Variant report

Variant	nsv428082
Chromosome Location	chr3:22397625-22539817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:407)
CpG islands
(count:916)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:22526923-22526941	GM12878	blood:	n/a	n/a
2	CEBPB	chr3:22533921-22533924	K562	blood:	n/a	n/a
3	CEBPB	chr3:22522306-22522616	IMR90	lung:	n/a	n/a
4	CEBPB	chr3:22461953-22462276	A549	lung:	n/a	chr3:22462116-22462127
5	CEBPB	chr3:22413324-22413641	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr3:22419951-22420223	HepG2	liver:	n/a	n/a
7	CEBPB	chr3:22402562-22402664	H1-hESC	embryonic stem cell:	n/a	chr3:22402566-22402577
8	CEBPB	chr3:22414157-22414309	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:22461971-22462246	HepG2	liver:	n/a	chr3:22462116-22462127
10	CEBPB	chr3:22522295-22522589	A549	lung:	n/a	n/a
11	CEBPB	chr3:22415022-22415091	A549	lung:	n/a	n/a
12	CEBPB	chr3:22402436-22402728	HepG2	liver:	n/a	chr3:22402566-22402577
13	CEBPB	chr3:22522316-22522614	HepG2	liver:	n/a	n/a
14	CHD1	chr3:22414077-22414100	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr3:22414063-22414253	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTBP2	chr3:22413206-22414448	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr3:22449080-22449114	GM10266	blood:	n/a	n/a
18	CTCF	chr3:22475900-22476050	HepG2	liver:	n/a	n/a
19	CTCF	chr3:22481586-22481720	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr3:22481540-22481690	GM12873	blood:	n/a	n/a
21	CTCF	chr3:22426085-22426120	LNCaP	prostate:	n/a	n/a
22	CTCF	chr3:22481540-22481690	HEK293	kidney:	n/a	n/a
23	CTCF	chr3:22413520-22413670	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr3:22502588-22502712	Lung_OC	lung:	n/a	n/a
25	CTCF	chr3:22535692-22535744	Lung_OC	lung:	n/a	n/a
26	CTCF	chr3:22398897-22398915	K562	blood:	n/a	n/a
27	CTCF	chr3:22459244-22459356	LNCaP	prostate:	n/a	n/a
28	CTCF	chr3:22503480-22503690	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr3:22455440-22455590	HepG2	liver:	n/a	n/a
30	CTCF	chr3:22450319-22450368	LNCaP	prostate:	n/a	n/a
31	CTCF	chr3:22399740-22399890	K562	blood:	n/a	n/a
32	CTCF	chr3:22495780-22495930	NHLF	lung:	n/a	n/a
33	CTCF	chr3:22484317-22484341	GM10266	blood:	n/a	n/a
34	CTCF	chr3:22423219-22423304	GM20000	blood:	n/a	n/a
35	CTCF	chr3:22414060-22414210	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr3:22399880-22400030	MCF-7	breast:	n/a	chr3:22399969-22399977
37	CTCF	chr3:22517420-22517570	HPF	lung:	n/a	n/a
38	CTCF	chr3:22423241-22423280	GM10266	blood:	n/a	n/a
39	CTCF	chr3:22412620-22412770	HMF	breast:	n/a	n/a
40	E2F4	chr3:22499539-22499754	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr3:22518923-22519197	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr3:22516988-22517602	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr3:22419036-22419309	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr3:22516092-22516481	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr3:22521863-22522063	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr3:22465905-22466012	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr3:22402346-22402782	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr3:22433470-22433653	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F6	chr3:22413329-22414541	H1-hESC	embryonic stem cell:	n/a	chr3:22413804-22413819 chr3:22413811-22413820
50	E2F6	chr3:22413318-22414589	H1-hESC	embryonic stem cell:	n/a	chr3:22413804-22413819 chr3:22413811-22413820

