Variant report

Variant	nsv1047838
Chromosome Location	chr10:43234590-43379219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2540)
CpG islands
(count:3358)
Chromatin interactive
region (count:96)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2540 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43277876-43278461	K562	blood:	n/a	n/a
2	ARID3A	chr10:43277794-43278837	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:43264291-43264671	K562	blood:	n/a	n/a
4	ARID3A	chr10:43366883-43366989	HepG2	liver:	n/a	n/a
5	ATF1	chr10:43277837-43279020	K562	blood:	n/a	n/a
6	ATF1	chr10:43239265-43239373	K562	blood:	n/a	n/a
7	ATF1	chr10:43264252-43264654	K562	blood:	n/a	n/a
8	ATF1	chr10:43362943-43363029	K562	blood:	n/a	n/a
9	ATF1	chr10:43327236-43327383	K562	blood:	n/a	n/a
10	ATF2	chr10:43296575-43296964	GM12878	blood:	n/a	n/a
11	ATF2	chr10:43277906-43278566	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr10:43277895-43278451	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr10:43277891-43278637	GM12878	blood:	n/a	n/a
14	ATF2	chr10:43277935-43278664	GM12878	blood:	n/a	n/a
15	ATF3	chr10:43277853-43278406	A549	lung:	n/a	n/a
16	ATF3	chr10:43277721-43278499	A549	lung:	n/a	n/a
17	ATF3	chr10:43278350-43278642	K562	blood:	n/a	n/a
18	BACH1	chr10:43360208-43360382	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr10:43248608-43248903	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr10:43277990-43278352	K562	blood:	n/a	n/a
21	BACH1	chr10:43362173-43362398	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr10:43361855-43361897	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr10:43277956-43278287	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr10:43323789-43323995	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr10:43277973-43278382	GM12878	blood:	n/a	n/a
26	BATF	chr10:43296561-43297027	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:43312407-43312659	H1-hESC	embryonic stem cell:	n/a	n/a
28	BCL11A	chr10:43277864-43278662	GM12878	blood:	n/a	n/a
29	BCL3	chr10:43278061-43278405	GM12878	blood:	n/a	n/a
30	BCL3	chr10:43371657-43371891	GM12878	blood:	n/a	n/a
31	BCL3	chr10:43277861-43278491	A549	lung:	n/a	n/a
32	BCL3	chr10:43365040-43365394	GM12878	blood:	n/a	n/a
33	BCL3	chr10:43375696-43375924	GM12878	blood:	n/a	n/a
34	BCL3	chr10:43277795-43278523	A549	lung:	n/a	n/a
35	BCL3	chr10:43371612-43371871	GM12878	blood:	n/a	n/a
36	BCL3	chr10:43278010-43278387	GM12878	blood:	n/a	n/a
37	BCL3	chr10:43375692-43375971	GM12878	blood:	n/a	n/a
38	BCLAF1	chr10:43277828-43278426	K562	blood:	n/a	n/a
39	BCLAF1	chr10:43277681-43278535	GM12878	blood:	n/a	n/a
40	BCLAF1	chr10:43277795-43278504	K562	blood:	n/a	n/a
41	BCLAF1	chr10:43277746-43278546	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:43277879-43278655	GM12878	blood:	n/a	n/a
43	BHLHE40	chr10:43264879-43264880	K562	blood:	n/a	n/a
44	BHLHE40	chr10:43264256-43264646	K562	blood:	n/a	n/a
45	BHLHE40	chr10:43366559-43366917	HepG2	liver:	n/a	chr10:43366705-43366726 chr10:43366712-43366721
46	BHLHE40	chr10:43362265-43362383	K562	blood:	n/a	n/a
47	BHLHE40	chr10:43375436-43375595	K562	blood:	n/a	chr10:43375480-43375489 chr10:43375479-43375488 chr10:43375478-43375491 chr10:43375480-43375489
48	BHLHE40	chr10:43277825-43278574	K562	blood:	n/a	n/a
49	BHLHE40	chr10:43366623-43366760	K562	blood:	n/a	chr10:43366705-43366726 chr10:43366712-43366721
50	BHLHE40	chr10:43265256-43265443	K562	blood:	n/a	n/a

(count:3358 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43277850-43277900	Hela-S3	cervix:	n/a
2	chr10:43335974-43336024	GM12892	blood:	n/a
3	chr10:43278230-43278280	AG09319	gingival:	n/a
4	chr10:43277850-43277900	Hela-S3	cervix:	n/a
5	chr10:43335974-43336024	GM12892	blood:	n/a
6	chr10:43278230-43278280	AG09319	gingival:	n/a
7	chr10:43331952-43332002	HCPEpiC	choroid plexus:	n/a
8	chr10:43280976-43281026	T-47D	breast:	n/a
9	chr10:43249924-43249974	NHBE	bronchial:	n/a
10	chr10:43250800-43250850	T-47D	breast:	n/a
11	chr10:43334380-43334430	HCF	heart:	n/a
12	chr10:43251951-43252001	HRCEpiC	kidney:	n/a
13	chr10:43252305-43252355	HCM	heart:	n/a
14	chr10:43354902-43354952	SK-N-MC	brain:	n/a
15	chr10:43362076-43362126	ProgFib	skin:	n/a
16	chr10:43361618-43361668	BE2_C	brain:	n/a
17	chr10:43277862-43277912	IMR90	lung:	fetal
18	chr10:43277534-43277584	SK-N-MC	brain:	n/a
19	chr10:43361605-43361655	BE2_C	brain:	n/a
20	chr10:43278349-43278399	HRCEpiC	kidney:	n/a
21	chr10:43331952-43332002	SK-N-SH	brain:	n/a
22	chr10:43278214-43278264	GM06990	blood:	n/a
23	chr10:43277938-43277988	GM06990	blood:	n/a
24	chr10:43248870-43248920	GM12891	blood:	n/a
25	chr10:43362202-43362252	GM12892	blood:	n/a
26	chr10:43362626-43362676	HAEpiC	amniotic membrane:	n/a
