Variant report

Variant	nsv831796
Chromosome Location	chr10:16240111-16393044
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:63)
Chromatin interactive
region (count:15)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:16284761-16285320	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr10:16284800-16285382	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr10:16284893-16285288	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL11A	chr10:16284861-16285310	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr10:16360145-16360392	A549	lung:	n/a	chr10:16360248-16360259
6	CEBPB	chr10:16305474-16305784	IMR90	lung:	n/a	chr10:16305614-16305625
7	CEBPB	chr10:16305434-16305798	A549	lung:	n/a	chr10:16305614-16305625
8	CEBPB	chr10:16274441-16274545	A549	lung:	n/a	chr10:16274475-16274486
9	CEBPB	chr10:16341886-16342012	A549	lung:	n/a	n/a
10	CEBPB	chr10:16294338-16294677	IMR90	lung:	n/a	chr10:16294501-16294512
11	CEBPB	chr10:16305458-16305799	HepG2	liver:	n/a	chr10:16305614-16305625
12	CEBPB	chr10:16305551-16305724	H1-hESC	embryonic stem cell:	n/a	chr10:16305614-16305625
13	CEBPB	chr10:16320617-16320901	A549	lung:	n/a	n/a
14	CEBPB	chr10:16360259-16360296	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:16380964-16381117	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:16274419-16274579	HepG2	liver:	n/a	chr10:16274475-16274486
17	CEBPB	chr10:16320584-16320820	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:16254419-16254431	A549	lung:	n/a	n/a
19	CEBPB	chr10:16294351-16294578	HepG2	liver:	n/a	chr10:16294501-16294512
20	CHD1	chr10:16376499-16376535	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr10:16356373-16356483	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr10:16319239-16319255	K562	blood:	n/a	n/a
23	CHD2	chr10:16383305-16383496	K562	blood:	n/a	n/a
24	CHD2	chr10:16340364-16340635	K562	blood:	n/a	n/a
25	CTBP2	chr10:16284886-16285249	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr10:16281420-16281570	Caco-2	colon:	n/a	n/a
27	CTCF	chr10:16356360-16356510	NHEK	skin:	n/a	n/a
28	CTCF	chr10:16356383-16356497	GM10248	blood:	n/a	n/a
29	CTCF	chr10:16356340-16356552	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:16356370-16356498	GM10266	blood:	n/a	n/a
31	CTCF	chr10:16245640-16245790	HCFaa	heart:	n/a	n/a
32	CTCF	chr10:16356400-16356550	HCT-116	colon:	n/a	n/a
33	CTCF	chr10:16356300-16356450	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:16356360-16356510	HRE	kidney:	n/a	n/a
35	CTCF	chr10:16356320-16356470	HEK293	kidney:	n/a	n/a
36	CTCF	chr10:16356360-16356510	GM12869	blood:	n/a	n/a
37	CTCF	chr10:16248960-16249015	GM10266	blood:	n/a	n/a
38	CTCF	chr10:16356328-16356542	HepG2	liver:	n/a	n/a
39	CTCF	chr10:16258575-16258666	GM10248	blood:	n/a	n/a
40	CTCF	chr10:16356424-16356464	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr10:16280979-16281093	GM20000	blood:	n/a	n/a
42	CTCF	chr10:16356400-16356550	GM12865	blood:	n/a	n/a
43	CTCF	chr10:16356320-16356470	GM12873	blood:	n/a	n/a
44	CTCF	chr10:16356345-16356553	MCF-7	breast:	n/a	n/a
45	CTCF	chr10:16356440-16356590	A549	lung:	n/a	n/a
46	CTCF	chr10:16356332-16356556	GM19238	blood:	n/a	n/a
47	CTCF	chr10:16356320-16356470	SAEC	small airway:	n/a	n/a
48	CTCF	chr10:16356360-16356519	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr10:16356340-16356490	GM12873	blood:	n/a	n/a
50	CTCF	chr10:16356300-16356450	GM12873	blood:	n/a	n/a

