Variant report

Variant	nsv880833
Chromosome Location	chr5:52502168-52544231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:231)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:231 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:52541926-52542291	K562	blood:	n/a	n/a
2	BATF	chr5:52514994-52515362	GM12878	blood:	n/a	n/a
3	BATF	chr5:52507703-52507918	GM12878	blood:	n/a	chr5:52507794-52507805
4	BATF	chr5:52507674-52507927	GM12878	blood:	n/a	chr5:52507794-52507805
5	CCNT2	chr5:52541887-52542140	K562	blood:	n/a	n/a
6	CEBPB	chr5:52513522-52513715	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:52532352-52532430	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:52507773-52507830	IMR90	lung:	n/a	n/a
9	CEBPB	chr5:52541894-52542245	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:52527102-52527252	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:52513515-52513749	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:52541885-52542210	K562	blood:	n/a	n/a
13	CEBPD	chr5:52541722-52542181	K562	blood:	n/a	n/a
14	CTCF	chr5:52515223-52515247	ProgFib	skin:	n/a	n/a
15	CTCF	chr5:52532126-52532155	Lung_OC	lung:	n/a	n/a
16	CTCF	chr5:52539340-52539490	MCF-7	breast:	n/a	chr5:52539433-52539446
17	CTCF	chr5:52539380-52539530	GM12874	blood:	n/a	chr5:52539433-52539446
18	CTCF	chr5:52507734-52507800	A549	lung:	n/a	n/a
19	CTCF	chr5:52539380-52539530	HBMEC	blood vessel:	n/a	chr5:52539433-52539446
20	CTCF	chr5:52539380-52539530	GM12864	blood:	n/a	chr5:52539433-52539446
21	CTCF	chr5:52539480-52539630	NHEK	skin:	n/a	n/a
22	CTCF	chr5:52539330-52539570	K562	blood:	n/a	chr5:52539433-52539446
23	CTCF	chr5:52539400-52539550	HCT-116	colon:	n/a	chr5:52539433-52539446
24	CTCF	chr5:52539420-52539570	MCF-7	breast:	n/a	chr5:52539433-52539446
25	CTCF	chr5:52539360-52539510	GM12873	blood:	n/a	chr5:52539433-52539446
26	CTCF	chr5:52507753-52507827	ProgFib	skin:	n/a	n/a
27	CTCF	chr5:52532731-52532762	Fibrobl	skin:	n/a	n/a
28	CTCF	chr5:52539280-52539430	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr5:52539379-52539456	GM12878	blood:	n/a	chr5:52539433-52539446
30	CTCF	chr5:52539434-52539502	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:52539360-52539523	Gliobla	brain:	n/a	chr5:52539433-52539446
32	CTCF	chr5:52507700-52507850	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr5:52539400-52539550	Caco-2	colon:	n/a	chr5:52539433-52539446
34	CTCF	chr5:52539300-52539450	GM12869	blood:	n/a	chr5:52539433-52539446
35	CTCF	chr5:52539360-52539510	A549	lung:	n/a	chr5:52539433-52539446
36	CTCF	chr5:52539440-52539590	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:52515160-52515310	GM12865	blood:	n/a	n/a
38	CTCF	chr5:52507600-52507750	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr5:52507698-52507830	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr5:52541940-52542090	Caco-2	colon:	n/a	n/a
41	CTCF	chr5:52539320-52539470	HPAF	blood vessel:	n/a	chr5:52539433-52539446
42	CTCF	chr5:52539315-52539554	H1-hESC	embryonic stem cell:	n/a	chr5:52539433-52539446
43	CTCF	chr5:52539303-52539577	K562	blood:	n/a	chr5:52539433-52539446
44	CTCF	chr5:52507760-52507790	GM19240	blood:	n/a	n/a
45	CTCF	chr5:52539280-52539430	HCT-116	colon:	n/a	n/a
46	CTCF	chr5:52539348-52539521	Hela-S3	cervix:	n/a	chr5:52539433-52539446
