Variant report

Variant	nsv963576
Chromosome Location	chr3:97825434-98041343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:852)
CpG islands
(count:915)
Chromatin interactive
region (count:9)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:97962650-97963075	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:98010485-98010670	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:97827090-97827290	HepG2	liver:	n/a	n/a
4	ATF2	chr3:97915093-97915523	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:97859032-97859037	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:97856959-97857324	GM12878	blood:	n/a	n/a
7	BATF	chr3:97959089-97959288	GM12878	blood:	n/a	chr3:97959202-97959213
8	BATF	chr3:97952380-97952574	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:97952351-97952515	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:97895161-97895345	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:97951400-97951563	GM12878	blood:	n/a	n/a
12	BCL3	chr3:97916362-97916553	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:97907429-97907720	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:97951405-97952685	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:97943474-97943485	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:97962720-97963131	HepG2	liver:	n/a	n/a
17	BRCA1	chr3:97939937-97940001	GM12878	blood:	n/a	n/a
18	BRCA1	chr3:97907317-97907430	GM12878	blood:	n/a	n/a
19	CEBPB	chr3:97922385-97922691	A549	lung:	n/a	chr3:97922556-97922567
20	CEBPB	chr3:97873705-97874032	HepG2	liver:	n/a	chr3:97873850-97873861
21	CEBPB	chr3:97922385-97922736	HepG2	liver:	n/a	chr3:97922556-97922567
22	CEBPB	chr3:97984146-97984209	HepG2	liver:	n/a	chr3:97984150-97984161
23	CEBPB	chr3:98010377-98010684	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:98010460-98010640	HepG2	liver:	n/a	n/a
25	CEBPB	chr3:97962794-97963080	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:97856954-97857153	K562	blood:	n/a	n/a
27	CHD1	chr3:97952484-97952829	GM12878	blood:	n/a	n/a
28	CHD1	chr3:97907603-97907803	GM12878	blood:	n/a	n/a
29	CHD1	chr3:97942962-97942975	GM12878	blood:	n/a	n/a
30	CHD1	chr3:97959991-97960022	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:98010479-98010628	HepG2	liver:	n/a	n/a
32	CHD2	chr3:97952077-97952654	GM12878	blood:	n/a	n/a
33	CHD2	chr3:97907426-97907647	GM12878	blood:	n/a	n/a
34	CTCF	chr3:97904131-97904293	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:97978720-97978870	HMEC	breast:	n/a	n/a
36	CTCF	chr3:97904100-97904250	RPTEC	kidney:	n/a	n/a
37	CTCF	chr3:97907640-97907790	A549	lung:	n/a	n/a
38	CTCF	chr3:97907520-97907670	HCFaa	heart:	n/a	n/a
39	CTCF	chr3:97907540-97907690	AG09309	skin:	n/a	n/a
40	CTCF	chr3:97907316-97907821	HCT-116	colon:	n/a	n/a
41	CTCF	chr3:97907480-97907630	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr3:97904183-97904274	GM10266	blood:	n/a	n/a
43	CTCF	chr3:97978686-97978866	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr3:97907446-97907701	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:97907520-97907670	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr3:97967723-97967796	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:97978640-97978790	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr3:97978667-97978879	A549	lung:	n/a	n/a
49	CTCF	chr3:97907518-97907673	K562	blood:	n/a	n/a
50	CTCF	chr3:97978720-97978870	GM12871	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:97886603-97886653	GM19239	blood:	n/a
2	chr3:97867758-97867808	CMK	blood:	n/a
3	chr3:97850862-97850912	PANC-1	pancreas:	n/a
4	chr3:97867758-97867808	U87	brain:	n/a
5	chr3:97982397-97982447	Jurkat	blood:	n/a
6	chr3:97850378-97850428	SK-N-MC	brain:	n/a
7	chr3:97887864-97887914	SK-N-SH	brain:	n/a
8	chr3:97983253-97983303	CMK	blood:	n/a
9	chr3:97887864-97887914	HEK293	kidney:	embryo
10	chr3:97850862-97850912	HRE	kidney:	n/a
11	chr3:98001269-98001319	HAEpiC	amniotic membrane:	n/a
12	chr3:98000733-98000783	GM19239	blood:	n/a
13	chr3:97852335-97852385	HAEpiC	amniotic membrane:	n/a
14	chr3:97886603-97886653	ProgFib	skin:	n/a
15	chr3:97850862-97850912	SK-N-SH	brain:	n/a
16	chr3:97983540-97983590	HNPCEpiC	eye:	n/a
17	chr3:97886603-97886653	HCPEpiC	choroid plexus:	n/a
18	chr3:97887864-97887914	BE2_C	brain:	n/a
19	chr3:97868656-97868706	AG10803	skin:	n/a
20	chr3:97868656-97868706	HL-60	blood:	n/a
21	chr3:97886467-97886517	NH-A	brain:	n/a
22	chr3:97852335-97852385	GM12892	blood:	n/a
23	chr3:97983253-97983303	PANC-1	pancreas:	n/a
24	chr3:97983540-97983590	GM06990	blood:	n/a
25	chr3:97850862-97850912	HCM	heart:	n/a
26	chr3:97886467-97886517	HCF	heart:	n/a
27	chr3:97982397-97982447	K562	blood:	n/a
28	chr3:98001269-98001319	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:98001736-98001786	HepG2	liver:	n/a
30	chr3:97852335-97852385	HepG2	liver:	n/a
31	chr3:98001269-98001319	HRPEpiC	eye:	n/a
32	chr3:97886467-97886517	GM12891	blood:	n/a
33	chr3:97982830-97982880	SK-N-SH	brain:	n/a
34	chr3:97886467-97886517	HRPEpiC	eye:	n/a
35	chr3:97983253-97983303	NB4	blood:	n/a
36	chr3:97868656-97868706	HNPCEpiC	eye:	n/a
37	chr3:97868656-97868706	PANC-1	pancreas:	n/a
38	chr3:97983540-97983590	AG04449	skin:	fetal
39	chr3:97886603-97886653	GM12892	blood:	n/a
40	chr3:97886603-97886653	HAEpiC	amniotic membrane:	n/a
41	chr3:97886467-97886517	PrEC	prostate:	n/a
42	chr3:97983253-97983303	SK-N-SH	brain:	n/a
43	chr3:97886467-97886517	CMK	blood:	n/a
44	chr3:97982830-97982880	NH-A	brain:	n/a
45	chr3:97886603-97886653	NT2-D1	testis:	n/a
