Variant report

Variant	nsv881216
Chromosome Location	chr5:27361816-27464184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:197)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:197 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:27428887-27428920	K562	blood:	n/a	n/a
2	BHLHE40	chr5:27390071-27390112	K562	blood:	n/a	n/a
3	BRCA1	chr5:27403373-27403840	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:27444220-27444223	A549	lung:	n/a	n/a
5	CEBPB	chr5:27434396-27434708	A549	lung:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545
6	CEBPB	chr5:27402580-27402860	HepG2	liver:	n/a	chr5:27402684-27402697 chr5:27402755-27402766
7	CEBPB	chr5:27402961-27403754	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:27390852-27391121	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr5:27448587-27448827	HepG2	liver:	n/a	chr5:27448671-27448682
10	CEBPB	chr5:27434401-27434672	HepG2	liver:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545
11	CEBPB	chr5:27434380-27434748	ECC-1	luminal epithelium:	n/a	chr5:27434536-27434547 chr5:27434534-27434547 chr5:27434534-27434545 chr5:27434726-27434743
12	CEBPB	chr5:27390811-27391135	HepG2	liver:	n/a	n/a
13	CEBPB	chr5:27459726-27459987	HepG2	liver:	n/a	chr5:27459841-27459854 chr5:27459841-27459852 chr5:27459842-27459853
14	CEBPB	chr5:27403393-27403602	A549	lung:	n/a	n/a
15	CEBPB	chr5:27376600-27376800	A549	lung:	n/a	chr5:27376717-27376728
16	CEBPB	chr5:27376585-27376872	HepG2	liver:	n/a	chr5:27376717-27376728
17	CEBPB	chr5:27459716-27459960	A549	lung:	n/a	chr5:27459841-27459854 chr5:27459841-27459852 chr5:27459842-27459853
18	CEBPB	chr5:27431090-27431379	A549	lung:	n/a	n/a
19	CEBPB	chr5:27390828-27391122	IMR90	lung:	n/a	n/a
20	CEBPB	chr5:27448645-27448696	Hela-S3	cervix:	n/a	chr5:27448671-27448682
21	CEBPB	chr5:27414276-27414476	HepG2	liver:	n/a	n/a
22	CTCF	chr5:27407120-27407270	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:27389900-27390050	GM12878	blood:	n/a	n/a
24	CTCF	chr5:27407040-27407190	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr5:27407146-27407214	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:27407121-27407236	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr5:27447980-27448130	HEK293	kidney:	n/a	n/a
28	CTCF	chr5:27386060-27386095	GM13976	blood:	n/a	n/a
29	CTCF	chr5:27431090-27431148	GM13976	blood:	n/a	n/a
30	CTCF	chr5:27407060-27407210	GM12873	blood:	n/a	n/a
31	CTCF	chr5:27395703-27395756	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:27425814-27425866	GM13977	blood:	n/a	n/a
33	CTCF	chr5:27407040-27407190	GM12866	blood:	n/a	n/a
34	CTCF	chr5:27437551-27437605	GM20000	blood:	n/a	n/a
35	CTCF	chr5:27407029-27407367	GM12878	blood:	n/a	n/a
36	CTCF	chr5:27371372-27371377	K562	blood:	n/a	n/a
37	CTCF	chr5:27407160-27407310	GM06990	blood:	n/a	n/a
38	CTCF	chr5:27402800-27402950	HepG2	liver:	n/a	n/a
39	CTCF	chr5:27407040-27407190	GM06990	blood:	n/a	n/a
40	CTCF	chr5:27407060-27407210	Hela-S3	cervix:	n/a	n/a
41	E2F4	chr5:27398247-27398399	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr5:27402564-27402764	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr5:27437782-27437926	MCF10A-Er-Src	breast:	n/a	n/a
44	EP300	chr5:27388832-27389149	HepG2	liver:	n/a	n/a
45	EP300	chr5:27387629-27387924	HepG2	liver:	n/a	chr5:27387731-27387741
46	EP300	chr5:27387532-27387952	HepG2	liver:	n/a	chr5:27387731-27387741
47	EP300	chr5:27437899-27438420	ECC-1	luminal epithelium:	n/a	chr5:27438190-27438204
48	EP300	chr5:27403312-27403762	Hela-S3	cervix:	n/a	n/a
49	ESR1	chr5:27437902-27438206	ECC-1	luminal epithelium:	n/a	n/a
50	FOS	chr5:27418114-27418340	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:27387958-27388008	T-47D	breast:	n/a
2	chr5:27438836-27438886	HEEpiC	esophagus:	n/a
3	chr5:27387958-27388008	ovcar-3	ovarian:	n/a
4	chr5:27438836-27438886	NHDF-neo	bronchial:	n/a
5	chr5:27387958-27388008	BJ	skin:	n/a
6	chr5:27387958-27388008	ECC-1	luminal epithelium:	n/a
7	chr5:27387958-27388008	SK-N-SH_RA	brain:	n/a
8	chr5:27387958-27388008	HL-60	blood:	n/a
9	chr5:27387958-27388008	AoSMC	blood vessel:	n/a
10	chr5:27387958-27388008	SKMC	muscle:	n/a
11	chr5:27438836-27438886	CMK	blood:	n/a
12	chr5:27438836-27438886	AG04449	skin:	fetal
13	chr5:27438836-27438886	HRPEpiC	eye:	n/a
14	chr5:27387958-27388008	HCT-116	colon:	n/a
15	chr5:27438836-27438886	A549	lung:	n/a
16	chr5:27387958-27388008	HIPEpiC	eye:	n/a
17	chr5:27438836-27438886	ovcar-3	ovarian:	n/a
18	chr5:27438836-27438886	AG09319	gingival:	n/a
19	chr5:27438836-27438886	HCF	heart:	n/a
20	chr5:27387958-27388008	Caco-2	colon:	n/a
21	chr5:27387958-27388008	AG09309	skin:	n/a
22	chr5:27438836-27438886	HepG2	liver:	n/a
23	chr5:27438836-27438886	MCF10A-Er-Src	breast:	n/a
24	chr5:27438836-27438886	K562	blood:	n/a
25	chr5:27438836-27438886	GM12878	blood:	n/a
26	chr5:27438836-27438886	SK-N-SH	brain:	n/a
27	chr5:27387958-27388008	HUVEC	blood vessel:	n/a
28	chr5:27438836-27438886	Hepatocyte	liver:	n/a
29	chr5:27438836-27438886	AG09309	skin:	n/a
30	chr5:27438836-27438886	NHBE	bronchial:	n/a
31	chr5:27438836-27438886	SAEC	small airway:	n/a
32	chr5:27387958-27388008	SK-N-MC	brain:	n/a
33	chr5:27387958-27388008	NHBE	bronchial:	n/a
34	chr5:27438836-27438886	GM12892	blood:	n/a
35	chr5:27387958-27388008	PrEC	prostate:	n/a
36	chr5:27387958-27388008	GM12892	blood:	n/a
37	chr5:27387958-27388008	AG10803	skin:	n/a
