Variant report

Variant	esv15195
Chromosome Location	chr5:17481743-17517271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:140)
CpG islands
(count:549)
Chromatin interactive
region (count:3)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:140 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:17492224-17492379	K562	blood:	n/a	n/a
2	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:17499619-17499851	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:17499603-17499787	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:17483315-17483373	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:17486902-17487265	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:17504178-17504267	HepG2	liver:	n/a	n/a
8	CTCF	chr5:17507228-17507340	GM13976	blood:	n/a	n/a
9	CTCF	chr5:17481860-17482010	Caco-2	colon:	n/a	n/a
10	CTCF	chr5:17481740-17481890	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr5:17508150-17508159	LNCaP	prostate:	n/a	n/a
12	CTCF	chr5:17481840-17481990	BE2_C	brain:	n/a	n/a
13	CTCF	chr5:17481862-17482016	Gliobla	brain:	n/a	n/a
14	CTCF	chr5:17481700-17481850	A549	lung:	n/a	n/a
15	CTCF	chr5:17481912-17481950	Medullo	brain:	n/a	n/a
16	CTCF	chr5:17486619-17486669	Fibrobl	skin:	n/a	n/a
17	CTCF	chr5:17495120-17495270	Caco-2	colon:	n/a	n/a
18	CTCF	chr5:17509784-17509815	Medullo	brain:	n/a	n/a
19	CTCF	chr5:17481880-17482030	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:17481780-17481930	A549	lung:	n/a	n/a
21	CTCF	chr5:17481780-17481930	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:17511524-17511588	LNCaP	prostate:	n/a	n/a
23	CTCF	chr5:17481900-17482050	BE2_C	brain:	n/a	n/a
24	CTCF	chr5:17491692-17491836	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr5:17488800-17488950	HPF	lung:	n/a	n/a
26	CTCF	chr5:17499727-17499747	LNCaP	prostate:	n/a	n/a
27	CTCF	chr5:17481839-17481971	GM12878	blood:	n/a	n/a
28	CTCF	chr5:17491694-17491823	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:17481946-17481996	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr5:17500777-17500832	GM13976	blood:	n/a	n/a
31	CTCF	chr5:17481912-17482004	MCF-7	breast:	n/a	n/a
32	EBF1	chr5:17490158-17490500	GM12878	blood:	n/a	chr5:17490277-17490290 chr5:17490278-17490289
33	EP300	chr5:17487009-17487549	Hela-S3	cervix:	n/a	chr5:17487416-17487425 chr5:17487084-17487098
34	EP300	chr5:17482969-17483245	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr5:17482937-17483232	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr5:17482980-17483238	K562	blood:	n/a	n/a
37	EP300	chr5:17499644-17499832	GM12878	blood:	n/a	n/a
38	EP300	chr5:17499500-17499859	GM12878	blood:	n/a	n/a
39	EP300	chr5:17498495-17498839	GM12878	blood:	n/a	n/a
40	EP300	chr5:17485346-17485854	SK-N-SH_RA	brain:	n/a	chr5:17485360-17485370
41	EP300	chr5:17482475-17483479	SK-N-SH	brain:	n/a	n/a
42	FOSL2	chr5:17499590-17499879	HepG2	liver:	n/a	n/a
43	FOSL2	chr5:17487168-17487692	MCF-7	breast:	n/a	chr5:17487415-17487425 chr5:17487415-17487424 chr5:17487416-17487425
44	FOSL2	chr5:17487115-17487592	A549	lung:	n/a	chr5:17487130-17487138 chr5:17487131-17487138 chr5:17487415-17487425 chr5:17487415-17487424 chr5:17487416-17487425
