Variant report

Variant	esv3450032
Chromosome Location	chr5:17496567-17670408
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1877)
CpG islands
(count:1161)
Chromatin interactive
region (count:5)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1877 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17526839-17526866	K562	blood:	n/a	n/a
2	ARID3A	chr5:17517830-17517852	K562	blood:	n/a	n/a
3	ATF1	chr5:17517811-17517870	K562	blood:	n/a	n/a
4	ATF3	chr5:17517759-17517894	K562	blood:	n/a	n/a
5	BACH1	chr5:17526845-17526876	K562	blood:	n/a	n/a
6	BATF	chr5:17587321-17587686	GM12878	blood:	n/a	n/a
7	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
8	BATF	chr5:17581121-17581401	GM12878	blood:	n/a	n/a
9	BATF	chr5:17588369-17588646	GM12878	blood:	n/a	n/a
10	BATF	chr5:17631481-17631659	GM12878	blood:	n/a	n/a
11	BATF	chr5:17632271-17632495	GM12878	blood:	n/a	n/a
12	BATF	chr5:17524295-17524851	GM12878	blood:	n/a	n/a
13	BATF	chr5:17581115-17581413	GM12878	blood:	n/a	n/a
14	BATF	chr5:17599128-17599665	GM12878	blood:	n/a	n/a
15	BATF	chr5:17586894-17587691	GM12878	blood:	n/a	n/a
16	BATF	chr5:17518382-17520848	GM12878	blood:	n/a	n/a
17	BATF	chr5:17595225-17595440	GM12878	blood:	n/a	n/a
18	BATF	chr5:17595045-17595501	GM12878	blood:	n/a	n/a
19	BATF	chr5:17528684-17530686	GM12878	blood:	n/a	n/a
20	BATF	chr5:17633076-17633247	GM12878	blood:	n/a	n/a
21	BATF	chr5:17525255-17528049	GM12878	blood:	n/a	n/a
22	BATF	chr5:17595471-17597904	GM12878	blood:	n/a	n/a
23	BATF	chr5:17586589-17586869	GM12878	blood:	n/a	n/a
24	BATF	chr5:17592098-17594464	GM12878	blood:	n/a	n/a
25	BATF	chr5:17599390-17599669	GM12878	blood:	n/a	n/a
26	BATF	chr5:17586583-17586881	GM12878	blood:	n/a	n/a
27	BATF	chr5:17520861-17521352	GM12878	blood:	n/a	n/a
28	BATF	chr5:17591806-17592083	GM12878	blood:	n/a	n/a
29	BATF	chr5:17595530-17597898	GM12878	blood:	n/a	n/a
30	BATF	chr5:17588661-17591031	GM12878	blood:	n/a	n/a
31	BATF	chr5:17527729-17528285	GM12878	blood:	n/a	n/a
32	BATF	chr5:17633787-17633984	GM12878	blood:	n/a	n/a
33	BATF	chr5:17528689-17530680	GM12878	blood:	n/a	n/a
34	BATF	chr5:17632982-17633256	GM12878	blood:	n/a	n/a
35	BATF	chr5:17581436-17582365	GM12878	blood:	n/a	n/a
36	BATF	chr5:17521821-17524301	GM12878	blood:	n/a	n/a
37	BATF	chr5:17588377-17588634	GM12878	blood:	n/a	n/a
38	BATF	chr5:17525250-17527716	GM12878	blood:	n/a	n/a
39	BATF	chr5:17591814-17594470	GM12878	blood:	n/a	n/a
40	BATF	chr5:17586875-17587277	GM12878	blood:	n/a	n/a
41	BATF	chr5:17632734-17632883	GM12878	blood:	n/a	n/a
42	BATF	chr5:17583178-17585829	GM12878	blood:	n/a	n/a
43	BATF	chr5:17583170-17583447	GM12878	blood:	n/a	n/a
44	BATF	chr5:17521816-17524282	GM12878	blood:	n/a	n/a
45	BATF	chr5:17524307-17524569	GM12878	blood:	n/a	n/a
46	BATF	chr5:17583462-17585828	GM12878	blood:	n/a	n/a
47	BATF	chr5:17588662-17591030	GM12878	blood:	n/a	n/a
48	BATF	chr5:17518387-17521181	GM12878	blood:	n/a	n/a
49	BATF	chr5:17581407-17582352	GM12878	blood:	n/a	n/a
50	BATF	chr5:17580902-17581080	GM12878	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17524561-17524611	MCF10A-Er-Src	breast:	n/a
2	chr5:17522582-17522632	GM12891	blood:	n/a
3	chr5:17524561-17524611	MCF10A-Er-Src	breast:	n/a
4	chr5:17522582-17522632	GM12891	blood:	n/a
5	chr5:17654594-17654644	PANC-1	pancreas:	n/a
6	chr5:17522582-17522632	HEK293	kidney:	embryo
7	chr5:17522582-17522632	AG04449	skin:	fetal
8	chr5:17655356-17655406	HepG2	liver:	n/a
9	chr5:17633640-17633690	AG09309	skin:	n/a
10	chr5:17633640-17633690	ECC-1	luminal epithelium:	n/a
11	chr5:17595441-17595491	T-47D	breast:	n/a
12	chr5:17604867-17604917	HEEpiC	esophagus:	n/a
13	chr5:17580826-17580876	HL-60	blood:	n/a
14	chr5:17595441-17595491	NHBE	bronchial:	n/a
15	chr5:17524561-17524611	Hela-S3	cervix:	n/a
16	chr5:17528991-17529041	HNPCEpiC	eye:	n/a
17	chr5:17633640-17633690	U87	brain:	n/a
18	chr5:17519013-17519063	NH-A	brain:	n/a
19	chr5:17517201-17517251	HEK293	kidney:	embryo
20	chr5:17632536-17632586	GM12878	blood:	n/a
21	chr5:17528991-17529041	AoSMC	blood vessel:	n/a
22	chr5:17664567-17664617	NHDF-neo	bronchial:	n/a
23	chr5:17631696-17631746	Caco-2	colon:	n/a
24	chr5:17631696-17631746	LNCaP	prostate:	n/a
25	chr5:17604867-17604917	IMR90	lung:	fetal
26	chr5:17631696-17631746	HRCEpiC	kidney:	n/a
27	chr5:17527430-17527480	MCF10A-Er-Src	breast:	n/a
28	chr5:17632536-17632586	IMR90	lung:	fetal
29	chr5:17656637-17656687	GM12891	blood:	n/a
30	chr5:17632043-17632093	Jurkat	blood:	n/a
31	chr5:17524561-17524611	PANC-1	pancreas:	n/a
32	chr5:17528991-17529041	HMEC	breast:	n/a
33	chr5:17528991-17529041	GM12878	blood:	n/a
34	chr5:17522582-17522632	H1-hESC	embryonic stem cell:	embryo
35	chr5:17632557-17632607	Jurkat	blood:	n/a
36	chr5:17655356-17655406	ProgFib	skin:	n/a
37	chr5:17654594-17654644	U87	brain:	n/a
38	chr5:17655356-17655406	Jurkat	blood:	n/a
39	chr5:17654594-17654644	BE2_C	brain:	n/a
40	chr5:17633640-17633690	AG04450	lung:	fetal
41	chr5:17528991-17529041	AG04449	skin:	fetal
42	chr5:17632557-17632607	BE2_C	brain:	n/a
43	chr5:17524561-17524611	AG09309	skin:	n/a
44	chr5:17655356-17655406	PANC-1	pancreas:	n/a
45	chr5:17595441-17595491	HAEpiC	amniotic membrane:	n/a
46	chr5:17631696-17631746	NH-A	brain:	n/a
47	chr5:17631696-17631746	GM19239	blood:	n/a
48	chr5:17631696-17631746	GM12891	blood:	n/a
