Variant report

Variant	esv16395
Chromosome Location	chr10:38693709-38772324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr10:38731742-38731980	GM12878	blood:	n/a	n/a
2	BHLHE40	chr10:38767051-38767303	HepG2	liver:	n/a	n/a
3	BHLHE40	chr10:38770634-38770874	HepG2	liver:	n/a	n/a
4	CBX3	chr10:38738233-38738485	K562	blood:	n/a	n/a
5	CEBPB	chr10:38726503-38726522	HepG2	liver:	n/a	chr10:38726511-38726522
6	CEBPB	chr10:38738268-38738409	HepG2	liver:	n/a	n/a
7	CEBPB	chr10:38738701-38739205	HepG2	liver:	n/a	n/a
8	CEBPB	chr10:38738324-38738533	K562	blood:	n/a	n/a
9	CEBPB	chr10:38729575-38729703	K562	blood:	n/a	n/a
10	CEBPB	chr10:38759806-38760305	K562	blood:	n/a	n/a
11	CEBPB	chr10:38738721-38738938	K562	blood:	n/a	n/a
12	CEBPB	chr10:38726323-38726688	IMR90	lung:	n/a	chr10:38726511-38726522
13	CEBPB	chr10:38738140-38738564	K562	blood:	n/a	n/a
14	CEBPD	chr10:38754891-38755311	K562	blood:	n/a	n/a
15	CEBPD	chr10:38759787-38760324	K562	blood:	n/a	n/a
16	CTCF	chr10:38770755-38770860	Kidney_OC	kidney:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
17	CTCF	chr10:38770761-38770955	GM12878	blood:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
18	CTCF	chr10:38736002-38736409	K562	blood:	n/a	n/a
19	CTCF	chr10:38705040-38705190	GM12871	blood:	n/a	n/a
20	CTCF	chr10:38737848-38738144	K562	blood:	n/a	chr10:38737969-38737982
21	CTCF	chr10:38770680-38770830	Caco-2	colon:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
22	CTCF	chr10:38770700-38770850	MCF-7	breast:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
23	CTCF	chr10:38770660-38770810	Caco-2	colon:	n/a	n/a
24	CTCF	chr10:38770727-38770872	Gliobla	brain:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
25	CTCF	chr10:38770660-38770810	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr10:38741240-38741390	K562	blood:	n/a	n/a
27	CTCF	chr10:38770720-38770870	RPTEC	kidney:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
28	CTCF	chr10:38770680-38770830	HA-sp	spinal cord:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
29	CTCF	chr10:38770712-38770902	MCF-7	breast:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
30	CTCF	chr10:38741260-38741410	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr10:38735940-38736090	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr10:38737816-38738174	K562	blood:	n/a	chr10:38737969-38737982
33	CTCF	chr10:38770680-38770830	AG04450	lung:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
34	CTCF	chr10:38770772-38770892	GM10248	blood:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
35	CTCF	chr10:38770680-38770830	GM12875	blood:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
36	CTCF	chr10:38735940-38736090	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr10:38770739-38770893	LNCaP	prostate:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
38	CTCF	chr10:38770680-38770830	HepG2	liver:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
39	CTCF	chr10:38770700-38770850	RPTEC	kidney:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
40	CTCF	chr10:38705133-38705217	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:38770640-38770790	NHEK	skin:	n/a	n/a
42	CTCF	chr10:38770715-38770911	Hela-S3	cervix:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
43	CTCF	chr10:38737072-38737492	K562	blood:	n/a	chr10:38737453-38737462 chr10:38737449-38737462 chr10:38737447-38737465 chr10:38737450-38737460 chr10:38737191-38737209 chr10:38737442-38737463
44	CTCF	chr10:38770725-38770850	GM19240	blood:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
45	CTCF	chr10:38735960-38736110	RPTEC	kidney:	n/a	n/a
46	CTCF	chr10:38705136-38705221	MCF-7	breast:	n/a	n/a
47	CTCF	chr10:38735968-38736226	K562	blood:	n/a	n/a
48	CTCF	chr10:38737340-38737490	A549	lung:	n/a	chr10:38737453-38737462 chr10:38737449-38737462 chr10:38737447-38737465 chr10:38737450-38737460 chr10:38737442-38737463
49	CTCF	chr10:38770527-38771017	A549	lung:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825
50	CTCF	chr10:38770720-38770870	HCT-116	colon:	n/a	chr10:38770805-38770818 chr10:38770805-38770813 chr10:38770802-38770820 chr10:38770804-38770825

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:38739506-38739556	NHDF-neo	bronchial:	n/a
2	chr10:38739506-38739556	NHDF-neo	bronchial:	n/a
3	chr10:38716268-38716318	HEEpiC	esophagus:	n/a
4	chr10:38716291-38716341	Hela-S3	cervix:	n/a
5	chr10:38739885-38739935	GM12891	blood:	n/a
