Variant report

Variant	nsv895884
Chromosome Location	chr10:91861413-91959144
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	ATF2	chr10:91890317-91890862	GM12878	blood:	n/a	n/a
2	ATF2	chr10:91927258-91927862	GM12878	blood:	n/a	n/a
3	ATF2	chr10:91890093-91890911	GM12878	blood:	n/a	n/a
4	ATF2	chr10:91927400-91927804	GM12878	blood:	n/a	n/a
5	ATF3	chr10:91939363-91939912	HCT-116	colon:	n/a	n/a
6	BATF	chr10:91871473-91871730	GM12878	blood:	n/a	chr10:91871572-91871582
7	BATF	chr10:91927387-91927750	GM12878	blood:	n/a	n/a
8	BATF	chr10:91890152-91890374	GM12878	blood:	n/a	n/a
9	BATF	chr10:91890157-91890885	GM12878	blood:	n/a	chr10:91890837-91890847
10	BATF	chr10:91927485-91927777	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:91890115-91890841	GM12878	blood:	n/a	chr10:91890270-91890279
12	BCL11A	chr10:91927479-91927794	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:91871449-91871701	GM12878	blood:	n/a	n/a
14	BCL3	chr10:91927465-91927749	GM12878	blood:	n/a	n/a
15	BCLAF1	chr10:91896461-91896791	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:91927540-91927714	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:91890242-91890882	GM12878	blood:	n/a	n/a
18	BRCA1	chr10:91908318-91908467	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr10:91907039-91908782	HCT-116	colon:	n/a	n/a
20	CBX3	chr10:91896482-91896801	K562	blood:	n/a	n/a
21	CBX3	chr10:91939280-91939970	HCT-116	colon:	n/a	n/a
22	CBX3	chr10:91896309-91897039	HCT-116	colon:	n/a	n/a
23	CBX3	chr10:91896466-91896862	K562	blood:	n/a	n/a
24	CBX3	chr10:91871218-91872034	HCT-116	colon:	n/a	n/a
25	CBX3	chr10:91896401-91897009	HCT-116	colon:	n/a	n/a
26	CEBPB	chr10:91902785-91903021	Hela-S3	cervix:	n/a	chr10:91902891-91902902
27	CEBPB	chr10:91862909-91863194	HepG2	liver:	n/a	chr10:91863019-91863030
28	CEBPB	chr10:91885885-91885964	A549	lung:	n/a	chr10:91885912-91885923
29	CEBPB	chr10:91921659-91921850	HepG2	liver:	n/a	chr10:91921727-91921738 chr10:91921728-91921739
30	CEBPB	chr10:91939218-91940011	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
31	CEBPB	chr10:91927556-91927750	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:91907213-91908758	HCT-116	colon:	n/a	chr10:91908254-91908266 chr10:91907431-91907442
33	CEBPB	chr10:91939385-91939711	HepG2	liver:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
34	CEBPB	chr10:91939420-91939777	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
35	CEBPB	chr10:91939318-91939779	A549	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
36	CEBPB	chr10:91939168-91940050	HCT-116	colon:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
37	CEBPB	chr10:91927401-91927883	HCT-116	colon:	n/a	chr10:91927539-91927550
38	CEBPB	chr10:91862941-91863191	A549	lung:	n/a	chr10:91863019-91863030
39	CEBPB	chr10:91902748-91903062	HepG2	liver:	n/a	chr10:91902891-91902902
40	CEBPB	chr10:91885896-91885946	IMR90	lung:	n/a	chr10:91885912-91885923
41	CEBPB	chr10:91891142-91891155	A549	lung:	n/a	n/a
42	CEBPB	chr10:91927610-91927719	HepG2	liver:	n/a	n/a
43	CEBPB	chr10:91907712-91908308	HCT-116	colon:	n/a	chr10:91908254-91908266
44	CEBPB	chr10:91893492-91893648	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr10:91902812-91902978	A549	lung:	n/a	chr10:91902891-91902902
46	CEBPB	chr10:91927487-91927750	Hela-S3	cervix:	n/a	chr10:91927539-91927550
47	CEBPB	chr10:91939310-91939832	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
48	CEBPB	chr10:91862945-91863195	IMR90	lung:	n/a	chr10:91863019-91863030
49	CEBPB	chr10:91939266-91939861	MCF-7	breast:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566
50	CEBPB	chr10:91939390-91939807	IMR90	lung:	n/a	chr10:91939553-91939564 chr10:91939555-91939564 chr10:91939553-91939566 chr10:91939555-91939566

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91919031-91919081	A549	lung:	n/a
2	chr10:91919031-91919081	AG10803	skin:	n/a
3	chr10:91919031-91919081	MCF-7	breast:	n/a
4	chr10:91919031-91919081	AG04449	skin:	fetal
5	chr10:91919031-91919081	AG09309	skin:	n/a
6	chr10:91919031-91919081	HPAEpiC	pulmonary alveolar:	n/a
7	chr10:91919031-91919081	Caco-2	colon:	n/a
8	chr10:91919031-91919081	CMK	blood:	n/a
9	chr10:91919031-91919081	PFSK-1	brain:	n/a
10	chr10:91919031-91919081	AG04450	lung:	fetal
11	chr10:91919031-91919081	HRE	kidney:	n/a
12	chr10:91919031-91919081	GM19239	blood:	n/a
13	chr10:91919031-91919081	AoSMC	blood vessel:	n/a
14	chr10:91919031-91919081	ProgFib	skin:	n/a
15	chr10:91919031-91919081	BJ	skin:	n/a
16	chr10:91919031-91919081	HUVEC	blood vessel:	n/a
17	chr10:91919031-91919081	AG09319	gingival:	n/a
18	chr10:91919031-91919081	NB4	blood:	n/a
19	chr10:91919031-91919081	SK-N-MC	brain:	n/a
20	chr10:91919031-91919081	HCPEpiC	choroid plexus:	n/a
21	chr10:91919031-91919081	NHBE	bronchial:	n/a
22	chr10:91919031-91919081	GM06990	blood:	n/a
23	chr10:91919031-91919081	HCF	heart:	n/a
24	chr10:91919031-91919081	HAEpiC	amniotic membrane:	n/a
25	chr10:91919031-91919081	Hela-S3	cervix:	n/a
26	chr10:91919031-91919081	H1-hESC	embryonic stem cell:	embryo
27	chr10:91919031-91919081	U87	brain:	n/a
28	chr10:91919031-91919081	MCF10A-Er-Src	breast:	n/a
29	chr10:91919031-91919081	GM12891	blood:	n/a
30	chr10:91919031-91919081	IMR90	lung:	fetal
