Variant report

Variant	esv1795420
Chromosome Location	chr10:61637271-61669227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1885)
CpG islands
(count:733)
Chromatin interactive
region (count:83)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:61667540-61668663	K562	blood:	n/a	n/a
2	ARID3A	chr10:61666208-61666941	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:61655323-61655775	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:61666398-61667284	K562	blood:	n/a	n/a
5	ARID3A	chr10:61640194-61640941	K562	blood:	n/a	n/a
6	ARID3A	chr10:61667807-61667973	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:61652795-61652803	K562	blood:	n/a	n/a
8	ARID3A	chr10:61655233-61655731	K562	blood:	n/a	n/a
9	ATF1	chr10:61667625-61668620	K562	blood:	n/a	n/a
10	ATF1	chr10:61652481-61652819	K562	blood:	n/a	n/a
11	ATF1	chr10:61655415-61655842	K562	blood:	n/a	n/a
12	ATF2	chr10:61664457-61665198	GM12878	blood:	n/a	n/a
13	ATF2	chr10:61640752-61641336	GM12878	blood:	n/a	n/a
14	ATF2	chr10:61664628-61665058	GM12878	blood:	n/a	n/a
15	ATF2	chr10:61639067-61639636	GM12878	blood:	n/a	n/a
16	ATF2	chr10:61666170-61666616	GM12878	blood:	n/a	n/a
17	ATF2	chr10:61640594-61641447	GM12878	blood:	n/a	n/a
18	ATF2	chr10:61666420-61666944	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr10:61645095-61645675	GM12878	blood:	n/a	n/a
20	ATF2	chr10:61667526-61668554	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr10:61667352-61668051	GM12878	blood:	n/a	n/a
22	ATF2	chr10:61665908-61667042	GM12878	blood:	n/a	n/a
23	ATF2	chr10:61645030-61645630	GM12878	blood:	n/a	n/a
24	ATF2	chr10:61667534-61668628	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr10:61667403-61668126	GM12878	blood:	n/a	n/a
26	ATF3	chr10:61666074-61666889	A549	lung:	n/a	chr10:61666659-61666668
27	ATF3	chr10:61667592-61668014	K562	blood:	n/a	n/a
28	ATF3	chr10:61666244-61666657	K562	blood:	n/a	n/a
29	BACH1	chr10:61666439-61666922	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr10:61668215-61668608	H1-hESC	embryonic stem cell:	n/a	n/a
31	BATF	chr10:61645250-61645577	GM12878	blood:	n/a	n/a
32	BATF	chr10:61639154-61639634	GM12878	blood:	n/a	n/a
33	BATF	chr10:61640707-61641258	GM12878	blood:	n/a	n/a
34	BATF	chr10:61640129-61640402	GM12878	blood:	n/a	n/a
35	BATF	chr10:61640676-61641314	GM12878	blood:	n/a	n/a
36	BATF	chr10:61664650-61665154	GM12878	blood:	n/a	n/a
37	BATF	chr10:61664697-61665056	GM12878	blood:	n/a	n/a
38	BCL11A	chr10:61645141-61645595	GM12878	blood:	n/a	n/a
39	BCL11A	chr10:61640741-61641352	GM12878	blood:	n/a	chr10:61641156-61641165
40	BCL11A	chr10:61640843-61641286	GM12878	blood:	n/a	chr10:61641156-61641165
41	BCL11A	chr10:61645230-61645518	GM12878	blood:	n/a	n/a
42	BCL3	chr10:61666119-61666914	A549	lung:	n/a	chr10:61666184-61666193 chr10:61666343-61666356 chr10:61666219-61666232
43	BCL3	chr10:61640769-61641247	GM12878	blood:	n/a	chr10:61641156-61641165
44	BCLAF1	chr10:61665982-61667013	GM12878	blood:	n/a	chr10:61666184-61666193 chr10:61666343-61666356 chr10:61666219-61666232
45	BCLAF1	chr10:61666083-61667015	GM12878	blood:	n/a	chr10:61666184-61666193 chr10:61666343-61666356 chr10:61666219-61666232
46	BCLAF1	chr10:61645154-61645646	GM12878	blood:	n/a	n/a
47	BCLAF1	chr10:61640566-61641223	GM12878	blood:	n/a	chr10:61641156-61641165
48	BCLAF1	chr10:61640548-61641305	GM12878	blood:	n/a	chr10:61641156-61641165
49	BCLAF1	chr10:61666078-61666739	K562	blood:	n/a	chr10:61666184-61666193 chr10:61666343-61666356 chr10:61666219-61666232
50	BCLAF1	chr10:61645051-61645759	GM12878	blood:	n/a	chr10:61645669-61645682 chr10:61645675-61645684

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:61666281-61666331	Hela-S3	cervix:	n/a
2	chr10:61666281-61666331	Hela-S3	cervix:	n/a
3	chr10:61666281-61666331	ProgFib	skin:	n/a
4	chr10:61663157-61663207	SK-N-SH_RA	brain:	n/a
5	chr10:61666263-61666313	HUVEC	blood vessel:	n/a
6	chr10:61667761-61667811	NB4	blood:	n/a
7	chr10:61666281-61666331	NHBE	bronchial:	n/a
8	chr10:61666667-61666717	GM12891	blood:	n/a
9	chr10:61666263-61666313	HRCEpiC	kidney:	n/a
10	chr10:61664954-61665004	HEEpiC	esophagus:	n/a
11	chr10:61667761-61667811	IMR90	lung:	fetal
12	chr10:61665557-61665607	H1-hESC	embryonic stem cell:	embryo
13	chr10:61666263-61666313	AG04450	lung:	fetal
14	chr10:61666543-61666593	Caco-2	colon:	n/a
15	chr10:61665557-61665607	A549	lung:	n/a
16	chr10:61663157-61663207	HCM	heart:	n/a
17	chr10:61666263-61666313	AG09319	gingival:	n/a
18	chr10:61666667-61666717	HMEC	breast:	n/a
19	chr10:61665557-61665607	NT2-D1	testis:	n/a
20	chr10:61666824-61666874	IMR90	lung:	fetal
