Variant report

Variant	esv1792771
Chromosome Location	chr10:21874152-22013644
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1268)
CpG islands
(count:183)
Chromatin interactive
region (count:111)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:22013360-22013970	K562	blood:	n/a	n/a
2	ARID3A	chr10:21950782-21950786	K562	blood:	n/a	n/a
3	ARID3A	chr10:21912298-21912489	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:21964142-21964505	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:21955681-21955702	K562	blood:	n/a	n/a
6	ARID3A	chr10:22013511-22014320	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:21877283-21877407	HepG2	liver:	n/a	n/a
8	ATF1	chr10:21950124-21950374	K562	blood:	n/a	n/a
9	ATF1	chr10:21976658-21976858	K562	blood:	n/a	n/a
10	ATF1	chr10:22009018-22009361	K562	blood:	n/a	n/a
11	ATF1	chr10:21944988-21945293	K562	blood:	n/a	n/a
12	ATF1	chr10:21991603-21991760	K562	blood:	n/a	n/a
13	ATF1	chr10:22013180-22013997	K562	blood:	n/a	n/a
14	ATF2	chr10:21991403-21992133	GM12878	blood:	n/a	n/a
15	ATF2	chr10:21999461-22000047	GM12878	blood:	n/a	n/a
16	ATF2	chr10:21991423-21992167	GM12878	blood:	n/a	n/a
17	ATF2	chr10:21999479-22000064	GM12878	blood:	n/a	n/a
18	ATF3	chr10:22013564-22013930	K562	blood:	n/a	n/a
19	BACH1	chr10:21975911-21975997	K562	blood:	n/a	n/a
20	BACH1	chr10:21995995-21995999	K562	blood:	n/a	n/a
21	BATF	chr10:21999624-21999995	GM12878	blood:	n/a	n/a
22	BATF	chr10:22013608-22013889	GM12878	blood:	n/a	n/a
23	BCL11A	chr10:21999723-22000032	GM12878	blood:	n/a	n/a
24	BCL3	chr10:22013383-22014056	A549	lung:	n/a	n/a
25	BCLAF1	chr10:21991700-21992222	GM12878	blood:	n/a	n/a
26	BHLHE40	chr10:22009095-22009442	GM12878	blood:	n/a	n/a
27	BHLHE40	chr10:21999562-21999999	GM12878	blood:	n/a	n/a
28	BRCA1	chr10:21938750-21938763	GM12878	blood:	n/a	n/a
29	BRCA1	chr10:21937177-21937201	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr10:21989263-21989756	K562	blood:	n/a	n/a
31	CBX3	chr10:21989357-21989806	K562	blood:	n/a	n/a
32	CBX3	chr10:21896856-21897194	K562	blood:	n/a	n/a
33	CCNT2	chr10:22013459-22013981	K562	blood:	n/a	n/a
34	CCNT2	chr10:21990699-21990809	K562	blood:	n/a	n/a
35	CEBPB	chr10:22013381-22014050	HCT-116	colon:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
36	CEBPB	chr10:22001673-22001761	K562	blood:	n/a	chr10:22001714-22001725
37	CEBPB	chr10:22013397-22014018	ECC-1	luminal epithelium:	n/a	chr10:22013720-22013733 chr10:22013717-22013734 chr10:22013722-22013731 chr10:22013721-22013732 chr10:22013722-22013731 chr10:22013722-22013731
38	CEBPB	chr10:22009004-22009414	ECC-1	luminal epithelium:	n/a	chr10:22009205-22009216
39	CEBPB	chr10:21976642-21976928	K562	blood:	n/a	n/a
40	CEBPB	chr10:21966511-21966811	HepG2	liver:	n/a	chr10:21966655-21966672 chr10:21966658-21966669
41	CEBPB	chr10:21897960-21898160	K562	blood:	n/a	n/a
42	CEBPB	chr10:22008376-22008627	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:21901626-21901643	K562	blood:	n/a	n/a
44	CEBPB	chr10:21906213-21906580	IMR90	lung:	n/a	n/a
45	CEBPB	chr10:21906220-21906695	A549	lung:	n/a	n/a
46	CEBPB	chr10:21976609-21977266	Hela-S3	cervix:	n/a	chr10:21977189-21977202 chr10:21977189-21977200
47	CEBPB	chr10:22001546-22001871	IMR90	lung:	n/a	chr10:22001714-22001725
48	CEBPB	chr10:21996427-21996633	A549	lung:	n/a	chr10:21996517-21996528
49	CEBPB	chr10:21897612-21897657	K562	blood:	n/a	n/a
50	CEBPB	chr10:21980068-21980177	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:21958473-21958523	T-47D	breast:	n/a
2	chr10:21958473-21958523	AG09319	gingival:	n/a
3	chr10:21958473-21958523	SK-N-MC	brain:	n/a
4	chr10:21982589-21982639	HRCEpiC	kidney:	n/a
5	chr10:21958473-21958523	HAEpiC	amniotic membrane:	n/a
6	chr10:21982589-21982639	HMEC	breast:	n/a
7	chr10:21926911-21926961	SAEC	small airway:	n/a
8	chr10:21926911-21926961	NB4	blood:	n/a
9	chr10:21982589-21982639	HRE	kidney:	n/a
10	chr10:21982589-21982639	AoSMC	blood vessel:	n/a
11	chr10:21958473-21958523	HEK293	kidney:	embryo
12	chr10:21982589-21982639	K562	blood:	n/a
13	chr10:21982589-21982639	Hepatocyte	liver:	n/a
14	chr10:21926911-21926961	PANC-1	pancreas:	n/a
15	chr10:21926911-21926961	HUVEC	blood vessel:	n/a
16	chr10:21926911-21926961	AG09309	skin:	n/a
17	chr10:21958473-21958523	GM12891	blood:	n/a
18	chr10:21982589-21982639	U87	brain:	n/a
19	chr10:21958473-21958523	HRPEpiC	eye:	n/a
20	chr10:21982589-21982639	NH-A	brain:	n/a
21	chr10:21958473-21958523	AoSMC	blood vessel:	n/a
22	chr10:21926911-21926961	HCM	heart:	n/a
23	chr10:21926911-21926961	MCF10A-Er-Src	breast:	n/a
