Variant report

Variant	nsv883264
Chromosome Location	chr5:178887482-178936722
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	ARID3A	chr5:178921008-178921368	K562	blood:	n/a	n/a
2	ARID3A	chr5:178920984-178921396	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
4	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:178901832-178902147	K562	blood:	n/a	n/a
6	CEBPB	chr5:178918660-178918869	IMR90	lung:	n/a	chr5:178918811-178918822
7	CEBPB	chr5:178898880-178899073	MCF-7	breast:	n/a	n/a
8	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:178901844-178902195	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:178898795-178899125	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:178901817-178902203	MCF-7	breast:	n/a	n/a
13	CEBPB	chr5:178898849-178899101	K562	blood:	n/a	n/a
14	CEBPB	chr5:178901917-178902069	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:178898812-178899126	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:178901859-178902134	K562	blood:	n/a	n/a
17	CEBPB	chr5:178920783-178920906	K562	blood:	n/a	n/a
18	CEBPB	chr5:178901904-178902149	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:178898817-178899053	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:178901823-178902191	MCF-7	breast:	n/a	n/a
21	CEBPB	chr5:178901825-178902196	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr5:178918785-178918864	HepG2	liver:	n/a	chr5:178918811-178918822
23	CEBPB	chr5:178901832-178902156	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr5:178913800-178913866	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:178918772-178918946	K562	blood:	n/a	chr5:178918811-178918822
26	CEBPB	chr5:178921088-178921413	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:178913744-178914042	IMR90	lung:	n/a	chr5:178913860-178913871
28	CTCF	chr5:178923000-178923150	HCPEpiC	choroid plexus:	n/a	chr5:178923029-178923037
29	CTCF	chr5:178921160-178921310	AG09319	gingival:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
30	CTCF	chr5:178902920-178903070	HepG2	liver:	n/a	n/a
31	CTCF	chr5:178923020-178923170	NHEK	skin:	n/a	chr5:178923029-178923037
32	CTCF	chr5:178921160-178921310	HRPEpiC	eye:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
33	CTCF	chr5:178921192-178921349	Fibrobl	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
34	CTCF	chr5:178922823-178923253	MCF-7	breast:	n/a	chr5:178923029-178923037
35	CTCF	chr5:178921180-178921330	HPF	lung:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
36	CTCF	chr5:178923003-178923169	MCF-7	breast:	n/a	chr5:178923029-178923037
37	CTCF	chr5:178921023-178921318	SK-N-SH_RA	brain:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
38	CTCF	chr5:178922980-178923130	GM12865	blood:	n/a	chr5:178923029-178923037
39	CTCF	chr5:178900994-178901013	GM10248	blood:	n/a	n/a
40	CTCF	chr5:178922980-178923130	HPAF	blood vessel:	n/a	chr5:178923029-178923037
41	CTCF	chr5:178923000-178923150	Caco-2	colon:	n/a	chr5:178923029-178923037
42	CTCF	chr5:178921179-178921324	GM20000	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
43	CTCF	chr5:178921160-178921310	AG04449	skin:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
44	CTCF	chr5:178921140-178921290	GM12865	blood:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
45	CTCF	chr5:178921120-178921270	SAEC	small airway:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
46	CTCF	chr5:178922923-178923285	H1-hESC	embryonic stem cell:	n/a	chr5:178923029-178923037
47	CTCF	chr5:178921160-178921310	HPF	lung:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
48	CTCF	chr5:178921160-178921310	Caco-2	colon:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
49	CTCF	chr5:178921098-178921350	A549	lung:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240
50	CTCF	chr5:178921125-178921357	A549	lung:	n/a	chr5:178921225-178921241 chr5:178921224-178921242 chr5:178921219-178921240

