Variant report

Variant	nsv1017901
Chromosome Location	chr5:105847628-106298378
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1640)
CpG islands
(count:61)
Chromatin interactive
region (count:27)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1640 , 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	chr5:106185067-106185290	HepG2	liver:	n/a	n/a
2	ATF1	chr5:105859633-105859780	K562	blood:	n/a	n/a
3	ATF2	chr5:105937147-105937733	GM12878	blood:	n/a	n/a
4	BACH1	chr5:106298185-106298529	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr5:106198610-106198771	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr5:106133692-106133983	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr5:106217759-106218099	H1-hESC	embryonic stem cell:	n/a	chr5:106217913-106217927
8	BATF	chr5:105952746-105952947	GM12878	blood:	n/a	n/a
9	BATF	chr5:105952737-105952935	GM12878	blood:	n/a	n/a
10	BATF	chr5:105889044-105889346	GM12878	blood:	n/a	n/a
11	BATF	chr5:106016002-106016273	GM12878	blood:	n/a	n/a
12	BATF	chr5:105889076-105889285	GM12878	blood:	n/a	n/a
13	BATF	chr5:105871246-105871400	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:106133704-106134047	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr5:105889001-105889386	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:105871234-105871399	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:106015965-106016276	GM12878	blood:	n/a	chr5:106016208-106016217
18	BHLHE40	chr5:105887552-105887806	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:106209310-106209646	HepG2	liver:	n/a	n/a
20	BHLHE40	chr5:106212434-106212567	K562	blood:	n/a	n/a
21	BHLHE40	chr5:105889035-105889258	HepG2	liver:	n/a	n/a
22	BHLHE40	chr5:105937145-105937565	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:106212411-106212637	HepG2	liver:	n/a	n/a
24	BHLHE40	chr5:105938056-105938340	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:106035012-106035163	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:105871319-105871346	GM12878	blood:	n/a	n/a
27	CBX3	chr5:106212458-106212675	K562	blood:	n/a	n/a
28	CEBPB	chr5:106297159-106297333	HepG2	liver:	n/a	chr5:106297280-106297291
29	CEBPB	chr5:105937304-105937803	MCF-7	breast:	n/a	n/a
30	CEBPB	chr5:106092296-106092480	HepG2	liver:	n/a	chr5:106092396-106092407
31	CEBPB	chr5:105902109-105902237	A549	lung:	n/a	n/a
32	CEBPB	chr5:106263028-106263328	HepG2	liver:	n/a	chr5:106263175-106263186
33	CEBPB	chr5:106216448-106216737	H1-hESC	embryonic stem cell:	n/a	chr5:106216591-106216602
34	CEBPB	chr5:106263043-106263302	A549	lung:	n/a	chr5:106263175-106263186
35	CEBPB	chr5:105891868-105892016	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr5:106072244-106072341	H1-hESC	embryonic stem cell:	n/a	chr5:106072263-106072274
37	CEBPB	chr5:106216397-106216708	ECC-1	luminal epithelium:	n/a	chr5:106216591-106216602
38	CEBPB	chr5:106064429-106064545	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr5:106280198-106280466	A549	lung:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
40	CEBPB	chr5:105893053-105893322	HepG2	liver:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
41	CEBPB	chr5:106216419-106216706	A549	lung:	n/a	chr5:106216591-106216602
42	CEBPB	chr5:106280169-106280451	IMR90	lung:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
43	CEBPB	chr5:106072855-106073076	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr5:105859114-105859462	IMR90	lung:	n/a	chr5:105859114-105859125 chr5:105859284-105859295
45	CEBPB	chr5:106216454-106216807	MCF-7	breast:	n/a	chr5:106216591-106216602
46	CEBPB	chr5:106212411-106212611	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr5:105893027-105893313	A549	lung:	n/a	chr5:105893187-105893198 chr5:105893189-105893200 chr5:105893187-105893200
48	CEBPB	chr5:106104189-106104416	H1-hESC	embryonic stem cell:	n/a	chr5:106104282-106104293 chr5:106104283-106104294 chr5:106104284-106104293 chr5:106104282-106104295 chr5:106104282-106104295
49	CEBPB	chr5:106216294-106216749	HCT-116	colon:	n/a	chr5:106216388-106216400 chr5:106216591-106216602
50	CEBPB	chr5:106212456-106212683	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:106269670-106269720	MCF-7	breast:	n/a
2	chr5:106269670-106269720	SK-N-MC	brain:	n/a
3	chr5:106269670-106269720	HEK293	kidney:	embryo
4	chr5:106269670-106269720	Hepatocyte	liver:	n/a
