Variant report

Variant	nsv428081
Chromosome Location	chr3:22077893-22256869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

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	chr3:22164128-22164369	GM12878	blood:	n/a	chr3:22164265-22164276
3	BATF	chr3:22164137-22164374	GM12878	blood:	n/a	chr3:22164265-22164276
4	BHLHE40	chr3:22159971-22159994	GM12878	blood:	n/a	n/a
5	BHLHE40	chr3:22130865-22131163	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:22159425-22159426	K562	blood:	n/a	n/a
7	BHLHE40	chr3:22164062-22164443	GM12878	blood:	n/a	n/a
8	BRCA1	chr3:22147560-22148537	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr3:22200899-22201125	HepG2	liver:	n/a	chr3:22201008-22201021
10	CEBPB	chr3:22200864-22201215	Hela-S3	cervix:	n/a	chr3:22201008-22201021
11	CEBPB	chr3:22147693-22148379	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:22200917-22201096	HepG2	liver:	n/a	chr3:22201008-22201021
13	CEBPB	chr3:22237586-22237702	A549	lung:	n/a	n/a
14	CEBPB	chr3:22159289-22159588	K562	blood:	n/a	n/a
15	CEBPB	chr3:22157049-22157445	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:22148135-22148381	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr3:22137588-22137831	A549	lung:	n/a	chr3:22137755-22137766
18	CEBPB	chr3:22137582-22137905	IMR90	lung:	n/a	chr3:22137755-22137766
19	CEBPB	chr3:22137595-22137886	HepG2	liver:	n/a	chr3:22137755-22137766
20	CEBPB	chr3:22162691-22163152	HepG2	liver:	n/a	chr3:22163128-22163139
21	CEBPB	chr3:22150505-22150716	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:22227764-22227995	A549	lung:	n/a	n/a
23	CEBPB	chr3:22137626-22137809	K562	blood:	n/a	chr3:22137755-22137766
24	CEBPB	chr3:22252947-22253151	A549	lung:	n/a	n/a
25	CEBPB	chr3:22200829-22201208	HepG2	liver:	n/a	chr3:22201008-22201021
26	CEBPB	chr3:22147569-22148482	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr3:22148066-22148387	MCF-7	breast:	n/a	n/a
28	CHD2	chr3:22147753-22148435	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr3:22164016-22164425	GM12878	blood:	n/a	n/a
30	CTCF	chr3:22159344-22159534	Pancreas_OC	pancreas:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
31	CTCF	chr3:22130760-22130910	HUVEC	blood vessel:	n/a	n/a
32	CTCF	chr3:22159340-22159490	HRE	kidney:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
33	CTCF	chr3:22159360-22159510	AoAF	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
34	CTCF	chr3:22130800-22130950	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr3:22159254-22159651	MCF-7	breast:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
36	CTCF	chr3:22109381-22109414	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr3:22159304-22159575	Medullo	brain:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
38	CTCF	chr3:22130873-22131054	GM12892	blood:	n/a	n/a
39	CTCF	chr3:22217520-22217670	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr3:22159338-22159530	Lung_OC	lung:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
41	CTCF	chr3:22159379-22159511	MCF-7	breast:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
42	CTCF	chr3:22217540-22217690	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:22159340-22159490	AG09319	gingival:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
44	CTCF	chr3:22217480-22217630	HMEC	breast:	n/a	n/a
45	CTCF	chr3:22130904-22131037	GM12891	blood:	n/a	n/a
46	CTCF	chr3:22159296-22159580	HUVEC	blood vessel:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
47	CTCF	chr3:22159320-22159470	NB4	blood:	n/a	chr3:22159423-22159444 chr3:22159428-22159446
48	CTCF	chr3:22130860-22131010	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr3:22130820-22130970	NHEK	skin:	n/a	n/a
50	CTCF	chr3:22130840-22130990	HCPEpiC	choroid plexus:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22192127-22192177	HRCEpiC	kidney:	n/a
2	chr3:22192127-22192177	Hela-S3	cervix:	n/a
3	chr3:22192127-22192177	GM12878	blood:	n/a
4	chr3:22192127-22192177	HNPCEpiC	eye:	n/a
5	chr3:22192127-22192177	AG09319	gingival:	n/a
6	chr3:22192127-22192177	SKMC	muscle:	n/a
7	chr3:22192127-22192177	PANC-1	pancreas:	n/a
8	chr3:22192127-22192177	PFSK-1	brain:	n/a
9	chr3:22192127-22192177	HIPEpiC	eye:	n/a
10	chr3:22192127-22192177	ovcar-3	ovarian:	n/a
11	chr3:22192127-22192177	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:22192127-22192177	HRE	kidney:	n/a
13	chr3:22192127-22192177	HepG2	liver:	n/a
14	chr3:22192127-22192177	SK-N-SH_RA	brain:	n/a
15	chr3:22192127-22192177	AG04449	skin:	fetal
16	chr3:22192127-22192177	NH-A	brain:	n/a
17	chr3:22192127-22192177	SAEC	small airway:	n/a
18	chr3:22192127-22192177	HAEpiC	amniotic membrane:	n/a
19	chr3:22192127-22192177	IMR90	lung:	fetal
20	chr3:22192127-22192177	A549	lung:	n/a
21	chr3:22192127-22192177	GM19239	blood:	n/a
22	chr3:22192127-22192177	SK-N-MC	brain:	n/a
23	chr3:22192127-22192177	MCF-7	breast:	n/a
24	chr3:22192127-22192177	GM12892	blood:	n/a
25	chr3:22192127-22192177	LNCaP	prostate:	n/a
26	chr3:22192127-22192177	T-47D	breast:	n/a
27	chr3:22192127-22192177	RPTEC	kidney:	n/a
