Variant report

Variant	esv3344393
Chromosome Location	chr5:114937053-114938901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:462)
CpG islands
(count:671)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:114937281-114937791	GM12878	blood:	n/a	n/a
2	ATF2	chr5:114937958-114938507	GM12878	blood:	n/a	n/a
3	ATF2	chr5:114937257-114937744	GM12878	blood:	n/a	n/a
4	ATF3	chr5:114938066-114938296	K562	blood:	n/a	n/a
5	BACH1	chr5:114938065-114938286	K562	blood:	n/a	n/a
6	BACH1	chr5:114937814-114938326	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr5:114938019-114938314	GM12878	blood:	n/a	n/a
8	BATF	chr5:114937295-114937797	GM12878	blood:	n/a	n/a
9	BATF	chr5:114937319-114937692	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:114937323-114937709	GM12878	blood:	n/a	chr5:114937585-114937594
11	BCL3	chr5:114937298-114938465	GM12878	blood:	n/a	chr5:114937585-114937594
12	BCLAF1	chr5:114937314-114938529	GM12878	blood:	n/a	chr5:114937585-114937594
13	BCLAF1	chr5:114937272-114937742	GM12878	blood:	n/a	chr5:114937585-114937594
14	BCLAF1	chr5:114937744-114938571	GM12878	blood:	n/a	n/a
15	BHLHE40	chr5:114938084-114938417	K562	blood:	n/a	n/a
16	BHLHE40	chr5:114937335-114938650	GM12878	blood:	n/a	n/a
17	CBX3	chr5:114937959-114938379	K562	blood:	n/a	n/a
18	CCNT2	chr5:114937353-114938280	K562	blood:	n/a	n/a
19	CEBPB	chr5:114937260-114937728	GM12878	blood:	n/a	n/a
20	CHD1	chr5:114937799-114938757	GM12878	blood:	n/a	n/a
21	CHD2	chr5:114938191-114938289	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr5:114938211-114938284	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr5:114937826-114938247	K562	blood:	n/a	n/a
24	CHD2	chr5:114937393-114938625	GM12878	blood:	n/a	chr5:114937623-114937633
25	CHD2	chr5:114938650-114938834	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr5:114937844-114938220	A549	lung:	n/a	n/a
27	CTCF	chr5:114938142-114938147	GM13977	blood:	n/a	n/a
28	CTCF	chr5:114937620-114937770	GM12864	blood:	n/a	n/a
29	CTCF	chr5:114937610-114937671	GM12878	blood:	n/a	n/a
30	CTCF	chr5:114937700-114937850	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr5:114937700-114937850	GM12869	blood:	n/a	n/a
32	CTCF	chr5:114938075-114938184	GM19239	blood:	n/a	n/a
33	CTCF	chr5:114938000-114938150	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr5:114937585-114937900	GM12891	blood:	n/a	n/a
35	CTCF	chr5:114937720-114937870	GM12868	blood:	n/a	n/a
36	CTCF	chr5:114937780-114937930	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr5:114938000-114938250	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr5:114937720-114937870	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr5:114937720-114937870	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr5:114937740-114937890	AG09309	skin:	n/a	n/a
41	CTCF	chr5:114937761-114937856	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr5:114937540-114937690	AG09319	gingival:	n/a	n/a
43	CTCF	chr5:114938120-114938270	GM12878	blood:	n/a	n/a
44	CTCF	chr5:114937760-114937910	AG09309	skin:	n/a	n/a
45	CTCF	chr5:114937740-114937890	Caco-2	colon:	n/a	n/a
46	CTCF	chr5:114937740-114937890	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr5:114937700-114937850	GM12873	blood:	n/a	n/a
48	CTCF	chr5:114937760-114937910	AG04449	skin:	n/a	n/a
49	CTCF	chr5:114938080-114938230	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr5:114937700-114937850	NHDF-neo	bronchial:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114937784-114937834	AG09309	skin:	n/a
2	chr5:114937784-114937834	HEK293	kidney:	embryo
3	chr5:114938002-114938052	GM12892	blood:	n/a
4	chr5:114937614-114937664	A549	lung:	n/a
5	chr5:114937919-114937969	PrEC	prostate:	n/a
6	chr5:114938002-114938052	ProgFib	skin:	n/a
7	chr5:114938236-114938286	GM19239	blood:	n/a
8	chr5:114938439-114938489	MCF10A-Er-Src	breast:	n/a
9	chr5:114937614-114937664	AG04450	lung:	fetal
10	chr5:114938439-114938489	MCF-7	breast:	n/a
11	chr5:114937535-114937585	CMK	blood:	n/a
12	chr5:114937614-114937664	Hela-S3	cervix:	n/a
13	chr5:114937919-114937969	BE2_C	brain:	n/a
14	chr5:114937614-114937664	NB4	blood:	n/a
15	chr5:114938002-114938052	AG09309	skin:	n/a
16	chr5:114937614-114937664	IMR90	lung:	fetal
17	chr5:114938148-114938198	AG10803	skin:	n/a
18	chr5:114937784-114937834	AG09319	gingival:	n/a
19	chr5:114937535-114937585	HepG2	liver:	n/a
20	chr5:114938389-114938439	BE2_C	brain:	n/a
21	chr5:114938439-114938489	GM12878	blood:	n/a
22	chr5:114937919-114937969	NHBE	bronchial:	n/a
23	chr5:114938148-114938198	ECC-1	luminal epithelium:	n/a
24	chr5:114938148-114938198	GM06990	blood:	n/a
25	chr5:114937535-114937585	RPTEC	kidney:	n/a
26	chr5:114938236-114938286	PANC-1	pancreas:	n/a
27	chr5:114938148-114938198	HEK293	kidney:	embryo
28	chr5:114938389-114938439	AG04450	lung:	fetal
29	chr5:114937614-114937664	HRE	kidney:	n/a
30	chr5:114937648-114937698	GM06990	blood:	n/a
31	chr5:114938236-114938286	HRCEpiC	kidney:	n/a
32	chr5:114937784-114937834	H1-hESC	embryonic stem cell:	embryo
33	chr5:114938439-114938489	K562	blood:	n/a
34	chr5:114937535-114937585	MCF10A-Er-Src	breast:	n/a
