Variant report

Variant	nsv1031853
Chromosome Location	chr5:178846260-178917347
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:1038)
Chromatin interactive
region (count:20)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

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	chr5:178868515-178868770	K562	blood:	n/a	chr5:178868635-178868644 chr5:178868636-178868645 chr5:178868634-178868647 chr5:178868630-178868651 chr5:178868636-178868645 chr5:178868637-178868646
3	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
4	CBX3	chr5:178882860-178883255	K562	blood:	n/a	n/a
5	CEBPB	chr5:178901859-178902134	K562	blood:	n/a	n/a
6	CEBPB	chr5:178882230-178882319	A549	lung:	n/a	n/a
7	CEBPB	chr5:178858362-178858799	MCF-7	breast:	n/a	n/a
8	CEBPB	chr5:178882280-178882457	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a
10	CEBPB	chr5:178901904-178902149	IMR90	lung:	n/a	n/a
11	CEBPB	chr5:178858409-178858867	MCF-7	breast:	n/a	n/a
12	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
13	CEBPB	chr5:178858441-178858825	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:178858440-178858814	A549	lung:	n/a	n/a
15	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr5:178858455-178858788	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:178913744-178914042	IMR90	lung:	n/a	chr5:178913860-178913871
18	CEBPB	chr5:178858431-178858818	A549	lung:	n/a	n/a
19	CEBPB	chr5:178858452-178858788	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
21	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:178901917-178902069	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr5:178898849-178899101	K562	blood:	n/a	n/a
29	CEBPB	chr5:178858474-178858798	K562	blood:	n/a	n/a
30	CEBPB	chr5:178858449-178858788	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
32	CEBPZ	chr5:178853499-178853583	HepG2	liver:	n/a	n/a
33	CTCF	chr5:178879995-178880012	HepG2	liver:	n/a	n/a
34	CTCF	chr5:178901300-178901450	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:178859583-178859733	HepG2	liver:	n/a	n/a
36	CTCF	chr5:178909474-178909529	HepG2	liver:	n/a	chr5:178909484-178909502
37	CTCF	chr5:178859620-178859770	K562	blood:	n/a	n/a
38	CTCF	chr5:178876788-178876810	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:178899780-178899930	HepG2	liver:	n/a	n/a
40	CTCF	chr5:178909360-178909510	HEK293	kidney:	n/a	chr5:178909484-178909502
41	CTCF	chr5:178859660-178859810	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr5:178853240-178853390	GM12873	blood:	n/a	n/a
43	CTCF	chr5:178847360-178847510	GM12871	blood:	n/a	n/a
44	CTCF	chr5:178900994-178901013	GM10248	blood:	n/a	n/a
45	CTCF	chr5:178869865-178869914	GM13976	blood:	n/a	n/a
46	CTCF	chr5:178859580-178859730	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:178873420-178873570	GM12866	blood:	n/a	n/a
48	CTCF	chr5:178859620-178859770	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr5:178859643-178859771	K562	blood:	n/a	n/a
50	CTCF	chr5:178877536-178877604	Lung_OC	lung:	n/a	n/a

