Variant report

Variant	nsv522807
Chromosome Location	chr5:142417658-142529960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1720)
CpG islands
(count:916)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1720 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:142485784-142486106	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:142431074-142431487	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:142518683-142518809	K562	blood:	n/a	n/a
4	ARID3A	chr5:142431121-142431415	K562	blood:	n/a	n/a
5	ARID3A	chr5:142443944-142443971	K562	blood:	n/a	n/a
6	ATF1	chr5:142436597-142436732	K562	blood:	n/a	n/a
7	ATF1	chr5:142504183-142504601	K562	blood:	n/a	n/a
8	ATF1	chr5:142492301-142492352	K562	blood:	n/a	n/a
9	ATF1	chr5:142431121-142431414	K562	blood:	n/a	n/a
10	ATF1	chr5:142518406-142518694	K562	blood:	n/a	n/a
11	ATF1	chr5:142420269-142420551	K562	blood:	n/a	n/a
12	ATF1	chr5:142434009-142434266	K562	blood:	n/a	n/a
13	ATF2	chr5:142433842-142434901	GM12878	blood:	n/a	n/a
14	ATF2	chr5:142435017-142437730	GM12878	blood:	n/a	n/a
15	ATF2	chr5:142445684-142447108	GM12878	blood:	n/a	n/a
16	ATF2	chr5:142418458-142418855	GM12878	blood:	n/a	n/a
17	ATF2	chr5:142473233-142473673	GM12878	blood:	n/a	n/a
18	ATF2	chr5:142433807-142437775	GM12878	blood:	n/a	n/a
19	ATF2	chr5:142418388-142418938	GM12878	blood:	n/a	n/a
20	ATF2	chr5:142498866-142499401	GM12878	blood:	n/a	n/a
21	ATF2	chr5:142445530-142447020	GM12878	blood:	n/a	n/a
22	ATF3	chr5:142420126-142420613	HCT-116	colon:	n/a	n/a
23	ATF3	chr5:142466425-142467109	A549	lung:	n/a	n/a
24	BACH1	chr5:142527742-142527798	K562	blood:	n/a	n/a
25	BACH1	chr5:142473449-142474015	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr5:142480637-142481024	GM12878	blood:	n/a	n/a
27	BATF	chr5:142514461-142514825	GM12878	blood:	n/a	n/a
28	BATF	chr5:142435873-142436097	GM12878	blood:	n/a	chr5:142436015-142436026
29	BATF	chr5:142429818-142430086	GM12878	blood:	n/a	n/a
30	BATF	chr5:142436349-142436641	GM12878	blood:	n/a	n/a
31	BATF	chr5:142502214-142502436	GM12878	blood:	n/a	n/a
32	BATF	chr5:142474159-142474552	GM12878	blood:	n/a	chr5:142474385-142474396
33	BATF	chr5:142494082-142494413	GM12878	blood:	n/a	n/a
34	BATF	chr5:142514465-142514810	GM12878	blood:	n/a	n/a
35	BATF	chr5:142446030-142446407	GM12878	blood:	n/a	n/a
36	BATF	chr5:142468345-142468609	GM12878	blood:	n/a	chr5:142468467-142468478 chr5:142468495-142468506
37	BATF	chr5:142437148-142437610	GM12878	blood:	n/a	n/a
38	BATF	chr5:142418440-142418782	GM12878	blood:	n/a	chr5:142418700-142418711 chr5:142418701-142418711
39	BATF	chr5:142435810-142436162	GM12878	blood:	n/a	chr5:142436015-142436026
40	BATF	chr5:142418486-142418886	GM12878	blood:	n/a	chr5:142418700-142418711 chr5:142418701-142418711
41	BATF	chr5:142433891-142434450	GM12878	blood:	n/a	n/a
42	BATF	chr5:142446003-142446877	GM12878	blood:	n/a	n/a
43	BCL11A	chr5:142433913-142434458	GM12878	blood:	n/a	n/a
44	BCL11A	chr5:142445992-142446675	GM12878	blood:	n/a	n/a
45	BCL11A	chr5:142434004-142434391	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:142437104-142437572	GM12878	blood:	n/a	chr5:142437173-142437180
47	BCL11A	chr5:142437109-142437569	GM12878	blood:	n/a	chr5:142437173-142437180
48	BCL11A	chr5:142418534-142418744	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:142436291-142436755	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:142418488-142418877	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:142444988-142445038	HEK293	kidney:	embryo
2	chr5:142444988-142445038	HEK293	kidney:	embryo
3	chr5:142444988-142445038	PrEC	prostate:	n/a
4	chr5:142487917-142487967	HMEC	breast:	n/a
5	chr5:142445604-142445654	T-47D	breast:	n/a
6	chr5:142487917-142487967	HepG2	liver:	n/a
7	chr5:142487917-142487967	PANC-1	pancreas:	n/a
8	chr5:142455060-142455110	ECC-1	luminal epithelium:	n/a
9	chr5:142490096-142490146	HRCEpiC	kidney:	n/a
10	chr5:142490096-142490146	HMEC	breast:	n/a
11	chr5:142431272-142431322	GM12892	blood:	n/a
12	chr5:142422241-142422291	Jurkat	blood:	n/a
13	chr5:142444988-142445038	Hela-S3	cervix:	n/a
14	chr5:142511729-142511779	NH-A	brain:	n/a
15	chr5:142458116-142458166	Hepatocyte	liver:	n/a
16	chr5:142432538-142432588	HCF	heart:	n/a
