Variant report

Variant	nsv882679
Chromosome Location	chr5:106263197-106399718
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	ATF2	chr5:106314497-106314745	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:106320004-106320377	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:106298185-106298529	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr5:106364723-106364998	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:106364704-106364911	GM12878	blood:	n/a	n/a
6	BRCA1	chr5:106393872-106394255	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:106355939-106356101	A549	lung:	n/a	chr5:106356040-106356051
8	CEBPB	chr5:106280169-106280451	IMR90	lung:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
9	CEBPB	chr5:106309912-106310179	IMR90	lung:	n/a	chr5:106310029-106310040 chr5:106310031-106310040 chr5:106310031-106310040 chr5:106310031-106310040 chr5:106310031-106310042 chr5:106310031-106310040
10	CEBPB	chr5:106393863-106394272	Hela-S3	cervix:	n/a	chr5:106394042-106394053 chr5:106394042-106394053
11	CEBPB	chr5:106371345-106371404	H1-hESC	embryonic stem cell:	n/a	chr5:106371373-106371390 chr5:106371376-106371387
12	CEBPB	chr5:106263043-106263302	A549	lung:	n/a	chr5:106263175-106263186
13	CEBPB	chr5:106388001-106388201	A549	lung:	n/a	n/a
14	CEBPB	chr5:106348535-106348815	A549	lung:	n/a	n/a
15	CEBPB	chr5:106348574-106348718	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:106393883-106394226	A549	lung:	n/a	chr5:106394042-106394053 chr5:106394042-106394053
17	CEBPB	chr5:106280198-106280466	A549	lung:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
18	CEBPB	chr5:106348540-106348816	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:106348625-106348770	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:106280150-106280371	K562	blood:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
21	CEBPB	chr5:106355896-106356117	IMR90	lung:	n/a	chr5:106356040-106356051
22	CEBPB	chr5:106309914-106310183	HepG2	liver:	n/a	chr5:106310029-106310040 chr5:106310031-106310040 chr5:106310031-106310040 chr5:106310031-106310040 chr5:106310031-106310042 chr5:106310031-106310040
23	CEBPB	chr5:106280201-106280432	HepG2	liver:	n/a	chr5:106280318-106280329 chr5:106280317-106280330
24	CEBPB	chr5:106263028-106263328	HepG2	liver:	n/a	chr5:106263175-106263186
25	CEBPB	chr5:106263049-106263272	H1-hESC	embryonic stem cell:	n/a	chr5:106263175-106263186
26	CEBPB	chr5:106297159-106297333	HepG2	liver:	n/a	chr5:106297280-106297291
27	CEBPB	chr5:106371237-106371419	HepG2	liver:	n/a	chr5:106371246-106371257 chr5:106371373-106371390 chr5:106371376-106371387
28	CEBPB	chr5:106355968-106356172	HepG2	liver:	n/a	chr5:106356040-106356051
29	CEBPB	chr5:106390801-106391001	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:106278689-106278999	HepG2	liver:	n/a	chr5:106278860-106278869 chr5:106278860-106278871
31	CEBPB	chr5:106263019-106263332	IMR90	lung:	n/a	chr5:106263175-106263186
32	CHD1	chr5:106319972-106320916	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr5:106363756-106363786	GM12878	blood:	n/a	n/a
34	CHD1	chr5:106315310-106316217	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr5:106319848-106320228	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr5:106293059-106293510	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr5:106292040-106292190	HCT-116	colon:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
38	CTCF	chr5:106337000-106337150	GM12878	blood:	n/a	n/a
39	CTCF	chr5:106348844-106348878	GM20000	blood:	n/a	n/a
40	CTCF	chr5:106340180-106340330	GM12864	blood:	n/a	n/a
41	CTCF	chr5:106291960-106292110	HRPEpiC	eye:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
42	CTCF	chr5:106291980-106292130	HEK293	kidney:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
43	CTCF	chr5:106303120-106303270	HCPEpiC	choroid plexus:	n/a	chr5:106303142-106303163 chr5:106303147-106303165
44	CTCF	chr5:106291940-106292090	BE2_C	brain:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
45	CTCF	chr5:106292067-106292125	A549	lung:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
46	CTCF	chr5:106292020-106292170	HRE	kidney:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
47	CTCF	chr5:106291980-106292130	HA-sp	spinal cord:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
48	CTCF	chr5:106291980-106292130	WERI-Rb-1	eye:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088
49	CTCF	chr5:106264858-106264940	GM13976	blood:	n/a	n/a
50	CTCF	chr5:106292000-106292150	Hela-S3	cervix:	n/a	chr5:106292072-106292090 chr5:106292073-106292089 chr5:106292067-106292088

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:106311004-106311054	GM12892	blood:	n/a
2	chr5:106311004-106311054	HCF	heart:	n/a
3	chr5:106311004-106311054	HCM	heart:	n/a
4	chr5:106269670-106269720	NHBE	bronchial:	n/a
5	chr5:106311004-106311054	HMEC	breast:	n/a
6	chr5:106311004-106311054	Jurkat	blood:	n/a
7	chr5:106269670-106269720	GM12878	blood:	n/a
8	chr5:106269670-106269720	LNCaP	prostate:	n/a
9	chr5:106269670-106269720	GM06990	blood:	n/a
10	chr5:106312235-106312285	Hepatocyte	liver:	n/a
11	chr5:106312235-106312285	HCF	heart:	n/a
12	chr5:106269670-106269720	HAEpiC	amniotic membrane:	n/a
13	chr5:106312235-106312285	HEK293	kidney:	embryo
14	chr5:106312235-106312285	NB4	blood:	n/a
15	chr5:106269670-106269720	H1-hESC	embryonic stem cell:	embryo
16	chr5:106269670-106269720	HL-60	blood:	n/a
17	chr5:106311004-106311054	PANC-1	pancreas:	n/a
18	chr5:106312235-106312285	T-47D	breast:	n/a
19	chr5:106312235-106312285	ECC-1	luminal epithelium:	n/a
20	chr5:106312235-106312285	HL-60	blood:	n/a
