Variant report

Variant	nsv876621
Chromosome Location	chr3:22147707-22228577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:22162549-22162915	HepG2	liver:	n/a	n/a
2	BATF	chr3:22164137-22164374	GM12878	blood:	n/a	chr3:22164265-22164276
3	BATF	chr3:22164128-22164369	GM12878	blood:	n/a	chr3:22164265-22164276
4	BHLHE40	chr3:22164062-22164443	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:22159425-22159426	K562	blood:	n/a	n/a
6	BHLHE40	chr3:22159971-22159994	GM12878	blood:	n/a	n/a
7	BRCA1	chr3:22147560-22148537	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:22157049-22157445	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr3:22150505-22150716	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:22147693-22148379	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:22148066-22148387	MCF-7	breast:	n/a	n/a
12	CEBPB	chr3:22162691-22163152	HepG2	liver:	n/a	chr3:22163128-22163139
13	CEBPB	chr3:22200917-22201096	HepG2	liver:	n/a	chr3:22201008-22201021
14	CEBPB	chr3:22200829-22201208	HepG2	liver:	n/a	chr3:22201008-22201021
15	CEBPB	chr3:22227764-22227995	A549	lung:	n/a	n/a
16	CEBPB	chr3:22200899-22201125	HepG2	liver:	n/a	chr3:22201008-22201021
17	CEBPB	chr3:22148135-22148381	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:22147569-22148482	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:22159289-22159588	K562	blood:	n/a	n/a
20	CEBPB	chr3:22200864-22201215	Hela-S3	cervix:	n/a	chr3:22201008-22201021
21	CHD2	chr3:22164016-22164425	GM12878	blood:	n/a	n/a
22	CHD2	chr3:22147753-22148435	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr3:22152571-22152649	K562	blood:	n/a	n/a
24	CTCF	chr3:22159340-22159490	HPAF	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
25	CTCF	chr3:22159540-22159690	GM06990	blood:	n/a	n/a
26	CTCF	chr3:22217500-22217650	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr3:22159748-22159868	Medullo	brain:	n/a	n/a
28	CTCF	chr3:22159329-22159543	GM13977	blood:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
29	CTCF	chr3:22159400-22159550	HPAF	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
30	CTCF	chr3:22159328-22159543	K562	blood:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
31	CTCF	chr3:22159300-22159450	HEK293	kidney:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
32	CTCF	chr3:22217480-22217630	HMEC	breast:	n/a	n/a
33	CTCF	chr3:22159426-22159464	MCF-7	breast:	n/a	chr3:22159428-22159446
34	CTCF	chr3:22217460-22217610	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr3:22159360-22159510	BJ	skin:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
36	CTCF	chr3:22159340-22159490	GM12867	blood:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
37	CTCF	chr3:22159720-22159870	AG10803	skin:	n/a	n/a
38	CTCF	chr3:22217480-22217630	AG10803	skin:	n/a	n/a
39	CTCF	chr3:22159338-22159530	Lung_OC	lung:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
40	CTCF	chr3:22159360-22159510	AG04449	skin:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
41	CTCF	chr3:22159298-22159609	HepG2	liver:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
42	CTCF	chr3:22217500-22217650	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr3:22159380-22159530	GM12878	blood:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
44	CTCF	chr3:22159320-22159470	NHEK	skin:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
45	CTCF	chr3:22159254-22159651	MCF-7	breast:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
46	CTCF	chr3:22159340-22159490	AoAF	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
47	CTCF	chr3:22159332-22159561	LNCaP	prostate:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
48	CTCF	chr3:22217480-22217630	HPF	lung:	n/a	n/a
49	CTCF	chr3:22159360-22159510	AoAF	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
50	CTCF	chr3:22217440-22217590	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22192127-22192177	RPTEC	kidney:	n/a
2	chr3:22192127-22192177	AG10803	skin:	n/a
3	chr3:22192127-22192177	GM06990	blood:	n/a
4	chr3:22192127-22192177	HEEpiC	esophagus:	n/a
5	chr3:22192127-22192177	NB4	blood:	n/a
6	chr3:22192127-22192177	HepG2	liver:	n/a
7	chr3:22192127-22192177	HIPEpiC	eye:	n/a
8	chr3:22192127-22192177	ovcar-3	ovarian:	n/a
9	chr3:22192127-22192177	NH-A	brain:	n/a
10	chr3:22192127-22192177	Hela-S3	cervix:	n/a
11	chr3:22192127-22192177	SK-N-MC	brain:	n/a
12	chr3:22192127-22192177	AG04449	skin:	fetal
13	chr3:22192127-22192177	AG09319	gingival:	n/a
14	chr3:22192127-22192177	HL-60	blood:	n/a
15	chr3:22192127-22192177	BJ	skin:	n/a
16	chr3:22192127-22192177	AG09309	skin:	n/a
17	chr3:22192127-22192177	H1-hESC	embryonic stem cell:	embryo
18	chr3:22192127-22192177	HCF	heart:	n/a
19	chr3:22192127-22192177	HUVEC	blood vessel:	n/a
20	chr3:22192127-22192177	PANC-1	pancreas:	n/a
21	chr3:22192127-22192177	LNCaP	prostate:	n/a
22	chr3:22192127-22192177	Jurkat	blood:	n/a
23	chr3:22192127-22192177	GM12892	blood:	n/a
24	chr3:22192127-22192177	HMEC	breast:	n/a
