Variant report

Variant	nsv517747
Chromosome Location	chr10:58296224-58473735
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	ATF2	chr10:58393859-58394401	GM12878	blood:	n/a	n/a
2	ATF2	chr10:58413072-58413421	GM12878	blood:	n/a	n/a
3	ATF2	chr10:58393677-58394392	GM12878	blood:	n/a	n/a
4	ATF2	chr10:58412944-58413514	GM12878	blood:	n/a	n/a
5	BACH1	chr10:58297730-58298115	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr10:58393849-58394184	GM12878	blood:	n/a	n/a
7	BATF	chr10:58356028-58356235	GM12878	blood:	n/a	chr10:58356125-58356136
8	BATF	chr10:58413137-58413422	GM12878	blood:	n/a	n/a
9	BATF	chr10:58392302-58392666	GM12878	blood:	n/a	chr10:58392517-58392528
10	BCL11A	chr10:58393892-58394170	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:58393836-58394267	GM12878	blood:	n/a	n/a
12	BCLAF1	chr10:58393692-58394349	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:58310956-58311145	HepG2	liver:	n/a	n/a
14	BHLHE40	chr10:58393840-58394442	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:58422586-58422736	GM12878	blood:	n/a	n/a
16	CBX3	chr10:58330110-58330379	K562	blood:	n/a	n/a
17	CEBPB	chr10:58454387-58454781	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:58364906-58365392	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:58306645-58306911	K562	blood:	n/a	chr10:58306737-58306746
20	CEBPB	chr10:58458348-58458586	Hela-S3	cervix:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
21	CEBPB	chr10:58310793-58311237	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:58427588-58427860	IMR90	lung:	n/a	chr10:58427746-58427757
23	CEBPB	chr10:58458311-58458645	IMR90	lung:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
24	CEBPB	chr10:58458326-58458658	HepG2	liver:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
25	CEBPB	chr10:58458325-58458631	K562	blood:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
26	CEBPB	chr10:58458331-58458523	H1-hESC	embryonic stem cell:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
27	CEBPB	chr10:58397140-58397340	A549	lung:	n/a	chr10:58397224-58397235
28	CEBPB	chr10:58454437-58454792	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:58310788-58311246	MCF-7	breast:	n/a	n/a
30	CEBPB	chr10:58473662-58473927	IMR90	lung:	n/a	chr10:58473775-58473786 chr10:58473775-58473788
31	CEBPB	chr10:58389499-58389707	A549	lung:	n/a	chr10:58389639-58389650
32	CEBPB	chr10:58454489-58454756	K562	blood:	n/a	n/a
33	CEBPB	chr10:58397073-58397273	HepG2	liver:	n/a	chr10:58397224-58397235
34	CEBPB	chr10:58458309-58458622	A549	lung:	n/a	chr10:58458469-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458471-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480 chr10:58458469-58458482 chr10:58458471-58458480
35	CEBPB	chr10:58389538-58389770	HepG2	liver:	n/a	chr10:58389639-58389650
36	CEBPB	chr10:58473719-58473849	K562	blood:	n/a	chr10:58473775-58473786 chr10:58473775-58473788
37	CEBPB	chr10:58306624-58307014	HepG2	liver:	n/a	chr10:58306737-58306746
38	CEBPB	chr10:58427632-58427869	HepG2	liver:	n/a	chr10:58427746-58427757
39	CEBPB	chr10:58310819-58311202	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:58454369-58454740	A549	lung:	n/a	n/a
41	CEBPZ	chr10:58390422-58390450	HepG2	liver:	n/a	n/a
42	CHD1	chr10:58393767-58394099	GM12878	blood:	n/a	n/a
43	CHD2	chr10:58393742-58394425	GM12878	blood:	n/a	n/a
44	CHD2	chr10:58422681-58422872	GM12878	blood:	n/a	n/a
45	CREB1	chr10:58310870-58311150	HepG2	liver:	n/a	n/a
46	CTCF	chr10:58346260-58346410	HMEC	breast:	n/a	n/a
47	CTCF	chr10:58393998-58394096	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr10:58392418-58392512	GM12878	blood:	n/a	n/a
49	CTCF	chr10:58392420-58392570	GM12872	blood:	n/a	n/a
50	CTCF	chr10:58393880-58394363	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:58346379-58346429	NT2-D1	testis:	n/a
2	chr10:58346379-58346429	ProgFib	skin:	n/a
3	chr10:58346379-58346429	HRE	kidney:	n/a
4	chr10:58346379-58346429	GM19239	blood:	n/a
5	chr10:58346379-58346429	NHDF-neo	bronchial:	n/a
6	chr10:58346379-58346429	NH-A	brain:	n/a
7	chr10:58346379-58346429	SKMC	muscle:	n/a
8	chr10:58346379-58346429	HCPEpiC	choroid plexus:	n/a
9	chr10:58346379-58346429	ovcar-3	ovarian:	n/a
10	chr10:58346379-58346429	LNCaP	prostate:	n/a
11	chr10:58346379-58346429	HAEpiC	amniotic membrane:	n/a
12	chr10:58346379-58346429	HEK293	kidney:	embryo
13	chr10:58346379-58346429	IMR90	lung:	fetal
14	chr10:58346379-58346429	MCF-7	breast:	n/a
15	chr10:58346379-58346429	BJ	skin:	n/a
16	chr10:58346379-58346429	NHBE	bronchial:	n/a
17	chr10:58346379-58346429	HRCEpiC	kidney:	n/a
18	chr10:58346379-58346429	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:58346379-58346429	HCT-116	colon:	n/a
20	chr10:58346379-58346429	T-47D	breast:	n/a
21	chr10:58346379-58346429	GM12878	blood:	n/a
22	chr10:58346379-58346429	HMEC	breast:	n/a
23	chr10:58346379-58346429	HepG2	liver:	n/a
24	chr10:58346379-58346429	GM12891	blood:	n/a
25	chr10:58346379-58346429	SK-N-SH_RA	brain:	n/a
26	chr10:58346379-58346429	HCM	heart:	n/a
27	chr10:58346379-58346429	CMK	blood:	n/a
28	chr10:58346379-58346429	A549	lung:	n/a
29	chr10:58346379-58346429	SAEC	small airway:	n/a
30	chr10:58346379-58346429	Hepatocyte	liver:	n/a
