Variant report

Variant	nsv831815
Chromosome Location	chr10:28235661-28407533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:1159)
Chromatin interactive
region (count:29)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:28394597-28394764	HepG2	liver:	n/a	n/a
2	ATF1	chr10:28376983-28377135	K562	blood:	n/a	n/a
3	ATF3	chr10:28366569-28367286	HCT-116	colon:	n/a	n/a
4	ATF3	chr10:28366621-28367459	HCT-116	colon:	n/a	n/a
5	ATF3	chr10:28376858-28377229	K562	blood:	n/a	n/a
6	BACH1	chr10:28287456-28288113	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr10:28303649-28303856	GM12878	blood:	n/a	n/a
8	BHLHE40	chr10:28292280-28292417	HepG2	liver:	n/a	n/a
9	BRCA1	chr10:28360041-28360159	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr10:28343044-28344269	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr10:28287365-28287591	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr10:28394414-28395110	HCT-116	colon:	n/a	n/a
13	CBX3	chr10:28343062-28344178	HCT-116	colon:	n/a	n/a
14	CBX3	chr10:28366620-28367434	HCT-116	colon:	n/a	n/a
15	CBX3	chr10:28352410-28352924	HCT-116	colon:	n/a	n/a
16	CBX3	chr10:28366538-28367501	HCT-116	colon:	n/a	n/a
17	CBX3	chr10:28400571-28401319	HCT-116	colon:	n/a	n/a
18	CEBPB	chr10:28366677-28367223	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:28343032-28344369	HCT-116	colon:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
20	CEBPB	chr10:28376875-28377187	K562	blood:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
21	CEBPB	chr10:28378480-28379045	IMR90	lung:	n/a	n/a
22	CEBPB	chr10:28249586-28249739	IMR90	lung:	n/a	chr10:28249710-28249722
23	CEBPB	chr10:28310152-28310467	A549	lung:	n/a	chr10:28310438-28310455 chr10:28310181-28310192 chr10:28310441-28310454
24	CEBPB	chr10:28343960-28344312	A549	lung:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
25	CEBPB	chr10:28299790-28300010	H1-hESC	embryonic stem cell:	n/a	chr10:28299923-28299934
26	CEBPB	chr10:28299743-28300105	HepG2	liver:	n/a	chr10:28299923-28299934
27	CEBPB	chr10:28342807-28344444	Hela-S3	cervix:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
28	CEBPB	chr10:28376880-28377203	A549	lung:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
29	CEBPB	chr10:28376940-28377165	K562	blood:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
30	CEBPB	chr10:28407470-28409997	HCT-116	colon:	n/a	chr10:28409196-28409207 chr10:28409505-28409518
31	CEBPB	chr10:28376790-28377170	A549	lung:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
32	CEBPB	chr10:28376542-28377444	HCT-116	colon:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
33	CEBPB	chr10:28284642-28284723	Hela-S3	cervix:	n/a	chr10:28284683-28284696
34	CEBPB	chr10:28366639-28367132	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr10:28310072-28310585	HepG2	liver:	n/a	chr10:28310438-28310455 chr10:28310181-28310192 chr10:28310441-28310454
36	CEBPB	chr10:28310413-28310448	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr10:28299801-28300098	K562	blood:	n/a	chr10:28299923-28299934
38	CEBPB	chr10:28340148-28340426	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:28376821-28377275	IMR90	lung:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
40	CEBPB	chr10:28363346-28363611	IMR90	lung:	n/a	n/a
41	CEBPB	chr10:28342807-28344334	IMR90	lung:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
42	CEBPB	chr10:28344016-28344256	K562	blood:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
43	CEBPB	chr10:28340170-28340438	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:28342918-28344491	HCT-116	colon:	n/a	chr10:28344148-28344161 chr10:28344148-28344159
45	CEBPB	chr10:28376820-28377266	Hela-S3	cervix:	n/a	chr10:28377028-28377039 chr10:28377028-28377041 chr10:28377030-28377041
46	CEBPB	chr10:28310369-28310561	IMR90	lung:	n/a	chr10:28310438-28310455 chr10:28310441-28310454
47	CEBPB	chr10:28336963-28337123	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:28366502-28367436	HCT-116	colon:	n/a	n/a
49	CEBPB	chr10:28400656-28400933	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr10:28290421-28290475	K562	blood:	n/a	n/a

(count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:28287707-28287757	NHDF-neo	bronchial:	n/a
2	chr10:28288024-28288074	NHBE	bronchial:	n/a
3	chr10:28285416-28285466	AoSMC	blood vessel:	n/a
4	chr10:28287983-28288033	HRPEpiC	eye:	n/a
5	chr10:28287388-28287438	IMR90	lung:	fetal
6	chr10:28285416-28285466	U87	brain:	n/a