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22413680-22413730	Hepatocyte	liver:	n/a
2	chr3:22413680-22413730	Hepatocyte	liver:	n/a
3	chr3:22412746-22412796	LNCaP	prostate:	n/a
4	chr3:22423260-22423310	ovcar-3	ovarian:	n/a
5	chr3:22413232-22413282	HNPCEpiC	eye:	n/a
6	chr3:22412124-22412174	AG09309	skin:	n/a
7	chr3:22423260-22423310	BE2_C	brain:	n/a
8	chr3:22414843-22414893	SK-N-MC	brain:	n/a
9	chr3:22423260-22423310	Hepatocyte	liver:	n/a
10	chr3:22413680-22413730	HAEpiC	amniotic membrane:	n/a
11	chr3:22414349-22414399	BJ	skin:	n/a
12	chr3:22410416-22410466	HEEpiC	esophagus:	n/a
13	chr3:22414339-22414389	HIPEpiC	eye:	n/a
14	chr3:22414364-22414414	K562	blood:	n/a
15	chr3:22412124-22412174	AG04450	lung:	fetal
16	chr3:22414843-22414893	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:22414843-22414893	RPTEC	kidney:	n/a
18	chr3:22414843-22414893	PANC-1	pancreas:	n/a
19	chr3:22413232-22413282	MCF-7	breast:	n/a
20	chr3:22413960-22414010	SAEC	small airway:	n/a
21	chr3:22413582-22413632	Jurkat	blood:	n/a
22	chr3:22413232-22413282	ECC-1	luminal epithelium:	n/a
23	chr3:22413680-22413730	PrEC	prostate:	n/a
24	chr3:22412385-22412435	NT2-D1	testis:	n/a
25	chr3:22413680-22413730	ovcar-3	ovarian:	n/a
26	chr3:22413582-22413632	Hela-S3	cervix:	n/a
27	chr3:22422855-22422905	HRE	kidney:	n/a
28	chr3:22422855-22422905	GM06990	blood:	n/a
29	chr3:22414349-22414399	HIPEpiC	eye:	n/a
30	chr3:22414364-22414414	SAEC	small airway:	n/a
31	chr3:22422855-22422905	MCF-7	breast:	n/a
32	chr3:22413582-22413632	ProgFib	skin:	n/a
33	chr3:22423260-22423310	HNPCEpiC	eye:	n/a
34	chr3:22412746-22412796	RPTEC	kidney:	n/a
35	chr3:22414843-22414893	GM12878	blood:	n/a
36	chr3:22413680-22413730	HCPEpiC	choroid plexus:	n/a
37	chr3:22414349-22414399	HAEpiC	amniotic membrane:	n/a
38	chr3:22417573-22417623	AG04450	lung:	fetal
39	chr3:22414364-22414414	HCM	heart:	n/a
40	chr3:22412746-22412796	ProgFib	skin:	n/a
41	chr3:22412124-22412174	SK-N-SH	brain:	n/a
42	chr3:22413232-22413282	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:22412746-22412796	NHDF-neo	bronchial:	n/a
44	chr3:22423260-22423310	MCF-7	breast:	n/a
45	chr3:22412124-22412174	HRPEpiC	eye:	n/a
46	chr3:22412746-22412796	AG09319	gingival:	n/a
47	chr3:22414339-22414389	T-47D	breast:	n/a
48	chr3:22414349-22414399	NHDF-neo	bronchial:	n/a
49	chr3:22413680-22413730	GM19239	blood:	n/a
50	chr3:22412124-22412174	HRE	kidney:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:22499125..22501406-chr3:22508186..22509688,2	K562	blood:
2	chr3:22531582..22534400-chr3:23151408..23153228,2	K562	blood:
3	chr3:22499125..22501406-chr3:22508186..22509688,2	K562	blood:
4	chr3:22531342..22533092-chr3:22535706..22538633,2	K562	blood:
5	chr3:22402745..22404325-chr3:22406779..22409343,2	K562	blood:
6	chr3:22402745..22404325-chr3:22406779..22409343,2	K562	blood:
7	chr3:22531342..22533092-chr3:22535706..22538633,2	K562	blood:
8	chr3:22413816..22414336-chr3:133969155..133969870,2	HCT-116	colon:
9	chr3:22408287..22411021-chr3:22415658..22417538,2	K562	blood:
10	chr3:22420213..22422752-chr3:22425859..22427632,2	K562	blood:
11	chr3:22408287..22411021-chr3:22415658..22417538,2	K562	blood:
12	chr3:22501026..22503450-chr3:22509731..22511752,2	K562	blood:
13	chr3:22454300..22456299-chr3:22460627..22462261,2	K562	blood:
14	chr3:22501026..22503450-chr3:22509731..22511752,2	K562	blood:
15	chr3:22454300..22456299-chr3:22460627..22462261,2	K562	blood:
16	chr3:22420213..22422752-chr3:22425859..22427632,2	K562	blood:
17	chr3:22527480..22530262-chr3:22542907..22545144,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF385D-2	chr3:22498045-22498151	l_2331_chr3:22495715-22498151_testes
2	lnc-UBE2E2-6	chr3:22424046-22424420	NONHSAT088657
3	lnc-ZNF385D-2	chr3:22495716-22495905	l_2331_chr3:22495715-22498151_testes

