Variant report

Variant	nsv466879
Chromosome Location	chr10:42862079-42925487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:671)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr10:42863291-42863724	K562	blood:	n/a	n/a
2	CCNT2	chr10:42876568-42876697	K562	blood:	n/a	n/a
3	CCNT2	chr10:42863141-42863422	K562	blood:	n/a	n/a
4	CEBPB	chr10:42886922-42886990	HepG2	liver:	n/a	chr10:42886933-42886944
5	CEBPB	chr10:42903832-42903893	IMR90	lung:	n/a	chr10:42903853-42903864
6	CEBPB	chr10:42903805-42903926	HepG2	liver:	n/a	chr10:42903853-42903864
7	CEBPB	chr10:42862252-42862433	K562	blood:	n/a	n/a
8	CEBPD	chr10:42876429-42876788	K562	blood:	n/a	n/a
9	CHD2	chr10:42863523-42863535	GM12878	blood:	n/a	n/a
10	CHD2	chr10:42863371-42863685	K562	blood:	n/a	n/a
11	CTCF	chr10:42924080-42924230	GM12874	blood:	n/a	n/a
12	CTCF	chr10:42924080-42924230	GM12870	blood:	n/a	n/a
13	CTCF	chr10:42924120-42924270	BJ	skin:	n/a	n/a
14	CTCF	chr10:42924103-42924291	MCF-7	breast:	n/a	n/a
15	CTCF	chr10:42924100-42924250	SAEC	small airway:	n/a	n/a
16	CTCF	chr10:42924060-42924210	AG04449	skin:	n/a	n/a
17	CTCF	chr10:42924062-42924324	LNCaP	prostate:	n/a	n/a
18	CTCF	chr10:42924080-42924230	GM12871	blood:	n/a	n/a
19	CTCF	chr10:42924080-42924230	AG09319	gingival:	n/a	n/a
20	CTCF	chr10:42924220-42924370	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr10:42924060-42924210	HepG2	liver:	n/a	n/a
22	CTCF	chr10:42924080-42924230	GM12872	blood:	n/a	n/a
23	CTCF	chr10:42924100-42924250	AG09319	gingival:	n/a	n/a
24	CTCF	chr10:42924100-42924250	AG04450	lung:	n/a	n/a
25	CTCF	chr10:42924080-42924230	SAEC	small airway:	n/a	n/a
26	CTCF	chr10:42924097-42924298	Gliobla	brain:	n/a	n/a
27	CTCF	chr10:42924100-42924250	HPF	lung:	n/a	n/a
28	CTCF	chr10:42863288-42863344	Spleen_OC	spleen:	n/a	chr10:42863316-42863324
29	CTCF	chr10:42924000-42924150	GM12864	blood:	n/a	n/a
30	CTCF	chr10:42924100-42924250	AG09309	skin:	n/a	n/a
31	CTCF	chr10:42924120-42924270	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr10:42924080-42924230	GM12864	blood:	n/a	n/a
33	CTCF	chr10:42924160-42924310	GM12875	blood:	n/a	n/a
34	CTCF	chr10:42924120-42924270	HepG2	liver:	n/a	n/a
35	CTCF	chr10:42924080-42924230	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr10:42906695-42906729	GM13976	blood:	n/a	n/a
37	CTCF	chr10:42924127-42924274	GM13977	blood:	n/a	n/a
38	CTCF	chr10:42924100-42924250	HRE	kidney:	n/a	n/a
39	CTCF	chr10:42924100-42924250	GM12868	blood:	n/a	n/a
40	CTCF	chr10:42924120-42924270	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr10:42924139-42924247	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr10:42924180-42924330	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr10:42924160-42924310	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr10:42924087-42924281	HepG2	liver:	n/a	n/a
45	CTCF	chr10:42924100-42924250	AG10803	skin:	n/a	n/a
46	CTCF	chr10:42924006-42924414	K562	blood:	n/a	n/a
47	CTCF	chr10:42869883-42869979	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr10:42924060-42924210	HCM	heart:	n/a	n/a
49	CTCF	chr10:42924100-42924250	BE2_C	brain:	n/a	n/a
50	CTCF	chr10:42923963-42924370	MCF-7	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42864912-42864962	HRCEpiC	kidney:	n/a
2	chr10:42863550-42863600	NHBE	bronchial:	n/a
3	chr10:42864912-42864962	GM12892	blood:	n/a
4	chr10:42863068-42863118	HIPEpiC	eye:	n/a
5	chr10:42862876-42862926	AG09319	gingival:	n/a
6	chr10:42863444-42863494	BE2_C	brain:	n/a
7	chr10:42863594-42863644	HUVEC	blood vessel:	n/a
8	chr10:42864912-42864962	H1-hESC	embryonic stem cell:	embryo
9	chr10:42862876-42862926	NH-A	brain:	n/a
10	chr10:42863173-42863223	PrEC	prostate:	n/a
11	chr10:42863173-42863223	HNPCEpiC	eye:	n/a
12	chr10:42864633-42864683	AG09319	gingival:	n/a
13	chr10:42863444-42863494	K562	blood:	n/a
14	chr10:42864633-42864683	HepG2	liver:	n/a
15	chr10:42862876-42862926	NHDF-neo	bronchial:	n/a
16	chr10:42863508-42863558	HRE	kidney:	n/a
17	chr10:42863068-42863118	NH-A	brain:	n/a
18	chr10:42863539-42863589	HCF	heart:	n/a
19	chr10:42862978-42863028	HUVEC	blood vessel:	n/a
20	chr10:42864912-42864962	SK-N-MC	brain:	n/a
21	chr10:42862876-42862926	MCF-7	breast:	n/a
22	chr10:42863550-42863600	AoSMC	blood vessel:	n/a
23	chr10:42863539-42863589	AG09309	skin:	n/a
24	chr10:42863550-42863600	H1-hESC	embryonic stem cell:	embryo
25	chr10:42863508-42863558	HUVEC	blood vessel:	n/a
26	chr10:42863594-42863644	ovcar-3	ovarian:	n/a
27	chr10:42863550-42863600	HCPEpiC	choroid plexus:	n/a
28	chr10:42863550-42863600	HAEpiC	amniotic membrane:	n/a
29	chr10:42863508-42863558	SAEC	small airway:	n/a
30	chr10:42864633-42864683	HCPEpiC	choroid plexus:	n/a
31	chr10:42863594-42863644	ProgFib	skin:	n/a
32	chr10:42863539-42863589	HUVEC	blood vessel:	n/a
33	chr10:42863068-42863118	AG04449	skin:	fetal
34	chr10:42863068-42863118	IMR90	lung:	fetal
