Variant report

Variant	esv2759195
Chromosome Location	chr3:161449993-161593770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:795)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:161569866-161570024	HepG2	liver:	n/a	n/a
2	ATF2	chr3:161488305-161488790	GM12878	blood:	n/a	n/a
3	ATF2	chr3:161569700-161570087	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:161488337-161488752	GM12878	blood:	n/a	n/a
5	BACH1	chr3:161504615-161504661	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:161541802-161541998	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr3:161488271-161488720	GM12878	blood:	n/a	n/a
8	BCL11A	chr3:161488253-161488765	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:161488389-161488674	GM12878	blood:	n/a	n/a
10	BCL3	chr3:161551481-161551803	GM12878	blood:	n/a	n/a
11	BCL3	chr3:161488407-161488728	GM12878	blood:	n/a	n/a
12	BCLAF1	chr3:161488182-161488765	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:161488384-161489161	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:161569945-161569969	K562	blood:	n/a	n/a
15	BHLHE40	chr3:161569816-161570041	GM12878	blood:	n/a	n/a
16	CEBPB	chr3:161456021-161456143	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:161566191-161566415	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:161539126-161539564	A549	lung:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
19	CEBPB	chr3:161529583-161529774	K562	blood:	n/a	n/a
20	CEBPB	chr3:161576847-161577106	MCF-7	breast:	n/a	chr3:161577042-161577051 chr3:161577040-161577053
21	CEBPB	chr3:161477631-161477939	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:161539263-161539518	H1-hESC	embryonic stem cell:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
23	CEBPB	chr3:161576865-161577188	A549	lung:	n/a	chr3:161577042-161577051 chr3:161577040-161577053
24	CEBPB	chr3:161511062-161511366	A549	lung:	n/a	n/a
25	CEBPB	chr3:161477731-161477931	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:161455952-161456211	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:161508558-161508610	A549	lung:	n/a	n/a
28	CEBPB	chr3:161455943-161456209	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:161576868-161577210	H1-hESC	embryonic stem cell:	n/a	chr3:161577042-161577051 chr3:161577040-161577053
30	CEBPB	chr3:161529555-161529754	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr3:161566223-161566453	A549	lung:	n/a	n/a
32	CEBPB	chr3:161539002-161539550	MCF-7	breast:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
33	CEBPB	chr3:161529517-161529827	IMR90	lung:	n/a	n/a
34	CEBPB	chr3:161529582-161529777	MCF-7	breast:	n/a	n/a
35	CEBPB	chr3:161539178-161539513	HepG2	liver:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
36	CEBPB	chr3:161477709-161477941	A549	lung:	n/a	n/a
37	CEBPB	chr3:161576940-161577199	HepG2	liver:	n/a	chr3:161577042-161577051 chr3:161577040-161577053
38	CEBPB	chr3:161539192-161539511	A549	lung:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
39	CEBPB	chr3:161456026-161456063	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:161539202-161539496	IMR90	lung:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
41	CEBPB	chr3:161576863-161577227	IMR90	lung:	n/a	chr3:161577042-161577051 chr3:161577040-161577053
42	CEBPB	chr3:161511048-161511487	A549	lung:	n/a	n/a
43	CEBPB	chr3:161455871-161456197	A549	lung:	n/a	n/a
44	CEBPB	chr3:161488287-161488818	GM12878	blood:	n/a	n/a
45	CEBPB	chr3:161539040-161539599	MCF-7	breast:	n/a	chr3:161539354-161539363 chr3:161539354-161539363 chr3:161539354-161539363
46	CHD2	chr3:161488043-161488771	GM12878	blood:	n/a	n/a
47	CHD2	chr3:161569968-161570039	HepG2	liver:	n/a	n/a
48	CREB1	chr3:161488226-161488772	GM12878	blood:	n/a	n/a
49	CTCF	chr3:161470291-161470359	A549	lung:	n/a	chr3:161470333-161470351
50	CTCF	chr3:161569480-161569630	GM12868	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:161577612-161577662	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:161577612-161577662	AoSMC	blood vessel:	n/a
3	chr3:161577612-161577662	HRCEpiC	kidney:	n/a
4	chr3:161577612-161577662	IMR90	lung:	fetal
5	chr3:161577612-161577662	MCF-7	breast:	n/a
6	chr3:161577612-161577662	MCF10A-Er-Src	breast:	n/a
7	chr3:161577612-161577662	ProgFib	skin:	n/a
8	chr3:161577612-161577662	SK-N-SH_RA	brain:	n/a
9	chr3:161577612-161577662	HIPEpiC	eye:	n/a
10	chr3:161577612-161577662	GM12891	blood:	n/a
11	chr3:161577612-161577662	GM06990	blood:	n/a
12	chr3:161577612-161577662	AG04449	skin:	fetal
13	chr3:161577612-161577662	LNCaP	prostate:	n/a
14	chr3:161577612-161577662	GM12892	blood:	n/a
15	chr3:161577612-161577662	AG09319	gingival:	n/a
16	chr3:161577612-161577662	Jurkat	blood:	n/a
17	chr3:161577612-161577662	SAEC	small airway:	n/a
18	chr3:161577612-161577662	BJ	skin:	n/a
19	chr3:161577612-161577662	ovcar-3	ovarian:	n/a
20	chr3:161577612-161577662	HEEpiC	esophagus:	n/a
21	chr3:161577612-161577662	HUVEC	blood vessel:	n/a
22	chr3:161577612-161577662	HMEC	breast:	n/a
23	chr3:161577612-161577662	U87	brain:	n/a
24	chr3:161577612-161577662	RPTEC	kidney:	n/a
25	chr3:161577612-161577662	GM12878	blood:	n/a
26	chr3:161577612-161577662	HepG2	liver:	n/a
27	chr3:161577612-161577662	K562	blood:	n/a
28	chr3:161577612-161577662	NB4	blood:	n/a
29	chr3:161577612-161577662	A549	lung:	n/a
