Variant report

Variant	nsv895347
Chromosome Location	chr10:48664066-49299273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1870)
CpG islands
(count:1281)
Chromatin interactive
region (count:0)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr10:48989552-48989844	GM12878	blood:	n/a	n/a
2	BATF	chr10:48951827-48952054	GM12878	blood:	n/a	chr10:48951972-48951982
3	BATF	chr10:48989549-48989912	GM12878	blood:	n/a	n/a
4	BATF	chr10:48956676-48956928	GM12878	blood:	n/a	chr10:48956771-48956782
5	BATF	chr10:48714324-48714566	GM12878	blood:	n/a	n/a
6	BATF	chr10:48956627-48956981	GM12878	blood:	n/a	chr10:48956771-48956782
7	BATF	chr10:48952428-48952658	GM12878	blood:	n/a	n/a
8	BCL11A	chr10:48952136-48952344	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:49005020-49005346	GM12878	blood:	n/a	n/a
10	BCL11A	chr10:48989531-48989902	GM12878	blood:	n/a	chr10:48989690-48989699
11	BCL11A	chr10:48989616-48989790	GM12878	blood:	n/a	chr10:48989690-48989699
12	BCL11A	chr10:48956689-48956877	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:48956608-48956947	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:49005038-49005190	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:49080042-49080383	HepG2	liver:	n/a	n/a
16	BHLHE40	chr10:49045988-49046173	HepG2	liver:	n/a	n/a
17	BRCA1	chr10:49199990-49200190	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr10:48952273-48952700	K562	blood:	n/a	n/a
19	CBX3	chr10:49249785-49250052	K562	blood:	n/a	n/a
20	CEBPB	chr10:48751748-48752065	K562	blood:	n/a	n/a
21	CEBPB	chr10:49046671-49046868	IMR90	lung:	n/a	chr10:49046694-49046707 chr10:49046696-49046705 chr10:49046696-49046705 chr10:49046696-49046705
22	CEBPB	chr10:48813184-48813461	K562	blood:	n/a	n/a
23	CEBPB	chr10:49272320-49272583	K562	blood:	n/a	n/a
24	CEBPB	chr10:49199799-49200207	Hela-S3	cervix:	n/a	chr10:49199988-49199999
25	CEBPB	chr10:49068108-49068463	K562	blood:	n/a	n/a
26	CEBPB	chr10:49197254-49197290	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr10:49004870-49005359	GM12878	blood:	n/a	n/a
28	CEBPB	chr10:48813073-48813507	K562	blood:	n/a	n/a
29	CEBPB	chr10:49199814-49200190	A549	lung:	n/a	chr10:49199988-49199999
30	CEBPB	chr10:49068168-49068380	K562	blood:	n/a	n/a
31	CEBPB	chr10:49199984-49200016	HepG2	liver:	n/a	chr10:49199988-49199999
32	CEBPD	chr10:49245923-49246196	K562	blood:	n/a	n/a
33	CEBPD	chr10:48954264-48954686	K562	blood:	n/a	n/a
34	CEBPD	chr10:48813141-48813550	K562	blood:	n/a	n/a
35	CEBPD	chr10:48929222-48929557	K562	blood:	n/a	n/a
36	CEBPD	chr10:48876061-48876445	K562	blood:	n/a	n/a
37	CEBPD	chr10:48723545-48723962	K562	blood:	n/a	n/a
38	CHD2	chr10:49199811-49200185	Hela-S3	cervix:	n/a	chr10:49199901-49199911
39	CTCF	chr10:49084298-49084343	GM20000	blood:	n/a	n/a
40	CTCF	chr10:48892050-48892092	Pancreas_OC	pancreas:	n/a	n/a
41	CTCF	chr10:48746195-48746340	LNCaP	prostate:	n/a	n/a
42	CTCF	chr10:48775821-48775847	MCF-7	breast:	n/a	n/a
43	CTCF	chr10:48714273-48714600	NHEK	skin:	n/a	chr10:48714421-48714437 chr10:48714420-48714438 chr10:48714415-48714436 chr10:48714427-48714434
44	CTCF	chr10:48691408-48691782	K562	blood:	n/a	chr10:48691583-48691596 chr10:48691576-48691597 chr10:48691581-48691599 chr10:48691582-48691598 chr10:48691587-48691596 chr10:48691583-48691596 chr10:48691584-48691594
45	CTCF	chr10:48743923-48743997	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr10:48725187-48725379	K562	blood:	n/a	chr10:48725283-48725301
47	CTCF	chr10:48676210-48676419	MCF-7	breast:	n/a	n/a
48	CTCF	chr10:49050023-49050106	GM13976	blood:	n/a	n/a
49	CTCF	chr10:48952644-48952789	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr10:48870985-48871291	A549	lung:	n/a	n/a