47	CTCF	chr5:52539340-52539490	HFF-Myc	foreskin:	n/a	chr5:52539433-52539446
48	CTCF	chr5:52539340-52539490	HMEC	breast:	n/a	chr5:52539433-52539446
49	CTCF	chr5:52507733-52507814	HepG2	liver:	n/a	n/a
50	CTCF	chr5:52515140-52515290	GM06990	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:52543882-52543932	K562	blood:	n/a
2	chr5:52543882-52543932	K562	blood:	n/a
3	chr5:52536202-52536252	AG04449	skin:	fetal
4	chr5:52536202-52536252	HCPEpiC	choroid plexus:	n/a
5	chr5:52543882-52543932	Caco-2	colon:	n/a
6	chr5:52543882-52543932	NHBE	bronchial:	n/a
7	chr5:52536202-52536252	Hepatocyte	liver:	n/a
8	chr5:52543882-52543932	HCPEpiC	choroid plexus:	n/a
9	chr5:52543882-52543932	H1-hESC	embryonic stem cell:	embryo
10	chr5:52536202-52536252	MCF10A-Er-Src	breast:	n/a
11	chr5:52543882-52543932	MCF-7	breast:	n/a
12	chr5:52543882-52543932	GM06990	blood:	n/a
13	chr5:52536202-52536252	Jurkat	blood:	n/a
14	chr5:52536202-52536252	HCM	heart:	n/a
15	chr5:52536202-52536252	HCT-116	colon:	n/a
16	chr5:52543882-52543932	NT2-D1	testis:	n/a
17	chr5:52536202-52536252	HMEC	breast:	n/a
18	chr5:52543882-52543932	ECC-1	luminal epithelium:	n/a
19	chr5:52543882-52543932	SK-N-SH_RA	brain:	n/a
20	chr5:52543882-52543932	AG04449	skin:	fetal
21	chr5:52536202-52536252	ECC-1	luminal epithelium:	n/a
22	chr5:52543882-52543932	HRCEpiC	kidney:	n/a
23	chr5:52536202-52536252	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:52543882-52543932	PANC-1	pancreas:	n/a
25	chr5:52543882-52543932	PFSK-1	brain:	n/a
26	chr5:52536202-52536252	SKMC	muscle:	n/a
27	chr5:52543882-52543932	ovcar-3	ovarian:	n/a
28	chr5:52543882-52543932	LNCaP	prostate:	n/a
29	chr5:52543882-52543932	PrEC	prostate:	n/a
30	chr5:52543882-52543932	Hepatocyte	liver:	n/a
31	chr5:52543882-52543932	HL-60	blood:	n/a
32	chr5:52543882-52543932	HRPEpiC	eye:	n/a
33	chr5:52543882-52543932	HPAEpiC	pulmonary alveolar:	n/a
34	chr5:52543882-52543932	AG10803	skin:	n/a
35	chr5:52543882-52543932	HCF	heart:	n/a
36	chr5:52536202-52536252	BE2_C	brain:	n/a
37	chr5:52543882-52543932	U87	brain:	n/a
38	chr5:52536202-52536252	ProgFib	skin:	n/a
39	chr5:52536202-52536252	HRCEpiC	kidney:	n/a
40	chr5:52536202-52536252	HAEpiC	amniotic membrane:	n/a
41	chr5:52536202-52536252	GM19239	blood:	n/a
42	chr5:52543882-52543932	AG09319	gingival:	n/a
43	chr5:52536202-52536252	NT2-D1	testis:	n/a
44	chr5:52543882-52543932	BJ	skin:	n/a
45	chr5:52536202-52536252	HCF	heart:	n/a
46	chr5:52536202-52536252	HEK293	kidney:	embryo
47	chr5:52536202-52536252	GM06990	blood:	n/a
48	chr5:52543882-52543932	HepG2	liver:	n/a
49	chr5:52536202-52536252	SAEC	small airway:	n/a
50	chr5:52536202-52536252	CMK	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:52514986..52517115-chr5:52518136..52519755,2	MCF-7	breast:
2	chr5:52537239..52539717-chr5:52539892..52542383,2	K562	blood:
3	chr5:52537239..52539717-chr5:52539892..52542383,2	K562	blood:
4	chr5:52541978..52544639-chr5:52547451..52550337,2	K562	blood:
5	chr5:52532240..52534104-chr5:52535420..52537788,2	K562	blood:
6	chr5:52514986..52517115-chr5:52518136..52519755,2	MCF-7	breast:
7	chr5:52532240..52534104-chr5:52535420..52537788,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MOCS2-5	chr5:52543829-52544029	NONHSAT101427
2	lnc-MOCS2-5	chr5:52514226-52514749	NONHSAT101427

