Variant report

Variant	nsv5055
Chromosome Location	chr5:146812672-146857424
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	ATF2	chr5:146833767-146834161	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:146835769-146835770	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:146833380-146833758	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:146834990-146835178	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:146816232-146816481	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:146833592-146833681	H1-hESC	embryonic stem cell:	n/a	n/a
7	CCNT2	chr5:146832990-146833091	K562	blood:	n/a	n/a
8	CEBPB	chr5:146814864-146815146	A549	lung:	n/a	chr5:146814998-146815009
9	CEBPB	chr5:146841652-146841860	A549	lung:	n/a	n/a
10	CEBPB	chr5:146822231-146822508	A549	lung:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
11	CEBPB	chr5:146838965-146839417	IMR90	lung:	n/a	n/a
12	CEBPB	chr5:146833488-146833727	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:146834904-146835277	IMR90	lung:	n/a	n/a
14	CEBPB	chr5:146822137-146822514	IMR90	lung:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
15	CEBPB	chr5:146822182-146822510	HepG2	liver:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
16	CEBPB	chr5:146814842-146815119	HepG2	liver:	n/a	chr5:146814998-146815009
17	CEBPB	chr5:146821950-146822461	H1-hESC	embryonic stem cell:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
18	CEBPB	chr5:146821980-146822455	Hela-S3	cervix:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
19	CEBPB	chr5:146822189-146822392	K562	blood:	n/a	chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822331-146822342 chr5:146822330-146822343 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822332-146822341 chr5:146822330-146822341
20	CEBPB	chr5:146847717-146848114	IMR90	lung:	n/a	n/a
21	CEBPB	chr5:146847748-146848111	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:146836943-146836954	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr5:146834914-146835273	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD1	chr5:146832499-146834412	H1-hESC	embryonic stem cell:	n/a	chr5:146833828-146833835 chr5:146833608-146833618
25	CHD1	chr5:146843773-146843846	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr5:146835405-146835644	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr5:146833613-146833783	HepG2	liver:	n/a	n/a
28	CHD2	chr5:146833456-146834120	H1-hESC	embryonic stem cell:	n/a	chr5:146833828-146833835 chr5:146833608-146833618
29	CHD2	chr5:146832213-146832311	GM12878	blood:	n/a	n/a
30	CREB1	chr5:146833422-146833805	A549	lung:	n/a	n/a
31	CTBP2	chr5:146816321-146817144	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr5:146831494-146833991	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr5:146833560-146833710	HRE	kidney:	n/a	chr5:146833598-146833619 chr5:146833596-146833614 chr5:146833599-146833608 chr5:146833599-146833612 chr5:146833599-146833612 chr5:146833601-146833611 chr5:146833597-146833613
34	CTCF	chr5:146843880-146844030	A549	lung:	n/a	n/a
35	CTCF	chr5:146843846-146844081	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:146833520-146833670	SK-N-SH_RA	brain:	n/a	chr5:146833598-146833619 chr5:146833596-146833614 chr5:146833599-146833608 chr5:146833599-146833612 chr5:146833599-146833612 chr5:146833601-146833611 chr5:146833597-146833613
37	CTCF	chr5:146843920-146844070	GM12866	blood:	n/a	n/a
38	CTCF	chr5:146843880-146844030	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr5:146843900-146844050	GM12878	blood:	n/a	n/a
40	CTCF	chr5:146830320-146830470	GM12866	blood:	n/a	chr5:146830404-146830417
41	CTCF	chr5:146833840-146833990	BJ	skin:	n/a	n/a
42	CTCF	chr5:146833520-146833670	NHDF-neo	bronchial:	n/a	chr5:146833598-146833619 chr5:146833596-146833614 chr5:146833599-146833608 chr5:146833599-146833612 chr5:146833599-146833612 chr5:146833601-146833611 chr5:146833597-146833613
43	CTCF	chr5:146830260-146830410	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr5:146843880-146844030	HCFaa	heart:	n/a	n/a
45	CTCF	chr5:146843860-146844069	HepG2	liver:	n/a	n/a
46	CTCF	chr5:146833172-146833177	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr5:146843900-146844050	GM12868	blood:	n/a	n/a
48	CTCF	chr5:146833520-146833670	HPF	lung:	n/a	chr5:146833598-146833619 chr5:146833596-146833614 chr5:146833599-146833608 chr5:146833599-146833612 chr5:146833599-146833612 chr5:146833601-146833611 chr5:146833597-146833613
49	CTCF	chr5:146843860-146844010	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:146843860-146844010	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:146849919-146849969	AG04449	skin:	fetal
2	chr5:146849919-146849969	AG04449	skin:	fetal
3	chr5:146833961-146834011	SK-N-SH	brain:	n/a
4	chr5:146829385-146829435	NB4	blood:	n/a
5	chr5:146829385-146829435	HIPEpiC	eye:	n/a
6	chr5:146829385-146829435	GM06990	blood:	n/a
7	chr5:146845196-146845246	ProgFib	skin:	n/a
8	chr5:146832182-146832232	HCT-116	colon:	n/a
9	chr5:146831209-146831259	MCF-7	breast:	n/a
10	chr5:146826146-146826196	RPTEC	kidney:	n/a
11	chr5:146849919-146849969	NT2-D1	testis:	n/a
12	chr5:146832257-146832307	NHBE	bronchial:	n/a
13	chr5:146832182-146832232	Hepatocyte	liver:	n/a
14	chr5:146833665-146833715	SK-N-SH_RA	brain:	n/a
15	chr5:146849919-146849969	MCF-7	breast:	n/a
16	chr5:146832298-146832348	ovcar-3	ovarian:	n/a
17	chr5:146833961-146834011	CMK	blood:	n/a
18	chr5:146832356-146832406	HIPEpiC	eye:	n/a
