Variant report

Variant	esv1812313
Chromosome Location	chr5:17634065-17710478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:307)
CpG islands
(count:428)
Chromatin interactive
region (count:8)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:17680992-17681026	K562	blood:	n/a	n/a
2	BATF	chr5:17633718-17634065	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:17633698-17634114	GM12878	blood:	n/a	n/a
4	BCL3	chr5:17694847-17695529	A549	lung:	n/a	chr5:17695250-17695259
5	BRCA1	chr5:17679984-17680257	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr5:17694481-17695921	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr5:17691746-17692676	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:17635259-17635326	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:17679965-17680281	MCF-7	breast:	n/a	chr5:17680161-17680172
10	CEBPB	chr5:17679987-17680283	HepG2	liver:	n/a	chr5:17680161-17680172
11	CEBPB	chr5:17680006-17680300	IMR90	lung:	n/a	chr5:17680161-17680172
12	CEBPB	chr5:17679986-17680295	A549	lung:	n/a	chr5:17680161-17680172
13	CEBPB	chr5:17694967-17695397	MCF-7	breast:	n/a	n/a
14	CEBPB	chr5:17694461-17695782	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:17676779-17677058	HepG2	liver:	n/a	chr5:17676912-17676923
16	CEBPB	chr5:17679962-17680276	A549	lung:	n/a	chr5:17680161-17680172
17	CEBPB	chr5:17694967-17695479	A549	lung:	n/a	n/a
18	CEBPB	chr5:17691832-17692471	Hela-S3	cervix:	n/a	chr5:17692053-17692070
19	CEBPB	chr5:17679832-17680634	Hela-S3	cervix:	n/a	chr5:17680161-17680172
20	CEBPB	chr5:17680008-17680237	ECC-1	luminal epithelium:	n/a	chr5:17680161-17680172
21	CEBPB	chr5:17676882-17676947	K562	blood:	n/a	chr5:17676912-17676923
22	CEBPB	chr5:17676818-17677046	A549	lung:	n/a	chr5:17676912-17676923
23	CEBPB	chr5:17694987-17695485	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:17679981-17680265	ECC-1	luminal epithelium:	n/a	chr5:17680161-17680172
25	CEBPB	chr5:17676850-17677041	IMR90	lung:	n/a	chr5:17676912-17676923
26	CEBPB	chr5:17679822-17680468	A549	lung:	n/a	chr5:17680161-17680172
27	CEBPB	chr5:17691305-17691412	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr5:17695079-17695387	A549	lung:	n/a	n/a
29	CEBPB	chr5:17667008-17667264	A549	lung:	n/a	n/a
30	CEBPB	chr5:17667048-17667244	IMR90	lung:	n/a	n/a
31	CEBPB	chr5:17694817-17695648	A549	lung:	n/a	n/a
32	CHD2	chr5:17679972-17680355	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr5:17694498-17695438	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr5:17670510-17670678	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr5:17655420-17655570	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:17670503-17670697	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:17670539-17670602	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:17655460-17655610	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:17637019-17637082	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr5:17670580-17670730	NB4	blood:	n/a	n/a
41	CTCF	chr5:17655429-17655640	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:17655477-17655549	Gliobla	brain:	n/a	n/a
43	CTCF	chr5:17674280-17674430	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:17688800-17688950	GM06990	blood:	n/a	n/a
45	CTCF	chr5:17670480-17670630	K562	blood:	n/a	n/a
46	CTCF	chr5:17655516-17655567	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:17670517-17670622	A549	lung:	n/a	n/a
48	CTCF	chr5:17670580-17670730	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr5:17670340-17670590	HEK293	kidney:	n/a	n/a
50	CTCF	chr5:17670567-17670622	Hela-S3	cervix:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:17670475-17670525	HepG2	liver:	n/a
2	chr5:17670475-17670525	HepG2	liver:	n/a
3	chr5:17634462-17634512	HCF	heart:	n/a
4	chr5:17656637-17656687	HUVEC	blood vessel:	n/a
5	chr5:17670475-17670525	HL-60	blood:	n/a
6	chr5:17655356-17655406	HNPCEpiC	eye:	n/a
7	chr5:17670442-17670492	AoSMC	blood vessel:	n/a
8	chr5:17664567-17664617	Jurkat	blood:	n/a
9	chr5:17670475-17670525	IMR90	lung:	fetal
10	chr5:17655356-17655406	HPAEpiC	pulmonary alveolar:	n/a
11	chr5:17670442-17670492	HRCEpiC	kidney:	n/a
12	chr5:17670442-17670492	K562	blood:	n/a
13	chr5:17656637-17656687	PFSK-1	brain:	n/a
14	chr5:17654594-17654644	HRE	kidney:	n/a
15	chr5:17654594-17654644	HMEC	breast:	n/a
16	chr5:17656637-17656687	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:17654594-17654644	U87	brain:	n/a
18	chr5:17654594-17654644	SK-N-MC	brain:	n/a
19	chr5:17654594-17654644	HIPEpiC	eye:	n/a
20	chr5:17670475-17670525	HRPEpiC	eye:	n/a
21	chr5:17664567-17664617	K562	blood:	n/a
22	chr5:17670442-17670492	AG04449	skin:	fetal
23	chr5:17655356-17655406	Caco-2	colon:	n/a
24	chr5:17655356-17655406	HRPEpiC	eye:	n/a
25	chr5:17670475-17670525	GM12892	blood:	n/a
26	chr5:17634462-17634512	MCF-7	breast:	n/a
27	chr5:17670442-17670492	HRPEpiC	eye:	n/a
28	chr5:17664567-17664617	CMK	blood:	n/a
29	chr5:17664567-17664617	HMEC	breast:	n/a
30	chr5:17664567-17664617	T-47D	breast:	n/a
31	chr5:17670475-17670525	AG09309	skin:	n/a
