Variant report

Variant	esv1813526
Chromosome Location	chr10:94446041-94449749
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:466)
CpG islands
(count:307)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:466 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:94449623-94449834	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:94449642-94449923	K562	blood:	n/a	n/a
3	ARID3A	chr10:94448575-94448749	K562	blood:	n/a	n/a
4	BHLHE40	chr10:94449745-94450830	K562	blood:	n/a	chr10:94450146-94450162
5	BHLHE40	chr10:94449290-94449318	K562	blood:	n/a	n/a
6	BHLHE40	chr10:94448577-94448982	K562	blood:	n/a	n/a
7	BHLHE40	chr10:94448540-94450445	HepG2	liver:	n/a	chr10:94449270-94449286 chr10:94450146-94450162 chr10:94449642-94449658
8	CBX3	chr10:94448327-94449135	K562	blood:	n/a	n/a
9	CCNT2	chr10:94448631-94451909	K562	blood:	n/a	chr10:94449521-94449530 chr10:94451255-94451264
10	CEBPB	chr10:94448390-94448651	K562	blood:	n/a	n/a
11	CEBPB	chr10:94445970-94446248	K562	blood:	n/a	chr10:94446100-94446111
12	CEBPB	chr10:94445969-94446189	HepG2	liver:	n/a	chr10:94446100-94446111
13	CEBPB	chr10:94448399-94448626	HepG2	liver:	n/a	n/a
14	CEBPD	chr10:94449168-94449517	HepG2	liver:	n/a	n/a
15	CEBPD	chr10:94449571-94450015	HepG2	liver:	n/a	n/a
16	CEBPD	chr10:94449523-94449905	HepG2	liver:	n/a	n/a
17	CHD2	chr10:94449342-94449343	K562	blood:	n/a	n/a
18	CHD2	chr10:94448750-94448936	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr10:94449248-94450546	Hela-S3	cervix:	n/a	chr10:94449522-94449532 chr10:94449385-94449395
20	CREB1	chr10:94449053-94450362	A549	lung:	n/a	n/a
21	CTBP2	chr10:94449746-94452477	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr10:94448629-94449382	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr10:94448600-94448750	HCFaa	heart:	n/a	n/a
24	CTCF	chr10:94448620-94448770	GM12871	blood:	n/a	n/a
25	CTCF	chr10:94448660-94448810	AG04450	lung:	n/a	n/a
26	CTCF	chr10:94448631-94448802	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr10:94448700-94448950	HAc	cerebellar:	n/a	n/a
28	CTCF	chr10:94448937-94448950	A549	lung:	n/a	n/a
29	CTCF	chr10:94449600-94449750	GM12874	blood:	n/a	n/a
30	CTCF	chr10:94448639-94448813	ProgFib	skin:	n/a	n/a
31	CTCF	chr10:94448640-94448790	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr10:94448700-94448850	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr10:94448740-94448890	NB4	blood:	n/a	n/a
34	CTCF	chr10:94448820-94448970	HMF	breast:	n/a	n/a
35	CTCF	chr10:94448700-94448850	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:94448880-94449030	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr10:94448620-94448770	HVMF	connective:	n/a	n/a
38	CTCF	chr10:94448674-94448682	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr10:94448608-94448975	HepG2	liver:	n/a	n/a
40	CTCF	chr10:94448680-94448830	HFF	foreskin:	n/a	n/a
41	CTCF	chr10:94448680-94448830	GM12874	blood:	n/a	n/a
42	CTCF	chr10:94448700-94448850	SAEC	small airway:	n/a	n/a
43	CTCF	chr10:94449469-94449489	GM12878	blood:	n/a	n/a
44	CTCF	chr10:94448780-94448930	GM12873	blood:	n/a	n/a
45	CTCF	chr10:94448677-94448684	GM10266	blood:	n/a	n/a
46	CTCF	chr10:94448860-94449010	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr10:94448640-94448790	GM12864	blood:	n/a	n/a
48	CTCF	chr10:94448640-94448790	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr10:94448841-94448947	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr10:94448863-94448879	Medullo	brain:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:94449250-94449300	BE2_C	brain:	n/a
2	chr10:94449567-94449617	SAEC	small airway:	n/a
3	chr10:94449250-94449300	BE2_C	brain:	n/a
4	chr10:94449567-94449617	SAEC	small airway:	n/a
5	chr10:94448532-94448582	GM12891	blood:	n/a
6	chr10:94448702-94448752	ovcar-3	ovarian:	n/a
7	chr10:94448702-94448752	LNCaP	prostate:	n/a
8	chr10:94449567-94449617	HRE	kidney:	n/a
9	chr10:94448532-94448582	U87	brain:	n/a
10	chr10:94449250-94449300	AG10803	skin:	n/a
11	chr10:94449250-94449300	AG09309	skin:	n/a
12	chr10:94448728-94448778	SKMC	muscle:	n/a
13	chr10:94448728-94448778	U87	brain:	n/a
14	chr10:94448532-94448582	MCF10A-Er-Src	breast:	n/a
15	chr10:94449567-94449617	BE2_C	brain:	n/a
16	chr10:94448702-94448752	H1-hESC	embryonic stem cell:	embryo
17	chr10:94448728-94448778	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:94449250-94449300	NHDF-neo	bronchial:	n/a
19	chr10:94448532-94448582	T-47D	breast:	n/a
20	chr10:94448728-94448778	PrEC	prostate:	n/a
21	chr10:94449250-94449300	HPAEpiC	pulmonary alveolar:	n/a
22	chr10:94448702-94448752	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:94449250-94449300	AG04450	lung:	fetal
24	chr10:94448702-94448752	BE2_C	brain:	n/a
25	chr10:94448728-94448778	GM12892	blood:	n/a
26	chr10:94449567-94449617	PFSK-1	brain:	n/a
27	chr10:94448728-94448778	BJ	skin:	n/a
28	chr10:94448702-94448752	HCM	heart:	n/a
29	chr10:94448728-94448778	HNPCEpiC	eye:	n/a
30	chr10:94449567-94449617	LNCaP	prostate:	n/a
31	chr10:94448702-94448752	AG09309	skin:	n/a
32	chr10:94448702-94448752	MCF-7	breast:	n/a
33	chr10:94448702-94448752	Jurkat	blood:	n/a
34	chr10:94448728-94448778	AG10803	skin:	n/a
