Variant report

Variant	nsv895055
Chromosome Location	chr10:42771774-42947627
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1455)
CpG islands
(count:978)
Chromatin interactive
region (count:13)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1455 , 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	chr10:42799540-42800192	HepG2	liver:	n/a	n/a
2	ATF1	chr10:42801380-42801410	K562	blood:	n/a	n/a
3	ATF1	chr10:42799538-42800192	K562	blood:	n/a	n/a
4	ATF1	chr10:42797113-42797490	K562	blood:	n/a	n/a
5	ATF1	chr10:42815222-42815574	K562	blood:	n/a	n/a
6	ATF1	chr10:42817203-42817917	K562	blood:	n/a	n/a
7	BACH1	chr10:42813274-42813746	K562	blood:	n/a	n/a
8	BATF	chr10:42790414-42790906	GM12878	blood:	n/a	n/a
9	BATF	chr10:42791008-42791549	GM12878	blood:	n/a	n/a
10	BATF	chr10:42791867-42792344	GM12878	blood:	n/a	n/a
11	BATF	chr10:42796760-42798052	GM12878	blood:	n/a	n/a
12	BATF	chr10:42790411-42790908	GM12878	blood:	n/a	n/a
13	BATF	chr10:42794125-42794872	GM12878	blood:	n/a	n/a
14	BATF	chr10:42843892-42844051	GM12878	blood:	n/a	chr10:42843938-42843949
15	BATF	chr10:42794103-42794967	GM12878	blood:	n/a	n/a
16	BATF	chr10:42814968-42815467	GM12878	blood:	n/a	n/a
17	BATF	chr10:42775977-42776265	GM12878	blood:	n/a	n/a
18	BATF	chr10:42816795-42818369	GM12878	blood:	n/a	n/a
19	BATF	chr10:42815938-42818365	GM12878	blood:	n/a	n/a
20	BATF	chr10:42791080-42791784	GM12878	blood:	n/a	n/a
21	BATF	chr10:42802384-42802603	GM12878	blood:	n/a	n/a
22	BATF	chr10:42799184-42800297	GM12878	blood:	n/a	n/a
23	BATF	chr10:42801201-42801861	GM12878	blood:	n/a	n/a
24	BATF	chr10:42792510-42793190	GM12878	blood:	n/a	n/a
25	BATF	chr10:42799191-42800355	GM12878	blood:	n/a	n/a
26	BATF	chr10:42843878-42844039	GM12878	blood:	n/a	chr10:42843938-42843949
27	BATF	chr10:42810326-42810760	GM12878	blood:	n/a	n/a
28	BCL11A	chr10:42794300-42794905	GM12878	blood:	n/a	n/a
29	BCL11A	chr10:42816269-42818366	GM12878	blood:	n/a	n/a
30	BCL11A	chr10:42790409-42790946	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:42816771-42818395	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:42799172-42800370	GM12878	blood:	n/a	n/a
33	BCL11A	chr10:42790997-42791796	GM12878	blood:	n/a	n/a
34	BCL11A	chr10:42797687-42798021	GM12878	blood:	n/a	n/a
35	BCL3	chr10:42797112-42797375	K562	blood:	n/a	n/a
36	BHLHE40	chr10:42815145-42815520	HepG2	liver:	n/a	n/a
37	BHLHE40	chr10:42805345-42805717	K562	blood:	n/a	n/a
38	BHLHE40	chr10:42810371-42810796	HepG2	liver:	n/a	n/a
39	BHLHE40	chr10:42816960-42818341	HepG2	liver:	n/a	n/a
40	BHLHE40	chr10:42799294-42800192	HepG2	liver:	n/a	n/a
41	BRCA1	chr10:42805344-42805718	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr10:42809116-42809143	GM12878	blood:	n/a	n/a
43	BRCA1	chr10:42813274-42813759	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr10:42813274-42813756	GM12878	blood:	n/a	n/a
45	CBX3	chr10:42832408-42832737	K562	blood:	n/a	n/a
46	CBX3	chr10:42863291-42863724	K562	blood:	n/a	n/a
47	CBX3	chr10:42831412-42831715	K562	blood:	n/a	n/a
48	CBX3	chr10:42799259-42800350	K562	blood:	n/a	n/a
49	CCNT2	chr10:42863141-42863422	K562	blood:	n/a	n/a
50	CCNT2	chr10:42876568-42876697	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:42777525-42777575	NHDF-neo	bronchial:	n/a
2	chr10:42863068-42863118	SK-N-SH_RA	brain:	n/a
3	chr10:42777525-42777575	NHDF-neo	bronchial:	n/a