19	chr5:146833937-146833987	AG04450	lung:	fetal
20	chr5:146833665-146833715	PANC-1	pancreas:	n/a
21	chr5:146833961-146834011	HAEpiC	amniotic membrane:	n/a
22	chr5:146833470-146833520	HAEpiC	amniotic membrane:	n/a
23	chr5:146849919-146849969	ProgFib	skin:	n/a
24	chr5:146818610-146818660	NT2-D1	testis:	n/a
25	chr5:146832387-146832437	PFSK-1	brain:	n/a
26	chr5:146833431-146833481	PANC-1	pancreas:	n/a
27	chr5:146832356-146832406	Caco-2	colon:	n/a
28	chr5:146832387-146832437	NHBE	bronchial:	n/a
29	chr5:146832257-146832307	NH-A	brain:	n/a
30	chr5:146831209-146831259	H1-hESC	embryonic stem cell:	embryo
31	chr5:146833961-146834011	HNPCEpiC	eye:	n/a
32	chr5:146832257-146832307	Jurkat	blood:	n/a
33	chr5:146826146-146826196	GM12891	blood:	n/a
34	chr5:146832356-146832406	NHDF-neo	bronchial:	n/a
35	chr5:146837147-146837197	ProgFib	skin:	n/a
36	chr5:146832257-146832307	AoSMC	blood vessel:	n/a
37	chr5:146849919-146849969	Hepatocyte	liver:	n/a
38	chr5:146831209-146831259	GM12878	blood:	n/a
39	chr5:146837147-146837197	AG04450	lung:	fetal
40	chr5:146833937-146833987	HRE	kidney:	n/a
41	chr5:146833171-146833221	GM12891	blood:	n/a
42	chr5:146832182-146832232	LNCaP	prostate:	n/a
43	chr5:146849919-146849969	CMK	blood:	n/a
44	chr5:146832933-146832983	BJ	skin:	n/a
45	chr5:146833431-146833481	HMEC	breast:	n/a
46	chr5:146826146-146826196	ovcar-3	ovarian:	n/a
47	chr5:146832518-146832568	H1-hESC	embryonic stem cell:	embryo
48	chr5:146833665-146833715	AoSMC	blood vessel:	n/a
49	chr5:146833961-146834011	T-47D	breast:	n/a
50	chr5:146833937-146833987	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:146813910..146815673-chr5:146829270..146831419,2	K562	blood:
2	chr5:146843864..146844427-chr5:146939683..146940421,2	MCF-7	breast:
3	chr5:146802902..146805345-chr5:146810324..146812732,2	K562	blood:
4	chr5:146813910..146815673-chr5:146829270..146831419,2	K562	blood:
5	chr5:146843342..146844495-chr5:146957725..146958288,5	MCF-7	breast:
6	chr5:146841686..146842370-chr5:146957260..146958248,2	MCF-7	breast:
7	chr5:146843533..146844497-chr5:146938186..146939120,6	MCF-7	breast:
8	chr5:146852615..146855525-chr5:146856529..146860037,3	K562	blood:
9	chr5:146843544..146844324-chr5:146956668..146957286,3	MCF-7	breast:
10	chr5:146852615..146855525-chr5:146856529..146860037,3	K562	blood:

Variant related genes	Relation type
DPYSL3	TF binding region
DPYSL3	CpG island

Extended variants
information (count: 1479 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142844228	chr5:146812744-146812745	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs191407131	chr5:146812854-146812855	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531324769	chr5:146812867-146812868	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551036901	chr5:146812899-146812900	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571103963	chr5:146812949-146812950	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs73794725	chr5:146812966-146812967	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs183172926	chr5:146812986-146812987	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs55842239	chr5:146813038-146813039	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535560963	chr5:146813152-146813153	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555433911	chr5:146813198-146813199	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575279177	chr5:146813240-146813241	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544176488	chr5:146813279-146813280	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs115994611	chr5:146813318-146813319	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370303437	chr5:146813322-146813323	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540127088	chr5:146813325-146813326	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs111464435	chr5:146813330-146813331	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs386693330	chr5:146813332-146813333	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142635159	chr5:146813334-146813335	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs569542300	chr5:146813337-146813338	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531363185	chr5:146813356-146813357	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551342104	chr5:146813367-146813368	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555141089	chr5:146813368-146813369	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533704017	chr5:146813393-146813394	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538578847	chr5:146813407-146813408	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557985011	chr5:146813424-146813425	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571520245	chr5:146813451-146813452	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566735212	chr5:146813452-146813453	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116330551	chr5:146813463-146813464	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192329049	chr5:146813482-146813483	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148840905	chr5:146813508-146813509	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141367712	chr5:146813509-146813510	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150956460	chr5:146813549-146813550	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200679218	chr5:146813569-146813570	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560885821	chr5:146813591-146813592	