Variant report

Variant	nsv1038046
Chromosome Location	chr10:56916197-57213690
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	ATF1	chr10:56923483-56923663	K562	blood:	n/a	n/a
3	ATF3	chr10:57082402-57082655	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:56963172-56963378	GM12878	blood:	n/a	n/a
5	BATF	chr10:56963158-56963370	GM12878	blood:	n/a	n/a
6	BATF	chr10:57142366-57142608	GM12878	blood:	n/a	chr10:57142479-57142489 chr10:57142478-57142489
7	BHLHE40	chr10:57206631-57206648	GM12878	blood:	n/a	n/a
8	BRCA1	chr10:56952521-56952565	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr10:57091511-57091621	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr10:57094577-57094601	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr10:56997255-56997585	HepG2	liver:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
12	CEBPB	chr10:56975295-56975404	H1-hESC	embryonic stem cell:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
13	CEBPB	chr10:56997308-56997584	H1-hESC	embryonic stem cell:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
14	CEBPB	chr10:57014429-57014701	Hela-S3	cervix:	n/a	chr10:57014540-57014553
15	CEBPB	chr10:57129864-57130320	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr10:56997293-56997588	K562	blood:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
17	CEBPB	chr10:56980747-56981119	IMR90	lung:	n/a	chr10:56980929-56980940
18	CEBPB	chr10:57023727-57023998	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr10:56997265-56997554	Hela-S3	cervix:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
20	CEBPB	chr10:57000080-57000434	Hela-S3	cervix:	n/a	chr10:57000251-57000262
21	CEBPB	chr10:57023791-57024033	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:56934020-56934033	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr10:57014403-57014700	HepG2	liver:	n/a	chr10:57014540-57014553
24	CEBPB	chr10:56975198-56975541	HepG2	liver:	n/a	chr10:56975355-56975368 chr10:56975355-56975368 chr10:56975355-56975366
25	CEBPB	chr10:57060433-57060785	HepG2	liver:	n/a	chr10:57060613-57060624
26	CEBPB	chr10:57014490-57014614	H1-hESC	embryonic stem cell:	n/a	chr10:57014540-57014553
27	CEBPB	chr10:57128479-57128741	A549	lung:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
28	CEBPB	chr10:56980767-56981087	A549	lung:	n/a	chr10:56980929-56980940
29	CEBPB	chr10:57060537-57060765	K562	blood:	n/a	chr10:57060613-57060624
30	CEBPB	chr10:57060454-57060783	IMR90	lung:	n/a	chr10:57060613-57060624
31	CEBPB	chr10:56989960-56990287	HepG2	liver:	n/a	chr10:56990029-56990042 chr10:56990029-56990042 chr10:56990031-56990042 chr10:56990031-56990042
32	CEBPB	chr10:57000100-57000403	IMR90	lung:	n/a	chr10:57000251-57000262
33	CEBPB	chr10:56980832-56981047	H1-hESC	embryonic stem cell:	n/a	chr10:56980929-56980940
34	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
35	CEBPB	chr10:56990068-56990243	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr10:57014366-57014664	A549	lung:	n/a	chr10:57014540-57014553
37	CEBPB	chr10:57000106-57000426	HepG2	liver:	n/a	chr10:57000251-57000262
38	CEBPB	chr10:57038695-57038853	H1-hESC	embryonic stem cell:	n/a	chr10:57038777-57038788 chr10:57038777-57038788
39	CEBPB	chr10:57129959-57130282	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr10:57000172-57000294	A549	lung:	n/a	chr10:57000251-57000262
41	CEBPB	chr10:57022653-57022930	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr10:56980787-56981098	K562	blood:	n/a	chr10:56980929-56980940
43	CEBPB	chr10:57020877-57021146	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:57014381-57014683	IMR90	lung:	n/a	chr10:57014540-57014553
45	CEBPB	chr10:56997263-56997570	A549	lung:	n/a	chr10:56997430-56997439 chr10:56997428-56997439 chr10:56997428-56997441 chr10:56997430-56997441
46	CEBPB	chr10:57112618-57112952	HepG2	liver:	n/a	chr10:57112784-57112795
47	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
48	CEBPB	chr10:57128461-57128779	HepG2	liver:	n/a	chr10:57128618-57128631 chr10:57128620-57128629 chr10:57128620-57128629 chr10:57128620-57128629
49	CEBPB	chr10:57082447-57082681	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr10:56975189-56975523	IMR90	lung:	n/a	chr10:56975355-56975368 chr10:56975193-56975206 chr10:56975355-56975368 chr10:56975355-56975366

