Variant report

Variant	esv2762864
Chromosome Location	chr10:52030945-52107415
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1668)
CpG islands
(count:62)
Chromatin interactive
region (count:72)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1668 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52090227-52090559	K562	blood:	n/a	n/a
2	ARID3A	chr10:52081241-52082196	K562	blood:	n/a	n/a
3	ARID3A	chr10:52099381-52099787	K562	blood:	n/a	n/a
4	ARID3A	chr10:52051151-52051887	K562	blood:	n/a	chr10:52051843-52051859
5	ARID3A	chr10:52055144-52055451	K562	blood:	n/a	n/a
6	ARID3A	chr10:52035412-52035803	K562	blood:	n/a	n/a
7	ARID3A	chr10:52063453-52063845	K562	blood:	n/a	n/a
8	ARID3A	chr10:52078573-52079065	K562	blood:	n/a	n/a
9	ARID3A	chr10:52076596-52077385	K562	blood:	n/a	n/a
10	ARID3A	chr10:52072531-52073538	K562	blood:	n/a	n/a
11	ARID3A	chr10:52084484-52089746	K562	blood:	n/a	chr10:52089059-52089075 chr10:52089058-52089074
12	ARID3A	chr10:52096785-52097419	K562	blood:	n/a	n/a
13	ARID3A	chr10:52075129-52075588	K562	blood:	n/a	n/a
14	ARID3A	chr10:52070534-52070946	K562	blood:	n/a	n/a
15	ARID3A	chr10:52091151-52092344	K562	blood:	n/a	n/a
16	ARID3A	chr10:52077960-52078184	K562	blood:	n/a	n/a
17	ATF1	chr10:52072566-52073079	K562	blood:	n/a	n/a
18	ATF1	chr10:52085140-52085785	K562	blood:	n/a	n/a
19	ATF1	chr10:52086523-52087559	K562	blood:	n/a	n/a
20	ATF2	chr10:52106973-52107749	GM12878	blood:	n/a	n/a
21	ATF2	chr10:52085076-52085573	GM12878	blood:	n/a	n/a
22	ATF2	chr10:52107026-52107665	GM12878	blood:	n/a	n/a
23	ATF3	chr10:52086482-52087108	K562	blood:	n/a	n/a
24	ATF3	chr10:52085055-52085796	K562	blood:	n/a	n/a
25	BACH1	chr10:52091726-52092287	K562	blood:	n/a	n/a
26	BACH1	chr10:52100879-52101325	K562	blood:	n/a	n/a
27	BACH1	chr10:52039339-52039690	H1-hESC	embryonic stem cell:	n/a	chr10:52039520-52039534
28	BACH1	chr10:52042451-52042475	K562	blood:	n/a	n/a
29	BACH1	chr10:52076598-52077012	K562	blood:	n/a	n/a
30	BACH1	chr10:52092573-52092805	K562	blood:	n/a	n/a
31	BACH1	chr10:52035455-52035788	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr10:52086440-52087663	K562	blood:	n/a	n/a
33	BACH1	chr10:52079541-52079637	K562	blood:	n/a	n/a
34	BACH1	chr10:52073601-52073850	K562	blood:	n/a	n/a
35	BACH1	chr10:52035377-52035783	K562	blood:	n/a	n/a
36	BACH1	chr10:52039370-52039740	K562	blood:	n/a	chr10:52039520-52039534
37	BATF	chr10:52085169-52085457	GM12878	blood:	n/a	chr10:52085345-52085356
38	BCL11A	chr10:52107291-52107599	GM12878	blood:	n/a	n/a
39	BCL11A	chr10:52107331-52107617	GM12878	blood:	n/a	n/a
40	BCL3	chr10:52107189-52107656	GM12878	blood:	n/a	n/a
41	BCL3	chr10:52061272-52062611	K562	blood:	n/a	n/a
42	BCL3	chr10:52086449-52087296	K562	blood:	n/a	chr10:52086565-52086574
43	BCL3	chr10:52062694-52065056	K562	blood:	n/a	chr10:52063446-52063453
44	BCLAF1	chr10:52086332-52087197	K562	blood:	n/a	chr10:52086565-52086574
45	BCLAF1	chr10:52035522-52035798	GM12878	blood:	n/a	n/a
46	BCLAF1	chr10:52107061-52107659	GM12878	blood:	n/a	n/a
47	BCLAF1	chr10:52107248-52107597	GM12878	blood:	n/a	n/a
48	BCLAF1	chr10:52085079-52085537	GM12878	blood:	n/a	n/a
49	BHLHE40	chr10:52095774-52096375	K562	blood:	n/a	n/a
50	BHLHE40	chr10:52085135-52085893	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52066867-52066917	AG09319	gingival:	n/a
2	chr10:52066867-52066917	AG09319	gingival:	n/a
3	chr10:52066867-52066917	SK-N-SH	brain:	n/a
4	chr10:52066867-52066917	GM06990	blood:	n/a
5	chr10:52066867-52066917	HEK293	kidney:	embryo
6	chr10:52066867-52066917	SKMC	muscle:	n/a
7	chr10:52066867-52066917	SAEC	small airway:	n/a
8	chr10:52066867-52066917	HL-60	blood:	n/a
9	chr10:52066867-52066917	AG09309	skin:	n/a