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178903057-178903107	SAEC	small airway:	n/a
2	chr5:178903057-178903107	SAEC	small airway:	n/a
3	chr5:178882605-178882655	HL-60	blood:	n/a
4	chr5:178882605-178882655	U87	brain:	n/a
5	chr5:178899789-178899839	HCT-116	colon:	n/a
6	chr5:178899850-178899900	SK-N-SH	brain:	n/a
7	chr5:178899789-178899839	GM19239	blood:	n/a
8	chr5:178913683-178913733	AG10803	skin:	n/a
9	chr5:178902956-178903006	H1-hESC	embryonic stem cell:	embryo
10	chr5:178902790-178902840	BJ	skin:	n/a
11	chr5:178854202-178854252	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:178899850-178899900	Hepatocyte	liver:	n/a
13	chr5:178913683-178913733	SK-N-MC	brain:	n/a
14	chr5:178882605-178882655	BE2_C	brain:	n/a
15	chr5:178854502-178854552	PFSK-1	brain:	n/a
16	chr5:178882605-178882655	AG04450	lung:	fetal
17	chr5:178899812-178899862	MCF-7	breast:	n/a
18	chr5:178854758-178854808	GM12892	blood:	n/a
19	chr5:178899789-178899839	SAEC	small airway:	n/a
20	chr5:178854265-178854315	GM12878	blood:	n/a
21	chr5:178882763-178882813	NH-A	brain:	n/a
22	chr5:178854265-178854315	U87	brain:	n/a
23	chr5:178899812-178899862	GM06990	blood:	n/a
24	chr5:178854758-178854808	LNCaP	prostate:	n/a
25	chr5:178902956-178903006	HUVEC	blood vessel:	n/a
26	chr5:178899812-178899862	AG09319	gingival:	n/a
27	chr5:178854202-178854252	NH-A	brain:	n/a
28	chr5:178854586-178854636	HCM	heart:	n/a
29	chr5:178902699-178902749	Jurkat	blood:	n/a
30	chr5:178882605-178882655	NHBE	bronchial:	n/a
31	chr5:178854586-178854636	AoSMC	blood vessel:	n/a
32	chr5:178913683-178913733	HepG2	liver:	n/a
33	chr5:178902790-178902840	SK-N-SH_RA	brain:	n/a
34	chr5:178899812-178899862	HNPCEpiC	eye:	n/a
35	chr5:178903057-178903107	HCF	heart:	n/a
36	chr5:178846740-178846790	GM12878	blood:	n/a
37	chr5:178899789-178899839	MCF10A-Er-Src	breast:	n/a
38	chr5:178846740-178846790	AG04450	lung:	fetal
39	chr5:178899850-178899900	Jurkat	blood:	n/a
40	chr5:178902790-178902840	HIPEpiC	eye:	n/a
41	chr5:178854265-178854315	NHBE	bronchial:	n/a
42	chr5:178902790-178902840	AG09319	gingival:	n/a
43	chr5:178902790-178902840	AG04450	lung:	fetal
44	chr5:178902790-178902840	HRE	kidney:	n/a
45	chr5:178899850-178899900	U87	brain:	n/a
46	chr5:178899812-178899862	NH-A	brain:	n/a
47	chr5:178902699-178902749	GM12891	blood:	n/a
48	chr5:178903057-178903107	HEEpiC	esophagus:	n/a
49	chr5:178846740-178846790	T-47D	breast:	n/a
50	chr5:178903057-178903107	MCF-7	breast:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178834706..178836824-chr5:178848454..178851441,2	K562	blood:
2	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
3	chr5:178871548..178873217-chr5:178880850..178883062,2	MCF-7	breast:
4	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
5	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
6	chr5:178843393..178845957-chr5:178846634..178848163,2	K562	blood:
7	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
8	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
9	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
10	chr5:178847716..178849702-chr5:178850729..178853201,2	K562	blood:
11	chr5:178837251..178839356-chr5:178856114..178858488,2	MCF-7	breast:
12	chr5:178844770..178846299-chr5:178846428..178847929,2	MCF-7	breast:
13	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
14	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
15	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
16	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
17	chr5:178848461..178850011-chr5:178850961..178853110,2	MCF-7	breast:
18	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
19	chr12:72186780..72187498-chr5:178846162..178846680,2	MCF-7	breast:
20	chr5:178882272..178884920-chr5:179049238..179052060,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAMTS2-2	chr5:178893834-178894126	NONHSAT105584
2	lnc-RUFY1-1	chr5:178882416-178882818	XLOC_004674
3	lnc-RUFY1-1	chr5:178882939-178883096	XLOC_004674

No data

Variant related genes	Relation type
ENSG00000250674	TF binding region
RN7SL71P	TF binding region
ENSG00000250674	CpG island
RN7SL71P	CpG island
ENSG00000250674	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000264205	chromatin interactions
ENSG00000176783	chromatin interactions

