Variant report

Variant	nsv883236
Chromosome Location	chr5:178720968-178774860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:1957)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:178729527-178729868	K562	blood:	n/a	n/a
2	ATF2	chr5:178753597-178754030	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr5:178763657-178763929	K562	blood:	n/a	n/a
4	BACH1	chr5:178770779-178771405	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:178753623-178753861	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr5:178746077-178746614	GM12878	blood:	n/a	n/a
7	BCL3	chr5:178746298-178746633	GM12878	blood:	n/a	n/a
8	BHLHE40	chr5:178722893-178723057	K562	blood:	n/a	chr5:178723031-178723040 chr5:178723031-178723040
9	BHLHE40	chr5:178763708-178763938	K562	blood:	n/a	n/a
10	BRCA1	chr5:178754565-178754676	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr5:178729517-178729803	K562	blood:	n/a	n/a
12	CCNT2	chr5:178772466-178772783	K562	blood:	n/a	n/a
13	CCNT2	chr5:178771882-178771973	K562	blood:	n/a	n/a
14	CEBPB	chr5:178749384-178749670	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:178734831-178734994	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:178771987-178772057	IMR90	lung:	n/a	n/a
17	CEBPB	chr5:178731436-178731883	IMR90	lung:	n/a	n/a
18	CHD1	chr5:178769622-178773044	IMR90	lung:	n/a	chr5:178772444-178772454
19	CHD1	chr5:178771062-178771490	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr5:178771804-178771970	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr5:178729729-178729764	K562	blood:	n/a	n/a
22	CHD2	chr5:178771048-178771541	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr5:178772523-178772566	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr5:178729457-178729948	K562	blood:	n/a	n/a
25	CTBP2	chr5:178770889-178772047	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTBP2	chr5:178772320-178773389	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:178721141-178721175	Lung_OC	lung:	n/a	n/a
28	CTCF	chr5:178721960-178722110	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr5:178769800-178769950	BJ	skin:	n/a	chr5:178769882-178769895
30	CTCF	chr5:178770986-178771385	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:178727920-178728070	BJ	skin:	n/a	chr5:178728020-178728033
32	CTCF	chr5:178746454-178746547	GM19239	blood:	n/a	n/a
33	CTCF	chr5:178721980-178722130	AG09309	skin:	n/a	n/a
34	CTCF	chr5:178769860-178770010	BE2_C	brain:	n/a	chr5:178769882-178769895
35	CTCF	chr5:178721960-178722110	HMF	breast:	n/a	n/a
36	CTCF	chr5:178770400-178770550	AG09319	gingival:	n/a	chr5:178770517-178770530
37	CTCF	chr5:178771060-178771210	HPF	lung:	n/a	n/a
38	CTCF	chr5:178771060-178771210	GM12873	blood:	n/a	n/a
39	CTCF	chr5:178771071-178771166	GM19238	blood:	n/a	n/a
40	CTCF	chr5:178771040-178771190	BE2_C	brain:	n/a	n/a
41	CTCF	chr5:178769780-178769930	HMF	breast:	n/a	chr5:178769882-178769895
42	CTCF	chr5:178772280-178772430	AG04449	skin:	n/a	chr5:178772410-178772423
43	CTCF	chr5:178771040-178771190	SAEC	small airway:	n/a	n/a
44	CTCF	chr5:178771060-178771210	HCM	heart:	n/a	n/a
45	CTCF	chr5:178722040-178722099	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr5:178770960-178771110	A549	lung:	n/a	n/a
47	CTCF	chr5:178771060-178771210	AG10803	skin:	n/a	n/a
48	CTCF	chr5:178769857-178769871	HepG2	liver:	n/a	n/a
49	CTCF	chr5:178769780-178769930	HVMF	connective:	n/a	chr5:178769882-178769895
50	CTCF	chr5:178769875-178769907	Kidney_OC	kidney:	n/a	chr5:178769882-178769895