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146353824	chr5:146813592-146813593	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs398109522	chr5:146813605-146813606	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184601958	chr5:146813626-146813627	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs537916313	chr5:146813649-146813650	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558153417	chr5:146813681-146813682	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572243068	chr5:146813689-146813690	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139537408	chr5:146813692-146813693	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187822429	chr5:146813724-146813725	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149695198	chr5:146813728-146813729	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574110949	chr5:146813788-146813789	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542822815	chr5:146813797-146813798	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73794726	chr5:146813813-146813814	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs540034798	chr5:146813814-146813815	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146651092	chr5:146813822-146813823	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7725771	chr5:146813845-146813846	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs527255149	chr5:146813868-146813869	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	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
Breast cancer	21858162	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
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	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
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:146798200-146815600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:146799000-146818400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr5:146804400-146815800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr5:146804800-146831600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr5:146805800-146819200	Enhancers	Colon Smooth Muscle	Colon
6	chr5:146806000-146814800	Enhancers	Fetal Brain Male	brain
7	chr5:146807600-146812800	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr5:146808000-146816200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:146808200-146816400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:146808200-146816600	Weak transcription	Osteobl	bone
11	chr5:146808200-146818800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:146809000-146816600	Weak transcription	Esophagus	oesophagus
13	chr5:146809400-146819200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:146809800-146814000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:146810000-146823400	Weak transcription	Small Intestine	intestine
16	chr5:146810200-146812800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:146810400-146813200	Enhancers	Fetal Brain Female	brain
18	chr5:146810400-146815600	Enhancers	Duodenum Smooth Muscle	Duodenum
19	chr5:146810800-146812800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr5:146810800-146813400	Enhancers	Ovary	ovary
21	chr5:146810800-146814200	Enhancers	Fetal Intestine Large	intestine
22	chr5:146810800-146817600	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:146810800-146819400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr5:146810800-146822600	Genic enhancers	HUES48 Cell Line	embryonic stem cell
25	chr5:146811000-146813200	Genic enhancers	Brain Germinal Matrix	brain
26	chr5:146811200-146812800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr5:146811200-146813000	Enhancers	Left Ventricle	heart
28	chr5:146811400-146813000	Enhancers	Fetal Intestine Small	intestine
29	chr5:146811400-146818800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr5:146811600-146815400	Weak transcription	Brain Anterior Caudate	brain
31	chr5:146811600-146815400	Weak transcription	Lung	lung
32	chr5:146811600-146815600	Weak transcription	NH-A	brain
33	chr5:146811600-146818800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr5:146811800-146813000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:146811800-146813000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr5:146811800-146813600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr5:146811800-146813800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:146812000-146812800	Flanking Active TSS	Stomach Smooth Muscle	stomach
39	chr5:146812000-146815400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:146812000-146815400	Weak transcription	Psoas Muscle	Psoas
41	chr5:146812000-146816200	Weak transcription	Brain Substantia Nigra	brain
42	chr5:146812000-146816400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr5:146812000-146816400	Weak transcription	Brain Hippocampus Middle	brain
44	chr5:146812000-146816800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr5:146812200-146813600	Strong transcription	HUES64 Cell Line	embryonic stem cell
46	chr5:146812200-146814000	Enhancers	Rectal Smooth Muscle	rectum
47	chr5:146812200-146815000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:146812200-146815200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr5:146812200-146815400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr5:146812200-146815400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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