46	chr3:97886603-97886653	HL-60	blood:	n/a
47	chr3:98001269-98001319	HRE	kidney:	n/a
48	chr3:97982830-97982880	HPAEpiC	pulmonary alveolar:	n/a
49	chr3:97850378-97850428	SKMC	muscle:	n/a
50	chr3:98001736-98001786	BJ	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:97904894..97907628-chr3:98045904..98048505,2	K562	blood:
2	chr3:97978738..97980851-chr3:98012803..98015207,2	MCF-7	breast:
3	chr3:97978738..97980851-chr3:98012803..98015207,2	MCF-7	breast:
4	chr3:97758293..97759189-chr3:97903652..97904697,9	MCF-7	breast:
5	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:
6	chr3:97907135..97908080-chr3:98062563..98063391,2	MCF-7	breast:
7	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:
8	chr3:97907135..97908282-chr3:98048120..98049025,6	MCF-7	breast:
9	chr3:97757849..97759434-chr3:97903672..97904727,17	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5H1-1	chr3:97838051-97838558	NONHSAT090785
2	lnc-MINA-6	chr3:97916789-97916922	NONHSAT090787
3	lnc-OR5H15-1	chr3:97910049-97910454	XLOC_002733
4	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
5	lnc-OR5H6-1	chr3:98030730-98030852	ENSG00000251088.1
6	lnc-MINA-2	chr3:97956121-97956211	XLOC_003187
7	lnc-MINA-6	chr3:97923366-97923509	NONHSAT090787
8	lnc-OR5H15-1	chr3:97912268-97912342	XLOC_002733
9	lnc-MINA-6	chr3:97925331-97925450	NONHSAT090787
10	lnc-MINA-1	chr3:97866885-97866978	ENSG00000249225.1
11	lnc-OR5H6-1	chr3:97952495-97952520	ENSG00000251088.1
12	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
13	lnc-MINA-2	chr3:97954345-97954692	XLOC_003187
14	lnc-MINA-6	chr3:97904268-97904295	NONHSAT090787
15	lnc-OR5H15-1	chr3:97915250-97915894	XLOC_002733
16	lnc-OR5H15-1	chr3:97910049-97910454	XLOC_002733
17	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
18	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
19	lnc-OR5H15-1	chr3:97912268-97912342	XLOC_002733
20	lnc-OR5H15-1	chr3:97915253-97915894	XLOC_002733
21	lnc-MINA-2	chr3:97956121-97956217	XLOC_003187
22	lnc-MINA-2	chr3:97956121-97956219	XLOC_003187
23	lnc-MINA-2	chr3:97954530-97954692	XLOC_003187
24	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187

No data

Variant related genes	Relation type
OR5H1	TF binding region
OR5H14	TF binding region
OR5H5P	TF binding region
OR5H6	TF binding region
OR5H3P	TF binding region
ENSG00000251088	TF binding region
OR5H7P	TF binding region
OR5H15	TF binding region
POU5F1P7	TF binding region
OR5H4P	TF binding region
OR5H2	TF binding region
ENSG00000249225	TF binding region
OR5H8P	TF binding region
OR5H1	CpG island
OR5H14	CpG island
OR5H5P	CpG island
OR5H6	CpG island
OR5H3P	CpG island
ENSG00000251088	CpG island
OR5H7P	CpG island
OR5H15	CpG island
POU5F1P7	CpG island
OR5H4P	CpG island
OR5H2	CpG island
ENSG00000249225	CpG island
OR5H8P	CpG island
FAM46C	miRNA target sites
LYPD3	miRNA target sites
TGFB2	miRNA target sites
POU2F1	miRNA target sites

Extended variants
information (count: 6139 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6139 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555273039	chr3:97825484-97825485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114025560	chr3:97825539-97825540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545529033	chr3:97825561-97825562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564333832	chr3:97825567-97825568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114488234	chr3:97825568-97825569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4857318	chr3:97825585-97825586	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs4857319	chr3:97825606-97825607	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs4857320	chr3:97825613-97825614	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs113439492	chr3:97825634-97825635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531604924	chr3:97825653-97825654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563265422	chr3:97825724-97825725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548164324	chr3:97825743-97825744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs138532935	chr3:97825749-97825750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4857321	chr3:97825757-97825758	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs547421218	chr3:97825765-97825766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112749634	chr3:97825825-97825826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9855512	chr3:97825901-97825902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs552184345	chr3:97825923-97825924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539557206	chr3:97825950-97825951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376721516	chr3:97825976-97825977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs552711986	chr3:97826066-97826067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369563491	chr3:97826085-97826086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569189025	chr3:97826154-97826155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373979253	chr3:97826179-97826180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538468250	chr3:97826221-97826222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545435903	chr3:97826222-97826223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554955590	chr3:97826243-97826244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574841665	chr3:97826258-97826259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs533886562	chr3:97826287-97826288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs553759377	