28	chr3:22192127-22192177	CMK	blood:	n/a
29	chr3:22192127-22192177	HL-60	blood:	n/a
30	chr3:22192127-22192177	HCPEpiC	choroid plexus:	n/a
31	chr3:22192127-22192177	Caco-2	colon:	n/a
32	chr3:22192127-22192177	BJ	skin:	n/a
33	chr3:22192127-22192177	HCM	heart:	n/a
34	chr3:22192127-22192177	MCF10A-Er-Src	breast:	n/a
35	chr3:22192127-22192177	K562	blood:	n/a
36	chr3:22192127-22192177	NB4	blood:	n/a
37	chr3:22192127-22192177	SK-N-SH	brain:	n/a
38	chr3:22192127-22192177	NHBE	bronchial:	n/a
39	chr3:22192127-22192177	H1-hESC	embryonic stem cell:	embryo
40	chr3:22192127-22192177	PrEC	prostate:	n/a
41	chr3:22192127-22192177	HCT-116	colon:	n/a
42	chr3:22192127-22192177	HMEC	breast:	n/a
43	chr3:22192127-22192177	NHDF-neo	bronchial:	n/a
44	chr3:22192127-22192177	BE2_C	brain:	n/a
45	chr3:22192127-22192177	GM12891	blood:	n/a
46	chr3:22192127-22192177	HRPEpiC	eye:	n/a
47	chr3:22192127-22192177	ECC-1	luminal epithelium:	n/a
48	chr3:22192127-22192177	Hepatocyte	liver:	n/a
49	chr3:22192127-22192177	AoSMC	blood vessel:	n/a
50	chr3:22192127-22192177	HUVEC	blood vessel:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
2	chr3:22218049..22218903-chr9:120895826..120896702,2	MCF-7	breast:
3	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
4	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
5	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
6	chr3:22195364..22197977-chr3:22208185..22210526,2	K562	blood:
7	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
8	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
9	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
10	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
11	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
12	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
13	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
14	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
15	chr3:22217113..22218017-chr3:22727091..22727719,2	MCF-7	breast:
16	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
17	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
18	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
19	chr3:22130623..22131453-chr3:22928892..22930144,3	K562	blood:

(count:4 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4808 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4808 , 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	rs114986593	chr3:22079819-22079820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541182122	chr3:22079827-22079828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114619440	chr3:22079829-22079830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529958546	chr3:22079837-22079838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185704255	chr3:22079888-22079889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563466320	chr3:22079930-22079931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372324004	chr3:22079955-22079956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560039699	chr3:22079977-22079978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs74738023	chr3:22079992-22079993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200793413	chr3:22080020-22080021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370627800	chr3:22080024-22080025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs145109246	chr3:22080066-22080067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571672785	chr3:22080102-22080103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532471535	chr3:22080164-22080165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11924399	chr3:22080196-22080197	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs711690	chr3:22080210-22080211	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs577131317	chr3:22080213-22080214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536482050	chr3:22080241-22080242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188668069	chr3:22080245-22080246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570269196	chr3:22080247-22080248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546095078	chr3:22080254-22080255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113750123	chr3:22080274-22080275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558271716	chr3:22080310-22080311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs528062927	chr3:22080321-22080322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375734502	chr3:22080332-22080333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576960525	chr3:22080345-22080346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113432212	chr3:22080363-22080364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147175571	chr3:22080377-22080378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373303916	chr3:22080378-22080379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs115709993	chr3:22080381-22080382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11928454	chr3:22080389-22080390	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs810429	