32	chr5:17656637-17656687	AG04449	skin:	fetal
33	chr5:17664567-17664617	HCF	heart:	n/a
34	chr5:17664567-17664617	SAEC	small airway:	n/a
35	chr5:17655356-17655406	PFSK-1	brain:	n/a
36	chr5:17634462-17634512	ProgFib	skin:	n/a
37	chr5:17655356-17655406	AG04450	lung:	fetal
38	chr5:17664567-17664617	HRE	kidney:	n/a
39	chr5:17670442-17670492	HIPEpiC	eye:	n/a
40	chr5:17670442-17670492	HL-60	blood:	n/a
41	chr5:17655356-17655406	GM12891	blood:	n/a
42	chr5:17656637-17656687	ProgFib	skin:	n/a
43	chr5:17655356-17655406	CMK	blood:	n/a
44	chr5:17670442-17670492	NH-A	brain:	n/a
45	chr5:17664567-17664617	RPTEC	kidney:	n/a
46	chr5:17655356-17655406	HMEC	breast:	n/a
47	chr5:17664567-17664617	HCT-116	colon:	n/a
48	chr5:17634462-17634512	T-47D	breast:	n/a
49	chr5:17664567-17664617	HRCEpiC	kidney:	n/a
50	chr5:17670475-17670525	Hepatocyte	liver:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:17693367..17696364-chr5:17702400..17704641,2	MCF-7	breast:
2	chr5:17644806..17646667-chr5:17648582..17651312,2	MCF-7	breast:
3	chr5:17216395..17218536-chr5:17655025..17657774,2	MCF-7	breast:
4	chr5:17632983..17635813-chr5:17637711..17640599,2	K562	blood:
5	chr5:17693367..17696364-chr5:17702400..17704641,2	MCF-7	breast:
6	chr5:17702899..17705763-chr5:17710587..17714118,3	MCF-7	breast:
7	chr5:17217433..17219821-chr5:17690448..17693197,3	MCF-7	breast:
8	chr5:17635261..17638059-chr5:17641232..17643907,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO10-19	chr5:17654482-17654752	NONHSAT100661
2	lnc-BASP1-7	chr5:17684693-17684796	ENSG00000249937
3	lnc-MYO10-17	chr5:17643071-17643337	NONHSAT100659
4	lnc-BASP1-7	chr5:17684693-17684796	NONHSAT100665

No data

Variant related genes	Relation type
ENSG00000248542	TF binding region
ENSG00000248471	TF binding region
ENSG00000269466	TF binding region
ENSG00000250715	TF binding region
ENSG00000248337	TF binding region
ENSG00000248160	TF binding region
ENSG00000250782	TF binding region
ENSG00000249937	TF binding region
ENSG00000248542	CpG island
ENSG00000248471	CpG island
ENSG00000269466	CpG island
ENSG00000250715	CpG island
ENSG00000248337	CpG island
ENSG00000248160	CpG island
ENSG00000250782	CpG island
ENSG00000249937	CpG island
ENSG00000215196	chromatin interactions
ENSG00000248471	chromatin interactions
ENSG00000248542	chromatin interactions
ENSG00000250782	chromatin interactions
ENSG00000176788	chromatin interactions

Extended variants
information (count: 1525 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2005391	chr5:17634065-17634066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs113279788	chr5:17634078-17634079	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs573214534	chr5:17634079-17634080	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs534584905	chr5:17634081-17634082	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs79816064	chr5:17634085-17634086	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557499061	chr5:17634086-17634087	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577653672	chr5:17634093-17634094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs543196336	chr5:17634098-17634099	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs563496433	chr5:17634103-17634104	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs72742666	chr5:17634119-17634120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs573835093	chr5:17634171-17634172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs542853611	chr5:17634188-17634189	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142236797	chr5:17634470-17634471	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs186828857	chr5:17634486-17634487	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs112373095	chr5:17634487-17634488	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs190854903	chr5:17634490-17634491	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs555139150	chr5:17635267-17635268	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs111675494	chr5:17635278-17635279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564094838	chr5:17635296-17635297	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188236494	chr5:17635330-17635331	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371246411	chr5:17635343-17635344	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs180734752	chr5:17635393-17635394	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148817983	chr5:17635399-17635400	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532663045	chr5:17635407-17635408	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs184911555	chr5:17635410-17635411	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189759042	chr5:17635433-17635434	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181902731	chr5:17635442-17635443	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548852495	chr5:17635446-17635447	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568778820	chr5:17635452-17635453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200490046	