10	chr10:52066867-52066917	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:52066867-52066917	CMK	blood:	n/a
12	chr10:52066867-52066917	NHBE	bronchial:	n/a
13	chr10:52066867-52066917	HIPEpiC	eye:	n/a
14	chr10:52066867-52066917	PrEC	prostate:	n/a
15	chr10:52066867-52066917	ECC-1	luminal epithelium:	n/a
16	chr10:52066867-52066917	A549	lung:	n/a
17	chr10:52066867-52066917	GM12891	blood:	n/a
18	chr10:52066867-52066917	GM12892	blood:	n/a
19	chr10:52066867-52066917	SK-N-MC	brain:	n/a
20	chr10:52066867-52066917	HCM	heart:	n/a
21	chr10:52066867-52066917	U87	brain:	n/a
22	chr10:52066867-52066917	NB4	blood:	n/a
23	chr10:52066867-52066917	Jurkat	blood:	n/a
24	chr10:52066867-52066917	PANC-1	pancreas:	n/a
25	chr10:52066867-52066917	Hela-S3	cervix:	n/a
26	chr10:52066867-52066917	MCF10A-Er-Src	breast:	n/a
27	chr10:52066867-52066917	LNCaP	prostate:	n/a
28	chr10:52066867-52066917	HCF	heart:	n/a
29	chr10:52066867-52066917	RPTEC	kidney:	n/a
30	chr10:52066867-52066917	IMR90	lung:	fetal
31	chr10:52066867-52066917	AoSMC	blood vessel:	n/a
32	chr10:52066867-52066917	HNPCEpiC	eye:	n/a
33	chr10:52066867-52066917	AG04450	lung:	fetal
34	chr10:52066867-52066917	BE2_C	brain:	n/a
35	chr10:52066867-52066917	HAEpiC	amniotic membrane:	n/a
36	chr10:52066867-52066917	HMEC	breast:	n/a
37	chr10:52066867-52066917	Caco-2	colon:	n/a
38	chr10:52066867-52066917	HRE	kidney:	n/a
39	chr10:52066867-52066917	GM12878	blood:	n/a
40	chr10:52066867-52066917	HepG2	liver:	n/a
41	chr10:52066867-52066917	HRCEpiC	kidney:	n/a
42	chr10:52066867-52066917	GM19239	blood:	n/a
43	chr10:52066867-52066917	BJ	skin:	n/a
44	chr10:52066867-52066917	AG10803	skin:	n/a
45	chr10:52066867-52066917	T-47D	breast:	n/a
46	chr10:52066867-52066917	HCPEpiC	choroid plexus:	n/a
47	chr10:52066867-52066917	HCT-116	colon:	n/a
48	chr10:52066867-52066917	Hepatocyte	liver:	n/a
49	chr10:52066867-52066917	AG04449	skin:	fetal
50	chr10:52066867-52066917	H1-hESC	embryonic stem cell:	embryo

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:52036642..52039011-chr10:52040195..52041719,2	K562	blood:
2	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
3	chr10:52105040..52107754-chr10:52130504..52132718,2	MCF-7	breast:
4	chr10:52104092..52107025-chr10:52382873..52384665,2	MCF-7	breast:
5	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
6	chr10:52040114..52042581-chr10:52049836..52051714,2	K562	blood:
7	chr10:52084925..52086838-chr10:52120229..52123147,2	K562	blood:
8	chr10:52038390..52041263-chr10:52085010..52087882,2	K562	blood:
9	chr10:52064205..52066621-chr10:52082912..52084606,2	K562	blood:
10	chr10:52064687..52067489-chr10:52072620..52075726,3	K562	blood:
11	chr10:52079847..52082788-chr10:52084797..52086833,2	MCF-7	breast:
12	chr10:52078609..52080735-chr10:52099175..52100683,2	MCF-7	breast:
13	chr10:52033462..52036031-chr10:52039236..52041874,2	K562	blood:
14	chr10:52084222..52086810-chr10:52173871..52176505,2	K562	blood:
15	chr10:52065089..52067181-chr10:52085442..52087556,2	K562	blood:
16	chr10:52085739..52087419-chr10:52285865..52287749,2	K562	blood:
17	chr10:52047341..52049235-chr10:52083279..52085507,2	K562	blood:
18	chr10:52071869..52074741-chr10:52080323..52082329,2	MCF-7	breast:
19	chr10:52014263..52015864-chr10:52038453..52040858,2	K562	blood:
20	chr10:52046559..52050186-chr10:52057567..52060183,3	K562	blood:
21	chr10:52050989..52051888-chr10:52180720..52181237,2	K562	blood:
22	chr10:52059289..52061333-chr10:52068987..52071568,2	MCF-7	breast:
23	chr10:52075208..52077138-chr10:52380386..52382972,2	K562	blood:
24	chr10:52039584..52041526-chr10:52044440..52046214,2	MCF-7	breast:
25	chr10:52038390..52041263-chr10:52085010..52087882,2	K562	blood:
26	chr10:52030038..52033991-chr10:52034749..52038715,4	MCF-7	breast:
27	chr10:52100945..52103388-chr10:52103997..52106988,2	MCF-7	breast:
28	chr10:52033462..52036031-chr10:52039236..52041874,2	K562	blood:
29	chr10:52046559..52050186-chr10:52057567..52060183,3	K562	blood:
30	chr10:52053125..52055994-chr10:52093315..52095681,2	K562	blood:
31	chr10:52058612..52061385-chr10:52062063..52064503,2	K562	blood:
32	chr10:52047341..52049235-chr10:52083279..52085507,2	K562	blood:
33	chr10:52043739..52044593-chr2:55242128..55242713,2	K562	blood:
34	chr10:52032843..52037067-chr10:52037860..52041874,6	K562	blood:
35	chr10:52062509..52064058-chr10:52071657..52073815,2	K562	blood:
36	chr10:52084908..52086579-chr10:52176958..52179360,2	K562	blood:
37	chr10:52030038..52033991-chr10:52034749..52038715,4	MCF-7	breast:
38	chr10:52087443..52089388-chr10:52116523..52119614,3	K562	blood:
39	chr10:52050788..52053473-chr10:52085482..52088054,2	K562	blood:
40	chr10:52039584..52041526-chr10:52044440..52046214,2	MCF-7	breast:
41	chr10:52063071..52064625-chr10:52072402..52074193,2	MCF-7	breast:
42	chr10:52089314..52090958-chr10:52289108..52291926,2	K562	blood:
43	chr10:52040531..52043332-chr10:52062739..52065495,2	K562	blood:
44	chr10:52100945..52103388-chr10:52103997..52106988,2	MCF-7	breast:
45	chr10:52044776..52046727-chr10:52383268..52385118,2	K562	blood:
46	chr10:52069285..52071040-chr10:52072375..52074305,2	K562	blood:
47	chr10:52091344..52092956-chr10:52110761..52113396,2	MCF-7	breast:
48	chr10:52064687..52067489-chr10:52072620..52075726,3	K562	blood:
49	chr10:52032843..52037067-chr10:52037860..52041874,6	K562	blood:
50	chr10:52090051..52092656-chr10:52383474..52386447,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM21A-2	chr10:52062175-52063940	l_311_chr10:52061403-52063940_testes
2	lnc-ASAH2-4	chr10:52102202-52102561	NONHSAT013378
3	lnc-ASAH2-5	chr10:52096448-52096864	l_312_chr10:52096258-52104698_testes
4	lnc-FAM21A-2	chr10:52061404-52061522	l_311_chr10:52061403-52063940_testes
5	lnc-ASAH2-6	chr10:52103896-52104105	NONHSAT013379
6	lnc-ASAH2-5	chr10:52104168-52104349	l_312_chr10:52096258-52104698_testes
7	lnc-ASAH2-5	chr10:52104608-52104698	l_312_chr10:52096258-52104698_testes
8	lnc-ASAH2-5	chr10:52096259-52096435	l_312_chr10:52096258-52104698_testes

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SGMS1	hsa-miR-33a-5p	chr10:52066188-52066208
2	SGMS1	hsa-miR-124-3p	chr10:52066157-52066151
3	SGMS1	hsa-miR-33a-5p	chr10:52065390-52065409
4	SGMS1	hsa-miR-130b-3p	chr10:52066406-52066429
5	SGMS1	hsa-miR-124-3p	chr10:52066151-52066170
6	SGMS1	hsa-miR-130b-3p	chr10:52065388-52065411
7	SGMS1	hsa-miR-93-5p	chr10:52065386-52065408
8	SGMS1	hsa-miR-130b-3p	chr10:52066686-52066707
9	SGMS1	hsa-miR-130b-3p	chr10:52066046-52066067

Variant related genes	Relation type
SGMS1	TF binding region
ENSG00000269165	TF binding region
SGMS1	CpG island
ENSG00000269165	CpG island
ENSG00000198964	chromatin interactions
ENSG00000269165	chromatin interactions
ENSG00000226200	chromatin interactions

Extended variants
information (count: 2759 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2759 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs80025149	chr10:52031007-52031008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148149428	chr10:52031034-52031035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75207667	chr10:52031041-52031042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs12258132	chr10:52031048-52031049	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs557805304	chr10:52031081-52031082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577885976	