25	chr3:22192127-22192177	NHBE	bronchial:	n/a
26	chr3:22192127-22192177	ECC-1	luminal epithelium:	n/a
27	chr3:22192127-22192177	K562	blood:	n/a
28	chr3:22192127-22192177	ProgFib	skin:	n/a
29	chr3:22192127-22192177	Caco-2	colon:	n/a
30	chr3:22192127-22192177	BE2_C	brain:	n/a
31	chr3:22192127-22192177	SK-N-SH_RA	brain:	n/a
32	chr3:22192127-22192177	A549	lung:	n/a
33	chr3:22192127-22192177	Hepatocyte	liver:	n/a
34	chr3:22192127-22192177	SK-N-SH	brain:	n/a
35	chr3:22192127-22192177	HRE	kidney:	n/a
36	chr3:22192127-22192177	GM12878	blood:	n/a
37	chr3:22192127-22192177	HNPCEpiC	eye:	n/a
38	chr3:22192127-22192177	HAEpiC	amniotic membrane:	n/a
39	chr3:22192127-22192177	NHDF-neo	bronchial:	n/a
40	chr3:22192127-22192177	MCF10A-Er-Src	breast:	n/a
41	chr3:22192127-22192177	PFSK-1	brain:	n/a
42	chr3:22192127-22192177	SAEC	small airway:	n/a
43	chr3:22192127-22192177	U87	brain:	n/a
44	chr3:22192127-22192177	HRCEpiC	kidney:	n/a
45	chr3:22192127-22192177	GM12891	blood:	n/a
46	chr3:22192127-22192177	HCT-116	colon:	n/a
47	chr3:22192127-22192177	IMR90	lung:	fetal
48	chr3:22192127-22192177	SKMC	muscle:	n/a
49	chr3:22192127-22192177	AoSMC	blood vessel:	n/a
50	chr3:22192127-22192177	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
2	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
3	chr3:22218049..22218903-chr9:120895826..120896702,2	MCF-7	breast:
4	chr3:22195364..22197977-chr3:22208185..22210526,2	K562	blood:
5	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
6	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
7	chr3:22217113..22218017-chr3:22727091..22727719,2	MCF-7	breast:
8	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
9	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SGOL1-3	chr3:22175074-22175484	NONHSAT088653
2	lnc-SGOL1-3	chr3:22175811-22175883	NONHSAT088653
3	lnc-SGOL1-3	chr3:22210309-22210443	NONHSAT088650
4	lnc-SGOL1-3	chr3:22210309-22210508	NONHSAT088653

Variant related genes	Relation type
ZNF385D	TF binding region
ZNF385D	CpG island
ENSG00000151789	chromatin interactions

Extended variants
information (count: 3002 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:3002 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs779183	chr3:22147707-22147708	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138387612	chr3:22147723-22147724	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs543925357	chr3:22147724-22147725	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs562624882	chr3:22147739-22147740	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs143939331	chr3:22147744-22147745	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs561831025	chr3:22147770-22147771	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs779182	chr3:22147772-22147773	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs809037	chr3:22147791-22147792	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs79152006	chr3:22147805-22147806	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs779181	chr3:22147814-22147815	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs529289456	chr3:22147830-22147831	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs550766926	chr3:22147840-22147841	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs569387315	chr3:22147845-22147846	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs539971655	chr3:22147849-22147850	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs147294371	chr3:22147869-22147870	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs139843601	chr3:22147877-22147878	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs75876966	chr3:22147893-22147894	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs536477423	chr3:22147901-22147902	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs533358749	chr3:22147932-22147933	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531414698	chr3:22147945-22147946	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs779180	chr3:22148001-22148002	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556033997	chr3:22148008-22148009	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs779179	chr3:22148015-22148016	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs544211795	chr3:22148017-22148018	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs149830156	chr3:22148029-22148030	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs144813130	chr3:22148037-22148038	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs779178	chr3:22148064-22148065	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs183356988	chr3:22148095-22148096	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs148588037	chr3:22148124-22148125	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs542507247	chr3:22148144-22148145	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561255744	chr3:22148148-22148149	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs2969106	chr3:22148157-22148158	