Variant report

Variant	nsv550692
Chromosome Location	chr10:42860042-42925487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:673)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 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	chr10:42863141-42863422	K562	blood:	n/a	n/a
3	CCNT2	chr10:42876568-42876697	K562	blood:	n/a	n/a
4	CEBPB	chr10:42861983-42862018	K562	blood:	n/a	n/a
5	CEBPB	chr10:42903805-42903926	HepG2	liver:	n/a	chr10:42903853-42903864
6	CEBPB	chr10:42886922-42886990	HepG2	liver:	n/a	chr10:42886933-42886944
7	CEBPB	chr10:42903832-42903893	IMR90	lung:	n/a	chr10:42903853-42903864
8	CEBPB	chr10:42862252-42862433	K562	blood:	n/a	n/a
9	CEBPD	chr10:42876429-42876788	K562	blood:	n/a	n/a
10	CHD2	chr10:42863523-42863535	GM12878	blood:	n/a	n/a
11	CHD2	chr10:42863371-42863685	K562	blood:	n/a	n/a
12	CTCF	chr10:42924060-42924210	HCM	heart:	n/a	n/a
13	CTCF	chr10:42924120-42924270	GM12873	blood:	n/a	n/a
14	CTCF	chr10:42924120-42924270	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr10:42924099-42924285	GM12878	blood:	n/a	n/a
16	CTCF	chr10:42924000-42924259	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr10:42924200-42924350	NHLF	lung:	n/a	n/a
18	CTCF	chr10:42924140-42924290	HCT-116	colon:	n/a	n/a
19	CTCF	chr10:42924080-42924230	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr10:42924139-42924247	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr10:42924120-42924270	AG10803	skin:	n/a	n/a
22	CTCF	chr10:42924070-42924304	K562	blood:	n/a	n/a
23	CTCF	chr10:42924220-42924370	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr10:42924120-42924270	NHEK	skin:	n/a	n/a
25	CTCF	chr10:42924029-42924326	GM12878	blood:	n/a	n/a
26	CTCF	chr10:42924080-42924230	AG09319	gingival:	n/a	n/a
27	CTCF	chr10:42906656-42906711	GM13977	blood:	n/a	n/a
28	CTCF	chr10:42885484-42885503	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr10:42924120-42924270	Caco-2	colon:	n/a	n/a
30	CTCF	chr10:42924080-42924230	MCF-7	breast:	n/a	n/a
31	CTCF	chr10:42924080-42924230	NHEK	skin:	n/a	n/a
32	CTCF	chr10:42924121-42924263	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr10:42924160-42924310	GM12875	blood:	n/a	n/a
34	CTCF	chr10:42906695-42906729	GM13976	blood:	n/a	n/a
35	CTCF	chr10:42924060-42924210	HepG2	liver:	n/a	n/a
36	CTCF	chr10:42924100-42924250	AG10803	skin:	n/a	n/a
37	CTCF	chr10:42924100-42924250	GM12869	blood:	n/a	n/a
38	CTCF	chr10:42910465-42910525	MCF-7	breast:	n/a	n/a
39	CTCF	chr10:42923920-42924321	T-47D	breast:	n/a	n/a
40	CTCF	chr10:42924160-42924310	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr10:42923830-42924420	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr10:42924120-42924270	AG04449	skin:	n/a	n/a