49	chr5:17664567-17664617	HCF	heart:	n/a
50	chr5:17655356-17655406	HRPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:17216395..17218536-chr5:17655025..17657774,2	MCF-7	breast:
2	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
3	chr5:17635261..17638059-chr5:17641232..17643907,2	MCF-7	breast:
4	chr5:17632983..17635813-chr5:17637711..17640599,2	K562	blood:
5	chr5:17644806..17646667-chr5:17648582..17651312,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-17	chr5:17643071-17643337	NONHSAT100659
2	lnc-MYO10-19	chr5:17654482-17654752	NONHSAT100661
3	lnc-MYO10-12	chr5:17587399-17587632	NONHSAT100653

No data

Variant related genes	Relation type
ENSG00000248542	TF binding region
ENSG00000249427	TF binding region
ENSG00000249282	TF binding region
ENSG00000248861	TF binding region
ENSG00000250558	TF binding region
ENSG00000248205	TF binding region
ENSG00000248471	TF binding region
ENSG00000250807	TF binding region
ENSG00000250667	TF binding region
ENSG00000250296	TF binding region
ENSG00000250055	TF binding region
ENSG00000248422	TF binding region
ENSG00000269466	TF binding region
ENSG00000249339	TF binding region
ENSG00000271296	TF binding region
ENSG00000250386	TF binding region
ENSG00000250351	TF binding region
ENSG00000249329	TF binding region
ENSG00000249666	TF binding region
ENSG00000249357	TF binding region
ENSG00000249156	TF binding region
ENSG00000248337	TF binding region
ENSG00000250088	TF binding region
ENSG00000248160	TF binding region
ENSG00000250782	TF binding region
ENSG00000268799	TF binding region
ENSG00000185041	TF binding region
ENSG00000249620	TF binding region
ENSG00000248542	CpG island
ENSG00000249427	CpG island
ENSG00000249282	CpG island
ENSG00000248861	CpG island
ENSG00000250558	CpG island
ENSG00000248205	CpG island
ENSG00000248471	CpG island
ENSG00000250807	CpG island
ENSG00000250667	CpG island
ENSG00000250296	CpG island
ENSG00000250055	CpG island
ENSG00000248422	CpG island
ENSG00000269466	CpG island
ENSG00000249339	CpG island
ENSG00000271296	CpG island
ENSG00000250386	CpG island
ENSG00000250351	CpG island
ENSG00000249329	CpG island
ENSG00000249666	CpG island
ENSG00000249357	CpG island
ENSG00000249156	CpG island
ENSG00000248337	CpG island
ENSG00000250088	CpG island
ENSG00000248160	CpG island
ENSG00000250782	CpG island
ENSG00000268799	CpG island
ENSG00000185041	CpG island
ENSG00000249620	CpG island
ENSG00000215196	chromatin interactions
ENSG00000248542	chromatin interactions
ENSG00000250782	chromatin interactions
ENSG00000268799	chromatin interactions
ENSG00000248471	chromatin interactions
ENSG00000176788	chromatin interactions

Extended variants
information (count: 2445 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368938919	chr5:17496616-17496617	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs185566032	chr5:17496620-17496621	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs541417739	chr5:17496626-17496627	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs561763015	chr5:17496636-17496637	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs527390501	chr5:17496655-17496656	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs541147822	chr5:17496683-17496684	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs113377116	chr5:17496722-17496723	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs533124871	chr5:17496735-17496736	Inactive region	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs550022610	chr5:17496756-17496757	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569919213	chr5:17496760-17496761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs141934199	chr5:17496777-17496778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542079455	chr5:17496792-17496793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549100080	chr5:17496827-17496828	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566115159	chr5:17496833-17496834	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs534787760	chr5:17496854-17496855	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188933068	chr5:17496882-17496883	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191477468	chr5:17496902-17496903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183719363	chr5:17496910-17496911	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557140074	chr5:17496986-17496987	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188777383	chr5:17497059-17497060	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs201450853	chr5:17497112-17497113	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs552845386	chr5:17497134-17497135	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375725157	chr5:17497142-17497143	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377691620	chr5:17497153-17497154	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2457753	chr5:17497219-17497220	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs77693388	chr5:17497261-17497262	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536998876	chr5:17497266-17497267	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74399882	chr5:17497291-17497292	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs145360588	chr5:17497315-17497316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200116269	