Variant report

Variant	nsv549884
Chromosome Location	chr10:5037926-5065248
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:903)
CpG islands
(count:610)
Chromatin interactive
region (count:18)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:5044421-5044450	K562	blood:	n/a	n/a
2	ARID3A	chr10:5061188-5061367	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:5062394-5062740	K562	blood:	n/a	n/a
4	ARID3A	chr10:5051271-5051707	HepG2	liver:	n/a	n/a
5	ATF1	chr10:5044389-5044572	K562	blood:	n/a	n/a
6	ATF3	chr10:5051280-5051719	A549	lung:	n/a	n/a
7	ATF3	chr10:5051152-5051727	A549	lung:	n/a	n/a
8	ATF3	chr10:5043740-5045168	A549	lung:	n/a	n/a
9	BACH1	chr10:5062431-5062668	K562	blood:	n/a	n/a
10	BACH1	chr10:5054805-5055071	K562	blood:	n/a	n/a
11	BACH1	chr10:5062492-5062763	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr10:5051200-5051819	A549	lung:	n/a	n/a
13	BCL3	chr10:5040385-5041259	A549	lung:	n/a	n/a
14	BCL3	chr10:5051407-5051659	GM12878	blood:	n/a	n/a
15	BCL3	chr10:5041450-5041896	A549	lung:	n/a	n/a
16	BCL3	chr10:5062256-5062847	A549	lung:	n/a	n/a
17	BCL3	chr10:5043019-5045474	A549	lung:	n/a	chr10:5043544-5043553
18	BCL3	chr10:5045778-5046158	A549	lung:	n/a	n/a
19	BCL3	chr10:5045658-5046322	A549	lung:	n/a	n/a
20	BCL3	chr10:5042025-5043017	A549	lung:	n/a	n/a
21	BCL3	chr10:5039784-5041366	A549	lung:	n/a	n/a
22	BCL3	chr10:5051336-5051703	GM12878	blood:	n/a	n/a
23	BCL3	chr10:5042177-5042783	A549	lung:	n/a	n/a
24	BCL3	chr10:5039213-5039693	A549	lung:	n/a	n/a
25	BCL3	chr10:5050987-5051835	A549	lung:	n/a	n/a
26	BCL3	chr10:5043450-5044764	A549	lung:	n/a	chr10:5043544-5043553
27	BHLHE40	chr10:5062449-5062685	K562	blood:	n/a	n/a
28	CCNT2	chr10:5062405-5062731	K562	blood:	n/a	chr10:5062519-5062528 chr10:5062579-5062599
29	CEBPB	chr10:5062558-5062813	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr10:5064109-5064365	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:5051354-5051745	K562	blood:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
32	CEBPB	chr10:5051242-5051750	A549	lung:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
33	CEBPB	chr10:5039354-5039384	A549	lung:	n/a	n/a
34	CEBPB	chr10:5051199-5051864	A549	lung:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
35	CEBPB	chr10:5045994-5046240	A549	lung:	n/a	n/a
36	CEBPB	chr10:5051236-5051663	MCF-7	breast:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
37	CEBPB	chr10:5051236-5051854	MCF-7	breast:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
38	CEBPB	chr10:5051249-5051751	Hela-S3	cervix:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
39	CEBPB	chr10:5051377-5051633	HepG2	liver:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
40	CEBPB	chr10:5051291-5051683	HCT-116	colon:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
41	CEBPB	chr10:5046025-5046201	K562	blood:	n/a	n/a
42	CEBPB	chr10:5048613-5048680	K562	blood:	n/a	n/a
43	CEBPB	chr10:5048696-5048802	IMR90	lung:	n/a	n/a
44	CEBPB	chr10:5051213-5051659	A549	lung:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
45	CEBPB	chr10:5046019-5046239	K562	blood:	n/a	n/a
46	CEBPB	chr10:5051334-5051733	K562	blood:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
47	CEBPB	chr10:5045702-5046324	K562	blood:	n/a	n/a
48	CEBPB	chr10:5051317-5051763	HepG2	liver:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
49	CEBPB	chr10:5051312-5051638	ECC-1	luminal epithelium:	n/a	chr10:5051545-5051558 chr10:5051377-5051390 chr10:5051545-5051556
50	CEBPB	chr10:5051392-5051650	ECC-1	luminal epithelium:	n/a	chr10:5051545-5051558 chr10:5051545-5051556

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:5060432-5060482	A549	lung:	n/a
2	chr10:5060566-5060616	PrEC	prostate:	n/a
3	chr10:5060566-5060616	K562	blood:	n/a
4	chr10:5046097-5046147	GM12891	blood:	n/a
5	chr10:5046097-5046147	U87	brain:	n/a
6	chr10:5061094-5061144	Caco-2	colon:	n/a
7	chr10:5047456-5047506	SK-N-SH_RA	brain:	n/a
8	chr10:5047456-5047506	AG04450	lung:	fetal
9	chr10:5060566-5060616	HEEpiC	esophagus:	n/a
10	chr10:5044992-5045042	HPAEpiC	pulmonary alveolar:	n/a
