Variant report

Variant	nsv882232
Chromosome Location	chr5:80393949-80436584
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	ARID3A	chr5:80404255-80404596	HepG2	liver:	n/a	n/a
2	ATF1	chr5:80433255-80433447	K562	blood:	n/a	n/a
3	ATF1	chr5:80394276-80394595	K562	blood:	n/a	n/a
4	CEBPB	chr5:80421869-80422165	K562	blood:	n/a	chr5:80421894-80421905
5	CEBPB	chr5:80421813-80421953	HepG2	liver:	n/a	chr5:80421894-80421905
6	CEBPB	chr5:80404338-80404657	HepG2	liver:	n/a	n/a
7	CEBPB	chr5:80429943-80430224	MCF-7	breast:	n/a	chr5:80429975-80429987 chr5:80430058-80430071
8	CEBPB	chr5:80421821-80422106	MCF-7	breast:	n/a	chr5:80421894-80421905
9	CEBPB	chr5:80421850-80422102	HepG2	liver:	n/a	chr5:80421894-80421905
10	CEBPB	chr5:80421727-80422215	HepG2	liver:	n/a	chr5:80421894-80421905
11	CEBPB	chr5:80421912-80422060	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr5:80421818-80422198	Hela-S3	cervix:	n/a	chr5:80421894-80421905
13	CEBPB	chr5:80421742-80422135	A549	lung:	n/a	chr5:80421894-80421905
14	CEBPB	chr5:80421738-80422228	IMR90	lung:	n/a	chr5:80421894-80421905
15	CTCF	chr5:80404300-80404450	BE2_C	brain:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
16	CTCF	chr5:80404340-80404490	WERI-Rb-1	eye:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
17	CTCF	chr5:80404316-80404521	NHEK	skin:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
18	CTCF	chr5:80404300-80404450	HA-sp	spinal cord:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
19	CTCF	chr5:80404337-80404556	A549	lung:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
20	CTCF	chr5:80404360-80404510	GM12867	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
21	CTCF	chr5:80404218-80404623	GM12878	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
22	CTCF	chr5:80404142-80404622	MCF-7	breast:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
23	CTCF	chr5:80404003-80404769	A549	lung:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
24	CTCF	chr5:80404231-80404516	HepG2	liver:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
25	CTCF	chr5:80404340-80404490	GM06990	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
26	CTCF	chr5:80398305-80398420	GM20000	blood:	n/a	n/a
27	CTCF	chr5:80404360-80404510	HMF	breast:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
28	CTCF	chr5:80404268-80404570	H1-hESC	embryonic stem cell:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
29	CTCF	chr5:80404300-80404450	HCT-116	colon:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
30	CTCF	chr5:80404298-80404555	K562	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
31	CTCF	chr5:80404420-80404570	GM12870	blood:	n/a	n/a
32	CTCF	chr5:80404320-80404470	GM12864	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
33	CTCF	chr5:80404460-80404610	A549	lung:	n/a	n/a
34	CTCF	chr5:80404320-80404470	GM12867	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
35	CTCF	chr5:80404279-80404564	MCF-7	breast:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
36	CTCF	chr5:80404294-80404538	HepG2	liver:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
37	CTCF	chr5:80404340-80404490	HRPEpiC	eye:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
38	CTCF	chr5:80404320-80404470	AoAF	blood vessel:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
39	CTCF	chr5:80404314-80404545	K562	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
40	CTCF	chr5:80404340-80404490	AG09309	skin:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
41	CTCF	chr5:80404400-80404550	RPTEC	kidney:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
42	CTCF	chr5:80404360-80404510	HCPEpiC	choroid plexus:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
43	CTCF	chr5:80404262-80404572	GM12878	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
44	CTCF	chr5:80404360-80404510	HUVEC	blood vessel:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
45	CTCF	chr5:80404180-80404603	IMR90	lung:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
46	CTCF	chr5:80404340-80404490	MCF-7	breast:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
47	CTCF	chr5:80404288-80404552	Gliobla	brain:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
48	CTCF	chr5:80404320-80404470	GM12878	blood:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
49	CTCF	chr5:80404320-80404470	HBMEC	blood vessel:	n/a	chr5:80404403-80404421 chr5:80404406-80404416
50	CTCF	chr5:80404320-80404470	Hela-S3	cervix:	n/a	chr5:80404403-80404421 chr5:80404406-80404416

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80394254-80394304	U87	brain:	n/a
2	chr5:80408936-80408986	SK-N-SH_RA	brain:	n/a
3	chr5:80394254-80394304	HAEpiC	amniotic membrane:	n/a
4	chr5:80394254-80394304	GM06990	blood:	n/a
5	chr5:80394254-80394304	PANC-1	pancreas:	n/a
6	chr5:80408936-80408986	HCF	heart:	n/a
7	chr5:80394254-80394304	SK-N-MC	brain:	n/a
8	chr5:80394254-80394304	HRCEpiC	kidney:	n/a
9	chr5:80394254-80394304	HEK293	kidney:	embryo
10	chr5:80408936-80408986	HNPCEpiC	eye:	n/a
11	chr5:80408936-80408986	HRPEpiC	eye:	n/a
12	chr5:80408936-80408986	H1-hESC	embryonic stem cell:	embryo
13	chr5:80394254-80394304	HNPCEpiC	eye:	n/a