7	chr10:28342666-28342716	AG10803	skin:	n/a
8	chr10:28342666-28342716	ProgFib	skin:	n/a
9	chr10:28288192-28288242	HIPEpiC	eye:	n/a
10	chr10:28287983-28288033	U87	brain:	n/a
11	chr10:28287999-28288049	CMK	blood:	n/a
12	chr10:28287999-28288049	SAEC	small airway:	n/a
13	chr10:28287999-28288049	ProgFib	skin:	n/a
14	chr10:28287983-28288033	ovcar-3	ovarian:	n/a
15	chr10:28288669-28288719	Jurkat	blood:	n/a
16	chr10:28288669-28288719	LNCaP	prostate:	n/a
17	chr10:28288005-28288055	SK-N-SH_RA	brain:	n/a
18	chr10:28289379-28289429	HAEpiC	amniotic membrane:	n/a
19	chr10:28288192-28288242	HCT-116	colon:	n/a
20	chr10:28287879-28287929	GM12892	blood:	n/a
21	chr10:28287543-28287593	MCF10A-Er-Src	breast:	n/a
22	chr10:28288003-28288053	NH-A	brain:	n/a
23	chr10:28288024-28288074	MCF-7	breast:	n/a
24	chr10:28288669-28288719	ECC-1	luminal epithelium:	n/a
25	chr10:28288003-28288053	Hela-S3	cervix:	n/a
26	chr10:28287707-28287757	HCM	heart:	n/a
27	chr10:28288005-28288055	AG09309	skin:	n/a
28	chr10:28287999-28288049	A549	lung:	n/a
29	chr10:28289379-28289429	SK-N-SH_RA	brain:	n/a
30	chr10:28288115-28288165	Jurkat	blood:	n/a
31	chr10:28238789-28238839	NHBE	bronchial:	n/a
32	chr10:28287388-28287438	Caco-2	colon:	n/a
33	chr10:28342666-28342716	MCF-7	breast:	n/a
34	chr10:28288115-28288165	AoSMC	blood vessel:	n/a
35	chr10:28287983-28288033	SK-N-SH	brain:	n/a
36	chr10:28287707-28287757	AG09309	skin:	n/a
37	chr10:28287983-28288033	HIPEpiC	eye:	n/a
38	chr10:28288115-28288165	GM12878	blood:	n/a
39	chr10:28287543-28287593	HUVEC	blood vessel:	n/a
40	chr10:28285416-28285466	AG09309	skin:	n/a
41	chr10:28287983-28288033	HUVEC	blood vessel:	n/a
42	chr10:28287879-28287929	BJ	skin:	n/a
43	chr10:28288115-28288165	Hepatocyte	liver:	n/a
44	chr10:28291599-28291649	HCM	heart:	n/a
45	chr10:28342666-28342716	SK-N-MC	brain:	n/a
46	chr10:28288005-28288055	GM19239	blood:	n/a
47	chr10:28238789-28238839	HRE	kidney:	n/a
48	chr10:28288003-28288053	SK-N-SH_RA	brain:	n/a
49	chr10:28288192-28288242	AG09319	gingival:	n/a
50	chr10:28288115-28288165	HUVEC	blood vessel:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:28317069..28320040-chr10:28334616..28337378,2	MCF-7	breast:
2	chr10:28289668..28291874-chr10:28295671..28297553,2	K562	blood:
3	chr10:28384110..28385653-chr10:28390069..28392151,2	MCF-7	breast:
4	chr10:28397069..28398753-chr10:28400190..28402343,2	K562	blood:
5	chr10:28397069..28398753-chr10:28400190..28402343,2	K562	blood:
6	chr10:28362265..28365237-chr10:28365253..28367161,2	K562	blood:
7	chr10:28280780..28284678-chr10:28290006..28293445,3	MCF-7	breast:
8	chr10:28329005..28330814-chr10:28337139..28340091,2	K562	blood:
9	chr10:28288287..28290743-chr10:28297361..28299658,2	K562	blood:
10	chr10:28364402..28367665-chr10:28377622..28380231,3	MCF-7	breast:
11	chr10:28332388..28334708-chr10:28335974..28338490,2	K562	blood:
12	chr10:28372312..28376657-chr10:28391120..28396968,5	K562	blood:
13	chr10:28364402..28367665-chr10:28377622..28380231,3	MCF-7	breast:
14	chr10:28308451..28310712-chr10:28313933..28317202,3	MCF-7	breast:
15	chr10:28308451..28310712-chr10:28313933..28317202,3	MCF-7	breast:
16	chr10:28290909..28293718-chr10:28295058..28297556,2	K562	blood:
17	chr10:28387058..28389693-chr6:27776467..27779114,2	MCF-7	breast:
18	chr10:28372312..28376657-chr10:28391120..28396968,5	K562	blood:
19	chr10:28384110..28385653-chr10:28390069..28392151,2	MCF-7	breast:
20	chr10:28310448..28312369-chr10:28329135..28331454,2	K562	blood:
21	chr10:28329005..28330814-chr10:28337139..28340091,2	K562	blood:
22	chr10:27551467..27554348-chr10:28282862..28284378,2	K562	blood:
23	chr10:28362265..28365237-chr10:28365253..28367161,2	K562	blood:
24	chr10:28317069..28320040-chr10:28334616..28337378,2	MCF-7	breast:
25	chr10:28310448..28312369-chr10:28329135..28331454,2	K562	blood:
26	chr10:28280780..28284678-chr10:28290006..28293445,3	MCF-7	breast:
27	chr10:28406473..28409563-chr10:28410652..28413187,3	MCF-7	breast:
28	chr10:28289668..28291874-chr10:28295671..28297553,2	K562	blood:
29	chr10:28332388..28334708-chr10:28335974..28338490,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB18-2	chr10:28338321-28338544	ENSG00000233472.1
2	lnc-RAB18-2	chr10:28311360-28311460	ENSG00000233472.1
3	lnc-RAB18-7	chr10:28293631-28293861	NONHSAT011921
4	lnc-RAB18-6	chr10:28283997-28284120	NONHSAT011919
5	lnc-RAB18-6	chr10:28272081-28272210	NONHSAT011919
6	lnc-RAB18-2	chr10:28332853-28332885	ENSG00000233472.1
