Variant report

Variant	nsv877210
Chromosome Location	chr3:97866177-97992964
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:666)
CpG islands
(count:549)
Chromatin interactive
region (count:8)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	ATF2	chr3:97915093-97915523	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr3:97959089-97959288	GM12878	blood:	n/a	chr3:97959202-97959213
4	BATF	chr3:97952380-97952574	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:97895161-97895345	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:97951400-97951563	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:97952351-97952515	GM12878	blood:	n/a	n/a
8	BCL3	chr3:97916362-97916553	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:97943474-97943485	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:97951405-97952685	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:97907429-97907720	GM12878	blood:	n/a	n/a
12	BHLHE40	chr3:97962720-97963131	HepG2	liver:	n/a	n/a
13	BRCA1	chr3:97939937-97940001	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:97907317-97907430	GM12878	blood:	n/a	n/a
15	CEBPB	chr3:97922385-97922736	HepG2	liver:	n/a	chr3:97922556-97922567
16	CEBPB	chr3:97984146-97984209	HepG2	liver:	n/a	chr3:97984150-97984161
17	CEBPB	chr3:97962794-97963080	HepG2	liver:	n/a	n/a
18	CEBPB	chr3:97873705-97874032	HepG2	liver:	n/a	chr3:97873850-97873861
19	CEBPB	chr3:97922385-97922691	A549	lung:	n/a	chr3:97922556-97922567
20	CHD1	chr3:97959991-97960022	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr3:97952484-97952829	GM12878	blood:	n/a	n/a
22	CHD1	chr3:97907603-97907803	GM12878	blood:	n/a	n/a
23	CHD1	chr3:97942962-97942975	GM12878	blood:	n/a	n/a
24	CHD2	chr3:97907426-97907647	GM12878	blood:	n/a	n/a
25	CHD2	chr3:97952077-97952654	GM12878	blood:	n/a	n/a
26	CTCF	chr3:97904183-97904274	GM10266	blood:	n/a	n/a
27	CTCF	chr3:97952340-97952490	GM06990	blood:	n/a	n/a
28	CTCF	chr3:97978660-97978810	HCFaa	heart:	n/a	n/a
29	CTCF	chr3:97904200-97904350	A549	lung:	n/a	n/a
30	CTCF	chr3:97907483-97907663	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:97978440-97978590	GM12872	blood:	n/a	n/a
32	CTCF	chr3:97978677-97978902	GM19240	blood:	n/a	n/a
33	CTCF	chr3:97907540-97907690	AG04450	lung:	n/a	n/a
34	CTCF	chr3:97907480-97907630	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr3:97978760-97978910	GM12865	blood:	n/a	n/a
36	CTCF	chr3:97903808-97904617	HCT-116	colon:	n/a	n/a
37	CTCF	chr3:97904160-97904310	GM12869	blood:	n/a	n/a
38	CTCF	chr3:97907540-97907690	GM12864	blood:	n/a	n/a
39	CTCF	chr3:97907480-97907630	HFF	foreskin:	n/a	n/a
40	CTCF	chr3:97978700-97978850	HMEC	breast:	n/a	n/a
41	CTCF	chr3:97904080-97904230	GM12870	blood:	n/a	n/a
42	CTCF	chr3:97978700-97978850	AG04450	lung:	n/a	n/a
43	CTCF	chr3:97907465-97907743	IMR90	lung:	n/a	n/a
44	CTCF	chr3:97907500-97907650	HepG2	liver:	n/a	n/a
45	CTCF	chr3:97907820-97907970	GM12865	blood:	n/a	n/a
46	CTCF	chr3:97978675-97978877	GM12878	blood:	n/a	n/a
47	CTCF	chr3:97907500-97907669	GM20000	blood:	n/a	n/a
48	CTCF	chr3:97978726-97978848	GM10266	blood:	n/a	n/a
49	CTCF	chr3:97978720-97978870	GM12864	blood:	n/a	n/a
50	CTCF	chr3:97907520-97907670	SAEC	small airway:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:97982830-97982880	HNPCEpiC	eye:	n/a
2	chr3:97887864-97887914	GM12878	blood:	n/a
3	chr3:97886603-97886653	HEEpiC	esophagus:	n/a
4	chr3:97983540-97983590	AG09319	gingival:	n/a
5	chr3:97982397-97982447	SK-N-SH_RA	brain:	n/a
6	chr3:97982830-97982880	Jurkat	blood:	n/a
7	chr3:97886467-97886517	SKMC	muscle:	n/a
8	chr3:97867758-97867808	AoSMC	blood vessel:	n/a
9	chr3:97886603-97886653	GM12891	blood:	n/a
10	chr3:97868656-97868706	SK-N-SH_RA	brain:	n/a
11	chr3:97886603-97886653	MCF10A-Er-Src	breast:	n/a
12	chr3:97983253-97983303	T-47D	breast:	n/a
13	chr3:97887864-97887914	ovcar-3	ovarian:	n/a
14	chr3:97983253-97983303	HCT-116	colon:	n/a
15	chr3:97868656-97868706	GM12892	blood:	n/a
16	chr3:97887864-97887914	HCM	heart:	n/a
17	chr3:97982397-97982447	HIPEpiC	eye:	n/a
18	chr3:97868656-97868706	HL-60	blood:	n/a
19	chr3:97868656-97868706	HNPCEpiC	eye:	n/a
20	chr3:97983540-97983590	BE2_C	brain:	n/a
21	chr3:97982397-97982447	MCF10A-Er-Src	breast:	n/a
22	chr3:97886467-97886517	HepG2	liver:	n/a
23	chr3:97983253-97983303	HCM	heart:	n/a
24	chr3:97983253-97983303	SK-N-SH_RA	brain:	n/a
25	chr3:97982830-97982880	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:97982830-97982880	AG09309	skin:	n/a
27	chr3:97867758-97867808	GM06990	blood:	n/a
28	chr3:97983253-97983303	NB4	blood:	n/a
29	chr3:97886603-97886653	LNCaP	prostate:	n/a
30	chr3:97867758-97867808	Hela-S3	cervix:	n/a
31	chr3:97867758-97867808	HL-60	blood:	n/a
32	chr3:97886467-97886517	HRPEpiC	eye:	n/a
33	chr3:97983540-97983590	GM12878	blood:	n/a
34	chr3:97867758-97867808	Hepatocyte	liver:	n/a
35	chr3:97983540-97983590	HCT-116	colon:	n/a
36	chr3:97887864-97887914	SKMC	muscle:	n/a
37	chr3:97867758-97867808	BE2_C	brain:	n/a
38	chr3:97983253-97983303	AG10803	skin:	n/a
39	chr3:97868656-97868706	HepG2	liver:	n/a
40	chr3:97982830-97982880	RPTEC	kidney:	n/a
41	chr3:97982830-97982880	A549	lung:	n/a
42	chr3:97886603-97886653	Hepatocyte	liver:	n/a
43	chr3:97983253-97983303	ProgFib	skin:	n/a
44	chr3:97983540-97983590	Hela-S3	cervix:	n/a
45	chr3:97887864-97887914	PANC-1	pancreas:	n/a
46	chr3:97983253-97983303	HUVEC	blood vessel:	n/a
47	chr3:97867758-97867808	SK-N-SH_RA	brain:	n/a
48	chr3:97982830-97982880	HRPEpiC	eye:	n/a
49	chr3:97887864-97887914	HCT-116	colon:	n/a
50	chr3:97887864-97887914	HRPEpiC	eye:	n/a