31	chr10:91919031-91919081	HL-60	blood:	n/a
32	chr10:91919031-91919081	ECC-1	luminal epithelium:	n/a
33	chr10:91919031-91919081	Hepatocyte	liver:	n/a
34	chr10:91919031-91919081	RPTEC	kidney:	n/a
35	chr10:91919031-91919081	HEEpiC	esophagus:	n/a
36	chr10:91919031-91919081	T-47D	breast:	n/a
37	chr10:91919031-91919081	SAEC	small airway:	n/a
38	chr10:91919031-91919081	GM12878	blood:	n/a
39	chr10:91919031-91919081	HEK293	kidney:	embryo
40	chr10:91919031-91919081	SK-N-SH	brain:	n/a
41	chr10:91919031-91919081	HepG2	liver:	n/a
42	chr10:91919031-91919081	HCT-116	colon:	n/a
43	chr10:91919031-91919081	NH-A	brain:	n/a
44	chr10:91919031-91919081	HCM	heart:	n/a
45	chr10:91919031-91919081	LNCaP	prostate:	n/a
46	chr10:91919031-91919081	NHDF-neo	bronchial:	n/a
47	chr10:91919031-91919081	Jurkat	blood:	n/a
48	chr10:91919031-91919081	NT2-D1	testis:	n/a
49	chr10:91919031-91919081	SK-N-SH_RA	brain:	n/a
50	chr10:91919031-91919081	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:91900968..91904082-chr10:91905876..91909843,4	MCF-7	breast:
2	chr10:91905536..91908500-chr10:91908685..91910985,2	K562	blood:
3	chr10:91886442..91889438-chr10:91891894..91894771,2	MCF-7	breast:
4	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
5	chr10:91908033..91909093-chr10:92411955..92412824,3	MCF-7	breast:
6	chr10:91908037..91908636-chr10:92339006..92340002,2	MCF-7	breast:
7	chr10:91553240..91554032-chr10:91898333..91899226,2	MCF-7	breast:
8	chr10:91908451..91909024-chr10:92048226..92048868,2	MCF-7	breast:
9	chr10:91931353..91933621-chr10:91948075..91950614,2	K562	blood:
10	chr10:91899658..91901656-chr3:161118536..161120894,2	MCF-7	breast:
11	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:
12	chr10:91907918..91908914-chr10:92477743..92478315,2	MCF-7	breast:
13	chr10:91938353..91941143-chr10:91951885..91953423,2	MCF-7	breast:
14	chr10:91908029..91908801-chr10:92352406..92353300,3	MCF-7	breast:
15	chr10:91553149..91554039-chr10:91898323..91899074,3	MCF-7	breast:
16	chr10:91886442..91889438-chr10:91891894..91894771,2	MCF-7	breast:
17	chr10:91905536..91908500-chr10:91908685..91910985,2	K562	blood:
18	chr10:91900968..91904082-chr10:91905876..91909843,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF20B-5	chr10:91923670-91923893	XLOC_008555
2	lnc-KIF20B-8	chr10:91939472-91939926	NONHSAT015584
3	lnc-PANK1-8	chr10:91923408-91923717	NONHSAT015582
4	lnc-KIF20B-8	chr10:91924526-91924552	NONHSAT015584

Variant related genes	Relation type
RN7SKP143	TF binding region
RN7SKP143	CpG island

Extended variants
information (count: 3804 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3804 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10444056	chr10:91861413-91861414	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10444057	chr10:91861432-91861433	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs369032267	chr10:91861446-91861447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537588681	chr10:91861461-91861462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371437776	chr10:91861518-91861519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35016286	chr10:91861626-91861627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs397845926	chr10:91861628-91861629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11819051	chr10:91861644-91861645	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs151325946	chr10:91861650-91861651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546340832	chr10:91861664-91861665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553410280	chr10:91861673-91861674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140566085	chr10:91861677-91861678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186518840	chr10:91861690-91861691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369772178	chr10:91861720-91861721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560597812	chr10:91861751-91861752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529598045	chr10:91861761-91861762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367956583	chr10:91861766-91861767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374574857	chr10:91861767-91861768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3078014	chr10:91861802-91861803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71306845	chr10:91861803-91861804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543124122	chr10:91861819-91861820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57972880	chr10:91861851-91861852	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532228663	chr10:91861861-91861862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552376926	chr10:91861911-91861912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565721008	chr10:91861914-91861915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554261679	chr10:91861923-91861924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574423326	chr10:91861941-91861942	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528436673	chr10:91861950-91861951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548500088	chr10:91861954-91861955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs568466377	