Variant report

Variant	esv3421637
Chromosome Location	chr5:68258596-68263994
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:68258751-68259013	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr5:68260450-68262189	GM12878	blood:	n/a	n/a
3	BCL3	chr5:68260303-68262196	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:68258726-68258984	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr5:68258746-68258988	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr5:68258653-68259071	HepG2	liver:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
7	CTCF	chr5:68258880-68259030	GM12870	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
8	CTCF	chr5:68258780-68258930	GM12867	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
9	CTCF	chr5:68258840-68258990	K562	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
10	CTCF	chr5:68258820-68258970	HEEpiC	esophagus:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
11	CTCF	chr5:68258840-68258990	GM06990	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
12	CTCF	chr5:68258687-68259114	GM12878	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
13	CTCF	chr5:68258770-68258996	ECC-1	luminal epithelium:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
14	CTCF	chr5:68258840-68258990	Caco-2	colon:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
15	CTCF	chr5:68258820-68258970	BE2_C	brain:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
16	CTCF	chr5:68258794-68259047	MCF-7	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
17	CTCF	chr5:68261862-68261988	GM19239	blood:	n/a	n/a
18	CTCF	chr5:68258840-68258990	AG10803	skin:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
19	CTCF	chr5:68258689-68259111	T-47D	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
20	CTCF	chr5:68258789-68259004	Lung_OC	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
21	CTCF	chr5:68258840-68258990	HA-sp	spinal cord:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
22	CTCF	chr5:68258532-68259209	HCT-116	colon:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
23	CTCF	chr5:68258860-68259010	GM12868	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
24	CTCF	chr5:68258820-68258970	HCT-116	colon:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
25	CTCF	chr5:68258840-68258990	HRPEpiC	eye:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
26	CTCF	chr5:68261771-68261782	GM13976	blood:	n/a	n/a
27	CTCF	chr5:68258792-68259042	MCF-7	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
28	CTCF	chr5:68258820-68258970	GM12872	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
29	CTCF	chr5:68258820-68258970	Hela-S3	cervix:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
30	CTCF	chr5:68258800-68259032	MCF-7	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
31	CTCF	chr5:68258880-68259030	HL-60	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
32	CTCF	chr5:68258820-68258970	HBMEC	blood vessel:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
33	CTCF	chr5:68258788-68259030	LNCaP	prostate:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
34	CTCF	chr5:68258780-68258930	HPF	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
35	CTCF	chr5:68258820-68258970	NHLF	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
36	CTCF	chr5:68258840-68258990	HBMEC	blood vessel:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
37	CTCF	chr5:68258800-68258950	GM12869	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
38	CTCF	chr5:68258840-68258990	HCPEpiC	choroid plexus:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
39	CTCF	chr5:68258681-68259188	IMR90	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
40	CTCF	chr5:68258720-68259012	A549	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
41	CTCF	chr5:68259140-68259290	AG04449	skin:	n/a	n/a
42	CTCF	chr5:68258840-68258990	GM12868	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
43	CTCF	chr5:68258840-68258990	GM12867	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
44	CTCF	chr5:68258790-68259034	GM19240	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
45	CTCF	chr5:68259240-68259390	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr5:68258820-68258970	HMF	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
47	CTCF	chr5:68258800-68258950	MCF-7	breast:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
48	CTCF	chr5:68258816-68259020	GM13976	blood:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
49	CTCF	chr5:68258727-68259043	H1-hESC	embryonic stem cell:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904
50	CTCF	chr5:68258288-68259284	A549	lung:	n/a	chr5:68258888-68258906 chr5:68258890-68258903 chr5:68258883-68258904

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:68258016..68260416-chr5:68261824..68264961,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC30A5-1	chr5:68259073-68259310	XLOC_004417
2	lnc-SLC30A5-1	chr5:68263494-68263672	XLOC_004417
3	lnc-CCDC125-4	chr5:68263568-68264283	XLOC_004860
4	lnc-CCDC125-4	chr5:68263568-68264283	NONHSAT101876

Variant related genes	Relation type
ENSG00000250066	TF binding region
ENSG00000249335	TF binding region
ENSG00000250066	chromatin interactions