35	chr10:94449567-94449617	NT2-D1	testis:	n/a
36	chr10:94448702-94448752	HCPEpiC	choroid plexus:	n/a
37	chr10:94449567-94449617	PrEC	prostate:	n/a
38	chr10:94449567-94449617	A549	lung:	n/a
39	chr10:94448702-94448752	T-47D	breast:	n/a
40	chr10:94448532-94448582	SK-N-SH_RA	brain:	n/a
41	chr10:94449250-94449300	BJ	skin:	n/a
42	chr10:94449250-94449300	SAEC	small airway:	n/a
43	chr10:94448532-94448582	NHBE	bronchial:	n/a
44	chr10:94448532-94448582	Jurkat	blood:	n/a
45	chr10:94448702-94448752	SK-N-MC	brain:	n/a
46	chr10:94448532-94448582	LNCaP	prostate:	n/a
47	chr10:94448532-94448582	IMR90	lung:	fetal
48	chr10:94448532-94448582	RPTEC	kidney:	n/a
49	chr10:94448702-94448752	HMEC	breast:	n/a
50	chr10:94449250-94449300	AG09319	gingival:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94349533..94354628-chr10:94448059..94453493,12	K562	blood:
2	chr10:94449475..94450112-chr19:14529907..14530785,2	Hela-S3	cervix:
3	chr10:94449603..94452740-chr10:94589464..94592452,3	K562	blood:
4	chr10:94449237..94450232-chr6:27805942..27806496,2	NB4	blood:
5	chr10:94449314..94450224-chr16:30388710..30389229,2	NB4	blood:
6	chr10:94449678..94450357-chr11:62359130..62359860,2	Hela-S3	cervix:
7	chr10:94449635..94450319-chr15:59396946..59397778,2	NB4	blood:
8	chr10:94448193..94452899-chr10:94604769..94609293,6	K562	blood:
9	chr10:94333616..94336720-chr10:94448718..94451044,3	K562	blood:
10	chr10:94349533..94356622-chr10:94447410..94453498,11	K562	blood:
11	chr10:94332371..94335153-chr10:94446165..94448467,2	K562	blood:

No data

Variant related genes	Relation type
HHEX	TF binding region
HHEX	CpG island
ENSG00000138160	chromatin interactions
ENSG00000123136	chromatin interactions
ENSG00000233822	chromatin interactions
ENSG00000138190	chromatin interactions
ENSG00000119912	chromatin interactions
ENSG00000149016	chromatin interactions
ENSG00000184348	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000180209	chromatin interactions

Extended variants
information (count: 150 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:150 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2488087	chr10:94446041-94446042	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77880651	chr10:94446083-94446084	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs61861455	chr10:94446085-94446086	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs192250866	chr10:94446112-94446113	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs12262390	chr10:94446123-94446124	ZNF genes & repeats Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183894112	chr10:94446168-94446169	ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573624002	chr10:94446227-94446228	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs78090142	chr10:94446241-94446242	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs144862493	chr10:94446262-94446263	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576115933	chr10:94446295-94446296	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs138771989	chr10:94446323-94446324	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs188663158	chr10:94446328-94446329	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181309101	chr10:94446344-94446345	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs184360015	chr10:94446346-94446347	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs375828365	chr10:94446380-94446381	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539885380	chr10:94446399-94446400	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs560864996	chr10:94446430-94446431	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs370912284	chr10:94446444-94446445	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs141496830	chr10:94446455-94446456	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543719151	chr10:94446464-94446465	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530946471	chr10:94446468-94446469	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs563912426	chr10:94446469-94446470	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs532572679	chr10:94446565-94446566	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs10786052	chr10:94446635-94446636	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs117306673	chr10:94446642-94446643	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528540686	chr10:94446688-94446689	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs190078465	chr10:94446757-94446758	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs568102382	chr10:94446768-94446769	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs117176247	chr10:94446778-94446779	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs556137400	chr10:94446812-94446813	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569853560	chr10:94446848-94446849	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs538421605	chr10:94446856-94446857	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542537113	chr10:94446895-94446896	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs547064048	chr10:94446950-94446951	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs144446092	