38	chr5:27438836-27438886	NT2-D1	testis:	n/a
39	chr5:27387958-27388008	HEEpiC	esophagus:	n/a
40	chr5:27438836-27438886	GM19239	blood:	n/a
41	chr5:27387958-27388008	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:27438836-27438886	PFSK-1	brain:	n/a
43	chr5:27387958-27388008	H1-hESC	embryonic stem cell:	embryo
44	chr5:27438836-27438886	RPTEC	kidney:	n/a
45	chr5:27438836-27438886	BJ	skin:	n/a
46	chr5:27387958-27388008	NB4	blood:	n/a
47	chr5:27438836-27438886	GM06990	blood:	n/a
48	chr5:27387958-27388008	GM06990	blood:	n/a
49	chr5:27387958-27388008	HepG2	liver:	n/a
50	chr5:27387958-27388008	RPTEC	kidney:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:27410717..27413698-chr5:27423274..27425658,2	K562	blood:
2	chr5:27386479..27389149-chr5:27394969..27398145,3	K562	blood:
3	chr5:27384451..27386814-chr5:27398781..27400428,2	K562	blood:
4	chr5:27356861..27358465-chr5:27382622..27384445,2	K562	blood:
5	chr3:133852407..133853154-chr5:27377165..27378018,2	MCF-7	breast:
6	chr5:27367781..27370478-chr5:27378982..27381299,2	MCF-7	breast:
7	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:
8	chr5:27384539..27388630-chr5:27389237..27391656,3	K562	blood:
9	chr5:27386479..27389149-chr5:27394969..27398145,3	K562	blood:
10	chr5:27415884..27418944-chr5:27423264..27427119,3	K562	blood:
11	chr5:27441556..27444509-chr5:27447634..27449803,2	K562	blood:
12	chr5:27384539..27388630-chr5:27389237..27391656,3	K562	blood:
13	chr5:27410717..27413698-chr5:27423274..27425658,2	K562	blood:
14	chr5:27415884..27418944-chr5:27423264..27427119,3	K562	blood:
15	chr5:27422999..27425291-chr5:27429898..27432218,2	K562	blood:
16	chr5:27384451..27386814-chr5:27398781..27400428,2	K562	blood:
17	chr5:27367781..27370478-chr5:27378982..27381299,2	MCF-7	breast:
18	chr5:27422999..27425291-chr5:27429898..27432218,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
2	lnc-CDH9-2	chr5:27412775-27412796	XLOC_004761
3	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
4	lnc-CDH9-2	chr5:27413322-27413758	XLOC_004761
5	lnc-CDH9-2	chr5:27410327-27410387	XLOC_004761
6	lnc-CDH9-9	chr5:27448470-27448525	l_2893_chr5:27442393-27446144_testes
7	lnc-CDH9-2	chr5:27412713-27412768	XLOC_004761
8	lnc-CDH9-2	chr5:27409693-27409751	XLOC_004761
9	lnc-CDH9-9	chr5:27446084-27446144	l_2893_chr5:27442393-27446144_testes
10	lnc-CDH9-2	chr5:27406639-27406877	XLOC_004761
11	lnc-CDH9-2	chr5:27413322-27413758	XLOC_004761
12	lnc-CDH9-9	chr5:27442394-27442634	l_2893_chr5:27442393-27446144_testes
13	lnc-CDH9-2	chr5:27412713-27412796	XLOC_004761
14	lnc-CDH9-2	chr5:27412720-27412796	XLOC_004761
15	lnc-CDH9-2	chr5:27423608-27423708	XLOC_004761
16	lnc-CDH9-2	chr5:27436260-27436518	XLOC_004761
17	lnc-CDH9-2	chr5:27428267-27428320	XLOC_004761
18	lnc-CDH9-2	chr5:27406640-27406877	XLOC_004761

No data

Variant related genes	Relation type
ENSG00000248490	TF binding region
ENSG00000248490	CpG island
CHEK1	miRNA target sites
YWHAQ	miRNA target sites

Extended variants
information (count: 1130 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2561649	chr5:27371244-27371245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115767896	chr5:27371249-27371250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536953813	chr5:27371261-27371262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558767911	chr5:27371287-27371288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs325353	chr5:27371289-27371290	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183436700	chr5:27371298-27371299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187288187	chr5:27371305-27371306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142945551	chr5:27371317-27371318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543073498	chr5:27371336-27371337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541517099	chr5:27371348-27371349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs561496265	chr5:27371385-27371386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561333891	chr5:27371410-27371411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531887685	chr5:27371424-27371425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543653373	chr5:27371452-27371453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575132474	chr5:27371461-27371462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7716017	chr5:27371470-27371471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs532654136	chr5:27371501-27371502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565253520	chr5:27371525-27371526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146136673	chr5:27371529-27371530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565306746	chr5:27371539-27371540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193188322	chr5:27371575-27371576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57760953	chr5:27377811-27377812	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374937523	chr5:27377822-27377823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191327421	chr5:27377824-27377825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149399326	chr5:27377853-27377854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183794108	chr5:27377855-27377856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576180543	chr5:27377903-27377904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188624449	