chr10:52031087-52031088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180818727	chr10:52031088-52031089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73328926	chr10:52031119-52031120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567481239	chr10:52031160-52031161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200513925	chr10:52031162-52031163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368709275	chr10:52031207-52031208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372406599	chr10:52031210-52031211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185710130	chr10:52031249-52031250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111438206	chr10:52031262-52031263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2574948	chr10:52031278-52031279	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs80048455	chr10:52031291-52031292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141994860	chr10:52031295-52031296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35906501	chr10:52031318-52031319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs190565296	chr10:52031400-52031401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565410556	chr10:52031407-52031408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372315969	chr10:52031415-52031416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561972889	chr10:52031443-52031444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549322635	chr10:52031444-52031445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78306298	chr10:52031462-52031463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528950245	chr10:52031483-52031484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548693961	chr10:52031484-52031485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs139675185	chr10:52031520-52031521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143602724	chr10:52031524-52031525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs73328927	chr10:52031552-52031553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181838996	chr10:52031602-52031603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368142556	chr10:52031642-52031643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537352932	chr10:52031700-52031701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557384021	chr10:52031706-52031707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574129869	chr10:52031734-52031735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375332983	chr10:52031814-52031815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536722790	chr10:52031820-52031821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs549824089	chr10:52031850-52031851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553469093	chr10:52031855-52031856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113889775	chr10:52031856-52031857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34466638	chr10:52031865-52031866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560661737	chr10:52031917-52031918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142454228	chr10:52031925-52031926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545223327	chr10:52031928-52031929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs565482284	chr10:52031931-52031932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575836776	chr10:52031948-52031949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146319042	chr10:52032005-52032006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs10508923	chr10:52032024-52032025	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs116480110	chr10:52032078-52032079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7082758	chr10:52032084-52032085	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs201167628	chr10:52032095-52032096	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	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