chr3:97826297-97826298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9843054	chr3:97826310-97826311	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546002769	chr3:97826330-97826331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563025277	chr3:97826331-97826332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576140502	chr3:97826332-97826333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551950214	chr3:97826342-97826343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542045712	chr3:97826344-97826345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs145175402	chr3:97826375-97826376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115178888	chr3:97826405-97826406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527595749	chr3:97826426-97826427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547384433	chr3:97826431-97826432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148342773	chr3:97826434-97826435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532973906	chr3:97826440-97826441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141540801	chr3:97826510-97826511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569773781	chr3:97826534-97826535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs193106934	chr3:97826608-97826609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116205456	chr3:97826627-97826628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185545882	chr3:97826632-97826633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568373093	chr3:97826634-97826635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569796457	chr3:97826644-97826645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186728135	chr3:97826664-97826665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:225 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97823800-97828200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:97828400-97828600	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:97828400-97828600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr3:97828400-97829000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr3:97828400-97829000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr3:97828400-97829800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:97828600-97829000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr3:97829000-97829800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr3:97829000-97830200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr3:97830200-97830400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr3:97830200-97830400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
12	chr3:97834800-97835000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr3:97837600-97838000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:97855400-97855600	Enhancers	GM12878-XiMat	blood
15	chr3:97855800-97856800	Weak transcription	GM12878-XiMat	blood
16	chr3:97856800-97857400	Enhancers	GM12878-XiMat	blood
17	chr3:97857800-97858800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:97858200-97858400	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:97858200-97858600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr3:97858200-97859200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:97858200-97859200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:97858200-97859800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr3:97858200-97860000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:97858200-97866400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr3:97858400-97858800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr3:97858800-97859400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr3:97858800-97859600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr3:97859200-97859800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr3:97859800-97860800	Enhancers	Fetal Brain Male	brain
30	chr3:97860000-97860200	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr3:97870000-97870600	Enhancers	Fetal Heart	heart
32	chr3:97889000-97890800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr3:97899200-97899400	Active TSS	Monocytes-CD14+_RO01746	blood
34	chr3:97899400-97899800	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr3:97899400-97900000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr3:97899400-97900800	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr3:97900000-97900200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr3:97900400-97902000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr3:97900400-97902400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:97901000-97901800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr3:97901000-97902200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr3:97901400-97902000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr3:97901400-97902000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr3:97901400-97902200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:97902000-97907000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr3:97902200-97906400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:97902200-97907200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr3:97902400-97907000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr3:97906400-97906800	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr3:97906800-97907000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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