43	CTCF	chr10:42924120-42924270	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr10:42924000-42924150	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr10:42924180-42924330	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr10:42924170-42924239	GM13976	blood:	n/a	n/a
47	CTCF	chr10:42924120-42924270	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr10:42924040-42924190	GM12865	blood:	n/a	n/a
49	CTCF	chr10:42924083-42924295	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr10:42924100-42924250	AG09309	skin:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42863068-42863118	HCM	heart:	n/a
2	chr10:42863539-42863589	HCPEpiC	choroid plexus:	n/a
3	chr10:42863068-42863118	HCM	heart:	n/a
4	chr10:42863539-42863589	HCPEpiC	choroid plexus:	n/a
5	chr10:42864912-42864962	HRE	kidney:	n/a
6	chr10:42863508-42863558	SK-N-SH	brain:	n/a
7	chr10:42862978-42863028	SK-N-SH	brain:	n/a
8	chr10:42863550-42863600	Hepatocyte	liver:	n/a
9	chr10:42864633-42864683	CMK	blood:	n/a
10	chr10:42864633-42864683	SK-N-SH_RA	brain:	n/a
11	chr10:42863594-42863644	HL-60	blood:	n/a
12	chr10:42863550-42863600	PANC-1	pancreas:	n/a
13	chr10:42863068-42863118	PANC-1	pancreas:	n/a
14	chr10:42863550-42863600	HRCEpiC	kidney:	n/a
15	chr10:42862876-42862926	HMEC	breast:	n/a
16	chr10:42863508-42863558	HUVEC	blood vessel:	n/a
17	chr10:42864912-42864962	Jurkat	blood:	n/a
18	chr10:42863508-42863558	HepG2	liver:	n/a
19	chr10:42863594-42863644	HRCEpiC	kidney:	n/a
20	chr10:42863444-42863494	NHBE	bronchial:	n/a
21	chr10:42864912-42864962	HNPCEpiC	eye:	n/a
22	chr10:42863539-42863589	IMR90	lung:	fetal
23	chr10:42863173-42863223	HEEpiC	esophagus:	n/a
24	chr10:42862876-42862926	IMR90	lung:	fetal
25	chr10:42864633-42864683	HRCEpiC	kidney:	n/a
26	chr10:42864912-42864962	HCT-116	colon:	n/a
27	chr10:42863550-42863600	NHBE	bronchial:	n/a
28	chr10:42863444-42863494	AG10803	skin:	n/a
29	chr10:42863594-42863644	Hepatocyte	liver:	n/a
30	chr10:42864633-42864683	Jurkat	blood:	n/a
31	chr10:42863550-42863600	Hela-S3	cervix:	n/a
32	chr10:42864912-42864962	SK-N-SH	brain:	n/a
33	chr10:42863444-42863494	AG04449	skin:	fetal
34	chr10:42862876-42862926	HCF	heart:	n/a
35	chr10:42863550-42863600	HAEpiC	amniotic membrane:	n/a
36	chr10:42863444-42863494	HIPEpiC	eye:	n/a
37	chr10:42863539-42863589	T-47D	breast:	n/a
38	chr10:42863444-42863494	Jurkat	blood:	n/a
39	chr10:42864633-42864683	AG04449	skin:	fetal
40	chr10:42863550-42863600	AG09309	skin:	n/a
41	chr10:42864633-42864683	HCPEpiC	choroid plexus:	n/a
42	chr10:42863550-42863600	GM12878	blood:	n/a
43	chr10:42862876-42862926	NHDF-neo	bronchial:	n/a
44	chr10:42863068-42863118	HUVEC	blood vessel:	n/a
45	chr10:42863173-42863223	IMR90	lung:	fetal
46	chr10:42863550-42863600	K562	blood:	n/a
47	chr10:42863444-42863494	PFSK-1	brain:	n/a
48	chr10:42863550-42863600	HCF	heart:	n/a
49	chr10:42863508-42863558	IMR90	lung:	fetal
50	chr10:42863173-42863223	Hepatocyte	liver:	n/a