Extended variants
information (count: 3189 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:3189 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549898684	chr5:178846317-178846318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73336932	chr5:178846331-178846332	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs539240684	chr5:178846348-178846349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553558682	chr5:178846388-178846389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565690345	chr5:178846436-178846437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145847237	chr5:178846451-178846452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148564919	chr5:178846458-178846459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs372695539	chr5:178846459-178846460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576658000	chr5:178846491-178846492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146122817	chr5:178846554-178846555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376600707	chr5:178846562-178846563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35963244	chr5:178846563-178846564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs58972144	chr5:178846581-178846582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs78950663	chr5:178846582-178846583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78125647	chr5:178846584-178846585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200580334	chr5:178846588-178846589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543418488	chr5:178846594-178846595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375797631	chr5:178846600-178846601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs555545087	chr5:178846646-178846647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573773616	chr5:178846676-178846677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs7718190	chr5:178846679-178846680	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs188404562	chr5:178846722-178846723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142898049	chr5:178846740-178846741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546491951	chr5:178846743-178846744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115501864	chr5:178846769-178846770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531760838	chr5:178846771-178846772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376953833	chr5:178846773-178846774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574655540	chr5:178846788-178846789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs193192513	chr5:178846803-178846804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185145099	chr5:178846804-178846805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529349307	chr5:178846840-178846841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs369027617	chr5:178846847-178846848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149325276	chr5:178846895-178846896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569390974	chr5:178846937-178846938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200680500	chr5:178846967-178846968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547458211	chr5:178847000-178847001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62394880	chr5:178847001-178847002	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs557721451	chr5:178847002-178847003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7705649	chr5:178847029-178847030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs569847671	chr5:178847034-178847035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560061427	chr5:178847037-178847038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537086041	chr5:178847043-178847044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62394881	chr5:178847056-178847057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs573635748	chr5:178847108-178847109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187110637	chr5:178847144-178847145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540852636	chr5:178847217-178847218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138320397	chr5:178847219-178847220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552759706	chr5:178847226-178847227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7702097	chr5:178847300-178847301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7378933	chr5:178847302-178847303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178842600-178848400	Weak transcription	Spleen	Spleen
2	chr5:178847400-178848000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:178847800-178848600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:178848000-178848400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178848400-178849200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:178848400-178850400	Enhancers	Spleen	Spleen
7	chr5:178849200-178849400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:178849200-178850000	Bivalent Enhancer	Fetal Stomach	stomach
9	chr5:178849200-178850400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr5:178849200-178850800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr5:178849400-178849600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr5:178849400-178850000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:178849400-178850200	Enhancers	Fetal Muscle Leg	muscle
14	chr5:178849400-178850600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr5:178849600-178850000	Enhancers	Osteobl	bone
16	chr5:178849600-178850600	Enhancers	NHDF-Ad	bronchial
17	chr5:178849800-178850200	Bivalent Enhancer	Placenta	Placenta
18	chr5:178850000-178850200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr5:178850200-178854000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr5:178851800-178852000	Enhancers	Fetal Intestine Large	intestine
21	chr5:178853000-178854200	Enhancers	H1 Cell Line	embryonic stem cell
22	chr5:178853200-178854000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:178853400-178854000	Enhancers	Pancreas	Pancrea
24	chr5:178853400-178855000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr5:178853600-178854800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr5:178853800-178854600	Bivalent Enhancer	Fetal Stomach	stomach
27	chr5:178854000-178854200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:178854000-178854600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr5:178854000-178854600	Enhancers	Fetal Muscle Leg	muscle
30	chr5:178854200-178854400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:178854400-178854600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr5:178854400-178855000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:178854600-178856200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr5:178855000-178856000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:178855000-178856000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:178855400-178856400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:178856000-178856200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:178856000-178856200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr5:178856200-178856400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr5:178856200-178859600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:178859600-178860400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:178860400-178864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:178862600-178862800	Enhancers	Fetal Lung	lung
44	chr5:178862800-178863000	Bivalent Enhancer	Right Ventricle	heart
45	chr5:178862800-178864200	Weak transcription	Fetal Lung	lung
46	chr5:178863000-178866200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr5:178863000-178866600	Enhancers	Spleen	Spleen
48	chr5:178863200-178863400	Enhancers	Placenta	Placenta
49	chr5:178863200-178863600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
50	chr5:178863400-178863800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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