Variant report

Variant	nsv965604
Chromosome Location	chr5:61171281-61182073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:61176515-61176583	Kidney_OC	kidney:	n/a	n/a
2	FOS	chr5:61177713-61178001	MCF10A-Er-Src	breast:	n/a	chr5:61177874-61177886 chr5:61177874-61177885 chr5:61177876-61177884 chr5:61177877-61177888 chr5:61177879-61177886
3	FOS	chr5:61177736-61178008	MCF10A-Er-Src	breast:	n/a	chr5:61177874-61177886 chr5:61177874-61177885 chr5:61177876-61177884 chr5:61177877-61177888 chr5:61177879-61177886
4	FOS	chr5:61177817-61178035	MCF10A-Er-Src	breast:	n/a	chr5:61177874-61177886 chr5:61177874-61177885 chr5:61177876-61177884 chr5:61177877-61177888 chr5:61177879-61177886
5	FOS	chr5:61177704-61178000	MCF10A-Er-Src	breast:	n/a	chr5:61177874-61177886 chr5:61177874-61177885 chr5:61177876-61177884 chr5:61177877-61177888 chr5:61177879-61177886
6	FOXP2	chr5:61177593-61177897	PFSK-1	brain:	n/a	n/a
7	GATA2	chr5:61174510-61175002	SH-SY5Y	brain:	n/a	n/a
8	GATA2	chr5:61180148-61180603	SH-SY5Y	brain:	n/a	n/a
9	GATA3	chr5:61180298-61180578	SH-SY5Y	brain:	n/a	n/a
10	GATA3	chr5:61174699-61175041	SH-SY5Y	brain:	n/a	n/a
11	MAX	chr5:61177604-61177939	K562	blood:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
12	MAX	chr5:61177664-61177992	ECC-1	luminal epithelium:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
13	MAX	chr5:61177691-61177931	H1-hESC	embryonic stem cell:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
14	MAX	chr5:61177588-61178010	H1-hESC	embryonic stem cell:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
15	MAX	chr5:61177699-61177841	K562	blood:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
16	MYC	chr5:61177600-61177981	MCF10A-Er-Src	breast:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
17	MYC	chr5:61177723-61177853	MCF-7	breast:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
18	MYC	chr5:61177667-61177934	MCF10A-Er-Src	breast:	n/a	chr5:61177784-61177797 chr5:61177786-61177796 chr5:61177785-61177796 chr5:61177784-61177797 chr5:61177786-61177795 chr5:61177781-61177800 chr5:61177785-61177796 chr5:61177785-61177795 chr5:61177876-61177885 chr5:61177786-61177796 chr5:61177785-61177795 chr5:61177785-61177796 chr5:61177784-61177797
19	NFIC	chr5:61182043-61182446	ECC-1	luminal epithelium:	n/a	chr5:61182238-61182254 chr5:61182226-61182254 chr5:61182237-61182254
20	POLR2A	chr5:61177841-61177852	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr5:61179730-61179897	GM12878	blood:	n/a	n/a
22	POLR2A	chr5:61177533-61178069	PFSK-1	brain:	n/a	n/a
23	POLR2A	chr5:61174244-61174872	SK-N-MC	brain:	n/a	n/a
24	REST	chr5:61177637-61177907	PFSK-1	brain:	n/a	chr5:61177802-61177820
25	SIN3AK20	chr5:61177567-61177973	PFSK-1	brain:	n/a	n/a
26	STAT3	chr5:61177882-61177936	MCF10A-Er-Src	breast:	n/a	n/a
27	STAT3	chr5:61179205-61179275	MCF10A-Er-Src	breast:	n/a	n/a
28	TAF1	chr5:61177546-61178004	PFSK-1	brain:	n/a	n/a
29	USF1	chr5:61177723-61177974	ECC-1	luminal epithelium:	n/a	n/a
30	USF1	chr5:61177677-61177984	H1-hESC	embryonic stem cell:	n/a	n/a
31	USF1	chr5:61177630-61178022	ECC-1	luminal epithelium:	n/a	n/a
32	USF2	chr5:61177756-61177803	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61180442-61180492	HUVEC	blood vessel:	n/a
2	chr5:61180442-61180492	RPTEC	kidney:	n/a
3	chr5:61180442-61180492	HIPEpiC	eye:	n/a
4	chr5:61180442-61180492	NT2-D1	testis:	n/a
5	chr5:61180442-61180492	AG10803	skin:	n/a
6	chr5:61180442-61180492	IMR90	lung:	fetal
7	chr5:61180442-61180492	NH-A	brain:	n/a
8	chr5:61180442-61180492	SAEC	small airway:	n/a
9	chr5:61180442-61180492	HCF	heart:	n/a
10	chr5:61180442-61180492	HEK293	kidney:	embryo
11	chr5:61180442-61180492	PrEC	prostate:	n/a
12	chr5:61180442-61180492	HCT-116	colon:	n/a
13	chr5:61180442-61180492	GM06990	blood:	n/a
14	chr5:61180442-61180492	HPAEpiC	pulmonary alveolar:	n/a
15	chr5:61180442-61180492	AoSMC	blood vessel:	n/a
16	chr5:61180442-61180492	HNPCEpiC	eye:	n/a
17	chr5:61180442-61180492	U87	brain:	n/a
18	chr5:61180442-61180492	AG09319	gingival:	n/a
19	chr5:61180442-61180492	NHBE	bronchial:	n/a
20	chr5:61180442-61180492	T-47D	breast:	n/a
21	chr5:61180442-61180492	HAEpiC	amniotic membrane:	n/a
22	chr5:61180442-61180492	A549	lung:	n/a
23	chr5:61180442-61180492	Jurkat	blood:	n/a
24	chr5:61180442-61180492	BJ	skin:	n/a
25	chr5:61180442-61180492	Hela-S3	cervix:	n/a
26	chr5:61180442-61180492	HRCEpiC	kidney:	n/a
27	chr5:61180442-61180492	LNCaP	prostate:	n/a
28	chr5:61180442-61180492	ovcar-3	ovarian:	n/a
29	chr5:61180442-61180492	SK-N-MC	brain:	n/a
30	chr5:61180442-61180492	AG04450	lung:	fetal
