Variant report

Variant	nsv1015741
Chromosome Location	chr5:116525936-116665270
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	BATF	chr5:116580819-116581174	GM12878	blood:	n/a	n/a
2	BATF	chr5:116580825-116581108	GM12878	blood:	n/a	n/a
3	BATF	chr5:116566174-116566340	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:116580910-116581145	GM12878	blood:	n/a	n/a
5	BCL11A	chr5:116566325-116566509	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:116549749-116549920	HepG2	liver:	n/a	n/a
7	BRCA1	chr5:116562068-116562221	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:116597951-116598197	H1-hESC	embryonic stem cell:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116597968-116597977 chr5:116598098-116598109 chr5:116597966-116597977
9	CEBPB	chr5:116635780-116636181	MCF-7	breast:	n/a	chr5:116635987-116636004
10	CEBPB	chr5:116597932-116598252	A549	lung:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116597968-116597977 chr5:116598098-116598109 chr5:116597966-116597977
11	CEBPB	chr5:116597900-116598274	Hela-S3	cervix:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116597968-116597977 chr5:116598098-116598109 chr5:116597966-116597977
12	CEBPB	chr5:116584812-116585151	H1-hESC	embryonic stem cell:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
13	CEBPB	chr5:116584811-116585198	IMR90	lung:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
14	CEBPB	chr5:116597942-116598268	IMR90	lung:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116597968-116597977 chr5:116598098-116598109 chr5:116597966-116597977
15	CEBPB	chr5:116628372-116628472	A549	lung:	n/a	n/a
16	CEBPB	chr5:116642854-116643009	H1-hESC	embryonic stem cell:	n/a	chr5:116642923-116642936 chr5:116642923-116642936 chr5:116642925-116642936
17	CEBPB	chr5:116584813-116585163	HepG2	liver:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
18	CEBPB	chr5:116584833-116585178	K562	blood:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
19	CEBPB	chr5:116584821-116585176	A549	lung:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
20	CEBPB	chr5:116531544-116531834	HepG2	liver:	n/a	chr5:116531655-116531666 chr5:116531653-116531664
21	CEBPB	chr5:116597875-116598292	HepG2	liver:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116597968-116597977 chr5:116598098-116598109 chr5:116597966-116597977
22	CEBPB	chr5:116617917-116618117	HepG2	liver:	n/a	n/a
23	CEBPB	chr5:116597983-116598221	K562	blood:	n/a	chr5:116598100-116598109 chr5:116598099-116598110 chr5:116598098-116598109
24	CEBPB	chr5:116584862-116585125	MCF-7	breast:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
25	CEBPB	chr5:116584776-116585176	MCF-7	breast:	n/a	chr5:116584992-116585001 chr5:116584990-116585003 chr5:116584992-116585001 chr5:116584992-116585001 chr5:116584991-116585002 chr5:116584990-116585001 chr5:116584906-116584917 chr5:116584992-116585001 chr5:116584990-116585003
26	CEBPB	chr5:116531523-116531755	IMR90	lung:	n/a	chr5:116531655-116531666 chr5:116531653-116531664
27	CHD2	chr5:116542751-116543211	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr5:116602020-116602170	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:116654300-116654450	NHEK	skin:	n/a	chr5:116654405-116654418
30	CTCF	chr5:116654340-116654490	RPTEC	kidney:	n/a	chr5:116654405-116654418
31	CTCF	chr5:116654340-116654490	HAc	cerebellar:	n/a	chr5:116654405-116654418
32	CTCF	chr5:116654317-116654469	H1-hESC	embryonic stem cell:	n/a	chr5:116654405-116654418
33	CTCF	chr5:116616220-116616370	GM12869	blood:	n/a	n/a
34	CTCF	chr5:116654300-116654450	HBMEC	blood vessel:	n/a	chr5:116654405-116654418
35	CTCF	chr5:116662840-116662990	BE2_C	brain:	n/a	n/a
36	CTCF	chr5:116654333-116654500	MCF-7	breast:	n/a	chr5:116654405-116654418
37	CTCF	chr5:116654347-116654484	MCF-7	breast:	n/a	chr5:116654405-116654418
38	CTCF	chr5:116662740-116662890	GM12873	blood:	n/a	n/a
39	CTCF	chr5:116662733-116663013	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr5:116654364-116654478	Pancreas_OC	pancreas:	n/a	chr5:116654405-116654418
41	CTCF	chr5:116528979-116529013	Lung_OC	lung:	n/a	n/a