7	lnc-RAB18-2	chr10:28288717-28288827	ENSG00000233472.1
8	lnc-RAB18-6	chr10:28283238-28283321	NONHSAT011919

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MPP7	hsa-miR-32-5p	chr10:28342051-28342072

Variant related genes	Relation type
ENSG00000233472	TF binding region
ENSG00000226395	TF binding region
ARMC4	TF binding region
ENSG00000233472	CpG island
ENSG00000226395	CpG island
ARMC4	CpG island
ENSG00000203813	chromatin interactions
ENSG00000238021	chromatin interactions
ENSG00000226395	chromatin interactions
ENSG00000233472	chromatin interactions

Extended variants
information (count: 5610 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:5610 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553630647	chr10:28235672-28235673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs1931889	chr10:28235673-28235674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs149616301	chr10:28235711-28235712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144318239	chr10:28235743-28235744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61842727	chr10:28235752-28235753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs563663185	chr10:28235753-28235754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565367943	chr10:28235836-28235837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532739259	chr10:28235847-28235848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187197740	chr10:28235849-28235850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560061882	chr10:28235872-28235873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs368091306	chr10:28235876-28235877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527287345	chr10:28235879-28235880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532424742	chr10:28235951-28235952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79853268	chr10:28235955-28235956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77728719	chr10:28235976-28235977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544916316	chr10:28235990-28235991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs143495131	chr10:28236004-28236005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192287760	chr10:28236060-28236061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376192907	chr10:28236066-28236067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372389546	chr10:28236081-28236082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547308466	chr10:28236110-28236111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569327654	chr10:28236117-28236118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77007927	chr10:28236188-28236189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7094709	chr10:28236190-28236191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs554714686	chr10:28236210-28236211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369574339	chr10:28236268-28236269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541472505	chr10:28236345-28236346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181722569	chr10:28236353-28236354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561218493	chr10:28236367-28236368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537184643	chr10:28236368-28236369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558976728	chr10:28236375-28236376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577536611	chr10:28236406-28236407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574925379	chr10:28236446-28236447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538266717	chr10:28236473-28236474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376820055	chr10:28236475-28236476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186026620	chr10:28236525-28236526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560099198	chr10:28236649-28236650	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs575247800	chr10:28236720-28236721	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs190344770	chr10:28236748-28236749	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs182744669	chr10:28236780-28236781	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs147147096	chr10:28236782-28236783	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs531319315	chr10:28236787-28236788	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs188124014	chr10:28236791-28236792	