31	chr10:58346379-58346429	PANC-1	pancreas:	n/a
32	chr10:58346379-58346429	SK-N-MC	brain:	n/a
33	chr10:58346379-58346429	U87	brain:	n/a
34	chr10:58346379-58346429	NB4	blood:	n/a
35	chr10:58346379-58346429	PFSK-1	brain:	n/a
36	chr10:58346379-58346429	AoSMC	blood vessel:	n/a
37	chr10:58346379-58346429	GM06990	blood:	n/a
38	chr10:58346379-58346429	PrEC	prostate:	n/a
39	chr10:58346379-58346429	HEEpiC	esophagus:	n/a
40	chr10:58346379-58346429	SK-N-SH	brain:	n/a
41	chr10:58346379-58346429	K562	blood:	n/a
42	chr10:58346379-58346429	HIPEpiC	eye:	n/a
43	chr10:58346379-58346429	HRPEpiC	eye:	n/a
44	chr10:58346379-58346429	AG10803	skin:	n/a
45	chr10:58346379-58346429	HCF	heart:	n/a
46	chr10:58346379-58346429	GM12892	blood:	n/a
47	chr10:58346379-58346429	AG04449	skin:	fetal
48	chr10:58346379-58346429	MCF10A-Er-Src	breast:	n/a
49	chr10:58346379-58346429	HL-60	blood:	n/a
50	chr10:58346379-58346429	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:121484861..121485361-chr10:58418252..58418753,2	MCF-7	breast:
2	chr10:58403682..58405609-chr10:58417401..58419090,2	K562	blood:
3	chr10:58360207..58362204-chr10:58364540..58367315,2	K562	blood:
4	chr10:58351002..58353905-chr5:28242920..28245430,2	MCF-7	breast:
5	chr10:58424561..58425526-chr10:58543081..58543976,4	MCF-7	breast:
6	chr10:58360207..58362204-chr10:58364540..58367315,2	K562	blood:
7	chr10:58346871..58349130-chr10:58356428..58359069,2	MCF-7	breast:
8	chr10:58424658..58425526-chr10:58543096..58544051,4	MCF-7	breast:
9	chr10:58412864..58414828-chr10:58418444..58421274,2	MCF-7	breast:
10	chr10:58458032..58460416-chr10:58460857..58463853,2	K562	blood:
11	chr10:58412864..58414828-chr10:58418444..58421274,2	MCF-7	breast:
12	chr10:58310627..58311484-chr10:58424524..58425160,3	MCF-7	breast:
13	chr10:58118622..58121394-chr10:58364437..58368069,3	K562	blood:
14	chr10:58338696..58340505-chr10:58341566..58344213,2	K562	blood:
15	chr10:58387072..58387735-chr9:109982409..109983123,2	MCF-7	breast:
16	chr10:58407921..58410026-chr12:33604212..33606934,2	MCF-7	breast:
17	chr10:58310627..58311484-chr10:58424524..58425160,3	MCF-7	breast:
18	chr10:58346871..58349130-chr10:58356428..58359069,2	MCF-7	breast:
19	chr10:58338696..58340505-chr10:58341566..58344213,2	K562	blood:
20	chr10:58458032..58460416-chr10:58460857..58463853,2	K562	blood:
21	chr10:58293053..58295597-chr10:58297273..58300708,4	K562	blood:
22	chr10:58403682..58405609-chr10:58417401..58419090,2	K562	blood:

Variant related genes	Relation type
ENSG00000238707	TF binding region
ENSG00000238707	CpG island
ENSG00000122952	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56934435	chr10:58297209-58297210	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs57835860	chr10:58297241-58297242	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs35180428	chr10:58297294-58297295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192323583	chr10:58297310-58297311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78627687	chr10:58297318-58297319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577029452	chr10:58297332-58297333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79666754	chr10:58297341-58297342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559816110	chr10:58297364-58297365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7919770	chr10:58297379-58297380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138644114	chr10:58297389-58297390	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs140411437	chr10:58297390-58297391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531547152	chr10:58297391-58297392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183695782	chr10:58297393-58297394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549912392	chr10:58297399-58297400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs16908959	chr10:58297400-58297401	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs145399195	chr10:58297440-58297441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs138047720	chr10:58297448-58297449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142419254	chr10:58297535-58297536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531262622	chr10:58297577-58297578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530032369	chr10:58297599-58297600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548290904	chr10:58297634-58297635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143943621	chr10:58297654-58297655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188017696	chr10:58297656-58297657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs61855101	chr10:58297663-58297664	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570681344	chr10:58297680-58297681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73275470	chr10:58297709-58297710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148227324	chr10:58297722-58297723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553564216	chr10:58297732-58297733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77971566	chr10:58297737-58297738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72802984	chr10:58297755-58297756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554595824	