Variant report

Variant	esv1842860
Chromosome Location	chr3:97934241-98075543
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1063)
CpG islands
(count:610)
Chromatin interactive
region (count:19)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1063 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

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	ATF2	chr3:98045698-98046184	GM12878	blood:	n/a	n/a
4	ATF2	chr3:98050104-98050581	GM12878	blood:	n/a	n/a
5	ATF2	chr3:98045677-98046241	GM12878	blood:	n/a	n/a
6	BATF	chr3:98050107-98050554	GM12878	blood:	n/a	n/a
7	BATF	chr3:98045742-98046208	GM12878	blood:	n/a	n/a
8	BATF	chr3:98045659-98046193	GM12878	blood:	n/a	n/a
9	BATF	chr3:97959089-97959288	GM12878	blood:	n/a	chr3:97959202-97959213
10	BATF	chr3:97952380-97952574	GM12878	blood:	n/a	n/a
11	BATF	chr3:98050208-98050500	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:98045737-98046165	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:98050132-98050565	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:98050243-98050485	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:97952351-97952515	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:97951400-97951563	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:98062746-98063153	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:97962720-97963131	HepG2	liver:	n/a	n/a
19	BHLHE40	chr3:98062891-98063160	K562	blood:	n/a	n/a
20	BHLHE40	chr3:98062760-98063061	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:97943474-97943485	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:97951405-97952685	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:98045895-98046126	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:98048379-98048647	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:98048430-98048676	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr3:98043403-98043413	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr3:97939937-97940001	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:98044286-98044467	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:98010460-98010640	HepG2	liver:	n/a	n/a
30	CEBPB	chr3:98053127-98053379	HepG2	liver:	n/a	chr3:98053236-98053247
31	CEBPB	chr3:98069049-98069253	K562	blood:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
32	CEBPB	chr3:98068963-98069272	ECC-1	luminal epithelium:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
33	CEBPB	chr3:98068948-98069309	H1-hESC	embryonic stem cell:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
34	CEBPB	chr3:98010377-98010684	HepG2	liver:	n/a	n/a
35	CEBPB	chr3:97984146-97984209	HepG2	liver:	n/a	chr3:97984150-97984161
36	CEBPB	chr3:98068961-98069314	IMR90	lung:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
37	CEBPB	chr3:98048409-98048634	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:98067971-98068208	K562	blood:	n/a	n/a
39	CEBPB	chr3:97962794-97963080	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:98069002-98069319	A549	lung:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
41	CEBPB	chr3:98068959-98069305	HepG2	liver:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
42	CEBPB	chr3:98068982-98069307	A549	lung:	n/a	chr3:98069128-98069137 chr3:98069126-98069139 chr3:98069128-98069137 chr3:98069128-98069137 chr3:98069128-98069137
43	CHD1	chr3:98048613-98048751	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:97952484-97952829	GM12878	blood:	n/a	n/a
45	CHD1	chr3:98044229-98044718	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr3:97959991-97960022	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr3:98060210-98060264	GM12878	blood:	n/a	n/a
48	CHD1	chr3:98045157-98045436	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr3:98043379-98043837	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr3:97942962-97942975	GM12878	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:97983253-97983303	PFSK-1	brain:	n/a
2	chr3:97983540-97983590	Hela-S3	cervix:	n/a
3	chr3:98072423-98072473	A549	lung:	n/a
4	chr3:98001269-98001319	PFSK-1	brain:	n/a
