Variant report

Variant	nsv948006
Chromosome Location	chr10:52127164-52177684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1394)
CpG islands
(count:428)
Chromatin interactive
region (count:101)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1394 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:52176070-52176490	K562	blood:	n/a	n/a
2	ARID3A	chr10:52147139-52147416	K562	blood:	n/a	n/a
3	ARID3A	chr10:52156721-52157006	K562	blood:	n/a	n/a
4	ARID3A	chr10:52164318-52164640	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:52152230-52152647	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:52127535-52127844	K562	blood:	n/a	n/a
7	ARID3A	chr10:52132787-52132975	K562	blood:	n/a	n/a
8	ARID3A	chr10:52154906-52155475	HepG2	liver:	n/a	n/a
9	ARID3A	chr10:52172153-52172477	K562	blood:	n/a	n/a
10	ARID3A	chr10:52167220-52167329	K562	blood:	n/a	n/a
11	ARID3A	chr10:52153154-52153949	HepG2	liver:	n/a	n/a
12	ARID3A	chr10:52153043-52153961	K562	blood:	n/a	n/a
13	ARID3A	chr10:52145464-52145662	HepG2	liver:	n/a	n/a
14	ARID3A	chr10:52158346-52158930	K562	blood:	n/a	n/a
15	ARID3A	chr10:52169837-52170213	K562	blood:	n/a	n/a
16	ATF1	chr10:52153039-52153886	K562	blood:	n/a	n/a
17	ATF2	chr10:52156449-52157208	GM12878	blood:	n/a	n/a
18	ATF2	chr10:52134583-52135111	GM12878	blood:	n/a	n/a
19	ATF2	chr10:52156486-52157137	GM12878	blood:	n/a	n/a
20	ATF3	chr10:52153507-52153922	K562	blood:	n/a	n/a
21	ATF3	chr10:52167009-52167518	HCT-116	colon:	n/a	n/a
22	ATF3	chr10:52166990-52167643	HCT-116	colon:	n/a	n/a
23	ATF3	chr10:52167103-52167485	K562	blood:	n/a	n/a
24	ATF3	chr10:52152945-52153352	K562	blood:	n/a	n/a
25	ATF3	chr10:52163202-52163479	K562	blood:	n/a	n/a
26	ATF3	chr10:52167129-52167475	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr10:52167193-52167471	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr10:52139666-52139687	K562	blood:	n/a	n/a
29	BACH1	chr10:52137292-52137448	K562	blood:	n/a	n/a
30	BATF	chr10:52156551-52157040	GM12878	blood:	n/a	n/a
31	BATF	chr10:52156516-52157121	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:52156618-52157050	GM12878	blood:	n/a	chr10:52156873-52156882
33	BCLAF1	chr10:52177193-52178450	GM12878	blood:	n/a	chr10:52178049-52178062 chr10:52178237-52178246
34	BCLAF1	chr10:52175846-52176466	K562	blood:	n/a	n/a
35	BCLAF1	chr10:52156520-52157226	GM12878	blood:	n/a	chr10:52156873-52156882
36	BCLAF1	chr10:52177256-52178277	GM12878	blood:	n/a	chr10:52178237-52178246 chr10:52178049-52178062
37	BHLHE40	chr10:52177190-52177508	HepG2	liver:	n/a	chr10:52177324-52177333
38	BHLHE40	chr10:52176770-52177842	K562	blood:	n/a	chr10:52177324-52177333
39	BHLHE40	chr10:52156460-52156754	K562	blood:	n/a	n/a
40	BHLHE40	chr10:52153361-52153865	HepG2	liver:	n/a	n/a
41	BHLHE40	chr10:52157034-52157392	K562	blood:	n/a	n/a
42	BHLHE40	chr10:52172283-52172399	K562	blood:	n/a	n/a
43	BHLHE40	chr10:52153156-52153821	K562	blood:	n/a	n/a
44	BHLHE40	chr10:52176834-52178282	GM12878	blood:	n/a	chr10:52178062-52178078 chr10:52177324-52177333
45	BHLHE40	chr10:52131610-52131907	K562	blood:	n/a	n/a
46	BHLHE40	chr10:52177211-52177491	A549	lung:	n/a	chr10:52177324-52177333
47	BRCA1	chr10:52156229-52156417	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr10:52169686-52170018	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr10:52154884-52155413	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr10:52152819-52153936	Hela-S3	cervix:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52162583-52162633	HIPEpiC	eye:	n/a
2	chr10:52162583-52162633	HIPEpiC	eye:	n/a
3	chr10:52176755-52176805	SK-N-SH	brain:	n/a
4	chr10:52167630-52167680	HEK293	kidney:	embryo
5	chr10:52170429-52170479	Hepatocyte	liver:	n/a
6	chr10:52174504-52174554	Caco-2	colon:	n/a
7	chr10:52156632-52156682	GM12878	blood:	n/a
8	chr10:52174504-52174554	GM06990	blood:	n/a
9	chr10:52156632-52156682	HepG2	liver:	n/a
10	chr10:52176755-52176805	HL-60	blood:	n/a
11	chr10:52156632-52156682	NT2-D1	testis:	n/a
12	chr10:52167630-52167680	AG09319	gingival:	n/a
13	chr10:52156632-52156682	AG04450	lung:	fetal
14	chr10:52170429-52170479	SKMC	muscle:	n/a
15	chr10:52162583-52162633	HAEpiC	amniotic membrane:	n/a
16	chr10:52167630-52167680	LNCaP	prostate:	n/a
17	chr10:52174504-52174554	GM19239	blood:	n/a
18	chr10:52162583-52162633	HRCEpiC	kidney:	n/a
19	chr10:52170429-52170479	A549	lung:	n/a
20	chr10:52156632-52156682	NHDF-neo	bronchial:	n/a
21	chr10:52176755-52176805	SK-N-SH_RA	brain:	n/a
22	chr10:52145861-52145911	GM12892	blood:	n/a
