Variant report

Variant	esv2762523
Chromosome Location	chr5:60166108-60229718
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
2	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
4	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
5	BHLHE40	chr5:60168934-60168938	GM12878	blood:	n/a	n/a
6	CBX3	chr5:60166733-60166960	K562	blood:	n/a	n/a
7	CEBPB	chr5:60168749-60169059	IMR90	lung:	n/a	chr5:60168912-60168923
8	CEBPB	chr5:60168744-60169095	HepG2	liver:	n/a	chr5:60168912-60168923
9	CEBPB	chr5:60168783-60169063	K562	blood:	n/a	chr5:60168912-60168923
10	CEBPB	chr5:60168796-60169050	A549	lung:	n/a	chr5:60168912-60168923
11	CEBPB	chr5:60189614-60189869	HepG2	liver:	n/a	chr5:60189735-60189746 chr5:60189694-60189705
12	CHD1	chr5:60187619-60187641	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr5:60179180-60179330	GM12866	blood:	n/a	n/a
14	CTCF	chr5:60179200-60179350	HCT-116	colon:	n/a	n/a
15	CTCF	chr5:60224978-60225137	LNCaP	prostate:	n/a	n/a
16	CTCF	chr5:60178988-60179441	MCF-7	breast:	n/a	n/a
17	CTCF	chr5:60179066-60179354	A549	lung:	n/a	n/a
18	CTCF	chr5:60225020-60225170	GM06990	blood:	n/a	n/a
19	CTCF	chr5:60179260-60179410	HA-sp	spinal cord:	n/a	n/a
20	CTCF	chr5:60179140-60179290	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr5:60179240-60179390	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:60179180-60179330	HCM	heart:	n/a	n/a
23	CTCF	chr5:60224940-60225090	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr5:60224953-60225120	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr5:60224920-60225070	AoAF	blood vessel:	n/a	n/a
26	CTCF	chr5:60224960-60225110	HMF	breast:	n/a	n/a
27	CTCF	chr5:60179200-60179350	GM12875	blood:	n/a	n/a
28	CTCF	chr5:60225001-60225126	GM13977	blood:	n/a	n/a
29	CTCF	chr5:60224940-60225090	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr5:60179120-60179270	GM12874	blood:	n/a	n/a
31	CTCF	chr5:60179180-60179330	AG04450	lung:	n/a	n/a
32	CTCF	chr5:60179180-60179330	HCFaa	heart:	n/a	n/a
33	CTCF	chr5:60224980-60225130	GM12873	blood:	n/a	n/a
34	CTCF	chr5:60224980-60225130	AG04450	lung:	n/a	n/a
35	CTCF	chr5:60178983-60179529	HCT-116	colon:	n/a	n/a
36	CTCF	chr5:60179140-60179290	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr5:60179100-60179250	GM12878	blood:	n/a	n/a
38	CTCF	chr5:60179200-60179350	GM12869	blood:	n/a	n/a
39	CTCF	chr5:60179160-60179310	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr5:60179180-60179330	AG09319	gingival:	n/a	n/a
41	CTCF	chr5:60179160-60179310	AG09319	gingival:	n/a	n/a
42	CTCF	chr5:60179146-60179358	GM13977	blood:	n/a	n/a
43	CTCF	chr5:60179120-60179270	WI-38	lung:	n/a	n/a
44	CTCF	chr5:60225040-60225190	GM12864	blood:	n/a	n/a
45	CTCF	chr5:60225020-60225170	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:60224980-60225130	BJ	skin:	n/a	n/a
47	CTCF	chr5:60225240-60225390	NHLF	lung:	n/a	n/a
48	CTCF	chr5:60179120-60179270	GM12871	blood:	n/a	n/a
49	CTCF	chr5:60179160-60179310	GM12874	blood:	n/a	n/a
50	CTCF	chr5:60179120-60179270	HL-60	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60170058-60170108	Hela-S3	cervix:	n/a
2	chr5:60187211-60187261	Hepatocyte	liver:	n/a
3	chr5:60187211-60187261	A549	lung:	n/a
4	chr5:60187211-60187261	NHDF-neo	bronchial:	n/a
5	chr5:60187211-60187261	AoSMC	blood vessel:	n/a
6	chr5:60187211-60187261	BJ	skin:	n/a
7	chr5:60170058-60170108	CMK	blood:	n/a
8	chr5:60170058-60170108	U87	brain:	n/a
9	chr5:60187211-60187261	HCT-116	colon:	n/a
10	chr5:60170058-60170108	RPTEC	kidney:	n/a
11	chr5:60170058-60170108	HEK293	kidney:	embryo
12	chr5:60170058-60170108	LNCaP	prostate:	n/a
13	chr5:60170058-60170108	HMEC	breast:	n/a
14	chr5:60187211-60187261	SK-N-SH_RA	brain:	n/a
15	chr5:60170058-60170108	SAEC	small airway:	n/a
16	chr5:60170058-60170108	HCT-116	colon:	n/a
17	chr5:60187211-60187261	Jurkat	blood:	n/a
18	chr5:60170058-60170108	NB4	blood:	n/a
19	chr5:60187211-60187261	ProgFib	skin:	n/a
20	chr5:60170058-60170108	NT2-D1	testis:	n/a
21	chr5:60187211-60187261	HMEC	breast:	n/a
22	chr5:60187211-60187261	AG10803	skin:	n/a
23	chr5:60170058-60170108	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:60187211-60187261	Hela-S3	cervix:	n/a
25	chr5:60187211-60187261	HepG2	liver:	n/a
26	chr5:60170058-60170108	Hepatocyte	liver:	n/a
27	chr5:60187211-60187261	HEEpiC	esophagus:	n/a
28	chr5:60187211-60187261	GM12878	blood:	n/a
29	chr5:60170058-60170108	PrEC	prostate:	n/a
30	chr5:60170058-60170108	AG10803	skin:	n/a
31	chr5:60170058-60170108	H1-hESC	embryonic stem cell:	embryo
32	chr5:60187211-60187261	K562	blood:	n/a
33	chr5:60187211-60187261	HEK293	kidney:	embryo
34	chr5:60170058-60170108	MCF10A-Er-Src	breast:	n/a
35	chr5:60187211-60187261	AG04449	skin:	fetal
36	chr5:60187211-60187261	AG09309	skin:	n/a
37	chr5:60170058-60170108	SK-N-SH	brain:	n/a
38	chr5:60187211-60187261	HAEpiC	amniotic membrane:	n/a
39	chr5:60170058-60170108	GM06990	blood:	n/a
40	chr5:60170058-60170108	Caco-2	colon:	n/a
41	chr5:60170058-60170108	HIPEpiC	eye:	n/a
