Variant report

Variant	esv3349779
Chromosome Location	chr5:17491735-17620964
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1639)
CpG islands
(count:672)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1639 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:17517830-17517852	K562	blood:	n/a	n/a
2	ARID3A	chr5:17526839-17526866	K562	blood:	n/a	n/a
3	ATF1	chr5:17492224-17492379	K562	blood:	n/a	n/a
4	ATF1	chr5:17517811-17517870	K562	blood:	n/a	n/a
5	ATF3	chr5:17517759-17517894	K562	blood:	n/a	n/a
6	BACH1	chr5:17526845-17526876	K562	blood:	n/a	n/a
7	BATF	chr5:17580902-17581080	GM12878	blood:	n/a	n/a
8	BATF	chr5:17586875-17587277	GM12878	blood:	n/a	n/a
9	BATF	chr5:17520861-17521352	GM12878	blood:	n/a	n/a
10	BATF	chr5:17588369-17588646	GM12878	blood:	n/a	n/a
11	BATF	chr5:17527729-17528285	GM12878	blood:	n/a	n/a
12	BATF	chr5:17524295-17524851	GM12878	blood:	n/a	n/a
13	BATF	chr5:17588661-17591031	GM12878	blood:	n/a	n/a
14	BATF	chr5:17581407-17582352	GM12878	blood:	n/a	n/a
15	BATF	chr5:17581115-17581413	GM12878	blood:	n/a	n/a
16	BATF	chr5:17528689-17530680	GM12878	blood:	n/a	n/a
17	BATF	chr5:17581121-17581401	GM12878	blood:	n/a	n/a
18	BATF	chr5:17583462-17585828	GM12878	blood:	n/a	n/a
19	BATF	chr5:17586894-17587691	GM12878	blood:	n/a	n/a
20	BATF	chr5:17595530-17597898	GM12878	blood:	n/a	n/a
21	BATF	chr5:17528684-17530686	GM12878	blood:	n/a	n/a
22	BATF	chr5:17525255-17528049	GM12878	blood:	n/a	n/a
23	BATF	chr5:17521821-17524301	GM12878	blood:	n/a	n/a
24	BATF	chr5:17591806-17592083	GM12878	blood:	n/a	n/a
25	BATF	chr5:17587321-17587686	GM12878	blood:	n/a	n/a
26	BATF	chr5:17595225-17595440	GM12878	blood:	n/a	n/a
27	BATF	chr5:17583170-17583447	GM12878	blood:	n/a	n/a
28	BATF	chr5:17588662-17591030	GM12878	blood:	n/a	n/a
29	BATF	chr5:17599128-17599665	GM12878	blood:	n/a	n/a
30	BATF	chr5:17524307-17524569	GM12878	blood:	n/a	n/a
31	BATF	chr5:17581436-17582365	GM12878	blood:	n/a	n/a
32	BATF	chr5:17592098-17594464	GM12878	blood:	n/a	n/a
33	BATF	chr5:17518387-17521181	GM12878	blood:	n/a	n/a
34	BATF	chr5:17586589-17586869	GM12878	blood:	n/a	n/a
35	BATF	chr5:17595045-17595501	GM12878	blood:	n/a	n/a
36	BATF	chr5:17518382-17520848	GM12878	blood:	n/a	n/a
37	BATF	chr5:17588377-17588634	GM12878	blood:	n/a	n/a
38	BATF	chr5:17521816-17524282	GM12878	blood:	n/a	n/a
39	BATF	chr5:17525250-17527716	GM12878	blood:	n/a	n/a
40	BATF	chr5:17499625-17499833	GM12878	blood:	n/a	n/a
41	BATF	chr5:17591814-17594470	GM12878	blood:	n/a	n/a
42	BATF	chr5:17599390-17599669	GM12878	blood:	n/a	n/a
43	BATF	chr5:17583178-17585829	GM12878	blood:	n/a	n/a
44	BATF	chr5:17586583-17586881	GM12878	blood:	n/a	n/a
45	BATF	chr5:17595471-17597904	GM12878	blood:	n/a	n/a
46	BCL11A	chr5:17528686-17530695	GM12878	blood:	n/a	n/a
47	BCL11A	chr5:17580920-17582358	GM12878	blood:	n/a	n/a
48	BCL11A	chr5:17499619-17499851	GM12878	blood:	n/a	n/a
49	BCL11A	chr5:17595036-17597994	GM12878	blood:	n/a	n/a
50	BCL11A	chr5:17517610-17517929	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17522582-17522632	ECC-1	luminal epithelium:	n/a
2	chr5:17522582-17522632	ECC-1	luminal epithelium:	n/a
3	chr5:17517201-17517251	Hepatocyte	liver:	n/a
4	chr5:17522582-17522632	HNPCEpiC	eye:	n/a
5	chr5:17491941-17491991	GM06990	blood:	n/a
6	chr5:17519013-17519063	HUVEC	blood vessel:	n/a
7	chr5:17595441-17595491	MCF10A-Er-Src	breast:	n/a
8	chr5:17595441-17595491	U87	brain:	n/a
9	chr5:17528991-17529041	NHBE	bronchial:	n/a
10	chr5:17580826-17580876	Hela-S3	cervix:	n/a
11	chr5:17519013-17519063	AG09309	skin:	n/a
12	chr5:17580826-17580876	ProgFib	skin:	n/a
13	chr5:17495781-17495831	NT2-D1	testis:	n/a
14	chr5:17604867-17604917	HEK293	kidney:	embryo
15	chr5:17527430-17527480	BJ	skin:	n/a
16	chr5:17527430-17527480	H1-hESC	embryonic stem cell:	embryo
17	chr5:17495781-17495831	AG10803	skin:	n/a
18	chr5:17527430-17527480	AG09319	gingival:	n/a
19	chr5:17519013-17519063	GM06990	blood:	n/a
20	chr5:17528991-17529041	HMEC	breast:	n/a
21	chr5:17528991-17529041	GM12892	blood:	n/a
22	chr5:17580826-17580876	AG04450	lung:	fetal
23	chr5:17522582-17522632	Jurkat	blood:	n/a
24	chr5:17524561-17524611	Jurkat	blood:	n/a
25	chr5:17580826-17580876	CMK	blood:	n/a
26	chr5:17595441-17595491	Jurkat	blood:	n/a
27	chr5:17495781-17495831	A549	lung:	n/a
28	chr5:17517201-17517251	SK-N-SH	brain:	n/a
29	chr5:17604867-17604917	HCM	heart:	n/a
30	chr5:17595441-17595491	LNCaP	prostate:	n/a
31	chr5:17522582-17522632	Caco-2	colon:	n/a
32	chr5:17491941-17491991	HUVEC	blood vessel:	n/a
33	chr5:17524561-17524611	HUVEC	blood vessel:	n/a
34	chr5:17604867-17604917	BE2_C	brain:	n/a
35	chr5:17595441-17595491	HCPEpiC	choroid plexus:	n/a
