Variant report

Variant	nsv1007224
Chromosome Location	chr3:22612682-22809139
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:61)
Chromatin interactive
region (count:33)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:22613243-22613483	GM12878	blood:	n/a	n/a
2	CCNT2	chr3:22648660-22648860	K562	blood:	n/a	n/a
3	CEBPB	chr3:22758158-22758414	IMR90	lung:	n/a	chr3:22758288-22758299
4	CEBPB	chr3:22808988-22809235	HepG2	liver:	n/a	chr3:22809074-22809085
5	CEBPB	chr3:22668949-22669200	HepG2	liver:	n/a	chr3:22669047-22669058
6	CEBPB	chr3:22723551-22723746	HepG2	liver:	n/a	chr3:22723644-22723657 chr3:22723644-22723655
7	CEBPB	chr3:22619113-22619421	HepG2	liver:	n/a	chr3:22619269-22619280
8	CEBPB	chr3:22727018-22727459	MCF-7	breast:	n/a	n/a
9	CEBPB	chr3:22807874-22808037	Hela-S3	cervix:	n/a	chr3:22807955-22807966
10	CEBPB	chr3:22727073-22727381	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr3:22746512-22746771	A549	lung:	n/a	chr3:22746555-22746566
12	CEBPB	chr3:22758161-22758406	K562	blood:	n/a	chr3:22758288-22758299
13	CEBPB	chr3:22807788-22808115	IMR90	lung:	n/a	chr3:22807955-22807966
14	CEBPB	chr3:22807857-22808071	H1-hESC	embryonic stem cell:	n/a	chr3:22807955-22807966
15	CEBPB	chr3:22645226-22645457	A549	lung:	n/a	chr3:22645317-22645328
16	CEBPB	chr3:22807797-22808121	HepG2	liver:	n/a	chr3:22807955-22807966
17	CEBPB	chr3:22808930-22809139	K562	blood:	n/a	chr3:22809074-22809085
18	CEBPB	chr3:22755354-22755751	A549	lung:	n/a	chr3:22755560-22755571
19	CEBPB	chr3:22743267-22743453	A549	lung:	n/a	n/a
20	CEBPB	chr3:22755368-22755710	A549	lung:	n/a	chr3:22755560-22755571
21	CEBPB	chr3:22668942-22669130	A549	lung:	n/a	chr3:22669047-22669058
22	CEBPB	chr3:22755375-22755728	A549	lung:	n/a	chr3:22755560-22755571
23	CEBPB	chr3:22654523-22654875	HepG2	liver:	n/a	chr3:22654692-22654703
24	CEBPB	chr3:22645176-22645507	HepG2	liver:	n/a	chr3:22645317-22645328
25	CEBPB	chr3:22619152-22619433	IMR90	lung:	n/a	chr3:22619269-22619280
26	CEBPB	chr3:22755417-22755764	HepG2	liver:	n/a	chr3:22755560-22755571
27	CEBPB	chr3:22654553-22654756	HepG2	liver:	n/a	chr3:22654692-22654703
28	CEBPB	chr3:22755378-22755811	Hela-S3	cervix:	n/a	chr3:22755560-22755571
29	CEBPB	chr3:22808900-22809217	A549	lung:	n/a	chr3:22809074-22809085
30	CEBPB	chr3:22772271-22772583	HepG2	liver:	n/a	chr3:22772429-22772440
31	CEBPB	chr3:22758144-22758436	HepG2	liver:	n/a	chr3:22758288-22758299
32	CEBPB	chr3:22807813-22808145	A549	lung:	n/a	chr3:22807955-22807966
33	CEBPB	chr3:22619117-22619436	A549	lung:	n/a	chr3:22619269-22619280
34	CTCF	chr3:22727220-22727370	NHEK	skin:	n/a	n/a
35	CTCF	chr3:22746151-22746255	ProgFib	skin:	n/a	n/a
36	CTCF	chr3:22771560-22771710	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr3:22771500-22771650	HCM	heart:	n/a	n/a
38	CTCF	chr3:22771594-22771729	HepG2	liver:	n/a	n/a
39	CTCF	chr3:22771580-22771730	HMEC	breast:	n/a	n/a
40	CTCF	chr3:22727180-22727330	GM12868	blood:	n/a	n/a
41	CTCF	chr3:22771580-22771730	Caco-2	colon:	n/a	n/a
42	CTCF	chr3:22713440-22713590	HMEC	breast:	n/a	n/a
43	CTCF	chr3:22746200-22746350	WERI-Rb-1	eye:	n/a	chr3:22746264-22746285 chr3:22746269-22746287
44	CTCF	chr3:22771560-22771710	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr3:22727200-22727350	HMF	breast:	n/a	n/a
46	CTCF	chr3:22771640-22771790	GM06990	blood:	n/a	n/a
47	CTCF	chr3:22771700-22771850	RPTEC	kidney:	n/a	n/a
48	CTCF	chr3:22771620-22771770	GM12875	blood:	n/a	n/a
49	CTCF	chr3:22771538-22771803	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr3:22727240-22727390	GM12870	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22732998-22733048	AoSMC	blood vessel:	n/a
2	chr3:22732998-22733048	PrEC	prostate:	n/a
3	chr3:22732998-22733048	CMK	blood:	n/a
4	chr3:22732998-22733048	SK-N-SH_RA	brain:	n/a
5	chr3:22732998-22733048	GM06990	blood:	n/a
6	chr3:22732998-22733048	MCF10A-Er-Src	breast:	n/a
7	chr3:22732998-22733048	Jurkat	blood:	n/a
8	chr3:22732998-22733048	AG09319	gingival:	n/a
9	chr3:22732998-22733048	NB4	blood:	n/a
10	chr3:22732998-22733048	U87	brain:	n/a
11	chr3:22732998-22733048	AG10803	skin:	n/a
12	chr3:22732998-22733048	NH-A	brain:	n/a