35	chr5:114937648-114937698	SK-N-SH_RA	brain:	n/a
36	chr5:114938389-114938439	BJ	skin:	n/a
37	chr5:114937784-114937834	HUVEC	blood vessel:	n/a
38	chr5:114937648-114937698	GM12878	blood:	n/a
39	chr5:114938389-114938439	NHDF-neo	bronchial:	n/a
40	chr5:114937648-114937698	LNCaP	prostate:	n/a
41	chr5:114937614-114937664	SK-N-MC	brain:	n/a
42	chr5:114938459-114938509	GM12891	blood:	n/a
43	chr5:114937784-114937834	K562	blood:	n/a
44	chr5:114937535-114937585	NB4	blood:	n/a
45	chr5:114937648-114937698	ovcar-3	ovarian:	n/a
46	chr5:114938439-114938489	RPTEC	kidney:	n/a
47	chr5:114938236-114938286	GM12878	blood:	n/a
48	chr5:114937784-114937834	NHBE	bronchial:	n/a
49	chr5:114937535-114937585	PFSK-1	brain:	n/a
50	chr5:114937784-114937834	PrEC	prostate:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:114877886..114879457-chr5:114935009..114937600,2	K562	blood:
2	chr5:114934797..114939548-chr5:114953575..114961976,8	K562	blood:
3	chr5:114936247..114938177-chr5:114959534..114962655,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP3S1-4	chr5:114937844-114938157	NONHSAT103312
2	lnc-AP3S1-4	chr5:114938743-114938853	NONHSAT103312
3	lnc-AP3S1-4	chr5:114938378-114938404	NONHSAT103313
4	lnc-AP3S1-4	chr5:114938743-114938853	NONHSAT103313
5	lnc-AP3S1-4	chr5:114938743-114938853	NR_109874
6	lnc-AP3S1-4	chr5:114937852-114938157	NR_109875
7	lnc-AP3S1-4	chr5:114937852-114938157	NR_109874
8	lnc-AP3S1-4	chr5:114938743-114938853	NR_109875
9	lnc-TMED7-3	chr5:114937794-114937886	NONHSAT103310

No data

Variant related genes	Relation type
ENSG00000249249	TF binding region
TICAM2	TF binding region
ENSG00000249249	CpG island
TICAM2	CpG island
ENSG00000251201	chromatin interactions
ENSG00000243414	chromatin interactions
ENSG00000134970	chromatin interactions

Extended variants
information (count: 76 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:76 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147054403	chr5:114937079-114937080	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs190925463	chr5:114937085-114937086	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs568477504	chr5:114937105-114937106	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs138227153	chr5:114937126-114937127	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs562453768	chr5:114937157-114937158	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs533283221	chr5:114937166-114937167	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs182329186	chr5:114937167-114937168	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs566554559	chr5:114937200-114937201	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs546558391	chr5:114937216-114937217	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs256967	chr5:114937228-114937229	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs548900180	chr5:114937280-114937281	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs376109338	chr5:114937298-114937299	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs149552474	chr5:114937342-114937343	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs373141449	chr5:114937358-114937359	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs560914289	chr5:114937374-114937375	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs529758692	chr5:114937375-114937376	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs144236978	chr5:114937376-114937377	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs256966	chr5:114937385-114937386	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs76081272	chr5:114937391-114937392	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs13153908	chr5:114937416-114937417	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs148376638	chr5:114937425-114937426	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs539767070	chr5:114937462-114937463	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs528334664	chr5:114937465-114937466	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs548198881	chr5:114937467-114937468	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs568393692	chr5:114937480-114937481	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs537155963	chr5:114937516-114937517	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs557415652	chr5:114937529-114937530	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs571002894	chr5:114937569-114937570	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs11741198	chr5:114937575-114937576	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs540024325	chr5:114937669-114937670	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs553571540	chr5:114937729-114937730	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs573603275	chr5:114937750-114937751	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs171773	chr5:114937759-114937760	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs554277643	chr5:114937765-114937766	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs574365080	chr5:114937782-114937783	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs577854159	chr5:114937825-114937826	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs112100886	chr5:114937857-114937858	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs376035550	chr5:114937866-114937867	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs563375984	chr5:114937875-114937876	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs576660724	chr5:114937889-114937890	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
