Variant report

Variant	nsv1016610
Chromosome Location	chr5:74403611-74627654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1997)
CpG islands
(count:854)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1997 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74532687-74532790	K562	blood:	n/a	n/a
2	ARID3A	chr5:74621072-74621420	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:74463323-74463328	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74522901-74522920	K562	blood:	n/a	n/a
5	ARID3A	chr5:74510856-74511041	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74532794-74533010	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74556537-74556906	HepG2	liver:	n/a	n/a
8	ARID3A	chr5:74627149-74627662	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:74485211-74485511	HepG2	liver:	n/a	n/a
10	ARID3A	chr5:74616865-74617129	K562	blood:	n/a	n/a
11	ATF1	chr5:74616834-74617147	K562	blood:	n/a	n/a
12	ATF3	chr5:74532653-74532914	HepG2	liver:	n/a	chr5:74532787-74532796
13	ATF3	chr5:74616654-74617281	A549	lung:	n/a	n/a
14	ATF3	chr5:74616760-74617137	K562	blood:	n/a	n/a
15	ATF3	chr5:74532621-74532936	K562	blood:	n/a	chr5:74532787-74532796
16	BACH1	chr5:74532667-74533059	K562	blood:	n/a	n/a
17	BACH1	chr5:74493604-74493975	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:74532117-74532129	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:74532563-74533094	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr5:74616848-74617152	H1-hESC	embryonic stem cell:	n/a	chr5:74617004-74617018
21	BACH1	chr5:74493585-74493943	K562	blood:	n/a	n/a
22	BATF	chr5:74620644-74620968	GM12878	blood:	n/a	n/a
23	BCL3	chr5:74442051-74442314	GM12878	blood:	n/a	n/a
24	BCL3	chr5:74616489-74617234	A549	lung:	n/a	n/a
25	BCL3	chr5:74616528-74617339	A549	lung:	n/a	n/a
26	BCLAF1	chr5:74532480-74533071	GM12878	blood:	n/a	chr5:74532712-74532725 chr5:74532807-74532816
27	BHLHE40	chr5:74616798-74617273	K562	blood:	n/a	n/a
28	BHLHE40	chr5:74532532-74533117	GM12878	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
29	BHLHE40	chr5:74614935-74615164	K562	blood:	n/a	n/a
30	BHLHE40	chr5:74532228-74533127	K562	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
31	BHLHE40	chr5:74519635-74519784	K562	blood:	n/a	n/a
32	BRCA1	chr5:74409126-74409996	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr5:74407638-74408236	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr5:74532830-74533048	GM12878	blood:	n/a	n/a
35	BRCA1	chr5:74532796-74532900	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr5:74616781-74617420	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr5:74561550-74561750	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr5:74532701-74532945	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr5:74535454-74536020	HCT-116	colon:	n/a	n/a
40	CBX3	chr5:74463153-74463586	HCT-116	colon:	n/a	n/a
41	CBX3	chr5:74532596-74533042	K562	blood:	n/a	n/a
42	CBX3	chr5:74457355-74457583	K562	blood:	n/a	n/a
43	CBX3	chr5:74577498-74578097	HCT-116	colon:	n/a	n/a
44	CCNT2	chr5:74532202-74533086	K562	blood:	n/a	chr5:74532787-74532796
45	CCNT2	chr5:74616844-74617206	K562	blood:	n/a	n/a
46	CCNT2	chr5:74493718-74493858	K562	blood:	n/a	n/a
47	CEBPB	chr5:74616615-74617464	A549	lung:	n/a	n/a
48	CEBPB	chr5:74513259-74513547	A549	lung:	n/a	chr5:74513393-74513404
49	CEBPB	chr5:74610474-74610558	HepG2	liver:	n/a	chr5:74610507-74610518
50	CEBPB	chr5:74570363-74570609	HepG2	liver:	n/a	chr5:74570432-74570443

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74531185-74531235	HNPCEpiC	eye:	n/a
2	chr5:74616750-74616800	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:74533042-74533092	Hepatocyte	liver:	n/a
4	chr5:74532862-74532912	NT2-D1	testis:	n/a
5	chr5:74532880-74532930	ProgFib	skin:	n/a
6	chr5:74438852-74438902	PFSK-1	brain:	n/a
7	chr5:74532894-74532944	T-47D	breast:	n/a
8	chr5:74532852-74532902	Caco-2	colon:	n/a
9	chr5:74532852-74532902	CMK	blood:	n/a
10	chr5:74533279-74533329	HEK293	kidney:	embryo
11	chr5:74533066-74533116	SK-N-SH	brain:	n/a
12	chr5:74532835-74532885	AG09319	gingival:	n/a
13	chr5:74532862-74532912	AG09309	skin:	n/a
14	chr5:74438852-74438902	GM12891	blood:	n/a
15	chr5:74533042-74533092	MCF10A-Er-Src	breast:	n/a
16	chr5:74533279-74533329	HepG2	liver:	n/a
17	chr5:74531185-74531235	HCT-116	colon:	n/a
18	chr5:74532852-74532902	HCT-116	colon:	n/a