14	chr5:80408936-80408986	AG09309	skin:	n/a
15	chr5:80408936-80408986	Hela-S3	cervix:	n/a
16	chr5:80408936-80408986	HAEpiC	amniotic membrane:	n/a
17	chr5:80394254-80394304	SKMC	muscle:	n/a
18	chr5:80394254-80394304	Jurkat	blood:	n/a
19	chr5:80394254-80394304	BE2_C	brain:	n/a
20	chr5:80408936-80408986	HUVEC	blood vessel:	n/a
21	chr5:80408936-80408986	LNCaP	prostate:	n/a
22	chr5:80394254-80394304	ProgFib	skin:	n/a
23	chr5:80394254-80394304	MCF-7	breast:	n/a
24	chr5:80408936-80408986	HPAEpiC	pulmonary alveolar:	n/a
25	chr5:80394254-80394304	A549	lung:	n/a
26	chr5:80408936-80408986	SKMC	muscle:	n/a
27	chr5:80394254-80394304	AG04449	skin:	fetal
28	chr5:80394254-80394304	HMEC	breast:	n/a
29	chr5:80408936-80408986	HRE	kidney:	n/a
30	chr5:80408936-80408986	AoSMC	blood vessel:	n/a
31	chr5:80394254-80394304	SAEC	small airway:	n/a
32	chr5:80408936-80408986	NB4	blood:	n/a
33	chr5:80394254-80394304	AG04450	lung:	fetal
34	chr5:80394254-80394304	CMK	blood:	n/a
35	chr5:80394254-80394304	GM12878	blood:	n/a
36	chr5:80394254-80394304	AG10803	skin:	n/a
37	chr5:80408936-80408986	GM19239	blood:	n/a
38	chr5:80408936-80408986	ECC-1	luminal epithelium:	n/a
39	chr5:80394254-80394304	AoSMC	blood vessel:	n/a
40	chr5:80408936-80408986	PFSK-1	brain:	n/a
41	chr5:80394254-80394304	HUVEC	blood vessel:	n/a
42	chr5:80408936-80408986	GM12878	blood:	n/a
43	chr5:80394254-80394304	RPTEC	kidney:	n/a
44	chr5:80408936-80408986	ProgFib	skin:	n/a
45	chr5:80394254-80394304	NB4	blood:	n/a
46	chr5:80394254-80394304	HRE	kidney:	n/a
47	chr5:80408936-80408986	U87	brain:	n/a
48	chr5:80394254-80394304	HIPEpiC	eye:	n/a
49	chr5:80408936-80408986	SAEC	small airway:	n/a
50	chr5:80408936-80408986	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:80166800..80167382-chr5:80403557..80404427,2	MCF-7	breast:
2	chr5:80403945..80404890-chr5:80490639..80491442,3	MCF-7	breast:
3	chr5:79982530..79983116-chr5:80403919..80404506,2	K562	blood:
4	chr5:80231781..80232515-chr5:80403933..80404736,2	MCF-7	breast:
5	chr5:80403993..80404836-chr5:80461066..80461682,2	MCF-7	breast:
6	chr5:80415691..80417581-chr5:80419844..80422171,2	K562	blood:
7	chr5:80415691..80417581-chr5:80419844..80422171,2	K562	blood:

Variant related genes	Relation type
ENSG00000249772	TF binding region
ENSG00000249772	CpG island

Extended variants
information (count: 1600 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs455461	chr5:80393949-80393950	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182185955	chr5:80393983-80393984	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555349901	chr5:80394137-80394138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563033363	chr5:80394153-80394154	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531953796	chr5:80394174-80394175	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548357123	chr5:80394181-80394182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs115385267	chr5:80394209-80394210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573149776	chr5:80394221-80394222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376495896	chr5:80394223-80394224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186815369	chr5:80394270-80394271	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191603735	chr5:80394275-80394276	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369890749	chr5:80394415-80394416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs375279000	chr5:80394473-80394474	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs248993	chr5:80394515-80394516	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs527651730	chr5:80394588-80394589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556040715	chr5:80394602-80394603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182524077	chr5:80394749-80394750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9293833	chr5:80394855-80394856	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114453652	chr5:80394905-80394906	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73127196	chr5:80394987-80394988	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs367904424	chr5:80395021-80395022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146562705	chr5:80395026-80395027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185639403	chr5:80395031-80395032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs424196	chr5:80395067-80395068	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs139929956	chr5:80395117-80395118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546474599	chr5:80395121-80395122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73766189	chr5:80395131-80395132	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576543143	chr5:80395141-80395142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189660477	chr5:80395160-80395161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182284437	chr5:80395169-80395170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527826947	chr5:80395200-80395201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532351378	chr5:80395226-80395227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140505578	