6	chr10:38739885-38739935	H1-hESC	embryonic stem cell:	embryo
7	chr10:38739819-38739869	HRE	kidney:	n/a
8	chr10:38716291-38716341	K562	blood:	n/a
9	chr10:38739478-38739528	Hela-S3	cervix:	n/a
10	chr10:38716268-38716318	Jurkat	blood:	n/a
11	chr10:38715824-38715874	HRCEpiC	kidney:	n/a
12	chr10:38716291-38716341	AG09319	gingival:	n/a
13	chr10:38740319-38740369	HMEC	breast:	n/a
14	chr10:38739506-38739556	MCF10A-Er-Src	breast:	n/a
15	chr10:38763980-38764030	HMEC	breast:	n/a
16	chr10:38740029-38740079	HCPEpiC	choroid plexus:	n/a
17	chr10:38739849-38739899	ProgFib	skin:	n/a
18	chr10:38738647-38738697	IMR90	lung:	fetal
19	chr10:38738647-38738697	GM06990	blood:	n/a
20	chr10:38740029-38740079	SK-N-MC	brain:	n/a
21	chr10:38738647-38738697	K562	blood:	n/a
22	chr10:38716268-38716318	SK-N-MC	brain:	n/a
23	chr10:38739478-38739528	MCF-7	breast:	n/a
24	chr10:38740319-38740369	RPTEC	kidney:	n/a
25	chr10:38715824-38715874	HNPCEpiC	eye:	n/a
26	chr10:38763980-38764030	Hela-S3	cervix:	n/a
27	chr10:38763980-38764030	H1-hESC	embryonic stem cell:	embryo
28	chr10:38763980-38764030	HPAEpiC	pulmonary alveolar:	n/a
29	chr10:38763980-38764030	HCM	heart:	n/a
30	chr10:38738647-38738697	SK-N-SH	brain:	n/a
31	chr10:38738941-38738991	AG04449	skin:	fetal
32	chr10:38739849-38739899	HCM	heart:	n/a
33	chr10:38763980-38764030	ProgFib	skin:	n/a
34	chr10:38739506-38739556	PrEC	prostate:	n/a
35	chr10:38743472-38743522	NH-A	brain:	n/a
36	chr10:38743472-38743522	BE2_C	brain:	n/a
37	chr10:38762797-38762847	MCF10A-Er-Src	breast:	n/a
38	chr10:38740029-38740079	IMR90	lung:	fetal
39	chr10:38739506-38739556	Hela-S3	cervix:	n/a
40	chr10:38739819-38739869	BE2_C	brain:	n/a
41	chr10:38762797-38762847	HRCEpiC	kidney:	n/a
42	chr10:38739885-38739935	HRPEpiC	eye:	n/a
43	chr10:38738647-38738697	Jurkat	blood:	n/a
44	chr10:38715824-38715874	GM06990	blood:	n/a
45	chr10:38715824-38715874	AG04449	skin:	fetal
46	chr10:38716268-38716318	HepG2	liver:	n/a
47	chr10:38763980-38764030	HL-60	blood:	n/a
48	chr10:38715824-38715874	K562	blood:	n/a
49	chr10:38716268-38716318	K562	blood:	n/a
50	chr10:38715824-38715874	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:38770309..38770829-chr14:75039895..75040581,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF37A-3	chr10:38711696-38711926	ENSG00000225119.2
2	lnc-ZNF37A-3	chr10:38714747-38714811	ENSG00000225119.2
3	lnc-ZNF37A-3	chr10:38736592-38737700	ENSG00000225119.2
4	lnc-ZNF37A-3	chr10:38705610-38706132	ENSG00000225119.2
5	lnc-ZNF37A-4	chr10:38754897-38755311	ENSG00000203496
6	lnc-ZNF37A-3	chr10:38736592-38736649	ENSG00000225119.2
7	lnc-ZNF37A-4	chr10:38742109-38742458	ENSG00000203496.4
8	lnc-ZNF37A-3	chr10:38724058-38724181	ENSG00000225119.2
9	lnc-ZNF37A-3	chr10:38734345-38734535	ENSG00000225119.2
10	lnc-ZNF37A-4	chr10:38746609-38746777	ENSG00000203496.4
11	lnc-ZNF37A-4	chr10:38742109-38742458	ENSG00000203496
12	lnc-ZNF37A-3	chr10:38724228-38724691	XLOC_008461
13	lnc-ZNF37A-3	chr10:38717074-38717224	ENSG00000225119.2
14	lnc-ZNF37A-3	chr10:38736591-38736649	XLOC_008461
15	lnc-ZNF37A-3	chr10:38726472-38726679	ENSG00000225119.2
16	lnc-ZNF37A-3	chr10:38727786-38727798	NONHSAT012824
17	lnc-ZNF37A-3	chr10:38704472-38704530	ENSG00000225119.2
18	lnc-ZNF37A-3	chr10:38701156-38701371	ENSG00000225119.2
19	lnc-ZNF37A-3	chr10:38725679-38725788	ENSG00000225119.2
20	lnc-ZNF37A-3	chr10:38724058-38724486	XLOC_008461
21	lnc-ZNF37A-3	chr10:38734345-38734535	ENSG00000225119.2
22	lnc-ZNF37A-4	chr10:38754897-38755104	ENSG00000203496.4
23	lnc-ZNF37A-3	chr10:38696559-38696668	ENSG00000225119.2
24	lnc-ZNF37A-3	chr10:38702255-38702320	ENSG00000225119.2
25	lnc-ZNF37A-3	chr10:38734345-38734535	XLOC_008461
26	lnc-ZNF37A-3	chr10:38727786-38727850	ENSG00000225119.2
27	lnc-ZNF37A-3	chr10:38733470-38733591	XLOC_008461
28	lnc-ZNF37A-3	chr10:38714747-38714811	XLOC_008461
29	lnc-ZNF37A-3	chr10:38727786-38727954	ENSG00000225119.2
30	lnc-ZNF37A-3	chr10:38697731-38697862	ENSG00000225119.2
31	lnc-ZNF37A-3	chr10:38726018-38726134	ENSG00000225119.2
32	lnc-ZNF37A-3	chr10:38724058-38724184	XLOC_008461
33	lnc-ZNF37A-3	chr10:38733473-38733591	ENSG00000225119.2
34	lnc-ZNF37A-3	chr10:38736592-38736649	XLOC_008461
35	lnc-ZNF37A-3	chr10:38726472-38726668	ENSG00000225119.2
36	lnc-ZNF37A-3	chr10:38736743-38736820	ENSG00000225119.2
37	lnc-ZNF37A-3	chr10:38726018-38726134	ENSG00000225119.2
38	lnc-ZNF37A-3	chr10:38716834-38717224	XLOC_008461
39	lnc-ZNF37A-3	chr10:38701657-38701810	ENSG00000225119.2