chr5:17635473-17635474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs386685943	chr5:17635474-17635475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546638044	chr5:17635487-17635488	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186061166	chr5:17635492-17635493	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs72742668	chr5:17635494-17635495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190482229	chr5:17635497-17635498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs72742669	chr5:17635503-17635504	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111437544	chr5:17635518-17635519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181936442	chr5:17635524-17635525	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs72494140	chr5:17635530-17635531	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142541265	chr5:17635537-17635538	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs186352755	chr5:17635539-17635540	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs74193983	chr5:17635541-17635542	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1965384	chr5:17635546-17635547	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs139160074	chr5:17635555-17635556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111594048	chr5:17635561-17635562	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs190850504	chr5:17635564-17635565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372086449	chr5:17635582-17635583	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564805514	chr5:17635585-17635586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182781118	chr5:17635586-17635587	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34709437	chr5:17635602-17635603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17639200-17640000	Enhancers	Liver	Liver
2	chr5:17652200-17652400	Enhancers	HSMM	muscle
3	chr5:17662200-17662800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:17662800-17663000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:17662800-17663400	Enhancers	Fetal Muscle Trunk	muscle
6	chr5:17663000-17669200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:17664200-17664800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr5:17664200-17665400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr5:17664200-17665600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr5:17664200-17665800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:17664400-17664800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr5:17664400-17664800	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr5:17664400-17665000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:17664400-17665000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:17664400-17665800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr5:17664600-17664800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:17664800-17665800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:17665600-17668000	Enhancers	Primary B cells from cord blood	blood
19	chr5:17666000-17668000	Enhancers	Primary B cells from peripheral blood	blood
20	chr5:17670400-17670800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:17678800-17680000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr5:17678800-17680000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr5:17678800-17680800	Enhancers	HMEC	breast
24	chr5:17678800-17681400	Enhancers	Hela-S3	cervix
25	chr5:17679000-17680600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr5:17679200-17680800	Enhancers	A549	lung
27	chr5:17679600-17680000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:17679600-17680600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr5:17679800-17680200	Enhancers	NHEK	skin
30	chr5:17681400-17684400	Weak transcription	Hela-S3	cervix
31	chr5:17682800-17683000	Enhancers	Ovary	ovary
32	chr5:17683000-17684400	Weak transcription	Ovary	ovary
33	chr5:17684400-17684800	Flanking Active TSS	Ovary	ovary
34	chr5:17684400-17685200	Active TSS	Hela-S3	cervix
35	chr5:17684800-17685200	Enhancers	Ovary	ovary
36	chr5:17690200-17690800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:17690200-17690800	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr5:17690200-17691600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:17691400-17697000	Enhancers	Hela-S3	cervix
40	chr5:17692000-17692200	Enhancers	HMEC	breast
41	chr5:17692200-17692400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr5:17692200-17692600	Enhancers	Placenta	Placenta
43	chr5:17692600-17694200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr5:17694200-17696400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr5:17694200-17696600	Enhancers	NHEK	skin
46	chr5:17694400-17696600	Enhancers	HMEC	breast
47	chr5:17694600-17695000	Enhancers	A549	lung
48	chr5:17694600-17696400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:17695000-17695800	Flanking Active TSS	A549	lung
50	chr5:17695400-17696000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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