Variant report

Variant	nsv877227
Chromosome Location	chr3:102067254-102184308
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:102068555-102068558	HepG2	liver:	n/a	n/a
2	ATF1	chr3:102074053-102074309	K562	blood:	n/a	n/a
3	BACH1	chr3:102179530-102179782	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:102067835-102068058	GM12878	blood:	n/a	n/a
5	BATF	chr3:102067808-102068106	GM12878	blood:	n/a	n/a
6	BRCA1	chr3:102072821-102073099	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr3:102119533-102120062	HCT-116	colon:	n/a	n/a
8	CEBPB	chr3:102114402-102114715	IMR90	lung:	n/a	chr3:102114550-102114561
9	CEBPB	chr3:102073599-102074459	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:102166171-102166464	A549	lung:	n/a	n/a
11	CEBPB	chr3:102166120-102166510	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr3:102073648-102074490	HCT-116	colon:	n/a	n/a
13	CEBPB	chr3:102115233-102115532	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:102179492-102179804	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:102072233-102073122	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:102159861-102160061	HepG2	liver:	n/a	chr3:102160001-102160012 chr3:102160001-102160014
17	CEBPB	chr3:102073621-102074366	HCT-116	colon:	n/a	n/a
18	CEBPB	chr3:102160622-102160959	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:102166142-102166464	IMR90	lung:	n/a	n/a
20	CEBPB	chr3:102114404-102114695	HepG2	liver:	n/a	chr3:102114550-102114561
21	CEBPB	chr3:102175820-102176059	Hela-S3	cervix:	n/a	chr3:102175966-102175977
22	CEBPB	chr3:102072288-102072505	A549	lung:	n/a	n/a
23	CEBPB	chr3:102157789-102157983	A549	lung:	n/a	chr3:102157930-102157941 chr3:102157819-102157828
24	CTCF	chr3:102095800-102095950	GM12878	blood:	n/a	n/a
25	CTCF	chr3:102102160-102102310	HPF	lung:	n/a	n/a
26	CTCF	chr3:102143663-102143729	Lung_OC	lung:	n/a	n/a
27	CTCF	chr3:102091640-102091679	GM10248	blood:	n/a	n/a
28	CTCF	chr3:102091736-102091755	GM10266	blood:	n/a	n/a
29	CTCF	chr3:102084509-102084618	GM20000	blood:	n/a	n/a
30	CTCF	chr3:102074400-102074550	A549	lung:	n/a	n/a
31	CTCF	chr3:102091686-102091731	GM10248	blood:	n/a	n/a
32	CTCF	chr3:102071980-102072130	GM12867	blood:	n/a	n/a
33	CTCF	chr3:102088480-102088630	GM12878	blood:	n/a	n/a
34	E2F4	chr3:102183693-102183827	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr3:102123458-102123491	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr3:102097256-102097623	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr3:102074479-102074679	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr3:102166182-102166469	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr3:102068337-102068515	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr3:102168057-102168131	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr3:102126188-102126521	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr3:102137436-102137854	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:102089297-102089497	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:102075612-102075812	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:102072667-102073095	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:102164819-102164993	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr3:102072119-102072180	GM12878	blood:	n/a	n/a
48	EBF1	chr3:102067796-102067906	GM12878	blood:	n/a	n/a
49	ELK1	chr3:102119839-102119927	Hela-S3	cervix:	n/a	n/a
50	EP300	chr3:102119617-102119932	SK-N-SH_RA	brain:	n/a	chr3:102119818-102119827 chr3:102119817-102119826

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:102154087-102154137	U87	brain:	n/a
2	chr3:102154087-102154137	HRPEpiC	eye:	n/a
3	chr3:102156072-102156122	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:102156072-102156122	HRE	kidney:	n/a
5	chr3:102154087-102154137	Caco-2	colon:	n/a
6	chr3:102156072-102156122	CMK	blood:	n/a
7	chr3:102154087-102154137	A549	lung:	n/a
8	chr3:102154087-102154137	AG09319	gingival:	n/a
9	chr3:102154087-102154137	SKMC	muscle:	n/a
10	chr3:102156072-102156122	BJ	skin:	n/a
11	chr3:102154087-102154137	HRCEpiC	kidney:	n/a
12	chr3:102156072-102156122	AG04449	skin:	fetal
13	chr3:102154087-102154137	PrEC	prostate:	n/a
14	chr3:102154087-102154137	AG04450	lung:	fetal
15	chr3:102154087-102154137	AG04449	skin:	fetal
16	chr3:102156072-102156122	HEEpiC	esophagus:	n/a
17	chr3:102154087-102154137	LNCaP	prostate:	n/a
18	chr3:102154087-102154137	GM12878	blood:	n/a
19	chr3:102156072-102156122	AG04450	lung:	fetal
20	chr3:102156072-102156122	Hepatocyte	liver:	n/a
21	chr3:102156072-102156122	IMR90	lung:	fetal
22	chr3:102154087-102154137	K562	blood:	n/a
23	chr3:102154087-102154137	NB4	blood:	n/a
24	chr3:102156072-102156122	Caco-2	colon:	n/a
25	chr3:102156072-102156122	ProgFib	skin:	n/a
26	chr3:102156072-102156122	HRPEpiC	eye:	n/a
27	chr3:102156072-102156122	RPTEC	kidney:	n/a
28	chr3:102156072-102156122	HAEpiC	amniotic membrane:	n/a
29	chr3:102156072-102156122	NB4	blood:	n/a
30	chr3:102154087-102154137	HL-60	blood:	n/a
31	chr3:102156072-102156122	AoSMC	blood vessel:	n/a