42	CTCF	chr5:116602079-116602241	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:116654300-116654450	SAEC	small airway:	n/a	chr5:116654405-116654418
44	CTCF	chr5:116654366-116654434	LNCaP	prostate:	n/a	chr5:116654405-116654418
45	CTCF	chr5:116654380-116654530	GM12872	blood:	n/a	chr5:116654405-116654418
46	CTCF	chr5:116654290-116654545	MCF-7	breast:	n/a	chr5:116654405-116654418
47	CTCF	chr5:116654326-116654530	MCF-7	breast:	n/a	chr5:116654405-116654418
48	CTCF	chr5:116654300-116654450	BE2_C	brain:	n/a	chr5:116654405-116654418
49	CTCF	chr5:116654340-116654490	HMEC	breast:	n/a	chr5:116654405-116654418
50	CTCF	chr5:116654320-116654470	Caco-2	colon:	n/a	chr5:116654405-116654418

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:116553827-116553877	GM12892	blood:	n/a
2	chr5:116553827-116553877	Jurkat	blood:	n/a
3	chr5:116553827-116553877	K562	blood:	n/a
4	chr5:116553827-116553877	HRCEpiC	kidney:	n/a
5	chr5:116553827-116553877	GM12891	blood:	n/a
6	chr5:116640666-116640716	HCF	heart:	n/a
7	chr5:116553827-116553877	NB4	blood:	n/a
8	chr5:116640666-116640716	PFSK-1	brain:	n/a
9	chr5:116640666-116640716	IMR90	lung:	fetal
10	chr5:116553827-116553877	ECC-1	luminal epithelium:	n/a
11	chr5:116553827-116553877	NHDF-neo	bronchial:	n/a
12	chr5:116553827-116553877	ovcar-3	ovarian:	n/a
13	chr5:116640666-116640716	HRE	kidney:	n/a
14	chr5:116640666-116640716	GM19239	blood:	n/a
15	chr5:116553827-116553877	A549	lung:	n/a
16	chr5:116640666-116640716	SAEC	small airway:	n/a
17	chr5:116640666-116640716	NB4	blood:	n/a
18	chr5:116640666-116640716	GM12891	blood:	n/a
19	chr5:116640666-116640716	Jurkat	blood:	n/a
20	chr5:116553827-116553877	AG09319	gingival:	n/a
21	chr5:116553827-116553877	HRE	kidney:	n/a
22	chr5:116553827-116553877	HCPEpiC	choroid plexus:	n/a
23	chr5:116640666-116640716	HAEpiC	amniotic membrane:	n/a
24	chr5:116553827-116553877	MCF10A-Er-Src	breast:	n/a
25	chr5:116553827-116553877	GM12878	blood:	n/a
26	chr5:116553827-116553877	GM19239	blood:	n/a
27	chr5:116640666-116640716	BE2_C	brain:	n/a
28	chr5:116553827-116553877	U87	brain:	n/a
29	chr5:116553827-116553877	HNPCEpiC	eye:	n/a
30	chr5:116553827-116553877	Hepatocyte	liver:	n/a
31	chr5:116640666-116640716	ProgFib	skin:	n/a
32	chr5:116553827-116553877	SK-N-SH_RA	brain:	n/a
33	chr5:116553827-116553877	HepG2	liver:	n/a
34	chr5:116553827-116553877	HMEC	breast:	n/a
35	chr5:116640666-116640716	HCT-116	colon:	n/a
36	chr5:116553827-116553877	H1-hESC	embryonic stem cell:	embryo
37	chr5:116640666-116640716	GM06990	blood:	n/a
38	chr5:116640666-116640716	HNPCEpiC	eye:	n/a
39	chr5:116640666-116640716	SKMC	muscle:	n/a
40	chr5:116553827-116553877	RPTEC	kidney:	n/a
41	chr5:116640666-116640716	SK-N-SH_RA	brain:	n/a
42	chr5:116553827-116553877	LNCaP	prostate:	n/a
43	chr5:116553827-116553877	AG10803	skin:	n/a
44	chr5:116640666-116640716	LNCaP	prostate:	n/a
45	chr5:116553827-116553877	HEEpiC	esophagus:	n/a
46	chr5:116553827-116553877	T-47D	breast:	n/a
47	chr5:116640666-116640716	K562	blood:	n/a
48	chr5:116553827-116553877	HCT-116	colon:	n/a
49	chr5:116553827-116553877	MCF-7	breast:	n/a
50	chr5:116640666-116640716	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:116648124..116649695-chr5:116650114..116652832,2	MCF-7	breast:
2	chr5:116591259..116593842-chr5:116596466..116598545,2	K562	blood:
3	chr5:116654194..116654786-chr5:116790174..116790911,2	MCF-7	breast:
4	chr5:116649673..116651747-chr5:116653579..116656311,3	MCF-7	breast:
5	chr13:54966032..54966839-chr5:116662215..116662871,2	MCF-7	breast:
6	chr5:116648124..116649695-chr5:116650114..116652832,2	MCF-7	breast:
7	chr5:116640598..116642872-chr5:116653886..116656099,2	MCF-7	breast:
8	chr5:116640598..116642872-chr5:116653886..116656099,2	MCF-7	breast:
9	chr5:116649673..116651747-chr5:116653579..116656311,3	MCF-7	breast:
10	chr5:116412565..116413464-chr5:116601306..116602202,3	MCF-7	breast:
11	chr5:116591259..116593842-chr5:116596466..116598545,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEMA6A-9	chr5:116636800-116637138	NONHSAT103385