27	chr10:43277745-43277795	NB4	blood:	n/a
28	chr10:43278230-43278280	Caco-2	colon:	n/a
29	chr10:43361605-43361655	GM12892	blood:	n/a
30	chr10:43375618-43375668	Hela-S3	cervix:	n/a
31	chr10:43277938-43277988	Hela-S3	cervix:	n/a
32	chr10:43250063-43250113	ovcar-3	ovarian:	n/a
33	chr10:43335974-43336024	HIPEpiC	eye:	n/a
34	chr10:43361618-43361668	Jurkat	blood:	n/a
35	chr10:43277938-43277988	AG04450	lung:	fetal
36	chr10:43362370-43362420	NHDF-neo	bronchial:	n/a
37	chr10:43252305-43252355	AG04450	lung:	fetal
38	chr10:43362370-43362420	Hela-S3	cervix:	n/a
39	chr10:43252305-43252355	GM06990	blood:	n/a
40	chr10:43278700-43278750	LNCaP	prostate:	n/a
41	chr10:43277757-43277807	HRPEpiC	eye:	n/a
42	chr10:43361618-43361668	HUVEC	blood vessel:	n/a
43	chr10:43329092-43329142	HCF	heart:	n/a
44	chr10:43365572-43365622	PFSK-1	brain:	n/a
45	chr10:43335974-43336024	Jurkat	blood:	n/a
46	chr10:43251951-43252001	HCT-116	colon:	n/a
47	chr10:43252305-43252355	HEEpiC	esophagus:	n/a
48	chr10:43329092-43329142	IMR90	lung:	fetal
49	chr10:43362370-43362420	Caco-2	colon:	n/a
50	chr10:43332443-43332493	HCF	heart:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:43366376..43368491-chr10:43369258..43371520,2	MCF-7	breast:
2	chr10:43368762..43369411-chr10:43606065..43606957,2	MCF-7	breast:
3	chr10:43355311..43356829-chr10:43360308..43362900,2	MCF-7	breast:
4	chr10:43291799..43294495-chr10:43296598..43299321,2	MCF-7	breast:
5	chr10:43278228..43281116-chr10:43281806..43285386,3	K562	blood:
6	chr10:43287294..43289602-chr10:43294220..43295848,2	K562	blood:
7	chr10:43361854..43362671-chr10:43600633..43601533,4	K562	blood:
8	chr10:43282048..43284162-chr10:43286079..43288954,3	K562	blood:
9	chr10:43359833..43360692-chr10:43600708..43601545,3	MCF-7	breast:
10	chr10:43360509..43362298-chr10:43627787..43629550,2	MCF-7	breast:
11	chr10:43265661..43268257-chr10:43275827..43278080,2	K562	blood:
12	chr10:43360364..43363685-chr10:43571830..43575400,3	MCF-7	breast:
13	chr10:43272289..43273994-chr10:43276021..43278160,2	MCF-7	breast:
14	chr10:43287294..43289602-chr10:43294220..43295848,2	K562	blood:
15	chr10:43132519..43135183-chr10:43271199..43273394,3	K562	blood:
16	chr10:43278046..43280773-chr10:43285758..43288568,2	MCF-7	breast:
17	chr10:43363801..43367756-chr10:43571423..43575718,4	MCF-7	breast:
18	chr10:43283711..43286231-chr10:43299028..43301664,2	K562	blood:
19	chr10:43270031..43271737-chr10:43276984..43278616,2	K562	blood:
20	chr10:43263552..43268206-chr10:43276275..43279426,5	MCF-7	breast:
21	chr10:43276828..43279728-chr10:43292956..43295036,2	MCF-7	breast:
22	chr10:43278278..43279935-chr10:43297692..43300575,2	K562	blood:
23	chr10:43258843..43262487-chr10:43264254..43267473,3	K562	blood:
24	chr10:43363351..43366348-chr2:91758287..91761339,3	K562	blood:
25	chr10:43277427..43280552-chr10:43294891..43296896,3	K562	blood:
26	chr10:43291912..43294159-chr10:43296262..43298525,2	K562	blood:
27	chr10:43263804..43266604-chr10:43268900..43270663,2	MCF-7	breast:
28	chr10:43365921..43366623-chr10:43521643..43522303,3	MCF-7	breast:
29	chr10:43272289..43273994-chr10:43276021..43278160,2	MCF-7	breast:
30	chr10:43265661..43268257-chr10:43275827..43278080,2	K562	blood:
31	chr10:43278278..43279935-chr10:43297692..43300575,2	K562	blood:
32	chr10:43285592..43290643-chr10:43292360..43294489,4	K562	blood:
33	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
34	chr10:43147543..43150157-chr10:43264028..43266927,2	K562	blood:
35	chr10:43250283..43253153-chr10:43277432..43279955,3	MCF-7	breast:
36	chr10:43291799..43294495-chr10:43296598..43299321,2	MCF-7	breast:
37	chr10:43132662..43134552-chr10:43265373..43268238,2	MCF-7	breast:
38	chr10:43285411..43287004-chr10:43291005..43292621,2	K562	blood:
39	chr10:43132954..43135205-chr10:43277445..43279937,2	K562	blood:
40	chr10:43277931..43278431-chr11:62608637..62609557,2	Hela-S3	cervix:
41	chr10:43285411..43287004-chr10:43291005..43292621,2	K562	blood:
42	chr10:43132863..43135217-chr10:43276470..43279459,4	K562	blood:
43	chr10:43292432..43295311-chr10:43296307..43298120,2	MCF-7	breast:
44	chr10:43360554..43363791-chr10:43570974..43576100,9	MCF-7	breast:
45	chr10:43361913..43362690-chr10:43470789..43471679,3	MCF-7	breast:
46	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
47	chr10:43132020..43136600-chr10:43277441..43279853,5	MCF-7	breast:
48	chr10:43285592..43290643-chr10:43292360..43294489,4	K562	blood:
49	chr10:43364725..43366400-chr10:43449208..43451181,2	MCF-7	breast:
50	chr10:43270690..43272215-chr10:43274653..43276562,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BMS1-1	chr10:43367957-43369508	XLOC_008465
2	lnc-BMS1-1	chr10:43366969-43367130	XLOC_008465
