Variant report

Variant	nsv971859
Chromosome Location	chr10:28070066-28271252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:28072636-28072933	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr10:28198307-28198666	HCT-116	colon:	n/a	n/a
3	CBX3	chr10:28182087-28183106	HCT-116	colon:	n/a	n/a
4	CBX3	chr10:28154005-28154773	HCT-116	colon:	n/a	n/a
5	CBX3	chr10:28182088-28183104	HCT-116	colon:	n/a	n/a
6	CEBPB	chr10:28234176-28234297	H1-hESC	embryonic stem cell:	n/a	chr10:28234235-28234246 chr10:28234233-28234244 chr10:28234233-28234246 chr10:28234230-28234247
7	CEBPB	chr10:28072688-28072929	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:28183488-28183587	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr10:28121512-28121801	HepG2	liver:	n/a	chr10:28121636-28121647 chr10:28121636-28121649
10	CEBPB	chr10:28121500-28121774	IMR90	lung:	n/a	chr10:28121636-28121647 chr10:28121636-28121649
11	CEBPB	chr10:28182317-28182706	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:28234080-28234349	HepG2	liver:	n/a	chr10:28234235-28234246 chr10:28234233-28234244 chr10:28234233-28234246 chr10:28234230-28234247
13	CEBPB	chr10:28214250-28214383	A549	lung:	n/a	chr10:28214342-28214353
14	CEBPB	chr10:28121482-28121751	A549	lung:	n/a	chr10:28121636-28121647 chr10:28121636-28121649
15	CEBPB	chr10:28108564-28108729	K562	blood:	n/a	chr10:28108646-28108657
16	CEBPB	chr10:28234068-28234385	IMR90	lung:	n/a	chr10:28234235-28234246 chr10:28234233-28234244 chr10:28234233-28234246 chr10:28234230-28234247
17	CEBPB	chr10:28200640-28200961	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr10:28234177-28234390	K562	blood:	n/a	chr10:28234235-28234246 chr10:28234233-28234244 chr10:28234233-28234246 chr10:28234230-28234247
19	CEBPB	chr10:28199600-28199739	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr10:28119349-28119577	A549	lung:	n/a	n/a
21	CEBPB	chr10:28176894-28177177	A549	lung:	n/a	chr10:28177025-28177036
22	CEBPB	chr10:28268242-28268579	IMR90	lung:	n/a	n/a
23	CEBPB	chr10:28176989-28177088	H1-hESC	embryonic stem cell:	n/a	chr10:28177025-28177036
24	CEBPB	chr10:28109183-28109490	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr10:28222006-28222180	K562	blood:	n/a	chr10:28222129-28222140
26	CEBPB	chr10:28182072-28183091	HCT-116	colon:	n/a	chr10:28182273-28182286
27	CEBPB	chr10:28108641-28108667	HepG2	liver:	n/a	chr10:28108646-28108657
28	CEBPB	chr10:28221987-28222254	IMR90	lung:	n/a	chr10:28222129-28222140
29	CEBPB	chr10:28176893-28177191	HepG2	liver:	n/a	chr10:28177025-28177036
30	CEBPB	chr10:28176854-28177197	IMR90	lung:	n/a	chr10:28177025-28177036
31	CEBPB	chr10:28238458-28239003	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:28196399-28196599	Hela-S3	cervix:	n/a	chr10:28196462-28196473 chr10:28196463-28196472
33	CEBPB	chr10:28249586-28249739	IMR90	lung:	n/a	chr10:28249710-28249722
34	CEBPB	chr10:28234103-28234376	MCF-7	breast:	n/a	chr10:28234235-28234246 chr10:28234233-28234244 chr10:28234233-28234246 chr10:28234230-28234247
35	CEBPB	chr10:28268321-28268469	A549	lung:	n/a	n/a
36	CEBPB	chr10:28268307-28268510	MCF-7	breast:	n/a	n/a
37	CEBPB	chr10:28196308-28196605	HepG2	liver:	n/a	chr10:28196462-28196473 chr10:28196463-28196472
38	CEBPB	chr10:28268317-28268501	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr10:28221996-28222240	Hela-S3	cervix:	n/a	chr10:28222129-28222140
40	CEBPB	chr10:28250905-28251026	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:28214190-28214488	HepG2	liver:	n/a	chr10:28214342-28214353
42	CEBPB	chr10:28222086-28222223	H1-hESC	embryonic stem cell:	n/a	chr10:28222129-28222140
43	CEBPB	chr10:28268281-28268530	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:28182121-28183068	HCT-116	colon:	n/a	chr10:28182273-28182286
45	CEBPB	chr10:28108553-28108768	IMR90	lung:	n/a	chr10:28108646-28108657
46	CEBPB	chr10:28221971-28222300	HepG2	liver:	n/a	chr10:28222129-28222140
47	CEBPB	chr10:28196422-28196551	K562	blood:	n/a	chr10:28196462-28196473 chr10:28196463-28196472
48	CEBPB	chr10:28125984-28125995	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:28221989-28222237	A549	lung:	n/a	chr10:28222129-28222140