Variant related genes	Relation type
RPL35AP15	TF binding region
RPL35AP15	CpG island

Extended variants
information (count: 3349 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:3349 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538397274	chr5:116525971-116525972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551688636	chr5:116525973-116525974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150672309	chr5:116525983-116525984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534052207	chr5:116526009-116526010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77961446	chr5:116526028-116526029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111542361	chr5:116526031-116526032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536690381	chr5:116526076-116526077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142125882	chr5:116526080-116526081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575618494	chr5:116526083-116526084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs146221806	chr5:116526127-116526128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182743470	chr5:116526143-116526144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs115042106	chr5:116526144-116526145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111579761	chr5:116526154-116526155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11283876	chr5:116526168-116526169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376526725	chr5:116526177-116526178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs60582265	chr5:116526182-116526183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs78982475	chr5:116526183-116526184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs201785230	chr5:116526189-116526190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369913563	chr5:116526195-116526196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191380511	chr5:116526201-116526202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528850153	chr5:116526256-116526257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542226349	chr5:116526335-116526336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537344559	chr5:116526360-116526361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139194989	chr5:116526391-116526392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201320587	chr5:116526400-116526401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs144010316	chr5:116526445-116526446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs144871248	chr5:116526460-116526461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376004119	chr5:116526489-116526490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112209108	chr5:116526496-116526497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527911793	chr5:116526526-116526527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111391479	chr5:116526529-116526530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6861258	chr5:116526546-116526547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529141250	chr5:116526583-116526584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567798740	chr5:116526586-116526587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536607698	chr5:116526610-116526611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs556599845	chr5:116526623-116526624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569105227	chr5:116526629-116526630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545288322	chr5:116526630-116526631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199527807	chr5:116526631-116526632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533917215	chr5:116526634-116526635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182389271	chr5:116526640-116526641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558061475	chr5:116526650-116526651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572464825	chr5:116526679-116526680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13189024	chr5:116526710-116526711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375498476	chr5:116526733-116526734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535155706	chr5:116526739-116526740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187394061	chr5:116526750-116526751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540463139	chr5:116526760-116526761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35484030	chr5:116526767-116526768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151199990	chr5:116526831-116526832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116525400-116526000	Enhancers	Brain Angular Gyrus	brain
