Variant report

Variant	nsv883259
Chromosome Location	chr5:178828854-178878869
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	BACH1	chr5:178867641-178867777	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr5:178867642-178867915	K562	blood:	n/a	chr5:178867741-178867750 chr5:178867742-178867751 chr5:178867742-178867751 chr5:178867743-178867752 chr5:178867736-178867757 chr5:178867740-178867753
3	BHLHE40	chr5:178868515-178868770	K562	blood:	n/a	chr5:178868635-178868644 chr5:178868636-178868645 chr5:178868634-178868647 chr5:178868630-178868651 chr5:178868636-178868645 chr5:178868637-178868646
4	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
5	CEBPB	chr5:178858440-178858814	A549	lung:	n/a	n/a
6	CEBPB	chr5:178858441-178858825	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:178858455-178858788	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:178858362-178858799	MCF-7	breast:	n/a	n/a
9	CEBPB	chr5:178858474-178858798	K562	blood:	n/a	n/a
10	CEBPB	chr5:178858409-178858867	MCF-7	breast:	n/a	n/a
11	CEBPB	chr5:178858449-178858788	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:178858452-178858788	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPZ	chr5:178853499-178853583	HepG2	liver:	n/a	n/a
14	CTCF	chr5:178831380-178831634	Gliobla	brain:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
15	CTCF	chr5:178831420-178831570	BJ	skin:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
16	CTCF	chr5:178831420-178831570	HCPEpiC	choroid plexus:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
17	CTCF	chr5:178831360-178831510	HVMF	connective:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
18	CTCF	chr5:178859600-178859750	HCT-116	colon:	n/a	n/a
19	CTCF	chr5:178831420-178831570	HCM	heart:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
20	CTCF	chr5:178831421-178831569	K562	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
21	CTCF	chr5:178831210-178831765	HCT-116	colon:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
22	CTCF	chr5:178831420-178831570	GM12865	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
23	CTCF	chr5:178831444-178831577	H1-hESC	embryonic stem cell:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
24	CTCF	chr5:178853240-178853390	GM12873	blood:	n/a	n/a
25	CTCF	chr5:178831440-178831590	HCM	heart:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
26	CTCF	chr5:178859700-178859850	HEK293	kidney:	n/a	n/a
27	CTCF	chr5:178859640-178859790	HepG2	liver:	n/a	n/a
28	CTCF	chr5:178831480-178831630	HFF-Myc	foreskin:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
29	CTCF	chr5:178831420-178831570	AG09319	gingival:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
30	CTCF	chr5:178869865-178869914	GM13976	blood:	n/a	n/a
31	CTCF	chr5:178831300-178831590	GM12873	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
32	CTCF	chr5:178831345-178831644	K562	blood:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
33	CTCF	chr5:178831440-178831590	RPTEC	kidney:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
34	CTCF	chr5:178831420-178831570	AG10803	skin:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
35	CTCF	chr5:178831390-178831668	MCF-7	breast:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
36	CTCF	chr5:178831420-178831570	BE2_C	brain:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
37	CTCF	chr5:178831440-178831590	K562	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
38	CTCF	chr5:178873420-178873570	GM12866	blood:	n/a	n/a
39	CTCF	chr5:178831420-178831570	NHDF-neo	bronchial:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
40	CTCF	chr5:178831454-178831542	GM12891	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
41	CTCF	chr5:178831420-178831570	HA-sp	spinal cord:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
42	CTCF	chr5:178831416-178831599	K562	blood:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
43	CTCF	chr5:178831440-178831590	HCFaa	heart:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
44	CTCF	chr5:178831400-178831550	HCT-116	colon:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
45	CTCF	chr5:178831420-178831570	HPAF	blood vessel:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503
46	CTCF	chr5:178831660-178831810	WI-38	lung:	n/a	n/a
47	CTCF	chr5:178831300-178831691	IMR90	lung:	n/a	chr5:178831604-178831622 chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831606-178831627 chr5:178831482-178831503
48	CTCF	chr5:178859643-178859771	K562	blood:	n/a	n/a
49	CTCF	chr5:178859580-178859730	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr5:178831462-178831558	NHEK	skin:	n/a	chr5:178831487-178831505 chr5:178831489-178831502 chr5:178831482-178831503

