Variant report

Variant	nsv894795
Chromosome Location	chr10:5286600-5348491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1119)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1119 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5326370-5326774	K562	blood:	n/a	n/a
2	ARID3A	chr10:5325483-5325825	HepG2	liver:	n/a	n/a
3	ATF1	chr10:5300425-5300441	K562	blood:	n/a	n/a
4	ATF1	chr10:5339509-5339711	K562	blood:	n/a	n/a
5	ATF1	chr10:5326291-5326744	K562	blood:	n/a	n/a
6	ATF1	chr10:5337658-5338224	K562	blood:	n/a	n/a
7	ATF1	chr10:5325479-5325806	K562	blood:	n/a	n/a
8	ATF1	chr10:5333613-5334043	K562	blood:	n/a	n/a
9	ATF3	chr10:5333695-5334079	K562	blood:	n/a	n/a
10	ATF3	chr10:5333465-5334182	A549	lung:	n/a	n/a
11	ATF3	chr10:5326289-5326817	K562	blood:	n/a	n/a
12	ATF3	chr10:5333223-5334296	A549	lung:	n/a	n/a
13	BACH1	chr10:5325193-5325762	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr10:5326467-5326786	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr10:5314029-5314452	H1-hESC	embryonic stem cell:	n/a	chr10:5314219-5314233
16	BACH1	chr10:5333705-5333941	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:5336196-5336356	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr10:5314040-5314410	K562	blood:	n/a	chr10:5314219-5314233
19	BACH1	chr10:5326454-5327033	K562	blood:	n/a	n/a
20	BCL3	chr10:5333183-5334316	A549	lung:	n/a	n/a
21	BCL3	chr10:5325157-5327103	A549	lung:	n/a	chr10:5326539-5326548
22	BCL3	chr10:5325009-5326832	A549	lung:	n/a	chr10:5326539-5326548
23	BCL3	chr10:5333309-5334562	A549	lung:	n/a	n/a
24	BHLHE40	chr10:5337719-5337915	K562	blood:	n/a	n/a
25	BHLHE40	chr10:5339529-5339545	K562	blood:	n/a	n/a
26	BHLHE40	chr10:5333619-5333920	K562	blood:	n/a	n/a
27	BHLHE40	chr10:5326335-5326780	K562	blood:	n/a	n/a
28	BRCA1	chr10:5333574-5334170	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr10:5336152-5336386	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr10:5333327-5334314	K562	blood:	n/a	n/a
31	CBX3	chr10:5336027-5336413	K562	blood:	n/a	n/a
32	CBX3	chr10:5336091-5336370	K562	blood:	n/a	n/a
33	CBX3	chr10:5326216-5326887	K562	blood:	n/a	n/a
34	CCNT2	chr10:5326424-5326723	K562	blood:	n/a	n/a
35	CEBPB	chr10:5294448-5294773	A549	lung:	n/a	n/a
36	CEBPB	chr10:5333532-5333776	K562	blood:	n/a	n/a
37	CEBPB	chr10:5294450-5294655	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:5326460-5326848	K562	blood:	n/a	n/a
39	CEBPB	chr10:5333787-5334021	K562	blood:	n/a	n/a
40	CEBPB	chr10:5326281-5326926	A549	lung:	n/a	n/a
41	CEBPB	chr10:5326307-5326933	A549	lung:	n/a	n/a
42	CEBPB	chr10:5326531-5326679	HepG2	liver:	n/a	n/a
43	CEBPB	chr10:5333435-5334384	K562	blood:	n/a	chr10:5333459-5333476
44	CEBPB	chr10:5326351-5326856	A549	lung:	n/a	n/a
45	CEBPB	chr10:5325100-5325739	A549	lung:	n/a	chr10:5325630-5325642
46	CEBPB	chr10:5326460-5326723	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr10:5326389-5326882	K562	blood:	n/a	n/a
48	CEBPB	chr10:5333274-5334468	A549	lung:	n/a	chr10:5333459-5333476
49	CEBPB	chr10:5333517-5334091	IMR90	lung:	n/a	n/a
50	CEBPB	chr10:5339428-5339796	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5333615-5333665	PFSK-1	brain:	n/a
2	chr10:5302629-5302679	A549	lung:	n/a
3	chr10:5333615-5333665	HUVEC	blood vessel:	n/a
4	chr10:5333615-5333665	SK-N-SH_RA	brain:	n/a
5	chr10:5333615-5333665	SK-N-SH	brain:	n/a
6	chr10:5333615-5333665	HL-60	blood:	n/a
7	chr10:5333615-5333665	T-47D	breast:	n/a
8	chr10:5302629-5302679	PrEC	prostate:	n/a
9	chr10:5302629-5302679	NB4	blood:	n/a
10	chr10:5333615-5333665	NB4	blood:	n/a
11	chr10:5302629-5302679	MCF-7	breast:	n/a
12	chr10:5333615-5333665	HRCEpiC	kidney:	n/a
13	chr10:5302629-5302679	HEEpiC	esophagus:	n/a
14	chr10:5302629-5302679	HAEpiC	amniotic membrane:	n/a
15	chr10:5302629-5302679	HRCEpiC	kidney:	n/a
16	chr10:5333615-5333665	IMR90	lung:	fetal
17	chr10:5302629-5302679	HL-60	blood:	n/a
18	chr10:5302629-5302679	HCPEpiC	choroid plexus:	n/a
19	chr10:5333615-5333665	GM12892	blood:	n/a
20	chr10:5302629-5302679	IMR90	lung:	fetal
21	chr10:5302629-5302679	SK-N-MC	brain:	n/a