2	chr5:116525400-116526400	Enhancers	Colon Smooth Muscle	Colon
3	chr5:116525600-116526400	Enhancers	Fetal Stomach	stomach
4	chr5:116526400-116530200	Weak transcription	Fetal Stomach	stomach
5	chr5:116530200-116531000	Enhancers	Fetal Stomach	stomach
6	chr5:116530200-116532000	Enhancers	Fetal Lung	lung
7	chr5:116532000-116536400	Weak transcription	Fetal Lung	lung
8	chr5:116535200-116536800	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:116536000-116538000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:116536200-116536600	Enhancers	Stomach Smooth Muscle	stomach
11	chr5:116536200-116537400	Enhancers	Colon Smooth Muscle	Colon
12	chr5:116536400-116537000	Enhancers	Rectal Smooth Muscle	rectum
13	chr5:116536400-116537400	Enhancers	Fetal Lung	lung
14	chr5:116536600-116537000	Active TSS	Stomach Smooth Muscle	stomach
15	chr5:116536600-116537200	Enhancers	Brain Substantia Nigra	brain
16	chr5:116536600-116538000	Enhancers	Fetal Kidney	kidney
17	chr5:116536800-116537200	Enhancers	Fetal Muscle Leg	muscle
18	chr5:116536800-116537600	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr5:116537200-116540400	Weak transcription	Brain Substantia Nigra	brain
20	chr5:116537200-116540600	Weak transcription	Fetal Muscle Leg	muscle
21	chr5:116537400-116541000	Weak transcription	Fetal Lung	lung
22	chr5:116537600-116538000	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr5:116538000-116538200	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:116538000-116538200	Enhancers	Brain Inferior Temporal Lobe	brain
25	chr5:116538200-116540400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr5:116538200-116543000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr5:116539800-116540600	Enhancers	Brain Angular Gyrus	brain
28	chr5:116540000-116541000	Enhancers	Brain Anterior Caudate	brain
29	chr5:116540000-116541000	Enhancers	Brain Cingulate Gyrus	brain
30	chr5:116540200-116541000	Enhancers	Brain Hippocampus Middle	brain
31	chr5:116540400-116540600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr5:116540400-116541000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr5:116540400-116541400	Enhancers	Brain Substantia Nigra	brain
34	chr5:116540400-116541600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr5:116540600-116541200	Weak transcription	Brain Angular Gyrus	brain
36	chr5:116540600-116541400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr5:116540600-116541600	Enhancers	Fetal Muscle Leg	muscle
38	chr5:116540800-116541400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:116540800-116541800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr5:116540800-116541800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr5:116541000-116541200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr5:116541000-116541400	Active TSS	Brain Hippocampus Middle	brain
43	chr5:116541000-116541400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
44	chr5:116541000-116541400	Enhancers	Fetal Lung	lung
45	chr5:116541000-116541600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:116541000-116541600	Flanking Active TSS	Brain Cingulate Gyrus	brain
47	chr5:116541000-116541600	Enhancers	Fetal Heart	heart
48	chr5:116541000-116541800	Flanking Active TSS	Brain Anterior Caudate	brain
49	chr5:116541000-116542000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr5:116541200-116541400	Enhancers	H1 Cell Line	embryonic stem cell

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