Variant report

Variant	nsv540458
Chromosome Location	chr10:3839308-3874184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1480)
CpG islands
(count:612)
Chromatin interactive
region (count:82)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1480 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:3856113-3856144	K562	blood:	n/a	n/a
2	ARID3A	chr10:3845156-3848452	K562	blood:	n/a	chr10:3845447-3845463
3	ARID3A	chr10:3867500-3867806	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:3852227-3853805	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:3873074-3873542	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:3855521-3855746	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:3870774-3871266	K562	blood:	n/a	n/a
8	ARID3A	chr10:3852306-3852934	K562	blood:	n/a	n/a
9	ARID3A	chr10:3847392-3847682	HepG2	liver:	n/a	n/a
10	ARID3A	chr10:3856109-3856619	HepG2	liver:	n/a	n/a
11	ATF1	chr10:3870442-3871021	K562	blood:	n/a	n/a
12	ATF1	chr10:3841209-3841407	K562	blood:	n/a	n/a
13	ATF1	chr10:3847428-3847793	K562	blood:	n/a	n/a
14	ATF1	chr10:3852316-3852744	K562	blood:	n/a	n/a
15	ATF1	chr10:3845667-3847024	K562	blood:	n/a	n/a
16	ATF1	chr10:3867490-3867798	K562	blood:	n/a	n/a
17	ATF2	chr10:3853309-3854255	GM12878	blood:	n/a	n/a
18	ATF2	chr10:3853521-3854167	GM12878	blood:	n/a	n/a
19	ATF2	chr10:3852111-3853035	GM12878	blood:	n/a	n/a
20	ATF2	chr10:3852179-3853147	GM12878	blood:	n/a	n/a
21	ATF2	chr10:3847925-3848629	GM12878	blood:	n/a	n/a
22	ATF2	chr10:3847271-3847916	GM12878	blood:	n/a	n/a
23	ATF2	chr10:3847378-3847800	GM12878	blood:	n/a	n/a
24	ATF2	chr10:3847981-3848681	GM12878	blood:	n/a	n/a
25	ATF3	chr10:3852183-3852802	A549	lung:	n/a	chr10:3852558-3852571
26	ATF3	chr10:3852126-3852872	HCT-116	colon:	n/a	chr10:3852558-3852571
27	ATF3	chr10:3852340-3852659	HepG2	liver:	n/a	chr10:3852558-3852571
28	ATF3	chr10:3846041-3846464	K562	blood:	n/a	n/a
29	ATF3	chr10:3847990-3848445	K562	blood:	n/a	n/a
30	ATF3	chr10:3867417-3867854	A549	lung:	n/a	n/a
31	BACH1	chr10:3845453-3846599	K562	blood:	n/a	n/a
32	BACH1	chr10:3845548-3846004	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr10:3847205-3847223	K562	blood:	n/a	n/a
34	BATF	chr10:3852131-3852646	GM12878	blood:	n/a	chr10:3852363-3852374
35	BATF	chr10:3847473-3847713	GM12878	blood:	n/a	chr10:3847548-3847559 chr10:3847549-3847559
36	BATF	chr10:3847381-3847792	GM12878	blood:	n/a	chr10:3847548-3847559 chr10:3847549-3847559
37	BATF	chr10:3853539-3854134	GM12878	blood:	n/a	n/a
38	BATF	chr10:3848038-3848494	GM12878	blood:	n/a	chr10:3848190-3848200
39	BATF	chr10:3852253-3852589	GM12878	blood:	n/a	chr10:3852363-3852374
40	BCL11A	chr10:3852290-3852572	GM12878	blood:	n/a	n/a
41	BCL11A	chr10:3853430-3854034	GM12878	blood:	n/a	n/a
42	BCL11A	chr10:3852197-3852923	GM12878	blood:	n/a	n/a
43	BCL11A	chr10:3848194-3848538	GM12878	blood:	n/a	n/a
44	BCL3	chr10:3852190-3852887	GM12878	blood:	n/a	n/a
45	BCL3	chr10:3847400-3847917	GM12878	blood:	n/a	n/a
46	BCL3	chr10:3848180-3848562	GM12878	blood:	n/a	chr10:3848189-3848198
47	BCL3	chr10:3852163-3852638	GM12878	blood:	n/a	n/a
48	BCL3	chr10:3844593-3845220	GM12878	blood:	n/a	n/a
49	BCL3	chr10:3844615-3845340	GM12878	blood:	n/a	n/a
50	BCL3	chr10:3853554-3854016	GM12878	blood:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:3862735-3862785	HCPEpiC	choroid plexus:	n/a
2	chr10:3868224-3868274	HRE	kidney:	n/a
3	chr10:3862735-3862785	HCPEpiC	choroid plexus:	n/a
4	chr10:3868224-3868274	HRE	kidney:	n/a
5	chr10:3850160-3850210	A549	lung:	n/a
6	chr10:3868224-3868274	AG04449	skin:	fetal
7	chr10:3871234-3871284	GM12892	blood:	n/a
8	chr10:3862735-3862785	GM19239	blood:	n/a
9	chr10:3870178-3870228	HCT-116	colon:	n/a
10	chr10:3862796-3862846	BE2_C	brain:	n/a
11	chr10:3870178-3870228	HCM	heart:	n/a
12	chr10:3862796-3862846	PFSK-1	brain:	n/a
13	chr10:3868224-3868274	AG09309	skin:	n/a
14	chr10:3853668-3853718	GM12892	blood:	n/a
15	chr10:3870178-3870228	PrEC	prostate:	n/a
16	chr10:3868336-3868386	PANC-1	pancreas:	n/a
17	chr10:3870178-3870228	NHDF-neo	bronchial:	n/a
18	chr10:3868493-3868543	SK-N-MC	brain:	n/a
19	chr10:3853668-3853718	SKMC	muscle:	n/a
20	chr10:3868336-3868386	H1-hESC	embryonic stem cell:	embryo
21	chr10:3862796-3862846	CMK	blood:	n/a
22	chr10:3868493-3868543	NH-A	brain:	n/a
