Variant report

Variant	nsv1028476
Chromosome Location	chr5:120232873-120525748
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:750)
CpG islands
(count:427)
Chromatin interactive
region (count:26)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:750 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:120321426-120321583	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:120480659-120480718	K562	blood:	n/a	n/a
3	BHLHE40	chr5:120355613-120355776	K562	blood:	n/a	n/a
4	CBX3	chr5:120289176-120289482	K562	blood:	n/a	n/a
5	CEBPB	chr5:120254721-120255092	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:120497839-120498066	HepG2	liver:	n/a	chr5:120497966-120497977
7	CEBPB	chr5:120489377-120489704	K562	blood:	n/a	chr5:120489508-120489519
8	CEBPB	chr5:120489367-120489679	A549	lung:	n/a	chr5:120489508-120489519
9	CEBPB	chr5:120254718-120255097	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr5:120344818-120345134	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:120324365-120324487	K562	blood:	n/a	n/a
12	CEBPB	chr5:120518577-120518857	K562	blood:	n/a	chr5:120518723-120518734
13	CEBPB	chr5:120362867-120363103	K562	blood:	n/a	chr5:120362980-120362991
14	CEBPB	chr5:120254687-120255099	A549	lung:	n/a	n/a
15	CEBPB	chr5:120254745-120255040	K562	blood:	n/a	n/a
16	CEBPB	chr5:120497904-120498020	A549	lung:	n/a	chr5:120497966-120497977
17	CEBPB	chr5:120388756-120389126	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr5:120313455-120313746	K562	blood:	n/a	chr5:120313575-120313586
19	CEBPB	chr5:120409404-120409415	K562	blood:	n/a	n/a
20	CEBPB	chr5:120344767-120345102	A549	lung:	n/a	n/a
21	CEBPB	chr5:120254788-120255079	A549	lung:	n/a	n/a
22	CEBPB	chr5:120518614-120519156	HepG2	liver:	n/a	chr5:120518723-120518734
23	CEBPB	chr5:120313451-120313786	HepG2	liver:	n/a	chr5:120313575-120313586
24	CEBPB	chr5:120243945-120244154	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:120500288-120500607	K562	blood:	n/a	n/a
26	CEBPB	chr5:120236959-120237290	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:120382637-120382812	A549	lung:	n/a	chr5:120382770-120382783
28	CEBPB	chr5:120500293-120500606	K562	blood:	n/a	n/a
29	CEBPB	chr5:120254653-120255046	HCT-116	colon:	n/a	n/a
30	CEBPB	chr5:120497794-120498111	K562	blood:	n/a	chr5:120497966-120497977
31	CEBPB	chr5:120490481-120490746	A549	lung:	n/a	chr5:120490627-120490638
32	CEBPB	chr5:120511816-120512016	HepG2	liver:	n/a	chr5:120511903-120511914
33	CEBPB	chr5:120344890-120345090	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:120407480-120407657	HepG2	liver:	n/a	chr5:120407589-120407602
35	CEBPB	chr5:120497807-120498101	IMR90	lung:	n/a	chr5:120497966-120497977
36	CEBPB	chr5:120278273-120278630	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr5:120465336-120465526	K562	blood:	n/a	chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447 chr5:120465434-120465445 chr5:120465434-120465447 chr5:120465436-120465445 chr5:120465436-120465445 chr5:120465434-120465447
38	CEBPB	chr5:120254722-120255094	K562	blood:	n/a	n/a
39	CEBPB	chr5:120362842-120363162	H1-hESC	embryonic stem cell:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
40	CEBPB	chr5:120509430-120509502	K562	blood:	n/a	chr5:120509449-120509462 chr5:120509449-120509460
41	CEBPB	chr5:120315991-120316249	HepG2	liver:	n/a	chr5:120316125-120316136
42	CEBPB	chr5:120254692-120255072	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr5:120321723-120321990	HepG2	liver:	n/a	chr5:120321831-120321842
44	CEBPB	chr5:120362833-120363079	IMR90	lung:	n/a	chr5:120362980-120362991
45	CEBPB	chr5:120260548-120260826	HepG2	liver:	n/a	chr5:120260680-120260691
46	CEBPB	chr5:120254719-120255091	A549	lung:	n/a	n/a
47	CEBPB	chr5:120362859-120363138	HepG2	liver:	n/a	chr5:120363105-120363118 chr5:120362980-120362991
48	CEBPB	chr5:120254753-120255060	MCF-7	breast:	n/a	n/a
49	CEBPB	chr5:120254751-120255081	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:120489328-120489659	H1-hESC	embryonic stem cell:	n/a	chr5:120489508-120489519