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178903057-178903107	U87	brain:	n/a
2	chr5:178903057-178903107	U87	brain:	n/a
3	chr5:178902699-178902749	HMEC	breast:	n/a
4	chr5:178903057-178903107	H1-hESC	embryonic stem cell:	embryo
5	chr5:178899812-178899862	Hela-S3	cervix:	n/a
6	chr5:178903087-178903137	IMR90	lung:	fetal
7	chr5:178902699-178902749	AG04450	lung:	fetal
8	chr5:178902699-178902749	SKMC	muscle:	n/a
9	chr5:178903087-178903137	GM12878	blood:	n/a
10	chr5:178913683-178913733	Hela-S3	cervix:	n/a
11	chr5:178902790-178902840	HRCEpiC	kidney:	n/a
12	chr5:178903057-178903107	HNPCEpiC	eye:	n/a
13	chr5:178899789-178899839	BE2_C	brain:	n/a
14	chr5:178899812-178899862	HCF	heart:	n/a
15	chr5:178902790-178902840	SK-N-SH	brain:	n/a
16	chr5:178903087-178903137	AG04450	lung:	fetal
17	chr5:178913683-178913733	AG04449	skin:	fetal
18	chr5:178903057-178903107	AG09309	skin:	n/a
19	chr5:178913683-178913733	NB4	blood:	n/a
20	chr5:178913683-178913733	HCM	heart:	n/a
21	chr5:178902956-178903006	ovcar-3	ovarian:	n/a
22	chr5:178902790-178902840	HL-60	blood:	n/a
23	chr5:178899789-178899839	HNPCEpiC	eye:	n/a
24	chr5:178902790-178902840	HepG2	liver:	n/a
25	chr5:178902790-178902840	SK-N-SH_RA	brain:	n/a
26	chr5:178902956-178903006	HRCEpiC	kidney:	n/a
27	chr5:178899812-178899862	Caco-2	colon:	n/a
28	chr5:178903057-178903107	PFSK-1	brain:	n/a
29	chr5:178899812-178899862	HEK293	kidney:	embryo
30	chr5:178902790-178902840	HEK293	kidney:	embryo
31	chr5:178902699-178902749	AG09319	gingival:	n/a
32	chr5:178902956-178903006	AG04449	skin:	fetal
33	chr5:178903057-178903107	BJ	skin:	n/a
34	chr5:178913683-178913733	HEK293	kidney:	embryo
35	chr5:178903057-178903107	AG10803	skin:	n/a
36	chr5:178902956-178903006	HRE	kidney:	n/a
37	chr5:178899850-178899900	HRPEpiC	eye:	n/a
38	chr5:178902790-178902840	T-47D	breast:	n/a
39	chr5:178899789-178899839	AG04450	lung:	fetal
40	chr5:178899850-178899900	GM19239	blood:	n/a
41	chr5:178899850-178899900	SK-N-SH	brain:	n/a
42	chr5:178902956-178903006	SK-N-SH_RA	brain:	n/a
43	chr5:178902699-178902749	BJ	skin:	n/a
44	chr5:178899789-178899839	NH-A	brain:	n/a
45	chr5:178899850-178899900	ProgFib	skin:	n/a
46	chr5:178902790-178902840	HCM	heart:	n/a
47	chr5:178903087-178903137	HAEpiC	amniotic membrane:	n/a
48	chr5:178899812-178899862	U87	brain:	n/a
49	chr5:178899812-178899862	ovcar-3	ovarian:	n/a
50	chr5:178903057-178903107	T-47D	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:177708522..177710701-chr5:178921263..178923252,2	K562	blood:
2	chr5:178921207..178921791-chr5:179095335..179095939,2	K562	blood:
3	chr5:178687965..178688655-chr5:178920708..178921301,2	K562	blood:
4	chr5:178688082..178688899-chr5:178920410..178921212,2	MCF-7	breast:
5	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
6	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
7	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
8	chr5:178219922..178220838-chr5:178920668..178921270,2	MCF-7	breast:
9	chr5:178912346..178914624-chr5:178918648..178920688,2	K562	blood:
10	chr5:178892938..178894678-chr5:178896634..178898137,2	K562	blood:
11	chr5:178219841..178220793-chr5:178920740..178921735,2	MCF-7	breast:
12	chr5:178593773..178595177-chr5:178920715..178921686,6	MCF-7	breast:
13	chr5:178901161..178903409-chr5:178906875..178908641,2	MCF-7	breast:
14	chr5:178907766..178909631-chr5:178910623..178913270,3	K562	blood:
15	chr5:178662646..178664463-chr5:178900746..178903231,2	K562	blood:
16	chr5:178594236..178594749-chr5:178920299..178921066,2	K562	blood:
17	chr5:178905653..178907978-chr5:178976399..178978448,2	MCF-7	breast:
18	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652
2	lnc-ADAMTS2-2	chr5:178893834-178894126	NONHSAT105584