19	chr5:74438852-74438902	HUVEC	blood vessel:	n/a
20	chr5:74533279-74533329	NB4	blood:	n/a
21	chr5:74532835-74532885	PFSK-1	brain:	n/a
22	chr5:74533042-74533092	HRPEpiC	eye:	n/a
23	chr5:74533279-74533329	U87	brain:	n/a
24	chr5:74531185-74531235	SK-N-MC	brain:	n/a
25	chr5:74533066-74533116	GM12892	blood:	n/a
26	chr5:74532268-74532318	AG04450	lung:	fetal
27	chr5:74531185-74531235	HAEpiC	amniotic membrane:	n/a
28	chr5:74531185-74531235	AG04449	skin:	fetal
29	chr5:74533279-74533329	GM12891	blood:	n/a
30	chr5:74536793-74536843	SKMC	muscle:	n/a
31	chr5:74531185-74531235	Hepatocyte	liver:	n/a
32	chr5:74533066-74533116	NB4	blood:	n/a
33	chr5:74533279-74533329	HRE	kidney:	n/a
34	chr5:74532268-74532318	NT2-D1	testis:	n/a
35	chr5:74533279-74533329	BJ	skin:	n/a
36	chr5:74532862-74532912	GM06990	blood:	n/a
37	chr5:74532880-74532930	Caco-2	colon:	n/a
38	chr5:74571706-74571756	HEEpiC	esophagus:	n/a
39	chr5:74533066-74533116	GM12878	blood:	n/a
40	chr5:74531185-74531235	Jurkat	blood:	n/a
41	chr5:74438852-74438902	LNCaP	prostate:	n/a
42	chr5:74571706-74571756	HRE	kidney:	n/a
43	chr5:74532894-74532944	AG04450	lung:	fetal
44	chr5:74571706-74571756	ProgFib	skin:	n/a
45	chr5:74532880-74532930	AG09309	skin:	n/a
46	chr5:74616750-74616800	AG04450	lung:	fetal
47	chr5:74532880-74532930	K562	blood:	n/a
48	chr5:74531185-74531235	SAEC	small airway:	n/a
49	chr5:74532894-74532944	PFSK-1	brain:	n/a
50	chr5:74616750-74616800	HRCEpiC	kidney:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
2	chr5:74527339..74529345-chr5:74531111..74533787,2	K562	blood:
3	chr5:74439700..74441214-chr5:76362795..76365262,2	K562	blood:
4	chr5:74526525..74528959-chr5:74530851..74533698,2	MCF-7	breast:
5	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
6	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
7	chr5:74230558..74231547-chr5:74561170..74561749,2	MCF-7	breast:
8	chr5:74535747..74537406-chr5:74677465..74679427,2	K562	blood:
9	chr5:74601851..74604093-chr5:74606288..74608285,2	K562	blood:
10	chr5:74532315..74532928-chr5:74561101..74562172,4	MCF-7	breast:
11	chr5:74530643..74533204-chr5:74537611..74539237,3	K562	blood:
12	chr5:74569658..74571671-chr5:74631055..74633610,2	MCF-7	breast:
13	chr5:74459995..74462741-chr5:74463456..74465776,2	K562	blood:
14	chr5:74398898..74401626-chr5:74404084..74405845,2	K562	blood:
15	chr5:74624687..74627329-chr5:74632188..74633774,2	MCF-7	breast:
16	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
17	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
18	chr5:74348653..74349615-chr5:74462874..74463564,2	MCF-7	breast:
19	chr5:74619697..74622468-chr5:74630363..74633145,3	MCF-7	breast:
20	chr5:74606664..74608899-chr5:74628244..74629786,2	K562	blood:
21	chr5:74623256..74625820-chr5:74629134..74632022,2	K562	blood:
22	chr5:74601851..74604093-chr5:74606288..74608285,2	K562	blood:
23	chr5:74491047..74493376-chr5:74495534..74497598,2	K562	blood:
24	chr5:74575010..74575851-chr5:74632251..74632946,2	MCF-7	breast:
25	chr5:74345728..74346291-chr5:74523458..74524224,2	MCF-7	breast:
26	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
27	chr5:74220830..74221511-chr5:74561645..74562178,2	MCF-7	breast:
28	chr5:74504886..74507088-chr5:74507988..74510413,2	K562	blood:
29	chr5:74532153..74534047-chr5:74632305..74633924,2	MCF-7	breast:
30	chr5:74490335..74492474-chr5:74495385..74497140,2	K562	blood:
31	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
32	chr5:74573556..74575818-chr5:74631336..74632955,2	MCF-7	breast:
33	chr5:74626345..74628591-chr5:74631486..74633303,2	MCF-7	breast:
34	chr5:74345325..74346339-chr5:74561197..74562160,5	MCF-7	breast:
35	chr5:74409705..74412287-chr5:74414282..74416485,2	K562	blood:
36	chr5:74504360..74506170-chr5:74531534..74533618,3	K562	blood:
37	chr5:74518294..74520803-chr5:74529681..74531542,2	K562	blood:
38	chr5:74230538..74231300-chr5:74561168..74561757,3	MCF-7	breast:
39	chr5:74532409..74533382-chr5:74632361..74633307,2	Hela-S3	cervix:
40	chr5:74624109..74627608-chr5:74630494..74633773,3	K562	blood:
41	chr5:74505529..74508894-chr5:74510527..74513977,3	K562	blood:
42	chr5:74530660..74533161-chr5:74616119..74617776,2	K562	blood:
43	chr5:74481183..74484880-chr5:74486837..74490307,3	K562	blood:
44	chr5:74532313..74533315-chr5:74561168..74561902,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL4A3BP-1	chr5:74615980-74616308	ENSG00000247372.2