Extended variants
information (count: 295 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187780699	chr5:68258626-68258627	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs73771636	chr5:68258720-68258721	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs568792633	chr5:68258722-68258723	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs143462326	chr5:68258747-68258748	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs536067021	chr5:68258771-68258772	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs73771637	chr5:68258774-68258775	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs192445615	chr5:68258787-68258788	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs547578777	chr5:68258788-68258789	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs554422944	chr5:68258789-68258790	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs185039987	chr5:68258803-68258804	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs189940647	chr5:68258830-68258831	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs73124953	chr5:68258835-68258836	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs372734754	chr5:68258856-68258857	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs577180982	chr5:68258861-68258862	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs112000065	chr5:68258909-68258910	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs556351291	chr5:68258956-68258957	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs574547339	chr5:68258979-68258980	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs142503521	chr5:68258992-68258993	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs560033103	chr5:68259010-68259011	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs571994802	chr5:68259062-68259063	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs545512153	chr5:68259093-68259094	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs182167655	chr5:68259123-68259124	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs36070419	chr5:68259198-68259199	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs74722263	chr5:68259208-68259209	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs372639931	chr5:68259264-68259265	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs114617357	chr5:68259270-68259271	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs138559559	chr5:68259302-68259303	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs529510723	chr5:68259320-68259321	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572906926	chr5:68259354-68259355	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372845609	chr5:68259361-68259362	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533693740	chr5:68259381-68259382	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs372970272	chr5:68259390-68259391	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs539943792	chr5:68259463-68259464	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551763659	chr5:68259475-68259476	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs570073889	chr5:68259514-68259515	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs201432612	chr5:68259520-68259521	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs76662607	chr5:68259533-68259534	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs184550358	chr5:68259563-68259564	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs189892824	chr5:68259601-68259602	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558618841	chr5:68259607-68259608	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568239999	chr5:68259624-68259625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565958505	chr5:68259675-68259676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553811117	chr5:68259721-68259722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572019997	chr5:68259728-68259729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180727737	chr5:68259744-68259745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548631045	chr5:68259818-68259819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185170516	chr5:68259879-68259880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563986618	chr5:68259944-68259945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112861174	chr5:68259953-68259954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141750860	chr5:68259954-68259955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Lung adenocarcinoma	17086460	CNVD
Breast cancer	21045282	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Lung cancer	17086460	CNVD
Prostate cancer	16461572	CNVD
Myelodysplastic syndrome	18663149	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Sezary syndrome	18413736	CNVD
Ewing''s sarcoma	17952124	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68246200-68262200	Weak transcription	Esophagus	oesophagus
2	chr5:68249400-68258600	Weak transcription	Right Atrium	heart
3	chr5:68254400-68258600	Weak transcription	Fetal Kidney	kidney
4	chr5:68256400-68259200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr5:68256600-68258600	Weak transcription	Primary B cells from peripheral blood	blood
6	chr5:68257000-68258600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:68257800-68258600	Enhancers	Adipose Nuclei	Adipose
8	chr5:68257800-68259200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr5:68257800-68259200	Enhancers	Liver	Liver
10	chr5:68258000-68258800	Enhancers	Colon Smooth Muscle	Colon
11	chr5:68258000-68258800	Enhancers	Fetal Heart	heart
12	chr5:68258000-68259200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr5:68258000-68261800	Weak transcription	Spleen	Spleen
14	chr5:68258200-68258800	Enhancers	Fetal Muscle Trunk	muscle
15	chr5:68258200-68259000	Enhancers	Fetal Muscle Leg	muscle
16	chr5:68258400-68258600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:68258400-68258600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:68258400-68258600	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr5:68258400-68258600	Enhancers	Small Intestine	intestine
20	chr5:68258400-68258600	Enhancers	NHDF-Ad	bronchial
21	chr5:68258400-68258800	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:68258400-68258800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr5:68258400-68258800	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr5:68258400-68258800	Enhancers	Duodenum Smooth Muscle	Duodenum
25	chr5:68258400-68258800	Enhancers	Fetal Lung	lung
26	chr5:68258400-68259200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr5:68258400-68259200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr5:68258600-68258800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr5:68258600-68258800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr5:68258600-68258800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:68258600-68258800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:68258600-68258800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:68258600-68258800	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr5:68258600-68258800	Enhancers	Brain Hippocampus Middle	brain
35	chr5:68258600-68258800	Enhancers	Brain Substantia Nigra	brain
36	chr5:68258600-68258800	Enhancers	Fetal Kidney	kidney
37	chr5:68258600-68258800	Enhancers	Right Atrium	heart
38	chr5:68258600-68258800	Enhancers	Stomach Smooth Muscle	stomach
39	chr5:68258600-68258800	Enhancers	HepG2	liver
40	chr5:68258600-68258800	Flanking Active TSS	K562	blood
41	chr5:68258600-68258800	Flanking Active TSS	NHDF-Ad	bronchial
42	chr5:68258600-68259000	Enhancers	Primary B cells from peripheral blood	blood
43	chr5:68258600-68259000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:68258600-68259000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr5:68258600-68259000	Enhancers	Brain Anterior Caudate	brain
46	chr5:68258600-68259000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr5:68258600-68259000	Active TSS	A549	lung
48	chr5:68258600-68259000	Flanking Active TSS	Osteobl	bone
49	chr5:68258600-68259200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr5:68258600-68259200	Active TSS	Muscle Satellite Cultured Cells	--

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