chr5:17497318-17497319	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555040823	chr5:17497335-17497336	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs75878878	chr5:17497338-17497339	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575842104	chr5:17497352-17497353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79475218	chr5:17497358-17497359	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75211029	chr5:17497359-17497360	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs74708913	chr5:17497364-17497365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs115186699	chr5:17497375-17497376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139966456	chr5:17497385-17497386	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369547634	chr5:17497398-17497399	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564141942	chr5:17497409-17497410	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs78222197	chr5:17497410-17497411	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs79725460	chr5:17497411-17497412	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148349177	chr5:17497417-17497418	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs72740581	chr5:17497418-17497419	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72740582	chr5:17497419-17497420	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs72740583	chr5:17497433-17497434	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372932384	chr5:17497446-17497447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563516082	chr5:17497463-17497464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75626652	chr5:17497464-17497465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78847389	chr5:17497470-17497471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17500600-17500800	Enhancers	A549	lung
2	chr5:17500600-17500800	Enhancers	Hela-S3	cervix
3	chr5:17500600-17501000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:17500600-17501000	Active TSS	NHDF-Ad	bronchial
5	chr5:17502200-17503000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:17509000-17509400	Enhancers	Fetal Brain Male	brain
7	chr5:17512000-17512200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:17512200-17512400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr5:17512200-17512400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:17512400-17512600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:17512600-17517600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:17512600-17519400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr5:17513600-17514600	Enhancers	A549	lung
14	chr5:17517400-17517600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:17517600-17518000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr5:17517600-17518000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:17517800-17518000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
18	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Lung	lung
19	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
20	chr5:17517800-17518000	Bivalent/Poised TSS	Small Intestine	intestine
21	chr5:17517800-17518000	Bivalent/Poised TSS	Hela-S3	cervix
22	chr5:17526600-17527000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
23	chr5:17526600-17527000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr5:17526600-17527000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:17526600-17527000	ZNF genes & repeats	Brain Substantia Nigra	brain
26	chr5:17526800-17527000	Bivalent Enhancer	Small Intestine	intestine
27	chr5:17593600-17598800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr5:17604200-17604600	Enhancers	Lung	lung
29	chr5:17604200-17604600	Enhancers	Hela-S3	cervix
30	chr5:17607400-17607600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:17616600-17616800	ZNF genes & repeats	Brain Hippocampus Middle	brain
32	chr5:17619200-17620600	Enhancers	Hela-S3	cervix
33	chr5:17620600-17621000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:17639200-17640000	Enhancers	Liver	Liver
35	chr5:17652200-17652400	Enhancers	HSMM	muscle
36	chr5:17662200-17662800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr5:17662800-17663000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr5:17662800-17663400	Enhancers	Fetal Muscle Trunk	muscle
39	chr5:17663000-17669200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr5:17664200-17664800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr5:17664200-17665400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr5:17664200-17665600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:17664200-17665800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:17664400-17664800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:17664400-17664800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr5:17664400-17665000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:17664400-17665000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:17664400-17665800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr5:17664600-17664800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:17664800-17665800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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