Variant report

Variant	nsv971917
Chromosome Location	chr10:45547355-45595482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:146)
CpG islands
(count:306)
Chromatin interactive
region (count:6)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:45566602-45566816	K562	blood:	n/a	n/a
2	ATF3	chr10:45566507-45566845	K562	blood:	n/a	n/a
3	CBX3	chr10:45565950-45566252	K562	blood:	n/a	n/a
4	CEBPB	chr10:45559278-45559550	K562	blood:	n/a	chr10:45559447-45559458
5	CEBPB	chr10:45559289-45559602	IMR90	lung:	n/a	chr10:45559447-45559458
6	CEBPB	chr10:45565956-45566252	K562	blood:	n/a	chr10:45566097-45566108
7	CEBPB	chr10:45589668-45589979	HepG2	liver:	n/a	chr10:45589822-45589833
8	CEBPB	chr10:45559285-45559616	HepG2	liver:	n/a	chr10:45559447-45559458
9	CEBPB	chr10:45574104-45574189	HepG2	liver:	n/a	chr10:45574142-45574153
10	CEBPB	chr10:45553313-45553378	A549	lung:	n/a	chr10:45553343-45553354
11	CEBPB	chr10:45589729-45589928	IMR90	lung:	n/a	chr10:45589822-45589833
12	CEBPB	chr10:45561892-45562003	A549	lung:	n/a	n/a
13	CEBPB	chr10:45566008-45566198	HepG2	liver:	n/a	chr10:45566097-45566108
14	CEBPB	chr10:45565991-45566130	A549	lung:	n/a	chr10:45566097-45566108
15	CEBPB	chr10:45565996-45566259	H1-hESC	embryonic stem cell:	n/a	chr10:45566097-45566108
16	CEBPB	chr10:45553255-45553397	HepG2	liver:	n/a	chr10:45553343-45553354
17	CEBPB	chr10:45564057-45564233	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:45559292-45559598	A549	lung:	n/a	chr10:45559447-45559458
19	CTCF	chr10:45575960-45576110	HPAF	blood vessel:	n/a	n/a
20	CTCF	chr10:45576280-45576430	HCFaa	heart:	n/a	n/a
21	CTCF	chr10:45552547-45552552	GM10266	blood:	n/a	n/a
22	CTCF	chr10:45566920-45567150	GM06990	blood:	n/a	n/a
23	CTCF	chr10:45560460-45560610	NB4	blood:	n/a	n/a
24	CTCF	chr10:45558000-45558150	GM12865	blood:	n/a	n/a
25	CTCF	chr10:45575980-45576130	HCT-116	colon:	n/a	n/a
26	CTCF	chr10:45566880-45567030	K562	blood:	n/a	n/a
27	CTCF	chr10:45575940-45576090	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr10:45576040-45576190	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr10:45575940-45576090	HCFaa	heart:	n/a	n/a
30	CTCF	chr10:45575940-45576090	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr10:45575940-45576090	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr10:45576000-45576150	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr10:45568960-45569110	GM12866	blood:	n/a	n/a
34	CTCF	chr10:45567020-45567170	HEK293	kidney:	n/a	n/a
35	E2F4	chr10:45559084-45559602	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F6	chr10:45557639-45557859	K562	blood:	n/a	chr10:45557689-45557698 chr10:45557687-45557696
37	ELF1	chr10:45554176-45554438	K562	blood:	n/a	chr10:45554291-45554304
38	FOS	chr10:45557572-45557805	MCF10A-Er-Src	breast:	n/a	chr10:45557688-45557697
39	FOS	chr10:45549090-45549394	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr10:45557545-45557837	MCF10A-Er-Src	breast:	n/a	chr10:45557688-45557697
41	FOS	chr10:45549085-45549406	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr10:45553979-45554841	HUVEC	blood vessel:	n/a	chr10:45554185-45554196
43	FOS	chr10:45559060-45559555	MCF10A-Er-Src	breast:	n/a	chr10:45559239-45559250 chr10:45559317-45559329
44	FOS	chr10:45554627-45554889	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr10:45566504-45566884	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr10:45549067-45549409	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr10:45559114-45559549	MCF10A-Er-Src	breast:	n/a	chr10:45559239-45559250 chr10:45559317-45559329
48	FOS	chr10:45557340-45557733	MCF10A-Er-Src	breast:	n/a	chr10:45557688-45557697
49	FOS	chr10:45554083-45554375	MCF10A-Er-Src	breast:	n/a	chr10:45554185-45554196
50	FOS	chr10:45554063-45554943	MCF10A-Er-Src	breast:	n/a	chr10:45554185-45554196

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45567261-45567311	HRPEpiC	eye:	n/a
2	chr10:45567261-45567311	HRPEpiC	eye:	n/a
3	chr10:45567160-45567210	IMR90	lung:	fetal
4	chr10:45567160-45567210	H1-hESC	embryonic stem cell:	embryo
5	chr10:45567169-45567219	ProgFib	skin:	n/a
6	chr10:45567160-45567210	SK-N-SH_RA	brain:	n/a
7	chr10:45567169-45567219	GM12878	blood:	n/a
8	chr10:45567697-45567747	HRCEpiC	kidney:	n/a
9	chr10:45567169-45567219	NHBE	bronchial:	n/a