5	chr3:98000733-98000783	NH-A	brain:	n/a
6	chr3:98072423-98072473	ProgFib	skin:	n/a
7	chr3:98047673-98047723	A549	lung:	n/a
8	chr3:98073044-98073094	PFSK-1	brain:	n/a
9	chr3:97982830-97982880	IMR90	lung:	fetal
10	chr3:97983253-97983303	GM12892	blood:	n/a
11	chr3:97982397-97982447	NHBE	bronchial:	n/a
12	chr3:97983253-97983303	SK-N-SH_RA	brain:	n/a
13	chr3:98001736-98001786	IMR90	lung:	fetal
14	chr3:97982830-97982880	NB4	blood:	n/a
15	chr3:97982397-97982447	HRE	kidney:	n/a
16	chr3:98072423-98072473	GM06990	blood:	n/a
17	chr3:97982397-97982447	Jurkat	blood:	n/a
18	chr3:98073044-98073094	SK-N-SH_RA	brain:	n/a
19	chr3:98001736-98001786	RPTEC	kidney:	n/a
20	chr3:98072423-98072473	HRPEpiC	eye:	n/a
21	chr3:98001736-98001786	PANC-1	pancreas:	n/a
22	chr3:98000733-98000783	GM12878	blood:	n/a
23	chr3:98000733-98000783	GM19239	blood:	n/a
24	chr3:97982397-97982447	SK-N-SH_RA	brain:	n/a
25	chr3:98073044-98073094	GM12892	blood:	n/a
26	chr3:97982397-97982447	HAEpiC	amniotic membrane:	n/a
27	chr3:98073044-98073094	GM12891	blood:	n/a
28	chr3:98073044-98073094	Jurkat	blood:	n/a
29	chr3:97982830-97982880	HCT-116	colon:	n/a
30	chr3:98073044-98073094	HRE	kidney:	n/a
31	chr3:98072423-98072473	PFSK-1	brain:	n/a
32	chr3:97982397-97982447	U87	brain:	n/a
33	chr3:98072423-98072473	HCT-116	colon:	n/a
34	chr3:97982830-97982880	SK-N-SH_RA	brain:	n/a
35	chr3:98000733-98000783	LNCaP	prostate:	n/a
36	chr3:98000733-98000783	Hela-S3	cervix:	n/a
37	chr3:98047673-98047723	RPTEC	kidney:	n/a
38	chr3:98073044-98073094	A549	lung:	n/a
39	chr3:98072423-98072473	BE2_C	brain:	n/a
40	chr3:97983253-97983303	ovcar-3	ovarian:	n/a
41	chr3:98001269-98001319	LNCaP	prostate:	n/a
42	chr3:98001736-98001786	AoSMC	blood vessel:	n/a
43	chr3:97982830-97982880	HL-60	blood:	n/a
44	chr3:98073044-98073094	SKMC	muscle:	n/a
45	chr3:97983253-97983303	NH-A	brain:	n/a
46	chr3:97982397-97982447	Hela-S3	cervix:	n/a
47	chr3:97982397-97982447	HRCEpiC	kidney:	n/a
48	chr3:97982397-97982447	Caco-2	colon:	n/a
49	chr3:98001269-98001319	PrEC	prostate:	n/a
50	chr3:98073044-98073094	K562	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:97904894..97907628-chr3:98045904..98048505,2	K562	blood:
2	chr3:97758368..97758971-chr3:98062622..98063411,2	MCF-7	breast:
3	chr3:98067412..98069433-chr3:98072322..98074885,2	K562	blood:
4	chr3:97978738..97980851-chr3:98012803..98015207,2	MCF-7	breast:
5	chr3:97978738..97980851-chr3:98012803..98015207,2	MCF-7	breast:
6	chr3:98047998..98048939-chr3:98062458..98063084,2	MCF-7	breast:
7	chr3:98053614..98055772-chr3:98057619..98059779,2	K562	blood:
8	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:
9	chr3:97907135..97908282-chr3:98048120..98049025,6	MCF-7	breast:
10	chr3:98053614..98055772-chr3:98057619..98059779,2	K562	blood:
11	chr3:97758193..97758817-chr3:98047055..98047815,3	MCF-7	breast:
12	chr3:98043669..98046299-chr3:98046855..98049975,3	K562	blood:
13	chr3:98047998..98048939-chr3:98062458..98063084,2	MCF-7	breast:
14	chr3:97757871..97759038-chr3:98048078..98048948,5	K562	blood:
15	chr3:97907135..97908080-chr3:98062563..98063391,2	MCF-7	breast:
16	chr3:97757588..97759255-chr3:98048075..98049104,20	MCF-7	breast:
17	chr3:97977847..97980147-chr3:97980537..97982058,2	MCF-7	breast:
18	chr3:98043669..98046299-chr3:98046855..98049975,3	K562	blood:
19	chr3:97758056..97758983-chr3:98048226..98049035,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
2	lnc-OR5H6-1	chr3:97952495-97952520	ENSG00000251088.1
3	lnc-OR5H6-1	chr3:98061235-98061273	ENSG00000251088.1
4	lnc-OR5H6-1	chr3:98030730-98030852	ENSG00000251088.1
5	lnc-MINA-2	chr3:97954530-97954692	XLOC_003187
6	lnc-MINA-2	chr3:97956121-97956211	XLOC_003187
7	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
8	lnc-MINA-2	chr3:97956121-97956219	XLOC_003187
9	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
10	lnc-MINA-2	chr3:97949910-97950089	XLOC_003187
11	lnc-MINA-2	chr3:97956121-97956217	XLOC_003187
12	lnc-MINA-2	chr3:97955718-97955882	XLOC_003187
13	lnc-MINA-2	chr3:97954345-97954692	XLOC_003187

