Variant report

Variant	nsv877616
Chromosome Location	chr3:145921954-145983688
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	chr3:145939594-145940831	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:145936731-145937064	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:145941119-145941527	HepG2	liver:	n/a	n/a
4	ATF1	chr3:145959778-145959950	K562	blood:	n/a	n/a
5	BACH1	chr3:145968459-145969085	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:145936724-145936984	GM12878	blood:	n/a	chr3:145936966-145936975
7	BCL3	chr3:145939979-145940826	A549	lung:	n/a	n/a
8	BHLHE40	chr3:145940155-145940799	HepG2	liver:	n/a	n/a
9	BHLHE40	chr3:145968815-145968925	K562	blood:	n/a	n/a
10	BRCA1	chr3:145924542-145924588	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr3:145968563-145969088	K562	blood:	n/a	n/a
12	CEBPB	chr3:145967627-145968119	IMR90	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
13	CEBPB	chr3:145940113-145940674	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:145943966-145944149	Hela-S3	cervix:	n/a	chr3:145944070-145944081
15	CEBPB	chr3:145941324-145941541	A549	lung:	n/a	n/a
16	CEBPB	chr3:145943995-145944194	K562	blood:	n/a	chr3:145944070-145944081
17	CEBPB	chr3:145943941-145944226	HepG2	liver:	n/a	chr3:145944070-145944081
18	CEBPB	chr3:145928283-145928567	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:145965734-145966053	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:145936409-145936418	K562	blood:	n/a	n/a
21	CEBPB	chr3:145968381-145969227	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:145939105-145939296	A549	lung:	n/a	n/a
23	CEBPB	chr3:145982753-145983062	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:145933950-145934138	HepG2	liver:	n/a	chr3:145933968-145933979
25	CEBPB	chr3:145946758-145947067	A549	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
26	CEBPB	chr3:145975222-145975278	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:145946749-145947065	HepG2	liver:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
28	CEBPB	chr3:145967647-145967801	K562	blood:	n/a	n/a
29	CEBPB	chr3:145933941-145934099	H1-hESC	embryonic stem cell:	n/a	chr3:145933968-145933979
30	CEBPB	chr3:145968610-145968627	K562	blood:	n/a	n/a
31	CEBPB	chr3:145939060-145939389	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:145967646-145968183	A549	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
33	CEBPB	chr3:145967604-145968179	Hela-S3	cervix:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
34	CEBPB	chr3:145928233-145928556	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:145943940-145944249	IMR90	lung:	n/a	chr3:145944070-145944081
36	CEBPB	chr3:145946751-145947057	IMR90	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
37	CEBPB	chr3:145928359-145928465	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPZ	chr3:145940149-145940488	HepG2	liver:	n/a	n/a
39	CHD1	chr3:145983326-145983397	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr3:145968318-145969145	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr3:145940149-145940808	HepG2	liver:	n/a	n/a
42	CREB1	chr3:145968387-145969169	A549	lung:	n/a	n/a
43	CTBP2	chr3:145968207-145969151	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr3:145936760-145936910	GM12867	blood:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
45	CTCF	chr3:145936760-145936910	NHEK	skin:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
46	CTCF	chr3:145940007-145940131	HepG2	liver:	n/a	n/a
47	CTCF	chr3:145936485-145937317	A549	lung:	n/a	chr3:145936874-145936884 chr3:145936871-145936892 chr3:145936869-145936882 chr3:145936869-145936887 chr3:145936872-145936881 chr3:145936870-145936886
48	CTCF	chr3:145939280-145939430	HMEC	breast:	n/a	n/a
49	CTCF	chr3:145940546-145940812	A549	lung:	n/a	n/a
50	CTCF	chr3:145940267-145940268	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145968726-145968776	MCF10A-Er-Src	breast:	n/a
2	chr3:145969625-145969675	HepG2	liver:	n/a
3	chr3:145968696-145968746	HMEC	breast:	n/a
4	chr3:145968726-145968776	AG09319	gingival:	n/a
5	chr3:145968242-145968292	HRCEpiC	kidney:	n/a
6	chr3:145968726-145968776	MCF10A-Er-Src	breast:	n/a
7	chr3:145969625-145969675	HepG2	liver:	n/a
8	chr3:145968696-145968746	HMEC	breast:	n/a
9	chr3:145968726-145968776	AG09319	gingival:	n/a
10	chr3:145968242-145968292	HRCEpiC	kidney:	n/a
11	chr3:145969007-145969057	HIPEpiC	eye:	n/a
12	chr3:145968726-145968776	HRE	kidney:	n/a
13	chr3:145968700-145968750	PrEC	prostate:	n/a
14	chr3:145969625-145969675	GM12891	blood:	n/a
15	chr3:145968722-145968772	HCF	heart:	n/a
16	chr3:145969625-145969675	HCF	heart:	n/a
17	chr3:145970385-145970435	HAEpiC	amniotic membrane:	n/a
18	chr3:145969579-145969629	SK-N-MC	brain:	n/a
19	chr3:145968620-145968670	Hela-S3	cervix:	n/a
20	chr3:145969718-145969768	SK-N-MC	brain:	n/a
21	chr3:145969718-145969768	PrEC	prostate:	n/a
22	chr3:145968389-145968439	HEK293	kidney:	embryo
23	chr3:145968722-145968772	CMK	blood:	n/a
24	chr3:145969718-145969768	ovcar-3	ovarian:	n/a
25	chr3:145968726-145968776	PFSK-1	brain:	n/a
26	chr3:145968696-145968746	H1-hESC	embryonic stem cell:	embryo
27	chr3:145968696-145968746	SK-N-SH	brain:	n/a
28	chr3:145970385-145970435	IMR90	lung:	fetal
29	chr3:145968696-145968746	BE2_C	brain:	n/a
30	chr3:145969625-145969675	AoSMC	blood vessel:	n/a
