Variant report

Variant	nsv1048021
Chromosome Location	chr10:91703053-91748404
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	chr10:91719469-91719945	GM12878	blood:	n/a	n/a
2	BATF	chr10:91719496-91719906	GM12878	blood:	n/a	n/a
3	BATF	chr10:91714636-91715272	GM12878	blood:	n/a	n/a
4	BATF	chr10:91719389-91719943	GM12878	blood:	n/a	n/a
5	BCL11A	chr10:91719406-91719973	GM12878	blood:	n/a	chr10:91719732-91719741
6	BCL11A	chr10:91719240-91719880	GM12878	blood:	n/a	chr10:91719377-91719386 chr10:91719732-91719741
7	CEBPB	chr10:91703950-91704236	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr10:91717700-91717924	A549	lung:	n/a	chr10:91717835-91717846
9	CEBPB	chr10:91707769-91708041	HepG2	liver:	n/a	chr10:91707878-91707889
10	CEBPB	chr10:91707746-91708068	A549	lung:	n/a	chr10:91707878-91707889
11	CEBPB	chr10:91717668-91718002	HepG2	liver:	n/a	chr10:91717835-91717846
12	CEBPB	chr10:91739929-91740217	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:91707750-91708023	IMR90	lung:	n/a	chr10:91707878-91707889
14	CEBPB	chr10:91717719-91717919	IMR90	lung:	n/a	chr10:91717835-91717846
15	CTCF	chr10:91714620-91714770	GM12873	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
16	CTCF	chr10:91714368-91714413	Gliobla	brain:	n/a	n/a
17	CTCF	chr10:91714660-91714810	HPAF	blood vessel:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
18	CTCF	chr10:91714980-91715130	HRPEpiC	eye:	n/a	n/a
19	CTCF	chr10:91714556-91714870	HUVEC	blood vessel:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
20	CTCF	chr10:91714395-91714462	GM12878	blood:	n/a	n/a
21	CTCF	chr10:91714580-91714730	BJ	skin:	n/a	n/a
22	CTCF	chr10:91714060-91714210	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr10:91714360-91714510	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr10:91714500-91714650	GM12867	blood:	n/a	n/a
25	CTCF	chr10:91714600-91714750	WI-38	lung:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
26	CTCF	chr10:91714640-91714790	GM12874	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
27	CTCF	chr10:91714620-91714770	SK-N-SH_RA	brain:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
28	CTCF	chr10:91714680-91714830	AG09319	gingival:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
29	CTCF	chr10:91714540-91714690	GM06990	blood:	n/a	n/a
30	CTCF	chr10:91714643-91714815	LNCaP	prostate:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
31	CTCF	chr10:91714620-91714770	RPTEC	kidney:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
32	CTCF	chr10:91714445-91714921	GM12878	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
33	CTCF	chr10:91714674-91714795	GM10266	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
34	CTCF	chr10:91714560-91714710	SAEC	small airway:	n/a	n/a
35	CTCF	chr10:91715120-91715270	HCM	heart:	n/a	n/a
36	CTCF	chr10:91714600-91714750	HBMEC	blood vessel:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
37	CTCF	chr10:91714280-91714430	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr10:91714640-91714790	HCT-116	colon:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
39	CTCF	chr10:91714560-91714710	HVMF	connective:	n/a	n/a
40	CTCF	chr10:91714640-91714790	HMEC	breast:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
41	CTCF	chr10:91714640-91714790	AG04449	skin:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
42	CTCF	chr10:91714620-91714799	GM10248	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
43	CTCF	chr10:91714313-91714366	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr10:91714320-91714470	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr10:91714460-91714610	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr10:91714620-91714770	GM12871	blood:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
47	CTCF	chr10:91714580-91714730	GM12873	blood:	n/a	n/a
48	CTCF	chr10:91714720-91714870	HVMF	connective:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
49	CTCF	chr10:91714640-91714790	AG09319	gingival:	n/a	chr10:91714722-91714738 chr10:91714726-91714734 chr10:91714721-91714739 chr10:91714723-91714744
50	CTCF	chr10:91714480-91714630	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:91738713-91738763	Hela-S3	cervix:	n/a
2	chr10:91738713-91738763	Hela-S3	cervix:	n/a
3	chr10:91738713-91738763	HRCEpiC	kidney:	n/a
4	chr10:91738713-91738763	AG09309	skin:	n/a
5	chr10:91738713-91738763	PANC-1	pancreas:	n/a
6	chr10:91738713-91738763	HMEC	breast:	n/a
7	chr10:91738528-91738578	CMK	blood:	n/a
8	chr10:91738528-91738578	AG09319	gingival:	n/a
9	chr10:91738461-91738511	HNPCEpiC	eye:	n/a
10	chr10:91737463-91737513	BE2_C	brain:	n/a
11	chr10:91737463-91737513	PFSK-1	brain:	n/a
12	chr10:91737463-91737513	BJ	skin:	n/a
13	chr10:91738791-91738841	AG09319	gingival:	n/a
14	chr10:91738461-91738511	AG10803	skin:	n/a
15	chr10:91738528-91738578	H1-hESC	embryonic stem cell:	embryo
16	chr10:91738791-91738841	IMR90	lung:	fetal
17	chr10:91737463-91737513	PANC-1	pancreas:	n/a
18	chr10:91737463-91737513	ProgFib	skin:	n/a
19	chr10:91738461-91738511	HEEpiC	esophagus:	n/a
20	chr10:91737463-91737513	GM19239	blood:	n/a