45	FOSL2	chr5:17499533-17499889	HepG2	liver:	n/a	n/a
46	FOXA1	chr5:17499599-17499849	HepG2	liver:	n/a	n/a
47	FOXA1	chr5:17513472-17513776	HepG2	liver:	n/a	chr5:17513643-17513655
48	FOXA1	chr5:17483808-17484066	HepG2	liver:	n/a	n/a
49	FOXA1	chr5:17513527-17513816	HepG2	liver:	n/a	chr5:17513643-17513655
50	FOXA2	chr5:17483709-17484200	A549	lung:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17491604-17491654	U87	brain:	n/a
2	chr5:17491604-17491654	ovcar-3	ovarian:	n/a
3	chr5:17491586-17491636	HEK293	kidney:	embryo
4	chr5:17491941-17491991	SKMC	muscle:	n/a
5	chr5:17485435-17485485	HIPEpiC	eye:	n/a
6	chr5:17517201-17517251	U87	brain:	n/a
7	chr5:17517201-17517251	HCT-116	colon:	n/a
8	chr5:17491941-17491991	PrEC	prostate:	n/a
9	chr5:17490778-17490828	HRCEpiC	kidney:	n/a
10	chr5:17485435-17485485	GM06990	blood:	n/a
11	chr5:17495781-17495831	NB4	blood:	n/a
12	chr5:17491469-17491519	SK-N-MC	brain:	n/a
13	chr5:17485435-17485485	BE2_C	brain:	n/a
14	chr5:17491604-17491654	BE2_C	brain:	n/a
15	chr5:17488879-17488929	K562	blood:	n/a
16	chr5:17490778-17490828	PANC-1	pancreas:	n/a
17	chr5:17490778-17490828	Hela-S3	cervix:	n/a
18	chr5:17488879-17488929	Caco-2	colon:	n/a
19	chr5:17491586-17491636	HUVEC	blood vessel:	n/a
20	chr5:17488879-17488929	LNCaP	prostate:	n/a
21	chr5:17491469-17491519	K562	blood:	n/a
22	chr5:17491941-17491991	AG09319	gingival:	n/a
23	chr5:17491469-17491519	HPAEpiC	pulmonary alveolar:	n/a
24	chr5:17490778-17490828	Jurkat	blood:	n/a
25	chr5:17491469-17491519	RPTEC	kidney:	n/a
26	chr5:17488879-17488929	GM06990	blood:	n/a
27	chr5:17485435-17485485	AG10803	skin:	n/a
28	chr5:17490778-17490828	SK-N-MC	brain:	n/a
29	chr5:17488879-17488929	MCF10A-Er-Src	breast:	n/a
30	chr5:17491469-17491519	A549	lung:	n/a
31	chr5:17485435-17485485	NHBE	bronchial:	n/a
32	chr5:17488879-17488929	GM12878	blood:	n/a
33	chr5:17491586-17491636	AG04449	skin:	fetal
34	chr5:17491604-17491654	IMR90	lung:	fetal
35	chr5:17488879-17488929	MCF-7	breast:	n/a
36	chr5:17491941-17491991	PANC-1	pancreas:	n/a
37	chr5:17490778-17490828	AG10803	skin:	n/a
38	chr5:17485435-17485485	HL-60	blood:	n/a
39	chr5:17517201-17517251	HAEpiC	amniotic membrane:	n/a
40	chr5:17495781-17495831	Jurkat	blood:	n/a
41	chr5:17485435-17485485	RPTEC	kidney:	n/a
42	chr5:17495781-17495831	SKMC	muscle:	n/a
43	chr5:17491604-17491654	Hepatocyte	liver:	n/a
44	chr5:17517201-17517251	AoSMC	blood vessel:	n/a
45	chr5:17491586-17491636	BJ	skin:	n/a
46	chr5:17491941-17491991	HEK293	kidney:	embryo
47	chr5:17517201-17517251	NT2-D1	testis:	n/a
48	chr5:17491941-17491991	HepG2	liver:	n/a
49	chr5:17491586-17491636	HRE	kidney:	n/a
50	chr5:17491469-17491519	SK-N-SH_RA	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
2	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
3	chr5:17482145..17483996-chr5:17485919..17488626,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-4	chr5:17485639-17485937	XLOC_004309
2	lnc-BASP1-4	chr5:17483841-17484055	XLOC_004309
3	lnc-BASP1-11	chr5:17494578-17494846	l_2885_chr5:17456969-17494846_brain
4	lnc-BASP1-4	chr5:17483931-17484068	XLOC_004309