35	chr10:42863068-42863118	HCT-116	colon:	n/a
36	chr10:42863539-42863589	Hepatocyte	liver:	n/a
37	chr10:42862876-42862926	HNPCEpiC	eye:	n/a
38	chr10:42863550-42863600	HIPEpiC	eye:	n/a
39	chr10:42864912-42864962	Hela-S3	cervix:	n/a
40	chr10:42863508-42863558	GM19239	blood:	n/a
41	chr10:42864633-42864683	CMK	blood:	n/a
42	chr10:42863550-42863600	Hela-S3	cervix:	n/a
43	chr10:42863444-42863494	IMR90	lung:	fetal
44	chr10:42863550-42863600	ovcar-3	ovarian:	n/a
45	chr10:42863173-42863223	HUVEC	blood vessel:	n/a
46	chr10:42863508-42863558	HPAEpiC	pulmonary alveolar:	n/a
47	chr10:42864633-42864683	SK-N-SH	brain:	n/a
48	chr10:42863550-42863600	HRCEpiC	kidney:	n/a
49	chr10:42863444-42863494	HCPEpiC	choroid plexus:	n/a
50	chr10:42863594-42863644	PFSK-1	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
2	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000215146	TF binding region
ENSG00000215146	CpG island
ENSG00000215146	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000272373	chromatin interactions

Extended variants
information (count: 259 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:259 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2489684	chr10:42862079-42862080	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560681854	chr10:42862097-42862098	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs574158607	chr10:42862119-42862120	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs543076533	chr10:42862125-42862126	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562884279	chr10:42862184-42862185	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs551415172	chr10:42862185-42862186	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531707224	chr10:42862192-42862193	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs183230839	chr10:42862233-42862234	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564994909	chr10:42862262-42862263	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373560552	chr10:42862263-42862264	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527523817	chr10:42862305-42862306	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147222578	chr10:42862340-42862341	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372129534	chr10:42862392-42862393	Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs567051778	chr10:42862448-42862449	Active TSS ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs9732776	chr10:42862565-42862566	Active TSS ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
16	rs370728452	chr10:42862592-42862593	Active TSS ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546971505	chr10:42862661-42862662	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs567884733	chr10:42862669-42862670	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs367735513	chr10:42862674-42862675	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs368860034	chr10:42862675-42862676	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs115883678	chr10:42862722-42862723	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs371726613	chr10:42862738-42862739	Active TSS ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569332360	chr10:42862830-42862831	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538209402	chr10:42862834-42862835	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs536830862	chr10:42862842-42862843	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs546701340	chr10:42862863-42862864	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201006550	chr10:42862867-42862868	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs188692452	chr10:42862875-42862876	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs535518910	chr10:42862901-42862902	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs10400195	chr10:42862907-42862908	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs569134747	chr10:42862927-42862928	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs534431838	chr10:42862954-42862955	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs147257813	chr10:42862971-42862972	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370386513	chr10:42862980-42862981	Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs574248689	chr10:42863028-42863029	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs148714741	chr10:42863029-42863030	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs556644756	chr10:42863046-42863047	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
38	rs538417136	chr10:42863057-42863058	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
39	rs576512027	chr10:42863110-42863111	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
40	rs2505801	chr10:42863120-42863121	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs556828559	chr10:42863148-42863149	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