23	chr10:52145861-52145911	AG10803	skin:	n/a
24	chr10:52174504-52174554	HUVEC	blood vessel:	n/a
25	chr10:52145861-52145911	MCF10A-Er-Src	breast:	n/a
26	chr10:52167630-52167680	HNPCEpiC	eye:	n/a
27	chr10:52145861-52145911	AG09309	skin:	n/a
28	chr10:52167630-52167680	H1-hESC	embryonic stem cell:	embryo
29	chr10:52156632-52156682	NB4	blood:	n/a
30	chr10:52176755-52176805	H1-hESC	embryonic stem cell:	embryo
31	chr10:52174504-52174554	SKMC	muscle:	n/a
32	chr10:52167630-52167680	SAEC	small airway:	n/a
33	chr10:52170429-52170479	AoSMC	blood vessel:	n/a
34	chr10:52156632-52156682	A549	lung:	n/a
35	chr10:52156632-52156682	MCF-7	breast:	n/a
36	chr10:52162583-52162633	A549	lung:	n/a
37	chr10:52174504-52174554	HEEpiC	esophagus:	n/a
38	chr10:52176755-52176805	HRE	kidney:	n/a
39	chr10:52174504-52174554	SAEC	small airway:	n/a
40	chr10:52145861-52145911	SK-N-SH_RA	brain:	n/a
41	chr10:52170429-52170479	NHDF-neo	bronchial:	n/a
42	chr10:52156632-52156682	HMEC	breast:	n/a
43	chr10:52176755-52176805	PrEC	prostate:	n/a
44	chr10:52174504-52174554	PFSK-1	brain:	n/a
45	chr10:52167630-52167680	GM12891	blood:	n/a
46	chr10:52167630-52167680	IMR90	lung:	fetal
47	chr10:52174504-52174554	RPTEC	kidney:	n/a
48	chr10:52170429-52170479	GM12892	blood:	n/a
49	chr10:52167630-52167680	HRPEpiC	eye:	n/a
50	chr10:52145861-52145911	ovcar-3	ovarian:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:52139065..52141348-chr10:52143343..52146205,3	K562	blood:
2	chr10:52154508..52157227-chr10:52160159..52164764,6	MCF-7	breast:
3	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
4	chr10:52164829..52166437-chr10:52168704..52170422,2	MCF-7	breast:
5	chr10:52155995..52158141-chr10:52176386..52179255,3	K562	blood:
6	chr10:52153243..52155406-chr10:52158716..52160773,2	K562	blood:
7	chr10:52120330..52124092-chr10:52125493..52129232,4	K562	blood:
8	chr10:52149428..52151054-chr10:52153978..52156665,2	K562	blood:
9	chr10:52127857..52130924-chr10:52133934..52136011,3	K562	blood:
10	chr10:52173349..52175159-chr10:52175578..52178225,2	K562	blood:
11	chr10:52158173..52160799-chr10:52163076..52165080,2	MCF-7	breast:
12	chr10:52150758..52153271-chr10:52349900..52352192,2	K562	blood:
13	chr10:52177364..52178170-chr6:2999684..3000477,2	Hela-S3	cervix:
14	chr10:52127277..52127980-chr10:52180802..52181438,3	MCF-7	breast:
15	chr10:52136009..52138905-chr10:52161513..52164062,2	K562	blood:
16	chr10:52132102..52134129-chr10:52137496..52139624,2	K562	blood:
17	chr10:52173349..52175159-chr10:52175578..52178225,2	K562	blood:
18	chr10:52132102..52134129-chr10:52137496..52139624,2	K562	blood:
19	chr10:52140515..52144174-chr10:52145469..52147444,3	MCF-7	breast:
20	chr10:52131941..52133571-chr10:52135239..52137791,2	MCF-7	breast:
21	chr10:52164829..52166437-chr10:52168704..52170422,2	MCF-7	breast:
22	chr10:52084222..52086810-chr10:52173871..52176505,2	K562	blood:
23	chr10:52177553..52178230-chr9:34179387..34179965,2	Hela-S3	cervix:
24	chr10:52143975..52146783-chr10:52153265..52157154,4	K562	blood:
25	chr10:52175389..52176966-chr10:52179598..52182050,2	K562	blood:
26	chr10:52152624..52157680-chr10:52173844..52179255,6	K562	blood:
27	chr10:52149428..52151054-chr10:52153978..52156665,2	K562	blood:
28	chr10:52176588..52178104-chr10:52321160..52323318,2	MCF-7	breast:
29	chr10:52153243..52155406-chr10:52158716..52160773,2	K562	blood:
30	chr10:52127640..52130879-chr10:52134264..52136292,3	K562	blood:
31	chr10:52124299..52127180-chr10:52148333..52150881,2	K562	blood:
32	chr10:52163901..52167177-chr10:52381610..52384393,3	MCF-7	breast:
33	chr10:52152624..52157680-chr10:52173844..52179255,6	K562	blood:
34	chr10:52161910..52166825-chr10:52176564..52180969,7	MCF-7	breast:
35	chr10:52139930..52141788-chr10:52152560..52154138,2	MCF-7	breast:
36	chr10:52154324..52156059-chr10:52394056..52396919,2	K562	blood:
37	chr10:52164630..52167501-chr10:52173843..52176462,2	MCF-7	breast:
38	chr10:52156579..52161749-chr10:52162901..52167145,5	K562	blood:
39	chr10:52127520..52128296-chr10:52163800..52164644,2	MCF-7	breast:
40	chr10:52140574..52146052-chr10:52147232..52152526,7	K562	blood:
41	chr10:52154496..52159392-chr10:52160687..52163216,5	K562	blood:
42	chr10:52143975..52146783-chr10:52153265..52157154,4	K562	blood:
43	chr10:52152378..52155454-chr10:52174313..52178963,4	MCF-7	breast:
44	chr10:52133378..52136507-chr10:52147936..52151266,3	MCF-7	breast:
45	chr10:52160919..52162899-chr10:52165247..52167938,3	K562	blood:
46	chr10:52160595..52164108-chr10:52172645..52175372,3	MCF-7	breast:
47	chr10:52152378..52155454-chr10:52174313..52178963,4	MCF-7	breast:
48	chr10:52085312..52087982-chr10:52138618..52141238,2	K562	blood:
49	chr10:52164112..52165618-chr10:52174506..52177347,2	K562	blood:
50	chr10:52132819..52134741-chr10:52135257..52137397,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269700	TF binding region
ENSG00000269700	CpG island
ENSG00000269700	chromatin interactions
ENSG00000238523	chromatin interactions
ENSG00000225303	chromatin interactions
ENSG00000124588	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000198964	chromatin interactions

Extended variants
information (count: 1846 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1846 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111569127	chr10:52127169-52127170	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528998638	chr10:52127274-52127275	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559100349	chr10:52127279-52127280	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367796205	chr10:52127284-52127285	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569395252	chr10:52127288-52127289	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538433578	chr10:52127316-52127317	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186948609	chr10:52127321-52127322	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75504026	chr10:52127400-52127401	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs532127815	chr10:52127401-52127402	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542187673	chr10:52127426-52127427	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372087880	chr10:52127441-52127442	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190893364	chr10:52127442-52127443	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10508927	chr10:52127451-52127452	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375215238	chr10:52127471-52127472	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs2060560	chr10:52127483-52127484	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs534348375	chr10:52127564-52127565	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376910347	chr10:52127615-52127616	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146615912	chr10:52127629-52127630	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182706748	chr10:52127714-52127715	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566294760	chr10:52127718-52127719	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188842476	chr10:52127759-52127760	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547853141	chr10:52127770-52127771	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs561140117	chr10:52127775-52127776	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530046137	chr10:52127820-52127821	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs547003758	chr10:52127922-52127923	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566916014	chr10:52127928-52127929	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs193206069	chr10:52127953-52127954	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184900275	chr10:52127980-52127981	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569341254	chr10:52128023-52128024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141402279	chr10:52128075-52128076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113294101	chr10:52128085-52128086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs370656204	chr10:52128209-52128210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs372754257	chr10:52128210-52128211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568391582	chr10:52128242-52128243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7080963	chr10:52128248-52128249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552540717	chr10:52128370-52128371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151238920	chr10:52128374-52128375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75125396	chr10:52128396-52128397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558334984	chr10:52128409-52128410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187654656	chr10:52128453-52128454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544400215	chr10:52128457-52128458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369062142	chr10:52128472-52128473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111291663	chr10:52128505-52128506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192095045	chr10:52128513-52128514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184268249	chr10:52128534-52128535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560395949	chr10:52128538-52128539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532360074	chr10:52128552-52128553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536758425	chr10:52128573-52128574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140450262	chr10:52128608-52128609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115068668	chr10:52128711-52128712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