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:48760449-48760499	Hela-S3	cervix:	n/a
2	chr10:48807252-48807302	ovcar-3	ovarian:	n/a
3	chr10:48861038-48861088	MCF10A-Er-Src	breast:	n/a
4	chr10:49205543-49205593	Caco-2	colon:	n/a
5	chr10:48965159-48965209	RPTEC	kidney:	n/a
6	chr10:48981581-48981631	Hepatocyte	liver:	n/a
7	chr10:48826782-48826832	HMEC	breast:	n/a
8	chr10:49205543-49205593	NHBE	bronchial:	n/a
9	chr10:48826782-48826832	GM06990	blood:	n/a
10	chr10:48949616-48949666	GM19239	blood:	n/a
11	chr10:48855211-48855261	HRE	kidney:	n/a
12	chr10:48950242-48950292	ECC-1	luminal epithelium:	n/a
13	chr10:48826782-48826832	ProgFib	skin:	n/a
14	chr10:48952423-48952473	PANC-1	pancreas:	n/a
15	chr10:48902368-48902418	HCT-116	colon:	n/a
16	chr10:48807341-48807391	GM12892	blood:	n/a
17	chr10:48899772-48899822	HCPEpiC	choroid plexus:	n/a
18	chr10:48828106-48828156	Jurkat	blood:	n/a
19	chr10:48898075-48898125	RPTEC	kidney:	n/a
20	chr10:48760449-48760499	T-47D	breast:	n/a
21	chr10:48861038-48861088	PrEC	prostate:	n/a
22	chr10:48807252-48807302	HUVEC	blood vessel:	n/a
23	chr10:48952423-48952473	GM12892	blood:	n/a
24	chr10:48861038-48861088	HUVEC	blood vessel:	n/a
25	chr10:48952423-48952473	GM12878	blood:	n/a
26	chr10:48807252-48807302	SK-N-SH_RA	brain:	n/a
27	chr10:48826782-48826832	HAEpiC	amniotic membrane:	n/a
28	chr10:48855211-48855261	MCF-7	breast:	n/a
29	chr10:48855211-48855261	HCT-116	colon:	n/a
30	chr10:48905601-48905651	BE2_C	brain:	n/a
31	chr10:48861038-48861088	RPTEC	kidney:	n/a
32	chr10:49205543-49205593	NH-A	brain:	n/a
33	chr10:48807252-48807302	AG04449	skin:	fetal
34	chr10:48950242-48950292	A549	lung:	n/a
35	chr10:48855211-48855261	MCF10A-Er-Src	breast:	n/a
36	chr10:49218579-49218629	H1-hESC	embryonic stem cell:	embryo
37	chr10:48807252-48807302	NB4	blood:	n/a
38	chr10:48965159-48965209	HEK293	kidney:	embryo
39	chr10:48760449-48760499	BJ	skin:	n/a
40	chr10:48828680-48828730	MCF-7	breast:	n/a
41	chr10:48828109-48828159	MCF10A-Er-Src	breast:	n/a
42	chr10:48828109-48828159	H1-hESC	embryonic stem cell:	embryo
43	chr10:48902368-48902418	HRCEpiC	kidney:	n/a
44	chr10:48828680-48828730	HCPEpiC	choroid plexus:	n/a
45	chr10:48981581-48981631	K562	blood:	n/a
46	chr10:48998683-48998733	NHBE	bronchial:	n/a
47	chr10:48826782-48826832	K562	blood:	n/a
48	chr10:48899772-48899822	HUVEC	blood vessel:	n/a
49	chr10:48905601-48905651	GM12892	blood:	n/a
50	chr10:48905601-48905651	AG10803	skin:	n/a