24	chr10:21958473-21958523	U87	brain:	n/a
25	chr10:21958473-21958523	GM06990	blood:	n/a
26	chr10:21982589-21982639	AG04449	skin:	fetal
27	chr10:21982589-21982639	HNPCEpiC	eye:	n/a
28	chr10:21926911-21926961	K562	blood:	n/a
29	chr10:21926911-21926961	HCF	heart:	n/a
30	chr10:21926911-21926961	GM12892	blood:	n/a
31	chr10:21958473-21958523	HUVEC	blood vessel:	n/a
32	chr10:21926911-21926961	LNCaP	prostate:	n/a
33	chr10:21926911-21926961	AG04450	lung:	fetal
34	chr10:21958473-21958523	HNPCEpiC	eye:	n/a
35	chr10:21982589-21982639	GM12878	blood:	n/a
36	chr10:21958473-21958523	PrEC	prostate:	n/a
37	chr10:21958473-21958523	ProgFib	skin:	n/a
38	chr10:21982589-21982639	HPAEpiC	pulmonary alveolar:	n/a
39	chr10:21926911-21926961	GM12878	blood:	n/a
40	chr10:21958473-21958523	HEEpiC	esophagus:	n/a
41	chr10:21982589-21982639	T-47D	breast:	n/a
42	chr10:21958473-21958523	BJ	skin:	n/a
43	chr10:21926911-21926961	RPTEC	kidney:	n/a
44	chr10:21982589-21982639	HAEpiC	amniotic membrane:	n/a
45	chr10:21926911-21926961	MCF-7	breast:	n/a
46	chr10:21926911-21926961	IMR90	lung:	fetal
47	chr10:21926911-21926961	NH-A	brain:	n/a
48	chr10:21982589-21982639	ovcar-3	ovarian:	n/a
49	chr10:21958473-21958523	MCF10A-Er-Src	breast:	n/a
50	chr10:21982589-21982639	NHBE	bronchial:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:21871808..21874312-chr10:21879354..21881232,2	K562	blood:
2	chr10:21995574..21997205-chr10:22520645..22522648,2	K562	blood:
3	chr10:21821015..21823100-chr10:21941325..21943555,2	K562	blood:
4	chr10:21912943..21915292-chr10:21917187..21920065,2	K562	blood:
5	chr10:22007575..22010165-chr10:22014123..22016701,2	K562	blood:
6	chr10:21816369..21819253-chr10:22004806..22007546,2	MCF-7	breast:
7	chr10:21822599..21824193-chr10:21898159..21900268,3	K562	blood:
8	chr10:21961052..21963302-chr10:21964301..21966207,2	K562	blood:
9	chr10:21957343..21959730-chr10:21965989..21967764,2	K562	blood:
10	chr10:21956427..21959026-chr10:21960604..21963223,2	K562	blood:
11	chr10:21817690..21818555-chr10:21919238..21919922,2	MCF-7	breast:
12	chr10:21996482..21998429-chr10:22004832..22006508,2	K562	blood:
13	chr10:21897294..21899834-chr10:21908105..21909643,2	MCF-7	breast:
14	chr10:21996482..21998429-chr10:22004832..22006508,2	K562	blood:
15	chr10:21909889..21911580-chr10:21929468..21932103,2	K562	blood:
16	chr10:21919335..21919967-chr10:21931821..21932370,2	MCF-7	breast:
17	chr10:21814123..21816913-chr10:21995893..21998162,2	MCF-7	breast:
18	chr10:21938514..21940778-chr10:21955713..21957412,2	K562	blood:
19	chr10:21954505..21956388-chr10:21958814..21960336,2	K562	blood:
20	chr10:21909487..21912918-chr10:21916062..21919904,3	K562	blood:
21	chr10:21914982..21917959-chr10:21922446..21924222,2	K562	blood:
22	chr10:21813660..21816356-chr10:21896974..21899642,3	K562	blood:
23	chr10:21892363..21894156-chr10:21920730..21923308,2	MCF-7	breast:
24	chr10:21964215..21964716-chr10:22020856..22021759,2	MCF-7	breast:
25	chr10:21785072..21787206-chr10:22004943..22007364,2	MCF-7	breast:
26	chr10:21871808..21874312-chr10:21879354..21881232,2	K562	blood:
27	chr10:21932966..21934847-chr10:21935882..21937587,2	K562	blood:
28	chr10:21898129..21900750-chr10:21903688..21906433,3	K562	blood:
29	chr10:21939974..21941555-chr10:21943236..21945845,2	K562	blood:
30	chr10:21893811..21896382-chr10:21900964..21903749,2	MCF-7	breast:
31	chr10:21812847..21814748-chr10:21961916..21964331,2	MCF-7	breast:
32	chr10:21784768..21786630-chr10:21978936..21981188,2	K562	blood:
33	chr10:21822599..21824168-chr10:21898203..21900268,2	K562	blood:
34	chr10:21815978..21818479-chr10:21973475..21976355,2	K562	blood:
35	chr10:21883151..21884959-chr10:21942105..21944413,2	K562	blood:
36	chr10:21971952..21974355-chr10:21975605..21977585,2	K562	blood:
37	chr10:21967381..21969902-chr10:21970354..21972033,2	K562	blood:
38	chr10:21813812..21816552-chr10:22000725..22002586,2	K562	blood:
39	chr10:22001640..22004162-chr10:22017196..22019106,3	K562	blood:
40	chr10:21571237..21573748-chr10:21899490..21902266,2	MCF-7	breast:
41	chr10:21784668..21785216-chr10:21964281..21964790,2	K562	blood:
42	chr10:21860750..21863107-chr10:21896992..21899830,2	K562	blood:
43	chr10:21970179..21972315-chr10:21973680..21976595,2	K562	blood:
44	chr10:21932966..21934847-chr10:21935882..21937587,2	K562	blood:
45	chr10:21976494..21979598-chr10:21980267..21982775,3	K562	blood:
46	chr10:21814835..21816924-chr10:22010662..22012545,2	K562	blood:
47	chr10:22008975..22011385-chr10:22011817..22013721,2	K562	blood:
48	chr10:21970179..21972315-chr10:21973680..21976595,2	K562	blood:
49	chr10:21905679..21908459-chr10:21909977..21914285,3	K562	blood:
50	chr10:21927290..21929661-chr10:21936208..21938819,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf140-1	chr10:21913521-21915215	NONHSAT011721

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MLLT10	hsa-miR-132-3p	chr10:21940668-21940686

Variant related genes	Relation type
MLLT10	TF binding region
RNU6-1141P	TF binding region
HNRNPRP1	TF binding region
MLLT10	CpG island
RNU6-1141P	CpG island
HNRNPRP1	CpG island
ENSG00000078403	chromatin interactions
ENSG00000204682	chromatin interactions
ENSG00000180592	chromatin interactions
ENSG00000222071	chromatin interactions
ENSG00000223984	chromatin interactions
ENSG00000242622	chromatin interactions

Extended variants
information (count: 4960 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:4960 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11012745	chr10:21874152-21874153	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565293894	chr10:21874177-21874178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546660203	chr10:21874272-21874273	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs575679808	chr10:21874311-21874312	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549519749	chr10:21874336-21874337	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74120976	chr10:21874344-21874345	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568527616	chr10:21874355-21874356	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11012746	chr10:21874370-21874371	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557322999	chr10:21874535-21874536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564953460	chr10:21874582-21874583	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186220261	chr10:21874707-21874708	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535511426	chr10:21874709-21874710	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs191512823	chr10:21874720-21874721	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182811937	chr10:21874752-21874753	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560698340	chr10:21874772-21874773	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532683846	chr10:21874803-21874804	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs373541819	chr10:21874881-21874882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs143760010	chr10:21874890-21874891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571706121	chr10:21874917-21874918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530459223	chr10:21874918-21874919	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550542120	chr10:21874931-21874932	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs12247916	chr10:21874971-21874972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs116394251	chr10:21874983-21874984	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536298070	chr10:21874990-21874991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377421025	chr10:21875001-21875002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186001284	chr10:21875015-21875016	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190866306	chr10:21875019-21875020	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12570519	chr10:21875042-21875043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370231612	chr10:21875097-21875098	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202184436	chr10:21875185-21875186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368157812	chr10:21875201-21875202	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544655093	chr10:21875207-21875208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75432462	chr10:21875218-21875219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201734317	chr10:21875219-21875220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374122460	chr10:21875240-21875241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139468248	chr10:21875263-21875264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574849261	chr10:21875286-21875287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367750602	chr10:21875325-21875326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540690896	chr10:21875490-21875491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549843067	chr10:21875528-21875529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532597799	chr10:21875569-21875570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545973690	chr10:21875584-21875585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573049512	