31	chr5:61180442-61180492	SK-N-SH	brain:	n/a
32	chr5:61180442-61180492	HepG2	liver:	n/a
33	chr5:61180442-61180492	CMK	blood:	n/a
34	chr5:61180442-61180492	GM12892	blood:	n/a
35	chr5:61180442-61180492	AG04449	skin:	fetal
36	chr5:61180442-61180492	PANC-1	pancreas:	n/a
37	chr5:61180442-61180492	ProgFib	skin:	n/a
38	chr5:61180442-61180492	Caco-2	colon:	n/a
39	chr5:61180442-61180492	NB4	blood:	n/a
40	chr5:61180442-61180492	HEEpiC	esophagus:	n/a
41	chr5:61180442-61180492	HCM	heart:	n/a
42	chr5:61180442-61180492	MCF10A-Er-Src	breast:	n/a
43	chr5:61180442-61180492	MCF-7	breast:	n/a
44	chr5:61180442-61180492	HMEC	breast:	n/a
45	chr5:61180442-61180492	GM12878	blood:	n/a
46	chr5:61180442-61180492	ECC-1	luminal epithelium:	n/a
47	chr5:61180442-61180492	K562	blood:	n/a
48	chr5:61180442-61180492	SKMC	muscle:	n/a
49	chr5:61180442-61180492	GM19239	blood:	n/a
50	chr5:61180442-61180492	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:60628455..60630619-chr5:61175090..61177005,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf64-2	chr5:61173936-61174226	XLOC_004406
2	lnc-C5orf64-2	chr5:61181794-61181956	XLOC_004406

Variant related genes	Relation type
ENSG00000248199	TF binding region
ENSG00000248199	CpG island

Extended variants
information (count: 416 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6859572	chr5:61171312-61171313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575226890	chr5:61171329-61171330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572041558	chr5:61171344-61171345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544231369	chr5:61171363-61171364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371444437	chr5:61171472-61171473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563217213	chr5:61171481-61171482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576747016	chr5:61171484-61171485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545562036	chr5:61171489-61171490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191901554	chr5:61171496-61171497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552187998	chr5:61171510-61171511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545707045	chr5:61171522-61171523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374130221	chr5:61171552-61171553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183951813	chr5:61171585-61171586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530504688	chr5:61171628-61171629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs563910056	chr5:61171643-61171644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570504652	chr5:61171695-61171696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550623987	chr5:61171701-61171702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571131854	chr5:61171705-61171706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1445878	chr5:61171733-61171734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76958694	chr5:61171747-61171748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs566947459	chr5:61171748-61171749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188448947	chr5:61171753-61171754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555562148	chr5:61171772-61171773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1445877	chr5:61171872-61171873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1445876	chr5:61171915-61171916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs374856164	chr5:61171953-61171954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537816918	chr5:61171966-61171967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562879222	chr5:61171974-61171975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557749151	chr5:61172008-61172009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530101051	chr5:61172068-61172069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149468589	chr5:61172086-61172087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190327884	chr5:61172103-61172104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567157387	chr5:61172114-61172115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559648996	chr5:61172148-61172149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530764810	chr5:61172179-61172180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572944438	chr5:61172182-61172183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182528330	chr5:61172183-61172184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34469886	chr5:61172200-61172201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs530645227	