23	chr10:3868493-3868543	HepG2	liver:	n/a
24	chr10:3868493-3868543	ECC-1	luminal epithelium:	n/a
25	chr10:3868493-3868543	GM06990	blood:	n/a
26	chr10:3853668-3853718	GM12891	blood:	n/a
27	chr10:3848384-3848434	HCT-116	colon:	n/a
28	chr10:3871234-3871284	HCF	heart:	n/a
29	chr10:3862796-3862846	H1-hESC	embryonic stem cell:	embryo
30	chr10:3870178-3870228	GM12878	blood:	n/a
31	chr10:3862735-3862785	AoSMC	blood vessel:	n/a
32	chr10:3868336-3868386	HRCEpiC	kidney:	n/a
33	chr10:3850160-3850210	ProgFib	skin:	n/a
34	chr10:3862796-3862846	HRCEpiC	kidney:	n/a
35	chr10:3868224-3868274	ECC-1	luminal epithelium:	n/a
36	chr10:3868224-3868274	SK-N-SH_RA	brain:	n/a
37	chr10:3868493-3868543	MCF-7	breast:	n/a
38	chr10:3862735-3862785	SK-N-MC	brain:	n/a
39	chr10:3862735-3862785	HRE	kidney:	n/a
40	chr10:3862796-3862846	HepG2	liver:	n/a
41	chr10:3848384-3848434	NT2-D1	testis:	n/a
42	chr10:3870178-3870228	PANC-1	pancreas:	n/a
43	chr10:3853668-3853718	NT2-D1	testis:	n/a
44	chr10:3868493-3868543	Caco-2	colon:	n/a
45	chr10:3862796-3862846	HL-60	blood:	n/a
46	chr10:3862796-3862846	A549	lung:	n/a
47	chr10:3850160-3850210	SK-N-MC	brain:	n/a
48	chr10:3862735-3862785	CMK	blood:	n/a
49	chr10:3848384-3848434	HIPEpiC	eye:	n/a
50	chr10:3862735-3862785	HRCEpiC	kidney:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:3847634..3849590-chr10:3852996..3855309,2	MCF-7	breast:
2	chr10:3829858..3831695-chr10:3839872..3841495,2	MCF-7	breast:
3	chr10:3854297..3857056-chr10:3857370..3862242,4	MCF-7	breast:
4	chr10:3846213..3848385-chr10:3895031..3897147,2	K562	blood:
5	chr10:3862123..3864079-chr10:3866800..3868917,2	K562	blood:
6	chr10:3851273..3854029-chr10:3860569..3863821,3	MCF-7	breast:
7	chr10:3848174..3849677-chr10:3873437..3875106,2	MCF-7	breast:
8	chr10:3873629..3875241-chr10:3930072..3932141,2	MCF-7	breast:
9	chr10:3851780..3854214-chr10:3872954..3875359,2	MCF-7	breast:
10	chr10:3866153..3869765-chr10:3871825..3874573,4	MCF-7	breast:
11	chr10:3847592..3850445-chr10:3893287..3894960,2	MCF-7	breast:
12	chr10:3838224..3841156-chr10:3850289..3853010,2	MCF-7	breast:
13	chr10:3847326..3850608-chr10:3890273..3893795,3	K562	blood:
14	chr10:3851673..3853403-chr10:3866040..3867619,2	MCF-7	breast:
15	chr10:3822110..3831216-chr10:3843525..3857606,41	MCF-7	breast:
16	chr10:3846136..3847799-chr10:3877909..3879695,2	K562	blood:
17	chr10:3844115..3845978-chr10:3894603..3897488,2	K562	blood:
18	chr10:3863367..3864956-chr10:3865204..3867871,2	MCF-7	breast:
19	chr10:3856210..3857914-chr10:3861188..3862923,2	K562	blood:
20	chr10:3872000..3874925-chr10:3876840..3879256,2	MCF-7	breast:
21	chr10:3824763..3831324-chr10:3865342..3876834,32	MCF-7	breast:
22	chr10:3872230..3874819-chr10:3880173..3882288,2	MCF-7	breast:
23	chr10:3864738..3867822-chr10:3868245..3870935,5	K562	blood:
24	chr10:3851797..3855219-chr10:3870977..3874184,3	MCF-7	breast:
25	chr10:3847609..3850397-chr10:3850957..3853100,3	MCF-7	breast:
26	chr10:3820450..3836478-chr10:3861249..3889254,84	K562	blood:
27	chr10:3851780..3854214-chr10:3872954..3875359,2	MCF-7	breast:
28	chr10:3851733..3853926-chr10:3916076..3917752,2	MCF-7	breast:
29	chr10:3847634..3849590-chr10:3852996..3855309,2	MCF-7	breast:
30	chr10:3856210..3857914-chr10:3861188..3862923,2	K562	blood:
31	chr10:3838224..3841156-chr10:3850289..3853010,2	MCF-7	breast:
32	chr10:3842625..3845056-chr10:3845647..3847558,3	MCF-7	breast:
33	chr10:3871384..3873040-chr10:3893634..3895396,2	MCF-7	breast:
34	chr10:3847609..3850397-chr10:3850957..3853100,3	MCF-7	breast:
35	chr10:3850418..3854705-chr10:3877438..3880204,3	K562	blood:
36	chr10:3844661..3847626-chr10:3892286..3894671,2	K562	blood:
37	chr10:3845321..3847632-chr10:3930350..3933088,2	K562	blood:
38	chr10:3544672..3546393-chr10:3846136..3849063,2	K562	blood:
39	chr10:3851797..3855219-chr10:3870977..3874184,3	MCF-7	breast:
40	chr10:3795979..3797716-chr10:3852548..3854370,2	MCF-7	breast:
41	chr10:3841262..3842953-chr10:3844726..3846302,2	MCF-7	breast:
42	chr10:3862123..3864079-chr10:3866800..3868917,2	K562	blood:
43	chr10:3845249..3847045-chr10:3927599..3930581,2	MCF-7	breast:
44	chr10:3872888..3874797-chr10:3878426..3880060,2	MCF-7	breast:
45	chr10:3864738..3867822-chr10:3868245..3870935,5	K562	blood:
46	chr10:3851673..3853403-chr10:3866040..3867619,2	MCF-7	breast:
47	chr10:3846512..3848264-chr10:3935343..3937709,2	K562	blood:
48	chr10:3854297..3857056-chr10:3857370..3862242,4	MCF-7	breast:
49	chr10:3872742..3874480-chr10:3876071..3877683,2	K562	blood:
50	chr10:3848332..3850077-chr10:3898448..3900637,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PFKP-32	chr10:3866142-3866429	NONHSAT011055
2	lnc-PFKP-32	chr10:3866673-3866920	NONHSAT011055

No data

Variant related genes	Relation type
ENSG00000230573	TF binding region
ENSG00000230573	CpG island
ENSG00000233321	chromatin interactions
ENSG00000067082	chromatin interactions
ENSG00000230573	chromatin interactions

Extended variants
information (count: 1710 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566211248	chr10:3839345-3839346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141139481	chr10:3839361-3839362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112300613	chr10:3839449-3839450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs180918778	chr10:3839451-3839452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs12253022	chr10:3839520-3839521	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs72771221	chr10:3839559-3839560	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs528960023	chr10:3839564-3839565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550701357	chr10:3839570-3839571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs568932686	chr10:3839601-3839602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539633027	chr10:3839625-3839626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7919841	chr10:3839642-3839643	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs555618577	chr10:3839659-3839660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2388851	chr10:3839746-3839747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs139217129	chr10:3839757-3839758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555331822	chr10:3839765-3839766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573706516	chr10:3839785-3839786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537901380	chr10:3839793-3839794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71477839	chr10:3839815-3839816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs74113831	chr10:3839836-3839837	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370774118	chr10:3839864-3839865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556221607	chr10:3839891-3839892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs117991696	chr10:3839916-3839917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184936131	chr10:3839993-3839994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs386740160	chr10:3840012-3840013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs79644013	chr10:3840013-3840014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10508266	chr10:3840014-3840015	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs371476002	chr10:3840022-3840023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190130766	chr10:3840041-3840042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560086938	chr10:3840057-3840058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562586318	chr10:3840069-3840070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs17249564	chr10:3840101-3840102	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551548135	chr10:3840145-3840146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183462070	chr10:3840226-3840227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566367783	chr10:3840236-3840237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186325257	chr10:3840293-3840294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542747693	chr10:3840307-3840308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548868265	chr10:3840318-3840319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76010946	chr10:3840342-3840343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537864513	chr10:3840366-3840367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11252107	chr10:3840374-3840375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192027430	chr10:3840382-3840383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs578047428	