10	chr10:45567169-45567219	AG10803	skin:	n/a
11	chr10:45567169-45567219	AG09319	gingival:	n/a
12	chr10:45567261-45567311	GM12892	blood:	n/a
13	chr10:45567697-45567747	A549	lung:	n/a
14	chr10:45567261-45567311	ProgFib	skin:	n/a
15	chr10:45567169-45567219	Hela-S3	cervix:	n/a
16	chr10:45567169-45567219	HEK293	kidney:	embryo
17	chr10:45567697-45567747	AG09319	gingival:	n/a
18	chr10:45567160-45567210	HCPEpiC	choroid plexus:	n/a
19	chr10:45567169-45567219	ECC-1	luminal epithelium:	n/a
20	chr10:45567697-45567747	HepG2	liver:	n/a
21	chr10:45567160-45567210	HEK293	kidney:	embryo
22	chr10:45567048-45567098	GM06990	blood:	n/a
23	chr10:45567169-45567219	HCPEpiC	choroid plexus:	n/a
24	chr10:45567048-45567098	AG09319	gingival:	n/a
25	chr10:45567261-45567311	SAEC	small airway:	n/a
26	chr10:45567048-45567098	Hela-S3	cervix:	n/a
27	chr10:45567160-45567210	PANC-1	pancreas:	n/a
28	chr10:45567169-45567219	RPTEC	kidney:	n/a
29	chr10:45567169-45567219	Jurkat	blood:	n/a
30	chr10:45567048-45567098	HNPCEpiC	eye:	n/a
31	chr10:45567697-45567747	HIPEpiC	eye:	n/a
32	chr10:45567697-45567747	U87	brain:	n/a
33	chr10:45567261-45567311	LNCaP	prostate:	n/a
34	chr10:45567697-45567747	MCF10A-Er-Src	breast:	n/a
35	chr10:45567697-45567747	PrEC	prostate:	n/a
36	chr10:45567048-45567098	GM12891	blood:	n/a
37	chr10:45567697-45567747	SK-N-MC	brain:	n/a
38	chr10:45567697-45567747	ProgFib	skin:	n/a
39	chr10:45567160-45567210	SK-N-MC	brain:	n/a
40	chr10:45567169-45567219	HPAEpiC	pulmonary alveolar:	n/a
41	chr10:45567697-45567747	Hepatocyte	liver:	n/a
42	chr10:45567160-45567210	GM12892	blood:	n/a
43	chr10:45567160-45567210	AoSMC	blood vessel:	n/a
44	chr10:45567697-45567747	IMR90	lung:	fetal
45	chr10:45567261-45567311	NT2-D1	testis:	n/a
46	chr10:45567169-45567219	AoSMC	blood vessel:	n/a
47	chr10:45567048-45567098	PANC-1	pancreas:	n/a
48	chr10:45567169-45567219	GM12891	blood:	n/a
49	chr10:45567160-45567210	NB4	blood:	n/a
50	chr10:45567697-45567747	HEK293	kidney:	embryo

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:45570815..45572617-chr10:45574192..45576399,2	K562	blood:
2	chr10:45547265..45549115-chr10:45552966..45555091,2	K562	blood:
3	chr10:45551775..45554609-chr10:45555349..45558284,2	K562	blood:
4	chr10:45496059..45498031-chr10:45560561..45563072,2	K562	blood:
5	chr10:45547265..45549115-chr10:45552966..45555091,2	K562	blood:
6	chr10:45551775..45554609-chr10:45555349..45558284,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf25-2	chr10:45561781-45561970	NONHSAT013066
2	lnc-ZNF22-5	chr10:45551104-45551716	NONHSAT013064
3	lnc-C10orf25-2	chr10:45571370-45571666	XLOC_008802
4	lnc-C10orf25-2	chr10:45565926-45566430	NONHSAT013067
5	lnc-C10orf25-2	chr10:45561781-45561970	NONHSAT013067
6	lnc-ZNF22-1	chr10:45586675-45586698	XLOC_008477
7	lnc-C10orf25-2	chr10:45566996-45567042	NONHSAT013069
8	lnc-C10orf25-2	chr10:45561623-45561669	NONHSAT013065
9	lnc-C10orf25-2	chr10:45566996-45567068	NONHSAT013065
10	lnc-C10orf25-2	chr10:45561620-45561669	NONHSAT013067
11	lnc-C10orf25-2	chr10:45561623-45561669	NONHSAT013066
12	lnc-C10orf25-2	chr10:45565926-45566111	NONHSAT013066
13	lnc-C10orf25-2	chr10:45561805-45561970	NONHSAT013068
14	lnc-C10orf25-2	chr10:45594933-45595947	NONHSAT013077
15	lnc-C10orf25-2	chr10:45560975-45561061	NONHSAT013062
16	lnc-C10orf25-2	chr10:45561805-45561970	NONHSAT013069
17	lnc-C10orf25-2	chr10:45567013-45567049	NONHSAT013068
18	lnc-C10orf25-2	chr10:45557710-45558032	NONHSAT013065
19	lnc-ZNF22-1	chr10:45587756-45587949	XLOC_008477
20	lnc-C10orf25-2	chr10:45566695-45567014	NONHSAT013066
21	lnc-C10orf25-2	chr10:45561018-45561061	NONHSAT013066
22	lnc-C10orf25-2	chr10:45560975-45561061	NONHSAT013065
23	lnc-C10orf25-2	chr10:45556875-45557088	NONHSAT013065
24	lnc-C10orf25-2	chr10:45572101-45572131	XLOC_008802
25	lnc-C10orf25-2	chr10:45566695-45566819	NONHSAT013062
26	lnc-C10orf25-2	chr10:45566240-45566657	NONHSAT013070
27	lnc-C10orf25-2	chr10:45567013-45567068	NONHSAT013067
28	lnc-C10orf25-2	chr10:45594924-45595947	NR_024472
29	lnc-C10orf25-2	chr10:45566695-45566757	NONHSAT013069
30	lnc-C10orf25-2	chr10:45565926-45566430	NONHSAT013062
31	lnc-C10orf25-2	chr10:45561623-45561669	NONHSAT013062

No data

Variant related genes	Relation type
ENSG00000228462	TF binding region