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:120254714-120254764	HCPEpiC	choroid plexus:	n/a
2	chr5:120254714-120254764	HAEpiC	amniotic membrane:	n/a
3	chr5:120272625-120272675	PrEC	prostate:	n/a
4	chr5:120254714-120254764	PFSK-1	brain:	n/a
5	chr5:120272625-120272675	AG10803	skin:	n/a
6	chr5:120272574-120272624	AG04450	lung:	fetal
7	chr5:120400115-120400165	HEK293	kidney:	embryo
8	chr5:120272625-120272675	BJ	skin:	n/a
9	chr5:120254714-120254764	IMR90	lung:	fetal
10	chr5:120272625-120272675	HRCEpiC	kidney:	n/a
11	chr5:120248381-120248431	AG10803	skin:	n/a
12	chr5:120272574-120272624	NHDF-neo	bronchial:	n/a
13	chr5:120278165-120278215	ProgFib	skin:	n/a
14	chr5:120254714-120254764	U87	brain:	n/a
15	chr5:120248381-120248431	HAEpiC	amniotic membrane:	n/a
16	chr5:120248381-120248431	GM12892	blood:	n/a
17	chr5:120444080-120444130	CMK	blood:	n/a
18	chr5:120272574-120272624	Jurkat	blood:	n/a
19	chr5:120272574-120272624	CMK	blood:	n/a
20	chr5:120254714-120254764	AoSMC	blood vessel:	n/a
21	chr5:120272574-120272624	SK-N-SH	brain:	n/a
22	chr5:120254714-120254764	T-47D	breast:	n/a
23	chr5:120254714-120254764	RPTEC	kidney:	n/a
24	chr5:120400115-120400165	AoSMC	blood vessel:	n/a
25	chr5:120248381-120248431	GM06990	blood:	n/a
26	chr5:120248381-120248431	HEK293	kidney:	embryo
27	chr5:120254714-120254764	AG04449	skin:	fetal
28	chr5:120254714-120254764	AG04450	lung:	fetal
29	chr5:120444080-120444130	AG09319	gingival:	n/a
30	chr5:120272625-120272675	HIPEpiC	eye:	n/a
31	chr5:120272574-120272624	U87	brain:	n/a
32	chr5:120272574-120272624	ovcar-3	ovarian:	n/a
33	chr5:120400115-120400165	PrEC	prostate:	n/a
34	chr5:120254714-120254764	AG09309	skin:	n/a
35	chr5:120400115-120400165	HIPEpiC	eye:	n/a
36	chr5:120272625-120272675	AG04450	lung:	fetal
37	chr5:120272574-120272624	Hepatocyte	liver:	n/a
38	chr5:120272625-120272675	MCF10A-Er-Src	breast:	n/a
39	chr5:120278165-120278215	Hepatocyte	liver:	n/a
40	chr5:120248381-120248431	Caco-2	colon:	n/a
41	chr5:120248381-120248431	PANC-1	pancreas:	n/a
42	chr5:120272625-120272675	MCF-7	breast:	n/a
43	chr5:120400115-120400165	HMEC	breast:	n/a
44	chr5:120254714-120254764	HL-60	blood:	n/a
45	chr5:120444080-120444130	Hela-S3	cervix:	n/a
46	chr5:120254714-120254764	HCT-116	colon:	n/a
47	chr5:120248381-120248431	SK-N-SH_RA	brain:	n/a
48	chr5:120400115-120400165	GM12892	blood:	n/a
49	chr5:120248381-120248431	AG04449	skin:	fetal
50	chr5:120400115-120400165	AG09319	gingival:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
2	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
3	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
4	chr5:120449899..120451786-chr5:120452739..120454812,2	K562	blood:
5	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
6	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
7	chr5:120435633..120438376-chr5:120443596..120446057,2	MCF-7	breast:
8	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
9	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
10	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
11	chr5:120525427..120527646-chr5:120529318..120531590,2	K562	blood:
12	chr5:120250931..120253908-chr5:120254077..120258114,3	K562	blood:
13	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
14	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
15	chr5:120509173..120511287-chr5:120514590..120516648,2	MCF-7	breast:
16	chr5:120250931..120253908-chr5:120255261..120258114,2	K562	blood:
17	chr5:120430789..120432374-chr5:120435217..120437128,2	K562	blood:
18	chr5:120344504..120347250-chr5:120354364..120356375,2	K562	blood:
19	chr5:120466262..120468152-chr5:120477634..120479866,2	K562	blood:
20	chr5:120466262..120468288-chr5:120477634..120479614,2	K562	blood:
21	chr5:120300949..120302956-chr5:121296548..121298304,2	K562	blood:
22	chr5:120480813..120483324-chr5:120484034..120486935,2	MCF-7	breast:
23	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
24	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:
25	chr5:120324000..120326925-chr5:120354314..120357069,2	K562	blood:
26	chr5:120471143..120473520-chr5:120475370..120477496,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR16-2	chr5:120376385-120376432	NONHSAT103450
2	lnc-PRR16-2	chr5:120379384-120379727	NONHSAT103450
3	lnc-PRR16-3	chr5:120394939-120395040	NONHSAT103451
4	lnc-PRR16-3	chr5:120396085-120396648	NONHSAT103451
5	lnc-PRR16-2	chr5:120375785-120376277	NONHSAT103450