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs532176595	chr10:28236800-28236801	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs369786019	chr10:28236806-28236807	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs142240280	chr10:28236820-28236821	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs9299594	chr10:28236846-28236847	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548451134	chr10:28236852-28236853	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs563707304	chr10:28236859-28236860	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs376459541	chr10:28236862-28236863	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Autism	21439084	CNVD
Maculopathy	20981449	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	22341455	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22048815	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28223800-28238400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:28224200-28253000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr10:28226800-28237400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr10:28236400-28236600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:28236600-28236800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:28236600-28236800	Bivalent Enhancer	HSMMtube	muscle
7	chr10:28236600-28237400	Bivalent Enhancer	Osteobl	bone
8	chr10:28236600-28237600	Enhancers	Adipose Nuclei	Adipose
9	chr10:28236600-28237800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:28236600-28238600	Enhancers	Fetal Lung	lung
11	chr10:28236600-28239200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr10:28236800-28238200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:28237000-28237200	Enhancers	Fetal Stomach	stomach
14	chr10:28237200-28238400	Weak transcription	Fetal Stomach	stomach
15	chr10:28237200-28238600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:28237400-28239200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr10:28238000-28239200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr10:28238000-28239200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr10:28238200-28239000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:28238200-28239200	Enhancers	Fetal Muscle Leg	muscle
21	chr10:28238200-28239800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr10:28238400-28238800	Enhancers	Fetal Muscle Trunk	muscle
23	chr10:28238400-28239000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr10:28238400-28239000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr10:28238400-28239000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr10:28238400-28239000	Enhancers	Fetal Stomach	stomach
27	chr10:28238400-28239800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:28238800-28239200	Enhancers	H1 Cell Line	embryonic stem cell
29	chr10:28238800-28239200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr10:28239000-28239200	Enhancers	Ovary	ovary
31	chr10:28239200-28243200	Weak transcription	Ovary	ovary
32	chr10:28239800-28287200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr10:28243200-28243400	Active TSS	Ovary	ovary
34	chr10:28243200-28243600	Enhancers	Osteobl	bone
35	chr10:28247000-28247200	Enhancers	Primary B cells from cord blood	blood
36	chr10:28247000-28247200	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr10:28247000-28247200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr10:28247000-28247400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr10:28247000-28247400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr10:28247000-28248000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr10:28247000-28248600	Enhancers	Dnd41	blood
42	chr10:28247200-28247400	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr10:28247200-28247400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:28247200-28247400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr10:28247200-28247600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr10:28247200-28247800	Active TSS	Primary B cells from cord blood	blood
47	chr10:28247200-28247800	Active TSS	Primary T helper cells fromperipheralblood	blood
48	chr10:28247200-28247800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr10:28247200-28247800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr10:28247200-28248000	Active TSS	Primary T cells fromperipheralblood	blood

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