22	chr10:5302629-5302679	GM12892	blood:	n/a
23	chr10:5302629-5302679	AG09309	skin:	n/a
24	chr10:5302629-5302679	ProgFib	skin:	n/a
25	chr10:5333615-5333665	GM12878	blood:	n/a
26	chr10:5333615-5333665	Hela-S3	cervix:	n/a
27	chr10:5333615-5333665	H1-hESC	embryonic stem cell:	embryo
28	chr10:5302629-5302679	GM19239	blood:	n/a
29	chr10:5302629-5302679	SK-N-SH	brain:	n/a
30	chr10:5333615-5333665	HEK293	kidney:	embryo
31	chr10:5333615-5333665	GM12891	blood:	n/a
32	chr10:5302629-5302679	HIPEpiC	eye:	n/a
33	chr10:5333615-5333665	HNPCEpiC	eye:	n/a
34	chr10:5302629-5302679	K562	blood:	n/a
35	chr10:5333615-5333665	SK-N-MC	brain:	n/a
36	chr10:5333615-5333665	NH-A	brain:	n/a
37	chr10:5333615-5333665	AoSMC	blood vessel:	n/a
38	chr10:5333615-5333665	A549	lung:	n/a
39	chr10:5333615-5333665	ProgFib	skin:	n/a
40	chr10:5333615-5333665	NHDF-neo	bronchial:	n/a
41	chr10:5302629-5302679	U87	brain:	n/a
42	chr10:5333615-5333665	BJ	skin:	n/a
43	chr10:5302629-5302679	GM12878	blood:	n/a
44	chr10:5302629-5302679	SAEC	small airway:	n/a
45	chr10:5333615-5333665	PrEC	prostate:	n/a
46	chr10:5333615-5333665	AG04450	lung:	fetal
47	chr10:5333615-5333665	HIPEpiC	eye:	n/a
48	chr10:5302629-5302679	T-47D	breast:	n/a
49	chr10:5333615-5333665	HAEpiC	amniotic membrane:	n/a
50	chr10:5333615-5333665	AG10803	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5300898..5303251-chr10:5486479..5488838,2	K562	blood:
2	chr10:5131798..5132693-chr10:5325154..5326138,5	MCF-7	breast:
3	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
4	chr10:5344285..5346013-chr10:5348255..5349922,2	K562	blood:
5	chr10:5308367..5310948-chr10:5323905..5325582,2	K562	blood:
6	chr10:5241329..5242148-chr10:5325053..5325709,2	MCF-7	breast:
7	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
8	chr10:5325782..5327303-chr10:5331354..5334117,2	K562	blood:
9	chr10:5344285..5346013-chr10:5348255..5349922,2	K562	blood:
10	chr10:5347252..5349655-chr10:5350748..5353704,2	K562	blood:
11	chr10:5285721..5288092-chr10:5296102..5298963,2	K562	blood:
12	chr10:4857887..4858608-chr10:5325585..5326522,2	K562	blood:
13	chr10:5082340..5083456-chr10:5325202..5326034,4	MCF-7	breast:
14	chr10:5314790..5316685-chr10:5325493..5327295,2	K562	blood:
15	chr10:5327837..5330329-chr10:5330922..5333846,2	K562	blood:
16	chr10:5336010..5336717-chr10:5425689..5426611,2	MCF-7	breast:
17	chr10:5338258..5343485-chr10:5345968..5350797,5	K562	blood:
18	chr10:4891638..4892533-chr10:5325193..5326077,4	MCF-7	breast:
19	chr10:5024232..5024860-chr10:5325292..5325936,2	K562	blood:
20	chr10:5061036..5061618-chr10:5325622..5326440,2	MCF-7	breast:
21	chr10:5336048..5336657-chr10:5385291..5386158,2	MCF-7	breast:
22	chr10:4856147..4859117-chr10:5323721..5326556,2	K562	blood:
23	chr10:5308367..5310948-chr10:5323905..5325582,2	K562	blood:
24	chr10:5335891..5336750-chr10:5390020..5390722,2	MCF-7	breast:
25	chr10:5309166..5310938-chr10:5312604..5314202,2	K562	blood:
26	chr10:4891547..4892555-chr10:5325301..5326118,4	MCF-7	breast:
27	chr10:5189042..5190566-chr10:5324451..5326870,2	MCF-7	breast:
28	chr10:5343873..5346040-chr10:5352452..5353968,2	MCF-7	breast:
29	chr10:5210740..5212996-chr10:5319959..5322251,2	MCF-7	breast:
30	chr10:5285994..5288790-chr10:5292059..5294701,2	MCF-7	breast:
31	chr10:5325782..5327303-chr10:5331354..5334117,2	K562	blood:
32	chr10:4869978..4871994-chr10:5334140..5336719,2	K562	blood:
33	chr10:5314790..5316685-chr10:5325493..5327295,2	K562	blood:
34	chr10:5056816..5057785-chr10:5335747..5336705,2	MCF-7	breast:
35	chr10:5333712..5336149-chr10:5487099..5489733,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C4-1	chr10:5304928-5305371	ENSG00000231039.2
2	lnc-AKR1CL1-3	chr10:5297996-5298648	NONHSAT011146
3	lnc-AKR1CL1-3	chr10:5303161-5303199	NONHSAT011146
4	lnc-AKR1CL1-1	chr10:5307996-5308648	XLOC_008706
5	lnc-AKR1CL1-1	chr10:5313161-5313199	XLOC_008706
6	lnc-AKR1C4-3	chr10:5294924-5295165	NONHSAT011143
7	lnc-TUBAL3-1	chr10:5346394-5346828	NONHSAT011148
8	lnc-AKR1C4-1	chr10:5304924-5305165	XLOC_008363

No data

Variant related genes	Relation type