3	lnc-ZNF33B-2	chr10:43246626-43247593	ENSG00000259869.1
4	lnc-RET-4	chr10:43306923-43307499	l_299_chr10:43299976-43307499_brain
5	lnc-BMS1-4	chr10:43236406-43236520	NONHSAT012928
6	lnc-RET-4	chr10:43306826-43306918	l_299_chr10:43299976-43307499_brain
7	lnc-BMS1-4	chr10:43237124-43237260	NONHSAT012928
8	lnc-RET-4	chr10:43299977-43300625	l_299_chr10:43299976-43307499_brain
9	lnc-ZNF33B-5	chr10:43274740-43277953	NONHSAT012930
10	lnc-BMS1-4	chr10:43236053-43236103	NONHSAT012928

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BMS1	hsa-miR-30a-5p	chr10:43327447-43327468

Variant related genes	Relation type
ENSG00000259869	TF binding region
ENSG00000234944	TF binding region
RNU6-885P	TF binding region
ENSG00000238732	TF binding region
DUXAP3	TF binding region
BMS1	TF binding region
ENSG00000259869	CpG island
ENSG00000234944	CpG island
RNU6-885P	CpG island
ENSG00000238732	CpG island
DUXAP3	CpG island
BMS1	CpG island
ENSG00000273008	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000185904	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000234420	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000234944	chromatin interactions
ENSG00000179950	chromatin interactions
ENSG00000269893	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 5675 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5675 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527238226	chr10:43234590-43234591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551764068	chr10:43234607-43234608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563829485	chr10:43234610-43234611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531348552	chr10:43234619-43234620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549924119	chr10:43234631-43234632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146730924	chr10:43234693-43234694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535652277	chr10:43234709-43234710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139260878	chr10:43234722-43234723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376659434	chr10:43234751-43234752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369803723	chr10:43234776-43234777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373031241	chr10:43234779-43234780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565985867	chr10:43234784-43234785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113472840	chr10:43234811-43234812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558227427	chr10:43234830-43234831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561553231	chr10:43234840-43234841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575442689	chr10:43234845-43234846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576236279	chr10:43234884-43234885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576608258	chr10:43234888-43234889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150055499	chr10:43234946-43234947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537178282	chr10:43234947-43234948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555913421	chr10:43234985-43234986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574118369	chr10:43235003-43235004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541615354	chr10:43235060-43235061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs61844760	chr10:43235073-43235074	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs577957898	chr10:43235083-43235084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545391402	chr10:43235129-43235130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563764699	chr10:43235141-43235142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs180717831	chr10:43235188-43235189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs678572	chr10:43235200-43235201	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs561840999	chr10:43235223-43235224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113194537	chr10:43235235-43235236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113624259	chr10:43235239-43235240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186119044	chr10:43235313-43235314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533333763	chr10:43235314-43235315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35736554	chr10:43235319-43235320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139247678	chr10:43235343-43235344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs191411061	chr10:43235395-43235396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540376731	chr10:43235410-43235411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183117201	