No data

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPN20B-2	chr10:48987655-48988451	NONHSAT013251
2	lnc-PTPN20B-2	chr10:48987596-48988451	NONHSAT013249
3	lnc-MAPK8-2	chr10:48954138-48954797	NONHSAT013243
4	lnc-PTPN20B-2	chr10:48989140-48989262	XLOC_008814
5	lnc-PTPN20B-1	chr10:49244690-49248867	NONHSAT013237
6	lnc-MAPK8-2	chr10:48980202-48980269	NONHSAT013243
7	lnc-PTPN20B-2	chr10:48989109-48989268	XLOC_008814
8	lnc-PTPN20B-2	chr10:48988121-48988451	XLOC_008814
9	lnc-PTPN20B-2	chr10:48989082-48989267	NONHSAT013249
10	lnc-MAPK8-2	chr10:48968560-48968623	NONHSAT013243
11	lnc-PTPN20B-2	chr10:48989082-48989262	XLOC_008814
12	lnc-GDF10-4	chr10:48737040-48738686	NONHSAT013232
13	lnc-PTPN20B-2	chr10:48998570-48998768	NONHSAT013251
14	lnc-GDF10-4	chr10:48827861-48827934	NONHSAT013232
15	lnc-GDF10-4	chr10:48795347-48795444	NONHSAT013233
16	lnc-GDF10-4	chr10:48792520-48792799	NONHSAT013234
17	lnc-MAPK8-2	chr10:48971070-48971153	NONHSAT013243
18	lnc-GDF10-4	chr10:48739388-48739450	NONHSAT013232
19	lnc-FAM25C-1	chr10:49199649-49199824	NONHSAT013257
20	lnc-GDF10-4	chr10:48738573-48738686	NONHSAT013233
21	lnc-GDF10-4	chr10:48795347-48795444	NONHSAT013232
22	lnc-MAPK8-2	chr10:48966878-48966933	NONHSAT013243
23	lnc-PTPN20B-2	chr10:48998570-48998766	XLOC_008814
24	lnc-PTPN20B-2	chr10:48987596-48988451	NONHSAT013248
25	lnc-GDF10-4	chr10:48795347-48795444	NONHSAT013234
26	lnc-GDF10-4	chr10:48792687-48792799	NONHSAT013233
27	lnc-GDF10-4	chr10:48792687-48792799	NONHSAT013232
28	lnc-PTPN20B-2	chr10:48989140-48989267	NONHSAT013248
29	lnc-PTPN20B-2	chr10:48987630-48988451	XLOC_008814
30	lnc-PTPN20B-2	chr10:48988121-48988451	XLOC_008814
31	lnc-MAPK8-2	chr10:48954322-48954975	NONHSAT013244
32	lnc-MAPK8-2	chr10:48962529-48962620	NONHSAT013242
33	lnc-MAPK8-2	chr10:48966878-48966933	NONHSAT013244
34	lnc-FAM25C-3	chr10:49090136-49090419	NONHSAT013255
35	lnc-MAPK8-2	chr10:48954405-48958083	NONHSAT013245
36	lnc-PTPN20B-2	chr10:48989140-48989262	NONHSAT013251
37	lnc-GDF10-4	chr10:48827520-48827581	NONHSAT013233
38	lnc-MAPK8-2	chr10:48953761-48954799	NONHSAT013242
39	lnc-FAM25C-1	chr10:49205711-49205776	NONHSAT013257
40	lnc-PTPN20B-2	chr10:49018309-49018413	XLOC_008814
41	lnc-GDF10-4	chr10:48739388-48739450	NONHSAT013233
42	lnc-FAM25C-1	chr10:49195626-49195779	NONHSAT013256
43	lnc-FAM25C-1	chr10:49199717-49199881	NONHSAT013256
44	lnc-PTPN20B-1	chr10:48927413-48927432	NONHSAT013237
45	lnc-GDF10-4	chr10:48806829-48806896	NONHSAT013234

No data

Variant related genes	Relation type
FAM25C	TF binding region
BMS1P7	TF binding region
PTPN20B	TF binding region
DUSP8P1	TF binding region
RNA5SP315	TF binding region
BMS1P5	TF binding region
RN7SL527P	TF binding region
FAM35EP	TF binding region
FRMPD2P1	TF binding region
CTGLF12P	TF binding region
CTSLP3	TF binding region
ENSG00000232426	TF binding region
GLUD1P2	TF binding region
RNA5SP314	TF binding region
FAM25C	CpG island
BMS1P7	CpG island
PTPN20B	CpG island
DUSP8P1	CpG island
RNA5SP315	CpG island
BMS1P5	CpG island
RN7SL527P	CpG island
FAM35EP	CpG island
FRMPD2P1	CpG island
CTGLF12P	CpG island
CTSLP3	CpG island
ENSG00000232426	CpG island
GLUD1P2	CpG island
RNA5SP314	CpG island
MED6	miRNA target sites
MED28	miRNA target sites
MED8	miRNA target sites