No data

Variant related genes	Relation type
ENSG00000213940	TF binding region
ENSG00000213940	CpG island

Extended variants
information (count: 2041 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2041 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541510455	chr5:52502188-52502189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560002036	chr5:52502191-52502192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs114589219	chr5:52502212-52502213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182815132	chr5:52502231-52502232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570250696	chr5:52502247-52502248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187462929	chr5:52502275-52502276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs549518501	chr5:52502310-52502311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73756636	chr5:52502330-52502331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs73756637	chr5:52502331-52502332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs193038677	chr5:52502365-52502366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571714041	chr5:52502416-52502417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565568365	chr5:52502427-52502428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538720232	chr5:52502439-52502440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536038742	chr5:52502440-52502441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554486531	chr5:52502442-52502443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576267068	chr5:52502443-52502444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184093308	chr5:52502453-52502454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557419962	chr5:52502469-52502470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558703068	chr5:52502475-52502476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577137069	chr5:52502484-52502485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566069358	chr5:52502487-52502488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187442282	chr5:52502491-52502492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559862357	chr5:52502516-52502517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2548321	chr5:52502526-52502527	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs77701314	chr5:52502607-52502608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs251513	chr5:52502644-52502645	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs531112271	chr5:52502647-52502648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555277968	chr5:52502650-52502651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35609378	chr5:52502654-52502655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs34881433	chr5:52502677-52502678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573565304	chr5:52502681-52502682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534338899	chr5:52502715-52502716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564764307	chr5:52502726-52502727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146903448	chr5:52502779-52502780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547139061	chr5:52502791-52502792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78286555	chr5:52502808-52502809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535903624	chr5:52502811-52502812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139391259	chr5:52502814-52502815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569806184	chr5:52502840-52502841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116938810	chr5:52502867-52502868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192711534	chr5:52502873-52502874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs251514	chr5:52502876-52502877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs553544745	chr5:52502883-52502884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574993328	chr5:52502892-52502893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542294889	chr5:52502901-52502902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563749526	chr5:52502903-52502904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575758755	chr5:52502916-52502917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546209898	chr5:52502924-52502925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183946851	chr5:52502970-52502971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188588100	chr5:52502975-52502976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	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
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:137 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52489000-52507000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:52489600-52507800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:52506800-52508200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:52506800-52508200	Enhancers	HMEC	breast
5	chr5:52506800-52508200	Enhancers	NHEK	skin
6	chr5:52507000-52507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:52507000-52507400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr5:52507000-52508200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:52507400-52507800	Enhancers	HUVEC	blood vessel
10	chr5:52507400-52508200	Enhancers	Muscle Satellite Cultured Cells	--
11	chr5:52507400-52508200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:52507400-52508400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:52507800-52508000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr5:52508200-52508400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:52508200-52509600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr5:52509600-52540000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:52515200-52515600	Active TSS	GM12878-XiMat	blood
18	chr5:52525400-52526000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
19	chr5:52526000-52526600	Active TSS	Fetal Heart	heart
20	chr5:52526600-52526800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr5:52526800-52528000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:52528000-52529000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:52529000-52535200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:52530200-52540000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr5:52532000-52532200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr5:52533200-52535400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:52533600-52534200	Enhancers	HSMM	muscle
28	chr5:52533600-52534200	Enhancers	HSMMtube	muscle
29	chr5:52534200-52540600	Weak transcription	HSMM	muscle
30	chr5:52535000-52536600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:52535000-52536600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:52535200-52535600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr5:52535200-52535600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr5:52535200-52535600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:52535200-52535600	Enhancers	Adipose Nuclei	Adipose
36	chr5:52535200-52535600	Enhancers	HMEC	breast
37	chr5:52535200-52535600	Enhancers	NHDF-Ad	bronchial
38	chr5:52535200-52535800	Enhancers	NHEK	skin
39	chr5:52535200-52535800	Enhancers	Osteobl	bone
40	chr5:52535400-52535600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:52535400-52535800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr5:52535400-52536800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:52535400-52536800	Enhancers	NHLF	lung
44	chr5:52535600-52539200	Weak transcription	HMEC	breast
45	chr5:52535600-52539800	Weak transcription	NHDF-Ad	bronchial
46	chr5:52535600-52540600	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr5:52535600-52540600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr5:52535600-52540600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:52535600-52541200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:52535800-52540600	Weak transcription	NHEK	skin

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