No data

Variant related genes	Relation type
ENSG00000251304	TF binding region
ENSG00000249339	TF binding region
ENSG00000268799	TF binding region
ENSG00000249620	TF binding region
ENSG00000248861	TF binding region
ENSG00000248205	TF binding region
ENSG00000250667	TF binding region
ENSG00000185041	TF binding region
ENSG00000251304	CpG island
ENSG00000249339	CpG island
ENSG00000268799	CpG island
ENSG00000249620	CpG island
ENSG00000248861	CpG island
ENSG00000248205	CpG island
ENSG00000250667	CpG island
ENSG00000185041	CpG island
ENSG00000268799	chromatin interactions
ENSG00000251304	chromatin interactions
ENSG00000250667	chromatin interactions

Extended variants
information (count: 1090 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575238875	chr5:17481792-17481793	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs537544622	chr5:17481835-17481836	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs117810177	chr5:17481849-17481850	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs537936769	chr5:17481911-17481912	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs540006702	chr5:17481922-17481923	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs549648374	chr5:17481938-17481939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180977465	chr5:17481955-17481956	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546118322	chr5:17481990-17481991	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551021604	chr5:17482024-17482025	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs142357216	chr5:17482109-17482110	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs567802446	chr5:17482134-17482135	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs537475231	chr5:17482192-17482193	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531758985	chr5:17482195-17482196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs185000709	chr5:17482257-17482258	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550338204	chr5:17482260-17482261	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190299943	chr5:17482345-17482346	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs527807239	chr5:17482427-17482428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183240464	chr5:17482437-17482438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs13178095	chr5:17482438-17482439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs540129912	chr5:17482439-17482440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs550058732	chr5:17482446-17482447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs146355118	chr5:17482455-17482456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375472790	chr5:17482504-17482505	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs13178787	chr5:17482576-17482577	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs187825100	chr5:17482593-17482594	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs147651747	chr5:17482646-17482647	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554283736	chr5:17482673-17482674	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs538731662	chr5:17482720-17482721	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369571874	chr5:17482771-17482772	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs574168244	chr5:17482773-17482774	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536833699	chr5:17482777-17482778	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553540229	chr5:17482801-17482802	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373662970	chr5:17482818-17482819	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs576672931	chr5:17482828-17482829	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545757590	chr5:17482829-17482830	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs562834449	chr5:17482846-17482847	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576271108	chr5:17482867-17482868	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149100576	chr5:17482887-17482888	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs377572172	chr5:17482901-17482902	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114948252	chr5:17482908-17482909	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372619261	chr5:17482928-17482929	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527747579	chr5:17483047-17483048	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541581578	chr5:17483085-17483086	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200681759	chr5:17483127-17483128	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370094679	chr5:17483128-17483129	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373848165	chr5:17483147-17483148	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150659933	chr5:17483156-17483157	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116233768	chr5:17483162-17483163	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs533605448	chr5:17483181-17483182	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550192168	chr5:17483185-17483186	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21364760	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Myoepithelioma	18604193	CNVD
Lung cancer	16740712	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Melanoma	22183965	CNVD
Renal cell carcinoma	18194544	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19287141	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17476400-17486200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr5:17481400-17482000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr5:17481400-17482000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr5:17481400-17482000	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:17481400-17482000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr5:17481400-17482000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr5:17481400-17482200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:17481400-17483000	Enhancers	A549	lung
9	chr5:17481600-17481800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:17481600-17482000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:17481600-17482000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:17481600-17482000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:17483000-17487000	Weak transcription	A549	lung
14	chr5:17486200-17487800	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr5:17487000-17487600	Enhancers	A549	lung
16	chr5:17487200-17487400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr5:17487200-17487600	Enhancers	Hela-S3	cervix
18	chr5:17487400-17488200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:17488200-17489000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr5:17494400-17496200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr5:17500600-17500800	Enhancers	A549	lung
22	chr5:17500600-17500800	Enhancers	Hela-S3	cervix
23	chr5:17500600-17501000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr5:17500600-17501000	Active TSS	NHDF-Ad	bronchial
25	chr5:17502200-17503000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr5:17509000-17509400	Enhancers	Fetal Brain Male	brain
27	chr5:17512000-17512200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr5:17512200-17512400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:17512200-17512400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:17512400-17512600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:17512600-17517600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr5:17512600-17519400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr5:17513600-17514600	Enhancers	A549	lung

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