No data

Variant related genes	Relation type
HMGB1P5	TF binding region
ZNF385D	TF binding region
HMGB1P5	CpG island
ZNF385D	CpG island
ENSG00000163785	chromatin interactions

Extended variants
information (count: 2429 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2429 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556252837	chr3:22397670-22397671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs570005884	chr3:22397686-22397687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370823684	chr3:22397690-22397691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535960479	chr3:22397713-22397714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs545199715	chr3:22397718-22397719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79877006	chr3:22397774-22397775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183597083	chr3:22397783-22397784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs74532072	chr3:22397785-22397786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73142210	chr3:22397800-22397801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532418062	chr3:22397818-22397819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555733984	chr3:22397856-22397857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531367145	chr3:22397907-22397908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7635394	chr3:22397945-22397946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs370522183	chr3:22397969-22397970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs80057874	chr3:22398001-22398002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17011245	chr3:22398002-22398003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs186524843	chr3:22398009-22398010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528522111	chr3:22398011-22398012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578169600	chr3:22398033-22398034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529897631	chr3:22398057-22398058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73142213	chr3:22398113-22398114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs547592830	chr3:22398114-22398115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569579757	chr3:22398122-22398123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191114722	chr3:22398126-22398127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142866410	chr3:22398131-22398132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571416530	chr3:22398187-22398188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555900447	chr3:22398194-22398195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145092617	chr3:22398248-22398249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567317120	chr3:22398260-22398261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200159818	chr3:22398285-22398286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536431658	chr3:22398291-22398292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376553366	chr3:22398295-22398296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138982126	chr3:22398315-22398316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541525440	chr3:22398340-22398341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183263717	chr3:22398376-22398377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575954605	chr3:22398421-22398422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141572571	chr3:22398433-22398434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576784314	chr3:22398465-22398466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs543448790	chr3:22398490-22398491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186807566	chr3:22398522-22398523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540815362	chr3:22398571-22398572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559379236	chr3:22398585-22398586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529882597	chr3:22398591-22398592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113009832	chr3:22398638-22398639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541531502	chr3:22398702-22398703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552201620	chr3:22398739-22398740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552043437	chr3:22398764-22398765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138330758	chr3:22398797-22398798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149234589	chr3:22398801-22398802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547608435	chr3:22398808-22398809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22393600-22402200	Weak transcription	Fetal Lung	lung
2	chr3:22394600-22398800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr3:22394800-22398800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:22398800-22399600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:22398800-22399600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr3:22399400-22400400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr3:22399600-22402400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:22399600-22402600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:22400400-22402600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:22401400-22402800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:22401800-22403200	Enhancers	Adipose Nuclei	Adipose
12	chr3:22402200-22402800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:22402200-22403000	Enhancers	Fetal Lung	lung
14	chr3:22402200-22403200	Enhancers	NHDF-Ad	bronchial
15	chr3:22402200-22403400	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr3:22402400-22403000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr3:22402600-22403000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr3:22402600-22403000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:22402800-22403000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:22402800-22403400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:22403000-22403200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:22403000-22403400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:22403000-22403400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr3:22403200-22403400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:22403400-22404200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr3:22403400-22406200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr3:22403400-22406200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr3:22403400-22406400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:22406200-22406400	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr3:22406200-22408200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:22406400-22406600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr3:22406400-22410400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr3:22406600-22407000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:22407000-22408400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:22408200-22409400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr3:22408400-22409400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:22409400-22410400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:22409400-22411000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr3:22410400-22411600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:22410400-22415200	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr3:22411000-22411400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr3:22411400-22412400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:22411600-22412200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:22411800-22412600	Bivalent Enhancer	Fetal Lung	lung
45	chr3:22412000-22412200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr3:22412200-22413400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr3:22412200-22415000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:22412400-22412600	Bivalent Enhancer	Adipose Nuclei	Adipose
49	chr3:22412400-22415000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:22412600-22412800	Flanking Bivalent TSS/Enh	Fetal Lung	lung

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