Variant report

Variant	nsv895474
Chromosome Location	chr10:56993816-57207096
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	BHLHE40	chr10:57206631-57206648	GM12878	blood:	n/a	n/a
5	BRCA1	chr10:57094577-57094601	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr10:57091511-57091621	Hela-S3	cervix:	n/a	n/a
7	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
8	CEBPB	chr10:57128470-57128745	IMR90	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
9	CEBPB	chr10:57000172-57000294	A549	lung:	n/a	chr10:57000251-57000262
10	CEBPB	chr10:57060537-57060765	K562	blood:	n/a	chr10:57060613-57060624
11	CEBPB	chr10:57090142-57090629	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:56997308-56997584	H1-hESC	embryonic stem cell:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
13	CEBPB	chr10:57020877-57021146	HepG2	liver:	n/a	n/a
14	CEBPB	chr10:57112618-57112952	HepG2	liver:	n/a	chr10:57112784-57112795
15	CEBPB	chr10:57022653-57022930	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr10:57060510-57060769	A549	lung:	n/a	chr10:57060613-57060624
17	CEBPB	chr10:57000100-57000403	IMR90	lung:	n/a	chr10:57000251-57000262
18	CEBPB	chr10:57128479-57128741	A549	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
19	CEBPB	chr10:57014366-57014664	A549	lung:	n/a	chr10:57014540-57014553
20	CEBPB	chr10:57000080-57000434	Hela-S3	cervix:	n/a	chr10:57000251-57000262
21	CEBPB	chr10:57014381-57014683	IMR90	lung:	n/a	chr10:57014540-57014553
22	CEBPB	chr10:56997255-56997585	HepG2	liver:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
23	CEBPB	chr10:57023791-57024033	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr10:57129959-57130282	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr10:57023727-57023998	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:57082447-57082681	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr10:57014403-57014700	HepG2	liver:	n/a	chr10:57014540-57014553
28	CEBPB	chr10:57162077-57162382	HepG2	liver:	n/a	chr10:57162197-57162208
29	CEBPB	chr10:57014429-57014701	Hela-S3	cervix:	n/a	chr10:57014540-57014553
30	CEBPB	chr10:57014490-57014614	H1-hESC	embryonic stem cell:	n/a	chr10:57014540-57014553
31	CEBPB	chr10:56997293-56997588	K562	blood:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
32	CEBPB	chr10:56997254-56997579	IMR90	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
33	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
34	CEBPB	chr10:57060454-57060783	IMR90	lung:	n/a	chr10:57060613-57060624
35	CEBPB	chr10:57129864-57130320	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr10:57130666-57130959	HepG2	liver:	n/a	chr10:57130811-57130822
37	CEBPB	chr10:57000106-57000426	HepG2	liver:	n/a	chr10:57000251-57000262
38	CEBPB	chr10:56997263-56997570	A549	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
39	CEBPB	chr10:56997265-56997554	Hela-S3	cervix:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
40	CEBPB	chr10:57128461-57128779	HepG2	liver:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
41	CEBPB	chr10:57130696-57130958	IMR90	lung:	n/a	chr10:57130811-57130822
42	CEBPB	chr10:57060433-57060785	HepG2	liver:	n/a	chr10:57060613-57060624
43	CEBPB	chr10:57128529-57128721	K562	blood:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
44	CEBPB	chr10:57060444-57060785	Hela-S3	cervix:	n/a	chr10:57060613-57060624
45	CEBPB	chr10:57038695-57038853	H1-hESC	embryonic stem cell:	n/a	chr10:57038777-57038788 chr10:57038777-57038788
46	CTCF	chr10:57023729-57024212	A549	lung:	n/a	n/a
47	CTCF	chr10:57023820-57023970	HRE	kidney:	n/a	n/a
48	CTCF	chr10:57068040-57068190	GM12873	blood:	n/a	n/a
49	CTCF	chr10:57170418-57170701	Medullo	brain:	n/a	chr10:57170551-57170572
50	CTCF	chr10:57023826-57023953	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57026776-57026826	HepG2	liver:	n/a
2	chr10:57026776-57026826	AG04450	lung:	fetal
3	chr10:57026776-57026826	A549	lung:	n/a
4	chr10:57026776-57026826	SK-N-MC	brain:	n/a
5	chr10:57026776-57026826	HRCEpiC	kidney:	n/a
6	chr10:57026776-57026826	T-47D	breast:	n/a
7	chr10:57026776-57026826	U87	brain:	n/a
8	chr10:57026776-57026826	AG09319	gingival:	n/a
9	chr10:57026776-57026826	HCT-116	colon:	n/a
10	chr10:57026776-57026826	K562	blood:	n/a
11	chr10:57026776-57026826	HL-60	blood:	n/a
12	chr10:57026776-57026826	NHDF-neo	bronchial:	n/a
13	chr10:57026776-57026826	NB4	blood:	n/a
14	chr10:57026776-57026826	LNCaP	prostate:	n/a
15	chr10:57026776-57026826	H1-hESC	embryonic stem cell:	embryo
16	chr10:57026776-57026826	HCM	heart:	n/a
17	chr10:57026776-57026826	GM06990	blood:	n/a
18	chr10:57026776-57026826	HAEpiC	amniotic membrane:	n/a
19	chr10:57026776-57026826	MCF10A-Er-Src	breast:	n/a
20	chr10:57026776-57026826	IMR90	lung:	fetal
21	chr10:57026776-57026826	AoSMC	blood vessel:	n/a
22	chr10:57026776-57026826	AG10803	skin:	n/a
23	chr10:57026776-57026826	SK-N-SH	brain:	n/a
