Variant report

Variant	nsv540465
Chromosome Location	chr10:5108345-5261482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2016)
CpG islands
(count:917)
Chromatin interactive
region (count:78)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2016 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5112815-5114610	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:5123254-5123638	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5138000-5138153	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:5189270-5191011	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:5113567-5114862	K562	blood:	n/a	n/a
6	ARID3A	chr10:5147856-5147891	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:5120586-5121209	K562	blood:	n/a	n/a
8	ARID3A	chr10:5237741-5238762	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:5239083-5239264	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:5136259-5137212	HepG2	liver:	n/a	n/a
11	ARID3A	chr10:5136891-5137133	K562	blood:	n/a	n/a
12	ARID3A	chr10:5110678-5110878	K562	blood:	n/a	n/a
13	ARID3A	chr10:5261272-5261624	HepG2	liver:	n/a	n/a
14	ARID3A	chr10:5122054-5122324	HepG2	liver:	n/a	n/a
15	ARID3A	chr10:5236523-5236713	HepG2	liver:	n/a	n/a
16	ATF1	chr10:5113912-5114323	K562	blood:	n/a	n/a
17	ATF3	chr10:5113430-5114380	A549	lung:	n/a	n/a
18	ATF3	chr10:5136385-5137238	A549	lung:	n/a	n/a
19	ATF3	chr10:5112971-5114564	A549	lung:	n/a	n/a
20	ATF3	chr10:5113911-5114354	K562	blood:	n/a	n/a
21	ATF3	chr10:5189307-5189866	A549	lung:	n/a	n/a
22	ATF3	chr10:5190304-5190995	A549	lung:	n/a	n/a
23	ATF3	chr10:5121895-5122433	A549	lung:	n/a	n/a
24	ATF3	chr10:5136661-5137163	K562	blood:	n/a	n/a
25	ATF3	chr10:5207727-5207953	K562	blood:	n/a	n/a
26	BACH1	chr10:5136593-5136915	K562	blood:	n/a	chr10:5136819-5136833
27	BACH1	chr10:5113506-5114634	K562	blood:	n/a	n/a
28	BACH1	chr10:5113866-5114859	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr10:5121194-5121208	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr10:5121040-5121383	K562	blood:	n/a	n/a
31	BCL3	chr10:5237721-5238466	A549	lung:	n/a	n/a
32	BCL3	chr10:5136379-5137271	A549	lung:	n/a	chr10:5136770-5136779
33	BCL3	chr10:5141308-5142213	A549	lung:	n/a	n/a
34	BCL3	chr10:5149405-5152719	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
35	BCL3	chr10:5121933-5122486	A549	lung:	n/a	n/a
36	BCL3	chr10:5121775-5122553	A549	lung:	n/a	n/a
37	BCL3	chr10:5190290-5191005	A549	lung:	n/a	n/a
38	BCL3	chr10:5112966-5115139	A549	lung:	n/a	n/a
39	BCL3	chr10:5149846-5152451	A549	lung:	n/a	chr10:5151173-5151180 chr10:5151748-5151757
40	BCL3	chr10:5112642-5114508	A549	lung:	n/a	n/a
41	BCL3	chr10:5134993-5138735	A549	lung:	n/a	chr10:5137586-5137595 chr10:5136770-5136779
42	BCL3	chr10:5189224-5190092	A549	lung:	n/a	n/a
43	BCL3	chr10:5189111-5191215	A549	lung:	n/a	n/a
44	BHLHE40	chr10:5113493-5114242	HepG2	liver:	n/a	n/a
45	BHLHE40	chr10:5190346-5190928	HepG2	liver:	n/a	n/a
46	BHLHE40	chr10:5207857-5208008	K562	blood:	n/a	n/a
47	BHLHE40	chr10:5185410-5185563	HepG2	liver:	n/a	n/a
48	BHLHE40	chr10:5113561-5114284	K562	blood:	n/a	n/a
49	BHLHE40	chr10:5120759-5121300	K562	blood:	n/a	n/a
50	BRCA1	chr10:5113573-5114550	Hela-S3	cervix:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5136782-5136832	SK-N-SH_RA	brain:	n/a
2	chr10:5246625-5246675	HMEC	breast:	n/a
3	chr10:5136782-5136832	SK-N-SH_RA	brain:	n/a
4	chr10:5246625-5246675	HMEC	breast:	n/a
5	chr10:5237853-5237903	HEEpiC	esophagus:	n/a
6	chr10:5228106-5228156	H1-hESC	embryonic stem cell:	embryo
7	chr10:5238881-5238931	HUVEC	blood vessel:	n/a
8	chr10:5237869-5237919	BJ	skin:	n/a
9	chr10:5238881-5238931	NH-A	brain:	n/a
10	chr10:5237881-5237931	HAEpiC	amniotic membrane:	n/a
11	chr10:5149799-5149849	Jurkat	blood:	n/a
12	chr10:5135453-5135503	RPTEC	kidney:	n/a
13	chr10:5135453-5135503	AG09319	gingival:	n/a
14	chr10:5227312-5227362	IMR90	lung:	fetal
15	chr10:5149799-5149849	RPTEC	kidney:	n/a
16	chr10:5136782-5136832	HCF	heart:	n/a
17	chr10:5246625-5246675	HCM	heart:	n/a
18	chr10:5246625-5246675	IMR90	lung:	fetal
19	chr10:5238881-5238931	HAEpiC	amniotic membrane:	n/a
20	chr10:5260740-5260790	ECC-1	luminal epithelium:	n/a
21	chr10:5237869-5237919	AG09319	gingival:	n/a
22	chr10:5227162-5227212	Jurkat	blood:	n/a
23	chr10:5238881-5238931	U87	brain:	n/a
24	chr10:5227162-5227212	GM12892	blood:	n/a
