Variant report

Variant	esv34133
Chromosome Location	chr5:76138696-76239330
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:765)
CpG islands
(count:488)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:765 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76145750-76146088	K562	blood:	n/a	n/a
2	ARID3A	chr5:76147455-76147464	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76169967-76170322	K562	blood:	n/a	n/a
4	ARID3A	chr5:76163911-76164256	K562	blood:	n/a	n/a
5	ARID3A	chr5:76165986-76166156	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:76163901-76164233	HepG2	liver:	n/a	n/a
7	ATF1	chr5:76152591-76152875	K562	blood:	n/a	n/a
8	ATF1	chr5:76170064-76170385	K562	blood:	n/a	n/a
9	ATF2	chr5:76163943-76164306	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr5:76145745-76146124	K562	blood:	n/a	n/a
11	BACH1	chr5:76169930-76170265	K562	blood:	n/a	n/a
12	BACH1	chr5:76170008-76170259	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:76233684-76233893	GM12878	blood:	n/a	n/a
14	BATF	chr5:76236874-76237087	GM12878	blood:	n/a	n/a
15	BATF	chr5:76234063-76234276	GM12878	blood:	n/a	n/a
16	BATF	chr5:76233915-76234338	GM12878	blood:	n/a	n/a
17	BHLHE40	chr5:76164044-76164139	K562	blood:	n/a	n/a
18	BHLHE40	chr5:76165863-76166236	HepG2	liver:	n/a	n/a
19	BHLHE40	chr5:76163936-76164249	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:76169996-76170347	K562	blood:	n/a	n/a
21	BHLHE40	chr5:76145340-76145346	K562	blood:	n/a	n/a
22	BHLHE40	chr5:76145594-76146150	K562	blood:	n/a	n/a
23	BHLHE40	chr5:76152823-76152904	K562	blood:	n/a	n/a
24	BHLHE40	chr5:76145717-76145893	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:76142105-76142119	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:76163801-76164243	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:76151671-76152135	K562	blood:	n/a	n/a
28	CBX3	chr5:76145641-76146136	K562	blood:	n/a	n/a
29	CBX3	chr5:76177673-76177972	K562	blood:	n/a	n/a
30	CBX3	chr5:76145548-76146197	K562	blood:	n/a	n/a
31	CCNT2	chr5:76145582-76146271	K562	blood:	n/a	chr5:76145946-76145966 chr5:76146151-76146160 chr5:76146143-76146152
32	CCNT2	chr5:76223541-76223650	K562	blood:	n/a	n/a
33	CCNT2	chr5:76170068-76170405	K562	blood:	n/a	chr5:76170251-76170271
34	CEBPB	chr5:76233200-76233932	A549	lung:	n/a	chr5:76233528-76233539
35	CEBPB	chr5:76233346-76233726	A549	lung:	n/a	chr5:76233528-76233539
36	CEBPB	chr5:76233349-76233725	IMR90	lung:	n/a	chr5:76233528-76233539
37	CEBPB	chr5:76189100-76189418	MCF-7	breast:	n/a	chr5:76189318-76189329
38	CEBPB	chr5:76233318-76233790	A549	lung:	n/a	chr5:76233528-76233539
39	CEBPB	chr5:76206311-76206596	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:76163632-76164208	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr5:76233345-76233719	HepG2	liver:	n/a	chr5:76233528-76233539
42	CEBPB	chr5:76233350-76233725	Hela-S3	cervix:	n/a	chr5:76233528-76233539
43	CEBPB	chr5:76155503-76155786	K562	blood:	n/a	chr5:76155681-76155692
44	CEBPB	chr5:76155552-76155794	A549	lung:	n/a	chr5:76155681-76155692
45	CEBPB	chr5:76155472-76155919	MCF-7	breast:	n/a	chr5:76155681-76155692
46	CEBPB	chr5:76163720-76163973	A549	lung:	n/a	n/a
47	CEBPB	chr5:76155499-76155815	HepG2	liver:	n/a	chr5:76155681-76155692
48	CEBPB	chr5:76233264-76233729	K562	blood:	n/a	chr5:76233528-76233539
49	CEBPB	chr5:76233312-76233707	ECC-1	luminal epithelium:	n/a	chr5:76233528-76233539
50	CEBPB	chr5:76163684-76164152	MCF-7	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76145903-76145953	HCM	heart:	n/a
2	chr5:76145809-76145859	GM06990	blood:	n/a
3	chr5:76210838-76210888	IMR90	lung:	fetal
4	chr5:76145809-76145859	ovcar-3	ovarian:	n/a
5	chr5:76210838-76210888	SK-N-MC	brain:	n/a
6	chr5:76238976-76239026	ProgFib	skin:	n/a
7	chr5:76170418-76170468	PFSK-1	brain:	n/a
8	chr5:76210838-76210888	Hela-S3	cervix:	n/a
9	chr5:76238976-76239026	GM12878	blood:	n/a
10	chr5:76144940-76144990	AG10803	skin:	n/a
11	chr5:76145809-76145859	NT2-D1	testis:	n/a
12	chr5:76238976-76239026	Jurkat	blood:	n/a
13	chr5:76144940-76144990	AoSMC	blood vessel:	n/a
14	chr5:76145903-76145953	HCT-116	colon:	n/a
15	chr5:76171906-76171956	HIPEpiC	eye:	n/a
16	chr5:76238976-76239026	HEK293	kidney:	embryo
17	chr5:76144940-76144990	U87	brain:	n/a
18	chr5:76170418-76170468	GM06990	blood:	n/a
19	chr5:76145903-76145953	NB4	blood:	n/a
20	chr5:76144940-76144990	AG09319	gingival:	n/a
21	chr5:76144940-76144990	SKMC	muscle:	n/a
22	chr5:76210838-76210888	SAEC	small airway:	n/a
23	chr5:76238976-76239026	H1-hESC	embryonic stem cell:	embryo
24	chr5:76146148-76146198	K562	blood:	n/a
25	chr5:76170418-76170468	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:76146148-76146198	NT2-D1	testis:	n/a
27	chr5:76171906-76171956	PANC-1	pancreas:	n/a
28	chr5:76145903-76145953	LNCaP	prostate:	n/a
29	chr5:76238976-76239026	NB4	blood:	n/a
30	chr5:76171906-76171956	AG10803	skin:	n/a
31	chr5:76144940-76144990	HUVEC	blood vessel:	n/a
32	chr5:76210838-76210888	HepG2	liver:	n/a
33	chr5:76170418-76170468	HMEC	breast:	n/a
34	chr5:76210838-76210888	PrEC	prostate:	n/a
35	chr5:76210838-76210888	HMEC	breast:	n/a
36	chr5:76210838-76210888	MCF-7	breast:	n/a
37	chr5:76146148-76146198	GM06990	blood:	n/a
38	chr5:76144940-76144990	HCM	heart:	n/a
39	chr5:76170418-76170468	Jurkat	blood:	n/a
40	chr5:76144940-76144990	Jurkat	blood:	n/a
41	chr5:76238976-76239026	Hepatocyte	liver:	n/a
42	chr5:76144940-76144990	PrEC	prostate:	n/a
43	chr5:76144940-76144990	HEK293	kidney:	embryo