13	chr3:22732998-22733048	NHDF-neo	bronchial:	n/a
14	chr3:22732998-22733048	ovcar-3	ovarian:	n/a
15	chr3:22732998-22733048	HRCEpiC	kidney:	n/a
16	chr3:22732998-22733048	AG04450	lung:	fetal
17	chr3:22732998-22733048	IMR90	lung:	fetal
18	chr3:22732998-22733048	NHBE	bronchial:	n/a
19	chr3:22732998-22733048	MCF-7	breast:	n/a
20	chr3:22732998-22733048	A549	lung:	n/a
21	chr3:22732998-22733048	HIPEpiC	eye:	n/a
22	chr3:22732998-22733048	HCF	heart:	n/a
23	chr3:22732998-22733048	PFSK-1	brain:	n/a
24	chr3:22732998-22733048	AG04449	skin:	fetal
25	chr3:22732998-22733048	GM12892	blood:	n/a
26	chr3:22732998-22733048	SAEC	small airway:	n/a
27	chr3:22732998-22733048	GM19239	blood:	n/a
28	chr3:22732998-22733048	GM12878	blood:	n/a
29	chr3:22732998-22733048	Hepatocyte	liver:	n/a
30	chr3:22732998-22733048	Caco-2	colon:	n/a
31	chr3:22732998-22733048	Hela-S3	cervix:	n/a
32	chr3:22732998-22733048	RPTEC	kidney:	n/a
33	chr3:22732998-22733048	GM12891	blood:	n/a
34	chr3:22732998-22733048	HEK293	kidney:	embryo
35	chr3:22732998-22733048	HMEC	breast:	n/a
36	chr3:22732998-22733048	HL-60	blood:	n/a
37	chr3:22732998-22733048	SK-N-SH	brain:	n/a
38	chr3:22732998-22733048	T-47D	breast:	n/a
39	chr3:22732998-22733048	HRPEpiC	eye:	n/a
40	chr3:22732998-22733048	HCPEpiC	choroid plexus:	n/a
41	chr3:22732998-22733048	HEEpiC	esophagus:	n/a
42	chr3:22732998-22733048	BE2_C	brain:	n/a
43	chr3:22732998-22733048	HAEpiC	amniotic membrane:	n/a
44	chr3:22732998-22733048	SKMC	muscle:	n/a
45	chr3:22732998-22733048	BJ	skin:	n/a
46	chr3:22732998-22733048	ECC-1	luminal epithelium:	n/a
47	chr3:22732998-22733048	ProgFib	skin:	n/a
48	chr3:22732998-22733048	AG09309	skin:	n/a
49	chr3:22732998-22733048	HNPCEpiC	eye:	n/a
50	chr3:22732998-22733048	PANC-1	pancreas:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:22762695..22766191-chr3:22767247..22769971,3	MCF-7	breast:
2	chr3:22785472..22787166-chr3:22787468..22789169,2	MCF-7	breast:
3	chr3:22656088..22657056-chr4:29865254..29865836,2	MCF-7	breast:
4	chr3:22762494..22764619-chr3:22766448..22769090,2	K562	blood:
5	chr3:22757830..22758594-chr3:195658318..195659105,2	MCF-7	breast:
6	chr3:22771212..22772136-chr3:22903356..22904056,6	MCF-7	breast:
7	chr3:22621236..22623407-chr3:22624012..22625741,2	K562	blood:
8	chr3:22771477..22772449-chr3:22985846..22986742,2	MCF-7	breast:
9	chr3:22804037..22805757-chr3:23957373..23959128,2	K562	blood:
10	chr3:22771112..22772132-chr3:22928764..22929789,6	MCF-7	breast:
11	chr3:22605258..22606015-chr3:22726589..22727722,7	MCF-7	breast:
12	chr3:22771239..22772148-chr3:22928875..22929886,10	MCF-7	breast:
13	chr3:22771584..22772119-chr3:23001665..23002525,2	MCF-7	breast:
14	chr3:22794268..22797124-chr3:22799597..22801489,2	MCF-7	breast:
15	chr3:22762695..22766191-chr3:22767247..22769971,3	MCF-7	breast:
16	chr20:52236011..52236894-chr3:22635315..22635889,2	MCF-7	breast:
17	chr3:22808136..22810861-chr3:22815889..22818179,2	K562	blood:
18	chr3:22770781..22772111-chr3:23001246..23002368,7	MCF-7	breast:
19	chr3:22606338..22606850-chr3:22713171..22713815,2	MCF-7	breast:
20	chr3:22803714..22805482-chr3:22807294..22809398,2	K562	blood:
21	chr3:22605202..22606238-chr3:22726881..22727802,6	MCF-7	breast:
22	chr3:22786053..22788405-chr3:22793906..22796307,2	MCF-7	breast:
23	chr3:22784017..22786866-chr3:22809414..22812166,2	MCF-7	breast:
24	chr3:22770066..22771939-chr3:22999640..23001789,2	MCF-7	breast:
25	chr3:22605358..22606044-chr3:22713391..22713898,2	MCF-7	breast:
26	chr3:22605347..22606025-chr3:22726006..22726863,2	MCF-7	breast:
27	chr3:22794268..22797124-chr3:22799597..22801489,2	MCF-7	breast:
28	chr3:22785472..22787166-chr3:22787468..22789169,2	MCF-7	breast:
29	chr3:22217113..22218017-chr3:22727091..22727719,2	MCF-7	breast:
30	chr3:22762494..22764619-chr3:22766448..22769090,2	K562	blood:
31	chr3:22786053..22788405-chr3:22793906..22796307,2	MCF-7	breast:
32	chr3:22803714..22805482-chr3:22807294..22809398,2	K562	blood:
33	chr3:22621236..22623407-chr3:22624012..22625741,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF385D-3	chr3:22711799-22712025	NONHSAT088658
2	lnc-ZNF385D-3	chr3:22711692-22711772	NONHSAT088658