17	chr5:142458116-142458166	HAEpiC	amniotic membrane:	n/a
18	chr5:142511729-142511779	HNPCEpiC	eye:	n/a
19	chr5:142458116-142458166	HNPCEpiC	eye:	n/a
20	chr5:142444988-142445038	AG09319	gingival:	n/a
21	chr5:142499847-142499897	K562	blood:	n/a
22	chr5:142422241-142422291	HUVEC	blood vessel:	n/a
23	chr5:142431272-142431322	NH-A	brain:	n/a
24	chr5:142445604-142445654	MCF-7	breast:	n/a
25	chr5:142455060-142455110	SK-N-SH	brain:	n/a
26	chr5:142442486-142442536	HAEpiC	amniotic membrane:	n/a
27	chr5:142445604-142445654	GM19239	blood:	n/a
28	chr5:142499847-142499897	CMK	blood:	n/a
29	chr5:142432538-142432588	AG04450	lung:	fetal
30	chr5:142514108-142514158	ovcar-3	ovarian:	n/a
31	chr5:142422241-142422291	HRCEpiC	kidney:	n/a
32	chr5:142458116-142458166	CMK	blood:	n/a
33	chr5:142490096-142490146	HNPCEpiC	eye:	n/a
34	chr5:142442486-142442536	IMR90	lung:	fetal
35	chr5:142527658-142527708	HCT-116	colon:	n/a
36	chr5:142490096-142490146	ovcar-3	ovarian:	n/a
37	chr5:142442486-142442536	GM12892	blood:	n/a
38	chr5:142458116-142458166	GM06990	blood:	n/a
39	chr5:142458116-142458166	GM19239	blood:	n/a
40	chr5:142445604-142445654	SK-N-MC	brain:	n/a
41	chr5:142422241-142422291	A549	lung:	n/a
42	chr5:142442486-142442536	AG04449	skin:	fetal
43	chr5:142432538-142432588	HRPEpiC	eye:	n/a
44	chr5:142455060-142455110	AG09319	gingival:	n/a
45	chr5:142422241-142422291	HCT-116	colon:	n/a
46	chr5:142527658-142527708	HIPEpiC	eye:	n/a
47	chr5:142422241-142422291	BE2_C	brain:	n/a
48	chr5:142487917-142487967	HNPCEpiC	eye:	n/a
49	chr5:142511729-142511779	SK-N-SH	brain:	n/a
50	chr5:142499847-142499897	Caco-2	colon:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:142505307..142507084-chr5:142517845..142520293,2	K562	blood:
2	chr5:142417100..142419470-chr5:142782951..142784921,2	K562	blood:
3	chr5:142480535..142484269-chr5:142501795..142505704,3	K562	blood:
4	chr5:142480535..142484269-chr5:142501795..142505704,3	K562	blood:
5	chr5:142505307..142507084-chr5:142517845..142520293,2	K562	blood:
6	chr5:142412112..142414029-chr5:142495778..142497487,2	K562	blood:
7	chr5:142429610..142433984-chr5:142435999..142437847,3	K562	blood:
8	chr5:142436823..142439027-chr5:142442525..142445366,2	K562	blood:
9	chr5:142496471..142498126-chr5:142504184..142505736,2	MCF-7	breast:
10	chr5:142528267..142530513-chr5:142797463..142798963,2	K562	blood:
11	chr5:142489594..142492192-chr5:142492646..142494592,2	K562	blood:
12	chr5:142489594..142492192-chr5:142492646..142494592,2	K562	blood:
13	chr5:142496471..142498126-chr5:142504184..142505736,2	MCF-7	breast:
14	chr5:142487174..142489706-chr5:142493078..142495363,2	MCF-7	breast:
15	chr11:58965619..58966464-chr5:142419606..142420543,2	MCF-7	breast:
16	chr5:142478262..142480394-chr5:142625617..142627473,2	K562	blood:
17	chr5:142428903..142431537-chr5:142442552..142444300,2	MCF-7	breast:
18	chr5:142521035..142524889-chr5:142526288..142527900,3	MCF-7	breast:
19	chr5:142436823..142439027-chr5:142442525..142445366,2	K562	blood:
20	chr5:142428903..142431537-chr5:142442552..142444300,2	MCF-7	breast:
21	chr5:142521035..142524889-chr5:142526288..142527900,3	MCF-7	breast:
22	chr5:142527880..142530221-chr5:142549020..142551278,3	MCF-7	breast:
23	chr5:142429610..142433984-chr5:142435999..142437847,3	K562	blood:
24	chr5:142517877..142520038-chr5:142523506..142526391,2	K562	blood:
25	chr5:142487174..142489706-chr5:142493078..142495363,2	MCF-7	breast:
26	chr5:142517877..142520038-chr5:142523506..142526391,2	K562	blood:
27	chr5:142498526..142500168-chr5:142783082..142784755,2	MCF-7	breast:
28	chr5:142414825..142417650-chr5:142419145..142423301,4	K562	blood:

No data

Variant related genes	Relation type
ARHGAP26	TF binding region
ARHGAP26	CpG island
ENSG00000145819	chromatin interactions
ENSG00000113580	chromatin interactions

Extended variants