chr10:58297763-58297764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576111371	chr10:58297941-58297942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192775251	chr10:58297949-58297950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564989964	chr10:58297968-58297969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532281480	chr10:58297969-58297970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74137685	chr10:58298022-58298023	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs146189763	chr10:58298026-58298027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs530249499	chr10:58298041-58298042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs372983191	chr10:58298047-58298048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141148741	chr10:58298053-58298054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548477152	chr10:58298138-58298139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569664950	chr10:58298156-58298157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530832901	chr10:58298160-58298161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535487555	chr10:58298168-58298169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60791414	chr10:58298175-58298176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570594804	chr10:58298195-58298196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116568365	chr10:58298198-58298199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150729582	chr10:58298240-58298241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190166929	chr10:58298241-58298242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547730664	chr10:58298260-58298261	Enhancers	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
Autism	20858243	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:58297200-58298600	Enhancers	HMEC	breast
2	chr10:58297400-58298600	Enhancers	NHEK	skin
3	chr10:58297600-58298000	Enhancers	A549	lung
4	chr10:58297600-58298200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr10:58297600-58298200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr10:58297600-58298200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr10:58297600-58298200	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:58297600-58298400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:58297600-58298400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr10:58297600-58298400	Enhancers	NH-A	brain
11	chr10:58297600-58298600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr10:58297600-58298600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:58297800-58298200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr10:58297800-58298200	Enhancers	Placenta Amnion	Placenta Amnion
15	chr10:58297800-58298400	Enhancers	Hela-S3	cervix
16	chr10:58297800-58298600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr10:58310800-58311200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr10:58330000-58330200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr10:58341800-58344000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:58341800-58344000	Enhancers	HMEC	breast
21	chr10:58341800-58344000	Enhancers	NHEK	skin
22	chr10:58341800-58344200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:58342000-58342200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:58342200-58343200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr10:58343200-58343600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr10:58343200-58344000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:58343200-58345600	Enhancers	Fetal Heart	heart
28	chr10:58343600-58346200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr10:58343800-58344000	Enhancers	Left Ventricle	heart
30	chr10:58343800-58344000	Enhancers	Right Ventricle	heart
31	chr10:58344000-58346000	Weak transcription	HMEC	breast
32	chr10:58344000-58346200	Weak transcription	NHEK	skin
33	chr10:58344200-58345400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:58344800-58346000	Enhancers	Right Atrium	heart
35	chr10:58345400-58345600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr10:58345400-58346200	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr10:58345400-58347200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr10:58345600-58346000	Flanking Active TSS	Fetal Heart	heart
39	chr10:58345600-58346200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr10:58345600-58346400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr10:58345600-58346400	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr10:58345600-58346400	Enhancers	Left Ventricle	heart
43	chr10:58345600-58346400	Enhancers	Right Ventricle	heart
44	chr10:58345600-58346600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr10:58345600-58346600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr10:58345600-58346600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr10:58345600-58347200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr10:58345800-58346400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr10:58345800-58346400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr10:58345800-58346400	Enhancers	Esophagus	oesophagus

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