42	chr5:60170058-60170108	HL-60	blood:	n/a
43	chr5:60187211-60187261	ovcar-3	ovarian:	n/a
44	chr5:60187211-60187261	NH-A	brain:	n/a
45	chr5:60187211-60187261	HNPCEpiC	eye:	n/a
46	chr5:60187211-60187261	NB4	blood:	n/a
47	chr5:60170058-60170108	A549	lung:	n/a
48	chr5:60187211-60187261	HCPEpiC	choroid plexus:	n/a
49	chr5:60170058-60170108	HCF	heart:	n/a
50	chr5:60170058-60170108	PFSK-1	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
2	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
3	chr5:59973507..59975333-chr5:60177921..60180223,2	MCF-7	breast:
4	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
5	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
6	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
7	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
8	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
9	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
10	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
11	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
12	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
13	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
14	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
15	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
2	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
3	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1

No data

Variant related genes	Relation type
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
ENSG00000272308	TF binding region
ERCC8	TF binding region
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000272308	CpG island
ERCC8	CpG island
ENSG00000164182	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000233847	chromatin interactions

Extended variants
information (count: 2478 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2478 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4700400	chr5:60166111-60166112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138603460	chr5:60166125-60166126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560937220	chr5:60166153-60166154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552131814	chr5:60166154-60166155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13178869	chr5:60166165-60166166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141503205	chr5:60166182-60166183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs17332824	chr5:60166187-60166188	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs554345959	chr5:60166193-60166194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146191650	chr5:60166194-60166195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565268268	chr5:60166198-60166199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79416340	chr5:60166199-60166200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555027647	chr5:60166208-60166209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200148352	chr5:60166269-60166270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs60600383	chr5:60166296-60166297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559175329	chr5:60166310-60166311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57423118	chr5:60166339-60166340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113144636	chr5:60166350-60166351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183397249	chr5:60166420-60166421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376930526	chr5:60166421-60166422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28642275	chr5:60166440-60166441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149650551	chr5:60166445-60166446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369066254	chr5:60166446-60166447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542978992	chr5:60166488-60166489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78653477	chr5:60166489-60166490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199755813	chr5:60166500-60166501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560320408	chr5:60166511-60166512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573721913	chr5:60166517-60166518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543177784	chr5:60166520-60166521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562949467	chr5:60166529-60166530	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs35526496	chr5:60166561-60166562	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs537651805	chr5:60166605-60166606	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs531786929	chr5:60166612-60166613	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186208760	chr5:60166711-60166712	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs78177828	chr5:60166773-60166774	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs529788512	chr5:60166778-60166779	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs191111540	chr5:60166779-60166780	