42	rs527571562	chr10:42863177-42863178	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
43	rs578193639	chr10:42863190-42863191	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
44	rs541256525	chr10:42863195-42863196	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
45	rs142355150	chr10:42863209-42863210	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
46	rs553688268	chr10:42863217-42863218	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
47	rs529812303	chr10:42863226-42863227	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
48	rs573796209	chr10:42863241-42863242	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
49	rs117426521	chr10:42863247-42863248	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs569402923	chr10:42863253-42863254	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Lung cancer	18438408	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
Breast cancer	21509527	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	20622171	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Hirschsprung''s Disease	19925665	CNVD
Hirschsprung''s Disease	20456320	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42848000-42862600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:42850600-42862200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr10:42850600-42862200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:42852200-42862600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr10:42854200-42862600	Weak transcription	Colon Smooth Muscle	Colon
6	chr10:42854800-42862600	Weak transcription	Adipose Nuclei	Adipose
7	chr10:42855400-42862600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr10:42855600-42862600	Weak transcription	Brain Angular Gyrus	brain
9	chr10:42857800-42862800	Weak transcription	Aorta	Aorta
10	chr10:42858000-42862600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:42858000-42862800	Weak transcription	Gastric	stomach
12	chr10:42858200-42862400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr10:42859000-42863600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr10:42859200-42862400	Weak transcription	Ovary	ovary
15	chr10:42859200-42862600	Weak transcription	Left Ventricle	heart
16	chr10:42860200-42862200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr10:42860400-42863800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
18	chr10:42860600-42863400	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr10:42860600-42863600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr10:42861000-42862800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:42861600-42862200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr10:42861600-42862200	ZNF genes & repeats	HMEC	breast
23	chr10:42861600-42862600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr10:42861600-42863600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr10:42861600-42863600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:42861600-42863600	ZNF genes & repeats	Fetal Stomach	stomach
27	chr10:42861800-42862600	Weak transcription	Brain Anterior Caudate	brain
28	chr10:42861800-42862800	Weak transcription	Fetal Lung	lung
29	chr10:42861800-42863800	Active TSS	K562	blood
30	chr10:42862000-42862800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr10:42862000-42862800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr10:42862000-42863400	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr10:42862000-42863400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:42862000-42863600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr10:42862000-42863600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr10:42862000-42863600	ZNF genes & repeats	Pancreas	Pancrea
37	chr10:42862000-42863800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr10:42862000-42864200	Active TSS	Stomach Smooth Muscle	stomach
39	chr10:42862200-42862600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr10:42862200-42862600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:42862200-42863600	Active TSS	HMEC	breast
42	chr10:42862200-42863800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:42862200-42863800	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr10:42862400-42862800	Enhancers	Primary B cells from peripheral blood	blood
45	chr10:42862400-42863000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
46	chr10:42862400-42863000	Active TSS	Fetal Brain Female	brain
47	chr10:42862400-42863600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:42862400-42863600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:42862400-42863600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr10:42862400-42863800	Active TSS	Ovary	ovary

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