50	CEBPB	chr10:28196351-28196607	IMR90	lung:	n/a	chr10:28196462-28196473 chr10:28196463-28196472

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:28233188-28233238	ovcar-3	ovarian:	n/a
2	chr10:28238789-28238839	ovcar-3	ovarian:	n/a
3	chr10:28233188-28233238	ovcar-3	ovarian:	n/a
4	chr10:28238789-28238839	ovcar-3	ovarian:	n/a
5	chr10:28238789-28238839	U87	brain:	n/a
6	chr10:28200623-28200673	AG10803	skin:	n/a
7	chr10:28233188-28233238	HL-60	blood:	n/a
8	chr10:28101242-28101292	HCF	heart:	n/a
9	chr10:28233109-28233159	HIPEpiC	eye:	n/a
10	chr10:28101242-28101292	HepG2	liver:	n/a
11	chr10:28233109-28233159	T-47D	breast:	n/a
12	chr10:28233140-28233190	NHDF-neo	bronchial:	n/a
13	chr10:28200623-28200673	HIPEpiC	eye:	n/a
14	chr10:28233109-28233159	HRCEpiC	kidney:	n/a
15	chr10:28233109-28233159	AG04450	lung:	fetal
16	chr10:28200623-28200673	H1-hESC	embryonic stem cell:	embryo
17	chr10:28101242-28101292	ECC-1	luminal epithelium:	n/a
18	chr10:28200623-28200673	RPTEC	kidney:	n/a
19	chr10:28233109-28233159	CMK	blood:	n/a
20	chr10:28233140-28233190	SK-N-MC	brain:	n/a
21	chr10:28233188-28233238	HIPEpiC	eye:	n/a
22	chr10:28233188-28233238	AG10803	skin:	n/a
23	chr10:28200623-28200673	SK-N-SH	brain:	n/a
24	chr10:28233188-28233238	GM12891	blood:	n/a
25	chr10:28233140-28233190	NT2-D1	testis:	n/a
26	chr10:28238789-28238839	SK-N-MC	brain:	n/a
27	chr10:28101242-28101292	HMEC	breast:	n/a
28	chr10:28233109-28233159	HEEpiC	esophagus:	n/a
29	chr10:28101242-28101292	SK-N-MC	brain:	n/a
30	chr10:28101242-28101292	PrEC	prostate:	n/a
31	chr10:28101242-28101292	HAEpiC	amniotic membrane:	n/a
32	chr10:28233109-28233159	HCT-116	colon:	n/a
33	chr10:28238789-28238839	HIPEpiC	eye:	n/a
34	chr10:28233188-28233238	HPAEpiC	pulmonary alveolar:	n/a
35	chr10:28238789-28238839	HRPEpiC	eye:	n/a
36	chr10:28101242-28101292	Caco-2	colon:	n/a
37	chr10:28101242-28101292	AG04449	skin:	fetal
38	chr10:28233140-28233190	MCF-7	breast:	n/a
39	chr10:28233188-28233238	Jurkat	blood:	n/a
40	chr10:28238789-28238839	HAEpiC	amniotic membrane:	n/a
41	chr10:28238789-28238839	HRE	kidney:	n/a
42	chr10:28101242-28101292	NHBE	bronchial:	n/a
43	chr10:28238789-28238839	ECC-1	luminal epithelium:	n/a
44	chr10:28200623-28200673	GM06990	blood:	n/a
45	chr10:28238789-28238839	SAEC	small airway:	n/a
46	chr10:28200623-28200673	IMR90	lung:	fetal
47	chr10:28200623-28200673	HMEC	breast:	n/a
48	chr10:28200623-28200673	NH-A	brain:	n/a
49	chr10:28238789-28238839	Hepatocyte	liver:	n/a
50	chr10:28233109-28233159	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:28177944..28180786-chr10:28185411..28187145,2	K562	blood:
2	chr10:28096701..28099351-chr10:28115513..28118158,2	K562	blood:
3	chr10:28166524..28168170-chr10:28169949..28171674,2	K562	blood:
4	chr10:28178111..28179847-chr10:28182667..28184534,2	K562	blood:
5	chr10:28138203..28140544-chr10:28141785..28143922,2	K562	blood:
6	chr10:28194965..28197519-chr10:28200097..28202641,2	MCF-7	breast:
7	chr10:28108136..28110708-chr10:28110807..28112653,2	K562	blood:
8	chr10:28096701..28099351-chr10:28115513..28118158,2	K562	blood:
9	chr10:28138203..28140544-chr10:28141785..28143922,2	K562	blood:
10	chr10:28177944..28180786-chr10:28185411..28187145,2	K562	blood:
11	chr10:28101558..28104290-chr10:28106943..28109516,2	MCF-7	breast:
12	chr10:28153808..28154667-chr10:28468156..28469155,3	MCF-7	breast:
13	chr10:28198019..28200299-chr10:28200413..28203306,2	K562	blood:
14	chr10:28198019..28200299-chr10:28200413..28203306,2	K562	blood:
15	chr10:28194965..28197519-chr10:28200097..28202641,2	MCF-7	breast:
16	chr10:28178111..28179847-chr10:28182667..28184534,2	K562	blood:
17	chr10:28108136..28110708-chr10:28110807..28112653,2	K562	blood:
18	chr10:28222012..28225002-chr17:57922450..57924037,2	MCF-7	breast:
19	chr10:28166524..28168170-chr10:28169949..28171674,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB18-4	chr10:28127445-28130140	NONHSAT011917
2	lnc-RAB18-5	chr10:28193928-28194091	NONHSAT011918
3	lnc-RAB18-5	chr10:28193138-28193278	NONHSAT011918
4	lnc-MKX-1	chr10:28072775-28072982	NONHSAT011914