2	lnc-HMGCR-3	chr5:74521249-74521493	NONHSAT102199

No data

Variant related genes	Relation type
HMGCR	TF binding region
ANKRD31	TF binding region
SUMO2P5	TF binding region
HMGCR	CpG island
ANKRD31	CpG island
SUMO2P5	CpG island
ENSG00000113161	chromatin interactions
ENSG00000250889	chromatin interactions
ENSG00000145700	chromatin interactions
ENSG00000247372	chromatin interactions
ENSG00000113163	chromatin interactions

Extended variants
information (count: 6698 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:6698 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9293645	chr5:74404281-74404282	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538759184	chr5:74404330-74404331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570651024	chr5:74404425-74404426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371388742	chr5:74404428-74404429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537778105	chr5:74404484-74404485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189281599	chr5:74404492-74404493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147258509	chr5:74404538-74404539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6875035	chr5:74404558-74404559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192368332	chr5:74404570-74404571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184651077	chr5:74404572-74404573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs139669140	chr5:74404686-74404687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564521614	chr5:74404690-74404691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578155108	chr5:74404738-74404739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs4340901	chr5:74404905-74404906	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73127392	chr5:74404958-74404959	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188526867	chr5:74404981-74404982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181278186	chr5:74405053-74405054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561699538	chr5:74405072-74405073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs4361493	chr5:74405097-74405098	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs374564797	chr5:74405106-74405107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113572751	chr5:74405129-74405130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570543985	chr5:74405131-74405132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs533105616	chr5:74405136-74405137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549589481	chr5:74405141-74405142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569582261	chr5:74405202-74405203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149855095	chr5:74405366-74405367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185797460	chr5:74405371-74405372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565782918	chr5:74405476-74405477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs534799934	chr5:74405518-74405519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112899807	chr5:74405520-74405521	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578035577	chr5:74405528-74405529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543967424	chr5:74405619-74405620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145848230	chr5:74405626-74405627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148565795	chr5:74405650-74405651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543369077	chr5:74405718-74405719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542921528	chr5:74405719-74405720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565237769	chr5:74405723-74405724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6862740	chr5:74405749-74405750	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs182273853	chr5:74405980-74405981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540677479	chr5:74406004-74406005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72768330	chr5:74406013-74406014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532902530	chr5:74406032-74406033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549552703	chr5:74406074-74406075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79051905	chr5:74406079-74406080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536428501	chr5:74406126-74406127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368585645	chr5:74406246-74406247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547299807	chr5:74406267-74406268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9763362	chr5:74406316-74406317	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190870249	chr5:74406332-74406333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182532949	chr5:74406402-74406403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	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