(count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:16285821-16285871	SK-N-MC	brain:	n/a
2	chr10:16285821-16285871	IMR90	lung:	fetal
3	chr10:16285821-16285871	SK-N-MC	brain:	n/a
4	chr10:16285821-16285871	IMR90	lung:	fetal
5	chr10:16285821-16285871	K562	blood:	n/a
6	chr10:16285821-16285871	Hela-S3	cervix:	n/a
7	chr10:16285821-16285871	Jurkat	blood:	n/a
8	chr10:16285821-16285871	HL-60	blood:	n/a
9	chr10:16285821-16285871	H1-hESC	embryonic stem cell:	embryo
10	chr10:16285821-16285871	SKMC	muscle:	n/a
11	chr10:16285821-16285871	T-47D	breast:	n/a
12	chr10:16285821-16285871	GM12891	blood:	n/a
13	chr10:16285821-16285871	HUVEC	blood vessel:	n/a
14	chr10:16285821-16285871	NHDF-neo	bronchial:	n/a
15	chr10:16285821-16285871	AG04450	lung:	fetal
16	chr10:16285821-16285871	HepG2	liver:	n/a
17	chr10:16285821-16285871	HRCEpiC	kidney:	n/a
18	chr10:16285821-16285871	HNPCEpiC	eye:	n/a
19	chr10:16285821-16285871	SK-N-SH	brain:	n/a
20	chr10:16285821-16285871	RPTEC	kidney:	n/a
21	chr10:16285821-16285871	SK-N-SH_RA	brain:	n/a
22	chr10:16285821-16285871	ovcar-3	ovarian:	n/a
23	chr10:16285821-16285871	ECC-1	luminal epithelium:	n/a
24	chr10:16285821-16285871	HCM	heart:	n/a
25	chr10:16285821-16285871	PrEC	prostate:	n/a
26	chr10:16285821-16285871	HCPEpiC	choroid plexus:	n/a
27	chr10:16285821-16285871	LNCaP	prostate:	n/a
28	chr10:16285821-16285871	AG04449	skin:	fetal
29	chr10:16285821-16285871	HRE	kidney:	n/a
30	chr10:16285821-16285871	ProgFib	skin:	n/a
31	chr10:16285821-16285871	GM12878	blood:	n/a
32	chr10:16285821-16285871	HCT-116	colon:	n/a
33	chr10:16285821-16285871	AG10803	skin:	n/a
34	chr10:16285821-16285871	HEEpiC	esophagus:	n/a
35	chr10:16285821-16285871	NT2-D1	testis:	n/a
36	chr10:16285821-16285871	U87	brain:	n/a
37	chr10:16285821-16285871	AoSMC	blood vessel:	n/a
38	chr10:16285821-16285871	Hepatocyte	liver:	n/a
39	chr10:16285821-16285871	AG09319	gingival:	n/a
40	chr10:16285821-16285871	BE2_C	brain:	n/a
41	chr10:16285821-16285871	GM06990	blood:	n/a
42	chr10:16285821-16285871	HAEpiC	amniotic membrane:	n/a
43	chr10:16285821-16285871	HIPEpiC	eye:	n/a
44	chr10:16285821-16285871	MCF-7	breast:	n/a
45	chr10:16285821-16285871	PFSK-1	brain:	n/a
46	chr10:16285821-16285871	GM12892	blood:	n/a
47	chr10:16285821-16285871	A549	lung:	n/a
48	chr10:16285821-16285871	GM19239	blood:	n/a
49	chr10:16285821-16285871	CMK	blood:	n/a
50	chr10:16285821-16285871	PANC-1	pancreas:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:16327734..16329898-chr10:16330970..16332624,2	K562	blood:
2	chr10:16275723..16278095-chr10:16278831..16281522,2	K562	blood:
3	chr10:16337821..16339620-chr10:16340390..16342255,2	K562	blood:
4	chr10:16272567..16275355-chr10:16277483..16279973,2	K562	blood:
5	chr10:16327319..16329234-chr10:16331124..16332628,2	K562	blood:
6	chr10:16356271..16356862-chr10:16819173..16819762,2	MCF-7	breast:
7	chr10:16378750..16381635-chr10:16385964..16388665,2	K562	blood:
8	chr10:16337821..16339620-chr10:16340390..16342255,2	K562	blood:
9	chr10:16378750..16381635-chr10:16385964..16388665,2	K562	blood:
10	chr10:16356096..16356854-chr10:16560586..16561200,2	MCF-7	breast:
11	chr10:16327319..16329234-chr10:16331124..16332628,2	K562	blood:
12	chr10:16272567..16275355-chr10:16277483..16279973,2	K562	blood:
13	chr10:16275723..16278095-chr10:16278831..16281522,2	K562	blood:
14	chr10:16327734..16329898-chr10:16330970..16332624,2	K562	blood:
15	chr10:16280790..16281457-chr9:86888651..86889166,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTER-4	chr10:16360706-16360754	NONHSAT011593
2	lnc-PTER-4	chr10:16365735-16365913	NONHSAT011593
3	lnc-PTER-4	chr10:16360706-16360754	NONHSAT011592
4	lnc-PTER-2	chr10:16320700-16320748	XLOC_008401
5	lnc-PTER-2	chr10:16320700-16320748	XLOC_008401
6	lnc-PTER-2	chr10:16330841-16331047	XLOC_008401
7	lnc-PTER-4	chr10:16377694-16377863	NONHSAT011593
8	lnc-PTER-2	chr10:16337688-16337857	XLOC_008401
9	lnc-PTER-2	chr10:16330841-16330900	XLOC_008401
10	lnc-PTER-4	chr10:16370847-16370906	NONHSAT011593
11	lnc-PTER-4	chr10:16365735-16365913	NONHSAT011592
12	lnc-PTER-2	chr10:16325729-16325907	XLOC_008401
13	lnc-PTER-4	chr10:16370847-16371053	NONHSAT011592
14	lnc-PTER-2	chr10:16325729-16325907	XLOC_008401
15	lnc-C1QL3-2	chr10:16380643-16380732	NONHSAT011594