(count:8 , 50 per page) page: 1

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

(count:22 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 3991 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3991 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4857072	chr3:97866177-97866178	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370364957	chr3:97866181-97866182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370931030	chr3:97866202-97866203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182533062	chr3:97866212-97866213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565354263	chr3:97866238-97866239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563517797	chr3:97866247-97866248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150276968	chr3:97866248-97866249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567352137	chr3:97866266-97866267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530012814	chr3:97866310-97866311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368008276	chr3:97866318-97866319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201067806	chr3:97866332-97866333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111863902	chr3:97866345-97866346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372439109	chr3:97866362-97866363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575646771	chr3:97866902-97866903	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs544426866	chr3:97866916-97866917	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs545516776	chr3:97866960-97866961	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs539867084	chr3:97867758-97867759	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
18	rs566770717	chr3:97867763-97867764	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
19	rs539310184	chr3:97867764-97867765	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
20	rs72927982	chr3:97867772-97867773	Inactive region	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs573543283	chr3:97867779-97867780	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
22	rs144295217	chr3:97867794-97867795	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
23	rs34031148	chr3:97867806-97867807	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
24	rs541769203	chr3:97868216-97868217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs143136689	chr3:97868231-97868232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs374375074	chr3:97868245-97868246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139958192	chr3:97868257-97868258	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs112019994	chr3:97868258-97868259	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs7433910	chr3:97868296-97868297	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369829680	chr3:97868297-97868298	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs146669592	chr3:97868307-97868308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs540702892	chr3:97868314-97868315	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs113602332	chr3:97868323-97868324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs373319419	chr3:97868331-97868332	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs143981381	chr3:97868342-97868343	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs146466887	chr3:97868389-97868390	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs143765725	chr3:97868391-97868392	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs146577101	chr3:97868656-97868657	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs149145758	chr3:97868657-97868658	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs377657013	chr3:97868665-97868666	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs148337288	chr3:97868670-97868671	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs374940876	chr3:97868673-97868674	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs145464091	chr3:97868675-97868676	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs528002845	chr3:97868677-97868678	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs78410857	chr3:97868683-97868684	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs368007526	chr3:97868690-97868691	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs181133249	chr3:97868703-97868704	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs139547938	chr3:97869057-97869058	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558065491	chr3:97869072-97869073	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs576225122	chr3:97869074-97869075	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:97858200-97866400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:97870000-97870600	Enhancers	Fetal Heart	heart
3	chr3:97889000-97890800	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr3:97899200-97899400	Active TSS	Monocytes-CD14+_RO01746	blood
5	chr3:97899400-97899800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr3:97899400-97900000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
7	chr3:97899400-97900800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:97900000-97900200	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr3:97900400-97902000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:97900400-97902400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr3:97901000-97901800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr3:97901000-97902200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:97901400-97902000	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:97901400-97902000	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr3:97901400-97902200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:97902000-97907000	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr3:97902200-97906400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr3:97902200-97907200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:97902400-97907000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr3:97906400-97906800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr3:97906800-97907000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr3:97906800-97907000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:97906800-97908000	Enhancers	Primary hematopoietic stem cells	blood
24	chr3:97906800-97908400	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr3:97907000-97907400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr3:97907000-97908000	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr3:97907000-97908000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr3:97907000-97908200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr3:97907000-97910200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:97907200-97907600	Enhancers	Primary T cells from cord blood	blood
31	chr3:97907200-97907600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr3:97907200-97907600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:97907200-97907600	Enhancers	GM12878-XiMat	blood
34	chr3:97907200-97907800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:97907400-97908400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr3:97908200-97908600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr3:97908400-97910000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr3:97908600-97908800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:97908800-97910800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr3:97910000-97912200	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr3:97910200-97910400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:97910200-97910800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:97910400-97913600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:97910800-97911400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:97910800-97913800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr3:97911400-97911600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr3:97911600-97912000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr3:97912000-97912600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr3:97912200-97914600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr3:97912600-97916000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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