Hepatocellular carcinoma	16750200	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
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	21720365	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1145 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74404200-74405600	Enhancers	NHEK	skin
2	chr5:74404200-74405800	Enhancers	Hela-S3	cervix
3	chr5:74404200-74406200	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr5:74404400-74405400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:74404400-74405600	Enhancers	HMEC	breast
6	chr5:74404400-74405800	Enhancers	Primary T cells from cord blood	blood
7	chr5:74404400-74405800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr5:74405000-74405400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:74405000-74405600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr5:74405000-74405800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr5:74405000-74405800	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr5:74405000-74405800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr5:74405000-74405800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr5:74405000-74405800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr5:74405000-74405800	Enhancers	Fetal Thymus	thymus
16	chr5:74405000-74406200	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr5:74405200-74405600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:74405200-74405600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:74405200-74405600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:74405200-74405800	Enhancers	Primary T killer memory cells from peripheral blood	blood
21	chr5:74405200-74405800	Enhancers	Thymus	Thymus
22	chr5:74405400-74405800	Enhancers	Primary T cells fromperipheralblood	blood
23	chr5:74405400-74407600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:74405600-74407400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr5:74405600-74407400	Weak transcription	NHEK	skin
26	chr5:74405600-74407600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr5:74405600-74407600	Weak transcription	HMEC	breast
28	chr5:74405800-74406200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr5:74405800-74406800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr5:74405800-74406800	Weak transcription	Hela-S3	cervix
31	chr5:74405800-74407200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr5:74405800-74407400	Weak transcription	Primary T cells from cord blood	blood
33	chr5:74405800-74407400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr5:74405800-74407600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:74406200-74406400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr5:74406200-74407200	Weak transcription	Primary T helper cells PMA-I stimulated	--
37	chr5:74406200-74407400	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr5:74406400-74407400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr5:74406800-74407600	Enhancers	Hela-S3	cervix
40	chr5:74406800-74407800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr5:74407200-74407800	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr5:74407200-74408000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr5:74407400-74407600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr5:74407400-74407800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr5:74407400-74408000	Enhancers	Primary T cells from cord blood	blood
46	chr5:74407400-74408000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr5:74407400-74409200	Enhancers	NHEK	skin
48	chr5:74407600-74407800	Enhancers	Primary T helper naive cells from peripheral blood	blood
49	chr5:74407600-74407800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr5:74407600-74407800	Flanking Active TSS	Hela-S3	cervix

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