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178854202-178854252	NHBE	bronchial:	n/a
2	chr5:178835980-178836030	U87	brain:	n/a
3	chr5:178835980-178836030	AG04449	skin:	fetal
4	chr5:178835885-178835935	AG09309	skin:	n/a
5	chr5:178854265-178854315	LNCaP	prostate:	n/a
6	chr5:178854265-178854315	NHDF-neo	bronchial:	n/a
7	chr5:178835885-178835935	HIPEpiC	eye:	n/a
8	chr5:178854502-178854552	AG04449	skin:	fetal
9	chr5:178833490-178833540	HAEpiC	amniotic membrane:	n/a
10	chr5:178854586-178854636	AG04450	lung:	fetal
11	chr5:178854586-178854636	GM06990	blood:	n/a
12	chr5:178835980-178836030	Jurkat	blood:	n/a
13	chr5:178833490-178833540	HRCEpiC	kidney:	n/a
14	chr5:178854586-178854636	HEEpiC	esophagus:	n/a
15	chr5:178854265-178854315	GM06990	blood:	n/a
16	chr5:178854265-178854315	IMR90	lung:	fetal
17	chr5:178833490-178833540	HCT-116	colon:	n/a
18	chr5:178854758-178854808	NH-A	brain:	n/a
19	chr5:178835885-178835935	HEK293	kidney:	embryo
20	chr5:178835943-178835993	HRPEpiC	eye:	n/a
21	chr5:178854758-178854808	AG04449	skin:	fetal
22	chr5:178854502-178854552	GM12891	blood:	n/a
23	chr5:178835943-178835993	IMR90	lung:	fetal
24	chr5:178835943-178835993	RPTEC	kidney:	n/a
25	chr5:178854586-178854636	RPTEC	kidney:	n/a
26	chr5:178835980-178836030	IMR90	lung:	fetal
27	chr5:178835943-178835993	CMK	blood:	n/a
28	chr5:178835943-178835993	SK-N-SH_RA	brain:	n/a
29	chr5:178854265-178854315	BJ	skin:	n/a
30	chr5:178854758-178854808	HRE	kidney:	n/a
31	chr5:178854265-178854315	H1-hESC	embryonic stem cell:	embryo
32	chr5:178854202-178854252	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:178854502-178854552	NHDF-neo	bronchial:	n/a
34	chr5:178846740-178846790	RPTEC	kidney:	n/a
35	chr5:178833490-178833540	GM12892	blood:	n/a
36	chr5:178854265-178854315	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:178833490-178833540	PrEC	prostate:	n/a
38	chr5:178854202-178854252	SK-N-SH_RA	brain:	n/a
39	chr5:178854758-178854808	H1-hESC	embryonic stem cell:	embryo
40	chr5:178854586-178854636	BJ	skin:	n/a
41	chr5:178854758-178854808	AoSMC	blood vessel:	n/a
42	chr5:178854202-178854252	IMR90	lung:	fetal
43	chr5:178854502-178854552	HCF	heart:	n/a
44	chr5:178835943-178835993	Hepatocyte	liver:	n/a
45	chr5:178835885-178835935	CMK	blood:	n/a
46	chr5:178835943-178835993	SK-N-SH	brain:	n/a
47	chr5:178835885-178835935	Jurkat	blood:	n/a
48	chr5:178854502-178854552	Hela-S3	cervix:	n/a
49	chr5:178854202-178854252	ovcar-3	ovarian:	n/a
50	chr5:178854586-178854636	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
2	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
3	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
4	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
5	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
6	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
7	chr5:178871548..178873217-chr5:178880850..178883062,2	MCF-7	breast:
8	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
9	chr5:178840253..178841953-chr5:178842013..178844118,2	K562	blood:
10	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
11	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
12	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
13	chr5:178811806..178815884-chr5:178836936..178839970,3	MCF-7	breast:
14	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
15	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
16	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
17	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:

Variant related genes	Relation type
ENSG00000250674	TF binding region
ENSG00000250674	CpG island
ENSG00000250674	chromatin interactions
ENSG00000253617	chromatin interactions