21	chr10:91717815-91717865	NB4	blood:	n/a
22	chr10:91717815-91717865	H1-hESC	embryonic stem cell:	embryo
23	chr10:91738713-91738763	PFSK-1	brain:	n/a
24	chr10:91738461-91738511	PrEC	prostate:	n/a
25	chr10:91738791-91738841	CMK	blood:	n/a
26	chr10:91738528-91738578	HMEC	breast:	n/a
27	chr10:91738461-91738511	HCM	heart:	n/a
28	chr10:91717815-91717865	AG04449	skin:	fetal
29	chr10:91738791-91738841	GM12892	blood:	n/a
30	chr10:91717815-91717865	HCF	heart:	n/a
31	chr10:91738791-91738841	GM12878	blood:	n/a
32	chr10:91738461-91738511	LNCaP	prostate:	n/a
33	chr10:91717815-91717865	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:91738791-91738841	Hela-S3	cervix:	n/a
35	chr10:91738461-91738511	HCPEpiC	choroid plexus:	n/a
36	chr10:91738461-91738511	MCF-7	breast:	n/a
37	chr10:91738791-91738841	HRPEpiC	eye:	n/a
38	chr10:91738461-91738511	Hela-S3	cervix:	n/a
39	chr10:91737463-91737513	MCF-7	breast:	n/a
40	chr10:91738528-91738578	HIPEpiC	eye:	n/a
41	chr10:91738528-91738578	AoSMC	blood vessel:	n/a
42	chr10:91738713-91738763	PrEC	prostate:	n/a
43	chr10:91738528-91738578	ECC-1	luminal epithelium:	n/a
44	chr10:91738713-91738763	NT2-D1	testis:	n/a
45	chr10:91717815-91717865	A549	lung:	n/a
46	chr10:91737463-91737513	AG04449	skin:	fetal
47	chr10:91738791-91738841	T-47D	breast:	n/a
48	chr10:91737463-91737513	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:91738461-91738511	HEK293	kidney:	embryo
50	chr10:91738528-91738578	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:
2	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:
3	chr10:91718660..91720369-chr10:91722902..91725645,2	MCF-7	breast:
4	chr10:91722915..91725484-chr10:91726332..91728860,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PANK1-7	chr10:91706886-91707110	NONHSAT015579
2	lnc-PANK1-7	chr10:91705952-91706174	NONHSAT015579
3	lnc-PANK1-7	chr10:91705612-91705740	NONHSAT015579
4	lnc-PANK1-4	chr10:91715632-91715760	XLOC_008900
5	lnc-PANK1-4	chr10:91715972-91716194	XLOC_008900
6	lnc-PANK1-4	chr10:91716906-91717130	XLOC_008900

Variant related genes	Relation type
SNRPD2P1	TF binding region
ENSG00000226159	TF binding region
SNRPD2P1	CpG island
ENSG00000226159	CpG island
HMGA2	miRNA target sites
TGFBR2	miRNA target sites

Extended variants
information (count: 1387 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1387 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571518804	chr10:91703057-91703058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs527578871	chr10:91703105-91703106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116903273	chr10:91703112-91703113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182166349	chr10:91703171-91703172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536371842	chr10:91703187-91703188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556209698	chr10:91703204-91703205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569928645	chr10:91703215-91703216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148900293	chr10:91703227-91703228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143568420	chr10:91703263-91703264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572693476	chr10:91703264-91703265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541698228	chr10:91703287-91703288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs57308670	chr10:91703359-91703360	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573553492	chr10:91703448-91703449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542761528	chr10:91703449-91703450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562530591	chr10:91703471-91703472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576310948	chr10:91703530-91703531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200852998	chr10:91703541-91703542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187649445	chr10:91703565-91703566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542435021	chr10:91703586-91703587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150977734	chr10:91703666-91703667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190886143	chr10:91703742-91703743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558757194	chr10:91703743-91703744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547645720	chr10:91703847-91703848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577089856	chr10:91703848-91703849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567570311	chr10:91703975-91703976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140508321	chr10:91703983-91703984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549870117	chr10:91704005-91704006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541256557	chr10:91704076-91704077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182991842	chr10:91704094-91704095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538739547	chr10:91704126-91704127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77632951	chr10:91704127-91704128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372528148	