chr10:94446976-94446977	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182259703	chr10:94447009-94447010	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541118919	chr10:94447049-94447050	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs185406723	chr10:94447086-94447087	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs187742658	chr10:94447096-94447097	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs145636332	chr10:94447100-94447101	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs554616292	chr10:94447102-94447103	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs574308005	chr10:94447106-94447107	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs375738070	chr10:94447131-94447132	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs10531158	chr10:94447143-94447144	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs61861456	chr10:94447155-94447156	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs544120183	chr10:94447216-94447217	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369474448	chr10:94447266-94447267	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566979617	chr10:94447296-94447297	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374201154	chr10:94447371-94447372	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539206641	chr10:94447407-94447408	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Sezary syndrome	18413736	CNVD
Intracranial aneurysm	16715129	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94437600-94447600	Weak transcription	Liver	Liver
2	chr10:94440600-94448600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:94441800-94446200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr10:94441800-94448600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:94442000-94446600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr10:94442800-94448000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:94444200-94446800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
8	chr10:94444400-94448400	Weak transcription	Pancreas	Pancrea
9	chr10:94444600-94446200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
10	chr10:94444600-94448400	Weak transcription	Lung	lung
11	chr10:94446200-94448200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr10:94446200-94448400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr10:94446600-94447600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr10:94446600-94448600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:94446800-94448600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr10:94447400-94447600	Enhancers	K562	blood
17	chr10:94447600-94447800	Flanking Active TSS	K562	blood
18	chr10:94447600-94448200	Enhancers	Liver	Liver
19	chr10:94447600-94448600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr10:94447800-94448000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr10:94447800-94448200	Enhancers	HepG2	liver
22	chr10:94447800-94448400	Transcr. at gene 5' and 3'	K562	blood
23	chr10:94447800-94450600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr10:94448000-94448200	Enhancers	Primary B cells from cord blood	blood
25	chr10:94448000-94448200	Enhancers	A549	lung
26	chr10:94448000-94448600	Enhancers	Primary B cells from peripheral blood	blood
27	chr10:94448000-94449200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
28	chr10:94448000-94449400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr10:94448200-94448400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:94448200-94448400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr10:94448200-94448400	Enhancers	Colon Smooth Muscle	Colon
32	chr10:94448200-94448400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
33	chr10:94448200-94448400	Bivalent/Poised TSS	Fetal Lung	lung
34	chr10:94448200-94448400	Enhancers	Rectal Smooth Muscle	rectum
35	chr10:94448200-94448400	Enhancers	HUVEC	blood vessel
36	chr10:94448200-94448600	Active TSS	Primary hematopoietic stem cells short term culture	blood
37	chr10:94448200-94448600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr10:94448200-94448600	Flanking Active TSS	HepG2	liver
39	chr10:94448200-94448800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
40	chr10:94448200-94448800	Flanking Active TSS	A549	lung
41	chr10:94448200-94449000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr10:94448200-94449000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
43	chr10:94448200-94449000	Flanking Active TSS	Liver	Liver
44	chr10:94448200-94449400	Flanking Active TSS	Primary B cells from cord blood	blood
45	chr10:94448400-94448600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr10:94448400-94448600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
47	chr10:94448400-94448600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
48	chr10:94448400-94448600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:94448400-94448600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
50	chr10:94448400-94448600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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