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

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

No data

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

Extended variants
information (count: 320 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2466482	chr10:42860042-42860043	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs544394652	chr10:42860064-42860065	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs145748285	chr10:42860104-42860105	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs376004082	chr10:42860170-42860171	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs368040599	chr10:42860171-42860172	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs111344685	chr10:42860174-42860175	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs564471853	chr10:42860213-42860214	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs535700374	chr10:42860228-42860229	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs142977066	chr10:42860272-42860273	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs114838468	chr10:42860324-42860325	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs566874262	chr10:42860416-42860417	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559350365	chr10:42860440-42860441	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529258361	chr10:42860454-42860455	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs74417471	chr10:42860642-42860643	Strong transcription ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372546341	chr10:42860656-42860657	Strong transcription ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112984716	chr10:42860754-42860755	Strong transcription ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs569162176	chr10:42860758-42860759	Strong transcription ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538083945	chr10:42860809-42860810	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs555496042	chr10:42860862-42860863	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs186985054	chr10:42860874-42860875	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191829795	chr10:42860894-42860895	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs533900915	chr10:42860921-42860922	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs146628107	chr10:42860922-42860923	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573588598	chr10:42860941-42860942	Strong transcription ZNF genes & repeats Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140818486	chr10:42861003-42861004	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs530741910	chr10:42861103-42861104	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs555682949	chr10:42861110-42861111	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs183340360	chr10:42861116-42861117	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs376816729	chr10:42861126-42861127	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544432688	chr10:42861147-42861148	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs554411381	chr10:42861155-42861156	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144624648	chr10:42861158-42861159	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs577598327	chr10:42861161-42861162	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs186569995	chr10:42861162-42861163	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs540743286	chr10:42861205-42861206	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs189639771	chr10:42861212-42861213	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs201812148	chr10:42861240-42861241	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113974623	chr10:42861251-42861252	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200803548	chr10:42861255-42861256	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs11284178	chr10:42861256-42861257	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374744472	chr10:42861259-42861260	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs560036828	chr10:42861344-42861345	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs529346374	chr10:42861392-42861393	Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs374126591	chr10:42861423-42861424	Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs576536797	chr10:42861448-42861449	Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549394076	chr10:42861535-42861536	Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182302663	chr10:42861569-42861570	Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs138518211	chr10:42861619-42861620	ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs117029902	chr10:42861640-42861641	ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140247102	chr10:42861660-42861661	ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	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:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42847000-42860600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr10:42848000-42862600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:42848800-42862000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr10:42850600-42862200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
5	chr10:42850600-42862200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:42852200-42862600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr10:42854000-42861600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr10:42854200-42862600	Weak transcription	Colon Smooth Muscle	Colon
9	chr10:42854800-42862600	Weak transcription	Adipose Nuclei	Adipose
10	chr10:42855400-42862600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr10:42855600-42862600	Weak transcription	Brain Angular Gyrus	brain
12	chr10:42857000-42861000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
13	chr10:42857800-42862800	Weak transcription	Aorta	Aorta
14	chr10:42858000-42860200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr10:42858000-42862000	Weak transcription	Pancreas	Pancrea
16	chr10:42858000-42862600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr10:42858000-42862800	Weak transcription	Gastric	stomach
18	chr10:42858200-42862400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr10:42858800-42860400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr10:42859000-42863600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr10:42859200-42860200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr10:42859200-42860200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:42859200-42862400	Weak transcription	Ovary	ovary
24	chr10:42859200-42862600	Weak transcription	Left Ventricle	heart
25	chr10:42859400-42860400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:42859800-42860800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr10:42859800-42860800	ZNF genes & repeats	K562	blood
28	chr10:42860200-42860800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:42860200-42862000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr10:42860200-42862000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr10:42860200-42862200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr10:42860400-42860800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr10:42860400-42863800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr10:42860600-42861000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
35	chr10:42860600-42863400	Active TSS	iPS-15b Cell Line	embryonic stem cell
36	chr10:42860600-42863600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
37	chr10:42860800-42861400	Strong transcription	K562	blood
38	chr10:42860800-42861600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr10:42860800-42862000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:42860800-42862000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr10:42861000-42861600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr10:42861000-42862800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr10:42861400-42861800	Transcr. at gene 5' and 3'	K562	blood
44	chr10:42861600-42861800	ZNF genes & repeats	Fetal Lung	lung
45	chr10:42861600-42862000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr10:42861600-42862200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr10:42861600-42862200	ZNF genes & repeats	HMEC	breast
48	chr10:42861600-42862600	Active TSS	H9 Cell Line	embryonic stem cell
49	chr10:42861600-42863600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:42861600-42863600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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