chr5:80395228-80395229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547494911	chr5:80395243-80395244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs372446214	chr5:80395267-80395268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538879837	chr5:80395313-80395314	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187662413	chr5:80395321-80395322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563129629	chr5:80395326-80395327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35431512	chr5:80395330-80395331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs549630697	chr5:80395331-80395332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139184196	chr5:80395402-80395403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569969160	chr5:80395410-80395411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535272358	chr5:80395434-80395435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs73766190	chr5:80395458-80395459	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs114987475	chr5:80395503-80395504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368279987	chr5:80395598-80395599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183910180	chr5:80395601-80395602	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs143361081	chr5:80395618-80395619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201731569	chr5:80395714-80395715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199755685	chr5:80395721-80395722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80343200-80394400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:80375000-80422600	Weak transcription	Left Ventricle	heart
3	chr5:80375200-80401000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:80375800-80400400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr5:80377000-80401000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr5:80382800-80400600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr5:80383200-80409800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:80383200-80413600	Weak transcription	Ovary	ovary
9	chr5:80383400-80400600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr5:80383400-80408400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr5:80383400-80414800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr5:80383400-80421600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr5:80383600-80394200	Weak transcription	Small Intestine	intestine
14	chr5:80383600-80394400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr5:80383600-80400800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr5:80383600-80409000	Weak transcription	Adipose Nuclei	Adipose
17	chr5:80383600-80412600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr5:80383800-80394400	Weak transcription	Brain Hippocampus Middle	brain
19	chr5:80383800-80400600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr5:80384200-80400600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr5:80387400-80394200	Weak transcription	Pancreas	Pancrea
22	chr5:80387800-80395400	Strong transcription	Primary T cells fromperipheralblood	blood
23	chr5:80388400-80394400	Strong transcription	Primary T cells from cord blood	blood
24	chr5:80388400-80394600	Strong transcription	HepG2	liver
25	chr5:80388600-80397000	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr5:80389000-80400600	Weak transcription	Brain Substantia Nigra	brain
27	chr5:80390200-80400400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr5:80390200-80400800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:80390600-80409200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr5:80392400-80394200	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr5:80392400-80394600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr5:80392400-80394600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr5:80392600-80408200	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr5:80393400-80394200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr5:80393600-80394400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:80393600-80395200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr5:80393800-80394000	Enhancers	NHLF	lung
38	chr5:80394000-80417000	Weak transcription	NHLF	lung
39	chr5:80394200-80397200	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr5:80394200-80408200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:80394400-80394600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr5:80394400-80394600	Enhancers	Brain Hippocampus Middle	brain
43	chr5:80394400-80394600	Enhancers	Lung	lung
44	chr5:80394400-80395400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr5:80394400-80400600	Weak transcription	Primary T cells from cord blood	blood
46	chr5:80394600-80400600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr5:80394600-80408400	Weak transcription	HepG2	liver
48	chr5:80394800-80395000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr5:80395200-80400600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr5:80395400-80396400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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