21	chr10:61665557-61665607	Hela-S3	cervix:	n/a
22	chr10:61665557-61665607	HCF	heart:	n/a
23	chr10:61664954-61665004	Jurkat	blood:	n/a
24	chr10:61666667-61666717	MCF10A-Er-Src	breast:	n/a
25	chr10:61665988-61666038	HRE	kidney:	n/a
26	chr10:61666667-61666717	NHBE	bronchial:	n/a
27	chr10:61667009-61667059	HMEC	breast:	n/a
28	chr10:61665988-61666038	GM19239	blood:	n/a
29	chr10:61666281-61666331	Jurkat	blood:	n/a
30	chr10:61667761-61667811	GM12878	blood:	n/a
31	chr10:61668184-61668234	MCF-7	breast:	n/a
32	chr10:61668184-61668234	BJ	skin:	n/a
33	chr10:61665988-61666038	IMR90	lung:	fetal
34	chr10:61665988-61666038	ovcar-3	ovarian:	n/a
35	chr10:61666824-61666874	NB4	blood:	n/a
36	chr10:61667009-61667059	HRPEpiC	eye:	n/a
37	chr10:61666263-61666313	AoSMC	blood vessel:	n/a
38	chr10:61668184-61668234	K562	blood:	n/a
39	chr10:61666263-61666313	NHBE	bronchial:	n/a
40	chr10:61667009-61667059	HepG2	liver:	n/a
41	chr10:61666281-61666331	AG09319	gingival:	n/a
42	chr10:61668184-61668234	HepG2	liver:	n/a
43	chr10:61667761-61667811	RPTEC	kidney:	n/a
44	chr10:61664954-61665004	MCF10A-Er-Src	breast:	n/a
45	chr10:61667009-61667059	GM12892	blood:	n/a
46	chr10:61667761-61667811	GM12891	blood:	n/a
47	chr10:61665557-61665607	GM06990	blood:	n/a
48	chr10:61668184-61668234	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:61663157-61663207	HIPEpiC	eye:	n/a
50	chr10:61666543-61666593	HEEpiC	esophagus:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:61615566..61617712-chr10:61637129..61639962,2	MCF-7	breast:
2	chr10:61632628..61635950-chr10:61647299..61651205,3	K562	blood:
3	chr10:61635533..61637804-chr10:61638300..61641205,3	K562	blood:
4	chr10:61645960..61647887-chr10:61649262..61651552,2	MCF-7	breast:
5	chr10:61594890..61595766-chr10:61639203..61639741,2	MCF-7	breast:
6	chr10:61634142..61636332-chr10:61636728..61639636,2	MCF-7	breast:
7	chr10:61639233..61641192-chr10:61644964..61647007,2	MCF-7	breast:
8	chr10:61603804..61606777-chr10:61661880..61663736,2	K562	blood:
9	chr10:61655581..61657205-chr10:61658249..61660092,2	K562	blood:
10	chr10:61646248..61649681-chr10:61659057..61661794,4	MCF-7	breast:
11	chr10:61633143..61635751-chr10:61635824..61637359,2	K562	blood:
12	chr10:61661963..61664576-chr10:61749051..61751954,2	MCF-7	breast:
13	chr10:61639063..61643015-chr10:61647185..61650219,3	MCF-7	breast:
14	chr10:61655581..61657205-chr10:61658249..61660092,2	K562	blood:
15	chr10:61647386..61652939-chr10:61663740..61669349,9	K562	blood:
16	chr10:61649784..61652594-chr10:61664669..61667678,3	MCF-7	breast:
17	chr10:61638896..61642309-chr10:61665188..61667493,3	K562	blood:
18	chr10:61652458..61655140-chr10:61737942..61740337,2	K562	blood:
19	chr10:61648268..61650504-chr10:61650711..61652681,2	MCF-7	breast:
20	chr10:61643762..61645786-chr10:61664123..61666003,2	MCF-7	breast:
21	chr10:61593371..61594213-chr10:61664532..61665492,2	MCF-7	breast:
22	chr10:61666545..61669325-chr10:61676846..61678686,2	MCF-7	breast:
23	chr10:61636740..61643413-chr10:61643807..61649213,6	K562	blood:
24	chr10:61648268..61650504-chr10:61650711..61652681,2	MCF-7	breast:
25	chr10:61633677..61637740-chr10:61638115..61642166,4	K562	blood:
26	chr10:61666876..61669628-chr10:61791272..61793178,2	MCF-7	breast:
27	chr10:61666623..61668608-chr10:61670476..61672736,2	MCF-7	breast:
28	chr10:61629487..61631429-chr10:61653201..61655597,2	K562	blood:
29	chr10:61641674..61643594-chr10:61648088..61650811,2	K562	blood:
30	chr10:61645422..61647388-chr10:61657593..61660192,2	K562	blood:
31	chr10:61648057..61649845-chr10:61652542..61654790,2	MCF-7	breast:
32	chr10:61654182..61656949-chr10:61658544..61661969,6	MCF-7	breast:
33	chr10:61632812..61634893-chr10:61666626..61669207,2	K562	blood:
34	chr10:61646248..61649681-chr10:61659057..61661794,4	MCF-7	breast:
35	chr10:61643704..61646293-chr10:61656724..61658823,2	MCF-7	breast:
36	chr10:61640293..61643125-chr10:61664795..61666558,2	MCF-7	breast:
37	chr10:61642094..61644181-chr10:61649311..61651720,2	K562	blood:
38	chr10:61654182..61656949-chr10:61658544..61661969,6	MCF-7	breast:
39	chr10:61631763..61634620-chr10:61659289..61660920,2	MCF-7	breast:
40	chr10:61641536..61643091-chr10:61645394..61647753,2	MCF-7	breast:
41	chr10:61595408..61597026-chr10:61643896..61645826,2	MCF-7	breast:
42	chr10:61665935..61666585-chr7:123388569..123389135,2	Hela-S3	cervix:
43	chr10:61629487..61632652-chr10:61653201..61655969,3	K562	blood:
44	chr10:61594610..61596651-chr10:61661878..61664205,2	K562	blood:
45	chr10:61648057..61649845-chr10:61652542..61654790,2	MCF-7	breast:
46	chr10:61632628..61634680-chr10:61647299..61649721,2	K562	blood:
47	chr10:61638398..61641573-chr10:61642787..61646612,4	K562	blood:
48	chr10:61645006..61647125-chr10:61664294..61667425,3	K562	blood:
49	chr10:61628053..61630048-chr10:61661857..61663658,2	K562	blood:
50	chr10:61630214..61632918-chr10:61637567..61639312,2	MCF-7	breast:

No data

Variant related genes	Relation type
CCDC6	TF binding region
CCDC6	CpG island
ENSG00000122557	chromatin interactions
ENSG00000233621	chromatin interactions
ENSG00000272686	chromatin interactions
ENSG00000108091	chromatin interactions
ENSG00000271122	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000163874	chromatin interactions
ENSG00000106299	chromatin interactions

Extended variants
information (count: 1177 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1177 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189872869	chr10:61637274-61637275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs570428071	chr10:61637283-61637284	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs539776593	chr10:61637291-61637292	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs558968660	chr10:61637322-61637323	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs577279751	chr10:61637331-61637332	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs535029399	chr10:61637380-61637381	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs72811515	chr10:61637391-61637392	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs7899565	chr10:61637436-61637437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs557468244	chr10:61637448-61637449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542050919	chr10:61637455-61637456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563943286	chr10:61637462-61637463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182432381	chr10:61637473-61637474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577521147	chr10:61637474-61637475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564456120	chr10:61637477-61637478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12571977	chr10:61637493-61637494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539845719	chr10:61637502-61637503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs147725311	chr10:61637633-61637634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529023921	chr10:61637645-61637646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140887928	chr10:61637647-61637648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569060190	chr10:61637648-61637649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572311013	chr10:61637732-61637733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537825232	chr10:61637749-61637750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533181488	chr10:61637768-61637769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551664782	chr10:61637769-61637770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142357378	chr10:61637777-61637778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186775695	chr10:61637799-61637800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553376039	chr10:61637809-61637810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568448904	chr10:61637878-61637879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535975461	chr10:61637898-61637899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557198210	chr10:61637956-61637957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140471640	chr10:61637980-61637981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545996443	chr10:61638053-61638054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs193279441	chr10:61638087-61638088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557983006	chr10:61638088-61638089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116164437	chr10:61638179-61638180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150397998	chr10:61638212-61638213	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs561756911	chr10:61638222-61638223	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs183810983	chr10:61638284-61638285	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541599576	chr10:61638297-61638298	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs374346600	chr10:61638310-61638311	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs544265442	chr10:61638334-61638335	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs578223770	chr10:61638568-61638569	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs117502156	chr10:61638573-61638574	