11	chr10:5061094-5061144	NB4	blood:	n/a
12	chr10:5042313-5042363	LNCaP	prostate:	n/a
13	chr10:5060318-5060368	ECC-1	luminal epithelium:	n/a
14	chr10:5047487-5047537	GM19239	blood:	n/a
15	chr10:5047456-5047506	HepG2	liver:	n/a
16	chr10:5060291-5060341	H1-hESC	embryonic stem cell:	embryo
17	chr10:5060318-5060368	NHDF-neo	bronchial:	n/a
18	chr10:5061094-5061144	ProgFib	skin:	n/a
19	chr10:5046097-5046147	H1-hESC	embryonic stem cell:	embryo
20	chr10:5060566-5060616	U87	brain:	n/a
21	chr10:5046097-5046147	NT2-D1	testis:	n/a
22	chr10:5060291-5060341	LNCaP	prostate:	n/a
23	chr10:5046097-5046147	HRE	kidney:	n/a
24	chr10:5061094-5061144	SK-N-SH_RA	brain:	n/a
25	chr10:5047487-5047537	HIPEpiC	eye:	n/a
26	chr10:5061094-5061144	HCPEpiC	choroid plexus:	n/a
27	chr10:5042313-5042363	HEK293	kidney:	embryo
28	chr10:5060318-5060368	SK-N-SH_RA	brain:	n/a
29	chr10:5047487-5047537	AG09309	skin:	n/a
30	chr10:5047456-5047506	K562	blood:	n/a
31	chr10:5047456-5047506	Caco-2	colon:	n/a
32	chr10:5060291-5060341	GM19239	blood:	n/a
33	chr10:5060318-5060368	MCF10A-Er-Src	breast:	n/a
34	chr10:5047456-5047506	HL-60	blood:	n/a
35	chr10:5060291-5060341	PANC-1	pancreas:	n/a
36	chr10:5046097-5046147	MCF-7	breast:	n/a
37	chr10:5042313-5042363	SK-N-SH	brain:	n/a
38	chr10:5044992-5045042	T-47D	breast:	n/a
39	chr10:5044992-5045042	K562	blood:	n/a
40	chr10:5060291-5060341	SK-N-SH_RA	brain:	n/a
41	chr10:5047456-5047506	Hepatocyte	liver:	n/a
42	chr10:5060291-5060341	GM12892	blood:	n/a
43	chr10:5060318-5060368	Hepatocyte	liver:	n/a
44	chr10:5042313-5042363	GM12878	blood:	n/a
45	chr10:5047487-5047537	CMK	blood:	n/a
46	chr10:5044992-5045042	CMK	blood:	n/a
47	chr10:5061094-5061144	HPAEpiC	pulmonary alveolar:	n/a
48	chr10:5044992-5045042	Jurkat	blood:	n/a
49	chr10:5046097-5046147	HCPEpiC	choroid plexus:	n/a
50	chr10:5042313-5042363	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5039943..5042485-chr10:5047433..5049901,2	MCF-7	breast:
2	chr10:5026070..5027592-chr10:5040944..5042648,2	K562	blood:
3	chr10:5061036..5061618-chr10:5325622..5326440,2	MCF-7	breast:
4	chr10:4891883..4892464-chr10:5057320..5057832,2	MCF-7	breast:
5	chr10:5049047..5051331-chr10:5062456..5064553,2	MCF-7	breast:
6	chr10:5049047..5051331-chr10:5062456..5064553,2	MCF-7	breast:
7	chr10:5040612..5043134-chr10:5043757..5046328,2	K562	blood:
8	chr10:4997960..5000911-chr10:5049814..5051321,2	MCF-7	breast:
9	chr10:4892321..4893891-chr10:5065026..5067152,2	MCF-7	breast:
10	chr10:5030937..5032573-chr10:5043050..5044672,2	MCF-7	breast:
11	chr10:4873120..4874675-chr10:5065165..5067364,2	K562	blood:
12	chr10:5048912..5051298-chr10:5054151..5056215,2	MCF-7	breast:
13	chr10:5048912..5051298-chr10:5054151..5056215,2	MCF-7	breast:
14	chr10:5039943..5042485-chr10:5047433..5049901,2	MCF-7	breast:
15	chr10:5060824..5061816-chr10:5136872..5137424,2	MCF-7	breast:
16	chr10:5054978..5056571-chr10:5059008..5060514,2	K562	blood:
17	chr10:5052203..5054008-chr10:5065761..5068228,2	MCF-7	breast:
18	chr10:5008134..5010940-chr10:5050778..5053121,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1C1-2	chr10:5038229-5038338	ENSG00000224251.2
2	lnc-AKR1C2-6	chr10:5058029-5058084	NONHSAT011131
3	lnc-AKR1C2-6	chr10:5060092-5060126	NONHSAT011130
4	lnc-AKR1C1-2	chr10:5039432-5039566	ENSG00000224251.2
5	lnc-AKR1C1-2	chr10:5039432-5039572	ENSG00000224251.1
6	lnc-AKR1C2-6	chr10:5049599-5049698	NONHSAT011129
7	lnc-AKR1C2-6	chr10:5060092-5060223	NONHSAT011129
8	lnc-AKR1C2-6	chr10:5052655-5052845	NONHSAT011131
9	lnc-AKR1C1-2	chr10:5038045-5038338	ENSG00000224251.1
10	lnc-AKR1C1-2	chr10:5038074-5038124	ENSG00000224251.1
11	lnc-AKR1C2-6	chr10:5048654-5048784	NONHSAT011130
12	lnc-AKR1C2-6	chr10:5049599-5049698	NONHSAT011130
13	lnc-AKR1C2-6	chr10:5052536-5052845	NONHSAT011129
14	lnc-AKR1C1-2	chr10:5038229-5038338	ENSG00000224251.1
15	lnc-AKR1C2-6	chr10:5057095-5057426	NONHSAT011131
16	lnc-AKR1C2-6	chr10:5052536-5052845	NONHSAT011130
17	lnc-AKR1C2-6	chr10:5048187-5048244	NONHSAT011129
18	lnc-AKR1C1-2	chr10:5039432-5039569	ENSG00000224251.1

No data

Variant related genes	Relation type
AKR1C2	TF binding region