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

Extended variants
information (count: 2406 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2406 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6871253	chr5:178887482-178887483	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs28671020	chr5:178887506-178887507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568396779	chr5:178887544-178887545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147311659	chr5:178887586-178887587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs180847484	chr5:178887590-178887591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572012031	chr5:178887592-178887593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545443411	chr5:178887623-178887624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557852086	chr5:178887625-178887626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575706068	chr5:178887626-178887627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186441111	chr5:178887628-178887629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs4701158	chr5:178887633-178887634	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs530367385	chr5:178887670-178887671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542114979	chr5:178887677-178887678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375420931	chr5:178887691-178887692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369707443	chr5:178887772-178887773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs372561004	chr5:178887799-178887800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374189294	chr5:178887815-178887816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112673033	chr5:178887819-178887820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs35609887	chr5:178887820-178887821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs386405811	chr5:178887826-178887827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60071778	chr5:178887833-178887834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202082873	chr5:178887834-178887835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4700822	chr5:178887854-178887855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs190803474	chr5:178887894-178887895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs4700823	chr5:178887897-178887898	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs141701957	chr5:178887907-178887908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527674640	chr5:178887935-178887936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181648948	chr5:178887951-178887952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568257374	chr5:178887952-178887953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373442597	chr5:178887959-178887960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535600446	chr5:178887983-178887984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547846092	chr5:178888113-178888114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185730186	chr5:178888131-178888132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561260405	chr5:178888132-178888133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4700824	chr5:178888144-178888145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs539444602	chr5:178888172-178888173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs190119605	chr5:178888287-178888288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539944160	chr5:178888323-178888324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575767534	chr5:178888352-178888353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536521592	chr5:178888382-178888383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552052550	chr5:178888408-178888409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28494775	chr5:178888424-178888425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs139463721	chr5:178888427-178888428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537704120	chr5:178888438-178888439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542022330	chr5:178888441-178888442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374010307	chr5:178888513-178888514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs28454143	chr5:178888530-178888531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570530434	chr5:178888581-178888582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs59965534	chr5:178888599-178888600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs28415352	chr5:178888608-178888609	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178884600-178889000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:178886800-178887600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:178889000-178889200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178889200-178889600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:178889600-178896000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:178892800-178893200	ZNF genes & repeats	Pancreas	Pancrea
7	chr5:178893200-178893600	Weak transcription	Pancreas	Pancrea
8	chr5:178895800-178896200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:178896000-178896400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:178896200-178897400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr5:178896400-178897200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:178897200-178897600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:178897400-178897800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr5:178897600-178899600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr5:178897800-178902200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:178899600-178900000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr5:178899800-178900000	Enhancers	Brain Germinal Matrix	brain
18	chr5:178899800-178900000	Enhancers	Placenta	Placenta
19	chr5:178899800-178900000	Enhancers	Pancreas	Pancrea
20	chr5:178900000-178902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:178900000-178902200	Weak transcription	Placenta	Placenta
22	chr5:178900200-178901400	Weak transcription	Brain Germinal Matrix	brain
23	chr5:178900800-178902200	Enhancers	Fetal Lung	lung
24	chr5:178901400-178903200	Enhancers	Brain Germinal Matrix	brain
25	chr5:178901800-178902800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr5:178901800-178903200	Enhancers	Fetal Brain Male	brain
27	chr5:178902000-178902400	Enhancers	Primary hematopoietic stem cells	blood
28	chr5:178902000-178902800	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr5:178902000-178902800	Enhancers	Fetal Brain Female	brain
30	chr5:178902000-178902800	Enhancers	HSMMtube	muscle
31	chr5:178902000-178903200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr5:178902000-178903200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr5:178902000-178903400	Enhancers	Fetal Kidney	kidney
34	chr5:178902200-178902400	Bivalent Enhancer	Brain Angular Gyrus	brain
35	chr5:178902200-178902600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:178902200-178902600	Enhancers	H1 Cell Line	embryonic stem cell
37	chr5:178902200-178902600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:178902200-178902600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr5:178902200-178902600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
40	chr5:178902200-178902600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr5:178902200-178902600	Flanking Active TSS	Fetal Lung	lung
42	chr5:178902200-178902600	Enhancers	Fetal Muscle Leg	muscle
43	chr5:178902200-178902600	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr5:178902200-178902800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr5:178902200-178902800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:178902200-178902800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr5:178902200-178902800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr5:178902200-178902800	Enhancers	Placenta	Placenta
49	chr5:178902200-178902800	Enhancers	Fetal Stomach	stomach
50	chr5:178902200-178902800	Enhancers	Spleen	Spleen

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