25	chr10:5237869-5237919	HCPEpiC	choroid plexus:	n/a
26	chr10:5136782-5136832	PANC-1	pancreas:	n/a
27	chr10:5237869-5237919	NHBE	bronchial:	n/a
28	chr10:5136782-5136832	NT2-D1	testis:	n/a
29	chr10:5149799-5149849	HUVEC	blood vessel:	n/a
30	chr10:5246625-5246675	H1-hESC	embryonic stem cell:	embryo
31	chr10:5227312-5227362	RPTEC	kidney:	n/a
32	chr10:5227757-5227807	HPAEpiC	pulmonary alveolar:	n/a
33	chr10:5227162-5227212	HRCEpiC	kidney:	n/a
34	chr10:5135453-5135503	AG04449	skin:	fetal
35	chr10:5136782-5136832	MCF10A-Er-Src	breast:	n/a
36	chr10:5237869-5237919	K562	blood:	n/a
37	chr10:5227162-5227212	AG04450	lung:	fetal
38	chr10:5237853-5237903	GM06990	blood:	n/a
39	chr10:5135453-5135503	HL-60	blood:	n/a
40	chr10:5203419-5203469	BJ	skin:	n/a
41	chr10:5227162-5227212	HCT-116	colon:	n/a
42	chr10:5203419-5203469	SK-N-SH	brain:	n/a
43	chr10:5203419-5203469	Hepatocyte	liver:	n/a
44	chr10:5237869-5237919	MCF-7	breast:	n/a
45	chr10:5227757-5227807	SK-N-MC	brain:	n/a
46	chr10:5135453-5135503	HCPEpiC	choroid plexus:	n/a
47	chr10:5227757-5227807	HAEpiC	amniotic membrane:	n/a
48	chr10:5227162-5227212	HCPEpiC	choroid plexus:	n/a
49	chr10:5237853-5237903	MCF-7	breast:	n/a
50	chr10:5238881-5238931	AG04449	skin:	fetal

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:5082218..5083019-chr10:5136925..5137462,2	MCF-7	breast:
2	chr10:5231335..5234110-chr10:5249009..5251135,2	MCF-7	breast:
3	chr10:5227828..5229662-chr10:5232988..5235057,2	K562	blood:
4	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
5	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
6	chr10:5169411..5171944-chr10:5173509..5175691,2	K562	blood:
7	chr10:5112364..5115030-chr10:5137295..5139055,2	K562	blood:
8	chr10:5114807..5118123-chr10:5118660..5122292,3	MCF-7	breast:
9	chr10:5113654..5115809-chr10:5119275..5121684,2	MCF-7	breast:
10	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
11	chr10:5139751..5141653-chr10:5142229..5144051,2	K562	blood:
12	chr10:5171829..5174408-chr10:5176222..5177928,2	MCF-7	breast:
13	chr10:5157749..5160543-chr10:5164093..5166584,2	MCF-7	breast:
14	chr10:5250240..5252491-chr10:5252736..5256514,3	K562	blood:
15	chr10:5118736..5120512-chr10:5120642..5122422,2	MCF-7	breast:
16	chr10:5166174..5167900-chr10:5189108..5191670,2	MCF-7	breast:
17	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
18	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
19	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
20	chr10:5135013..5137947-chr10:5149855..5151840,2	MCF-7	breast:
21	chr10:5196320..5198098-chr10:5207185..5208709,2	MCF-7	breast:
22	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
23	chr10:5228162..5230153-chr10:5232988..5235199,2	K562	blood:
24	chr10:5159415..5162131-chr10:5167591..5169595,2	MCF-7	breast:
25	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
26	chr10:5198281..5200177-chr10:5228677..5230787,2	K562	blood:
27	chr10:5140998..5143202-chr10:5149820..5152620,2	K562	blood:
28	chr10:5138883..5141588-chr10:5142729..5145007,2	K562	blood:
29	chr10:5135730..5138906-chr10:5144094..5147673,3	K562	blood:
30	chr10:5248069..5249924-chr10:5250712..5252871,2	K562	blood:
31	chr10:5198281..5200177-chr10:5228677..5230787,2	K562	blood:
32	chr10:5247043..5249924-chr10:5250707..5254146,4	K562	blood:
33	chr10:5135730..5137727-chr10:5144800..5147673,2	K562	blood:
34	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
35	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
36	chr10:5256183..5258752-chr10:5259686..5261941,2	K562	blood:
37	chr10:4867516..4869900-chr10:5135201..5137283,2	K562	blood:
38	chr10:5228162..5230153-chr10:5232988..5235199,2	K562	blood:
39	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
40	chr10:5111978..5114211-chr10:5116578..5119006,2	MCF-7	breast:
41	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
42	chr10:5210740..5212996-chr10:5319959..5322251,2	MCF-7	breast:
43	chr10:5115990..5119268-chr10:5120160..5123753,3	K562	blood:
44	chr10:5239744..5241358-chr10:5244602..5246718,2	K562	blood:
45	chr10:5136517..5137515-chr10:5241491..5242054,2	MCF-7	breast:
46	chr10:5149764..5151896-chr10:5189814..5192281,2	MCF-7	breast:
47	chr10:5254857..5257683-chr10:5259686..5261466,3	K562	blood:
48	chr10:5193912..5196444-chr10:5202827..5204457,2	K562	blood:
49	chr10:4891149..4892494-chr10:5136639..5137645,6	MCF-7	breast:
50	chr10:5163399..5166048-chr10:5166871..5170286,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1CL1-2	chr10:5186655-5187952	ucscGeneNc_uc009xhz_1
2	lnc-AKR1C4-2	chr10:5237425-5237538	NONHSAT011140
3	lnc-AKR1C4-2	chr10:5238192-5238885	NONHSAT011140
4	lnc-AKR1CL1-2	chr10:5192082-5192149	ucscGeneNc_uc009xhz_1
5	lnc-AKR1C3-5	chr10:5249132-5249705	NONHSAT011142
6	lnc-AKR1CL1-2	chr10:5189836-5190001	ucscGeneNc_uc009xhz_1

No data

Variant related genes	Relation type
AKR1C3	TF binding region
ENSG00000251909	TF binding region
AKR1C4	TF binding region
ENSG00000239142	TF binding region
ENSG00000228291	TF binding region
AKR1C5P	TF binding region
AKR1CL1	TF binding region
AKR1C3	CpG island
ENSG00000251909	CpG island
AKR1C4	CpG island
ENSG00000239142	CpG island
ENSG00000228291	CpG island
AKR1C5P	CpG island
AKR1CL1	CpG island
ENSG00000196326	chromatin interactions
ENSG00000165568	chromatin interactions
ENSG00000228291	chromatin interactions
ENSG00000239142	chromatin interactions
ENSG00000225418	chromatin interactions
ENSG00000196139	chromatin interactions

Extended variants
information (count: 7548 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7548 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577616735	chr10:5108346-5108347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs148671764	chr10:5108351-5108352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs142863051	chr10:5108365-5108366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572657065	chr10:5108380-5108381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191935357	chr10:5108427-5108428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561532107	chr10:5108428-5108429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562801214	chr10:5108461-5108462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113655256	chr10:5108470-5108471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532045965	chr10:5108487-5108488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs7100778	chr10:5108506-5108507	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs565124907	chr10:5108522-5108523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs77619356	chr10:5108541-5108542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547550113	chr10:5108556-5108557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565856701	chr10:5108571-5108572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183269470	chr10:5108576-5108577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187539859	chr10:5108585-5108586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191456758	chr10:5108618-5108619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs72772187	chr10:5108620-5108621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146582561	chr10:5108636-5108637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566954726	chr10:5108637-5108638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141192807	chr10:5108683-5108684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143596633	chr10:5108684-5108685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553559648	chr10:5108700-5108701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs537548586	chr10:5108701-5108702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543204007	chr10:5108752-5108753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146867049	chr10:5108753-5108754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs118015663	chr10:5108760-5108761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367543317	chr10:5108772-5108773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532372586	chr10:5108785-5108786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548927692	chr10:5108817-5108818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4881390	chr10:5108821-5108822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557127733	chr10:5108822-5108823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530135200	chr10:5108885-5108886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548325198	chr10:5108899-5108900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567116472	chr10:5108910-5108911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184431920	chr10:5108913-5108914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368168956	