31	chr3:145968389-145968439	U87	brain:	n/a
32	chr3:145968726-145968776	NHBE	bronchial:	n/a
33	chr3:145968722-145968772	NHDF-neo	bronchial:	n/a
34	chr3:145969579-145969629	Hepatocyte	liver:	n/a
35	chr3:145968620-145968670	HIPEpiC	eye:	n/a
36	chr3:145969007-145969057	NHDF-neo	bronchial:	n/a
37	chr3:145968722-145968772	U87	brain:	n/a
38	chr3:145968242-145968292	SKMC	muscle:	n/a
39	chr3:145969718-145969768	NHDF-neo	bronchial:	n/a
40	chr3:145968620-145968670	H1-hESC	embryonic stem cell:	embryo
41	chr3:145968692-145968742	HMEC	breast:	n/a
42	chr3:145968692-145968742	NB4	blood:	n/a
43	chr3:145968722-145968772	PFSK-1	brain:	n/a
44	chr3:145968389-145968439	Hepatocyte	liver:	n/a
45	chr3:145968700-145968750	AoSMC	blood vessel:	n/a
46	chr3:145969625-145969675	GM06990	blood:	n/a
47	chr3:145969718-145969768	NB4	blood:	n/a
48	chr3:145968700-145968750	NB4	blood:	n/a
49	chr3:145968700-145968750	HL-60	blood:	n/a
50	chr3:145968242-145968292	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:145940254..145941134-chr3:146295120..146295978,3	MCF-7	breast:
2	chr3:145878599..145881384-chr3:145968449..145970595,2	MCF-7	breast:
3	chr3:145936462..145937370-chr3:146044619..146045821,9	MCF-7	breast:
4	chr3:145938109..145938869-chr3:146044708..146045495,2	MCF-7	breast:
5	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
6	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
7	chr3:145936744..145937271-chr3:146358471..146359250,3	K562	blood:
8	chr3:145936366..145937318-chr3:146295230..146296148,3	K562	blood:
9	chr3:145936448..145937286-chr3:146358746..146359294,2	MCF-7	breast:
10	chr3:145938654..145939295-chr3:146044870..146045659,2	MCF-7	breast:
11	chr3:145937350..145938198-chr3:146044684..146045576,2	K562	blood:
12	chr3:145961600..145965107-chr3:145968575..145970473,3	K562	blood:
13	chr3:145940299..145941372-chr3:146044662..146045624,8	MCF-7	breast:
14	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
15	chr3:145936710..145937294-chr3:146312292..146312926,2	K562	blood:
16	chr3:145979759..145981408-chr3:145991775..145993643,2	K562	blood:
17	chr3:145938152..145938842-chr3:146358330..146358865,2	MCF-7	breast:
18	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
19	chr3:145936384..145937370-chr3:146044670..146045567,4	MCF-7	breast:

Variant related genes	Relation type
PLSCR4	TF binding region
PLSCR4	CpG island
ENSG00000152952	chromatin interactions
ENSG00000114698	chromatin interactions

Extended variants
information (count: 2553 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9839874	chr3:145921954-145921955	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35366505	chr3:145921970-145921971	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544350876	chr3:145921987-145921988	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77652194	chr3:145922007-145922008	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116266281	chr3:145922064-145922065	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs180771314	chr3:145922076-145922077	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541851048	chr3:145922084-145922085	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560012683	chr3:145922142-145922143	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527620989	chr3:145922176-145922177	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs35499991	chr3:145922230-145922231	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564082999	chr3:145922251-145922252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531558827	chr3:145922282-145922283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs549579752	chr3:145922359-145922360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568196931	chr3:145922470-145922471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201262946	chr3:145922491-145922492	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs540708979	chr3:145922501-145922502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183900219	chr3:145922547-145922548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568910018	chr3:145922593-145922594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142575955	chr3:145922709-145922710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565685670	chr3:145922754-145922755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150501101	chr3:145922760-145922761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35823914	chr3:145922772-145922773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34511784	chr3:145922786-145922787	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559224122	chr3:145922805-145922806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139468900	chr3:145922831-145922832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536532955	chr3:145922836-145922837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540754918	chr3:145922845-145922846	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143435455	chr3:145922849-145922850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6808115	chr3:145922874-145922875	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs537537242	chr3:145922902-145922903	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189412321	chr3:145922975-145922976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577345896	chr3:145922976-145922977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541812334	