Variant report

Variant	nsv589856
Chromosome Location	chr3:20305232-20436493
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:754)
CpG islands
(count:245)
Chromatin interactive
region (count:55)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:754 , 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	chr3:20366598-20367214	K562	blood:	n/a	n/a
2	ARID3A	chr3:20362800-20363279	K562	blood:	n/a	n/a
3	ARID3A	chr3:20361861-20362463	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:20368591-20368761	K562	blood:	n/a	n/a
5	ARID3A	chr3:20363620-20364094	K562	blood:	n/a	chr3:20363734-20363750
6	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:20364750-20365312	K562	blood:	n/a	n/a
8	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
9	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
10	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
11	ARID3A	chr3:20371522-20371864	K562	blood:	n/a	n/a
12	ATF1	chr3:20364790-20365451	K562	blood:	n/a	n/a
13	ATF1	chr3:20366606-20366910	K562	blood:	n/a	n/a
14	ATF1	chr3:20346503-20346616	K562	blood:	n/a	n/a
15	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
17	BACH1	chr3:20366536-20366578	K562	blood:	n/a	n/a
18	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:20363669-20363903	K562	blood:	n/a	n/a
20	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
21	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
22	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:20371437-20371693	H1-hESC	embryonic stem cell:	n/a	n/a
24	BHLHE40	chr3:20394266-20394730	K562	blood:	n/a	n/a
25	BHLHE40	chr3:20306641-20306956	K562	blood:	n/a	n/a
26	BHLHE40	chr3:20371536-20371904	K562	blood:	n/a	n/a
27	BHLHE40	chr3:20361903-20362390	HepG2	liver:	n/a	n/a
28	BHLHE40	chr3:20381816-20382255	K562	blood:	n/a	n/a
29	BHLHE40	chr3:20364697-20365365	K562	blood:	n/a	n/a
30	BHLHE40	chr3:20366210-20366396	K562	blood:	n/a	n/a
31	BHLHE40	chr3:20355407-20355580	A549	lung:	n/a	n/a
32	BRCA1	chr3:20381852-20382113	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr3:20347626-20347963	K562	blood:	n/a	n/a
34	CBX3	chr3:20347694-20347925	K562	blood:	n/a	n/a
35	CBX3	chr3:20394150-20394723	K562	blood:	n/a	chr3:20394644-20394655
36	CBX3	chr3:20346385-20346769	K562	blood:	n/a	n/a
37	CBX3	chr3:20324264-20324647	K562	blood:	n/a	n/a
38	CBX3	chr3:20364770-20365367	K562	blood:	n/a	n/a
39	CBX3	chr3:20366551-20367349	K562	blood:	n/a	n/a
40	CBX3	chr3:20324344-20324598	K562	blood:	n/a	n/a
41	CCNT2	chr3:20364768-20365575	K562	blood:	n/a	n/a
42	CCNT2	chr3:20366682-20366882	K562	blood:	n/a	n/a
43	CCNT2	chr3:20371431-20371945	K562	blood:	n/a	n/a
44	CCNT2	chr3:20394423-20394638	K562	blood:	n/a	n/a
45	CCNT2	chr3:20372976-20373098	K562	blood:	n/a	n/a
46	CCNT2	chr3:20361414-20361646	K562	blood:	n/a	n/a
47	CCNT2	chr3:20362758-20363417	K562	blood:	n/a	chr3:20363078-20363098
48	CEBPB	chr3:20364877-20365116	Hela-S3	cervix:	n/a	chr3:20364966-20364977
49	CEBPB	chr3:20394100-20394376	HepG2	liver:	n/a	chr3:20394224-20394235
50	CEBPB	chr3:20381826-20382192	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20371290-20371340	HEEpiC	esophagus:	n/a
2	chr3:20371290-20371340	HEEpiC	esophagus:	n/a
3	chr3:20418856-20418906	HEK293	kidney:	embryo
4	chr3:20321584-20321634	AG10803	skin:	n/a
5	chr3:20412342-20412392	HIPEpiC	eye:	n/a
6	chr3:20321584-20321634	SK-N-SH	brain:	n/a
7	chr3:20418856-20418906	Jurkat	blood:	n/a
8	chr3:20371290-20371340	GM12892	blood:	n/a
9	chr3:20321584-20321634	PFSK-1	brain:	n/a
10	chr3:20321584-20321634	ProgFib	skin:	n/a
11	chr3:20418856-20418906	NHDF-neo	bronchial:	n/a
12	chr3:20371290-20371340	PANC-1	pancreas:	n/a
13	chr3:20412342-20412392	MCF-7	breast:	n/a
14	chr3:20321584-20321634	HAEpiC	amniotic membrane:	n/a
15	chr3:20412342-20412392	AG10803	skin:	n/a
16	chr3:20371290-20371340	K562	blood:	n/a
17	chr3:20371290-20371340	HNPCEpiC	eye:	n/a
18	chr3:20418856-20418906	AoSMC	blood vessel:	n/a
19	chr3:20321584-20321634	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:20321584-20321634	GM06990	blood:	n/a
21	chr3:20418856-20418906	AG09309	skin:	n/a
22	chr3:20371290-20371340	HL-60	blood:	n/a
23	chr3:20371290-20371340	HCF	heart:	n/a
24	chr3:20321584-20321634	K562	blood:	n/a
25	chr3:20418856-20418906	K562	blood:	n/a
26	chr3:20371290-20371340	AG09319	gingival:	n/a
27	chr3:20418856-20418906	AG04449	skin:	fetal
28	chr3:20418856-20418906	RPTEC	kidney:	n/a
29	chr3:20418856-20418906	Hepatocyte	liver:	n/a
30	chr3:20371290-20371340	ProgFib	skin:	n/a