CEP164P1	TF binding region
DUXAP4	TF binding region
ENSG00000228462	CpG island
CEP164P1	CpG island
DUXAP4	CpG island
ENSG00000226937	chromatin interactions
ENSG00000165511	chromatin interactions
ADARB1	miRNA target sites
VAMP8	miRNA target sites

Extended variants
information (count: 1536 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185931330	chr10:45548329-45548330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs60575180	chr10:45548353-45548354	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7478211	chr10:45548366-45548367	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139011142	chr10:45548543-45548544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12359377	chr10:45548585-45548586	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs142295656	chr10:45548621-45548622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114547656	chr10:45548693-45548694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556140201	chr10:45548743-45548744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143365368	chr10:45548746-45548747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550745720	chr10:45548752-45548753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552484903	chr10:45548755-45548756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572160647	chr10:45548767-45548768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568995568	chr10:45548807-45548808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148877207	chr10:45548819-45548820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377438278	chr10:45548820-45548821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534785931	chr10:45548846-45548847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191575210	chr10:45548856-45548857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78547547	chr10:45548882-45548883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146348703	chr10:45548975-45548976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566251265	chr10:45549031-45549032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533510544	chr10:45549041-45549042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12250724	chr10:45549045-45549046	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs570807376	chr10:45549061-45549062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538197138	chr10:45549074-45549075	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs139365433	chr10:45549077-45549078	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574890317	chr10:45549088-45549089	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs554443113	chr10:45549141-45549142	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs542433116	chr10:45549159-45549160	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs535786637	chr10:45549183-45549184	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs374998308	chr10:45549184-45549185	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs554276847	chr10:45549187-45549188	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149896618	chr10:45549233-45549234	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs546194569	chr10:45549394-45549395	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs564516756	chr10:45549538-45549539	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs112853181	chr10:45549546-45549547	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs368143649	chr10:45549549-45549550	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532436501	chr10:45549550-45549551	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs372499086	chr10:45549615-45549616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544136188	chr10:45549634-45549635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562803566	chr10:45549649-45549650	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs543137262	chr10:45549658-45549659	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs143965067	chr10:45549805-45549806	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs372500929	chr10:45549811-45549812	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs148646033	chr10:45549826-45549827	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs527431730	chr10:45549848-45549849	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs572153146	chr10:45549865-45549866	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs570075411	chr10:45549912-45549913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144190426	chr10:45549926-45549927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4526732	chr10:45549934-45549935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556553513	chr10:45550005-45550006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
