Variant report

Variant	nsv895544
Chromosome Location	chr10:58938552-59282980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:59098888-59099216	HepG2	liver:	n/a	n/a
2	ATF1	chr10:58978298-58978471	K562	blood:	n/a	n/a
3	BACH1	chr10:59063455-59063655	K562	blood:	n/a	n/a
4	BACH1	chr10:59217955-59218146	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:59035982-59036219	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr10:58981377-58982645	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:59226296-59226323	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:59063324-59063718	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr10:58982383-58982665	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr10:58982420-58982633	H1-hESC	embryonic stem cell:	n/a	n/a
11	CCNT2	chr10:59112963-59113085	K562	blood:	n/a	n/a
12	CCNT2	chr10:59152075-59152417	K562	blood:	n/a	n/a
13	CEBPB	chr10:59021105-59021342	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:59278581-59278781	K562	blood:	n/a	chr10:59278696-59278707
15	CEBPB	chr10:59254315-59254530	HepG2	liver:	n/a	n/a
16	CEBPB	chr10:59178284-59178619	H1-hESC	embryonic stem cell:	n/a	chr10:59178462-59178473
17	CEBPB	chr10:59208678-59208892	H1-hESC	embryonic stem cell:	n/a	chr10:59208795-59208812 chr10:59208798-59208809
18	CEBPB	chr10:58977793-58978645	MCF-7	breast:	n/a	chr10:58978274-58978286
19	CEBPB	chr10:59254274-59254601	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:59232552-59232999	Hela-S3	cervix:	n/a	chr10:59232716-59232725 chr10:59232714-59232725 chr10:59232716-59232725 chr10:59232716-59232725 chr10:59232715-59232726 chr10:59232716-59232725
21	CEBPB	chr10:59278586-59278818	IMR90	lung:	n/a	chr10:59278696-59278707
22	CEBPB	chr10:59178334-59178606	HepG2	liver:	n/a	chr10:59178462-59178473
23	CEBPB	chr10:59055250-59055409	HepG2	liver:	n/a	chr10:59055288-59055299
24	CEBPB	chr10:59182290-59182570	Hela-S3	cervix:	n/a	chr10:59182426-59182437 chr10:59182426-59182435 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182437 chr10:59182424-59182435
25	CEBPB	chr10:58970964-58971188	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:59090496-59090747	HepG2	liver:	n/a	chr10:59090592-59090603
27	CEBPB	chr10:59020004-59020333	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:59208776-59208824	A549	lung:	n/a	chr10:59208795-59208812 chr10:59208798-59208809
29	CEBPB	chr10:59208672-59208938	IMR90	lung:	n/a	chr10:59208795-59208812 chr10:59208798-59208809
30	CEBPB	chr10:59155783-59155901	A549	lung:	n/a	n/a
31	CEBPB	chr10:59178283-59178604	A549	lung:	n/a	chr10:59178462-59178473
32	CEBPB	chr10:59156867-59157094	HepG2	liver:	n/a	chr10:59156964-59156975
33	CEBPB	chr10:59232563-59233028	A549	lung:	n/a	chr10:59232716-59232725 chr10:59232714-59232725 chr10:59232716-59232725 chr10:59232716-59232725 chr10:59232715-59232726 chr10:59232716-59232725
34	CEBPB	chr10:59232622-59232926	A549	lung:	n/a	chr10:59232716-59232725 chr10:59232714-59232725 chr10:59232716-59232725 chr10:59232716-59232725 chr10:59232715-59232726 chr10:59232716-59232725
35	CEBPB	chr10:59130426-59130642	HepG2	liver:	n/a	n/a
36	CEBPB	chr10:58985759-58986003	HepG2	liver:	n/a	n/a
37	CEBPB	chr10:59182372-59182442	K562	blood:	n/a	chr10:59182426-59182437 chr10:59182426-59182435 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182437 chr10:59182424-59182435
38	CEBPB	chr10:58996972-58997083	A549	lung:	n/a	n/a
39	CEBPB	chr10:59178294-59178628	Hela-S3	cervix:	n/a	chr10:59178462-59178473
40	CEBPB	chr10:59182363-59182520	A549	lung:	n/a	chr10:59182426-59182437 chr10:59182426-59182435 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182437 chr10:59182424-59182435
41	CEBPB	chr10:59232607-59232816	HepG2	liver:	n/a	chr10:59232716-59232725 chr10:59232714-59232725 chr10:59232716-59232725 chr10:59232716-59232725 chr10:59232715-59232726 chr10:59232716-59232725
42	CEBPB	chr10:59182281-59182505	HepG2	liver:	n/a	chr10:59182426-59182437 chr10:59182426-59182435 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182424-59182437 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182435 chr10:59182426-59182437 chr10:59182424-59182435
43	CEBPB	chr10:59278572-59278868	HepG2	liver:	n/a	chr10:59278696-59278707
44	CEBPB	chr10:59208683-59208933	HepG2	liver:	n/a	chr10:59208795-59208812 chr10:59208798-59208809
45	CEBPB	chr10:59178305-59178618	K562	blood:	n/a	chr10:59178462-59178473
46	CEBPB	chr10:59004244-59004316	A549	lung:	n/a	n/a
47	CEBPB	chr10:59178281-59178623	IMR90	lung:	n/a	chr10:59178462-59178473