32	chr3:102156072-102156122	HUVEC	blood vessel:	n/a
33	chr3:102154087-102154137	IMR90	lung:	fetal
34	chr3:102154087-102154137	GM12891	blood:	n/a
35	chr3:102156072-102156122	HEK293	kidney:	embryo
36	chr3:102154087-102154137	AG10803	skin:	n/a
37	chr3:102156072-102156122	GM19239	blood:	n/a
38	chr3:102154087-102154137	HMEC	breast:	n/a
39	chr3:102154087-102154137	HAEpiC	amniotic membrane:	n/a
40	chr3:102154087-102154137	ovcar-3	ovarian:	n/a
41	chr3:102156072-102156122	HCT-116	colon:	n/a
42	chr3:102154087-102154137	HCPEpiC	choroid plexus:	n/a
43	chr3:102156072-102156122	AG09319	gingival:	n/a
44	chr3:102154087-102154137	T-47D	breast:	n/a
45	chr3:102156072-102156122	PrEC	prostate:	n/a
46	chr3:102156072-102156122	HCM	heart:	n/a
47	chr3:102156072-102156122	NH-A	brain:	n/a
48	chr3:102154087-102154137	MCF-7	breast:	n/a
49	chr3:102154087-102154137	Jurkat	blood:	n/a
50	chr3:102156072-102156122	AG09309	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:102170010..102172131-chr3:102173986..102176853,2	K562	blood:
2	chr3:102065265..102067946-chr3:102070779..102072872,2	K562	blood:
3	chr3:102115274..102117462-chr3:102120586..102123538,2	MCF-7	breast:
4	chr3:102043009..102043544-chr3:102172789..102173389,2	MCF-7	breast:
5	chr3:102043009..102043823-chr3:102172889..102173620,2	MCF-7	breast:
6	chr3:102178264..102180140-chr3:102180823..102183403,2	MCF-7	breast:
7	chr3:102184197..102185596-chr3:102248087..102248957,3	MCF-7	breast:
8	chr3:102170010..102172131-chr3:102173986..102176853,2	K562	blood:
9	chr3:102113340..102116015-chr3:102116422..102118729,2	MCF-7	breast:
10	chr3:102115274..102117462-chr3:102120586..102123538,2	MCF-7	breast:
11	chr3:102113340..102116015-chr3:102116422..102118729,2	MCF-7	breast:
12	chr3:102065265..102067946-chr3:102070779..102072872,2	K562	blood:
13	chr3:102178264..102180140-chr3:102180823..102183403,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZPLD1	TF binding region
ZPLD1	CpG island

Extended variants
information (count: 3209 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3209 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs985374	chr3:102067254-102067255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111588146	chr3:102067319-102067320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146316714	chr3:102067329-102067330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547719234	chr3:102067362-102067363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190389830	chr3:102067373-102067374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536494530	chr3:102067376-102067377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182588316	chr3:102067533-102067534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548293527	chr3:102067632-102067633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368295740	chr3:102067637-102067638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185391293	chr3:102067678-102067679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs536770927	chr3:102067686-102067687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113229913	chr3:102067693-102067694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576763143	chr3:102067703-102067704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534980419	chr3:102067721-102067722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542544721	chr3:102067722-102067723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574676437	chr3:102067793-102067794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370944750	chr3:102067810-102067811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563751549	chr3:102067817-102067818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575658815	chr3:102067872-102067873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144331320	chr3:102067875-102067876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564458677	chr3:102067877-102067878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528543568	chr3:102067900-102067901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543001658	chr3:102067912-102067913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146115167	chr3:102067954-102067955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190888137	chr3:102068010-102068011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148763652	chr3:102068066-102068067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569769182	chr3:102068088-102068089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183913951	chr3:102068116-102068117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554780001	chr3:102068126-102068127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375427632	chr3:102068159-102068160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188868481	chr3:102068164-102068165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552030175	chr3:102068165-102068166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs373425327	chr3:102068195-102068196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570416039	