Breast cancer	21785460	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Glioblastoma multiforme	21138945	CNVD
Autism	19287141	CNVD
Intellectual disability	21948486	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:202 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45548200-45548400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:45548200-45548600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr10:45548400-45549000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:45549000-45549200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:45549200-45554200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:45551800-45552000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:45552000-45559600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:45552400-45552800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr10:45552800-45553200	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr10:45553200-45553800	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr10:45553400-45555000	Enhancers	HUVEC	blood vessel
12	chr10:45553400-45555600	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr10:45553800-45554400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr10:45553800-45554600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr10:45553800-45554600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:45553800-45555000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr10:45553800-45555000	Enhancers	NHEK	skin
18	chr10:45554000-45554800	Enhancers	HMEC	breast
19	chr10:45554000-45555000	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr10:45554000-45555000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr10:45554200-45554600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr10:45554200-45554600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr10:45554200-45555200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr10:45554400-45554600	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr10:45554400-45558800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:45554600-45557200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:45554600-45558800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:45554800-45557200	Weak transcription	HMEC	breast
29	chr10:45555000-45555400	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr10:45555000-45557200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:45555000-45557200	Weak transcription	NHEK	skin
32	chr10:45555000-45557600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr10:45555200-45557200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:45555400-45558800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr10:45555600-45558800	Weak transcription	Primary monocytes fromperipheralblood	blood
36	chr10:45556000-45556200	Enhancers	Fetal Brain Male	brain
37	chr10:45557000-45558000	Enhancers	Fetal Brain Female	brain
38	chr10:45557200-45558000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr10:45557200-45558200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr10:45557200-45559000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:45557200-45559600	Enhancers	NHEK	skin
42	chr10:45557200-45560200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr10:45557200-45560800	Enhancers	HMEC	breast
44	chr10:45557400-45557600	Enhancers	Fetal Brain Male	brain
45	chr10:45557400-45557800	Enhancers	Aorta	Aorta
46	chr10:45557400-45557800	Enhancers	Brain Anterior Caudate	brain
47	chr10:45557400-45558000	Enhancers	Placenta	Placenta
48	chr10:45557400-45558200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr10:45557600-45557800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr10:45557600-45557800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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