40	lnc-ZNF37A-3	chr10:38714788-38714811	XLOC_008461
41	lnc-ZNF37A-3	chr10:38726276-38726679	NONHSAT012824
42	lnc-ZNF37A-3	chr10:38736743-38736965	XLOC_008461
43	lnc-ZNF37A-4	chr10:38746609-38746777	ENSG00000203496
44	lnc-ZNF37A-3	chr10:38717035-38717224	XLOC_008461

Variant related genes	Relation type
CICP9	TF binding region
RNU6-1118P	TF binding region
SEPT7P9	TF binding region
ENSG00000203496	TF binding region
LINC00999	TF binding region
CICP9	CpG island
RNU6-1118P	CpG island
SEPT7P9	CpG island
ENSG00000203496	CpG island
LINC00999	CpG island
SAPS3	miRNA target sites

Extended variants
information (count: 1963 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:1963 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145633148	chr10:38693855-38693856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs548494500	chr10:38693860-38693861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61837220	chr10:38693873-38693874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568212754	chr10:38693878-38693879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536391519	chr10:38693896-38693897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556611296	chr10:38693902-38693903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377256137	chr10:38693906-38693907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576392701	chr10:38693916-38693917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376249220	chr10:38693944-38693945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372244126	chr10:38694130-38694131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538999613	chr10:38694131-38694132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558491482	chr10:38694155-38694156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572418794	chr10:38694179-38694180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541284040	chr10:38694203-38694204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112845149	chr10:38694209-38694210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2754373	chr10:38694218-38694219	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs368098103	chr10:38694221-38694222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574968694	chr10:38694225-38694226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372602897	chr10:38694226-38694227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs371887645	chr10:38694242-38694243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543190282	chr10:38694261-38694262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563375749	chr10:38694283-38694284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532081658	chr10:38694335-38694336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113654826	chr10:38694339-38694340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552219597	chr10:38694347-38694348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372899223	chr10:38694352-38694353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373398868	chr10:38694389-38694390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370137884	chr10:38694432-38694433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373100522	chr10:38694434-38694435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528396996	chr10:38694435-38694436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11498332	chr10:38694539-38694540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11498333	chr10:38694544-38694545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11498334	chr10:38694575-38694576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11498335	chr10:38694585-38694586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548498292	chr10:38694606-38694607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs3897151	chr10:38694671-38694672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568203635	chr10:38694685-38694686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530716161	chr10:38694701-38694702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550032207	chr10:38694710-38694711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189737892	chr10:38694729-38694730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538710929	chr10:38694759-38694760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558536239	chr10:38694760-38694761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192437095	chr10:38694763-38694764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536775659	chr10:38694766-38694767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535028050	chr10:38694813-38694814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374524311	chr10:38694828-38694829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184416189	chr10:38694847-38694848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7097955	chr10:38694857-38694858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566892069	chr10:38694878-38694879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7082201	chr10:38694886-38694887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Lung cancer	21569311	CNVD