chr10:91704130-91704131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535029835	chr10:91704191-91704192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149163123	chr10:91704205-91704206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs555209766	chr10:91704217-91704218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573567605	chr10:91704246-91704247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs35426563	chr10:91704359-91704360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536207789	chr10:91704433-91704434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1777941	chr10:91704440-91704441	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs28658287	chr10:91704442-91704443	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs371408640	chr10:91704456-91704457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1324698	chr10:91704474-91704475	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs187321098	chr10:91704475-91704476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564527158	chr10:91704482-91704483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572174458	chr10:91704491-91704492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190179716	chr10:91704548-91704549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540980981	chr10:91704595-91704596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs71022588	chr10:91704608-91704609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561194725	chr10:91704614-91704615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs147052618	chr10:91704615-91704616	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:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91700200-91704000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr10:91700200-91704200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:91700200-91705600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:91701000-91704000	Weak transcription	HMEC	breast
5	chr10:91703000-91703800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:91703800-91704600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr10:91704000-91704400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:91704000-91704400	Enhancers	HMEC	breast
9	chr10:91704200-91704400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr10:91704600-91705000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:91705000-91706000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr10:91705200-91706000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr10:91705200-91706200	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr10:91705400-91706000	Enhancers	Primary B cells from peripheral blood	blood
15	chr10:91705400-91706000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr10:91705400-91706400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr10:91705600-91706000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr10:91705800-91706200	Enhancers	Primary T cells from cord blood	blood
19	chr10:91705800-91706200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr10:91705800-91706200	Flanking Active TSS	Dnd41	blood
21	chr10:91705800-91706200	Active TSS	NHDF-Ad	bronchial
22	chr10:91705800-91706200	Active TSS	NHLF	lung
23	chr10:91705800-91706400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:91706200-91706400	Enhancers	Dnd41	blood
25	chr10:91708600-91710200	Enhancers	Fetal Brain Male	brain
26	chr10:91709600-91713000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:91710200-91712000	Weak transcription	Fetal Brain Male	brain
28	chr10:91711600-91712000	ZNF genes & repeats	Fetal Stomach	stomach
29	chr10:91712000-91712400	Enhancers	Fetal Brain Male	brain
30	chr10:91712000-91713800	Weak transcription	Fetal Stomach	stomach
31	chr10:91712400-91713600	Weak transcription	Fetal Brain Male	brain
32	chr10:91712400-91714200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr10:91713600-91714200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr10:91713600-91714200	Enhancers	Fetal Brain Female	brain
35	chr10:91713600-91714400	Enhancers	Fetal Brain Male	brain
36	chr10:91713800-91714000	Enhancers	Right Atrium	heart
37	chr10:91713800-91714600	Enhancers	Fetal Stomach	stomach
38	chr10:91714200-91714400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr10:91714200-91714400	Enhancers	HMEC	breast
40	chr10:91714400-91715400	Enhancers	GM12878-XiMat	blood
41	chr10:91714400-91722600	Weak transcription	HMEC	breast
42	chr10:91715400-91718800	Weak transcription	GM12878-XiMat	blood
43	chr10:91717800-91718200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr10:91718600-91725600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr10:91718800-91719600	Enhancers	Primary B cells from peripheral blood	blood
46	chr10:91718800-91720400	ZNF genes & repeats	GM12878-XiMat	blood
47	chr10:91719600-91719800	Enhancers	Primary B cells from cord blood	blood
48	chr10:91719800-91720000	Enhancers	NHEK	skin
49	chr10:91719800-91739800	Weak transcription	Primary B cells from cord blood	blood
50	chr10:91721800-91724400	Enhancers	NHEK	skin

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