Variant report

Variant	esv1796699
Chromosome Location	chr3:20278414-20335900
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:169)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:169 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
2	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
3	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
4	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
5	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:20306641-20306956	K562	blood:	n/a	n/a
8	CBX3	chr3:20324264-20324647	K562	blood:	n/a	n/a
9	CBX3	chr3:20324344-20324598	K562	blood:	n/a	n/a
10	CEBPB	chr3:20287304-20287598	MCF-7	breast:	n/a	n/a
11	CEBPB	chr3:20325166-20325366	K562	blood:	n/a	chr3:20325251-20325264 chr3:20325252-20325263 chr3:20325251-20325262 chr3:20325251-20325264 chr3:20325251-20325264
12	CEBPB	chr3:20298924-20299012	K562	blood:	n/a	chr3:20298947-20298958
13	CEBPB	chr3:20325107-20325384	HepG2	liver:	n/a	chr3:20325251-20325264 chr3:20325252-20325263 chr3:20325116-20325127 chr3:20325251-20325262 chr3:20325251-20325264 chr3:20325251-20325264
14	CEBPB	chr3:20298810-20299031	HepG2	liver:	n/a	chr3:20298947-20298958
15	CTCF	chr3:20287320-20287470	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr3:20287380-20287530	GM12866	blood:	n/a	n/a
17	CTCF	chr3:20287360-20287510	GM12865	blood:	n/a	n/a
18	CTCF	chr3:20287348-20287558	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr3:20287379-20287547	MCF-7	breast:	n/a	n/a
20	CTCF	chr3:20287420-20287570	HCFaa	heart:	n/a	n/a
21	CTCF	chr3:20288240-20288390	HepG2	liver:	n/a	n/a
22	CTCF	chr3:20287400-20287550	GM12871	blood:	n/a	n/a
23	CTCF	chr3:20287320-20287470	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr3:20287460-20287610	GM12875	blood:	n/a	n/a
25	CTCF	chr3:20287420-20287570	GM12871	blood:	n/a	n/a
26	CTCF	chr3:20287397-20287528	Gliobla	brain:	n/a	n/a
27	CTCF	chr3:20287420-20287570	RPTEC	kidney:	n/a	n/a
28	CTCF	chr3:20287380-20287530	RPTEC	kidney:	n/a	n/a
29	CTCF	chr3:20287340-20287490	GM12872	blood:	n/a	n/a
30	CTCF	chr3:20287400-20287550	GM12873	blood:	n/a	n/a
31	CTCF	chr3:20287380-20287530	GM12873	blood:	n/a	n/a
32	CTCF	chr3:20287420-20287514	GM12878	blood:	n/a	n/a
33	CTCF	chr3:20287360-20287510	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr3:20294743-20294821	Lung_OC	lung:	n/a	n/a
35	CTCF	chr3:20287400-20287550	GM12869	blood:	n/a	n/a
36	CTCF	chr3:20287340-20287490	HMEC	breast:	n/a	n/a
37	CTCF	chr3:20287320-20287470	HCT-116	colon:	n/a	n/a
38	CTCF	chr3:20287360-20287510	HMF	breast:	n/a	n/a
39	CTCF	chr3:20287440-20287590	HCT-116	colon:	n/a	n/a
40	CTCF	chr3:20291860-20292010	GM12865	blood:	n/a	n/a
41	CTCF	chr3:20334566-20334612	GM10266	blood:	n/a	n/a
42	CTCF	chr3:20287400-20287550	HEK293	kidney:	n/a	n/a
43	CTCF	chr3:20287400-20287550	HA-sp	spinal cord:	n/a	n/a
44	CTCF	chr3:20287460-20287610	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr3:20287380-20287530	GM12872	blood:	n/a	n/a
46	CTCF	chr3:20287340-20287490	GM12864	blood:	n/a	n/a
47	CTCF	chr3:20287300-20287450	NHEK	skin:	n/a	n/a
48	CTCF	chr3:20287440-20287590	HRE	kidney:	n/a	n/a
49	CTCF	chr3:20287308-20287625	K562	blood:	n/a	n/a