information (count: 4143 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:4143 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13163604	chr5:142417658-142417659	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs137997602	chr5:142417664-142417665	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs537362080	chr5:142417665-142417666	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs13182178	chr5:142417674-142417675	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186730515	chr5:142417692-142417693	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs546222403	chr5:142417712-142417713	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs149476981	chr5:142417747-142417748	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs573033780	chr5:142417813-142417814	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541897993	chr5:142417822-142417823	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs245825	chr5:142417823-142417824	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs112770960	chr5:142417824-142417825	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189919534	chr5:142417834-142417835	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529804330	chr5:142417843-142417844	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs200474854	chr5:142417888-142417889	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs143350579	chr5:142417924-142417925	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs245824	chr5:142417941-142417942	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs563647326	chr5:142417996-142417997	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548055681	chr5:142418028-142418029	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs561451936	chr5:142418087-142418088	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs148340977	chr5:142418093-142418094	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs73799523	chr5:142418102-142418103	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs34722383	chr5:142418110-142418111	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373740575	chr5:142418111-142418112	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565659186	chr5:142418142-142418143	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10045391	chr5:142418143-142418144	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs182086153	chr5:142418166-142418167	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568683029	chr5:142418202-142418203	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs185947149	chr5:142418221-142418222	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550242565	chr5:142418231-142418232	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144594882	chr5:142418250-142418251	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs60428049	chr5:142418275-142418276	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs80288163	chr5:142418276-142418277	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs74936428	chr5:142418280-142418281	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111662577	chr5:142418283-142418284	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577504559	chr5:142418322-142418323	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs245823	chr5:142418325-142418326	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs13186856	chr5:142418329-142418330	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs201456767	chr5:142418344-142418345	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190756723	chr5:142418356-142418357	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs541934951	chr5:142418361-142418362	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561804804	chr5:142418373-142418374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs575332176	chr5:142418389-142418390	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543642844	chr5:142418401-142418402	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181897126	chr5:142418417-142418418	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs245822	chr5:142418449-142418450	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs569056095	chr5:142418480-142418481	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs559409344	chr5:142418510-142418511	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs11960157	chr5:142418611-142418612	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs150607209	chr5:142418637-142418638	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568205013	chr5:142418676-142418677	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Bipolar disorder	18458673	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