chr3:102068231-102068232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193093008	chr3:102068262-102068263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367948612	chr3:102068281-102068282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183025160	chr3:102068284-102068285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543546905	chr3:102068289-102068290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187310335	chr3:102068324-102068325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142413705	chr3:102068346-102068347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575752012	chr3:102068358-102068359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546277235	chr3:102068367-102068368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564599540	chr3:102068387-102068388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573261137	chr3:102068508-102068509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576434436	chr3:102068537-102068538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9873657	chr3:102068544-102068545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191778504	chr3:102068549-102068550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77542177	chr3:102068565-102068566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541758651	chr3:102068601-102068602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562175755	chr3:102068664-102068665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102066400-102073400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr3:102066800-102072000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:102066800-102072000	Weak transcription	NHEK	skin
4	chr3:102067800-102068000	Enhancers	GM12878-XiMat	blood
5	chr3:102072000-102072600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:102072000-102072600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:102072000-102074200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr3:102072000-102074800	Enhancers	NHEK	skin
9	chr3:102072000-102075000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr3:102072000-102075000	Enhancers	HMEC	breast
11	chr3:102072000-102076600	Enhancers	Hela-S3	cervix
12	chr3:102072400-102074000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:102072600-102080000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:102073400-102074600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:102073400-102074600	Enhancers	Muscle Satellite Cultured Cells	--
16	chr3:102073600-102073800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:102073600-102074400	Enhancers	HSMMtube	muscle
18	chr3:102073600-102076600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr3:102073800-102074000	Enhancers	Ovary	ovary
20	chr3:102073800-102074400	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:102073800-102074800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr3:102073800-102076600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:102074600-102074800	Enhancers	Ovary	ovary
24	chr3:102074600-102077200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr3:102074800-102076400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr3:102075000-102075200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr3:102075000-102075400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr3:102075000-102075800	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:102075200-102079000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr3:102075400-102075600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:102075600-102075800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:102075600-102076400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr3:102075600-102096600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr3:102075800-102078800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr3:102076000-102079400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr3:102076400-102076600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr3:102076400-102078600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr3:102076400-102078800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr3:102076600-102077200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:102077200-102077600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr3:102077200-102078400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr3:102078400-102080400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:102078600-102079200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:102078600-102080200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr3:102078800-102080400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:102078800-102080400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:102079000-102079600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:102079000-102080200	Enhancers	Brain Germinal Matrix	brain
49	chr3:102079200-102079400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr3:102079400-102079600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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