4	chr10:42863068-42863118	SK-N-SH_RA	brain:	n/a
5	chr10:42864912-42864962	HEEpiC	esophagus:	n/a
6	chr10:42863539-42863589	MCF-7	breast:	n/a
7	chr10:42864912-42864962	NHDF-neo	bronchial:	n/a
8	chr10:42863539-42863589	HEEpiC	esophagus:	n/a
9	chr10:42863173-42863223	CMK	blood:	n/a
10	chr10:42864912-42864962	HCM	heart:	n/a
11	chr10:42863539-42863589	Jurkat	blood:	n/a
12	chr10:42864912-42864962	A549	lung:	n/a
13	chr10:42863444-42863494	HepG2	liver:	n/a
14	chr10:42862876-42862926	MCF10A-Er-Src	breast:	n/a
15	chr10:42863068-42863118	HRE	kidney:	n/a
16	chr10:42863550-42863600	AG10803	skin:	n/a
17	chr10:42862876-42862926	HNPCEpiC	eye:	n/a
18	chr10:42863508-42863558	GM19239	blood:	n/a
19	chr10:42862876-42862926	PANC-1	pancreas:	n/a
20	chr10:42864633-42864683	T-47D	breast:	n/a
21	chr10:42777525-42777575	H1-hESC	embryonic stem cell:	embryo
22	chr10:42931123-42931173	NB4	blood:	n/a
23	chr10:42931123-42931173	ovcar-3	ovarian:	n/a
24	chr10:42862978-42863028	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:42863508-42863558	HL-60	blood:	n/a
26	chr10:42863508-42863558	T-47D	breast:	n/a
27	chr10:42931123-42931173	NH-A	brain:	n/a
28	chr10:42859004-42859054	A549	lung:	n/a
29	chr10:42863550-42863600	HNPCEpiC	eye:	n/a
30	chr10:42931123-42931173	HCPEpiC	choroid plexus:	n/a
31	chr10:42863508-42863558	Jurkat	blood:	n/a
32	chr10:42777525-42777575	ProgFib	skin:	n/a
33	chr10:42863594-42863644	BJ	skin:	n/a
34	chr10:42777375-42777425	AoSMC	blood vessel:	n/a
35	chr10:42864633-42864683	PrEC	prostate:	n/a
36	chr10:42863068-42863118	PrEC	prostate:	n/a
37	chr10:42863508-42863558	ovcar-3	ovarian:	n/a
38	chr10:42862876-42862926	AG10803	skin:	n/a
39	chr10:42859004-42859054	AoSMC	blood vessel:	n/a
40	chr10:42862978-42863028	IMR90	lung:	fetal
41	chr10:42777525-42777575	HL-60	blood:	n/a
42	chr10:42864912-42864962	SK-N-SH	brain:	n/a
43	chr10:42859004-42859054	PrEC	prostate:	n/a
44	chr10:42862876-42862926	A549	lung:	n/a
45	chr10:42863539-42863589	Hepatocyte	liver:	n/a
46	chr10:42863594-42863644	HUVEC	blood vessel:	n/a
47	chr10:42863550-42863600	A549	lung:	n/a
48	chr10:42863508-42863558	HEK293	kidney:	embryo
49	chr10:42863539-42863589	AG09309	skin:	n/a
50	chr10:42863173-42863223	HCT-116	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
2	chr10:42861377..42864864-chr10:42876467..42879026,3	K562	blood:
3	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
4	chr10:42846704..42848638-chr10:42856458..42859194,2	K562	blood:
5	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
6	chr10:42843787..42846463-chr10:42857739..42859504,2	K562	blood:
7	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
8	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:
9	chr10:42843787..42846463-chr10:42856590..42859504,3	K562	blood:
10	chr10:42860335..42863039-chr10:43132551..43135299,2	K562	blood:
11	chr10:42939273..42941878-chr10:42945639..42947236,2	K562	blood:
12	chr10:42822722..42825307-chr10:42828970..42830910,2	K562	blood:
13	chr10:42851804..42854724-chr10:42857105..42858652,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNYL2-5	chr10:42794471-42794553	NONHSAT012863
2	lnc-CCNYL2-5	chr10:42796822-42796961	NONHSAT012863
3	lnc-CCNYL2-6	chr10:42775182-42777267	NONHSAT012861
4	lnc-CCNYL2-5	chr10:42795737-42796013	NONHSAT012863
5	lnc-BMS1-6	chr10:42791078-42791322	NONHSAT012862