(count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178771329-178771379	AG09309	skin:	n/a
2	chr5:178753803-178753853	HL-60	blood:	n/a
3	chr5:178736443-178736493	GM12892	blood:	n/a
4	chr5:178774760-178774810	SAEC	small airway:	n/a
5	chr5:178763293-178763343	K562	blood:	n/a
6	chr5:178771329-178771379	AG09309	skin:	n/a
7	chr5:178753803-178753853	HL-60	blood:	n/a
8	chr5:178736443-178736493	GM12892	blood:	n/a
9	chr5:178774760-178774810	SAEC	small airway:	n/a
10	chr5:178763293-178763343	K562	blood:	n/a
11	chr5:178767472-178767522	AG10803	skin:	n/a
12	chr5:178741004-178741054	HEEpiC	esophagus:	n/a
13	chr5:178772390-178772440	HMEC	breast:	n/a
14	chr5:178771781-178771831	BJ	skin:	n/a
15	chr5:178752999-178753049	AG04450	lung:	fetal
16	chr5:178772203-178772253	Caco-2	colon:	n/a
17	chr5:178770629-178770679	LNCaP	prostate:	n/a
18	chr5:178741205-178741255	GM19239	blood:	n/a
19	chr5:178772203-178772253	HEEpiC	esophagus:	n/a
20	chr5:178772782-178772832	ovcar-3	ovarian:	n/a
21	chr5:178735241-178735291	ovcar-3	ovarian:	n/a
22	chr5:178741205-178741255	K562	blood:	n/a
23	chr5:178770629-178770679	HCF	heart:	n/a
24	chr5:178753803-178753853	GM12878	blood:	n/a
25	chr5:178741205-178741255	ProgFib	skin:	n/a
26	chr5:178772203-178772253	PFSK-1	brain:	n/a
27	chr5:178741004-178741054	GM12878	blood:	n/a
28	chr5:178772385-178772435	HEEpiC	esophagus:	n/a
29	chr5:178753432-178753482	NHBE	bronchial:	n/a
30	chr5:178722726-178722776	HRE	kidney:	n/a
31	chr5:178763293-178763343	HRCEpiC	kidney:	n/a
32	chr5:178763771-178763821	NH-A	brain:	n/a
33	chr5:178772390-178772440	SK-N-SH	brain:	n/a
34	chr5:178772793-178772843	HL-60	blood:	n/a
35	chr5:178748193-178748243	CMK	blood:	n/a
36	chr5:178763293-178763343	HIPEpiC	eye:	n/a
37	chr5:178763771-178763821	CMK	blood:	n/a
38	chr5:178722726-178722776	NH-A	brain:	n/a
39	chr5:178771329-178771379	Caco-2	colon:	n/a
40	chr5:178774760-178774810	HEK293	kidney:	embryo
41	chr5:178748193-178748243	AG09319	gingival:	n/a
42	chr5:178771393-178771443	GM06990	blood:	n/a
43	chr5:178772203-178772253	GM12891	blood:	n/a
44	chr5:178772969-178773019	HCF	heart:	n/a
45	chr5:178753803-178753853	NH-A	brain:	n/a
46	chr5:178748193-178748243	HIPEpiC	eye:	n/a
47	chr5:178770998-178771048	HAEpiC	amniotic membrane:	n/a
48	chr5:178774760-178774810	SKMC	muscle:	n/a
49	chr5:178772782-178772832	NHBE	bronchial:	n/a
50	chr5:178753803-178753853	AG04449	skin:	fetal

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:
2	chr5:178763364..178765890-chr5:178804717..178806886,2	K562	blood:
3	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
4	chr5:178762053..178764261-chr5:178817559..178819340,2	K562	blood:
5	chr5:178770291..178772174-chr5:178775649..178777213,2	MCF-7	breast:
6	chr5:178751231..178753197-chr5:178755873..178757949,2	MCF-7	breast:
7	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
8	chr5:178774195..178776525-chr5:178779659..178783563,3	K562	blood:
9	chr5:178719721..178723694-chr5:178743933..178746463,3	K562	blood:
10	chr5:178748584..178750238-chr5:178758412..178760319,2	MCF-7	breast:

No data

Variant related genes	Relation type
ADAMTS2	TF binding region
ADAMTS2	CpG island
ENSG00000253163	chromatin interactions