36	chr5:17519013-17519063	MCF-7	breast:	n/a
37	chr5:17491941-17491991	BJ	skin:	n/a
38	chr5:17595441-17595491	GM12892	blood:	n/a
39	chr5:17524561-17524611	Hepatocyte	liver:	n/a
40	chr5:17527430-17527480	NB4	blood:	n/a
41	chr5:17495781-17495831	K562	blood:	n/a
42	chr5:17580826-17580876	HCPEpiC	choroid plexus:	n/a
43	chr5:17522582-17522632	IMR90	lung:	fetal
44	chr5:17580826-17580876	GM19239	blood:	n/a
45	chr5:17595441-17595491	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:17517201-17517251	NT2-D1	testis:	n/a
47	chr5:17524561-17524611	HNPCEpiC	eye:	n/a
48	chr5:17580826-17580876	HRCEpiC	kidney:	n/a
49	chr5:17595441-17595491	SK-N-SH	brain:	n/a
50	chr5:17491941-17491991	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:
2	chr5:17491440..17494172-chr5:17495062..17497549,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BASP1-11	chr5:17494578-17494846	l_2885_chr5:17456969-17494846_brain
2	lnc-MYO10-12	chr5:17587399-17587632	NONHSAT100653

No data

Variant related genes	Relation type
ENSG00000249427	TF binding region
ENSG00000249282	TF binding region
ENSG00000248861	TF binding region
ENSG00000250558	TF binding region
ENSG00000248205	TF binding region
ENSG00000250807	TF binding region
ENSG00000250667	TF binding region
ENSG00000250296	TF binding region
ENSG00000250055	TF binding region
ENSG00000248422	TF binding region
ENSG00000249339	TF binding region
ENSG00000271296	TF binding region
ENSG00000249329	TF binding region
ENSG00000249357	TF binding region
ENSG00000249156	TF binding region
ENSG00000250088	TF binding region
ENSG00000268799	TF binding region
ENSG00000185041	TF binding region
ENSG00000249620	TF binding region
ENSG00000249427	CpG island
ENSG00000249282	CpG island
ENSG00000248861	CpG island
ENSG00000250558	CpG island
ENSG00000248205	CpG island
ENSG00000250807	CpG island
ENSG00000250667	CpG island
ENSG00000250296	CpG island
ENSG00000250055	CpG island
ENSG00000248422	CpG island
ENSG00000249339	CpG island
ENSG00000271296	CpG island
ENSG00000249329	CpG island
ENSG00000249357	CpG island
ENSG00000249156	CpG island
ENSG00000250088	CpG island
ENSG00000268799	CpG island
ENSG00000185041	CpG island
ENSG00000249620	CpG island
ENSG00000268799	chromatin interactions
ENSG00000250667	chromatin interactions

Extended variants
information (count: 1419 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1419 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573804624	chr5:17491773-17491774	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs542798613	chr5:17491778-17491779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545722944	chr5:17491787-17491788	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559510396	chr5:17491799-17491800	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs528370671	chr5:17491803-17491804	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs61745031	chr5:17491829-17491830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551680206	chr5:17491845-17491846	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565116758	chr5:17491860-17491861	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs569451426	chr5:17491863-17491864	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs530776816	chr5:17491867-17491868	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs377256071	chr5:17491871-17491872	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550583327	chr5:17491876-17491877	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200861628	chr5:17491953-17491954	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs564399944	chr5:17491955-17491956	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567375861	chr5:17491968-17491969	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs536354777	chr5:17491970-17491971	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546867764	chr5:17491987-17491988	Inactive region	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs191906398	chr5:17492006-17492007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs538943034	chr5:17492034-17492035	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs73756920	chr5:17492077-17492078	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs143192095	chr5:17492109-17492110	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs576023733	chr5:17492127-17492128	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537018525	chr5:17492130-17492131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs557001837	chr5:17492131-17492132	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573739552	chr5:17492146-17492147	