50	CTCF	chr3:20287354-20287559	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20321584-20321634	AG04450	lung:	fetal
2	chr3:20321584-20321634	PrEC	prostate:	n/a
3	chr3:20321584-20321634	AG04449	skin:	fetal
4	chr3:20321584-20321634	SKMC	muscle:	n/a
5	chr3:20321584-20321634	K562	blood:	n/a
6	chr3:20321584-20321634	RPTEC	kidney:	n/a
7	chr3:20321584-20321634	NT2-D1	testis:	n/a
8	chr3:20321584-20321634	A549	lung:	n/a
9	chr3:20321584-20321634	SK-N-SH	brain:	n/a
10	chr3:20321584-20321634	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:20321584-20321634	MCF-7	breast:	n/a
12	chr3:20321584-20321634	GM12892	blood:	n/a
13	chr3:20321584-20321634	HCT-116	colon:	n/a
14	chr3:20321584-20321634	HCM	heart:	n/a
15	chr3:20321584-20321634	HL-60	blood:	n/a
16	chr3:20321584-20321634	HIPEpiC	eye:	n/a
17	chr3:20321584-20321634	GM12891	blood:	n/a
18	chr3:20321584-20321634	MCF10A-Er-Src	breast:	n/a
19	chr3:20321584-20321634	HCF	heart:	n/a
20	chr3:20321584-20321634	U87	brain:	n/a
21	chr3:20321584-20321634	GM19239	blood:	n/a
22	chr3:20321584-20321634	ECC-1	luminal epithelium:	n/a
23	chr3:20321584-20321634	HEEpiC	esophagus:	n/a
24	chr3:20321584-20321634	T-47D	breast:	n/a
25	chr3:20321584-20321634	AG09309	skin:	n/a
26	chr3:20321584-20321634	ovcar-3	ovarian:	n/a
27	chr3:20321584-20321634	HCPEpiC	choroid plexus:	n/a
28	chr3:20321584-20321634	NHDF-neo	bronchial:	n/a
29	chr3:20321584-20321634	SAEC	small airway:	n/a
30	chr3:20321584-20321634	HEK293	kidney:	embryo
31	chr3:20321584-20321634	HUVEC	blood vessel:	n/a
32	chr3:20321584-20321634	Hela-S3	cervix:	n/a
33	chr3:20321584-20321634	IMR90	lung:	fetal
34	chr3:20321584-20321634	GM12878	blood:	n/a
35	chr3:20321584-20321634	AoSMC	blood vessel:	n/a
36	chr3:20321584-20321634	Caco-2	colon:	n/a
37	chr3:20321584-20321634	Jurkat	blood:	n/a
38	chr3:20321584-20321634	NB4	blood:	n/a
39	chr3:20321584-20321634	H1-hESC	embryonic stem cell:	embryo
40	chr3:20321584-20321634	PANC-1	pancreas:	n/a
41	chr3:20321584-20321634	NHBE	bronchial:	n/a
42	chr3:20321584-20321634	AG09319	gingival:	n/a
43	chr3:20321584-20321634	HRCEpiC	kidney:	n/a
44	chr3:20321584-20321634	NH-A	brain:	n/a
45	chr3:20321584-20321634	LNCaP	prostate:	n/a
46	chr3:20321584-20321634	HMEC	breast:	n/a
47	chr3:20321584-20321634	HRE	kidney:	n/a
48	chr3:20321584-20321634	HAEpiC	amniotic membrane:	n/a
49	chr3:20321584-20321634	SK-N-MC	brain:	n/a
50	chr3:20321584-20321634	SK-N-SH_RA	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:
2	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
3	chr3:20333199..20337962-chr3:20339317..20343120,4	K562	blood:
4	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
5	chr3:20329415..20331770-chr3:20333391..20336112,2	K562	blood:
6	chr3:20320265..20323041-chr3:20324824..20326695,2	K562	blood:
7	chr3:20248922..20251335-chr3:20323167..20325698,2	K562	blood:
8	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
9	chr3:20335611..20337962-chr3:20339317..20341435,2	K562	blood:
10	chr3:20275707..20278612-chr3:20280261..20282928,2	K562	blood:
11	chr3:20316601..20319465-chr3:20319672..20321888,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619

