Variant report

Variant	nsv540640
Chromosome Location	chr10:56939249-57201820
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	chr10:57023730-57024067	HepG2	liver:	n/a	n/a
2	ATF3	chr10:57082402-57082655	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr10:57142366-57142608	GM12878	blood:	n/a	chr10:57142479-57142489 chr10:57142478-57142489
4	BATF	chr10:56963172-56963378	GM12878	blood:	n/a	n/a
5	BATF	chr10:56963158-56963370	GM12878	blood:	n/a	n/a
6	BRCA1	chr10:57091511-57091621	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr10:57094577-57094601	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr10:56952521-56952565	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr10:56990068-56990243	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr10:57129864-57130320	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr10:57070782-57071102	IMR90	lung:	n/a	chr10:57070961-57070978 chr10:57070962-57070973 chr10:57070830-57070841 chr10:57070932-57070945 chr10:57070932-57070943 chr10:57070963-57070975 chr10:57070828-57070841
12	CEBPB	chr10:56997263-56997570	A549	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
13	CEBPB	chr10:57000172-57000294	A549	lung:	n/a	chr10:57000251-57000262
14	CEBPB	chr10:57082447-57082681	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr10:57060433-57060785	HepG2	liver:	n/a	chr10:57060613-57060624
16	CEBPB	chr10:56980832-56981047	H1-hESC	embryonic stem cell:	n/a	chr10:56980929-56980940
17	CEBPB	chr10:57020877-57021146	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:57162077-57162382	HepG2	liver:	n/a	chr10:57162197-57162208
19	CEBPB	chr10:56997255-56997585	HepG2	liver:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
20	CEBPB	chr10:56975189-56975523	IMR90	lung:	n/a	chr10:56975355-56975368 chr10:56975193-56975206 chr10:56975355-56975368 chr10:56975355-56975366
21	CEBPB	chr10:57128529-57128721	K562	blood:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
22	CEBPB	chr10:56980759-56981124	HepG2	liver:	n/a	chr10:56980929-56980940
23	CEBPB	chr10:56975198-56975541	HepG2	liver:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
24	CEBPB	chr10:57000106-57000426	HepG2	liver:	n/a	chr10:57000251-57000262
25	CEBPB	chr10:57129959-57130282	ECC-1	luminal epithelium:	n/a	n/a
26	CEBPB	chr10:57014381-57014683	IMR90	lung:	n/a	chr10:57014540-57014553
27	CEBPB	chr10:57130696-57130958	IMR90	lung:	n/a	chr10:57130811-57130822
28	CEBPB	chr10:57070762-57071104	HepG2	liver:	n/a	chr10:57070961-57070978 chr10:57070962-57070973 chr10:57070830-57070841 chr10:57070932-57070945 chr10:57070932-57070943 chr10:57070963-57070975 chr10:57070828-57070841
29	CEBPB	chr10:56980767-56981087	A549	lung:	n/a	chr10:56980929-56980940
30	CEBPB	chr10:56997308-56997584	H1-hESC	embryonic stem cell:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
31	CEBPB	chr10:56997293-56997588	K562	blood:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
32	CEBPB	chr10:56975295-56975404	H1-hESC	embryonic stem cell:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
33	CEBPB	chr10:57022653-57022930	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr10:57014366-57014664	A549	lung:	n/a	chr10:57014540-57014553
35	CEBPB	chr10:56980747-56981119	IMR90	lung:	n/a	chr10:56980929-56980940
36	CEBPB	chr10:56975199-56975467	A549	lung:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
37	CEBPB	chr10:57000080-57000434	Hela-S3	cervix:	n/a	chr10:57000251-57000262
38	CEBPB	chr10:57000100-57000403	IMR90	lung:	n/a	chr10:57000251-57000262
39	CEBPB	chr10:57128470-57128745	IMR90	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
40	CEBPB	chr10:57090142-57090629	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:56989960-56990287	HepG2	liver:	n/a	chr10:56990029-56990042 chr10:56990029-56990042 chr10:56990031-56990042 chr10:56990031-56990042
42	CEBPB	chr10:57023727-57023998	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr10:57128479-57128741	A549	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
44	CEBPB	chr10:57038695-57038853	H1-hESC	embryonic stem cell:	n/a	chr10:57038777-57038788 chr10:57038777-57038788
45	CEBPB	chr10:56987661-56987948	HepG2	liver:	n/a	chr10:56987791-56987802 chr10:56987855-56987868
46	CEBPB	chr10:57128461-57128779	HepG2	liver:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
47	CEBPB	chr10:56997254-56997579	IMR90	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
48	CEBPB	chr10:57112618-57112952	HepG2	liver:	n/a	chr10:57112784-57112795
49	CEBPB	chr10:57014403-57014700	HepG2	liver:	n/a	chr10:57014540-57014553
50	CEBPB	chr10:56980787-56981098	K562	blood:	n/a	chr10:56980929-56980940

