Variant report

Variant	esv2759350
Chromosome Location	chr5:74433760-74611714
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1598)
CpG islands
(count:795)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1598 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:74522901-74522920	K562	blood:	n/a	n/a
2	ARID3A	chr5:74532687-74532790	K562	blood:	n/a	n/a
3	ARID3A	chr5:74463323-74463328	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:74510856-74511041	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:74532794-74533010	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:74556537-74556906	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:74485211-74485511	HepG2	liver:	n/a	n/a
8	ATF3	chr5:74532621-74532936	K562	blood:	n/a	chr5:74532787-74532796
9	ATF3	chr5:74532653-74532914	HepG2	liver:	n/a	chr5:74532787-74532796
10	BACH1	chr5:74532563-74533094	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:74532117-74532129	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:74532667-74533059	K562	blood:	n/a	n/a
13	BACH1	chr5:74493604-74493975	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:74493585-74493943	K562	blood:	n/a	n/a
15	BCL3	chr5:74442051-74442314	GM12878	blood:	n/a	n/a
16	BCLAF1	chr5:74532480-74533071	GM12878	blood:	n/a	chr5:74532712-74532725 chr5:74532807-74532816
17	BHLHE40	chr5:74532228-74533127	K562	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
18	BHLHE40	chr5:74532532-74533117	GM12878	blood:	n/a	chr5:74532785-74532801 chr5:74533055-74533071
19	BHLHE40	chr5:74519635-74519784	K562	blood:	n/a	n/a
20	BRCA1	chr5:74561550-74561750	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr5:74532830-74533048	GM12878	blood:	n/a	n/a
22	BRCA1	chr5:74532796-74532900	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr5:74532701-74532945	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr5:74532596-74533042	K562	blood:	n/a	n/a
25	CBX3	chr5:74577498-74578097	HCT-116	colon:	n/a	n/a
26	CBX3	chr5:74535454-74536020	HCT-116	colon:	n/a	n/a
27	CBX3	chr5:74457355-74457583	K562	blood:	n/a	n/a
28	CBX3	chr5:74463153-74463586	HCT-116	colon:	n/a	n/a
29	CCNT2	chr5:74532202-74533086	K562	blood:	n/a	chr5:74532787-74532796
30	CCNT2	chr5:74493718-74493858	K562	blood:	n/a	n/a
31	CEBPB	chr5:74532392-74532649	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:74535558-74535876	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr5:74454985-74455100	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr5:74536380-74536580	K562	blood:	n/a	chr5:74536486-74536495 chr5:74536486-74536497 chr5:74536484-74536495
35	CEBPB	chr5:74513259-74513547	A549	lung:	n/a	chr5:74513393-74513404
36	CEBPB	chr5:74610474-74610558	HepG2	liver:	n/a	chr5:74610507-74610518
37	CEBPB	chr5:74582095-74582337	Hela-S3	cervix:	n/a	chr5:74582226-74582237
38	CEBPB	chr5:74441751-74441886	HepG2	liver:	n/a	chr5:74441789-74441800 chr5:74441789-74441802 chr5:74441789-74441802 chr5:74441790-74441801
39	CEBPB	chr5:74454858-74455117	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:74573557-74573876	K562	blood:	n/a	chr5:74573741-74573752 chr5:74573740-74573751 chr5:74573742-74573751
41	CEBPB	chr5:74582159-74582312	H1-hESC	embryonic stem cell:	n/a	chr5:74582226-74582237
42	CEBPB	chr5:74532284-74532970	K562	blood:	n/a	n/a
43	CEBPB	chr5:74577633-74577829	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:74466982-74467091	K562	blood:	n/a	chr5:74467037-74467048
45	CEBPB	chr5:74577319-74578148	HCT-116	colon:	n/a	n/a
46	CEBPB	chr5:74513309-74513508	K562	blood:	n/a	chr5:74513393-74513404
47	CEBPB	chr5:74573206-74573384	A549	lung:	n/a	n/a
48	CEBPB	chr5:74610472-74610557	H1-hESC	embryonic stem cell:	n/a	chr5:74610507-74610518
49	CEBPB	chr5:74570249-74570634	MCF-7	breast:	n/a	chr5:74570432-74570443
50	CEBPB	chr5:74573190-74573835	HepG2	liver:	n/a	chr5:74573741-74573752 chr5:74573740-74573751 chr5:74573742-74573751