21	chr5:106312235-106312285	GM12892	blood:	n/a
22	chr5:106269670-106269720	HRPEpiC	eye:	n/a
23	chr5:106269670-106269720	PFSK-1	brain:	n/a
24	chr5:106312235-106312285	GM12891	blood:	n/a
25	chr5:106311004-106311054	RPTEC	kidney:	n/a
26	chr5:106312235-106312285	AoSMC	blood vessel:	n/a
27	chr5:106269670-106269720	HMEC	breast:	n/a
28	chr5:106311004-106311054	HRE	kidney:	n/a
29	chr5:106312235-106312285	HMEC	breast:	n/a
30	chr5:106311004-106311054	GM06990	blood:	n/a
31	chr5:106311004-106311054	HIPEpiC	eye:	n/a
32	chr5:106312235-106312285	Caco-2	colon:	n/a
33	chr5:106269670-106269720	NB4	blood:	n/a
34	chr5:106269670-106269720	SK-N-SH_RA	brain:	n/a
35	chr5:106312235-106312285	HNPCEpiC	eye:	n/a
36	chr5:106269670-106269720	Hela-S3	cervix:	n/a
37	chr5:106312235-106312285	GM06990	blood:	n/a
38	chr5:106311004-106311054	T-47D	breast:	n/a
39	chr5:106269670-106269720	MCF-7	breast:	n/a
40	chr5:106311004-106311054	HEEpiC	esophagus:	n/a
41	chr5:106269670-106269720	BE2_C	brain:	n/a
42	chr5:106312235-106312285	ovcar-3	ovarian:	n/a
43	chr5:106311004-106311054	BJ	skin:	n/a
44	chr5:106312235-106312285	PFSK-1	brain:	n/a
45	chr5:106311004-106311054	AoSMC	blood vessel:	n/a
46	chr5:106269670-106269720	SAEC	small airway:	n/a
47	chr5:106311004-106311054	ProgFib	skin:	n/a
48	chr5:106311004-106311054	MCF10A-Er-Src	breast:	n/a
49	chr5:106311004-106311054	HepG2	liver:	n/a
50	chr5:106269670-106269720	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:105577057..105577825-chr5:106276409..106277049,3	MCF-7	breast:
2	chr5:106378357..106381255-chr5:106381782..106384639,2	K562	blood:
3	chr5:106353118..106354798-chr5:106355082..106357442,2	K562	blood:
4	chr5:106335059..106337350-chr5:106341839..106343537,2	MCF-7	breast:
5	chr5:106335059..106337350-chr5:106341839..106343537,2	MCF-7	breast:
6	chr5:106354055..106355877-chr5:106363964..106366429,2	MCF-7	breast:
7	chr5:106341177..106343472-chr5:106344792..106347005,2	K562	blood:
8	chr5:106354055..106355877-chr5:106363964..106366429,2	MCF-7	breast:
9	chr5:106378357..106381255-chr5:106381782..106384639,2	K562	blood:
10	chr5:106338383..106341187-chr5:106343308..106346258,2	MCF-7	breast:
11	chr5:105577109..105578026-chr5:106276409..106277185,3	MCF-7	breast:
12	chr5:106338383..106341187-chr5:106343308..106346258,2	MCF-7	breast:
13	chr5:106353118..106354798-chr5:106355082..106357442,2	K562	blood:
14	chr5:106389025..106391862-chr5:106427124..106429120,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFNA5-2	chr5:106316465-106316570	XLOC_004951
2	lnc-EFNA5-7	chr5:106374540-106374642	l_2991_chr5:106178796-106374642_testes
3	lnc-EFNA5-5	chr5:106318910-106319012	NONHSAT103110
4	lnc-EFNA5-6	chr5:106318191-106318244	NONHSAT103109
5	lnc-EFNA5-2	chr5:106305585-106305652	XLOC_004951
6	lnc-EFNA5-5	chr5:106319129-106319282	NONHSAT103110
7	lnc-FER-15	chr5:106300101-106300653	NONHSAT103107
8	lnc-EFNA5-6	chr5:106320260-106321329	NONHSAT103109

Variant related genes	Relation type
ENSG00000251027	TF binding region
ENSG00000251027	CpG island
ENSG00000251027	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 4096 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4096 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115562112	chr5:106264828-106264829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549695932	chr5:106264853-106264854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35946199	chr5:106264902-106264903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149991044	chr5:106264903-106264904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556106545	chr5:106264927-106264928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572627547	chr5:106264932-106264933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535229301	chr5:106264951-106264952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11950719	chr5:106264964-106264965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11950720	chr5:106264965-106264966	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562761626	chr5:106264975-106264976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141121719	chr5:106264995-106264996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs67607822	chr5:106264996-106264997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs36110581	chr5:106264998-106264999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376698330	chr5:106264999-106265000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192125302	chr5:106267096-106267097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140075772	chr5:106267142-106267143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs201206474	chr5:106267202-106267203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566086362	chr5:106267203-106267204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536228735	chr5:106267250-106267251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538627408	chr5:106267251-106267252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558312316	chr5:106267316-106267317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376309083	chr5:106267324-106267325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs200521190	chr5:106267336-106267337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575479709	chr5:106267359-106267360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544209087	chr5:106267360-106267361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76964947	chr5:106267363-106267364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560702417	chr5:106268808-106268809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532607104	