No data

Variant related genes	Relation type
ENSG00000226140	TF binding region
RNU6-1075P	TF binding region
ENSG00000226140	CpG island
RNU6-1075P	CpG island
SEPT9	miRNA target sites
SERBP1	miRNA target sites
SEPT7	miRNA target sites
AUH	miRNA target sites

Extended variants
information (count: 3477 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:3477 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549217270	chr10:16247209-16247210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs556545117	chr10:16247231-16247232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113454087	chr10:16247253-16247254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184269399	chr10:16247300-16247301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12778353	chr10:16247310-16247311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553230584	chr10:16247314-16247315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs571753415	chr10:16247316-16247317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539099540	chr10:16247353-16247354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574879457	chr10:16247377-16247378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1578265	chr10:16247399-16247400	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs61065714	chr10:16249989-16249990	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537945293	chr10:16250037-16250038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552029482	chr10:16250062-16250063	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs570435075	chr10:16250076-16250077	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs370791833	chr10:16257408-16257409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112639595	chr10:16257417-16257418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572950453	chr10:16257427-16257428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147902079	chr10:16257451-16257452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564947534	chr10:16257460-16257461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141586310	chr10:16257466-16257467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs71493247	chr10:16257479-16257480	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs562499149	chr10:16257532-16257533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530073251	chr10:16257545-16257546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1340139	chr10:16257548-16257549	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147032008	chr10:16257591-16257592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1340138	chr10:16257615-16257616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570982419	chr10:16257622-16257623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148067797	chr10:16257644-16257645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117347518	chr10:16257648-16257649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575303102	chr10:16257686-16257687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs56380644	chr10:16257694-16257695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536301090	chr10:16257715-16257716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374251746	chr10:16257722-16257723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554884383	chr10:16257739-16257740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1340137	chr10:16257742-16257743	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs540177783	chr10:16257750-16257751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187158656	chr10:16257763-16257764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs565044281	chr10:16257765-16257766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190989182	chr10:16257769-16257770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576973747	chr10:16257794-16257795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536509107	chr10:16257815-16257816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10904688	chr10:16257823-16257824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs374399442	chr10:16257827-16257828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530012370	chr10:16257854-16257855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112530964	chr10:16257872-16257873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548210754	chr10:16257884-16257885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10904689	chr10:16257952-16257953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs1934638	chr10:16257990-16257991	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184938068	chr10:16258069-16258070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs150144832	chr10:16258070-16258071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Renal cell carcinoma	18765545	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
DiGeorge-Velo cardiofacial	22470819	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
Adrenocortical carcinoma	18281524	CNVD
Digeorge syndrome	17576883	CNVD
Lung cancer	16773561	CNVD
Velocardiofacial syndrome	17576883	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	22048815	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Hepatocellular carcinoma	16750200	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Thymic lymphomas tumor	22700994	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:16247200-16247400	Weak transcription	Aorta	Aorta
2	chr10:16257400-16257800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr10:16257800-16262200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr10:16264200-16264600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:16264400-16264600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
6	chr10:16264600-16266600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr10:16267000-16267200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr10:16270000-16271600	Weak transcription	Fetal Brain Male	brain
9	chr10:16271000-16271400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr10:16271000-16271400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr10:16271400-16273600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr10:16271600-16271800	Enhancers	Fetal Brain Male	brain
13	chr10:16271800-16272200	Weak transcription	Fetal Brain Male	brain
14	chr10:16272200-16274800	Enhancers	Fetal Brain Male	brain
15	chr10:16273200-16273400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr10:16273600-16273800	Enhancers	Fetal Brain Female	brain
17	chr10:16273600-16274000	Enhancers	H9 Cell Line	embryonic stem cell
18	chr10:16273800-16274200	Flanking Active TSS	Fetal Brain Female	brain
19	chr10:16274200-16274400	Enhancers	Fetal Brain Female	brain
20	chr10:16274800-16276800	Weak transcription	Fetal Brain Male	brain
21	chr10:16276800-16277400	Enhancers	Fetal Brain Male	brain
22	chr10:16281000-16282000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
23	chr10:16281000-16282600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr10:16281800-16282400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
25	chr10:16282400-16284400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr10:16282600-16285400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:16283200-16283400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
28	chr10:16283600-16284400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr10:16284200-16286600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr10:16284400-16284600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr10:16284400-16284600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr10:16284400-16284800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr10:16284400-16285000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
34	chr10:16284400-16285000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
35	chr10:16284400-16286200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr10:16284600-16284800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr10:16284600-16284800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr10:16284600-16285000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr10:16284600-16285000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
40	chr10:16284600-16285800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:16284800-16285000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
42	chr10:16284800-16285400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr10:16284800-16285600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr10:16284800-16285600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr10:16284800-16285600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
46	chr10:16284800-16285800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr10:16284800-16286000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr10:16285000-16285200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr10:16285000-16285200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr10:16285000-16285200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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