30	chr3:161577612-161577662	NH-A	brain:	n/a
31	chr3:161577612-161577662	SK-N-MC	brain:	n/a
32	chr3:161577612-161577662	HCM	heart:	n/a
33	chr3:161577612-161577662	NHDF-neo	bronchial:	n/a
34	chr3:161577612-161577662	Hela-S3	cervix:	n/a
35	chr3:161577612-161577662	BE2_C	brain:	n/a
36	chr3:161577612-161577662	AG04450	lung:	fetal
37	chr3:161577612-161577662	ECC-1	luminal epithelium:	n/a
38	chr3:161577612-161577662	PANC-1	pancreas:	n/a
39	chr3:161577612-161577662	AG10803	skin:	n/a
40	chr3:161577612-161577662	HRPEpiC	eye:	n/a
41	chr3:161577612-161577662	GM19239	blood:	n/a
42	chr3:161577612-161577662	AG09309	skin:	n/a
43	chr3:161577612-161577662	CMK	blood:	n/a
44	chr3:161577612-161577662	PrEC	prostate:	n/a
45	chr3:161577612-161577662	T-47D	breast:	n/a
46	chr3:161577612-161577662	HCF	heart:	n/a
47	chr3:161577612-161577662	H1-hESC	embryonic stem cell:	embryo
48	chr3:161577612-161577662	HCPEpiC	choroid plexus:	n/a
49	chr3:161577612-161577662	NHBE	bronchial:	n/a
50	chr3:161577612-161577662	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:161518824..161521549-chr3:161537494..161539506,2	MCF-7	breast:
2	chr3:161472760..161474501-chr3:161478505..161480497,2	K562	blood:
3	chr3:161469489..161471513-chr3:161473255..161475165,2	K562	blood:
4	chr3:161277802..161278537-chr3:161469868..161470746,2	MCF-7	breast:
5	chr3:161545972..161548808-chr3:161568962..161570462,2	MCF-7	breast:
6	chr16:89006271..89008204-chr3:161471043..161472567,2	MCF-7	breast:
7	chr3:161587513..161590442-chr3:161590834..161592884,2	MCF-7	breast:
8	chr3:161588066..161590743-chr3:161592762..161595576,2	MCF-7	breast:
9	chr3:161588066..161590743-chr3:161592762..161595576,2	MCF-7	breast:
10	chr3:161545972..161548808-chr3:161568962..161570462,2	MCF-7	breast:
11	chr3:161587513..161590442-chr3:161590834..161592884,2	MCF-7	breast:
12	chr3:161547471..161549402-chr3:161554856..161557293,2	MCF-7	breast:
13	chr3:161518824..161521549-chr3:161537494..161539506,2	MCF-7	breast:
14	chr3:161547471..161549402-chr3:161554856..161557293,2	MCF-7	breast:
15	chr3:161472760..161474501-chr3:161478505..161480497,2	K562	blood:
16	chr3:161469489..161471513-chr3:161473255..161475165,2	K562	blood:
17	chr3:161536736..161539708-chr3:161543704..161546343,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPTSSB-1	chr3:161539485-161539696	XLOC_003310
2	lnc-SPTSSB-1	chr3:161534697-161534967	XLOC_003310

No data

Variant related genes	Relation type
ENSG00000240354	TF binding region
ENSG00000240354	CpG island
ENSG00000129993	chromatin interactions
ENSG00000240354	chromatin interactions

Extended variants
information (count: 2861 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2861 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115144696	chr3:161454223-161454224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545715889	chr3:161454224-161454225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35847327	chr3:161454231-161454232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs558854526	chr3:161454281-161454282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73877474	chr3:161454303-161454304	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532602	chr3:161454363-161454364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539934846	chr3:161454403-161454404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560220367	chr3:161454447-161454448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs528854446	chr3:161454526-161454527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373472700	chr3:161454535-161454536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542254829	chr3:161454540-161454541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562148026	chr3:161454552-161454553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9881156	chr3:161454572-161454573	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs142142858	chr3:161454576-161454577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571338576	chr3:161454581-161454582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192322394	chr3:161454597-161454598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547572970	chr3:161454598-161454599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566324361	chr3:161454629-161454630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113567840	chr3:161454729-161454730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372415995	chr3:161454731-161454732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184858238	chr3:161454749-161454750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189742930	chr3:161454764-161454765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570084390	chr3:161454783-161454784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538062932	chr3:161454785-161454786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192079724	chr3:161454809-161454810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17490325	chr3:161454863-161454864	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372875319	chr3:161454905-161454906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541656320	chr3:161454997-161454998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4376051	chr3:161455035-161455036	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs77854092	