3	lnc-ZNF385D-3	chr3:22712093-22712202	NONHSAT088658

No data

Variant related genes	Relation type
ENSG00000234723	TF binding region
ENSG00000234723	CpG island
ENSG00000197885	chromatin interactions
ENSG00000174748	chromatin interactions

Extended variants
information (count: 4413 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4413 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549044744	chr3:22622410-22622411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180918977	chr3:22622448-22622449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537646217	chr3:22622502-22622503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377109021	chr3:22622641-22622642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78878166	chr3:22622653-22622654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35303673	chr3:22622655-22622656	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs185278858	chr3:22622662-22622663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557889532	chr3:22622694-22622695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573158510	chr3:22622745-22622746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377507914	chr3:22622750-22622751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9810744	chr3:22622763-22622764	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191612455	chr3:22622778-22622779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142867951	chr3:22622806-22622807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74757819	chr3:22622900-22622901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553899536	chr3:22622910-22622911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74707023	chr3:22622917-22622918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs977612	chr3:22622954-22622955	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs545646639	chr3:22622962-22622963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559925681	chr3:22622989-22622990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151099772	chr3:22623007-22623008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181204681	chr3:22623011-22623012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200729956	chr3:22623035-22623036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141033898	chr3:22623049-22623050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562038570	chr3:22623052-22623053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71316089	chr3:22623076-22623077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370976197	chr3:22623087-22623088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571082204	chr3:22623095-22623096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9852231	chr3:22623140-22623141	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201303098	chr3:22623183-22623184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146868512	chr3:22623224-22623225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370666516	chr3:22623341-22623342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140812719	chr3:22623346-22623347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187116694	chr3:22623411-22623412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144565691	chr3:22623419-22623420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs113497148	chr3:22623426-22623427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78644564	chr3:22623471-22623472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs556808266	chr3:22623475-22623476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs115281801	chr3:22623486-22623487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs6809842	chr3:22623495-22623496	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs543476613	chr3:22623580-22623581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1531160	chr3:22623604-22623605	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs542615648	chr3:22623614-22623615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533283122	chr3:22623622-22623623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs111973700	