48	CEBPB	chr10:59232641-59232855	A549	lung:	n/a	chr10:59232716-59232725 chr10:59232714-59232725 chr10:59232716-59232725 chr10:59232716-59232725 chr10:59232715-59232726 chr10:59232716-59232725
49	CEBPB	chr10:59278559-59278828	A549	lung:	n/a	chr10:59278696-59278707
50	CHD1	chr10:58981736-58983074	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:59066158-59066208	LNCaP	prostate:	n/a
2	chr10:59066158-59066208	HNPCEpiC	eye:	n/a
3	chr10:59066158-59066208	AG10803	skin:	n/a
4	chr10:59081375-59081425	NHBE	bronchial:	n/a
5	chr10:59081375-59081425	U87	brain:	n/a
6	chr10:59066158-59066208	RPTEC	kidney:	n/a
7	chr10:59081375-59081425	PrEC	prostate:	n/a
8	chr10:59081375-59081425	Jurkat	blood:	n/a
9	chr10:59155846-59155896	GM06990	blood:	n/a
10	chr10:59155846-59155896	GM12878	blood:	n/a
11	chr10:59081346-59081396	SK-N-SH	brain:	n/a
12	chr10:59066158-59066208	HCT-116	colon:	n/a
13	chr10:59081375-59081425	LNCaP	prostate:	n/a
14	chr10:59155846-59155896	HCPEpiC	choroid plexus:	n/a
15	chr10:59066158-59066208	T-47D	breast:	n/a
16	chr10:59066158-59066208	AoSMC	blood vessel:	n/a
17	chr10:59081375-59081425	PANC-1	pancreas:	n/a
18	chr10:59081346-59081396	Caco-2	colon:	n/a
19	chr10:59081346-59081396	GM06990	blood:	n/a
20	chr10:59155846-59155896	Caco-2	colon:	n/a
21	chr10:59155846-59155896	HRCEpiC	kidney:	n/a
22	chr10:59081375-59081425	MCF10A-Er-Src	breast:	n/a
23	chr10:59066158-59066208	NT2-D1	testis:	n/a
24	chr10:59081346-59081396	CMK	blood:	n/a
25	chr10:59066158-59066208	HRPEpiC	eye:	n/a
26	chr10:59081375-59081425	SK-N-SH_RA	brain:	n/a
27	chr10:59081346-59081396	GM19239	blood:	n/a
28	chr10:59081346-59081396	HL-60	blood:	n/a
29	chr10:59081375-59081425	GM06990	blood:	n/a
30	chr10:59066158-59066208	A549	lung:	n/a
31	chr10:59081346-59081396	SK-N-MC	brain:	n/a
32	chr10:59081375-59081425	Hepatocyte	liver:	n/a
33	chr10:59066158-59066208	HIPEpiC	eye:	n/a
34	chr10:59155846-59155896	GM12892	blood:	n/a
35	chr10:59066158-59066208	HPAEpiC	pulmonary alveolar:	n/a
36	chr10:59155846-59155896	HMEC	breast:	n/a
37	chr10:59066158-59066208	SK-N-SH_RA	brain:	n/a
38	chr10:59155846-59155896	Hepatocyte	liver:	n/a
39	chr10:59081375-59081425	SK-N-MC	brain:	n/a
40	chr10:59155846-59155896	HEK293	kidney:	embryo
41	chr10:59081375-59081425	HAEpiC	amniotic membrane:	n/a
42	chr10:59066158-59066208	GM12878	blood:	n/a
43	chr10:59155846-59155896	HCT-116	colon:	n/a
44	chr10:59066158-59066208	HCM	heart:	n/a
45	chr10:59155846-59155896	ECC-1	luminal epithelium:	n/a
46	chr10:59066158-59066208	HEEpiC	esophagus:	n/a
47	chr10:59081375-59081425	SKMC	muscle:	n/a
48	chr10:59155846-59155896	SK-N-SH_RA	brain:	n/a
49	chr10:59081346-59081396	HCPEpiC	choroid plexus:	n/a
50	chr10:59081346-59081396	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:58957814..58958334-chr4:116457976..116458496,2	MCF-7	breast:
2	chr10:59119517..59121118-chr10:59121352..59123797,2	K562	blood:
3	chr10:59141917..59143760-chr10:59167909..59170297,2	K562	blood:
4	chr10:59098744..59099488-chr10:59416761..59417512,2	MCF-7	breast:
5	chr10:59028011..59029703-chr10:59035060..59037128,2	MCF-7	breast:
6	chr10:58983000..58985770-chr10:58990490..58992498,2	K562	blood:
7	chr10:59098430..59099263-chr10:59609222..59610076,2	MCF-7	breast:
8	chr10:58975934..58977805-chr10:58980347..58981945,2	K562	blood:
9	chr10:59173064..59175096-chr10:59176934..59178723,2	K562	blood:
10	chr10:58981686..58984044-chr10:59073048..59074981,2	MCF-7	breast:
11	chr10:59141917..59143760-chr10:59167909..59170297,2	K562	blood:
12	chr10:58983000..58985770-chr10:58990490..58992498,2	K562	blood:
13	chr10:59028011..59029703-chr10:59035060..59037128,2	MCF-7	breast:
14	chr10:58981686..58984044-chr10:59073048..59074981,2	MCF-7	breast:
15	chr10:59273221..59275068-chr10:59277123..59280013,2	MCF-7	breast:
16	chr10:58964683..58966262-chr10:58967768..58970622,2	K562	blood:
17	chr10:59020826..59022562-chr10:59023852..59026093,2	MCF-7	breast:
18	chr10:58964683..58966262-chr10:58967768..58970622,2	K562	blood:
19	chr10:59173064..59175096-chr10:59176934..59178723,2	K562	blood:
20	chr10:59162193..59163830-chr10:59170301..59171826,2	K562	blood:
21	chr10:59273221..59275068-chr10:59277123..59280013,2	MCF-7	breast:
22	chr10:59162193..59163830-chr10:59170301..59171826,2	K562	blood:
23	chr10:58978500..58980701-chr10:58984657..58986549,2	MCF-7	breast:
24	chr1:202718635..202720646-chr10:59027468..59029112,2	MCF-7	breast:
25	chr10:59020826..59022562-chr10:59023852..59026093,2	MCF-7	breast:
26	chr10:59098466..59099424-chr10:59352866..59354001,3	MCF-7	breast:
27	chr10:58975934..58977805-chr10:58980347..58981945,2	K562	blood:
28	chr10:59098621..59099527-chr10:59416327..59417352,4	MCF-7	breast:
29	chr10:59098757..59099315-chr10:59825173..59825685,2	MCF-7	breast:
30	chr10:59119517..59121118-chr10:59121352..59123797,2	K562	blood:
31	chr10:58978500..58980701-chr10:58984657..58986549,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-3	chr10:58982372-58982557	XLOC_008830
2	lnc-CISD1-6	chr10:59272917-59273185	NONHSAT013479

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3924	chr10:59064249-59064270	MIMAT0018199

Variant related genes	Relation type
ENSG00000235810	TF binding region
MIR3924	TF binding region
ENSG00000235810	CpG island
MIR3924	CpG island
C2orf29	miRNA target sites

Extended variants
information (count: 4977 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4977 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6481257	chr10:58938552-58938553	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566813109	chr10:58938603-58938604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188726988	chr10:58938614-58938615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143218604	chr10:58938620-58938621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150844154	chr10:58938625-58938626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201280174	chr10:58938626-58938627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140346799	chr10:58938633-58938634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567797245	chr10:58938641-58938642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10690398	chr10:58938643-58938644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555485578	chr10:58938647-58938648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72801956	chr10:58938704-58938705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397956385	chr10:58938720-58938721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142754911	chr10:58938729-58938730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140966658	chr10:58938731-58938732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145078107	chr10:58938732-58938733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371463089	chr10:58938735-58938736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373929847	chr10:58938736-58938737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116304225	chr10:58938739-58938740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6481258	chr10:58938741-58938742	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs146826806	chr10:58938744-58938745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143207854	chr10:58938748-58938749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143527695	chr10:58938773-58938774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140016405	chr10:58938778-58938779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150981839	chr10:58938780-58938781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs180853983	chr10:58938784-58938785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146918535	chr10:58938786-58938787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141965234	chr10:58938799-58938800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs578212263	chr10:58938827-58938828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6481259	chr10:58938884-58938885	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs72801960	chr10:58938900-58938901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144165321	chr10:58938910-58938911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201676230	chr10:58938914-58938915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76705583	chr10:58938929-58938930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370145688	chr10:58938934-58938935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371514207	chr10:58938964-58938965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545616884	chr10:58938982-58938983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192187398	chr10:58938990-58938991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183961178	chr10:58939000-58939001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185952188	chr10:58939017-58939018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs561802854	chr10:58939049-58939050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7915950	chr10:58939059-58939060	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs140738290	