chr3:22080461-22080462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542070785	chr3:22080479-22080480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs711689	chr3:22080522-22080523	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs77173811	chr3:22080535-22080536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114092219	chr3:22080576-22080577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192750731	chr3:22080596-22080597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532409569	chr3:22080603-22080604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554436920	chr3:22080612-22080613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547470342	chr3:22080613-22080614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528757702	chr3:22080620-22080621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs59798829	chr3:22080631-22080632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs813582	chr3:22080653-22080654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548507035	chr3:22080662-22080663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183928661	chr3:22080667-22080668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140424520	chr3:22080705-22080706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552875476	chr3:22080715-22080716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76167625	chr3:22080746-22080747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77558320	chr3:22080747-22080748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397877237	chr3:22080748-22080749	Enhancers	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
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:131 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22079800-22081800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:22087400-22087800	Enhancers	H1 Cell Line	embryonic stem cell
3	chr3:22087400-22087800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:22087400-22088200	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:22088000-22088200	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr3:22089400-22089600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:22106800-22107000	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr3:22129800-22130200	Enhancers	Fetal Lung	lung
9	chr3:22129800-22130800	Enhancers	Colon Smooth Muscle	Colon
10	chr3:22130600-22130800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:22130600-22130800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:22130800-22131000	Active TSS	Hela-S3	cervix
13	chr3:22130800-22131200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:22130800-22131200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:22130800-22131200	Enhancers	Adipose Nuclei	Adipose
16	chr3:22130800-22132400	Enhancers	Liver	Liver
17	chr3:22131000-22131200	Enhancers	Pancreas	Pancrea
18	chr3:22131000-22131200	Flanking Active TSS	Hela-S3	cervix
19	chr3:22131200-22133000	Enhancers	Hela-S3	cervix
20	chr3:22132800-22133200	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr3:22133200-22133800	Active TSS	Skeletal Muscle Male	skeletal muscle
22	chr3:22135000-22135400	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr3:22135400-22139600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:22138200-22139000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:22139000-22139800	Enhancers	Hela-S3	cervix
26	chr3:22139600-22139800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr3:22139600-22140200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr3:22139600-22140200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:22142800-22144000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr3:22142800-22144000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr3:22143400-22144000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:22144000-22146600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr3:22145600-22147000	Enhancers	Hela-S3	cervix
34	chr3:22147000-22147400	Flanking Active TSS	Hela-S3	cervix
35	chr3:22147000-22147800	Enhancers	Liver	Liver
36	chr3:22147400-22147600	Enhancers	Hela-S3	cervix
37	chr3:22147600-22148600	Flanking Active TSS	Hela-S3	cervix
38	chr3:22147800-22148200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr3:22147800-22148400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:22147800-22148400	Flanking Active TSS	Liver	Liver
41	chr3:22148000-22148400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:22148000-22148800	Enhancers	Placenta	Placenta
43	chr3:22148400-22148600	Enhancers	Liver	Liver
44	chr3:22148400-22152800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:22148600-22149600	Enhancers	Hela-S3	cervix
46	chr3:22152800-22153400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:22153200-22153400	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr3:22153200-22153600	Enhancers	Fetal Brain Male	brain
49	chr3:22153400-22153800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:22153400-22158400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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