24	chr10:57026776-57026826	HUVEC	blood vessel:	n/a
25	chr10:57026776-57026826	HMEC	breast:	n/a
26	chr10:57026776-57026826	Caco-2	colon:	n/a
27	chr10:57026776-57026826	HPAEpiC	pulmonary alveolar:	n/a
28	chr10:57026776-57026826	ovcar-3	ovarian:	n/a
29	chr10:57026776-57026826	HNPCEpiC	eye:	n/a
30	chr10:57026776-57026826	MCF-7	breast:	n/a
31	chr10:57026776-57026826	ProgFib	skin:	n/a
32	chr10:57026776-57026826	GM12892	blood:	n/a
33	chr10:57026776-57026826	HEEpiC	esophagus:	n/a
34	chr10:57026776-57026826	HCF	heart:	n/a
35	chr10:57026776-57026826	HRE	kidney:	n/a
36	chr10:57026776-57026826	SK-N-SH_RA	brain:	n/a
37	chr10:57026776-57026826	GM12878	blood:	n/a
38	chr10:57026776-57026826	NT2-D1	testis:	n/a
39	chr10:57026776-57026826	ECC-1	luminal epithelium:	n/a
40	chr10:57026776-57026826	GM19239	blood:	n/a
41	chr10:57026776-57026826	NH-A	brain:	n/a
42	chr10:57026776-57026826	PrEC	prostate:	n/a
43	chr10:57026776-57026826	BE2_C	brain:	n/a
44	chr10:57026776-57026826	HCPEpiC	choroid plexus:	n/a
45	chr10:57026776-57026826	Jurkat	blood:	n/a
46	chr10:57026776-57026826	SAEC	small airway:	n/a
47	chr10:57026776-57026826	RPTEC	kidney:	n/a
48	chr10:57026776-57026826	SKMC	muscle:	n/a
49	chr10:57026776-57026826	NHBE	bronchial:	n/a
50	chr10:57026776-57026826	GM12891	blood:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZWINT-4	chr10:57125852-57125973	ENSG00000236744.2
2	lnc-ZWINT-4	chr10:57007515-57007648	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
ENSG00000150275	chromatin interactions
ENSG00000099860	chromatin interactions

Extended variants
information (count: 2832 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2832 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191913573	chr10:56998855-56998856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182860491	chr10:56998863-56998864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1899910	chr10:56998878-56998879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142832220	chr10:56998917-56998918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545705537	chr10:56998934-56998935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549727135	chr10:56998950-56998951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs151034730	chr10:56999052-56999053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113671289	chr10:56999099-56999100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140863313	chr10:56999102-56999103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561198072	chr10:56999187-56999188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187946713	chr10:56999201-56999202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575697506	chr10:56999217-56999218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs540014578	chr10:56999270-56999271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559908720	chr10:56999394-56999395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544301002	chr10:56999418-56999419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79514064	chr10:56999446-56999447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552033470	chr10:56999447-56999448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192409877	chr10:56999511-56999512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184491164	chr10:56999515-56999516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs12268534	chr10:56999518-56999519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147892204	chr10:56999649-56999650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187747790	chr10:56999708-56999709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536861588	chr10:56999744-56999745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73267509	chr10:56999769-56999770	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs569594006	chr10:56999797-56999798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs539368985	chr10:56999806-56999807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559278243	chr10:56999859-56999860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575730591	chr10:56999889-56999890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs72803813	chr10:56999944-56999945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530906755	chr10:56999950-56999951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529814106	chr10:56999995-56999996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192754582	chr10:57000023-57000024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs71492650	chr10:57000035-57000036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17611988	chr10:57000058-57000059	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184703497	chr10:57000093-57000094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527692167	chr10:57000134-57000135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538498537	chr10:57000169-57000170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76822115	