chr5:27377926-27377927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs543605606	chr5:27377927-27377928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565274477	chr5:27377935-27377936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547403831	chr5:27377953-27377954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs115448616	chr5:27377964-27377965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541052005	chr5:27378005-27378006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200573043	chr5:27378032-27378033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143785581	chr5:27378054-27378055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529130456	chr5:27378083-27378084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs193247738	chr5:27378103-27378104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185659575	chr5:27378122-27378123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs148007035	chr5:27378127-27378128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372131142	chr5:27378148-27378149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530773408	chr5:27378156-27378157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs552391176	chr5:27378171-27378172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs190172283	chr5:27378188-27378189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182728	chr5:27378197-27378198	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs547783480	chr5:27378217-27378218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs565894388	chr5:27378239-27378240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73747005	chr5:27378256-27378257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181587682	chr5:27378257-27378258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6872538	chr5:27378322-27378323	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs141658233	chr5:27378336-27378337	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:27371200-27371600	Enhancers	Esophagus	oesophagus
2	chr5:27377800-27378400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr5:27378000-27378400	Enhancers	Placenta Amnion	Placenta Amnion
4	chr5:27387000-27389200	Enhancers	HepG2	liver
5	chr5:27387400-27388200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:27387600-27388000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:27387600-27388200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:27387600-27388200	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:27387600-27388200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr5:27387600-27388200	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr5:27387600-27388800	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr5:27388200-27389800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr5:27388600-27389800	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr5:27388800-27389800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr5:27389200-27389600	Weak transcription	HepG2	liver
16	chr5:27389600-27390000	Enhancers	HepG2	liver
17	chr5:27389800-27390000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr5:27389800-27390200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:27392000-27393400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:27392400-27393600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr5:27402600-27404200	Active TSS	A549	lung
22	chr5:27403000-27403200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr5:27403000-27403200	Enhancers	Hela-S3	cervix
24	chr5:27403200-27403800	Active TSS	Hela-S3	cervix
25	chr5:27403200-27404000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:27403400-27403800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr5:27403400-27403800	Active TSS	Fetal Muscle Leg	muscle
28	chr5:27403400-27404000	Active TSS	HMEC	breast
29	chr5:27403400-27404000	Active TSS	Osteobl	bone
30	chr5:27403400-27404200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:27403600-27404000	Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr5:27410400-27411000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:27417800-27418200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr5:27434000-27435200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:27434200-27435200	Enhancers	NHEK	skin
36	chr5:27435000-27435200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:27435000-27435400	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr5:27435000-27435400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr5:27435000-27435600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr5:27435200-27436200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr5:27436200-27436600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr5:27436400-27436600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:27436800-27449400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr5:27442800-27443200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr5:27446600-27449200	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr5:27447600-27448400	ZNF genes & repeats	Spleen	Spleen
47	chr5:27450600-27451200	Enhancers	Fetal Heart	heart
48	chr5:27450800-27451000	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr5:27450800-27451200	Enhancers	Rectal Smooth Muscle	rectum
50	chr5:27450800-27451400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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