chr3:22623719-22623720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs143489636	chr3:22623734-22623735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370629307	chr3:22623735-22623736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191642484	chr3:22623737-22623738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6550700	chr3:22623784-22623785	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs148041395	chr3:22623833-22623834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9815839	chr3:22623846-22623847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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	22037309	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22622400-22622600	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:22622400-22622800	Enhancers	HepG2	liver
3	chr3:22622600-22623000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr3:22622600-22626600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:22623200-22623800	Enhancers	Brain Angular Gyrus	brain
6	chr3:22623200-22624000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr3:22623200-22624000	Enhancers	Brain Substantia Nigra	brain
8	chr3:22623200-22624600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr3:22623200-22625000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:22623400-22623800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr3:22623400-22624000	Enhancers	Brain Cingulate Gyrus	brain
12	chr3:22623400-22624000	Enhancers	Brain Hippocampus Middle	brain
13	chr3:22623600-22623800	Enhancers	Rectal Smooth Muscle	rectum
14	chr3:22623600-22624000	Enhancers	Fetal Kidney	kidney
15	chr3:22624000-22624400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr3:22624000-22624600	Weak transcription	Brain Substantia Nigra	brain
17	chr3:22624400-22624800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr3:22624600-22624800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:22624600-22624800	Enhancers	Brain Substantia Nigra	brain
20	chr3:22624600-22625000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr3:22625800-22627000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:22626000-22626600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:22626200-22627800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:22626200-22628200	Enhancers	HMEC	breast
25	chr3:22626200-22629200	Enhancers	Brain Germinal Matrix	brain
26	chr3:22626600-22627200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr3:22626600-22627200	Enhancers	NHDF-Ad	bronchial
28	chr3:22626600-22627400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:22626600-22627400	Enhancers	Fetal Lung	lung
30	chr3:22626600-22627800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr3:22626600-22627800	Enhancers	NH-A	brain
32	chr3:22626600-22627800	Enhancers	NHEK	skin
33	chr3:22626800-22627800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:22626800-22628000	Enhancers	Fetal Brain Male	brain
35	chr3:22627000-22627200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:22627000-22627400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:22627000-22627400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr3:22627000-22627400	Enhancers	Ovary	ovary
39	chr3:22627000-22627600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr3:22627000-22627800	Enhancers	Fetal Stomach	stomach
41	chr3:22627000-22628200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr3:22627400-22627600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:22627600-22628600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:22627800-22629000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr3:22628600-22628800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:22629200-22629400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr3:22635000-22636600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr3:22636000-22636200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr3:22636200-22648200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:22638600-22639200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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