P1	TF binding region
ENSG00000260251	TF binding region
RNU6-845P	TF binding region
ENSG00000261356	TF binding region
ANKRD26P1	CpG island
ENSG00000260251	CpG island
RNU6-845P	CpG island
ENSG00000261356	CpG island
ENSG00000260251	chromatin interactions
ENSG00000261239	chromatin interactions
ENSG00000171241	chromatin interactions
GJA1	miRNA target sites
UTRN	miRNA target sites

Extended variants
information (count: 604 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:604 , 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	rs529910558	chr16:46500679-46500680	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs548356534	chr16:46500729-46500730	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs143718457	chr16:46500756-46500757	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs527545862	chr16:46500767-46500768	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs552180621	chr16:46500788-46500789	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs531348486	chr16:46508035-46508036	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs549462856	chr16:46508060-46508061	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs567770432	chr16:46508108-46508109	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs530242094	chr16:46508118-46508119	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs548729813	chr16:46508127-46508128	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs567071667	chr16:46508159-46508160	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs148559586	chr16:46508175-46508176	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs550593234	chr16:46508189-46508190	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs142946146	chr16:46508214-46508215	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs146145318	chr16:46509850-46509851	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs549184032	chr16:46509904-46509905	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs552760645	chr16:46509906-46509907	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs560669783	chr16:46512248-46512249	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs187715554	chr16:46512315-46512316	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs574311033	chr16:46512330-46512331	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs561387663	chr16:46513432-46513433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528284912	chr16:46513553-46513554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188483726	chr16:46513566-46513567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35511509	chr16:46513653-46513654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs371548979	chr16:46513654-46513655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs4255804	chr16:46513656-46513657	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs113634119	chr16:46513659-46513660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs4614751	chr16:46513660-46513661	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs565203634	chr16:46513667-46513668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs532428317	chr16:46513682-46513683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs4541096	chr16:46513683-46513684	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs550632147	chr16:46513687-46513688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs375442511	chr16:46513714-46513715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs536391823	chr16:46513723-46513724	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs547981811	chr16:46513731-46513732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532976436	chr16:46513837-46513838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs9328598	chr16:46513848-46513849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs139860952	chr16:46513852-46513853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553123201	chr16:46513882-46513883	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139237952	chr16:46516456-46516457	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568428713	chr16:46516771-46516772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs537388968	chr16:46516891-46516892	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs115039296	chr16:46516918-46516919	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565672476	chr16:46516976-46516977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs71380958	chr16:46517000-46517001	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs115703327	chr16:46517003-46517004	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs557381267	chr16:46517025-46517026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs192334891	chr16:46517034-46517035	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184546573	chr16:46517076-46517077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs555453011	chr16:46517118-46517119	Inactive region	TF binding region	1 gene(s)	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:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46497800-46500800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr16:46522600-46523000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr16:46552600-46553800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr16:46558600-46559200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr16:46581800-46583000	Enhancers	Fetal Lung	lung
6	chr16:46588400-46588600	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr16:46588400-46588600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr16:46588400-46588600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr16:46588400-46588600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr16:46588400-46588600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr16:46588400-46588600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr16:46588400-46588600	Enhancers	Adipose Nuclei	Adipose
13	chr16:46588400-46588600	Active TSS	K562	blood
14	chr16:46588400-46588800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr16:46588400-46588800	Active TSS	Muscle Satellite Cultured Cells	--
16	chr16:46588400-46588800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr16:46588400-46588800	Active TSS	Brain Angular Gyrus	brain
18	chr16:46588400-46588800	Active TSS	Brain Cingulate Gyrus	brain
19	chr16:46588400-46588800	Enhancers	Fetal Muscle Trunk	muscle
20	chr16:46588400-46588800	Enhancers	Stomach Mucosa	stomach
21	chr16:46588400-46588800	Active TSS	HepG2	liver
22	chr16:46588400-46588800	Active TSS	NHDF-Ad	bronchial
23	chr16:46588600-46588800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr16:46588600-46588800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
25	chr16:46588600-46588800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr16:46588600-46588800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr16:46588600-46588800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr16:46588600-46588800	Flanking Active TSS	K562	blood
29	chr16:46588800-46589400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr16:46588800-46589600	Weak transcription	NHDF-Ad	bronchial
31	chr16:46588800-46590800	Weak transcription	K562	blood
32	chr16:46589600-46591600	Enhancers	NHDF-Ad	bronchial
33	chr16:46589800-46590000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr16:46589800-46590200	Enhancers	Osteobl	bone
35	chr16:46589800-46590400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr16:46590200-46594000	Weak transcription	Osteobl	bone
37	chr16:46590400-46591400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr16:46590800-46591000	Bivalent/Poised TSS	HepG2	liver
39	chr16:46590800-46591000	Flanking Active TSS	K562	blood
40	chr16:46591000-46591200	Enhancers	K562	blood
41	chr16:46591000-46591600	Bivalent Enhancer	HepG2	liver
42	chr16:46591200-46591600	Flanking Active TSS	K562	blood
43	chr16:46591400-46592000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr16:46591600-46592000	Enhancers	K562	blood
45	chr16:46594000-46594200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr16:46594000-46594200	Enhancers	Osteobl	bone
47	chr16:46599800-46600000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr16:46600000-46602000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr16:46600400-46602800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr16:46601400-46603000	Weak transcription	Right Atrium	heart

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