chr10:58939101-58939102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7912607	chr10:58939126-58939127	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs150620014	chr10:58939144-58939145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182514189	chr10:58939151-58939152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150305295	chr10:58939164-58939165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187173997	chr10:58939171-58939172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78398317	chr10:58939191-58939192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549048552	chr10:58939196-58939197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567447505	chr10:58939201-58939202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:287 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:58930200-58959200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:58933000-58947200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:58945800-58946200	Enhancers	Fetal Kidney	kidney
4	chr10:58945800-58946400	Enhancers	Fetal Lung	lung
5	chr10:58947800-58949200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr10:58952400-58968400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr10:58959000-58960000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:58959200-58960200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr10:58960200-58966600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:58963600-58963800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:58963800-58970000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr10:58966600-58967400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:58967400-58970600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:58968400-58969200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr10:58969200-58970800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr10:58970000-58973400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
17	chr10:58970600-58971000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr10:58970600-58972200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
19	chr10:58970800-58971200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:58970800-58972200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr10:58971000-58972600	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr10:58971200-58972000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr10:58971400-58972000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:58972000-58972800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr10:58972000-58978800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:58972600-58977400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr10:58972800-58973400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr10:58973400-58976000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr10:58973600-58973800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr10:58973600-58973800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr10:58973800-58974200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr10:58973800-58977600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr10:58974200-58977600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr10:58975800-58980800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:58976000-58976600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr10:58976200-58976400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr10:58976200-58976400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr10:58976400-58977600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:58976400-58977600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr10:58976600-58977200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr10:58976600-58982000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr10:58977200-58980400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr10:58977400-58979800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr10:58977600-58977800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:58977600-58977800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr10:58977600-58978000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr10:58977600-58978000	Enhancers	H9 Cell Line	embryonic stem cell
48	chr10:58977600-58978200	Enhancers	Placenta	Placenta
49	chr10:58977600-58978400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:58977600-58978600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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