chr10:57000197-57000198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558079651	chr10:57000261-57000262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552202583	chr10:57000354-57000355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545704970	chr10:57000372-57000373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570492859	chr10:57000378-57000379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562411369	chr10:57000423-57000424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189118840	chr10:57000431-57000432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547833184	chr10:57000432-57000433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368079067	chr10:57000452-57000453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561714025	chr10:57000465-57000466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146975943	chr10:57000472-57000473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369587580	chr10:57000493-57000494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549831169	chr10:57000534-57000535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Acute myeloid leukemia	20962326	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56998800-56999800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr10:56999200-56999600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr10:56999200-57000000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr10:56999800-57002200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr10:57002000-57002800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr10:57002200-57002800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr10:57002400-57003200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr10:57005400-57005600	Enhancers	HUVEC	blood vessel
9	chr10:57005600-57005800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr10:57005600-57006000	Active TSS	Colonic Mucosa	Colon
11	chr10:57005600-57006000	Enhancers	Ovary	ovary
12	chr10:57005600-57006000	Flanking Active TSS	HUVEC	blood vessel
13	chr10:57005600-57006200	Active TSS	Stomach Smooth Muscle	stomach
14	chr10:57005600-57006200	Active TSS	NHDF-Ad	bronchial
15	chr10:57005600-57006400	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr10:57005800-57006200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr10:57006000-57006400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr10:57006000-57006400	Active TSS	HUVEC	blood vessel
19	chr10:57006200-57007200	Weak transcription	Stomach Smooth Muscle	stomach
20	chr10:57006800-57007600	Enhancers	Fetal Lung	lung
21	chr10:57007200-57007400	Enhancers	Stomach Smooth Muscle	stomach
22	chr10:57019800-57020600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr10:57019800-57020800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr10:57019800-57020800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr10:57020200-57021000	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr10:57020600-57026400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:57020800-57021000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr10:57020800-57024000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr10:57021000-57026200	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr10:57021000-57026600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr10:57022800-57023400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr10:57022800-57026400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr10:57023000-57023400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr10:57023000-57023400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr10:57024000-57024200	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr10:57024000-57024200	Enhancers	Stomach Smooth Muscle	stomach
37	chr10:57024000-57024400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr10:57024200-57026200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr10:57024400-57024600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr10:57024400-57026200	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr10:57024600-57026200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr10:57026200-57026800	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr10:57026200-57026800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr10:57026200-57026800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr10:57026200-57027000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr10:57026200-57027000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr10:57026200-57027000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:57026400-57026800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr10:57026400-57026800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr10:57026400-57026800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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