chr10:21875596-21875597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562885726	chr10:21875616-21875617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374181589	chr10:21875633-21875634	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs550308361	chr10:21875696-21875697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183452026	chr10:21875707-21875708	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529766956	chr10:21875748-21875749	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113177460	chr10:21875775-21875776	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs370736792	chr10:21875776-21875777	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Intracranial arachnoid cysts	20187927	CNVD
Cancer	17440070	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute myeloid leukemia	19651600	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:3637 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21824600-21930400	Weak transcription	Gastric	stomach
2	chr10:21832000-21876400	Weak transcription	Aorta	Aorta
3	chr10:21839400-21878200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr10:21839800-21880200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr10:21840000-21877200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr10:21841200-21897200	Weak transcription	Fetal Kidney	kidney
7	chr10:21842200-21897200	Weak transcription	Fetal Brain Male	brain
8	chr10:21844600-21896600	Weak transcription	Hela-S3	cervix
9	chr10:21846800-21874800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr10:21846800-21882200	Weak transcription	Brain Germinal Matrix	brain
11	chr10:21846800-21889600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr10:21846800-21892800	Weak transcription	HSMMtube	muscle
13	chr10:21846800-21913600	Weak transcription	Rectal Smooth Muscle	rectum
14	chr10:21847000-21901200	Weak transcription	HUVEC	blood vessel
15	chr10:21848800-21914200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr10:21849400-21889600	Weak transcription	NHEK	skin
17	chr10:21849400-21913600	Weak transcription	Esophagus	oesophagus
18	chr10:21849800-21874400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:21849800-21889400	Weak transcription	Brain Hippocampus Middle	brain
20	chr10:21849800-21894600	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr10:21849800-21897000	Weak transcription	Fetal Brain Female	brain
22	chr10:21850400-21875600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr10:21850800-21889600	Weak transcription	HMEC	breast
24	chr10:21853400-21875000	Weak transcription	Fetal Intestine Large	intestine
25	chr10:21856400-21876000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr10:21856600-21874400	Weak transcription	Thymus	Thymus
27	chr10:21856600-21874800	Weak transcription	Placenta	Placenta
28	chr10:21856600-21876000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr10:21856600-21876000	Weak transcription	Fetal Muscle Leg	muscle
30	chr10:21856600-21877400	Weak transcription	Fetal Lung	lung
31	chr10:21856800-21913400	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr10:21859200-21875600	Weak transcription	Left Ventricle	heart
33	chr10:21859400-21889800	Weak transcription	Pancreas	Pancrea
34	chr10:21860400-21886600	Weak transcription	Small Intestine	intestine
35	chr10:21860600-21876200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr10:21860600-21879000	Weak transcription	Lung	lung
37	chr10:21860600-21895400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr10:21860800-21874200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr10:21860800-21878200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr10:21861200-21883000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr10:21861200-21890000	Weak transcription	Colon Smooth Muscle	Colon
42	chr10:21861400-21875600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr10:21861400-21898400	Weak transcription	Brain Angular Gyrus	brain
44	chr10:21861400-21902800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr10:21861600-21875600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr10:21861800-21878800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr10:21861800-21889600	Weak transcription	Brain Cingulate Gyrus	brain
48	chr10:21861800-21895400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr10:21861800-21898400	Weak transcription	Brain Anterior Caudate	brain
50	chr10:21861800-21913800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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