chr10:43235469-43235470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560201177	chr10:43235474-43235475	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143208386	chr10:43235504-43235505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112150292	chr10:43235505-43235506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567756333	chr10:43235512-43235513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534894702	chr10:43235514-43235515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138319506	chr10:43235541-43235542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186030928	chr10:43235554-43235555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149465851	chr10:43235577-43235578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557246549	chr10:43235592-43235593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190499281	chr10:43235593-43235594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183105338	chr10:43235596-43235597	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Lung cancer	18438408	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
Mental retardation	21062444	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3308 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43232600-43235200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr10:43233200-43235600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:43235200-43235400	Enhancers	Gastric	stomach
4	chr10:43241400-43241600	Enhancers	K562	blood
5	chr10:43241600-43242400	Active TSS	K562	blood
6	chr10:43248000-43248200	Active TSS	Duodenum Mucosa	Duodenum
7	chr10:43248000-43248800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr10:43248200-43248400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr10:43248200-43248400	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
10	chr10:43248200-43248400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:43248200-43248400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:43248200-43248400	Enhancers	Adipose Nuclei	Adipose
13	chr10:43248200-43248400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr10:43248200-43248400	Bivalent Enhancer	Fetal Intestine Small	intestine
15	chr10:43248200-43248400	Enhancers	Pancreas	Pancrea
16	chr10:43248200-43248400	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
17	chr10:43248200-43248400	Bivalent/Poised TSS	Right Ventricle	heart
18	chr10:43248200-43248400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
19	chr10:43248200-43248600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
20	chr10:43248200-43248600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
21	chr10:43248200-43248600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:43248200-43248600	Flanking Active TSS	Duodenum Mucosa	Duodenum
23	chr10:43248200-43248600	Flanking Bivalent TSS/Enh	Placenta	Placenta
24	chr10:43248200-43248600	Bivalent/Poised TSS	HUVEC	blood vessel
25	chr10:43248200-43248800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
26	chr10:43248200-43248800	Bivalent Enhancer	Stomach Mucosa	stomach
27	chr10:43248200-43249000	Active TSS	A549	lung
28	chr10:43248200-43249000	Bivalent/Poised TSS	Osteobl	bone
29	chr10:43248200-43250000	Active TSS	Rectal Smooth Muscle	rectum
30	chr10:43248200-43250200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr10:43248200-43250800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:43248200-43251000	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr10:43248200-43251200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
34	chr10:43248400-43248600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr10:43248400-43248600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
37	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
38	chr10:43248400-43248600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
39	chr10:43248400-43248600	Bivalent/Poised TSS	Cortex derived primary cultured neurospheres	brain
40	chr10:43248400-43248600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:43248400-43248600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr10:43248400-43248600	Enhancers	Liver	Liver
43	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
44	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
45	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
46	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
47	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
48	chr10:43248400-43248600	Active TSS	Ovary	ovary
49	chr10:43248400-43248600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
50	chr10:43248400-43248600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle

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