ENSG00000223987	TF binding region
ENSG00000224034	TF binding region
AKR1C7P	TF binding region
ENSG00000223987	CpG island
ENSG00000224034	CpG island
AKR1C7P	CpG island
ENSG00000223987	chromatin interactions
ENSG00000151632	chromatin interactions
ENSG00000215267	chromatin interactions
ENSG00000173848	chromatin interactions
ENSG00000224034	chromatin interactions
LRP1B	miRNA target sites
OLIG3	miRNA target sites

Extended variants
information (count: 2532 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2532 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7895816	chr10:5286600-5286601	Enhancers Active TSS Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370272296	chr10:5286635-5286636	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574299302	chr10:5286637-5286638	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142351337	chr10:5286649-5286650	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144652656	chr10:5286650-5286651	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577917357	chr10:5286685-5286686	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181411863	chr10:5286733-5286734	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545432989	chr10:5286749-5286750	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560362510	chr10:5286802-5286803	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572241058	chr10:5286806-5286807	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558710216	chr10:5286819-5286820	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368526210	chr10:5286824-5286825	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542731531	chr10:5286831-5286832	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7908061	chr10:5286855-5286856	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs529058866	chr10:5286898-5286899	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550421706	chr10:5286901-5286902	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562840298	chr10:5286902-5286903	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs532785778	chr10:5286950-5286951	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551382608	chr10:5286973-5286974	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151320589	chr10:5287011-5287012	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570545886	chr10:5287012-5287013	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184656401	chr10:5287013-5287014	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs549119768	chr10:5287018-5287019	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375606545	chr10:5287025-5287026	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140649468	chr10:5287039-5287040	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190370075	chr10:5287050-5287051	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556577920	chr10:5287063-5287064	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7911385	chr10:5287088-5287089	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs561910458	chr10:5287092-5287093	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs554102668	chr10:5287103-5287104	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9423570	chr10:5287110-5287111	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs542668143	chr10:5287145-5287146	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375995438	chr10:5287153-5287154	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11595920	chr10:5287177-5287178	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs9423396	chr10:5287192-5287193	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7896353	chr10:5287193-5287194	Flanking Active TSS Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs562617384	chr10:5287236-5287237	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs533289681	chr10:5287243-5287244	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544987246	chr10:5287252-5287253	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560162783	chr10:5287255-5287256	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181787117	