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57026776-57026826	NH-A	brain:	n/a
2	chr10:57026776-57026826	AoSMC	blood vessel:	n/a
3	chr10:57026776-57026826	ovcar-3	ovarian:	n/a
4	chr10:57026776-57026826	AG10803	skin:	n/a
5	chr10:57026776-57026826	A549	lung:	n/a
6	chr10:57026776-57026826	Hela-S3	cervix:	n/a
7	chr10:57026776-57026826	PFSK-1	brain:	n/a
8	chr10:57026776-57026826	HRE	kidney:	n/a
9	chr10:57026776-57026826	GM12891	blood:	n/a
10	chr10:57026776-57026826	GM06990	blood:	n/a
11	chr10:57026776-57026826	LNCaP	prostate:	n/a
12	chr10:57026776-57026826	HCF	heart:	n/a
13	chr10:57026776-57026826	SKMC	muscle:	n/a
14	chr10:57026776-57026826	U87	brain:	n/a
15	chr10:57026776-57026826	PrEC	prostate:	n/a
16	chr10:57026776-57026826	HNPCEpiC	eye:	n/a
17	chr10:57026776-57026826	Hepatocyte	liver:	n/a
18	chr10:57026776-57026826	HAEpiC	amniotic membrane:	n/a
19	chr10:57026776-57026826	HMEC	breast:	n/a
20	chr10:57026776-57026826	GM12878	blood:	n/a
21	chr10:57026776-57026826	AG04450	lung:	fetal
22	chr10:57026776-57026826	HCPEpiC	choroid plexus:	n/a
23	chr10:57026776-57026826	SAEC	small airway:	n/a
24	chr10:57026776-57026826	NHDF-neo	bronchial:	n/a
25	chr10:57026776-57026826	ProgFib	skin:	n/a
26	chr10:57026776-57026826	HCT-116	colon:	n/a
27	chr10:57026776-57026826	SK-N-SH_RA	brain:	n/a
28	chr10:57026776-57026826	GM19239	blood:	n/a
29	chr10:57026776-57026826	T-47D	breast:	n/a
30	chr10:57026776-57026826	CMK	blood:	n/a
31	chr10:57026776-57026826	H1-hESC	embryonic stem cell:	embryo
32	chr10:57026776-57026826	MCF10A-Er-Src	breast:	n/a
33	chr10:57026776-57026826	GM12892	blood:	n/a
34	chr10:57026776-57026826	K562	blood:	n/a
35	chr10:57026776-57026826	NB4	blood:	n/a
36	chr10:57026776-57026826	AG09309	skin:	n/a
37	chr10:57026776-57026826	HEK293	kidney:	embryo
38	chr10:57026776-57026826	AG04449	skin:	fetal
39	chr10:57026776-57026826	HRCEpiC	kidney:	n/a
40	chr10:57026776-57026826	HRPEpiC	eye:	n/a
41	chr10:57026776-57026826	HUVEC	blood vessel:	n/a
42	chr10:57026776-57026826	Caco-2	colon:	n/a
43	chr10:57026776-57026826	NT2-D1	testis:	n/a
44	chr10:57026776-57026826	HIPEpiC	eye:	n/a
45	chr10:57026776-57026826	RPTEC	kidney:	n/a
46	chr10:57026776-57026826	MCF-7	breast:	n/a
47	chr10:57026776-57026826	NHBE	bronchial:	n/a
48	chr10:57026776-57026826	BJ	skin:	n/a
49	chr10:57026776-57026826	AG09319	gingival:	n/a
50	chr10:57026776-57026826	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr10:56851202..56852127-chr10:57023430..57024403,6	MCF-7	breast:
2	chr10:57012609..57015608-chr6:34209555..34212466,2	K562	blood:
3	chr10:57177168..57179759-chr10:57181346..57183496,2	K562	blood:
4	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
5	chr10:55757466..55757977-chr10:57022925..57023910,2	MCF-7	breast:
6	chr10:57045296..57046208-chr13:38876652..38877471,2	MCF-7	breast:
7	chr10:57177168..57179759-chr10:57181346..57183496,2	K562	blood:
8	chr10:57077687..57079914-chr10:57092227..57093981,2	K562	blood:
9	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
10	chr10:57047149..57047763-chr10:57389634..57390254,2	MCF-7	breast:
11	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
12	chr10:57046804..57047423-chr10:57260630..57261301,2	MCF-7	breast:
13	chr10:57046815..57047629-chr10:57390561..57391169,3	MCF-7	breast:
14	chr10:57154707..57155371-chr10:83749526..83750393,2	MCF-7	breast:
15	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
16	chr10:56856112..56857067-chr10:57023573..57024305,2	MCF-7	breast:
17	chr10:57063877..57064377-chr19:2475827..2476338,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-4	chr10:57007515-57007648	ENSG00000236744.2
2	lnc-ZWINT-4	chr10:57125852-57125973	ENSG00000236744.2
3	lnc-ZWINT-4	chr10:57125852-57125973	ENSG00000236744.1
4	lnc-ZWINT-4	chr10:57007508-57007648	ENSG00000236744.1

Variant related genes	Relation type
PCDH15	TF binding region
PCDH15	CpG island
ENSG00000099860	chromatin interactions
ENSG00000150275	chromatin interactions