No data

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

Extended variants
information (count: 1874 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1874 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532990611	chr3:20278445-20278446	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370664452	chr3:20278461-20278462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148807978	chr3:20278463-20278464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143896433	chr3:20278464-20278465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112341753	chr3:20278511-20278512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549121033	chr3:20278554-20278555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542938354	chr3:20278557-20278558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188929418	chr3:20278558-20278559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375618740	chr3:20278560-20278561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112789590	chr3:20278663-20278664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556268858	chr3:20278694-20278695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577601562	chr3:20278699-20278700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139704375	chr3:20278721-20278722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375952393	chr3:20278735-20278736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551601544	chr3:20278736-20278737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554043156	chr3:20278739-20278740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572656020	chr3:20278820-20278821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542963766	chr3:20278934-20278935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561502897	chr3:20279031-20279032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6801725	chr3:20279048-20279049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544306950	chr3:20279049-20279050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562612008	chr3:20279055-20279056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532953892	chr3:20279090-20279091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551348914	chr3:20279091-20279092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560199559	chr3:20279113-20279114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527546364	chr3:20279124-20279125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373676042	chr3:20279152-20279153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567434214	chr3:20279171-20279172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201992788	chr3:20279210-20279211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370444039	chr3:20279300-20279301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549855821	chr3:20279355-20279356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs374440084	chr3:20279417-20279418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368846602	chr3:20279421-20279422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571457281	chr3:20279430-20279431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538754228	chr3:20279475-20279476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553712554	chr3:20279499-20279500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565958732	chr3:20279511-20279512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370455986	chr3:20279529-20279530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527743343	chr3:20279535-20279536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371982626	chr3:20279661-20279662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs199751748	chr3:20279669-20279670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367940499	chr3:20279715-20279716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371960366	chr3:20279718-20279719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536927545	chr3:20279736-20279737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554996016	chr3:20279748-20279749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576568690	chr3:20279751-20279752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186197001	chr3:20279757-20279758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559198269	chr3:20279764-20279765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577771762	chr3:20279845-20279846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs545140815	chr3:20279863-20279864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20276600-20278600	Enhancers	Liver	Liver
2	chr3:20278000-20278600	Enhancers	Fetal Intestine Large	intestine
3	chr3:20278000-20278600	Enhancers	Stomach Mucosa	stomach
4	chr3:20278400-20282200	Weak transcription	Fetal Intestine Small	intestine
5	chr3:20278600-20282000	Weak transcription	Liver	Liver
6	chr3:20281200-20282400	Enhancers	Ovary	ovary
7	chr3:20281400-20282800	Enhancers	Aorta	Aorta
8	chr3:20281600-20282000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:20281600-20282000	Enhancers	Spleen	Spleen
10	chr3:20281600-20282600	Enhancers	Esophagus	oesophagus
11	chr3:20282800-20284000	Weak transcription	Aorta	Aorta
12	chr3:20284000-20284200	Enhancers	Aorta	Aorta
13	chr3:20287200-20289000	Enhancers	GM12878-XiMat	blood
14	chr3:20291800-20292200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:20291800-20292400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:20291800-20292400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr3:20291800-20293400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr3:20291800-20293400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:20291800-20293600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr3:20292000-20292200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:20292000-20293200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr3:20292000-20293200	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:20292000-20293200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:20292000-20293200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:20292200-20292400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr3:20292200-20292400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr3:20292200-20292800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr3:20292200-20293400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:20292200-20293400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr3:20292400-20292600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:20292400-20292800	Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr3:20292400-20293200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:20292400-20296000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:20292600-20292800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr3:20292600-20293200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:20292600-20296800	Weak transcription	Ovary	ovary
37	chr3:20292800-20293000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr3:20292800-20293600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:20293000-20293200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:20293200-20293400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr3:20293400-20295600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr3:20293400-20295800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:20293600-20295600	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr3:20293600-20297600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr3:20295600-20296200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:20295600-20296400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr3:20295800-20296000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:20295800-20296200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:20295800-20296200	Active TSS	A549	lung
50	chr3:20295800-20296400	Active TSS	Hela-S3	cervix

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