No data

Variant related genes	Relation type
ENSG00000251135	TF binding region
ENSG00000248853	TF binding region
ENSG00000251135	CpG island
ENSG00000248853	CpG island
ENSG00000151304	chromatin interactions

Extended variants
information (count: 6864 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6864 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550692440	chr5:120236864-120236865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562541277	chr5:120236866-120236867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149134682	chr5:120236867-120236868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529867203	chr5:120236881-120236882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184983462	chr5:120236957-120236958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566398327	chr5:120236960-120236961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191024049	chr5:120237020-120237021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74358743	chr5:120237031-120237032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570862724	chr5:120237063-120237064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556656108	chr5:120237080-120237081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114628323	chr5:120237098-120237099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4131762	chr5:120237099-120237100	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs6894107	chr5:120237131-120237132	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs113308872	chr5:120237135-120237136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553720730	chr5:120237136-120237137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561638887	chr5:120237152-120237153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs539341583	chr5:120237163-120237164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536023050	chr5:120237167-120237168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554428318	chr5:120237215-120237216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138862688	chr5:120237315-120237316	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs572023119	chr5:120237326-120237327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141783903	chr5:120237331-120237332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564718323	chr5:120237434-120237435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576820022	chr5:120237435-120237436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543949957	chr5:120237475-120237476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11959456	chr5:120237497-120237498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529757252	chr5:120237534-120237535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547957401	chr5:120237561-120237562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13163243	chr5:120246211-120246212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs13163625	chr5:120246214-120246215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74853031	chr5:120246216-120246217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556997136	chr5:120246274-120246275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs151185950	chr5:120246329-120246330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs542786527	chr5:120246343-120246344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs561547267	chr5:120246349-120246350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140396386	chr5:120246358-120246359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114923773	chr5:120246373-120246374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184747067	chr5:120246376-120246377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187677251	chr5:120246392-120246393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371539463	chr5:120246414-120246415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113909577	chr5:120246445-120246446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73262984	chr5:120246533-120246534	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530643086	chr5:120246540-120246541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13359522	chr5:120246565-120246566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs192541524	chr5:120246571-120246572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs552617332	chr5:120246595-120246596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147023194	chr5:120246657-120246658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7733696	chr5:120246666-120246667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs571462742	chr5:120246718-120246719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs544886489	chr5:120246737-120246738	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	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
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:120236800-120237600	Enhancers	Dnd41	blood
2	chr5:120246200-120246800	Enhancers	Fetal Lung	lung
3	chr5:120246600-120247000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:120247000-120249000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr5:120248400-120248800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr5:120248800-120254200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr5:120249000-120249400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr5:120249000-120249400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:120249000-120249400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:120249400-120253000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr5:120249400-120253000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:120253000-120253400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:120253000-120253400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr5:120254200-120254600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:120254200-120254600	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr5:120254200-120254800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr5:120254200-120254800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:120263400-120264000	Enhancers	Liver	Liver
19	chr5:120269200-120269400	Enhancers	Dnd41	blood
20	chr5:120269400-120274200	Weak transcription	Dnd41	blood
21	chr5:120272400-120273400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr5:120273200-120273400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr5:120273400-120289200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr5:120273600-120274600	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr5:120274000-120274600	Enhancers	Liver	Liver
26	chr5:120274200-120275200	Enhancers	Dnd41	blood
27	chr5:120274600-120275600	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr5:120275200-120277800	Weak transcription	Dnd41	blood
29	chr5:120275800-120276000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr5:120277400-120278800	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr5:120277400-120279000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr5:120277400-120279000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr5:120277600-120278200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr5:120277600-120278600	Enhancers	H9 Cell Line	embryonic stem cell
35	chr5:120277600-120278600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:120277600-120279000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr5:120277600-120279400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr5:120277600-120279400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:120277800-120278800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr5:120277800-120279000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr5:120277800-120280200	Enhancers	Dnd41	blood
42	chr5:120278200-120278600	Enhancers	HMEC	breast
43	chr5:120278400-120279000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr5:120278400-120279200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:120278400-120279600	Enhancers	Fetal Lung	lung
46	chr5:120278600-120279000	Enhancers	Colon Smooth Muscle	Colon
47	chr5:120279000-120286600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr5:120279400-120284600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr5:120284600-120284800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr5:120284600-120285000	Enhancers	H1 Cell Line	embryonic stem cell

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