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57026776-57026826	BE2_C	brain:	n/a
2	chr10:57026776-57026826	HL-60	blood:	n/a
3	chr10:57026776-57026826	PrEC	prostate:	n/a
4	chr10:57026776-57026826	HUVEC	blood vessel:	n/a
5	chr10:57026776-57026826	PFSK-1	brain:	n/a
6	chr10:57026776-57026826	HIPEpiC	eye:	n/a
7	chr10:57026776-57026826	SK-N-SH_RA	brain:	n/a
8	chr10:57026776-57026826	HNPCEpiC	eye:	n/a
9	chr10:57026776-57026826	GM19239	blood:	n/a
10	chr10:57026776-57026826	HAEpiC	amniotic membrane:	n/a
11	chr10:57026776-57026826	PANC-1	pancreas:	n/a
12	chr10:57026776-57026826	GM12878	blood:	n/a
13	chr10:57026776-57026826	AoSMC	blood vessel:	n/a
14	chr10:57026776-57026826	HCM	heart:	n/a
15	chr10:57026776-57026826	HPAEpiC	pulmonary alveolar:	n/a
16	chr10:57026776-57026826	BJ	skin:	n/a
17	chr10:57026776-57026826	T-47D	breast:	n/a
18	chr10:57026776-57026826	NT2-D1	testis:	n/a
19	chr10:57026776-57026826	MCF10A-Er-Src	breast:	n/a
20	chr10:57026776-57026826	NHDF-neo	bronchial:	n/a
21	chr10:57026776-57026826	AG10803	skin:	n/a
22	chr10:57026776-57026826	H1-hESC	embryonic stem cell:	embryo
23	chr10:57026776-57026826	GM06990	blood:	n/a
24	chr10:57026776-57026826	SKMC	muscle:	n/a
25	chr10:57026776-57026826	HEK293	kidney:	embryo
26	chr10:57026776-57026826	A549	lung:	n/a
27	chr10:57026776-57026826	AG09309	skin:	n/a
28	chr10:57026776-57026826	AG09319	gingival:	n/a
29	chr10:57026776-57026826	ECC-1	luminal epithelium:	n/a
30	chr10:57026776-57026826	HCF	heart:	n/a
31	chr10:57026776-57026826	SK-N-SH	brain:	n/a
32	chr10:57026776-57026826	HCPEpiC	choroid plexus:	n/a
33	chr10:57026776-57026826	HepG2	liver:	n/a
34	chr10:57026776-57026826	LNCaP	prostate:	n/a
35	chr10:57026776-57026826	MCF-7	breast:	n/a
36	chr10:57026776-57026826	Hela-S3	cervix:	n/a
37	chr10:57026776-57026826	K562	blood:	n/a
38	chr10:57026776-57026826	IMR90	lung:	fetal
39	chr10:57026776-57026826	AG04450	lung:	fetal
40	chr10:57026776-57026826	Hepatocyte	liver:	n/a
41	chr10:57026776-57026826	ProgFib	skin:	n/a
42	chr10:57026776-57026826	HRE	kidney:	n/a
43	chr10:57026776-57026826	NHBE	bronchial:	n/a
44	chr10:57026776-57026826	SAEC	small airway:	n/a
45	chr10:57026776-57026826	Jurkat	blood:	n/a
46	chr10:57026776-57026826	U87	brain:	n/a
47	chr10:57026776-57026826	HCT-116	colon:	n/a
48	chr10:57026776-57026826	NB4	blood:	n/a
49	chr10:57026776-57026826	HEEpiC	esophagus:	n/a
50	chr10:57026776-57026826	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:57046804..57047423-chr10:57260630..57261301,2	MCF-7	breast:
2	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
3	chr10:56851202..56852127-chr10:57023430..57024403,6	MCF-7	breast:
4	chr10:57209977..57212489-chr10:57214390..57216525,2	K562	blood:
5	chr10:56926801..56928606-chr10:56934525..56937343,2	K562	blood:
6	chr10:57046815..57047629-chr10:57390561..57391169,3	MCF-7	breast:
7	chr10:57177168..57179759-chr10:57181346..57183496,2	K562	blood:
8	chr10:57047149..57047763-chr10:57389634..57390254,2	MCF-7	breast:
9	chr10:56930146..56932824-chr10:56934216..56936608,2	K562	blood:
10	chr10:55757466..55757977-chr10:57022925..57023910,2	MCF-7	breast:
11	chr10:57045296..57046208-chr13:38876652..38877471,2	MCF-7	breast:
12	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
13	chr10:57070275..57072956-chr10:57073924..57076698,2	K562	blood:
14	chr10:57154707..57155371-chr10:83749526..83750393,2	MCF-7	breast:
15	chr10:56930146..56932824-chr10:56934216..56936608,2	K562	blood:
16	chr10:57128438..57131267-chr10:57136615..57139314,2	K562	blood:
17	chr10:56926801..56928606-chr10:56934525..56937343,2	K562	blood:
18	chr10:57177168..57179759-chr10:57181346..57183496,2	K562	blood:
19	chr10:56856112..56857067-chr10:57023573..57024305,2	MCF-7	breast:
20	chr10:57012609..57015608-chr6:34209555..34212466,2	K562	blood:
21	chr10:57077687..57079914-chr10:57092227..57093981,2	K562	blood:
22	chr10:57063877..57064377-chr19:2475827..2476338,2	HCT-116	colon:

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

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

Extended variants
information (count: 3659 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:3659 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150269647	chr10:56916220-56916221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116761624	chr10:56916226-56916227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115955599	chr10:56916231-56916232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs36107985	chr10:56916237-56916238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531318596	chr10:56916238-56916239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541888737	chr10:56916254-56916255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548843958	chr10:56916258-56916259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186227481	chr10:56916259-56916260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190496717	chr10:56916269-56916270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547526182	chr10:56916279-56916280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181984221	chr10:56916284-56916285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574930311	chr10:56916290-56916291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11004759	chr10:56916347-56916348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs527836858	chr10:56916350-56916351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548079825	chr10:56916366-56916367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187193923	chr10:56916376-56916377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190810252	chr10:56916386-56916387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369812017	chr10:56916400-56916401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554494991	chr10:56916422-56916423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568122822	chr10:56916452-56916453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533993873	chr10:56916471-56916472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553995016	chr10:56916486-56916487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183001274	chr10:56916492-56916493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2680318	chr10:56916543-56916544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs185932436	chr10:56916575-56916576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576452737	chr10:56916633-56916634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1838453	chr10:56916637-56916638	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs367829212	chr10:56916647-56916648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561630279	chr10:56916668-56916669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141975062	chr10:56916720-56916721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557710148	chr10:56916748-56916749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147002930	chr10:56916749-56916750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1838454	chr10:56916788-56916789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs372343292	chr10:56916824-56916825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564058631	chr10:56916832-56916833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2799576	chr10:56916841-56916842	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs71461282	chr10:56916886-56916887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200682692	chr10:56916887-56916888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs201601381	chr10:56916892-56916893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201029876	chr10:56916896-56916897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs71014455	chr10:56916897-56916898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs543785713	chr10:56916910-56916911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10825477	chr10:56916940-56916941	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs10825478	chr10:56916962-56916963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531844553	chr10:56916969-56916970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548485990	chr10:56916992-56916993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190225190	chr10:56916997-56916998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541162184	chr10:56917000-56917001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9733594	chr10:56917012-56917013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs9733596	chr10:56917040-56917041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:278 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:56915000-56918200	Weak transcription	Fetal Heart	heart
2	chr10:56918200-56919000	Enhancers	Fetal Heart	heart
3	chr10:56918400-56918800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr10:56918400-56918800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr10:56918800-56920600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:56920000-56920600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr10:56920000-56920800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:56920000-56921800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr10:56920200-56920800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr10:56920200-56921400	Enhancers	HMEC	breast
11	chr10:56920400-56921200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr10:56920400-56921600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr10:56920600-56920800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:56920600-56921800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr10:56920800-56922400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr10:56921200-56921600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr10:56921600-56922800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr10:56922200-56922400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr10:56922400-56922600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr10:56932200-56932600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr10:56932200-56932800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr10:56932200-56933000	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr10:56932200-56933200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr10:56932600-56933000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
25	chr10:56932600-56933000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr10:56932800-56933000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr10:56932800-56934000	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr10:56933000-56934000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:56933000-56934000	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr10:56933000-56934000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr10:56933000-56934400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr10:56933200-56933600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr10:56933600-56934400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr10:56934000-56934200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr10:56934000-56934400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr10:56934000-56934600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr10:56934000-56934600	Enhancers	Fetal Stomach	stomach
38	chr10:56934200-56934400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr10:56934200-56934400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr10:56934200-56934400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr10:56934800-56937200	Weak transcription	Psoas Muscle	Psoas
42	chr10:56943200-56943800	Enhancers	HMEC	breast
43	chr10:56943600-56944000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr10:56943800-56944200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr10:56947200-56947800	Enhancers	Fetal Stomach	stomach
46	chr10:56951000-56951200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr10:56951200-56951600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr10:56961400-56961800	Enhancers	Fetal Stomach	stomach
49	chr10:56961800-56962200	Weak transcription	Fetal Stomach	stomach
50	chr10:56962200-56962400	Enhancers	Fetal Stomach	stomach

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