chr10:5287269-5287270	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200976420	chr10:5287295-5287296	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549058184	chr10:5287300-5287301	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186854188	chr10:5287314-5287315	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531921247	chr10:5287318-5287319	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550384354	chr10:5287319-5287320	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571763157	chr10:5287320-5287321	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539294060	chr10:5287321-5287322	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554175251	chr10:5287322-5287323	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565698830	chr10:5287338-5287339	Active TSS Weak transcription	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	23223014	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5284200-5287200	Enhancers	HepG2	liver
2	chr10:5286200-5286600	Strong transcription	A549	lung
3	chr10:5286200-5287000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr10:5286400-5287200	Active TSS	Liver	Liver
5	chr10:5286600-5293800	Weak transcription	A549	lung
6	chr10:5287000-5287200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr10:5287000-5287400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr10:5287200-5287400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr10:5293800-5294400	Enhancers	A549	lung
10	chr10:5293800-5295000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr10:5293800-5295000	Enhancers	HepG2	liver
12	chr10:5294200-5294600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr10:5294200-5294600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr10:5294200-5294600	Enhancers	Esophagus	oesophagus
15	chr10:5294200-5294600	Enhancers	Placenta	Placenta
16	chr10:5294200-5294600	Bivalent Enhancer	Left Ventricle	heart
17	chr10:5294200-5294600	Enhancers	Stomach Mucosa	stomach
18	chr10:5294200-5294600	Enhancers	HMEC	breast
19	chr10:5294200-5294800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr10:5294200-5294800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:5294200-5294800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr10:5294400-5294600	Flanking Active TSS	A549	lung
23	chr10:5294400-5294800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr10:5294600-5295200	Enhancers	A549	lung
25	chr10:5294600-5296000	Weak transcription	Esophagus	oesophagus
26	chr10:5294600-5296400	Weak transcription	Stomach Mucosa	stomach
27	chr10:5295000-5300600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr10:5295000-5301400	Weak transcription	HepG2	liver
29	chr10:5295200-5301400	Weak transcription	A549	lung
30	chr10:5296000-5296400	Enhancers	Esophagus	oesophagus
31	chr10:5296000-5296600	Enhancers	Colonic Mucosa	Colon
32	chr10:5296200-5296600	Enhancers	Duodenum Mucosa	Duodenum
33	chr10:5296200-5296600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr10:5296200-5296600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr10:5296200-5296600	Enhancers	NHEK	skin
36	chr10:5296400-5296800	Enhancers	Stomach Mucosa	stomach
37	chr10:5300600-5302000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr10:5300800-5303200	Enhancers	Liver	Liver
39	chr10:5301200-5301600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr10:5301400-5302400	Enhancers	HepG2	liver
41	chr10:5301400-5303400	Strong transcription	A549	lung
42	chr10:5302200-5302600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr10:5302400-5304400	Weak transcription	HepG2	liver
44	chr10:5302600-5303000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr10:5302800-5303600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr10:5303200-5305000	Weak transcription	Liver	Liver
47	chr10:5303400-5307400	Weak transcription	A549	lung
48	chr10:5304400-5305200	Enhancers	HepG2	liver
49	chr10:5305000-5305200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:5305400-5306600	Weak transcription	Liver	Liver

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