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74532880-74532930	CMK	blood:	n/a
2	chr5:74531185-74531235	HRE	kidney:	n/a
3	chr5:74532880-74532930	CMK	blood:	n/a
4	chr5:74531185-74531235	HRE	kidney:	n/a
5	chr5:74533042-74533092	SAEC	small airway:	n/a
6	chr5:74536793-74536843	K562	blood:	n/a
7	chr5:74536793-74536843	SAEC	small airway:	n/a
8	chr5:74532835-74532885	HRE	kidney:	n/a
9	chr5:74532894-74532944	AG04449	skin:	fetal
10	chr5:74438852-74438902	SK-N-SH_RA	brain:	n/a
11	chr5:74533279-74533329	HNPCEpiC	eye:	n/a
12	chr5:74533066-74533116	RPTEC	kidney:	n/a
13	chr5:74438852-74438902	AoSMC	blood vessel:	n/a
14	chr5:74532862-74532912	HCPEpiC	choroid plexus:	n/a
15	chr5:74438852-74438902	AG04449	skin:	fetal
16	chr5:74532862-74532912	Hepatocyte	liver:	n/a
17	chr5:74532880-74532930	AG09319	gingival:	n/a
18	chr5:74532268-74532318	LNCaP	prostate:	n/a
19	chr5:74532862-74532912	BE2_C	brain:	n/a
20	chr5:74532862-74532912	PrEC	prostate:	n/a
21	chr5:74438852-74438902	MCF10A-Er-Src	breast:	n/a
22	chr5:74532862-74532912	SK-N-MC	brain:	n/a
23	chr5:74532880-74532930	LNCaP	prostate:	n/a
24	chr5:74438852-74438902	HCM	heart:	n/a
25	chr5:74536793-74536843	SK-N-SH	brain:	n/a
26	chr5:74571706-74571756	HPAEpiC	pulmonary alveolar:	n/a
27	chr5:74532268-74532318	SK-N-MC	brain:	n/a
28	chr5:74532268-74532318	SKMC	muscle:	n/a
29	chr5:74438852-74438902	T-47D	breast:	n/a
30	chr5:74532880-74532930	BJ	skin:	n/a
31	chr5:74532835-74532885	U87	brain:	n/a
32	chr5:74533042-74533092	AG10803	skin:	n/a
33	chr5:74438852-74438902	GM12878	blood:	n/a
34	chr5:74536793-74536843	NT2-D1	testis:	n/a
35	chr5:74533042-74533092	RPTEC	kidney:	n/a
36	chr5:74438852-74438902	HUVEC	blood vessel:	n/a
37	chr5:74438852-74438902	LNCaP	prostate:	n/a
38	chr5:74532852-74532902	MCF10A-Er-Src	breast:	n/a
39	chr5:74532862-74532912	HMEC	breast:	n/a
40	chr5:74533066-74533116	LNCaP	prostate:	n/a
41	chr5:74532852-74532902	NT2-D1	testis:	n/a
42	chr5:74532862-74532912	GM12878	blood:	n/a
43	chr5:74533279-74533329	SAEC	small airway:	n/a
44	chr5:74531185-74531235	HIPEpiC	eye:	n/a
45	chr5:74532862-74532912	RPTEC	kidney:	n/a
46	chr5:74532268-74532318	HL-60	blood:	n/a
47	chr5:74571706-74571756	T-47D	breast:	n/a
48	chr5:74533066-74533116	PFSK-1	brain:	n/a
49	chr5:74533042-74533092	Hepatocyte	liver:	n/a
50	chr5:74532852-74532902	HRE	kidney:	n/a