5	chr5:106269670-106269720	PANC-1	pancreas:	n/a
6	chr5:106269670-106269720	ECC-1	luminal epithelium:	n/a
7	chr5:106269670-106269720	ovcar-3	ovarian:	n/a
8	chr5:106269670-106269720	HAEpiC	amniotic membrane:	n/a
9	chr5:106269670-106269720	NHDF-neo	bronchial:	n/a
10	chr5:106269670-106269720	CMK	blood:	n/a
11	chr5:106269670-106269720	PFSK-1	brain:	n/a
12	chr5:106269670-106269720	BJ	skin:	n/a
13	chr5:106269670-106269720	HMEC	breast:	n/a
14	chr5:106269670-106269720	HCPEpiC	choroid plexus:	n/a
15	chr5:106269670-106269720	AG04449	skin:	fetal
16	chr5:106269670-106269720	SAEC	small airway:	n/a
17	chr5:106269670-106269720	HepG2	liver:	n/a
18	chr5:106269670-106269720	BE2_C	brain:	n/a
19	chr5:106269670-106269720	ProgFib	skin:	n/a
20	chr5:106269670-106269720	SK-N-SH_RA	brain:	n/a
21	chr5:106269670-106269720	Jurkat	blood:	n/a
22	chr5:106269670-106269720	LNCaP	prostate:	n/a
23	chr5:106269670-106269720	RPTEC	kidney:	n/a
24	chr5:106269670-106269720	PrEC	prostate:	n/a
25	chr5:106269670-106269720	U87	brain:	n/a
26	chr5:106269670-106269720	IMR90	lung:	fetal
27	chr5:106269670-106269720	AG09309	skin:	n/a
28	chr5:106269670-106269720	GM12892	blood:	n/a
29	chr5:106269670-106269720	GM12878	blood:	n/a
30	chr5:106269670-106269720	SKMC	muscle:	n/a
31	chr5:106269670-106269720	HCM	heart:	n/a
32	chr5:106269670-106269720	NH-A	brain:	n/a
33	chr5:106269670-106269720	A549	lung:	n/a
34	chr5:106269670-106269720	H1-hESC	embryonic stem cell:	embryo
35	chr5:106269670-106269720	NHBE	bronchial:	n/a
36	chr5:106269670-106269720	NT2-D1	testis:	n/a
37	chr5:106269670-106269720	AoSMC	blood vessel:	n/a
38	chr5:106269670-106269720	GM06990	blood:	n/a
39	chr5:106269670-106269720	MCF10A-Er-Src	breast:	n/a
40	chr5:106269670-106269720	HUVEC	blood vessel:	n/a
41	chr5:106269670-106269720	AG04450	lung:	fetal
42	chr5:106269670-106269720	HRPEpiC	eye:	n/a
43	chr5:106269670-106269720	HPAEpiC	pulmonary alveolar:	n/a
44	chr5:106269670-106269720	AG09319	gingival:	n/a
45	chr5:106269670-106269720	HL-60	blood:	n/a
46	chr5:106269670-106269720	AG10803	skin:	n/a
47	chr5:106269670-106269720	K562	blood:	n/a
48	chr5:106269670-106269720	SK-N-SH	brain:	n/a
49	chr5:106269670-106269720	HEEpiC	esophagus:	n/a
50	chr5:106269670-106269720	HNPCEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:106113493..106115491-chr5:106132534..106134120,2	MCF-7	breast:
2	chr5:106210052..106213021-chr5:107006073..107010056,3	MCF-7	breast:
3	chr5:106220156..106222310-chr5:106223090..106225336,2	K562	blood:
4	chr5:52211080..52211594-chr5:105856085..105856865,2	MCF-7	breast:
5	chr5:105938151..105940256-chr5:105942344..105944925,2	MCF-7	breast:
6	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
7	chr5:105971307..105972912-chr5:105974720..105977019,2	MCF-7	breast:
8	chr5:105577109..105578026-chr5:106276409..106277185,3	MCF-7	breast:
9	chr5:106131520..106133910-chr5:106135475..106137782,2	MCF-7	breast:
10	chr5:106185229..106189035-chr5:106199699..106201875,3	MCF-7	breast:
11	chr5:106091111..106094042-chr5:106098260..106100095,2	K562	blood:
12	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:
13	chr5:105938151..105940256-chr5:105942344..105944925,2	MCF-7	breast:
14	chr5:105577057..105577825-chr5:106276409..106277049,3	MCF-7	breast:
15	chr5:106113493..106115491-chr5:106132534..106134120,2	MCF-7	breast:
16	chr5:105907774..105910252-chr5:105911884..105914582,2	K562	blood:
17	chr5:105907051..105910252-chr5:105911452..105914582,3	K562	blood:
18	chr5:106131520..106133910-chr5:106135475..106137782,2	MCF-7	breast:
19	chr5:106091111..106094042-chr5:106098260..106100095,2	K562	blood:
20	chr5:106186315..106188102-chr5:107007477..107009162,2	MCF-7	breast:
21	chr5:106185229..106189035-chr5:106199699..106201875,3	MCF-7	breast:
22	chr5:105577079..105577587-chr5:106153989..106154803,2	MCF-7	breast:
23	chr5:105982713..105983578-chr7:143652953..143653920,2	MCF-7	breast:
24	chr5:105971307..105972912-chr5:105974720..105977019,2	MCF-7	breast:
25	chr5:105577079..105577846-chr5:106153949..106154767,2	MCF-7	breast:
26	chr5:106220156..106222310-chr5:106223090..106225336,2	K562	blood:
27	chr17:56709318..56712109-chr5:106181952..106184880,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFNA5-7	chr5:106181999-106182077	l_2991_chr5:106178796-106374642_testes
2	lnc-EFNA5-2	chr5:106154100-106154178	XLOC_004951