chr10:5108979-5108980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59007330	chr10:5108980-5108981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2398192	chr10:5109012-5109013	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555752396	chr10:5109032-5109033	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2398191	chr10:5109048-5109049	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577060539	chr10:5109061-5109062	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150494764	chr10:5109083-5109084	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2105451	chr10:5109092-5109093	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189728516	chr10:5109215-5109216	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs546264232	chr10:5109226-5109227	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs541781294	chr10:5109230-5109231	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs144988666	chr10:5109237-5109238	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs200399201	chr10:5109248-5109249	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs192867755	chr10:5109257-5109258	Flanking Active TSS Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1005 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5095400-5120800	Weak transcription	Right Atrium	heart
2	chr10:5105800-5109600	Weak transcription	Adipose Nuclei	Adipose
3	chr10:5106000-5108400	Enhancers	NHDF-Ad	bronchial
4	chr10:5107000-5112800	Weak transcription	Liver	Liver
5	chr10:5107200-5109000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:5108000-5113000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr10:5108200-5113200	Weak transcription	HSMM	muscle
8	chr10:5108400-5110000	Weak transcription	NHDF-Ad	bronchial
9	chr10:5109000-5109200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:5109200-5109400	ZNF genes & repeats	A549	lung
11	chr10:5109200-5111000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr10:5109400-5110800	Weak transcription	A549	lung
13	chr10:5109400-5112600	Enhancers	HepG2	liver
14	chr10:5109400-5113200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:5109600-5111200	Enhancers	Adipose Nuclei	Adipose
16	chr10:5109800-5112800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr10:5110000-5111000	Enhancers	NHDF-Ad	bronchial
18	chr10:5110400-5110800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr10:5110800-5111000	Enhancers	Gastric	stomach
20	chr10:5110800-5111000	Enhancers	Pancreas	Pancrea
21	chr10:5110800-5111000	Enhancers	Rectal Mucosa Donor 31	rectum
22	chr10:5110800-5112400	Enhancers	A549	lung
23	chr10:5110800-5112800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:5111000-5112200	Weak transcription	NHDF-Ad	bronchial
25	chr10:5111000-5112800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr10:5111200-5112000	Weak transcription	Adipose Nuclei	Adipose
27	chr10:5111200-5112400	Weak transcription	Psoas Muscle	Psoas
28	chr10:5111800-5116200	Enhancers	Fetal Intestine Large	intestine
29	chr10:5112000-5113200	Enhancers	Duodenum Mucosa	Duodenum
30	chr10:5112000-5113200	ZNF genes & repeats	Fetal Intestine Small	intestine
31	chr10:5112000-5115200	Enhancers	Adipose Nuclei	Adipose
32	chr10:5112200-5112400	ZNF genes & repeats	K562	blood
33	chr10:5112200-5112800	Enhancers	NHDF-Ad	bronchial
34	chr10:5112200-5114000	Enhancers	Ovary	ovary
35	chr10:5112400-5112600	Flanking Active TSS	A549	lung
36	chr10:5112400-5112600	Weak transcription	K562	blood
37	chr10:5112400-5112600	Weak transcription	NHLF	lung
38	chr10:5112400-5113400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:5112400-5113400	Enhancers	Small Intestine	intestine
40	chr10:5112400-5113800	Enhancers	Psoas Muscle	Psoas
41	chr10:5112600-5112800	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr10:5112600-5113000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr10:5112600-5113000	Transcr. at gene 5' and 3'	A549	lung
44	chr10:5112600-5113200	ZNF genes & repeats	NHLF	lung
45	chr10:5112600-5113400	Genic enhancers	K562	blood
46	chr10:5112600-5113600	Enhancers	Colonic Mucosa	Colon
47	chr10:5112600-5114000	Flanking Active TSS	HepG2	liver
48	chr10:5112800-5113000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr10:5112800-5113400	Enhancers	Liver	Liver
50	chr10:5112800-5113400	Enhancers	Hela-S3	cervix

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