(count:35 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGCR-3	chr5:74521249-74521493	NONHSAT102199

No data

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

Extended variants
information (count: 4704 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4704 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs717587	chr5:74433835-74433836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371367483	chr5:74433839-74433840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs397786843	chr5:74433850-74433851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76455020	chr5:74433853-74433854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559395709	chr5:74433863-74433864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192401868	chr5:74433864-74433865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567378812	chr5:74433870-74433871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143056868	chr5:74433872-74433873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148197487	chr5:74433919-74433920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533189671	chr5:74433942-74433943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs79592501	chr5:74433995-74433996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs141501360	chr5:74434047-74434048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553141993	chr5:74434120-74434121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573281168	chr5:74434145-74434146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78373781	chr5:74434146-74434147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532123598	chr5:74434186-74434187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs575406862	chr5:74434206-74434207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544419278	chr5:74434312-74434313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551933251	chr5:74434431-74434432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184995937	chr5:74434453-74434454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575075864	chr5:74434552-74434553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs77973805	chr5:74434554-74434555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553347205	chr5:74434560-74434561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573181451	chr5:74434573-74434574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538887058	chr5:74434579-74434580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189300030	chr5:74434604-74434605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10044478	chr5:74434617-74434618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555503715	chr5:74434718-74434719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192285141	chr5:74434754-74434755	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530707158	chr5:74434867-74434868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575558712	chr5:74434909-74434910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184670081	chr5:74434919-74434920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544412271	chr5:74435100-74435101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140802847	chr5:74435112-74435113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374308936	chr5:74435116-74435117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189485648	chr5:74435190-74435191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562378631	chr5:74435195-74435196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536196822	chr5:74435204-74435205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1308231	chr5:74435227-74435228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113241702	chr5:74435267-74435268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150575585	chr5:74435282-74435283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539046670	chr5:74435289-74435290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558593898	chr5:74435308-74435309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370335390	chr5:74435323-74435324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4704178	chr5:74435324-74435325	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115987478	chr5:74435358-74435359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74876356	chr5:74435361-74435362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554782878	chr5:74435363-74435364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574986724	chr5:74435380-74435381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540520915	chr5:74435403-74435404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:900 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74427600-74434600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:74434200-74434600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr5:74434200-74435000	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr5:74434400-74434800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr5:74434600-74435000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr5:74434600-74438400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:74434800-74438200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:74435000-74438400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr5:74436600-74436800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:74437600-74438600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:74438000-74439400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr5:74438200-74439200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr5:74438400-74438800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr5:74438400-74439200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr5:74438400-74439200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr5:74438400-74439200	Enhancers	Primary T cells from cord blood	blood
17	chr5:74438400-74439200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr5:74438400-74439200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr5:74438400-74439200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:74438400-74439400	Enhancers	H1 Cell Line	embryonic stem cell
21	chr5:74438400-74439400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr5:74438400-74439400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:74438600-74439400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:74438600-74439400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:74438600-74439600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr5:74438800-74439200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
27	chr5:74438800-74439200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr5:74438800-74439200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:74438800-74439600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:74439200-74439800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr5:74439200-74441600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr5:74439200-74441600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:74439200-74441800	Weak transcription	Primary T cells from cord blood	blood
34	chr5:74439200-74442200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr5:74439400-74440000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr5:74439600-74449000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr5:74440000-74442600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr5:74440400-74448000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr5:74441600-74442000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:74441600-74443800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:74441800-74443400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chr5:74441800-74443800	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr5:74441800-74444600	Enhancers	Primary T cells from cord blood	blood
44	chr5:74441800-74444600	Enhancers	Primary hematopoietic stem cells	blood
45	chr5:74442000-74442400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr5:74442000-74442400	Enhancers	Fetal Thymus	thymus
47	chr5:74442000-74442600	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr5:74442000-74442600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:74442000-74442800	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr5:74442000-74443200	Enhancers	Primary T helper cells PMA-I stimulated	--

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