3	lnc-EFNA5-2	chr5:106150903-106151247	XLOC_004951
4	lnc-EFNA5-2	chr5:106150906-106151247	XLOC_004951
5	lnc-EFNA5-7	chr5:106178797-106179146	l_2991_chr5:106178796-106374642_testes
6	lnc-EFNA5-2	chr5:106179762-106179915	XLOC_004951

No data

Variant related genes	Relation type
ENSG00000250145	TF binding region
ENSG00000252337	TF binding region
ENSG00000250145	CpG island
ENSG00000252337	CpG island
ENSG00000184349	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 6366 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6366 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373370232	chr5:105847648-105847649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs542105974	chr5:105847656-105847657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138470788	chr5:105847688-105847689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528249118	chr5:105847690-105847691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555931506	chr5:105847721-105847722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs112384007	chr5:105847741-105847742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553389190	chr5:105847761-105847762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541768052	chr5:105847781-105847782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564047955	chr5:105847801-105847802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12657564	chr5:105847867-105847868	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs148627018	chr5:105847877-105847878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs142115220	chr5:105847936-105847937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189025211	chr5:105847946-105847947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201189925	chr5:105847948-105847949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181024477	chr5:105847963-105847964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565557705	chr5:105847967-105847968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570904709	chr5:105848011-105848012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186255800	chr5:105848018-105848019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146656218	chr5:105848031-105848032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570498777	chr5:105848033-105848034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35402012	chr5:105848061-105848062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547073473	chr5:105848065-105848066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539491051	chr5:105848067-105848068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs115993481	chr5:105848118-105848119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570007055	chr5:105848165-105848166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377629390	chr5:105848216-105848217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140241599	chr5:105848271-105848272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555652401	chr5:105848274-105848275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191623084	chr5:105848288-105848289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182863310	chr5:105848378-105848379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145881321	chr5:105848393-105848394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs67878037	chr5:105848396-105848397	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs185718358	chr5:105848408-105848409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563302379	chr5:105848441-105848442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573618279	chr5:105848477-105848478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542732073	chr5:105848497-105848498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559102933	chr5:105848501-105848502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533169560	chr5:105855010-105855011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573401327	chr5:105855019-105855020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113055746	chr5:105855021-105855022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368477587	chr5:105855027-105855028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs112428659	chr5:105855061-105855062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527824524	