ENSG00000239148	TF binding region
ENSG00000224251	TF binding region
AKR1C2	CpG island
ENSG00000239148	CpG island
ENSG00000224251	CpG island
ENSG00000151632	chromatin interactions

Extended variants
information (count: 1499 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1499 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550209837	chr10:5037936-5037937	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs374253499	chr10:5037962-5037963	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200650974	chr10:5037977-5037978	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs571588082	chr10:5037980-5037981	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs138437499	chr10:5038000-5038001	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs149560142	chr10:5038011-5038012	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566167986	chr10:5038019-5038020	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs111932774	chr10:5038022-5038023	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs536442138	chr10:5038032-5038033	Strong transcription Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555081842	chr10:5038100-5038101	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs111999542	chr10:5038105-5038106	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs573408906	chr10:5038111-5038112	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs543860135	chr10:5038116-5038117	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs2518034	chr10:5038149-5038150	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs577535131	chr10:5038158-5038159	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs548057107	chr10:5038179-5038180	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs560375110	chr10:5038186-5038187	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs572316911	chr10:5038261-5038262	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs189362843	chr10:5038295-5038296	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs180751645	chr10:5038296-5038297	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs531863949	chr10:5038300-5038301	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs369014332	chr10:5038307-5038308	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs201933166	chr10:5038309-5038310	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs565169026	chr10:5038314-5038315	Strong transcription Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs532515117	chr10:5038370-5038371	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs116519120	chr10:5038420-5038421	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566020813	chr10:5038432-5038433	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs536506322	chr10:5038449-5038450	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs117952235	chr10:5038464-5038465	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs569889481	chr10:5038473-5038474	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs78379963	chr10:5038481-5038482	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs200462318	chr10:5038492-5038493	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs145300678	chr10:5038515-5038516	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs577597857	chr10:5038533-5038534	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs184937102	chr10:5038540-5038541	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs538625349	chr10:5038551-5038552	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575018401	chr10:5038670-5038671	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189419944	chr10:5038673-5038674	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs553822241	chr10:5038693-5038694	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs181616930	chr10:5038737-5038738	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs371538926	chr10:5038739-5038740	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs377061764	chr10:5038740-5038741	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs200451297	chr10:5038753-5038754	