Extended variants
information (count: 2682 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2682 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs166031	chr5:178720968-178720969	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566717710	chr5:178721001-178721002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527434211	chr5:178721031-178721032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552508269	chr5:178721032-178721033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117769086	chr5:178721095-178721096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs537467340	chr5:178721096-178721097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6894857	chr5:178721129-178721130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567951198	chr5:178721167-178721168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535577973	chr5:178721170-178721171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553448207	chr5:178721302-178721303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540437695	chr5:178721315-178721316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573105439	chr5:178721341-178721342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534087067	chr5:178721347-178721348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs372706925	chr5:178721364-178721365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs578015492	chr5:178721382-178721383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs111849414	chr5:178721434-178721435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577492933	chr5:178721452-178721453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114830435	chr5:178721488-178721489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562940802	chr5:178721489-178721490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574736257	chr5:178721522-178721523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs151278496	chr5:178721549-178721550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189593340	chr5:178721561-178721562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528195715	chr5:178721595-178721596	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6869283	chr5:178721631-178721632	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs552374566	chr5:178721671-178721672	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs461652	chr5:178721679-178721680	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs187218335	chr5:178721821-178721822	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs531668604	chr5:178721852-178721853	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs113838816	chr5:178721877-178721878	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs140483903	chr5:178721919-178721920	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs564575640	chr5:178721955-178721956	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs535061061	chr5:178721984-178721985	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs547100282	chr5:178722007-178722008	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs376223241	chr5:178722008-178722009	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs340117	chr5:178722024-178722025	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs372944745	chr5:178722079-178722080	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs539123906	chr5:178722080-178722081	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs150403440	chr5:178722086-178722087	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs577356778	chr5:178722108-178722109	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs538574331	chr5:178722110-178722111	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs542315319	chr5:178722114-178722115	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs574783771	chr5:178722155-178722156	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs191590371	chr5:178722170-178722171	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs183846911	chr5:178722189-178722190	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs572602930	chr5:178722204-178722205	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs186055418	chr5:178722238-178722239	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs564349054	chr5:178722251-178722252	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs531403571	chr5:178722285-178722286	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs550053913	chr5:178722292-178722293	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs561795262	chr5:178722341-178722342	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	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	18451855	CNVD

Chromatin state (count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178712600-178722200	Weak transcription	Fetal Intestine Small	intestine
2	chr5:178713400-178727200	Weak transcription	NHLF	lung
3	chr5:178715200-178722000	Weak transcription	Right Ventricle	heart
4	chr5:178715800-178722400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr5:178716000-178721400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr5:178716000-178721400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr5:178716000-178722800	Weak transcription	Spleen	Spleen
8	chr5:178716200-178730800	Weak transcription	HSMM	muscle
9	chr5:178717200-178724400	Weak transcription	Ovary	ovary
10	chr5:178718200-178722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:178718200-178725000	Weak transcription	Gastric	stomach
12	chr5:178718400-178722800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:178718800-178721400	Weak transcription	Fetal Stomach	stomach
14	chr5:178719600-178721600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr5:178719800-178722400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:178719800-178722800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr5:178719800-178725200	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:178720000-178722400	Enhancers	NHDF-Ad	bronchial
19	chr5:178720000-178726000	Enhancers	Osteobl	bone
20	chr5:178720600-178721600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:178720600-178721800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:178720600-178721800	Weak transcription	Adipose Nuclei	Adipose
23	chr5:178720600-178721800	Weak transcription	Fetal Lung	lung
24	chr5:178720600-178722000	Weak transcription	Right Atrium	heart
25	chr5:178720600-178724200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr5:178720600-178728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:178720800-178721200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:178720800-178721200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:178721000-178722200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr5:178721200-178722800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:178721200-178723400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr5:178721400-178722400	Enhancers	Fetal Brain Male	brain
33	chr5:178721400-178722800	Enhancers	Stomach Smooth Muscle	stomach
34	chr5:178721400-178723000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr5:178721400-178723600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr5:178721400-178725200	Enhancers	Fetal Stomach	stomach
37	chr5:178721600-178721800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr5:178721600-178722800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr5:178721600-178723000	Enhancers	Fetal Brain Female	brain
40	chr5:178721600-178723200	Enhancers	Colon Smooth Muscle	Colon
41	chr5:178721600-178723800	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr5:178721600-178724600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr5:178721800-178722000	Enhancers	Fetal Lung	lung
44	chr5:178721800-178722400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:178721800-178722600	Enhancers	Fetal Muscle Leg	muscle
46	chr5:178721800-178723000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr5:178721800-178723000	Enhancers	Rectal Smooth Muscle	rectum
48	chr5:178721800-178725200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr5:178721800-178725400	Enhancers	Adipose Nuclei	Adipose
50	chr5:178722000-178722600	Weak transcription	Fetal Lung	lung

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