chr5:105855116-105855117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148659519	chr5:105855134-105855135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368795999	chr5:105855184-105855185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183921661	chr5:105855188-105855189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs188660809	chr5:105855229-105855230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570118189	chr5:105855242-105855243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529420734	chr5:105855255-105855256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs117390680	chr5:105855256-105855257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
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
Retinoblastoma	22278416	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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:105846200-105847800	Weak transcription	Fetal Heart	heart
2	chr5:105847800-105848600	Enhancers	Fetal Heart	heart
3	chr5:105855000-105855200	Enhancers	A549	lung
4	chr5:105855200-105855800	Weak transcription	A549	lung
5	chr5:105855800-105857200	Enhancers	A549	lung
6	chr5:105857000-105858800	Enhancers	HUVEC	blood vessel
7	chr5:105857200-105857600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:105857200-105857800	Enhancers	Brain Hippocampus Middle	brain
9	chr5:105857200-105858000	Flanking Active TSS	A549	lung
10	chr5:105857200-105858600	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr5:105857200-105859800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr5:105857600-105858200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:105857600-105858400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:105857600-105858400	Enhancers	Brain Cingulate Gyrus	brain
15	chr5:105857800-105858200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:105857800-105858200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr5:105857800-105858200	Enhancers	NH-A	brain
18	chr5:105858000-105858400	Active TSS	A549	lung
19	chr5:105858400-105859200	Weak transcription	A549	lung
20	chr5:105858800-105859200	Weak transcription	HUVEC	blood vessel
21	chr5:105859200-105860000	Enhancers	HUVEC	blood vessel
22	chr5:105859200-105860200	Enhancers	A549	lung
23	chr5:105859600-105859800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr5:105860200-105860400	Weak transcription	A549	lung
25	chr5:105860400-105861800	ZNF genes & repeats	A549	lung
26	chr5:105862200-105862600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr5:105870800-105871200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr5:105871000-105871600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:105871200-105871600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr5:105871200-105871600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr5:105871200-105871600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
32	chr5:105871200-105871600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr5:105871200-105871600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
34	chr5:105871200-105871600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr5:105871200-105871600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:105871200-105871600	ZNF genes & repeats	Esophagus	oesophagus
37	chr5:105871200-105871600	ZNF genes & repeats	Fetal Kidney	kidney
38	chr5:105871200-105871600	ZNF genes & repeats	Pancreas	Pancrea
39	chr5:105871400-105871600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
40	chr5:105871400-105871600	ZNF genes & repeats	Brain Anterior Caudate	brain
41	chr5:105871400-105871600	Flanking Bivalent TSS/Enh	Gastric	stomach
42	chr5:105871600-105877000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:105877000-105877200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr5:105879200-105880600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr5:105910800-105911000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr5:105916000-105916600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr5:105916200-105916600	Enhancers	Brain Germinal Matrix	brain
48	chr5:105916200-105916600	Enhancers	Fetal Brain Female	brain
49	chr5:105916400-105919800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:105916600-105919800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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