chr3:161455054-161455055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542336516	chr3:161455058-161455059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553340042	chr3:161455089-161455090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562110571	chr3:161455101-161455102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs17424676	chr3:161455109-161455110	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs76568570	chr3:161455133-161455134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140341664	chr3:161455140-161455141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527487703	chr3:161455162-161455163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547532262	chr3:161455163-161455164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567469971	chr3:161455174-161455175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184429551	chr3:161455185-161455186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs9819763	chr3:161455195-161455196	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs147006160	chr3:161455209-161455210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs189138249	chr3:161455226-161455227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181800021	chr3:161455308-161455309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs147648880	chr3:161455325-161455326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79044746	chr3:161455326-161455327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186449799	chr3:161455349-161455350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554715488	chr3:161455374-161455375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141516280	chr3:161455398-161455399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535928557	chr3:161455405-161455406	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161454200-161455400	Enhancers	Liver	Liver
2	chr3:161454400-161455800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:161454800-161455800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr3:161455000-161455600	Enhancers	Dnd41	blood
5	chr3:161455200-161455600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr3:161457200-161459200	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr3:161457200-161459400	Enhancers	Fetal Lung	lung
8	chr3:161457600-161458800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:161458800-161459000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr3:161459000-161459400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:161463400-161464600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:161463600-161465200	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr3:161463600-161465200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:161463600-161465200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:161473400-161474000	Enhancers	Dnd41	blood
16	chr3:161474000-161476400	Weak transcription	Dnd41	blood
17	chr3:161476400-161477800	Enhancers	Dnd41	blood
18	chr3:161476600-161476800	Enhancers	Placenta	Placenta
19	chr3:161477400-161477600	Enhancers	Placenta	Placenta
20	chr3:161483400-161484200	Enhancers	Placenta Amnion	Placenta Amnion
21	chr3:161483800-161484800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:161483800-161485000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:161484200-161484600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr3:161484200-161484600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:161484200-161484600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr3:161484200-161484600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr3:161484200-161484800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr3:161484200-161484800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:161484600-161484800	Enhancers	Placenta Amnion	Placenta Amnion
30	chr3:161484800-161486000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr3:161486000-161486200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr3:161486200-161486600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:161486200-161488400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr3:161487600-161488000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:161487600-161489600	Enhancers	Primary hematopoietic stem cells	blood
36	chr3:161487800-161488800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr3:161487800-161489200	Enhancers	GM12878-XiMat	blood
38	chr3:161487800-161489400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr3:161488000-161488200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr3:161488000-161488600	Enhancers	NH-A	brain
41	chr3:161488000-161490400	Enhancers	Dnd41	blood
42	chr3:161488200-161488600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr3:161488400-161488600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr3:161488600-161489000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:161488800-161490400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:161489000-161489400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:161489200-161489400	Enhancers	Rectal Mucosa Donor 31	rectum
48	chr3:161490400-161490800	Weak transcription	Dnd41	blood
49	chr3:161490800-161492800	Enhancers	Dnd41	blood
50	chr3:161497000-161507200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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