31	chr3:20371290-20371340	NHDF-neo	bronchial:	n/a
32	chr3:20418856-20418906	GM06990	blood:	n/a
33	chr3:20371290-20371340	HAEpiC	amniotic membrane:	n/a
34	chr3:20418856-20418906	HCF	heart:	n/a
35	chr3:20412342-20412392	NH-A	brain:	n/a
36	chr3:20412342-20412392	BE2_C	brain:	n/a
37	chr3:20418856-20418906	PrEC	prostate:	n/a
38	chr3:20371290-20371340	HepG2	liver:	n/a
39	chr3:20412342-20412392	NT2-D1	testis:	n/a
40	chr3:20321584-20321634	HMEC	breast:	n/a
41	chr3:20321584-20321634	Caco-2	colon:	n/a
42	chr3:20371290-20371340	HCM	heart:	n/a
43	chr3:20412342-20412392	SK-N-MC	brain:	n/a
44	chr3:20371290-20371340	GM06990	blood:	n/a
45	chr3:20412342-20412392	ECC-1	luminal epithelium:	n/a
46	chr3:20321584-20321634	MCF10A-Er-Src	breast:	n/a
47	chr3:20321584-20321634	T-47D	breast:	n/a
48	chr3:20321584-20321634	HepG2	liver:	n/a
49	chr3:20418856-20418906	SK-N-SH_RA	brain:	n/a
50	chr3:20371290-20371340	Hela-S3	cervix:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
2	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
3	chr3:20344022..20346742-chr3:20354498..20357355,2	K562	blood:
4	chr3:20225982..20227551-chr3:20349845..20352725,2	K562	blood:
5	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
6	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
7	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
8	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
9	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
10	chr3:20361855..20364563-chr3:20364654..20366618,2	K562	blood:
11	chr3:20358544..20361265-chr3:20365566..20368705,3	K562	blood:
12	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
13	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
14	chr20:55749599..55750399-chr3:20381742..20382481,2	MCF-7	breast:
15	chr3:20342900..20345810-chr3:20347041..20349478,2	K562	blood:
16	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
17	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
18	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
19	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
20	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
21	chr3:20352341..20352841-chr6:144261197..144261734,2	MCF-7	breast:
22	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
23	chr3:20248922..20251335-chr3:20323167..20325698,2	K562	blood:
24	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
25	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:
26	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
27	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
28	chr3:20365682..20367813-chr3:20369993..20373801,3	K562	blood:
29	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
30	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
31	chr3:20361855..20364563-chr3:20364654..20366618,2	K562	blood:
32	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
33	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
34	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
35	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
36	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
37	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
38	chr3:20369262..20370826-chr3:20371574..20373222,2	K562	blood:
39	chr3:20381671..20382483-chr3:21592493..21593315,3	MCF-7	breast:
40	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
41	chr3:20381763..20382471-chr3:21525223..21526354,4	MCF-7	breast:
42	chr3:20358467..20362257-chr3:20366935..20370675,4	K562	blood:
43	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
44	chr3:20346246..20348359-chr3:20361269..20362788,2	K562	blood:
45	chr3:20363426..20365605-chr3:20367558..20369154,2	K562	blood:
46	chr3:20368039..20370603-chr3:20372170..20374733,2	K562	blood:
47	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
48	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
49	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
50	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
2	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
3	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
4	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
5	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595
6	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
7	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
8	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
9	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
10	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595