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
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
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
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1666 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52104000-52134000	Weak transcription	Primary T helper cells fromperipheralblood	blood
2	chr10:52104000-52141400	Weak transcription	Pancreas	Pancrea
3	chr10:52104200-52133600	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr10:52104200-52134200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr10:52104200-52157000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr10:52109400-52134400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr10:52115800-52142200	Weak transcription	Fetal Intestine Small	intestine
8	chr10:52117400-52133400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr10:52119000-52129400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:52119000-52133200	Weak transcription	Colon Smooth Muscle	Colon
11	chr10:52119400-52127400	Weak transcription	Hela-S3	cervix
12	chr10:52119400-52134000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:52119400-52136000	Weak transcription	Fetal Brain Male	brain
14	chr10:52120400-52133000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr10:52120600-52133800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:52120600-52141400	Weak transcription	HSMM	muscle
17	chr10:52120800-52133000	Weak transcription	HSMMtube	muscle
18	chr10:52120800-52133400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr10:52120800-52133600	Weak transcription	Osteobl	bone
20	chr10:52121200-52134400	Weak transcription	Fetal Stomach	stomach
21	chr10:52121200-52136600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr10:52121200-52141600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:52121400-52133000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr10:52121400-52139400	Weak transcription	Placenta	Placenta
25	chr10:52121600-52127200	Weak transcription	Psoas Muscle	Psoas
26	chr10:52121600-52132400	Weak transcription	Brain Hippocampus Middle	brain
27	chr10:52121600-52134000	Weak transcription	Esophagus	oesophagus
28	chr10:52121800-52127200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr10:52121800-52131000	Weak transcription	Adipose Nuclei	Adipose
30	chr10:52121800-52131200	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr10:52121800-52132800	Weak transcription	Brain Substantia Nigra	brain
32	chr10:52121800-52134000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr10:52121800-52134000	Weak transcription	Liver	Liver
34	chr10:52121800-52134000	Weak transcription	Right Atrium	heart
35	chr10:52121800-52134400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr10:52121800-52135000	Weak transcription	H9 Cell Line	embryonic stem cell
37	chr10:52122000-52134000	Weak transcription	Brain Anterior Caudate	brain
38	chr10:52122200-52133000	Weak transcription	NHDF-Ad	bronchial
39	chr10:52122800-52134600	Weak transcription	HUVEC	blood vessel
40	chr10:52123400-52134000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr10:52123400-52134400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr10:52123400-52134400	Weak transcription	Primary T cells from cord blood	blood
43	chr10:52123400-52134400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr10:52123400-52134400	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr10:52123400-52134800	Weak transcription	Primary hematopoietic stem cells	blood
46	chr10:52123400-52136800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr10:52124600-52130800	Weak transcription	Fetal Lung	lung
48	chr10:52124600-52139400	Weak transcription	Primary B cells from cord blood	blood
49	chr10:52124800-52132800	Weak transcription	Fetal Heart	heart
50	chr10:52125400-52134000	Weak transcription	Left Ventricle	heart

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