chr5:61172230-61172231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552928190	chr5:61172241-61172242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1445875	chr5:61172249-61172250	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs186994109	chr5:61172276-61172277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533004154	chr5:61172297-61172298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546967623	chr5:61172335-61172336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs191435985	chr5:61172361-61172362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182509126	chr5:61172384-61172385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189165658	chr5:61172385-61172386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143871789	chr5:61172387-61172388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374301257	chr5:61172430-61172431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537961396	chr5:61172441-61172442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
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

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61168800-61174000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:61173600-61175000	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:61173600-61175000	Enhancers	HMEC	breast
4	chr5:61173800-61174400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr5:61173800-61174800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:61173800-61175200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr5:61174000-61174800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr5:61174000-61174800	Enhancers	NHEK	skin
9	chr5:61174800-61177200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:61174800-61177200	Weak transcription	NHEK	skin
11	chr5:61174800-61177600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr5:61175000-61177200	Weak transcription	HMEC	breast
13	chr5:61175200-61177000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr5:61177000-61178000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:61177200-61177600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:61177200-61177600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:61177200-61177800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:61177200-61178000	Enhancers	HMEC	breast
19	chr5:61177200-61178000	Enhancers	NHEK	skin
20	chr5:61177200-61178200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr5:61177400-61177600	Active TSS	Brain Anterior Caudate	brain
22	chr5:61177400-61177600	Active TSS	HSMMtube	muscle
23	chr5:61177400-61177800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:61177400-61177800	Enhancers	HSMM	muscle
25	chr5:61177400-61178000	Enhancers	H9 Cell Line	embryonic stem cell
26	chr5:61177400-61178000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr5:61177400-61178200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:61177400-61178200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr5:61177400-61178200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr5:61177400-61178200	Enhancers	NH-A	brain
31	chr5:61177400-61178400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:61177600-61177800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:61177600-61177800	Flanking Active TSS	Brain Anterior Caudate	brain
34	chr5:61177600-61177800	Flanking Active TSS	HSMMtube	muscle
35	chr5:61177600-61178000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:61177600-61178000	Enhancers	Osteobl	bone
37	chr5:61177600-61178200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:61177600-61178200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:61177800-61178200	Enhancers	Brain Anterior Caudate	brain
40	chr5:61178000-61178200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr5:61178000-61180000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr5:61178000-61180200	Weak transcription	HMEC	breast
43	chr5:61178200-61180000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:61178200-61183000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr5:61178400-61178800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:61178800-61180600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:61179400-61181000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:61179600-61180000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
49	chr5:61179600-61181000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr5:61180000-61180600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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