Extended variants
information (count: 702 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535268767	chr10:48691103-48691104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555062660	chr10:48691104-48691105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573219290	chr10:48691127-48691128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540238662	chr10:48691152-48691153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558566277	chr10:48691168-48691169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9422337	chr10:48691328-48691329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536194886	chr10:48737695-48737696	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs548249915	chr10:48737696-48737697	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs566474420	chr10:48737702-48737703	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs534111887	chr10:48737710-48737711	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs537880867	chr10:48737781-48737782	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs570676100	chr10:48737813-48737814	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs537615987	chr10:48737824-48737825	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs557430114	chr10:48737834-48737835	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs143087149	chr10:48739404-48739405	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs202027139	chr10:48739410-48739411	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs75140225	chr10:48792663-48792664	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs556939578	chr10:48807178-48807179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs142238406	chr10:48807252-48807253	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs184543817	chr10:48807253-48807254	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs374581517	chr10:48807341-48807342	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs559735879	chr10:48807773-48807774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs61846360	chr10:48807817-48807818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs541557050	chr10:48816015-48816016	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546696514	chr10:48816611-48816612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs564780725	chr10:48816619-48816620	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs532140551	chr10:48816622-48816623	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575218980	chr10:48818596-48818597	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs377240984	chr10:48818672-48818673	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542927918	chr10:48818812-48818813	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs200154793	chr10:48818824-48818825	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374281582	chr10:48818826-48818827	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs377631141	chr10:48820510-48820511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs546137459	chr10:48828438-48828439	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs554852267	chr10:48828681-48828682	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs61846371	chr10:48871281-48871282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536889622	chr10:48924070-48924071	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs555534325	chr10:48924071-48924072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs574871661	chr10:48924169-48924170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs528992718	chr10:48925481-48925482	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs547058869	chr10:48925532-48925533	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200118216	chr10:48926125-48926126	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201492642	chr10:48926684-48926685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs201176393	chr10:48926739-48926740	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs76918336	chr10:48926757-48926758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200369842	chr10:48926761-48926762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs539005212	chr10:48926773-48926774	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs550951538	chr10:48926776-48926777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs569898589	chr10:48926816-48926817	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs534612051	chr10:48928820-48928821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:48691000-48691400	Enhancers	Primary T cells fromperipheralblood	blood
2	chr10:48828000-48828400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr10:48940400-48951800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:48942800-48952000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr10:48947200-48948800	Weak transcription	Fetal Stomach	stomach
6	chr10:48947400-48951800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:48947600-48951600	Weak transcription	K562	blood
8	chr10:48948800-48949400	Strong transcription	Fetal Stomach	stomach
9	chr10:48949200-48951600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr10:48949200-48951600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:48949400-48952200	Weak transcription	Fetal Stomach	stomach
12	chr10:48951400-48952200	Active TSS	Hela-S3	cervix
13	chr10:48951600-48952400	Active TSS	K562	blood
14	chr10:48951600-48952600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr10:48951600-48952600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr10:48951600-48952600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:48951600-48952600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:48951800-48952200	Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr10:48951800-48952200	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr10:48951800-48952200	Active TSS	HUVEC	blood vessel
21	chr10:48951800-48952400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:48951800-48952400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr10:48951800-48952400	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr10:48951800-48952400	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr10:48951800-48952400	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr10:48951800-48952400	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr10:48951800-48952400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:48951800-48952400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr10:48951800-48952400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr10:48951800-48952400	Active TSS	Fetal Brain Female	brain
31	chr10:48951800-48952400	Active TSS	Psoas Muscle	Psoas
32	chr10:48951800-48952400	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr10:48951800-48952600	Active TSS	H9 Cell Line	embryonic stem cell
34	chr10:48951800-48952600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:48951800-48952600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr10:48951800-48952600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr10:48951800-48952600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr10:48951800-48952600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr10:48951800-48952600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
40	chr10:48951800-48952600	Active TSS	Right Ventricle	heart
41	chr10:48951800-48952600	Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr10:48951800-48952600	Active TSS	Dnd41	blood
43	chr10:48951800-48952600	Active TSS	HMEC	breast
44	chr10:48952000-48952400	Active TSS	Adipose Nuclei	Adipose
45	chr10:48952000-48952400	Active TSS	Rectal Smooth Muscle	rectum
46	chr10:48952000-48952400	Active TSS	Stomach Smooth Muscle	stomach
47	chr10:48952000-48952600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr10:48952000-48952600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:48952000-48952600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr10:48952000-48952600	Active TSS	Fetal Muscle Trunk	muscle

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