chr10:91862016-91862017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189697116	chr10:91862025-91862026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537399239	chr10:91862032-91862033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555675615	chr10:91862039-91862040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145780951	chr10:91862062-91862063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553451486	chr10:91862071-91862072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577504412	chr10:91862077-91862078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376992365	chr10:91862094-91862095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539538583	chr10:91862219-91862220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs180861796	chr10:91862225-91862226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573101315	chr10:91862232-91862233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542123008	chr10:91862250-91862251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555600598	chr10:91862308-91862309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574110544	chr10:91862325-91862326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546513582	chr10:91862335-91862336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs552588819	chr10:91862349-91862350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547185238	chr10:91862362-91862363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139625562	chr10:91862377-91862378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs137944609	chr10:91862407-91862408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112613746	chr10:91862432-91862433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140876469	chr10:91862469-91862470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
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
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	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
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91847200-91869400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:91860000-91862000	Strong transcription	Primary B cells from cord blood	blood
3	chr10:91862000-91870200	Weak transcription	Primary B cells from cord blood	blood
4	chr10:91868200-91869600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr10:91869400-91869600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr10:91871000-91872800	Enhancers	HMEC	breast
7	chr10:91871200-91872400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:91871200-91872600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:91871400-91871800	Enhancers	Osteobl	bone
10	chr10:91871400-91872400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:91871600-91872200	Enhancers	NH-A	brain
12	chr10:91871600-91872400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:91871600-91872400	Enhancers	Aorta	Aorta
14	chr10:91871800-91872000	Flanking Active TSS	Osteobl	bone
15	chr10:91871800-91872400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr10:91871800-91872400	Enhancers	HSMM	muscle
17	chr10:91872000-91872200	Enhancers	Osteobl	bone
18	chr10:91872200-91872400	Flanking Active TSS	Osteobl	bone
19	chr10:91872400-91884400	Weak transcription	Aorta	Aorta
20	chr10:91879400-91880000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:91883600-91885200	Enhancers	Osteobl	bone
22	chr10:91883800-91884000	Enhancers	NHLF	lung
23	chr10:91883800-91885200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr10:91884000-91885000	Weak transcription	NHLF	lung
25	chr10:91884200-91886600	Enhancers	Brain Germinal Matrix	brain
26	chr10:91884400-91884600	Enhancers	Aorta	Aorta
27	chr10:91884400-91885400	Enhancers	Stomach Smooth Muscle	stomach
28	chr10:91884400-91885600	Enhancers	Brain Hippocampus Middle	brain
29	chr10:91884400-91886400	Enhancers	Fetal Muscle Leg	muscle
30	chr10:91884600-91885200	Weak transcription	Aorta	Aorta
31	chr10:91884600-91886000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr10:91884600-91886600	Enhancers	Fetal Stomach	stomach
33	chr10:91884600-91886600	Enhancers	NH-A	brain
34	chr10:91884800-91886200	Enhancers	Fetal Brain Female	brain
35	chr10:91884800-91886400	Enhancers	Brain Angular Gyrus	brain
36	chr10:91884800-91886400	Enhancers	Brain Anterior Caudate	brain
37	chr10:91885000-91886000	Enhancers	Brain Cingulate Gyrus	brain
38	chr10:91885000-91886200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr10:91885000-91886200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr10:91885000-91886400	Enhancers	Fetal Lung	lung
41	chr10:91885000-91886400	Enhancers	NHLF	lung
42	chr10:91885000-91887200	Enhancers	Brain Substantia Nigra	brain
43	chr10:91885200-91885400	Enhancers	Psoas Muscle	Psoas
44	chr10:91885200-91885600	Flanking Active TSS	Osteobl	bone
45	chr10:91885200-91885800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:91885200-91886000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr10:91885200-91886000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr10:91885200-91886000	Enhancers	Fetal Brain Male	brain
49	chr10:91885200-91886000	Enhancers	HSMM	muscle
50	chr10:91885200-91886200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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