No data

Variant related genes	Relation type
PABPC1P8	TF binding region
ENSG00000215146	TF binding region
PABPC1P8	CpG island
ENSG00000215146	CpG island
ENSG00000272373	chromatin interactions
ENSG00000215146	chromatin interactions
ENSG00000196693	chromatin interactions

Extended variants
information (count: 5506 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5506 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7898538	chr10:42775202-42775203	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs11595040	chr10:42775233-42775234	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs61853486	chr10:42775240-42775241	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs7898552	chr10:42775242-42775243	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs200632054	chr10:42775268-42775269	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs560502998	chr10:42775275-42775276	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs2954849	chr10:42775285-42775286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs529570344	chr10:42775290-42775291	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs549619918	chr10:42775292-42775293	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs75581741	chr10:42775304-42775305	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs371197729	chr10:42775325-42775326	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs540781268	chr10:42775345-42775346	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs199884009	chr10:42775352-42775353	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs531964046	chr10:42775360-42775361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs9783150	chr10:42775390-42775391	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs79649522	chr10:42775393-42775394	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs551986652	chr10:42775400-42775401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs9783151	chr10:42775401-42775402	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs571806650	chr10:42775404-42775405	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs4948905	chr10:42775414-42775415	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs534283547	chr10:42775427-42775428	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs200091595	chr10:42775438-42775439	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs201067276	chr10:42775442-42775443	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs202177966	chr10:42775468-42775469	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs547813817	chr10:42775483-42775484	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs200182467	chr10:42775501-42775502	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs151039500	chr10:42775513-42775514	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs202200020	chr10:42775514-42775515	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs201038285	chr10:42775531-42775532	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs202037046	chr10:42775570-42775571	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs200166063	chr10:42775572-42775573	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs201277166	chr10:42775574-42775575	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs202152491	chr10:42775605-42775606	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs111598079	chr10:42775628-42775629	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs9783153	chr10:42775661-42775662	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs9783211	chr10:42775671-42775672	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs200527859	chr10:42775678-42775679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs9783165	chr10:42775720-42775721	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs201432815	chr10:42775723-42775724	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs368588254	chr10:42775745-42775746	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs199505939	chr10:42775772-42775773	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs200674841	chr10:42775776-42775777	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs201179882	chr10:42775782-42775783	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs200214805	chr10:42775830-42775831	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs201197970	chr10:42775901-42775902	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs199646387	chr10:42775992-42775993	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs567622964	chr10:42775999-42776000	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs200575676	chr10:42776004-42776005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs201853279	chr10:42776052-42776053	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs200193111	chr10:42776057-42776058	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	17440070	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:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:42790400-42790600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr10:42790400-42818200	ZNF genes & repeats	Liver	Liver
3	chr10:42790600-42795200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
4	chr10:42790600-42795400	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
5	chr10:42790600-42795400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
6	chr10:42790600-42818000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
7	chr10:42790600-42818000	ZNF genes & repeats	Brain Substantia Nigra	brain
8	chr10:42790600-42818000	ZNF genes & repeats	Colonic Mucosa	Colon
9	chr10:42790600-42818000	ZNF genes & repeats	Sigmoid Colon	Sigmoid Colon
10	chr10:42790600-42818000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
11	chr10:42790600-42818200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
12	chr10:42790600-42818200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr10:42790600-42818200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr10:42790600-42818200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr10:42790600-42818200	ZNF genes & repeats	Primary T cells from cord blood	blood
16	chr10:42790600-42818200	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr10:42790600-42818200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
18	chr10:42790600-42818400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
19	chr10:42790600-42818400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr10:42790600-42818400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:42790600-42818400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
22	chr10:42790600-42818600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:42790800-42792800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
24	chr10:42790800-42793200	ZNF genes & repeats	Fetal Heart	heart
25	chr10:42790800-42795200	ZNF genes & repeats	Primary T helper naive cells from peripheral blood	blood
26	chr10:42790800-42795200	ZNF genes & repeats	Rectal Smooth Muscle	rectum
27	chr10:42790800-42818000	ZNF genes & repeats	Brain Angular Gyrus	brain
28	chr10:42790800-42818000	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
29	chr10:42790800-42818000	ZNF genes & repeats	Rectal Mucosa Donor 29	rectum
30	chr10:42790800-42818000	ZNF genes & repeats	Dnd41	blood
31	chr10:42790800-42818200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
32	chr10:42790800-42818200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:42790800-42818200	ZNF genes & repeats	Primary B cells from cord blood	blood
34	chr10:42790800-42818200	ZNF genes & repeats	Brain Hippocampus Middle	brain
35	chr10:42790800-42818200	ZNF genes & repeats	Colon Smooth Muscle	Colon
36	chr10:42790800-42818200	ZNF genes & repeats	Fetal Brain Male	brain
37	chr10:42790800-42818200	ZNF genes & repeats	Fetal Lung	lung
38	chr10:42790800-42818200	ZNF genes & repeats	Gastric	stomach
39	chr10:42791000-42791600	ZNF genes & repeats	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr10:42791000-42791600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
41	chr10:42791000-42791600	ZNF genes & repeats	Right Atrium	heart
42	chr10:42791000-42791800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr10:42791000-42791800	ZNF genes & repeats	Pancreas	Pancrea
44	chr10:42791000-42791800	ZNF genes & repeats	K562	blood
45	chr10:42791000-42791800	ZNF genes & repeats	NH-A	brain
46	chr10:42791000-42792000	ZNF genes & repeats	HepG2	liver
47	chr10:42791000-42792000	ZNF genes & repeats	HSMM	muscle
48	chr10:42791000-42792200	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
49	chr10:42791000-42792600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
50	chr10:42791000-42792600	ZNF genes & repeats	Spleen	Spleen

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