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs77785202	chr10:61638597-61638598	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs572552997	chr10:61638641-61638642	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs546445151	chr10:61638657-61638658	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566765089	chr10:61638658-61638659	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs527621440	chr10:61638670-61638671	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs201104575	chr10:61638673-61638674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs4146652	chr10:61638677-61638678	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Obesity	21956041	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
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Urothelial carcinoma	21177765	CNVD
abnormal development	18461090	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	20643615	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2169 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61583200-61640600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:61624800-61641000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr10:61625000-61638800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr10:61625000-61655400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:61625200-61639200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr10:61628600-61638600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr10:61630000-61647800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr10:61633000-61637600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr10:61633000-61638200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:61633000-61638400	Weak transcription	Primary T cells from cord blood	blood
11	chr10:61633000-61638400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr10:61633000-61638400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr10:61633000-61639200	Weak transcription	Spleen	Spleen
14	chr10:61633000-61640600	Weak transcription	Gastric	stomach
15	chr10:61633200-61638600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:61633200-61638600	Weak transcription	A549	lung
17	chr10:61633200-61639400	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr10:61633200-61640600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:61633200-61641800	Weak transcription	Lung	lung
20	chr10:61633400-61637400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr10:61633400-61638000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr10:61633400-61638200	Weak transcription	Psoas Muscle	Psoas
23	chr10:61633400-61638600	Weak transcription	Thymus	Thymus
24	chr10:61633400-61638800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr10:61633400-61639400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:61633400-61643200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr10:61633400-61645200	Weak transcription	Fetal Thymus	thymus
28	chr10:61633400-61647800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr10:61633400-61647800	Weak transcription	Fetal Muscle Leg	muscle
30	chr10:61633400-61647800	Weak transcription	Fetal Stomach	stomach
31	chr10:61633400-61648600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr10:61633600-61637400	Weak transcription	NHDF-Ad	bronchial
33	chr10:61633600-61645200	Weak transcription	Brain Germinal Matrix	brain
34	chr10:61633800-61638400	Weak transcription	Liver	Liver
35	chr10:61634000-61637600	Weak transcription	Fetal Heart	heart
36	chr10:61634000-61640400	Weak transcription	Duodenum Mucosa	Duodenum
37	chr10:61634000-61645000	Weak transcription	Stomach Smooth Muscle	stomach
38	chr10:61634000-61645600	Weak transcription	Fetal Lung	lung
39	chr10:61634000-61646800	Weak transcription	Adipose Nuclei	Adipose
40	chr10:61634200-61637400	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr10:61634400-61637400	Weak transcription	Rectal Smooth Muscle	rectum
42	chr10:61634400-61638000	Weak transcription	Aorta	Aorta
43	chr10:61634400-61638200	Enhancers	GM12878-XiMat	blood
44	chr10:61634400-61640200	Enhancers	Colon Smooth Muscle	Colon
45	chr10:61634400-61648800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr10:61634400-61649000	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr10:61634400-61651200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr10:61634600-61638800	Weak transcription	Pancreas	Pancrea
49	chr10:61634600-61640600	Weak transcription	Left Ventricle	heart
50	chr10:61634800-61638200	Weak transcription	Sigmoid Colon	Sigmoid Colon

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