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550935974	chr3:22148184-22148185	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs567948308	chr3:22148186-22148187	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs530829908	chr3:22148188-22148189	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs533460695	chr3:22148189-22148190	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs188094723	chr3:22148220-22148221	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs567030084	chr3:22148237-22148238	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550561493	chr3:22148243-22148244	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs192884260	chr3:22148248-22148249	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs143154787	chr3:22148273-22148274	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs570717824	chr3:22148277-22148278	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567934009	chr3:22148283-22148284	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs183607010	chr3:22148289-22148290	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs17593897	chr3:22148294-22148295	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs576154235	chr3:22148313-22148314	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs111894734	chr3:22148323-22148324	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs11917630	chr3:22148340-22148341	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs538308396	chr3:22148342-22148343	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs553456477	chr3:22148369-22148370	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:89 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22147000-22147800	Enhancers	Liver	Liver
2	chr3:22147600-22148600	Flanking Active TSS	Hela-S3	cervix
3	chr3:22147800-22148200	Enhancers	Skeletal Muscle Male	skeletal muscle
4	chr3:22147800-22148400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:22147800-22148400	Flanking Active TSS	Liver	Liver
6	chr3:22148000-22148400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:22148000-22148800	Enhancers	Placenta	Placenta
8	chr3:22148400-22148600	Enhancers	Liver	Liver
9	chr3:22148400-22152800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:22148600-22149600	Enhancers	Hela-S3	cervix
11	chr3:22152800-22153400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:22153200-22153400	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr3:22153200-22153600	Enhancers	Fetal Brain Male	brain
14	chr3:22153400-22153800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:22153400-22158400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:22153600-22157200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr3:22153800-22157800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:22154200-22154600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr3:22156000-22159000	Enhancers	Hela-S3	cervix
20	chr3:22156600-22157600	Enhancers	HUVEC	blood vessel
21	chr3:22157000-22158600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr3:22157200-22157400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr3:22157400-22161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:22157800-22158600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:22158400-22159000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:22158800-22159400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:22160000-22160200	Enhancers	Liver	Liver
28	chr3:22160200-22161600	Weak transcription	Liver	Liver
29	chr3:22161600-22162400	Enhancers	HepG2	liver
30	chr3:22161600-22162600	Enhancers	Liver	Liver
31	chr3:22161800-22162400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:22161800-22162400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr3:22162400-22162600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr3:22162400-22162800	Active TSS	HepG2	liver
35	chr3:22162600-22163000	Active TSS	GM12878-XiMat	blood
36	chr3:22162600-22163200	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr3:22162600-22163400	Flanking Active TSS	Liver	Liver
38	chr3:22162800-22163400	Flanking Active TSS	HepG2	liver
39	chr3:22163000-22163600	Enhancers	Pancreas	Pancrea
40	chr3:22163200-22163600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr3:22163400-22163800	Enhancers	Liver	Liver
42	chr3:22163400-22163800	Enhancers	HepG2	liver
43	chr3:22163600-22163800	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr3:22163800-22164200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr3:22164200-22164600	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr3:22170400-22171600	Enhancers	HMEC	breast
47	chr3:22170400-22171800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr3:22170800-22171200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr3:22170800-22172400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:22183000-22183600	Enhancers	Skeletal Muscle Male	skeletal muscle

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