Malignant fibrous histiocytomas	21085701	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Prostate cancer	21965145	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Schizophrenia	19546859	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	21062161	CNVD
Developmental delay	19128483	CNVD
Leukoplakia	24403051	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD

Chromatin state (count:3300 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:142390200-142420200	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr5:142397000-142431000	Weak transcription	Small Intestine	intestine
3	chr5:142400000-142442600	Weak transcription	Spleen	Spleen
4	chr5:142403600-142421200	Weak transcription	Gastric	stomach
5	chr5:142403600-142445000	Weak transcription	Colonic Mucosa	Colon
6	chr5:142404200-142421000	Weak transcription	Fetal Intestine Small	intestine
7	chr5:142404200-142421400	Weak transcription	Brain Angular Gyrus	brain
8	chr5:142404200-142421400	Weak transcription	Lung	lung
9	chr5:142404400-142421400	Weak transcription	Colon Smooth Muscle	Colon
10	chr5:142405400-142421400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr5:142405400-142430800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr5:142405800-142421400	Weak transcription	Brain Anterior Caudate	brain
13	chr5:142405800-142430800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:142406200-142421200	Weak transcription	Fetal Heart	heart
15	chr5:142406200-142421400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr5:142406200-142421400	Weak transcription	Right Ventricle	heart
17	chr5:142408800-142421200	Weak transcription	Left Ventricle	heart
18	chr5:142410200-142421600	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr5:142410200-142430400	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr5:142410400-142421400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr5:142410400-142428200	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr5:142410400-142435800	Weak transcription	Dnd41	blood
23	chr5:142410600-142421400	Weak transcription	Adipose Nuclei	Adipose
24	chr5:142410600-142433800	Weak transcription	Primary hematopoietic stem cells	blood
25	chr5:142410800-142421000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
26	chr5:142410800-142421200	Weak transcription	Fetal Thymus	thymus
27	chr5:142410800-142421200	Weak transcription	Thymus	Thymus
28	chr5:142410800-142434000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr5:142410800-142436200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr5:142411000-142421000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr5:142411000-142421400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr5:142411000-142421400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:142411000-142421400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr5:142411000-142429600	Weak transcription	Brain Hippocampus Middle	brain
35	chr5:142411000-142433600	Weak transcription	Primary B cells from peripheral blood	blood
36	chr5:142411200-142421000	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr5:142411800-142418200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr5:142412000-142421400	Weak transcription	Fetal Muscle Trunk	muscle
39	chr5:142412000-142421400	Weak transcription	Stomach Mucosa	stomach
40	chr5:142412400-142421400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr5:142412600-142421400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:142413200-142421400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr5:142413400-142421200	Weak transcription	Fetal Stomach	stomach
44	chr5:142413400-142430600	Weak transcription	A549	lung
45	chr5:142414000-142420400	Weak transcription	Hela-S3	cervix
46	chr5:142414200-142417800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:142414200-142420200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr5:142414200-142421000	Weak transcription	HSMMtube	muscle
49	chr5:142415600-142417800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr5:142415600-142418000	Enhancers	HUES64 Cell Line	embryonic stem cell

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