chr10:3840502-3840503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183346846	chr10:3840516-3840517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187984590	chr10:3840632-3840633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs534471971	chr10:3840633-3840634	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561411917	chr10:3840673-3840674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs376681139	chr10:3840688-3840689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142415474	chr10:3840794-3840795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543316740	chr10:3840827-3840828	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376753612	chr10:3840865-3840866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
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
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD

Chromatin state (count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:3829200-3843000	Weak transcription	Fetal Heart	heart
2	chr10:3829200-3844800	Weak transcription	Right Ventricle	heart
3	chr10:3833000-3847600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:3834800-3846600	Weak transcription	NHLF	lung
5	chr10:3835200-3843200	Weak transcription	Spleen	Spleen
6	chr10:3838600-3844800	Weak transcription	Gastric	stomach
7	chr10:3839400-3841000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr10:3840000-3840400	Enhancers	K562	blood
9	chr10:3840000-3840800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr10:3840000-3842000	Enhancers	Dnd41	blood
11	chr10:3840000-3846400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr10:3840200-3840400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr10:3840200-3840400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr10:3840400-3840600	Enhancers	HepG2	liver
15	chr10:3840400-3842400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr10:3840400-3844400	Weak transcription	K562	blood
17	chr10:3840600-3842000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr10:3840600-3843400	Weak transcription	HepG2	liver
19	chr10:3840800-3841800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr10:3841000-3841400	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr10:3841400-3844800	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr10:3841800-3846400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
23	chr10:3842000-3843600	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr10:3842000-3844600	Weak transcription	Dnd41	blood
25	chr10:3842000-3844800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr10:3842400-3843600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr10:3842400-3843800	Enhancers	Primary T cells from cord blood	blood
28	chr10:3842800-3843800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr10:3842800-3843800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr10:3842800-3846400	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr10:3842800-3846400	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr10:3843000-3843200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr10:3843000-3844600	Enhancers	Fetal Heart	heart
34	chr10:3843000-3847800	Enhancers	Primary T cells fromperipheralblood	blood
35	chr10:3843000-3852000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr10:3843200-3843400	Enhancers	Primary hematopoietic stem cells	blood
37	chr10:3843200-3843400	Enhancers	Placenta	Placenta
38	chr10:3843200-3843400	Enhancers	Lung	lung
39	chr10:3843200-3843400	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr10:3843200-3843400	Enhancers	Spleen	Spleen
41	chr10:3843200-3843600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr10:3843200-3844400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr10:3843200-3844600	Enhancers	Fetal Muscle Leg	muscle
44	chr10:3843400-3843600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr10:3843400-3843600	Enhancers	Fetal Lung	lung
46	chr10:3843400-3843800	Enhancers	Fetal Thymus	thymus
47	chr10:3843400-3843800	Enhancers	HepG2	liver
48	chr10:3843400-3844400	Weak transcription	Primary hematopoietic stem cells	blood
49	chr10:3843400-3844600	Weak transcription	Lung	lung
50	chr10:3843400-3845400	Enhancers	Left Ventricle	heart

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