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs373454885	chr10:5038754-5038755	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557578968	chr10:5038767-5038768	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs61856064	chr10:5038829-5038830	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs76906176	chr10:5038831-5038832	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576288342	chr10:5038838-5038839	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs543496759	chr10:5038880-5038881	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs186090261	chr10:5038900-5038901	Strong transcription Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5005800-5045800	Weak transcription	HSMMtube	muscle
2	chr10:5008200-5044000	Weak transcription	Fetal Brain Male	brain
3	chr10:5011600-5044200	Weak transcription	Fetal Brain Female	brain
4	chr10:5011800-5043800	Weak transcription	Psoas Muscle	Psoas
5	chr10:5019400-5044600	Weak transcription	Brain Germinal Matrix	brain
6	chr10:5021800-5044400	Weak transcription	NHDF-Ad	bronchial
7	chr10:5024400-5039400	Weak transcription	Ovary	ovary
8	chr10:5024400-5040400	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr10:5024400-5040600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:5024400-5056800	Weak transcription	Esophagus	oesophagus
11	chr10:5024800-5044400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:5024800-5051400	Weak transcription	Fetal Intestine Small	intestine
13	chr10:5025000-5045800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr10:5025200-5044200	Weak transcription	K562	blood
15	chr10:5027400-5042400	Weak transcription	Gastric	stomach
16	chr10:5027600-5045000	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr10:5027800-5038600	Weak transcription	Left Ventricle	heart
18	chr10:5027800-5043200	Weak transcription	HepG2	liver
19	chr10:5027800-5045800	Weak transcription	Fetal Stomach	stomach
20	chr10:5027800-5045800	Weak transcription	Stomach Smooth Muscle	stomach
21	chr10:5027800-5050600	Weak transcription	Pancreas	Pancrea
22	chr10:5028000-5045800	Weak transcription	Fetal Muscle Leg	muscle
23	chr10:5030200-5042200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr10:5030400-5039200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:5033800-5039800	Weak transcription	Liver	Liver
26	chr10:5033800-5040000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:5033800-5040000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr10:5033800-5040200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr10:5033800-5044600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr10:5034000-5040000	Weak transcription	Adipose Nuclei	Adipose
31	chr10:5034800-5042800	Weak transcription	Fetal Intestine Large	intestine
32	chr10:5036800-5043200	Weak transcription	Right Atrium	heart
33	chr10:5037800-5040000	Active TSS	A549	lung
34	chr10:5039200-5041200	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr10:5039800-5041800	Strong transcription	Liver	Liver
36	chr10:5040000-5041200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:5040000-5041200	Genic enhancers	Adipose Nuclei	Adipose
38	chr10:5040000-5041600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr10:5040000-5045200	Transcr. at gene 5' and 3'	A549	lung
40	chr10:5040000-5045600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr10:5040200-5041200	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr10:5040400-5041200	Strong transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:5040600-5041000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr10:5041000-5044600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr10:5041200-5042200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr10:5041200-5042200	Strong transcription	Adipose Nuclei	Adipose
47	chr10:5041200-5043800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr10:5041200-5044000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:5041200-5044200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr10:5041600-5045800	Weak transcription	HMEC	breast

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