44	chr5:76145809-76145859	HCT-116	colon:	n/a
45	chr5:76145903-76145953	AG10803	skin:	n/a
46	chr5:76144940-76144990	HRCEpiC	kidney:	n/a
47	chr5:76171906-76171956	AG04450	lung:	fetal
48	chr5:76144940-76144990	HL-60	blood:	n/a
49	chr5:76144940-76144990	HCPEpiC	choroid plexus:	n/a
50	chr5:76146148-76146198	HCT-116	colon:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76145559..76148481-chr5:76149405..76151711,4	K562	blood:
2	chr5:76201621..76204477-chr5:76206976..76209585,2	K562	blood:
3	chr5:76115175..76117196-chr5:76160540..76162682,2	MCF-7	breast:
4	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
5	chr5:75973826..75975865-chr5:76141935..76143640,2	MCF-7	breast:
6	chr5:76144979..76147946-chr5:76325039..76327688,2	K562	blood:
7	chr5:76163711..76164616-chr5:76311702..76312587,6	MCF-7	breast:
8	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
9	chr5:76163618..76164624-chr5:76373134..76374055,4	K562	blood:
10	chr5:76150968..76153966-chr5:76157599..76160236,2	K562	blood:
11	chr5:76219477..76221427-chr5:76228225..76229868,2	K562	blood:
12	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
13	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
14	chr5:76170197..76172032-chr5:76326129..76328554,2	MCF-7	breast:
15	chr5:76163643..76164600-chr5:76311594..76312851,8	K562	blood:
16	chr5:76216275..76218652-chr5:76220966..76223336,2	K562	blood:
17	chr5:76201621..76204477-chr5:76206976..76209585,2	K562	blood:
18	chr5:76132665..76134749-chr5:76137165..76139299,2	K562	blood:
19	chr5:76163387..76165111-chr5:76366962..76369589,2	K562	blood:
20	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
21	chr5:76163760..76164637-chr5:76311217..76312283,3	MCF-7	breast:
22	chr5:76221898..76224119-chr5:76227208..76231002,3	K562	blood:
23	chr5:76219477..76221427-chr5:76228225..76229868,2	K562	blood:
24	chr5:76163515..76164197-chr5:76787927..76788778,2	K562	blood:
25	chr5:76136037..76139434-chr5:76141594..76145921,5	K562	blood:
26	chr5:76162914..76165922-chr5:76372633..76374807,3	K562	blood:
27	chr5:76150968..76153966-chr5:76157599..76160236,2	K562	blood:
28	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
29	chr5:76163903..76164537-chr5:76440482..76441271,2	MCF-7	breast:
30	chr5:76221898..76224119-chr5:76227208..76231002,3	K562	blood:
31	chr5:76216275..76218652-chr5:76220966..76223336,2	K562	blood:
32	chr5:76163632..76164571-chr5:76382049..76382765,2	MCF-7	breast:

No data

Variant related genes	Relation type
S100Z	TF binding region
S100Z	CpG island
ENSG00000164253	chromatin interactions
ENSG00000164251	chromatin interactions
ENSG00000264391	chromatin interactions
ENSG00000164252	chromatin interactions
ENSG00000250802	chromatin interactions
ENSG00000171643	chromatin interactions

Extended variants
information (count: 4224 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4224 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7712957	chr5:76138696-76138697	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538299622	chr5:76138745-76138746	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555114229	chr5:76138754-76138755	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs567317367	chr5:76138759-76138760	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs115063428	chr5:76138852-76138853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs4704367	chr5:76138879-76138880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs7730074	chr5:76138900-76138901	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs377464479	chr5:76138922-76138923	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs7731262	chr5:76138940-76138941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs193071268	chr5:76138941-76138942	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534640203	chr5:76138954-76138955	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs7731415	chr5:76138998-76138999	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530217507	chr5:76139082-76139083	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs540865693	chr5:76139112-76139113	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs75214623	chr5:76139117-76139118	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs534318463	chr5:76139118-76139119	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75662060	chr5:76139119-76139120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs368216737	chr5:76139122-76139123	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs560622936	chr5:76139198-76139199	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114728016	chr5:76139223-76139224	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs552915813	chr5:76139226-76139227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs12186919	chr5:76139269-76139270	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531759248	chr5:76139319-76139320	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548369690	chr5:76139372-76139373	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs558880353	chr5:76139420-76139421	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs568572370	chr5:76139444-76139445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575261638	chr5:76139457-76139458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs536048969	chr5:76139475-76139476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116169014	chr5:76139479-76139480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs566550466	chr5:76139490-76139491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538504093	