No data

Variant related genes	Relation type
RNU6-822P	TF binding region
ENSG00000231304	TF binding region
ENSG00000261734	TF binding region
RNU6-822P	CpG island
ENSG00000231304	CpG island
ENSG00000261734	CpG island

Extended variants
information (count: 4820 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4820 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1395988	chr3:20305232-20305233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9854447	chr3:20305234-20305235	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs548757456	chr3:20305249-20305250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567354330	chr3:20305268-20305269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531245063	chr3:20305269-20305270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193070495	chr3:20305276-20305277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs954797	chr3:20305293-20305294	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs538520837	chr3:20305327-20305328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79626153	chr3:20305338-20305339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565698479	chr3:20305356-20305357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs1395987	chr3:20305362-20305363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs142620334	chr3:20305369-20305370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576602307	chr3:20305378-20305379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs954798	chr3:20305396-20305397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558970099	chr3:20305399-20305400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146847058	chr3:20305436-20305437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10552096	chr3:20305444-20305445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs1395986	chr3:20305445-20305446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs151299053	chr3:20305449-20305450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530276722	chr3:20305489-20305490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542398263	chr3:20305505-20305506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11707483	chr3:20305516-20305517	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs73818868	chr3:20305529-20305530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs540909864	chr3:20305537-20305538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549391219	chr3:20305551-20305552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140525190	chr3:20305646-20305647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs1507801	chr3:20305654-20305655	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370176710	chr3:20305707-20305708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs547330390	chr3:20305721-20305722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565963450	chr3:20305745-20305746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567369174	chr3:20305758-20305759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536098438	chr3:20305775-20305776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554734459	chr3:20305843-20305844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570192468	chr3:20305849-20305850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373828455	chr3:20305886-20305887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11916194	chr3:20305912-20305913	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs9837930	chr3:20305925-20305926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs11923947	chr3:20305930-20305931	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs541411162	chr3:20305931-20305932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553428747	chr3:20305972-20305973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556157690	chr3:20306034-20306035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575059792	chr3:20306042-20306043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542083499	chr3:20306071-20306072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142796074	chr3:20306100-20306101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144973454	chr3:20306134-20306135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138781050	chr3:20306135-20306136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185070374	chr3:20306164-20306165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368961415	chr3:20306170-20306171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200276228	chr3:20306183-20306184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75152424	chr3:20306186-20306187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20296200-20310800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:20296600-20306200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:20306200-20306600	Enhancers	Placenta	Placenta
4	chr3:20306200-20306800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:20306200-20306800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:20306200-20307000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:20306400-20306800	Enhancers	HepG2	liver
8	chr3:20306800-20307000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:20309600-20312000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:20316600-20318600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:20317600-20329000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:20317800-20318200	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr3:20318600-20319400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:20319400-20319800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:20319400-20320400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr3:20319800-20320800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:20320400-20322400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr3:20320400-20322600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:20320800-20322200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:20321600-20322200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr3:20321600-20322200	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr3:20321600-20322200	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr3:20321600-20322200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr3:20321600-20322400	Enhancers	Primary B cells from peripheral blood	blood
25	chr3:20321600-20322400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
26	chr3:20321800-20322000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:20321800-20322200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr3:20322000-20329800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr3:20322200-20322600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:20322200-20322600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr3:20322600-20322800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:20322600-20325800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:20322800-20323000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr3:20324000-20324800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:20325600-20325800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
36	chr3:20325600-20325800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:20325800-20330200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:20326200-20331000	Weak transcription	Pancreas	Pancrea
39	chr3:20327400-20331000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:20328800-20331200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chr3:20329000-20329800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
42	chr3:20329000-20330200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
43	chr3:20329200-20329600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
44	chr3:20331000-20331200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:20331000-20331200	ZNF genes & repeats	Pancreas	Pancrea
46	chr3:20336600-20337000	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
47	chr3:20337000-20344800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr3:20344000-20344800	Enhancers	Fetal Heart	heart
49	chr3:20344200-20345000	Enhancers	Fetal Brain Male	brain
50	chr3:20347000-20347200	Active TSS	K562	blood

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