41	rs545606926	chr5:114937897-114937898	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
42	rs559090880	chr5:114937924-114937925	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
43	rs528369608	chr5:114937964-114937965	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
44	rs256965	chr5:114937967-114937968	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs561980721	chr5:114937974-114937975	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
46	rs534431845	chr5:114937996-114937997	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
47	rs372626154	chr5:114938019-114938020	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
48	rs530930334	chr5:114938073-114938074	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs550822281	chr5:114938088-114938089	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs570942084	chr5:114938093-114938094	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	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
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:114914800-114937400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:114925000-114937400	Weak transcription	Pancreas	Pancrea
3	chr5:114930200-114937400	Weak transcription	Hela-S3	cervix
4	chr5:114933000-114937400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr5:114933800-114937200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:114934600-114937200	Enhancers	Primary B cells from peripheral blood	blood
7	chr5:114935000-114937200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:114935000-114937400	Enhancers	Brain Anterior Caudate	brain
9	chr5:114935200-114937200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:114935200-114937200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:114935200-114937200	Enhancers	HSMMtube	muscle
12	chr5:114935200-114937200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr5:114935200-114937400	Enhancers	Brain Cingulate Gyrus	brain
14	chr5:114935600-114937400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr5:114935600-114937400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:114935600-114937400	Weak transcription	NHEK	skin
17	chr5:114935800-114937200	Weak transcription	Placenta	Placenta
18	chr5:114935800-114937200	Weak transcription	Ovary	ovary
19	chr5:114935800-114937400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr5:114935800-114937400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr5:114935800-114938400	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr5:114936000-114937200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr5:114936000-114937400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr5:114936000-114937400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr5:114936000-114938400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:114936000-114938400	Active TSS	Aorta	Aorta
27	chr5:114936200-114937200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr5:114936200-114937400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr5:114936200-114937400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr5:114936200-114937400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr5:114936200-114937400	Enhancers	Stomach Mucosa	stomach
32	chr5:114936400-114937200	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr5:114936400-114937200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr5:114936400-114937400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr5:114936400-114937400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr5:114936400-114937400	Weak transcription	Gastric	stomach
37	chr5:114936400-114937400	Enhancers	A549	lung
38	chr5:114936400-114938200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:114936400-114938400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr5:114936600-114937200	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr5:114936600-114937200	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr5:114936600-114937200	Enhancers	Primary T cells from cord blood	blood
43	chr5:114936600-114937200	Flanking Active TSS	Liver	Liver
44	chr5:114936600-114937400	Weak transcription	Brain Angular Gyrus	brain
45	chr5:114936600-114937600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
46	chr5:114936600-114938400	Active TSS	Muscle Satellite Cultured Cells	--
47	chr5:114936600-114938400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr5:114936600-114938400	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr5:114936600-114938400	Active TSS	NHLF	lung
50	chr5:114936800-114937200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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