Variant related genes	Relation type
ARMC4	TF binding region
RPL36AP55	TF binding region
RN7SKP132	TF binding region
ARMC4	CpG island
RPL36AP55	CpG island
RN7SKP132	CpG island
ENSG00000169126	chromatin interactions

Extended variants
information (count: 7367 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:7367 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551026080	chr10:28072203-28072204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569903924	chr10:28072245-28072246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191804118	chr10:28072262-28072263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149610461	chr10:28072277-28072278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571091600	chr10:28072321-28072322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570872320	chr10:28072344-28072345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571248481	chr10:28072358-28072359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553461399	chr10:28072382-28072383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549544160	chr10:28072383-28072384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572011648	chr10:28072396-28072397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34599208	chr10:28072437-28072438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs112712747	chr10:28072454-28072455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539729291	chr10:28072506-28072507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576303073	chr10:28072538-28072539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs539781362	chr10:28072542-28072543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565172275	chr10:28072563-28072564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532274818	chr10:28072634-28072635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368317905	chr10:28072644-28072645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184600762	chr10:28072674-28072675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187952999	chr10:28072675-28072676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530073181	chr10:28072710-28072711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553643419	chr10:28072727-28072728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34569067	chr10:28072740-28072741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548271735	chr10:28072761-28072762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569840814	chr10:28072830-28072831	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs192431653	chr10:28072881-28072882	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs530992178	chr10:28072890-28072891	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs552459920	chr10:28072895-28072896	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs571046420	chr10:28072901-28072902	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs12413349	chr10:28072904-28072905	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs534959311	chr10:28072908-28072909	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs547281826	chr10:28072933-28072934	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs145375303	chr10:28072936-28072937	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs536301042	chr10:28072953-28072954	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs137933222	chr10:28072977-28072978	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs576241253	chr10:28073010-28073011	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs537161152	chr10:28073050-28073051	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558442102	chr10:28073071-28073072	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs554695041	chr10:28073087-28073088	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs576974969	chr10:28073098-28073099	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs553097147	chr10:28073110-28073111	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs573109602	chr10:28073177-28073178	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs573238112	chr10:28073182-28073183	