chr5:76139513-76139514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112062356	chr5:76139514-76139515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371008293	chr5:76139562-76139563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558666560	chr5:76139564-76139565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374412759	chr5:76139565-76139566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71606213	chr5:76139569-76139570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75631669	chr5:76139581-76139582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376042039	chr5:76139594-76139595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543840266	chr5:76139632-76139633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554361310	chr5:76139662-76139663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs574524556	chr5:76139723-76139724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539957964	chr5:76139750-76139751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189436864	chr5:76139752-76139753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142724495	chr5:76139753-76139754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546488926	chr5:76139784-76139785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371745463	chr5:76139797-76139798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370367703	chr5:76139810-76139811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181806278	chr5:76139811-76139812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528643684	chr5:76139815-76139816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184991693	chr5:76139869-76139870	Weak 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
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
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	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76130400-76140400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:76132200-76145800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:76135000-76139800	Weak transcription	Small Intestine	intestine
4	chr5:76135200-76140200	Weak transcription	HUVEC	blood vessel
5	chr5:76135200-76140800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:76135400-76145600	Weak transcription	Gastric	stomach
7	chr5:76136000-76140400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr5:76136000-76146400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:76136200-76140000	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr5:76136200-76140200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr5:76136400-76140000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr5:76136800-76140000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr5:76137600-76140000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr5:76137600-76140000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr5:76137600-76140000	Weak transcription	Pancreas	Pancrea
16	chr5:76137600-76144400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr5:76138800-76139000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr5:76140000-76140600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr5:76140000-76140600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr5:76140000-76140600	Enhancers	Pancreas	Pancrea
21	chr5:76140000-76141200	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr5:76140000-76141200	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr5:76140000-76141200	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr5:76140200-76140600	Enhancers	Adipose Nuclei	Adipose
25	chr5:76140200-76140600	Enhancers	HUVEC	blood vessel
26	chr5:76140200-76140800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:76140400-76140600	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr5:76140400-76140600	Enhancers	Duodenum Mucosa	Duodenum
29	chr5:76140600-76143000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr5:76140600-76145000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:76140600-76145800	Weak transcription	Adipose Nuclei	Adipose
32	chr5:76140800-76141200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr5:76140800-76141200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:76140800-76141200	Enhancers	HMEC	breast
35	chr5:76140800-76143200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:76141200-76143200	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr5:76141200-76143200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr5:76141200-76144400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr5:76142600-76145800	Weak transcription	Right Atrium	heart
40	chr5:76143000-76143200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:76143200-76143600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:76143200-76143600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr5:76143200-76143800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr5:76143200-76145800	Enhancers	Primary hematopoietic stem cells	blood
45	chr5:76143200-76145800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:76143600-76143800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr5:76143600-76145600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr5:76143800-76144800	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr5:76143800-76144800	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr5:76144200-76144400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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