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs542788437	chr5:17492151-17492152	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187590039	chr5:17492154-17492155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs573024363	chr5:17492166-17492167	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544889268	chr5:17492205-17492206	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35465459	chr5:17492230-17492231	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs192998784	chr5:17492238-17492239	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs543152393	chr5:17492256-17492257	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550519971	chr5:17492297-17492298	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs150858139	chr5:17492362-17492363	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs139302730	chr5:17492371-17492372	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533583910	chr5:17492398-17492399	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149565860	chr5:17492442-17492443	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566936487	chr5:17492499-17492500	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs182567372	chr5:17492506-17492507	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs369906519	chr5:17492512-17492513	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186838538	chr5:17492535-17492536	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs530819971	chr5:17492548-17492549	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs375338254	chr5:17492570-17492571	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs2457755	chr5:17492589-17492590	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73756921	chr5:17492591-17492592	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs192185881	chr5:17492607-17492608	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556989256	chr5:17492651-17492652	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573705381	chr5:17492665-17492666	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs371177449	chr5:17492674-17492675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184223349	chr5:17492716-17492717	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:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17494400-17496200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr5:17500600-17500800	Enhancers	A549	lung
3	chr5:17500600-17500800	Enhancers	Hela-S3	cervix
4	chr5:17500600-17501000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:17500600-17501000	Active TSS	NHDF-Ad	bronchial
6	chr5:17502200-17503000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:17509000-17509400	Enhancers	Fetal Brain Male	brain
8	chr5:17512000-17512200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr5:17512200-17512400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr5:17512200-17512400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:17512400-17512600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:17512600-17517600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:17512600-17519400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:17513600-17514600	Enhancers	A549	lung
15	chr5:17517400-17517600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:17517600-17518000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr5:17517600-17518000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr5:17517800-17518000	ZNF genes & repeats	Duodenum Mucosa	Duodenum
19	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Lung	lung
20	chr5:17517800-17518000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
21	chr5:17517800-17518000	Bivalent/Poised TSS	Small Intestine	intestine
22	chr5:17517800-17518000	Bivalent/Poised TSS	Hela-S3	cervix
23	chr5:17526600-17527000	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
24	chr5:17526600-17527000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr5:17526600-17527000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:17526600-17527000	ZNF genes & repeats	Brain Substantia Nigra	brain
27	chr5:17526800-17527000	Bivalent Enhancer	Small Intestine	intestine
28	chr5:17593600-17598800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr5:17604200-17604600	Enhancers	Lung	lung
30	chr5:17604200-17604600	Enhancers	Hela-S3	cervix
31	chr5:17607400-17607600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:17616600-17616800	ZNF genes & repeats	Brain Hippocampus Middle	brain
33	chr5:17619200-17620600	Enhancers	Hela-S3	cervix
34	chr5:17620600-17621000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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