Extended variants
information (count: 3027 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3027 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551782726	chr10:56943202-56943203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140057176	chr10:56943270-56943271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536419248	chr10:56943376-56943377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571280224	chr10:56943418-56943419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs530929566	chr10:56943437-56943438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs397813494	chr10:56943446-56943447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs398114363	chr10:56943447-56943448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375794691	chr10:56943448-56943449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368234183	chr10:56943449-56943450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554918552	chr10:56943488-56943489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs111634643	chr10:56943507-56943508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1822760	chr10:56943548-56943549	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146236227	chr10:56943580-56943581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139455081	chr10:56943584-56943585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534190557	chr10:56943629-56943630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375223135	chr10:56943653-56943654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs3930839	chr10:56943658-56943659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149957275	chr10:56943668-56943669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145045059	chr10:56943697-56943698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189175646	chr10:56943699-56943700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs149036391	chr10:56943751-56943752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537947638	chr10:56943782-56943783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78125068	chr10:56943789-56943790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141207916	chr10:56943798-56943799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543240208	chr10:56943806-56943807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577162451	chr10:56943847-56943848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11004770	chr10:56943953-56943954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573503634	chr10:56943975-56943976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192569266	chr10:56943977-56943978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs74136388	chr10:56944014-56944015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139231974	chr10:56944015-56944016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544405985	chr10:56944028-56944029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570739093	chr10:56944057-56944058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76185274	chr10:56944094-56944095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561083991	chr10:56944108-56944109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373448473	chr10:56944137-56944138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111814216	chr10:56944154-56944155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184319288	chr10:56944164-56944165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs12265891	chr10:56947230-56947231	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556742838	chr10:56947237-56947238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373909435	chr10:56947251-56947252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111428554	chr10:56947345-56947346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112465259	chr10:56947359-56947360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538202576	chr10:56947375-56947376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs541695251	chr10:56947527-56947528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs561901432	chr10:56947598-56947599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529126154	chr10:56947603-56947604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572269065	chr10:56947606-56947607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370707675	chr10:56947684-56947685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs187441826	chr10:56947739-56947740	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Breast cancer	22522925	CNVD
Usher type I cohort	17277737	CNVD
Usher type I cohort	21436283	CNVD
Leukemia	21357790	CNVD
Medulloblastoma	22832581	CNVD
small cell lung cancer	17426248	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	20962326	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56943200-56943800	Enhancers	HMEC	breast
2	chr10:56943600-56944000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:56943800-56944200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:56947200-56947800	Enhancers	Fetal Stomach	stomach
5	chr10:56951000-56951200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:56951200-56951600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:56961400-56961800	Enhancers	Fetal Stomach	stomach
8	chr10:56961800-56962200	Weak transcription	Fetal Stomach	stomach
9	chr10:56962200-56962400	Enhancers	Fetal Stomach	stomach
10	chr10:56962400-56963400	Weak transcription	Fetal Stomach	stomach
11	chr10:56963600-56963800	Enhancers	Fetal Stomach	stomach
12	chr10:56977800-56978400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr10:56992200-56993600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr10:56992400-56992600	Enhancers	GM12878-XiMat	blood
15	chr10:56992400-56992600	Enhancers	Hela-S3	cervix
16	chr10:56992400-56992800	Active TSS	Stomach Smooth Muscle	stomach
17	chr10:56992400-56993400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:56992400-56993400	Active TSS	Duodenum Mucosa	Duodenum
19	chr10:56992600-56993000	Enhancers	Liver	Liver
20	chr10:56992600-56993400	Active TSS	GM12878-XiMat	blood
21	chr10:56992800-56993200	Active TSS	Rectal Mucosa Donor 29	rectum
22	chr10:56993000-56993400	Active TSS	Duodenum Smooth Muscle	Duodenum
23	chr10:56993000-56993600	Active TSS	Liver	Liver
24	chr10:56998800-56999800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:56999200-56999600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr10:56999200-57000000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr10:56999800-57002200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr10:57002000-57002800	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr10:57002200-57002800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr10:57002400-57003200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr10:57005400-57005600	Enhancers	HUVEC	blood vessel
32	chr10:57005600-57005800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr10:57005600-57006000	Active TSS	Colonic Mucosa	Colon
34	chr10:57005600-57006000	Enhancers	Ovary	ovary
35	chr10:57005600-57006000	Flanking Active TSS	HUVEC	blood vessel
36	chr10:57005600-57006200	Active TSS	Stomach Smooth Muscle	stomach
37	chr10:57005600-57006200	Active TSS	NHDF-Ad	bronchial
38	chr10:57005600-57006400	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr10:57005800-57006200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr10:57006000-57006400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr10:57006000-57006400	Active TSS	HUVEC	blood vessel
42	chr10:57006200-57007200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr10:57006800-57007600	Enhancers	Fetal Lung	lung
44	chr10:57007200-57007400	Enhancers	Stomach Smooth Muscle	stomach
45	chr10:57019800-57020600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr10:57019800-57020800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr10:57019800-57020800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr10:57020200-57021000	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr10:57020600-57026400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr10:57020800-57021000	Enhancers	HUES6 Cell Line	embryonic stem cell

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