No data

Variant related genes	Relation type
OR5K4	TF binding region
OR5H6	TF binding region
ENSG00000251088	TF binding region
OR5H7P	TF binding region
OR5H4P	TF binding region
OR5H2	TF binding region
OR5H8P	TF binding region
OR5K4	CpG island
OR5H6	CpG island
ENSG00000251088	CpG island
OR5H7P	CpG island
OR5H4P	CpG island
OR5H2	CpG island
OR5H8P	CpG island
ENSG00000196098	chromatin interactions
POU2F1	miRNA target sites

Extended variants
information (count: 3431 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3431 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9821499	chr3:97934241-97934242	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572479214	chr3:97934242-97934243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150017328	chr3:97934259-97934260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563982002	chr3:97934272-97934273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532971431	chr3:97934273-97934274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375511431	chr3:97934274-97934275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573714165	chr3:97934296-97934297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545329918	chr3:97934318-97934319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111536159	chr3:97934350-97934351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372819535	chr3:97934351-97934352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73853707	chr3:97934360-97934361	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73853708	chr3:97934369-97934370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs55956513	chr3:97934382-97934383	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183087250	chr3:97934441-97934442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528241246	chr3:97934489-97934490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112529340	chr3:97934511-97934512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs545007214	chr3:97934516-97934517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11720576	chr3:97934521-97934522	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112444001	chr3:97934528-97934529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570288713	chr3:97934542-97934543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187423511	chr3:97934559-97934560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113707559	chr3:97934567-97934568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555527692	chr3:97934604-97934605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199919699	chr3:97934611-97934612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78591056	chr3:97934612-97934613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572200113	chr3:97934618-97934619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541087845	chr3:97934619-97934620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs55655921	chr3:97934649-97934650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs192073359	chr3:97934680-97934681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11708500	chr3:97934693-97934694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543266056	chr3:97934698-97934699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183526175	chr3:97934716-97934717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531784251	chr3:97934718-97934719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188742447	chr3:97934744-97934745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34979809	chr3:97934747-97934748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141083499	chr3:97934763-97934764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6439692	chr3:97934799-97934800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs542605064	chr3:97934809-97934810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192813228	chr3:97934810-97934811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528101510	chr3:97934854-97934855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs16839374	chr3:97934902-97934903	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs386663710	chr3:97934918-97934919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142598958	chr3:97934919-97934920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1497533	chr3:97934961-97934962	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs565900523	chr3:97935000-97935001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570328908	chr3:97935064-97935065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147990147	chr3:97935102-97935103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535816235	chr3:97935113-97935114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549662664	chr3:97935118-97935119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1497534	chr3:97935125-97935126	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:60)

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
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97928200-97936800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr3:97932800-97936200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:97933800-97938000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr3:97934000-97934400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:97936200-97936800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr3:97936800-97937600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:97936800-97937800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:97937600-97938000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:97937800-97942400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:97938000-97938200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr3:97942400-97943400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:97943400-97944000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr3:97944000-97944200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr3:97945200-97945600	Active TSS	Esophagus	oesophagus
15	chr3:97951200-97952800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr3:97951400-97952200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:97951600-97952800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr3:97951800-97952200	Enhancers	Primary hematopoietic stem cells	blood
19	chr3:97952200-97952600	Flanking Active TSS	Primary hematopoietic stem cells	blood
20	chr3:97952200-97952600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:97952600-97953400	Enhancers	Primary hematopoietic stem cells	blood
22	chr3:97952600-97953600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:97958600-97959400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr3:97959000-97959600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:97959000-97961600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:97959200-97960600	Enhancers	H9 Cell Line	embryonic stem cell
27	chr3:97959200-97961400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr3:97959200-97961400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr3:97959200-97961800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr3:97959400-97961400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr3:97959600-97960000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr3:97959800-97960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:97959800-97960600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:97959800-97962000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr3:97960000-97961800	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr3:97962600-97964000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:97970200-97973400	Weak transcription	Fetal Heart	heart
38	chr3:97974200-97974400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr3:97974400-97975000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr3:97974600-97975400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr3:97974600-97975800	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr3:97974600-97975800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr3:97974800-97975400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr3:97974800-97975400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr3:97975000-97975600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr3:97975200-97975600	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr3:97989600-97990000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr3:97990000-97991000	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr3:97990400-97991600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr3:97991000-97991200	Enhancers	HUES6 Cell Line	embryonic stem cell

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