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs567879604	chr5:60166790-60166791	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs559237199	chr5:60166793-60166794	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs528341772	chr5:60166796-60166797	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200150974	chr5:60166799-60166800	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs536425535	chr5:60166800-60166801	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs74424641	chr5:60166808-60166809	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568604182	chr5:60166814-60166815	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs537509097	chr5:60166819-60166820	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs76133371	chr5:60166909-60166910	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs527320644	chr5:60166925-60166926	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs577541618	chr5:60166939-60166940	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs182100144	chr5:60166942-60166943	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553767125	chr5:60166964-60166965	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs144334856	chr5:60166974-60166975	ZNF genes & repeats Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:869 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60162600-60166800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr5:60165400-60166600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:60165600-60166600	Weak transcription	Primary B cells from cord blood	blood
4	chr5:60165800-60167400	Weak transcription	Primary T cells from cord blood	blood
5	chr5:60165800-60167800	Weak transcription	Esophagus	oesophagus
6	chr5:60166600-60166800	ZNF genes & repeats	Primary B cells from cord blood	blood
7	chr5:60166600-60167200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:60166600-60177000	Weak transcription	Ovary	ovary
9	chr5:60166800-60167400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:60167000-60167200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
11	chr5:60167200-60192600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:60167400-60167800	ZNF genes & repeats	Primary T cells from cord blood	blood
13	chr5:60167400-60186000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:60167800-60168000	ZNF genes & repeats	Esophagus	oesophagus
15	chr5:60167800-60182000	Weak transcription	Left Ventricle	heart
16	chr5:60167800-60187800	Weak transcription	Primary T cells from cord blood	blood
17	chr5:60167800-60188400	Weak transcription	Liver	Liver
18	chr5:60167800-60192800	Weak transcription	Primary hematopoietic stem cells	blood
19	chr5:60167800-60228200	Weak transcription	Psoas Muscle	Psoas
20	chr5:60168400-60169000	ZNF genes & repeats	Adipose Nuclei	Adipose
21	chr5:60168400-60191000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr5:60169000-60185800	Weak transcription	Adipose Nuclei	Adipose
23	chr5:60169800-60191000	Weak transcription	NH-A	brain
24	chr5:60175200-60188400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:60175200-60188400	Weak transcription	Right Ventricle	heart
26	chr5:60175400-60177000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr5:60175400-60177000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:60175400-60177000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:60175800-60188200	Weak transcription	Gastric	stomach
30	chr5:60175800-60188200	Weak transcription	Stomach Smooth Muscle	stomach
31	chr5:60175800-60239400	Weak transcription	NHEK	skin
32	chr5:60176400-60220400	Weak transcription	Esophagus	oesophagus
33	chr5:60176600-60176800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr5:60176600-60178000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr5:60176600-60178200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:60176600-60179600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr5:60176600-60188000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr5:60176800-60177200	ZNF genes & repeats	Fetal Lung	lung
39	chr5:60176800-60178000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:60176800-60180000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:60176800-60188200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr5:60177000-60177200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr5:60177000-60177400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:60177000-60177400	ZNF genes & repeats	Ovary	ovary
45	chr5:60177000-60178000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr5:60177000-60178400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr5:60177000-60178600	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr5:60177000-60178600	ZNF genes & repeats	Fetal Stomach	stomach
49	chr5:60177000-60190400	Weak transcription	HSMM	muscle
50	chr5:60177200-60178400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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