chr5:106268820-106268821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141835718	chr5:106268883-106268884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527879841	chr5:106268887-106268888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs186781542	chr5:106268895-106268896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531475501	chr5:106268941-106268942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548192912	chr5:106268992-106268993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374631514	chr5:106269022-106269023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542182620	chr5:106269122-106269123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568088704	chr5:106269138-106269139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527554059	chr5:106269146-106269147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150627445	chr5:106269160-106269161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570584187	chr5:106269249-106269250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539255680	chr5:106269263-106269264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140719337	chr5:106269284-106269285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145276790	chr5:106269394-106269395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537979361	chr5:106269416-106269417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs575297279	chr5:106269454-106269455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368096384	chr5:106269469-106269470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574509021	chr5:106269504-106269505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73204147	chr5:106269544-106269545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112650735	chr5:106269558-106269559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191204592	chr5:106269559-106269560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs57502629	chr5:106269573-106269574	Enhancers	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106264800-106265000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:106267000-106267400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:106268800-106269800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:106268800-106269800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:106268800-106269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr5:106269000-106269800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:106269200-106269600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:106269600-106269800	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:106269800-106270800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:106269800-106271000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr5:106270800-106271000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr5:106270800-106271200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr5:106273600-106276000	Weak transcription	Stomach Mucosa	stomach
14	chr5:106276000-106276400	Enhancers	A549	lung
15	chr5:106276000-106277600	Enhancers	Stomach Mucosa	stomach
16	chr5:106276000-106278000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr5:106276200-106277400	Enhancers	Fetal Intestine Small	intestine
18	chr5:106276200-106277600	Enhancers	Gastric	stomach
19	chr5:106276200-106277800	Enhancers	HUVEC	blood vessel
20	chr5:106276400-106277200	Flanking Active TSS	A549	lung
21	chr5:106276800-106277400	Enhancers	Pancreas	Pancrea
22	chr5:106277000-106277600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:106277200-106277800	Enhancers	A549	lung
24	chr5:106287600-106288000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
25	chr5:106288400-106302000	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr5:106289200-106292800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr5:106291600-106292200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr5:106292000-106292200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:106292200-106292400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:106292200-106295200	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:106292400-106302000	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr5:106294800-106295000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr5:106294800-106295800	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr5:106295000-106295200	Enhancers	Psoas Muscle	Psoas
35	chr5:106295000-106295800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:106295000-106295800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:106295000-106295800	Enhancers	Stomach Mucosa	stomach
38	chr5:106295000-106295800	Enhancers	Hela-S3	cervix
39	chr5:106295000-106296600	Enhancers	HUVEC	blood vessel
40	chr5:106295200-106295600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:106295200-106295800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:106295200-106295800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr5:106295600-106298400	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr5:106295800-106298600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr5:106295800-106299200	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr5:106295800-106302200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr5:106295800-106309400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr5:106296600-106299800	Weak transcription	HUVEC	blood vessel
49	chr5:106298200-106300800	Enhancers	A549	lung
50	chr5:106298400-106298600	Enhancers	Skeletal Muscle Female	skeletal muscle

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