chr3:145923052-145923053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368991177	chr3:145923059-145923060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs35616919	chr3:145923144-145923145	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs545753643	chr3:145923151-145923152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564424255	chr3:145923163-145923164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377573688	chr3:145923218-145923219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386666791	chr3:145923266-145923267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543646839	chr3:145923267-145923268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146754955	chr3:145923323-145923324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528953381	chr3:145923352-145923353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547516355	chr3:145923438-145923439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565650876	chr3:145923451-145923452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182568652	chr3:145923515-145923516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs563086581	chr3:145923532-145923533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113432957	chr3:145923540-145923541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78653873	chr3:145923607-145923608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146562352	chr3:145923663-145923664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs145014457	chr3:145923678-145923679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Bipolar disorder	18458673	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
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145897000-145933600	Weak transcription	Fetal Stomach	stomach
2	chr3:145901000-145923800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr3:145902800-145923000	Weak transcription	Osteobl	bone
4	chr3:145902800-145923600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:145903000-145934800	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr3:145905000-145933600	Weak transcription	NHLF	lung
7	chr3:145907000-145938600	Weak transcription	Fetal Intestine Small	intestine
8	chr3:145907600-145939200	Weak transcription	Brain Anterior Caudate	brain
9	chr3:145908200-145936400	Weak transcription	A549	lung
10	chr3:145909600-145939200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:145910400-145932400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:145910400-145940000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr3:145912200-145923800	Weak transcription	Fetal Muscle Leg	muscle
14	chr3:145912600-145923600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:145913200-145923200	Weak transcription	Colon Smooth Muscle	Colon
16	chr3:145913800-145939200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:145914000-145923400	Weak transcription	Fetal Intestine Large	intestine
18	chr3:145914200-145937000	Weak transcription	Placenta	Placenta
19	chr3:145914600-145940200	Weak transcription	Gastric	stomach
20	chr3:145914800-145924200	Weak transcription	Aorta	Aorta
21	chr3:145914800-145940200	Weak transcription	Psoas Muscle	Psoas
22	chr3:145914800-145940400	Weak transcription	Spleen	Spleen
23	chr3:145917400-145925200	Strong transcription	Adipose Nuclei	Adipose
24	chr3:145917800-145923000	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr3:145917800-145923800	Weak transcription	HSMMtube	muscle
26	chr3:145917800-145940400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr3:145918000-145940400	Weak transcription	Pancreas	Pancrea
28	chr3:145918200-145924200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr3:145918200-145924200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:145918400-145940400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr3:145918600-145923200	Weak transcription	Stomach Smooth Muscle	stomach
32	chr3:145918600-145923600	Weak transcription	HepG2	liver
33	chr3:145918800-145924200	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr3:145918800-145925200	Weak transcription	Fetal Kidney	kidney
35	chr3:145919000-145934800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:145920400-145922800	Strong transcription	HUVEC	blood vessel
37	chr3:145920400-145925800	Strong transcription	Liver	Liver
38	chr3:145920600-145922200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:145920600-145940600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:145920800-145922400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr3:145921000-145922000	Strong transcription	Left Ventricle	heart
42	chr3:145921400-145922200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:145921400-145922200	Enhancers	NHDF-Ad	bronchial
44	chr3:145921400-145923200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr3:145921400-145923200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:145921400-145923200	Weak transcription	Fetal Lung	lung
47	chr3:145921400-145923400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr3:145921400-145923400	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr3:145921600-145923600	Weak transcription	Ovary	ovary
50	chr3:145921600-145940200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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