Colorectal cancer	20459617	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Central neurocytomas	17123091	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:221 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38691800-38698000	Weak transcription	Spleen	Spleen
2	chr10:38692200-38741000	Weak transcription	Aorta	Aorta
3	chr10:38692400-38739600	Weak transcription	Gastric	stomach
4	chr10:38692600-38698000	Weak transcription	Ovary	ovary
5	chr10:38692600-38699400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:38692600-38716400	Weak transcription	Primary T cells from cord blood	blood
7	chr10:38692600-38736800	Weak transcription	Pancreas	Pancrea
8	chr10:38692600-38737200	Weak transcription	Esophagus	oesophagus
9	chr10:38692800-38698000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:38692800-38698000	Weak transcription	Lung	lung
11	chr10:38692800-38699800	Weak transcription	Fetal Stomach	stomach
12	chr10:38692800-38700000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr10:38692800-38700200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr10:38692800-38701800	Weak transcription	Fetal Intestine Small	intestine
15	chr10:38692800-38703200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:38692800-38709200	Weak transcription	Adipose Nuclei	Adipose
17	chr10:38692800-38714600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr10:38692800-38728800	Weak transcription	Brain Substantia Nigra	brain
19	chr10:38692800-38736800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr10:38692800-38736800	Weak transcription	Brain Anterior Caudate	brain
21	chr10:38692800-38736800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr10:38692800-38737200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr10:38692800-38737200	Weak transcription	Brain Hippocampus Middle	brain
24	chr10:38692800-38737400	Weak transcription	Fetal Intestine Large	intestine
25	chr10:38692800-38737600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr10:38692800-38741200	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:38693000-38697200	Weak transcription	Liver	Liver
28	chr10:38693000-38698000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr10:38693000-38698000	Weak transcription	Left Ventricle	heart
30	chr10:38693000-38700000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:38693000-38700200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr10:38693000-38714000	Weak transcription	Right Ventricle	heart
33	chr10:38693000-38716000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr10:38693000-38736800	Weak transcription	Stomach Smooth Muscle	stomach
35	chr10:38693000-38737200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr10:38693000-38737200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr10:38693000-38737200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr10:38693000-38737200	Weak transcription	Fetal Muscle Leg	muscle
39	chr10:38693000-38737400	Weak transcription	Placenta	Placenta
40	chr10:38693000-38739200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr10:38693200-38698000	Weak transcription	Fetal Muscle Trunk	muscle
42	chr10:38693200-38699800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr10:38697200-38700600	Strong transcription	Liver	Liver
44	chr10:38698000-38698600	Genic enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:38698000-38698600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr10:38698000-38698600	Strong transcription	Ovary	ovary
47	chr10:38698000-38698600	Strong transcription	Spleen	Spleen
48	chr10:38698000-38698800	Strong transcription	Fetal Muscle Trunk	muscle
49	chr10:38698000-38698800	Strong transcription	Left Ventricle	heart
50	chr10:38698000-38698800	Strong transcription	Lung	lung

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