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs73604066	chr10:28073342-28073343	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189479984	chr10:28073441-28073442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs16928283	chr10:28073449-28073450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112421810	chr10:28073469-28073470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs563356570	chr10:28073490-28073491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs565399366	chr10:28073503-28073504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs575888584	chr10:28073542-28073543	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

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
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28072200-28074000	Enhancers	Aorta	Aorta
2	chr10:28072200-28074200	Enhancers	Ovary	ovary
3	chr10:28074000-28080200	Weak transcription	Aorta	Aorta
4	chr10:28074200-28074800	Weak transcription	Ovary	ovary
5	chr10:28074800-28075000	Enhancers	Ovary	ovary
6	chr10:28077400-28078000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr10:28077600-28078200	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr10:28077600-28078400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr10:28077800-28078200	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr10:28080200-28080600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr10:28080200-28080600	Enhancers	Aorta	Aorta
12	chr10:28080400-28080600	Enhancers	Esophagus	oesophagus
13	chr10:28081800-28096600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:28088000-28088200	Enhancers	Ovary	ovary
15	chr10:28088200-28092800	Weak transcription	Ovary	ovary
16	chr10:28089000-28089400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr10:28089600-28090800	Enhancers	Placenta Amnion	Placenta Amnion
18	chr10:28090000-28090800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr10:28090000-28091000	Enhancers	HMEC	breast
20	chr10:28090200-28090600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr10:28090200-28090600	Enhancers	Esophagus	oesophagus
22	chr10:28090200-28090800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:28090200-28090800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr10:28090200-28090800	Enhancers	NHEK	skin
25	chr10:28090800-28092400	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr10:28092400-28094000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr10:28092800-28094600	Enhancers	Ovary	ovary
28	chr10:28093400-28094000	Enhancers	Stomach Smooth Muscle	stomach
29	chr10:28094000-28094600	Enhancers	Colon Smooth Muscle	Colon
30	chr10:28094000-28094600	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr10:28094400-28094600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr10:28094400-28094600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr10:28094600-28094800	Enhancers	Stomach Smooth Muscle	stomach
34	chr10:28094600-28099400	Weak transcription	Ovary	ovary
35	chr10:28099200-28100200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr10:28099400-28099600	Enhancers	Ovary	ovary
37	chr10:28099600-28100000	Weak transcription	Ovary	ovary
38	chr10:28099800-28100200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr10:28100000-28101000	Active TSS	Ovary	ovary
40	chr10:28100200-28104000	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr10:28101000-28108000	Weak transcription	Ovary	ovary
42	chr10:28103600-28103800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:28103600-28104600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr10:28103600-28105600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr10:28103800-28104400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:28104000-28105400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr10:28104400-28105400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr10:28104400-28105600	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr10:28105600-28127600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr10:28108000-28109400	Enhancers	Ovary	ovary

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