skeletal anomalies	21948486	CNVD
Autism	21948486	CNVD
speech delay	21948486	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1595 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52031000-52033200	Enhancers	K562	blood
2	chr10:52033200-52034800	Weak transcription	K562	blood
3	chr10:52034800-52036600	Enhancers	K562	blood
4	chr10:52035200-52035400	Enhancers	Aorta	Aorta
5	chr10:52038800-52042200	Enhancers	K562	blood
6	chr10:52039000-52039400	Enhancers	Hela-S3	cervix
7	chr10:52039000-52039600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr10:52039000-52039600	Flanking Active TSS	A549	lung
9	chr10:52039000-52039800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr10:52039000-52039800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:52039000-52040400	Enhancers	HepG2	liver
12	chr10:52039200-52039400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr10:52039200-52039600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr10:52039200-52039600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:52039200-52039800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr10:52039200-52040000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr10:52039200-52040400	Enhancers	Stomach Mucosa	stomach
18	chr10:52039200-52040800	Enhancers	Liver	Liver
19	chr10:52039400-52039600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:52039400-52039600	Enhancers	Gastric	stomach
21	chr10:52039600-52040000	Enhancers	A549	lung
22	chr10:52040200-52040400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:52040200-52040400	Enhancers	Gastric	stomach
24	chr10:52040800-52045600	Weak transcription	Liver	Liver
25	chr10:52042200-52046600	Weak transcription	K562	blood
26	chr10:52044800-52047000	Enhancers	Fetal Lung	lung
27	chr10:52045400-52048000	Enhancers	Fetal Brain Male	brain
28	chr10:52045600-52046600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:52045600-52048000	Enhancers	Liver	Liver
30	chr10:52045800-52046000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr10:52045800-52047200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr10:52046000-52046400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr10:52046000-52047000	Enhancers	Brain Cingulate Gyrus	brain
34	chr10:52046000-52047200	Enhancers	Brain Hippocampus Middle	brain
35	chr10:52046000-52047400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr10:52046000-52047600	Enhancers	Adipose Nuclei	Adipose
37	chr10:52046000-52048000	Enhancers	NHDF-Ad	bronchial
38	chr10:52046200-52046600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr10:52046200-52047000	Enhancers	Brain Anterior Caudate	brain
40	chr10:52046200-52047200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr10:52046200-52047200	Enhancers	NHLF	lung
42	chr10:52046200-52048000	Enhancers	Fetal Stomach	stomach
43	chr10:52046400-52046800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr10:52046400-52046800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr10:52046400-52047400	Enhancers	Fetal Thymus	thymus
46	chr10:52046600-52047000	Enhancers	Brain Angular Gyrus	brain
47	chr10:52046600-52047000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr10:52046600-52047200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:52046600-52047200	Enhancers	K562	blood
50	chr10:52046600-52047200	Enhancers	Osteobl	bone

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