Extended variants
information (count: 2046 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2046 , 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	rs186682585	chr5:178829659-178829660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538455078	chr5:178829669-178829670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550377126	chr5:178829688-178829689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568819398	chr5:178829783-178829784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535764182	chr5:178829873-178829874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554405447	chr5:178829879-178829880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11738978	chr5:178829906-178829907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112845901	chr5:178829933-178829934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191478143	chr5:178829938-178829939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557847412	chr5:178829940-178829941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562108579	chr5:178829983-178829984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576114660	chr5:178830008-178830009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543238662	chr5:178830011-178830012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555137269	chr5:178830017-178830018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs182852037	chr5:178830037-178830038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373986023	chr5:178830039-178830040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187877504	chr5:178830041-178830042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559551298	chr5:178830090-178830091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532811846	chr5:178830130-178830131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs139130420	chr5:178830150-178830151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563405216	chr5:178830159-178830160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577143632	chr5:178830164-178830165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189676303	chr5:178830182-178830183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550438365	chr5:178830232-178830233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs568680984	chr5:178830238-178830239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529444988	chr5:178830257-178830258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200290006	chr5:178830258-178830259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs398000073	chr5:178830267-178830268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62396788	chr5:178830270-178830271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9329073	chr5:178830284-178830285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561442237	chr5:178830292-178830293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566330618	chr5:178830303-178830304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115706227	chr5:178830373-178830374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182252511	chr5:178830406-178830407	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569860869	chr5:178830481-178830482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75792983	chr5:178830514-178830515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558850564	chr5:178830526-178830527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576823	chr5:178830540-178830541	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs9329074	chr5:178830574-178830575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541192757	chr5:178830589-178830590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553007128	chr5:178830602-178830603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149449998	chr5:178830672-178830673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116344233	chr5:178830689-178830690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563264779	chr5:178830696-178830697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577883	chr5:178830704-178830705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144146563	chr5:178830726-178830727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188069150	chr5:178830729-178830730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192444357	chr5:178830759-178830760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529482258	chr5:178830771-178830772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578640	chr5:178830774-178830775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
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
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:173 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178829600-178833200	Weak transcription	Ovary	ovary
2	chr5:178830400-178830600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:178831200-178831400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:178831200-178831400	Enhancers	Osteobl	bone
5	chr5:178831600-178832200	Enhancers	Spleen	Spleen
6	chr5:178831800-178832000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr5:178831800-178832000	Bivalent Enhancer	Fetal Stomach	stomach
8	chr5:178832200-178832600	Weak transcription	Spleen	Spleen
9	chr5:178832200-178832800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:178832200-178834800	Enhancers	Fetal Muscle Leg	muscle
11	chr5:178832600-178832800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:178832600-178832800	Enhancers	Spleen	Spleen
13	chr5:178832600-178835200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr5:178832800-178833400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:178832800-178833600	Bivalent Enhancer	Fetal Stomach	stomach
16	chr5:178832800-178834400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
17	chr5:178832800-178834600	Weak transcription	Spleen	Spleen
18	chr5:178832800-178835200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr5:178833000-178833200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr5:178833000-178834800	Enhancers	Placenta	Placenta
21	chr5:178833000-178835000	Enhancers	Fetal Lung	lung
22	chr5:178833200-178833600	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr5:178833200-178833800	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr5:178833200-178834200	Enhancers	NHDF-Ad	bronchial
25	chr5:178833200-178834800	Enhancers	Ovary	ovary
26	chr5:178833200-178835000	Enhancers	Adipose Nuclei	Adipose
27	chr5:178833200-178835800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr5:178833400-178834600	Enhancers	Osteobl	bone
29	chr5:178833400-178834800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr5:178833400-178835000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:178833400-178835200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr5:178833400-178835800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr5:178833600-178834000	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr5:178833600-178835200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr5:178833600-178835400	Enhancers	Fetal Stomach	stomach
36	chr5:178833800-178834400	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr5:178833800-178834600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:178833800-178834800	Enhancers	Fetal Intestine Small	intestine
39	chr5:178834000-178834600	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr5:178834200-178834800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr5:178834400-178834600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:178834400-178834600	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr5:178834400-178834800	Enhancers	Colonic Mucosa	Colon
44	chr5:178834400-178835200	Enhancers	Right Atrium	heart
45	chr5:178834600-178834800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:178834600-178835200	Enhancers	Spleen	Spleen
47	chr5:178834800-178837600	Weak transcription	Fetal Muscle Leg	muscle
48	chr5:178835200-178836800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr5:178835200-178837200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:178835200-178840600	Weak transcription	Spleen	Spleen

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